Management of non-ST-elevation acute coronary syndromes: how cost-effective are glycoprotein IIb/IIIA antagonists in the UK National Health Service?. Palmer, S., Sculpher, M. J., Philips, Z., Robinson, M., Ginnelly, L., Bakhai, A., Abrams, K. R., Cooper, N. J., Packham, C., Alfakih, K., Hall, A., & Gray, D. International Journal of Cardiology, 100(2):229–240, April, 2005.
doi  abstract   bibtex   
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 pound4605 to pound10,343. 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.
@article{palmer_management_2005-1,
	title = {Management of non-{ST}-elevation acute coronary syndromes: how cost-effective are glycoprotein {IIb}/{IIIA} antagonists in the {UK} {National} {Health} {Service}?},
	volume = {100},
	issn = {0167-5273},
	shorttitle = {Management of non-{ST}-elevation acute coronary syndromes},
	doi = {10.1016/j.ijcard.2004.08.042},
	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 pound4605 to pound10,343. 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.},
	language = {eng},
	number = {2},
	journal = {International Journal of Cardiology},
	author = {Palmer, S. and Sculpher, M. J. and Philips, Z. and Robinson, M. and Ginnelly, L. and Bakhai, A. and Abrams, K. R. and Cooper, N. J. and Packham, C. and Alfakih, K. and Hall, A. and Gray, D.},
	month = apr,
	year = {2005},
	pmid = {15823630},
	keywords = {Cardiovascular Diseases, Coronary Disease, Cost-Benefit Analysis, Drug Costs, Econometric, Humans, Models, Myocardial Infarction, Platelet Aggregation Inhibitors, Platelet Glycoprotein GPIIb-IIIa Complex, Quality-Adjusted Life Years, Risk, State Medicine, United Kingdom},
	pages = {229--240},
}

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