Chronic heart failure: Difference between revisions
From IDWiki
No edit summary |
No edit summary |
||
(3 intermediate revisions by the same user not shown) | |||
Line 4: | Line 4: | ||
*A syndrome of volume overload and poor tissue perfusion that is caused by cardiac dysfunction and is characterized by dyspnea, fatigue, and edema |
*A syndrome of volume overload and poor tissue perfusion that is caused by cardiac dysfunction and is characterized by dyspnea, fatigue, and edema |
||
*Two broad types: |
|||
=== Classification by LVEF === |
|||
⚫ | |||
{| class="wikitable sortable" |
|||
⚫ | |||
!LVEF |
|||
!Classification |
|||
|- |
|||
|≤40% |
|||
⚫ | |||
|- |
|||
|≤40% that improves >40% on repeat |
|||
|Heart failure with improved ejection fraction (HFimpEF) |
|||
|- |
|||
|41-49% |
|||
|Heart failure with mildly reduced ejection fraction (HFmrEF) |
|||
|- |
|||
|≥50% |
|||
⚫ | |||
|} |
|||
===Stages=== |
===Stages=== |
||
*'''Stage A:''' no structural heart disease or symptoms but high risk for developing HF (e.g., patients with diabetes mellitus or hypertension) |
*'''Stage A:''' no structural heart disease or symptoms but high risk for developing HF (e.g., patients with [[diabetes mellitus]] or [[hypertension]]) |
||
*'''Stage B:''' structural heart disease without symptoms of HF (e.g., patients with a previous MI and asymptomatic LV dysfunction) |
*'''Stage B:''' structural heart disease without symptoms of HF (e.g., patients with a previous MI and asymptomatic LV dysfunction) |
||
*'''Stage C:''' structural heart disease with symptoms of HF (e.g., patients with a previous MI with dyspnea and fatigue) |
*'''Stage C:''' structural heart disease with symptoms of HF (e.g., patients with a previous MI with dyspnea and fatigue) |
||
Line 36: | Line 51: | ||
====By Cardiomyopathy==== |
====By Cardiomyopathy==== |
||
*Dilated cardiomyopathy: toxins (alcohol, cocaine, chemotherapy), myocarditis, Chagas disease, peripartum cardiopmyopathy, familial cardiomyopathies |
*Dilated cardiomyopathy: toxins (alcohol, cocaine, chemotherapy), myocarditis, [[Chagas disease]], [[peripartum cardiopmyopathy]], familial cardiomyopathies |
||
*Hypertrophic cardiomyopathy: hypertension |
*Hypertrophic cardiomyopathy: [[hypertension]] |
||
*Restrictive cardiomyopathy |
*Restrictive cardiomyopathy |
||
*Arrhythmogenic right ventricular cardiomyopathy |
*Arrhythmogenic right ventricular cardiomyopathy |
||
Line 48: | Line 63: | ||
**Valvular heart disease |
**Valvular heart disease |
||
**If CAD risk factors: |
**If CAD risk factors: |
||
***Coronary artery disease |
***[[Coronary artery disease]] |
||
***Hypertensive cardiomyopathy |
***Hypertensive cardiomyopathy |
||
*Other risks |
*Other risks |
||
**Toxic agents: alcohol, amphetamines, cocaine, steroids, chemotherapy, heavy metals, radiation |
**Toxic agents: alcohol, amphetamines, cocaine, steroids, chemotherapy, heavy metals, radiation |
||
**Pregnancy: PPCM, pre-eclampsia, gestational diabetes |
**Pregnancy: [[PPCM]], [[pre-eclampsia]], [[gestational diabetes]] |
||
**Inflammatory or infectious: myocarditis, sarcoidosis, infectious hypereosinophilia, giant |
**Inflammatory or infectious: [[myocarditis]], [[sarcoidosis]], infectious hypereosinophilia, giant cell lymphocytic, auto-immune diseases |
||
**Metabolic: diabetes, thyroid disease, adrenal insufficiency, pheochromocytoma, Cushing disease |
**Metabolic: [[Diabetes mellitus|diabetes]], thyroid disease, [[adrenal insufficiency]], [[pheochromocytoma]], [[Cushing disease]] |
||
**Nutritional: thiamine deficiency, selenium deficiency, malnutrition, obesity |
**Nutritional: [[thiamine deficiency]], [[selenium deficiency]], malnutrition, obesity |
||
**Infiltrative: amyloidosis, glycogen storage disease, Fabry disease |
**Infiltrative: [[amyloidosis]], glycogen storage disease, [[Fabry disease]] |
||
**Hereditary: hypertrophic cardiomyopathy, ARVC, LV noncompaction, hemochromatosis |
**Hereditary: [[hypertrophic obstructive cardiomyopathy]], ARVC, LV noncompaction, [[hereditary hemochromatosis]] |
||
**Acute respiratory distress syndrome (ARDS) |
**[[Acute respiratory distress syndrome]] (ARDS) |
||
===Epidemiology=== |
===Epidemiology=== |
||
Line 77: | Line 92: | ||
===History=== |
===History=== |
||
* |
*History of heart failure, MI, or CAD |
||
*Dyspnea on exertion |
*Dyspnea on exertion |
||
*Paroxysmal nocturnal dyspnea |
*Paroxysmal nocturnal dyspnea |
||
Line 115: | Line 130: | ||
*Lab |
*Lab |
||
**Troponins |
**Troponins |
||
**B-type natriuretic peptide |
|||
**Natriuretic peptide (if diagnosis uncertain) |
|||
***NT-proBNP > 450 pg/mL if age < 50 years and > 900 pg/mL if age > 50 years; <100 pg/mL helps rule it out |
***NT-proBNP > 450 pg/mL if age < 50 years and > 900 pg/mL if age > 50 years; <100 pg/mL helps rule it out |
||
***Can be used in diagnosis of heart failure as a cause of dyspnea |
|||
***Can also be used for risk stratification in patients with chronic HF and prognosis in patients admitted for HF |
|||
***Predischarge BNP can also help with ongoing management |
|||
**Routine initial investigations: CBC, urinalysis, electrolytes, creatinine, glucose, lipid panel, liver panel, iron studies, TSH |
|||
*Imaging |
*Imaging |
||
**Chest X-ray showing pulmonary venous or interstitial edema, cardiomegaly, or pleural effusions |
**Chest X-ray showing pulmonary venous or interstitial edema, cardiomegaly, or pleural effusions |
||
Line 130: | Line 149: | ||
==Management== |
==Management== |
||
*See also [[Acute heart failure management]] |
*See also [[Acute heart failure#Management|Acute heart failure management]] |
||
===Non-Pharmacologic Management=== |
===Non-Pharmacologic Management=== |
||
Line 159: | Line 178: | ||
==== HFrEF ==== |
==== HFrEF ==== |
||
*For symptomatic HFrEF ≤40%, the overall approach is quadruple therapy: ARNI or ACEi/ARB, β-blockers, aldosterone agonists, and SGLT2 inhibitors |
*For symptomatic HFrEF ≤40%, the overall approach is '''quadruple therapy: ARNI or ACEi/ARB, β-blockers, aldosterone agonists, and SGLT2 inhibitors''' |
||
**Start with β-blocker plus SGLT2i, then ARNI, then MRA, so that they are on all four after a few weeks |
**Start with β-blocker plus SGLT2i, then ARNI, then MRA, so that they are on all four after a few weeks |
||
***SGLT2i has very quick benefit, regardless of diabetes, and should be started early |
***SGLT2i has very quick benefit, regardless of diabetes, and should be started early |
||
Line 319: | Line 338: | ||
|- |
|- |
||
|[[valsartan/sacubitril]] |
|[[valsartan/sacubitril]] |
||
|24/26 mg bid |
|24/26 mg bid to 49/51 mg bid |
||
| |
| |
||
|97/103 mg bid |
|97/103 mg bid |
||
Line 326: | Line 345: | ||
! colspan="5" |SGLT2 Inhibitors |
! colspan="5" |SGLT2 Inhibitors |
||
|- |
|- |
||
|[[dapagliflozin]] |
|||
|10 mg daily |
|||
| |
| |
||
|10 mg daily |
|||
| |
| |
||
|- |
|||
|[[empagliflozin]] |
|||
|10 mg daily |
|||
| |
| |
||
|10 mg daily |
|||
| |
| |
||
|- |
|||
! colspan="5" |Others |
|||
|- |
|||
|ISDN and hydralazine |
|||
|20-30 mg and 25-50 mg tid to qid |
|||
| |
|||
|120 mg TDD and 300 mg TDD |
|||
| |
|||
|- |
|||
|[[ivabradine]] |
|||
|5 mg bid |
|||
| |
|||
|7.5 mg bid |
|||
| |
|||
|- |
|||
|[[vericiguat]] |
|||
|2.5 mg daily |
|||
| |
|||
|10 mg daily |
|||
| |
|||
|- |
|||
|[[digoxin]] |
|||
|0.125-0.25 mg daily |
|||
| |
|||
|serum concentration 0.5-0.9 ng/mL |
|||
| |
| |
||
|} |
|} |
||
Line 364: | Line 415: | ||
**Cardiac cachexia |
**Cardiac cachexia |
||
**Unable to tolerate ADLs |
**Unable to tolerate ADLs |
||
=== HFpEF === |
|||
* Manage risk factors: |
|||
** Treat [[hypertension]] |
|||
** Treat [[atrial fibrillation]] |
|||
* '''SGLT2 inhibitors''' decrease hospitalizations and cardiovascular mortality |
|||
* In some patients with LVEF at the lower end: mineralocorticoid agonists and ARBs (or even ARNi) |
|||
* Diuretics as needed |
|||
==Prognosis== |
==Prognosis== |
||
Line 369: | Line 429: | ||
*30-40% of patients die within 1 year of diagnosis and 60-70% die within 5 years |
*30-40% of patients die within 1 year of diagnosis and 60-70% die within 5 years |
||
*NYHA II have a 5-10% annual mortality rate |
*NYHA II have a 5-10% annual mortality rate |
||
*NYHA IV have a 30 |
*NYHA IV have a 30-70% annual mortality rate |
||
*[https://www.mdcalc.com/maggic-risk-calculator-heart-failure MAGGIC risk score] |
*[https://www.mdcalc.com/maggic-risk-calculator-heart-failure MAGGIC risk score] |
||
**Estimates 1 and 3 year survival |
**Estimates 1 and 3 year survival |
||
==Palliative Care== |
|||
==Further Reading== |
==Further Reading== |
||
*[http://accessmedicine.mhmedical.com.myaccess.library.utoronto.ca/content.aspx?bookid=331§ionid=40727009 Harrison's 19e (Ch 234)] |
*[http://accessmedicine.mhmedical.com.myaccess.library.utoronto.ca/content.aspx?bookid=331§ionid=40727009 Harrison's 19e (Ch 234)] |
||
*[https://doi.org/10.1161/CIR.0000000000001063 AHA/ACC/HFSA Guidelines 2022] |
|||
*[http://www.ccs.ca/images/Guidelines/Guidelines_POS_Library/HF_CC_2006.pdf CCS Heart Failure Guidelines Update 2006] |
|||
*[https://doi.org/10.1001/jama.294.15.1944 Does this dyspneic patient in the emergency department have congestive heart failure? JAMA RCE 2005] |
*[https://doi.org/10.1001/jama.294.15.1944 Does this dyspneic patient in the emergency department have congestive heart failure? JAMA RCE 2005] |
||
Latest revision as of 16:20, 9 December 2024
Background
Definition
- A syndrome of volume overload and poor tissue perfusion that is caused by cardiac dysfunction and is characterized by dyspnea, fatigue, and edema
Classification by LVEF
LVEF | Classification |
---|---|
≤40% | Heart failure with reduced ejection fraction (HFrEF) |
≤40% that improves >40% on repeat | Heart failure with improved ejection fraction (HFimpEF) |
41-49% | Heart failure with mildly reduced ejection fraction (HFmrEF) |
≥50% | Heart failure with preserved ejection fraction (HFpEF) |
Stages
- Stage A: no structural heart disease or symptoms but high risk for developing HF (e.g., patients with diabetes mellitus or hypertension)
- Stage B: structural heart disease without symptoms of HF (e.g., patients with a previous MI and asymptomatic LV dysfunction)
- Stage C: structural heart disease with symptoms of HF (e.g., patients with a previous MI with dyspnea and fatigue)
- Stage D: refractory HF requiring special interventions (e.g., patients with refractory HF who are awaiting cardiac transplantation).
Etiologies
By Subtype
- Reduced ejection fraction (LVEF ≤40%)
- Coronary artery disease (most common)
- Hypertension (most common)
- Myocarditis, including viral infection
- Chronic alcohol use
- Valvular heart disease
- Chemotherapy, such as doxorubicin or trastuzumab
- Peripartum cardiomyopathy
- Idiopathic dilated cardiomyopathy
- Genetic causes of cardiomyopathy
- Preserved ejection fraction (LVEF ≥50%)
- Hypertension (most common)
- Myocardial infarction
- Mildly reduced ejection fraction (LVEF 41-49%)
By Cardiomyopathy
- Dilated cardiomyopathy: toxins (alcohol, cocaine, chemotherapy), myocarditis, Chagas disease, peripartum cardiopmyopathy, familial cardiomyopathies
- Hypertrophic cardiomyopathy: hypertension
- Restrictive cardiomyopathy
- Arrhythmogenic right ventricular cardiomyopathy
- Unclassified cardiomyopathy: Takotsubo cardiomyopathy, non-compaction cardiomyopathy
By Risk Factor
- Common
- Tachyarrhythmia
- Valvular heart disease
- If CAD risk factors:
- Coronary artery disease
- Hypertensive cardiomyopathy
- Other risks
- Toxic agents: alcohol, amphetamines, cocaine, steroids, chemotherapy, heavy metals, radiation
- Pregnancy: PPCM, pre-eclampsia, gestational diabetes
- Inflammatory or infectious: myocarditis, sarcoidosis, infectious hypereosinophilia, giant cell lymphocytic, auto-immune diseases
- Metabolic: diabetes, thyroid disease, adrenal insufficiency, pheochromocytoma, Cushing disease
- Nutritional: thiamine deficiency, selenium deficiency, malnutrition, obesity
- Infiltrative: amyloidosis, glycogen storage disease, Fabry disease
- Hereditary: hypertrophic obstructive cardiomyopathy, ARVC, LV noncompaction, hereditary hemochromatosis
- Acute respiratory distress syndrome (ARDS)
Epidemiology
- 6-10% of people over age 65
Risk Factors
- Previous episode of acute heart failure
- Prior atrial fibrillation or coronary artery bypass surgery
- Myocardial infarction
- Coronary artery disease
- Diabetes mellitus
- Hypertension
Clinical Manifestations
History
- History of heart failure, MI, or CAD
- Dyspnea on exertion
- Paroxysmal nocturnal dyspnea
- Orthopnea
- Fatigue
- Determine NYHA classification of functional status
Signs & Symptoms
- Cardiac exam: S3 present, abdominojugular reflux, elevated JVP
- Respiratory exam: crackles/rales
- Lower extremity edema
Dry | Wet | |
---|---|---|
Warm | Less congested Better-perfused |
More congested Better-perfused |
Cold | Less congested Poorly perfused |
Less congested Poorly perfused |
Prognosis
- Following an admission, 25% risk of 30-day readmission and 37% 1-year mortality
- 3-year all-cause mortality is 24% in HFpEF and 32% in HFrEF
- Sudden cardiac death is the cause of 50% of deaths
- Many risk calculators exist, including the MAGICC risk score
Investigations
- Lab
- Troponins
- B-type natriuretic peptide
- NT-proBNP > 450 pg/mL if age < 50 years and > 900 pg/mL if age > 50 years; <100 pg/mL helps rule it out
- Can be used in diagnosis of heart failure as a cause of dyspnea
- Can also be used for risk stratification in patients with chronic HF and prognosis in patients admitted for HF
- Predischarge BNP can also help with ongoing management
- Routine initial investigations: CBC, urinalysis, electrolytes, creatinine, glucose, lipid panel, liver panel, iron studies, TSH
- Imaging
- Chest X-ray showing pulmonary venous or interstitial edema, cardiomegaly, or pleural effusions
- Other
- EKG showing new atrial fibrillation, ischemic changes, or any other abnormality
- Echocardiography
- Systolic heart failure
- Reduced LV ejection fraction (LVEF)
- Diastolic heart failure
- E/A ratio less than 1
- MV deceleration time > 220ms
- Systolic heart failure
Management
- See also Acute heart failure management
Non-Pharmacologic Management
- Consider referral to multidisciplinary outpatient clinic
- Diet
- No-added-salt diet (2-3 g/day); 1-2g/day if severe fluid retention
- Fluid limited to 1.5 L/day to 2 L/day from all sources, if diuretics fail
- Exercise: regular exercise 3-5 times a week for 30-45 min per session (after stress test)
- Lifestyle
- Smoking cessation
- Decrease or eliminate alcohol intake
- Monitor body weight regularly for sudden increases (e.g. 2 kg increase in 3 days)
- Pneumococcal and annual influenza vaccines
- Avoid, when possible: NSAIDs (including COX-2 inhibitors), glucocorticoids, class I antiarrhythmics, sotalol and ibutilide,TCAs, dronedarone, verapamil and diltiazem (except in HFpEF), α-blockers, moxonidine, metformin, thiazolidinediones, anthracyclines
Manage Comorbidities
- Replace iron-deficiency with IV iron (improves quality of life)
- Avoid treating diabetes with glitazones, prefer SGLT-2 inhibitors
- Treat hypertension, especially in HFpEF
Pharmacologic Treatments
- Treat cardiovascular risk factors (hypertension, dyslipidemia, atherosclerotic disease)
- Previous MI: ASA 81 mg PO daily if indicated for secondary prevention
- Atrial fibrillation: warfarin or other anticoagulation
HFrEF
- For symptomatic HFrEF ≤40%, the overall approach is quadruple therapy: ARNI or ACEi/ARB, β-blockers, aldosterone agonists, and SGLT2 inhibitors
- Start with β-blocker plus SGLT2i, then ARNI, then MRA, so that they are on all four after a few weeks
- SGLT2i has very quick benefit, regardless of diabetes, and should be started early
- ARNIs have diuretic effect, so may need to decrease furosemide
- Titrate up every 4 to 8 weeks
- Monitor renal function and electrolytes 1 and 4 weeks after any increase, then monthly for 2 months, every 3 months for 9 months, and every 4 months indefinitely
- Start with β-blocker plus SGLT2i, then ARNI, then MRA, so that they are on all four after a few weeks
- Reassess NYHA class after maximizing treatment
- NYHA I: continue
- NYHA II-IV and sinus rhythm with resting HR ≥70: consider adding ivabradine
- NYHA III/IV: consider referral for advanced HF therapies including mechanical supprot
- Reassess LVEF after maximizing treatment
- If NYHA I-III and LVEF ≤35%: consider ICD/CRT
- NYHA IV: consider hydralazine/nitrates, referral for mechanical support or transplant, refer to palliative care
- If congestive symptoms:
- First-line: loop diuretic at lowest minimal dose required to control symptoms
- Second-line: consider adding thiazide or low-dose metolazone
- Last-line: consider adding digoxin if severe symptoms or poorly-controlled atrial fibrillation
SGLT2 Inhibitors
- Contraindicated in GFR <25ish (depending on agent)
- Increased risk of genital mycotic infections
Doses
Medication | Starting Dose | Titration | Usual Dose | Notes |
---|---|---|---|---|
Diuretics: Loop | ||||
furosemide | 20-40 mg/d | 40-240 mg/d | ||
torasemide | 5-10 mg/d | 10-20 mg/d | ||
Diuretics: Thiazide-Like | ||||
chlorthalidone | 12.5-25 mg/d | 25-100 mg/d | ||
hydrochlorothiazide | 25 mg/d | 12.5-100 mg/d | ||
indapamide | 2.5 mg/d | 2.5-5 mg/d | ||
Diuretics: Potassium-Sparing | ||||
amiloride | 2.5 mg/d | 5-10 mg/d | ||
eplerenone | 25 mg/d | 50 mg/d | ||
spirolonactone | 12.5-25 mg/d | 50 mg/d | ||
β-Blockers | ||||
bisoprolol | 1.25 mg daily | 2.5, 3.75, 5, 7, 10 | ||
carvedilol | 3.125 mg bid | 6.25, 12.5, 25, 50 | ||
metoprolol succinate CR | 12.5-25 mg daily | 25, 50, 100, 200 | ||
Angiotensin Antagonists: ACE Inhibitors | ||||
enalapril | 2.5 mg bid | 10-20 mg bid | ||
captopril | 6.25 mg tid | 50 mg tid | ||
lisinopril | 2.5-5 mg daily | 20-35 mg daily | ||
ramipril | 2.5 mg daily | 5 mg daily | ||
trandolapril | 0.5 mg daily | 4 mg daily | ||
Angiotensin Antagonists: ARBs | ||||
candesartan | 4-8 mg daily | 32 mg daily | ||
valsartan | 40 mg bid | 160 mg bid | ||
losartan | 50 mg daily | 150 mg daily | ||
Angiotensin Antagonists: ARB/ARNI | ||||
valsartan/sacubitril | 24/26 mg bid to 49/51 mg bid | 97/103 mg bid | If on ACEi, need 36 hour washout period before starting | |
SGLT2 Inhibitors | ||||
dapagliflozin | 10 mg daily | 10 mg daily | ||
empagliflozin | 10 mg daily | 10 mg daily | ||
Others | ||||
ISDN and hydralazine | 20-30 mg and 25-50 mg tid to qid | 120 mg TDD and 300 mg TDD | ||
ivabradine | 5 mg bid | 7.5 mg bid | ||
vericiguat | 2.5 mg daily | 10 mg daily | ||
digoxin | 0.125-0.25 mg daily | serum concentration 0.5-0.9 ng/mL |
Procedures
- Cardiac resynchronization therapy is indicated when LVEF<30%, LBBB, and QRS > 150ms
- Devices
- ICD if EF <35%
- CRT +/- ICD if reduced EF and LBBB
- Implantable hemodynamic monitor (CardioMEMS)
- Pulmonary artery pressure sensor
- Better than daily weights for predicting heart failure exacerbations
- Reduces hospitalizations by 30%
- Studied in HFpEF and HFrEF
- Expensive! $20k
- Surgery: see advanced therapies, below
Advanced Therapies
- Consider advanced therapies such as left ventricular assist device or cardiac transplantation when heart failure is severe and refractory
- Possible indications include:
- LVEF <25%
- End-organ dysfunction
- Recurrent hospitalizations 2x/12months unexplained
- Unable to tolerate medical therapies, including hypotension
- Diuretic refractory
- Inotropic support
- Pulmonary hypertension and right heart failure
- Six-minute walk test <300m
- Increased 1yr mortality >20%
- Renal or hepatic dysfunction
- Chronic hyponatremia <134 chronically
- Cardiac cachexia
- Unable to tolerate ADLs
HFpEF
- Manage risk factors:
- Treat hypertension
- Treat atrial fibrillation
- SGLT2 inhibitors decrease hospitalizations and cardiovascular mortality
- In some patients with LVEF at the lower end: mineralocorticoid agonists and ARBs (or even ARNi)
- Diuretics as needed
Prognosis
- 30-40% of patients die within 1 year of diagnosis and 60-70% die within 5 years
- NYHA II have a 5-10% annual mortality rate
- NYHA IV have a 30-70% annual mortality rate
- MAGGIC risk score
- Estimates 1 and 3 year survival