Management of CHF Exacerbation in the Emergency Department
The management of congestive heart failure (CHF) exacerbation in the emergency department should follow a systematic approach focusing on rapid assessment, oxygen therapy, ventilatory support, and appropriate medication administration based on the patient's hemodynamic status.
Initial Assessment and Triage
- Patients with significant dyspnea or hemodynamic instability should be immediately triaged to a resuscitation area where emergency interventions can be provided 1
- Initial vital sign monitoring should include pulse oximetry, blood pressure, respiratory rate, and continuous ECG 1
- Severity assessment should evaluate for respiratory distress (RR >25/min, SpO2 <90%, increased work of breathing) and hemodynamic instability (abnormal blood pressure, severe arrhythmias, HR <40 or >130 bpm) 1
- Laboratory tests should include BNP/NT-proBNP, troponin, BUN/urea, creatinine, electrolytes, glucose, and complete blood count 1
- ECG and chest radiography should be performed promptly to rule out alternative diagnoses 1
Oxygen Therapy and Ventilatory Support
- Oxygen therapy should be considered in patients with AHF having SpO2 <90% 1
- Non-invasive ventilation (NIV) is indicated in patients with respiratory distress and should be started as soon as possible to reduce respiratory distress and decrease the rate of endotracheal intubation 1, 2
- For patients with respiratory distress, CPAP is recommended in the prehospital setting as it is simpler than pressure-support positive end-expiratory pressure (PS-PEEP) 1
- In patients with acidosis and hypercapnia, particularly those with COPD history or signs of fatigue, PS-PEEP is preferred upon hospital arrival 1
Medication Management Based on Blood Pressure
For Patients with Normal to High Blood Pressure (SBP >110 mmHg):
- Intravenous vasodilators should be administered along with diuretics as first-line therapy for patients with normal to high blood pressure 1
- Sublingual nitrates may be considered as an initial therapy 1
- Intravenous diuretics (furosemide) should be administered with the following dosing recommendations:
For Patients with Low Blood Pressure (SBP <90 mmHg):
- Patients with hypotension and signs of hypoperfusion (oliguria, cold peripheries, altered mental status, lactate >2 mmol/L, metabolic acidosis) should be assessed for cardiogenic shock 1
- In cardiogenic shock, dobutamine may be indicated for inotropic support in the short-term treatment of cardiac decompensation due to depressed contractility 4
- Invasive monitoring with arterial line is needed in cardiogenic shock cases 1
Monitoring During Treatment
- Patients should be continuously monitored for:
- Dyspnea (using Visual Analog Scale, respiratory rate)
- Blood pressure, SpO2, heart rate and rhythm
- Urine output and peripheral perfusion 1
- Renal function and electrolytes should be measured daily 1
- Daily weight and accurate fluid balance charts should be maintained 1
Criteria for Admission vs. Discharge
Patients requiring ICU/CCU admission include those with:
- RR >25, SaO2 <90%, use of accessory muscles for breathing
- Systolic BP <90 mmHg
- Need for intubation
- Signs of hypoperfusion (oliguria, cold peripheries, altered mental status, lactate >2 mmol/L, metabolic acidosis) 1
Indicators of good response to initial therapy that might allow discharge consideration include:
- Patient-reported subjective improvement
- Resting HR <100 bpm
- No hypotension when standing up
- Adequate urine output
- Oxygen saturation >95% in room air 1
Common Pitfalls and Caveats
- Hyperoxia should be avoided unless specifically indicated 1
- Inotropes are not recommended unless the patient has symptomatic hypotension or evidence of hypoperfusion due to safety concerns 5
- ECG and blood pressure monitoring are mandatory when using inotropes and vasopressors, as they can cause arrhythmias and myocardial ischemia 5
- Parenteral diuretic therapy should be replaced with oral furosemide as soon as practical 3
- Neither dobutamine nor any other cyclic-AMP-dependent inotrope has been shown in controlled trials to be safe or effective in long-term treatment of CHF 4