Background: Infantile hypertrophic pyloric stenosis (IHPS) has several known risk factors. The association between prematurity and IHPS and the timeline of presentation are poorly defined. Our aim was to evaluate the associations between IHPS and prematurity. Methods: We performed a retrospective cohort study of 1,074,236 children born between June 2001 and April 2012 in the US Military Health System. IHPS cases and gestational ages (GA) were identified using billing codes. Additional risk factors for IHPS were controlled for in a multivariable logistic regression model. results: The incidence of IHPS was 2.99 per 1,000 in preterm infants and 2.25 per 1,000 in full term (relative risk (RR) = 1.33, 95% confidence interval (CI) 1.16-1.54). The adjusted odds ratio for prematurity was 1.26 (95% CI 1.08-1.46). The median (interquartile range (IQR)) chronological age at presentation was 40 d (30-56) in preterm infants vs. 33 d (26)(27)(28)(29)(30)(31)(32)(33)(34)(35)(36)(37)(38)(39)(40)(41)(42)(43)(44)(45) in full term (P < 0.001). Median postmenstrual age at presentation was 42 wk in preterm infants (40-42) vs. 45 wk (44-46) in full term (P < 0.001). conclusion: Prematurity is associated with IHPS. Premature infants develop IHPS at a later chronological age, but earlier postmenstrual age, than term infants. Providers should have an increased concern for IHPS development in premature infants. i nfantile hypertrophic pyloric stenosis (IHPS) is a common cause of gastric outlet obstruction in young infants. IHPS is a significant source of infant morbidity and, left untreated, can cause severe dehydration and life-threatening metabolic alkalosis. IHPS is now recognized earlier in its clinical course and is managed successfully with surgical pyloromyotomy (1-4). There are several established prenatal and perinatal risk factors for IHPS, including macrolide antibiotic use, bottle-feeding, male sex, family history, and birth order (5-8). The etiology of IHPS remains unclear, but current research suggests that it is caused by an interplay of environmental and genetic factors (9). Retrospective studies and post-hoc analysis with large populations continue to add important information about the potential causes and clinical course of IHPS.The rate of preterm birth in the United States, defined as delivery at <37 wk gestation, was around 11.7% in 2011 (10). The unique risks and clinical course of diseases in preterm populations are often underappreciated. The understanding of a relationship between IHPS and prematurity has evolved. Previous literature suggested that preterm infants rarely present with IHPS (11,12). Several recent epidemiological studies have found variable evidence that prematurity might be associated with increased risk of developing IHPS, although this association remains unclear (7,8,13,14).Full-term infants with IHPS typically present in the first 2-7 wk of life (7). The presentation age of preterm infants that develop IHPS is defined less clearly. Some studies suggest that preterm infants may present with ...