Neonatal Services, Royal Women's Hospital, Melbourne, Australia.
The University of Melbourne, Melbourne, Australia.
Cochrane Database Syst Rev. 2021 Aug 4;8(8):CD005249. doi: 10.1002/14651858.CD005249.pub3.
Many small, sick, and preterm infants are unable to co-ordinate sucking, swallowing, and breathing, and therefore require gavage feeding. In gavage feeding, milk feeds are delivered through a tube passed via the nose or the mouth into the stomach. Intermittent bolus milk feeds may be administered by a syringe to gently push milk into the infant's stomach (push feed). Alternatively, milk can be poured into a syringe attached to the tube and allowed to drip in by gravity (gravity feed).
To determine whether use of push feeding compared with gravity feeding results in more rapid establishment of full gavage feeds without increasing adverse events among preterm or low birth weight infants, or both, who require intermittent bolus tube feeding.
We used the standard search strategy of Cochrane Neonatal to search the Cochrane Central Register of Controlled Trials (CENTRAL; 2020, Issue 7), in the Cochrane Library; Ovid MEDLINE(R) and Epub Ahead of Print, In-Process & Other Non-Indexed Citations, Daily and Versions(R); and the Cumulative Index to Nursing and Allied Health Literature (CINAHL), on 30 July 2020. We also searched clinical trials databases and the reference lists of retrieved articles for randomised controlled trials (RCTs) and quasi-RCTs.
We included RCTs and quasi-RCTs comparing push versus gravity intermittent gavage tube feeding in preterm (less than 37 weeks' gestation) or low birth weight (less than 2500 grams) infants, or both.
We assessed the methods of trials regarding blinding of randomisation and outcome measurement. We evaluated treatment effects with a fixed-effect model using risk ratio (RR), relative risk reduction, risk difference (RD), and number needed to treat for an additional beneficial outcome (NNTB) for categorical data; and using mean, standard deviation, and mean difference (MD) for continuous data. We analysed outcomes measured as count data, for example, frequency of apnoea, bradycardia, and episodes of pulse oximeter oxygen (SpO₂) desaturation, by comparing rates of events and the rate ratio. We evaluated heterogeneity to help determine the suitability of pooling results. We used the GRADE approach to assess the certainty of evidence.
One small cross-over trial (31 infants) met the criteria for inclusion in this review. The certainty of evidence for all outcomes was very low due to imprecision of estimates, wide confidence intervals, and unclear risk of bias. The primary outcome - time taken to establish full gavage feeding (days) and feeding intolerance (number of episodes per day) - was not reported in the included study. The evidence is very uncertain about the effects of push versus gravity intermittent gavage tube feeding on all other outcomes. Investigators reported respiratory rate (breaths per minute) at completion of feeding (MD 0.58, 95% confidence interval (CI) -5.97 to 7.13; 1 study, 31 participants; very low-certainty evidence); respiratory rate (breaths per minute) 10 to 30 minutes after completion of feeding (MD 3.1, 95% CI -3.43 to 9.63; 1 study, 31 participants; very low-certainty evidence); heart rate (beats per minute) at completion of feeding (MD 2.6, 95% CI -9.71 to 4.51; 1 study, 31 participants; very low-certainty evidence); and heart rate (beats per minute) 10 to 30 minutes after completion of feeding (MD 2.4, 95% CI -9.16 to 4.36; 1 study, 31 participants; very low-certainty evidence). We are very uncertain of the effects of push versus gravity intermittent gavage feeding on respiratory rate during and after feeding.
AUTHORS' CONCLUSIONS: We do not have sufficient evidence to determine the effects of intermittent bolus gavage feeding for preterm and low birth weight infants. The single small study of 31 infants comparing effects of push versus gravity bolus gavage feeding did not report the primary outcome identified in this review. Thus, evidence is insufficient to show whether use of push compared with gravity gavage feeding results in more rapid establishment of full gavage feeds without increasing adverse events in preterm or low birth weight infants who receive intermittent bolus gavage feeding. In addition, the included study was too small to measure potential adverse events that can occur during gavage tube feeding, for example, episodes of oxygen desaturation, apnoea, or bradycardia.
许多较小、患病和早产的婴儿无法协调吸吮、吞咽和呼吸,因此需要管饲喂养。在管饲喂养中,通过经鼻或经口插入胃中的管子输送牛奶喂养。通过注射器间歇推注牛奶可以将牛奶轻轻推入婴儿的胃中(推注喂养)。或者,可以将牛奶倒入连接到管子上的注射器中,让牛奶通过重力滴入(重力喂养)。
确定与重力喂养相比,推注喂养是否可以更快地建立全管饲喂养,而不会增加需要间歇性推注管饲喂养的早产儿或低出生体重儿(或两者)的不良事件。
我们使用 Cochrane 新生儿中心的标准搜索策略来搜索 Cochrane 图书馆中的 Cochrane 对照试验中心注册库(CENTRAL;2020 年,第 7 期);Ovid MEDLINE(R)和 Epub 提前在线、处理中和其他非索引引文、每日和版本(R);以及 Cumulative Index to Nursing and Allied Health Literature (CINAHL),于 2020 年 7 月 30 日。我们还搜索了临床试验数据库和检索文章的参考文献列表,以寻找随机对照试验(RCT)和准随机对照试验。
我们纳入了 RCT 和准 RCT,比较了早产儿(妊娠不足 37 周)或低出生体重儿(体重不足 2500 克)或两者的推注与重力间歇性管饲喂养。
我们评估了试验方法在随机分组和结局测量方面的盲法。我们使用固定效应模型评估治疗效果,使用风险比(RR)、相对风险降低、风险差异(RD)和额外有益结局的需要治疗数(NNTB)来表示分类数据;使用均值、标准差和均值差(MD)来表示连续数据。我们分析了以计数数据表示的结局,例如呼吸暂停、心动过缓和脉搏血氧饱和度(SpO₂)下降的发作频率,通过比较事件发生率和比率比来进行分析。我们评估了异质性,以帮助确定结果是否适合汇总。我们使用 GRADE 方法评估证据的确定性。
一项小型交叉试验(31 名婴儿)符合纳入本综述的标准。由于估计值不精确、置信区间较宽和偏倚风险不明确,所有结局的证据确定性都非常低。纳入研究未报告主要结局-建立全管饲喂养所需的时间(天数)和喂养不耐受(每天发作次数)。与重力间歇性管饲喂养相比,推注喂养对所有其他结局的影响的证据非常不确定。研究人员报告了完成喂养时的呼吸频率(每分钟呼吸次数)(MD 0.58,95%置信区间(CI)-5.97 至 7.13;1 项研究,31 名参与者;极低确定性证据);完成喂养后 10 至 30 分钟的呼吸频率(MD 3.1,95%CI-3.43 至 9.63;1 项研究,31 名参与者;极低确定性证据);完成喂养时的心率(每分钟心跳次数)(MD 2.6,95%CI-9.71 至 4.51;1 项研究,31 名参与者;极低确定性证据);完成喂养后 10 至 30 分钟的心率(MD 2.4,95%CI-9.16 至 4.36;1 项研究,31 名参与者;极低确定性证据)。我们非常不确定推注与重力间歇性管饲喂养对喂养期间和之后的呼吸频率的影响。
我们没有足够的证据来确定早产儿和低出生体重儿间歇性推注管饲喂养的效果。这项比较推注与重力推注管饲喂养对 31 名婴儿影响的小型单一研究没有报告本综述中确定的主要结局。因此,证据不足,无法表明与重力管饲喂养相比,使用推注管饲喂养是否可以更快地建立全管饲喂养,而不会增加接受间歇性推注管饲喂养的早产儿或低出生体重儿的不良事件。此外,纳入的研究规模太小,无法测量管饲喂养过程中可能发生的潜在不良事件,例如血氧饱和度下降、呼吸暂停或心动过缓的发作。