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Risk of bacterial bloodstream infection does not vary by central-line type during neutropenic periods in pediatric acute myeloid leukemia.
Elgarten, Caitlin W; Otto, William R; Shenton, Luke; Stein, Madison T; Horowitz, Joseph; Aftandilian, Catherine; Arnold, Staci D; Bona, Kira O; Caywood, Emi; Collier, Anderson B; Gramatges, M Monica; Henry, Meret; Lotterman, Craig; Maloney, Kelly; Modi, Arunkumar J; Mian, Amir; Mody, Rajen; Morgan, Elaine; Raetz, Elizabeth A; Verma, Anupam; Winick, Naomi; Wilkes, Jennifer J; Yu, Jennifer C; Aplenc, Richard; Fisher, Brian T; Getz, Kelly D.
Affiliation
  • Elgarten CW; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Otto WR; Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Shenton L; Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Stein MT; Division of Infectious Diseases, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Horowitz J; Drexel University College of Medicine, Philadelphia, Pennsylvania.
  • Aftandilian C; Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Arnold SD; College of Medicine, University of Illinois.
  • Bona KO; Division of Pediatric Hematology-Oncology, Department of Pediatrics, Stanford University, Palo Alto, California.
  • Caywood E; Children's Healthcare of Atlanta/Emory University, Atlanta, Georgia.
  • Collier AB; Pediatric Hematology-Oncology, Children's Hospital Boston, Boston, Massachusetts.
  • Gramatges MM; A.I. Dupont Hospital for Children-Nemours, Wilmington, Delaware.
  • Henry M; University of Mississippi Medical Center, Jackson, Mississippi.
  • Lotterman C; Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
  • Maloney K; Children's Hospital of Michigan, Detroit, Michigan.
  • Modi AJ; Ochsner Medical Center for Children, New Orleans, Lousisiana.
  • Mian A; Children's Hospital Colorado and the Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado.
  • Mody R; Arkansas Children's Hospital, Little Rock, Arkansas.
  • Morgan E; Arkansas Children's Hospital, Little Rock, Arkansas.
  • Raetz EA; University of Michigan, Ann Arbor, Michigan.
  • Verma A; Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
  • Winick N; Stephen D. Hassenfeld Children's Center for Cancer and Blood Disorders, New York, New York.
  • Wilkes JJ; Division of Pediatric Hematology-Oncology, Department of Pediatrics, University of Utah, Salt Lake City, Utah.
  • Yu JC; Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Aplenc R; Department of Pediatric Hematology Oncology, University of Texas Southwestern Medical Center, Dallas, Texas.
  • Fisher BT; Department of Pediatrics, University of Washington, Division of Hematology-Oncology, Seattle Children's Hospital, Seattle, Washington.
  • Getz KD; Division of Pediatric Hematology-Oncology, Rady Children's Hospital San Diego, San Diego, California.
Infect Control Hosp Epidemiol ; 44(2): 222-229, 2023 02.
Article in En | MEDLINE | ID: mdl-35465865
BACKGROUND: 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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Infections / Catheterization, Central Venous / Leukemia, Myeloid, Acute / Sepsis / Catheter-Related Infections / Central Venous Catheters / Neutropenia Type of study: Etiology_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Infect Control Hosp Epidemiol Journal subject: DOENCAS TRANSMISSIVEIS / ENFERMAGEM / EPIDEMIOLOGIA / HOSPITAIS Year: 2023 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacterial Infections / Catheterization, Central Venous / Leukemia, Myeloid, Acute / Sepsis / Catheter-Related Infections / Central Venous Catheters / Neutropenia Type of study: Etiology_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Infect Control Hosp Epidemiol Journal subject: DOENCAS TRANSMISSIVEIS / ENFERMAGEM / EPIDEMIOLOGIA / HOSPITAIS Year: 2023 Document type: Article Country of publication: United States