NationalLatest Updates to the Canadian VAP Guidelines - What's New?
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Transcript of NationalLatest Updates to the Canadian VAP Guidelines - What's New?
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LATEST UPDATES TO THE CANADIAN VAP GUIDELINES
Tuesday, September 30 2014 Mardi 30 Septembre 2014
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Your Hosts & Presenters Vos hôtes et présentateurs
Bruce Harries, Collaborative Director Denny Laporta, MD, MSc, FRCPC; ICU Collaborative Chair Intensivist, Dept of Adult Critical Care; Jewish General Hospital; Faculty of Medicine, McGill University John Muscedere, MD, FRCPC Associate Professor, Department of Medicine & Critical Care Program, Queen’s University; Research Director, Critical Care Program; Physician, Kingston General Hospital, Faculty Member Canadian ICU Collaborative Leanne Couves, Improvement Advisor
Ardis Eliason, Technical Host
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08/05/2014
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Dr. John Muscedere
Latest Updates to the Canadian VAP Guidelines
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Canadian Clinical Practice Guidelines
for Ventilator Associated
Pneumonia (VAP) Dr. John Muscedere Queen’s University
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Learning Objectives
1. To understand the epidemiology of VAP.
2. To review the principles of diagnosis for VAP
3. To review Clinical Practice Guidelines for VAP:
1. Prevention 2. Diagnosis 3. Treatment
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Epidemiology of VAP
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Hospital-Acquired Pneumonia (HAP): Definitions Hospital Acquired Pneumonia:
Arises 48 hours or more after hospital admission
Is not incubating at the time of admission Ventilator-associated pneumonia (VAP):
Arises 48-72 hours or more after endotracheal intubation (up to 48 -72 hours after endotracheal intubation)
Healthcare-associated pneumonia (HCAP): Arises within 90 days of admission to an
acute care facility or residence in NH/LTCF.
(American Thoracic Society/IDSA. Am J Respir Crit Care Med 2005;171:388-416)
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Hospital Location & Relative Frequency of HAP & VAP
HAP
ICU HAP
Non-ICU HAP VAP
Non-ICU HAP ICU HAP VAP ICU HAP
HAP ICU
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Why the focus on VAP? Increased Mortality
Depends on population Adequacy and timeliness of antibiotic treatment
Melsen et al, Crit Care Med, 2009
Baekert et al, AJRCCM, 2011
Melsen et al, SR and MA of 52 Obs. studies, 17,000 patients RR 1.27 (1.15,1.39)
Relative: 4- 6% of ICU Mortality Absolute: 1 – 1.5% Mortality
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VAP: Impact Increases ICU Stay, Increases duration of
Mechanical Ventilation and Increases duration of Hospital Stay Extra days in the hospital: 4-9 days Average extra days in ICU: 4.3 days
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VAP: Canadian Healthcare Costs
1Based on attributable mortality of 5.8% 2Ontario cost cost methodology Muscedere et al, J Crit Care, 2008
Cost per Case $11,450 Burden of Illness per year: Assuming 10.6
cases/1000 Vent days Excess Vent
days 16,000 days
(55 ICU beds) Excess Deaths1 216
Excess Cost2 $46,000,000
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Incidence
• Depends on how hard one looks • Surveillance underestimates true
incidence • Reported rates vary:
• USA: NHSN 2-10 Cases/1000 vent days • Ontario: 2.8 Cases/1000 vent days • Multi-center Canadian study: 9 Cases/ 1000
vent days
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Pathogenesis of HAP/VAP
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Pathogenesis of VAP
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Causative Pathogens
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Classification of HAP & VAP: Risk Stratification
Time from Hospitalization (days)
Time from Intubation (days)
Early-onset VAP Late-onset VAP
Late-onset HAP Early-onset HAP
0 1 2 3 4 5 6 7
0 1 2 3 4 5 6 7
(American Thoracic Society. Am J Respir Crit Care Med 2005;171:388-416)
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Pathogens to Consider When Treating HAP/VAP
Early HAP/VAP Late HAP/VAP
Timing Within five days of admission or mechanical ventilation
Five days or more after admission or mechanical ventilation
Bacteriology S. pneumoniae H. influenzae Methicillin-sensitive S. aureus Susceptible gram-negative bacteria
P. aeruginosa Acinetobacter Methicillin-resistant S. aureus Other multi-resistant organisms
Prognosis Less severe, little impact on outcome Mortality minimal
Higher attributable mortality and morbidity
(American Thoracic Society/IDSA. Am J Respir Crit Care Med 2005;171:388-416)
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Diagnosis of VAP
• No reference standard for VAP • Clinical features are non-specific and can
be found in many other diseases • CXRay:
– Neither sensitive nor specific – Normal xray can help rule out VAP (? VAT) – No pathognomic features of VAP
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Diagnosis of VAP
Clinical + Microbiology
• Purulent secretions • Increasing oxygen requirements
• Core temp > 38.0o C
• WBC <3.5 or > 11.0
+ Chest X-Ray
Pathogenic Bacteria
New or Persistent Infiltrates
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Invasive
ETT Aspirate
Obtaining Microbiological Sample for Diagnosis of VAP
Bronchoscopy
Non-Invasive
Quantitative Cultures
Non-Quantitative
Cultures
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Mortality of BAL vs ETA
Meta-Analysis of All trials comparing ETA with BAL
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VAT
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Possible pneumonia
Probable pneumonia
VAC ventilator-associated condition
New and sustained respiratory deterioration
New respiratory deterioration with
concurrent infection
IVAC Infection-related
ventilator-associated complication
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Definition: ≥2 days of stable or decreasing daily minimum PEEP or FiO2
followed by
Rise in daily minimum PEEP ≥3 cm H2O sustained ≥2 days or Rise in daily minimum FiO2 ≥20 points sustained ≥2 days
An alternative paradigm for surveillance:
Implemented in NHSN in January 2013
Ventilator Associate Conditions (VAC)
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Definition: VAC associated with alterations in WBC (< to 4 or ≥ 12) or temperature (< 36 or ≥ 38o C) within 2 days and Prescription of antibiotics continued ≥ 4 days
An alternative paradigm for surveillance: Infection Related Ventilator Associate Conditions (iVAC)
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VAP Guideline Recommendations
• Prevention • Diagnosis • Treatment
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Ann Intern Med. 2004;141:305-13. J Crit Care, 2008
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• Use Oral Route for intubation May not apply to pts with:
• Maxillofacial trauma/surgery • ENT surgery • Difficult intubation
VAP Guideline Recommendations: Prevention
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Sub-glottic Secretion Drainage
VAP Guideline Recommendations: Prevention
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Sub-glottic Secretion Drainage
Muscedere et al, CCM 2011
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• Subglottic Secretion Drainage • Requirement for prolonged
mechanical ventilation
May not apply to pts with: • Nasally intubation • Tracheostomy tube • Difficult endotracheal intubation
VAP Guideline Recommendations: Prevention
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• Semi-recumbent positioning at 45 degree angle
May not apply to pts with:
• Patient on vasopressors or undergoing resuscitation • Spine unstable or not cleared • Pelvic instability or fractures • Prone position • Intra aortic balloon pump • Unable to raise HOB because of obesity • Procedures (includes bathing)
VAP Guideline Recommendations: Prevention
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VAP and Semi-recumbency: The evidence
Outcome: The occurrence of VAP
Patient population: • Total of 409 patients studied • Head of bed elevation achieved only
measured in van Nieuwenhoven study
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• Chlorhexidine Oral Antiseptic May not apply to pts with:
• Chlorhexidine Allergy • Lack of access to patient’s oral cavity
VAP Guideline Recommendations: Prevention
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CHX decontamination compared with no prophylaxis on risk of VAP
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VAP Guidelines: Diagnosis
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• No improvement in clinical outcomes (mortality, length of stay, antibiotic use) compared to endotracheal aspirate
• May lead to delays in initiation of antibiotic therapy
• Requires expertise, time and personnel without added benefit
Diagnostic Bronchoscopy NOT RECOMMENDED
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• Diagnosis of suspected VAP • Endotracheal aspirates with nonquantitative
culture
May not apply to pts with: • Immunocompromised patients at physician’s
discretion
VAP Guideline Recommendations: Diagnosis
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Clinical Suspicion of VAP
New or persistent infiltrate on CXR plus 2 of the following: •Purulent endotracheal secretions •Increasing FiO2 requirements •Elevated temperature (> 38.0) •Increased WBC (>11.0) or decreased WBC (<3.5)
Diagnosis of VAP
Endotracheal aspirate
Consider diagnostic bronchoscopy for immunosuppressed patients
VAP Diagnosis
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VAP Guidelines: Treatment
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Treatment of VAP
• Initial inadequate empiric therapy of VAP is associated with worse outcome
• Delays in therapy associated with worse outcome
ATS Guidelines, 2005
Kuti, JCC 2009
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Impact of adequacy of empiric therapy on outcome
Adequate Inadequate p-value*
(n=313) (n=37)
Died within 14 days 33 (10.5%) 9 (24.3%) 0.01
Died within 28 days 51 (16.3%) 12 (32.4%) 0.02
Died in ICU 37 (11.8%) 13 (35.1%) 0.0001
Died in Hospital 61 (19.5%) 18 (48.7%) <0.0001
Muscedere, JCC 2011
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• Initiation of empiric treatment for VAP • Start antibiotics at time of VAP
suspicion (do not wait for culture results)
May not apply to pts with: none
VAP Guideline Recommendations: Treatment
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• Antibiotics for empiric treatment of VAP • Single effective agent for each suspected
organism May not apply to pts with:
• Patients known to be colonized or previously infected with Pseudomonas sp. or multidrug resistant organisms
• Immunocompromised patients
VAP Guideline Recommendations: Treatment
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VAP Guideline Recommendations: Treatment
Monotherapy vs. Combination Therapy: Mortality
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• Choice of antibiotics for empiric treatment of VAP
• Based on local ICU resistance patterns and patient factors
May not apply to pts with: none
VAP Guideline Recommendations: Treatment
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• Discontinuation of empiric antibiotics for VAP
• If noninfectious etiology of infiltrates is found
OR • If signs and symptoms of active infection
have resolved
May not apply to pts with: none
VAP Guideline Recommendations: Treatment
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• Choice of Antibiotic for Confirmed VAP
• “A” vs. “B”: No evidence to favor one agent over another – Multiple non-inferiority trials (approx. 30 trials)
• MRSA pneumonia – Linezolid vs. Glycopeptides (Vancomycin)
VAP Guideline Recommendations: Treatment
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MRSA VAP Pneumonia
In the three studies • Mortality at different time points reported • No effect on mortality was reported
Clinical cure rate
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• Duration of antibiotic treatment for confirmed VAP
• Maximum of 8 days in patients in whom initial empiric therapy was appropriate
May not apply to pts with:
• Immunocompromised patients
VAP Guideline Recommendations: Treatment
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TREATMENT OF VAP
•Stop empiric antibiotics for suspected VAP if another reason for patient’s signs & symptoms found •Stop antibiotics for confirmed VAP after 8 days of therapy
Reassess each antibiotic daily based on culture results,
and patient’s signs and symptoms
•Choose antibiotic on the basis of the microbiology and resistance patterns in the ICU •Choose one effective antibiotic active against each potential pathogen
Start empiric antibiotics at the time of clinical suspicion of VAP
Empiric Therapy
Antibiotic Selection
Duration of Antibiotic Therapy
Antibiotic
Management
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Thank You
Questions?
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QUESTIONS?
RAISE YOUR HAND / LEVEZ LA MAIN
OR/OU
CHAT TO “ALL PARTICIPANTS”
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“Taking the Pulse” Poll
08/05/2014 60
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Instructions to download certificate
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Canadian ICU Collaborative Faculty
Paule Bernier, P.Dt., Msc, Présidente, Ordre professionnel des diététistes du Québec; Sir MB David Jewish General Hospital (McGill University), Montreal
Paul Boiteau MD, Department Head, Critical Care Medicine, Alberta Health Services; Professor of Medicine, University of Calgary Mike Cass, BSc, RN, MScN, Advanced Practice Nurse, Trillium Health Centre Leanne Couves, Improvement Advisor, Improvement Associates Ltd. Carla Williams, Patient Safety Improvement Lead, CPSI Bruce Harries, Collaborative Director, Improvement Associates Ltd. Denny Laporta MD, Intensivist, Department of Adult Critical Care, Jewish General Hospital; Faculty of Medicine, McGill University Claudio Martin MD,Intensivist, London Health Sciences Centre, Critical Care Trauma Centre; Professor of Medicine and Physiology,
University of Western Ontario; Chair/Chief of Critical Care Western Cathy Mawdsley, RN, MScN, CNCC; Clinical Nurse Specialist – Critical Care, London Health Sciences Centre; John Muscedere MD, Assistant Professor of Medicine, Queens University; Intensivist, Kingston General Hospital Yoanna Skrobik MD, Intensivist, Hôpital Maisonneuve Rosemont, Montréal; Expert Panel for the new Pain, Sedation and Delirium
Guidelines, Society of Critical Care Medline (SCCM)
62 08/05/2014
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Reminders Rappels
Call is recorded Slides and links to
recordings will be available on Safer Healthcare Now! Communities of Practice
Additional resources are available on the SHN Website and Communities of Practice
L'appel est enregistré Les diapositives et liens
vers les enregistrements seront disponibles sur Des soins de santé plus sécuritaires maintenant! Communautés de pratique
Des ressources supplémentaires sont disponibles sur le site Web SSPSM et Communautés de Pratique
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THANK YOU MERCI
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