国际医药卫生导报 ›› 2023, Vol. 29 ›› Issue (3): 377-380.DOI: 10.3760/cma.j.issn.1007-1245.2023.03.018

• 科研课题 • 上一篇    下一篇

拉贝洛尔联合酚妥拉明对妊娠期高血压患者的疗效

邵帅1  门贵香1  孙菊香1  洪善玲2  任国华2   

  1. 1临沂市人民医院产科六病区,临沂 2765002临沂市人民医院产科二病区,临沂 276500

  • 收稿日期:2022-09-28 出版日期:2023-02-01 发布日期:2023-03-03
  • 通讯作者: 任国华,Email:r.guohua@163.com
  • 基金资助:

    山东省医药卫生科技发展计划项目(2019WS122

Effect of labetalol combined with phentolamine on patients with gestational hypertension

Shao Shuai1, Men Guixiang1, Sun Juxiang1, Hong Shanling2, Ren Guohua2   

  1. 1 Ward 6, Department of Obstetrics, Linyi People's Hospital, Linyi 276500, China; 2 Ward 2, Department of Obstetrics, Linyi People's Hospital, Linyi 276500, China

  • Received:2022-09-28 Online:2023-02-01 Published:2023-03-03
  • Contact: Ren Guohua, Email: r.guohua@163.com
  • Supported by:

    Health Science and Technology Development Program of Shandong Province (2019WS122)

摘要:

目的 探讨拉贝洛尔联合酚妥拉明对妊娠期高血压患者妊娠结局及爱帕琳肽(Apelin)、血栓调节蛋白(PTM)水平的影响。方法 本研究为随机对照试验。选择20192月至20222月临沂市人民医院收治的86例妊娠期高血压患者为研究对象,以随机数字表法分为观察组(43例)与对照组(43例)。对照组年龄(29.12±3.93)岁,孕周(29.63±4.12)周;观察组年龄(28.23±3.19)岁,孕周(31.01±4.13)周。对照组采用酚妥拉明治疗,观察组在对照组的基础上给予拉贝洛尔治疗,两组均持续治疗7 d后观察效果。对比两组患者的临床疗效及不良妊娠结局,比较治疗前后ApelinPTM水平。统计学方法采用χ2检验、独立样本t检验、配对t检验。结果 观察组患者的临床总有效率高于对照组[93.02%40/43)比76.74%33/43)],两组比较差异有统计学意义(χ2=4.440P=0.035)。治疗前,两组患者的ApelinPTM水平比较差异均无统计学意义(均P>0.05);治疗后,两组的ApelinPTM均降低,且观察组患者的ApelinPTM水平均低于对照组[(38.52±5.12ng/L比(43.25±6.25ng/L、(201.32±18.25ng/L比(281.51±19.25ng/L],差异均有统计学意义(t=3.83919.824P<0.001)。观察组不良妊娠结局总发生率低于对照组[4.65%2/43)比20.93%9/45)],差异有统计学意义(χ2=5.108P=0.024)。结论 拉贝洛尔联合酚妥拉明治疗妊娠期高血压患者,有利于提高治疗效果,降低ApelinPTM水平及不良妊娠结局发生率。

关键词:

妊娠期高血压, 拉贝洛尔, 酚妥拉明, 爱帕琳肽, 不良妊娠结局

Abstract:

Objective To investigate the effects of labetalol combined with phentolamine on the pregnancy outcomes and levels of Apelin and thrombomodulin (PTM) in patients with gestational hypertension. Methods It was a randomized controlled trial. A total of 86 patients with gestational hypertension admitted to Linyi People's Hospital from February 2019 to February 2022 were selected as the research objects. They were divided into an observation group (43 cases) and a control group (43 cases) by the random number table method. The age of the control group was (29.12±3.93) years old and the gestational age was (29.63±4.12) weeks; the age of the observation group was (28.23±3.19) years old and the gestational age was (31.01±4.13) weeks. The control group was treated with phentolamine, and the observation group was treated with labetalol on the basis of the control group. The effects of both groups were observed after 7 days of continuous treatment. The clinical effects and adverse pregnancy outcomes of the two groups were compared, and the levels of Apelin and PTM before and after treatment were compared. χ2 test, independent sample t test, and paired t test were used. Results The clinical effective rate of the observation group was higher than that of the control group [93.02% (40/43) vs. 76.74% (33/43)], with a statistically significant difference between the two groups (χ2=4.440, P=0.035). Before treatment, there were no statistically significant differences in the levels of Apelin and PTM between the two groups (both P>0.05). After treatment, the levels of Apelin and PTM decreased in both groups, and the levels of Apelin and PTM in the observation group were lower than those in the control group [(38.52±5.12) ng/L vs. (43.25±6.25) ng/L, (201.32±18.25) ng/L vs. (281.51±19.25) ng/L], with statistically significant differences (t=3.839 and 19.824; both P<0.001). The incidence of adverse pregnancy outcomes in the observation group was lower than that in the control group [4.65% (2/43) vs. 20.93% (9/45)] (χ2=5.108, P=0.024). Conclusion Labetalol combined with phentolamine can improve the therapeutic effect in patients with gestational hypertension, reduce the levels of Apelin and PTM, and reduce the incidence of adverse pregnancy outcomes.

Key words:

Gestational hypertension, Labetalol, Phentolamine, Apelin, Adverse pregnancy outcomes