Author/Authors :
Stephen Palmer، نويسنده , , Mark Sculpher، نويسنده , , Zoë Philips، نويسنده , , Mike Robinson، نويسنده , , Laura Ginnelly، نويسنده , , Ameet Bakhai، نويسنده , , Keith Abrams، نويسنده , , Nicola Cooper، نويسنده , , Chris Packham، نويسنده , , Khaled Alfakih، نويسنده , , Alistair Hall، نويسنده , , David Gray، نويسنده ,
Abstract :
Background
The glycoprotein IIb/IIIa antagonists (GPAs) represent a new class of drugs to prevent platelet aggregation in the acute treatment of non-ST-elevation acute coronary syndromes (NSTE-ACS). Systematic reviews have identified serious limitations in published cost-effectiveness analyses, including a lack of UK-specific studies and an absence of studies comparing different protocols for the use of GPAs.
Methods
A model was developed to assess the cost effectiveness of a variety of protocols employing GPAs for patients presenting with NSTE-ACS in the UK. The perspective of the UK National Health Service was adopted, with outcomes in terms of quality-adjusted life-years (QALYs). Four treatment strategies were evaluated: GPAs as part of initial medical management (Strategy 1); GPAs in patients with planned percutaneous coronary interventions (PCIs; Strategy 2); GPAs as an adjunct to the PCI procedure (Strategy 3); and no GPAs (Strategy 4). Baseline event rates and costs were taken from a UK observational study of ACS patients and relative risk reductions from GPAs were taken from a meta analysis of trials. Long-term costs and QALYs were estimated using data from a UK longitudinal study.
Results
The most cost-effective use of GPAs is likely to be Strategy 1, with an incremental cost per QALY gained of between £4605 to £10,343. Focusing this use of GPAs only on the subgroup of patients at high risk appears to represent the most cost-effective use of NHS resources.
Conclusions
Medical management of patients with NSTE-ACS using GPAs is the most cost-effective use of resources, particularly if targeted to higher risk subgroups.
Keywords :
Non-ST-elevation acute coronary syndromes , Cost-effectiveness analysis , Quality-adjusted life-years , Glycoprotein IIb/IIIa antagonists