Eur J Pediatr Surg 2019; 29(05): 425-430
DOI: 10.1055/s-0038-1667040
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Accuracy of Suction Rectal Biopsy for Diagnosis of Hirschsprung's Disease in Neonates

Ashley Rebekah Allen
1   Department of Pediatric Surgery, School of Medicine, University of Utah Hospital, Salt Lake City, Utah, United States
,
Angelica R. Putnam
2   Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, United States
,
Angela P. Presson
3   Division of Epidemiology, University of Utah Hospital, Salt Lake City, Utah, United States
,
Chelsea McCarty Allen
3   Division of Epidemiology, University of Utah Hospital, Salt Lake City, Utah, United States
,
Douglas C. Barnhart
4   Division of Pediatric Surgery, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, United States
,
Michael D. Rollins
4   Division of Pediatric Surgery, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, United States
› Author Affiliations
Further Information

Publication History

10 March 2018

04 June 2018

Publication Date:
01 August 2018 (online)

Abstract

Introduction Recent publications have questioned the sensitivity of suction rectal biopsy (SRB) for diagnosis of Hirschsprung's disease (HD) in newborns. A recent European survey reported that 39% of pediatric surgeons performed full-thickness transanal biopsies due to concerns about the accuracy of SRB. We sought to examine our contemporary SRB experience in infants.

Materials and Methods A review was performed (2007–2016) of patients under 6 months of age who had a SRB at our children's hospital. The cohort was subdivided by postmenstrual age at time of SRB: preterm (< 40 weeks, A), term neonate (40–44 weeks, B), and infant (> 44 weeks, C). The pathology reports from endorectal pull-through were used as gold standard confirmation. One-year follow-up of patients with negative SRB was used to confirm accurate diagnosis.

Results A total of 153 patients met the criteria and a total of 159 SRBs (< 2,500 g; n = 26) were performed (A = 60, B = 58, C = 35). Forty-three patients were diagnosed with HD (A = 25, B = 15, C = 3). A second SRB was performed in 6 (3.9%) patients due to inadequate tissue (A = 2, B = 2, C = 2) with HD diagnosed in 5. No complications occurred. Sensitivity and specificity of SRB was 100% in all age groups. Half of the patients with a negative SRB had at least 1 year follow-up, with none subsequently diagnosed with HD.

Conclusion SRB results in adequate tissue for evaluation of HD in nearly all patients less than 6 months of age on the first attempt and is highly accurate in the preterm and newborn infants. No complications occurred, even among infants less than 2,500 g.

 
  • References

  • 1 Teerlink CC, Bernhisel R, Cannon-Albright LA, Rollins MD. A population-based description of familial clustering of Hirschsprung's disease. J Pediatr Surg 2017; DOI: 10.1016/j.jpedsurg.2017.08.024.
  • 2 Kessmann J. Hirschsprung's disease: diagnosis and management. Am Fam Physician 2006; 74 (08) 1319-1322
  • 3 Bhatnagar SN. Hirschsprung's disease in newborns. J Neonatal Surg 2013; 2 (04) 51
  • 4 Friedmacher F, Puri P. Current practice patterns of rectal suction biopsy in the diagnostic work-up of Hirschsprung's disease: results from an international survey. Pediatr Surg Int 2016; 32 (08) 717-722
  • 5 Meinds RJ, Kuiper GA, Parry K. , et al. Infant's age influences the accuracy of rectal suction biopsies for diagnosing of Hirschsprung's disease. Clin Gastroenterol Hepatol 2015; 13 (10) 1801-1807
  • 6 Zani A, Eaton S, Morini F. , et al; EUPSA Network Office. European Paediatric Surgeons' Association survey on the management of Hirschsprung disease. Eur J Pediatr Surg 2017; 27 (01) 96-101
  • 7 R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing; 2017. Available at: https://www.R-project.org/ . Accessed June 23, 2018
  • 8 Barshack I, Fridman E, Goldberg I, Chowers Y, Kopolovic J. The loss of calretinin expression indicates aganglionosis in Hirschsprung's disease. J Clin Pathol 2004; 57 (07) 712-716
  • 9 Keyzer-Dekker CM, Sloots CE, Schokker-van Linschoten IK, Biermann K, Meeussen C, Doukas M. Effectiveness of rectal suction biopsy in diagnosing Hirschsprung disease. Eur J Pediatr Surg 2016; 26 (01) 100-105
  • 10 Friedmacher F, Puri P. Rectal suction biopsy for the diagnosis of Hirschsprung's disease: a systematic review of diagnostic accuracy and complications. Pediatr Surg Int 2015; 31 (09) 821-830
  • 11 Swenson O. Hirschsprung's disease: a review. Pediatrics 2002; 109 (05) 914-918
  • 12 Muise ED, Cowles RA. Rectal biopsy for Hirschsprung's disease: a review of techniques, pathology, and complications. World J Pediatr 2016; 12 (02) 135-141
  • 13 Rahman Z, Hannan J, Islam S. Hirschsprung's disease: role of rectal suction biopsy - data on 216 specimens. J Indian Assoc Pediatr Surg 2010; 15 (02) 56-58
  • 14 Muise ED, Hardee S, Morotti RA, Cowles RA. A comparison of suction and full-thickness rectal biopsy in children. J Surg Res 2016; 201 (01) 149-155
  • 15 Martucciello G, Pini Prato A, Puri P. , et al. Controversies concerning diagnostic guidelines for anomalies of the enteric nervous system: a report from the Fourth International Symposium on Hirschsprung's Disease and Related Neurocristopathies. J Pediatr Surg 2005; 40 (10) 1527-1531
  • 16 Kapur RP. Submucosal nerve diameter of greater than 40 μm is not a valid diagnostic index of transition zone pull-through. J Pediatr Surg 2016; 51 (10) 1585-1591