Long-Term Surgical Outcomes and Adulthood Transitional Care Planning for Hirschsprung’s Disease: A Single-Center Retrospective Study

<b>Introduction:</b> Hirschsprung's disease, despite its typical diagnosis and surgical treatment in infancy, profoundly impacts the lifelong health of affected individuals. There is a growing recognition of the necessity to establish a structured transition process for patients transitioning from pediatric to general surgical care, with the inclusion of gastroenterologists and psychologists in this process.<b>Aim:</b> This study aimed to characterize the demographic profile of patients who underwent surgery for Hirschsprung's disease, assess prevalent complications, determine reoperation rates, and evaluate the demand for gastroenterological care.<b>Materials and methods:</b> A retrospective analysis was conducted on data from adolescents and young adults born between 2000 and 2013 who underwent surgery for Hirschsprung's disease at the University Children's Hospital of Krakow, totaling 119 children meeting the inclusion criteria.<b>Results:</b> Findings reveal that despite active management by pediatric surgeons, follow-up duration remains insufficient, with 38.9% of patients monitored only until the age of 5. As many as 31.8% of patients were consulted by a pediatric surgeon during adolescence, and only 15% just before turning 18. Concurrent gastroenterological conditions were identified in 15.8% of patients, emphasizing the potential benefit of early diagnosis in symptom management. As many as 18.4% of patients required a procedure under general anesthesia, with 9.6% undergoing major abdominal surgery. Special attention should be given to patients with Crohn's disease and anorectal malformation. They require regular monitoring and multidisciplinary care.<b>Conclusions:</b> Patients treated for Hirschsprung's disease require long-term follow-up and a personalized approach, taking into account the possibility of additional conditions and the need for further medical interventions. Developing a standardized transition process is crucial, involving collaboration within a multidisciplinary team. Special attention should be given to patients with comorbidities, as they face an elevated risk of complications.

Authors

Institutions

Publication Details

Journal
Polish Journal of Surgery
Published
2024-10-24
DOI
https://doi.org/10.5604/01.3001.0054.8144
Primary Topic
Congenital gastrointestinal and neural anomalies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Long-Term Surgical Outcomes and Adulthood Transitional Care Planning for Hirschsprung’s Disease: A Single-Center Retrospective Study

Wojciech Górecki, Bartosz Bogusz, Małgorzata Smolec - Zamora, Karolina Tokarska et al.
Polish Journal of Surgery
Congenital gastrointestinal and neural anomalies
article

Long-Term Surgical Outcomes and Adulthood Transitional Care Planning for Hirschsprung’s Disease: A Single-Center Retrospective Study

Wojciech Górecki, Bartosz Bogusz, Małgorzata Smolec - Zamora, Karolina Tokarska, Miłosz Saryusz-Romiszewski
article en

Abstract

<b>Introduction:</b> Hirschsprung's disease, despite its typical diagnosis and surgical treatment in infancy, profoundly impacts the lifelong health of affected individuals. There is a growing recognition of the necessity to establish a structured transition process for patients transitioning from pediatric to general surgical care, with the inclusion of gastroenterologists and psychologists in this process.<b>Aim:</b> This study aimed to characterize the demographic profile of patients who underwent surgery for Hirschsprung's disease, assess prevalent complications, determine reoperation rates, and evaluate the demand for gastroenterological care.<b>Materials and methods:</b> A retrospective analysis was conducted on data from adolescents and young adults born between 2000 and 2013 who underwent surgery for Hirschsprung's disease at the University Children's Hospital of Krakow, totaling 119 children meeting the inclusion criteria.<b>Results:</b> Findings reveal that despite active management by pediatric surgeons, follow-up duration remains insufficient, with 38.9% of patients monitored only until the age of 5. As many as 31.8% of patients were consulted by a pediatric surgeon during adolescence, and only 15% just before turning 18. Concurrent gastroenterological conditions were identified in 15.8% of patients, emphasizing the potential benefit of early diagnosis in symptom management. As many as 18.4% of patients required a procedure under general anesthesia, with 9.6% undergoing major abdominal surgery. Special attention should be given to patients with Crohn's disease and anorectal malformation. They require regular monitoring and multidisciplinary care.<b>Conclusions:</b> Patients treated for Hirschsprung's disease require long-term follow-up and a personalized approach, taking into account the possibility of additional conditions and the need for further medical interventions. Developing a standardized transition process is crucial, involving collaboration within a multidisciplinary team. Special attention should be given to patients with comorbidities, as they face an elevated risk of complications.

Polish Journal of SurgeryVol. 97(1)
Jagiellonian University (PL), Uniwersytecki Szpital Dziecięcy (PL)
Openalex Percentile: Top 54%
Congenital gastrointestinal and neural anomalies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.