持续气道正压通气(CPAP)治疗早产儿呼吸暂停。
Continuous positive airway pressure (CPAP) for apnoea of prematurity.
机构信息
Department of Paediatrics, RCSI & UCD Malaysia Campus (formerly Penang Medical College), George Town, Malaysia.
Department of Clinical Skills, University of Split School of Medicine, Split, Croatia.
出版信息
Cochrane Database Syst Rev. 2023 Jul 18;7(7):CD013660. doi: 10.1002/14651858.CD013660.pub2.
BACKGROUND
Apnoea of prematurity (AoP) is defined as a pause in breathing for 20 seconds or longer, or for less than 20 seconds when accompanied by bradycardia and hypoxaemia, in a preterm infant. An association between the severity of apnoea and neurodevelopmental delay has been reported. Continuous positive airway pressure (CPAP) is a form of non-invasive ventilatory assistance that has been shown to be relatively safe and effective in preventing and treating respiratory distress among preterm infants. It is less clear whether CPAP treatment is safe and effective in the prevention and treatment of AoP.
OBJECTIVES
- To assess the effects of CPAP on AoP in preterm infants (this may be compared to supportive care or mechanical ventilation). 2. To assess the effects of different CPAP delivery systems on AoP in preterm infants.
SEARCH METHODS
Searches were conducted in September 2022 in the following databases: Cochrane Library, MEDLINE, Embase, and CINAHL. We also searched clinical trial registries and the reference lists of studies selected for inclusion.
SELECTION CRITERIA
We included all randomised and quasi-randomised controlled trials (RCTs) in which researchers determined that CPAP was necessary for AoP in preterm infants (born before 37 weeks). Cross-over studies were also included, provided sufficient data were available for analysis.
DATA COLLECTION AND ANALYSIS
We used the standard methods of Cochrane and Cochrane Neonatal, including independent assessment of risk of bias and extraction of data by at least two review authors. Discrepancies were resolved by involvement of a third author. We used the GRADE approach to assess the certainty of evidence for the following outcomes: 1) failed CPAP; 2) apnoea; 3) adverse effects of CPAP.
MAIN RESULTS
We included four single-centre trials conducted in Malaysia, Spain, Germany, and North America, involving 138 infants with a mean/median gestation of 26 to 28 weeks. Two studies were parallel-group RCTs and two were cross-over trials. None of the studies compared CPAP with supportive care. All trials compared one form of CPAP with another. Two compared a variable flow device with ventilator CPAP, one compared two different variable flow devices, and one compared a variable flow device with bubble CPAP. Interventions were administered for periods ranging between six and 48 hours, with pressures between 4 and 6 cm HO. We assessed all trials as having a high risk of bias for blinding of participants and personnel, and two studies for blinding of outcome assessors. We found a high risk of a carry-over effect in two studies where the washout period was not adequately described, and a high risk of bias in a study that appeared to use an analysis method not generally accepted for cross-over studies. Comparison 1. CPAP and supportive care compared to supportive care alone We did not identify any study for inclusion in this comparison. Comparison 2. CPAP delivered by different types of devices 2a. Variable flow compared to ventilator CPAP Two studies were included in this comparison. We are very uncertain whether there is any difference in the incidence of failed CPAP, defined as the need for mechanical ventilation (risk ratio (RR) 0.16, 95% confidence interval (CI) 0.01 to 2.90; 1 study, 26 participants; very low-certainty). We are very uncertain whether there is any difference in the frequency of apnoea events (mean difference (MD) per four-hour interval -0.10, 95% CI -1.30 to 1.10; 1 study, 26 participants; very low-certainty). We are uncertain whether there is any difference in adverse events. Neurodevelopmental outcomes were not reported. 2b. Variable flow compared to bubble CPAP We included one study in this comparison, but it did not report our pre-specified outcomes. 2c. Infant Flow variable flow CPAP compared to Medijet variable flow CPAP We are very uncertain whether there is any difference in the incidence of failed CPAP (RR 2.62, 95% CI 0.91 to 7.53; 1 study, 80 participants; very low-certainty). The frequency of apnoea was not reported, and we do not know whether there is any difference in adverse events. Neurodevelopmental outcomes were not reported. Comparison 3. CPAP compared to mechanical ventilation We did not identify any studies for inclusion in this comparison.
AUTHORS' CONCLUSIONS: Due to the limited available evidence, we are very uncertain whether any CPAP device is more effective than other forms of supportive care, other CPAP devices, or mechanical ventilation for the prevention and treatment of AoP. The devices used in these studies included two types of variable flow CPAP device: bubble CPAP and ventilator CPAP. For each comparison, data were only available from a single study. There are theoretical reasons why these devices might have different effects on AoP, therefore further trials are indicated.
背景
早产儿呼吸暂停(AoP)是指早产儿在呼吸暂停 20 秒或更长时间,或呼吸暂停持续时间小于 20 秒但伴有心动过缓和低氧血症。已有研究报道呼吸暂停的严重程度与神经发育延迟有关。持续气道正压通气(CPAP)是一种非侵入性通气辅助形式,已被证明在预防和治疗早产儿呼吸窘迫方面相对安全有效。CPAP 治疗在预防和治疗 AoP 中的安全性和有效性尚不清楚。
目的
- 评估 CPAP 对早产儿 AoP 的作用(可与支持性护理或机械通气进行比较)。2. 评估不同 CPAP 输送系统对早产儿 AoP 的作用。
检索方法
2022 年 9 月,在 Cochrane 图书馆、MEDLINE、Embase 和 CINAHL 等数据库中进行了检索。我们还检索了临床试验注册处和纳入研究的参考文献列表。
选择标准
我们纳入了所有随机和半随机对照试验(RCT),其中研究人员确定 CPAP 对早产儿(出生于 37 周之前)的 AoP 是必要的。也纳入了交叉研究,只要有足够的数据进行分析。
数据收集和分析
我们使用 Cochrane 和 Cochrane 新生儿的标准方法,包括由至少两名综述作者独立评估偏倚风险和提取数据。存在分歧时,由第三名作者参与解决。我们使用 GRADE 方法评估以下结局的证据确定性:1)CPAP 失败;2)呼吸暂停;3)CPAP 的不良反应。
主要结果
我们纳入了四项单中心试验,分别在马来西亚、西班牙、德国和北美进行,涉及 138 名平均/中位胎龄为 26 至 28 周的婴儿。两项研究为平行组 RCT,两项为交叉研究。没有一项研究将 CPAP 与支持性护理进行比较。所有试验均比较了一种 CPAP 与另一种 CPAP。两项比较了可变流量装置与呼吸机 CPAP,一项比较了两种不同的可变流量装置,一项比较了可变流量装置与气泡 CPAP。干预措施的持续时间在 6 至 48 小时之间,压力在 4 至 6 cmHO 之间。我们评估所有试验的参与者和人员的盲法以及两项试验的结局评估者的盲法都存在高偏倚风险。我们发现两项研究的洗脱期描述不充分,存在高偏倚风险,而另一项研究似乎使用了一种不被普遍接受的交叉研究分析方法。
比较 1. CPAP 和支持性护理与支持性护理单独比较
我们没有发现任何符合纳入标准的研究。
比较 2. 不同类型的 CPAP 设备的效果
2a. 可变流量与呼吸机 CPAP
两项研究被纳入这一比较。我们非常不确定 CPAP 失败的发生率是否存在差异,CPAP 失败定义为需要机械通气(风险比(RR)0.16,95%置信区间(CI)0.01 至 2.90;1 项研究,26 名参与者;极低确定性)。我们也非常不确定呼吸暂停事件的频率是否存在差异(每四小时间隔的平均差值-0.10,95%CI-1.30 至 1.10;1 项研究,26 名参与者;极低确定性)。我们不确定是否存在不良反应差异。神经发育结局未报告。
2b. 可变流量与气泡 CPAP
我们纳入了一项研究,但它没有报告我们预先指定的结局。
2c. Infant Flow 可变流量 CPAP 与 Medijet 可变流量 CPAP
我们非常不确定 CPAP 失败的发生率是否存在差异(RR 2.62,95%CI 0.91 至 7.53;1 项研究,80 名参与者;极低确定性)。呼吸暂停的频率没有报告,我们也不知道不良反应是否存在差异。神经发育结局未报告。
比较 3. CPAP 与机械通气
我们没有发现任何符合纳入标准的研究。
作者结论
由于可用证据有限,我们非常不确定任何 CPAP 设备在预防和治疗 AoP 方面是否比其他形式的支持性护理、其他 CPAP 设备或机械通气更有效。这些研究中使用的设备包括两种类型的可变流量 CPAP 设备:气泡 CPAP 和呼吸机 CPAP。对于每个比较,只有一项研究提供了数据。这些设备在理论上可能对 AoP 有不同的影响,因此需要进一步的试验。
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