Cleland P G
Sunderland District General Hospital, England.
Drug Saf. 1991 Jan-Feb;6(1):70-81. doi: 10.2165/00002018-199106010-00007.
Problems with anticonvulsants in women of child-bearing potential include potential adverse effects on appearance, contraception and pregnancy. These effects must be weighed against the overwhelming benefits of anticonvulsant treatment in the majority of women with epilepsy. Coarsened features, hirsutism and acne may occur in both men and women, particularly if they are exposed to phenytoin. Valproic acid may cause weight gain and hair loss, while carbamazepine treatment carries a significant risk of skin rashes. Anticonvulsants which are liver enzyme inducers (phenytoin, phenobarbital, primidone and carbamazepine) reduce the efficacy of the oral contraceptive pill. No 'pill failure' has been reported with valproic acid. There is a risk of increased seizure frequency in pregnancy irrespective of whether anticonvulsant treatment is taken. Individual seizures carry little risk to the mother or the fetus but status epilepticus has a significant maternal and fetal mortality. The risk of status epilepticus must be taken into account when deciding whether to stop anticonvulsant treatment before pregnancy. There is a 2 to 3 times increased malformation rate in the offspring of epileptic women on treatment. This is primarily due to the drug treatment, but epilepsy itself may also increase the malformation rate. Most malformations are mild and include facial clefts, congenital heart disease and skeletal abnormalities. Valproic acid, however, carries a 1% risk of causing neural tube defects: women receiving this drug who become pregnant should have an ultrasound and alpha-fetoprotein estimation at 16 to 18 weeks of pregnancy. If any abnormality is detected then amniocentesis should be carried out. Women with epilepsy should be counselled before conception and during pregnancy. Before achieving pregnancy a women should be on optimum treatment, preferably on one anticonvulsant. Consideration should be given to withdrawal of anticonvulsant drugs in any woman who has been seizure free for 2 years or who has only mild and infrequent seizures. Folate supplementation should be started prior to conception and should continue during pregnancy. There is a tendency for anticonvulsant drug concentrations to fall during pregnancy, and the dose may need to be increased if clinically indicated. Over 90% of epileptic women who become pregnant will have uneventful pregnancies and will produce healthy infants.
育龄期女性使用抗惊厥药物存在的问题包括对外观、避孕和妊娠的潜在不良影响。在大多数癫痫女性中,必须将这些影响与抗惊厥治疗的显著益处相权衡。男性和女性都可能出现面容粗糙、多毛和痤疮,尤其是在接触苯妥英的情况下。丙戊酸可能导致体重增加和脱发,而卡马西平治疗有发生皮疹的重大风险。作为肝酶诱导剂的抗惊厥药物(苯妥英、苯巴比妥、扑米酮和卡马西平)会降低口服避孕药的疗效。尚未有丙戊酸导致“避孕失败”的报道。无论是否进行抗惊厥治疗,妊娠期间癫痫发作频率都有增加的风险。单次发作对母亲或胎儿的风险较小,但癫痫持续状态有显著的母婴死亡率。在决定妊娠前是否停用抗惊厥药物时,必须考虑癫痫持续状态的风险。接受治疗的癫痫女性后代的畸形率增加2至3倍。这主要归因于药物治疗,但癫痫本身也可能增加畸形率。大多数畸形为轻度,包括唇腭裂、先天性心脏病和骨骼异常。然而,丙戊酸有致神经管缺陷的1%风险:服用此药的孕妇在妊娠16至18周时应进行超声检查和甲胎蛋白测定。如果检测到任何异常,则应进行羊膜穿刺术。癫痫女性在受孕前和孕期都应接受咨询。在怀孕前,女性应接受最佳治疗,最好使用一种抗惊厥药物。对于任何已无癫痫发作达2年或仅有轻微且不频繁发作的女性,应考虑停用抗惊厥药物。应在受孕前开始补充叶酸,并在孕期持续。妊娠期间抗惊厥药物浓度有下降趋势,如果有临床指征,可能需要增加剂量。超过90%怀孕的癫痫女性将有顺利的妊娠并产下健康婴儿。