Maryland Acute Care Hospitals Michael McAllaster 2011-2012 PHASE - - PowerPoint PPT Presentation

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Maryland Acute Care Hospitals Michael McAllaster 2011-2012 PHASE - - PowerPoint PPT Presentation

The Prevalence of Carbapenem Resistant Enterobacteriaecea in Maryland Acute Care Hospitals Michael McAllaster 2011-2012 PHASE Internship Overview Organization of PHASE and DHMH Internship Carbapenem-resistant Enterobacteriaceae


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The Prevalence of Carbapenem Resistant Enterobacteriaecea in Maryland Acute Care Hospitals

Michael McAllaster 2011-2012 PHASE Internship

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Overview

  • Organization of PHASE and DHMH Internship
  • Carbapenem-resistant Enterobacteriaceae
  • Objectives
  • Methods
  • Results
  • Discussion: Public health implications,

challenges limitations and lessons learned

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Organization: PHASE and Maryland Department of Health and Mental Hygiene

Internship Maryland Department of Health and Mental Hygiene Emerging Infections Program Healthcare Associated Infections Johns Hopkins School of Public Health PHASE

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Carbapenem

  • β-lactam antimicrobial

agents with a broad spectrum of activity

  • Inhibit bacterial cell

wall synthesis

  • Include: Imipenem,

meropenem, etrapenem, doripenem and razupenem

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Resistant

  • Class of bacterial enzymes that inactivate

carbapenem antibiotics called carbapenemases

  • Plasmid mediated
  • Carbapenemases first found in Klebsiella

pneumoniae (KPC)

  • Found in other organisms:

– Proteus, Salmonella, Citrobacter, Serrratia

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Enterobacteriaecea

  • Stain Gram-negative, facultative anaerobes
  • Found in normal human flora in the gastrointestinal tract

Carbapenem Resistant Enterobacteriaecea Gram negative bacteria carrying genes that confer resistance to carbapenem antibiotics Or CRE

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CRE is a Healthcare Associated Infection (HAI)

  • In 2002, HAIs accounted for 99,000 deaths

and a financial burden of $28-33 billion in excess healthcare spending1

  • Increasing incidence of CRE in tertiary care

centers, hospitals and nursing homes2-4

  • High mortality rates among CRE infected

patients, even higher in long term care facilities5

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CRE in the United States, 2011

Yellow: Confirmed CRE cases caused by the KPC enzyme. Blue dot: confirmation of CRE caused by the NDM-1 enzyme. Orange dot: CRE caused by a VIM or IMP enzyme.

Centers for Disease Control and Prevention, 2011.

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CRE in Maryland Acute Care Hospitals, 2010

Southern – 9 (2%) Central – 394 (68%) Capital - 114 (20%) Eastern Shore – 33 (6%) Western - 22 (4%)

0-5 6-15 16-68 2 4 6 8 10 12 14 16 18

Number of Maryland Hospitals Number of CRE+ Individuals Distritbution of CRE Cases in Maryland Hospitals September 2009 - August 2010

  • 572 CRE positive patients from 42 reporting hospitals (36 clinical laboratories)
  • Mean number of cases was 14
  • Heterogeneous surveillance
  • Wide distribution

Patricia Lawson, David Blythe, et al. 2011

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Objectives

  • Survey the prevalence of CRE in acute care

hospitals in Maryland from September 2010 to August 2011

  • Survey the methods to detect and confirm

CRE in clinical specimens in Maryland

  • Compare the prevalence of cases observed in

Maryland from 2010 to 2011

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Project Timeline

April 2012 – May 2012 Analyze data Interpret results January 2012 – March 2012 Data entry Follow-up with clinical laboratories October 2011 – December 2011 Finalize survey Disseminate survey

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Methods: Survey

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Methods: Dissemination of Survey

  • There are 36 clinical laboratories serving 42

Maryland acute care hospitals

  • Distributed to clinical laboratory staff of

Maryland acute care hospital microbiology laboratories at 2011 Laboratory Response Network Sentinel Laboratory Bioterrorism Preparedness Training

  • Three follow up phone calls or e-mails per

clinical laboratory

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2011 CRE Prevalence Survey Results

10 20 30 40 50 60 70 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z AA BB CC DD EE FF GG HH II NUMBER OF CRE POSITIVE CASES Maryland Acute Care Hospital

36 reporting hospitals 21 clinical laboratories 269 CRE positive patients Mean: 8 Median: 3 Mode: 0

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Southern – 9 (2%) Central – 394 (68%) Capital - 114 (20%) Eastern Shore – 33 (6%) Western - 22 (4%)

Western – 1 (0.4%) Capital – 13 (5%)

  • Central – 193 (71%)

Southern – 22 (8%) Eastern Shore – 40 (15%)

Distribution of CRE in Maryland Acute Care Hospitals 2011

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CRE Clinical Laboratory Testing Methods, 2011

Test Category Laboratory Test Number (%) laboratories performing tests Automated Automated antibiotic susceptibility (Vitek, Microscan, Phoenix) 14 (67%) Manual Manual screening (E-test) 2 (10%) Manual Kirby-Bauer (disk diffusion) 1 (5%) Confirmatory Modified Hodge Test 14 (67%) Confirmatory PCR 1 (5%) Confirmatory Reference Laboratory (confirmatory testing) 4 (19%) Unknown Unknown screening test 2 (10%)

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CRE Case Comparison 2010 vs. 2011

2 4 6 8 10 12 14 16 18 <10 10 to 20 20 to 30 30 to 40 60 to 70 Number of Maryland Hospitals Number of CRE+ Individuals 2010 2011

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Limitations and Challenges

  • Data collection

– Non-responders – Out of phase with clinical lab reporting cycle – Electronic queries, 86% have capability

  • Project timeline beyond PHASE internship

– Policy implications – 2012 survey

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Policy and Practice Implications

  • CRE is not a reportable disease in Maryland

– Not reportable nationally – Variable response by clinical labs to a CRE positive case

  • Standardized testing

– Feasible?

  • 2012 CRE Survey

– Leave it to the epidemiologists? – A single survey for all HAIs – MuGSI

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Lessons Learned

  • Public health practice is challenging
  • Public health practice is rewarding
  • Friday outbreak meetings are cool!

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Acknowledgements

DHMH Brenda Roup, PhD, RN, CIC Patricia Lawson, MPH, MSN, RN, CIC Malorie Givan, MPH Katie Richards, MPH Lucy Wilson, ScM, MD PHASE Dipti Shaw, MPH Patricia Truant

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References

1. Public Health update of Carbapenem-Resistant Enterobacteriaceae (CRE) producing metallo-beta- lactamases (NDM, VIM, IMP) in the U.S. reported to CDC. http://www.cdc.gov/HAI/organisms/cre.html. Accessed April 10, 2012.

2. Perez, F. et al. Carbapenem-resistant Acinetobacter baumannii and Klebsiella pneumoniae across a hospital system : impact of post-acute care facilities on dissemination. Access 1807-1818 (2010).doi:10.1093/jac/dkq191 3. Endimiani, A. et al. Characterization of bla KPC -containing Klebsiella pneumoniae isolates detected in different institutions in the Eastern USA. Journal of Antimicrobial Chemotherapy 427-437 (2009).doi:10.1093/jac/dkn547 4. Endimiani, A. et al. Emergence of bla KPC -containing Klebsiella pneumoniae in a long-term acute care hospital : a new challenge to our healthcare system. Journal of Antimicrobial Chemotherapy 1102-1110 (2009).doi:10.1093/jac/dkp327 5. Investigation, O. Rapid Spread of Carbapenem-Resistant. 165, 1430-1435 (2012). 6. Bonomo, R. a New Delhi metallo-β-lactamase and multidrug resistance: a global SOS? Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 52, 485-7 (2011). 7. Sidjabat, H. et al. Carbapenem resistance in Klebsiella pneumoniae due to the New Delhi Metallo-β-lactamase. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 52, 481-4 (2011). 8. Crespo, M.P. et al. Outbreak of Carbapenem-Resistant Pseudomonas aeruginosa Producing VIM-8 , a Novel Metallo- ␤ -Lactamase , in a Tertiary Care Center in Cali , Colombia. Society 42, 5094-5101 (2004). 9. Siegel, J.D. et al. Management of Organisms In Healthcare Settings , 2006. Infection Control 1-74 (2006). 10. Nordmann, P., Gniadkowski, M., Giske, C. G., Poirel, L., Woodford, N., Miriagou, V. and the European Network on Carbapenemases (2012), Identification and screening of carbapenemase-producing Enterobacteriaceae. Clinical Microbiology and Infection, 18: 432–438. doi: 10.1111/j.1469-0691.2012.03815.x 11. Performance Standards for Antimicrobial Susceptibility Testing ; Twenty-First Informational Supplement. Control 31, (2011).

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Questions?