Under-utilization of evidence-based drug treatment in patients with heart failure is only partially explained by dissimilarity to patients enrolled in landmark trials: a report from the Euro Heart Survey on Heart Failure

被引:128
作者
Lenzen, MJ
Boersma, E
Scholte op Reimer, WJM
Balk, AHMM
Komajda, M
Swedberg, K
Follath, F
Jimenez-Navarro, M
Simoons, ML
Cleland, JGF
机构
[1] Erasmus MC, Dept Cardiol, NL-3000 CA Rotterdam, Netherlands
[2] Hop La Pitie Salpetriere, Dept Cardiol, Paris, France
[3] Univ Gothenburg, Gothenburg, Sweden
[4] Sahlgrens Univ Hosp, S-41345 Gothenburg, Sweden
[5] Univ Zurich Hosp, Dept Internal Med, CH-8091 Zurich, Switzerland
[6] Univ Malaga, Hosp Clin Virgen Victoria, Dept Cardiol, E-29071 Malaga, Spain
[7] Castle Hill Hosp, Dept Cardiol, Kingston Upon Hull, Yorks, England
关键词
heart failure; randomized clinical trials; treatment; under-utilization;
D O I
10.1093/eurheartj/ehi499
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Surveys on heart failure management suggest under-utilization of life-saving evidence-based treatment. Evidence-based medicine and clinical guidelines are based on the results of randomized controlled trials. Therefore, we investigated how patients who fulfilled the enrolment criteria of randomized trials were treated in real life. Methods and results We selected three large placebo-controlled trials of patients with chronic heart failure, in which ACE-inhibitors (ACE-Is), beta-blockers, and spironolactone proved to be safe and effective. The major enrolment criteria of trials were identified and applied to patients enrolled in the Euro Heart Survey on Heart Failure to identify the proportion of patients eligible for treatment and also treated appropriately. Of the 10 701 patients who were enrolled in the Euro Heart Survey on Heart Failure, only a small percentage (13%) would have qualified for participation in at least one of the selected trials. Patients who fulfilled enrolment criteria of the identified trials were more likely to be treated with ACE-Is (83% of SOLVD-eligible patients), beta-blockers (54% of MERIT-HF-eligible patients), and aldosterone antagonists (43% of RALES-eligible patients) than trial-ineligible patients. Almost half of SOLVD-eligible patients who were treated with ACE-Is received the target dose as recommended in the guidelines, but only < 10% of MERIT-HF eligible patients who were treated with beta-blockers received the target dose. Conclusion ACE-Is are widely utilized but given in lower doses than proven effective in clinical trials. beta-Blockers are underused and given in lower doses to patients who fulfil the enrolment criteria of relevant landmark trials.
引用
收藏
页码:2706 / 2713
页数:8
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