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拉贝洛尔联合硝苯地平治疗子痫前期患者的效果

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目的:观察拉贝洛尔联合硝苯地平治疗子痫前期患者的效果.方法:选取 2021 年 6 月至 2023 年 6 月该院收治的 80 例子痫前期患者进行前瞻性研究,按照随机数字表法将其分为对照组和观察组各 40 例.两组均予以常规治疗,在此基础上,对照组予以硝苯地平治疗,观察组在对照组基础上联合拉贝洛尔治疗,两组均连续治疗 1 个月.比较两组临床疗效,治疗前后血压(收缩压、舒张压)、24 h尿蛋白定量、凝血功能指标[凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、凝血酶时间(TT)、纤维蛋白原(FIB)]、胎儿脐动脉血流指标[收缩压与舒张压的比值(S/D)、搏动指数(PI)、阻力指数(RI)]水平,不良妊娠结局发生率,以及不良反应发生率.结果:观察组治疗总有效率为97.50%(39/40),高于对照组的80.00%(32/40),差异有统计学意义(P<0.05);治疗后,观察组收缩压、舒张压、24 h尿蛋白定量水平均低于对照组,差异有统计学意义(P<0.05);治疗后,观察组PT、APTT、TT长于对照组,FIB水平低于对照组,差异均有统计学意义(P<0.05);治疗后,观察组胎儿脐动脉S/D、PI、RI均低于对照组,差异有统计学意义(P<0.05);随访至分娩结束,观察组不良妊娠结局发生率为 17.50%(7/40),低于对照组的 55.00%(22/40),差异有统计学意义(P<0.05);两组不良反应发生率比较,差异无统计学意义(P>0.05).结论:拉贝洛尔联合硝苯地平治疗子痫前期患者可提高治疗总有效率,降低血压、24 h尿蛋白定量、胎儿脐动脉血流指标水平和不良妊娠结局发生率,改善凝血功能指标水平,效果优于单纯硝苯地平治疗.
Effects of Labetalol combined with Nifedipine in treatment of patients with preeclampsia
Objective:To observe effects of Labetalol combined with Nifedipine in treatment of patients with preeclampsia.Methods:A prospective study was conducted on 80 patients with preeclampsia admitted to the hospital from June 2021 to June 2023.According to the random number table method,they were divided into control group and observation group,40 cases in each group.Both groups were given routine treatment.On this basis,the control group was treated with Nifedipine,while the observation group was treated with Labetalol on the basis of that of the control group.Both groups were treated continuously for 1 month.The clinical efficacy,the levels of blood pressure(systolic blood pressure,diastolic blood pressure),the 24 h urine protein quantitative,the coagulation function index[prothrombin time(PT),activated partial thromboplastin time(APTT),thrombin time(TT),fibrinogen(FIB)],and the fetal umbilical artery blood flow index[ratio of systolic blood pressure to diastolic blood pressure(S/D),pulsatility index(PI),resistance index(RI)],the incidence of adverse pregnancy outcomes,and the incidence of adverse reactions were compared between the two groups.Results:The total effective rate of the observation group was 97.50%(39/40),which was higher than 80.00%(32/40)of the control group,and the difference was statistically significant(P<0.05).After the treatment,the levels of systolic blood pressure,diastolic blood pressure and 24 h urinary protein in the observation group were lower than those in the control group,and the differences were statistically significant(P<0.05).After the treatment,the PT,APTT and TT in the observation group were longer than those in the control group,the level of FIB was lower than that in the control group,and the differences were statistically significant(P<0.05).After the treatment,the fetal umbilical artery S/D,PI and RI in the observation group were lower than those in the control group,and the differences were statistically significant(P<0.05).From follow-up to delivery,the incidence of adverse pregnancy outcomes in the observation group was 17.50%(7/40),which was lower than 55.00%(22/40)in the control group,the difference was statistically significant(P<0.05).However,there was no significant difference in the incidence of adverse reactions between the two groups(P>0.05).Conclusions:Labetalol combined with Nifedipine in the treatment of the patients with preeclampsia can improve the total effective rate of treatment,reduce the blood pressure,24 h urine protein quantification,fetal umbilical artery blood flow index levels and incidence of adverse pregnancy outcomes,and improve the levels of coagulation function indexes.Moreover,it is superior to single Nifedipine treatment.

PreeclampsiaLabetalolNifedipineBlood pressurePregnancy outcomeCoagulation functionAdverse reaction

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焦作市妇幼保健院产科一区,河南 焦作 454000

子痫前期 拉贝洛尔 硝苯地平 血压 妊娠结局 凝血功能 不良反应

2024

中国民康医学
中国社会工作协会

中国民康医学

影响因子:0.649
ISSN:1672-0369
年,卷(期):2024.36(13)