Decreased organ failure in patients with severe SIRS and septic shock treated with the platelet-activating factor antagonist TCV-309: A prospective, multicenter, double-blind, randomized phase II trial

被引:43
作者
Poeze, M [1 ]
Froon, AHM [1 ]
Ramsay, G [1 ]
Buurman, WA [1 ]
Greve, JWM [1 ]
机构
[1] Univ Hosp Maastricht, Dept Surg, Maastricht, Netherlands
来源
SHOCK | 2000年 / 14卷 / 04期
关键词
sepsis; mortality; multiple organ failure; clinical trial; intensive care; human; immunomodulation;
D O I
10.1097/00024382-200014040-00001
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Sepsis and organ failure remain the main cause of death on the ICU. Sepsis is characterized by a severe inflammatory response, in which platelet-activating factor (PAF) is considered to play an important role. This study investigated whether treatment with the PAF-antagonist TCV-309 reduces morbidity and mortality in patients with septic shock. The study was conducted as a double-blind, randomized, placebo controlled multicenter study. The included patients had to fulfill the SIRS criteria with a clinical suspicion of infection, an admission APACHE II score greater than 15, and shock, defined as a mean arterial pressure <70 mmHg and/or a decrease <greater than or equal to>40 mmHg despite adequate fluid resuscitation. Patients received 1.0 mg/kg TCV-309 or placebo, twice daily, intravenously during 14 days. The prospectively set goals were MOF score, recovery from shock, mortality, and assessment of the safety of the medication. A total of 98 patients were included of which 97 were analyzed on an intention-to-treat basis. The overall survival at day 56 of TCV-309 treated patients was similar compared to placebo treated patients (51.0% vs. 41.7%, P = 0.47). In contrast, the mean percentage of failed organs per patient present after 14 days in the TCV-309 treated patients was significantly lower compared to the placebo treated patients (11.9% vs. 25.1%, P = 0.04), leading to a reduced need for vasopressors, dialysis, and ventilatory support. Furthermore, the mean APACHE-II score during treatment with TCV-309 was significantly lower and the number of patients recovered from shock after day 14 was significantly higher in the TCV-309 treated patient group (2/32 vs. 9/29, P = 0.01). The number of adverse events was not significantly different between the TCV-309 and placebo treated patients. TCV-309 did not change overall mortality of septic shock, however a substantial reduction in organ dysfunction and morbidity, frequently associated with septic shock was achieved, without significant adverse events.
引用
收藏
页码:421 / 428
页数:8
相关论文
共 44 条
[1]  
Ayala A, 1996, New Horiz, V4, P265
[2]   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
[3]   Sequential systemic platelet-activating factor and interleukin 8 primes neutrophils in patients with trauma at risk of multiple organ failure [J].
Botha, AJ ;
Moore, FA ;
Moore, EE ;
Peterson, VM ;
Silliman, CC ;
Goode, AW .
BRITISH JOURNAL OF SURGERY, 1996, 83 (10) :1407-1412
[4]  
BOUMA MG, 1994, J IMMUNOL, V153, P4159
[5]  
BRAQUET P, 1987, PHARMACOL REV, V39, P97
[6]   PLATELET-ACTIVATING-FACTOR MEDIATES HEMODYNAMIC-CHANGES AND LUNG INJURY IN ENDOTOXIN-TREATED RATS [J].
CHANG, SW ;
FEDDERSEN, CO ;
HENSON, PM ;
VOELKEL, NF .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (05) :1498-1509
[7]   INTERSEPT: An international, multicenter, placebo-controlled trial of monoclonal antibody to human tumor necrosis factor-alpha in patients with sepsis [J].
Cohen, J ;
Carlet, J .
CRITICAL CARE MEDICINE, 1996, 24 (09) :1431-1440
[8]   Systemic inflammatory response syndrome [J].
Davies, MG ;
Hagen, PO .
BRITISH JOURNAL OF SURGERY, 1997, 84 (07) :920-935
[9]  
DENTENER MA, 1993, J IMMUNOL, V150, P2885
[10]  
DHAINAUT JF, 1990, UPDATE INTENSIVE CAR, P100