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Neonatology ; 112(4): 347-353, 2017.
Article in English | MEDLINE | ID: mdl-28768263

ABSTRACT

BACKGROUND: Meconium retention is associated with feeding intolerance. Trials using glycerol and Gastrografin to expedite the evacuation of meconium have failed to generate clinically valid results for efficacy and safety. OBJECTIVE: We assessed the feasibility of aggressive meconium evacuation with saline rectal washout (RW) in very-low-birth-weight infants to reduce the time it took them to reach full enteral feeds. METHODS: We conducted an open-label, pilot, randomized controlled trial (RCT) (birth weight stratified, i.e., to 750-999 g and 1,000-1,500 g) of early aggressive meconium evacuation with twice-daily normal saline RW compared to conventional management with glycerin suppositories (GS), until full enteral feeds (110 mL/kg/day) were reached. Primary outcome was time to reach full enteral feeds. Safety, process, and secondary efficacy outcomes were also evaluated. RESULTS: Sixty-one infants were randomized, 28 to RW and 33 to GS. The process and feasibility outcomes were met. RW was found to be safe; none of the RW-randomized infants developed necrotizing enterocolitis (≥ stage II) or complications secondary to RW. Evidence of efficacy was supported: in the 750-999 g stratum (n = 15), the median time to full enteral feeds was shorter with RW (11.0 days, 95% CI: 10.4-11.6) than with GS (15.6 days, 95% CI: 13.0-18.2) by a reduction of 4.6 days (p = 0.027). In the 1,000-1,500 g stratum (n = 46), there was no evidence of benefit: RW 10.2 days (95% CI 8.3-12.1) and GS 10.1 days (95% CI 9.3-10.9, p = 0.304). CONCLUSION: Our protocol was feasible and an adequately powered RCT is required to confirm the findings of this trial.


Subject(s)
Enteral Nutrition , Glycerol/administration & dosage , Infant, Premature , Infant, Very Low Birth Weight , Intestinal Obstruction/therapy , Meconium , Sodium Chloride/administration & dosage , Therapeutic Irrigation/methods , Adult , Birth Weight , Enema , Enteral Nutrition/adverse effects , Feasibility Studies , Female , Gestational Age , Glycerol/adverse effects , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Intestinal Obstruction/etiology , Intestinal Obstruction/physiopathology , Male , Pilot Projects , Singapore , Sodium Chloride/adverse effects , Suppositories , Therapeutic Irrigation/adverse effects , Time Factors , Treatment Outcome
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