Morag Iris, Xiao Yu-Tian, Bruschettini Matteo
School of Medicine, Tel- Aviv University, Tel-Aviv, Israel.
Pediatrics, Shamir Medical Center, Zeriffin, Israel.
Cochrane Database Syst Rev. 2024 Dec 19;12(12):CD006982. doi: 10.1002/14651858.CD006982.pub5.
Preterm and low birth weight infants are at an early stage of development, and do not receive adequate maternal circadian signals. They are often cared for over prolonged periods of hospitalisation in neonatal intensive care units (NICU), where environmental circadian stimuli are lacking. Exposure to artificial light-dark cycles may stimulate the development of the circadian system and improve clinical outcomes. However, it remains uncertain whether cycled light (CL) is preferable to near darkness (ND) or continuous bright light (CBL) in fostering development and maturation, and reducing adverse neonatal health outcomes. This is an update of an earlier Cochrane review, last published in 2016.
To evaluate the benefits and harms of CL in preterm and low birth weight infants compared to ND or CBL.
We searched CENTRAL, PubMed, Embase, and two trial registries to September 2023. We also checked reference lists, and searched for retractions of included studies.
We included randomised controlled trials (RCTs) or quasi-RCTs in preterm infants (< 37 weeks' postmenstrual age (PMA)), or those with a low birth weight (< 2500 g), admitted and cared for in an NICU or a step-down unit, comparing CL with ND or CBL.
We used the standard review methods of the Cochrane Neonatal Review Group to assess the methodological quality of studies. We used the fixed-effect model with risk ratio (RR) and mean difference (MD), with their 95% confidence intervals (CIs) for dichotomous data. Our primary outcomes were (1) growth at three and six months' corrected age, (2) major neurodevelopmental disability, and (3) adverse effects. Our secondary outcomes were (4) retinopathy of prematurity, (5) duration of initial hospitalisation, (6) duration of oxygen treatment, and (7) parent satisfaction. We used GRADE to assess the certainty of evidence for each outcome.
We included 20 studies with 1633 infants. Data for meta-analysis were available for 11 studies (1126 infants). One study with multiple arms was included in both comparisons. We rated the overall risk of bias at the study level as high or unclear for all 20 studies that had one or several unclear or high risk of bias judgements across the domains. Cycled light versus dimmed light or near darkness (10 studies) The evidence is very uncertain about the effect of cycled light compared to dimmed light (reduction of illumination levels) or near darkness on weight at three months (MD 24.79, 95% CI -262.33 to 311.91; 2 studies, 187 infants; very low-certainty evidence), and weight at six months (MD 202, 95% CI -109.68 to 513.68; 1 study, 147 infants; very low-certainty evidence). The studies did not report any data for major neurodevelopmental disability. No data are available for adverse effects; it is uncertain if the absence of adverse effects is because none occurred, or because they were not identified and recorded. The evidence is very uncertain about the effect of cycled light compared to dimmed light or near darkness on the likelihood of developing retinopathy of prematurity of any stage (RR 0.89, 95% CI 0.76 to 1.03; 3 studies, 307 infants; very low-certainty evidence), and severe retinopathy of prematurity of stage 3 or higher (RR 0.98, 95% CI 0.59 to 1.61; 4 studies, 454 infants; very low-certainty evidence). Cycled light compared to dimmed light or near darkness may have little to no effect on the duration of initial hospitalisation (MD -3.04, 95% CI -7.86 to 1.78; 5 studies, 550 infants; very low-certainty evidence), but the evidence is very uncertain. Cycled light versus continuous bright light (11 studies) No data are available on the following primary outcomes, as no studies reported them: growth at three and six months' corrected age, major neurodevelopmental disability, and adverse effects. It is uncertain if the absence of adverse effects is because none occurred or because they were not identified and recorded. No data are available on retinopathy of prematurity, as no studies reported it. Cycled light compared to continuous bright light may reduce the duration of initial hospitalisation, but the evidence is very uncertain (MD -9.86, 95% CI -10.09 to -9.63; 5 studies, 499 infants; very low-certainty evidence).
AUTHORS' CONCLUSIONS: Despite identifying 20 studies, we remain uncertain about the effect of CL compared to ND or CBL on all outcomes of interest in this review. In addition, a few critical outcomes were not reported by any of the included studies. The evidence remains uncertain about whether CL is the right choice in the NICU. The physician should always weigh the benefits and risks, based on the effects of the different options in the specific setting.
早产和低出生体重婴儿处于发育早期,未接收到足够的母体昼夜节律信号。他们通常在新生儿重症监护病房(NICU)接受长时间住院治疗,而那里缺乏环境昼夜节律刺激。暴露于人工明暗循环可能会刺激昼夜节律系统的发育并改善临床结局。然而,在促进发育和成熟以及减少不良新生儿健康结局方面,循环光(CL)是否优于近乎黑暗(ND)或持续强光(CBL)仍不确定。这是对2016年最后发表的一篇早期Cochrane综述的更新。
评估与ND或CBL相比,CL对早产和低出生体重婴儿的益处和危害。
我们检索了截至2023年9月的Cochrane系统评价数据库、PubMed、Embase和两个试验注册库。我们还检查了参考文献列表,并搜索了纳入研究的撤稿情况。
我们纳入了针对胎龄小于37周(月经龄(PMA))或出生体重小于2500g的早产儿,在NICU或降级病房住院并接受护理的随机对照试验(RCT)或半随机对照试验,比较CL与ND或CBL。
我们采用Cochrane新生儿综述小组的标准综述方法来评估研究的方法学质量。对于二分数据,我们使用固定效应模型,计算风险比(RR)和均值差(MD)及其95%置信区间(CI)。我们的主要结局包括:(1)矫正年龄3个月和6个月时的生长情况;(2)主要神经发育障碍;(3)不良反应。次要结局包括:(4)早产儿视网膜病变;(5)首次住院时间;(6)吸氧治疗时间;(7)家长满意度。我们使用GRADE评估每个结局的证据确定性。
我们纳入了20项研究,共1633名婴儿。11项研究(1126名婴儿)可获得用于荟萃分析的数据。一项有多组对照的研究在两项比较中均被纳入。在所有20项研究中,若在各个领域有一项或多项偏倚风险判断为不明确或高风险,则我们将研究水平的总体偏倚风险评为高或不明确。循环光与暗光或近乎黑暗(10项研究)与暗光(降低照明水平)或近乎黑暗相比,关于循环光对3个月时体重的影响(MD 24.79,95%CI -262.33至311.91;2项研究,187名婴儿;极低确定性证据)以及6个月时体重的影响(MD 202,95%CI -109.68至513.68;1项研究,147名婴儿;极低确定性证据),证据非常不确定。这些研究未报告任何关于主要神经发育障碍的数据。无不良反应数据;不确定未出现不良反应是因为未发生,还是因为未被识别和记录。与暗光或近乎黑暗相比,关于循环光对任何阶段早产儿视网膜病变发生可能性的影响(RR 0.89,95%CI 0.76至1.03;3项研究,307名婴儿;极低确定性证据)以及3期或更高期严重早产儿视网膜病变的影响(RR 0.98,95%CI 0.59至1.61;4项研究,454名婴儿;极低确定性证据),证据非常不确定。与暗光或近乎黑暗相比,循环光可能对首次住院时间影响很小或无影响(MD -3.04,95%CI -7.86至1.78;5项研究,550名婴儿;极低确定性证据),但证据非常不确定。循环光与持续强光(11项研究)以下主要结局无数据,因为没有研究报告:矫正年龄3个月和6个月时的生长情况、主要神经发育障碍和不良反应。不确定未出现不良反应是因为未发生,还是因为未被识别和记录。无早产儿视网膜病变的数据,因为没有研究报告。与持续强光相比,循环光可能会缩短首次住院时间,但证据非常不确定(MD -9.86,95%CI -10.09至-9.63;5项研究,499名婴儿;极低确定性证据)。
尽管识别出20项研究,但与ND或CBL相比,我们仍不确定CL对本综述中所有感兴趣结局的影响。此外,纳入的任何研究均未报告一些关键结局。关于CL是否是NICU中的正确选择,证据仍然不确定。医生应始终根据特定环境中不同选择的效果权衡利弊。