Am. J. Respir. Crit. Care Med., Vol 150, No. 1, 07 1994, 113-122.
Evolution of bronchoalveolar cell populations in the adult respiratory distress syndrome
KP Steinberg, JA Milberg, TR Martin, RJ Maunder, BA Cockrill and LD Hudson
Harborview Medical Center, Department of Veterans Affairs Medical Center, Seattle, Washington.
To characterize the evolution of inflammation in the adult respiratory
distress syndrome (ARDS) and test the hypothesis that sustained alveolar
inflammation is associated with a poor outcome in patients with ARDS, we
performed fiberoptic bronchoscopy and bronchoalveolar lavage (BAL) in 125
patients and compared BAL cells and protein concentrations in survivors and
nonsurvivors. ARDS followed sepsis syndrome in 35 patients, major trauma in
41, and other causes in 49. When possible, BAL was performed on Days 3, 7,
and 14 after the onset of ARDS. Sixty-five patients (52%) had more than one
BAL. We first performed analyses on each BAL day using information from all
212 BAL in the 125 patients (cross-sectional analysis). All patients had
increased leukocytes and total protein in the first BAL (Day 3 after onset
of ARDS). In patients with ARDS following sepsis, the percentage of BAL
polymorphonuclear leukocytes (PMN) was higher on Day 7 (p = 0.11) and
particularly Day 14 (p = 0.02) in patients who died; there was a consistent
trend of a higher PMN concentration on all days in patients who died then
in those who lived. In patients with ARDS following trauma and other risks,
however, BAL PMN measures did not distinguish survivors from patients who
died. Analysis of serial data from the patients with more than one BAL
showed that alveolar macrophages (AM) increased in survivors of ARDS, both
in absolute numbers and as a percentage of total cells; this pattern was
most pronounced in the sepsis patients. The cross-sectional data analysis
suggests that sustained alveolar inflammation occurs frequently in patients
with ARDS following sepsis and is associated with a high mortality.
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Copyright © 1994 American Thoracic Society
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