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去氧孕烯、诺孕酯和孕二烯酮:新型孕激素。

Desogestrel, norgestimate, and gestodene: the newer progestins.

作者信息

Kaplan B

机构信息

School of Medicine, West Virginia University, Robert C Byrd Health Sciences Center, Charleston 25304, USA.

出版信息

Ann Pharmacother. 1995 Jul-Aug;29(7-8):736-42. doi: 10.1177/106002809502907-817.

Abstract

OBJECTIVE

To review and compare the newer progestins desogestrel, norgestimate, and gestodene with regard to chemistry, pharmacokinetics, efficacy, and tolerability.

DATA SOURCES

Primary literature on desogestrel, norgestimate, and gestodene was identified from a comprehensive MEDLINE English-literature search from 1984 through 1994, with additional studies selected by review of the references. Indexing terms included progestins, desogestrel, gestodene, norgestimate, levonorgestrel, and norgestrel.

STUDY SELECTION

Only human clinical and pharmacokinetic trials performed in Europe, Canada, and the US were included.

DATA EXTRACTION

All available data from human studies were reviewed; both comparative and noncomparative studies were included because of the paucity of direct comparative information available.

DATA SYNTHESIS

The newer progestins were designed to minimize the adverse effects (e.g., acne, hirsuitism, nausea, carbohydrate and lipid metabolism changes) observed with older oral contraceptives (OCs) while maintaining efficacy and good menstrual cycle control. Desogestrel, norgestimate, and gestodene have minimal amounts of androgenicity and antiestrogenic potential. All of these agents are pharmacokinetically similar to older agents: they are highly bioavailable when administered orally, hepatically metabolized, and obtain steady-state concentrations after 8-10 days of continuous administration. The newer agents have similar Pearl Indexes and slightly better cycle control. Furthermore, the new progestins appear to cause fewer adverse effects, such as acne and hirsuitism, and similar rates of weight gain, blood pressure changes, and lipid and carbohydrate metabolism changes.

CONCLUSIONS

Desogestrel, norgestimate, and gestodene appear to offer clinical advantages because of their decreased androgenicity. Women whose cycles are currently well controlled with other OCs should not be switched to a newer progestin. However, any of the combination OC products that contain these progestins may be prescribed for women intolerant of older agents or to first-time users of OCs. The newer progestins appear to be efficacious and offer similar cycle control, improved safety and tolerability profiles, and comparable price with the older agents.

摘要

目的

对新型孕激素去氧孕烯、诺孕酯和孕二烯酮在化学结构、药代动力学、疗效和耐受性方面进行综述和比较。

资料来源

通过对1984年至1994年全面的MEDLINE英文文献检索,确定了关于去氧孕烯、诺孕酯和孕二烯酮的原始文献,并通过参考文献回顾选择了其他研究。索引词包括孕激素、去氧孕烯、孕二烯酮、诺孕酯、左炔诺孕酮和炔诺孕酮。

研究选择

仅纳入在欧洲、加拿大和美国进行的人体临床和药代动力学试验。

资料提取

回顾了人体研究的所有可用数据;由于缺乏直接的比较信息,纳入了比较性和非比较性研究。

资料综合

新型孕激素的设计目的是在保持疗效和良好月经周期控制的同时,尽量减少与 older口服避孕药(OCs)相关的不良反应(如痤疮、多毛症、恶心、碳水化合物和脂质代谢变化)。去氧孕烯、诺孕酯和孕二烯酮的雄激素活性和抗雌激素潜力极小。所有这些药物在药代动力学上与 older药物相似:口服给药时生物利用度高,经肝脏代谢,连续给药8-10天后达到稳态浓度。新型药物的Pearl指数相似,周期控制稍好。此外,新型孕激素似乎引起的不良反应较少,如痤疮和多毛症,体重增加、血压变化以及脂质和碳水化合物代谢变化的发生率相似。

结论

去氧孕烯、诺孕酯和孕二烯酮因其雄激素活性降低而似乎具有临床优势。目前使用其他OCs月经周期控制良好的女性不应改用新型孕激素。然而,任何含有这些孕激素的复方OC产品都可开给不耐受 older药物的女性或初次使用OCs的女性。新型孕激素似乎有效,提供相似的周期控制、改善的安全性和耐受性,且价格与 older药物相当。

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