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Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study
BACKGROUND: Many clinical guidelines have adopted a multifactorial cardiovascular risk assessment to identify high-risk individuals for treatment. The Framingham risk chart is a widely used risk engine to calculate the absolute cardiovascular risk of an individual. Cost-effective analyses are typica...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Clinics Cardive Publishing
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975215/ https://www.ncbi.nlm.nih.gov/pubmed/18516355 |
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author | Ker, J A Oosthuizen, H Rheeder, P |
author_facet | Ker, J A Oosthuizen, H Rheeder, P |
author_sort | Ker, J A |
collection | PubMed |
description | BACKGROUND: Many clinical guidelines have adopted a multifactorial cardiovascular risk assessment to identify high-risk individuals for treatment. The Framingham risk chart is a widely used risk engine to calculate the absolute cardiovascular risk of an individual. Cost-effective analyses are typically used to evaluate therapeutic strategies, but it is more problematic for a clinician when faced with alternative therapeutic strategies to calculate cost effectiveness. AIM: We used a single simulated-patient model to explore the effect of different drug treatments on the calculated absolute cardiovascular risk. METHODS: The Framingham risk score was calculated on a hypothetical patient, and drug treatment was initiated. After every drug introduced, the score was recalculated. Single-exit pricing of the various drugs in South Africa was used to calculate the cost of reducing predicted cardiovascular risk. RESULTS: The cost-effective ratio of an antihypertensive treatment strategy was calculated to be R21.35 per percentage of risk reduction. That of a statin treatment strategy was R22.93 per percentage of risk reduction. Using a high-dose statin, the cost-effective ratio was R12.81 per percentage of risk reduction. Combining the antihypertensive and statin strategy demonstrated a cost-effective ratio of R23.84 per percentage of risk reduction. A combination of several drugs enabled the hypothetical patient to reduce the risk to 14% at a cost-effective ratio of R17.18 per percentage of risk reduction. CONCLUSION: This model demonstrates a method to compare different therapeutic strategies to reduce cardiovascular risk with their cost-effective ratios. |
format | Online Article Text |
id | pubmed-3975215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Clinics Cardive Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-39752152014-05-07 Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study Ker, J A Oosthuizen, H Rheeder, P Cardiovasc J Afr Cardiovascular Topics BACKGROUND: Many clinical guidelines have adopted a multifactorial cardiovascular risk assessment to identify high-risk individuals for treatment. The Framingham risk chart is a widely used risk engine to calculate the absolute cardiovascular risk of an individual. Cost-effective analyses are typically used to evaluate therapeutic strategies, but it is more problematic for a clinician when faced with alternative therapeutic strategies to calculate cost effectiveness. AIM: We used a single simulated-patient model to explore the effect of different drug treatments on the calculated absolute cardiovascular risk. METHODS: The Framingham risk score was calculated on a hypothetical patient, and drug treatment was initiated. After every drug introduced, the score was recalculated. Single-exit pricing of the various drugs in South Africa was used to calculate the cost of reducing predicted cardiovascular risk. RESULTS: The cost-effective ratio of an antihypertensive treatment strategy was calculated to be R21.35 per percentage of risk reduction. That of a statin treatment strategy was R22.93 per percentage of risk reduction. Using a high-dose statin, the cost-effective ratio was R12.81 per percentage of risk reduction. Combining the antihypertensive and statin strategy demonstrated a cost-effective ratio of R23.84 per percentage of risk reduction. A combination of several drugs enabled the hypothetical patient to reduce the risk to 14% at a cost-effective ratio of R17.18 per percentage of risk reduction. CONCLUSION: This model demonstrates a method to compare different therapeutic strategies to reduce cardiovascular risk with their cost-effective ratios. Clinics Cardive Publishing 2008-04 /pmc/articles/PMC3975215/ /pubmed/18516355 Text en Copyright © 2010 Clinics Cardive Publishing http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cardiovascular Topics Ker, J A Oosthuizen, H Rheeder, P Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
title | Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
title_full | Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
title_fullStr | Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
title_full_unstemmed | Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
title_short | Decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
title_sort | decision-making using absolute cardiovascular risk reduction and incremental cost-effectiveness ratios: a case study |
topic | Cardiovascular Topics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975215/ https://www.ncbi.nlm.nih.gov/pubmed/18516355 |
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