Abiramalatha Thangaraj, Thanigainathan Sivam, Balakrishnan Umamaheswari
Neonatology, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India.
Cochrane Database Syst Rev. 2019 Jul 8;7(7):CD012940. doi: 10.1002/14651858.CD012940.pub2.
Routine monitoring of gastric residuals in preterm infants on gavage feeds is a common practice in many neonatal intensive care units and is used to guide the initiation and advancement of feeds. No guidelines or consensus is available on whether to re-feed or discard the aspirated gastric residuals. Although re-feeding gastric residuals may replace partially digested milk, gastrointestinal enzymes, hormones, and trophic substances that aid in digestion and promote gastrointestinal motility and maturation, re-feeding abnormal residuals may result in emesis, necrotising enterocolitis, or sepsis.
To assess the efficacy and safety of re-feeding compared to discarding gastric residuals in preterm infants. The allocation should have been started in the first week of life and should have been continued at least until the baby reached full enteral feeds. The investigator could have chosen to discard the gastric residual in the re-feeding group, if the gastric residual quality was not satisfactory. However, the criteria for discarding gastric residual should have been predefined.To conduct subgroup analysis based on gestational age (≤ 27 weeks, 28 weeks to 31 weeks, ≥ 32 weeks), birth weight (< 1000 g, 1000 g to 1499 g, ≥ 1500 g), type of milk (human milk or formula milk), quality of the gastric residual (fresh milk, curded milk, or bile-stained gastric residual), volume of gastric residual replaced (total volume, 50% of the volume, volume of the next feed, or prespecified volume, irrespective of the volume of the aspirate, e.g. 2 mL, 3 mL), and whether the volume of gastric residual that is re-fed is included in or excluded from the volume of the next feed (see "Subgroup analysis and investigation of heterogeneity").
We used the standard search strategy of Cochrane Neonatal to search the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 1), MEDLINE via PubMed (1966 to 19 February 2018), Embase (1980 to 19 February 2018), and the Cumulative Index to Nursing and Allied Health Literature (CINAHL) (1982 to 19 February 2018). We also searched clinical trial databases, conference proceedings, and the reference lists of retrieved articles for randomised controlled trials and quasi-randomised trials.
Randomised and quasi-randomised controlled trials that compared re-feeding versus discarding gastric residuals in preterm infants.
Two review authors assessed trial eligibility and risk of bias and independently extracted data. We analysed treatment effects in individual trials and reported the risk ratio and risk difference for dichotomous data, and the mean difference for continuous data, with respective 95% confidence intervals. We used the GRADE approach to assess the quality of evidence.
We found one eligible trial that included 72 preterm infants. This trial was not blinded.We are uncertain as to the effect of re-feeding gastric residual on efficacy outcomes such as time to regain birth weight (mean difference (MD) 0.40 days, 95% confidence interval (CI) -2.89 to 3.69 days; very low quality evidence), time to reach enteral feeds ≥ 120 mL/kg/d (MD -1.30 days, 95% CI -2.93 to 0.33 days; very low quality evidence), number of infants with extrauterine growth restriction at discharge (risk ratio (RR) 1.29, 95% CI 0.38 to 4.34; very low quality evidence), duration of total parenteral nutrition (MD -0.30 days, 95% CI -2.07 to 1.47 days; very low quality evidence), and length of hospital stay (MD -1.90 days, 95% CI -25.27 to 21.47 days; very low quality evidence).Similarly, we are uncertain as to the effect of re-feeding gastric residual on safety outcomes such as incidence of stage 2 or 3 necrotising enterocolitis and/or spontaneous intestinal perforation (RR 0.71, 95% CI 0.25 to 2.04; very low quality evidence), number of episodes of feed interruption lasting ≥ 12 hours (RR 0.80, 95% CI 0.42 to 1.52; very low quality evidence), or mortality before discharge (RR 0.50, 95% CI 0.14 to 1.85; low-quality evidence). We are uncertain as to the effect of re-feeding gastric residual in the subgroups of human milk-fed and formula-fed infants. We found no data on other outcomes such as linear and head growth during hospital stay, postdischarge growth, number of infants with parenteral nutrition-associated liver disease, and neurodevelopmental outcomes.
AUTHORS' CONCLUSIONS: We found only limited data from one small unblinded trial on the efficacy and safety of re-feeding gastric residuals in preterm infants. The quality of evidence was low to very low. Hence, available evidence is insufficient to support or refute re-feeding of gastric residuals in preterm infants. A large, randomised controlled trial is needed to provide data of sufficient quality and precision to inform policy and practice.
在许多新生儿重症监护病房,常规监测经口喂养的早产儿胃残余量是一种常见做法,用于指导喂养的开始和推进。对于吸出的胃残余物是重新喂食还是丢弃,目前尚无指南或共识。虽然重新喂食胃残余物可能会补充部分消化的乳汁、胃肠酶、激素以及有助于消化并促进胃肠蠕动和成熟的营养物质,但重新喂食异常的残余物可能会导致呕吐、坏死性小肠结肠炎或败血症。
评估与丢弃胃残余物相比,重新喂食早产儿胃残余物的疗效和安全性。分配应在出生后第一周开始,并应至少持续到婴儿完全经口喂养。如果胃残余物质量不令人满意,研究人员可以选择在重新喂食组中丢弃胃残余物。然而,丢弃胃残余物的标准应该预先定义。根据胎龄(≤27周、28周至31周、≥32周)、出生体重(<1000g、1000g至1499g、≥1500g)、乳汁类型(母乳或配方奶)、胃残余物质量(新鲜乳汁、凝乳或胆汁染色的胃残余物)、重新喂食的胃残余物替代量(总量、吸出量的50%、下次喂食量或预先指定的量,例如2mL、3mL,与吸出量无关)以及重新喂食的胃残余物量是否包含在下一次喂食量中或从中排除进行亚组分析(见“亚组分析和异质性研究”)。
我们使用Cochrane新生儿组的标准检索策略,检索Cochrane对照试验中心注册库(CENTRAL;2018年第1期)、通过PubMed检索的MEDLINE(1966年至2018年2月19日)、Embase(1980年至2018年2月19日)以及护理及相关健康文献累积索引(CINAHL)(1982年至2018年2月19日)。我们还检索了临床试验数据库、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。
比较重新喂食与丢弃早产儿胃残余物的随机和半随机对照试验。
两位综述作者评估试验的合格性和偏倚风险,并独立提取数据。我们分析了各个试验中的治疗效果,并报告了二分数据的风险比和风险差异,以及连续数据的平均差异,并给出各自的95%置信区间。我们使用GRADE方法评估证据质量。
我们找到一项符合条件的试验,该试验纳入了72名早产儿。该试验未设盲。我们不确定重新喂食胃残余物对以下疗效结局的影响,如恢复出生体重的时间(平均差异(MD)0.40天,95%置信区间(CI)-2.89至3.69天;极低质量证据)、达到经口喂养≥120mL/kg/d的时间(MD -1.30天,95%CI -2.93至0.33天;极低质量证据)、出院时宫外生长受限婴儿的数量(风险比(RR)1.29,95%CI 0.38至4.34;极低质量证据)、全胃肠外营养的持续时间(MD -0.30天,95%CI -2.07至1.47天;极低质量证据)以及住院时间(MD -1.90天,95%CI -25.27至21.47天;极低质量证据)。同样,我们不确定重新喂食胃残余物对以下安全性结局的影响,如2期或3期坏死性小肠结肠炎和/或自发性肠穿孔的发生率(RR 0.71,95%CI 0.25至2.04;极低质量证据)、持续≥12小时的喂养中断次数(RR 0.80,95%CI 0.42至1.52;极低质量证据)或出院前死亡率(RR 0.50,95%CI 0.14至1.85;低质量证据)。我们不确定重新喂食胃残余物在母乳喂养和配方奶喂养婴儿亚组中的效果。我们未找到关于其他结局的数据,如住院期间的线性生长和头围生长、出院后生长、患有肠外营养相关肝病的婴儿数量以及神经发育结局。
我们仅从一项小型非盲法试验中获得了关于重新喂食早产儿胃残余物的疗效和安全性的有限数据。证据质量低至极低。因此,现有证据不足以支持或反驳对早产儿重新喂食胃残余物。需要进行一项大型随机对照试验,以提供足够质量和精度的数据来指导政策和实践。