Congestive Heart Failure
By the end of this post you will be able to:
- Classify heart failure by ejection fraction and identify common etiologies.
- Initiate acute management of decompensated heart failure.
- Name the four pillars of GDMT for HFrEF and their target doses.
TL;DR
What you need to know before seeing your first patient on your IM rotation with this condition
Estimated read time: 4 minutes
- What it is: A clinical syndrome where the heart cannot pump enough blood to meet the body’s metabolic demands. Classified by LVEF: HFrEF (≤40%), HFmrEF (41–49%), HFpEF (≥50%).
- Common etiologies: Ischemic heart disease (most common), hypertension, valvular disease, dilated cardiomyopathy, toxins (alcohol, chemotherapy), myocarditis, arrhythmia (e.g., tachycardia-mediated).
- How it presents: Dyspnea (on exertion → at rest), orthopnea, PND, fatigue, peripheral edema. Exam: elevated JVP, S3 gallop, displaced PMI, pulmonary crackles, hepatomegaly. The JAMA Rational Clinical Exam highlights key findings for volume overload: S3 gallop (LR+ 11), JVP >3 cm above sternal angle (LR+ 4.1, specificity 92%), BNP ≥100 pg/mL (LR+ 6.9), PND (LR+ 2.6), crackles (LR+ 2.7), and peripheral edema (LR+ 2.2).
- Initial workup: ECG, CXR (pulmonary edema, cardiomegaly), troponin, BNP/NT-proBNP, basic labs (CBC, lytes, Cr, glucose, TSH, LFTs), iron studies (ferritin, TSAT). Echocardiogram to assess LVEF, valves, and wall motion.
- Acute management:
• Oxygenate: supplemental O2 (target SpO2 ≥92%); NIPPV/BiPAP if ongoing respiratory distress
• IV diuresis: furosemide 1–2.5× the home PO dose as IV bolus (CCS; DOSE trial)
• Vasodilation: IV nitroglycerin if SBP >90 with persistent pulmonary edema
• Treat reversible causes: ischemia, arrhythmia, infection, dietary/medication non-adherence - When to call for help: Cardiogenic shock (hypotension, end-organ hypoperfusion), refractory pulmonary edema despite initial therapy, need for inotropes/vasopressors or mechanical circulatory support.
Listen: The Intern at Work
Read Around the Case
Based on the CCS 2021 HFrEF Update, the CCS 2021 HF Pocket Guide, and the CCS 2025 HFnrEF Pocket Guide
Estimated read time: 15 minutes
HF Classification
Heart failure is classified by left ventricular ejection fraction (LVEF):
- HFrEF (LVEF ≤40%): Reduced systolic function. Most evidence-based therapies target this group.
- HFmrEF (LVEF 41–49%): Mildly reduced. Emerging evidence supports GDMT similar to HFrEF.
- HFpEF (LVEF ≥50%): Preserved systolic function, impaired diastolic filling. The CCS 2025 guidelines now group HFmrEF and HFpEF together as HFnrEF (non-reduced EF, LVEF >40%).
NYHA functional classification grades symptom severity from I (no limitation) to IV (symptoms at rest) and guides therapy decisions.
Etiology & Workup
Identifying the underlying cause of HF is essential — some etiologies are reversible, and treatment differs accordingly. Common causes include:
- Ischemic heart disease: The most common cause of HFrEF in developed countries. All new HF patients should be assessed for CAD (coronary angiography or non-invasive testing as appropriate).
- Hypertension: Chronic pressure overload leads to LVH and eventually diastolic then systolic dysfunction. A major contributor to HFpEF.
- Valvular heart disease: Aortic stenosis, mitral regurgitation — may require surgical or percutaneous intervention.
- Non-ischemic cardiomyopathy: Dilated (idiopathic, familial), hypertrophic, restrictive, peripartum, stress (Takotsubo).
- Toxins: Alcohol (reversible with abstinence), chemotherapy (anthracyclines, trastuzumab), stimulants.
- Tachycardia-mediated cardiomyopathy: Prolonged uncontrolled tachyarrhythmia (e.g., AF with rapid ventricular response). Often reversible with rate/rhythm control.
- Infiltrative: Amyloidosis (cardiac), sarcoidosis, hemochromatosis — consider in unexplained HFpEF or HF with LVH and low voltage on ECG.
- Other: Myocarditis, thyroid disease (hyper- or hypothyroidism), high-output states (anemia, AV fistula), pericardial disease.
Etiologic workup for new HF includes echocardiography (LVEF, wall motion, valves, diastolic function), coronary assessment, and targeted investigations based on clinical suspicion (e.g., cardiac MRI for infiltrative disease, iron studies for hemochromatosis, thyroid function).
Acute Decompensated HF Management
The CCS pocket guide outlines a stepwise approach to acute decompensated HF:
Acute Decompensated HF — Initial Management
Supplemental O2 (target SpO2 ≥92%). NIPPV/BiPAP if ongoing respiratory distress
Furosemide 1–2.5× home PO dose as IV bolus. May repeat q2–4h
IV NTG if SBP >90 with persistent pulmonary edema
Ischemia, arrhythmia, infection, dietary/medication non-adherence, etc.
Diuretic dosing: For patients on chronic oral furosemide, the CCS recommends an initial IV bolus of 1–2.5× the home PO dose (e.g., home dose 40 mg PO daily → 40–100 mg IV). The ADVOR trial showed that adding acetazolamide (500 mg IV daily) to IV loop diuretics improved decongestion in acute decompensated HF, though adoption of this strategy varies across centres. For diuretic-naive patients, 20–40 mg IV furosemide is a reasonable starting dose.
In-Hospital Diuretic Management
Managing diuresis day-to-day on the ward is a core internal medicine skill. Reassess volume status daily and adjust accordingly:
- Daily weights & I/Os: Target net negative 1–2 L/day (or ~0.5–1 kg/day weight loss). Weigh at the same time each morning.
- Reassess the exam daily: JVP, crackles, edema, orthopnea. Use the JAMA Rational Clinical Exam findings — JVP (LR+ 4.1) and S3 (LR+ 11) are the most specific bedside signs of persistent congestion.
- Inadequate response? First, re-consider the diagnosis — is this truly decompensated HF, or could there be another cause (e.g., hepatic cirrhosis, nephrotic syndrome, PE)? If HF is confirmed: consider adding metolazone (2.5–5 mg PO 30 min before furosemide) for sequential nephron blockade, or double the IV furosemide dose. Continuous furosemide infusion (5–20 mg/h) is an option but typically requires CCU/ICU-level monitoring.
- Monitor renal function and electrolytes: Check Cr, K+, Mg2+, and bicarbonate at least daily during active diuresis. Mild rises in Cr (“pseudo-worsening renal function”) are acceptable if decongestion is occurring. A rising bicarbonate (“contraction alkalosis”) can signal over-diuresis or dehydration — reassess volume status and consider slowing the rate of diuresis.
- Transition to PO before discharge: When euvolemic, convert IV to PO furosemide (IV:PO ratio ~1:2). Observe for 24–48h on the oral dose to confirm stability before discharge.
The Four Pillars of GDMT for HFrEF
The CCS 2021 guidelines define four standard therapies for HFrEF. All four should be initiated early and titrated to target doses within 3–6 months:
Titration principles: Start low, titrate every 1–2 weeks as tolerated. Aim for target doses within 3–6 months. Do not withhold one pillar while waiting to optimize another — initiate all four early, even at low doses. The STRONG-HF trial showed that rapid uptitration (within 2 weeks of discharge) reduced 180-day HF readmission and death.
Additional Therapies
- Hydralazine/ISDN: Add for self-identified Black patients already on optimal GDMT, or as alternative if ACEi/ARB/ARNi not tolerated (e.g., hyperkalemia, renal dysfunction).
- Ivabradine: For patients in sinus rhythm with resting HR >70 bpm despite maximally tolerated beta-blocker.
- Digoxin: For persistent symptoms despite optimal GDMT. Aim trough 0.5–0.9 ng/mL. No mortality benefit — symptom relief and reduced hospitalization only.
- Loop diuretics: For volume management. No mortality benefit — use the lowest effective dose for euvolemia. Not a “pillar” of GDMT.
Transition of Care
- IV iron (ferric carboxymaltose): Recommended for HFrEF with iron deficiency (ferritin <100 µg/L, or 100–299 with TSAT <20%). Improves symptoms, functional capacity, and quality of life (AFFIRM-AHF). Check iron studies on all HF patients.
- In-hospital ARNi initiation: The PIONEER-HF trial showed that starting sacubitril-valsartan in hospital (once hemodynamically stable ≥24h) led to greater NT-proBNP reduction vs. enalapril. Consider initiating ARNi before discharge in eligible patients.
“GDMT for HFrEF should be continued at the usual dose during acute intercurrent illness unless they are not tolerated or could potentially worsen severity of illness.” — CCS 2021. Common mistake: reflexively holding all HF meds during a decompensation. The CCS explicitly recommends continuing GDMT unless there is cardiogenic shock, symptomatic hypotension, or hyperkalemia. Unnecessary interruptions delay recovery and worsen outcomes.
HFpEF and HFnrEF — Chronic Management

The CCS 2025 guidelines introduce HFnrEF (LVEF >40%) as a unified category combining HFmrEF and HFpEF. The following recommendations apply to chronic outpatient management:
- SGLT2 inhibitors (dapagliflozin or empagliflozin): Strong recommendation for all HFnrEF. Supported by EMPEROR-Preserved and DELIVER.
- MRA (spironolactone or eplerenone): Strong recommendation. Supported by TOPCAT.
- ARNi (sacubitril-valsartan): Weak recommendation (may be considered). Based on PARAGON-HF.
- GLP-1 RA (semaglutide): For LVEF ≥45% with BMI ≥30 kg/m². Supported by STEP-HFpEF / SUMMIT.
- Diuretics for volume management and treatment of comorbidities (HTN, AF, CAD, obesity, sleep apnea) remain central to HFpEF care.
Lifestyle & Non-Pharmacologic Management
The CCS guidelines emphasize that pharmacotherapy alone is insufficient. Key non-pharmacologic recommendations include:
- Sodium restriction: Limit to <2 g/day. Counsel on reading food labels and avoiding processed foods.
- Exercise: Regular aerobic exercise (e.g., 30 min/day, 5 days/week) is safe and improves functional capacity and quality of life in stable HF patients. Cardiac rehabilitation referral is recommended.
- Daily weight monitoring: Patients should weigh themselves daily and have a plan for weight gain >1.5–2 kg over 2 days (e.g., prn diuretic adjustment, contact clinic).
- Multidisciplinary HF care: HF clinics with nurse-led follow-up, pharmacist medication reviews, and dietitian counselling reduce readmissions and mortality.
- Advance care planning: Discuss goals of care early, especially in patients with advanced HF (NYHA III–IV) or frequent hospitalizations. Include discussions about ICD deactivation if appropriate.
- Remote monitoring: Telemonitoring programs (daily weights, symptoms, vital signs) can facilitate early intervention and reduce hospitalizations.
Related Trial Files
MRAs for HFrEF — RALES & EMPHASIS-HF
Trial Files Throwback →
Acetazolamide in CHF (ADVOR)
Trial Files →
Furosemide Dosing in CHF (DOSE Trial)
Trial Files Throwback →
IV Iron for HFrEF (AFFIRM-AHF)
Trial Files Throwback →
Liberal Fluid Intake vs. Fluid Restriction in Chronic HF
Trial Files →
Finerenone for Preserved EF & Beta-Blockers After MI
Trial Files →
Digitoxin for HFrEF (ESC 2025 Special Edition)
Trial Files →
Thoracentesis in Acute Heart Failure
Trial Files Throwback →
Hydralazine-ISDN for HFrEF (A-HeFT)
Trial Files Throwback →
Tirzepatide for HFpEF & Obesity (SUMMIT)
Trial Files →
Listen: Deep Dives
Test Yourself
MCQ 1 for medical students · MCQ 2 for residents
A 72-year-old woman with a history of HFrEF (LVEF 30%) who takes furosemide 40 mg PO daily, ramipril, bisoprolol, and spironolactone presents to the emergency department with worsening dyspnea over 3 days. On exam, her BP is 138/82 mmHg, HR 96 bpm, SpO2 91% on room air. She has bilateral crackles to the mid-lung fields, elevated JVP, and 2+ peripheral edema. You apply supplemental O2 with improvement to SpO2 95%. What is the most appropriate next step?
A 58-year-old man is diagnosed with HFrEF (LVEF 28%) after presenting with new-onset dyspnea on exertion. He has no significant past medical history beyond hypertension controlled with amlodipine 10 mg daily. His BP is 124/78 mmHg and his renal function is normal. Which combination represents the four standard therapies (“four pillars”) recommended by the CCS 2021 guidelines for HFrEF?
Reflect
Your patient with HFrEF (LVEF 25%) is being discharged after their third admission for decompensated HF in six months. They’re on low-dose carvedilol and furosemide only — the previous teams each started one medication but never uptitrated. What would you do differently, and what barriers might explain why this keeps happening?
Please do not include patient identifying details — no names, initials, dates, medical record numbers, or any detail that could identify a specific patient or encounter. Write about your reasoning, not about a real person.
Further Reading
-
Canadian Guideline
CCS 2021 Update on Heart Failure with Reduced Ejection Fraction — Ezekowitz et al. CJC 2021. -
Pocket Guide
CCS 2021 Heart Failure Pocket Guide -
Canadian Guideline
CCS 2025 HFnrEF Pocket Guide -
International Guideline
2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure — Heidenreich et al. Circulation 2022. -
Clinical Exam
JAMA Rational Clinical Examination: Does This Patient Have Volume Overload? — Likelihood ratios for bedside findings in heart failure. -
Clinical Resource
Trial Files — MedicinePods — Evidence summaries for key HF trials.
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