Congestive heart failure

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Congestive heart failure









Risk factors and pathophysiology


Asymptomatic left ventricular systolic dysfunction (ALVSD) frequently progresses to congestive heart failure (CHF). This progression can be retarded by angiotensin-converting enzyme (ACE) inhibitors.3 ALVSD is a function of age. In community-based studies, almost all the young people with left [ventricular] systolic dysfunction (left ventricular ejection fraction [LVEF] greater than 30) are asymptomatic; in men older than age 65, half were asymptomatic, and in older women, only 27% were asymptomatic.4 This may be because the symptoms of CHF are manifestations of compensatory mechanisms used to maintain cardiac output. Data for patients older than age 75 are not available.


Left ventricular systolic dysfunction is the cause of CHF in the elderly patient in 50% to 60% of CHF cases. In the remainder, LVEF is normal but evidence of impaired ventricular filling is present.5 If significant valvular or pericardial disease is absent, CHF is then attributed to diastolic dysfunction. Normal LVEF, determined by echocardiography or nuclear techniques, is generally 50% or more. Significant left ventricular systolic dysfunction is defined as an LVEF less than 40%. There is no simple measure of diastolic function. CHF resulting from diastolic dysfunction may be so common in the elderly because aging itself results in a stiff, poorly relaxing left ventricle. Disease processes add to these aging effects.


CHF, a more advanced stage of heart failure (strictly defined as impairment in heart function leading to symptoms such as fatigue and dyspnea because of inadequate cardiac output), is defined as the presence of evidence of fluid retention manifested clinically by edema and congestion of the veins of the pulmonary and systemic circuits.



Differential diagnosis and assessment



Diagnosis


Classically, the diagnosis of CHF is based on history, physical examination, and chest x-ray (CXR) examination.6 Brain natriuretic peptide (BNP) testing has altered this approach. Diagnosis of CHF in the elderly may be difficult because the history is often atypical (Box 38-1), or unobtainable, or because the symptoms are minimized by the patient or attributed to age. One of the most common atypical presentations of CHF is delirium, which is frequently superimposed on preexisting dementia.



Physical signs of CHF are often overlooked. Jugular venous distention (JVD) and hepatojugular reflux are excellent signs of “right-sided failure.” S3 gallop remains reliable but is often difficult to hear. In contrast, the S4 is a common finding in otherwise healthy older patients. Crackles or rales on lung auscultation are nonspecific. Ankle edema often merely reflects inactivity or associated dependency of the legs.




A good-quality CXR may be difficult to obtain, especially in frail, older patients. Persistence until an adequate film is obtained pays rich diagnostic dividends. Consider performing the CXR examination with the patient sitting upright in the wheelchair. Key findings are an enlarged heart, enlarged hila with indistinct margins (perivascular edema), and prominent veins draining the upper lobes (cephalization of flow).


The measurement of BNP has revolutionized the diagnosis of CHF. BNP is specific to the ventricles, reflects stretch or tension of the left ventricle, and correlates well with the severity of CHF. BNP is elevated in both systolic and diastolic CHF. Patients with dyspnea and normal BNP are unlikely to have CHF as the cause of their symptoms. BNP levels decrease as CHF patients improve so monitoring BNP may be helpful. Healthy women have higher levels than do men, and BNP increases with age; thresholds used to discriminate normal from CHF may need age and sex adjustment. In addition, BNP is cleared by the kidneys so renal function influences BNP. Various parts of the peptide have been assayed but all appear to provide similar information.7 BNP has beneficial effects: natriuresis, diuresis, vasodilation, and antagonism of endothelin, aldosterone, and renin. Nesiritide (recombinant human BNP) produces these effects when infused in decompensated patients despite their preexisting BNP elevations. Nesiritide may be less arrhythmogenic than is dobutamine, but experience in elderly patients is limited. BNP, for diagnosis and monitoring, is valuable in the elderly, whereas the use of nesiritide is still being defined.7





Precipitating factors


Conditions increasing cardiovascular demand or interfering with compensatory mechanisms can precipitate CHF in otherwise compensated patients (Box 38-2). Frequent precipitating factors form the mnemonic DAMN IT:




Drugs—including withdrawal of ACE inhibitors, digitalis, or beta-blockers, and the administration of steroids or nonsteroidal antiinflammatory drugs (NSAIDs)


Arrhythmias—bradyarrhythmias, including heart block and tachyarrhythmias, especially atrial fibrillation


Myocardial ischemia—often presenting atypically (consider stress testing if suspicion is high)


Noncompliance—such as with diet, fluid restriction, or medications


Intravenous fluid administration


Thyroid—hyperthyroidism (thyroid-stimulating hormone and free T4 should be considered) (Box 38-3).



Pharmacologic stress testing can be used if exercise testing is not obtainable. Once precipitants are treated, the ongoing CHF regimen may need to be modified.




Jun 8, 2016 | Posted by in GERIATRICS | Comments Off on Congestive heart failure

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