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Central Line–Associated Bloodstream Infections in Neonates with Gastrointestinal Conditions: Developing a Candidate Definition for Mucosal Barrier Injury Bloodstream Infections

Published online by Cambridge University Press:  10 May 2016

Susan E. Coffin*
Affiliation:
Division of Infectious Diseases, Center for Pediatric Clinical Effectiveness, and Department of Infection Prevention, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania
Sarah B. Klieger
Affiliation:
Division of Infectious Diseases, Center for Pediatric Clinical Effectiveness, and Department of Infection Prevention, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania
Christopher Duggan
Affiliation:
Division of Gastroenterology, Hepatology, and Nutrition, Boston Children’s Hospital, Boston, Massachusetts Department of Pediatrics, Harvard Medical School, Boston, Massachusetts
W. Charles Huskins
Affiliation:
Division of Pediatric Infectious Diseases, Mayo Clinic, Rochester, Minnesota
Aaron M. Milstone
Affiliation:
Division of Pediatric Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland
Gail Potter-Bynoe
Affiliation:
Infection Prevention and Control, Boston Children’s Hospital, Boston, Massachusetts
Bram Raphael
Affiliation:
Division of Gastroenterology, Hepatology, and Nutrition, Boston Children’s Hospital, Boston, Massachusetts Department of Pediatrics, Harvard Medical School, Boston, Massachusetts
Thomas J. Sandora
Affiliation:
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts Infection Prevention and Control, Boston Children’s Hospital, Boston, Massachusetts Division of Infectious Diseases, Boston Children’s Hospital, Boston, Massachusetts
Xiaoyan Song
Affiliation:
Division of Infectious Diseases and Department of Pediatrics, Children’s National Medical Center, Washington, D.C.
Danielle M. Zerr
Affiliation:
Division of Infectious Diseases and Department of Pediatrics, University of Washington, Seattle, Washington
Grace M. Lee
Affiliation:
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts Infection Prevention and Control, Boston Children’s Hospital, Boston, Massachusetts Division of Infectious Diseases, Boston Children’s Hospital, Boston, Massachusetts Harvard Pilgrim Healthcare Institute, Boston, Massachusetts
Pediatric Prevention EpiCenter Consortium
Affiliation:
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts Infection Prevention and Control, Boston Children’s Hospital, Boston, Massachusetts Division of Infectious Diseases, Boston Children’s Hospital, Boston, Massachusetts Harvard Pilgrim Healthcare Institute, Boston, Massachusetts
*
Division of Infectious Diseases, Children’s Hospital of Philadelphia, 3535 Market Street, Suite 1579, Philadelphia, PA 19104 ([email protected]).

Abstract

Objective.

To develop a candidate definition for central line–associated bloodstream infection (CLABSI) in neonates with presumed mucosal barrier injury due to gastrointestinal (MBI-GI) conditions and to evaluate epidemiology and microbiology of MBI-GI CLABSI in infants

Design.

Multicenter retrospective cohort study.

Setting.

Neonatal intensive care units from 14 US children’s hospitals and pediatric facilities.

Methods.

A multidisciplinary focus group developed a candidate MBI-GI CLABSI definition based on presence of an MBI-GI condition, parenteral nutrition (PN) exposure, and an eligible enteric organism. CLABSI surveillance data from participating hospitals were supplemented by chart review to identify MBI-GI conditions and PN exposure.

Results.

During 2009–2012, 410 CLABSIs occurred in 376 infants. MBI-GI conditions and PN exposure occurred in 149 (40%) and 324 (86%) of these 376 neonates, respectively. The distribution of pathogens was similar among neonates with versus without MBI-GI conditions and PN exposure. Fifty-nine (16%) of the 376 initial CLABSI episodes met the candidate MBI-GI CLABSI definition. Subsequent versus initial CLABSIs were more likely to be caused by an enteric organism (22 of 34 [65%] vs 151 of 376 [40%]; P = .009) and to meet the candidate MBI-GI CLABSI definition (19 of 34 [56%] vs 59 of 376 [16%]; P < .01).

Conclusions.

While MBI-GI conditions and PN exposure were common, only 16% of initial CLABSIs met the candidate definition of MBI-GI CLABSI. The high proportion of MBI-GI CLABSIs among subsequent infections suggests that infants with MBI-GI CLABSI should be a population targeted for further surveillance and interventional research.

Infect Control Hosp Epidemiol 2014;35(11):1391–1399

Type
Original Article
Copyright
© 2014 by The Society for Healthcare Epidemiology of America. All rights reserved.

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References

1. Dudeck, MA, Horan, T, Peterson, KD, et al. National Healthcare Safety Network report, data summary for 2011, device-associated module. Am J Infect Control 2013;41(4):286300. doi:10.1016/j.ajic.2013.01.002.CrossRefGoogle ScholarPubMed
2. Miller, MR, Griswold, M, Harris, JM, et al. Decreasing PICU catheter-associated bloodstream infections: NACHRI’s quality transformation efforts. Pediatrics 2010;125(2):206213. doi:10.1542/peds.2009–1382.Google Scholar
3. Wheeler, DS, Giaccone, MJ, Hutchinson, N, et al. A hospital-wide quality-improvement collaborative to reduce catheter-associated bloodstream infections. Pediatrics 2011;128(4):e995–e1007. doi:10.1542/peds.2010–2601.CrossRefGoogle ScholarPubMed
4. Bizzarro, MJ, Sabo, B, Noonan, M, Bonfiglio, MP, Northrup, V, Diefenbach, K. A quality improvement initiative to reduce central line–associated bloodstream infections in a neonatal intensive care unit. Infect Control Hosp Epidemiol 2010;31(3):241248. doi:10.1086/650448.Google Scholar
5. Schulman, J, Stricof, R, Stevens, TP, et al. Statewide NICU central-line-associated bloodstream infection rates decline after bundles and checklists. Pediatrics 2011;127(3):436444. doi:10.1542/peds.2010–2873.Google Scholar
6. Steinberg, JP, Robichaux, C, Tejedor, SC, Reyes, MD, Jacob, JT. Distribution of pathogens in central line–associated bloodstream infections among patients with and without neutropenia following chemotherapy: evidence for a proposed modification to the current surveillance definition. Infect Control Hosp Epidemiol 2013;34(2):171175. doi:10.1086/669082.Google Scholar
7. Fraser, TG, Gordon, SM. CLABSI rates in immunocompromised patients: a valuable patient centered outcome? Clin Infect Dis 2011;52(12):14461450. doi:10.1093/cid/cir200.Google Scholar
8. Beekmann, SE, Diekema, DJ, Huskins, WC, et al. Diagnosing and reporting of central line–associated bloodstream infections. Infect Control Hosp Epidemiol 2012;33(9):875882. doi:10.1086/667379.CrossRefGoogle ScholarPubMed
9. Sexton, DJ, Chen, LF, Anderson, DJ. Current definitions of central line–associated bloodstream infection: is the emperor wearing clothes? Infect Control Hosp Epidemiol 2010;31(12):12861289. doi:10.1086/657583.Google Scholar
10. Lukenbill, J, Rybicki, L, Sekeres, MA, et al. Defining incidence, risk factors, and impact on survival of central line-associated blood stream infections following hematopoietic cell transplantation in acute myeloid leukemia and myelodysplastic syndrome. Biol Blood Marrow Transplant 2013;19(5):720724. doi:10.1016/j.bbmt.2013.01.022.Google Scholar
11. DiGiorgio, MJ, Fatica, C, Oden, M, et al. Development of a modified surveillance definition of central line–associated bloodstream infections for patients with hematologic malignancies. Infect Control Hosp Epidemiol 2012;33(9):865868. doi:10.1086/667380.CrossRefGoogle ScholarPubMed
12. See, I, Iwamoto, M, Allen-Bridson, KT, Horan, T, Magill, SS, Thompson, ND. Mucosal barrier injury laboratory-confirmed bloodstream infection: results from a field test of a new National Healthcare Safety Network definition. Infect Control Hosp Epidemiol 2013;34(8):769776. doi:10.1086/671281.CrossRefGoogle ScholarPubMed
13. Cole, CR, Frem, JC, Schmotzer, B, et al. The rate of bloodstream infection is high in infants with short bowel syndrome. J Pediatr 2010;156:941947.Google Scholar
14. Centers for Disease Control and Prevention (CDC). 17 CDC NHSN surveillance definitions. Atlanta: CDC, 2012.Google Scholar
15. Squires, RH, Duggan, C, Teitelbaum, DH, et al. Natural history of pediatric intestinal failure: initial report from the pediatric intestinal failure consortium. J Pediatr 2012;161(4):723728.e2. doi:10.1016/j.jpeds.2012.03.062.Google Scholar
16. Graham, PL III, Begg, MD, Larson, E, Della-Latta, P, Allen, A, Saiman, L. Risk factors for late onset gram-negative sepsis in low birth weight infants hospitalized in the neonatal intensive care unit. Pediatr Infect Dis J 2006;25(2):113117. doi:10.1097/01.inf.0000199310.52875.10.Google Scholar
17. Niedner, MF, Huskins, WC, Colantuoni, E, et al. Epidemiology of central line–associated bloodstream infections in the pediatric intensive care unit. Infect Control Hosp Epidemiol 2011;32(12):12001208. doi:10.1086/662621.CrossRefGoogle ScholarPubMed
18. Blanchard, AC, Fortin, E, Rocher, I, et al. Central line–associated bloodstream infection in neonatal intensive care units. Infect Control Hosp Epidemiol 2013;34(11):11671173. doi:10.1086/673464.Google Scholar
19. Advani, S, Reich, NG, Sengupta, A, Gosey, L, Milstone, AM. Central line-associated bloodstream infection in hospitalized children with peripherally inserted central venous catheters: extending risk analyses outside the intensive care unit. Clin Infect Dis 2013;52(9):11081115. doi:10.1093/cid/cir145.CrossRefGoogle Scholar
20. Hocevar, SN, Edwards, JR, Horan, TC, Morrell, GOC, Iwamoto, M, Lessa, FC. Device-associated infections among neonatal intensive care unit patients: incidence and associated pathogens reported to the National Healthcare Safety Network, 2006–2008. Infect Control Hosp Epidemiol 2012;33(12):12001206. doi:10.1086/668425.CrossRefGoogle Scholar
21. MacFie, J, Reddy, BS, Gatt, M, Jain, PK, Sowdi, R, Mitchell, CJ. Bacterial translocation studied in 927 patients over 13 years. Br J Surg 2005;93(1):8793. doi:10.1002/bjs.5184.CrossRefGoogle Scholar
22. MacFie, J, O’Boyle, C, Mitchel, CJ, Buckley, PM, Johnstone, D, Sudworth, P. Gut origin of sepsis: a prospective study investigating associations between bacterial translocation, gastric microflora, and septic morbidity. Gut 1999;45:223228.Google Scholar
23. O’Boyle, C, MacFie, J, Mitchel, CJ, Johnstone, D, Sagar, PM, Sedman, AB. Microbiology of bacterial translocation in humans. Gut 1998;42:2935.Google Scholar
24. Taur, Y, Xavier, JB, Lipuma, L, et al. Intestinal domination and the risk of bacteremia in patients undergoing allogeneic hematopoietic stem cell transplantation. Clin Infect Dis 2012;55(7):905914. doi:10.1093/cid/cis580.CrossRefGoogle ScholarPubMed
25. Milisavljevic, V, Garg, M, Vuletic, I, et al. Prospective assessment of the gastroesophageal microbiome in VLBW neonates. BMC Pediatr 2013;13(1):11. doi:10.1371/journal.pbio.0050177.CrossRefGoogle ScholarPubMed
26. Cowan, ME, Frost, MR. A comparison between a detergent baby bath additive and baby soap on the skin flora of neonates. J Hosp Infect 1986;7:9195.Google Scholar
27. Polin, RA, Denson, S, Brady, MT; Committee on Fetus and Newborn; Committee on Infectious Diseases. Strategies for prevention of health care-associated infections in the NICU. Pediatrics 2012;129(4):e1085–e1093. doi:10.1542/peds.2012–0145.Google Scholar
28. Hull, MA, Jones, BA, Zurakowski, D, et al. Low serum citrulline concentration correlates with catheter-related bloodstream infections in children with intestinal failure. JPEN J Parenter Enteral Nutr 2011;35(2):181187. doi:10.1177/0148607110381406.Google Scholar
29. Ziegler, TR, Luo, M, Estívariz, CF, et al. Detectable serum flagellin and lipopolysaccharide and upregulated anti-flagellin and lipopolysaccharide immunoglobulins in human short bowel syndrome. Am J Physiol Regul Integr Comp Physiol 2008;294(2):R402R410. doi:10.1152/ajpregu.00650.2007.Google Scholar
30. Cole, CR, Hansen, NI, Higgins, R, et al. Bloodstream infections in very low birth weight infants with intestinal failure. J Pediatr 2012;160(1):5459.e2. doi:10.1016/j.jpeds.2011.06.034.CrossRefGoogle ScholarPubMed