Heart failure treatments: issues of safety versus issues of quality of life

J Feenstra1, J Lubsen, D E Grobbee

  • 1Drug Safety Unit, Inspectorate for Healthcare, The Hague, The Netherlands. feenstra@epib.fgg.eur.nl

Drug Safety
|February 6, 1999
PubMed

Insights

New congestive heart failure drugs may improve quality of life but reduce survival. Clinical trials must assess if improved quality of life justifies increased mortality risk for severe heart failure patients.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Trials

Background:

  • Congestive heart failure significantly impacts morbidity and mortality in Western countries.
  • Development of new heart failure drugs is ongoing due to the condition's profound effects on life expectancy and quality of life.

Purpose of the Study:

  • To evaluate the trade-off between improved quality of life and increased mortality risk with new congestive heart failure drugs.
  • To determine if quality of life improvements justify potential survival reduction in severe cases.

Main Methods:

  • Analysis of existing clinical trial data on new heart failure pharmacotherapies.
  • Assessment of studies evaluating both mortality and quality of life outcomes.

Main Results:

  • Some new heart failure agents show short-term quality of life benefits but reduced survival in trials.
  • Current trials often lack data on the composite probability of improved quality of life and survival.

Conclusions:

  • Drugs improving quality of life at the cost of mortality may benefit severe congestive heart failure patients.
  • Future clinical trials should assess composite probabilities of survival and quality of life benefits for innovative heart failure treatments.

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