Management of GDMT in Patients with ADHF
In patients with acute decompensated heart failure (ADHF) who are on guideline-directed medical therapy (GDMT), preexisting GDMT should be continued and optimized during hospitalization, unless specifically contraindicated. 1
Continuation of GDMT During ADHF Hospitalization
Evidence-Based Rationale
- Continuation of GDMT during hospitalization has been shown in registries to lower the risk of post-discharge death and readmission compared with discontinuation 1
- In the OPTIMIZE-HF registry, discontinuation of beta-blockers was associated with higher mortality compared to those continued on beta-blockers 1
- Withdrawal of ACEi/ARB among hospitalized patients with HFrEF was associated with higher rates of post-discharge mortality and readmission in the GWTG-HF registry 1
Specific Recommendations by Medication Class
Beta-blockers:
- Continue in most patients with ADHF
- Consider temporary withholding or dose reduction only in patients with:
- Marked volume overload
- Marginal/low cardiac output
- Cardiogenic shock
ACEi/ARB/ARNi:
- Continue during hospitalization
- Do not routinely discontinue for mild decreases in renal function
Mineralocorticoid Receptor Antagonists (MRAs):
- Continue unless severe hyperkalemia (>5.5 mEq/L) or acute kidney injury develops
- May need temporary discontinuation if creatinine clearance <30 mL/min
SGLT2 inhibitors:
- Can generally be continued during hospitalization for ADHF
- Exception: If patient is undergoing surgery, should be held 3-4 days before procedure 1
When to Consider Temporary Discontinuation
Temporary discontinuation of GDMT may be necessary in specific circumstances:
Hemodynamic instability:
- Cardiogenic shock
- Symptomatic hypotension (systolic BP <90 mmHg)
- Signs of hypoperfusion
Significant renal dysfunction:
- Acute kidney injury with creatinine increase >0.5 mg/dL from baseline
- Note: Mild increases in creatinine (up to 0.3 mg/dL) during decongestion should not prompt discontinuation 2
Severe electrolyte abnormalities:
- Hyperkalemia >5.5 mEq/L (particularly with MRAs)
Management Algorithm During ADHF
Initial Assessment:
- Evaluate hemodynamic status (blood pressure, heart rate, signs of hypoperfusion)
- Review renal function and electrolytes
- Assess volume status and congestion
Decision Framework:
- If hemodynamically stable: Continue all GDMT components
- If hypotensive but asymptomatic: Continue GDMT but monitor closely
- If symptomatic hypotension or shock: Temporarily hold vasodilators (ACEi/ARB/ARNi) and consider reducing/holding beta-blockers
During Diuresis:
- Monitor renal function and electrolytes daily
- Do not routinely discontinue GDMT for mild decreases in renal function or asymptomatic reduction in blood pressure 1
- Focus on achieving decongestion while maintaining GDMT
Before Discharge:
- If GDMT was temporarily discontinued, reinitiate and optimize as soon as clinical stability is achieved 1
- Ensure patient is on optimal doses of all appropriate GDMT components
Common Pitfalls to Avoid
Premature discontinuation of GDMT due to small increases in creatinine or asymptomatic hypotension
- This is associated with worse outcomes 3
Failure to reinitiate GDMT before discharge if temporarily discontinued
- Approximately 42% of patients are not prescribed GDMT within 30 days post-hospitalization 1
Discharging patients without optimizing GDMT
Overreaction to mild laboratory changes
- Small increases in creatinine (up to 0.3 mg/dL) during decongestion are acceptable 2
Special Considerations
Hypotensive symptoms may be due to over-diuresis, non-CV drugs with hemodynamic effects, or autonomic dysfunction - address these before reducing GDMT 1
Worsening renal function: Consider using lower than target doses of ACEi/ARB/ARNi rather than complete discontinuation 1
Diuretic therapy: Focus on achieving decongestion while maintaining GDMT; premature discontinuation of diuretics due to small increases in creatinine should be avoided 2
By following these evidence-based recommendations, clinicians can optimize outcomes for patients with ADHF while maintaining the mortality and morbidity benefits of GDMT.