Sampling methods for ventilator-associated pneumonia: validation using different histologic and microbiological references

Crit Care Med. 2000 Aug;28(8):2799-804. doi: 10.1097/00003246-200008000-00020.

Abstract

Objective: To validate sampling techniques (tracheobronchial aspirates, protected specimen brush, and bronchoalveolar lavage, both conventional and protected) for the detection of ventilator-associated pneumonia (VAP) and causative microorganisms according to different histologic and microbiological references.

Design: Immediate, multiple bilateral lung biopsy, postmortem study.

Setting: Respiratory intensive care unit of a 1,000-bed teaching hospital.

Patients: Twenty-five mechanically ventilated patients (>72 hrs) who died in our intensive care unit.

Measurements: Lung tissue histologic examination and quantitative cultures (16 specimens/patient). The following four references for the diagnostic techniques were used: histology of guided lung biopsy, histology of blind lung biopsy, combined guided and blind lung biopsy histology and microbiology of lung tissue, and microbiology of lung tissue.

Results: Sensitivities when histologic reference tests were used ranged from 16% to almost 40%, whereas specificity rates were always <80%. When we combined both lung histology of guided or blind specimens and microbiology of lung tissue, all diagnostic techniques achieved considerably higher but still limited diagnostic yields (sensitivity range 43% to 83%; specificity range 67% to 91%). Causative organisms were missed in a significant number of cases by all techniques (17% to 83%).

Conclusions: The diagnostic performances of different diagnostic techniques strongly depend on the reference used. All techniques for detecting VAP are of limited value. Finding a balance between clinical judgment and microbiological results is crucial to appropriately manage patients with VAP.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • Cadaver
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pneumonia, Bacterial / etiology
  • Pneumonia, Bacterial / microbiology*
  • Pneumonia, Bacterial / pathology*
  • Respiration, Artificial / adverse effects*