중환자에서 Dexmedetomidine의 Opioid-Sparing Effect를 고려한 Remifentanil 용량 조절
Dose Adjustment for Remifentanil with Regards to the Opioid- Sparing Effect of Dexmedetomidine in Critically Ill Patients
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Background : Since the ‘analgosedation’was emerged as an important concept forcritically ill patients, the recommendation for a combinational usage of remifentanil anddexmedetomidine as well as its usage has increased. Taking the opioid-sparing effect ofdexmedetomidine into account, the dosage of remifentanil can be reduced if the combination oftwo drugs is used for the purpose of analgosedation which may consequently lead to the reductionof total drug costs. However, no tapering protocol of remifentanil in case of dexmedetomidinecombined as sedative drug has been studied yet and there are no cost-effectiveness data for the opioid-sparing effect of dexmedetomidine. Methods : A retrospective cohort analysis was done on patients treated with remifentanil anddexmedetomidine at the medical intensive care unit (MICU) of a tertiary teaching hospital fromAugust 2013 to September 2013. The success rates of remifentanil reduction and cost reduction ofanalgesics were analyzed via the data of dosage and costs of remifentanil, dexmedetomidine andother rescue analgesics. Results : Of 63 patients admitted to the MICU, 29 patients were treated with remifentanil anddexmedetomidine for analgosedation under mechanical ventilator care and 10 patients weretreated with a half reduced dose of remifentanil. Eight (80%) patients succeeded in reducing theirdose of remifentanil since the used Richmond Agitation-Sedation Scale showed scores between-2and 0 and the numeric rating score for pain was maintained below 5. The rate of cost reductionwas 32.8% (from ₩159,059 to ₩105,283) in comparing the remifentanil-reduction succeeded groupto the failed group (p=0.044). The overall rate of cost reduction was 26.9% in the whole remifentanil-reduction trial group. Conclusions : The dose reduction of remifentanil was successfully achieved in critically illpatients under administration of remifentanil and dexmedetomidine, and it might be cost-effective. This study presents the possibility of an analgosedation adjustment that can be applied toMICU patients treated with both of dexmedetomidine and remifentanil.
Abstract
Background : Since the ‘analgosedation’was emerged as an important concept forcritically ill patients, the recommendation for a combinational usage of remifentanil anddexmedetomidine as well as its usage has increased. Taking the opioid-sparing effect ofdexmedetomidine into account, the dosage of remifentanil can be reduced if the combination oftwo drugs is used for the purpose of analgosedation which may consequently lead to the reductionof total drug costs. However, no tapering protocol of remifentanil in case of dexmedetomidinecombined as sedative drug has been studied yet and there are no cost-effectiveness data for the opioid-sparing effect of dexmedetomidine. Methods : A retrospective cohort analysis was done on patients treated with remifentanil anddexmedetomidine at the medical intensive care unit (MICU) of a tertiary teaching hospital fromAugust 2013 to September 2013. The success rates of remifentanil reduction and cost reduction ofanalgesics were analyzed via the data of dosage and costs of remifentanil, dexmedetomidine andother rescue analgesics. Results : Of 63 patients admitted to the MICU, 29 patients were treated with remifentanil anddexmedetomidine for analgosedation under mechanical ventilator care and 10 patients weretreated with a half reduced dose of remifentanil. Eight (80%) patients succeeded in reducing theirdose of remifentanil since the used Richmond Agitation-Sedation Scale showed scores between-2and 0 and the numeric rating score for pain was maintained below 5. The rate of cost reductionwas 32.8% (from ₩159,059 to ₩105,283) in comparing the remifentanil-reduction succeeded groupto the failed group (p=0.044). The overall rate of cost reduction was 26.9% in the whole remifentanil-reduction trial group. Conclusions : The dose reduction of remifentanil was successfully achieved in critically illpatients under administration of remifentanil and dexmedetomidine, and it might be cost-effective. This study presents the possibility of an analgosedation adjustment that can be applied toMICU patients treated with both of dexmedetomidine and remifentanil.
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