Late Diagnosis of Hirschsprung Disease: Clinical Presentation and Long-Term Functional Outcomes

被引:1
作者
Ostertag-Hill, Claire A. [1 ]
Nandivada, Prathima [1 ]
Dickie, Belinda H. [1 ,2 ]
机构
[1] Boston Childrens Hosp, Dept Surg, Boston, MA USA
[2] Boston Childrens Hosp, Dept Surg, 300 Longwood Ave Fegan 3, Boston, MA 02115 USA
关键词
Hirschsprung disease; Late diagnosis; Pull-through; Outcome; BOWEL FUNCTION; AGE;
D O I
10.1016/j.jpedsurg.2023.10.018
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: Hirschsprung Disease (HD) is typically diagnosed in the neonatal period. A small subset of patients have a prolonged course of abdominal distention and constipation prior to diagnosis. Late HD is defined as having been diagnosed at greater than or equal to one year of age. The literature is limited and offers conflicting data on the implications of a late diagnosis. We aim to investigate the presentation, operative approach, and functional outcomes of a large cohort of patients with a late HD diagnosis. Methods: All patients with a late diagnosis of HD (after 1 year of age) at our institution between 1997 and 2021 were included. Results: Twenty-eight patients were diagnosed with HD at a median age of 3.4 years. Chronic constipation, failure to thrive, and enterocolitis occurred in 100 %, 31 %, and 14 %, respectively. All patients underwent contrast enema and biopsies during their workup, identifying primarily rectosigmoid disease (n = 27) and total colonic aganglionosis (n = 1). Surgical intervention was performed in 27 patients, with 4 patients (15 %) needing a stoma (3 with plan for staged pull-through, 1 long-term stoma) and 23 patients (85 %) undergoing a single-stage pull-through. Postoperative complications included Hirschsprung-associated enterocolitis (n = 5), ostomy prolapse and revision (n = 2), abdominal distention requiring ileostomy creation (n = 2), redo pull-through (n = 2), retroperitoneal hematoma (n = 1), and cecostomy tube placement (n = 1). At a median follow-up of 5.4 years, 83 % of eligible patients achieved fecal continence with 43 % needing laxatives for persistent constipation. Conclusion: Recognizing a late presentation of HD requires a high index of suspicion. Patients with a late diagnosis did not experience an increased rate of permanent stoma, complications, or redo surgery compared to rates reported for the larger HD population. Similar long-term functional outcomes were achieved compared to the larger HD population. Level of Evidence: IV. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:220 / 224
页数:5
相关论文
共 25 条
  • [11] Comparison of clinical outcomes after total transanal and laparoscopic assisted endorectal pull-through in patients with rectosigmoid Hirschsprung disease
    Karlsen, Remi Andre
    Hoel, Anders Telle
    Fosby, Marianne Valeberg
    Ertresvag, Kjetil
    Austrheim, Astrid Ingeborg
    Stensrud, Kjetil Juul
    Bjornland, Kristin
    [J]. JOURNAL OF PEDIATRIC SURGERY, 2022, 57 (09) : 69 - 74
  • [12] Prevalence of Functional Defecation Disorders in Children: A Systematic Review and Meta-Analysis
    Koppen, Ilan J. N.
    Vriesman, Mana H.
    Saps, Miguel
    Rajindrajith, Shaman
    Shi, Xiaoxia
    van Etten-Jamaludin, Faridi S.
    Di Lorenzo, Carlo
    Benninga, Marc A.
    Tabbers, Merit M.
    [J]. JOURNAL OF PEDIATRICS, 2018, 198 : 121 - +
  • [13] Surgical approach to Hirschsprung disease
    Langer, Jacob C.
    [J]. SEMINARS IN PEDIATRIC SURGERY, 2022, 31 (02)
  • [14] Clinical Impacts of Delayed Diagnosis of Hirschsprung's Disease in Newborn Infants
    Lee, Chien-Chung
    Lien, Reyin
    Chian, Ming-Chou
    Yang, Peng-Hong
    Chu, Shih-Ming
    Fu, Jen-Hei
    Lai, Jin-Yao
    [J]. PEDIATRICS AND NEONATOLOGY, 2012, 53 (02) : 133 - 137
  • [15] Long-term functional outcomes and quality of life in patients with Hirschsprung's disease
    Meinds, R. J.
    van der Steeg, A. F. W.
    Sloots, C. E. J.
    Witvliet, M. J.
    de Blaauw, I.
    van Gemert, W. G.
    Trzpis, M.
    Broens, P. M. A.
    [J]. BRITISH JOURNAL OF SURGERY, 2019, 106 (04) : 499 - 507
  • [16] The science of Hirschsprung disease: What we know and where we are headed
    Mueller, Jessica L.
    Goldstein, Allan M.
    [J]. SEMINARS IN PEDIATRIC SURGERY, 2022, 31 (02)
  • [17] Transanal-only Swenson-like pull-through for late diagnosed Hirschsprung disease
    Rentea, Rebecca M.
    Halleran, Devin R.
    Ahmad, Hira
    Maloof, Elias
    Wood, Richard J.
    Levitt, Marc A.
    [J]. JOURNAL OF SURGICAL CASE REPORTS, 2019, (12):
  • [18] Fecal continence in patients having undergone posterior sagittal anorectoplasty procedure for a high anorectal malformation improves at adolescence, as constipation disappears
    Rintala, RJ
    Lindahl, HG
    [J]. JOURNAL OF PEDIATRIC SURGERY, 2001, 36 (08) : 1218 - 1221
  • [19] HIRSCHSPRUNG DISEASE IN A LARGE BIRTH COHORT
    SPOUGE, D
    BAIRD, PA
    [J]. TERATOLOGY, 1985, 32 (02) : 171 - 177
  • [20] Late diagnosis of Hirschsprung disease-patient characteristics and results
    Stensrud, Kjetil Juul
    Emblem, Ragnhild
    Bjornland, Kristin
    [J]. JOURNAL OF PEDIATRIC SURGERY, 2012, 47 (10) : 1874 - 1879