brand logo

Am Fam Physician. 2004;69(1):71-72

Clinical Scenario

A 63-year-old man with a history of congestive heart failure (CHF) and an ejection fraction of 25 percent presents with dyspnea on moderate exertion. He has a regular heartbeat, basilar crackles, and 3+ pitting edema on both legs.

Clinical Question

Should we prescribe digitalis for treatment of CHF in patients in normal sinus rhythm?

Evidence-Based Answer

Adding digitalis to treatment with angiotensin-converting enzyme (ACE) inhibitors and diuretics will reduce hospitalization rates and improve clinical status in patients in normal sinus rhythm with left ventricular systolic dysfunction (LVSD) and symptoms of CHF on moderate or mild exertion (New York Hospital Association [NYHA] class II or III). However, the addition of digitalis to ACE inhibitor or diuretic therapy will not reduce the risk of death. The incremental benefit of adding digitalis to regimens already including ACE inhibitors, beta blockers, and spironolactone (Aldactone) is unclear.

Cochrane Abstract

Background. Digitalis glycosides have been used clinically to treat CHF for more than 200 years. In recent years, several trials have been conducted to address concerns about the efficacy and potential toxicity of digitalis. Although a systematic review of the literature was published recently, an update is required to include more current trials.

Objectives. To examine the effectiveness of digitalis glycosides in treating CHF in patients with normal sinus rhythm and the effect of digitalis in patients taking diuretics, ACE inhibitors, and beta blockers; patients with varying severity and duration of disease; patients with prior exposure to digitalis compared with no prior exposure; and patients with diastolic versus systolic dysfunction.

Search Strategy. The authors1 searched electronic databases from 1966 to 2000. Dissertation Abstracts and annual meeting abstracts of the American Heart Association, American College of Cardiology, and European Society of Cardiology were searched from 1996 to 2000. In addition, reference lists provided by Glaxo Wellcome Inc. were searched.

Selection Criteria. The authors included randomized, placebo-controlled trials of 20 or more adult patients with symptomatic CHF who were studied for seven weeks or more. They excluded trials in which the prevalence of atrial fibrillation was 2 percent or greater, or in which any arrhythmia that might compromise cardiac function or any potentially reversible cause of heart failure (e.g., acute ischemic heart disease, myocarditis) was present.

Data Collection and Analysis. Selected articles were reviewed by one of the coauthors and validated by staff from the central office of the Heart Collaborative Review Group in Bristol, U.K.

Primary Results. Eleven articles meeting the defined criteria were identified, and eight, four, and 10 of these trials had end points of mortality, hospitalization, and clinical status, respectively. The data show that there is no evidence of a difference in mortality rates between treatment and control groups, although digitalis therapy is associated with lower rates of hospitalization and clinical deterioration.

Reviewers' Conclusions. The literature indicates that digitalis has a useful role in the treatment of patients with CHF who are in normal sinus rhythm.

These summaries have been derived from Cochrane reviews published in the Cochrane Database of Systematic Reviews in the Cochrane Library. Their content has, as far as possible, been checked with the authors of the originalreviews, but the summaries should not be regarded as an official product of the Cochrane Collaboration; minorediting changes have been made to the text (http://www.cochrane.org)

Practice Pointers

The most recent guidelines on evaluation and management of heart failure from the American College of Cardiology and the American Heart Association2 include a new staging system (see the accompanying table) and emphasize management of CHF. Risk factor reduction is recommended in patients at risk for heart failure who are asymptomatic and have structurally normal hearts (stage A), and ACE inhibitors and beta blockers are recommended in patients with asymptomatic LVSD (stage B). Digitalis is advised for use only in patients who need symptom control in stage C (equivalent to NYHA class II or III) or stage D (equivalent to NYHA class IV).3

This Cochrane review combines data from 11 studies—the large Digitalis Investigators Group (DIG) trial4 and 10 smaller trials—to assess the effect of digitalis on three patient-oriented end points: mortality rates, hospitalization rates, and clinical outcomes. Most patients in these studies had NYHA class II or III heart failure and an ejection fraction of 25 to 30 percent, and also were taking diuretics and ACE inhibitors.

Meta-analysis of the eight studies that addressed mortality found no evidence that treatment with digitalis decreased the risk of death. Combined data from the DIG study and three smaller, shorter studies found that digitalis reduced hospital admissions (25.4 versus 33.1 percent, P < .001); approximately 13 patients would need to be treated with digitalis to prevent one hospitalization over the three- to five-year study period of the DIG trial. Meta-analysis of the 10 smaller studies that addressed clinical outcomes found a 71 percent relative reduction in risk of clinical deterioration at three months of digitalis therapy, but the precise meaning of “clinical deterioration” varied between studies.

There have been no new major studies of digitalis in heart failure since this Cochrane review was revised in May 2001, but a retrospective review of the original DIG data suggests that lower serum digitalis concentrations may be most beneficial. When patients in the DIG study were grouped according to serum digitalis concentration (SDC) after the first month of therapy, patients with an SDC of 0.5 to 0.8 ng per mL had lower rates of death and hospitalization than the control patients, and patients with an SDC of 1.2 ng per mL or greater had a higher rate of death than control patients.5

NYHA functional classesACC/AHA stages
I. Asymptomatic LVSDA. Asymptomatic high risk
II. Symptoms with moderate exertionB. LVSD without symptoms
III. Symptoms with mild exertionC. LVSD and symptomatic heart failure
IV. Symptoms at restD. End-stage heart failure

Recent research has also highlighted the importance of beta blockers in NYHA class II to IV heart failure, and spironolactone in NYHA class IV heart failure. Although approximately 60 to 70 percent of the patients in the major studies of metoprolol,6 carvedilol,7 and spironolactone8 were taking digitalis, no retrospective or prospective information has been published on the impact of the addition of digitalis to therapy with ACE inhibitors, beta blockers, and spironolactone.

These are summaries of reviews from the Cochrane Library.

This series is coordinated by Corey D. Fogleman, MD, assistant medical editor.

A collection of Cochrane for Clinicians published in AFP is available at https://www.aafp.org/afp/cochrane.

Continue Reading


More in AFP

More in PubMed

Copyright © 2004 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP.  See permissions for copyright questions and/or permission requests.