Dg. Sinclair et al., PULMONARY ENDOTHELIAL PERMEABILITY IN PATIENTS WITH SEVERE LUNG INJURY - CLINICAL CORRELATES AND NATURAL-HISTORY, Chest, 106(2), 1994, pp. 535-539
Study objective: To establish the natural history of lung injury in ad
ult respiratory distress syndrome (ARDS) in terms of increased pulmona
ry vascular permeability. Secondly, to relate such changes to the numb
er of neutrophils in bronchoalveolar lavage (BAL) and a clinical score
of the severity of lung injury.Design: Prospective, open. Setting: Ad
ult intensive care unit of a tertiary (national) referral hospital.Pat
ients: Fourteen patients meeting accepted diagnostic criteria for ARDS
. Interventions: Mechanical ventilatory support. Conventional intensiv
e care and support for other failed organ systems as appropriate. Meas
urements and results: Pulmonary vascular permeability was estimated us
ing a dual isotope technique (protein accumulation index [PAI]), neutr
ophil numbers by BAL and the severity of ARDS by the lung injury score
(LIS). The PAI and LIS were measured simultaneously on three occasion
s as far apart as possible during the course of the illness. A single
BAL was performed immediately after one of the three PAI/LIS measureme
nts, the precise timing being dictated by the clinical stability of ea
ch patient. Fourteen patients (8 male; age range, 19 to 69 years) were
studied, 1.40 +/- 0.16, 11.36 +/- 1.79, and 20.90 +/- 2.30 days after
the onset of ARDS (mean +/- EM). Six patients died. The PAI (normal r
ange, 0 to 1.0x10(-3)) was 2.81 +/- 0.39, 2.94 +/- 0.48, and 2.80 +/-
0.87; and LIS (severe injury >2.5) was 2.18 +/- 0.25, 2.48 +/- 0.14, a
nd 2.06 +/- 0.27, respectively. The BAL neutrophil content was 54.09 /- 8.89. There were significant positive correlations between PAI and
LIS (r=0.73, p<0.001) and PAI and BAL neutrophil content (r=0.81, p<0.
001). Conclusions: These data suggest that increased pulmonary vascula
r permeability persists throughout the course of ARDS and is related t
o a clinical score of injury severity and BAL neutrophil content.