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双球囊导管用于宫颈成熟的66例临床分析

[Clinical analysis of double-balloon catheter for cervical ripening in 66 cases].

作者信息

He Yingdong, Hu Jun, Zhang Xiaowei, Huang He, Chen Qian

机构信息

Department of Obstetrics and Gynecology, Peking University First Hospital, Beijing 100034, China.

Department of Obstetrics and Gynecology, Peking University First Hospital, Beijing 100034, China. Email:

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2014 Oct;49(10):741-5.

Abstract

OBJECTIVE

To evaluate the efficacy and safety for cervical ripening by double-balloon catheter among full-term pregnancy women underwent labor induction.

METHODS

It was a prospective non-randomly controlled research. Totally 128 singleton-pregnancy women in full-term who had to undergo labor induction because of pregnancy complications or comorbidities from August 2011 to April 2013 in Peking University First Hospital were selected as study subjects. Participants were allocated to preinduction cervical ripening with either a double-balloon catheter (66 participants, study group) or prostaglandin vaginal insert (62 participants, control group). Compare the efficacy for cervical ripening and adverse reactions between the two groups.

RESULTS

The efficacy for cervical ripening (Bishop scores improved by ≥ 2) had no significant differences between study and control groups [82% (54/66) compared with 81% (50/62), P > 0.05]. The time interval between intervention and parturiency was significantly higher in the double balloon catheter group than in the prostaglandin vaginal insert group [(24.2 ± 8.5) compared with (14.5 ± 8.0) hours, P < 0.05]. The proportion of women who achieved parturiency within 12 hours was significantly lower in the double-balloon catheter group than that in the control group [9% (6/66) compared with 21% (13/62), P < 0.05]. The cesarean section rate showed no significant differences [41% (27/66) compared with 43% (27/62), P > 0.05]. The prevalence of intrauterine infection demonstrated by clinical diagnosis was significantly higher in the double- balloon catheter group [11% (7/66) compared with 6% (4/62), P < 0.05]. The double-balloon catheter group had significantly lower rates of contraction over frequency [0(0/66) compared with 42% (26/62), P < 0.05], hyperthermia [3% (2/66) compared with 19% (12/62), P < 0.05], fetal heart rate abnormalities before removing the device or drug [5% (3/66) compared with 19% (12/62), P < 0.05], as well as precipitate labour [2% (1/66) compared with 16% (10/62), P < 0.05].

CONCLUSIONS

The efficacy of a double- balloon transcervical catheter is similar to that of a prostaglandin vaginal insert. However, the double- balloon catheter cannot significantly reduce the cesarean section rate while it increases the risk of intrauterine infection. The maternal and fetal safety of transcervical catheter is superior to the prostaglandin vaginal insert. In cases of oligohydramnios, fetal growth restriction, pregnancy complicated with asthma, hypertension and scar uterine are in favor of a balloon catheter using for cervical ripening on account of high risk of using prostaglandin.

摘要

目的

评估双球囊导管用于足月妊娠引产孕妇促宫颈成熟的有效性及安全性。

方法

这是一项前瞻性非随机对照研究。选取2011年8月至2013年4月在北京大学第一医院因妊娠并发症或合并症而需引产的128名单胎足月孕妇作为研究对象。将参与者分为两组,分别采用双球囊导管进行引产术前促宫颈成熟(66例,研究组)和阴道放置前列腺素制剂(62例,对照组)。比较两组促宫颈成熟的效果及不良反应。

结果

研究组与对照组促宫颈成熟的效果(Bishop评分提高≥2分)差异无统计学意义[82%(54/66)与81%(50/62),P>0.05]。双球囊导管组干预至分娩的时间间隔显著长于阴道放置前列腺素制剂组[(24.2±8.5)小时与(14.5±8.0)小时,P<0.05]。双球囊导管组12小时内分娩的产妇比例显著低于对照组[9%(6/66)与21%(13/62),P<0.05]。剖宫产率差异无统计学意义[41%(27/66)与43%(27/62),P>0.05]。临床诊断的宫内感染发生率在双球囊导管组显著高于对照组[11%(7/66)与6%(4/62),P<0.05]。双球囊导管组宫缩过频发生率[0(0/66)与42%(26/62),P<0.05]、发热[3%(2/66)与19%(12/62),P<0.05]、去除装置或药物前胎儿心率异常[5%(3/66)与19%(12/62),P<0.05]以及急产[2%(1/66)与16%(10/62),P<0.05]的发生率均显著低于对照组。

结论

双球囊经宫颈导管促宫颈成熟的效果与阴道放置前列腺素制剂相似。然而,双球囊导管不能显著降低剖宫产率,同时增加了宫内感染的风险。经宫颈导管的母胎安全性优于阴道放置前列腺素制剂。对于羊水过少、胎儿生长受限、合并哮喘、高血压及瘢痕子宫的妊娠,因使用前列腺素风险高,双球囊导管更有利于促宫颈成熟。

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