Abstract
Purpose
Intestinal dysmotility in preterm infants has often been attributed to immature enteric nervous system. It is frequently reported that Hirschsprung’s disease (HD) is rare in premature infants. The exact prevalence of HD in premature infants is not well documented. The classical signs of HD may often not be identified due to the complexity of symptoms of prematurity itself. This systematic review was designed to determine the prevalence and presentation of HD in premature infants.
Methods
A systematic review of the literature using the keywords “Hirschsprung’s disease”, “aganglionosis”, “congenital megacolon”, “premature” and “preterm” was performed. Resulting publications were reviewed for epidemiology and morbidity. Only infants born <37 weeks of gestation or described as preterm birth by the authors were included. Reference lists were screened for additional relevant studies.
Results
Twenty-six publications from 1964 to 2013 reported data on premature infants with HD. Out of a total number of 4,147 infants, prematurity was recorded in 257 cases, giving a prevalence rate of 6 % of preterm infants diagnosed with HD. During 1964–1999, reported prevalence of HD in premature infants ranged from 1.7 to 9.2 % (overall prevalence 5 %) and during 2000–2013 prevalence ranged from 4 to 19.4 % (overall prevalence 14 %). The prevalence of total colonic aganglionosis in premature infants was 13 % (15 out of 118 infants). Mean gestational age of preterm infants was 34.5 (±0.7) weeks and mean age at diagnosis ranged from 18.3 days to 3.9 months. Abdominal distension was observed in 80 % of preterm infants, delayed passage of meconium in 57 and 37 % of premature infants presented with bile-stained vomiting.
Conclusion
In recent years, higher prevalence of HD has been reported in premature infants compared to previous years. Hirschsprung’s disease should be considered in preterm infants presenting with features of intestinal obstruction.
Similar content being viewed by others
References
Baxter KJ, Bhatia AM (2013) Hirschsprung’s disease in the preterm infant: implications for diagnosis and outcome. Am Surg 79(7):734–738
Escobar MA, Grosfeld JL, West KW, Scherer LR, Rouse TM, Engum SA, Rescorla FJ (2005) Long-term outcomes in total colonic aganglionosis: a 32-year experience. J Pediatr Surg 40(6):955–961
Puri P (2011) Hirschsprung’s disease. In: Puri P (ed) Newborn surgery, 3rd edn. Arnold, London, pp 554–565
Haricharan RN, Georgeson KE (2008) Hirschsprung disease. Semin Pediatr Surg 17(4):266–275
Tam PK, Garcia-Barcelo M (2009) Genetic basis of Hirschsprung’s disease. Pediatr Surg Int 25(7):543–558
Zhou Y, Yang J, Watkins DJ, Boomer LA, Matthews MA, Su Y, Besner GE (2013) Enteric nervous system abnormalities are present in human necrotizing enterocolitis: potential neurotransplantation therapy. Stem Cell Res Ther 4(6):157
Talishinskiy T, Tomita S (2013) Intestinal perforation in preterm infant as an unusual initial presentation of Hirschsprung’s disease. J Pediatr Surg Case Rep 1(11):381–382
Peres LC, Cohen MC (2013) Sudden unexpected early neonatal death due to undiagnosed Hirschsprung disease enterocolitis: a report of two cases and literature review. Forensic Sci Med Pathol 9(4):558–563
Bajaj R, Smith J, Trochet D, Pitkin J, Ouvrier R, Graf N, Sillence D, Kluckow M (2005) Congenital central hypoventilation syndrome and Hirschsprung’s disease in an extremely preterm infant. Pediatrics 115(6):e737–e738
Honein MA, Kirby RS, Meyer RE, Xing J, Skerrette NI, Yuskiv N, Marengo L, Petrini JR, Davidoff MJ, Mai CT, Druschel CM, Viner-Brown S, Sever LE (2009) The association between major birth defects and preterm birth. Matern Child Health J 13(2):164–175
Rescorla FJ, Morrison AM, Engles D, West KW, Grosfeld JL (1992) Hirschsprung’s disease. Evaluation of mortality and long-term function in 260 cases. Arch Surg 127(8):934–941 (Discussion 941–932)
Sharp NE, Pettiford-Cunningham J, Shah SR, Thomas P, Juang D, St Peter SD, Ostlie DJ (2013) The prevalence of Hirschsprung disease in premature infants after suction rectal biopsy. J Surg Res 184(1):374–377
Chen A, Du J, Du LZ (2013) Clinical characteristics of abdominal distention in early newborns. Zhongguo Dang Dai Er Ke Za Zhi 15(12):1074–1078
Hamrick SE, Strickland MJ, Shapira SK, Autry A, Schendel D (2010) Use of special education services among children with and without congenital gastrointestinal anomalies. Am J Intellect Dev Disabil 115(5):421–432
Anupama B, Zheng S, Xiao X (2007) Ten-year experience in the management of total colonic aganglionosis. J Pediatr Surg 42(10):1671–1676
Teitelbaum DH, Cilley RE, Sherman NJ, Bliss D, Uitvlugt ND, Renaud EJ, Kirstioglu I, Bengston T, Coran AG (2000) A decade of experience with the primary pull-through for Hirschsprung disease in the newborn period: a multicenter analysis of outcomes. Ann Surg 232(3):372–380
Sarioglu A, Tanyel FC, Buyukpamukcu N, Hicsonmez A (1997) Hirschsprung-associated congenital anomalies. Eur J Pediatr Surg 7(6):331–337
Jung PM (1995) Hirschsprung’s disease: one surgeon’s experience in one institution. J Pediatr Surg 30(5):646–651
Halevy H, Mares A, Cohen Z, Finaly R, Freud E, Pilpel D (1994) Hirschprung’s disease in the Negev. Harefuah 127(5–6):148–154 (216)
Klein MD, Philippart AI (1993) Hirschsprung’s disease: three decades’ experience at a single institution. J Pediatr Surg 28(10):1291–1293 (Discussion 1293–1294)
Ryan ET, Ecker JL, Christakis NA, Folkman J (1992) Hirschsprung’s disease: associated abnormalities and demography. J Pediatr Surg 27(1):76–81
Polley TZ Jr, Coran AG (1986) Hirschsprung’s disease in the newborn. Pediatr Surg Int 1(2):80–83
Klein MD, Coran AG, Wesley JR, Drongowski RA (1984) Hirschsprung’s disease in the newborn. J Pediatr Surg 19(4):370–374
Ikeda K, Goto S (1984) Diagnosis and treatment of Hirschsprung’s disease in Japan. An analysis of 1628 patients. Ann Surg 199(4):400–405
Cass DT, Myers N (1987) Total colonic aganglionosis: 30 years’ experience. Pediatr Surg Int 2(2):68–75
Rossello PJ, Lores ME (1979) Hirschsprung’s disease: analysis of cases at the University Hospital. Bol Asoc Med P R 71(1):6–16
Grosfeld JL, Ballantine VN, Csicsko JF (1978) A critical evaluation of the Duhamel operation for Hirschsprung’s disease. Arch Surg 113(4):454–460
Lister J (1977) Hirschsprung: the man and the disease. J R Coll Surg Edinb 22(6):378–384
Swenson O, Sherman JO, Fisher JH (1973) Diagnosis of congenital megacolon: an analysis of 501 patients. J Pediatr Surg 8(5):587–594
Sane SM, Girdany BR (1973) Total aganglionosis coli. Clinical and roentgenographic manifestations. Radiology 107(2):397–404
Bowring AC, Kern IB (1972) The management of Hirschsprung’s disease in the neonate. Aust Paediatr J 8(3):121–127
Fraser GC, Wilkinson AW (1967) Neonatal Hirschsprung’s disease. Br Med J 3(5556):7–10
Hofmann S, Rehbein F (1966) Hirschsprungsche Krankheit im Neugeborenenalter. Z Kinderchir 3:182–194
Madsen CM (1964) Hirschsprung's disease. Munksgaard, Copenhagen
McKeown SJ, Stamp L, Hao MM, Young HM (2013) Hirschsprung disease: a developmental disorder of the enteric nervous system. Wiley Interdiscip Rev Dev Biol 2(1):113–129
Lucchini R, Bizzarri B, Giampietro S, De Curtis M (2011) Feeding intolerance in preterm infants. How to understand the warning signs. J Matern Fetal Neonatal Med 24(Suppl 1):72–74
Kenny SE, Tam PK, Garcia-Barcelo M (2010) Hirschsprung’s disease. Semin Pediatr Surg 19(3):194–200
Lee CC, Lien R, Chiang MC, Yang PH, Chu SM, Fu JH, Lai JY (2012) Clinical impacts of delayed diagnosis of Hirschsprung’s disease in newborn infants. Pediatr Neonatol 53(2):133–137
Shahar E, Shinawi M (2003) Neurocristopathies presenting with neurologic abnormalities associated with Hirschsprung’s disease. Pediatr Neurol 28(5):385–391
Moore SW (2006) The contribution of associated congenital anomalies in understanding Hirschsprung’s disease. Pediatr Surg Int 22(4):305–315
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Duess, J.W., Hofmann, A.D. & Puri, P. Prevalence of Hirschsprung’s disease in premature infants: a systematic review. Pediatr Surg Int 30, 791–795 (2014). https://doi.org/10.1007/s00383-014-3540-8
Accepted:
Published:
Issue date:
DOI: https://doi.org/10.1007/s00383-014-3540-8
