PLASMA ELASTASE LEVELS AND THE DEVELOPMENT OF THE ADULT-RESPIRATORY-DISTRESS-SYNDROME

被引:126
作者
DONNELLY, SC
MACGREGOR, I
ZAMANI, A
GORDON, MWG
ROBERTSON, CE
STEEDMAN, DJ
LITTLE, K
HASLETT, C
机构
[1] UNIV EDINBURGH,SCH MED,RESP MED UNIT,RAYNE LAB,EDINBURGH EH8 9AG,MIDLOTHIAN,SCOTLAND
[2] SCOTTISH BLOOD TRANSFUS SERV,NATL SCI LAB,EDINBURGH,MIDLOTHIAN,SCOTLAND
[3] ROYAL INFIRM,DEPT ACCID & EMERGENCY MED,EDINBURGH,MIDLOTHIAN,SCOTLAND
关键词
D O I
10.1164/ajrccm.151.5.7735596
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Inflammatory cells, particularly neutrophil granulocytes, have been implicated in the pathogenesis of the adult respiratory distress syndrome (ARDS). In this study, we investigated whether a relationship exists between neutrophil elastase in the plasma of multiple-trauma patients on initial hospital presentation and the subsequent development of lung injury and ARDS. Sixty-one multiple-trauma patients were enrolled prospectively. Neutrophil elastase was measured by a specific radioimmunoassay, and analysis was performed by nonparametric statistical methods. A highly significantly elevated plasma elastase level was found in patients who progressed to ARDS (median 217 ng/ml, range 127 to 480) (n = 8) compared with those who did not (median 117 ng/ml, range 21.4 to 685) (n = 53) (p = 0.009). Significant correlation was found between initial elastase values and subsequent requirement for mechanical ventilation (p = 0.01), lowest arterial oxygen saturation/oxygen supplementation recorded (p = 0.003), and organ failure score (p = 0.006). This study shows that within minutes of the initiating trauma event, there is evidence of enhanced neutrophil degranulation as manifested by elevated levels of immunoreactive neutrophil elastase in the peripheral blood. The level of this enzyme correlates with the degree of subsequent lung injury and ARDS. These findings reinforce the importance of neutrophils and their secretory products in early ARDS disease pathogenesis.
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页码:1428 / 1433
页数:6
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  • [1] Repine J.E., Scientific perspectives on adult respiratory distress syndrome, Lancet, 339, pp. 466-469, (1992)
  • [2] McWhinney P.H.M., Gillespie S.H., Kibbler C.C., Hoffbrand A.V., Prentice H.G., Streptococcus mitis and ARDS in neutropenic patients, Lancet, 337, (1991)
  • [3] Rinaldo J.E., Rogers R.M., Adult respiratory distress syndrome: Changing concepts of lung injury and repair, N. Engl. J. Med., 306, pp. 900-910, (1982)
  • [4] Warshawski F.J., Sibbald W.J., Driedger A.A., Cheung H., Abnormal neutrophil-pulmonary interaction in the adult respiratory distress syndrome, Am. Rev. Respir. Dis., 133, pp. 797-804, (1986)
  • [5] Weiland J.E., Davis W.B., Holler J.F., Mohammed J.R., Dorinsky P.M., Gadek J.E., Lung neutrophils in the adult respiratory distress syndrome. Clinical and pathophysiological significance, Am. Rev. Respir. Dis., 133, pp. 218-225, (1986)
  • [6] Rocker G.M., Wiseman M.S., Pearson D., Shale D.J., Diagnostic criteria for adult respiratory distress syndrome: Time for reappraisal, Lancet, 1, pp. 120-123, (1989)
  • [7] Christner P., Fein A., Goldberg S., Zippman M., Abrams W., Weinbaum G., Collagenase in the lower respiratory tract of patients with the adult respiratory distress syndrome, Am. Rev. Respir. Dis., 131, pp. 690-695, (1985)
  • [8] Parsons P.E., Fowler A.A., Hyers T.M., Henson P.M., Chemotactic activity in bronchoalveolar lavage fluid from patients with the adult respiratory distress syndrome, Am. Rev. Respir. Dis., 132, pp. 490-493, (1985)
  • [9] Miller E.J., Nagao S., Cohen A.B., Griffith D., Maunder R.J., Martin T.R., Weiner-Kronish J.P., Sticherling M., Elevated levels of NAP-1/interleukin-8 are present in the airspaces of patients with the adult respiratory distress syndrome and are associated with increased mortality, Am. Rev. Respir. Dis., 146, pp. 427-432, (1992)
  • [10] Donnelly S.C., Strieter R.M., Kunkel S.L., Walz A., Robertson C.E., Carter D.C., Grant I.S., Pollok A.J., Haslett C., Interleukin-8 and the development of the adult respiratory distress syndrome (ARDS) in at-risk patient groups, Lancet, 341, pp. 643-647, (1993)