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International sepsis trial (INTERSEPT)Role and impact of a Clinical Evaluation Committee

 

作者: Charles L. MD Sprung,   Roger G. MD Finch,   Lambertus G. MD Thijs,   Michel P. MD Glauser,  

 

期刊: Critical Care Medicine  (OVID Available online 1996)
卷期: Volume 24, issue 9  

页码: 1441-1447

 

ISSN:0090-3493

 

年代: 1996

 

出版商: OVID

 

数据来源: OVID

 

摘要:

ObjectiveSeveral large clinical trials have recently evaluated a variety of potential therapeutic interventions for sepsis and have yielded negative results based on analyses of intention-to-treat cohorts. The present study was undertaken to evaluate the importance of a Clinical Evaluation Committee.DesignProspective, double-blind evaluation of a prospective, controlled, double-blind, randomized, multinational trial.SettingForty medical centers.PatientsFive hundred fifty-three infused patients with severe sepsis and septic shock.MethodsAs part of an international trial (INTERSEPT) of anti-tumor necrosis factor therapy, a Scientific Extramural Review Commitee prospectively defined and excluded patients with confounding events that objectively interfered with the potential of any intervention for sepsis to exercise its therapeutic effect. These confounding events included inappropriate antimicrobial therapy, inadequate medical-surgical management, underlying disorders, and forgoing life-sustaining therapies before management had failed. Patients who met all inclusion and exclusion criteria and who had no confounding events were defined as the Scientific Extramural Review Committee group.Measurements and Main ResultsFive hundred fifty-three patients were enrolled in INTERSEPT. Seventy-seven patients did not meet inclusion and exclusion criteria. Sixty patients had confounding events, including inappropriate antimicrobial therapy (n = 28), inadequate medical-surgical management (n = 16), underlying disorders (n = 17), and forgoing life-sustaining therapies (n = 7). Four hundred sixteen patients were in the Scientific Extramural Review Committee group and their mortality rates were different from the mortality rates of the intent-to-treat cohort. In the intent-to-treat analysis among shock patients, low-dose anti-tumor necrosis factor reduced 28-day mortality by 14.5% (p = .34), whereas in the Scientific Extramural Review Committee group, the study drug reduced mortality by 26.5% (p = .16). More patients in the high dose anti-tumor necrosis factor treatment arm (31/176) were in the invalid Scientific Extramural Review Committee group than in the other two arms (16/157 and 13/143, respectively, p < .05).ConclusionsIn large trials of sepsis, in addition to analyzing the intent-to-treat cohort, patients in compliance with the protocol and with no confounding events should also be analyzed. These results should assist in determining whether treatment groups are comparable and provide a greater likelihood of demonstrating the potential efficacy of a new therapy for sepsis. A Clinical Evaluation Committee is important to properly assess a clinical sepsis trial.(Crit Care Med 1996; 24:1441-1447)

 



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