Risk of bacterial bloodstream infection does not vary by central-line type during neutropenic periods in pediatric acute myeloid leukemia

Author:

Elgarten Caitlin W.ORCID,Otto William R.ORCID,Shenton LukeORCID,Stein Madison T.,Horowitz Joseph,Aftandilian CatherineORCID,Arnold Staci D.ORCID,Bona Kira O.ORCID,Caywood EmiORCID,Collier Anderson B.ORCID,Gramatges M. MonicaORCID,Henry Meret,Lotterman Craig,Maloney Kelly,Modi Arunkumar J.ORCID,Mian AmirORCID,Mody RajenORCID,Morgan ElaineORCID,Raetz Elizabeth A.,Verma Anupam,Winick NaomiORCID,Wilkes Jennifer J.ORCID,Yu Jennifer C.ORCID,Aplenc RichardORCID,Fisher Brian T.ORCID,Getz Kelly D.ORCID

Abstract

AbstractBackground:Bloodstream infections (BSIs) are a frequent cause of morbidity in patients with acute myeloid leukemia (AML), due in part to the presence of central venous access devices (CVADs) required to deliver therapy.Objective:To determine the differential risk of bacterial BSI during neutropenia by CVAD type in pediatric patients with AML.Methods:We performed a secondary analysis in a cohort of 560 pediatric patients (1,828 chemotherapy courses) receiving frontline AML chemotherapy at 17 US centers. The exposure was CVAD type at course start: tunneled externalized catheter (TEC), peripherally inserted central catheter (PICC), or totally implanted catheter (TIC). The primary outcome was course-specific incident bacterial BSI; secondary outcomes included mucosal barrier injury (MBI)-BSI and non-MBI BSI. Poisson regression was used to compute adjusted rate ratios comparing BSI occurrence during neutropenia by line type, controlling for demographic, clinical, and hospital-level characteristics.Results:The rate of BSI did not differ by CVAD type: 11 BSIs per 1,000 neutropenic days for TECs, 13.7 for PICCs, and 10.7 for TICs. After adjustment, there was no statistically significant association between CVAD type and BSI: PICC incident rate ratio [IRR] = 1.00 (95% confidence interval [CI], 0.75–1.32) and TIC IRR = 0.83 (95% CI, 0.49–1.41) compared to TEC. When MBI and non-MBI were examined separately, results were similar.Conclusions:In this large, multicenter cohort of pediatric AML patients, we found no difference in the rate of BSI during neutropenia by CVAD type. This may be due to a risk-profile for BSI that is unique to AML patients.

Publisher

Cambridge University Press (CUP)

Subject

Infectious Diseases,Microbiology (medical),Epidemiology

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