Antimicrobial stewardship program - School of Medicinesom.uci.edu/hospitalist/pdfs...
Transcript of Antimicrobial stewardship program - School of Medicinesom.uci.edu/hospitalist/pdfs...
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Antimicrobial Stewardship
Steven Park, MD/PhD
Associate Professor of Clinical Medicine
Director, Antimicrobial Stewardship Program
Director, Fellowship Program
Division of Infectious Diseases
UCI Medical Center
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Objectives
Review UCI Antimicrobial Stewardship Program (ASP)
Review Rapid Disc Diffusion Susceptibility Testing for GNR bacteremia
Discuss future plans for UCI ASP (focus on Hospitalist Teams)
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• Formulary restriction Certain antimicrobials require justification or approval from a designated
gatekeeper
• Prospective audit Post-prescription review of appropriateness of antibiotic use Performed at 48-72 hours after initial prescription
• Clinical guidelines and education Multi-disciplinary, evidence based guidelines on optimal treatment of
various infections Based on local antibiogram Educational lectures to specific subspecialties
• Others Computerized order entry and surveillance systems (EPIC) Rapid diagnostics (direct sensitivity, ACCELERATE) Biomarkers (pro-calcitonin) Antibiotic time out Allergy assessment Quality improvement projects (carbapenems and UTI’s)
UCI Antimicrobial Stewardship Program
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The California Antimicrobial Stewardship Program Initiative
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Antimicrobial Use at UCI
Stewardship interventions begin
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Stewardship interventions begin
Antimicrobial Use at UCI
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Antimicrobial Use at UCI
Stewardship interventions begin
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QI Project: Targeting carbapenem use for UTI’s
ID division performed literature review on efficacy of non-carbapenems (cefepime, Zosyn) for treatment of urinary tract infections (including bacteremia) with ESBL pathogens
Concluded that cefepime and Zosyn are effective and ID would no longer approve carbapenems if the urine ESBL pathogen is sensitive to cefepime or Zosyn even with bacteremia
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Carbapenem Use
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Rapid Disc Diffusion Susceptibility Testing for GNR bacteremia (RDDT)
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Advantage: Faster by 24-36 hours
Disadvantage: Not standardized, less experience, not CLSI approved.
How well does it correlate with standardized Kirby Bauer (DD) and Vitek tests?
RDDT: Advantages and Disadvantages
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Comparison of RDDT and Vitek and Kirby Bauer (DD)
Results - interpretation
• Agreement (A): rapid sens = DD/Vitek
• Very Major (VM): rapid sens (S) DD/Vitek (R)
• Major (M): rapid sens (R) DD/Vitek (S)
• minor (m): other discrepancies
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Rapid Disc Diffusion Susceptibility Testing for GNR bacteremia
Pilot study looking at 106 positive blood cx with GNR from July 2015 to Oct 2015
Rapid Disc Diffusion Susceptibility Testing conducted by the Microbiology laboratory in addition to standard susceptibility testing (Kirby Bauer (DD) and Vitek)
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Reference Control N % of Total
CLSI Disc Diffusion Discrepancies
Very Major (VM) 2 0.1
Major (M) 26 1.4
Minor (m) 188 10.1
Complete Agreement (A) 1644 88.4
Total 1860 100
Reference Control N % of Total
Vitek Discrepancies
Very Major (VM) 2 0.1
Major (M) 37 2.2
Minor (m) 146 8.9
Complete Agreement (A) 1463 88.8
Total 1648 100
*2 VM: TMP/SMX for Enterobacter, and Tobra for ESBL E.coli
Rapid Sens compared to Disc Diffusion and Vitek (N=106)
*2 VM: Amp/SBT for E.coli and imipenem for proteus
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The median time from BC positivity to RDDDT report was 17.5 hrs vs. 46 hrs for VITEK.
72/162 cases (44%) required antibiotic change with median time to optimization of 21 hrs based on RDDDT vs. 71 hrs based on prior baseline VITEK.
RDDT led to faster de-escalations but more escalations than Vitek RDDT was over calling resistance
Rapid Disc Diffusion Susceptibility Testing and ASP Intervention for GNR bacteremia
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Accelerate Pheno™ system
• The Accelerate Pheno™ system uses a broad panel of fluorescence in-situ hybridization assays for microorganism identification.
• Morphokinetic Cellular Analysis (MCA) using time-lapse imaging for antimicrobial susceptibility testing (AST).
• The system can identify 16 organisms (six Gram positive and eight Gram negative bacteria as well as two Candida species) from positive blood cultures.
• It provides results in 1.25 hours for identification (ID), and AST and resistance phenotypes in about 7 hours.
• FDA approved • UCI Microbiology currently testing
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Future ASP activities
ASP newsletter
Antibiotic allergy de-labelling (collaboration with Allergy and Immunology)
Comprehensive ID order set for EPIC
Physician dashboard providing feedback on antimicrobial use for individual physicians
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Hospitalist Teams and Stewardship
2015-2016 academic year: 97/549 interventions made by ASP including Family and IM for a rate of 17.6% 2017 year: 167/1067 interventions made by ASP for a rate of 15.6%
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How can we improve?
Skin/soft tissue infection Health care associated pneumonia Correlates with meeting metrics for PRIME
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Management of Skin/Soft Tissue Infection IDSA Practice Guidelines 2014
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Skin and Soft Tissue Infections: Proposal
No need to add vancomycin for cases of cellulitis given: • No purulent drainage • No evidence of abscess by exam and ultrasound (ED)
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Healthcare Associated Pneumonia
Overly broad and HCAP removed from 2016 IDSA practice guidelines for HAP AND VAP
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Healthcare Associated Pneumonia: Proposal
Retrospective chart review to identify risk factors for pseudomonas or MRSA pneumonia admitted to the hospital (not HAP or VAP)
If there are risk factors, cases undergo sputum collection in the ED
If sputum negative, antibiotics de-escalated or discontinued
Procalcitonin
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Procalcitonin in respiratory tract infections
Cochrane review looked at 14 randomized controlled trials looking at procalcitonin algorithms in antibiotic decision making for acute respiratory infections
Lowered antibiotic use by 65% in primary care, 35% in ED, and 30% in ICU
Decreased antibiotic exposure in hospital by 3.5 days No difference in treatment failure or mortality at 30 days No firm conclusions on cost-effectiveness
Schuetz P et al. Procalcitonin to initiate or discontinue antibiotics in acute respiratory tract infections. Cochrane Review. 2012.
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UCI Procalcitonin Algorithm1: Respiratory tract infections
PCT value
Antibiotic Recommendation
<0.1 mg/ml >0.24 mg/ml 0.1-0.24 mg/ml
Antibiotics strongly discouraged
Antibiotics discouraged
Antibiotics encouraged
PCT to initiate antibiotics
Consider viral infection Consider non-infectious cause
Repeat q2-3 days to consider stopping antibiotics See Algorithm 2
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UCI Procalcitonin Algorithm2: Respiratory tract infections
PCT value
Antibiotic Recommendation
<0.1 mg/ml >0.24 mg/ml
Strongly recommend antibiotics be stopped
Recommend continuation of antibiotics
PCT to stop antibiotics
Make sure there is appropriate clinical response
If PCT rising or not decreasing, consider broadening coverage and/or ID consult
0.1-0.24 mg/ml
Recommend antibiotics be stopped
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Antibiotics at time of admission
Proper antibiotic utilization at time of presentation to hospital is the most difficult to implement from stewardship perspective
Many times they are started on admission then discontinued or drastically de-escalated the next day
Pressure to discharge definitely a factor
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Summary
• UCI Antimicrobial Stewardship Program is now up and running using advanced methods to meet its goals
• Future methods will be coming in the future (ACCELERATE, allergy de-labelling, etc.)
• Hospitalist teams are doing an excellent job in antibiotic utilization • We need to address SST, HCAP, and antibiotics at admission