Hostname: page-component-848d4c4894-x5gtn Total loading time: 0 Render date: 2024-05-12T03:25:52.763Z Has data issue: false hasContentIssue false

Central-line–associated bloodstream infections in a pediatric oncology and hematology hospital at home program

Published online by Cambridge University Press:  01 August 2022

Sylvain C. Raimbault*
Affiliation:
Institute of Pediatric Hematology and Oncology (IHOPe), Lyon, France
Carine Domenech
Affiliation:
Institute of Pediatric Hematology and Oncology (IHOPe), Lyon, France Faculté de médecine et de maïeutique Lyon Sud, Université Claude Bernard Lyon 1, Hospices Civils de Lyon, Lyon, France Apoptosis, Cancer and Development Laboratory, Cancer Research of Center of Lyon, INSERM U1052-CNRS UMR5286, Lyon, France
Christine Fuhrmann
Affiliation:
Institut des agents infectieux et de pathologies infectieuses, Hospices Civils de Lyon, Lyon, France Centre Léon Bérard, Lyon, France
Amandine Bertrand
Affiliation:
Institute of Pediatric Hematology and Oncology (IHOPe), Lyon, France U1290, Research on Healthcare Performance (RESHAPE), Lyon, France
*
Author for correspondence: Sylvain C. Raimbault, E-mail: sylvain.raimbault@chu-lyon.fr

Abstract

Objective:

Central-line–associated bloodstream infections (CLABSIs) are associated with significant morbidity among pediatric oncology-hematology patients, and risk factors remain largely unknown in the setting of hospital at home (HAH). Children in HAH receive intensive treatment (eg, chemotherapy and parenteral nutrition), with frequent central-line handling; thus, they may be at higher risk for CLABSI.

Methods:

We conducted a monocentric retrospective study of patients with a central line included in our HAH program from January 1 to December 31, 2016. HAH patient characteristics for children developing CLABSIs were compared to those who did not, based on blood cultures positive for infection and clinical data of all patients included.

Results:

Overall, 492 HAH stays were analyzed, with 144 patients. The overall CLABSI rate in these patients was 2.6 per 1,000 central-line days. Children who developed CLABSIs were younger (median age, 2.5 vs 8.8 years; P < .001), suffered more from hematological pathologies (malignant or nonmalignant, 75% vs 52%; P = .02), and had more frequently undergone hematopoietic stem-cell transplantation (30.8% vs 6.5%; P = .01). In addition, these patients often had a tunneled externalized catheter as the central line and were more frequently given parenteral nutrition at home (46% vs 8%; P < .001).

Conclusions:

CLABSI rates for children in HAH were more similar to those of inpatients than to rates previously reported for ambulatory patients. The factors associated with infection identified herein should be further validated in multicentric studies and considered to improve HAH practices, parallel to prevention measures used in the inpatient setting.

Type
Original Article
Copyright
© The Author(s), 2022. Published by Cambridge University Press on behalf of The Society for Healthcare Epidemiology of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Rinke, ML, Milstone, AM, Chen, AR, et al. Ambulatory pediatric oncology CLABSIs: epidemiology and risk factors. Pediatr Blood Cancer 2013;60:18821889.CrossRefGoogle ScholarPubMed
Hord, JD, Lawlor, JP, Werner, EJ, et al. Central-line–associated bloodstream infections in pediatric hematology/oncology patients with different types of central lines. Pediatr Blood Cancer 2016;63:16031607.CrossRefGoogle ScholarPubMed
Rinke, ML, Chen, AR, Bundy, DG, et al. Implementation of a central-line maintenance care bundle in hospitalized pediatric oncology patients. Pediatrics 2012;130:e996e1004.CrossRefGoogle ScholarPubMed
Bertrand, A, Favier, B, Devaux, Y, et al. Intravenous chemotherapy at home: A pediatric monocentric experience. Bull Cancer 2018;105:155161.CrossRefGoogle Scholar
Lippert, M, Semmens, S, Tacey, L, et al. The Hospital at Home program: no place like home. Curr Oncol 2017;24:2327.CrossRefGoogle ScholarPubMed
Hansson, H, Kjaergaard, H, Johansen, C, et al. Hospital-based home care for children with cancer: feasibility and psychosocial impact on children and their families. Pediatr Blood Cancer 2013;60:865872.CrossRefGoogle ScholarPubMed
Rinke, ML, Chen, AR, Milstone, AM, et al. Bringing central-line–associated bloodstream infection prevention home: catheter maintenance practices and beliefs of pediatric oncology patients and families. Jt Comm J Qual Patient Saf 2015;41:177185.Google ScholarPubMed
Horan, TC, Andrus, M, Dudeck, MA. CDC/NHSN surveillance definition of healthcare-associated infection and criteria for specific types of infections in the acute-care setting. Am J Infect Control 2008;36:309332.CrossRefGoogle ScholarPubMed
Ammann, RA, Laws, HJ, Schrey, D, et al. Bloodstream infection in paediatric cancer centres—leukaemia and relapsed malignancies are independent risk factors. Eur J Pediatr 2015;174:675686.CrossRefGoogle ScholarPubMed
Smith, TL, Pullen, GT, Crouse, V, Rosenberg, J, Jarvis, WR. Bloodstream infections in pediatric oncology outpatients: a new healthcare systems challenge. Infect Control Hosp Epidemiol 2002;23:239243.CrossRefGoogle ScholarPubMed
Shah, SS, Manning, ML, Leahy, E, Magnusson, M, Rheingold, SR, Bell, LM. Central venous catheter–associated bloodstream infections in pediatric oncology home care. Infect Control Hosp Epidemiol 2002;23:99101.CrossRefGoogle ScholarPubMed
Simon, A, Ammann, RA, Bode, U, et al. Healthcare-associated infections in pediatric cancer patients: results of a prospective surveillance study from university hospitals in Germany and Switzerland. BMC Infect Dis 2008;8:70.CrossRefGoogle ScholarPubMed
Shenep, MA, Tanner, MR, Sun, Y, et al. Catheter-related complications in children with cancer receiving parenteral nutrition: change in risk is moderated by catheter type. J Parenter Enteral Nutr 2017;41:10631071.CrossRefGoogle ScholarPubMed
Kelly, MS, Conway, M, Wirth, KE, Potter-Bynoe, G, Billett, AL, Sandora, TJ. Microbiology and risk factors for central line-associated bloodstream infections among pediatric oncology outpatients: a single institution experience of 41 cases. J Pediatr Hematol Oncol 2013;35:e71e76.CrossRefGoogle ScholarPubMed
Nassar, R, Hazan, G, Leibovitz, EL, et al. Central venous catheter-associated bloodstream infections in children diagnosed with intestinal failure in southern Israel. Eur J Clin Microbiol Infect Dis 2020;39:517525.CrossRefGoogle ScholarPubMed
Moon, HM, Kim, S, Yun, KW, et al. Clinical characteristics and risk factors of long-term central venous catheter–associated bloodstream infections in children. Pediatr Infect Dis J 2018;37:401406.CrossRefGoogle ScholarPubMed
Christensen, ML, Hancock, ML, Gattuso, J, et al. Parenteral nutrition associated with increased infection rate in children with cancer. Cancer 1993;72:27322738.3.0.CO;2-E>CrossRefGoogle ScholarPubMed
Viana Taveira, MR, Lima, LS, de Araújo, CC, de Mello, MJG. Risk factors for central-line–associated bloodstream infection in pediatric oncology patients with a totally implantable venous access port: a cohort study. Pediatr Blood Cancer 2017;64:336342.CrossRefGoogle ScholarPubMed
Celebi, S, Sezgin, ME, Cakır, D, et al. Catheter-associated bloodstream infections in pediatric hematology-oncology patients. Pediatr Hematol Oncol 2013;30:187194.CrossRefGoogle ScholarPubMed
Rinke, ML, Bundy, DG, Chen, AR, et al. Central-line maintenance bundles and CLABSIs in ambulatory oncology patients. Pediatrics 2013;132:e1403e1412.CrossRefGoogle ScholarPubMed
Miedema, KGE, Winter, RHLJ, Ammann, RA, et al. Bacteria causing bacteremia in pediatric cancer patients presenting with febrile neutropenia—species distribution and susceptibility patterns. Support Care Cancer 2013;21:24172426.CrossRefGoogle ScholarPubMed
Supplementary material: File

Raimbault et al. supplementary material

Tables S1-S2

Download Raimbault et al. supplementary material(File)
File 15.7 KB