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宫缩抑制剂治疗的最新进展。

Update on tocolytic therapy.

作者信息

McCombs J

机构信息

College of Pharmacy, University of Georgia, Athens 30602, USA.

出版信息

Ann Pharmacother. 1995 May;29(5):515-22. doi: 10.1177/106002809502900511.

Abstract

OBJECTIVE

To review medications currently being used or investigated for the treatment of preterm labor. Adverse effects, pharmacoeconomic issues, and therapeutic controversies are included.

DATA SOURCES

A MEDLINE search, limited to English-language articles and publication years of 1989-1994, was used to identify pertinent literature. Additional references were identified from articles retrieved in the search.

STUDY SELECTION

Studies were chosen on drugs that are available or whose approval is anticipated in the US: ritodrine, terbutaline, hexoprenaline, and magnesium sulfate. Several studies comparing indomethacin and nifedipine with currently used medications are also included. Oxytocin antagonists, now in Phase II clinical trials, are discussed. Studies focusing on adverse reactions were included because of serious concerns that these reactions raise.

DATA EXTRACTION

Part of the controversy surrounding tocolytic agents involves the difficulty in comparing data from different trials, particularly because the criteria for diagnosis of preterm labor vary significantly. Therefore, no attempt was made to directly compare data from different sources; individual study data are presented.

DATA SYNTHESIS

Most studies reviewed using the beta-agonists showed each to be comparable in effectiveness when given parenterally during early preterm labor. These drugs usually delay delivery for 24-48 hours. There is less evidence that they are consistently effective in the long-term treatment of preterm labor. The adverse effects vary somewhat, but all beta-agonists have been reported to cause pulmonary edema, which is the most serious adverse effect associated with the use of these medications to inhibit labor. Indomethacin and nifedipine may be alternative choices for tocolytic therapy, but each has different adverse reactions that also make them less than ideal agents. Oxytocin antagonists may provide more specific therapy and are currently being investigated.

CONCLUSIONS

The beta-agonists are effective in delaying delivery for 24-48 hours in most patients; however, there are potential risks involved. Magnesium sulfate, prostaglandin synthetase inhibitors, calcium-channel blockers, and oxytocin antagonists may provide alternative choices for the treatment of preterm labor associated with neonatal morbidity and mortality. Each of the medications has advantages and disadvantages at different stages of gestation.

摘要

目的

综述目前用于治疗早产或正在研究的药物。包括不良反应、药物经济学问题及治疗方面的争议。

资料来源

利用MEDLINE检索,限于1989 - 1994年发表的英文文章来识别相关文献。从检索到的文章中确定其他参考文献。

研究选择

选择在美国已上市或预期批准的药物的研究:利托君、特布他林、己丙肾上腺素和硫酸镁。还纳入了几项比较吲哚美辛和硝苯地平与目前使用药物的研究。讨论了目前处于Ⅱ期临床试验阶段的缩宫素拮抗剂。由于对这些反应的严重关注,纳入了关注不良反应的研究。

资料提取

围绕宫缩抑制剂的部分争议涉及比较不同试验数据的困难,特别是因为早产的诊断标准差异很大。因此,未尝试直接比较不同来源的数据;呈现的是个别研究数据。

资料综合

大多数使用β - 激动剂的综述研究表明,在早产早期经胃肠外给药时,每种药物的有效性相当。这些药物通常可使分娩延迟24 - 48小时。较少有证据表明它们在早产的长期治疗中始终有效。不良反应有所不同,但据报道所有β - 激动剂都会引起肺水肿,这是与使用这些药物抑制宫缩相关的最严重不良反应。吲哚美辛和硝苯地平可能是宫缩抑制治疗的替代选择,但每种药物都有不同的不良反应,这也使其并非理想药物。缩宫素拮抗剂可能提供更具针对性的治疗,目前正在研究中。

结论

β - 激动剂对大多数患者可有效延迟分娩24 - 48小时;然而,存在潜在风险。硫酸镁、前列腺素合成酶抑制剂、钙通道阻滞剂和缩宫素拮抗剂可能为治疗与新生儿发病率和死亡率相关的早产提供替代选择。每种药物在妊娠不同阶段都有优缺点。

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