ARTICLE TYPE : CASE REPORT
Published on : 22 Dec 2025, Volume - 1
Journal Title : WebLog Journal of Pediatrics | WebLog J Pediatr
Source URL:
https://weblogoa.com/articles/wjp.2025.l2203
Permanent Identifier (DOI) :
https://doi.org/10.5281/zenodo.18058267
Infantile Acute Colonic Pseudo-Obstruction (Ogilvie’s Syndrome) Following Use of Dicyclomine in Infantile Colic- A Case Report
2Director for International Affairs (South Asia), Lincoln University College (LUC), School of Medicine, 2, Jalan Stadium, SS7/15 SS7. 47301 Petaling Jaya, Selangor, Malaysia
3J. Watumull Global Hospital & Research Centre, Delwara Road, Mount Abu, Rajasthan 307501, India Affiliated to Medical Faculty of God Fatherly Spiritual University, Mount Abu, Rajasthan, India
Abstract
Infantile colic is a common functional gastrointestinal disorder characterized by excessive crying in otherwise healthy infants, Infantile colic is a common, self-limiting condition. Pharmacological interventions, particularly anticholinergic agents, have historically been attempted and used but are associated with significant risks and not recommended due to safety concerns. We report a 6-week old female infant who developed acute colonic pseudo-obstruction following administration of anticolic medication, dicyclomine, an atropine derivative prescribed for colic relief. Patient was successfully treated conservatively for a prolonged period and who subsequently developed congenital colorectal motility disorder on longer term follow up. This case underscores the dangers of anticholinergic therapy in infants and highlights the importance of non-pharmacological management strategies.
Keywords: Atropine Derivatives; Colonic Pseudo-Obstruction; Congenital Colorectal Motility Disorder; Dicyclomine; Gastrointestinal Functional Obstruction Disorder; Infantile Colic; Ogilvie’s Syndrome
Citation
Govani DR, Swamy KB, Midha PK, Govani ND, Panchasara NG, Patel RR, et al. Infantile Acute Colonic Pseudo Obstruction (Ogilvie’s Syndrome) Following Use of Dicyclomine in Infantile Colic- A Case Report. WebLog J Pediatr. wjp.2025.l2203. https://doi.org/10.5281/zenodo.18058267