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

被引:22
作者
Dhainaut, Jean-Francois [1 ]
Payet, Stephanie [2 ]
Vallet, Benoit [3 ]
Franca, Lionel Riou [2 ]
Annane, Djillali [4 ]
Bollaert, Pierre-Edouard [5 ]
Le Tulzo, Yves [6 ]
Runge, Isabelle [7 ]
Malledant, Yannick [8 ]
Guidet, Bertrand [9 ]
Le Lay, Katell [2 ]
Launois, Robert [2 ]
机构
[1] Univ Paris 05, CHU Cochin Port Royal, Dept Intens Care, Paris, France
[2] Reseau Evaluat Econ Sante, Paris, France
[3] Univ Lille, Univ Hosp Lille, Dept Anesthesiol & Intens Care, Lille, France
[4] Univ Versailles, Raymund Poincare Hosp, Dept Intens Care, Garches, France
[5] Univ Nancy 1, Cent Hosp, Dept Intens Care, Nancy, France
[6] Univ Hosp Rennes, Dept Infect Dis & Med Intens Care, Rennes, France
[7] La Source Hosp, Dept Intens Care, Orleans, France
[8] Univ Hosp Rennes, Dept Anesthesiol & Intens Care, Rennes, France
[9] Univ Paris 06, St Antoine Hosp, Dept Intens Care, Paris, France
关键词
D O I
10.1186/cc6116
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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 ((sic)47,870 versus (sic)36,717, P < 0.05). The incremental cost-effectiveness ratios gained were as follows: (sic)20,278 per life-year gained and (sic)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 (sic)50,000 per life-year gained. The probability was 64.3% if there were willingness to pay (sic)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 (sic)50,000 per life-year gained is 74.5%.
引用
收藏
页数:14
相关论文
共 37 条
[1]  
Aegerter P, 1998, REV EPIDEMIOL SANTE, V46, P226
[2]   Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[3]   Cost-effectiveness of drotrecogin alfa (activated) in the treatment of severe sepsis [J].
Angus, DC ;
Linde-Zwirble, WT ;
Clermont, G ;
Ball, DE ;
Basson, BR ;
Ely, EW ;
Laterre, PF ;
Vincent, JL ;
Bernard, G ;
van Hout, B .
CRITICAL CARE MEDICINE, 2003, 31 (01) :1-11
[4]   Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock [J].
Annane, D ;
Sébille, V ;
Charpentier, C ;
Bollaert, PE ;
François, B ;
Korach, JM ;
Capellier, G ;
Cohen, Y ;
Azoulay, E ;
Troché, G ;
Chaumet-Riffaut, P ;
Bellissant, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (07) :862-871
[5]  
*ANT ADV COMM, 2001, CLIN REV DROTR ALF A
[6]   Efficacy and safety of recombinant human activated protein C for severe sepsis. [J].
Bernard, GR ;
Vincent, JL ;
Laterre, P ;
LaRosa, SP ;
Dhainaut, JF ;
Lopez-Rodriguez, A ;
Steingrub, JS ;
Garber, GE ;
Helterbrand, JD ;
Ely, EW ;
Fisher, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :699-709
[7]   An evaluation of the cost effectiveness of drotrecogin alfa (Activated) relative to the number of organ system failures [J].
Betancourt, M ;
McKinnon, PS ;
Massanari, RM ;
Kanji, S ;
Bach, D ;
Devlin, JW .
PHARMACOECONOMICS, 2003, 21 (18) :1331-1340
[8]   The death of cost-minimization analysis? [J].
Briggs, AH ;
O'Brien, BJ .
HEALTH ECONOMICS, 2001, 10 (02) :179-184
[9]   EPISEPSIS: a reappraisal of the epidemiology and outcome of severe sepsis in French intensive care units [J].
Brun-Buisson, C ;
Meshaka, P ;
Pinton, P ;
Vallet, B ;
Rodie-Talbere, P ;
Zahar, JR .
INTENSIVE CARE MEDICINE, 2004, 30 (04) :580-588
[10]   Prescribing indications based on successful clinical trials in sepsis: A difficult exercise [J].
Carlet, J .
CRITICAL CARE MEDICINE, 2006, 34 (02) :525-529