Corticosteroids in acute respiratory distress syndrome

被引:30
作者
Fernandes, ABS
Zin, WA
Rocco, PRM [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Lab Invest Pulmonar, CCS, BR-21949900 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Lab Fisol Resp, BR-21949900 Rio De Janeiro, Brazil
关键词
acute respiratory distress syndrome; collagen; cytokine; methylprednisolone; experimental models; clinical trials;
D O I
10.1590/S0100-879X2005000200003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Improving the course and outcome of patients with acute respiratory distress syndrome presents a challenge. By understanding the immune status of a patient, physicians can consider manipulating proinflammatory systems more rationally. In this context, corticosteroids could be a therapeutic tool in the armamentarium against acute respiratory distress syndrome. Corticosteroid therapy has been studied in three situations: prevention in high-risk patients, early treatment with high-dose, short-course therapy, and prolonged therapy in unresolving cases. There are differences be. tween the corticosteroid trials of the past and recent trials: today, treatment starts 2-10 days after disease onset in patients that failed to improve; in the past, the corticosteroid doses employed were 5140 times higher than those used now. Additionally, in the past treatment consisted of administering one to four doses every 6 h (methylprednisolone, 30 mg/kg) versus prolonging treatment as long as necessary in the new trials (2 mg kg(-1) day(-1) every 6 h). The variable response to corticosteroid treatment could be attributed to the heterogeneous biochemical and molecular mechanisms activated in response to different initial insults. Numerous factors need to be taken into account when corticosteroids are used to treat acute respiratory distress syndrome: the specificity of inhibition, the duration and degree of inhibition, and the timing of inhibition. The major continuing problem is when to administer corticosteroids and how to monitor their use. The inflammatory mechanisms are continuous and cyclic, sometimes causing deterioration or improvement of lung function. This article reviews the mechanisms of action of corticosteroids and the results of experimental and clinical studies regarding the use of corticosteroids in acute respiratory distress syndrome.
引用
收藏
页码:147 / 159
页数:13
相关论文
共 59 条
[1]   Negative regulation of nuclear factor-κB activation and function by glucocorticoids [J].
Almawi, WY ;
Melemedjian, OK .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2002, 28 (02) :69-78
[2]  
ALMAWI WY, 1991, J IMMUNOL, V146, P3523
[3]  
ASHBAUGH DG, 1967, LANCET, V2, P319
[4]  
ASHBAUGH DG, 1985, ARCH SURG-CHICAGO, V120, P530
[5]   Molecular determinants of glucocorticoid receptor function and tissue sensitivity to glucocorticoids [J].
Bamberger, CM ;
Schulte, HM ;
Chrousos, GP .
ENDOCRINE REVIEWS, 1996, 17 (03) :245-261
[6]   HIGH-DOSE CORTICOSTEROIDS IN PATIENTS WITH THE ADULT RESPIRATORY-DISTRESS SYNDROME [J].
BERNARD, GR ;
LUCE, JM ;
SPRUNG, CL ;
RINALDO, JE ;
TATE, RM ;
SIBBALD, WJ ;
KARIMAN, K ;
HIGGINS, S ;
BRADLEY, R ;
METZ, CA ;
HARRIS, TR ;
BRIGHAM, KL .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (25) :1565-1570
[7]   THE AMERICAN-EUROPEAN CONSENSUS CONFERENCE ON ARDS - DEFINITIONS, MECHANISMS, RELEVANT OUTCOMES, AND CLINICAL-TRIAL COORDINATION [J].
BERNARD, GR ;
ARTIGAS, A ;
BRIGHAM, KL ;
CARLET, J ;
FALKE, K ;
HUDSON, L ;
LAMY, M ;
LEGALL, JR ;
MORRIS, A ;
SPRAGG, R ;
COCHIN, B ;
LANKEN, PN ;
LEEPER, KV ;
MARINI, J ;
MURRAY, JF ;
OPPENHEIMER, L ;
PESENTI, A ;
REID, L ;
RINALDO, J ;
VILLAR, J ;
VANASBECK, BS ;
DHAINAUT, JF ;
MANCEBO, J ;
MATTHAY, M ;
MEYRICK, B ;
PAYEN, D ;
PERRET, C ;
FOWLER, AA ;
SCHALLER, MD ;
HUDSON, LD ;
HYERS, T ;
KNAUS, W ;
MATTHAY, R ;
PINSKY, M ;
BONE, RC ;
BOSKEN, C ;
JOHANSON, WG ;
LEWANDOWSKI, K ;
REPINE, J ;
RODRIGUEZROISIN, R ;
ROUSSOS, C ;
ANTONELLI, MA ;
BELOUCIF, S ;
BIHARI, D ;
BURCHARDI, H ;
LEMAIRE, F ;
MONTRAVERS, P ;
PETTY, TL ;
ROBOTHAM, J ;
ZAPOL, W .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (03) :818-824
[8]   ARE CORTICOSTEROIDS SALVAGE THERAPY FOR REFRACTORY ACUTE RESPIRATORY-DISTRESS SYNDROME [J].
BIFFL, WL ;
MOORE, FA ;
MOORE, EE ;
HAENEL, JB ;
MCINTYRE, RC ;
BURCH, JM .
AMERICAN JOURNAL OF SURGERY, 1995, 170 (06) :591-596
[9]   EARLY METHYLPREDNISOLONE TREATMENT FOR SEPTIC SYNDROME AND THE ADULT RESPIRATORY-DISTRESS SYNDROME [J].
BONE, RC ;
FISHER, CJ ;
CLEMMER, TP ;
SLOTMAN, GJ ;
METZ, CA .
CHEST, 1987, 92 (06) :1032-1036
[10]   A CONTROLLED TRIAL OF EARLY ADJUNCTIVE TREATMENT WITH CORTICOSTEROIDS FOR PNEUMOCYSTIS-CARINII PNEUMONIA IN THE ACQUIRED-IMMUNODEFICIENCY-SYNDROME [J].
BOZZETTE, SA ;
SATTLER, FR ;
CHIU, J ;
WU, AW ;
GLUCKSTEIN, D ;
KEMPER, C ;
BARTOK, A ;
NIOSI, J ;
ABRAMSON, I ;
COFFMAN, J ;
HUGHLETT, C ;
LOYA, R ;
CASSENS, B ;
AKIL, B ;
MENG, TC ;
BOYLEN, CT ;
NIELSEN, D ;
RICHMAN, DD ;
TILLES, JG ;
LEEDOM, J ;
MCCUTCHAN, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (21) :1451-1457