• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

β1肾上腺素能受体阻滞剂阿替洛尔对产前胎心监护的影响。

Influence of the beta 1-adrenoceptor blocker atenolol on antenatal cardiotocography.

作者信息

Montan S, Solum T, Sjöberg N O

出版信息

Acta Obstet Gynecol Scand Suppl. 1984;118:99-102. doi: 10.3109/00016348409157133.

DOI:10.3109/00016348409157133
PMID:6587734
Abstract

Forty term patients with pregnancy-induced hypertension were treated with the beta 1-adrenoceptor blocker atenolol (Tenormin R; ICI) for at least 7 days prior to parturition. The antenatal cardiotocography (CTG) was visually analysed before and during treatment. The mean basal fetal heart rate (FHR) decreased from 143 +/- 7 beats per minute (bpm) to 133 +/- 8 bpm. In 13.1% of the recordings in treated patients there was a decrease in long-term variability for a period of more than 20 minutes; this was observed in only 2.3% prior to treatment. The amplitude of the accelerations was reduced from 23 +/- 6 bpm to 18 +/- 4 bpm. It was demonstrated that atenolol affected antenatal CTG, and this has to be taken into consideration when interpreting antenatal CTG as one parameter for evaluation of fetal well-being.

摘要

四十名患有妊娠高血压的足月孕妇在分娩前至少7天接受了β1肾上腺素能受体阻滞剂阿替洛尔(Tenormin R;ICI)治疗。在治疗前和治疗期间对产前胎心监护(CTG)进行了视觉分析。平均基础胎心率(FHR)从每分钟143±7次心跳(bpm)降至133±8 bpm。在接受治疗的患者中,13.1%的记录显示长期变异性在超过20分钟的时间段内降低;而治疗前仅为2.3%。加速幅度从23±6 bpm降至18±4 bpm。结果表明,阿替洛尔会影响产前CTG,在将产前CTG作为评估胎儿健康状况的一个参数进行解读时必须考虑到这一点。

相似文献

1
Influence of the beta 1-adrenoceptor blocker atenolol on antenatal cardiotocography.β1肾上腺素能受体阻滞剂阿替洛尔对产前胎心监护的影响。
Acta Obstet Gynecol Scand Suppl. 1984;118:99-102. doi: 10.3109/00016348409157133.
2
Fetal heart rate during treatment of maternal hypertension with beta-adrenergic antagonists. A preliminary report.β-肾上腺素能拮抗剂治疗妊娠高血压时的胎儿心率。初步报告。
Acta Obstet Gynecol Scand Suppl. 1984;118:95-7. doi: 10.3109/00016348409157132.
3
Obstetric aspects of the use in pregnancy-associated hypertension of the beta-adrenoceptor antagonist atenolol.β-肾上腺素能受体拮抗剂阿替洛尔在妊娠相关性高血压治疗中的产科应用
Am J Obstet Gynecol. 1984 Oct 15;150(4):389-92. doi: 10.1016/s0002-9378(84)80145-3.
4
Atenolol in the treatment of essential hypertension during pregnancy.阿替洛尔在妊娠期原发性高血压治疗中的应用
Br J Clin Pharmacol. 1982 Aug;14(2):279-81. doi: 10.1111/j.1365-2125.1982.tb01974.x.
5
Effect of diazoxide on the antepartum cardiotocograph in severe pregnancy-associated hypertension.二氮嗪对重度妊娠高血压综合征产前胎心监护的影响
Aust N Z J Obstet Gynaecol. 1981 Feb;21(1):11-5. doi: 10.1111/j.1479-828x.1981.tb00116.x.
6
[Effect of 2 beta-blockers on arterial hypertension during pregnancy. Results of a prospective study on 56 pregnant hypertensive women treated with atenolol and labetalol].
J Gynecol Obstet Biol Reprod (Paris). 1983;12(8):891-900.
7
Which beta-blocker in pregnancy-induced hypertension?
Lancet. 1983 Nov 19;2(8360):1194. doi: 10.1016/s0140-6736(83)91239-4.
8
Randomised controlled trial of atenolol and pindolol in human pregnancy: effects on fetal haemodynamics.阿替洛尔与吲哚洛尔在人类妊娠中的随机对照试验:对胎儿血流动力学的影响。
BMJ. 1992 Apr 11;304(6832):946-9. doi: 10.1136/bmj.304.6832.946.
9
Treatment of hypertension in pregnancy with beta-adrenoceptor antagonists.妊娠期高血压使用β-肾上腺素能受体拮抗剂治疗。
Br J Clin Pharmacol. 1982;13(Suppl 2):375S-378S. doi: 10.1111/j.1365-2125.1982.tb01944.x.
10
Effect of dihydralazine on the fetus in the treatment of maternal hypertension.
Obstet Gynecol. 1980 Apr;55(4):519-22.

引用本文的文献

1
Effect of maternal beta-blocker treatment on mean fetal heart rate.母体β受体阻滞剂治疗对胎儿平均心率的影响。
AJOG Glob Rep. 2024 Nov 20;5(1):100423. doi: 10.1016/j.xagr.2024.100423. eCollection 2025 Feb.
2
Betaxolol: a pilot study of its pharmacological and therapeutic properties in pregnancy.倍他洛尔:关于其在妊娠期药理及治疗特性的一项初步研究。
Eur J Clin Pharmacol. 1990;38(6):535-9. doi: 10.1007/BF00278577.