Journal List > Ann Clin Microbiol > v.16(2) > 1078490

Hong, Kim, Park, Kim, and Kim: Active Surveillance for Multidrug-resistant Organisms

초록

Infections and outbreaks of antimicrobial-resistant ba-cteria, such as methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enteroco-ccus (VRE), have been increasing. Detection methods for antimicrobial-resistant bacteria have been changed from traditional culture methods to chromogenic media culture and molecular methods. Strain- typing methods using various molecular technologies are essential tools for epidemiologic surveillance. Furthermore, outbreak detection, using syndromic surveillance as well as passive and active surveillance, has been applied. However, it is difficult to establish effective and robust guidelines and systems for using these various methods to control antimicrobial-resi-stant bacteria. Therefore, clinical microbiologists and policy makers must possess expertise in the control of antimicrobial resistant bacteria, discuss the issue sufficiently, and, finally, create a system to accom-plish this control.

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Fig. 1.
Syndromic surveillance: rationale for early detection. *Time between detection by syndromic (prediagnostic) surveillance and detection by traditional (diagnosis-bases) surveillance. Figure is adapted from MMWR, 2004;53.
acm-16-53f1.tif
Fig. 2.
Legislative maps of methicillin-resistant Staphylococcus aureus in the United States. Figure is adapted from http://apic.org.
acm-16-53f2.tif
Table 1.
Sensitivity and specificity of currently available chromogenic media and molecular assays for methicillin-resistant Staphylococcus aureus
Direct inoculation or OE, h of incubation % sensitivity % specificity Reference
Chromogenic media
  ChromID Direct, 16-24 h 51.0-76.0 95.0-99.5 [7], [9], [11,12]
Direct, 42-48 h 77.0-90.0 85.6-98.0 [7], [12,13]
OE, 24 h 93.0-94.0 100.0 [9], [12]
  MSRA Select Direct, 16-24 h 65.0-99.0 98.0-100.0 [6], [8-12]
Direct, 42-48 h 60.0-100.0 66.0-99.3 [6], [8,9], [11,12]
OE, 24 h 96.0   [12]
  CHROMagar MRSA Direct, 16-24 h 40.0-82.9 88.0-100.0 [7], [9-11], [13]
Direct, 42-48 h 72.0-79.0 79.0-97.0 [9], [11], [13]
OE, 24 h 95.0 99.0 [9]
  ORSAB Direct, 16-24 h 47.0-91.9 67.0-99.0 [6,7], [9], [12,13]
Direct, 42-48 h 67.0-96.0 68.0-98.0 [6,7], [9], [12,13]
OE, 24 h 91.0   [12]
  Chromogen Oxacillin Direct, 24 h 1.0 5.0 [12]
  S. aureus medium Direct, 48 h 53.0 80.0 [12]
Molecular assay
  Hyplex StaphyloResist Direct 91.7 90.0 [14]
OE, 18 h 97.6 83.7 [18]
  LC Staphylococcus/ OE, 24 h 95.7 90.8 [16]
LC MRSA detection
  IDI-MRSA/ Direct 80.0-100.0 89.0-99.0 [11], [17], [19-21]
    GeneOhm MRSA OE, 24 h 96.0 96.0 [22]
  Genotype MRSA direct Direct 68.0-94.6 96.0-98.7 [11], [12], [15]
  GeneXpert MRSA Direct 94.3 93.2 [23]

Table is adapted from Malhotra-Kumar et al., 2008.

Abbreviation: OE, overnight enrichment.

Table 2.
Required elements of an effective active surveillance program
Screening test
  Must be timely, affordable, and reliable
Clinical efficacy
  Should reduce transmission rate to patients and healthcare workers
  Should reduce infection rate by preventing acquisition
Implementation
  Hospital and administrative financial support
  Systems and staff to screen patients
  Systems and staff to monitor effectiveness and compliance
  Education of patients, staff, and families
  Adequate physical plant and supplies
  (e.g., private rooms, gloves, gowns, and antimicrobial agents)
  Plan to manage social isolation and safety of patients under contact precautions

Table isadapted from Weber et al., 2007.

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