Hydrolysed formula for preterm infants

Review question: does feeding preterm infants with cow's milk formula containing predigested (hydrolysed) proteins rather than whole proteins improve digestion and reduce the risk of severe bowel problems?

Background: preterm infants often find cow's milk formula more difficult to digest than human milk, and cow's milk formula may increase the risk of severe bowel problems for preterm (born before their due date) infants. If preterm infants are fed with cow's milk formula (when human milk is unavailable), then using a formula in which the protein is already partially digested (called hydrolysed) rather than a standard formula (with intact proteins) might reduce the risk of these problems. However, hydrolysed formulas are more expensive than standard formulas, and may have specific side effects not seen with standard formulas. Given these concerns, we have reviewed all the available evidence from clinical trials that compared these types of formula for feeding preterm infants.

Study characteristics: in searches of medical databases up to April 2017, we found 11 trials; most were small (involving 665 infants in total) and had methodological weaknesses.

Key results: the data from these trials provided no strong or consistent evidence that feeding preterm infants with hydrolysed formula rather than standard formula improved digestion or reduced the risk of severe bowel problems.

Conclusions: the currently available evidence suggested that feeding preterm infants with hydrolysed formula (rather than standard formula) during their initial hospital admission has no important benefits or harms. However, this finding is not yet conclusive, and larger and better quality trials are needed to provide evidence to help clinicians and families make informed choices about this issue.

Authors' conclusions: 

The identified trials provide only low quality evidence about the effects of feeding preterm infants with protein hydrolysate versus standard formula. The existing data did not support conclusions that feeding with protein hydrolysate affects the risk of feed intolerance or necrotising enterocolitis. Further large, pragmatic trials are needed to provide more reliable and precise estimates of effectiveness and cost-effectiveness.

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Background: 

When human milk is not available for feeding preterm infants, protein hydrolysate rather than standard cow's milk formulas (with intact proteins) are often used because they are perceived as being tolerated better and less likely to lead to complications. However, protein hydrolysate formulas are more expensive than standard formulas, and concern exists that their use in practice is not supported by high-quality evidence.

Objectives: 

To assess the effect of feeding preterm infants with hydrolysed formula (versus standard cow's milk formulas) on the risk of feed intolerance, necrotising enterocolitis, and other morbidity and mortality in preterm infants.

Search strategy: 

We used the standard Cochrane Neonatal search strategy including electronic searches of the Cochrane Central Register of Controlled Trials (CENTRAL; 2017, Issue 4), Ovid MEDLINE, Ovid Embase, and the Cumulative Index to Nursing and Allied Health Literature (CINAHL) (to April 2017), as well as conference proceedings and previous reviews.

Selection criteria: 

Randomised and quasi-randomised controlled trials that compared feeding preterm infants with protein hydrolysate versus standard (non-hydrolysed) cow's milk formula.

Data collection and analysis: 

Two review authors assessed trial eligibility and risk of bias and extracted data independently. We analysed treatment effects as described in the individual trials and reported risk ratios and risk differences for dichotomous data, and mean differences for continuous data, with respective 95% confidence intervals (CI). We used a fixed-effect model in meta-analyses and explored potential causes of heterogeneity in sensitivity analyses. We assessed quality of evidence at the outcome level using the GRADE approach.

Main results: 

We identified 11 trials for inclusion in the review. All trials were small (total participants 665) and had various methodological limitations including uncertainty about methods to ensure allocation concealment and blinding. Most participants were clinically stable preterm infants of gestational age less than about 34 weeks or birth weight less than about 1750 g. Fewer participants were extremely preterm, extremely low birth weight, or growth-restricted. Most trials found no effects on feed intolerance assessed variously as mean prefeed gastric residual volume, incidence of abdominal distention or other concerning gastrointestinal signs, or time taken to achieve full enteral feeds (meta-analysis was limited because studies used different measures). Meta-analysis found no effect on the risk of necrotising enterocolitis (typical risk ratio 1.10, 95% CI 0.36 to 3.34; risk difference 0.00, 95% CI -0.03 to 0.04; 5 trials, 385 infants) (low quality evidence; downgraded for imprecision and design weaknesses).

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