Analysis of the Financial Impact of Using Cangrelor on the Safety and Efficacy Outcomes in Patients Undergoing Percutaneous Coronary Intervention in Whom Oral Therapy with P2Y12 Inhibitors is Not Feasible or Desirable, in Spain.

PURPOSE: Cangrelor is an intravenous, direct-acting, reversible P2Y12 inhibitor indicated for the reduction of thrombotic cardiovascular events in patients with coronary artery disease (CAD) undergoing percutaneous coronary intervention (PCI) in whom oral P2Y12 inhibitors are not feasible or desirable. The objective was to assess the financial impact of introducing cangrelor into the hospital formulary in Spain. PATIENTS AND METHODS: A budget impact model was developed to calculate the cost difference between two scenarios (without and with cangrelor) to treat CAD patients undergoing PCI in whom oral P2Y12 inhibitors are not feasible or desirable, over 3 years. Intravenous P2Y12 inhibitor (cangrelor), oral P2Y12 inhibitors (clopidogrel, prasugrel, and ticagrelor), and glycoprotein IIb-IIIa inhibitors (GPIs) for bail-out use were considered. Epidemiological, efficacy (thrombotic events including cardiac death), safety (bleeding events), and costs (€, 2019) data were based on Spanish registries, clinical trials, and meta-analyses. One-way sensitivity analysis established the effect of uncertainty on results.
RESULTS: For years 1, 2, and 3, the target population to receive cangrelor was 607, 1,822, and 3,340 patients, and cangrelor uptake was 23.70%, 58.30%, and 51.30%, respectively. The 3-year budget impact was 1,021,717€ varying from 50,245€ in year 1 to 599,272€ in year 3. The results were sensitive to the number of patients treated with GPIs in Spanish hospitals.
CONCLUSION: Based on our results, the financial effort needed to introduce the use of cangrelor in patients undergoing PCI in whom antiplatelet therapy with oral P2Y12 inhibitors is not feasible or desirable barely exceeds one million € over three years, in Spain.

Introduction

In Spain, acute coronary syndromes (ACS), including ST elevation myocardial infarction (STEMI), non-ST elevation myocardial infarction (NSTEMI), and unstable angina are the leading cause of morbidity and mortality, and of elevated healthcare costs.1 Percutaneous coronary intervention (PCI) is the recommended reperfusion strategy for both STEMI (primary PCI) and high-risk NSTEMI patients.2 In 2018, 72,520 PCIs were performed in 109 hospitals in Spain; 21,261 were done in acute myocardial infarction (91% primary PCI), exceeding the estimates of 400 primary PCIs per million population.3

Platelet inhibition is a key component of the periprocedural adjunctive therapy.4,5 Oral P2Y12 inhibitors (clopidogrel, prasugrel, or ticagrelor) with concomitant acetylsalicylic acid (ASA) are the standard of care.6 However, and despite the significant advances made in the use of adjunctive antiplatelet treatment and in the PCI procedure, 12% of STEMI and 4.3% of NSTEMI patients remain at risk for periprocedural thrombotic complications (including myocardial infarction and stent thrombosis), as well as at risk for major bleedings.7–10 In 2018, the budget impact of treating patients with ACS undergoing PCI with oral prasugrel, ticagrelor, or clopidogrel was calculated to reach 76 million € in Spain.11 Pharmacy, myocardial infarction, urgent revascularization, minor and major bleeding, and stroke were the major cost components.11 In patients with ACS presenting with cardiogenic shock (5–10% of STEMI and 2–3% of NSTEMI12,13), or with active vomiting (30% of STEMI patients14) in whom treatment with oral P2Y12 inhibitors may not be feasible, glycoprotein IIb-IIIa inhibitors (GPIs) are parenteral options.10,15 However, GPIs are recommended for bail-out use only, provided their narrow therapeutic window.4,5

Cangrelor is an intravenous (iv) P2Y12 receptor inhibitor that prevents adenosine diphosphate (ADP) signaling and platelet activation in a direct and reversible way within two minutes of administering a bolus followed by continuous infusion. The antiplatelet effect is consistently maintained along the duration of the infusion, and platelet function returns to normal within one hour following the cessation of it.16–18 Co-administered with ASA, cangrelor is indicated for the reduction of thrombotic cardiovascular events in adults with coronary disease undergoing PCI who have not received an oral P2Y12 inhibitor prior to the PCI procedure and in whom oral therapy with P2Y12 inhibitors is not feasible or desirable.18 The pooled analysis of 3 pivotal trials (CHAMPION program)7,19,20 evaluating the efficacy and safety of cangrelor vs clopidogrel reported that cangrelor significantly reduced the odds of the primary efficacy composite of all-cause death, myocardial infarction, ischemia-driven revascularization, or stent thrombosis at 48 h by 19% (p = 0.0007 vs clopidogrel), and stent thrombosis (key secondary endpoint) by 41% (p = 0.0008).18 As it might be expected for a potent and immediate antiplatelet strategy, cangrelor increased periprocedural GUSTO mild bleeding events (16.8% vs 13.0%, cangrelor vs clopidogrel; p<0.0001).18 Based on the evidence on the efficacy and safety of cangrelor provided by the CHAMPION program,7,18–20 the ESC guidelines recommend that cangrelor may be considered as an iv option to achieve an immediate inhibition of the ADP-induced platelet aggregation after iv bolus plus perfusion, and to allow the restoration of the normal platelet function within 1 h after the cessation of the perfusion.4,5

This study was undertaken to assess the financial impact of introducing cangrelor into the drug formulary of hospital pharmacies in Spain as adjunctive treatment to reduce the risk of periprocedural thrombotic events in candidate patients for PCI, in whom antiplatelet therapy with oral P2Y12 inhibitors is not feasible or desirable.

Patients and Methods

Budget Impact Model

A budget impact model was built in Excel for Microsoft® to calculate the difference in costs of two hypothetical scenarios from the perspective of the National Health System, over a three-year time horizon (2019–2021), in Spain:

1. Current scenario, without cangrelor assuming patients receive antiplatelet treatment with oral P2Y12 inhibitors (pre-treatment) or GPIs (bail-out).

2. Alternative scenario, with cangrelor assuming patients receive oral P2Y12 inhibitors (pre-treatment) or cangrelor or GPIs (bail-out).

Inputs and Data Sources

First, a conceptual budget impact model was defined to set the appropriate PCI scenarios to be compared. Second, the medical literature and diverse sources of pharmacoeconomic information were reviewed to identify the most relevant and consistent data which may reflect as best as possible usual clinical practice in Spain. The pivotal clinical trial of cangrelor was used to estimate the efficacy and safety of cangrelor compared with clopidogrel;18 in the absence of indirect comparisons, a meta-analysis was utilized to calculate the efficacy and safety of cangrelor compared with prasugrel and ticagrelor;21 Spanish interventional cardiology registries were searched to identify population data and typical use of GPIs;22–24 market research information was gathered to infer market share over three years.

Third, assumptions were made to solve data inconsistencies, and the opinion of clinical experts was sought for validation. Three interventional cardiologists working for more than ten years in reference PCI Cath-Labs in Spain gave their expert opinion and validated sources, inputs, assumptions, and calculations. For validation, a semi-structured questionnaire was distributed by email. Experts were asked to choose the most appropriate group of data from the entire set extracted from the literature. In case of discrepancies, an external expert was required for the final decision.

The model was finally nourished with a set of endorsed epidemiological, clinical, and direct healthcare costs data, as follows (Tables 1–3):

Table 1

Size and Distribution of the PCI Population in Spain Over Three Years

	Year 1	Year 2	Year 3	References
Population size
Total PCI, n	74,217	75,978	77,768	22,23
STEMI/Primary PCI population, %	100%	100%	100%	KOL
Primary/Total PCI, %	25%	25%	25%	23,25
Total PCI population in whom oral P2Y12 inhibitors are not feasible or desirable/Total PCI population, %	1.02%	3.00%	5.37%	13,26,27
Total population in whom oral P2Y12 inhibitors are not feasible or desirable, n	760	2,280	4,180
Three-years total population in whom oral P2Y12 inhibitors are not feasible or desirable, n	7,220
Patients in whom antiplatelet treatment with oral P2Y12 inhibitors would be needed, n	607	1,822	3,340
Three-years population in whom antiplatelet treatment with oral P2Y12 inhibitors would be needed, n	5,769
Population diagnosis
ST-elevation myocardial infarction (STEMI)	30%	30%	30%	11,23
Non-ST-elevation myocardial infarction (NSTEMI)	40%	40%	40%
Stable coronary artery disease (SCAD)	22%	22%	22%
Others	8%	8%	8%

Abbreviations: KOL, key opinion leader; PCI, percutaneous coronary intervention; STEMI, ST-elevation myocardial infarction.

Table 3

Efficacy and Safety Outcome Rates of P2Y12 Inhibitors in the PCI Population in Spain

P2Y12 Inhibitor	Efficacy Outcomes at 48 Hours of PCI				Safety Outcomes, TIMI, at 48 Hours of PCI		References
	ST	MI	IDR	Cardiac Death	Major	Minor
Clopidogrel	0.85%	3.65%	0.74%	0.36%	0.22%	0.41%	18
Prasugrel	0.42%	2.77%	0.59%	0.36%	0.65%	0.44%	Estimated from21
Ticagrelor	0.57%	2.74%	0.62%	0.34%	0.25%	0.65%
Cangrelor	0.50%	3.11%	0.53%	0.26%	0.25%	0.61%	18

Abbreviations: IDR, ischemia-driven revascularization; MI, myocardial infarction; PCI, percutaneous coronary intervention; ST, stent thrombosis; TIMI, thrombolysis in myocardial infarction bleeding classification.

1. Epidemiological data: total PCI population3,22,23 primary PCI population23,25 and population of PCI patients in whom the use of oral P2Y12 inhibitors is not feasible or desirable.13,26,27

2. Clinical data: diagnosis at entry (STEMI, NSTEMI, stable CAD and other, that included any cardiovascular event that according to the criteria of the responsible physician deserved a PCI);11,23 pharmacological treatment (before and during PCI);11,18,22,28,29 risk of ischemic and bleeding events with each antiplatelet strategy.18,21

3. Direct healthcare costs data: ischemic and bleeding events unitary costs;30 drugs unitary costs.31

The size, growth, and percentage distribution (primary PCI/total PCI) of the PCI population were estimated from the Spanish registry of interventional cardiology for the 2016 to 2018 period.3,22,23,25 A 2% steady growth of the total PCI population over the three years of analysis was assumed.

In a face-to-face interaction, the clinical experts validated the final version of the model and the budget impact results.

Target Population

The target population included STEMI and NSTEMI patients candidate for PCI, in whom antiplatelet therapy with oral P2Y12 inhibitors was not feasible or desirable.12–14 Its size was derived from the total PCI population in Spain (74,217 individuals in year 1, 75,978 in year 2, and 77,768 in year 3) (Table 1).3,22,23

The percentage of patients in whom antiplatelet therapy with oral P2Y12 inhibitors was not feasible or desirable was based on data from the national registry of interventional cardiology on the 2016 to 2018 period and PCI population growth, on the estimated incidence of cardiogenic shock in PCI candidates, and on the opinion of clinical experts on drugs usage. It was calculated in 1.02% of the total PCI population in year 1, and to grow to 5.37% in year 313,26,27 (Table 1). It reached a total of 7,220 patients over three years (Figure 1). It was forecasted that adjuvant antiplatelet treatment with oral P2Y12 inhibitors would be needed in 607, 1,822, and 3,340 of these patients, respectively. They totalized 5,769 patients over three years (Table 1).

Figure 1

Three years distribution of the total, primary PCI and PCI population in whom antiplatelet therapy with oral P2Y12 inhibitors is not feasible or desirable, in Spain.

Use of Antiplatelet Therapy in the PCI Population

In the scenario without cangrelor in the hospital formulary, it was considered that 80% of the PCI patients received oral P2Y12 inhibitors (pre-treatment) and 6.50% of the patients received GPIs (bail-out), based on data taken from national registries,24 the literature,11 and on the opinion of clinical experts (Table 2).

Table 2

Distribution (in Percentage) of the Use of GPIs and Oral P2Y12 Inhibitors without and with Cangrelor in the Hospital Formulary in the PCI Population in Spain

	Percentage Usage			References
	Year 1	Year 2	Year 3
Pharmacological treatment current scenario (without cangrelor)*
Proportion of patients with oral P2Y12 inhibitors, %	80%	80%	80%	11,28 and KOL
Clopidogrel, %	18.20%	18.20%	18.20%	Estimated from28
Prasugrel, %	9.10%	9.10%	9.10%
Ticagrelor, %	72.70%	72.70%	72.70%
Proportion of patients on GPIs (bail-out), %	6.5%	6.5%	6.5%	Estimated from22
Abciximab, %	93%	93%	93%	Estimated from22
Eptifibatide, %	3%	3%	3%
Tirofiban, %	4%	4%	4%
Pharmacological treatment alternative scenario (with cangrelor)
Proportion of patients with oral P2Y12 inhibitors and cangrelor, %	80%	80%	80%	11,28
Clopidogrel, %	17.50%	16.90%	16.80%	Use forecast
Prasugrel, %	9.00%	9.00%	9.00%	Use forecast
Ticagrelor, %	49.80%	15.80%	22.90%	Use forecast
Cangrelor, %	23.70%	58.30%	51.30%	Use forecast
Proportion of patients on GPIs (bail-out), %	6.3%	6.3%	6.3%	Estimated from18 and KOL
Abciximab, %	93%	93%	93%	Estimated from22
Eptifibatide, %	3%	3%	3%
Tirofiban, %	4%	4%	4%

Notes: *The current scenario is a scenario without cangrelor in the market; it reflects current practice, and it would be the same from year 1 to 3 in the model (assumption).

Abbreviations: GPIs, glycoprotein IIb-IIIa inhibitors; KOL, key opinion leader; PCI, percutaneous coronary intervention.

In the scenario with cangrelor in the hospital formulary, the population receiving P2Y12 inhibitors was distributed amongst those receiving oral P2Y12 inhibitors and those receiving cangrelor. The proportion of patients in whom the use of oral P2Y12 inhibitors would not be feasible or desirable and could therefore be treated with cangrelor was 23.70% in year 1, 58.30% in year 2, and 51.30% in year 3 of the total PCI population (Table 2). The proportion of patients treated with GPIs (bail-out) slightly decreased with cangrelor in the hospital formulary, based on the opinion of clinical experts.

Clinical Outcomes

Periprocedural clinical outcomes (up to 48h of PCI) were ischemic events (stent thrombosis, myocardial infarction, ischemia-driven revascularization, cardiac death) (efficacy),18 and major and minor bleeding events according to the Thrombolysis in Myocardial Infarction (TIMI) criteria21 (safety) with P2Y12 inhibitors (Table 3). The pooled analysis of the CHAMPION PROGRAM published by Steg et al (2013)18 that compared cangrelor to clopidogrel and the network metanalysis by Westman et al (2017)21 that allowed to compare cangrelor, ticagrelor, and prasugrel to clopidogrel were used to derive ischemic and bleeding data.

Costs Data

Costs data are shown in . Pharmacological costs included P2Y12 inhibitors and GPIs (bail-out) and were driven from official databases.31 A 7.5% discount was applied to the cost of ticagrelor and cangrelor, and a 15% discount was considered for abciximab and eptifibatide following national drug price regulations (Real Decreto Ley (RDL) 8/2010).32 No discounts were applied to generic antiplatelet drugs. Clinical events costs were estimated from the literature.30

Costs were updated to 2019 € based on the Consumer Price Index (CPI) percentage changes for Spain33 and it was assumed that they would remain unchanged from 2020 onwards.

Assumptions

Assumptions were made when data were unavailable or inconsistent. They are summarized in Table 4. Assumptions were validated by clinical experts to better represent the usual clinical practice in Spain.

Table 4

Assumptions Considered in the Budget Impact Model (Base Case)

Epidemiology
A steady 2% growth of PCI population occurs over three years in Spain.23
Clinical
The same frequency of clinical events (ischemic and bleeding) occurs in clinical trials and in usual clinical practice.7
Use of antiplatelet drugs in the current and alternative scenario reflects usual medical practice.
TIMI is the bleeding scale used in practice.18,43
Comparators
The use of P2Y12 inhibitors is redistributed within the same target population size after the introduction of cangrelor in the hospital formulary.
The introduction of cangrelor in the market mostly influence the size of the population with ticagrelor and clopidogrel.
The use of oral P2Y12 prasugrel remains unchanged at 9% in the scenario with cangrelor in the market.
The use of GPIs (bail-out) slightly decreases with cangrelor in the hospital formulary.
Other assumptions
The cost of ischemic events (stent thrombosis, myocardial infarction or ischemia-driven revascularization) is the same.
The cost of bleedings (minor or major) is the same.
Costs remain unchanged over three years (time horizon).
The cost of death is 0€.

Abbreviations: GPIs, glycoprotein IIb-IIIa inhibitors; PCI, percutaneous coronary intervention: TIMI, thrombolysis in myocardial infarction.

Sensitivity Analysis

A one-way sensitivity analysis was conducted to assess the impact of different parameters on the budget impact results. The parameters included in the sensitivity analysis were suggested by the clinical experts. Percentage use of GPIs [current scenario: mean, 6.50% (range: 3.00% - 12.70%); alternative scenario: mean, 6.35% (range: 2.60% - 12.40%)]; percentage use of generic clopidogrel [mean: 62% (range: 50% - 100%)]; and costs of clinical events (±20%) were considered to highly influence budget impact according to usual practice in Spain.18,25.

Ethical Considerations

This was a pharmacoeconomic, non-interventional study, based on the collection of data from the literature and from public health reports and registries without involvement of human subjects. Ethical approval was not required to conduct this study.

Results

In the base case scenario, PCI patients in whom oral P2Y12 inhibitors are not feasible or desirable reaches 7,220 over three years (Figure 1); 5,769 patients would benefit from cangrelor as shown in Tables 1 and 2 and would benefit from achieving the corresponding efficacy and safety outcomes as described in Table 3. In this scenario, it was calculated that adding cangrelor at a tentative ex-factory price of 336.70€ per vial (legal VAT and a 7.5% mandatory discount included) into the hospital formulary, for the acute care of PCI patients in whom the antiplatelet therapy with oral P2Y12 inhibitors is not feasible or desirable would represent 1,021,717€ over 3 years, in Spain (Table 5). The budget impact would be 50,245€ in year one, 372,200€ in year two, and 599,272€ in year three.

Table 5

Budget Impact Results for Cangrelor Amongst PCI Patients in Whom Antiplatelet Therapy with Oral P2Y12 Inhibitors is Not Feasible or Desirable in Spain (Three-Year Time Horizon)

	PCI Population in Whom Oral P2Y12 Inhibitors are Not Feasible or Desirable
	Year 1	Year 2	Year 3
Target population, n*	760	2,280	4,180
Population with pre-treatment with P2Y12 inhibitors, n**	607	1,822	3,340
Uptake cangrelor, %	23.70	58.30	51.30
Total costs current scenario (without cangrelor) ***	273,725.00€	821,174.00€	1,505,485.00€
Costs of GPIs use	20,965.00€	62,896.00€	115,310.00€
Cost of pre-treatment with oral P2Y12 inhibitors before PCI	2,014.00€	6,041.00€	11,074.00€
Cost of oral P2Y12 inhibitors after PCI	1,232.00€	3,695.00€	6,773.00€
Costs of clinical events (ischemic) at 48h of PCI	241,582.00€	724,746.00€	1,328,700.00€
Costs of adverse events (bleedings) at 48h of PCI	7,932.00€	23,797.00€	43,628.00€
Total costs alternative scenario (with cangrelor)	323,969.00€	1,193,374.00€	2,104,757.00€
Costs of GPIs use	20,470.00€	61,410.00€	112,586.00€
Cost of pre-treatment with P2Y12 inhibitors before PCI	50,163.00€	361,425.00€	584,342.00€
Cost of oral P2Y12 inhibitors after PCI	1,232.00€	3,695.00€	6,773.00€
Costs of clinical events (ischemic) at 48h of PCI	243,838.00€	742,319.00€	1,355,990.00€
Costs of adverse events (bleedings) at 48h of PCI	8,266.00€	24,525.00€	45,066.00€
Budget impact (per year)	50,245.00€	372,200.00€	599,272.00€
Total budget impact for 3 years	1,021,717.00€

Notes: *Total population in whom oral P2Y12 inhibitors are not feasible or desirable. **Patients in whom antiplatelet treatment with oral P2Y12 inhibitors would be needed. ***Total cost in the current and alternative scenario and the total budget impact for 3 years is highlighted in bold text in the table.

Abbreviations: GPIs, glycoprotein IIb-IIIa inhibitors; PCI, percutaneous coronary intervention.

The introduction of cangrelor would modify the costs associated with the use of P2Y12 inhibitors in the hospital (Figure 2). It may increase the hospital pharmacy costs associated to the use of P2Y12 inhibitors totalizing 976,802 € over three years. Patients will remain on their long-term oral antiplatelets after receiving cangrelor during PCI. The costs of GPIs use may be −4,705€ lower. There would also be differences in the number and costs of clinical events between the scenario without cangrelor compared with the scenario with cangrelor in the hospital formulary (Table 6). The costs of ischemic and bleeding events may represent 47,119€ and 2,500€ over three years, respectively. Greater differences may appear in the incidence of thrombotic events compared to the incidence of bleeding episodes. The budget impact would be sensitive to the size of the population using GPIs (bail-out) and to the number of clinical events over three years (Figure 3). The cost of clinical events or the percentage of usage of clopidogrel would have minor influence in the budget impact.

Figure 2

Pharmacological and clinical event costs before and after introducing cangrelor into the hospital formulary in Spain for managing PCI patients in whom oral P2Y12 inhibitors are not feasible or desirable (three-year time horizon).

Table 6

Distribution of Clinical (Ischemic and Bleeding) Events Amongst PCI in Whom Antiplatelet Therapy with Oral P2Y12 Inhibitors is Not Feasible or Desirable in the Scenarios without and with Cangrelor in the Hospital Formulary in Spain (Three-Year Time Horizon)

	Year 1	Year 2	Year 3
Current scenario (without cangrelor)
Total number of ischaemic events at 48h of PCI (efficacy)
ST, n	4	11	20
MI, n	18	53	97
IDR, n	4	12	21
Cardiac death, n	2	6	12
Total number of bleedings, TIMI scale at 48h of PCI (safety)
Major, n	2	5	9
Minor, n	4	11	20
Alternative scenario (with cangrelor)
Total number ischaemic events at 48h of PCI (efficacy)
ST, n	4	10	19
MI, n	18	57	103
IDR, n	4	11	20
Cardiac death, n	2	6	10
Total number of bleedings, TIMI scale at 48h of PCI (safety)
Major, n	2	5	10
Minor, n	4	11	20
Difference in clinical events per year, current vs alternative scenarios
Ischemic events at 48h of PCI (efficacy)
ST	0	−1	−1
MI	0	+4	+6
IDR	0	−1	−1
Cardiac death	0	0	−2
Bleeding events at 48h of PCI (safety)
Major	0	0	+1
Minor	0	0	0

Abbreviations: IDR, ischemia-driven revascularization; MI, myocardial infarction; PCI, percutaneous coronary intervention; ST, stent thrombosis; TIMI, thrombolysis in myocardial infarction.

Figure 3

Tornado diagram: influence of key inputs on the budget impact of cangrelor for managing PCI patients in whom oral P2Y12 inhibitors are not feasible or desirable, in Spain.

Discussion

The results of the present economic analysis demonstrate that the financial impact of introducing cangrelor into the drug formulary of hospital pharmacies for the adjunctive treatment of approximately 6,000 PCI patients in whom the use of oral P2Y12 inhibitors is not feasible or desirable, slightly exceeds one million € over three years, in Spain. Compared to the budget impact of adjunctive oral antiplatelet drugs, it was reported that increasing by 5% to 10% the use of oral prasugrel only, or prasugrel and ticagrelor, versus clopidogrel in ACS patients undergoing PCI reached 239 million € to 252 million € over 3 years in Spain (2017 €).11

Likewise, two previous economic studies conducted in Spain (in 2010 and 2012, respectively) analyzed the cost implications of replacing clopidogrel by prasugrel or ticagrelor in patients undergoing PCI.34,35 The first study anticipated a budget impact of 8,245 million € in one year if 5% of the patients treated with clopidogrel were given prasugrel instead.35 The second study showed a budget impact in the range of 63,000€ to 86,000€ per each avoided death due to thrombotic events after replacing clopidogrel by ticagrelor, without considering bleeding costs.34 Overall, these data revealed that an important financial effort was made to introduce the two potent oral P2Y12 inhibitors, prasugrel and ticagrelor, into the drug formulary in Spain. Introducing cangrelor into the formulary of hospital pharmacies in Spain implies higher pharmacological costs. However, compared to drug costs, revascularization procedures and length of hospital stay are greater contributors of direct medical costs during the first year following an acute coronary event. They may reach up to one billon € in Spain.36

Taking into account the frame of the present analysis, meaning early PCI (<2 h)4,5 under clinical conditions in which the adjuvant antiplatelet treatment with oral P2Y12 inhibitors may not be feasible or desirable, it should also be considered that the antiplatelet effect of crushed ticagrelor37 and chewed prasugrel38 were also investigated as potential alternatives to improve their oral bioavailability. Although the results showed that time to maximum plasma concentration was shorter in the crushed ticagrelor group versus the integral tablets group, the median time of 2 h vs 4 h, respectively, still represents the delayed onset of the ticagrelor antiplatelet effect.37 In line with these results, the recently published FABOLUS FASTER pharmacodynamic study compared the antiplatelet effect of chewed prasugrel vs a loading dose of integral prasugrel tablet and demonstrated that chewed prasugrel led to higher active metabolite concentration but not to a greater platelet aggregation inhibition.38 The results of these pharmacodynamic studies emphasize that even the faster oral P2Y12 alternatives may still not be desirable. In this context, cangrelor represents an affordable iv alternative for immediate P2Y12 inhibition.

The therapeutic value of cangrelor is well aligned to the expected for a highly effective antiplatelet strategy to be used in the acute setting of PCI.39,40 Antiplatelet drugs with a favorable benefit/risk profile are needed to improve the overall clinical and economic outcomes of PCI patients in Spain, including the reduction of the length of hospital stay and the decrease in the number of periprocedural clinical events.41 In this regard, cangrelor is an innovative iv antiplatelet adjunctive strategy to guarantee an immediate, potent, and rapidly reversible effect in patients undergoing PCI, in whom an oral P2Y12 inhibition is not feasible or desirable.42

There are limitations in the present budget impact model that should be considered. Although all the inputs used in the analysis were taken from published registries, clinical trials and metanalysis and were further validated by external clinical experts, it was not always possible to identify the precise factors that matched the model definitions and represented the acute hospital setting of ACS, in Spain. For instance, PCI population growth and percentage distributions for P2Y12 inhibitors usage may differ from the model assumptions in forthcoming years implying changes in the budget impact estimates. The same cost for both minor and major bleeding events were considered. As a consequence, bleeding costs may have been overestimated. Likewise, other cost assumptions may further influence these results, both positively and negatively. Adverse events associated to GPIs were not modelled and may have influenced the budget impact results. Differences in cases characterization, studies design and patients’ representativeness amongst publications made data selection difficult to carry out. For this reason, assumptions were made to solve this lack of available evidence.

Despite these limitations, this budget impact analysis provides an estimate of introducing a novel antiplatelet iv strategy for PCI patients in whom the use of oral P2Y12 inhibitors is not feasible or desirable. Further research should focus on determining the most cost-effective scenarios for using cangrelor in the clinical practice.

Conclusions

Cangrelor represents an innovative iv strategy for the adjunctive antiplatelet therapy in PCI patients in whom an oral P2Y12 inhibition is not feasible or desirable. The economic effort that would be needed to incorporate cangrelor into the hospital pharmacy formulary seems to be within reasonable margins in Spain, barely exceeding one million € over 3 years. However, further research with a more robust design is needed to confirm these findings.