D. M. Hook-Dufresne1, X. Yu4, A. Olsen1, L. Putnam1, S. D. Moore-Olufemi1 1University Of Texas Health Science Center At Houston,Pediatric Surgery,Houston, TX, USA 4Baylor College Of Medicine,Pediatric Epidemiology,Houston, TX, USA
Introduction: Gastroschisis (GS) is the most common congenital abdominal wall defect and is associated with poor clinical outcomes associated with the development of intestinal failure (IF). GS patients are often born at less than 37 weeks gestational age (GA), classifying them as premature, and are at increased risk for feeding difficulties associated with prematurity. The purpose of this study was to analyze the effect of prematurity on the development of IF in both GS and non-GS patients and analyze IF related outcomes between the two groups.
Methods: A single institutional database of GS patients born less than 37 weeks GA (N=49) was queried for the following: GA, birth weight, length of stay (LOS), time to initial feeds (TIF), time to full feeds (TFF) and days on total parenteral nutrition (TPN), rate of catheter related blood stream infections (CRBSI) and 30 day mortality. Control infants (N=343) with no gastrointestinal pathology were 7:1 matched with the GS infants on GA by week. We defined IF as requiring TPN for ≥ 60 days. The Wilcoxon rank sum test and Chi-square test were used to test the differences between two groups for the continuous and categorical variables respectively.
Results: Premature GS infants had significantly lower birth weight than non-GS premature infants (2145 vs. 2485 gm, p< 0.0007). Premature GS infants had significantly longer LOS, TPN days, TIF and TFF when compared to non-GS premature infants (Table 1). Premature GS infants had significantly higher incidence of CRBSI (20% vs. 0.3%, p<0.0001) and 30 day mortality (4% vs. 0.3%, p<0.04). No patients in the non-GS premature group were diagnosed with IF, while the IF rate in the GS group was 29% (14 of 49).
Conclusion: Premature GS infants have significantly longer LOS, time on TPN and time to inital and full feeds when compared to their non-GS counterparts. Our study demonstrates that the poor nutritional outcomes and the development of IF in premature patients with GS is more likely a function of the intestinal dysfunction associated with GS than of prematurity. Further research into the factors that promote the intestinal dysfunction associated with GS is needed to improve clinical outcomes for these patients.