Achiam CC, Fernandes CMB, McLeod SL, Salvadori M, John M, Seabrook JA, Theakston KD, Milburn S, Huss - PowerPoint PPT Presentation

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Achiam CC, Fernandes CMB, McLeod SL, Salvadori M, John M, Seabrook JA, Theakston KD, Milburn S, Huss

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Title: Achiam CC, Fernandes CMB, McLeod SL, Salvadori M, John M, Seabrook JA, Theakston KD, Milburn S, Huss


1
What Is the Prevalence of Methicillin-Resistant
Staphylococcus aureus in Skin and Soft Tissue
Infections presenting to the Emergency
Departments of a Canadian Academic Health Care
Center?
  • Achiam CC, Fernandes CMB, McLeod SL, Salvadori M,
    John M, Seabrook JA, Theakston KD, Milburn S,
    Hussain Z

June 7, 2009
2
Disclosure
X I do not have an affiliation (financial or
otherwise) with any commercial organization that
may have a direct or indirect connection to the
content of my presentation.
3
Background
  • 1960s Methicillin-resistant Staphylococcus
    aureus (MRSA) identified as a nosocomial pathogen
  • 1981 First Canadian case of MRSA reported
  • More recently, infections caused by MRSA have
    been identified in persons who have no known
    traditional risk factors, such as exposure to a
    health care facility
  • Community-acquired (CA) MRSA

4
CA- MRSA in the Emergency Department
  • Recent studies have shown
  • In United States, MRSA has emerged in many cities
    as the most common pathogen in skin and soft
    tissue infections (SSTIs)
  • 2003 Canadian Nosocomial Infection Surveillance
    Program (CNISP)
  • Data suggested that, in Canada, MRSA remains
    primarily a HA pathogen
  • Only 8 of cases community-acquired

5
CA- MRSA Canadian Emergency Departments
  • Borgundvaag, et al (2008) CJEM
  • 7 hospitals in the Greater Toronto Area
  • Of purulent SSTI caused by S. aureus 18 MRSA
  • No published study that prospectively examines
    the importance of CA-MRSA in managing purulent
    and non-purulent skin and soft tissue infections
    of all etiologies in the Canadian ED setting

6
Study Objectives
  • Primary Objective
  • Prospective observational study
  • Estimate the city-wide prevalence of MRSA and
    CA-MRSA
  • Adult patients (gt18yrs old)
  • Presenting with skin or soft tissue infections
    (SSTIs)
  • Emergency departments (EDs) of a Canadian
    academic tertiary care center

7
Study Objectives
  • Secondary Objectives
  • Identification of demographic and clinical
    variables associated with MRSA
  • Characterization of MRSA antimicrobial
    susceptibilities and genotypes

8
Methods
  • Prospective prevalence study
  • Approved by the Ethics Review Board at The
    University of Western Ontario
  • 3 Emergency departments in London, Ontario
  • 150,000 visits annually
  • Estimated sample size of 138 patients

9
Methods
  • Inclusion Criteria
  • gt 18 years of age
  • Diagnosed with any of the following skin or soft
    tissue infections
  • Cellulitis, necrotizing soft tissue infection,
    wound infection, ulcer, septic bursitis, acute
    lymphadenitis, pilonidal cyst without abscess,
    impetigo, or abscess (including furuncle,
    carbuncle, superficial skin abscess, paronychia,
    hordeolum, or pilonidal abscess)
  • Written, informed consent

10
Methods
  • Exclusion Criteria
  • Previously enrolled
  • Diagnosed with
  • Bartholin gland abscess, odontogenic infection,
    or perianal abscess

11
Methods
  • At enrolment, the following were obtained from
    each participant
  • Standardized health history and lifestyle
    questionnaire
  • Anterior nares and throat cultures
  • Infection site cultures

12
Statistical Analysis
  • Descriptive statistics were used to summarize
    patient characteristics and prevalence of MRSA
  • Patient characteristics associated with MRSA
    colonization or infection were determined with a
    backwards stepwise multivariate logistic
    regression model

13
Results
  • During 6 weeks from July to August 2008
  • 205 subjects enrolled
  • Mean (standard deviation) age was 45.3 (17.9)
    years
  • 52.2 Male

14
Results
  • Primary Outcome
  • 35 patients (17.1) were found to be infected or
    colonized with MRSA
  • 27 (13.2) patients were found to be infected /-
    colonized with MRSA
  • 8 (3.9) patients were found to be colonized with
    MRSA

15
Results
  • Primary Outcome
  • MRSA isolates were present in
  • 27 (13.2) infection site cultures
  • 21 (10.2) of the nares cultures
  • 12 (5.8) of the throat cultures
  • S aureus grew in 38.0 of infection site cultures
  • 34.6 MRSA

16
Results
  • Secondary Outcomes
  • Genotype
  • All 35 patients infected or colonized with MRSA
    had at least one isolate genotyped
  • Twenty-seven (77) had isolates identified as
    CMRSA 10 (USA 300), a recognized
    community-acquired strain of MRSA

17
Results- Antimicrobial Susceptibilities
18
Results Univariate Analysis of Predictor
Variables
  • Variables associated with colonization
  • Currently homeless
  • Variables associated infection
  • Currently homeless
  • Age 18-44 years
  • Incarcerated in past yr
  • Physical contact with incarcerated person in last
    year
  • Know anyone else with skin infection
  • Competitive sports
  • Known exposure to MRSA
  • Previous abscess within past year
  • IV drug user
  • Purulent skin infection currently

19
Results Table 2
20
Results Table 3
21
Limitations
  • Prevalence and clinical predictors of MRSA may
    lack of external validity to other times of year,
    practice settings and communities
  • Estimated prevalence of MRSA can not be
    generalized to our overall ED population
  • Definitive conclusions about the pathogenic
    etiology of participants with pure cellulitis can
    not be drawn from our data

22
Implications
  • In appropriate patients with SSTIs
  • MRSA coverage should be considered when choosing
    empiric antimicrobial therapy

23
Implications
  • Cultures of purulent SSTI are not part of routine
    care in many EDs
  • Recommended by The Centers for Disease Control
    and Prevention
  • We suggest that all SSTI with purulent drainage
    should be sent for culture to
  • Definitively identify the pathogenic organism
  • Track the changing epidemiology and antimicrobial
    susceptibility of MRSA in the community
  • Reduce nosocomial infections

24
Thank you
25
(No Transcript)
26
Future Areas of Research
  • External validation of patient characteristics
    identified as risk factors for MRSA
    carriage/infection
  • May lead to a clinical algorithm to guide
    empirical antibiotic therapy
  • Best practice for empiric antimicrobial therapy
    in patients suspected of being infected with MRSA

27
Sample Size Estimate
  • Sample Size Estimate
  • n Z2 P (1-P)
  • d2
  • Assuming Power of 80
  • Estimated MRSA prevalence of 10 based on a local
    retrospective review
  • Desired precision level of 5
  • To be 95 confident that the true proportion of
    MRSA positive patients was between 5 and 15
  • Estimated 138 patients needed to be enrolled in
    the study
  • Decided to increase our sample size by 10 to
    account for potential missing data from the
    questionnaire

28
Clinical Definition of CA-MRSA
  • Community-dwelling persons without risk factors
    for HA-MRSA
  • Hospitalization or surgery within the previous
    year, residence in a nursing facility, dialysis,
    or presence of an indwelling bladder catheter
  • 68.6 fit the clinical definition for CA-MRSA
  • 11 patients did not meet the definition
  • 10 hospitalized within last 12 months
  • 1 indwelling bladder catheter

29
Estimated Enrollment at Each Site
  • University Hospital ED
  • 96 patients diagnosed with SSTI
  • 11 enrolled (11.5)
  • Victoria Hospital ED
  • 126 patients diagnosed with SSTI
  • 81 enrolled (64.3)
  • St. Josephs Health Care Urgent Care Center
  • 244 Patients diagnosed
  • 113 enrolled (46.3)

30
Statistical Analysis
  • Statistical Analysis of Patient Characteristics
  • Descriptive statistics were used to summarize
    patient characteristics and MRSA prevalence with
    95 confidence intervals (CIs)
  • Using contingency tables, univariate analysis was
    conducted for each independent variable collected
    in the health history and lifestyle questionnaire
  • The likelihood ratio chi-square test with k-1
    degrees of freedom was used to measure the level
    of association between the dichotomous outcome
    variable (whether or not a patient was MRSA) and
    primary predictor variables.
  • In the univariate analysis, variables with a p
    value lt 0.1 were found to be associated with
    being colonized or infected with MRSA were
    considered in the multivariate logistic
    regression model
  • Likelihood ratio tests were then used to
    determine the appropriate inclusion of variables
    in the model.
  • Backwards stepwise logistic regression (using a
    likelihood ratio removal criterion of 0.1) was
    used to obtain odds ratios with 95 confidence
    intervals for the final model

31
Types of SSTI with MRSA Isolates on Infection
Site Culture
32
Genotypic Concordance
  • 27 subjects with MRSA at infection site
  • 15 (55.6) colonized with MRSA
  • 13 (86.7) had genetic typing of a colonized site
    infection site
  • 5 (38.5) had genetically identical clones in all
    3 sites
  • 8 (61.5) had genetically identical clones in at
    least 2 sites
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