Chapman S T
Clin Obstet Gynaecol. 1986 Jun;13(2):397-416.
Certain infections, such as UTI, may have an increased incidence during pregnancy owing to physiological changes. Between 2 and 10% of pregnant women have covert or asymptomatic bacteriuria which is associated with an increased incidence of acute symptomatic UTI in later pregnancy if left untreated. Thus antenatal screening to detect the presence of bacteriuria is justified. Most women will remain abacteriuric throughout the remainder of pregnancy after a single course of antibiotic therapy but a small percentage will fail to respond or have recurrent UTIs. Maternal infection with certain organisms, namely those which resist phagocytosis, may result in transplacental infection of the fetus in utero. Congenital syphilis is preventable and antenatal serological screening is usually routinely performed. Listeriosis following maternal infection in pregnancy is less predictable and the epidemiology of L. monocytogenes remains unclear. Genital tract carriage of sexually transmitted organisms, such as N. gonorrhoeae or C. trachomatis, may also be detected during pregnancy and antibiotic therapy will be indicated to eradicate such organisms and prevent maternal and neonatal morbidity. Antibiotic therapy during pregnancy will not, however, eradicate carriage of GBS from the genital tract, although carriage status at term can now be reliably predicted by using enriched culture techniques and swabbing multiple sites on more than one occasion. Where carriage is confirmed, the administration of intrapartum antibiotics to the mother appears a useful approach in the prevention of early onset neonatal GBS disease. Broad spectrum intrapartum antibiotics may also be indicated when there are complications, such as prolonged labour or premature rupture of membranes, which are associated with a higher incidence of maternal postpartum endometritis and morbidity than in women following uncomplicated vaginal delivery. Serious postnatal sepsis and shock is fortunately now rare. The pharmacokinetics of antibiotics in late pregnancy and the puerperium are altered and maternal serum levels may be reduced by 10-50%. Most antibiotics cross the placenta and are excreted in breast milk. Some agents, such as the beta-lactams, are considered safe in pregnancy and breast-feeding women while other antibiotics are contraindicated owing to risk of toxicity (often rare) or teratogenicity (often theoretical). Caution is necessary with many agents which may cause side effects or toxicity although this does not necessarily contraindicate their use in pregnancy.(ABSTRACT TRUNCATED AT 400 WORDS)
某些感染,如尿路感染(UTI),由于生理变化,在孕期的发病率可能会增加。2%至10%的孕妇有无症状菌尿,如果不治疗,这与后期妊娠急性症状性UTI的发病率增加有关。因此,进行产前筛查以检测菌尿的存在是合理的。大多数女性在接受一个疗程的抗生素治疗后,在孕期剩余时间内仍将保持无菌尿状态,但有一小部分女性可能无反应或反复发生UTI。母体感染某些微生物,即那些抵抗吞噬作用的微生物,可能导致胎儿在子宫内发生经胎盘感染。先天性梅毒是可预防的,产前血清学筛查通常是常规进行的。孕期母体感染后的李斯特菌病较难预测,单核细胞增生李斯特菌的流行病学仍不清楚。孕期也可能检测到性传播微生物,如淋病奈瑟菌或沙眼衣原体在生殖道的携带情况,此时需要进行抗生素治疗以根除这些微生物,预防母体和新生儿发病。然而,孕期使用抗生素并不能根除生殖道中的B族链球菌(GBS)携带,尽管现在通过使用富集培养技术和多次在多个部位擦拭取样,可以可靠地预测足月时的携带状态。如果确认有携带情况,在分娩时给母亲使用抗生素似乎是预防早发性新生儿GBS疾病的有效方法。当出现并发症,如产程延长或胎膜早破时,也可能需要使用广谱产时抗生素,这些并发症与母体产后子宫内膜炎和发病率较高有关,比无并发症的阴道分娩女性更高。幸运的是,严重的产后败血症和休克现在很少见。孕期晚期和产褥期抗生素的药代动力学发生改变,母体血清水平可能会降低10%至50%。大多数抗生素可穿过胎盘并在母乳中排泄。一些药物,如β-内酰胺类,被认为在孕期和哺乳期女性中是安全的,而其他抗生素由于存在毒性风险(通常很少见)或致畸性风险(通常是理论上的)而被禁用。许多可能引起副作用或毒性的药物需要谨慎使用,尽管这不一定意味着禁止在孕期使用。(摘要截选至400字)