Granulocyte transfusion improves survival in pediatric febrile neutropenia: a 15-year cohort study

dc.contributor.authorPhetsai W.
dc.contributor.authorSanpakit K.
dc.contributor.authorBuaboonnam J.
dc.contributor.authorPhuakpet K.
dc.contributor.authorVathana N.
dc.contributor.authorNarkbunnam N.
dc.contributor.authorKladed F.
dc.contributor.authorTakpradit C.
dc.contributor.correspondencePhetsai W.
dc.contributor.otherMahidol University
dc.date.accessioned2026-03-15T18:12:04Z
dc.date.available2026-03-15T18:12:04Z
dc.date.issued2026-03-01
dc.description.abstractBackground: Febrile neutropenia (FN) remains a leading cause of morbidity and mortality in pediatric patients with high-risk hematologic disorders, particularly in low-and middle-income countries (LMICs), where antimicrobial resistance limits treatment options. Granulocyte transfusion (GT) is considered an adjunctive therapy; however, pediatric data from LMICs are limited. Purpose: This study evaluates the effectiveness, timing, and safety of GT in a real-world LMIC setting. Methods: This 15-year retrospective cohort study included pediatric patients (≤18 years) with severe neutropenic infections treated at a national tertiary referral center in Thailand in 2009–2023. The patients received GT plus antimicrobial therapy or antimicrobial therapy alone. The primary outcome measure was 30-day survival. The analyses included multivariate logistic regression, Cox regression, propensity score matching (PSM), and inverse probability of treatment weighting (IPTW). Results: Among the 54 patients (26 GT recipients; 28 controls), GT was associated with improved 30-day survival in the full cohort (odds ratio [OR], 0.105; 95% confidence interval [CI], 0.016–0.700; P=0.020). IPTW confirmed this association (OR, 0.099; P=0.001), with consistent results in the PSM analysis (OR, 0.157; P=0.028). In the high-risk hematologic condition subgroup (n=48), GT was associated with increased survival (95.2% vs. 61.9%; hazard ratio [HR], 0.105; P=0.034). GT also accelerated the resolution of fever (HR, 2.24; P=0.028), FN recovery (HR, 2.35; P=0.017), and absolute neutrophil count recovery (HR, 2.10; P=0.047). No serious transfusion-related adverse events were observed. Conclusion: GT was associated with improved survival and faster clinical recovery in pediatric patients with FN. These real-world LMIC data support its use as a feasible adjunctive therapy and warrant prospective validation.
dc.identifier.citationClinical and Experimental Pediatrics Vol.69 No.3 (2026) , 236-246
dc.identifier.doi10.3345/cep.2025.01186
dc.identifier.eissn27134148
dc.identifier.scopus2-s2.0-105032255197
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/115684
dc.rights.holderSCOPUS
dc.subjectNursing
dc.subjectMedicine
dc.titleGranulocyte transfusion improves survival in pediatric febrile neutropenia: a 15-year cohort study
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105032255197&origin=inward
oaire.citation.endPage246
oaire.citation.issue3
oaire.citation.startPage236
oaire.citation.titleClinical and Experimental Pediatrics
oaire.citation.volume69
oairecerif.author.affiliationSiriraj Hospital

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