Suppr超能文献

一项基于人群的食欲抑制药物与心脏瓣膜反流风险的研究。

A population-based study of appetite-suppressant drugs and the risk of cardiac-valve regurgitation.

作者信息

Jick H, Vasilakis C, Weinrauch L A, Meier C R, Jick S S, Derby L E

机构信息

Boston Collaborative Drug Surveillance Program, Boston University Medical Center, Lexington, MA 02421, USA.

出版信息

N Engl J Med. 1998 Sep 10;339(11):719-24. doi: 10.1056/NEJM199809103391102.

Abstract

BACKGROUND

Recent case reports suggest that a combination of the appetite suppressants fenfluramine and phentermine is associated with an increased risk of cardiac-valve regurgitation. There are also reports of valvular disorders in persons taking fenfluramine or dexfenfluramine alone, particularly for more than three months.

METHODS

We conducted a population-based follow-up study and a nested case-control analysis of 6532 subjects who received dexfenfluramine, 2371 who received fenfluramine, and 862 who received phentermine to assess the risk of a subsequent clinical diagnosis of a valvular disorder of uncertain origin. For comparison, we identified a group of 9281 obese subjects who had not taken appetite suppressants who were matched to the treated subjects for age, sex, and weight. All subjects were free of diagnosed cardiovascular disease at the start of follow-up. The average duration of follow-up for all subjects was about four years.

RESULTS

There were 11 cases of newly diagnosed idiopathic valvular disorders, 5 after the use of dexfenfluramine and 6 after the use of fenfluramine. There were six cases of aortic regurgitation, two cases of mitral regurgitation, and three cases of combined aortic and mitral regurgitation. There were no cases of idiopathic cardiac-valve abnormalities among the subjects who had not taken appetite suppressants or among those who took only phentermine. The five-year cumulative incidence of idiopathic cardiac-valve disorders was 0 per 10,000 subjects among those who had not taken appetite suppressants (95 percent confidence interval, 0 to 15.4) and among those who took phentermine alone (95 percent confidence interval, 0 to 76.6), 7.1 per 10,000 subjects among those who took either fenfluramine or dexfenfluramine for less than four months (95 percent confidence interval, 3.6 to 17.8; P=0.02 for the comparison with subjects who had not taken appetite suppressants), and 35.0 per 10,000 subjects among those who received either of these medications for four or more months (95 percent confidence interval, 16.4 to 76.2; P<0.001).

CONCLUSIONS

The use of fenfluramine or dexfenfluramine, particularly for four months or longer, is associated with an increased risk of newly diagnosed cardiac-valve disorders, particularly aortic regurgitation.

摘要

背景

近期的病例报告表明,食欲抑制剂芬氟拉明和苯丁胺联合使用会增加心脏瓣膜反流的风险。也有报告称,单独服用芬氟拉明或右芬氟拉明的人出现瓣膜疾病,尤其是服用超过三个月的人。

方法

我们进行了一项基于人群的随访研究,并对6532名接受右芬氟拉明治疗的受试者、2371名接受芬氟拉明治疗的受试者和862名接受苯丁胺治疗的受试者进行了巢式病例对照分析,以评估随后临床诊断为不明原因瓣膜疾病的风险。为作比较,我们确定了一组9281名未服用食欲抑制剂的肥胖受试者,他们在年龄、性别和体重方面与接受治疗的受试者相匹配。所有受试者在随访开始时均无已诊断出的心血管疾病。所有受试者的平均随访时间约为四年。

结果

有11例新诊断的特发性瓣膜疾病,5例在使用右芬氟拉明后出现,6例在使用芬氟拉明后出现。有6例主动脉瓣反流,2例二尖瓣反流,3例主动脉瓣和二尖瓣联合反流。在未服用食欲抑制剂的受试者或仅服用苯丁胺的受试者中,没有特发性心脏瓣膜异常病例。未服用食欲抑制剂的受试者(95%置信区间,0至15.4)和仅服用苯丁胺的受试者(95%置信区间,0至76.6)中,特发性心脏瓣膜疾病的五年累积发病率为每10,000名受试者0例;服用芬氟拉明或右芬氟拉明少于四个月的受试者中,每10,000名受试者中有7.1例(95%置信区间,3.6至17.8;与未服用食欲抑制剂的受试者相比,P=0.02);接受这两种药物治疗四个月或更长时间的受试者中,每10,000名受试者中有35.0例(95%置信区间,16.4至76.2;P<0.001)。

结论

使用芬氟拉明或右芬氟拉明,尤其是使用四个月或更长时间,会增加新诊断的心脏瓣膜疾病的风险,尤其是主动脉瓣反流。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验