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. Author manuscript; available in PMC: 2021 Apr 29.
Published in final edited form as: Infect Control Hosp Epidemiol. 2013 Dec 3;35(1):31–41. doi: 10.1086/674385

TABLE 1.

Description of Studies included in Meta-Analysis

Variable Seybold et al32 Carrillo-Marquez et al22 Kempker et al27 Kreisel et al10 Haque et al33 Lessa et al20 Tattevin et al34 Sherwood et al35
Study year 2006 2010 2010 2011 2012 2012 2012 2013
Location Grady Memorial Hospital, Atlanta, GA Texas Children’s Hospital, Houston, TX Emerging Infections Program, Atlanta, GA Baltimore, MD; Buffalo, NY; Washington DC; Richmond, VA University of Louisville, KY; Ohio State University Medical Center, OH; Henry Ford Health System, MI; University of Miami/Jackson Memorial Hospital, FL; Summa Health System, OH Active Bacterial Core Surveillance (ABCs) system, CA, CO, GA, MI, NY, TN San Francisco General Hospital (public, tertiary care) and 13 city-wide outpatient clinics Walter Reed Army Medical Center and National Naval Medical Center
No. of centers Single Single 8 4 5 6 14 2
Study population All age groups; MRSA bacteremia Neonates, infants, children; SA-CRB All age groups; MRSA bacteremia Adults, older (≥65 years); MRSA bacteremia Adults, older (≥65 years); MRSA pneumonia (HAP, VAP, or HCAP) All age groups; invasive MRSA infection (CLABSI and PNEUMO) All age groups ≥5 years; MRSA BSI Adults, older (≥65 years); MRSA BSI
Study design Prospective cohort Prospective cohort Prospective cohort Retrospective cohort Retrospective cohort Prospective cohort Retrospective cohort Retrospective cohort
Comparison group/non-USA300 USA100, USA500, USA800 USA100, USA200, USA400, USA700, USA800, unique USA100, USA500, other (<1%) One half USA100 USA100, USA600, other USA100 USA100, USA1000, USA500, USA1100, Other (3%) Predominantly USA100
Staphylococcus aureus typing method PFGE, SCC mec, PCR for PVL, phenotyping PFGE, SCCmec, PCR for agr typing and PVL, phenotyping PFGE PCR for PVL, ACME, and spa typing, PFGE (used for validation), phenotyping PFGE, SCCmec, PCR for agr typing and PVL, phenotyping PFGE PCR for PVL, ACME, and spa typing, PFGE (used for validation), MLST PFGE phenotyping
No. identified with S. aureus invasive infection 132a 112 4,344b 271 251 336 549 245c
No. (%) with USA300 39 (33.6) 12 (41.4) 414 (37.5) 67 (25) 60 (23.9) 90 (26.8) 304 (55.37) 30 (19.87)
No. (%) with non-USA300 77 (66.4) 17 (58.6) 690 (62.5) 204 (75) 191 (76.1) 246 (73.2) 245 (44.63) 121 (80.13)
Mortality measured Crude in-hospital mortality Crude in-hospital mortality In-hospital mortality 90-day mortality 28-day all-cause mortality Attributable mortality within 30 days in hospital Attributable mortality Crude in-hospital mortality
Mortality no./total mortality (%) in invasive infections
USA300 3/25 (12) 2/5 (40) 68/204 (33.33) 20/121 (16.53) 16 (26.7) 19/102 (18.63) 24/47 (51.06) 5/30 (16.67)
Non-USA300 22/25 (88) 3/5 (60) 136/204 (66.67) 101/121 (83.47) 77 (40.3) 83/102 (81.37) 23/47 (48.94) 21/121 (17.35)

NOTE. ACME, arginine catabolic mobile element; agr, accessory gene regulator; BSI, bloodstream infection; CLABSI, central line-associated bloodstream infection; HAP, hospital-associated pneumonia; HCAP, healthcare-associated pneumonia; MLST, multilocus sequence typing; PCR, polymerase chain reaction; PFGE, pulsed-field gel electrophoresis; phenotyping, antibiotic susceptibility testing; PNEUMO, community-onset pneumonia; PVL, Panton-Valentine leukocidin; SA-CRB, S. aureus catheter-related bacteremia; SCCmec, staphylococcal cassette chromosome mec element; VAP, ventilator-associated pneumonia.

a

Final analysis included only 116 isolates.

b

Final analysis included 1,104 isolates typed by PFGE for USA300 vs non-USA300.

c

Final analysis included only 151 isolates.