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Journal of pediatric gastroenterology and nutrition

September 8, 2026 · via Europe PMC

Efficacy and safety of intrapyloric botulinum toxin injection in pediatrics: Current evidence and future directions.

Chidiac L, Xu B, Wolfson S, Benitez AJ, Pearlstein H, Kapavarapu P, Piccoli D, Mousa H.

ReviewAbstract only — full text under license

AI summary — for doctors, generated from the abstract only

This review finds that while most small studies report symptom improvement after intrapyloric botulinum toxin injection for pediatric gastroparesis, no objective test studied (gastric emptying scintigraphy, manometry, or functional lumen imaging) reliably predicts which children will respond, highlighting a need for better biomarkers and controlled trials before this treatment's role can be clarified.

What was studied

A narrative review summarizing current literature on intrapyloric botulinum toxin (IPBT) injection for pediatric gastroparesis, focusing on symptomatic outcomes and evaluating potential objective predictors of treatment response, including gastric emptying scintigraphy, antroduodenal manometry, and endoscopic functional luminal probe parameters.

Key findings

  • Most studies report some degree of symptomatic improvement following intrapyloric botulinum toxin injection, but these findings are derived from small, retrospective cohorts without control groups, limiting the strength of conclusions.
  • Gastric emptying scintigraphy did not show correlation with treatment response; similarly, antroduodenal manometry general impressions and endoscopic functional luminal probe parameters did not reliably predict symptomatic response to the injection.
  • Several studies describe repeated injections, although protocols for repeat dosing are unclear and response to repeat treatment is varied; emerging modalities like body surface gastric mapping, gastric emptying breath test, and gastric MRI may eventually provide better biomarkers to guide treatment, though pediatric data on these remain limited.

Clinical relevance

The findings suggest that while clinicians may consider intrapyloric botulinum toxin injection for children with refractory gastroparesis given the symptomatic improvement reported in uncontrolled studies, they should recognize that current objective tests cannot reliably identify which children will respond, meaning treatment decisions currently rely on clinical judgment rather than predictive testing, and that larger prospective controlled studies are needed to clarify this treatment's true role.

Who should care

Medical GastroenterologyPediatric GastroenterologyPediatricsSurgical GastroenterologyPediatric Hepatology

Limitations

The authors explicitly state the current pediatric evidence is limited by suboptimal study designs (small, retrospective, uncontrolled) and lack of objective assessments of treatment response, calling for future prospective controlled studies.

This review finds that intrapyloric botulinum toxin injection shows symptomatic benefit in small uncontrolled pediatric gastroparesis studies, but no tested objective measure reliably predicts which children will respond, highlighting a need for better biomarkers and controlled trials.

This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.

Abstract

Pediatric gastroparesis is a debilitating disease requiring more diverse and effective treatment options. Intrapyloric botulinum toxin (IPBT) injection has emerged as a therapeutic option, although evidence supporting its use in children remains limited. The aim of this review is to summarize the current literature on IPBT injection for pediatric gastroparesis, focusing on symptomatic outcomes and potential predictors of response. Overall, most studies report some degree of symptomatic improvement following the injection; however, these findings are derived from small, retrospective cohorts without control groups. Objective predictors of response evaluated include gastric emptying scintigraphy, which did not show correlation with treatment response. Similarly, antroduodenal manometry general impressions and endoscopic functional luminal probe parameters did not reliably predict symptomatic response to the injection. Several studies describe repeated injections, although protocols for repeat are unclear, and the response is varied. Body surface gastric mapping represents a novel modality that may provide gastric physiological data allowing its use as a biomarker guiding IPBT injection, although pediatric data is still limited. Other emerging modalities, including gastric emptying breath test and gastric magnetic resonance imaging, may further enhance assessment of gastroparesis and treatment response. The current pediatric evidence on IPBT injection for gastroparesis is limited by suboptimal study designs and lack of objective assessments of treatment response. Future prospective, controlled studies are needed to strengthen conclusions on IPBT injection efficacy for pediatric gastroparesis and to clarify its role in clinical practice.

DOI

10.1002/jpn3.70571

PMID

42711930

Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.

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