Shock resident survival guide: Difference between revisions
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==Complete Diagnostic Approach== | ==Complete Diagnostic Approach== |
Revision as of 03:51, 16 April 2014
Shock Resident Survival Guide |
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Overview |
Causes |
FIRE |
Diagnosis |
Do's |
Don'ts |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, MBChB. [2]
Overview
Shock is the syndrome of circulatory failure that results in inadequate cellular oxygen utilization. The diagnosis of shock is based on clinical signs (eg, altered mental status, oliguria, cold and clammy skin) and biochemical abnormalities (eg, hyperlactatemia) indicative of tissue hypoperfusion.[1] Management of shock consists of stabilization of the hemodynamic status and correction of the underlying cause.
Causes
Life Threatening Causes
Shock is a life-threatening condition and must be treated as such irrespective of the underlying cause.
Common Causes
Cardiogenic Shock
- Arrhythmic
- Mechanical
- Myopathic
- Pharmacologic
Obstructive Shock
- Decreased cardiac compliance
- Decreased ventricular preload
- Increased ventricular afterload
Hypovolemic Shock
- Fluid depletion
- Hemorrhage
Distributive Shock
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.
Boxes in the salmon color 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; MVO2, mixed venous oxygen saturation; 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; SMA-7, sequential multiple analysis-7.
Does the patient have cardinal findings that increase the pretest probability of shock?
❑ Arterial hypotension ❑ Signs of hypoperfusion | |||||||||||||||||||||||||||||||||||
YES | NO | ||||||||||||||||||||||||||||||||||
Ventilate—Infuse—Pump (VIP) ❑ Oxygen ± mechanical ventilation ❑ Normal saline 300–500 mL over 20–30 min ❑ ± Norepinephrine 0.1–2.0 μg/kg/min | Consider other causes (eg, chronic hypotension, syncope) | ||||||||||||||||||||||||||||||||||
Immediate Goals | |||||||||||||||||||||||||||||||||||
Initial investigation | |||||||||||||||||||||||||||||||||||
History of trauma? | YES, then consider
❑ Cardiac injury ❑ Cardiac tamponade ❑ Hemorrhagic shock ❑ Tension pneumothorax | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Evidence of gastrointestinal hemorrhage, vomiting, diarrhea? | YES, then consider and manage as hypovolemic shock | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Fever or hypothermia? | YES, then consider and manage as septic shock | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Ischemic findings on ECG and/or chest pain with coronary risk factors? | YES, then consider and manage as cardiogenic shock | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Unexplained bradycardia? | YES, then consider
❑ Negative inotropic agents ❑ Hypothyroidism ❑ Steroid withdrawal ❑ Adrenal crisis | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Unexplained hypoxemia? | YES, then consider acute pulmonary embolism | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Abdominal or low back pain? | YES, then consider abdominal processes and surgical consultation | ||||||||||||||||||||||||||||||||||
NO, then proceed to the next step | |||||||||||||||||||||||||||||||||||
Wheezing with hives or skin flushing? | YES, then consider abdominal processes and surgical consultation | ||||||||||||||||||||||||||||||||||
NO, then proceed to complete diagnostic approach below | |||||||||||||||||||||||||||||||||||
Complete Diagnostic Approach
History Review all medications
Findings suggestive of hypovolemic shock
Findings suggestive of cardiogenic shock
Findings suggestive of distributive shock
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Physical Examination Vital signs
Mental status
Cutaneous
Neck
Cardiovascular
Pulmonary
Abdominal
Rectal
Extremities
Genitals
Neurologic | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Laboratory Findings Complete blood count
Electrolytes
Coagulation panel (PT, PTT, INR, etc.)
Cardiac markers
Liver function
Renal function
Lactate
Amylase and lipase
Arterial blood gas
Cultures
Nasogastric aspirate
Pregnancy test
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ECG Findings ❑ ST segment elevation or depression, pathologic Q waves, hyperacute or negative T waves ❑ Sinus tachycardia with S1Q3T3 pattern ❑ Low QRS voltage with electrical alternans ❑ QS deflections in precordial leads with right axis deviation and low QRS voltage ❑ Bradyarrhythmias or tachyarrhythmias Radiographic Findings ❑ Chest radiograph may aid in establishing diagnosis in the following conditions:
❑ CT scan may aid in directing management in the following conditions: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hemodynamic Profiles and Echocardiography Findings
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Treatment
Management of shock consists of stabilization of the hemodynamic status and correction of the underlying cause once it is identified.
Cardiogenic shock
Obstructive shock
Distributive shock
Hypovolemic shock
Do's
- Initial Management
- Resuscitation should be initiated while investigation is ongoing. Correct the cause of shock immediately once it is identified.
- The VIP (Ventilate-Infuse-Pump) approach is useful for ensuring an orderly sequence of therapeutic-diagnostic maneuvers.[2]
- Ventilate
- Endotracheal intubation should be performed in patients with severe dyspnea, hypoxemia, or persistent or worsening acidemia (pH <7.30).
- Infuse
- A central venous catheter should be placed for the infusion of fluids and vasoactive agents and to guide fluid therapy.
- A pulmonary artery catheter should be inserted for monitoring of blood pressure and blood sampling unless shock is rapidly reversed. (Indications)
- An infusion of 300–500 ml of crystalloid fluid is usually administered during a period of 20–30 minutes.
- End point of fluid therapy can be defined as a central venous pressure (CVP) of a few millimeters of mercury (mmHg) above the baseline to prevent fluid overload.[3]
- Pump
- Vasopressors are indicated in hypotension that is severe or refractory to fluid challenge.
- Norepinephrine (0.1–2.0 μg/kg/min IV) is the first choice of vasopressor, while epinephrine (0.1–0.5 μg/kg/min IV) is reserved for severe hypotension as the second-line agent.
- Isoproterenol (0.5–5.0 μg/min IV) should be limited to the treatment of hypotensive patients with severe bradycardia.
- Adjunctive vasopressin (0.01–0.04 U/min IV) to norepinephrine should be considered only in hyperdynamic phase of distributive shock.
Don'ts
- Do not test orthostatic hypotension in hypotensive patients.
- Do not rely solely on SpO2 readings from pulse oximeter. SaO2 from blood gas analysis provides more precise status of oxygenation.
- Do not administer low-dose dopamine (<5 μg/kg/min) to preserve renal function in patients with shock.
References
- ↑ 1.0 1.1 Vincent, JL.; De Backer, D. (2013). "Circulatory shock". N Engl J Med. 369 (18): 1726–34. doi:10.1056/NEJMra1208943. PMID 24171518. Unknown parameter
|month=
ignored (help) - ↑ Weil, MH.; Shubin, H. (1969). "The VIP approach to the bedside management of shock". JAMA. 207 (2): 337–40. PMID 5818156. Unknown parameter
|month=
ignored (help) - ↑ Dellinger, RP.; Levy, MM.; Rhodes, A.; Annane, D.; Gerlach, H.; Opal, SM.; Sevransky, JE.; Sprung, CL.; Douglas, IS. (2013). "Surviving sepsis campaign: international guidelines for management of severe sepsis and septic shock: 2012". Crit Care Med. 41 (2): 580–637. doi:10.1097/CCM.0b013e31827e83af. PMID 23353941. Unknown parameter
|month=
ignored (help)