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Intraoperative Pyloric Botulinum Toxin Injection for Post Total Pancreatectomy With Islet Autotransplantation
Juan P Gurria1, Bhargava Mullapudi1, Colleen M O Lowe1
1Division of Pediatric General and Thoracic Surgery, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA.
Insights
Botulinum toxin (BT) injections into the pylorus may improve outcomes for children undergoing Total Pancreatectomy with Islet Autotransplantation (TPIAT). This treatment reduced time to full oral nutrition and gastrostomy tube days for post-operative gastroparesis.
Area of Science:
- Gastroenterology
- Pediatric Surgery
- Endocrinology
Background:
- Acute Recurrent Pancreatitis (ARP) and Chronic Pancreatitis (CP) significantly impact children's quality of life, leading to pain and malnutrition.
- Total Pancreatectomy with Islet Autotransplantation (TPIAT) is a last resort for severe pancreatitis, but surgery can worsen gastroparesis.
- Botulinum toxin (BT) injections are a potential treatment for pediatric gastroparesis.
Purpose of the Study:
- To evaluate the efficacy of pyloric Botulinum toxin (BT) injections in managing post-operative gastroparesis in pediatric patients undergoing TPIAT.
- To compare outcomes between pediatric TPIAT patients who received BT injections and those who did not.
Main Methods:
- A retrospective cohort study (Level of Evidence: III) compared 20 pediatric patients who received pyloric BT during TPIAT with 20 who did not.
- Outcomes assessed included time to full oral nutrition, weight change, emesis days, gastrostomy tube dependence, and length of stay.
- Patients underwent TPIAT between 2021 and 2023.
Main Results:
- Patients receiving BT injections achieved full oral nutrition significantly faster (29.4 vs. 40.9 days, p < 0.01) and required fewer gastrostomy tube days (7.2 vs. 10.1 days, p < 0.01).
- No significant differences were observed in emesis days, percent weight change at discharge, or length of stay between the groups.
- The study population predominantly consisted of patients with Chronic Pancreatitis (80% in the BT group, 65% in the non-BT group).
Conclusions:
- Pyloric BT injections appear to be a promising intervention for mitigating postoperative gastroparesis symptoms in pediatric TPIAT patients.
- This study represents the first pediatric investigation into the impact of BT on gastroparesis morbidity following TPIAT.
- Further research is warranted to confirm these findings in a larger cohort.
Background:
Acute Recurrent Pancreatitis (ARP) and Chronic Pancreatitis (CP) may cause abdominal pain, malnutrition, opioid dependency, and impairment in quality of life. Total Pancreatectomy with Islet Autotransplantation (TPIAT) is an option when other measures fail. Pancreatitis gastroparesis can be potentiated by surgery. Botulinum toxin (BT) injections into the pylorus have been used in children for gastroparesis. We evaluated outcomes of pyloric injection of BT for TPIAT in children.
Methods:
Retrospective cohort of children who underwent TPIAT (2021-2023). Twenty with-BT and 20 without-BT were evaluated for time to achieve full oral nutrition, percent weight change at discharge, days with emesis through post op day 14 (POD14), days when gastrostomy tube (G) required drainage for vomiting through POD14, length of stay (LOS). We hypothesized that pyloric BT during TPIAT would decrease post-operative gastroparesis symptoms.
Results:
CP diagnosis present in 80 % of with-BT & 65 % of the without-BT patients. The groups were similar by sex (with-BT, 45 % male vs 50 % in without-BT). With-BT patients had fewer days to full PO (29.4 (18.3) vs. 40.9 (15.9), p < 0.01), and fewer G tube days (mean 7.2 SD (2.6) vs 10.1(3.4)) (p < 0.01) but no significant difference in emesis days (2.7 (2.8) vs 4.2 (2.9)) (p = 0.21), percent weight change at discharge (-2.9 % (2.7) vs. -4.6 % (2.7)) (p = 0.07) and LOS (median 15.5 IQR(14-16.5) vs. 16 (13.5-19)) (p = 0.46).
Conclusion:
Pyloric BT may improve postoperative gastroparesis symptoms among pediatric patients undergoing TPIAT. To our knowledge, this is the first pediatric study evaluating morbidity associated with gastroparesis after TPIAT in an already high-risk population due to ARP or CP.
Type Of Study:
Retrospective Cohort Study LEVEL OF EVIDENCE: III.
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