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. 2010 Sep-Oct;31(5):706-15.
doi: 10.1097/BCR.0b013e3181eebee9.

Prevalence and risk factors for development of delirium in burn intensive care unit patients

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Prevalence and risk factors for development of delirium in burn intensive care unit patients

Vivek Agarwal et al. J Burn Care Res. 2010 Sep-Oct.

Abstract

Delirium affects 60 to 80% of ventilated patients and is associated with worse clinical outcomes including death. Unfortunately, there are limited data regarding the prevalence and risk factors of delirium in critically ill burn patients. The objectives of this study were to evaluate the prevalence of delirium in ventilated burn patients, using validated instruments, and to identify its risk factors. Adult ventilated burn patients at two tertiary centers were prospectively evaluated for delirium using the Confusion Assessment Method in the Intensive Care Unit (CAM-ICU) for 30 days or until intensive care unit discharge. Patients with neurologic injuries, severe dementia, and those not expected to survive >24 hours were excluded. Markov logistic regression was used to identify the risk factors of delirium, adjusting for clinically relevant covariates. The 82 ventilated burn patients had a median (interquartile range) age of 48 (38-62) years, Acute Physiology and Chronic Health Evaluation II scores 27 (21-30), and percent burns of 20 (7-32). Prevalence of delirium was 77% with a median duration of 3 (1-6) days. Exposure to benzodiazepines was an independent risk factor for the development of delirium (odds ratio: 6.8 [confidence interval: 3.1-15], P < .001), whereas exposure to both intravenous opiates (0.5 [0.4-0.6], P < .001) and methadone (0.7 [0.5-0.9], P = .02) was associated with a lower risk of delirium. In conclusion, delirium occurred at least once in approximately 80% of ventilated burn patients. Exposure to benzodiazepines was an independent risk factor for delirium, whereas opiates and methadone reduced the risk of developing delirium, possibly through reduction of pain in these patients.

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Conflict of interest statement

Potential financial conflict of interest:

Dr. Pandharipande has received research grant and honoraria from Hospira Inc. Ms. Pun has received honoraria from Hospira Inc. Dr. Ely has received research grant and honoraria from Hospira, Inc, Pfizer, Eli Lilly, GSK, and a research grant from Aspect Medical Systems. The other authors report no financial disclosures.

Figures

Figure 1
Figure 1. Richmond Agitation- Sedation Scale (RASS) and the Confusion Assessment Method of the ICU (CAM-ICU)
This sedation scale and delirium instrument can be used together as a two-step approach to assess consciousness and diagnose delirium. Patients are considered to have delirium, if they have RASS scores of −3 and above and are CAM-ICU positive by having Features 1 and 2, and either 3 or 4 positive. With permission from Dr. E. Wesley Ely from www.icudelirium.org
Figure 1
Figure 1. Richmond Agitation- Sedation Scale (RASS) and the Confusion Assessment Method of the ICU (CAM-ICU)
This sedation scale and delirium instrument can be used together as a two-step approach to assess consciousness and diagnose delirium. Patients are considered to have delirium, if they have RASS scores of −3 and above and are CAM-ICU positive by having Features 1 and 2, and either 3 or 4 positive. With permission from Dr. E. Wesley Ely from www.icudelirium.org
Figure 2
Figure 2. Benzodiazepines (midazolam equivalents) and the probability of developing delirium
The probability of developing delirium increased with the dose of benzodiazepines administered in the previous 24 h. For the purpose of this study, all benzodiazepines were converted to midazolam equivalents, such that 1 mg of midazolam was equal to 0.4 mg of lorazepam and 2 mg of diazepam. This incremental risk of developing delirium was large at low doses and plateaued at around 50 mg/day of midazolam equivalent benzodiazepine exposure.
Figure 3
Figure 3. Opioid exposure (fentanyl equivalents) and the probability of developing delirium
The probability of developing delirium decreased with the dose of opiates administered in the previous 24 h. For the purpose of this study, all intravenous opioids administered were converted to fentanyl equivalents, such that 10 mg of morphine was equal to 150 micrograms of fentanyl.
Figure 4
Figure 4. Methadone and the probability of developing delirium
The probability of developing delirium decreased with increasing dose of methadone administered in the previous 24 h.

References

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