Methicillin-Resistant Staphylococcal Colonization and Infection in a Long-Term Care Facility

Abstract

Objective: To determine the natural history of colonization by methicillin-resistant Staphylococcus aureus (MRSA) among patients in a long-term care facility. We specifically sought to determine if MRSA colonization was predictive of subsequent infection.

Design: Cohort study.

Setting: Long-term Veterans Affairs Medical Center.

Patients: A total of 197 patients residing on two units were followed with regular surveillance cultures of the anterior nares.

Main Outcome Measurement: The development of staphylococcal infection.

Results: Thirty-two patients were persistent carriers of MRSA and 44 were persistent carriers of methicillin-susceptible strains (MSSA). Twenty-five percent of MRSA carriers had an episode of staphylococcal infection compared with 4% of MSSA carriers and 4.5% of non-carriers (P < 0.01; relative risk 3.8; 95% CI, 2.0 to 6.4). The rate of development of infection among MRSA carriers was 15% for every 100 days of carriage. Using logistic regression analysis, persistent MRSA carriage was the most significant predictor of infection (P < 0.001; odds ratio, 3.7). Seventy-three percent of all MRSA infections occurred among MRSA carriers. Isolates of MRSA from 7 patients were typed. Colonizing and infecting strains had the same phage type in all 7 patients and the same pattern of plasmid EcoRI restriction endonuclease fragments in 5 patients.

Conclusions: Colonization of the anterior nares by MRSA predicts the development of staphylococcal infection in long-term care patients; most infections arise from endogenously carried strains. Colonization by MRSA indicates a significantly greater risk for infection than does colonization by MSSA. The results offer a theoretic rationale for reduction in MRSA infections by interventions aimed at eliminating the carrier state.

Article and Author Information

  • From the Pittsburgh Veterans Affairs Medical Center, Pittsburgh, Pennsylvania; University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; and the Centers for Disease Control, Atlanta, Georgia. For current author addresses, see end of text.

  • Requests for Reprints: Robert R. Muder, MD, Infectious Disease Section, Veterans Affairs Medical Center, University Drive C, Pittsburgh, PA 15240.

  • Current Author Addresses: Drs. Muder and Yu, Ms. Brennen, Ms. Wagener, Mr. Vickers, Mr. Rihs, and Mr. Yee: Veterans Affairs Medical Center, University Drive C, Pittsburgh, PA 15240. Mr. Hancock: Centers for Disease Control, Building 5, Room 210, Atlanta, GA 30333.

    Dr. Miller: Centers for Disease Control, Building 1, B341, COl, Atlanta, GA 30333.

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