TY - JOUR
T1 - Anorectal manometry under adequate sedation or anesthesia as a highly reliable diagnostic tool for Hirschsprung's disease in neonates and young infants
T2 - A multicenter retrospective study
AU - Sanmoto, Yohei
AU - Naoe, Atsuki
AU - Goto, Yudai
AU - Inoue, Mikihiro
AU - Masumoto, Kouji
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/6
Y1 - 2025/6
N2 - Background: Hirschsprung's disease is a congenital disorder characterized by the absence of enteric ganglion cells. The diagnostic gold standard for Hirschsprung's disease is a rectal mucosal biopsy; however, its accuracy in neonates and young infants remains limited. Although less invasive, the diagnostic performance of anorectal manometry (ARM) in these populations remains controversial. We evaluated the diagnostic performance of ARM in patients with Hirschsprung's disease by age group. Methods: This multicenter retrospective study compared the diagnostic outcomes of ARM and biopsy across three age categories: neonates (<28 days), infants ≤6 months, and children aged >6 months. Additionally, logistic regression analysis was performed to assess changes in the probability of accurate diagnosis and exclusion of Hirschsprung's disease by ARM with increasing age. Results: Overall, 113 patients were included in this study. The median patient age (range) at the time of ARM was 103 (3–3913) days. Most patients (83.2 %) underwent ARM under intravenous sedation or inhalation anesthesia. ARM revealed higher sensitivity than did biopsy in neonates (100 % vs. 45.5 %, P = 0.012) and infants aged ≤6 months (97.1 % vs. 79.6 %, P = 0.022). With increasing age, the probability of accurate diagnosis for Hirschsprung's disease by ARM significantly decreased (P = 0.031), although the probability of accurate exclusion showed no significant change (P = 0.35). Conclusion: ARM, when performed under appropriate sedation or anesthesia, yields superior sensitivity for diagnosing Hirschsprung's disease in young children than does biopsy. However, diagnostic accuracy decreases with age, requiring careful interpretation in patients aged >6 months.
AB - Background: Hirschsprung's disease is a congenital disorder characterized by the absence of enteric ganglion cells. The diagnostic gold standard for Hirschsprung's disease is a rectal mucosal biopsy; however, its accuracy in neonates and young infants remains limited. Although less invasive, the diagnostic performance of anorectal manometry (ARM) in these populations remains controversial. We evaluated the diagnostic performance of ARM in patients with Hirschsprung's disease by age group. Methods: This multicenter retrospective study compared the diagnostic outcomes of ARM and biopsy across three age categories: neonates (<28 days), infants ≤6 months, and children aged >6 months. Additionally, logistic regression analysis was performed to assess changes in the probability of accurate diagnosis and exclusion of Hirschsprung's disease by ARM with increasing age. Results: Overall, 113 patients were included in this study. The median patient age (range) at the time of ARM was 103 (3–3913) days. Most patients (83.2 %) underwent ARM under intravenous sedation or inhalation anesthesia. ARM revealed higher sensitivity than did biopsy in neonates (100 % vs. 45.5 %, P = 0.012) and infants aged ≤6 months (97.1 % vs. 79.6 %, P = 0.022). With increasing age, the probability of accurate diagnosis for Hirschsprung's disease by ARM significantly decreased (P = 0.031), although the probability of accurate exclusion showed no significant change (P = 0.35). Conclusion: ARM, when performed under appropriate sedation or anesthesia, yields superior sensitivity for diagnosing Hirschsprung's disease in young children than does biopsy. However, diagnostic accuracy decreases with age, requiring careful interpretation in patients aged >6 months.
KW - Anorectal manometry
KW - Diagnosis
KW - Hirschsprung's disease
KW - Infants
KW - Neonates
KW - Rectal mucosal biopsy
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U2 - 10.1016/j.gpeds.2025.100255
DO - 10.1016/j.gpeds.2025.100255
M3 - Article
AN - SCOPUS:105002016859
SN - 2667-0097
VL - 12
JO - Global Pediatrics
JF - Global Pediatrics
M1 - 100255
ER -