Needs C J, Brooks P M
Br J Rheumatol. 1985 Aug;24(3):282-90. doi: 10.1093/rheumatology/24.3.282.
Drug effects on fetal physiology as well as possible teratogenesis need to be considered before prescribing for women of child-bearing age. All nonsteroidal anti-inflammatory drugs (NSAIDs), because of their suppression of prostaglandin synthesis, may prolong gestation and labour. Aspirin is also associated with an increased risk of ante- and post-partum haemorrhage. Indomethacin may be teratogenic in humans and like aspirin may induce pulmonary hypertension in the neonate. To reduce the physiological alterations induced by NSAIDs, short-half-life drugs such as ibuprofen, flurbiprofen or ketoprofen should be used at the maximally tolerable dosage interval. Gold salts and corticosteroids show little human evidence of teratogenicity although the largest possible dosage interval of gold should be used. D-Penicillamine may be teratogenic thus it should not be commenced during pregnancy and if a patient becomes pregnant whilst receiving the drug, it should be slowly withdrawn or the dosage reduced. 4-Aminoquinoline compounds are contra-indicated in pregnancy.
在为育龄妇女开处方前,需要考虑药物对胎儿生理的影响以及可能的致畸作用。所有非甾体抗炎药(NSAIDs)由于抑制前列腺素合成,可能会延长妊娠期和产程。阿司匹林还与产前和产后出血风险增加有关。吲哚美辛在人类中可能具有致畸性,并且与阿司匹林一样,可能会诱发新生儿肺动脉高压。为减少NSAIDs引起的生理改变,应使用半衰期短的药物,如布洛芬、氟比洛芬或酮洛芬,并以最大耐受剂量间隔给药。金盐和皮质类固醇几乎没有人类致畸性的证据,不过应使用金的最大可能剂量间隔。青霉胺可能具有致畸性,因此在怀孕期间不应开始使用,如果患者在服药期间怀孕,应缓慢停药或减少剂量。4-氨基喹啉化合物在怀孕期间禁用。