Invasive and noninvasive neuromodulation show similar efficacy for pediatric gastrointestinal motility disorders
A prospective interventional trial at a single tertiary referral center enrolled 70 eligible pediatric patients with refractory gastrointestinal motility disorders, with 48 completing the 12-month study. Patients were assigned to either invasive sacral neuromodulation (SNM) via an implanted device or noninvasive enteral neuromodulation (ENM) via surface electrodes. Treatment success, defined as clinically significant improvement in at least two of four domains (abdominal pain, fecal incontinence, defecation frequency, stool consistency), was observed in 80% of ENM patients and 83% of SNM patients, with no significant difference between groups (P = 1.00). No significant differences were found for individual primary outcomes. Severe comorbidities were significantly more frequent in the SNM group (45%) compared to the ENM group (3%) (P = .0018). Regarding safety, minor adverse events occurred in 27% of ENM patients versus 17% of SNM patients, with no significant difference in this comparison (P = .50). No major complications were reported. Key limitations include the single-center design and the lack of reported data on absolute numbers, effect sizes, and discontinuation rates. The study suggests both SNM and ENM are effective and safe options that may be considered within a multimodal therapeutic approach for this challenging pediatric population, though patient selection factors, particularly comorbidity burden, warrant careful consideration.