Morag Iris, Ohlsson Arne
The Edmond & Lily Safra Children's Hospital Sheba Medical Center, Tel Hashomer, Israel.
Cochrane Database Syst Rev. 2016 Aug 10;2016(8):CD006982. doi: 10.1002/14651858.CD006982.pub4.
Potential benefits and harms of different lighting in neonatal units have not been quantified.
• To determine effectiveness and safety of cycled light (CL) (approximately 12 hours of light on and 12 hours of light off) for growth in preterm infants at three and six months' corrected age (CA).• In separate analyses, to compare effects of CL with those of irregularly dimmed light (DL) or near darkness (ND), and effects of CL with those of continuous bright light (CBL), on growth in preterm infants at three and six months' CA.• To assess, in subgroup analyses, the effectiveness and safety of CL (vs control interventions (DL, ND and CBL)) introduced at different postmenstrual ages (PMAs) - before 32 weeks', at 32 weeks' and from 36 weeks' PMA - and to compare effectiveness and safety of CL for small for gestational age (GA) infants versus appropriately grown infants.
We used the standard search strategy of the Cochrane Neonatal Review Group to search the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 12), MEDLINE via PubMed (1966 to January 2016), Embase (1980 to January 2016) and the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to January 2016). We searched clinical trials databases, conference proceedings and reference lists of retrieved articles for randomised controlled trials and quasi-randomised trials.
Randomised or quasi-randomised trials of CL versus ND or CBL in preterm and low birth weight infants.
We performed data collection and analyses according to the methods of the Cochrane Neonatal Review Group. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to assess the quality of evidence.
We identified one additional study enrolling 38 participants for inclusion in this update, for a total of nine studies reporting on 544 infants. In general, the quality of the studies was low, mainly owing to lack of blinding and small sample sizes.Six studies enrolling 424 infants compared CL versus ND. No study reported on weight at three or six months. One study (n = 40) found no statistically significant difference in weight at four months between CL and ND groups. In another study (n = 62), the ratio of day-night activity before discharge favoured the CL group (mean difference (MD) 0.18, 95% confidence interval (CI) 0.17 to 0.19), indicating 18% more activity during the day than during the night in the CL group compared with the ND group. Two studies (n = 189) reported on retinopathy of prematurity (stage ≥ 3) and reported no statistically significant differences between CL and ND groups (typical risk ratio (RR) 0.53, 95% CI 0.25 to 1.11, I(2) = 0%; typical risk difference (RD) -0.09, 95% CI -0.19 to 0.01, I(2) = 0%). Two studies (n = 77) reported length of hospital stay (days) and noted a significant reduction in length of stay between CL and ND groups favouring the CL group (weighted mean difference (WMD) -13 days, 95% CI -23 to -2, I(2) = 0%; no heterogeneity). The quality of the evidence according to GRADE was low for this outcome. One study (n = 37) reported less crying at 11 weeks' corrected age (CA) in the CL group compared with the ND group (MD -0.57 hours/24 h, 95% CI -1.09 to -0.05). Tests for heterogeneity were not applicable.Three studies enrolling 120 infants compared CL versus CBL. Two studies (n = 79) reported significantly shorter length of stay in the CL group compared with the CBL group (WMD -16.5 days, 95% CI -26.2 to -6.8, I(2) = 0%; no heterogeneity). The quality of the evidence according to GRADE was low for this outcome. One study (n = 41) reported higher mean weight at three months' CA among infants cared for in the CL nursery (P value < 0.02) and a lower mean number of hours spent awake in 24 hours at three months of age (P value < 0.005). Data could not be entered into RevMan or GRADE. One study (n = 41) reported shorter time on the ventilator in the CL compared with the CBL group (MD -18.2 days, 95% CI -31.40 to -5.0). One study (n = 41) reported a shorter time to first oral feeding in the CL group (MD -6.8 days, 95% CI -13.29 to -0.31). We identified no safety issues.
AUTHORS' CONCLUSIONS: Trials assessing the effects of CL have enrolled 544 infants. No study reported on our primary outcome of weight at three or six months. Results from one additional study strengthen our findings that CL versus CBL shortens length of stay, as does CL versus ND. The quality of the evidence on both comparisons for this outcome according to GRADE was low. Future research should focus on comparing CL versus ND.
新生儿病房不同光照的潜在益处和危害尚未得到量化。
• 确定周期性光照(CL)(约12小时光照和12小时熄灯)对矫正年龄3个月和6个月的早产儿生长发育的有效性和安全性。• 在单独分析中,比较CL与不规则调光(DL)或接近黑暗(ND)对矫正年龄3个月和6个月的早产儿生长发育的影响,以及CL与持续强光(CBL)的影响。• 在亚组分析中,评估在不同月经龄(PMA)——32周之前、32周时以及36周及以后引入CL(与对照干预措施(DL、ND和CBL)相比)的有效性和安全性,并比较CL对小于胎龄(GA)婴儿与发育正常婴儿的有效性和安全性。
我们采用Cochrane新生儿综述组的标准检索策略,检索Cochrane对照试验中心注册库(CENTRAL;2016年第12期)、通过PubMed检索MEDLINE(1966年至2016年1月)、Embase(1980年至2016年1月)以及护理及相关健康文献累积索引(CINAHL;1982年至2016年1月)。我们检索临床试验数据库、会议论文集以及检索到的文章的参考文献列表,以查找随机对照试验和半随机试验。
早产和低出生体重婴儿中CL与ND或CBL的随机或半随机试验。
我们根据Cochrane新生儿综述组的方法进行数据收集和分析。我们采用推荐分级评估、制定与评价(GRADE)方法来评估证据质量。
我们确定了一项纳入38名参与者的额外研究,纳入本次更新,共有9项研究报告了544名婴儿的情况。总体而言,研究质量较低,主要是由于缺乏盲法和样本量较小。六项纳入424名婴儿的研究比较了CL与ND。没有研究报告3个月或6个月时的体重情况。一项研究(n = 40)发现CL组和ND组在4个月时体重无统计学显著差异。另一项研究(n = 62)发现,出院前昼夜活动比例有利于CL组(平均差(MD)0.18,95%置信区间(CI)0.17至0.19),表明与ND组相比,CL组白天活动比夜间多18%。两项研究(n = 189)报告了早产儿视网膜病变(≥3期),并报告CL组和ND组之间无统计学显著差异(典型风险比(RR)0.53,95%CI 0.25至1.11,I² = 0%;典型风险差(RD)-0.09,95%CI -0.19至0.01,I² = 0%)。两项研究(n = 77)报告了住院天数,并指出CL组和ND组之间住院天数有显著减少,有利于CL组(加权平均差(WMD)-13天,95%CI -23至-2,I² = 0%;无异质性)。根据GRADE,该结果的证据质量较低。一项研究(n = 37)报告,与ND组相比,CL组在矫正年龄11周时哭闹较少(MD -0.57小时/24小时,95%CI -1.09至-0.05)。异质性检验不适用。三项纳入120名婴儿的研究比较了CL与CBL。两项研究(n = 79)报告,与CBL组相比,CL组住院时间显著缩短(WMD -16.5天,95%CI -26.2至-6.8,I² = 0%;无异质性)。根据GRADE,该结果的证据质量较低。一项研究(n = 41)报告,在CL育婴室护理的婴儿在矫正年龄3个月时平均体重较高(P值<0.02),在3个月龄时24小时内平均清醒时间较短(P值<0.005)。数据无法输入RevMan或GRADE。一项研究(n = 41)报告,与CBL组相比,CL组机械通气时间较短(MD -18.2天,95%CI -31.40至-5.0)。一项研究(n = 41)报告,CL组首次经口喂养时间较短(MD -6.8天,95%CI -13.29至-0.31)。我们未发现安全问题。
评估CL效果的试验共纳入了544名婴儿。没有研究报告我们的主要结局,即3个月或6个月时的体重。一项额外研究的结果强化了我们的发现,即CL与CBL相比可缩短住院时间,CL与ND相比也是如此。根据GRADE,该结局的两项比较证据质量均较低。未来的研究应侧重于比较CL与ND。