Role of glucocorticoids on inflammatory response in nonimmunosuppressed patients with pneumonia:: a pilot study

被引:113
作者
Montón, C
Ewig, S
Torres, A
El-Ebiary, M
Filella, X
Rañó, A
Xaubet, A
机构
[1] Univ Barcelona, Hosp Clin, IDIBAPS, Serv Bioquim, Barcelona 08036, Spain
[2] Univ Barcelona, Hosp Clin, IDIBAPS, Serv Pneumol & Allergia Resp, Barcelona 08036, Spain
[3] Med Univ Bonn, Poliklin Bonn, Bonn, Germany
关键词
cytokine expression; glucocorticoids; inflammatory response; pneumonia;
D O I
10.1034/j.1399-3003.1999.14a37.x
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The aim of the study was to assess the potential role of glucocorticoids (GC) in modulating systemic and pulmonary inflammatory responses in mechanically ventilated patients with severe pneumonia. Twenty mechanically ventilated patients with pneumonia treated at a respiratory intensive care unit (RICU) of a 1,000-bed teaching hospital were prospectively studied. All patients had received prior antimicrobial treatment. Eleven patients received Hospital Clinic GC (mean+/-SD dose of i.v. methylprednisolone 677+/-508 mg for 9+/-7 days), mainly for bronchial dilatation. Serum and bronchoalveolar lavage fluid (BALF) tumour necrosis sis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-6 and C-reactive protein levels were measured in all patients. The inflammatory response was attenuated in patients receiving GC, both systemically (IL-6 1,089+/-342 versus 630+/-385 pg.mL(-1), p=0.03; C-reactive protein 34+/-15 versus 19+/-15 mg.L-1 p=0.04) and locally in BALF (TNF-alpha 118+/-50 versus 24+/-5 pg.ml(-1), p= 0.05; neutrophil count: 2.4+/-1.1 x 10(9) cells.L-1 (93+/-3%) versus 1.9+/-1.8 x 10(9) cells.L-1 (57+/-16%), p=0.03). Four of the 11 (36%) patients receiving GC died compared to six (67%) who were not receiving GC (p=0.37). The present pilot study suggests that glucocorticoids decrease systemic and lung inflammatory responses in mechanically ventilated patients with severe pneumonia receiving antimicrobial treatment.
引用
收藏
页码:218 / 220
页数:3
相关论文
共 8 条
[1]   Cytokine modulation by glucocorticoids: Mechanisms and actions in cellular studies [J].
Brattsand, R ;
Linden, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1996, 10 :81-90
[2]   Granulocyte activation markers in induced sputum: Comparison between chronic obstructive pulmonary disease, asthma, and normal subjects [J].
Keatings, VM ;
Barnes, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 155 (02) :449-453
[3]   PERSISTENT ELEVATION OF INFLAMMATORY CYTOKINES PREDICTS A POOR OUTCOME IN ARDS - PLASMA IL-1-BETA AND IL-6 LEVELS ARE CONSISTENT AND EFFICIENT PREDICTORS OF OUTCOME OVER TIME [J].
MEDURI, GU ;
HEADLEY, S ;
KOHLER, G ;
STENTZ, F ;
TOLLEY, E ;
UMBERGER, R ;
LEEPER, K .
CHEST, 1995, 107 (04) :1062-1073
[4]  
MONTON C, 1999, IN PRESS CRIT CARE M
[5]   COMPARTMENTALIZATION OF INTRAALVEOLAR AND SYSTEMIC LIPOPOLYSACCHARIDE-INDUCED TUMOR NECROSIS FACTOR AND THE PULMONARY INFLAMMATORY RESPONSE [J].
NELSON, S ;
BAGBY, GJ ;
BAINTON, BG ;
WILSON, LA ;
THOMPSON, JJ ;
SUMMER, WR .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (02) :189-194
[6]  
SCHLEIMER RP, 1993, EUR J CLIN PHARM S1, V45, P3
[7]   MACROPHAGES AND POLYMORPHONUCLEAR NEUTROPHILS IN LUNG DEFENSE AND INJURY [J].
SIBILLE, Y ;
REYNOLDS, HY .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1990, 141 (02) :471-501
[8]   Multiple system organ failure - Is mechanical ventilation a contributing factor? [J].
Slutsky, AS ;
Tremblay, LN .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (06) :1721-1725