Shepherd Emily, Salam Rehana A, Middleton Philippa, Makrides Maria, McIntyre Sarah, Badawi Nadia, Crowther Caroline A
ARCH: Australian Research Centre for Health of Women and Babies, Robinson Research Institute, Discipline of Obstetrics and Gynaecology, The University of Adelaide, Adelaide, South Australia, Australia, 5006.
Cochrane Database Syst Rev. 2017 Aug 8;8(8):CD012077. doi: 10.1002/14651858.CD012077.pub2.
Cerebral palsy is an umbrella term encompassing disorders of movement and posture, attributed to non-progressive disturbances occurring in the developing fetal or infant brain. As there are diverse risk factors and causes, no one strategy will prevent all cerebral palsy. Therefore, there is a need to systematically consider all potentially relevant interventions for their contribution to prevention.
To summarise the evidence from Cochrane reviews regarding the effects of antenatal and intrapartum interventions for preventing cerebral palsy.
We searched the Cochrane Database of Systematic Reviews on 7 August 2016, for reviews of antenatal or intrapartum interventions reporting on cerebral palsy. Two authors assessed reviews for inclusion, extracted data, assessed review quality, using AMSTAR and ROBIS, and quality of the evidence, using the GRADE approach. We organised reviews by topic, and summarised findings in text and tables. We categorised interventions as effective (high-quality evidence of effectiveness); possibly effective (moderate-quality evidence of effectiveness); ineffective (high-quality evidence of harm or of lack of effectiveness); probably ineffective (moderate-quality evidence of harm or of lack of effectiveness); and no conclusions possible (low- to very low-quality evidence).
We included 15 Cochrane reviews. A further 62 reviews pre-specified the outcome cerebral palsy in their methods, but none of the included randomised controlled trials (RCTs) reported this outcome. The included reviews were high quality and at low risk of bias. They included 279 RCTs; data for cerebral palsy were available from 27 (10%) RCTs, involving 32,490 children. They considered interventions for: treating mild to moderate hypertension (two) and pre-eclampsia (two); diagnosing and preventing fetal compromise in labour (one); preventing preterm birth (four); preterm fetal maturation or neuroprotection (five); and managing preterm fetal compromise (one). Quality of evidence ranged from very low to high. Effective interventions: high-quality evidence of effectiveness There was a reduction in cerebral palsy in children born to women at risk of preterm birth who received magnesium sulphate for neuroprotection of the fetus compared with placebo (risk ratio (RR) 0.68, 95% confidence interval (CI) 0.54 to 0.87; five RCTs; 6145 children). Probably ineffective interventions: moderate-quality evidence of harm There was an increase in cerebral palsy in children born to mothers in preterm labour with intact membranes who received any prophylactic antibiotics versus no antibiotics (RR 1.82, 95% CI 0.99 to 3.34; one RCT; 3173 children). There was an increase in cerebral palsy in children, who as preterm babies with suspected fetal compromise, were born immediately compared with those for whom birth was deferred (RR 5.88, 95% CI 1.33 to 26.02; one RCT; 507 children). Probably ineffective interventions: moderate-quality evidence of lack of effectiveness There was no clear difference in the presence of cerebral palsy in children born to women at risk of preterm birth who received repeat doses of corticosteroids compared with a single course (RR 1.03, 95% CI 0.71 to 1.50; four RCTs; 3800 children). No conclusions possible: low- to very low-quality evidence Low-quality evidence found there was a possible reduction in cerebral palsy for children born to women at risk of preterm birth who received antenatal corticosteroids for accelerating fetal lung maturation compared with placebo (RR 0.60, 95% CI 0.34 to 1.03; five RCTs; 904 children). There was no clear difference in the presence of cerebral palsy with interventionist care for severe pre-eclampsia versus expectant care (RR 6.01, 95% CI 0.75 to 48.14; one RCT; 262 children); magnesium sulphate for pre-eclampsia versus placebo (RR 0.34, 95% CI 0.09 to 1.26; one RCT; 2895 children); continuous cardiotocography for fetal assessment during labour versus intermittent auscultation (average RR 1.75, 95% CI 0.84 to 3.63; two RCTs; 13,252 children); prenatal progesterone for prevention of preterm birth versus placebo (RR 0.14, 95% CI 0.01 to 3.48; one RCT; 274 children); and betamimetics for inhibiting preterm labour versus placebo (RR 0.19, 95% CI 0.02 to 1.63; one RCT; 246 children).Very low-quality found no clear difference for the presence of cerebral palsy with any antihypertensive drug (oral beta-blockers) for treatment of mild to moderate hypertension versus placebo (RR 0.33, 95% CI 0.01 to 8.01; one RCT; 110 children); magnesium sulphate for prevention of preterm birth versus other tocolytic agents (RR 0.13, 95% CI 0.01 to 2.51; one RCT; 106 children); and vitamin K and phenobarbital prior to preterm birth for prevention of neonatal periventricular haemorrhage versus placebo (RR 0.77, 95% CI 0.33 to 1.76; one RCT; 299 children).
AUTHORS' CONCLUSIONS: This overview summarises evidence from Cochrane reviews on the effects of antenatal and intrapartum interventions on cerebral palsy, and can be used by researchers, funding bodies, policy makers, clinicians and consumers to aid decision-making and evidence translation. We recommend that readers consult the included Cochrane reviews to formally assess other benefits or harms of included interventions, including impacts on risk factors for cerebral palsy (such as the reduction in intraventricular haemorrhage for preterm babies following exposure to antenatal corticosteroids).Magnesium sulphate for women at risk of preterm birth for fetal neuroprotection can prevent cerebral palsy. Prophylactic antibiotics for women in preterm labour with intact membranes, and immediate rather than deferred birth of preterm babies with suspected fetal compromise, may increase the risk of cerebral palsy. Repeat doses compared with a single course of antenatal corticosteroids for women at risk of preterm birth do not clearly impact the risk of cerebral palsy.Cerebral palsy is rarely diagnosed at birth, has diverse risk factors and causes, and is diagnosed in approximately one in 500 children. To date, only a small proportion of Cochrane reviews assessing antenatal and intrapartum interventions have been able to report on this outcome. There is an urgent need for long-term follow-up of RCTs of interventions addressing risk factors for cerebral palsy, and consideration of the use of relatively new interim assessments (including the General Movements Assessment). Such RCTs must be rigorous in their design, and aim for consistency in cerebral palsy outcome measurement and reporting to facilitate pooling of data, to focus research efforts on prevention.
脑瘫是一个概括性术语,涵盖运动和姿势障碍,其病因是胎儿或婴儿发育中的大脑发生非进行性紊乱。由于存在多种风险因素和病因,没有一种策略能够预防所有脑瘫病例。因此,有必要系统地考虑所有潜在相关干预措施对预防的作用。
总结Cochrane系统评价中关于产前和产时干预措施预防脑瘫效果的证据。
我们于2016年8月7日检索了Cochrane系统评价数据库,以查找报告脑瘫情况的产前或产时干预措施的系统评价。两位作者评估纳入的系统评价,提取数据,使用AMSTAR和ROBIS评估系统评价质量,并使用GRADE方法评估证据质量。我们按主题整理系统评价,并以文字和表格形式总结研究结果。我们将干预措施分为有效(高质量的有效性证据);可能有效(中等质量的有效性证据);无效(高质量的危害或无效证据);可能无效(中等质量的危害或无效证据);以及无法得出结论(低至极低质量的证据)。
我们纳入了15篇Cochrane系统评价。另有62篇系统评价在其方法中预先设定了脑瘫这一结局,但纳入的随机对照试验(RCT)均未报告该结局。纳入的系统评价质量高,偏倚风险低。它们包括279项RCT;有27项(10%)RCT提供了脑瘫数据,涉及32490名儿童。这些系统评价考虑的干预措施包括:治疗轻度至中度高血压(2项)和子痫前期(2项);诊断和预防分娩时胎儿窘迫(1项);预防早产(4项);早产胎儿成熟或神经保护(5项);以及处理早产胎儿窘迫(1项)。证据质量从极低到高不等。有效干预措施:高质量的有效性证据与安慰剂相比,接受硫酸镁进行胎儿神经保护的早产风险女性所生儿童的脑瘫发生率降低(风险比(RR)0.68,95%置信区间(CI)0.54至0.87;5项RCT;6145名儿童)。可能无效的干预措施:中等质量的危害证据与未使用任何预防性抗生素相比,胎膜完整的早产母亲所生儿童接受任何预防性抗生素治疗后脑瘫发生率增加(RR 1.82,95%CI 0.99至3.34;1项RCT;3173名儿童)。与延迟分娩的疑似胎儿窘迫早产婴儿相比,立即分娩的此类婴儿脑瘫发生率增加(RR 5.88,95%CI 1.33至26.02;1项RCT;507名儿童)。可能无效的干预措施:中等质量的无效证据与单疗程相比,接受重复剂量皮质类固醇激素治疗的早产风险女性所生儿童的脑瘫发生率无明显差异(RR 1.03,95%CI 0.71至1.50;4项RCT;3800名儿童)。无法得出结论:低至极低质量的证据低质量证据表明,与安慰剂相比,接受产前皮质类固醇激素以加速胎儿肺成熟的早产风险女性所生儿童的脑瘫发生率可能降低(RR 0.60,95%CI 0.34至1.03;5项RCT;904名儿童)。与期待治疗相比,重度子痫前期的干预性护理与脑瘫发生率无明显差异(RR 6.01,95%CI 0.75至48.14;1项RCT;262名儿童);子痫前期使用硫酸镁与安慰剂相比(RR 0.34,95%CI 0.09至1.26;1项RCT;2895名儿童);分娩期间连续胎心监护与间歇听诊相比(平均RR 1.75,95%CI 0.84至3.63;2项RCT;13252名儿童);产前使用孕激素预防早产与安慰剂相比(RR 0.14,95%CI 0.01至3.48;1项RCT;274名儿童);以及使用β-拟交感神经药抑制早产与安慰剂相比(RR 0.19,95%CI 0.02至1.63;1项RCT;246名儿童)。极低质量证据表明,治疗轻度至中度高血压使用任何抗高血压药物(口服β受体阻滞剂)与安慰剂相比,脑瘫发生率无明显差异(RR 0.33,95%CI 0.01至8.01;1项RCT;110名儿童);硫酸镁预防早产与其他宫缩抑制剂相比(RR 0.13,95%CI 0.01至2.51;1项RCT;106名儿童);早产前使用维生素K和苯巴比妥预防新生儿脑室周围出血与安慰剂相比(RR 0.77,95%CI 0.33至1.76;1项RCT;299名儿童)。
本综述总结了Cochrane系统评价中关于产前和产时干预措施对脑瘫影响的证据,可供研究人员、资助机构、政策制定者、临床医生和消费者用于辅助决策和证据转化。我们建议读者查阅纳入的Cochrane系统评价,以正式评估纳入干预措施的其他益处或危害,包括对脑瘫风险因素的影响(如产前皮质类固醇激素暴露后早产婴儿脑室内出血的减少)。对于有早产风险的女性,使用硫酸镁进行胎儿神经保护可预防脑瘫。胎膜完整的早产女性使用预防性抗生素,以及疑似胎儿窘迫的早产婴儿立即而非延迟分娩,可能会增加脑瘫风险。与单疗程相比,有早产风险的女性重复剂量使用产前皮质类固醇激素对脑瘫风险无明显影响。脑瘫在出生时很少被诊断出来,其风险因素和病因多种多样,约每500名儿童中就有1名被诊断为脑瘫。迄今为止,评估产前和产时干预措施的Cochrane系统评价中只有一小部分能够报告这一结局。迫切需要对针对脑瘫风险因素的干预措施进行长期随访的RCT研究,并考虑使用相对较新的中期评估方法(包括全身运动评估)。此类RCT研究在设计上必须严谨,旨在使脑瘫结局测量和报告保持一致,以便于数据汇总,将研究重点集中在预防方面。