Purpose At our institution, congenital duodenal atresia is repaired laparoscopically using duodenoduodenostomy with a parallel anastomosis. During our use of this technique, we noted that after mobilization, the distal duodenal segment naturally rested in either a cranial or caudal orientation relative to the proximal segment and that this resting orientation appeared to vary with the anatomical level of atresia. This study primarily evaluated the association between atresia location and the natural orientation of the distal duodenal segment. It secondarily compared perioperative outcomes between the cranial and caudal orientation groups.
Methods This retrospective cohort study was conducted at Samsung Medical Center (Seoul, South Korea) and included neonates who underwent laparoscopic duodenoduodenostomy with parallel anastomosis for congenital duodenal atresia from January 2008 to June 2021. After patients with annular pancreas or duodenal web were excluded, 22 neonates were analyzed and categorized into the cranial (n=16) or caudal (n=6) orientation group according to intraoperative findings. Perioperative outcomes were compared, and the relationship between atresia location and distal segment orientation was analyzed.
Results Operative time, postoperative ventilator support, time to feeding initiation, time to full feeding, and length of hospitalization did not differ significantly between groups. No patient required conversion to open surgery, developed an anastomotic stricture, or died during hospitalization. One patient in the cranial group developed an anastomotic leak, which was treated by laparoscopic reanastomosis. First-portion duodenal atresia was significantly more frequent in the caudal group than in the cranial group (83.3% vs. 25.0%, P=0.023).
Conclusion Laparoscopic duodenoduodenostomy with parallel anastomosis was feasible in both cranial and caudal orientations, with no conversions to open surgery. The natural orientation of the distal duodenal segment was significantly associated with the anatomical location of atresia, supporting an anatomical basis for orientation-guided parallel anastomosis.
Jinyoung Park, Dayoung Ko, Hyunhee Kwon, Dae Yeon Kim, Seong Chul Kim, Soo-Hong Kim, Wontae Kim, Hyun-Young Kim, So Hyun Nam, Jung-Man Namgoong, Sungjoo Park, Junbeom Park, Min-Jung Bang, Jeong-Meen Seo, Ji-Young Sul, Joohyun Sim, Soo Min Ahn, Hee-Beom Yang, Jung-Tak Oh, Chaeyoun Oh, Joong Kee Youn, Sanghoon Lee, Ju Yeon Lee, Cheolgu Lee, Kyong Ihn, Soo-Min Jung, Yeon Jun Jeong, Eunyoung Jung, Jae Hee Chung, Min Jeng Cho, Suhyeon Ha, Seok Joo Han, In Geol Ho
Adv Pediatr Surg 2026;32(1):18-26. Published online June 22, 2026
Purpose This study investigated the clinical characteristics, anatomical distribution, operative management, and postoperative outcomes of pediatric patients who underwent surgery for intestinal duplication and were registered through a nationwide multicenter survey conducted by the Korean Association of Pediatric Surgeons (KAPS).
Methods KAPS conducted a nationwide multicenter retrospective survey across 18 institutions between 2020 and 2024 and collected data from 144 patients.
Results Female patients accounted for 55.6% of surgically treated cases, corresponding to a male to female ratio of 1:1.25. Vomiting and abdominal pain were the most common presenting symptoms. Prenatal diagnosis was achieved in 43.7% of cases. The ileum was the most common site of intestinal duplication (41.0%). Cystic duplications predominated (82.6%), and communication with the native bowel was documented in 19.4% of cases. Elective surgery was performed in 83.3% of patients, with laparoscopic-assisted surgery being the most commonly used approach (52.8%). The most frequently performed surgical procedures were excision (49.3%) and bowel resection with anastomosis (47.2%). Recurrence occurred in three patients (2.1%), and mortality was reported in one patient (0.7%).
Conclusion This study represents the largest multicenter dataset on intestinal duplication in South Korea and provides comprehensive information regarding its clinical characteristics and surgical outcomes. These findings may serve as a useful reference for understanding the clinical spectrum and operative management of pediatric intestinal duplication in South Korea and may support the development of future standardized prospective studies.
Jinyoung Park, Dayoung Ko, Eun-jung Koo, Hyunhee Kwon, Ki Hoon Kim, Dae Yeon Kim, Seong Chul Kim, Soo-Hong Kim, Wontae Kim, HaeYoung Kim, Hyun-Young Kim, So Hyun Nam, Jung-Man Namgoong, Junbeom Park, Taejin Park, Min-Jung Bang, Jeong-Meen Seo, Ji-Young Sul, Joonhyuk Son, Joohyun Sim, Soo Min Ahn, Hee-Beom Yang, Jung-Tak Oh, Chaeyoun Oh, Joong Kee Youn, Sanghoon Lee, Ju Yeon Lee, Kyong Ihn, Hye Kyung Chang, Yeon Jun Jeong, Eunyoung Jung, Jae Hee Chung, Min Jeong Cho, Yun-Mee Choe, Seok Joo Han, In Geol Ho, Jeong Hong
Adv Pediatr Surg 2025;31(1):8-15. Published online May 28, 2025
Purpose This study aims to investigate and compare the incidence, demographic characteristics, clinical manifestations, preoperative diagnostic methods, anatomical classifications, associated anomalies, operative treatments, and postoperative outcomes of patients with intestinal atresia treated by the members of the Korean Association of Pediatric Surgeons (KAPS) through three nationwide surveys.
Methods KAPS conducted 3 national surveys in 1998, 2010, and 2024 to examine the patients diagnosed with intestinal atresia. In preparation for the survey, we developed a customized case registration form to obtain data on patient sex, birth weight, gestational age, clinical manifestations, preoperative diagnostic methods, anatomical types, associated anomalies, operative treatments, and postoperative outcomes. Authorized KAPS members completed the case registration form.
Results The first, second, and third national surveys included 218, 222, and 236 individuals diagnosed with intestinal atresia, respectively. The male-to-female ratios were 1.5:1, 1.1:1, and 1.1:1, respectively. The first, second, and third national surveys revealed that 34.3%, 43.3%, and 53.4% of patients were born before 37 weeks of gestation, respectively. Additionally, 28.7%, 32.0%, and 40.7% of patients had a birth weight under 2,500 g. In the third national survey, duodenoduodenostomy was the most common procedure, performed in 70 out of 82 patients diagnosed with duodenal atresia. Resection and anastomosis were the main surgical procedures conducted in 47 out of 54 cases of jejunal atresia and 74 out of 92 cases of ileal atresia. The mortality rates in the first, second, and third national surveys were 13.8%, 3.6%, and 1.3% respectively, with the lowest rate observed in the third national survey.
Conclusion These national surveys offer valuable insights into the current state of intestinal atresia, including specific surgical interventions and postoperative outcomes in South Korea. For pediatric surgeons aiming to enhance their understanding of intestinal atresia and its treatment options, these surveys could be an indispensable resource and guide.