Congestive Heart Failure (CHF)

Updated: July 17, 2024

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Background

Congestive heart failure is an ongoing long-term disease that occurs when the heart muscle is weak and does not pump blood as required in the body. It leads to the accumulation of fluids (congestion) in different areas of the body including lungs, liver and the lower limbs. There are different types of CHF based on the heart’s ability to contract and relax: 

Systolic Heart Failure: This is a situation where the pumping action of the heart becomes compromised due to a failure of the cardiac muscles to contract broadly enough to pump sufficient blood in every cycle. 

Diastolic Heart Failure (or HFpEF): In this type, the heart muscle becomes rigid and is unable to relax at the end of systole, thus causing the heart chambers to fill inadequately. 

Epidemiology

CHF is a common disease worldwide, which affects millions of people. While it is more frequent in elderly people, it may develop in anyone with various factors such as high blood pressure, diabetes, high body weight, and previous cardiovascular issues. 

Anatomy

Pathophysiology

Heart failure is a chronic and slowly progressive disease that can be caused by acute episodes or chronic factors such as mutation, infiltration of the cardiac tissue, or ischemic disorders. Firstly, compensatory adaptations increase preload, stroke volume and cardiac output; the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) are main participants in this process. However, chronic activation leads to changes such as myocardial hypertrophy and fibrosis which are deleterious to the heart. This cycle raises the oxygen demand of myocardial cells and leads to cell death, thus lowering cardiac output and resulting in pulmonary congestion. Decompensated HF is characterized by peripheral vasoconstriction and ineffective natriuretic peptide release 

Etiology

Ischemic heart disease is the leading cause of congestive heart failure (CHF) globally, occurring due to decreased blood flow to the heart muscles and subsequently low ejection fraction. CHF incidence is increasing globally especially in developing nations due to the adoption of western lifestyles and advancement in health care reducing original causes such as myocarditis. 

Valvular Heart Disease such as rheumatic heart disease which mostly affects children and young adults and degenerative diseases of the valves with aging especially the aortic valve also cause CHF. Hypertension without Coronary Artery Disease damages the myocardium by increasing the afterload and thus the ventricular mass, often with other conditions present. 

Hypertrophic, dilated, restrictive, arrhythmogenic right ventricular, and left ventricular noncompaction cardiomyopathies cause enlarged ventricles with impaired function from primary causes. Inflammatory and infiltrative cardiomyopathies originating from genetic predisposition, infections including viral or Chagas disease toxins, and autoimmune disorders worsen CHF conditions and its outcome. 

Genetics

Prognostic Factors

Lower Ejection Fraction (EF): A lower EF is linked to worse results and a worse prognosis. 

Severity of Symptoms: Prognosis and NYHA functional class are correlated, with higher classes denoting more severe illness. 

Underlying Cause: Prognosis is influenced by cardiomyopathies, valvular heart disease, and ischemic heart disease. 

Comorbidities: Obesity, diabetes, renal failure, and chronic lung disease make treatment more difficult and harm prognosis. 

Elevated Biomarkers: Higher levels of NT-proBNP are associated with a poorer prognosis and higher heart stress. 

Clinical History

Infants and Newborns 

Delayed growth, which is stunted growth because of insufficient oxygen intake and blue skin and mucous membranes referred to as cyanosis.
Symptoms related to breathing are difficult or abnormal breathing, accelerated breathing, and breathlessness. 

Failure to feed young children appropriate foods might lead to failure to gain weight as expected by their age. 

Children and adolescence 

Lack of exercise tolerance leads to exhaustion and problems with exercise or physical labor. 

Recurring respiratory infections: Susceptibility to becoming infected and consequently being infected by pathogens. 

Chest discomfort: In some cases, children and adolescents, especially older ones, may experience chest pains particularly during exercise. 

Delays in development: In severe instances, developmental milestones may be affected or even not be achieved at all. 

Physical Examination

Cyanosis: Look for signs of cyanosis in areas such as the lips, tongue, ear lobes and nails that denote reduced oxygen saturation. 

Clubbing: Joints must be inspected to ascertain if they are enlarged at the extremities, particularly if the hands and feet seem like light bulbs, due to chronic hypoxemia. 

Palpation 

Pulses: Feel peripheral pulses to estimate the adequacy of blood circulation. 

Thrills: Tremors; associated with turbulent blood flow especially in congenital heart diseases; palpate for thrills. 

Auscultation: 

Heart Sounds: Look for I, II, and V auscultatory areas for S1 and S2 heart sounds. 

Additional Sounds: Speaking of note S3 and S4 sounds which point at ventricular dysfunction. 

Murmurs: Classify heart murmurs into those are abnormal in location, timing, intensity and radiation. 

Clicks and Snaps: Someone might hear a clicking or snapping sound: as in the case of mitral valve prolapse. 

Rub: Check for pericardial rubs and recommend on the presence of pericardial inflammation. 

Chest Examination: 

Shape: Palpate for expansiveness and perceive for irregularities in reaching for chest wall to rule out congenital heart problems. 

Retractions: It is essential to observe symptoms such as intercostal retractions that point to respiratory distress. 

Age group

Associated comorbidity

Associated activity

Acuity of presentation

  • Critical Congenital Heart Disease (CCHD): There are some congenital heart diseases that cause severe signs and symptoms within the first weeks of life and need urgent medical intervention. Examples include instances of severe diaphragmatic herniation, parachute umbilical cord, and severely hypoplastic lungs. 
  • Acute Decompensation: CHD patients might have mild or more moderate disease and while they are free of symptoms, they can develop acute episode because of infections, stress and other reasons.
  • Gradual Onset: Less severe signs may develop slowly over time and the disease may not be detected during childhood or adolescence, but may be diagnosed during adult physical exams, or while the person is being evaluated for other diseases. 

Differential Diagnoses

Acquired Heart Diseases:  

  • Rheumatic heart disease  
  • Infective endocarditis  
  • Kawasaki disease  

Cardiomyopathies:  

  • Hypertrophic cardiomyopathy  
  • Dilated cardiomyopathy  
  • Restrictive cardiomyopathy  

Vascular Disorders:  

  • Coarctation of the aorta  
  • Aortic stenosis  
  • Pulmonary stenosis  
  • Patent ductus arteriosus  

Arrhythmias:  

  • Wolff-Parkinson-White syndrome  
  • Long QT syndrome  
  • Atrial septal defect with atrial fibrillation  

Laboratory Studies

Imaging Studies

Procedures

Histologic Findings

Staging

Treatment Paradigm

Medical Management: Several CHDs may be treated by ensuring proper heart function, eliminating fluid accumulation, regulating blood pressure, discouraging clot formation or relieving symptoms using drugs and medication. In certain cardiac diseases, preventative antibiotics might be advised before dental or certain medical procedures to reduce the risk of infective endocarditis. 

Catheter-Based Interventions: 

Balloon Angioplasty: Conditions like pulmonary stenosis and aortic stenosis can be treated using a catheter which has the shape of a balloon and is placed on the tip. 

Device Closure: Some patients have anomalous connections such as atrial septal defects (ASD) and ventricular septal defects (VSD) that may be closed without surgical procedure with intravascular devices.

by Stage

by Modality

Chemotherapy

Radiation Therapy

Surgical Interventions

Open-Heart Surgery: Most of the CHD are complex and are treated with open heart surgery. This may require surgery to fix or replace the heart valves, if there are defects in the structure of the heart, or if the vessels need to be redirected. 

Heart Transplant: Heart transplantation is the last option where the heart is severely damaged, and the structure cannot be fixed.

 

Hormone Therapy

Immunotherapy

Hyperthermia

Photodynamic Therapy

Stem Cell Transplant

Targeted Therapy

Palliative Care

Palliative Procedures: 

Temporary Shunts: In some situations, such as in newborns with severe congenital heart disease, initial palliative procedures like placing shunts may be used to increase blood flow to the lungs or other organs while a more definitive surgery is planned and performed. 

use-of-a-non-pharmacological-approach-for-treating-congestive-heart-failure

Lifestyle and Dietary Management: 

Nutritional Support: It is important to note that some infants born with congenital heart disease may need feeding modifications or even enteral tube feedings. 

Physical Activity: People with heart conditions may require limited recommendations depending on their type of condition or may require restrictions on their physical activity. 

Palliative Procedures: 

Temporary Shunts: Sometimes, especially in neonates with complicated CHD, patients may undergo placement of temporary shunts to aid in circulation until definitive repair is possible. 

Role of diuretics in the treatment of congenital heart disease

Furosemide (Lasix): This specific diuretic functions at the kidneys’ loop of Henle by inhibiting the reabsorption of salt and chloride within the renal tubules, thereby enhancing production of urine. Lasix is commonly used to treat cases of fluid overload especially in cases where the patient has been diagnosed with heart failure due to CHD. It also has a beneficial effect in decreasing edema and improving respiratory manifestations. 

Role of Inotropic agents for treating congenital heart disease 

Digoxin: It increases the intracellular calcium levels since it inhibits sodium potassium pump. This leads to increased positive inotropic effect and the better heart’s pumping ability. Digoxin is effective in the treatment of congestive heart failure resulting from CHD, particularly in the needy categories of patients, the children. It can consequently enhance the occurrence of symptoms and decrease important hospitalizations. 

Role of Beta-Blockers

Propranolol: It is a cardio selective beta-blocker, and it opposes both the beta-1 and the beta-2 adrenoreceptors. It decreases the rate and force of the heartbeat and decreases blood pressure. It is employed in the treatment of the arrhythmias most of which are characterized by tachycardia or fast heart rates. It may also be applied to control systemic/inorganic sign related to hypertrophic cardiomyopathy. 

 

Role of Angiotensin II Receptor Blockers

Losartan: In the management of hypertension with CHD, losartan is often recommended. It is also given in situations that involve formation of an aortic aneurysm. 

Valsartan: It is another drug belonging to the ARB class that can be used to treat hypertension and heart failure in people with CHD. 

use-of-intervention-with-a-procedure-in-treating-congestive-heart-failure

Coronary Artery Bypass Grafting (CABG): This surgery is done for patients who have severe blockages in the coronary arteries, to increase blood flow to the heart, to relieve symptoms and to enhance the overall function of the heart. 

Percutaneous Coronary Intervention (PCI): Known as angioplasty, this procedure involves passing a catheter fitted with an inflatable balloon into a blocked coronary artery. The balloon is inflated to open the blocked artery and it is usually thereafter backed up using a stent.

Implantable Cardioverter-Defibrillators (ICDs): These devices are inserted in patients with Implantable Cardioverter Defibrillators or ICDs due to ventricular arrhythmias. ICDs continuously record heart rate and pace and can treat cardiac arrhythmias by issuing electric shocks.

use-of-phases-in-managing-congestive-heart-failure

Acute Phase: 

Assess the patient clinically and use ECG, chest X-ray and biochemical profile including BNP/NT-proBNP. First, assess if there are any life-threatening conditions that needs immediate attention to stabilize the patient. 

Give diuretics to remove excess fluids in the body, venodilators to decrease after load and inotropic agents in case cardiac output needs to be boosted. Oxygen therapy or non-invasive ventilation may be needed for patients with hypoxia. 

Subacute Phase: 

Optimize the doses of ACE inhibitors or ARBs, beta-blockers, aldosterone antagonists, and diuretics to cope with possible manifestations. Teaching on CHF, which includes signs and symptoms of CHF worsening, importance of taking medication as instructed, no use of salt or foods high in sodium, and making positive behavioural changes. Discharge planning should involve regular follow-up visits, home healthcare services if required, and proper guidelines on signs and symptoms to look out for and when to seek healthcare services. 

Chronic Phase: 

To maintain the heart failure status and prevent further deterioration, all long-term medications prescribed should be continued and modified accordingly in case of inefficiency or occurrence of side effects. It is recommended to perform follow-up visits every 3 to 6 months to perform clinical examination, laboratory tests, and imaging for the assessment of heart function and signs of conversation. Promote and maintain a heart-healthy diet, exercise habits, monitoring the weight, quitting smoking, and the moderate consumption of alcoholic beverages. 

Medication

 

dobutamine

Initial dose: 0.5-1 mcg/kg IV infusion over 1 minute
Maintenance dose: 2-20 mcg/kg IV infusion over 1 minute
the maximum dose recommended is 40 mcg/kg IV infusion over 1 minute



dopamine

Indicated for treating heart problems and imbalances in shock caused by infections, injuries, septicemia, surgery, kidney issues, or heart failure

continuous infusion:

Initial dose: 2-10 mcg/kg/min intravenously (IV)

Maintenance dose: 2-50 mcg/kg/min intravenously (IV)



ramipril

2.5

mg

Orally 

twice a day

; increase up to 5 mg



ramipril

2.5

mg

Orally 

twice a day

; increase up to 5 mg



amiloride hydrochlorothiazide

5-10 mg/50-100 mg amiloride/hydrochlorothiazide orally every day



carvedilol

Immediate release:

3.125

mg

orally

every 12 hrs

14

days

then increase every two weeks tolerated to 6.25mg,12.5mg, or 25 mg orally twice a day
Maximum recommended dose:
Mild to moderate heart failure:
<85 kg,25mg orally every 12 hours
>85kg,50mg orally twice daily
Severe heart failure:
25mg orally twice a day
Extended-release
10mg/day orally for 1-2 weeks, then increase 20mg/day,40mg/day, and 80mg/day orally



eplerenone 

25

mg

Orally 

daily



trandolapril 

1

mg

orally

daily

or may be increased up to 4 mg



dapagliflozin 

To reduce the risk of hospital admission in case of heart failure, dapagliflozin is indicated 10 mg orally in the morning



empagliflozin 

The drug is not recommended in the case of renal impairment when eGFR <30 mL/min/1.73 m2
It is also contraindicated in dialysing patients :

Indicated for the reduction in death due to cardiovascular collapse and hospitalization
10 mg orally each day



creatine 

20 gms orally every day repeated for 5 to 10 days



nitroglycerin topical 

When treating Congestive Heart Failure, healthcare providers typically prescribe a starting medication dosage of 1.5 inches, which can be increased by 0.5-1 inch up to a maximum of 4 inches
The medication should be administered every four hours



ivabradine 

Initially, 5 mg orally each day with meals
2 weeks later, assess the patients and arrange the dose to get a resting heart rate- of 50-60 bpm
After the dose adjustment as required based on tolerance and rest heart rate, do not exceed the dose of more than 7.5 mg twice daily



ivabradine 

Initially, 5 mg orally each day with meals
2 weeks later, assess the patients and arrange the dose to get a resting heart rate- of 50-60 bpm
After the dose adjustment as required based on tolerance and rest heart rate, do not exceed the dose of more than 7.5 mg twice daily
Dose Adjustment
In case of heart rate is more than 60 bpm- Increase the dose by 2.5 mg twice daily to a maximum of 7.5
When the heart rate is 50-60 bpm, maintain the dose
When the heart rate is less than 50 bpm, decrease the dose by 2.5 mg
If the current dose is 2.5 mg twice daily, discontinue the therapy



ivabradine 

Initially, 5 mg orally each day with meals
2 weeks later, assess the patients and arrange the dose to get a resting heart rate- of 50-60 bpm
After the dose adjustment as required based on tolerance and rest heart rate, do not exceed the dose of more than 7.5 mg twice daily
Dose Adjustment
In case of heart rate is more than 60 bpm- Increase the dose by 2.5 mg twice daily to a maximum of 7.5
When the heart rate is 50-60 bpm, maintain the dose
When the heart rate is less than 50 bpm, decrease the dose by 2.5 mg
If the current dose is 2.5 mg twice daily, discontinue the therapy



inamrinone 


Indicated for Congestive Heart Failure
loading dose: 0.75 mg/kg intravenous bolus for 2-3 min, after that 5-10 mcg/kg/min intravenously
It should not exceed 10 mg/kg/day of total everyday dose (including load dose)
Range of therapeutic dosage: 0.5-7 mcg/ml
Note:
Renal impairment
Sr CrCl <10 ml/min: Reduce to 25-50% of the dose
Sr CrCl >10 ml/min: No adjustment needed



perindopril 

2

mg

Orally every day; increase up to 8-16 mg



spironolactone and hydrochlorothiazide 

Ascites, Edema:

1-4 tablets/day orally (hydrochlorothiazide 50 mg/ spironolactone 50 mg)
1-8 tablets/day orally (hydrochlorothiazide 25 mg/ spironolactone 25 mg)



hydralazine 

Take initial dose of 10 to 25 mg orally every 6 to 8 hours and titrate dose every 2 to 4 weeks
Take maintenance dose of 225 to 300 mg daily orally divided every 6 to 8 hour
Dosing considerations
Adjust dose according to individual response



cilazapril 

Take initial dose of 0.5 mg orally one time a day then raise to 1 mg once daily in five days
It may further titrate as required to maintenance dose of 2.5 mg one time a day
Maximum dose not more than 2.5 mg one time a day



enalapril 

Initial dose: 2.5 mg orally every day or 2 times a day
Maintenance dose: 5 to 40 mg/Day orally divided every 2 times a day; titrate slowly every 2Weeks
Intravenous: 1.25 to 5 mg every 4 times a day; avoid Intravenous administration incase of acute myocardial infarction or unstable heart failure
Conversion from IV to oral dosage form
For those who are not using diuretics, start with 5 mg orally every day; when it comes to taking diuretics and responding to 0.625 mg Intravenous every 4 times a day, start with 2.5 mg orally every day and titrate up as needed



Dose Adjustments

Dosage Modifications
Hepatic impairment: dose adjustment is not required
Renal impairment
CrCl less than 30 mL/min: Initiate 2.5 mg orally; titrate based on response; should not exceed more than 40 mg
Dialysis: 2.5 mg orally on day of the dialysis; adjust dosage on nondialysis days according to the BP
CrCl less than 30 mL/min: Initiate 0.625 mg intravenous every 4 times a day; titrate to response
CrCl more than 30 mL/min: Initiate 5 mg/day orally; titrate to the maximum of 40 mg
CrCl more than 30 mL/min: 1.25 mg intravenous every 4 times a day; titrate to response

isosorbide dinitrate/hydralazine 

1 tablet orally every 8 hours
Titrate the dose as required
Do not exceed the dose of more than 2 tablets orally every 8 hours
Decrease the dose to half-tablet every 8 hours if any side effects are not tolerated
Titrate the dose if side effects subside
The above dose is also indicated as an adjunct therapy for heart failure in self-proclaimed African Americans



iobenguane I-123 

Administer dose of 10 millicurie intravenously
Begin anterior planar imaging of the chest at 4 hours (plus or minus 10 minutes) after administration
Administration
Administer intravenous infusion over 1 to 2 minutes, then flush with 0.9% sodium chloride to guarantee of complete administration of the dose



valsartan 

40 mg orally 2 times daily
Increase up tp 80-160 mg
Consider lowering the dosage of any concurrent diuretics

Maximum daily dosage of 320 mg was given in split doses during clinical studies



levosimendan 

Load 6-12 mcg/kg as an infusion for 10 minutes
Maintenance dose- 0.1 mcg/kg intravenously each minute through infusion
Decrease the dose to 0.05 mcg/kg each minute if cardiac disturbances occur
The drug is contraindicated in the case of severe renal (CrCl<30 ml/min) and hepatic impairment



deslanoside 

Administer dose up to 1.6 mg intravenously as a single dose or in form of divided doses



digitoxin 

Rapid digitalization with an oral loading dose of 600 mcg, which after 4-6 hours is followed by 400 mcg, followed by 200 mcg for every 4 -6 hours if necessary, depending on the patient's condition and slow digitalization with an oral dose of 200 mcg twice daily for four days
The maintenance dose is 50 to 300 mcg once every 24 hours, whereas the usual dose is 150 mcg every 24 hours



Dose Adjustments

Renal dose adjustments
In renal impairment, if the CrCl is less than or below 10 mL/min, the recommended dose is 50% or 75% of the usual dose

sacubitril 

There is no sufficient data available



amiloride 

maintenance dose:

5

mg

Tablet

Orally 

every 24 hours

5-10mg orally every 24hours



neladenoson 

5 to 40 mg is given orally once a day for 5 months



spironolactone and hydrochlorothiazide 

(Ascites, Edema) :

1-4 tablets/day orally (hydrochlorothiazide 50 mg/ spironolactone 50 mg)
1-8 tablets/day orally (hydrochlorothiazide 25 mg/ spironolactone 25 mg)



acetyldigitoxin 

10 to 15 mcg/kg is given orally



candesartan/hydrochlorothiazide 

4 mg/day orally, for every 2 weeks double the dose. The maximum dose 32 mg/day orally



inamrinone 

Loading dose- 0.75 mg/kg intravenously as a bolus for 2-3 minutes Later, 5-10 mcg/kg/min intravenously
Do not increase the total dose to more than 10 mg/kg/day (inclusive of the loading dose)
Therapeutic range- 0.5-7 mcg/ml



fosinopril 

Dosing Considerations
Benefits include reducing the incidence of MI, stroke, diabetic nephropathy, microalbuminuria, and diabetes in patients who are at risk for heart disease even if there is no HTN or CHF, start an ACE inhibitor in high-risk patients may maintain renal function in DM and may prolong life in CHF may aid in preventing migraines
No side effects of sexual dysfunction
A good choice for patients with hyperli:

5-10 mg orally every Day initially, should not exceed more than 40 mg/day



 

dobutamine

Initial dose: 0.5-1 mcg/kg IV infusion over 1 minute
Maintenance dose: 2-20 mcg/kg IV infusion over 1 minute
the maximum dose recommended is 40 mcg/kg IV infusion over 1 minute



dopamine

continuous infusion:
2-10 mcg/kg/min IV
2-50 mcg/kg/min IV



nitroglycerin IV 

FDA Not approved
Initial dose: 0.25 to 0.5 mcg/kg/min Intravenous infusion; may be increased to 0.5–1 mcg/kg/min every 3–5 minutes when necessary.
Usual range: 1 to 5 mcg/kg/min intravenous infusion
Should not exceed 20 mcg/min



ivabradine 

For more than 6 months
<40 kg- Initially 0.05 mg/kg orally as a solution twice daily
Assess the patients every fortnight and adjust the dose by 0.05 mg/kg to target the reduction in heart rate of at least one-fifth based on tolerance
Maximum dose for 6 months-1 year- Do not exceed more than 0.2mg /kg twice daily
Maximum dose for more than 1 year- 0.3 mg/kg twice daily
Do not exceed more than 7.5 mg twice daily
≥40 kg- Initially 2.5 mg orally as a tablet twice daily
Assess the patients every fortnight and adjust the dose by 2.5 mg to target the reduction in heart rate of at least one-fifth based on tolerance
Do not exceed the dose of more than 7.5 mg twice daily



ivabradine 

For more than 6 months
<40 kg- Initially 0.05 mg/kg orally as a solution twice daily
Assess the patients every fortnight and adjust the dose by 0.05 mg/kg to target the reduction in heart rate of at least one-fifth based on tolerance
The maximum dose for 6 months-1 year
Do not exceed more than 0.2mg /kg twice daily
Maximum dose for more than 1 year- 0.3 mg/kg twice daily
Do not exceed more than 7.5 mg twice daily
≥40 kg- Initially 2.5 mg orally as a tablet twice daily
Assess the patients every fortnight and adjust the dose by 2.5 mg to target the reduction in heart rate of at least one-fifth based on tolerance Do not exceed the dose of more than 7.5 mg twice daily



inamrinone 


Indicated for Congestive Heart Failure
Age <28 days
loading dose as in the adults, 0.75 mg/kg intravenously for 3-5 min; after that, 3-5 mcg/kg/min intravenously as a maintenance infusion
After 30 min, the bolus dose might need to repeat it
It should not exceed 10 mg/kg/day of total everyday dose
Range of therapeutic dosage: 0.5-7 mcg/ml
Age >28 days
loading dose as in the adults, 0.75 mg/kg intravenously for 3-5 min; after that, 5-15 mcg/kg/min intravenously
It should not exceed 10 mg/kg/day
Range of therapeutic dosage: 0.5-7 mcg/ml
Renal impairment
Sr CrCl >30 ml/min: No adjustment needed
Sr CrCl 10-29 ml/min: Reduce to 50% of the dose
Sr CrCl <10 ml/min: Reduce to 25% of the dose



hydralazine 

For Infants:
Administer dose of 0.1 to 0.5 mg/kg intravenously every 6 to 8 hours and dose should not be more than 2 mg/kg
For Children and adolescents:
Administer dose of 0.15 to 0.2 mg/kg intravenously every 4 to 6 hours and dose should not be more than 20 mg
For oral administration
Infants and older:
Administer dose of 0.75 to 3 mg/kg daily orally divided every 6 to 12 hours and daily dose should not be more than 200 mg



iobenguane I-123 

Gamma Scintigraphy
Start anterior planar imaging of the chest at 4 hours (plus or minus 10 minutes) after administration
Neonates <1 month: Safety and efficacy not determined
<16 years old and ≥70 kg: 10 millicurie
Children ≥16 years: follow as per adult dosing instructions
Administration
Administer intravenous infusion over 1 to 2 minutes, then flush with 0.9% sodium chloride to guarantee of complete administration of the dose



digitoxin 

Injectable solutions are administered and divided into fractions at 6 to 8 hours, maintained for children below 10
It is used only for rapid digitalization, in which IV is preferred over IM
The usual dose which is recommended is 20 mcg/kg



acetyldigitoxin 

Premature: 20 to 30 mcg/kg
1- 24 months: 35 to 60 mcg/kg
2 - 5 years: 30 to 45 mcg/kg
5 - 10 years: 20 to 35 mcg/kg



inamrinone 

For less than 28 days-
Loading dose- 0.75 mg/kg intravenously for 3-5 minutes
3-5 mcg/kg/minute intravenously as a maintenance dose
If the bolus is administered, it needs to repeat after half an hour
Do not increase the daily dose to more than 10 mg/kg/day
Range of therapeutic dose- 0.5-7 mcg/ml
For more than 28 days-
Loading dose- 0.75 mg/kg intravenously for 3-5 minutes
5-15 mcg/kg/minute intravenously as a maintenance dose
Do not increase the daily dose to more than 10 mg/kg/day
Range of therapeutic dose- 0.5-7 mcg/ml



 

amiloride hydrochlorothiazide

Half to 1 tablet orally daily



isosorbide dinitrate/hydralazine 

1 tablet orally every 8 hours
Titrate the dose as required



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Congestive Heart Failure (CHF)

Updated : July 17, 2024

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Congestive heart failure is an ongoing long-term disease that occurs when the heart muscle is weak and does not pump blood as required in the body. It leads to the accumulation of fluids (congestion) in different areas of the body including lungs, liver and the lower limbs. There are different types of CHF based on the heart’s ability to contract and relax: 

Systolic Heart Failure: This is a situation where the pumping action of the heart becomes compromised due to a failure of the cardiac muscles to contract broadly enough to pump sufficient blood in every cycle. 

Diastolic Heart Failure (or HFpEF): In this type, the heart muscle becomes rigid and is unable to relax at the end of systole, thus causing the heart chambers to fill inadequately. 

CHF is a common disease worldwide, which affects millions of people. While it is more frequent in elderly people, it may develop in anyone with various factors such as high blood pressure, diabetes, high body weight, and previous cardiovascular issues. 

Heart failure is a chronic and slowly progressive disease that can be caused by acute episodes or chronic factors such as mutation, infiltration of the cardiac tissue, or ischemic disorders. Firstly, compensatory adaptations increase preload, stroke volume and cardiac output; the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) are main participants in this process. However, chronic activation leads to changes such as myocardial hypertrophy and fibrosis which are deleterious to the heart. This cycle raises the oxygen demand of myocardial cells and leads to cell death, thus lowering cardiac output and resulting in pulmonary congestion. Decompensated HF is characterized by peripheral vasoconstriction and ineffective natriuretic peptide release 

Ischemic heart disease is the leading cause of congestive heart failure (CHF) globally, occurring due to decreased blood flow to the heart muscles and subsequently low ejection fraction. CHF incidence is increasing globally especially in developing nations due to the adoption of western lifestyles and advancement in health care reducing original causes such as myocarditis. 

Valvular Heart Disease such as rheumatic heart disease which mostly affects children and young adults and degenerative diseases of the valves with aging especially the aortic valve also cause CHF. Hypertension without Coronary Artery Disease damages the myocardium by increasing the afterload and thus the ventricular mass, often with other conditions present. 

Hypertrophic, dilated, restrictive, arrhythmogenic right ventricular, and left ventricular noncompaction cardiomyopathies cause enlarged ventricles with impaired function from primary causes. Inflammatory and infiltrative cardiomyopathies originating from genetic predisposition, infections including viral or Chagas disease toxins, and autoimmune disorders worsen CHF conditions and its outcome. 

Lower Ejection Fraction (EF): A lower EF is linked to worse results and a worse prognosis. 

Severity of Symptoms: Prognosis and NYHA functional class are correlated, with higher classes denoting more severe illness. 

Underlying Cause: Prognosis is influenced by cardiomyopathies, valvular heart disease, and ischemic heart disease. 

Comorbidities: Obesity, diabetes, renal failure, and chronic lung disease make treatment more difficult and harm prognosis. 

Elevated Biomarkers: Higher levels of NT-proBNP are associated with a poorer prognosis and higher heart stress. 

Infants and Newborns 

Delayed growth, which is stunted growth because of insufficient oxygen intake and blue skin and mucous membranes referred to as cyanosis.
Symptoms related to breathing are difficult or abnormal breathing, accelerated breathing, and breathlessness. 

Failure to feed young children appropriate foods might lead to failure to gain weight as expected by their age. 

Children and adolescence 

Lack of exercise tolerance leads to exhaustion and problems with exercise or physical labor. 

Recurring respiratory infections: Susceptibility to becoming infected and consequently being infected by pathogens. 

Chest discomfort: In some cases, children and adolescents, especially older ones, may experience chest pains particularly during exercise. 

Delays in development: In severe instances, developmental milestones may be affected or even not be achieved at all. 

Cyanosis: Look for signs of cyanosis in areas such as the lips, tongue, ear lobes and nails that denote reduced oxygen saturation. 

Clubbing: Joints must be inspected to ascertain if they are enlarged at the extremities, particularly if the hands and feet seem like light bulbs, due to chronic hypoxemia. 

Palpation 

Pulses: Feel peripheral pulses to estimate the adequacy of blood circulation. 

Thrills: Tremors; associated with turbulent blood flow especially in congenital heart diseases; palpate for thrills. 

Auscultation: 

Heart Sounds: Look for I, II, and V auscultatory areas for S1 and S2 heart sounds. 

Additional Sounds: Speaking of note S3 and S4 sounds which point at ventricular dysfunction. 

Murmurs: Classify heart murmurs into those are abnormal in location, timing, intensity and radiation. 

Clicks and Snaps: Someone might hear a clicking or snapping sound: as in the case of mitral valve prolapse. 

Rub: Check for pericardial rubs and recommend on the presence of pericardial inflammation. 

Chest Examination: 

Shape: Palpate for expansiveness and perceive for irregularities in reaching for chest wall to rule out congenital heart problems. 

Retractions: It is essential to observe symptoms such as intercostal retractions that point to respiratory distress. 

  • Critical Congenital Heart Disease (CCHD): There are some congenital heart diseases that cause severe signs and symptoms within the first weeks of life and need urgent medical intervention. Examples include instances of severe diaphragmatic herniation, parachute umbilical cord, and severely hypoplastic lungs. 
  • Acute Decompensation: CHD patients might have mild or more moderate disease and while they are free of symptoms, they can develop acute episode because of infections, stress and other reasons.
  • Gradual Onset: Less severe signs may develop slowly over time and the disease may not be detected during childhood or adolescence, but may be diagnosed during adult physical exams, or while the person is being evaluated for other diseases. 

Acquired Heart Diseases:  

  • Rheumatic heart disease  
  • Infective endocarditis  
  • Kawasaki disease  

Cardiomyopathies:  

  • Hypertrophic cardiomyopathy  
  • Dilated cardiomyopathy  
  • Restrictive cardiomyopathy  

Vascular Disorders:  

  • Coarctation of the aorta  
  • Aortic stenosis  
  • Pulmonary stenosis  
  • Patent ductus arteriosus  

Arrhythmias:  

  • Wolff-Parkinson-White syndrome  
  • Long QT syndrome  
  • Atrial septal defect with atrial fibrillation  

Medical Management: Several CHDs may be treated by ensuring proper heart function, eliminating fluid accumulation, regulating blood pressure, discouraging clot formation or relieving symptoms using drugs and medication. In certain cardiac diseases, preventative antibiotics might be advised before dental or certain medical procedures to reduce the risk of infective endocarditis. 

Catheter-Based Interventions: 

Balloon Angioplasty: Conditions like pulmonary stenosis and aortic stenosis can be treated using a catheter which has the shape of a balloon and is placed on the tip. 

Device Closure: Some patients have anomalous connections such as atrial septal defects (ASD) and ventricular septal defects (VSD) that may be closed without surgical procedure with intravascular devices.

Open-Heart Surgery: Most of the CHD are complex and are treated with open heart surgery. This may require surgery to fix or replace the heart valves, if there are defects in the structure of the heart, or if the vessels need to be redirected. 

Heart Transplant: Heart transplantation is the last option where the heart is severely damaged, and the structure cannot be fixed.

 

Palliative Procedures: 

Temporary Shunts: In some situations, such as in newborns with severe congenital heart disease, initial palliative procedures like placing shunts may be used to increase blood flow to the lungs or other organs while a more definitive surgery is planned and performed. 

Cardiology, General

Lifestyle and Dietary Management: 

Nutritional Support: It is important to note that some infants born with congenital heart disease may need feeding modifications or even enteral tube feedings. 

Physical Activity: People with heart conditions may require limited recommendations depending on their type of condition or may require restrictions on their physical activity. 

Palliative Procedures: 

Temporary Shunts: Sometimes, especially in neonates with complicated CHD, patients may undergo placement of temporary shunts to aid in circulation until definitive repair is possible. 

Cardiology, General

Cardiology, Interventional

Pediatrics, Cardiology

Furosemide (Lasix): This specific diuretic functions at the kidneys’ loop of Henle by inhibiting the reabsorption of salt and chloride within the renal tubules, thereby enhancing production of urine. Lasix is commonly used to treat cases of fluid overload especially in cases where the patient has been diagnosed with heart failure due to CHD. It also has a beneficial effect in decreasing edema and improving respiratory manifestations. 

Cardiology, General

Digoxin: It increases the intracellular calcium levels since it inhibits sodium potassium pump. This leads to increased positive inotropic effect and the better heart’s pumping ability. Digoxin is effective in the treatment of congestive heart failure resulting from CHD, particularly in the needy categories of patients, the children. It can consequently enhance the occurrence of symptoms and decrease important hospitalizations. 

Cardiology, General

Propranolol: It is a cardio selective beta-blocker, and it opposes both the beta-1 and the beta-2 adrenoreceptors. It decreases the rate and force of the heartbeat and decreases blood pressure. It is employed in the treatment of the arrhythmias most of which are characterized by tachycardia or fast heart rates. It may also be applied to control systemic/inorganic sign related to hypertrophic cardiomyopathy. 

 

Cardiology, General

Losartan: In the management of hypertension with CHD, losartan is often recommended. It is also given in situations that involve formation of an aortic aneurysm. 

Valsartan: It is another drug belonging to the ARB class that can be used to treat hypertension and heart failure in people with CHD. 

Cardiology, General

Coronary Artery Bypass Grafting (CABG): This surgery is done for patients who have severe blockages in the coronary arteries, to increase blood flow to the heart, to relieve symptoms and to enhance the overall function of the heart. 

Percutaneous Coronary Intervention (PCI): Known as angioplasty, this procedure involves passing a catheter fitted with an inflatable balloon into a blocked coronary artery. The balloon is inflated to open the blocked artery and it is usually thereafter backed up using a stent.

Implantable Cardioverter-Defibrillators (ICDs): These devices are inserted in patients with Implantable Cardioverter Defibrillators or ICDs due to ventricular arrhythmias. ICDs continuously record heart rate and pace and can treat cardiac arrhythmias by issuing electric shocks.

Cardiology, General

Acute Phase: 

Assess the patient clinically and use ECG, chest X-ray and biochemical profile including BNP/NT-proBNP. First, assess if there are any life-threatening conditions that needs immediate attention to stabilize the patient. 

Give diuretics to remove excess fluids in the body, venodilators to decrease after load and inotropic agents in case cardiac output needs to be boosted. Oxygen therapy or non-invasive ventilation may be needed for patients with hypoxia. 

Subacute Phase: 

Optimize the doses of ACE inhibitors or ARBs, beta-blockers, aldosterone antagonists, and diuretics to cope with possible manifestations. Teaching on CHF, which includes signs and symptoms of CHF worsening, importance of taking medication as instructed, no use of salt or foods high in sodium, and making positive behavioural changes. Discharge planning should involve regular follow-up visits, home healthcare services if required, and proper guidelines on signs and symptoms to look out for and when to seek healthcare services. 

Chronic Phase: 

To maintain the heart failure status and prevent further deterioration, all long-term medications prescribed should be continued and modified accordingly in case of inefficiency or occurrence of side effects. It is recommended to perform follow-up visits every 3 to 6 months to perform clinical examination, laboratory tests, and imaging for the assessment of heart function and signs of conversation. Promote and maintain a heart-healthy diet, exercise habits, monitoring the weight, quitting smoking, and the moderate consumption of alcoholic beverages. 

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