Introduction
In Canada, about 400,000 Canadians are living with the effects of stroke costing the economy more than $3.6 billion per year. Reference Boulanger, Lindsay and Gubitz1 In the province of Alberta, 4500 first ischemic strokes occur annually 2 with a case fatality rate of 14%. 3 Endovascular therapy (EVT), a minimally invasive, catheter-based procedure for reperfusion of acute intracranial large vessel occlusion, has been proven to increase functional independence and reduce mortality among patients with acute ischemic stroke. Reference Goyal, Demchuk and Menon4 Accordingly, EVT has been recommended in Canada and globally since 2015. Reference Casaubon, Boulanger and Blacquiere5,Reference Powers, Derdeyn and Biller6
Within Alberta Health Services (AHS), Canada’s largest province-wide, fully integrated health system, responsible for delivering health services to nearly 4.4 million people, EVT is available in Calgary (Foothills Medical Centre) and Edmonton (University of Alberta Hospital) only. The Cardiovascular Health & Stroke Strategic Clinical Network™, in collaboration with provincial stakeholders, has been implementing the Endovascular Reperfusion Alberta (ERA) project since 2015, aiming to increase access to EVT for patients with acute ischemic stroke. Strategies to meet the goal included: (i) a revision of emergency medical services triage and transport pathways to establish clear destination policies and a rural field consultation pathway for paramedics and suspected acute stroke patients; (ii) revision of inter-hospital stroke referrals and transport including involvement of STARS air ambulance service; (iii) implementation of appropriate neurovascular imaging protocols in remote stroke centres to determine EVT eligibility; and (iv) a quality improvement process in acute care to reduce the time to treatment. 7
We conducted a return on investment (ROI) analysis of this project after 5 years of implementation to inform policy regarding sustainability, scale, and spread.
Methods
We used a decision tree analysis comparing Return (or Benefit, B) and Investment (or Cost, C) (Figure 1). The net benefit (NB) was calculated by subtracting C from B (NB = B – C) and the ROI was calculated by dividing B by C (ROI = B/C). In this case, B refers to cost avoidance associated with the intervention. Reference Thanh, Patil and Knudsen8
We used a population-wide healthcare system perspective, where C included investments that AHS contributed to the ERA initiative, including costs for stroke observational beds, personnel (nurses and rehabilitation supports), and diagnostic imaging (EVT and computed tomography angiography). 7 B included savings from reductions in EVT patients’ health services utilization (HSU), including inpatient, outpatient, long-term care, and physician services, as well as prescription drugs. Of the inpatient services, we included the acute (Savings 1) and the alternative level of care (Savings 2). Of the outpatient services, we included emergency department (ED) visits (Savings 3) and clinic visits (Savings 4). Of the physician services, we included general practitioner (GP) visits (Savings 5) and specialist visits (Savings 6). Of the long-term care services, we included length of stay (LOS) in long-term care facilities (Savings 7). Of prescription drugs, we included drugs dispensed from community pharmacies (Savings 8). In summary, Savings 1–8 each were calculated using the formula: Savings = N × (U1 – U2) × C, where N was the number of EVT patients increased by the intervention; U1 was the HSU of non-EVT patients (control group), U2 was the HSU of EVT patients (intervention group), and C was the unit cost. From this formula, a positive impact (U1 – U2) indicated a reduction in HSU (thereby savings) for the intervention and vice versa. Therefore, the summation of costs is represented by B = ∑ savings 1–8.
The time frame for the number of patients and investments was 2 fiscal years (from April 1st to March 31st) 2018 and 2019. The number of EVT patients increased by the intervention was the total number of EVT patients in each year less 30%. That is if the intervention had not been implemented, 30% of the patients would still have been treated by EVT. Of note, this assumption was based on the number of EVT cases in Alberta before 2015. To estimate both short and long-term impacts of EVT on individual patients, we separately analyzed HSU and associated costs occurring within three time horizons, including short (90 days), medium (1 year), and long-term (5 years) from the patients’ EVT enrollment date.
Statistical Methods Estimating Model Inputs
As all eligible patients were treated with EVT (there have been no observational controls since 2015) and to calculate the long-term impact, we used data from 99 Alberta patients enrolled in the ESCAPE randomized controlled trial in 2013–2014. Reference Boulanger, Lindsay and Gubitz1 After calculating the difference in HSU costs between intervention and control groups, we extrapolated it to all patients receiving EVT in Alberta. We linked patients’ unique lifetime identifiers to the Alberta Health Administrative Databases for retrieving their HSU. Baseline demographic and comorbidity characteristics were similar (Table 1); therefore, the outcomes between intervention and control patients were compared using a univariate analysis. As the outcomes of interest in this study were HSU and associated costs, we did not consider death as an outcome, but included it in the denominator. Reference Thanh, Toye, Savu, Kumar and Kaul9
EVT, endovascular therapy; N, number; SD, standard deviation.
Unit costs (C1 to C8) were estimated among patients in the control group because if EVT had not been performed, the unit costs of patients in the intervention group would have been the same as those of the control group. Specifically, C1 was cost per day of the acute LOS, C2 was cost per day of the alternative level of care LOS, C3 was cost per ED visit, C4 was cost per outpatient clinic visit, C5 was cost per GP visit, C6 was cost per specialist visit, C7 was cost per day of the long-term care LOS, and C8 was cost per prescription drug dispense in the community pharmacies. Unit costs for inpatient and outpatient services were based on the CIHI Case-Mix Group Plus (CMG+) methodology. 10 The cost for each CMG+ group was retrieved from the Alberta Health Interactive Health Data Application. 11 The cost for physician services was defined as paid amounts to physicians from the Alberta Health Care Insurance Plan. Costs for prescription drugs were based on prices per unit of the Alberta Drug Benefit List. 12 The cost per day in a long-term care facility was retrieved from the AHS finance.
For C1 we used the average and for C2, we used the “marginal cost” Reference Drummond, Sculpher, Torrance, O’Brien and Stoddart13 per hospital day for the stays that were shortened by EVT. The rationale was that during a hospital stay, the cost of health services in the last days of the stay is lower than the average and close or equal to the “hotel cost” because of the high treatment cost in the first few days when major procedures are done. We applied the “hotel cost” as a percentage of the average cost (43.5%) to estimate the marginal cost. Reference Lee, Mata and Ghitulescu14 “Hotel cost” includes the costs that are related to patient care where no treatment is provided. It includes the share of hospital fixed costs (e.g. admin, facility, and overheads) that are allocated to each bed with a patient. Additionally, it includes meals and cleaning, as well as staff costs that are related to those minimum levels of activities.
Data Sources
Intervention and control patients were from the ESCAPE trial. Reference Boulanger, Lindsay and Gubitz1 The total number of patients treated with EVT in Alberta was obtained from the Quality Improvement & Clinical Research database, a comprehensive pan-Alberta stroke registry. 15 The Alberta Health Administrative databases, 16 which are linkable by the patient’s unique lifetime identifiers, were used to identify HSU of the patients. Specifically, inpatient services were retrieved from the Discharge Abstract Database, which contains information about acute inpatient care. Outpatient services were retrieved from the National Ambulatory Care Reporting System, which includes information about ambulatory care, day surgery, and ED settings. Practitioner services were retrieved from the Alberta Health Care Insurance Plan Claims database, which consists of claims to pay medical doctors and other allied practitioners. Long-term care services were retrieved from the Alberta Continuing Care Information System. Prescription drugs were retrieved from the Pharmaceutical Information Network, in which a record is created each time a prescription is dispensed.
Sensitivity Analysis
In total, there were three scenarios, one for each time horizon (90 days, 1 year, and 5 years). We included both statistically significant and nonsignificant impacts of EVT because the costs of the nonsignificant HSU may still be substantial. Reference Stowers, Lemanu and Hill17 Within each scenario, we performed both deterministic and probabilistic sensitivity analyses for the uncertainty of all the input parameters. In the deterministic, we used a one-way sensitivity analysis (each variable varied at a time) using a range from the lower to the higher value of 95% confidence interval of each parameter. We also performed a threshold analysis on the number of EVT patients increased by the intervention to estimate the break-even point. In the probabilistic (all variables varied simultaneously), we assumed cost variations follow a gamma distribution and HSU (count data) variations follow a Poisson distribution. Reference Briggs, Claxton and Sculpher18 We ran 100,000 samples/trials and reported a probability for the intervention to be cost saving.
All costs/savings were inflated to 2019 Canadian dollars using the Bank of Canada Inflation Calculator. 19 Stata (www.stata.com) and TreeAge Pro (www.treeage.com) were used for data analyses.
Results
There were 99 patients in Alberta participating in the ESCAPE trial, of whom 52 received EVT and 47 were non-EVT treated (Table 1). In the EVT group, males accounted for 48.1%, the mean age was 70.8 (SD=12.7), and the mean Charlson comorbidity index Reference Quan, Li and Couris20 was 2.96 (SD = 2.05). In the control group, the corresponding numbers were 51.1%, 72.7 (SD = 14.3), and 2.87 (SD = 2.09). All the differences between intervention and control groups were not statistically significant.
Table 2 shows differences in HSU and costs between EVT and control groups by time horizon. Generally, EVT was associated with a reduced cost for all time horizons. The most gross savings per patient ($66,452) were found in the medium term, followed by the long term ($58,930), and least in the short term ($4,546).
ED, emergency department; EVT, endovascular therapy; GP, general practitioner; LOS, length of stay; LTC, long-term care.
Within the medium term, patients treated with EVT used less services than their control group counterparts in all services included in this study, except for ED visits. Specifically, per patient, acute LOS was reduced by 10.83 days, alternative level of care LOS by 15.96 days, outpatient clinic by 0.95 visits, GP by 8.68 visits, specialist by 9.68 visits, prescription drugs by 12.86 dispenses, and long-term care LOS by 36.72 days, while ED increased by 0.13 visits.
Within the long term, patients treated with EVT used less than their counterparts in six services and used more in two services. Specifically, per patient, acute LOS was reduced by 5.20 days, alternative level of care LOS by 24.65 days, outpatient clinic by 4.91 visits, GP by 19.36 visits, prescription drugs by 107.09 dispenses and long-term care LOS by 45.99 days, while ED was increased by 0.47 visits and specialist was increased by 9.57 visits.
Within the short term, patients treated with EVT used less than their counterparts in three services and used more in five services. Specifically, per patient, acute LOS was reduced by 2.72 days, specialist by 0.62 visits, and long-term care LOS by 15.43 days, while alternative level of care LOS was increased by 4.93 days, ED by 0.34 visits, outpatient clinic by 0.53 visits, GP by 0.15 visits, and prescription drugs by 4.46 dispensed prescriptions. Despite the increased HSU observed in five areas, a gross savings of $4,546 per patient was observed.
The total estimated costs for ERA were $2.04 million in 2018 and $3.73 million in 2019 (Table 3). Dividing these costs by the number of EVT patients increased by the ERA (172 in 2018 and 218 in 2019), the cost per patient was $11,860 in 2018 and $17,070 in 2019. Subtracting these costs from the gross savings, the net savings per patient were −$7,313, $54,592, and $47,070 for short, medium, and long-term, respectively, in 2018. Corresponding net savings per patient in 2019 were −$12,524, $49,381, and $41,859. Multiplying the net savings per patient with the number of patients, the total net savings for the province for short, medium, and long term were, respectively, −$1.26, $9.40, and $8.11 million in 2018 and −$2.74, $10.78, and $9.14 million in 2019. ROI ratios were, respectively, 0.4, 5.6 and 5.0 in 2018, and 0.3, 3.9 and 3.5 in 2019.
EVT, endovascular therapy; FY, fiscal year; M, million; ROI, return on investment.
Sensitivity analyses showed, for 2018, the range of net savings was −$6.38 to $3.86 million, $0.88 to $17.93 million, and −$1.72 to $17.93 million; and the probability for ERA to be cost saving was 39%, 97%, and 94%, in the short, medium, and long-term time horizons, respectively (Table 4). The corresponding numbers in 2019 were −$9.23 to $3.75 million, −$0.02 to $21.60 million, and −$3.32 to $21.60 million; and 31%, 96%, and 91%. The threshold analysis showed the break-even point for the medium and long-term time horizons was 86% in 2018 and 80% in 2019. That is the intervention would be cost saving if it increased the number of patients treated with EVT by 14–20%.
ERA, Endovascular Reperfusion Alberta; ROI, return on investment.
Discussion
The novelty of the result is the demonstration that investment in EVT stroke treatment on a population-wide basis is cost saving and results in a rapid ROI in less than a year. Using a modeling technique together with real-world data to estimate NB and ROI of the ERA implementation in Alberta, we show that the ERA implementation was cost saving and a dominant strategy. During 1–5 years of follow-up of patients, the net savings per patient were from $42,000 to $55,000 and ROI from 3.5 to 5.6, meaning that every invested dollar would return $3.5–$5.6. The probability for ERA to be cost saving was from 91% to 97%. The impacts of ERA were found to be smaller in the shortest time horizon, indicating that if only 90-day time horizon had been used, the benefits of ERA implementation would have been underestimated. As a one-time intervention, it is reasonable that the impact peaked and then decreased over time. For example, the enhanced recovery after surgery intervention for colorectal, pancreas, cystectomy, liver, and gynecologic oncology procedures, had the lowest impact at 30 days, peaked at 90 days, and then decreased at 365 days, after the surgery. Reference Thanh, Nelson and Wang21 Similarly, the EVT had the lowest impact at 90 days, peaked at 1 year and then decreased at 5 years. This follows the episodic nature of stroke such that survivors to one year do not have substantially different health care needs than age-matched controls.
In Alberta, bi-plane angiography, imaging equipment, expertise, personnel and systems of care already existed to manage neuro-interventional procedures. Building on top of this infrastructure was a smaller investment that could contribute to the ROI.
The finding that EVT is cost-saving is internationally consistent. In Canada, Sevick et al. reported that EVT is cost-effective if the time-horizon is 1 year or more, Reference Servick, Demchuk and Shuaib22 and Xie et al. reported a similar benefit using a cost-utility analysis. Reference Xie, Lambrinos and Chan23 In the US, by comparing the cost of EVT with the average reimbursement from insurance, Brinjikji et al. concluded that the improved patient outcomes associated with EVT may result in decreases in long-term costs. Reference Brinjikji, Kallmes, Rabinstein, Lanzino and Cloft24 Another study found a net financial gain of US$500 per patient associated with EVT, compared to the net financial loss of US$1800 in the control group. Reference Rai and Evans25 Recently, Kunz et al. found that EVT leads to long-term cost-savings. Reference Kunz, Almekhlafi and Menon26 In England, McMeekin et al. also found that EVT benefits are highly likely to be cost-saving over 5 years. Reference McMeekin, Flynn and Allen27
There are several limitations to be acknowledged. First, as there are no controls in the same time periods with the EVT patients to compare, we used ESCAPE trial Reference Boulanger, Lindsay and Gubitz1 data which is a few years older and modelled the impact of EVT as similar in 2018–2019. Improvements in diagnosis and treatment for stroke over the years could result in our estimates being under or overestimated. Similarly, our estimates could be under or overestimated because the efficacy of EVT in the ESCAPE trial is possibly different from the effectiveness of EVT in the real-world ERA implementation. Reference Kamal, Rogers and Stang28 However, with the sensitivity analysis, we believe that this bias was minimized. Second, as the sample size was small, variations of differences in HSU costs between EVT and control group were wide. Therefore, the variation of net savings was wide. However, the probabilistic sensitivity analysis showed a high probability for ERA to be cost-saving, especially in longer time-horizons. Third, the savings could be underestimated as deaths were included in HSU calculations given EVT could reduce mortality; that is, EVT patients would live longer and therefore would use more health services than their counterparts. Fourth, as the costs of the ERA project did not include potential additional physician billings and the costs associated with a greater number of rapid evaluations (e.g. imaging and nursing) for non-stroke and non-EVT eligible ischemic stroke patients, the NB estimated in this study could be overestimated. Finally, our estimated savings would have been larger if societal costs had been included given it is evident that out-of-pocket costs, Reference Dewey, Thrift and Mihalopoulos29 as well as indirect costs of lost productivity for stroke survivors and their caregivers, are substantial. Reference Dunbar, Khavjou and Bakas30–Reference Ganapathy, Graham and DiBonaventura32
In conclusion, a population-wide investment in EVT is a dominant, cost-saving strategy. Our results have emphasized that it is important to consider a broad range of HSU and long-term impact to capture the full return on investment.
Acknowledgements
We thank the AHS Analytics for providing data access.
Disclosures
Dr Demchuk reports personal fees from Medtronic, outside the submitted work. In addition, Dr Demchuk has a patent Circle NVI issued. Dr Hill reports grants from Covidien (Medtronic LLC), during the conduct of the study; personal fees from Sun Pharma, grants from Boehringer-Ingelheim, grants from NoNO Inc., grants from Medtronic LLC, grants from Biogen Inc., outside the submitted work; In addition, Dr Hill has a patent US Patent office Number: 62/086,077 licensed to Circle Neurovascular Inc., and a patent US Patent office Number: US 10,916,346 licensed to Circle Neurovascular Inc. and owns stock in Pure Web Incorporated, a company that makes, among other products, medical imaging software, is a director of the Canadian Federation of Neurological Sciences, a not-for-profit group, a director of the Canadian Stroke Consortium, a not-for-profit group, is a director of Circle NeuroVascular Inc., and has received grant support from Alberta Innovates Health Solutions, CIHR, Heart & Stroke Foundation of Canada, National Institutes of Neurological Disorders and Stroke. Dr Goyal reports grants and personal fees from Medtronic, personal fees from Stryker, personal fees from Mentice, personal fees from Microvention, outside the submitted work. All the other authors have nothing to disclose.
Statement of Authorship
All authors participated in study conception and design, and interpretation of results. All the co-authors contributed to the project implementation and data collection. The first author analyzed data and drafted the first version of manuscript. The last author supervised the whole process. All authors revised and approved the manuscript before submission and take responsibility for contents of the article.