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在一个健康维护组织中对接受异维甲酸治疗痤疮患者的观察性研究。

An observational study of isotretinoin recipients treated for acne in a health maintenance organization.

作者信息

McElwee N E, Schumacher M C, Johnson S C, Weir T W, Greene S L, Scotvold M J, Hunter J R, Dinan B J, Jick H

机构信息

Intermountain Regional Poison Control Center, Salt Lake City, UT 84132.

出版信息

Arch Dermatol. 1991 Mar;127(3):341-6.

PMID:1825596
Abstract

From September 1982 to June 1987, all members (N = 513) of the Group Health Cooperative of Puget Sound, Seattle, Wash, who were prescribed isotretinoin for acne were observed throughout the first 4- to 5-month course of therapy for effectiveness and adverse effects. The highest rates of use were among male subjects aged 15 to 24 years. Excluding 47 subjects whose prescriptions were stopped because of noncompliance or who left the care of Group Health Cooperative physicians, 39 (8.4%) of the remaining 466 discontinued taking the drug because of the following adverse effects: mucous/skin/musculoskeletal effects (17); elevated triglyceride levels (eight); headaches (five); increased liver enzyme levels (three); amenorrhea (two); and other (four). One subject, excluded from the 466 because of noncompliance, became pregnant while using medication from a previous prescription and had a therapeutic abortion; she was not under the care of a physician at the time of pregnancy. Most subjects (97%) developed a mucocutaneous symptom, and 42% developed musculoskeletal symptoms. Moderate elevations in liver enzyme levels developed in six (1.8%) of 341 subjects with normal baseline values. Of 389 subjects with normal baseline triglyceride values (less than 2.25 mmol/L), nine (2.3%) developed moderate elevations (4.5 to 9.0 mmol/L), and one (0.3%) developed a severe elevation (greater than or equal to 9.0 mmol/L). Of 24 subjects with elevated baseline triglyceride levels, three (12.5%) developed moderate elevations. Of an additional 53 subjects whose baseline serum triglyceride levels were not determined, two developed elevations during therapy, one up to 13.4 mmol/L. Subjects who were overweight or had elevated baseline serum triglyceride values had an increased risk of developing elevations in triglyceride levels during therapy (odds ratio, 6.0; 95% confidence interval, 1.6 to 22.0; and odds ratio, 4.35; 95% confidence interval, 0.9 to 20.2, respectively). Acne was improved for at least 94.0% of subjects.

摘要

1982年9月至1987年6月,华盛顿州西雅图普吉特海湾集团健康合作社的所有成员(N = 513),凡因痤疮而开具异维甲酸处方者,在治疗的头4至5个月疗程中均接受了疗效和不良反应观察。使用率最高的是年龄在15至24岁的男性受试者。排除47名因不依从或离开集团健康合作社医生诊疗而停药的受试者后,其余466名受试者中有39名(8.4%)因以下不良反应而停药:黏液/皮肤/肌肉骨骼效应(17例);甘油三酯水平升高(8例);头痛(5例);肝酶水平升高(3例);闭经(2例);以及其他(4例)。一名因不依从而被排除在466名受试者之外的受试者,在服用前一疗程药物时怀孕并接受了治疗性流产;她怀孕时未接受医生诊疗。大多数受试者(97%)出现了皮肤黏膜症状,42%出现了肌肉骨骼症状。341名基线值正常的受试者中有6名(1.8%)肝酶水平出现中度升高。在389名基线甘油三酯值正常(低于2.25 mmol/L)的受试者中,9名(2.3%)出现中度升高(4.5至9.0 mmol/L),1名(0.3%)出现重度升高(大于或等于9.0 mmol/L)。在24名基线甘油三酯水平升高的受试者中,3名(12.5%)出现中度升高。在另外53名未测定基线血清甘油三酯水平的受试者中,2名在治疗期间出现升高,其中1名高达13.4 mmol/L。超重或基线血清甘油三酯值升高的受试者在治疗期间甘油三酯水平升高的风险增加(优势比分别为6.0;95%置信区间为1.6至22.0;以及优势比为4.35;95%置信区间为0.9至20.2)。至少94.0%的受试者痤疮得到改善。

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