宫颈环扎术联合其他治疗方法用于预防单胎妊娠自发性早产。
Cervical stitch (cerclage) in combination with other treatments for preventing spontaneous preterm birth in singleton pregnancies.
作者信息
Eleje George U, Eke Ahizechukwu C, Ikechebelu Joseph I, Ezebialu Ifeanyichukwu U, Okam Princeston C, Ilika Chito P
机构信息
Effective Care Research Unit, Department of Obstetrics and Gynaecology, Faculty of Medicine, College of Health Sciences, Nnamdi Azikiwe University, Nnewi Campus, PMB 5001, Nnewi, Nigeria.
Division of Maternal Fetal Medicine, Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
出版信息
Cochrane Database Syst Rev. 2020 Sep 24;9(9):CD012871. doi: 10.1002/14651858.CD012871.pub2.
BACKGROUND
Preterm birth (PTB) remains the foremost global cause of perinatal morbidity and mortality. Thus, the prevention of spontaneous PTB still remains of critical importance. In an attempt to prevent PTB in singleton pregnancies, cervical cerclage, in combination with other treatments, has been advocated. This is because, cervical cerclage is an intervention that is commonly recommended in women with a short cervix at high risk of preterm birth but, despite this, many women still deliver prematurely, as the biological mechanism is incompletely understood. Additionally, previous Cochrane Reviews have been published on the effectiveness of cervical cerclage in singleton and multiple pregnancies, however, none has evaluated the effectiveness of using cervical cerclage in combination with other treatments.
OBJECTIVES
To assess whether antibiotics administration, vaginal pessary, reinforcing or second cerclage placement, tocolytic, progesterone, or other interventions at the time of cervical cerclage placement prolong singleton gestation in women at high risk of pregnancy loss based on prior history and/or ultrasound finding of 'short cervix' and/or physical examination. History-indicated cerclage is defined as a cerclage placed usually between 12 and 15 weeks gestation based solely on poor prior obstetrical history, e.g. multiple second trimester losses due to painless dilatation. Ultrasound-indicated cerclage is defined as a cerclage placed usually between 16 and 23 weeks gestation for transvaginal ultrasound cervical length < 20 mm in a woman without cervical dilatation. Physical exam-indicated cerclage is defined as a cerclage placed usually between 16 and 23 weeks gestation because of cervical dilatation of one or more centimetres detected on physical (manual) examination.
SEARCH METHODS
We searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform (ICTRP) (26 September 2019), and reference lists of retrieved studies.
SELECTION CRITERIA
We included published, unpublished or ongoing randomised controlled trial (RCTs). Studies using a cluster-RCT design were also eligible for inclusion in this review but none were identified. We excluded quasi-RCTs (e.g. those randomised by date of birth or hospital number) and studies using a cross-over design. We also excluded studies that specified addition of the combination therapy after cervical cerclage because the woman subsequently became symptomatic. We included studies comparing cervical cerclage in combination with one, two or more interventions with cervical cerclage alone in singleton pregnancies.
DATA COLLECTION AND ANALYSIS
Two review authors independently screened titles and abstracts of all retrieved articles, selected studies for inclusion, extracted data, assessed risk of bias, and evaluated the certainty of the evidence for this review's main outcomes. Data were checked for accuracy. Standard Cochrane review methods were used throughout.
MAIN RESULTS
We identified two studies (involving a total of 73 women) comparing cervical cerclage alone to a different comparator. We also identified three ongoing studies (one investigating vaginal progesterone after cerclage, and two investigating cerclage plus pessary). One study (20 women), conducted in the UK, comparing cervical cerclage in combination with a tocolytic (salbutamol) with cervical cerclage alone in women with singleton pregnancy did not provide any useable data for this review. The other study (involving 53 women, with data from 50 women) took place in the USA and compared cervical cerclage in combination with a tocolytic (indomethacin) and antibiotics (cefazolin or clindamycin) versus cervical cerclage alone - this study did provide useable data for this review (and the study authors also provided additional data on request) but meta-analyses were not possible. This study was generally at a low risk of bias, apart from issues relating to blinding. We downgraded the certainty of evidence for serious risk of bias and imprecision (few participants, few events and wide 95% confidence intervals). Cervical cerclage in combination with an antibiotic and tocolytic versus cervical cerclage alone (one study, 50 women/babies) We are unclear about the effect of cervical cerclage in combination with antibiotics and a tocolytic compared with cervical cerclage alone on the risk of serious neonatal morbidity (RR 0.62, 95% CI 0.31 to 1.24; very low-certainty evidence); perinatal loss (data for miscarriage and stillbirth only - data not available for neonatal death) (RR 0.46, 95% CI 0.13 to 1.64; very low-certainty evidence) or preterm birth < 34 completed weeks of pregnancy (RR 0.78, 95% CI 0.44 to 1.40; very low-certainty evidence). There were no stillbirths (intrauterine death at 24 or more weeks). The trial authors did not report on the numbers of babies discharged home healthy (without obvious pathology) or on the risk of neonatal death.
AUTHORS' CONCLUSIONS: Currently, there is insufficient evidence to evaluate the effect of combining a tocolytic (indomethacin) and antibiotics (cefazolin/clindamycin) with cervical cerclage compared with cervical cerclage alone for preventing spontaneous PTB in women with singleton pregnancies. Future studies should recruit sufficient numbers of women to provide meaningful results and should measure neonatal death and numbers of babies discharged home healthy, as well as other important outcomes listed in this review. We did not identify any studies looking at other treatments in combination with cervical cerclage. Future research needs to focus on the role of other interventions such as vaginal support pessary, reinforcing or second cervical cerclage placement, 17-alpha-hydroxyprogesterone caproate or dydrogesterone or vaginal micronised progesterone, omega-3 long chain polyunsaturated fatty acid supplementation and bed rest.
背景
早产仍然是全球围产期发病和死亡的首要原因。因此,预防自发性早产仍然至关重要。为了预防单胎妊娠的早产,有人主张采用宫颈环扎术并结合其他治疗方法。这是因为,宫颈环扎术是一种通常推荐给宫颈短且早产风险高的女性的干预措施,但尽管如此,许多女性仍会早产,因为其生物学机制尚未完全了解。此外,之前已经发表了关于宫颈环扎术在单胎和多胎妊娠中有效性的Cochrane系统评价,然而,尚无研究评估宫颈环扎术联合其他治疗方法的有效性。
目的
评估在宫颈环扎术时给予抗生素、阴道托、加强或二次环扎、宫缩抑制剂、孕激素或其他干预措施,是否能延长有妊娠丢失高风险的单胎妊娠女性的孕周,这些女性基于既往史和/或超声检查发现“宫颈短”和/或体格检查结果。既往史指征性环扎定义为通常在妊娠12至15周之间进行的环扎,仅基于既往不良产科史,例如因无痛扩张导致多次孕中期流产。超声指征性环扎定义为通常在妊娠16至23周之间进行的环扎,适用于经阴道超声检查宫颈长度<20mm且无宫颈扩张的女性。体格检查指征性环扎定义为通常在妊娠16至23周之间进行的环扎,原因是体格(手法)检查发现宫颈扩张1厘米或以上。
检索方法
我们检索了Cochrane妊娠与分娩试验注册库、ClinicalTrials.gov和世界卫生组织国际临床试验注册平台(ICTRP)(2019年9月26日),以及检索到的研究的参考文献列表。
选择标准
我们纳入已发表、未发表或正在进行的随机对照试验(RCT)。采用整群RCT设计的研究也符合纳入本综述的条件,但未检索到此类研究。我们排除了半随机对照试验(例如按出生日期或医院编号随机分组的试验)和采用交叉设计的研究。我们还排除了那些在宫颈环扎术后指定添加联合治疗的研究,因为这些女性随后出现了症状。我们纳入了比较单胎妊娠中宫颈环扎术联合一种、两种或更多种干预措施与单纯宫颈环扎术的研究。
数据收集与分析
两位综述作者独立筛选所有检索到的文章的标题和摘要,选择纳入的研究,提取数据,评估偏倚风险,并评估本综述主要结局的证据确定性。检查数据的准确性。始终采用标准的Cochrane综述方法。
主要结果
我们确定了两项研究(共涉及73名女性),比较了单纯宫颈环扎术与不同的对照措施。我们还确定了三项正在进行的研究(一项研究宫颈环扎术后使用阴道孕激素,两项研究宫颈环扎术加阴道托)。一项在英国进行的研究(20名女性),比较了单胎妊娠女性中宫颈环扎术联合宫缩抑制剂(沙丁胺醇)与单纯宫颈环扎术,未为本综述提供任何可用数据。另一项研究(涉及53名女性,50名女性的数据可用)在美国进行,比较了宫颈环扎术联合宫缩抑制剂(吲哚美辛)和抗生素(头孢唑林或克林霉素)与单纯宫颈环扎术——该研究为本综述提供了可用数据(研究作者也应要求提供了额外数据),但无法进行荟萃分析。除了与盲法相关的问题外,该研究总体偏倚风险较低。我们因严重的偏倚风险和不精确性(参与者少、事件少且95%置信区间宽)而降低了证据的确定性。宫颈环扎术联合抗生素和宫缩抑制剂与单纯宫颈环扎术相比(一项研究,50名女性/婴儿)我们不清楚宫颈环扎术联合抗生素和宫缩抑制剂与单纯宫颈环扎术相比,对严重新生儿发病率风险的影响(风险比0·62,95%置信区间0·31至1·24;极低确定性证据);围产期丢失(仅流产和死产数据——无新生儿死亡数据)(风险比0·46,95%置信区间0·13至1·64;极低确定性证据)或妊娠<34足周的早产(风险比0·78,95%置信区间0·44至1·40;极低确定性证据)。没有死产(24周或更晚的宫内死亡)。试验作者未报告健康出院(无明显病理情况)的婴儿数量或新生儿死亡风险。
作者结论
目前,尚无足够证据评估与单纯宫颈环扎术相比,宫颈环扎术联合宫缩抑制剂(吲哚美辛)和抗生素(头孢唑林/克林霉素)对预防单胎妊娠女性自发性早产的效果。未来的研究应招募足够数量的女性以提供有意义的结果,并应测量新生儿死亡和健康出院的婴儿数量,以及本综述中列出的其他重要结局。我们未发现任何研究探讨其他治疗方法与宫颈环扎术联合使用的情况。未来的研究需要关注其他干预措施的作用,如阴道支撑托、加强或二次宫颈环扎术、己酸17α-羟孕酮或地屈孕酮或阴道微粒化孕酮、补充ω-3长链多不饱和脂肪酸和卧床休息。
相似文献
Cochrane Database Syst Rev. 2020-9-24
Cochrane Database Syst Rev. 2022-12-1
Cochrane Database Syst Rev. 2017-6-6
Cochrane Database Syst Rev. 2014-9-10
Cochrane Database Syst Rev. 2019-9-25
Cochrane Database Syst Rev. 2021-4-19
Cochrane Database Syst Rev. 2012-4-18
Cochrane Database Syst Rev. 2017-9-22
Cochrane Database Syst Rev. 2018-11-15
引用本文的文献
BMC Pregnancy Childbirth. 2025-1-8
BMC Pregnancy Childbirth. 2024-11-30
Explor Res Hypothesis Med. 2024-3
Heliyon. 2023-10-18
Pharmaceutics. 2022-9-23
BMC Pregnancy Childbirth. 2022-4-23
本文引用的文献
Int J Gynaecol Obstet. 2020-1-23
N Engl J Med. 2019-4-4
J Matern Fetal Neonatal Med. 2020-10
J Matern Fetal Neonatal Med. 2020-9
Acta Obstet Gynecol Scand. 2018-11-18
Geburtshilfe Frauenheilkd. 2018-8
Am J Obstet Gynecol. 2018-7-11