Antithrombin III supplementation in severe sepsis: Beneficial effects on organ dysfunction

被引:111
作者
Inthorn, D
Hoffmann, JN
Hartl, WH
Muhlbayer, D
Jochum, M
机构
[1] UNIV MUNICH,KLINIKUM GROSSHADERN,DEPT CLIN CHEM,D-81377 MUNICH,GERMANY
[2] UNIV MUNICH,KLINIKUM INNENSTADT,DEPT SURG,DIV CLIN BIOCHEM,D-80336 MUNICH,GERMANY
来源
SHOCK | 1997年 / 8卷 / 05期
关键词
D O I
10.1097/00024382-199711000-00003
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Activation of thrombin and of the coagulation system plays an important role in the pathophysiology of sepsis-associated organ dysfunction. Antithrombin III (AT III) is a natural inhibitor of thrombin, a central procoagulatory factor with pleiotropic activities. Experimental supplementation of AT III improved coagulation parameters and ameliorated organ dysfunction. To determine whether long-term AT III supplementation has beneficial effects on organ function, we conducted a randomized, prospective study in surgical patients with severe sepsis. The study evaluated the long-term effect of AT III supplementation (duration of treatment: 14 days). After randomization (AT III vs. control group), AT III was infused continuously over 14 days to obtain plasma AT III activities > 120%. Forty consecutive patients were recruited (20 AT III/20 control group). Eleven patients had a rapid fatal course and did not met the criterion of a 14 day treatment period. From these 11 patients, 8 patients (5 AT III/3 control group) died within 72 h due to septic shock. The remaining 14 AT III patients and 15 controls survived 14 days and showed no differences in baseline parameters of organ function. AT III caused a disappearance of disseminated intravascular coagulation (DIC) in all patients with DIG, whereas in control patients, the frequency of DIC remained constant (p < .05). In AT III patients a progressive increase in oxygenation index (Pao(2)/FIO2 ratio) and a continuous decrease in pulmonary hypertension index (mean pulmonary artery pressure/mean arterial pressure (PAP/MAP) ratio) indicated an improvement of lung function (p < .05 vs. control). AT III prevented the continuous rise in total serum bilirubin concentration observed in control patients and diminished the frequency of artificial renal support therapy (p < .05). Long-term supplementation with AT III may improve lung function and prevent the development of septic liver and kidney failure in patients with severe sepsis.
引用
收藏
页码:328 / 334
页数:7
相关论文
共 31 条
[1]   EFFECT OF ANTITHROMBIN CONCENTRATE ON HEMOSTATIC VARIABLES IN CRITICALLY ILL PATIENTS [J].
ALBERT, J ;
BLOMQVIST, H ;
GARDLUND, B ;
JAKOBSSON, J ;
SVENSSON, J ;
BLOMBACK, M .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1992, 36 (08) :745-752
[2]   COMPARISON OF DISEASE SEVERITY SCORING SYSTEMS IN SEPTIC SHOCK [J].
ARREGUI, LM ;
MOYES, DG ;
LIPMAN, J ;
FATTI, LP .
CRITICAL CARE MEDICINE, 1991, 19 (09) :1165-1171
[3]   SUBSTITUTION OF ANTITHROMBIN-III IN SHOCK AND DIC - A RANDOMIZED STUDY [J].
BLAUHUT, B ;
KRAMAR, H ;
VINAZZER, H ;
BERGMANN, H .
THROMBOSIS RESEARCH, 1985, 39 (01) :81-89
[4]   THE PATHOGENESIS OF SEPSIS [J].
BONE, RC .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (06) :457-469
[6]   STRATEGIES FOR BLOCKING THE SYSTEMIC EFFECTS OF CYTOKINES IN THE SEPSIS SYNDROME [J].
CHRISTMAN, JW ;
HOLDEN, EP ;
BLACKWELL, TS .
CRITICAL CARE MEDICINE, 1995, 23 (05) :955-963
[7]  
DICKNEITE G, 1993, THROMB HAEMOSTASIS, V69, P98
[8]   EFFICACY OF ANTITHROMBIN-III SUPPLEMENTATION IN ANIMAL-MODELS OF FULMINANT ESCHERICHIA-COLI ENDOTOXEMIA OR BACTEREMIA [J].
EMERSON, TE ;
FOURNEL, MA ;
REDENS, TB ;
TAYLOR, FB .
AMERICAN JOURNAL OF MEDICINE, 1989, 87 (3B) :S27-S33
[9]   DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF ANTITHROMBIN-III CONCENTRATES IN SEPTIC SHOCK WITH DISSEMINATED INTRAVASCULAR COAGULATION [J].
FOURRIER, F ;
CHOPIN, C ;
HUART, JJ ;
RUNGE, I ;
CARON, C ;
GOUDEMAND, J .
CHEST, 1993, 104 (03) :882-888
[10]   STABILITY OF THE ARTERIAL-ALVEOLAR OXYGEN PARTIAL-PRESSURE RATIO - EFFECTS OF LOW VENTILATION-PERFUSION REGIONS [J].
GILBERT, R ;
AUCHINCLOSS, JH ;
KUPPINGER, M ;
THOMAS, MV .
CRITICAL CARE MEDICINE, 1979, 7 (06) :267-272