Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-04T21:49:17.907Z Has data issue: false hasContentIssue false

An Outbreak of Methicillin-Resistant Staphylococcus aureus Infections Related to Central Venous Catheters for Hemodialysis

Published online by Cambridge University Press:  02 January 2015

Sai-Cheong Lee*
Affiliation:
Division of Infectious Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Kuo-Su Chen
Affiliation:
Department of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Chi-Jen Tsai
Affiliation:
Department of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Ching-Chang Lee
Affiliation:
Department of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Hung Yu Chang
Affiliation:
Department of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Lai-Chu See
Affiliation:
Department of Public Health, Chang Gung University, Linkou, Taiwan, Republic of China
Yu-Chin Kao
Affiliation:
Division of Infectious Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Shu-Chu Chen
Affiliation:
Division of Infectious Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
Cheng-Hsu Wang
Affiliation:
Department of Internal Medicine, Chang Gung Memorial Hospital, Keelung, Taiwan, Republic of China
*
Division of Infectious Diseases, Chang Gung Memorial Hospital, 222 Mai Chin Road, Keelung, Taiwan, Republic of China

Abstract

Objectives:

To determine risk factors for hemodialysis catheter-related bloodstream infections (HCRBSIs) and investigate whether use of maximal sterile barrier precautions would prevent HCRBSIs.

Setting:

Tertiary-care medical center hemodialysis unit.

Design:

Open trial with historical comparison and case-control study of risk factors for HCRBSIs.

Methods:

Prospective surveillance was used to compare HCRBSI rates for 1 year before and after implementation of maximal sterile barrier precautions. A case–control study compared 50 case-patients with HCRBSI with 51 randomly selected control-patients.

Results:

The HCRBSI rate was 1.6% per 100 dialysis runs (CI95, 1.1%–2.3%) in the first year and 0.77% (CI95, 0.5%–1.1%) in the second year (P = .0106). The most frequent cause of HCRBSI was MRSA in the first year (15 of 32) and MSSA in the second year (13 of 18). Ten MRSA blood isolates in the first year were identical by PFGE. Diabetes mellitus was a risk factor for HCRBSI. Age, gender, site of hemodialysis central venous catheter (CVC), other underlying diseases, coma score, APACHE II score, serum albumin level, and cholesterol level were not associated with HCRBSI and did not change between the 2 years. Hospital stay was prolonged for case-patients (32.78 ± 20.96 days) versus control-patients (22.75 ± 17.33 days), but mortality did not differ.

Conclusions:

Use of maximal sterile barrier precautions during the insertion of CVCs reduced HCRBSIs in dialysis patients and seemed cost-effective. Diabetes mellitus was associated with HCRBSI. An outbreak of MRSA in the first year was likely caused by cross-infection via medical personnel.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2004

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

1.Churchill, DN, Taylor, DW, Cook, RJ, et al.Canadian hemodialysis morbidity study. Am J Kidney Dis 1992;19:214234.Google Scholar
2.Hoen, B, Kessler, M, Hestin, D, Mayeux, D. Risk factors for bacterial infections in chronic hemodialysis adult patients: a multicenter prospective survey. Nephrol Dial Transplant 1995;10:377381.Google Scholar
3.Taylor, GD, McKenzie, M, Buchanan-Chell, M, et al.Central venous catheters as a source of hemodialysis-related bacteremia. Infect Control Hosp Epidemiol 1998;19:643646.Google Scholar
4.Mermel, LA, McCormick, RD, Springman, SR, Maki, DG. The pathogenesis and epidemiology of catheter-related infection with pulmonary artery Swan-Ganz catheters: a prospective study utilizing molecular subtyping. Am J Med 1991;91(suppl 3B):197S205S.CrossRefGoogle ScholarPubMed
5.Raad, II, Hohn, DC, Gilbreath, BJ, Suleiman, N, Hill, LA, Bruso, PA. Prevention of central venous catheter-related infections by using maximal sterile barrier precautions during insertion. Infect Control Hosp Epidemiol 1994;15:231238.Google Scholar
6.Banerjee, SN, Emori, TG, Culver, DH, et al.Secular trends in nosocomial primary bloodstream infections in the United States, 1980-1988. Am J Med 1991;91(suppl 3B):86S89S.Google Scholar
7.Cheesbrough, JS, Finch, RG, Burden, RP. A prospective study of the mechanism of infection associated with hemodialysis catheters. J Infect Dis 1986;154:579589.Google Scholar
8.Chow, JW, Sorkin, M, Goetz, A, Yu, VL. Staphylococcal infections in the hemodialysis unit: prevention using infection control principles. Infect Control Hosp Epidemiol 1988;9:531533.Google Scholar
9.Pearson, ML, Hierholzer, WJ, Mayhall, CG, et al.Guideline for prevention of intravascular device-related infections. Am J Infect Control 1996;24:262293.Google ScholarPubMed
10.Timsit, JF. Scheduled replacement of central venous catheters is not necessary. Infect Control Hosp Epidemiol 2000;21:371374.Google Scholar
11.Kloos, WE, Bannerman, TL. Manual of Clinical Microbiology, ed. 7. Washington, DC: American Society of Microbiology; 1999:264-282, 442-458, 517525.Google Scholar
12.Knaus, WA, Draper, EA, Wagner, DP, Zimmerman, JE. APACHE II: a severity of disease classification system. Crit Care Med 1985;13:818829.CrossRefGoogle ScholarPubMed
13.Tenover, FC, Albeit, RD, Goering, RV, et al.Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995;33:22332239.Google Scholar
14.Dice, LR. Measures of the amount of ecological association between species. Ecology 1945;26:297302.Google Scholar
15.Maki, DG, Weise, CE, Sarafin, HW. A semi-quantitative culture method for identifying intravenous catheter-related infections N Engl J Med 1977;296:13051309.Google Scholar
16.Maki, DG, Ringer, M, Alvarado, CJ. Prospective randomized trial of povidone-iodine alcohol, and chlorhexidine for prevention of infection associated with central venous and arterial catheters. Lancet 1991;38:339343.Google Scholar
17.Fridkin, SK, Pear, SM, Williamson, TH, Galgiani, JN, Jarvis, WR. The role of understaffing in central venous catheter-associated bloodstream infections. Infect Control Hosp Epidemiol 1996;17:150158.Google Scholar
18.Beck-Sague, CM, Jarvis, WR. Epidemic bloodstream infections associated with pressure transducers: a persistent problem. Infect Control Hosp Epidemiol 1989;10:5459.Google Scholar
19.Snydman, DR, Murray, SA, Kornfeld, SJ, Majka, JA, Ellis, CA. Total parenteral nutrition-related infections: prospective epidemiologic study using semiquantitative methods. Am J Med 1982;73:695699.Google Scholar
20.Freeman, JB, Lemire, A, Maclean, LD. Intravenous alimentation and septicemia. Surgery, Gynecology and Obstetrics 1972;135:708712.Google ScholarPubMed
21.Nehme, AE. Nutritional support of the hospitalized patient: the team concept. JAMA 1980;243:19061908.Google Scholar
22.Faubion, WC, Wesley, JR, Khalidi, N, Silva, J. Total parenteral nutrition catheter sepsis: impact of the team approach. JPEN J Parenter Enteral Nutr 1986;10:642645.Google Scholar
23.Nelson, DB, Kien, CL, Mohr, B, Frank, S, Davis, SD. Dressing changes by specialized personnel reduce infection rates in patients receiving central venous parenteral nutrition. JPEN J Parenter Enteral Nutr 1985;10:220222.Google Scholar
24.Raad, I, Abi-Said, D, Carrasco, CH, Umphrey, J, Hill, LA. The risk of infection associated with intra-arterial catheters for cancer chemotherapy. Infect Control Hosp Epidemiol 1998;19:640642.CrossRefGoogle ScholarPubMed