Badano Luigi P, Di Lenarda Andrea, Bellotti Paolo, Albanese Maria C, Sinagra Gianfranco, Fioretti Paolo M
Cardiology Unit, Cardiovascular Science Department, S. Maria della Misericordia Hospital, Udine, Italy.
Ital Heart J. 2003 Feb;4(2):84-91.
BACKGROUND: The aim of this study was to compare the clinical characteristics of patients enrolled in randomized clinical trials on congestive heart failure treatment with those of real-world patients encountered in daily clinical practice. METHODS: We searched the Cochrane review methodology, Medline and SilverPlatter databases to obtain the clinical characteristics of both patients enrolled in therapeutic clinical trials and real-world patients with heart failure. We selected 27 clinical trials, and 8 prospective epidemiological studies or registries published between 1987 and 2001 which enrolled 53,859 and 18,207 patients, respectively. RESULTS: On average, compared to real-world heart failure patients, patients enrolled in clinical trials were younger (63 +/- 10 vs 75 +/- 11 years respectively, p < 0.0001), and more likely to be male (72 vs 54% respectively, p < 0.0001). Clinical trial patients showed a lower ejection fraction (26 +/- 7 vs 38 +/- 15% respectively, p < 0.0001) but a lower prevalence of NYHA functional class III-IV (62 vs 75% respectively, p < 0.0001) than real-world patients. In clinical trial patients, the prevalence of ischemic heart disease (67 vs 42% respectively, p < 0.0001) and a history of previous myocardial infarction (62 vs 42% respectively, p < 0.0001) were higher than in real-world patients. Conversely, the prevalence of chronic atrial fibrillation (12 vs 31% respectively, p < 0.0001) and of diabetes (22 vs 24% respectively, p < 0.02) was lower in trial patients than in real-world patients. CONCLUSIONS: Our data suggest that most clinical trials on congestive heart failure, on which the guidelines for clinical practice are based, have generally included patients who are not representative of the whole spectrum of patients actually managed in clinical practice.
背景:本研究旨在比较充血性心力衰竭治疗随机临床试验中纳入患者与日常临床实践中真实世界患者的临床特征。 方法:我们检索了Cochrane综述方法、Medline和SilverPlatter数据库,以获取治疗性临床试验中纳入患者及真实世界心力衰竭患者的临床特征。我们选取了27项临床试验,以及1987年至2001年间发表的8项前瞻性流行病学研究或登记研究,分别纳入了53859例和18207例患者。 结果:平均而言,与真实世界的心力衰竭患者相比,临床试验中的患者更年轻(分别为63±10岁和75±11岁,p<0.0001),且男性比例更高(分别为72%和54%,p<0.0001)。临床试验患者的射血分数较低(分别为26±7%和38±15%,p<0.0001),但纽约心脏协会(NYHA)心功能III-IV级的患病率低于真实世界患者(分别为62%和75%,p<0.0001)。在临床试验患者中,缺血性心脏病的患病率(分别为67%和42%,p<0.0001)和既往心肌梗死病史的患病率(分别为62%和42%,p<0.0001)高于真实世界患者。相反,试验患者中慢性心房颤动的患病率(分别为12%和31%,p<0.0001)和糖尿病的患病率(分别为22%和24%,p<0.02)低于真实世界患者。 结论:我们的数据表明,作为临床实践指南依据的大多数充血性心力衰竭临床试验,通常纳入的患者并不能代表临床实践中实际管理的所有患者类型。
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