CORTICOSTEROID RESCUE TREATMENT OF PROGRESSIVE FIBROPROLIFERATION IN LATE ARDS - PATTERNS OF RESPONSE AND PREDICTORS OF OUTCOME

被引:190
作者
MEDURI, GU
CHINN, AJ
LEEPER, KV
WUNDERINK, RG
TOLLEY, E
WINERMURAM, HT
KHARE, V
ELTORKY, M
机构
[1] UNIV TENNESSEE,MED CTR,REG MED CTR,DIV PULM & CRIT CARE,MEMPHIS,TN
[2] UNIV TENNESSEE,MED CTR,REG MED CTR,DEPT CLIN EPIDEMIOL & BIOSTAT,MEMPHIS,TN
[3] UNIV TENNESSEE,MED CTR,REG MED CTR,DEPT RADIOL,MEMPHIS,TN
[4] UNIV TENNESSEE,MED CTR,REG MED CTR,DEPT PATHOL,MEMPHIS,TN
[5] VET AFFAIRS MED CTR,MEMPHIS,TN
关键词
D O I
10.1378/chest.105.5.1516
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Pulmonary fibroproliferation (PFP) is directly or indirectly the leading cause of death in patients with late ARDS. We previously reported our experience using intravenous corticosteroids (IVC) in 8 patients with late ARDS and now have expanded our observation to a total of 25 patients with severe fibroproliferation (mean lung injury score [LIS] 3) and progressive respiratory failure (RF). Thirteen patients had open-lung biopsy before treatment. Patients were started on IVC treatment (IVCT) an average of 15+/-7.5 days into mechanical ventilation (MV). Significant physiologic improvement (SPI) to IVCT was defined as a reduction in LIS of greater than 1 point or an increase in PaO2:FIo(2) ratio of greater than 100. We observed three patterns of response: rapid responders (RR) had an SPI by day 7 (n=15); delayed responders (DR) had an SPI by day 14 (n=6); nonresponders (NR) were without SPI by day 14 (n=4). Overall, the following significant mean changes were seen within 7 days of IVCT: LIS from 3 to 2 (p=0.001), PaO2:FIo(2) from 162 to 234 (p=0.0004), PEEP from 11 to 6.8 cm H2O (p=0.001), chest radiograph score from 3.8 to 3.0 (p=0.009), and VE from 16 to 13.6 L/min (p=0.01). Development of pneumonia was related to the pattern of response. Surveillance bronchoscopy was effective in identifying pneumonia in eight afebrile patients. Nineteen of 25 (76 percent) patients survived the ICU admission. Comparisons were made between survivors (S) and nonsurvivors (NS) and among the three groups of responders. At the time ARDS developed, no physiologic or demographic variable could discriminate between S and NS. At the time of IVCT, only liver failure was more frequent in nonsurvivors (p=0.035). Histologic findings at open-lung biopsy and pattern of physiologic response clearly predicted outcome. The presence of preserved alveolar architecture (p=0.045), myxoid type fibrosis (p=0.045), coexistent intraluminal bronchiolar fibrosis (p=0.0045), and lack of arteriolar subintimal fibroproliferation (p=0.045) separated S from NS. ICU survival rate was 86 percent in responders and 25 percent in nonresponders (p=0.03), Only one death resulted from refractory respiratory failure.
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收藏
页码:1516 / 1527
页数:12
相关论文
共 50 条
[1]   DIAGNOSIS OF NOSOCOMIAL BACTERIAL PNEUMONIA IN ACUTE, DIFFUSE LUNG INJURY [J].
ANDREWS, CP ;
COALSON, JJ ;
SMITH, JD ;
JOHANSON, WG .
CHEST, 1981, 80 (03) :254-258
[2]  
ASHBAUGH DG, 1985, ARCH SURG-CHICAGO, V120, P530
[3]  
ASHBAUGH DG, 1972, SURG GYNECOL OBSTETR, V135, P865
[4]  
AULER JOC, 1986, EUR J RESPIR DIS, V69, P261
[5]   ALTERATIONS OF GAS-EXCHANGE APPARATUS IN ADULT RESPIRATORY INSUFFICIENCY ASSOCIATED WITH SEPTICEMIA [J].
BACHOFEN, M ;
WEIBEL, ER .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1977, 116 (04) :589-615
[6]   MULTIPLE ORGAN SYSTEM FAILURE AND INFECTION IN ADULT RESPIRATORY-DISTRESS SYNDROME [J].
BELL, RC ;
COALSON, JJ ;
SMITH, JD ;
JOHANSON, WG .
ANNALS OF INTERNAL MEDICINE, 1983, 99 (03) :293-298
[7]   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
[8]   ADULT RESPIRATORY-DISTRESS SYNDROME - SEQUENCE AND IMPORTANCE OF DEVELOPMENT OF MULTIPLE ORGAN FAILURE [J].
BONE, RC ;
BALK, R ;
SLOTMAN, G ;
MAUNDER, R ;
SIVVERMAN, H ;
MYERS, TM ;
KERSTEIN, MD ;
SZIDON, P ;
HANLEY, M ;
JACOBS, E ;
CALDWELL, E ;
ALTMAN, F ;
BAGWELL, S ;
COX, P ;
LAMBERT, R ;
WILLIAMS, W ;
CERRA, F ;
BERLAUK, J ;
GILMOUR, I ;
CLOUTIER, C ;
DAVIES, E ;
STEINBURG, S ;
FEIN, A ;
GRANT, M ;
MONTAVANI, R ;
NEIDERMAN, M ;
SKLAREK, H ;
GASKILL, H ;
LEVINE, B ;
HUDSON, L ;
DETTENMEIER, P ;
WEBB, W ;
BELZBERG, H ;
MENDOZA, J ;
BURCHARD, K ;
SMITH, J ;
BLACKBURN, J ;
BURNS, R ;
WEIGELT, J ;
URSPRUNG, JJ ;
MAILE, M ;
WILKS, NE ;
DRENNE, K .
CHEST, 1992, 101 (02) :320-326
[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]   DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ .
CHEST, 1992, 101 (06) :1644-1655