Thohan Vinay, Patel Shomeet
Department of Cardiology, Wake Forest University School of Medicine, Medical Center Boulevard, Watlington One, Winston-Salem 27157, North Carolina, USA.
Curr Opin Cardiol. 2009 May;24(3):230-8. doi: 10.1097/HCO.0b013e328329f8fd.
Diastolic heart failure (DHF) is the culmination of various cardiovascular insults, producing a proportionally greater alteration of diastolic performance, subtle reductions of systolic function and the clinical syndrome of heart failure. Over half of heart failure patients aged 65 years or older have DHF, which carries similar morbidity and mortality to systolic heart failure (SHF). The aging population and increased prevalence of hypertension, diabetes mellitus and obesity will result in disproportionately higher incidence of DHF.
To date, seven large placebo-controlled trials have been conducted in DHF and none have convincingly demonstrated substantial morbidity or mortality reductions. This review will highlight DHF clinical trial efforts and provide explanations for the discordance between clinical trial patients and clinical practice patients.
Greater parity between clinical trial and clinical practice can be achieved by selecting DHF patients in the context of a few general principles: trials should enroll patients on the basis of the diagnostic criteria set forth by the European Study Group on Diastolic Heart Failure. A history of (<6 months) or current hospitalization for heart failure along with prespecified higher grades of diastolic dysfunction insures that a sufficiently at-risk population is studied. Patients with DHF are older, with multiple noncardiovascular comorbidities, and longer trial duration (>3 years) may be plagued with competing risks.
舒张性心力衰竭(DHF)是各种心血管损伤的最终结果,导致舒张功能出现相对更大的改变、收缩功能轻微降低以及心力衰竭临床综合征。65岁及以上的心力衰竭患者中,超过半数患有DHF,其发病率和死亡率与收缩性心力衰竭(SHF)相似。人口老龄化以及高血压、糖尿病和肥胖症患病率的增加将导致DHF发病率不成比例地升高。
迄今为止,已针对DHF开展了7项大型安慰剂对照试验,但均未令人信服地证明能显著降低发病率或死亡率。本综述将重点介绍DHF临床试验的情况,并解释临床试验患者与临床实践患者之间存在差异的原因。
通过遵循一些一般原则来选择DHF患者,可以使临床试验与临床实践之间实现更大程度的一致性:试验应根据欧洲舒张性心力衰竭研究组制定的诊断标准纳入患者。有(<6个月)心力衰竭病史或目前因心力衰竭住院,以及预先设定的较高等级舒张功能障碍,可确保研究足够高危的人群。DHF患者年龄较大,伴有多种非心血管合并症,且试验持续时间较长(>3年)可能会受到竞争风险的困扰。