Sandbox/00008: Difference between revisions
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<div style="width: | <div style="width: 87%; -webkit-user-select: none;"> | ||
{| class="infobox" style="margin: 0 0 0 0; border: 0; float: right; width: 5%; background: #A8A8A8; position: fixed; top: 250px; right: 20px; border-radius: 10px 10px 10px 10px;" cellpadding="0" cellspacing="0"; | {| class="infobox" style="margin: 0 0 0 0; border: 0; float: right; width: 12.5%; background: #A8A8A8; position: fixed; top: 250px; right: 20px; border-radius: 10px 10px 10px 10px;" cellpadding="0" cellspacing="0"; | ||
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! style="padding: 0 5px; font-size: 80%; background: #A8A8A8;" align=center| {{fontcolor|#2B3B44|Cardiogenic Shock<BR>Resident Survival Guide}} | ! style="padding: 0 5px; font-size: 80%; background: #A8A8A8;" align=center| {{fontcolor|#2B3B44|Cardiogenic Shock<BR>Resident Survival Guide}} | ||
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|FIRE]] | ! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|FIRE]] | ||
|- | |- | ||
! style="font-size: | ! style="font-size: 60%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Emergency Revascularization [Return to FIRE]|Emergency Revascularization]] | ||
|- | |- | ||
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}# | ! style="font-size: 50%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Complete Diagnostic Approach [Return to FIRE]|Complete Diagnostic Approach]] | ||
|- | |||
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Diagnostic Criteria [Return to FIRE]|Diagnostic Criteria]] | |||
: <div style="font-size: 80%;">[[{{PAGENAME}}#Criteria for Cardiogenic Shock|Cardiogenic Shock]]</div> | |||
: <div style="font-size: 80%;">[[{{PAGENAME}}#Criteria for Acute Myocardial Infarction|Acute Myocardial Infarction]]</div> | |||
|- | |||
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Maintenance of Blood Pressure [Return to FIRE]|Blood Pressure Maintenance]] | |||
|- | |||
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Optimization of Hemodynamic Status [Return to FIRE]|Hemodynamic Optimization]] | |||
|- | |- | ||
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Do's|Do's]] | ! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Do's|Do's]] | ||
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Don'ts|Don'ts]] | ! style="font-size: 80%; padding: 0 5px; background: #DCDCDC; border-radius: 5px 5px 5px 5px;" align=left | [[{{PAGENAME}}#Don'ts|Don'ts]] | ||
|} | |} | ||
__NOEDITSECTION____NOTOC__ | |||
==Overview== | |||
The clinical definition of [[cardiogenic shock]] includes decreased [[cardiac output]] with evidence of tissue [[hypoxia]] in the presence of adequate intravascular volume.<ref name="Califf-1994">{{Cite journal | last1 = Califf | first1 = RM. | last2 = Bengtson | first2 = JR. | title = Cardiogenic shock. | journal = N Engl J Med | volume = 330 | issue = 24 | pages = 1724-30 | month = Jun | year = 1994 | doi = 10.1056/NEJM199406163302406 | PMID = 8190135 }}</ref> | |||
==Causes== | |||
===Life Threatening Causes=== | |||
Cardiogenic shock is a life-threatening condition and must be treated as such irrespective of the underlying cause. | |||
===Common Causes=== | |||
:* ''Arrhythmic'' | |||
::* [[Atrioventricular block]] | |||
::* [[Sinoatrial block]] | |||
::* [[Supraventricular tachycardia]] | |||
::* [[Ventricular tachycardia]] | |||
:* ''Mechanical'' | |||
::* [[Mitral regurgitation|Acute mitral regurgitation]] ([[papillary muscle rupture]], [[chordae tendinae]] [[rupture]]) | |||
::* [[Myocardial rupture|Free wall rupture]] | |||
::* [[Hypertrophic cardiomyopathy]] | |||
::* [[Left ventricle|Obstruction to left ventricular filling]] ([[mitral stenosis]], [[left atrial myxoma]]) | |||
::* [[Left ventricular outflow tract obstruction|Obstruction to left ventricular outflow tract]] ([[aortic stenosis]], [[hypertrophic obstructive cardiomyopathy]]) | |||
::* [[Ventricular septal defect]] | |||
:* ''Myopathic'' | |||
::* [[Cardiomyopathy]] | |||
::* [[Myocardial contusion]] | |||
::* [[Myocardial infarction]] | |||
::* [[Myocarditis]] | |||
::* [[Myxedema coma]] | |||
::* [[ischemia|Postischemic]] [[myocardial stunning]] | |||
::* [[Sepsis|Septic myocardial depression]] | |||
:* ''Pharmacologic'' | |||
::* [[Anthracycline]]s | |||
::* [[Calcium channel blockers]] | |||
''Click '''[[Cardiogenic shock causes|here]]''' for the complete list of causes.'' | |||
==FIRE: Focused Initial Rapid Evaluation== | ==FIRE: Focused Initial Rapid Evaluation== | ||
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A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients in need of immediate intervention.<ref name="Robin-2006">{{Cite journal | last1 = Robin | first1 = E. | last2 = Costecalde | first2 = M. | last3 = Lebuffe | first3 = G. | last4 = Vallet | first4 = B. | title = Clinical relevance of data from the pulmonary artery catheter. | journal = Crit Care | volume = 10 Suppl 3 | issue = | pages = S3 | month = | year = 2006 | doi = 10.1186/cc4830 | PMID = 17164015 }}</ref> | A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients in need of immediate intervention.<ref name="Robin-2006">{{Cite journal | last1 = Robin | first1 = E. | last2 = Costecalde | first2 = M. | last3 = Lebuffe | first3 = G. | last4 = Vallet | first4 = B. | title = Clinical relevance of data from the pulmonary artery catheter. | journal = Crit Care | volume = 10 Suppl 3 | issue = | pages = S3 | month = | year = 2006 | doi = 10.1186/cc4830 | PMID = 17164015 }}</ref> | ||
<span style="font-size:85%">Boxes in | <span style="font-size:85%">Boxes in <span style="background: #FEDAEC;">red</span> signify that an urgent management is needed.</span> | ||
<span style="font-size: 85%;"> | <span style="font-size: 85%;"> | ||
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LFT, liver function test; | LFT, liver function test; | ||
MAP, mean arterial pressure; | MAP, mean arterial pressure; | ||
PCWP, pulmonary capillary wedge pressure; | PCWP, pulmonary capillary wedge pressure; | ||
PT, prothrombin time; | PT, prothrombin time; | ||
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SBP, systolic blood pressure; | SBP, systolic blood pressure; | ||
ScvO2, central venous oxygen saturation; | ScvO2, central venous oxygen saturation; | ||
SvO2, mixed venous oxygen saturation; | |||
SMA-7, sequential multiple analysis-7. | SMA-7, sequential multiple analysis-7. | ||
</span> | </span> | ||
<div style="font-size: 80%;"> | |||
{{Family tree/start}} | {{Family tree/start}} | ||
{{Family tree|boxstyle=width: 400px; text-align: left; font-size: 90%; padding: 0px;| | | | | A01 | | | |A01=<div style="padding: 15px;"><BIG>'''Does the patient have cardinal findings that increase the pretest probability of [[cardiogenic shock|<span style="color: #000000;">cardiogenic shock</span>]]?'''</BIG> | {{Family tree|boxstyle=width: 400px; text-align: left; font-size: 90%; padding: 0px;| | | | | | | | A01 | | | |A01=<div style="padding: 15px;"><BIG>'''Does the patient have cardinal findings that increase the pretest probability of [[cardiogenic shock|<span style="color: #000000;">cardiogenic shock</span>]]?'''</BIG> | ||
❑ Evidence of end-organ [[hypoperfusion|<span style="color: #000000;">hypoperfusion</span>]] | ❑ Evidence of end-organ [[hypoperfusion|<span style="color: #000000;">hypoperfusion</span>]] | ||
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: ❑ [[Cyanosis|<span style="color: #000000;">Cyanosis</span>]] | : ❑ [[Cyanosis|<span style="color: #000000;">Cyanosis</span>]] | ||
: ❑ [[Oliguria|<span style="color: #000000;">Oliguria</span>]] ([[urine output|<span style="color: #000000;">urine output</span>]] <0.5 mL/kg/h) | : ❑ [[Oliguria|<span style="color: #000000;">Oliguria</span>]] ([[urine output|<span style="color: #000000;">urine output</span>]] <0.5 mL/kg/h) | ||
: ❑ Sustained [[hypotension|<span style="color: #000000;">hypotension</span>]] | : ❑ Sustained [[hypotension|<span style="color: #000000;">hypotension</span>]] (≥30 min) | ||
:: ❑ [[SBP|<span style="color: #000000;">SBP</span>]] <90 mm Hg | :: ❑ [[SBP|<span style="color: #000000;">SBP</span>]] <90 mm Hg ''or'' | ||
:: ❑ [[MAP|<span style="color: #000000;">MAP</span>]] ↓ >30 mm Hg below baseline | :: ❑ [[MAP|<span style="color: #000000;">MAP</span>]] ↓ >30 mm Hg below baseline | ||
❑ Presence of myocardial dysfunction after exclusion or correction of non-myocardial factors contributing to tissue [[hypoperfusion|<span style="color: #000000;">hypoperfusion</span>]]</div>}} | ❑ Presence of myocardial dysfunction after exclusion or correction of non-myocardial factors contributing to tissue [[hypoperfusion|<span style="color: #000000;">hypoperfusion</span>]]</div>}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%;| |,|-|-|-|^|-|-|-|.| |}} | {{Family tree|boxstyle=text-align: left; font-size: 90%;| | | | |,|-|-|-|^|-|-|-|.| |}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| A02 | | | | | | A03 |A02=<div style="text-align: center; background: # | {{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | A02 | | | | | | A03 |A02=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>YES</BIG></div>|A03=<div style="text-align: center; background: #FEDAEC; color: #000000; font-weight: bold; padding: 5px;"><BIG>NO</BIG></div>}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| |!| | | | | | | | | {{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; background: #FEDAEC; border-top: 0px;| | | | A04 | | | | | | A05 |A04=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>Cardiogenic shock suspected</BIG><BR>''[[{{PAGENAME}}#Criteria for Cardiogenic Shock|<span style="color: #000000;">(click for details on criteria)</span>]]''</div> | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; background: # | |A05=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>Proceed to</BIG><br>[[shock resident survival guide|<span style="color: #000000;">shock resident survival guide</span>]]</div>}} | ||
| | {{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | |!| | | | | | | | | |}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| |!| | | | | | | | | |}} | {{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | A06 | | | | | | | | |A06=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px;"><BIG>'''Immediate steps'''</BIG></div>}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | {{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | A07 | | | | | | | | |A07=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''Initial management'''''</BIG> | ||
❑ Oxygen ± [[mechanical ventilation|<span style="color: #000000;">ventilatory support</span>]] | |||
❑ [[ECG|<span style="color: #000000;">ECG monitor</span>]] | |||
❑ [[Pulse oximeter|<span style="color: #000000;">Pulse oximeter</span>]] | |||
❑ [[Sphygmomanometer|<span style="color: #000000;">Sphygmomanometer</span>]] or [[Arterial line|<span style="color: #000000;">arterial line</span>]] | |||
❑ [[Intravenous therapy#Peripheral IV lines|<span style="color: #000000;">Large-bore peripheral venous lines</span>]] | |||
❑ [[Central venous catheter|<span style="color: #000000;">Central venous catheter</span>]] | |||
❑ [[Foley catheter|<span style="color: #000000;">Bladder catheterization</span>]] | |||
❑ Hold [[antihypertensive|<span style="color: #000000;">antihypertensive medications</span>]] | |||
❑ ± Correct [[tachyarrhythmia|<span style="color: #000000;">tachy-</span>]] or [[bradyarrhythmia|<span style="color: #000000;">bradyarrhythmia</span>]]</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | A08 | | | | | | | | |A08=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''Initial workup'''''</BIG> | |||
❑ [[Arterial blood gas|<span style="color: #000000;">Arterial blood gas</span>]] | |||
❑ [[CBC|<span style="color: #000000;">CBC</span>]]/[[Differential blood count (patient information)|<span style="color: #000000;">DC</span>]]/[[Basic metabolic panel|<span style="color: #000000;">SMA-7</span>]]/[[LFT|<span style="color: #000000;">LFT</span>]]/[[PT|<span style="color: #000000;">PT</span>]]/[[PTT|<span style="color: #000000;">PTT</span>]]/[[INR|<span style="color: #000000;">INR</span>]] | |||
❑ [[Troponin|<span style="color: #000000;">Cardiac troponins</span>]], [[CK-MB|<span style="color: #000000;">CK-MB</span>]] | |||
❑ [[Brain natriuretic peptide|<span style="color: #000000;">BNP</span>]], [[Brain natriuretic peptide|<span style="color: #000000;">NT-proBNP</span>]] | |||
❑ [[Lactate|<span style="color: #000000;">Lactate</span>]] | |||
❑ [[ECG|<span style="color: #000000;">12-Lead ECG</span>]] | |||
❑ [[CXR|<span style="color: #000000;">Chest radiograph</span>]] | |||
❑ [[Echocardiography|<span style="color: #000000;">Echocardiography</span>]]</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | |!| | | | | | | | | |}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | A09 | | | | | | | | |A09=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>Maintain adequate blood pressure</BIG><BR>''[[{{PAGENAME}}#Maintenance of Blood Pressure [Return to FIRE]|<span style="color: #000000;">(click for details)</span>]]''</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | A10 | | | | | | | | |A10=<div style="background: #FEDAEC; color: #000000; padding: 15px;"> | |||
'''''SBP <70 mm Hg:''''' | |||
❑ [[Norepinephrine|<span style="color: #000000;">Norepinephrine</span>]] | |||
: ❑ Initial dose: 0.5–1.0 μg/min | |||
: ❑ Maximum dose: 30–40 μg/min | |||
: ❑ Titrate to [[SBP|<span style="color: #000000;">SBP</span>]] >90 mm Hg | |||
'''''SBP 70–100 mm Hg with symptoms:''''' | |||
❑ [[Dopamine|<span style="color: #000000;">Dopamine</span>]] | |||
: ❑ Cardiac dose: 5.0–10 μg/kg/min | |||
: ❑ Pressor dose: 10–20 μg/kg/min | |||
: ❑ Maximum dose: 20–50 μg/kg/min | |||
'''''SBP 70–100 mm Hg w/o symptoms:''''' | |||
❑ [[Dobutamine|<span style="color: #000000;">Dobutamine</span>]] | |||
: ❑ Usual dose: 2.0–20 μg/kg/min | |||
: ❑ Maximum dose: 40 μg/kg/min | |||
: ❑ Avoid ↑ HR by >10% of baseline | |||
'''''SBP >100 mm Hg:''''' | |||
❑ [[Nitroglycerin|<span style="color: #000000;">Nitroglycerin</span>]] | |||
: ❑ Initial dose: 5.0 μg/min | |||
: ❑ Titrate by 10–20 μg/min q 3–5 min | |||
❑ [[Nitroprusside|<span style="color: #000000;">Nitroprusside</span>]] | |||
: ❑ Initial dose: 0.3 μg/kg/min | |||
: ❑ Usual dose: 3.0–5.0 μg/kg/min | |||
: ❑ Maximum dose: 10 μg/kg/min</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | |!| | | | | | | | | |}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | A09 | | | | | | | | |A09=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>'''Acute coronary syndrome likely?'''</BIG><BR>''[[{{PAGENAME}}#Criteria for Acute Myocardial Infarction|<span style="color: #000000;">(click for details on criteria)</span>]]''</div>}} | |||
{{Family tree|boxstyle=text-align: left; background: #FEDAEC; font-size: 90%; padding: 15px; border-top: 0px;| | | | A20 | | | | | | | | |A20=<div style="color: #000000">❑ '''New ischemic ECG changes''' | |||
❑ '''Positive [[cardiac biomarkers|<span style="color: #000000;">cTnT, cTnI, or CK-MB</span>]]''' | |||
❑ '''Anginal pain'''</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| |,|-|-|^|-|-|-|.| | | | | | |}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| A09 | | | | | A10 | | | | | | | |A09=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>YES</BIG></div>|A10=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>NO</BIG></div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; background: #FEDAEC; padding: 0px; border-top: 0px;| A09 | | | | | A10 | | | | | | | |A09=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 15px; font-weight: bold;"><BIG>Proceed to<BR>[[{{PAGENAME}}#Emergency Revascularization [Return to FIRE]|<span style="color: #000000;">Emergency Revascularization</span>]]</BIG></div>|A10=<div style="background: #FEDAEC; color: #000000; padding: 15px; font-weight: bold;">❑ [[ICU|<span style="color: #000000;">ICU admission</span>]] | |||
❑ [[Pulmonary artery catheter|<span style="color: #000000;">Swan-Ganz catheter</span>]] | |||
❑ [[Cardiology|<span style="color: #000000;">Cardiology consultation</span>]]</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | | | | | |!| | | | | | |}} | |||
{{Family tree|boxstyle=text-align: center; font-size: 90%; padding: 0px;| | | | | | | | A09 | | | | | | | | |A09=<div style="background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>Optimize hemodynamic status</BIG><BR>''[[{{PAGENAME}}#Optimization of Hemodynamic Status [Return to FIRE]|<span style="color: #000000;">(click for details)</span>]]''</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | | | | | A10 | | | | | | | | |A10=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''[[{{PAGENAME}}#Preload Optimization|<span style="color: #000000;">Preload</span>]]'''''</BIG> | |||
'''Goal: [[PCWP|<span style="color: #000000;">PCWP</span>]] 15–18 mm Hg, [[Central venous pressure|<span style="color: #000000;">CVP</span>]] 8–12 cm H<sub>2</sub>O''' | |||
❑ [[{{PAGENAME}}#Fluid Challenge Protocol|<span style="color: #000000;">Fluid challenge protocol ''("TROL")''</span>]] | |||
❑ ± Correct [[pulmonary congestion|<span style="color: #000000;">pulmonary congestion</span>]] | |||
: ❑ [[Furosemide|<span style="color: #000000;">Furosemide</span>]] | |||
:: ❑ Usual dose: 40 mg slow IV injection | |||
:: ❑ May increase dose to 80 mg after 1 hour as needed | |||
: ❑ [[Morphine|<span style="color: #000000;">Morphine</span>]] | |||
:: ❑ Usual dose: 2–4 mg slow IV injection | |||
:: ❑ May repeat dose every 5–30 minutes as needed</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | | | | | A11 | | | | | | | | |A11=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''[[{{PAGENAME}}#Afterload Optimization|<span style="color: #000000;">Afterload</span>]]'''''</BIG> | |||
'''Goal: [[MAP|<span style="color: #000000;">MAP</span>]] >65 mm Hg, [[SVR|<span style="color: #000000;">SVR</span>]] 800–1200 dyn·s·cm<sup>−5</sup>''' | |||
❑ '''If ↑ MAP & ↑ SVR:''' | |||
❑ [[ | : ❑ Taper [[vasopressor|<span style="color: #000000;">vasopressor</span>]] | ||
❑ [[ | : ❑ ± [[Vasodilator|<span style="color: #000000;">Vasodilator</span>]] | ||
❑ [[ | :: ❑ [[Nitroglycerin|<span style="color: #000000;">Nitroglycerin</span>]] | ||
❑ | ::: ❑ Initial dose: 5.0 μg/min | ||
❑ | ::: ❑ Titrate by 10–20 μg/min q 3–5 min | ||
❑ [[ | :: ❑ [[Nitroprusside|<span style="color: #000000;">Nitroprusside</span>]] | ||
❑ | ::: ❑ Initial dose: 0.3 μg/kg/min | ||
❑ | ::: ❑ Usual dose: 3.0–5.0 μg/kg/min | ||
❑ | ::: ❑ Maximum dose: 10 μg/kg/min | ||
❑ | ❑ '''If ↓ MAP & ↓ SVR:''' | ||
❑ [[ | : ❑ [[vasopressor|<span style="color: #000000;">Vasopressor</span>]] | ||
❑ | :: ❑ [[Norepinephrine|<span style="color: #000000;">Norepinephrine</span>]] | ||
❑ | ::: ❑ Initial dose: 0.5–1.0 μg/min | ||
❑ | ::: ❑ Maximum dose: 30–40 μg/min | ||
❑ | ::: ❑ Titrate to SBP >90 mm Hg | ||
❑ [[ | :: ❑ [[Dopamine|<span style="color: #000000;">Dopamine</span>]] | ||
❑ | ::: ❑ Cardiac dose: 5.0–10 μg/kg/min | ||
❑ | ::: ❑ Pressor dose: 10–20 μg/kg/min | ||
❑ | ::: ❑ Maximum dose: 20–50 μg/kg/min | ||
❑ | :: ❑ [[Phenylephrine|<span style="color: #000000;">Phenylephrine</span>]] | ||
❑ | ::: ❑ Initial dose: 100–180 μg/min | ||
❑ | ::: ❑ Maintenance dose: 40–60 μg/min | ||
: ❑ ± [[ | :: ❑ ± [[vasopressin|<span style="color: #000000;">Vasopressin</span>]] | ||
: ❑ | ::: ❑ Adjunctive therapy to norepinephrine or dopamine | ||
❑ | ::: ❑ Usual dose: 0.01–0.03 U/min | ||
: ❑ | ::: ❑ Maximum dose: 0.04 U/min | ||
❑ '''If ↓ MAP & ↑ SVR:''' | |||
: ❑ | : ❑ Continue [[vasopressor|<span style="color: #000000;">vasopressor</span>]] | ||
❑ | : ❑ Optimize cardiac output with [[inotrope|<span style="color: #000000;">inotropic agent</span>]]</div>}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | | | | | A12 | | | | | | | | |A12=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''[[{{PAGENAME}}#Cardiac Output Optimization|<span style="color: #000000;">Cardiac index</span>]]'''''</BIG> | |||
: | '''Goal: [[CI|<span style="color: #000000;">CI</span>]] >2.2 L/min/m<sup>2</sup>''' | ||
❑ [[Dobutamine|<span style="color: #000000;">Dobutamine</span>]] | |||
: ❑ | : ❑ Usual dose: 2.0–20 μg/kg/min | ||
❑ | : ❑ Maximum dose: 40 μg/kg/min | ||
❑ | : ❑ Avoid ↑ HR by >10% of baseline | ||
❑ [[ | ❑ [[Milrinone|<span style="color: #000000;">Milrinone</span>]] | ||
❑ | : ❑ Loading dose: 50 μg/kg (slowly over 10 minutes) | ||
❑ | : ❑ Maintenance dose: 0.375–0.75 μg/kg/min</div>}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | | | | | |!| | | | | | | | | |}} | |||
{{Family tree|boxstyle=text-align: center; font-size: 90%; padding: 0px;| | | | | | | | A13 | | | | | | | | |A13=<div style="background: #FEDAEC; color: #000000; padding: 5px;"><BIG>'''Evaluate perfusion and oxygenation'''</BIG></div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | | | | | A14 | | | | | | | | |A14=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''Endpoints:'''''</BIG> | |||
❑ [[ | ❑ [[SaO2|<span style="color: #000000;">SaO2</span>]] >92% | ||
❑ | ❑ [[mixed venous oxygen saturation|<span style="color: #000000;">SvO2</span>]] >60% | ||
❑ | ❑ [[SCVO2|<span style="color: #000000;">ScvO2</span>]] >70% | ||
❑ [[ | ❑ [[urine output|<span style="color: #000000;">Urine output</span>]] >0.5 mL/kg/h | ||
❑ | ❑ [[Lactate|<span style="color: #000000;">Lactate</span>]] <2.2 mM/L | ||
❑ | ❑ [[Hematocrit|<span style="color: #000000;">Hematocrit</span>]] ≥30%</div>}} | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; border-top: 0px;| | | | | | | | A14 | | | | | | | | |A14=<div style="background: #FEDAEC; color: #000000; padding: 15px;"><BIG>'''''If hypoperfusion persists:'''''</BIG><BR>❑ Consider [[IABP|<span style="color: #000000;">IABP</span>]], [[VAD|<span style="color: #000000;">VAD</span>]], or [[ECMO|<span style="color: #000000;">ECMO</span>]] if indicated</div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | | | | | |!| | | | | | | | | |}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | | | | | | A17 | | | | | | | | |A17=<div style="text-align: center; background: #FEDAEC; color: #000000; font-weight: bold; padding: 15px;"><BIG>Proceed to <br> [[{{PAGENAME}}#Complete Diagnostic Approach xx|<span style="color: #000000;">complete diagnostic approach</span>]]</BIG></div>}} | |||
{{Family tree/end}} | |||
</div> | </div> | ||
| | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px;| | | ==Emergency Revascularization <SMALL><SMALL>'''[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|[Return to ''FIRE'']]]'''</SMALL></SMALL>== | ||
{{Family tree|boxstyle=text-align: left; font-size: 90%; | |||
<div style="font-size: 80%;"> | |||
{{Family tree/start}} | |||
{{Family tree|boxstyle=width: 400px; text-align: left; font-size: 90%; padding: 0px;| | | | | | | | B01 | | | |B01=<div style="text-align: center; background: #FEDAEC; color: #000000; padding: 5px; font-weight: bold;"><BIG>'''Acute coronary syndrome'''</BIG><BR>''[[{{PAGENAME}}#Criteria for Acute Myocardial Infarction|<span style="color: #000000;">(click for details on criteria)</span>]]''</div>}} | |||
{{Family tree|boxstyle=text-align: left; background: #FEDAEC; font-size: 90%; padding: 15px; border-top: 0px;| | | | | | | | B02 | | | | | | | | |B02=<div style="color: #000000">❑ '''New ischemic ECG changes''' | |||
: ❑ New or presumably new ST elevation at the J point in two contiguous leads with the cutoff points: | |||
:: ❑ ≥0.1 mV in all leads other than leads V<sub>2</sub>–V<sub>3</sub> | |||
:: ❑ ≥0.15 mV in women in leads V<sub>2</sub>–V<sub>3</sub> | |||
:: ❑ ≥0.2 mV in men ≥40 years in leads V<sub>2</sub>–V<sub>3</sub> | |||
:: ❑ ≥0.25 mV in men <40 years in leads V<sub>2</sub>–V<sub>3</sub> | |||
: ❑ New left bundle branch block | |||
:: ❑ QRS duration ≥120 ms | |||
:: ❑ Supraventricular rhythm | |||
:: ❑ Absence of WPW pattern | |||
:: ❑ Broad and notched or slurred R in I and V<sub>5</sub> or V<sub>6</sub> | |||
:: ❑ Absence of Q wave in I and V<sub>5</sub> and V<sub>6</sub> | |||
:: ❑ R peak times ≥60 ms in V<sub>5</sub> or V<sub>6</sub> | |||
: ❑ New or presumably new ST-segment–T wave changes | |||
:: ❑ Horizontal or down-sloping ST depression ≥0.05 mV in two contiguous leads | |||
:: ❑ T inversion ≥0.1 mV in two contiguous leads with prominent R wave or R/S ratio >1 | |||
❑ '''Positive [[cardiac biomarkers|<span style="color: #000000;">cardiac biomarkers</span>]] (cTnT, cTnI, or CK-MB)''' | |||
❑ '''Anginal pain''' | |||
<table style="border: 2px solid #DCDCDC; font-size: 80%; background: #F8F8FF;"> | |||
<caption> <i>ST elevation in contiguous leads and location of MI and coronary occlusion</i> | |||
</caption> | |||
<tr> | |||
<td align="center" style="background: #A8A8A8; width: 120px;"> <b>ECG Leads with STE</b> | |||
</td> | |||
<td align="center" style="background: #A8A8A8; width: 100px;"> <b>Location of MI</b> | |||
</td> | |||
<td align="center" style="background: #A8A8A8; width: 200px;"> <b>Location of Coronary Occlusion</b> | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> I, aVL | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Lateral, Apical | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Diagonal, Obtuse Marginal, Distal LAD | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #F5F5F5;" align="left"> II, III, aVF | |||
</td> | |||
<td style="padding: 0 5px; background: #F5F5F5;" align="left"> Inferior | |||
</td> | |||
<td style="padding: 0 5px; background: #F5F5F5;" align="left"> PDA, Wraparound LAD | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> V<sub>1</sub>, V<sub>2</sub> | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Septal | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Proximal LAD, Septal Perforators | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> V<sub>3</sub>, V<sub>4</sub> | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Anterior | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Proximal or Mid LAD, Diagonal | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> V<sub>5</sub>, V<sub>6</sub> | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Lateral, Apical | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Diagonal, Obtuse Marginal, Distal LAD | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #F5F5F5;" align="left"> V<sub>7</sub>, V<sub>8</sub>, V<sub>9</sub> | |||
</td> | |||
<td style="padding: 0 5px; background: #F5F5F5;" align="left"> Posterobasal | |||
</td> | |||
<td style="padding: 0 5px; background: #F5F5F5;" align="left"> LCx, RCA | |||
</td></tr> | |||
<tr> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> V<sub>3</sub>R, V<sub>4</sub>R | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> RV Free Wall | |||
</td> | |||
<td style="padding: 0 5px; background: #DCDCDC;" align="left"> Proximal RCA | |||
</td></tr></table></div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%;| | | | |,|-|-|-|^|-|-|-|.| |}} | |||
{{Family tree|boxstyle=text-align: center; font-size: 90%; padding: 5px; background: #FEDAEC; font-weight: bold;| | | | B03 | | | | | | B04 |B03=<div style="color: #000000; padding: 5px;"><BIG>STEMI</BIG></div>|B04=<div style="color: #000000; padding: 5px;"><BIG>UA/NSTEMI</BIG></div>}} | |||
{{Family tree|boxstyle=text-align: left; font-size: 90%; padding: 0px; background: #FEDAEC; border-top: 0px;| | | | B05 | | | | | | B06 |B05=<div style="color: #000000; padding: 15px;"></div>|B06=<div style="color: #000000; padding: 15px;"></div>}} | |||
{{Family tree/end}} | {{Family tree/end}} | ||
</div> | |||
==Complete Diagnostic Approach <SMALL><SMALL>'''[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|[Return to ''FIRE'']]]'''</SMALL></SMALL>== | |||
== | |||
==Diagnostic Criteria <SMALL><SMALL>'''[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|[Return to ''FIRE'']]]'''</SMALL></SMALL>== | |||
<div class="mw-collapsible mw-collapsed"> | |||
===Criteria for Cardiogenic Shock=== | |||
<div class="mw-collapsible-content"> | |||
* ''Clinical Criteria''<ref name="Califf-1994">{{Cite journal | last1 = Califf | first1 = RM. | last2 = Bengtson | first2 = JR. | title = Cardiogenic shock. | journal = N Engl J Med | volume = 330 | issue = 24 | pages = 1724-30 | month = Jun | year = 1994 | doi = 10.1056/NEJM199406163302406 | PMID = 8190135 }}</ref><ref name="Hollenberg-1999">{{Cite journal | last1 = Hollenberg | first1 = SM. | last2 = Kavinsky | first2 = CJ. | last3 = Parrillo | first3 = JE. | title = Cardiogenic shock. | journal = Ann Intern Med | volume = 131 | issue = 1 | pages = 47-59 | month = Jul | year = 1999 | doi = | PMID = 10391815 }}</ref><ref name="Goldberg-1991">{{Cite journal | last1 = Goldberg | first1 = RJ. | last2 = Gore | first2 = JM. | last3 = Alpert | first3 = JS. | last4 = Osganian | first4 = V. | last5 = de Groot | first5 = J. | last6 = Bade | first6 = J. | last7 = Chen | first7 = Z. | last8 = Frid | first8 = D. | last9 = Dalen | first9 = JE. | title = Cardiogenic shock after acute myocardial infarction. Incidence and mortality from a community-wide perspective, 1975 to 1988. | journal = N Engl J Med | volume = 325 | issue = 16 | pages = 1117-22 | month = Oct | year = 1991 | doi = 10.1056/NEJM199110173251601 | PMID = 1891019 }}</ref> | * ''Clinical Criteria''<ref name="Califf-1994">{{Cite journal | last1 = Califf | first1 = RM. | last2 = Bengtson | first2 = JR. | title = Cardiogenic shock. | journal = N Engl J Med | volume = 330 | issue = 24 | pages = 1724-30 | month = Jun | year = 1994 | doi = 10.1056/NEJM199406163302406 | PMID = 8190135 }}</ref><ref name="Hollenberg-1999">{{Cite journal | last1 = Hollenberg | first1 = SM. | last2 = Kavinsky | first2 = CJ. | last3 = Parrillo | first3 = JE. | title = Cardiogenic shock. | journal = Ann Intern Med | volume = 131 | issue = 1 | pages = 47-59 | month = Jul | year = 1999 | doi = | PMID = 10391815 }}</ref><ref name="Goldberg-1991">{{Cite journal | last1 = Goldberg | first1 = RJ. | last2 = Gore | first2 = JM. | last3 = Alpert | first3 = JS. | last4 = Osganian | first4 = V. | last5 = de Groot | first5 = J. | last6 = Bade | first6 = J. | last7 = Chen | first7 = Z. | last8 = Frid | first8 = D. | last9 = Dalen | first9 = JE. | title = Cardiogenic shock after acute myocardial infarction. Incidence and mortality from a community-wide perspective, 1975 to 1988. | journal = N Engl J Med | volume = 325 | issue = 16 | pages = 1117-22 | month = Oct | year = 1991 | doi = 10.1056/NEJM199110173251601 | PMID = 1891019 }}</ref> | ||
:* Sustained [[hypotension]] ([[systolic blood pressure|SBP]] <90 mm Hg or [[mean arterial pressure|MAP]] 30 mm Hg below baseline in preexisting [[hypertension]] for at least 30 minutes) | :* Sustained [[hypotension]] ([[systolic blood pressure|SBP]] <90 mm Hg or [[mean arterial pressure|MAP]] 30 mm Hg below baseline in preexisting [[hypertension]] for at least 30 minutes) | ||
:* Evidence of [[hypoperfusion|tissue hypoperfusion]] (such as [[oliguria]], [[cyanosis]], [[cool extremities]], and [[Altered mental status|altered mental status]]) | :* Evidence of [[hypoperfusion|tissue hypoperfusion]] (such as [[oliguria]], [[cyanosis]], [[cool extremities]], and [[Altered mental status|altered mental status]]) | ||
Line 192: | Line 470: | ||
* ''Hemodynamic Criteria''<ref name="Califf-1994">{{Cite journal | last1 = Califf | first1 = RM. | last2 = Bengtson | first2 = JR. | title = Cardiogenic shock. | journal = N Engl J Med | volume = 330 | issue = 24 | pages = 1724-30 | month = Jun | year = 1994 | doi = 10.1056/NEJM199406163302406 | PMID = 8190135 }}</ref><ref name="Goldberg-1991">{{Cite journal | last1 = Goldberg | first1 = RJ. | last2 = Gore | first2 = JM. | last3 = Alpert | first3 = JS. | last4 = Osganian | first4 = V. | last5 = de Groot | first5 = J. | last6 = Bade | first6 = J. | last7 = Chen | first7 = Z. | last8 = Frid | first8 = D. | last9 = Dalen | first9 = JE. | title = Cardiogenic shock after acute myocardial infarction. Incidence and mortality from a community-wide perspective, 1975 to 1988. | journal = N Engl J Med | volume = 325 | issue = 16 | pages = 1117-22 | month = Oct | year = 1991 | doi = 10.1056/NEJM199110173251601 | PMID = 1891019 }}</ref><ref name="Forrester-1976">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (first of two parts). | journal = N Engl J Med | volume = 295 | issue = 24 | pages = 1356-62 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612092952406 | PMID = 790191 }}</ref><ref name="Forrester-1976-2">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (second of two parts). | journal = N Engl J Med | volume = 295 | issue = 25 | pages = 1404-13 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612162952505 | PMID = 790194 }}</ref><ref name="Reynolds-2008">{{Cite journal | last1 = Reynolds | first1 = HR. | last2 = Hochman | first2 = JS. | title = Cardiogenic shock: current concepts and improving outcomes. | journal = Circulation | volume = 117 | issue = 5 | pages = 686-97 | month = Feb | year = 2008 | doi = 10.1161/CIRCULATIONAHA.106.613596 | PMID = 18250279 }}</ref> | * ''Hemodynamic Criteria''<ref name="Califf-1994">{{Cite journal | last1 = Califf | first1 = RM. | last2 = Bengtson | first2 = JR. | title = Cardiogenic shock. | journal = N Engl J Med | volume = 330 | issue = 24 | pages = 1724-30 | month = Jun | year = 1994 | doi = 10.1056/NEJM199406163302406 | PMID = 8190135 }}</ref><ref name="Goldberg-1991">{{Cite journal | last1 = Goldberg | first1 = RJ. | last2 = Gore | first2 = JM. | last3 = Alpert | first3 = JS. | last4 = Osganian | first4 = V. | last5 = de Groot | first5 = J. | last6 = Bade | first6 = J. | last7 = Chen | first7 = Z. | last8 = Frid | first8 = D. | last9 = Dalen | first9 = JE. | title = Cardiogenic shock after acute myocardial infarction. Incidence and mortality from a community-wide perspective, 1975 to 1988. | journal = N Engl J Med | volume = 325 | issue = 16 | pages = 1117-22 | month = Oct | year = 1991 | doi = 10.1056/NEJM199110173251601 | PMID = 1891019 }}</ref><ref name="Forrester-1976">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (first of two parts). | journal = N Engl J Med | volume = 295 | issue = 24 | pages = 1356-62 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612092952406 | PMID = 790191 }}</ref><ref name="Forrester-1976-2">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (second of two parts). | journal = N Engl J Med | volume = 295 | issue = 25 | pages = 1404-13 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612162952505 | PMID = 790194 }}</ref><ref name="Reynolds-2008">{{Cite journal | last1 = Reynolds | first1 = HR. | last2 = Hochman | first2 = JS. | title = Cardiogenic shock: current concepts and improving outcomes. | journal = Circulation | volume = 117 | issue = 5 | pages = 686-97 | month = Feb | year = 2008 | doi = 10.1161/CIRCULATIONAHA.106.613596 | PMID = 18250279 }}</ref> | ||
:* Sustained [[hypotension]] ([[systolic blood pressure|SBP]] <90 mm Hg or [[mean arterial pressure|MAP]] 30 mm Hg below baseline in preexisting [[hypertension]] for at least 30 minutes) | :* Sustained [[hypotension]] ([[systolic blood pressure|SBP]] <90 mm Hg or [[mean arterial pressure|MAP]] 30 mm Hg below baseline in preexisting [[hypertension]] for at least 30 minutes) | ||
:* Depressed [[cardiac index]] (<1.8 L/min/m<sup>2</sup> of [[body surface area|BSA]] without support or <2.0–2.2 L/min/m<sup>2</sup> of [[body surface area|BSA]] with support) in the presence of an elevated [[PCWP|wedge pressure]] (>15 mm Hg). | :* Depressed [[cardiac index]] (<1.8 L/min/m<sup>2</sup> of [[body surface area|BSA]] without support or <2.0–2.2 L/min/m<sup>2</sup> of [[body surface area|BSA]] with support) in the presence of an elevated [[PCWP|wedge pressure]] (>15 mm Hg). | ||
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--> | --> | ||
</div></div> | |||
= | <div class="mw-collapsible mw-collapsed"> | ||
===Criteria for Acute Myocardial Infarction=== | |||
<div class="mw-collapsible-content"> | |||
The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one of the following criteria meets the diagnosis for MI: | |||
* | * '''Detection of a rise and/or fall of [[cardiac biomarker]] values (preferably [[cardiac troponin]]) with at least one value above the 99<sup>th</sup> percentile upper reference limit (URL)''' and with at least one of the following:<ref name="Thygesen-2012">{{Cite journal | last1 = Thygesen | first1 = K. | last2 = Alpert | first2 = JS. | last3 = Jaffe | first3 = AS. | last4 = Simoons | first4 = ML. | last5 = Chaitman | first5 = BR. | last6 = White | first6 = HD. | last7 = Thygesen | first7 = K. | last8 = Alpert | first8 = JS. | last9 = White | first9 = HD. | title = Third universal definition of myocardial infarction. | journal = J Am Coll Cardiol | volume = 60 | issue = 16 | pages = 1581-98 | month = Oct | year = 2012 | doi = 10.1016/j.jacc.2012.08.001 | PMID = 22958960 }}</ref> | ||
:* | :* '''Symptoms of [[ischemia]]'''<ref name="Braunwald-2000">{{Cite journal | last1 = Braunwald | first1 = E. | last2 = Antman | first2 = EM. | last3 = Beasley | first3 = JW. | last4 = Califf | first4 = RM. | last5 = Cheitlin | first5 = MD. | last6 = Hochman | first6 = JS. | last7 = Jones | first7 = RH. | last8 = Kereiakes | first8 = D. | last9 = Kupersmith | first9 = J. | title = ACC/AHA guidelines for the management of patients with unstable angina and non-ST-segment elevation myocardial infarction. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on the Management of Patients With Unstable Angina). | journal = J Am Coll Cardiol | volume = 36 | issue = 3 | pages = 970-1062 | month = Sep | year = 2000 | doi = | PMID = 10987629 }}</ref><ref name="Anderson-2011">{{Cite journal | last1 = Anderson | first1 = JL. | last2 = Adams | first2 = CD. | last3 = Antman | first3 = EM. | last4 = Bridges | first4 = CR. | last5 = Califf | first5 = RM. | last6 = Casey | first6 = DE. | last7 = Chavey | first7 = WE. | last8 = Fesmire | first8 = FM. | last9 = Hochman | first9 = JS. | title = 2011 ACCF/AHA Focused Update Incorporated Into the ACC/AHA 2007 Guidelines for the Management of Patients With Unstable Angina/Non-ST-Elevation Myocardial Infarction: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. | journal = Circulation | volume = 123 | issue = 18 | pages = e426-579 | month = May | year = 2011 | doi = 10.1161/CIR.0b013e318212bb8b | PMID = 21444888 }}</ref><ref name="Gibbons-2003">{{Cite journal | last1 = Gibbons | first1 = RJ. | last2 = Abrams | first2 = J. | last3 = Chatterjee | first3 = K. | last4 = Daley | first4 = J. | last5 = Deedwania | first5 = PC. | last6 = Douglas | first6 = JS. | last7 = Ferguson | first7 = TB. | last8 = Fihn | first8 = SD. | last9 = Fraker | first9 = TD. | title = ACC/AHA 2002 guideline update for the management of patients with chronic stable angina--summary article: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on the Management of Patients With Chronic Stable Angina). | journal = Circulation | volume = 107 | issue = 1 | pages = 149-58 | month = Jan | year = 2003 | doi = | PMID = 12515758 }}</ref> | ||
::* Recent episode of typical ischemic discomfort that either is of new onset or is severe or that exhibits an accelerating pattern of previous stable angina (especially if it has occurred at rest or is within 2 weeks of a previously documented MI) | |||
::* ''Quality:'' squeezing, grip-like, pressure-like, suffocating, crushing, or heavy | |||
::* ''Location:'' diffuse, not localized, nor positional, nor affected by movement at substernal area ± radiation to the neck, jaw, epigastrium, shoulders, or arms | |||
::* ''Duration:'' usually >20 minutes | |||
::* ''Factors that provoke the pain:'' exertion or emotional stress | |||
::* ''Factors that relieve the pain:'' rest or sublingual nitroglycerin (usually within minutes) | |||
::* ''Accompanying symptoms:'' diaphoresis, nausea or syncope | |||
:* '''New or presumably new significant [[ST-segment]]–[[T wave]] changes or new [[LBBB|left bundle branch block (LBBB)]].''' | |||
:* '''Development of [[Pathologic Q Waves|pathological Q waves]] in the [[ECG]].''' | |||
:* '''Imaging evidence of new loss of viable [[myocardium]] or new regional wall motion abnormality.''' | |||
:* '''Identification of an intracoronary [[thrombus]] by [[angiography]] or [[autopsy]].''' | |||
* | * Cardiac death with symptoms suggestive of myocardial ischemia and presumed new ischemic ECG changes or new LBBB, but death occurred before cardiac biomarkers were obtained, or before cardiac biomarker values would be increased. | ||
* | * Percutaneous coronary intervention related MI is arbitrarily defined by elevation of cardiac troponin (cTn) values (>5 × 99<sup>th</sup> percentile URL) in patients with normal baseline values (≤99<sup>th</sup> percentile URL) or a rise of cTn values >20% if the baseline values are elevated and are stable or falling. In addition, either one of the followings is required: | ||
::* | :* Symptoms suggestive of myocardial ischemia | ||
:* New ischemic ECG changes | |||
:* Angiographic findings consistent with a procedural complication | |||
:* Imaging demonstration of new loss of viable myocardium or new regional wall motion abnormality | |||
* | * Stent thrombosis associated with MI when detected by coronary angiography or autopsy in the setting of myocardial ischemia and with a rise and/or fall of cardiac biomarker values with at least one value above the 99<sup>th</sup> percentile URL. | ||
* Coronary artery bypass grafting related MI is arbitrarily defined by elevation of cardiac biomarker values (>10 × 99<sup>th</sup> percentile URL) in patients with normal baseline cTn values (≤99<sup>th</sup> percentile URL). In addition, either one of the followings is required: | |||
:* New pathological Q waves or new LBBB | |||
:* Angiographic documented new graft or new native coronary artery occlusion | |||
:* Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality | |||
</div></div> | |||
==Maintenance of Blood Pressure <SMALL><SMALL>'''[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|[Return to ''FIRE'']]]'''</SMALL></SMALL>== | |||
<div class="mw-collapsible mw-collapsed"> | |||
:: | ======Norepinephrine====== | ||
< | <div class="mw-collapsible-content"> | ||
: | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="NOREPINEPHRINE BITARTRATE INJECTION">{{Cite web | last = | first = | title = NOREPINEPHRINE BITARTRATE INJECTION | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3352c7d0-e621-46ed-9a54-e4a9583cde10 | publisher = | date = | accessdate = }}</ref> | |||
::* | :* Suggested Dilution: | ||
::* Mix 4 mg of [[norepinephrine]] in 250 mL of [[Intravenous sugar solution|D5W]] or [[Intravenous sugar solution|D5NS]]. Avoid dilution in [[normal saline]] alone. | |||
:* Suggested Regimen: | |||
::* Start at a dose of 0.5–1.0 μg/min [[IV|IV infusion]]; titrate to maintain [[SBP]] at above 90 mm Hg (up to 30–40 μg/min). | |||
* Contraindications | |||
:* [[Norepinephrine]] should not be given to patients who are [[hypotensive]] from [[hypovolemia|blood volume deficits]] except as an emergency measure to maintain [[coronary]] and [[cerebral]] artery [[perfusion]] until blood volume replacement therapy can be completed. | |||
:* [[Norepinephrine]] should also not be given to patients with [[mesentery|mesenteric]] or peripheral vascular [[thrombosis]] unless it is necessary as a life-saving procedure. | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Dopamine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="DOPAMINE HCL injection, solution">{{Cite web | last = | first = | title = DOPAMINE HCL INJECTION, SOLUTION [AMERICAN REGENT, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e061fb3e-afd7-4188-b5fb-617ac1d3e38d | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Dilution: transfer contents of one or more ampuls or vials by aseptic technique to either 250 mL or 500 mL of one of the following sterile intravenous solutions | |||
::* Sodium Chloride Injection | |||
::* Dextrose (5%) Injection | |||
::* Dextrose (5%) and Sodium Chloride (0.9%) Injection | |||
::* 5% Dextrose in 0.45% Sodium Chloride Solution | |||
::* Dextrose (5%) in Lactated Ringer’s Solution | |||
::* Sodium Lactate (1/6 Molar) Injection | |||
::* Lactated Ringer’s Injection | |||
:* Suggested Regimen: | |||
::* Begin administration of diluted solution at doses of 2–5 μg/kg/minute in patients who are likely to respond to modest increments of heart force and renal perfusion. | |||
::* In more seriously ill patients, begin administration of diluted solution at doses of 5 μg/kg/minute and increase gradually, using 5–10 μg/kg/minute increments, up to 20–50 μg/kg/minute as needed. | |||
::* If doses of 50 μg/kg/minute are required, it is suggested that urine output be checked frequently. Should the urine flow begin to decrease in the absence of hypotension, reduction of dosage should be considered. | |||
::* Treatment of all patients requires constant evaluation of therapy in terms of the blood volume, augmentation of myocardial contractility, and distribution of peripheral perfusion. Dosage should be adjusted according to the patient’s response, with particular attention to diminution of established urine flow rate, increasing tachycardia or development of new dysrhythmias as indices for decreasing or temporarily suspending the dosage. | |||
* Contraindications | |||
:* Pheochromocytoma | |||
:* Uncorrected tachyarrhythmias or ventricular fibrillation | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Dobutamine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="DOBUTAMINE (DOBUTAMINE HYDROCHLORIDE) INJECTION, SOLUTION">{{Cite web | last = | first = | title = DOBUTAMINE (DOBUTAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb842dc2-fb15-48f9-e4b1-ea4280db0199 | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Dilution: dobutamine injection must be further diluted in an IV container. Dilute 20 mL of dobutamine in at least 50 mL of diluent and dilute 40 mL of dobutamine in at least 100 mL of diluent. Use one of the following intravenous solutions as a diluent: | |||
::* Dextrose Injection 5% | |||
::* Dextrose 5% and Sodium Chloride 0.45% Injection | |||
::* Dextrose 5% and Sodium Chloride 0.9% Injection | |||
::* Dextrose Injection 10%, Isolyte® M with 5% Dextrose Injection | |||
::* Lactated Ringer’s Injection | |||
::* 5% Dextrose in Lactated Ringer’s Injection | |||
::* Normosol®-M in D5-W | |||
::* 20% Osmitrol® in Water for Injection | |||
::* Sodium Chloride Injection 0.9% | |||
::* Sodium Lactate Injection | |||
:* Suggested Regimen: | |||
::* The rate of infusion needed to increase cardiac output usually ranged from 2.5 to 15 mcg/kg/min. | |||
::* On rare occasions, infusion rates up to 40 mcg/kg/min have been required to obtain the desired effect. | |||
* Contraindications | |||
:* Idiopathic hypertrophic subaortic stenosis | |||
:* Hypersensitivity to dobutamine | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Nitroglycerin====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="NITROGLYCERIN INJECTION, SOLUTION">{{Cite web | last = | first = | title = NITROGLYCERIN INJECTION, SOLUTION [AMERICAN REGENT, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8c52cdf6-87be-4719-b105-f08be096d462 | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Initial Dilution: | |||
::* Nitroglycerin must be diluted in dextrose (5%) injection or sodium chloride (0.9%) injection prior to its infusion. Transfer 50 mg of nitroglycerin into a 500 mL glass bottle of either dextrose (5%) injection or sodium chloride injection (0.9%). This yields a final concentration of 100 μg/mL. Diluting 5 mg nitroglycerin into 100 mL will yield a final concentration of 50 μg/mL. | |||
:* Suggested Maintenance Dilution: | |||
::* Consider the fluid requirements of the patient as well as the expected duration of infusion in selecting the appropriate dilution of Nitroglycerin Injection. | |||
::* The concentration of nitroglycerin should not exceed 400 μg/mL. | |||
:* Suggested Regimen: | |||
::* '''Severe hypotension and shock may occur with even small doses of nitroglycerin. This drug should therefore be used with caution in patients who may be volume depleted or who, for whatever reason, are already hypotensive. Hypotension induced by nitroglycerin may be accompanied by paradoxical bradycardia and increased angina pectoris.''' | |||
::* The initial dosage should be 5 μg/min delivered through an infusion pump. Subsequent titration must be adjusted to the clinical situation, with dose increments becoming more cautious as partial response is seen. | |||
::* Initial titration should be in 5 μg/min increments, with increases every 3–5 minutes until some response is noted. | |||
::* If no response is seen at 20 μg/min, increments of 10 and later 20 μg/min can be used. | |||
::* Once a partial blood pressure response is observed, the dose increase should be reduced and the interval between increases should be lengthened. | |||
* Contraindications | |||
:* Pericardial tamponade | |||
:* Restrictive cardiomyopathy | |||
:* Constrictive pericarditis | |||
:* Hypersensitivity to nitroglycerin | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Nitroprusside====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="NITROPRESS (SODIUM NITROPRUSSIDE) INJECTION">{{Cite web | last = | first = | title = NITROPRESS (SODIUM NITROPRUSSIDE) INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6a44bcac-a0e1-4069-5691-db7b83dbb4b7 | publisher = | date = | accessdate = }}</ref><ref name="Chatterjee-1973">{{Cite journal | last1 = Chatterjee | first1 = K. | last2 = Parmley | first2 = WW. | last3 = Ganz | first3 = W. | last4 = Forrester | first4 = J. | last5 = Walinsky | first5 = P. | last6 = Crexells | first6 = C. | last7 = Swan | first7 = HJ. | title = Hemodynamic and metabolic responses to vasodilator therapy in acute myocardial infarction. | journal = Circulation | volume = 48 | issue = 6 | pages = 1183-93 | month = Dec | year = 1973 | doi = | PMID = 4762476 }}</ref> | |||
:* Suggested Dilution: | |||
::* Depending on the desired concentration, the solution containing 50 mg of nitroprusside must be further diluted in 250–1000 mL of sterile 5% dextrose injection. | |||
:* Suggested Regimen: | |||
::* '''While the average effective rate in adult and pediatric patients is about 3 μg/kg/min, some patients will become dangerously hypotensive at this rate.''' | |||
::* '''Nitroprusside can induce essentially unlimited blood pressure reduction, the blood pressure must be continuously monitored, using either a continually reinflated sphygmomanometer or (preferably) an intra-arterial pressure sensor. Special caution should be used in elderly patients, since they may be more sensitive to the hypotensive effects of the drug.''' | |||
::* Infusion of sodium nitroprusside should be started at a very low rate (0.3 μg/kg/min), with upward titration every few minutes until the desired effect is achieved or the maximum recommended infusion rate (10 μg/kg/min) has been reached. | |||
* Contraindications | |||
:* Sodium nitroprusside should not be used for the treatment of acute congestive heart failure associated with reduced peripheral vascular resistance such as high-output heart failure that may be seen in endotoxic sepsis. | |||
:* Sodium nitroprusside should not be used in the treatment of compensatory hypertension, where the primary hemodynamic lesion is aortic coarctation or arteriovenous shunting. | |||
:* Sodium nitroprusside should not be used to produce hypotension during surgery in patients with known inadequate cerebral circulation, or in moribund patients coming to emergency surgery. | |||
:* Patients with congenital (Leber’s) optic atrophy or with toxic amblyopia have unusually high cyanide/thiocyanate ratios. These rare conditions are probably associated with defective or absent rhodanase, and sodium nitroprusside should be avoided in these patients. | |||
</div></div> | |||
==Optimization of Hemodynamic Status <SMALL><SMALL>'''[[{{PAGENAME}}#FIRE: Focused Initial Rapid Evaluation|[Return to ''FIRE'']]]'''</SMALL></SMALL>== | |||
===Preload Optimization=== | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Fluid Challenge Protocol====== | |||
<div class="mw-collapsible-content"> | |||
* Preload optimization involves scrupulous fluid loading, manipulation of [[PCWP]] and/or [[central venous pressure|CVP]] levels, and correction of [[pulmonary congestion]].<ref name="Forrester-1976">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (first of two parts). | journal = N Engl J Med | volume = 295 | issue = 24 | pages = 1356-62 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612092952406 | PMID = 790191 }}</ref><ref name="Forrester-1976-2">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (second of two parts). | journal = N Engl J Med | volume = 295 | issue = 25 | pages = 1404-13 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612162952505 | PMID = 790194 }}</ref><ref name="Reynolds-2008">{{Cite journal | last1 = Reynolds | first1 = HR. | last2 = Hochman | first2 = JS. | title = Cardiogenic shock: current concepts and improving outcomes. | journal = Circulation | volume = 117 | issue = 5 | pages = 686-97 | month = Feb | year = 2008 | doi = 10.1161/CIRCULATIONAHA.106.613596 | PMID = 18250279 }}</ref><ref name="Crexells-1973">{{Cite journal | last1 = Crexells | first1 = C. | last2 = Chatterjee | first2 = K. | last3 = Forrester | first3 = JS. | last4 = Dikshit | first4 = K. | last5 = Swan | first5 = HJ. | title = Optimal level of filling pressure in the left side of the heart in acute myocardial infarction. | journal = N Engl J Med | volume = 289 | issue = 24 | pages = 1263-6 | month = Dec | year = 1973 | doi = 10.1056/NEJM197312132892401 | PMID = 4749545 }}</ref> | |||
* Protocolized fluid administration titrated to hemodynamic and clinical endpoints secures the efficacy of tissue perfusion and oxygenation.<ref name="Weil-fluid1">{{Cite journal | last1 = Weil | first1 = MH. | last2 = Henning | first2 = RJ. | title = New concepts in the diagnosis and fluid treatment of circulatory shock. Thirteenth annual Becton, Dickinson and Company Oscar Schwidetsky Memorial Lecture. | journal = Anesth Analg | volume = 58 | issue = 2 | pages = 124-32 | month = | year = | doi = | PMID = 571235 }}</ref> | |||
* Four elements of the fluid challenge protocol: type of fluid (T), rate of fluid administration (R), objective (O), and limits (L).<ref name="Vincent-2011">{{Cite journal | last1 = Vincent | first1 = JL. | title = Let's give some fluid and see what happens versus the mini-fluid challenge. | journal = Anesthesiology | volume = 115 | issue = 3 | pages = 455-6 | month = Sep | year = 2011 | doi = 10.1097/ALN.0b013e318229a521 | PMID = 21792055 }}</ref> | |||
:* 1. Type of fluid (T) | |||
::* The choice of crystalloid or colloid solution should be made on the basis of the underlying disease, the nature of fluid deficit, the severity of circulatory failure, the serum albumin concentration, and the risk of bleeding.<ref name="Weil-fluid2">{{Cite journal | last1 = Vincent | first1 = JL. | last2 = Weil | first2 = MH. | title = Fluid challenge revisited. | journal = Crit Care Med | volume = 34 | issue = 5 | pages = 1333-7 | month = May | year = 2006 | doi = 10.1097/01.CCM.0000214677.76535.A5 | PMID = 16557164 }}</ref> | |||
::* There were no significant differences in mortality between saline and albumin infusion for critically ill patients.<ref name="Finfer-2004">{{Cite journal | last1 = Finfer | first1 = S. | last2 = Bellomo | first2 = R. | last3 = Boyce | first3 = N. | last4 = French | first4 = J. | last5 = Myburgh | first5 = J. | last6 = Norton | first6 = R. | title = A comparison of albumin and saline for fluid resuscitation in the intensive care unit. | journal = N Engl J Med | volume = 350 | issue = 22 | pages = 2247-56 | month = May | year = 2004 | doi = 10.1056/NEJMoa040232 | PMID = 15163774 }}</ref> | |||
::* [[Blood transfusion]] may be considered in the presence of profound [[anemia]] or massive [[hemorrhage]].<ref name="Weil-fluid1">{{Cite journal | last1 = Weil | first1 = MH. | last2 = Henning | first2 = RJ. | title = New concepts in the diagnosis and fluid treatment of circulatory shock. Thirteenth annual Becton, Dickinson and Company Oscar Schwidetsky Memorial Lecture. | journal = Anesth Analg | volume = 58 | issue = 2 | pages = 124-32 | month = | year = | doi = | PMID = 571235 }}</ref> | |||
::* [[Hyperchloremic acidosis]] may be associated with the use of isotonic saline solution.<ref name="Scheingraber-1999">{{Cite journal | last1 = Scheingraber | first1 = S. | last2 = Rehm | first2 = M. | last3 = Sehmisch | first3 = C. | last4 = Finsterer | first4 = U. | title = Rapid saline infusion produces hyperchloremic acidosis in patients undergoing gynecologic surgery. | journal = Anesthesiology | volume = 90 | issue = 5 | pages = 1265-70 | month = May | year = 1999 | doi = | PMID = 10319771 }}</ref> | |||
:* 2. Rate of fluid administration (R) | |||
::* Based on the level of [[pulmonary capillary wedge pressure]] or [[central venous pressure]], a volume of 50, 100, or 200 ml of fluid is administered over a 10-minute interval through a peripheral venous catheter.<ref name="Weil-fluid1">{{Cite journal | last1 = Weil | first1 = MH. | last2 = Henning | first2 = RJ. | title = New concepts in the diagnosis and fluid treatment of circulatory shock. Thirteenth annual Becton, Dickinson and Company Oscar Schwidetsky Memorial Lecture. | journal = Anesth Analg | volume = 58 | issue = 2 | pages = 124-32 | month = | year = | doi = | PMID = 571235 }}</ref> | |||
{| | |||
| style="width: 10%" | | |||
| style="width: 90%" | | |||
{| style="border: 2px solid #DCDCDC; font-size: 90%;" | |||
| align="center" style="background: #DCDCDC; width: 150px;" | '''Baseline PCWP (mm Hg)''' | |||
| align="center" style="background: #DCDCDC; width: 150px;" | '''Baseline CVP (cm H<sub>2</sub>O)''' | |||
| align="center" style="background: #DCDCDC; width: 300px;" | '''Rate of fluid administration''' | |||
|- | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | ≥16 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | ≥14 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=left | 50 mL over 10 minutes | |||
|- | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | <16 but ≥12 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | <14 but ≥8 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=left | 100 mL over 10 minutes | |||
|- | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | <12 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | <8 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=left | 200 mL over 10 minutes | |||
|} | |||
|} | |||
:* 3. Objective (O) | |||
::* Fluid administration should be titrated to reach predetermined clinical endpoints such as resolution of tachycardia or oliguria, improved skin perfusion or level of consciousness, normalization of lactate concentrations, and restoration of adequate blood pressure or ventricular filling pressure.<ref name="Weil-fluid2">{{Cite journal | last1 = Vincent | first1 = JL. | last2 = Weil | first2 = MH. | title = Fluid challenge revisited. | journal = Crit Care Med | volume = 34 | issue = 5 | pages = 1333-7 | month = May | year = 2006 | doi = 10.1097/01.CCM.0000214677.76535.A5 | PMID = 16557164 }}</ref> | |||
:* 4. Limits (L) | |||
::* Fluid administration should be stopped if the safety limits are violated to minimize the risk of developing [[pulmonary edema]]. | |||
::* Inotropes, vasodilators, or mechanical circulatory device may be required if signs of hypoperfusion persist despite optimal fluid loading. | |||
::* Hemodynamic safety limits based on PCWP (the 7–3 rule) or CVP (the 5–2 rule):<ref name="Weil-fluid1">{{Cite journal | last1 = Weil | first1 = MH. | last2 = Henning | first2 = RJ. | title = New concepts in the diagnosis and fluid treatment of circulatory shock. Thirteenth annual Becton, Dickinson and Company Oscar Schwidetsky Memorial Lecture. | journal = Anesth Analg | volume = 58 | issue = 2 | pages = 124-32 | month = | year = | doi = | PMID = 571235 }}</ref> | |||
{| | |||
| style="width: 10%" | | |||
| style="width: 90%" | | |||
{| style="border: 2px solid #DCDCDC; font-size: 90%;" | |||
| align="center" style="background: #DCDCDC; width: 150px;" | '''↑ PCWP (mm Hg)''' | |||
| align="center" style="background: #DCDCDC; width: 150px;" | '''↑ CVP (cm H<sub>2</sub>O)''' | |||
| align="center" style="background: #DCDCDC; width: 300px;" | '''Action''' | |||
|- | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | ≥7 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | ≥5 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=left | Stop fluid administration | |||
|- | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | <7 but >3 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | <5 but >2 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=left | Wait and recheck pressure after 10 minutes | |||
|- | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | ≤3 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=center | ≤2 | |||
| style="padding: 0 5px; background: #F5F5F5;" align=left | Continue fluid administration | |||
|} | |||
|} | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Pulmonary Congestion====== | ======Pulmonary Congestion====== | ||
::* Radiologic manifestations of [[pulmonary congestion]] reflect the extent of elevation in [[PCWP|wedge pressure]]: | <div class="mw-collapsible-content"> | ||
{| style="border: 2px solid #DCDCDC; font-size: 90%;" | |||
* Findings suggestive of cardiogenic pulmonary edema:<ref name="Ware-2005">{{Cite journal | last1 = Ware | first1 = LB. | last2 = Matthay | first2 = MA. | title = Clinical practice. Acute pulmonary edema. | journal = N Engl J Med | volume = 353 | issue = 26 | pages = 2788-96 | month = Dec | year = 2005 | doi = 10.1056/NEJMcp052699 | PMID = 16382065 }}</ref> | |||
:* History and clinical manifestations | |||
::* Cough | |||
::* Dyspnea | |||
::* Expectoration of frothy sputum | |||
::* Orthopnea | |||
::* Paroxysmal nocturnal dyspnea | |||
::* Signs and symptoms of heart failure | |||
::* Signs and symptoms of hypoxemia | |||
::* Signs and symptoms of myocardial ischemia | |||
::* Signs and symptoms of valvular dysfunction | |||
::* Tachypnea | |||
:* Physical examination | |||
::* Cool extremities | |||
::* Heart murmurs | |||
::* Hepatomegaly | |||
::* Inspiratory crackles or rhonchi | |||
::* Jugular venous distention | |||
::* S3 gallop | |||
::* Peripheral edema | |||
:* Laboratory and hemodynamic findings | |||
::* BNP > 500 pg/mL | |||
::* PCWP >18 mm Hg | |||
:* Radiologic findings | |||
::* Central infiltrates with peripheral sparing | |||
::* Cephalization of pulmonary vessels | |||
::* Enlarged cardiac silhouette | |||
::* Enlargement of peribronchovascular spaces | |||
::* Increased opacity of acinar areas that coalesce into frank consolidations | |||
::* Kerley B lines | |||
::* Peribronchial cuffing | |||
::* Pleural effusions | |||
::* Vascular pedicle width >70 mm | |||
* Radiologic manifestations of [[pulmonary congestion]] reflect the extent of elevation in [[PCWP|wedge pressure]]:<ref name="Forrester-1976">{{Cite journal | last1 = Forrester | first1 = JS. | last2 = Diamond | first2 = G. | last3 = Chatterjee | first3 = K. | last4 = Swan | first4 = HJ. | title = Medical therapy of acute myocardial infarction by application of hemodynamic subsets (first of two parts). | journal = N Engl J Med | volume = 295 | issue = 24 | pages = 1356-62 | month = Dec | year = 1976 | doi = 10.1056/NEJM197612092952406 | PMID = 790191 }}</ref> | |||
{| | |||
| style="width: 4%" | | |||
| style="width: 96%" | | |||
{| style="border: 2px solid #DCDCDC; font-size: 90%;" | |||
| align="center" style="background: #DCDCDC; width: 100px;"| '''PCWP (mm Hg)''' | | align="center" style="background: #DCDCDC; width: 100px;"| '''PCWP (mm Hg)''' | ||
| align="center" style="background: #DCDCDC; width: 200px;" | '''Phase of Pulmonary Congestion''' | | align="center" style="background: #DCDCDC; width: 200px;" | '''Phase of Pulmonary Congestion''' | ||
Line 263: | Line 781: | ||
| style="padding: 0 5px; background: #F5F5F5;" align=left | Coalescence of periacinar rosettes resulting in "Bat's wing" opacities | | style="padding: 0 5px; background: #F5F5F5;" align=left | Coalescence of periacinar rosettes resulting in "Bat's wing" opacities | ||
|} | |} | ||
|} | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Furosemide====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="FUROSEMIDE injection">{{Cite web | last = | first = | title = FUROSEMIDE INJECTION [AMERICAN REGENT, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d6a6ff9-3f12-4a6e-bba3-3f85fd54ffac | publisher = | date = | accessdate = }}</ref> | |||
:* For [[pulmonary edema|acute pulmonary edema]], the initial dose is 40 mg injected slowly intravenously (over 1 to 2 minutes). | |||
:* If a satisfactory response does not occur within 1 hour, the dose may be increased to 80 mg injected slowly intravenously (over 1 to 2 minutes). | |||
* Contraindications | |||
:* [[Anuria]] | |||
:* [[Hypersensitivity]] to [[furosemide]] | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Morphine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="MORPHINE SULFATE INJECTION">{{Cite web | last = | first = | title = MORPHINE SULFATE INJECTION, SOLUTION, CONCENTRATE | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cadc3fdb-8edc-44cd-aaea-89e68aaf9a04 | publisher = | date = | accessdate = }}</ref><ref name="O'Connor-2010">{{Cite journal | last1 = O'Connor | first1 = RE. | last2 = Brady | first2 = W. | last3 = Brooks | first3 = SC. | last4 = Diercks | first4 = D. | last5 = Egan | first5 = J. | last6 = Ghaemmaghami | first6 = C. | last7 = Menon | first7 = V. | last8 = O'Neil | first8 = BJ. | last9 = Travers | first9 = AH. | title = Part 10: acute coronary syndromes: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. | journal = Circulation | volume = 122 | issue = 18 Suppl 3 | pages = S787-817 | month = Nov | year = 2010 | doi = 10.1161/CIRCULATIONAHA.110.971028 | PMID = 20956226 }}</ref> | |||
:* '''Morphine may cause [[Hypoventilation|respiratory depression]] or exacerbate [[hypotension]] in [[hypovolemia|volume-depleted]] patients.''' | |||
:* Morphine may be used adjunctively in the treatment of acute pulmonary edema at a dose of 2–4 mg (slow [[IV|IV injection]] over 1–5 minutes) every 5–30 minutes as needed. | |||
* Contraindications | |||
:* [[Hypersensitivity]] to [[morphine sulfate]] is one of the contraindications to its use. | |||
:* [[Morphine]] should not be used in [[convulsion|convulsive states]], such as those occurring in [[status epilepticus]], [[tetanus]], and [[strychnine]] poisoning. | |||
:* [[Morphine]] is also contraindicated in the following conditions: [[respiratory insufficiency|respiratory insufficiency or depression]]; [[bronchial asthma]]; [[heart failure]] secondary to [[COPD|chronic lung disease]]; [[cardiac arrhythmia]]s; increased [[ICP|intracranial or cerebrospinal pressure]]; [[head injury|head injuries]]; [[brain tumor]]; acute [[alcoholism]]; and [[delirium tremens]]. | |||
</div></div> | |||
===Afterload Optimization=== | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Nitroglycerin====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="NITROGLYCERIN INJECTION, SOLUTION">{{Cite web | last = | first = | title = NITROGLYCERIN INJECTION, SOLUTION [AMERICAN REGENT, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8c52cdf6-87be-4719-b105-f08be096d462 | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Initial Dilution: | |||
::* Nitroglycerin must be diluted in dextrose (5%) injection or sodium chloride (0.9%) injection prior to its infusion. Transfer 50 mg of nitroglycerin into a 500 mL glass bottle of either dextrose (5%) injection or sodium chloride injection (0.9%). This yields a final concentration of 100 μg/mL. Diluting 5 mg nitroglycerin into 100 mL will yield a final concentration of 50 μg/mL. | |||
:* Suggested Maintenance Dilution: | |||
::* Consider the fluid requirements of the patient as well as the expected duration of infusion in selecting the appropriate dilution of Nitroglycerin Injection. | |||
::* The concentration of nitroglycerin should not exceed 400 μg/mL. | |||
:* Suggested Regimen: | |||
::* '''Severe hypotension and shock may occur with even small doses of nitroglycerin. This drug should therefore be used with caution in patients who may be volume depleted or who, for whatever reason, are already hypotensive. Hypotension induced by nitroglycerin may be accompanied by paradoxical bradycardia and increased angina pectoris.''' | |||
::* The initial dosage should be 5 μg/min delivered through an infusion pump. Subsequent titration must be adjusted to the clinical situation, with dose increments becoming more cautious as partial response is seen. | |||
::* Initial titration should be in 5 μg/min increments, with increases every 3–5 minutes until some response is noted. | |||
::* If no response is seen at 20 μg/min, increments of 10 and later 20 μg/min can be used. | |||
::* Once a partial blood pressure response is observed, the dose increase should be reduced and the interval between increases should be lengthened. | |||
* Contraindications | |||
:* Pericardial tamponade | |||
:* Restrictive cardiomyopathy | |||
:* Constrictive pericarditis | |||
:* Hypersensitivity to nitroglycerin | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Nitroprusside====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="NITROPRESS (SODIUM NITROPRUSSIDE) INJECTION">{{Cite web | last = | first = | title = NITROPRESS (SODIUM NITROPRUSSIDE) INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6a44bcac-a0e1-4069-5691-db7b83dbb4b7 | publisher = | date = | accessdate = }}</ref><ref name="Chatterjee-1973">{{Cite journal | last1 = Chatterjee | first1 = K. | last2 = Parmley | first2 = WW. | last3 = Ganz | first3 = W. | last4 = Forrester | first4 = J. | last5 = Walinsky | first5 = P. | last6 = Crexells | first6 = C. | last7 = Swan | first7 = HJ. | title = Hemodynamic and metabolic responses to vasodilator therapy in acute myocardial infarction. | journal = Circulation | volume = 48 | issue = 6 | pages = 1183-93 | month = Dec | year = 1973 | doi = | PMID = 4762476 }}</ref> | |||
:* Suggested Dilution: | |||
::* Depending on the desired concentration, the solution containing 50 mg of nitroprusside must be further diluted in 250–1000 mL of sterile 5% dextrose injection. | |||
:* Suggested Regimen: | |||
::* '''While the average effective rate in adult and pediatric patients is about 3 μg/kg/min, some patients will become dangerously hypotensive at this rate.''' | |||
::* '''Nitroprusside can induce essentially unlimited blood pressure reduction, the blood pressure must be continuously monitored, using either a continually reinflated sphygmomanometer or (preferably) an intra-arterial pressure sensor. Special caution should be used in elderly patients, since they may be more sensitive to the hypotensive effects of the drug.''' | |||
::* Infusion of sodium nitroprusside should be started at a very low rate (0.3 μg/kg/min), with upward titration every few minutes until the desired effect is achieved or the maximum recommended infusion rate (10 μg/kg/min) has been reached. | |||
* Contraindications | |||
:* Sodium nitroprusside should not be used for the treatment of acute congestive heart failure associated with reduced peripheral vascular resistance such as high-output heart failure that may be seen in endotoxic sepsis. | |||
:* Sodium nitroprusside should not be used in the treatment of compensatory hypertension, where the primary hemodynamic lesion is aortic coarctation or arteriovenous shunting. | |||
:* Sodium nitroprusside should not be used to produce hypotension during surgery in patients with known inadequate cerebral circulation, or in moribund patients coming to emergency surgery. | |||
:* Patients with congenital (Leber’s) optic atrophy or with toxic amblyopia have unusually high cyanide/thiocyanate ratios. These rare conditions are probably associated with defective or absent rhodanase, and sodium nitroprusside should be avoided in these patients. | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Norepinephrine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="NOREPINEPHRINE BITARTRATE INJECTION">{{Cite web | last = | first = | title = NOREPINEPHRINE BITARTRATE INJECTION | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3352c7d0-e621-46ed-9a54-e4a9583cde10 | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Dilution: | |||
::* Mix 4 mg of [[norepinephrine]] in 250 mL of [[Intravenous sugar solution|D5W]] or [[Intravenous sugar solution|D5NS]]. Avoid dilution in [[normal saline]] alone. | |||
:* Suggested Regimen: | |||
::* Start at a dose of 0.5–1.0 μg/min [[IV|IV infusion]]; titrate to maintain [[SBP]] at above 90 mm Hg (up to 30–40 μg/min). | |||
* Contraindications | |||
:* [[Norepinephrine]] should not be given to patients who are [[hypotensive]] from [[hypovolemia|blood volume deficits]] except as an emergency measure to maintain [[coronary]] and [[cerebral]] artery [[perfusion]] until blood volume replacement therapy can be completed. | |||
:* [[Norepinephrine]] should also not be given to patients with [[mesentery|mesenteric]] or peripheral vascular [[thrombosis]] unless it is necessary as a life-saving procedure. | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Dopamine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="DOPAMINE HCL injection, solution">{{Cite web | last = | first = | title = DOPAMINE HCL INJECTION, SOLUTION [AMERICAN REGENT, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e061fb3e-afd7-4188-b5fb-617ac1d3e38d | publisher = | date = | accessdate = }}</ref> | |||
:: | :* Suggested Dilution: transfer contents of one or more ampuls or vials by aseptic technique to either 250 mL or 500 mL of one of the following sterile intravenous solutions | ||
::* Sodium Chloride Injection | |||
::* Dextrose (5%) Injection | |||
::* | ::* Dextrose (5%) and Sodium Chloride (0.9%) Injection | ||
::* 5% Dextrose in 0.45% Sodium Chloride Solution | |||
::* Dextrose (5%) in Lactated Ringer’s Solution | |||
::* Sodium Lactate (1/6 Molar) Injection | |||
::* Lactated Ringer’s Injection | |||
:* Suggested Regimen: | |||
::* Begin administration of diluted solution at doses of 2–5 μg/kg/minute in patients who are likely to respond to modest increments of heart force and renal perfusion. | |||
::* In more seriously ill patients, begin administration of diluted solution at doses of 5 μg/kg/minute and increase gradually, using 5–10 μg/kg/minute increments, up to 20–50 μg/kg/minute as needed. | |||
--> | ::* If doses of 50 μg/kg/minute are required, it is suggested that urine output be checked frequently. Should the urine flow begin to decrease in the absence of hypotension, reduction of dosage should be considered. | ||
::* Treatment of all patients requires constant evaluation of therapy in terms of the blood volume, augmentation of myocardial contractility, and distribution of peripheral perfusion. Dosage should be adjusted according to the patient’s response, with particular attention to diminution of established urine flow rate, increasing tachycardia or development of new dysrhythmias as indices for decreasing or temporarily suspending the dosage. | |||
* Contraindications | |||
:* Pheochromocytoma | |||
:* Uncorrected tachyarrhythmias or ventricular fibrillation | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Phenylephrine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="Hollenberg-2011">{{Cite journal | last1 = Hollenberg | first1 = SM. | title = Vasoactive drugs in circulatory shock. | journal = Am J Respir Crit Care Med | volume = 183 | issue = 7 | pages = 847-55 | month = Apr | year = 2011 | doi = 10.1164/rccm.201006-0972CI | PMID = 21097695 }}</ref><ref name="PHENYLEPHRINE HYDROCHLORIDE INJECTION">{{Cite web | last = | first = | title = PHENYLEPHRINE HYDROCHLORIDE INJECTION [BAXTER HEALTHCARE CORPORATION] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=72348406-e74f-46c5-b93d-34d07cffe1fd | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Dilution: | |||
::* Add 10 mg of the drug (1 mL of 1 percent solution) to 500 mL of Dextrose Injection or Sodium Chloride Injection (providing a 1:50,000 solution). | |||
:* Suggested Regimen: | |||
::* To raise the blood pressure rapidly, start the infusion at about 100 μg to 180 μg per minute (based on 20 drops per mL this would be 100 to 180 drops per minute). | |||
::* When the blood pressure is stabilized (at a low normal level for the individual), a maintenance rate of 40 μg to 60 μg per minute usually suffices (based on 20 drops per mL this would be 40 to 60 drops per minute). | |||
::* If a prompt initial pressor response is not obtained, additional increments of phenylephrine (10 mg or more) are added to the infusion bottle. The rate of flow is then adjusted until the desired blood pressure level is obtained. | |||
* Contraindications | |||
:* Severe hypertension | |||
:* Ventricular tachycardia | |||
:* Hypersensitivity to phenylephrine | |||
</div></div> | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Vasopressin====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="Hollenberg-2011">{{Cite journal | last1 = Hollenberg | first1 = SM. | title = Vasoactive drugs in circulatory shock. | journal = Am J Respir Crit Care Med | volume = 183 | issue = 7 | pages = 847-55 | month = Apr | year = 2011 | doi = 10.1164/rccm.201006-0972CI | PMID = 21097695 }}</ref><ref name="VASOPRESSIN INJECTION">{{Cite web | last = | first = | title = PITRESSIN (VASOPRESSIN) INJECTION [JHP PHARMACEUTICALS LLC] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1b316ff5-b7f8-4509-acc4-fd263d0a1703 | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Regimen: | |||
::* Adjunctive use of a low dose of vasopressin (0.01–0.04 U/min) to catecholamine may reduce its dosage requirement in patients with refractory shock. | |||
* Contraindications | |||
:* Anaphylaxis or hypersensitivity to the drug or its components | |||
</div></div> | |||
===Cardiac Output Optimization=== | |||
<div class="mw-collapsible mw-collapsed"> | |||
======Dobutamine====== | |||
<div class="mw-collapsible-content"> | |||
* Dosage and Administration<ref name="isbn1616690003">{{cite book | author = | authorlink = | editor = | others = | title = Handbook of Emergency Cardiovascular Care for Healthcare Providers | edition = | language = | publisher = | location = | year = | origyear = | pages = | quote = | isbn = 1616690003 | oclc = | doi = | url = | accessdate = }}</ref><ref name="-2000">{{Cite journal | title = Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation. | journal = Circulation | volume = 102 | issue = 8 Suppl | pages = I172-203 | month = Aug | year = 2000 | doi = | PMID = 10966673 }}</ref><ref name="DOBUTAMINE (DOBUTAMINE HYDROCHLORIDE) INJECTION, SOLUTION">{{Cite web | last = | first = | title = DOBUTAMINE (DOBUTAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb842dc2-fb15-48f9-e4b1-ea4280db0199 | publisher = | date = | accessdate = }}</ref> | |||
:* Suggested Dilution: dobutamine injection must be further diluted in an IV container. Dilute 20 mL of dobutamine in at least 50 mL of diluent and dilute 40 mL of dobutamine in at least 100 mL of diluent. Use one of the following intravenous solutions as a diluent: | |||
::* Dextrose Injection 5% | |||
::* Dextrose 5% and Sodium Chloride 0.45% Injection | |||
::* Dextrose 5% and Sodium Chloride 0.9% Injection | |||
::* Dextrose Injection 10%, Isolyte® M with 5% Dextrose Injection | |||
::* Lactated Ringer’s Injection | |||
::* 5% Dextrose in Lactated Ringer’s Injection | |||
::* Normosol®-M in D5-W | |||
::* 20% Osmitrol® in Water for Injection | |||
::* Sodium Chloride Injection 0.9% | |||
::* Sodium Lactate Injection | |||
:* Suggested Regimen: | |||
::* The rate of infusion needed to increase cardiac output usually ranged from 2.5–15 mcg/kg/min. | |||
::* On rare occasions, infusion rates up to 40 mcg/kg/min have been required to obtain the desired effect. | |||
* Contraindications | |||
:* Idiopathic hypertrophic subaortic stenosis | |||
:* Hypersensitivity to dobutamine | |||
</div></div> | |||
= | <div class="mw-collapsible mw-collapsed"> | ||
======Milrinone====== | |||
<div class="mw-collapsible-content"> | |||
==== | * Dosage and Administration<ref name="Hollenberg-2011">{{Cite journal | last1 = Hollenberg | first1 = SM. | title = Vasoactive drugs in circulatory shock. | journal = Am J Respir Crit Care Med | volume = 183 | issue = 7 | pages = 847-55 | month = Apr | year = 2011 | doi = 10.1164/rccm.201006-0972CI | PMID = 21097695 }}</ref><ref name="MILRINONE LACTATE INJECTION">{{Cite web | last = | first = | title = MILRINONE LACTATE (MILRINONE LACTATE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=13705c4d-f47e-4158-88d9-4494324142d4 | publisher = | date = | accessdate = }}</ref> | ||
:* Suggested Regimen: | |||
::* Milrinone should be administered with a loading dose followed by a continuous infusion (maintenance dose). | |||
::* Loading dose: 50 μg/kg (slowly over 10 minutes) | |||
::* Maintenance dose: 0.50 μg/kg/min (0.375–0.75 μg/kg/min) | |||
* Contraindications | |||
:* Hypersensitivity to milrinone | |||
</div></div> | |||
==Do's== | |||
==Don'ts== | |||
Line 338: | Line 1,001: | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Resident survival guide]] | |||
</div><div class="mw-collapsible mw-collapsed"><div class="mw-collapsible-content"></div></div> |
Latest revision as of 00:09, 6 May 2014
Cardiogenic Shock Resident Survival Guide |
---|
Overview |
Causes |
FIRE |
Emergency Revascularization |
Complete Diagnostic Approach |
Diagnostic Criteria
|
Blood Pressure Maintenance |
Hemodynamic Optimization |
Do's |
Don'ts |
Overview
The clinical definition of cardiogenic shock includes decreased cardiac output with evidence of tissue hypoxia in the presence of adequate intravascular volume.[1]
Causes
Life Threatening Causes
Cardiogenic shock is a life-threatening condition and must be treated as such irrespective of the underlying cause.
Common Causes
- Arrhythmic
- Mechanical
- Acute mitral regurgitation (papillary muscle rupture, chordae tendinae rupture)
- Free wall rupture
- Hypertrophic cardiomyopathy
- Obstruction to left ventricular filling (mitral stenosis, left atrial myxoma)
- Obstruction to left ventricular outflow tract (aortic stenosis, hypertrophic obstructive cardiomyopathy)
- Ventricular septal defect
- Myopathic
- Pharmacologic
Click here for the complete list of causes.
FIRE: Focused Initial Rapid Evaluation
A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients in need of immediate intervention.[2]
Boxes in red signify that an urgent management is needed.
Abbreviations: CBC, complete blood count; CI, cardiac index; CK-MB, creatine kinase MB isoform; CVP, central venous pressure; DC, differential count; ICU, intensive care unit; INR, international normalized ratio; LFT, liver function test; MAP, mean arterial pressure; PCWP, pulmonary capillary wedge pressure; PT, prothrombin time; PTT, partial prothrombin time; SaO2, arterial oxygen saturation; SBP, systolic blood pressure; ScvO2, central venous oxygen saturation; SvO2, mixed venous oxygen saturation; SMA-7, sequential multiple analysis-7.
Does the patient have cardinal findings that increase the pretest probability of cardiogenic shock?
❑ Evidence of end-organ hypoperfusion
| |||||||||||||||||||||||||||||||||||||
YES | NO | ||||||||||||||||||||||||||||||||||||
Cardiogenic shock suspected (click for details on criteria) | Proceed to shock resident survival guide | ||||||||||||||||||||||||||||||||||||
Immediate steps | |||||||||||||||||||||||||||||||||||||
Initial management
❑ Oxygen ± ventilatory support ❑ Sphygmomanometer or arterial line ❑ Large-bore peripheral venous lines ❑ Hold antihypertensive medications ❑ ± Correct tachy- or bradyarrhythmia | |||||||||||||||||||||||||||||||||||||
Initial workup
❑ Lactate ❑ Echocardiography | |||||||||||||||||||||||||||||||||||||
Maintain adequate blood pressure (click for details) | |||||||||||||||||||||||||||||||||||||
SBP <70 mm Hg:
SBP 70–100 mm Hg with symptoms: ❑ Dopamine
SBP 70–100 mm Hg w/o symptoms:
SBP >100 mm Hg:
| |||||||||||||||||||||||||||||||||||||
Acute coronary syndrome likely? (click for details on criteria) | |||||||||||||||||||||||||||||||||||||
❑ New ischemic ECG changes
❑ Positive cTnT, cTnI, or CK-MB ❑ Anginal pain | |||||||||||||||||||||||||||||||||||||
YES | NO | ||||||||||||||||||||||||||||||||||||
Proceed to Emergency Revascularization | |||||||||||||||||||||||||||||||||||||
Optimize hemodynamic status (click for details) | |||||||||||||||||||||||||||||||||||||
Preload
Goal: PCWP 15–18 mm Hg, CVP 8–12 cm H2O ❑ Fluid challenge protocol ("TROL") ❑ ± Correct pulmonary congestion
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Afterload
Goal: MAP >65 mm Hg, SVR 800–1200 dyn·s·cm−5 ❑ If ↑ MAP & ↑ SVR:
❑ If ↓ MAP & ↓ SVR:
❑ If ↓ MAP & ↑ SVR:
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Cardiac index
Goal: CI >2.2 L/min/m2
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Evaluate perfusion and oxygenation | |||||||||||||||||||||||||||||||||||||
Endpoints:
❑ SaO2 >92% ❑ SvO2 >60% ❑ ScvO2 >70% ❑ Urine output >0.5 mL/kg/h ❑ Lactate <2.2 mM/L ❑ Hematocrit ≥30% | |||||||||||||||||||||||||||||||||||||
Proceed to complete diagnostic approach | |||||||||||||||||||||||||||||||||||||
Emergency Revascularization [Return to FIRE]
Acute coronary syndrome (click for details on criteria) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
❑ New ischemic ECG changes
❑ Positive cardiac biomarkers (cTnT, cTnI, or CK-MB) ❑ Anginal pain
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STEMI | UA/NSTEMI | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Complete Diagnostic Approach [Return to FIRE]
Diagnostic Criteria [Return to FIRE]
Criteria for Cardiogenic Shock
- Sustained hypotension (SBP <90 mm Hg or MAP 30 mm Hg below baseline in preexisting hypertension for at least 30 minutes)
- Evidence of tissue hypoperfusion (such as oliguria, cyanosis, cool extremities, and altered mental status)
- Presence of myocardial dysfunction after exclusion or correction of non-myocardial factors contributing to tissue hypoperfusion (such as hypovolemia, hypoxia, and acidosis)
- Sustained hypotension (SBP <90 mm Hg or MAP 30 mm Hg below baseline in preexisting hypertension for at least 30 minutes)
- Depressed cardiac index (<1.8 L/min/m2 of BSA without support or <2.0–2.2 L/min/m2 of BSA with support) in the presence of an elevated wedge pressure (>15 mm Hg).
Criteria for Acute Myocardial Infarction
The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one of the following criteria meets the diagnosis for MI:
- Detection of a rise and/or fall of cardiac biomarker values (preferably cardiac troponin) with at least one value above the 99th percentile upper reference limit (URL) and with at least one of the following:[8]
-
- Recent episode of typical ischemic discomfort that either is of new onset or is severe or that exhibits an accelerating pattern of previous stable angina (especially if it has occurred at rest or is within 2 weeks of a previously documented MI)
- Quality: squeezing, grip-like, pressure-like, suffocating, crushing, or heavy
- Location: diffuse, not localized, nor positional, nor affected by movement at substernal area ± radiation to the neck, jaw, epigastrium, shoulders, or arms
- Duration: usually >20 minutes
- Factors that provoke the pain: exertion or emotional stress
- Factors that relieve the pain: rest or sublingual nitroglycerin (usually within minutes)
- Accompanying symptoms: diaphoresis, nausea or syncope
- New or presumably new significant ST-segment–T wave changes or new left bundle branch block (LBBB).
- Development of pathological Q waves in the ECG.
- Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality.
- Identification of an intracoronary thrombus by angiography or autopsy.
- Cardiac death with symptoms suggestive of myocardial ischemia and presumed new ischemic ECG changes or new LBBB, but death occurred before cardiac biomarkers were obtained, or before cardiac biomarker values would be increased.
- Percutaneous coronary intervention related MI is arbitrarily defined by elevation of cardiac troponin (cTn) values (>5 × 99th percentile URL) in patients with normal baseline values (≤99th percentile URL) or a rise of cTn values >20% if the baseline values are elevated and are stable or falling. In addition, either one of the followings is required:
- Symptoms suggestive of myocardial ischemia
- New ischemic ECG changes
- Angiographic findings consistent with a procedural complication
- Imaging demonstration of new loss of viable myocardium or new regional wall motion abnormality
- Stent thrombosis associated with MI when detected by coronary angiography or autopsy in the setting of myocardial ischemia and with a rise and/or fall of cardiac biomarker values with at least one value above the 99th percentile URL.
- Coronary artery bypass grafting related MI is arbitrarily defined by elevation of cardiac biomarker values (>10 × 99th percentile URL) in patients with normal baseline cTn values (≤99th percentile URL). In addition, either one of the followings is required:
- New pathological Q waves or new LBBB
- Angiographic documented new graft or new native coronary artery occlusion
- Imaging evidence of new loss of viable myocardium or new regional wall motion abnormality
Maintenance of Blood Pressure [Return to FIRE]
Norepinephrine
- Suggested Dilution:
- Mix 4 mg of norepinephrine in 250 mL of D5W or D5NS. Avoid dilution in normal saline alone.
- Suggested Regimen:
- Start at a dose of 0.5–1.0 μg/min IV infusion; titrate to maintain SBP at above 90 mm Hg (up to 30–40 μg/min).
- Contraindications
- Norepinephrine should not be given to patients who are hypotensive from blood volume deficits except as an emergency measure to maintain coronary and cerebral artery perfusion until blood volume replacement therapy can be completed.
- Norepinephrine should also not be given to patients with mesenteric or peripheral vascular thrombosis unless it is necessary as a life-saving procedure.
Dopamine
- Suggested Dilution: transfer contents of one or more ampuls or vials by aseptic technique to either 250 mL or 500 mL of one of the following sterile intravenous solutions
- Sodium Chloride Injection
- Dextrose (5%) Injection
- Dextrose (5%) and Sodium Chloride (0.9%) Injection
- 5% Dextrose in 0.45% Sodium Chloride Solution
- Dextrose (5%) in Lactated Ringer’s Solution
- Sodium Lactate (1/6 Molar) Injection
- Lactated Ringer’s Injection
- Suggested Regimen:
- Begin administration of diluted solution at doses of 2–5 μg/kg/minute in patients who are likely to respond to modest increments of heart force and renal perfusion.
- In more seriously ill patients, begin administration of diluted solution at doses of 5 μg/kg/minute and increase gradually, using 5–10 μg/kg/minute increments, up to 20–50 μg/kg/minute as needed.
- If doses of 50 μg/kg/minute are required, it is suggested that urine output be checked frequently. Should the urine flow begin to decrease in the absence of hypotension, reduction of dosage should be considered.
- Treatment of all patients requires constant evaluation of therapy in terms of the blood volume, augmentation of myocardial contractility, and distribution of peripheral perfusion. Dosage should be adjusted according to the patient’s response, with particular attention to diminution of established urine flow rate, increasing tachycardia or development of new dysrhythmias as indices for decreasing or temporarily suspending the dosage.
- Contraindications
- Pheochromocytoma
- Uncorrected tachyarrhythmias or ventricular fibrillation
Dobutamine
- Suggested Dilution: dobutamine injection must be further diluted in an IV container. Dilute 20 mL of dobutamine in at least 50 mL of diluent and dilute 40 mL of dobutamine in at least 100 mL of diluent. Use one of the following intravenous solutions as a diluent:
- Dextrose Injection 5%
- Dextrose 5% and Sodium Chloride 0.45% Injection
- Dextrose 5% and Sodium Chloride 0.9% Injection
- Dextrose Injection 10%, Isolyte® M with 5% Dextrose Injection
- Lactated Ringer’s Injection
- 5% Dextrose in Lactated Ringer’s Injection
- Normosol®-M in D5-W
- 20% Osmitrol® in Water for Injection
- Sodium Chloride Injection 0.9%
- Sodium Lactate Injection
- Suggested Regimen:
- The rate of infusion needed to increase cardiac output usually ranged from 2.5 to 15 mcg/kg/min.
- On rare occasions, infusion rates up to 40 mcg/kg/min have been required to obtain the desired effect.
- Contraindications
- Idiopathic hypertrophic subaortic stenosis
- Hypersensitivity to dobutamine
Nitroglycerin
- Suggested Initial Dilution:
- Nitroglycerin must be diluted in dextrose (5%) injection or sodium chloride (0.9%) injection prior to its infusion. Transfer 50 mg of nitroglycerin into a 500 mL glass bottle of either dextrose (5%) injection or sodium chloride injection (0.9%). This yields a final concentration of 100 μg/mL. Diluting 5 mg nitroglycerin into 100 mL will yield a final concentration of 50 μg/mL.
- Suggested Maintenance Dilution:
- Consider the fluid requirements of the patient as well as the expected duration of infusion in selecting the appropriate dilution of Nitroglycerin Injection.
- The concentration of nitroglycerin should not exceed 400 μg/mL.
- Suggested Regimen:
- Severe hypotension and shock may occur with even small doses of nitroglycerin. This drug should therefore be used with caution in patients who may be volume depleted or who, for whatever reason, are already hypotensive. Hypotension induced by nitroglycerin may be accompanied by paradoxical bradycardia and increased angina pectoris.
- The initial dosage should be 5 μg/min delivered through an infusion pump. Subsequent titration must be adjusted to the clinical situation, with dose increments becoming more cautious as partial response is seen.
- Initial titration should be in 5 μg/min increments, with increases every 3–5 minutes until some response is noted.
- If no response is seen at 20 μg/min, increments of 10 and later 20 μg/min can be used.
- Once a partial blood pressure response is observed, the dose increase should be reduced and the interval between increases should be lengthened.
- Contraindications
- Pericardial tamponade
- Restrictive cardiomyopathy
- Constrictive pericarditis
- Hypersensitivity to nitroglycerin
Nitroprusside
- Suggested Dilution:
- Depending on the desired concentration, the solution containing 50 mg of nitroprusside must be further diluted in 250–1000 mL of sterile 5% dextrose injection.
- Suggested Regimen:
- While the average effective rate in adult and pediatric patients is about 3 μg/kg/min, some patients will become dangerously hypotensive at this rate.
- Nitroprusside can induce essentially unlimited blood pressure reduction, the blood pressure must be continuously monitored, using either a continually reinflated sphygmomanometer or (preferably) an intra-arterial pressure sensor. Special caution should be used in elderly patients, since they may be more sensitive to the hypotensive effects of the drug.
- Infusion of sodium nitroprusside should be started at a very low rate (0.3 μg/kg/min), with upward titration every few minutes until the desired effect is achieved or the maximum recommended infusion rate (10 μg/kg/min) has been reached.
- Contraindications
- Sodium nitroprusside should not be used for the treatment of acute congestive heart failure associated with reduced peripheral vascular resistance such as high-output heart failure that may be seen in endotoxic sepsis.
- Sodium nitroprusside should not be used in the treatment of compensatory hypertension, where the primary hemodynamic lesion is aortic coarctation or arteriovenous shunting.
- Sodium nitroprusside should not be used to produce hypotension during surgery in patients with known inadequate cerebral circulation, or in moribund patients coming to emergency surgery.
- Patients with congenital (Leber’s) optic atrophy or with toxic amblyopia have unusually high cyanide/thiocyanate ratios. These rare conditions are probably associated with defective or absent rhodanase, and sodium nitroprusside should be avoided in these patients.
Optimization of Hemodynamic Status [Return to FIRE]
Preload Optimization
Fluid Challenge Protocol
- Preload optimization involves scrupulous fluid loading, manipulation of PCWP and/or CVP levels, and correction of pulmonary congestion.[5][6][7][20]
- Protocolized fluid administration titrated to hemodynamic and clinical endpoints secures the efficacy of tissue perfusion and oxygenation.[21]
- Four elements of the fluid challenge protocol: type of fluid (T), rate of fluid administration (R), objective (O), and limits (L).[22]
- 1. Type of fluid (T)
- The choice of crystalloid or colloid solution should be made on the basis of the underlying disease, the nature of fluid deficit, the severity of circulatory failure, the serum albumin concentration, and the risk of bleeding.[23]
- There were no significant differences in mortality between saline and albumin infusion for critically ill patients.[24]
- Blood transfusion may be considered in the presence of profound anemia or massive hemorrhage.[21]
- Hyperchloremic acidosis may be associated with the use of isotonic saline solution.[25]
- 2. Rate of fluid administration (R)
- Based on the level of pulmonary capillary wedge pressure or central venous pressure, a volume of 50, 100, or 200 ml of fluid is administered over a 10-minute interval through a peripheral venous catheter.[21]
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- 3. Objective (O)
- Fluid administration should be titrated to reach predetermined clinical endpoints such as resolution of tachycardia or oliguria, improved skin perfusion or level of consciousness, normalization of lactate concentrations, and restoration of adequate blood pressure or ventricular filling pressure.[23]
- 4. Limits (L)
- Fluid administration should be stopped if the safety limits are violated to minimize the risk of developing pulmonary edema.
- Inotropes, vasodilators, or mechanical circulatory device may be required if signs of hypoperfusion persist despite optimal fluid loading.
- Hemodynamic safety limits based on PCWP (the 7–3 rule) or CVP (the 5–2 rule):[21]
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Pulmonary Congestion
- Findings suggestive of cardiogenic pulmonary edema:[26]
- History and clinical manifestations
- Cough
- Dyspnea
- Expectoration of frothy sputum
- Orthopnea
- Paroxysmal nocturnal dyspnea
- Signs and symptoms of heart failure
- Signs and symptoms of hypoxemia
- Signs and symptoms of myocardial ischemia
- Signs and symptoms of valvular dysfunction
- Tachypnea
- Physical examination
- Cool extremities
- Heart murmurs
- Hepatomegaly
- Inspiratory crackles or rhonchi
- Jugular venous distention
- S3 gallop
- Peripheral edema
- Laboratory and hemodynamic findings
- BNP > 500 pg/mL
- PCWP >18 mm Hg
- Radiologic findings
- Central infiltrates with peripheral sparing
- Cephalization of pulmonary vessels
- Enlarged cardiac silhouette
- Enlargement of peribronchovascular spaces
- Increased opacity of acinar areas that coalesce into frank consolidations
- Kerley B lines
- Peribronchial cuffing
- Pleural effusions
- Vascular pedicle width >70 mm
- Radiologic manifestations of pulmonary congestion reflect the extent of elevation in wedge pressure:[5]
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Furosemide
- For acute pulmonary edema, the initial dose is 40 mg injected slowly intravenously (over 1 to 2 minutes).
- If a satisfactory response does not occur within 1 hour, the dose may be increased to 80 mg injected slowly intravenously (over 1 to 2 minutes).
- Contraindications
Morphine
- Morphine may cause respiratory depression or exacerbate hypotension in volume-depleted patients.
- Morphine may be used adjunctively in the treatment of acute pulmonary edema at a dose of 2–4 mg (slow IV injection over 1–5 minutes) every 5–30 minutes as needed.
- Contraindications
- Hypersensitivity to morphine sulfate is one of the contraindications to its use.
- Morphine should not be used in convulsive states, such as those occurring in status epilepticus, tetanus, and strychnine poisoning.
- Morphine is also contraindicated in the following conditions: respiratory insufficiency or depression; bronchial asthma; heart failure secondary to chronic lung disease; cardiac arrhythmias; increased intracranial or cerebrospinal pressure; head injuries; brain tumor; acute alcoholism; and delirium tremens.
Afterload Optimization
Nitroglycerin
- Suggested Initial Dilution:
- Nitroglycerin must be diluted in dextrose (5%) injection or sodium chloride (0.9%) injection prior to its infusion. Transfer 50 mg of nitroglycerin into a 500 mL glass bottle of either dextrose (5%) injection or sodium chloride injection (0.9%). This yields a final concentration of 100 μg/mL. Diluting 5 mg nitroglycerin into 100 mL will yield a final concentration of 50 μg/mL.
- Suggested Maintenance Dilution:
- Consider the fluid requirements of the patient as well as the expected duration of infusion in selecting the appropriate dilution of Nitroglycerin Injection.
- The concentration of nitroglycerin should not exceed 400 μg/mL.
- Suggested Regimen:
- Severe hypotension and shock may occur with even small doses of nitroglycerin. This drug should therefore be used with caution in patients who may be volume depleted or who, for whatever reason, are already hypotensive. Hypotension induced by nitroglycerin may be accompanied by paradoxical bradycardia and increased angina pectoris.
- The initial dosage should be 5 μg/min delivered through an infusion pump. Subsequent titration must be adjusted to the clinical situation, with dose increments becoming more cautious as partial response is seen.
- Initial titration should be in 5 μg/min increments, with increases every 3–5 minutes until some response is noted.
- If no response is seen at 20 μg/min, increments of 10 and later 20 μg/min can be used.
- Once a partial blood pressure response is observed, the dose increase should be reduced and the interval between increases should be lengthened.
- Contraindications
- Pericardial tamponade
- Restrictive cardiomyopathy
- Constrictive pericarditis
- Hypersensitivity to nitroglycerin
Nitroprusside
- Suggested Dilution:
- Depending on the desired concentration, the solution containing 50 mg of nitroprusside must be further diluted in 250–1000 mL of sterile 5% dextrose injection.
- Suggested Regimen:
- While the average effective rate in adult and pediatric patients is about 3 μg/kg/min, some patients will become dangerously hypotensive at this rate.
- Nitroprusside can induce essentially unlimited blood pressure reduction, the blood pressure must be continuously monitored, using either a continually reinflated sphygmomanometer or (preferably) an intra-arterial pressure sensor. Special caution should be used in elderly patients, since they may be more sensitive to the hypotensive effects of the drug.
- Infusion of sodium nitroprusside should be started at a very low rate (0.3 μg/kg/min), with upward titration every few minutes until the desired effect is achieved or the maximum recommended infusion rate (10 μg/kg/min) has been reached.
- Contraindications
- Sodium nitroprusside should not be used for the treatment of acute congestive heart failure associated with reduced peripheral vascular resistance such as high-output heart failure that may be seen in endotoxic sepsis.
- Sodium nitroprusside should not be used in the treatment of compensatory hypertension, where the primary hemodynamic lesion is aortic coarctation or arteriovenous shunting.
- Sodium nitroprusside should not be used to produce hypotension during surgery in patients with known inadequate cerebral circulation, or in moribund patients coming to emergency surgery.
- Patients with congenital (Leber’s) optic atrophy or with toxic amblyopia have unusually high cyanide/thiocyanate ratios. These rare conditions are probably associated with defective or absent rhodanase, and sodium nitroprusside should be avoided in these patients.
Norepinephrine
- Suggested Dilution:
- Mix 4 mg of norepinephrine in 250 mL of D5W or D5NS. Avoid dilution in normal saline alone.
- Suggested Regimen:
- Start at a dose of 0.5–1.0 μg/min IV infusion; titrate to maintain SBP at above 90 mm Hg (up to 30–40 μg/min).
- Contraindications
- Norepinephrine should not be given to patients who are hypotensive from blood volume deficits except as an emergency measure to maintain coronary and cerebral artery perfusion until blood volume replacement therapy can be completed.
- Norepinephrine should also not be given to patients with mesenteric or peripheral vascular thrombosis unless it is necessary as a life-saving procedure.
Dopamine
- Suggested Dilution: transfer contents of one or more ampuls or vials by aseptic technique to either 250 mL or 500 mL of one of the following sterile intravenous solutions
- Sodium Chloride Injection
- Dextrose (5%) Injection
- Dextrose (5%) and Sodium Chloride (0.9%) Injection
- 5% Dextrose in 0.45% Sodium Chloride Solution
- Dextrose (5%) in Lactated Ringer’s Solution
- Sodium Lactate (1/6 Molar) Injection
- Lactated Ringer’s Injection
- Suggested Regimen:
- Begin administration of diluted solution at doses of 2–5 μg/kg/minute in patients who are likely to respond to modest increments of heart force and renal perfusion.
- In more seriously ill patients, begin administration of diluted solution at doses of 5 μg/kg/minute and increase gradually, using 5–10 μg/kg/minute increments, up to 20–50 μg/kg/minute as needed.
- If doses of 50 μg/kg/minute are required, it is suggested that urine output be checked frequently. Should the urine flow begin to decrease in the absence of hypotension, reduction of dosage should be considered.
- Treatment of all patients requires constant evaluation of therapy in terms of the blood volume, augmentation of myocardial contractility, and distribution of peripheral perfusion. Dosage should be adjusted according to the patient’s response, with particular attention to diminution of established urine flow rate, increasing tachycardia or development of new dysrhythmias as indices for decreasing or temporarily suspending the dosage.
- Contraindications
- Pheochromocytoma
- Uncorrected tachyarrhythmias or ventricular fibrillation
Phenylephrine
- Suggested Dilution:
- Add 10 mg of the drug (1 mL of 1 percent solution) to 500 mL of Dextrose Injection or Sodium Chloride Injection (providing a 1:50,000 solution).
- Suggested Regimen:
- To raise the blood pressure rapidly, start the infusion at about 100 μg to 180 μg per minute (based on 20 drops per mL this would be 100 to 180 drops per minute).
- When the blood pressure is stabilized (at a low normal level for the individual), a maintenance rate of 40 μg to 60 μg per minute usually suffices (based on 20 drops per mL this would be 40 to 60 drops per minute).
- If a prompt initial pressor response is not obtained, additional increments of phenylephrine (10 mg or more) are added to the infusion bottle. The rate of flow is then adjusted until the desired blood pressure level is obtained.
- Contraindications
- Severe hypertension
- Ventricular tachycardia
- Hypersensitivity to phenylephrine
Vasopressin
Cardiac Output Optimization
Dobutamine
- Suggested Dilution: dobutamine injection must be further diluted in an IV container. Dilute 20 mL of dobutamine in at least 50 mL of diluent and dilute 40 mL of dobutamine in at least 100 mL of diluent. Use one of the following intravenous solutions as a diluent:
- Dextrose Injection 5%
- Dextrose 5% and Sodium Chloride 0.45% Injection
- Dextrose 5% and Sodium Chloride 0.9% Injection
- Dextrose Injection 10%, Isolyte® M with 5% Dextrose Injection
- Lactated Ringer’s Injection
- 5% Dextrose in Lactated Ringer’s Injection
- Normosol®-M in D5-W
- 20% Osmitrol® in Water for Injection
- Sodium Chloride Injection 0.9%
- Sodium Lactate Injection
- Suggested Regimen:
- The rate of infusion needed to increase cardiac output usually ranged from 2.5–15 mcg/kg/min.
- On rare occasions, infusion rates up to 40 mcg/kg/min have been required to obtain the desired effect.
- Contraindications
- Idiopathic hypertrophic subaortic stenosis
- Hypersensitivity to dobutamine
Milrinone
- Suggested Regimen:
- Milrinone should be administered with a loading dose followed by a continuous infusion (maintenance dose).
- Loading dose: 50 μg/kg (slowly over 10 minutes)
- Maintenance dose: 0.50 μg/kg/min (0.375–0.75 μg/kg/min)
- Contraindications
- Hypersensitivity to milrinone
Do's
Don'ts
References
- ↑ 1.0 1.1 1.2 Califf, RM.; Bengtson, JR. (1994). "Cardiogenic shock". N Engl J Med. 330 (24): 1724–30. doi:10.1056/NEJM199406163302406. PMID 8190135. Unknown parameter
|month=
ignored (help) - ↑ Robin, E.; Costecalde, M.; Lebuffe, G.; Vallet, B. (2006). "Clinical relevance of data from the pulmonary artery catheter". Crit Care. 10 Suppl 3: S3. doi:10.1186/cc4830. PMID 17164015.
- ↑ Hollenberg, SM.; Kavinsky, CJ.; Parrillo, JE. (1999). "Cardiogenic shock". Ann Intern Med. 131 (1): 47–59. PMID 10391815. Unknown parameter
|month=
ignored (help) - ↑ 4.0 4.1 Goldberg, RJ.; Gore, JM.; Alpert, JS.; Osganian, V.; de Groot, J.; Bade, J.; Chen, Z.; Frid, D.; Dalen, JE. (1991). "Cardiogenic shock after acute myocardial infarction. Incidence and mortality from a community-wide perspective, 1975 to 1988". N Engl J Med. 325 (16): 1117–22. doi:10.1056/NEJM199110173251601. PMID 1891019. Unknown parameter
|month=
ignored (help) - ↑ 5.0 5.1 5.2 Forrester, JS.; Diamond, G.; Chatterjee, K.; Swan, HJ. (1976). "Medical therapy of acute myocardial infarction by application of hemodynamic subsets (first of two parts)". N Engl J Med. 295 (24): 1356–62. doi:10.1056/NEJM197612092952406. PMID 790191. Unknown parameter
|month=
ignored (help) - ↑ 6.0 6.1 Forrester, JS.; Diamond, G.; Chatterjee, K.; Swan, HJ. (1976). "Medical therapy of acute myocardial infarction by application of hemodynamic subsets (second of two parts)". N Engl J Med. 295 (25): 1404–13. doi:10.1056/NEJM197612162952505. PMID 790194. Unknown parameter
|month=
ignored (help) - ↑ 7.0 7.1 Reynolds, HR.; Hochman, JS. (2008). "Cardiogenic shock: current concepts and improving outcomes". Circulation. 117 (5): 686–97. doi:10.1161/CIRCULATIONAHA.106.613596. PMID 18250279. Unknown parameter
|month=
ignored (help) - ↑ Thygesen, K.; Alpert, JS.; Jaffe, AS.; Simoons, ML.; Chaitman, BR.; White, HD.; Thygesen, K.; Alpert, JS.; White, HD. (2012). "Third universal definition of myocardial infarction". J Am Coll Cardiol. 60 (16): 1581–98. doi:10.1016/j.jacc.2012.08.001. PMID 22958960. Unknown parameter
|month=
ignored (help) - ↑ Braunwald, E.; Antman, EM.; Beasley, JW.; Califf, RM.; Cheitlin, MD.; Hochman, JS.; Jones, RH.; Kereiakes, D.; Kupersmith, J. (2000). "ACC/AHA guidelines for the management of patients with unstable angina and non-ST-segment elevation myocardial infarction. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on the Management of Patients With Unstable Angina)". J Am Coll Cardiol. 36 (3): 970–1062. PMID 10987629. Unknown parameter
|month=
ignored (help) - ↑ Anderson, JL.; Adams, CD.; Antman, EM.; Bridges, CR.; Califf, RM.; Casey, DE.; Chavey, WE.; Fesmire, FM.; Hochman, JS. (2011). "2011 ACCF/AHA Focused Update Incorporated Into the ACC/AHA 2007 Guidelines for the Management of Patients With Unstable Angina/Non-ST-Elevation Myocardial Infarction: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines". Circulation. 123 (18): e426–579. doi:10.1161/CIR.0b013e318212bb8b. PMID 21444888. Unknown parameter
|month=
ignored (help) - ↑ Gibbons, RJ.; Abrams, J.; Chatterjee, K.; Daley, J.; Deedwania, PC.; Douglas, JS.; Ferguson, TB.; Fihn, SD.; Fraker, TD. (2003). "ACC/AHA 2002 guideline update for the management of patients with chronic stable angina--summary article: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on the Management of Patients With Chronic Stable Angina)". Circulation. 107 (1): 149–58. PMID 12515758. Unknown parameter
|month=
ignored (help) - ↑ 12.00 12.01 12.02 12.03 12.04 12.05 12.06 12.07 12.08 12.09 12.10 12.11 Handbook of Emergency Cardiovascular Care for Healthcare Providers. ISBN 1616690003.
- ↑ 13.0 13.1 13.2 13.3 13.4 13.5 13.6 13.7 13.8 13.9 "Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Part 7: the era of reperfusion: section 1: acute coronary syndromes (acute myocardial infarction). The American Heart Association in collaboration with the International Liaison Committee on Resuscitation". Circulation. 102 (8 Suppl): I172–203. 2000. PMID 10966673. Unknown parameter
|month=
ignored (help) - ↑ 14.0 14.1 "NOREPINEPHRINE BITARTRATE INJECTION".
- ↑ 15.0 15.1 "DOPAMINE HCL INJECTION, SOLUTION [AMERICAN REGENT, INC.]".
- ↑ 16.0 16.1 "DOBUTAMINE (DOBUTAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]".
- ↑ 17.0 17.1 "NITROGLYCERIN INJECTION, SOLUTION [AMERICAN REGENT, INC.]".
- ↑ 18.0 18.1 "NITROPRESS (SODIUM NITROPRUSSIDE) INJECTION, SOLUTION, CONCENTRATE [HOSPIRA, INC.]".
- ↑ 19.0 19.1 Chatterjee, K.; Parmley, WW.; Ganz, W.; Forrester, J.; Walinsky, P.; Crexells, C.; Swan, HJ. (1973). "Hemodynamic and metabolic responses to vasodilator therapy in acute myocardial infarction". Circulation. 48 (6): 1183–93. PMID 4762476. Unknown parameter
|month=
ignored (help) - ↑ Crexells, C.; Chatterjee, K.; Forrester, JS.; Dikshit, K.; Swan, HJ. (1973). "Optimal level of filling pressure in the left side of the heart in acute myocardial infarction". N Engl J Med. 289 (24): 1263–6. doi:10.1056/NEJM197312132892401. PMID 4749545. Unknown parameter
|month=
ignored (help) - ↑ 21.0 21.1 21.2 21.3 Weil, MH.; Henning, RJ. "New concepts in the diagnosis and fluid treatment of circulatory shock. Thirteenth annual Becton, Dickinson and Company Oscar Schwidetsky Memorial Lecture". Anesth Analg. 58 (2): 124–32. PMID 571235.
- ↑ Vincent, JL. (2011). "Let's give some fluid and see what happens versus the mini-fluid challenge". Anesthesiology. 115 (3): 455–6. doi:10.1097/ALN.0b013e318229a521. PMID 21792055. Unknown parameter
|month=
ignored (help) - ↑ 23.0 23.1 Vincent, JL.; Weil, MH. (2006). "Fluid challenge revisited". Crit Care Med. 34 (5): 1333–7. doi:10.1097/01.CCM.0000214677.76535.A5. PMID 16557164. Unknown parameter
|month=
ignored (help) - ↑ Finfer, S.; Bellomo, R.; Boyce, N.; French, J.; Myburgh, J.; Norton, R. (2004). "A comparison of albumin and saline for fluid resuscitation in the intensive care unit". N Engl J Med. 350 (22): 2247–56. doi:10.1056/NEJMoa040232. PMID 15163774. Unknown parameter
|month=
ignored (help) - ↑ Scheingraber, S.; Rehm, M.; Sehmisch, C.; Finsterer, U. (1999). "Rapid saline infusion produces hyperchloremic acidosis in patients undergoing gynecologic surgery". Anesthesiology. 90 (5): 1265–70. PMID 10319771. Unknown parameter
|month=
ignored (help) - ↑ Ware, LB.; Matthay, MA. (2005). "Clinical practice. Acute pulmonary edema". N Engl J Med. 353 (26): 2788–96. doi:10.1056/NEJMcp052699. PMID 16382065. Unknown parameter
|month=
ignored (help) - ↑ "FUROSEMIDE INJECTION [AMERICAN REGENT, INC.]".
- ↑ "MORPHINE SULFATE INJECTION, SOLUTION, CONCENTRATE".
- ↑ O'Connor, RE.; Brady, W.; Brooks, SC.; Diercks, D.; Egan, J.; Ghaemmaghami, C.; Menon, V.; O'Neil, BJ.; Travers, AH. (2010). "Part 10: acute coronary syndromes: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care". Circulation. 122 (18 Suppl 3): S787–817. doi:10.1161/CIRCULATIONAHA.110.971028. PMID 20956226. Unknown parameter
|month=
ignored (help) - ↑ 30.0 30.1 30.2 Hollenberg, SM. (2011). "Vasoactive drugs in circulatory shock". Am J Respir Crit Care Med. 183 (7): 847–55. doi:10.1164/rccm.201006-0972CI. PMID 21097695. Unknown parameter
|month=
ignored (help) - ↑ "PHENYLEPHRINE HYDROCHLORIDE INJECTION [BAXTER HEALTHCARE CORPORATION]".
- ↑ "PITRESSIN (VASOPRESSIN) INJECTION [JHP PHARMACEUTICALS LLC]".
- ↑ "MILRINONE LACTATE (MILRINONE LACTATE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]".