Sandbox/MS: Difference between revisions
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D01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Administer one of the following antiplatelet agents:'''<br> | |||
❑ [[Clopidogrel|<span style="color:white;">Clopidogrel </span>]]<br> | |||
:❑ Loading dose (300 mg)<br> | |||
:❑ Maintenance dose for up to 12 months (75 mg)<br> | |||
❑ [[Ticagrelor|<span style="color:white;">Ticagrelor </span>]] | |||
:❑ Loading dose (180 mg)<br> | |||
:❑ Maintenance dose for up to 12 months (90 mg twice daily)</div> | |||
|D02= <div style="float: left; text-align: left; width: 20em; padding:1em;"> | |||
'''Administer one of the following antiplatelet agents:'''<br> | |||
'''Before [[PCI|<span style="color:white;">PCI </span>]]'''<br> | |||
❑ [[P2Y12|<span style="color:white;">P2Y12 </span>]]receptor inhibitors <br> | |||
:❑ [[Clopidogrel|<span style="color:white;">Clopidogrel </span>]] (600 mg), or<br> | |||
:❑ [[Ticagrelor|<span style="color:white;">Ticagrelor </span>]](180 mg), or <br> | |||
❑ IV [[GP IIb/IIIa|<span style="color:white;">GP IIb/IIIa </span>]] inhibitors <br> | |||
:❑ [[Eptifibatide|<span style="color:white;">Eptifibatide </span>]]<br> | |||
::❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes<br> | |||
::❑ Maintenance dose 2 mcg/kg/min, or <br> | |||
:❑ [[Tirofiban|<span style="color:white;">Tirofiban </span>]]<br> | |||
::❑ Loading dose 25 mcg/kg<br> | |||
::❑ Maintenance dose 0.15 mcg/kg/min<br> | |||
'''At the time of [[PCI|<span style="color:white;">PCI </span>]]'''<br> | |||
❑ [[P2Y12|<span style="color:white;">P2Y12 </span>]] receptor inhibitors <br> | |||
:❑ [[Clopidogrel|<span style="color:white;">Clopidogrel </span>]] (600 mg), or<br> | |||
:❑ [[Ticagrelor|<span style="color:white;">Ticagrelor </span>]] (180 mg), or <br> | |||
:❑ Prasugrel (60 mg)<br> | |||
❑ IV [[GP IIb/IIIa|<span style="color:white;">GP IIb/IIIa </span>]] inhibitors <br> | |||
:❑ [[Eptifibatide|<span style="color:white;">Eptifibatide </span>]]<br> | |||
::❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes<br> | |||
::❑ Maintenance dose 2 mcg/kg/min, or <br> | |||
:❑ [[Tirofiban|<span style="color:white;">Tirofiban <br> | |||
::❑ Loading dose 25 mcg/kg<br> | |||
::❑ Maintenance dose 0.15 mcg/kg/min<br></div> </div> | |||
Revision as of 20:51, 9 May 2014
Identify cardinal findings of Unstable angina/ NSTEMI : ❑ Chest pain or chest discomfort
❑ Characteristic ECG changes consistent with unstable angina/ NSTEMI
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Rule out life threatening alternative diagnoses: ❑ Aortic dissection (suggestive findings: vomiting, subcutaneous emphysema) | |||||||||||||||||||||||||
Begin initial treatment: ❑ Administer 162 - 325 mg of non enteric aspirin
❑ Administer 2-4 L/min oxygen via nasal cannula when saturation <90%
❑ Administer beta-blockers (unless contraindicated) and titrate to the heart rate and blood pressure
❑ Administer sublingual nitroglycerin 0.4 mg every 5 minutes for a total of 3 doses
❑ Administer 80 mg atorvastatin | |||||||||||||||||||||||||
Determine if the patient has any of the following indications that require immediate angiography and revascularization:
❑ Hemodynamic instability or cardiogenic shock | |||||||||||||||||||||||||
YES | NO | ||||||||||||||||||||||||
Proceed to angiography | Low risk Initial conservative strategy | High risk Initial invasive strategy | |||||||||||||||||||||||
{{{ D01 }}} | {{{ D02 }}} | ||||||||||||||||||||||||
D01=
- ❑ Loading dose (300 mg)
- ❑ Maintenance dose for up to 12 months (75 mg)
- ❑ Loading dose (180 mg)
- ❑ Maintenance dose for up to 12 months (90 mg twice daily)
|D02=
Administer one of the following antiplatelet agents:
Before PCI
❑ P2Y12 receptor inhibitors
- ❑ Clopidogrel (600 mg), or
- ❑ Ticagrelor (180 mg), or
❑ IV GP IIb/IIIa inhibitors
- ❑ Eptifibatide
- ❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes
- ❑ Maintenance dose 2 mcg/kg/min, or
- ❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes
- ❑ Tirofiban
- ❑ Loading dose 25 mcg/kg
- ❑ Maintenance dose 0.15 mcg/kg/min
- ❑ Loading dose 25 mcg/kg
At the time of PCI
❑ P2Y12 receptor inhibitors
- ❑ Clopidogrel (600 mg), or
- ❑ Ticagrelor (180 mg), or
- ❑ Prasugrel (60 mg)
❑ IV GP IIb/IIIa inhibitors
- ❑ Eptifibatide
- ❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes
- ❑ Maintenance dose 2 mcg/kg/min, or
- ❑ Loading dose 180 mcg/kg IV bolus followed by another bolus after 10 minutes
- ❑ [[Tirofiban|Tirofiban
- ❑ Loading dose 25 mcg/kg
- ❑ Maintenance dose 0.15 mcg/kg/min
- ❑ Loading dose 25 mcg/kg
Unstable angina/ NSTEMI Resident Survival Guide Microchapters |
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Overview |
Causes |
FIRE |
Diagnosis |
Treatment |
Do's |
Don'ts |
Examine the patient: Vitals
❑ Pulse oximetry
Neck ❑ Sensation (e.g., by touch, pin, vibration, proprioception) | |||||||||||||||||||||||
Identify cardinal signs and symptoms that increase the pretest probability of hypertensive crisis: ❑ Acute severe elevation in blood pressure (usually systolic blood pressure greater >160 mm Hg or diastolic blood pressure >100 mm Hg) with or without end-organ damage like
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With evidence of end-organ damage | Without evidence of end-organ damage | ||||||||||||||||||||||||||||||||||||||||
Hypertensive emergency | Hypertensive urgency | ||||||||||||||||||||||||||||||||||||||||
Identify alarming signs and symptoms: ❑ Tachycardia ❑ Hypotension ❑ Loss of consciousness ❑ Tachypnea | ❑ Consider admission for observation or ❑ Consider treatment on outpatient basis | ||||||||||||||||||||||||||||||||||||||||
Identify cardinal findings that suggest any of the following: | |||||||||||||||||||||||
Measure the blood pressure | |||||||||||||||||||||||
BP ≥ 180/120 | BP < 180/120 | ||||||||||||||||||||||
Does the patient have any evidence of end organ damage? | |||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||
Identify alarming signs and symptoms: ❑ Tachycardia ❑ Hypotension ❑ Loss of consciousness ❑ Tachypnea | ❑ Consider admission for observation ❑ Consider treatment as an outpatient | ||||||||||||||||||||||
Stage A | Stage B | Stage C | Stage D |
❑ No symptoms ❑ Patient at risk of developing mitral stenosis ❑ Mild valve doming during diastole ❑ Normal transmitral flow velocity |
❑ No symptoms ❑ Progressive mitral stenosis ❑ Valve area > 1.5 cm² ❑ Rheumatic valve changes with commissural fusion and diastolic doming of the mitral valve leaflets ❑ Increased transmitral flow velocities ❑ Diastolic pressure half-time < 150 ms ❑ Mild to moderate left atrial enlargement ❑ Normal pulmonary pressure at rest |
❑ Asymptomatic severe mitral stenosis ❑ Valve area ≤ 1.5 cm² (≤ 1 cm² in severe mitral stenosis) ❑ Rheumatic valve changes with commissural fusion and diastolic doming of the mitral valve leaflets ❑ Diastolic pressure half-time ≥ 150 ms (≥ 220 ms with very severe mitral stenosis) ❑ Elevated pulmonary artery systolic pressure > 30 mmHg ❑ Severe left atrial enlargement |
❑ Symptomatic severe mitral stenosis ❑ Valve area ≤ 1.5 cm² (≤ 1 cm² in severe mitral stenosis) ❑ Rheumatic valve changes with commissural fusion and diastolic doming of the mitral valve leaflets ❑ Diastolic pressure half-time ≥ 150 ms (≥ 220 ms with very severe mitral stenosis) ❑ Elevated pulmonary artery systolic pressure > 30 mmHg ❑ Severe left atrial enlargement |
Classify mitral stenosis based on TTE: ❑ Valve anatomy ❑ Valve hemodynamics gradient ❑ Hemodynamic consequences | |||||||||||||||||||||||||||||||||||||
Stage A | Stage B | Stage C | Stage D | ||||||||||||||||||||||||||||||||||
❑ Yearly follow up is recommended with history and physical examination in asymptomatic patients with mild MS ❑ For mild MS repeat echocardiography every 3-5 years[1] ❑ For moderate MS repeat echocardiography every 1-2 years[1] ❑ The onset of symptoms require medical therapy and re-evaluation of the stage as the patient may also need intervention in moderate and severe disease | |||||||||||||||||||||||||||||||||||||
The presence of symptoms is an indication for intervention Indications for pharmacotherapy: No longer require antimicrobial prophylaxis | |||||||||||||||||||||||||||||||||||||
Classify mitral stenosis based on the following findings on TTE: ❑ Valve anatomy ❑ Valve hemodynamics gradient ❑ Hemodynamic consequences | |||||||||||||||||||||||||||||||||||||
Stage A ❑ Patient at risk of developing mitral stenosis ❑ Mild valve doming during diastole ❑ Normal transmitral flow velocity | Stage B ❑ Progressive mitral stenosis ❑ Valve area > 1.5 cm² ❑ Rheumatic valve changes with commissural fusion and diastolic doming of the mitral valve leaflets ❑ Increased transmitral flow velocities ❑ Diastolic pressure half-time < 150 ms ❑ Mild to moderate left atrial enlargement ❑ Normal pulmonary pressure at rest | Stage C ❑ Asymptomatic severe mitral stenosis ❑ Valve area ≤ 1.5 cm² (≤ 1 cm² in severe mitral stenosis) ❑ Rheumatic valve changes with commissural fusion and diastolic doming of the mitral valve leaflets ❑ Diastolic pressure half-time ≥ 150 ms (≥ 220 ms with very severe mitral stenosis) ❑ Elevated pulmonary artery systolic pressure > 30 mmHg ❑ Severe left atrial enlargement | Stage D ❑ Symptomatic severe mitral stenosis ❑ Valve area ≤ 1.5 cm² (≤ 1 cm² in severe mitral stenosis) ❑ Rheumatic valve changes with commissural fusion and diastolic doming of the mitral valve leaflets ❑ Diastolic pressure half-time ≥ 150 ms (≥ 220 ms with very severe mitral stenosis) ❑ Elevated pulmonary artery systolic pressure > 30 mmHg ❑ Severe left atrial enlargement | ||||||||||||||||||||||||||||||||||
Identify cardinal findings that increase the pretest probability of mitral stenosis ❑ Mid diastolic murmur
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Does the patient have any of the following findings of decompensated mitral stenosis that require urgent management? ❑ Tachycardia ❑ Hypotension ❑ Severe dyspnea ❑ Loss of consciousness ❑ Chest pain | |||||||||||||||||||||||||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||||||||||||||||||||||||
What is the complication of mitral stenosis that is causing decompensation? | |||||||||||||||||||||||||||||||||||||||||||||
❑ Suspect in case of:
| ❑ Suspect in case of palpitations ❑ Order an ECG immediately looking for | ❑ Suspect in case of:
| Pulmonary hypertension ± right sided heart failure ❑ Suspect in case of severe dyspnea ❑ Increased jugular venous pressure immediately ❑ Hepatomegaly ± pulsatile liver | ||||||||||||||||||||||||||||||||||||||||||
Summary of Recommendations for Mitral Stenosis Intervention
- PMBC is recommended for symptomatic patients with sever mitral stenosis (MVA ≤ 1.5 cm², stage D) and favorabale valve morphology in the absence of contraindications (Class I, level of evidence A)
- Mitral valve surgery is indicated in severely symptomatic patients (NYHA class III/IV) with severe mitral stenosis (MVA ≤ 1.5 cm², stage D) who are not high risk for surgery and who are not candidates for or failed previous PMBC (Class I, level of evidence B)
- Concomitant mitral valve surgery is indicated for patients with severe mitral stenosis (MVA ≤ 1.5 cm², stage C or D) undergoing other cardiac surgery (Class I, level of evidence C)
- PMBC is reasonable for asymptomatic patients with very severe mitral stenosis (MVA ≤ 1 cm², stage C) and favourable valve morphology in the absence of contraindications (Class IIa, level of evidence C)
- Mitral valve surgery is reasonable for severely symptomatic patients with severe mitral stenosis (MVA ≤ 1.5 cm², stage D) provided that there is other operative indications (Class IIa, level of evidence C)
- PMBC may be considered for asymptomatic patients with mitral stenosis (MVA ≤ 1.5 cm², stage C) and favourable valve morphology who have new onset of atrial fibrillation in the absence of contraindications (Class IIb, level of evidence C)
- PMBC may be considered for symptomatic patients with MVA > 1.5 cm² if there is evidence of hemodynamically significant mitral stenosis during exercise (Class IIb, level of evidence C)
- PMBC may be considered for severely symptomatic patients (NYHA III/IV) with severe mitral stenosis (MVA ≤ 1.5 cm², stage D) who have suboptimal valve anatomy and aren't candidates for surgery or at high risk for surgery (Class IIb, level of evidence C)
- Concomitant mitral valve surgery may be considered for patients with moderate mitral stenosis (MVA 1.6 - 2.0 cm²) undergoing other cardiac surgery (Class IIb, level of evidence C)
- Mitral valve surgery and excision of the left atrial appendage may be considered for patients with severe mitral stenosis (MVA ≤ 1.5 cm², stage C and D) who have recurrent embolic events while receiving adequate anticoagulation (Class IIb, level of evidence C)