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Ventilator Associated Pneumonia

Ventilator Associated Pneumonia. Jeremy Fisher, PGY-3 VA vascular Surgery July 2011. 62M w / Systolic dysfn , HTN, DMII, smoking hx , POD 7 s/p Aorto -bi-fem bypass Kept intubated for pressor requirement post-op Now off pressors

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Ventilator Associated Pneumonia

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  1. Ventilator Associated Pneumonia Jeremy Fisher, PGY-3 VA vascular Surgery July 2011

  2. 62M w/ Systolic dysfn, HTN, DMII, smoking hx, POD 7 s/pAorto-bi-fem bypass Kept intubated for pressor requirement post-op Now off pressors Increased FiO2 from 0.40 to 0.50 o/n and increased PEEP 5->8 CXR w RML infiltrate and generalized haziness across both lung fields WBC 13.5 (11.0)

  3. What is the diagnosis? Criteria? Further studies? Treatment? What could have prevented this?

  4. Overview 1. Diagnosis 2. Incidence and Impact 3. Treatment 4. Prevention

  5. Overview • Diagnosis What is VAP? Clinical Criteria Respiratory Sampling/Cx 2. Incidence and Impact 3. Treatment 4. Prevention

  6. What is VAP? Pneumonia that develops in someone who has been intubated • Usually refers to those intubated >48 hours • Early onset <4 days • Late onset >4 days

  7. Diagnosis of VAP • Clinical diagnosis is challenging and controversial • Suspect VAP when: • CXR – new or progressive infiltrate • AND • At least 2 of fever, abnormal WBC, purulent secretions • Obtain lower respiratory culture

  8. Diagnosis of VAP • Clinical diagnosis is challenging and controversial • Suspect VAP when: • CXR – new or progressive infiltrate • AND • At least 2 of fever, abnormal WBC, purulent secretions • Obtain lower respiratory culture - Klompas, 2007 - Review/Meta analysis, - 14 Studies LR 1.7; 95% CI,1.1-2.5 LR 0.35; 95% CI,0.14-.87 LR, 2.8; 95% CI, 0.97-7.9 Incidence 9.7% then likelihood 23% Probability 3.6%

  9. Diagnosis of VAP: CPIS Score

  10. Diagnosis of VAP: CPIS Score CPIS > 6 Sensitivity 72-93% Specificity 42-85%

  11. Diagnosis of VAP: CDC Criteria

  12. Diagnosis: Lower Respiratory Sampling Blind Bronchial Aspirate > 105CFUs • BronchoalveolarLavage • > 104CFUs Protected Brushings Mini–BAL

  13. Diagnosis of VAP: Culture Blind

  14. Diagnosis: Lower Respiratory Sampling If less than 50% of cells = Neutrophils VAP very unlikely (LR 0.05-0.10) Blind Bronchial Aspirate > 105CFUs • BronchoalveolarLavage • > 104CFUs Positive Gram Stain LR 2.1 for VAP Positive Gram Stain LR 18 for VAP Growth > 105CFUs LR 9.6 for VAP Growth > 104CFUs “Unhelpful”

  15. Respiratory Sampling: Comparing the Methods • 90 Trauma patients with suspected VAP • BAL, blind aspirate, bronchoscopy brushings, blind brushings -Compared GS and Cx -Calculated agreement between modalities (kappa values) No statistically significant difference in yield

  16. Diagnosis of VAP: Summary • Clinical diagnosis is challenging and controversial • Suspect VAP when: • CXR – new or progressive infiltrate • AND • At least 2 of fever, abnormal WBC, purulent secretions • Obtain lower respiratory culture • +GS more meaningful w/ deeper sample • +Cx >10,000 CFUs on BAL does not make diagnosis but may guide therapy (controversial) • >100,000 CFUs more convincing

  17. Overview 1. Diagnosis 2. Incidence and Impact 3. Treatment 4. Prevention

  18. Incidence and Impact VAP occurs in 9-27% all intubated patients 2.1-10.7 episodes of VAP per 1000 ventilator days Barsanti, MC, Woeltje KF. “Infection Prevention in the Intensive Care Unit.” Infect DisClin N Am 23 (2009) 703–725. Apr 2009. Chastre J, Fagon JY. Ventilator-associated pneumonia. Am J RespirCrit Care Med 2002;165(7):867–903.

  19. Incidence and Impact Patients w VAP are twice as likely to die Significantly longer duration of ventilation and hospital stay Additional $10,000-40,000 Safdar N et al. Clinical and economic consequences of ventilator-associated pneumonia: a systematic review. Crit Care Med. 2005 Oct;33(10):2184-93

  20. Overview 1. Diagnosis 2. Incidence and Impact 3. Treatment Bacteriology Strategy for Antibiosis Duration of Therapy 4. Prevention

  21. Current Recommendations Infect DisClin N Am 23 (2009) 521–533

  22. General Strategy Starting with broad spectrum antibiotic therapy improves mortality Choice of BS Abx regimen should be guided by institutional bacteriology Narrow coverage when possible (Cx guided) Double coverage for those at high risk for MDR

  23. At Risk for MDR

  24. Antibiotic Choice

  25. Abx Choice Algorithm

  26. Possible MRSA

  27. Duration of Therapy Reassess at 72 hours, narrow if possible, broaden if necessary Duration not well established in literature Some studies suggest 8 days is equivalent to 14 days (Chastre)

  28. Overview 1. Diagnosis 2. Incidence and Impact 3. Treatment 4. Prevention

  29. Prevention Evidence Driven Factors to Reduce VAP • High RN to Pt ratio • Reduced use of invasive ventilation • Semirecumbent positioning • Continuous aspiration of subglottic secretions • ET cuff pressure >20 cm H2O • Silver coated ET tubes Barsanti, MC, Woeltje KF. “Infection Prevention in the Intensive Care Unit.” Infect DisClin N Am 23 (2009) 703–725. Apr 2009.

  30. Prevention Controversial Interventions • Slightly decreased rate of VAP w/ use of sucralfate in place of ranitidine, but increased risk of GIB (8 trials) • Oral care w/ chlorhexidine decreases VAP rates for those intubated <48hrs • Abx w/o diagnosis of VAP not recommended Barsanti, MC, Woeltje KF. “Infection Prevention in the Intensive Care Unit.” Infect DisClin N Am 23 (2009) 703–725. Apr 2009.

  31. REMEMBER! 1.VAP is common and costly (in lives and $) 2. New/progressive infiltrate on CXR + 2 (fever, abnormal WBC, purulent secretions) -> high clinical suspicion for VAP 3. BS abx as guided by local bacteriology, double coverage for those at high risk for MDR (esp pseudomonas) 4. Good nursing w/ HOB elevated and suctioning can reduce rates of VAP

  32. References

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