Safety of dexmedetomidine for the control of agitation in critically ill traumatic brain injury patients: a descriptive study.


Journal

Journal of clinical pharmacy and therapeutics
ISSN: 1365-2710
Titre abrégé: J Clin Pharm Ther
Pays: England
ID NLM: 8704308

Informations de publication

Date de publication:
Aug 2021
Historique:
revised: 25 01 2021
received: 09 09 2020
accepted: 08 02 2021
pubmed: 20 2 2021
medline: 15 12 2021
entrez: 19 2 2021
Statut: ppublish

Résumé

Behavioural disturbances such as agitation are common following traumatic brain injury and can interfere with treatments, cause self-harm and delay rehabilitation. As there is a lack of evidence on the optimal approach to manage agitation in recovering TBI patients, various pharmacological agents are used including antipsychotics, anticonvulsants and sedative agents. Among sedatives, the safety and efficacy of dexmedetomidine to control agitation in traumatic brain injury patients is not well documented. To describe the safety, use and efficacy of dexmedetomidine for the management of agitation following traumatic brain injury in the intensive care unit. Medical records of all patients admitted to the intensive care unit of the Hôpital Sacré-Coeur de Montréal for a traumatic brain injury who received dexmedetomidine for agitation between 1 January 2017 and 31 December 2017 were reviewed. Patients who received dexmedetomidine for indications other than agitation were excluded. Data on dexmedetomidine prescription practices and safety were extracted. Frequency of agitation and concomitant psychoactive medication use was explored over a period starting two days prior to the initiation of dexmedetomidine to six days after or discontinuation, whichever came first. We identified 41 patients in whom dexmedetomidine was initiated. Dexmedetomidine was started on median ICU day 3 (25 Dexmedetomidine use was safe and associated with a reduction in agitation in traumatic brain injury patients in the 96 hours following its initiation.

Sections du résumé

BACKGROUND BACKGROUND
Behavioural disturbances such as agitation are common following traumatic brain injury and can interfere with treatments, cause self-harm and delay rehabilitation. As there is a lack of evidence on the optimal approach to manage agitation in recovering TBI patients, various pharmacological agents are used including antipsychotics, anticonvulsants and sedative agents. Among sedatives, the safety and efficacy of dexmedetomidine to control agitation in traumatic brain injury patients is not well documented.
OBJECTIVE OBJECTIVE
To describe the safety, use and efficacy of dexmedetomidine for the management of agitation following traumatic brain injury in the intensive care unit.
METHODS METHODS
Medical records of all patients admitted to the intensive care unit of the Hôpital Sacré-Coeur de Montréal for a traumatic brain injury who received dexmedetomidine for agitation between 1 January 2017 and 31 December 2017 were reviewed. Patients who received dexmedetomidine for indications other than agitation were excluded. Data on dexmedetomidine prescription practices and safety were extracted. Frequency of agitation and concomitant psychoactive medication use was explored over a period starting two days prior to the initiation of dexmedetomidine to six days after or discontinuation, whichever came first.
RESULTS RESULTS
We identified 41 patients in whom dexmedetomidine was initiated. Dexmedetomidine was started on median ICU day 3 (25
CONCLUSION CONCLUSIONS
Dexmedetomidine use was safe and associated with a reduction in agitation in traumatic brain injury patients in the 96 hours following its initiation.

Identifiants

pubmed: 33606290
doi: 10.1111/jcpt.13389
doi:

Substances chimiques

Antipsychotic Agents 0
Hypnotics and Sedatives 0
Benzodiazepines 12794-10-4
Dexmedetomidine 67VB76HONO

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1020-1026

Informations de copyright

© 2021 John Wiley & Sons Ltd.

Références

Corrigan JD, Selassie AW, Orman JA. The epidemiology of traumatic brain injury. J Head Trauma Rehabil. 2010;25:72-80.
Arciniegas DB. Addressing neuropsychiatric disturbances during rehabilitation after traumatic brain injury: current and future methods. Dialogues Clin Neurosci. 2011;13:325-345.
Bogner J, Barrett RS, Hammond FM, et al. Predictors of agitated behavior during inpatient rehabilitation for traumatic brain injury. Arch Phys Med Rehabil. 2015;96:S274-S81 e4.
Bogner JA, Corrigan JD, Fugate L, Mysiw WJ, Clinchot D. Role of agitation in prediction of outcomes after traumatic brain injury. Am J Phys Med Rehabil. 2001;80:636-644.
Williamson DR, Cherifa SI, Frenette AJ, et al. Agitation, confusion, and aggression in critically ill traumatic brain injury - a pilot cohort study. Pilot Feasibility Stud. 2020;6:193.
Ganau M, Lavinio A, Prisco L. Delirium and agitation in traumatic brain injury patients: an update on pathological hypotheses and treatment options. Minerva Anestesiol. 2018;84:632-640.
Perreault M, Talic J, Frenette A, Burry L, Bernard F, Williamson D. Agitation after mild to moderate traumatic brain injury in the intensive care unit. Crit Care. 2017;21(Suppl 1):P219.
Brooke MM, Questad KA, Patterson DR, Bashak KJ. Agitation and restlessness after closed head injury: a prospective study of 100 consecutive admissions. Arch Phys Med Rehabil. 1992;73:320-323.
Nott MT, Chapparo C, Baguley IJ. Agitation following traumatic brain injury: an Australian sample. Brain Inj. 2006;20:1175-1182.
Singh R, Venkateshwara G, Nair KP, Khan M, Saad R. Agitation after traumatic brain injury and predictors of outcome. Brain Inj. 2014;28:336-340.
Luaute J, Plantier D, Wiart L, Tell L, group S. Care management of the agitation or aggressiveness crisis in patients with TBI. Systematic review of the literature and practice recommendations. Ann Phys Rehabil Med. 2016;59:58-67.
Ponsford J, Bayley M, Wiseman-Hakes C, et al. INCOG recommendations for management of cognition following traumatic brain injury, part II: attention and information processing speed. J Head Trauma Rehabil. 2014;29:321-337.
Williamson D, Frenette AJ, Burry LD, et al. Pharmacological interventions for agitated behaviours in patients with traumatic brain injury: a systematic review. BMJ Open. 2019;9:e029604.
Fugate LP, Spacek LA, Kresty LA, Levy CE, Johnson JC, Mysiw WJ. Measurement and treatment of agitation following traumatic brain injury: II. a survey of the brain injury special interest group of the american academy of physical medicine and rehabilitation. Arch Phys Med Rehabil. 1997;78:924-928.
Pisa FE, Cosano G, Giangreco M, et al. Prescribing practice and off-label use of psychotropic medications in post-acute brain injury rehabilitation centres: a cross-sectional survey. Brain Inj. 2015;29:508-516.
Keating GM. Dexmedetomidine: a review of its use for sedation in the intensive care setting. Drugs. 2015;75:1119-1130.
Jakob SM, Ruokonen E, Grounds RM, et al. Dexmedetomidine vs midazolam or propofol for sedation during prolonged mechanical ventilation: two randomized controlled trials. JAMA. 2012;307:1151-1160.
Riker RR, Shehabi Y, Bokesch PM, et al. Dexmedetomidine vs midazolam for sedation of critically ill patients: a randomized trial. JAMA. 2009;301:489-499.
Pasin L, Landoni G, Nardelli P, et al. Dexmedetomidine reduces the risk of delirium, agitation and confusion in critically Ill patients: a meta-analysis of randomized controlled trials. J Cardiothorac Vasc Anesth. 2014;28:1459-1466.
Pandharipande PP, Pun BT, Herr DL, et al. Effect of sedation with dexmedetomidine vs lorazepam on acute brain dysfunction in mechanically ventilated patients: the MENDS randomized controlled trial. JAMA. 2007;298:2644-2653.
Devlin JW, Skrobik Y, Gelinas C, et al. Clinical practice guidelines for the prevention and management of pain, agitation/sedation, delirium, immobility, and sleep disruption in adult patients in the ICU. Crit Care Med. 2018;46:e825-e873.
Reade MC, Finfer S. Sedation and delirium in the intensive care unit. N Engl J Med. 2014;370:444-454.
Pajoumand M, Kufera JA, Bonds BW, et al. Dexmedetomidine as an adjunct for sedation in patients with traumatic brain injury. The journal of trauma and acute care surgery. 2016;81:345-351.
Humble SS, Wilson LD, Leath TC, et al. ICU sedation with dexmedetomidine after severe traumatic brain injury. Brain Inj. 2016;30:1266-1270.
Tang JF, Chen PL, Tang EJ, May TA, Stiver SI. Dexmedetomidine controls agitation and facilitates reliable, serial neurological examinations in a non-intubated patient with traumatic brain injury. Neurocrit Care. 2011;15:175-181.
Gagnon DJ, Fontaine GV, Smith KE, et al. Valproate for agitation in critically ill patients: A retrospective study. J Crit Care. 2017;37:119-125.
Zhang J, Yu Y, Miao S, et al. Effects of peri-operative intravenous administration of dexmedetomidine on emergence agitation after general anesthesia in adults: a meta-analysis of randomized controlled trials. Drug Des Devel Ther. 2019;13:2853-2864.
Reade MC, Eastwood GM, Bellomo R, et al. Effect of Dexmedetomidine added to standard care on ventilator-free time in patients with agitated delirium: a randomized clinical trial. JAMA. 2016;315:1460-1468.
Dupuis S, Brindamour D, Karzon S, et al. A systematic review of interventions to facilitate extubation in patients difficult-to-wean due to delirium, agitation, or anxiety and a meta-analysis of the effect of dexmedetomidine. Canadian journal of anaesthesia. Can J Anaesth. 2019;66:318-327.
Frenette AJ, Bebawi ER, Deslauriers LC, et al. Validation and comparison of CAM-ICU and ICDSC in mild and moderate traumatic brain injury patients. Intensive Care Med. 2016;42:122-123.
Larsen LK, Frokjaer VG, Nielsen JS, et al. Delirium assessment in neuro-critically ill patients: a validation study. Acta Anaesthesiol Scand. 2019;63:352-359.

Auteurs

Véronique Bilodeau (V)

Faculté de pharmacie, Université de Montréal, Montreal, Canada.

Mar Saavedra-Mitjans (M)

Faculté de pharmacie, Université de Montréal, Montreal, Canada.
Research center, Hôpital du Sacré-Cœur-de-Montréal, Montreal, Canada.

Anne Julie Frenette (AJ)

Faculté de pharmacie, Université de Montréal, Montreal, Canada.
Research center, Hôpital du Sacré-Cœur-de-Montréal, Montreal, Canada.
Pharmacy Department, Hôpital du Sacré-Cœur-de-Montréal, Montreal, Canada.

Lisa Burry (L)

Pharmacy Department, Mount Sinai Hospital, Toronto, Canada.
Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada.

Martin Albert (M)

Department of Critical Care, Hôpital du Sacré-Coeur de Montréal, Montreal, Canada.
Department of Medicine, Faculté de médecine, Université de Montréal, Montreal, Canada.

Francis Bernard (F)

Department of Critical Care, Hôpital du Sacré-Coeur de Montréal, Montreal, Canada.
Department of Medicine, Faculté de médecine, Université de Montréal, Montreal, Canada.

David R Williamson (DR)

Faculté de pharmacie, Université de Montréal, Montreal, Canada.
Research center, Hôpital du Sacré-Cœur-de-Montréal, Montreal, Canada.
Pharmacy Department, Hôpital du Sacré-Cœur-de-Montréal, Montreal, Canada.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH