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Cost-effectiveness of activated protein C in real-life clinical practice

BACKGROUND: Recombinant human activated protein C (rhAPC) has been reported to be cost-effective in severely ill septic patients in studies using data from a pivotal randomized trial. We evaluated the cost-effectiveness of rhAPC in patients with severe sepsis and multiple organ failure in real-life...

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Autores principales: Dhainaut, Jean-François, Payet, Stéphanie, Vallet, Benoit, França, Lionel Riou, Annane, Djillali, Bollaert, Pierre-Edouard, Tulzo, Yves Le, Runge, Isabelle, Malledant, Yannick, Guidet, Bertrand, Le Lay, Katell, Launois, Robert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556742/
https://www.ncbi.nlm.nih.gov/pubmed/17822547
http://dx.doi.org/10.1186/cc6116
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author Dhainaut, Jean-François
Payet, Stéphanie
Vallet, Benoit
França, Lionel Riou
Annane, Djillali
Bollaert, Pierre-Edouard
Tulzo, Yves Le
Runge, Isabelle
Malledant, Yannick
Guidet, Bertrand
Le Lay, Katell
Launois, Robert
author_facet Dhainaut, Jean-François
Payet, Stéphanie
Vallet, Benoit
França, Lionel Riou
Annane, Djillali
Bollaert, Pierre-Edouard
Tulzo, Yves Le
Runge, Isabelle
Malledant, Yannick
Guidet, Bertrand
Le Lay, Katell
Launois, Robert
author_sort Dhainaut, Jean-François
collection PubMed
description BACKGROUND: Recombinant human activated protein C (rhAPC) has been reported to be cost-effective in severely ill septic patients in studies using data from a pivotal randomized trial. We evaluated the cost-effectiveness of rhAPC in patients with severe sepsis and multiple organ failure in real-life intensive care practice. METHODS: We conducted a prospective observational study involving adult patients recruited before and after licensure of rhAPC in France. Inclusion criteria were applied according to the label approved in Europe. The expected recruitment bias was controlled by building a sample of patients matched for propensity score. Complete hospitalization costs were quantified using a regression equation involving intensive care units variables. rhAPC acquisition costs were added, assuming that all costs associated with rhAPC were already included in the equation. Cost comparisons were conducted using the nonparametric bootstrap method. Cost-effectiveness quadrants and acceptability curves were used to assess uncertainty of the cost-effectiveness ratio. RESULTS: In the initial cohort (n = 1096), post-license patients were younger, had less co-morbid conditions and had failure of more organs than did pre-license patients (for all: P < 0.0001). In the matched sample (n = 840) the mean age was 62.4 ± 14.9 years, Simplified Acute Physiology Score II was 56.7 ± 18.5, and the number of organ failures was 3.20 ± 0.83. When rhAPC was used, 28-day mortality tended to be reduced (34.1% post-license versus 37.4% pre-license, P = 0.34), bleeding events were more frequent (21.7% versus 13.6%, P = 0.002) and hospital costs were higher (€47,870 versus €36,717, P < 0.05). The incremental cost-effectiveness ratios gained were as follows: €20,278 per life-year gained and €33,797 per quality-adjusted life-year gained. There was a 74.5% probability that rhAPC would be cost-effective if there were willingness to pay €50,000 per life-year gained. The probability was 64.3% if there were willingness to pay €50,000 per quality-adjusted life-year gained. CONCLUSION: This study, conducted in matched patient populations, demonstrated that in real-life clinical practice the probability that rhAPC will be cost-effective if one is willing to pay €50,000 per life-year gained is 74.5%.
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spelling pubmed-25567422008-10-01 Cost-effectiveness of activated protein C in real-life clinical practice Dhainaut, Jean-François Payet, Stéphanie Vallet, Benoit França, Lionel Riou Annane, Djillali Bollaert, Pierre-Edouard Tulzo, Yves Le Runge, Isabelle Malledant, Yannick Guidet, Bertrand Le Lay, Katell Launois, Robert Crit Care Research BACKGROUND: Recombinant human activated protein C (rhAPC) has been reported to be cost-effective in severely ill septic patients in studies using data from a pivotal randomized trial. We evaluated the cost-effectiveness of rhAPC in patients with severe sepsis and multiple organ failure in real-life intensive care practice. METHODS: We conducted a prospective observational study involving adult patients recruited before and after licensure of rhAPC in France. Inclusion criteria were applied according to the label approved in Europe. The expected recruitment bias was controlled by building a sample of patients matched for propensity score. Complete hospitalization costs were quantified using a regression equation involving intensive care units variables. rhAPC acquisition costs were added, assuming that all costs associated with rhAPC were already included in the equation. Cost comparisons were conducted using the nonparametric bootstrap method. Cost-effectiveness quadrants and acceptability curves were used to assess uncertainty of the cost-effectiveness ratio. RESULTS: In the initial cohort (n = 1096), post-license patients were younger, had less co-morbid conditions and had failure of more organs than did pre-license patients (for all: P < 0.0001). In the matched sample (n = 840) the mean age was 62.4 ± 14.9 years, Simplified Acute Physiology Score II was 56.7 ± 18.5, and the number of organ failures was 3.20 ± 0.83. When rhAPC was used, 28-day mortality tended to be reduced (34.1% post-license versus 37.4% pre-license, P = 0.34), bleeding events were more frequent (21.7% versus 13.6%, P = 0.002) and hospital costs were higher (€47,870 versus €36,717, P < 0.05). The incremental cost-effectiveness ratios gained were as follows: €20,278 per life-year gained and €33,797 per quality-adjusted life-year gained. There was a 74.5% probability that rhAPC would be cost-effective if there were willingness to pay €50,000 per life-year gained. The probability was 64.3% if there were willingness to pay €50,000 per quality-adjusted life-year gained. CONCLUSION: This study, conducted in matched patient populations, demonstrated that in real-life clinical practice the probability that rhAPC will be cost-effective if one is willing to pay €50,000 per life-year gained is 74.5%. BioMed Central 2007 2007-09-06 /pmc/articles/PMC2556742/ /pubmed/17822547 http://dx.doi.org/10.1186/cc6116 Text en Copyright © 2007 Dhainaut et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dhainaut, Jean-François
Payet, Stéphanie
Vallet, Benoit
França, Lionel Riou
Annane, Djillali
Bollaert, Pierre-Edouard
Tulzo, Yves Le
Runge, Isabelle
Malledant, Yannick
Guidet, Bertrand
Le Lay, Katell
Launois, Robert
Cost-effectiveness of activated protein C in real-life clinical practice
title Cost-effectiveness of activated protein C in real-life clinical practice
title_full Cost-effectiveness of activated protein C in real-life clinical practice
title_fullStr Cost-effectiveness of activated protein C in real-life clinical practice
title_full_unstemmed Cost-effectiveness of activated protein C in real-life clinical practice
title_short Cost-effectiveness of activated protein C in real-life clinical practice
title_sort cost-effectiveness of activated protein c in real-life clinical practice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2556742/
https://www.ncbi.nlm.nih.gov/pubmed/17822547
http://dx.doi.org/10.1186/cc6116
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