Cambon David, Leclercq Florence
Department of Cardiology, University Hospital Montpellier, Montpellier, France.
Department of Cardiology, University Hospital Montpellier, Montpellier, France.
Arch Cardiovasc Dis. 2015 Mar;108(3):172-80. doi: 10.1016/j.acvd.2014.10.006. Epub 2015 Mar 6.
Fenfluramine and its derivatives have been associated with significant risk of developing valvular heart disease but its exact prevalence and severity are still debated.
To evaluate the clinical and echocardiographic characteristics of patients hospitalized in a cardiology centre and who had past exposure to these drugs.
Between July 2011 and February 2012, patients admitted to the hospitalization and intensive care units at the University Centre of Montpellier, France were questioned about past exposure to fenfluramine or its derivatives. In patients who reported exposure, a questionnaire assessing prescribing patterns and medical history was proposed and echocardiography performed. All of the usual echocardiographic variables were analysed. We applied criteria from a French multicentre registry for diagnosis of drug-induced valvulopathy: leaflets and subvalvular apparatus thickening and retraction, leaflets loss of coaptation, no calcification, and no stenosis.
Ninety-five patients exposed to these drugs were included. The majority were female (n=62, 65.3%), 53.2% (n=50) had diabetes and 90.5% (n=86) were exposed to benfluorex. Mean treatment duration was 52.3months (95% confidence interval [CI] 39.0-65.6). Valvular regurgitations were observed in 64.0% of patients (n=57) while 19.8% (n=17) had pulmonary hypertension. Highly probable fenfluramine-induced regurgitations were present in 18.6% (n=16) of patients, possibly fenfluramine-induced regurgitations in 38.2% (n=34) of patients, and unlikely fenfluramine-induced regurgitations in 25.8% (n=23) of patients. Highly probable fenfluramine-induced regurgitations were mild to moderate in severity in all except three patients.
Considering the frequency of probable or possible fenfluramine-induced regurgitations and in the absence of definite knowledge about the evolution of drug-induced valvular disease, systematic questioning about fenfluramine use may be advisable in hospitalized cardiac patients.
芬氟拉明及其衍生物与患心脏瓣膜病的重大风险相关,但其确切患病率和严重程度仍存在争议。
评估在心脏病中心住院且既往接触过这些药物的患者的临床和超声心动图特征。
2011年7月至2012年2月期间,对法国蒙彼利埃大学中心住院部和重症监护病房收治的患者询问其既往是否接触过芬氟拉明或其衍生物。对于报告有接触史的患者,发放一份评估用药模式和病史的问卷,并进行超声心动图检查。分析所有常规超声心动图变量。我们采用法国多中心登记处的标准来诊断药物性瓣膜病:瓣叶和瓣下结构增厚及回缩、瓣叶对合不良、无钙化且无狭窄。
纳入了95名接触过这些药物的患者。大多数为女性(n = 62,65.3%),53.2%(n = 50)患有糖尿病,90.5%(n = 86)接触过苄氟雷司。平均治疗时长为52.3个月(95%置信区间[CI] 39.0 - 65.6)。64.0%的患者(n = 57)观察到瓣膜反流,19.8%(n = 17)患有肺动脉高压。18.6%的患者(n = 16)存在极有可能由芬氟拉明引起的反流,38.2%的患者(n = 34)可能由芬氟拉明引起反流,25.8%的患者(n = 23)不太可能由芬氟拉明引起反流。除3名患者外,极有可能由芬氟拉明引起的反流严重程度均为轻度至中度。
考虑到可能或极有可能由芬氟拉明引起的反流的发生率,且在对药物性瓣膜病的演变缺乏确切了解的情况下,对于住院心脏病患者,建议系统性询问芬氟拉明的使用情况。