Feasibility, efficacy, and safety of antipsychotics for intensive care unit delirium: The MIND randomized, placebo-controlled trial

被引:293
作者
Girard, Timothy D. [1 ,2 ,10 ]
Pandharipande, Pratik P. [3 ,11 ]
Carson, Shannon S. [6 ]
Schmidt, Gregory A. [7 ]
Wright, Patrick E. [8 ]
Canonico, Angelo E. [9 ]
Pun, Brenda T. [1 ]
Thompson, Jennifer L. [4 ]
Shintani, Ayumi K. [4 ]
Meltzer, Herbert Y. [5 ]
Bernard, Gordon R. [1 ]
Dittus, Robert S. [2 ,10 ]
Ely, E. Wesley [1 ,2 ,10 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Div Allergy Pulm & Crit Care Med, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Sch Med, Ctr Hlth Serv Res, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Anesthesiol, Div Crit Care, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Dept Biostat, Nashville, TN 37212 USA
[5] Vanderbilt Univ, Sch Med, Dept Psychiat, Nashville, TN 37212 USA
[6] Univ N Carolina, Dept Med, Div Pulm & Crit Care Med, Chapel Hill, NC USA
[7] Univ Iowa, Dept Internal Med, Div Pulm Dis Crit Care & Occupat Med, Carver Coll Med, Iowa City, IA 52242 USA
[8] Moses Cone Mem Hosp, Greensboro, NC USA
[9] St Thomas Hosp, Dept Med, Nashville, TN USA
[10] Tennessee Valley Healthcare Syst, Geriatr Res Educ & Clin Ctr Serv, Dept Vet Affairs Med Ctr, Nashville, TN USA
[11] Tennessee Valley Healthcare Syst, Anesthesia Serv, Dept Vet Affairs Med Ctr, Nashville, TN USA
关键词
delirium; intensive care units; antipsychotic agents; haloperidol; ziprasidone; clinical trial; MECHANICALLY VENTILATED PATIENTS; CONFUSION ASSESSMENT METHOD; AGITATION-SEDATION SCALE; CRITICALLY-ILL PATIENTS; INFORMANT QUESTIONNAIRE; COGNITIVE DECLINE; ELDERLY IQCODE; HALOPERIDOL; RISK; RELIABILITY;
D O I
10.1097/CCM.0b013e3181c58715
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To demonstrate the feasibility of a placebo-controlled trial of antipsychotics for delirium in the intensive care unit and to test the hypothesis that antipsychotics would improve days alive without delirium or coma. Design: Randomized, double-blind, placebo-controlled trial. Setting. Six tertiary care medical centers in the US. Patients: One hundred one mechanically ventilated medical and surgical intensive care unit patients. Intervention: Patients were randomly assigned to receive haloperidol or ziprasidone or placebo every 6 hrs for up to 14 days. Twice each day, frequency of study drug administration was adjusted according to delirium status, level of sedation, and side effects. Measurements and Main Outcomes: The primary end point was the number of days patients were alive without delirium or coma. During the 21-day study period, patients in the haloperidol group spent a similar number days alive without delirium or coma(median [interquartile range], 14.0 [6.0-18.0] days) as did patients in the ziprasidone (15.0 [9.1-18.0] days) and placebo groups (12.5 [1.2-17.2] days; p = 0.66). No differences were found in secondary clinical outcomes, including ventilator-free days (p = .25), hospital length of stay (p = .68), and mortality (p = .81). Ten (29%) patients in the haloperidol group reported symptoms consistent with akathisia, compared with six (20%) patients in the ziprasidone group and seven (19%) patients in the placebo group (p = .60), and a global measure of extrapyramidal symptoms was similar between treatment groups (p = .46). Conclusions: A randomized, placebo-controlled trial of antipsychotics for delirium in mechanically ventilated intensive care unit patients is feasible. Treatment with antipsychotics in this limited pilot trial did not improve the number of days alive without delirium or coma, nor did it increase adverse outcomes. Thus, a large trial is needed to determine whether use of antipsychotics for intensive care unit delirium is appropriate. (Crit Care Med 2010; 38:428-437) Trial Registration: ClinicalTrials.gov, number NCT00096863.
引用
收藏
页码:428 / 437
页数:10
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