SynthesisThe Cochrane database of systematic reviews2013
Slow advancement of enteral feed volumes to prevent necrotising enterocolitis in very low birth weight infants.
Synthesis in The Cochrane database of systematic reviews, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.
- Slow advancement of enteral feed volumes to prevent necrotising enterocolitis in very low birth weight infants.The Cochrane database of systematic reviews · 2021Pooled it
- Slow advancement of enteral feed volumes to prevent necrotising enterocolitis in very low birth weight infants.The Cochrane database of systematic reviews · 2017Pooled it
- The Speed of Increasing milk Feeds: a randomised controlled trial.BMC pediatrics · 2017Trial
- Hour of Life at Enteral Feeding Initiation and Associated Clinical Morbidity in Extremely Low-Birth-Weight Infants.Nutrients · 2024Article
- Time to full enteral feeds in hospitalised preterm and very low birth weight infants in Nigeria and Kenya.PloS one · 2024Article
- Quality improvement initiative to decrease time to full feeds and central line utilization among infants born less than or equal to 32 0/7 weeks through compliance with standardized feeding guidelines.Journal of perinatology : official journal of the California Perinatal Association · 2019Article
- Comparative Effectiveness of Prophylactic Therapies for Necrotizing Enterocolitis in Preterm Infants: Protocol for a Network Meta-analysis of Randomized Trials.International journal of preventive medicine · 2018Article
- Article
- Impact of a new aggressive nutrition policy incorporating early introduction of parenteral nutrition and mother's own milk on growth of preterm infants.World journal of pediatrics : WJP · 2016Article
- Intestinal microbiota and its relationship with necrotizing enterocolitis.Pediatric research · 2015Review
- Enteral L-Arginine and Glutamine Supplementation for Prevention of NEC in Preterm Neonates.International journal of pediatrics · 2015Article
- Evidence-based feeding strategies before and after the development of necrotizing enterocolitis.Expert review of clinical immunology · 2014Review
- Pathophysiology and current management of necrotizing enterocolitis.Indian journal of pediatrics · 2014Review
- Necrotizing enterocolitis and focal intestinal perforation in neonatal intensive care units in the state of baden-württemberg, Germany.Pediatric reports · 2014Article
- Article
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundEarly enteral feeding practices are potentially modifiable risk factors for necrotising enterocolitis in very preterm or very low birth weight (VLBW) infants. Observational studies suggest that conservative feeding regimens that include slowly advancing enteral feed volumes reduce the risk of necrotising enterocolitis. However, slow feed advancement may delay establishment of full enteral feeding and be associated with metabolic and infectious morbidities secondary to prolonged exposure to parenteral nutrition.
objectivesTo determine the effect of slow rates of enteral feed advancement on the incidence of necrotising enterocolitis, mortality and other morbidities in very preterm or VLBW infants. SEARCH
methodsWe used the standard search strategy of the Cochrane Neonatal Review Group. We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2012, Issue 12), MEDLINE, EMBASE and CINAHL (to December 2012), conference proceedings, and previous reviews. SELECTION CRITERIA: Randomised or quasi-randomised controlled trials that assessed the effect of slow (up to 24 ml/kg/day) versus faster rates of advancement of enteral feed volumes upon the incidence of necrotising enterocolitis in very preterm or VLBW infants. DATA COLLECTION AND ANALYSIS: Data collection and analysis was performed using the standard methods of the Cochrane Neonatal Review Group. MAIN
resultsWe identified five randomised controlled trials in which a total of 588 infants participated. Few participants were extremely preterm, extremely low birth weight or growth restricted. The trials defined slow advancement as daily increments of 15 to 20 ml/kg and faster advancement as 30 to 35 ml/kg. Meta-analyses did not detect statistically significant effects on the risk of necrotising enterocolitis (typical risk ratio (RR) 0.97, 95% confidence interval (CI) 0.54 to 1.74) or all-cause mortality (RR 1.41, 95% CI 0.81 to 2.74). Infants who had slow advancement took significantly longer to regain birth weight (reported median differences two to six days) and to establish full enteral feeding (two to five days). AUTHORS'
conclusionsThe available trial data suggest that advancing enteral feed volumes at slow rather than faster rates does not reduce the risk of necrotising enterocolitis in very preterm or VLBW infants. Advancing the volume of enteral feeds at slow rates results in several days delay in regaining birth weight and establishing full enteral feeds but the long term clinical importance of these effects is unclear. The applicability of these findings to extremely preterm, extremely low birth weight or growth restricted infants is limited. Further randomised controlled trials in these populations may be warranted to resolve this uncertainty.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.