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前列腺素合成酶抑制剂治疗原发性痛经。疗效试验综述。

Prostaglandin synthetase inhibitors in the treatment of primary dysmenorrhea. Outcome trials reviewed.

作者信息

Owen P R

出版信息

Am J Obstet Gynecol. 1984 Jan 1;148(1):96-103. doi: 10.1016/s0002-9378(84)80039-3.

Abstract

Clinical trials of prostaglandin synthetase inhibitors (PGSIs) prescribed for the treatment of primary dysmenorrhea were reviewed as to pain relief effectiveness, frequency and nature of side effects, and methodological adequacy. The review investigated 51 PGSI trials for a total of 1,649 women and 682 menstrual cycles and found that, over all, 72% of dysmenorrheic women reported significant pain relief to PGSI, 18% reported minimal or no pain relief, and 15% showed placebo response. Comparisons among the fenamatic compounds, ibuprofen, indomethacin, and naproxen showed the fenamates to be more effective in providing pain relief. PGSI-associated side effects were minimal for all PGSIs with the exception of indomethacin. Results were evaluated with respect to several methodological problems. Conclusions were drawn that despite these shortcomings, PGSIs are undoubtedly effective and safe for the majority of women with primary dysmenorrhea.

摘要

对用于治疗原发性痛经的前列腺素合成酶抑制剂(PGSIs)的临床试验进行了回顾,内容涉及疼痛缓解效果、副作用的频率和性质以及方法学的充分性。该回顾调查了51项PGSIs试验,涉及总共1649名女性和682个月经周期,发现总体而言,72%的痛经女性报告PGSIs能显著缓解疼痛,18%报告疼痛缓解极少或无缓解,15%显示出安慰剂反应。在非那酸类化合物、布洛芬、吲哚美辛和萘普生之间的比较表明,非那酸类在缓解疼痛方面更有效。除吲哚美辛外,所有PGSIs与PGSI相关的副作用都极小。针对几个方法学问题对结果进行了评估。得出的结论是,尽管存在这些缺点,但PGSIs对大多数原发性痛经女性无疑是有效且安全的。

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