AI Article Synopsis

  • Overt gastrointestinal bleeding (GIB) is a serious condition commonly seen in children undergoing haploidentical hematopoietic stem cell transplantation (haplo-HSCT), with a noted incidence of 25.2%.
  • The study reviewed 123 pediatric patients over a median follow-up of 26.3 months and found that GIB negatively impacted overall survival and increased non-relapse mortality.
  • Key risk factors for developing overt GIB included severe gut acute graft versus-host disease, thrombotic microangiopathy, and cytomegalovirus viremia.

Article Abstract

Background: Overt gastrointestinal bleeding (GIB) is a potentially serious and life-threatening condition in patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, relatively little information is available regarding overt GIB in children.

Objectives: To assess the prevalence, clinical patterns, and outcomes of overt GIB in children undergoing haploidentical hematopoietic stem cell transplantation (haplo-HSCT).

Methods: A total of 123 consecutive patients with malignant or non-malignant blood disorders who received haplo-HSCT were reviewed in our hospital between October 2017 and October 2022. Overt GIB was determined as hematemesis, melena or hematochezia. Continuous variables were compared by Mann Whitney U test. Categorical parameters were compared by the χ test or Fisher's exact test. Kaplan-Meier curves and log-rank tests were used to assess overall survival (OS), non-relapse mortality (NRM) and relapse. Univariate and multivariate analyses were performed to identify potential risk factors of overt GIB development.

Results: The median follow-up was 26.3 (range,1.7-74.8) months. Overt GIB occurred in 31 patients (25.2% incidence), with a median time elapsed after haplo-HSCT of 376 days (range, 58-1275 days). Compared with the non-GIB group, patients with overt GIB had reduced OS and increased NRM. In multivariate analysis, grade III-IV gut acute graft versus-host disease (aGvHD), thrombotic microangiopathy (TMA) and cytomegalovirus (CMV) viremia were significant risk factors for the occurrence of overt GIB after haplo-HSCT.

Conclusions: Overt GIB is a frequent complication after haplo-HSCT in pediatric patients, and associated with worse survival. Grade III-IV gut aGvHD, TMA and CMV viremia were associated with its development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11282719PMC
http://dx.doi.org/10.1186/s12887-024-04950-5DOI Listing

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