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拉贝洛尔在妊娠期重度高血压治疗中的应用。

Use of labetalol in the treatment of severe hypertension during pregnancy.

作者信息

Michael C A

出版信息

Br J Clin Pharmacol. 1979;8(Suppl 2):211S-215S.

Abstract

1 Labetalol, a hypotensive agent combining alpha- and beta-adrenoceptor antagonist properties, was used to treat severe hypertensive disease complicating pregnancy. 2 Effective reduction in BP was achieved in all but 3 of the 25 patients treated. Careful monitoring of feto-placental function was undertaken to ensure the maintenance of fetal well-being. Maternal and fetal side-effects were minimal and it was not necessary to discontinue the drug in any patient. 3 Labetalol was estimated in the cord blood of the fetus at delivery as well as in the breast milk of mothers on day 3 post partum. There were no adverse effects of the drug on the infants and significant hypotension did not occur. 4 The reults suggest that labetalol has a direct action on fetal lung maturation and this, together with its effective hypotensive effect, contributes to the low perinatal mortality (3.5%) observed. 5 Oculotoxicity due to the labetalol was not observed in the infants delivered. 6 It is concluded that the efficient hypotensive action of labetalol, together with apparent freedom from maternal and fetal side-effects, and consequent improved perinatal mortality, suggest that it is a suitable drug for use in pregnancy complicated by hypertension.

摘要
  1. 拉贝洛尔是一种兼具α和β肾上腺素能受体拮抗特性的降压药,用于治疗妊娠合并重度高血压疾病。2. 在接受治疗的25例患者中,除3例之外,其余患者的血压均有效降低。对胎儿 - 胎盘功能进行了密切监测,以确保胎儿的健康。母体和胎儿的副作用极小,没有必要在任何患者中停用该药物。3. 在分娩时对胎儿的脐血以及产后第3天母亲的母乳中的拉贝洛尔进行了测定。该药物对婴儿没有不良影响,也未发生明显的低血压。4. 结果表明,拉贝洛尔对胎儿肺成熟有直接作用,这与其有效的降压作用一起,促成了所观察到的低围产期死亡率(3.5%)。5. 在分娩的婴儿中未观察到拉贝洛尔引起的眼毒性。6. 得出的结论是,拉贝洛尔有效的降压作用,以及明显不存在母体和胎儿副作用,并由此改善了围产期死亡率,表明它是用于治疗妊娠合并高血压的合适药物。

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本文引用的文献

1
A controlled trial of hypotensive agents in hypertension in pregnancy.
Lancet. 1968 Aug 31;2(7566):488-90. doi: 10.1016/s0140-6736(68)90650-8.
4
Fetal outcome in trial of antihypertensive treatment in pregnancy.
Lancet. 1976 Oct 9;2(7989):753-6. doi: 10.1016/s0140-6736(76)90597-3.

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