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Journal of Indian Association of Pediatric Surgeons logoLink to Journal of Indian Association of Pediatric Surgeons
letter
. 2021 Sep 16;26(5):365–366. doi: 10.4103/jiaps.JIAPS_60_21

Critical Review of the Original Article “Modified Duhamel Two-Stage Procedure for Hirschsprung's Disease: Further Modification for Improved Outcome” by Nitin J. Peters et al. in September–October, 2020 Issue of JIAPS Issue

Sumitra Kumar Biswas 1,
PMCID: PMC8515524  PMID: 34728933

Sir,

This letter to you is a critical appraisal of the Original Article published in JIAPS volume 25, issue 5, September–October 2020, entitled “Modified Duhamel's Two-Stage Procedure for Hirschsprung's Disease (HD): Further Modifications for Improved Outcome” from one of India's Premier Institutes.

I have gone through the article avidly but failed to understand how their “further modification of sacrificing sigmoid colon irrespective of the extent of aganglionosis and doing a Hartman's procedure as a first step” is achieving better result and they had not explained it either. They had done this operation in a select group of short segment HD and reported on their results. However, this was an “Overkill” for majority with rectosigmoid HD[1] and could not be justified. This may however be a choice in adolescents and adults with rectosigmoid HD, who may present with a sigmoid volvulus with an unmanageable tire-like colon loaded with stool.[2]

During definitive surgery, this aganglionic rectal segment, kept as Hartman pouch, poses great difficulty in identification and retro-rectal dissection, even with a Hagar's Dilator in place due to extensive fibrosis (personal experience of two cases). Consequently, chances of pelvic nerve damage are more and so its sequalae in adult life.[3]

Their method of colorectal anastomosis was at the “pecten zone” of the anal canal, which essentially damages a significant area of sensitive anal mucosa and internal sphincter. Good continence with this type of surgery is difficult to achieve.[4] They had not assessed the nocturnal continence/soiling in these children, which could affect Quality of Life to a great extent. The response at follow-up was only 45% (69/152) and these patients might be a select happier group; the good result was thus skewed by inherent selection bias.

From 1948 to 2020, over 72 years of our journey with HD, we now know that a significant number of them carries their difficulty into adulthood, irrespective of whatever procedure is done.[5] Hence, a maximum follow-up period of 11 years is very small compared to the lifespan of any individual. We will eagerly wait for follow-up of these select groups of children to adulthood, from the same institute in future and hope it will clarify the situation further.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

REFERENCES

  • 1.Puri P, Montedonico S. Hirschsprung’s Disease: Clinical Features. In: Holschneider A, Puri P, editors. Hirschsprung's Disease and Allied Disorders. 3rd ed. Berlin, Heidelberg: Springer; 2008. pp. 107–113. Ch 8. [Google Scholar]
  • 2.Zeng M, Amodio J, Schwarz S, Garrow E, Xu J, Rabinowitz SS. Hirschsprung disease presenting as sigmoid volvulus: A case report and review of the literature. J Pediatr Surg. 2013;48:243–6. doi: 10.1016/j.jpedsurg.2012.10.042. [DOI] [PubMed] [Google Scholar]
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