Cost-effectiveness of new pneumococcal conjugate vaccines in Turkey: a decision analytical model

被引:20
作者
Bakir, Mustafa [1 ]
Turel, Ozden [2 ]
Topachevskyi, Oleksandr [3 ]
机构
[1] Marmara Univ, Sch Med Hosp, Dept Pediat & Pediat Infect Dis, TR-34662 Istanbul, Turkey
[2] Bakirkoy Matern & Childrens Res Hosp, Dept Pediat & Pediat Infect Dis, Istanbul, Turkey
[3] GlaxoSmithKline Vaccines, Wavre, Belgium
关键词
NONTYPABLE HAEMOPHILUS-INFLUENZAE; ACUTE OTITIS-MEDIA; STREPTOCOCCUS-PNEUMONIAE; ANTIMICROBIAL RESISTANCE; BACTERIAL-MENINGITIS; ECONOMIC-EVALUATION; UNITED-STATES; PROTEIN-D; DISEASE; VACCINATION;
D O I
10.1186/1472-6963-12-386
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Streptococcus pneumoniae infections, which place a considerable burden on healthcare resources, can be reduced in a cost-effective manner using a 7-valent pneumococcal conjugate vaccine (PCV-7). We compare the cost effectiveness of a 13-valent PCV (PCV-13) and a 10-valent pneumococcal non-typeable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) with that of PCV-7 in Turkey. Methods: A cost-utility analysis was conducted and a decision analytical model was used to estimate the proportion of the Turkish population <10 years old that would experience 10 mutually exclusive outcomes over the course of 1 year from a perspective of a healthcare system. Model outcomes were adjusted according to the population demographics and region-specific serotype distribution in Turkey. Health outcomes and direct healthcare costs were simulated for PCV-7, PCV-13 and PHiD-CV. Results: PCV-13 and PHiD-CV are projected to have a substantial impact on pneumococcal disease in Turkey versus PCV-7, with 2,223 and 3,156 quality-adjusted life years (QALYs) and 2,146 and 2,081 life years, respectively, being saved under a 3+1 schedule. Projections of direct medical costs showed that a PHiD-CV vaccination programme would provide the greatest cost savings, offering additional savings of US$11,718,813 versus PCV-7 and US $8,235,010 versus PCV-13. Probabilistic sensitivity analysis showed that PHiD-CV dominated PCV-13 in terms of QALYs gained and cost savings in 58.3% of simulations. Conclusion: Under the modeled conditions, PHiD-CV would provide the most cost-effective intervention for reducing pneumococcal disease in Turkish children.
引用
收藏
页数:12
相关论文
共 63 条
[11]   Epidemiology, clinical characteristics and antimicrobial resistance patterns of community-acquired pneumonia in 1702 hospitalized children in Singapore [J].
Chiang, Wen C. ;
Teoh, Oon H. ;
Chong, Chia Y. ;
Goh, Anne ;
Tang, Jenny P. L. ;
Chay, Oh M. .
RESPIROLOGY, 2007, 12 (02) :254-261
[12]   Pharmacoeconomic evaluation of 10-and 13-valent pneumococcal conjugate vaccines [J].
Chuck, Anderson W. ;
Jacobs, Philip ;
Tyrrell, Gregory ;
Kellner, James D. .
VACCINE, 2010, 28 (33) :5485-5490
[13]  
Comite sur l'immunisation du Quebec, 2010, EV DEUX NOUV VACC PE
[14]  
De Schutter I, 2009, 27 EUR SOC PAED INF
[15]   Modeling the Impact of a New Vaccine on Pneumococcal and Nontypable Haemophilus influenzae Diseases: A New Simulation Model [J].
De Wals, Philippe ;
Black, Steven ;
Borrow, Ray ;
Pearce, David .
CLINICAL THERAPEUTICS, 2009, 31 (10) :2152-2169
[16]   How to compare the efficacy of conjugate vaccines to prevent acute otitis media? [J].
De Wals, Philippe ;
Erickson, Lonny ;
Poirier, Beatrice ;
Pepin, Jacques ;
Pichichero, Michael E. .
VACCINE, 2009, 27 (21) :2877-2883
[17]   The global value of vaccination [J].
Ehreth, J .
VACCINE, 2003, 21 (7-8) :596-600
[18]   Efficacy of a pneumococcal conjugate vaccine against acute otitis media [J].
Eskola, J ;
Kilpi, T ;
Palmu, A ;
Jokinen, J ;
Haapakoski, J ;
Herva, E ;
Takala, A ;
Käyhty, H ;
Karma, P ;
Kohberger, R ;
Siber, G ;
Mäkela, PH ;
Lockhart, S ;
Ecrola, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (06) :403-409
[19]   Has the licensing of respiratory quinolones for adults and the 7-valent pneumococcal conjugate vaccine (PCV-7) for children had herd effects with respect to antimicrobial non-susceptibility in invasive Streptococcus pneumoniae? [J].
Fenoll, A. ;
Aguilar, L. ;
Granizo, J. J. ;
Gimenez, M. J. ;
Aragoneses-Fenoll, L. ;
Mendez, C. ;
Tarrago, D. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 62 (06) :1430-1433
[20]  
Garces-Sanchez M, 2004, An Pediatr (Barc), V60, P125