Microbiology and Risk Factors for Hospital-Associated Bloodstream Infections Among Pediatric Hematopoietic Stem Cell Transplant Recipients

Author:

Akinboyo Ibukunoluwa C1ORCID,Young Rebecca R1,Spees Lisa P23,Heston Sarah M1,Smith Michael J1,Chang Yeh-Chung1,McGill Lauren E14,Martin Paul L4,Jenkins Kirsten1,Lugo Debra J1,Hazen Kevin C5,Seed Patrick C6,Kelly Matthew S1

Affiliation:

1. Division of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA

2. Department of Health Policy and Management, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina, USA

3. Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, USA

4. Division of Pediatric Blood and Marrow Transplantation, Duke University Medical Center, Durham, North Carolina, USA

5. Pathology, Duke University Medical Center, Durham, North Carolina, USA

6. Division of Pediatric Infectious Diseases, Northwestern Feinberg School of Medicine, Chicago, Illinois, USA

Abstract

Abstract Background Children undergoing hematopoietic stem cell transplantation (HSCT) are at high risk for hospital-associated bloodstream infections (HA-BSIs). This study aimed to describe the incidence, microbiology, and risk factors for HA-BSI in pediatric HSCT recipients. Methods We performed a single-center retrospective cohort study of children and adolescents (<18 years of age) who underwent HSCT over a 20-year period (1997–2016). We determined the incidence and case fatality rate of HA-BSI by causative organism. We used multivariable Poisson regression to identify risk factors for HA-BSI. Results Of 1294 patients, the majority (86%) received an allogeneic HSCT, most commonly with umbilical cord blood (63%). During the initial HSCT hospitalization, 334 HA-BSIs occurred among 261 (20%) patients. These were classified as gram-positive bacterial (46%), gram-negative bacterial (24%), fungal (12%), mycobacterial (<1%), or polymicrobial (19%). During the study period, there was a decline in the cumulative incidence of HA-BSI (P = .021) and, specifically, fungal HA-BSIs (P = .002). In multivariable analyses, older age (incidence rate ratio [IRR], 1.03; 95% confidence interval [CI], 1.01–1.06), umbilical cord blood donor source (vs bone marrow; IRR, 1.69; 95% CI, 1.19–2.40), and nonmyeloablative conditioning (vs myeloablative; IRR, 1.85; 95% CI, 1.21–2.82) were associated with a higher risk of HA-BSIs. The case fatality rate was higher for fungal HA-BSI than other HA-BSI categories (21% vs 6%; P = .002). Conclusions Over the past 2 decades, the incidence of HA-BSIs has declined among pediatric HSCT recipients at our institution. Older age, umbilical cord blood donor source, and nonmyeloablative conditioning regimens are independent risk factors for HA-BSI among children undergoing HSCT.

Funder

University of North Carolina at Chapel Hill

National Institutes of Health Career Development Award

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

Reference36 articles.

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