Hensrud D D, Connolly H M, Grogan M, Miller F A, Bailey K R, Jensen M D
Division of Preventive and Occupational Medicine and Internal Medicine, Mayo Clinic Rochester, Minn 55905, USA.
Mayo Clin Proc. 1999 Dec;74(12):1191-7. doi: 10.4065/74.12.1191.
To determine the echocardiographic changes over time of valvular heart lesions in patients who took the weight loss drugs fenfluramine and phentermine.
This prospective cohort study began at the termination of a randomized, double-blind, placebo-controlled weight loss trial of 18 obese women and 13 obese men (mean age, 42 years; mean body mass index, 33.4 kg/m2) who had been assigned randomly to treatment with fenfluramine and phentermine or to placebo. Echocardiograms were obtained at termination of the trial when fenfluramine was withdrawn from the market and 6 months later. They were interpreted independently by 3 cardiologists blinded to treatment assignment and temporal sequence of the echocardiograms. The main outcome measure was the change in drug-related valvular disease over time.
One subject assigned to receive the drugs was lost to follow-up, and 3 subjects who did not meet a weight loss goal of 10 kg crossed over from placebo to drug treatment. Echocardiograms were obtained in 19 subjects who received the drugs and 11 subjects who received placebo, and 6-month follow-up echocardiograms were obtained in 15 subjects who received the drugs and 3 who received placebo. Subjects had taken fenfluramine and phentermine a mean of 41 weeks (range, 8-73 weeks). Five of 19 subjects who received the drugs (26%; 95% confidence interval, 7%-46%) and 1 of 11 who received placebo (9%) (odds ratio, 3.6; 95% confidence interval, 0.4-35.6) had findings that met criteria established for drug-related valvular disease. All 5 subjects (4 women and 1 man) receiving the drugs had mild aortic regurgitation, and 1 also had pulmonary hypertension (estimated pulmonary artery pressure, 59 mm Hg). Six months later, the echocardiographic findings had improved in all 5 subjects (P=.06), and 3 no longer met the criteria for drug-related valvular disease. Pulmonary artery pressures decreased to near normal in the subject with pulmonary hypertension (37 mm Hg). Overall, the echocardiographic valvular features improved in 8 of 15 subjects who received the drugs and had echocardiograms performed at both time periods (P=.008).
Valvular heart disease did not appear to progress after cessation of use of fenfluramine and phentermine, and echocardiographic valvular features appeared to improve over time.
确定服用减肥药物芬氟拉明和苯丁胺的患者心脏瓣膜病变随时间的超声心动图变化。
这项前瞻性队列研究始于一项针对18名肥胖女性和13名肥胖男性(平均年龄42岁;平均体重指数33.4kg/m²)的随机、双盲、安慰剂对照减肥试验结束时,这些受试者被随机分配接受芬氟拉明和苯丁胺治疗或安慰剂治疗。在试验结束时(当时芬氟拉明已退市)及6个月后获取超声心动图。由3名对治疗分配和超声心动图时间顺序不知情的心脏病专家独立解读这些超声心动图。主要结局指标是药物相关瓣膜病随时间的变化。
1名被分配接受药物治疗的受试者失访,3名未达到10kg体重减轻目标的受试者从安慰剂组转至药物治疗组。对19名接受药物治疗的受试者和11名接受安慰剂治疗的受试者进行了超声心动图检查,对15名接受药物治疗的受试者和3名接受安慰剂治疗的受试者进行了6个月的随访超声心动图检查。受试者服用芬氟拉明和苯丁胺的平均时间为41周(范围8 - 73周)。19名接受药物治疗的受试者中有5名(26%;95%置信区间,7% - 46%)以及11名接受安慰剂治疗的受试者中有1名(9%)(比值比,3.6;95%置信区间,0.4 - 35.6)的检查结果符合药物相关瓣膜病的既定标准。所有5名接受药物治疗的受试者(4名女性和1名男性)均有轻度主动脉瓣反流,其中1名还患有肺动脉高压(估计肺动脉压59mmHg)。6个月后,所有5名受试者的超声心动图检查结果均有改善(P = 0.06),3名不再符合药物相关瓣膜病的标准。患有肺动脉高压的受试者肺动脉压降至接近正常水平(37mmHg)。总体而言,在两个时间段均进行了超声心动图检查的15名接受药物治疗的受试者中,有8名的超声心动图瓣膜特征有所改善(P = 0.008)。
停用芬氟拉明和苯丁胺后,心脏瓣膜病似乎并未进展,且超声心动图瓣膜特征似乎随时间有所改善。