Preventing ICU Subsyndromal Delirium Conversion to Delirium With Low-Dose IV Haloperidol: A Double-Blind, Placebo-Controlled Pilot Study*

被引:72
|
作者
Al-Qadheeb, Nada S. [1 ]
Skrobik, Yoanna [2 ]
Schumaker, Greg [3 ]
Pacheco, Manuel N. [4 ]
Roberts, Russel J. [5 ]
Ruthazer, Robin R. [6 ,7 ]
Devlin, John W. [1 ,3 ]
机构
[1] Northeastern Univ, Sch Pharm, Boston, MA 02115 USA
[2] McGill Univ, Ctr Hlth, Dept Med, Montreal, PQ, Canada
[3] Tufts Med Ctr, Div Pulm Crit Care & Sleep Med, Boston, MA USA
[4] Tufts Med Ctr, Dept Psychiat, Boston, MA USA
[5] Tufts Med Ctr, Dept Pharm, Boston, MA USA
[6] Tufts Med Ctr, Tufts Clin & Translat Sci Inst, Res Design Ctr, Boston, MA USA
[7] Tufts Med Ctr, Tufts Clin & Translat Sci Inst, Biostat Res Ctr, Boston, MA USA
基金
美国国家卫生研究院;
关键词
prevention; haloperidol; randomized controlled trial; delirium; CRITICALLY-ILL PATIENTS; INTENSIVE-CARE-UNIT; MECHANICALLY VENTILATED PATIENTS; PUMP CARDIAC-SURGERY; POSTOPERATIVE DELIRIUM; CONTROLLED-TRIAL; RISK-FACTORS; WAKE-UP; SEDATION; EFFICACY;
D O I
10.1097/CCM.0000000000001411
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To compare the efficacy and safety of scheduled low-dose haloperidol versus placebo for the prevention of delirium (Intensive Care Delirium Screening Checklist >= 4) administered to critically ill adults with subsyndromal delirium (Intensive Care Delirium Screening Checklist = 1-3). Design: Randomized, double-blind, placebo-controlled trial. Setting: Three 10-bed ICUs (two medical and one surgical) at an academic medical center in the United States. Patients: Sixty-eight mechanically ventilated patients with subsyndromal delirium without complicating neurologic conditions, cardiac surgery, or requiring deep sedation. Interventions: Patients were randomly assigned to receive IV haloperidol 1 mg or placebo every 6 hours until delirium occurred (Intensive Care Delirium Screening Checklist >= 4 with psychiatric confirmation), 10 days of therapy had elapsed, or ICU discharge. Measurements and Main Results: Baseline characteristics were similar between the haloperidol (n = 34) and placebo (n = 34) groups. A similar number of patients given haloperidol (12/34 [35%]) and placebo (8/34 [23%]) developed delirium (p = 0.29). Haloperidol use reduced the hours per study day spent agitated (Sedation Agitation Scale >= 5) (p = 0.008), but it did not influence the proportion of 12-hour ICU shifts patients spent alive without coma (Sedation Agitation Scale <= 2) or delirium (p = 0.36), the time to first delirium occurrence (p = 0.22), nor delirium duration (p = 0.26). Days of mechanical ventilation (p = 0.80), ICU mortality (p = 0.55), and ICU patient disposition (p = 0.22) were similar in the two groups. The proportion of patients who developed corrected QT-interval prolongation (p = 0.16), extrapyramidal symptoms (p = 0.31), excessive sedation (p = 0.31), or new-onset hypotension (p = 1.0) that resulted in study drug discontinuation was comparable between the two groups. Conclusions: Low-dose scheduled haloperidol, initiated early in the ICU stay, does not prevent delirium and has little therapeutic advantage in mechanically ventilated, critically ill adults with subsyndromal delirium.
引用
收藏
页码:583 / 591
页数:9
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