Jean Lachaine , Catherine BeaucheminABSTRACT
Background
Dexmedetomidine is an α 2 -receptor agonist administered by continuous infusion in the intensive care unit (ICU) for sedation of critically ill patients who are undergoing mechanical ventilation following intubation. Relative to ICU patients receiving midazolam (a γ-aminobutyric acid agonist) for sedation, those receiving dexmedetomidine spent less time on ventilation, had fewer episodes of delirium, and had a lower incidence of tachycardia and hypertension.
Objective
To assess the economic impact, in a Canadian context, of dexmedetomidine, relative to midazolam, for sedation in the ICU.
Methods
This economic evaluation was based on a cost–consequences analysis, from the perspective of the Canadian health care system. The selected time horizon was an ICU stay (maximum 30 days). Clinical data were obtained from a previously published prospective, randomized, double-blind trial comparing dexmedetomidine and midazolam. This evaluation considered the costs of the medications, mechanical ventilation, and delirium episodes, as well as costs associated with adverse events requiring an intervention. All costs were adjusted to 2010 and are reported in Canadian dollars.
Results
The average cost of the medication was higher for dexmedetomidine than midazolam ($1929.57 versus $180.10 per patient), but the average costs associated with mechanical ventilation and management of delirium were lower with dexmedetomidine than with midazolam ($2939 versus $4448 for ventilation; $2127 versus $3012 for delirium). The overall cost per patient was lower with dexmedetomidine than with midazolam ($7022 versus $7680). Deterministic sensitivity analysis confirmed the robustness of the difference.
Conclusions
The use of dexmedetomidine was, in most contexts, a more favourable strategy than the use of midazolam, in terms of clinical consequences and economic impact. Dexmedetomidine was less expensive than midazolam and was associated with lower occurrence of delirium and shorter duration of mechanical ventilation.
KEYWORDS: dexmedetomidine , sedation , intensive care unit , economic evaluation
RÉSUMÉ
Contexte
La dexmédétomidine est un agoniste des récepteurs alpha-2 adrénergiques qu’on administre par perfusion continue à l’unité de soins intensifs (USI) pour la sédation des patients en phase critique, mis sous ventilation artificielle après intubation. Par rapport aux patients de l’USI qui ont reçu du midazolam (un agoniste de l’acide gamma-aminobutyrique) comme sédatif, ceux qui ont reçu de la dexmédétomidine sont restés moins longtemps sous ventilation, ont éprouvé moins d’épisodes de délire et ont connu une incidence plus faible de tachycardie et d’hypertension.
Objectif
Comparer les coûts de l’emploi de la dexmédétomidine à ceux du midazolam pour la sédation des patients d’une USI dans un contexte canadien.
Méthodes
Une évaluation économique fondée sur une analyse coûts-conséquences a été menée dans le contexte du système de soins de santé canadien. La période d’évaluation retenue a été un séjour à l’USI d’un maximum de 30 jours. Les données cliniques ont été tirées des résultats publiés d’un essai prospectif, à répartition aléatoire et à double insu comparant la dexmédétomidine et le midazolam. Les coûts pris en compte dans cette évaluation étaient ceux des médicaments, de la ventilation artificielle, des épisodes de délire de même que ceux associés aux événements indésirables nécessitant une intervention. Tous les coûts ont été convertis en dollars de 2010 et sont présentés en dollars canadiens.
Résultats
Le coût moyen des médicaments était plus élevé pour la dexmédétomidine que pour le midazolam (1929,57 $ contre 180,10 $ par patient), mais les coûts moyens associés à la ventilation artificielle et à la prise en charge du délire étaient moins élevés avec la dexmédétomidine qu’avec le midazolam (2939 $ contre 4448 $ pour la ventilation; 2127 $ contre 3012 $ pour le délire). Le coût global par patient était inférieur avec la dexmédétomidine qu’avec le midazolam (7022 $ contre 7680 $). Une analyse de sensibilité déterministe a confirmé la robustesse de cette différence.
Conclusions
L’emploi de la dexmédétomidine était dans la plupart des cas une stratégie préférable à l’emploi du midazolam, pour ce qui est des conséquences cliniques et de la résultante financière. La dexmédétomidine s’est révélée moins chère que le midazolam et a été associée à une fréquence moindre de délire et à une durée moindre de la ventilation artificielle.
MOTS CLÉS: dexmédétomidine , sédation , unité de soins intensifs , évaluation économique
[Traduction par l’éditeur]
Life-saving treatments such as mechanical ventilation, dialysis, and use of central venous catheters administered in the intensive care unit (ICU) often require sedation and analgesia to help the healing process, to facilitate use of life-support technology, and to relieve anxiety and pain. Previous studies have shown that strategies for sedation, such as provision of analgesia before sedation according to specific protocols, use of a scoring system for both sedation and delirium (to help recognize serious adverse effects associated with the medications administered), and effective monitoring of pain and delirium, have potential effects on patient outcomes and therefore on utilization of health care resources.1–3
Currently, 2 classes of medications are commonly used for sedation: γ-aminobutyric acid (GABA) agonists, such as midazolam, lorazepam, and propofol; and α 2 -agonists, such as clonidine and dexmedetomidine. In Canada, midazolam and propofol are the most common sedatives,4 whereas in the United States, midazolam, lorazepam, and propofol tend to be used most frequently.5 GABA agonists generally cause prolonged sedation and are known to interact with other medications and to cause serious adverse events such as hypotension and respiratory depression. Because α 2 -agonists provide analgesia and sedation with little or no respiratory depression, they represent an interesting alternative to GABA agonists. The choice between these 2 drug classes also influences the occurrence of delirium, the duration of mechanical ventilation, the length of the ICU stay, and, consequently, health care costs.3
Precedex (dexmedetomidine; Hospira Canada) received its notice of compliance from Health Canada on December 9, 2009.6 Dexmedetomidine is administered by continuous infusion for sedation of critically ill ICU patients who have undergone intubation and are receiving mechanical ventilation. Clinical trials have already demonstrated its clinical efficacy and safety.7,8 In particular, dexmedetomidine was associated with shorter duration of mechanical ventilation, fewer episodes of delirium, and lower incidences of tachycardia and hypertension, relative to midazolam, but a higher incidence of bradycardia.8 Recently, a cost-minimization analysis conducted in the United States compared dexmedetomidine with midazolam for long-term sedation in the ICU.9 The objective of that study was to compare dexmedetomidine and midazolam in terms of the costs associated with administration to patients undergoing mechanical ventilation in the ICU and to identify the factors influencing these costs. The analysis took into account all costs incurred during the ICU stay, including costs associated with ICU care and mechanical ventilation, administration of the study drug, and treatment of adverse effects. Including drug acquisition cost, sedation with dexmedetomidine was much less expensive than sedation with midazolam. The savings were due mainly to a shorter stay in the ICU and lower costs of mechanical ventilation. However, until now, no economic evaluation has estimated the economic impact of dexmedetomidine from a Canadian perspective.
In the current Canadian context, there is enormous variability in clinicians’ sedation practices, not only in terms of choice of drugs but also in the use of standard protocols for and monitoring of sedation.10 Given the magnitude of potential savings associated with choice of treatment and the possible need to standardize sedation practices throughout Canada, it is even more relevant to consider the economic benefits that could result from using dexmedetomidine instead of other sedatives that are commonly used in Canada, such as midazolam and propofol.
The objective of this cost–consequences evaluation was to compare dexmedetomidine and midazolam in terms of the costs associated with administration of these drugs in critically ill patients in Canadian ICUs, with consideration of their respective efficacy and safety.
To assess the economic impact of dexmedetomidine for sedation in the ICU, relative to midazolam, this economic evaluation was based on a cost–consequences analysis. The analysis was performed in accordance with the latest guidelines for economic evaluation of health technologies developed in Canada, as recommended by the Canadian Agency for Drugs and Technology in Health (CADTH).11 Midazolam was chosen as the comparator to allow use of data from the clinical evaluation performed by Riker and others,8 but also because this agent is widely used in Canada for the sedation of ICU patients and because it represents a relatively inexpensive treatment choice.
A cost–consequences analysis is usually not a preferred method for economic evaluation. However, in this case, it was deemed to be the most appropriate for highlighting the features that differentiate dexmedetomidine and midazolam both clinically and economically, according to the results of the Safety and Efficacy of Dexmedetomidine COmpared with Midazolam (SEDCOM) study.8 Those results indicated no difference between dexmedetomidine and midazolam in terms of time to achieve the targeted sedation level in mechanically ventilated patients in the ICU. However, at comparable sedation levels, patients treated with dexmedetomidine spent less time on mechanical ventilation and experienced less delirium, and there was a lower incidence of tachycardia and hypertension. Since there is no clinical evidence supporting a difference in efficacy between these 2 treatments, a cost-effectiveness analysis or a cost-utility analysis would not be appropriate. Moreover, although control of sedation and avoidance of delirium have a positive impact on quality of life, these effects occur only for relatively short periods of time. Consequently, estimation of quality-adjusted life-years (QALYs) resulting from this intervention would be inadequate. Indeed, Bala and Zarkin12 used the dentistry example of local anesthesia for a root canal procedure to demonstrate that QALYs are not applicable for assessing short-term health states. Moreover, given that the 2 treatments being compared in the current study differ in terms of duration of mechanical ventilation and incidence of adverse events, it would be inappropriate to perform a cost-minimization analysis, which requires equivalence of treatments.
This economic evaluation was performed from the perspective of the Canadian health care system. An analysis from the societal perspective would also have been of interest, but available data did not allow us to identify differences between treatments that would affect costs incurred outside the health system, such as costs borne by the patient or the patient’s family or costs associated with productivity losses.
The clinical data for this economic evaluation were drawn from the SEDCOM study, which was undertaken to compare dexmedetomidine and midazolam in terms of the efficacy and safety of prolonged sedation induced by these 2 agents in patients undergoing mechanical ventilation. The SEDCOM study was a prospective randomized, double-blind trial conducted in 68 centres in 5 countries between March 2005 and August 2007. The study enrolled 375 patients in medical or surgical ICUs for whom mechanical ventilation and sedation for a period of 3 days or more were anticipated. The patients had no significant concurrent disease.
The level of sedation was assessed with the Richmond Agitation–Sedation Scale (RASS),13 and the level of delirium was assessed with the Confusion Assessment Method for the ICU (CAM-ICU).14
Dexmedetomidine (0.2–1.4 mg/kg per hour) was administered to 244 patients and midazolam (0.02–0.1 mg/kg per hour) was administered to 122 patients to achieve light sedation (RASS score between −2 and +1). The drug was given from the date of each patient’s recruitment until extubation or for a maximum of 30 days. The average duration of dexmedetomidine administration in the SEDCOM study was 3.5 days, whereas the Canadian product monograph indicates that dexmedetomidine infusion should not exceed 24 h.15 The primary outcome was the percentage of time that each patient spent within the target RASS range. Secondary outcomes were the prevalence and duration of delirium, the use of fentanyl and open-label midazolam, and nursing assessments. Other outcomes, such as duration of mechanical ventilation, length of stay in the ICU, and incidence of adverse events, were also considered. All outcome measures were defined within a time horizon corresponding to a maximum ICU stay of 30 days.
According to the results of the SEDCOM study,8 there was no significant difference between treatment arms in terms of the percentage of time spent within the target RASS range. However, the prevalence of delirium episodes was lower and the median time to extubation was shorter among patients treated with dexmedetomidine. Time in the ICU was shorter with dexmedetomidine than with midazolam, but this difference did not reach statistical significance. Bradycardia was more likely to develop in patients treated with dexmedetomidine (42.2% versus 18.9%; p < 0.001), but the difference in the proportion of patients requiring additional intervention was not significant. As well, there was a lower tendency for development of tachycardia and hypertension requiring treatment among patients treated with dexmedetomidine.
The following costs were considered in this analysis: costs associated with the sedatives (dexmedetomidine and midazolam), costs of open-label treatment involving additional administration of midazolam, costs of an ICU stay with mechanical ventilation, and costs associated with adverse events. The cost of an ICU stay with mechanical ventilation was derived from the fully allocated accounting system of St Paul’s Hospital in Vancouver, British Columbia, as reported by Anis and others.16 The cost associated with episodes of delirium (one of the adverse events) was adapted for Canada from a US study that specifically focused on extra costs incurred by the occurrence of delirium.17 The cost of dexmedetomidine (Precedex) was provided by the manufacturer (Hospira Canada), and the cost of midazolam was taken from Quebec’s Liste des médicaments .18 The overall cost of treatment took into account the doses administered in the SEDCOM study and the period over which treatment was administered. For adverse events necessitating intervention, the cost of medical consultation was added. Specifically, the physician’s fee for care of a patient in the ICU was $130, according to the current billing manual of the Régie de l’assurance maladie du Québec.19 All costs were adjusted to reflect the value in 2010, according to Statistics Canada’s consumer price index for health care.20 However, given the short time horizon of the study, it was not necessary to discount either costs or effects.
To estimate the robustness of the baseline results, deterministic sensitivity analyses were performed. These analyses took into account alternative values for the cost of an ICU stay, the cost of mechanical ventilation, and the cost of delirium episodes.
The outcome measures for the comparison of dexmedetomidine and midazolam, as determined in the SEDCOM study,8 are reported in Table 1. There was no significant difference between the 2 drugs in terms of the percentage of time in the target sedation range or duration of the ICU stay. However, the duration of mechanical ventilation was significantly longer with midazolam, and higher proportions of the patients receiving midazolam had delirium and hypertension episodes requiring intervention. Also, fewer patients treated with midazolam required open-label midazolam.8
Table 1
Efficacy and Safety of Treatment with Dexmedetomidine and Midazolam*
All costs associated with sedation with dexmedetomidine and midazolam, in addition to the costs associated with additional outcomes, are reported in Table 2. Taking into account the dose of each drug administered and the duration of administration, the estimated cost was significantly higher for dexmedetomidine than for midazolam. For some patients, adjunct therapy with additional doses of midazolam was needed. The average per-patient cost of this additional treatment, estimated on the basis of the proportion of patients for whom this additional therapy was required and the median dose used, was minimal.
Table 2
Calculation of Costs Associated with Sedation with Dexmedetomidine and Midazolam
Additional outcomes included the duration of mechanical ventilation, the length of stay in the ICU, and adverse effects. The cost of an ICU stay could be found for only one Canadian institution, specifically the estimate based on the fully allocated accounting system of St Paul’s Hospital in Vancouver, British Columbia (the St Paul’s Hospital Cost Model), reported by Anis and others.16 Dasta and others9 estimated that the average daily costs of mechanical ventilation represented 31.9% of the overall daily cost of intensive care. This proportion was applied to the average daily cost of ICU care in Canada to estimate the daily cost of mechanical ventilation. Given that patients treated with dexmedetomidine and midazolam required 3.7 and 5.6 days of mechanical ventilation in the ICU, respectively, the costs associated with mechanical ventilation were estimated as $2939 and $4448, respectively (Table 2).
The costs associated with delirium episodes were estimated using data collected by Milbrandt and others,17 who found that delirium was associated with a 39% (95% confidence interval [CI] 12%–72%) increase in the cost of ICU care. To estimate the cost associated with delirium per Canadian patient, this 39% increase was adjusted to take into account the fact that average ICU costs already include the costs for patients both with and without delirium. According to the recent Delirium Epidemiology in Critical Care (DECCA) study by Salluh and others,21 the percentage of ICU patients with delirium was 32.3%. On the basis of this adjustment, the 39% increase reported by Milbrandt and others17 corresponds to a 23.4% increase for Canadian patients (adjusted 95% CI 7.8%–39.5%). Because the lengths of stay in the ICU were not statistically different between the 2 groups, the average of the 2 group means was used as a conservative estimate of overall mean length of stay. The proportion of patients experiencing delirium was smaller in the dexmedetomidine group than in the midazolam group (54.1% and 76.6%, respectively), and the average costs per patient associated with delirium were therefore calculated as $2127 and $3012, respectively (Table 2).
In each treatment arm, some patients experienced adverse events, such as hypotension, bradycardia, tachycardia, and hypertension. Some of these adverse events required specific interventions, which resulted in additional costs. However, hypertension was the only adverse effect for which the percentage of patients requiring intervention differed significantly between the 2 groups ( p = 0.02; see Table 1). The exact cost of interventions for hypertension could not be estimated. Therefore, the cost of one medical consultation was added for each case of hypertension requiring intervention, which resulted in an average per-patient cost associated with hypertension of $24.57 for dexmedetomidine and $38.35 for midazolam (Table 2).
All costs and effects for which there was a statistically significant difference between the 2 treatments are reported in Table 3. In the dexmedetomidine treatment group, delirium occurred in fewer patients (difference of 22.5 percentage points), duration of mechanical ventilation was shorter (by 1.9 days), open-label midazolam treatment was required for more patients (difference of 13.5 percentage points), and intervention for hypertension was required for fewer patients (difference of 10.6 percentage points). As a result, the total per-patient cost of dexmedetomidine administration was $7022, $658 less than the total per-patient cost of midazolam administration ($7680).
Table 3
Summary of Cost–Consequences Analysis*
Sensitivity analyses were performed to take into account the uncertainties associated with the costs of ICU care, mechanical ventilation, and delirium. For time to extubation (i.e., duration of mechanical ventilation), worst-case and best-case scenarios, based on the confidence limits for time to extubation for dexmedetomidine and midazolam, were developed. The daily cost of ICU care was arbitrarily subjected to changes of +25% and −25%, as no confidence interval was available for this parameter. The cost of delirium was first subjected to the value of the confidence interval reported by Milbrandt and others17 in terms of the adjusted increase in ICU cost based on the DECCA study21 (12% [adjusted value 7.8%] to 72% [adjusted value 39.5%]). Likewise, the difference in the percentage of patients with delirium (a difference of 22.5 percentage points) was explored using the values of the confidence interval of this difference (14 to 33 percentage points). Finally, sensitivity analyses were performed for the worst-case and base-case scenarios combining these 2 parameters (i.e., 7.8% increased cost with difference of 14 percentage points and 39.5% increased cost with difference of 33 percentage points).
The results of all sensitivity analyses favoured dexmedetomidine, except when the highest value for time to extubation with dexmedetomidine and the lowest value for time to extubation with midazolam were used (Table 4).
Table 4
Results of Deterministic Sensitivity Analysis
The results of a previous cost-minimization analysis performed in the United States indicated that dexmedetomidine was less costly than midazolam for long-term sedation in the ICU.9 The results of the cost–consequences analysis reported here, which was performed from a Canadian perspective, lead to the same conclusion. Compared with midazolam, dexmedetomidine was associated with a lower incidence of delirium episodes and a shorter median time to extubation,8 while being a cost-saving alternative. The primary drivers of cost savings in both the cost-minimization study9 and the cost–consequences study were reduced costs associated with the ICU stay and reduced costs of mechanical ventilation.
The costs associated with ICU care are recognized to be substantial, but they have seldom been estimated. For the purpose of this economic evaluation, we relied on an average daily cost for an ICU stay, based on the fully allocated accounting system of St Paul’s Hospital in Vancouver. No other valid source for the cost of ICU care in Canada could be found. As well, the costs associated with mechanical ventilation and delirium have never been directly estimated in Canada, but their contribution to overall ICU cost has been estimated in US studies, and this information was used to determine their costs in the Canadian context. To estimate the robustness of the results, sensitivity analyses were performed for the main cost drivers of this economic evaluation. In most cases, the results of the sensitivity analysis indicated that dexmedetomidine was a cost-saving alternative to midazolam, except when the worst-case scenarios for time to intubation and for delirium were examined. In fact, optimizing sedation and analgesia in the ICU for critically ill patients may decrease the length of the ICU stay or reduce the duration of mechanical ventilation, which may significantly reduce the high costs of ICU care.
Until now, no other study has compared the economic impacts of dexmedetomidine and midazolam for sedation in the ICU in a Canadian context. However, a Canadian randomized multicentre study demonstrated that use of propofol reduced the time to extubation relative to midazolam and was associated with a potential cost saving, although there was no difference in the intensity of resource use or ICU length of stay.16
The results of this economic evaluation are based on the efficacy and safety results of the SEDCOM study.8 That study incorporated best sedation practices (light-to-moderate sedation level and daily assessments of arousal in both study groups) and was the first to demonstrate that using dexmedetomidine for prolonged sedation of patients in the ICU provides several advantages over midazolam. Since the economic evaluation was based on the SEDCOM study, some limitations of the current study are similar to those reported by the SEDCOM investigators.8 For example, although midazolam is widely used for long-term sedation in Canada, other sedatives, such as propofol, are also commonly used but were not compared with dexmedetomidine in the current study. However, in a smaller randomized study comparing dexmedetomidine with propofol, the reported incidence of delirium was 3% with dexmedetomidine and 50% with propofol.22 In the current economic evaluation, it was assumed that dexmedetomidine and midazolam were equivalent in terms of the time to achieve targeted sedation. However, the SEDCOM trial was not a non-inferiority trial, so even if the 2 products had the same time to achieve targeted sedation, it is not absolutely certain that they are equivalent.
Cost–consequences analyses usually provide information to decision-makers in a transparent and disaggregated format, which allows them to decide the impact of each outcome individually. One problem with this type of analysis is that the weighting of the relative importance of different costs and benefits is left to the individual decision-maker, which can hinder making a decision that should be as objective as possible.23 This is particularly true when the results do not all point in the same direction. In the current study, all of the outcomes considered were favourable to dexmedetomidine, which would facilitate decision-making. Moreover, for completeness, this cost-consequences analysis took into account all of the clinical outcomes with significant differences between dexmedetomidine and midazolam (i.e., duration of mechanical ventilation and proportions of patients who had episodes of delirium, who required open-label midazolam therapy, and who had episodes of hypertension requiring intervention).
The results of this cost–consequences analysis indicate that the use of dexmedetomidine is a more favourable strategy for sedation than use of midazolam, in most ICU contexts. In fact, although the initial cost of dexmedetomidine is higher than that of midazolam, the savings realized in terms of reductions in duration of mechanical ventilation and in occurrence of delirium episodes make it a less expensive option overall.
1
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This economic evaluation was funded by Hospira Canada. We thank Karine Mathurin for her assistance in writing and editing the manuscript.
Canadian Journal of Hospital Pharmacy , VOLUME 65 , NUMBER 2 , March-April 2012