Bérengère Macabeo
Sanofi Pasteur
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Featured researches published by Bérengère Macabeo.
Human Vaccines & Immunotherapeutics | 2014
Gábor Kovács; Zoltán Kaló; Karina Jahnz-Rozyk; Jan Kynčl; Agnes Csohan; Adriana Pistol; Mariya Leleka; Rafail Kipshakbaev; Laure Durand; Bérengère Macabeo
Influenza affects 5–15% of the population during an epidemic. In Western Europe, vaccination of at-risk groups forms the cornerstone of influenza prevention. However, vaccination coverage of the elderly (>65 y) is often low in Central and Eastern Europe (CEE); potentially because a paucity of country-specific data limits evidence-based policy making. Therefore the medical and economic burden of influenza were estimated in elderly populations in the Czech Republic, Hungary, Kazakhstan, Poland, Romania, and Ukraine. Data covering national influenza vaccination policies, surveillance and reporting, healthcare costs, populations, and epidemiology were obtained via literature review, open-access websites and databases, and interviews with experts. A simplified model of patient treatment flow incorporating cost, population, and incidence/prevalence data was used to calculate the influenza burden per country. In the elderly, influenza represented a large burden on the assessed healthcare systems, with yearly excess hospitalization rates of ~30/100 000. Burden varied between countries and was likely influenced by population size, surveillance system, healthcare provision, and vaccine coverage. The greatest burden was found in Poland, where direct costs were over EUR 5 million. Substantial differences in data availability and quality were identified, and to fully quantify the burden of influenza in CEE, influenza reporting systems should be standardized. This study most probably underestimates the real burden of influenza, however the public health problem is recognized worldwide, and will further increase with population aging. Extending influenza vaccination of the elderly may be a cost-effective way to reduce the burden of influenza in CEE.
Value in Health | 2014
Pieter T. de Boer; Pascal Crépey; Richard Pitman; Bérengère Macabeo; Ayman Chit; Maarten Postma
BACKGROUND Designed to overcome influenza B mismatch, new quadrivalent influenza vaccines (QIVs) contain one additional B strain compared with trivalent influenza vaccines (TIVs). OBJECTIVE To examine the expected public health impact, budget impact, and incremental cost-effectiveness of QIV versus TIV in the United States. METHODS A dynamic transmission model was used to predict the annual incidence of influenza over the 20-year-period of 2014 to 2034 under either a TIV program or a QIV program. A decision tree model was interfaced with the transmission model to estimate the public health impact and the cost-effectiveness of replacing TIV with QIV from a societal perspective. Our models were informed by published data from the United States on influenza complication probabilities and relevant costs. The incremental vaccine price of QIV as compared with that of TIV was set at US
Expert Review of Vaccines | 2017
Margaret Haugh; Viviane Gresset-Bourgeois; Bérengère Macabeo; Anne Woods; Sandrine I. Samson
5.40 per dose. RESULTS Over the next 20 years, replacing TIV with QIV may reduce the number of influenza B cases by 27.2% (16.0 million cases), resulting in the prevention of 137,600 hospitalizations and 16,100 deaths and a gain of 212,000 quality-adjusted life-years (QALYs). The net societal budget impact would be US
BMC Public Health | 2016
Aurélien Jamotte; Chui Fung Chong; Andrew Manton; Bérengère Macabeo; Mondher Toumi
5.8 billion and the incremental cost-effectiveness ratio US
Human Vaccines & Immunotherapeutics | 2017
Aurélien Jamotte; Emilie Clay; Bérengère Macabeo; Andrès Caicedo; Jg Lopez; Lucia Ferro Bricks; Martín Romero Prada; Rubén Marrugo; Pamela Alfonso; Brechla Moreno Arévalo; Danilo Franco; Lourdes Garcia Diaz; Yadira Isaza de Molto
27,411/QALY gained. In the probabilistic sensitivity analysis, 100% and 96.5% of the simulations fell below US
PLOS ONE | 2016
Levent Akin; Bérengère Macabeo; Zafer Çalişkan; Serdar Altinel; Ilhan Satman
100,000/QALY and US
Value in Health | 2015
L Bricks; Jg Lopez; Bérengère Macabeo; Ad Piedade; Oa Clark; Am Nishikawa; A Bottoni; T Gonçalves
50,000/QALY, respectively. CONCLUSIONS Introducing QIV into the US immunization program may prevent a substantial number of hospitalizations and deaths. QIV is also expected to be a cost-effective alternative option to TIV.
BMC Public Health | 2014
E. Préaud; Laure Durand; Bérengère Macabeo; Norbert Farkas; Brigitte Sloesen; Abraham Palache; Francis Shupo; Sandrine I. Samson
ABSTRACT Introduction: Vaxigrip, a trivalent split-virion, inactivated vaccine available since 1968 has been in use longer than any other influenza vaccine. It is the most widely-used influenza vaccine, with more than 1.8 billion doses distributed in more than 120 countries. Areas covered: The significant body of evidence that confirms the efficacy, effectiveness, immunogenicity, and safety of Vaxigrip in healthy individuals of all ages and at-risk populations is summarized. The results from at least 15 randomized efficacy trials and 15 other studies have demonstrated that vaccination with Vaxigrip is efficacious against various clinical endpoints. It was estimated that more than 37 million laboratory-confirmed influenza episodes, 476,000 influenza-related hospitalizations, and 67,000 influenza-related deaths have been avoided by the more than 1.8 billion doses of Vaxigrip that have been distributed, emphasizing its important public health impact. Expert commentary: This strong evidence base in favor of Vaxigrip provides a robust foundation to support the implementation of the quadrivalent formulation. This quadrivalent formulation of Vaxigrip contains two A and two B influenza strains (VaxigripTetra), and has a similar immunogenicity and safety profile to the trivalent formulation while offering broader protection due to the addition of the second influenza B strain.
Post-Print | 2016
Aurélien Jamotte; Chui Fung Chong; Andrew Manton; Bérengère Macabeo; Mondher Toumi
BackgroundAnnual trivalent influenza vaccines (TIV) containing three influenza strains (A/H1N1, A/H3N2, and one B) have been recommended for the prevention of influenza. However, worldwide co-circulation of two distinct B lineages (Victoria and Yamagata) and difficulties in predicting which lineage will predominate each season have led to the development of quadrivalent influenza vaccines (QIV), which include both B lineages. Our analysis evaluates the public health benefit and associated influenza-related costs avoided which would have been obtained by using QIV rather than TIV in Australia over the period 2002–2012.MethodsA static model stratified by age group was used, focusing on people at increased risk of influenza as defined by the Australian vaccination recommendations. B-lineage cross-protection was accounted for. We calculated the potential impact of QIV compared with TIV over the seasons 2002–2012 (2009 pandemic year excluded) using Australian data on influenza circulation, vaccine coverage, hospitalisation and mortality rates as well as unit costs, and international data on vaccine effectiveness, influenza attack rate, GP consultation rate and working days lost. Third-party payer and societal influenza-related costs were estimated in 2014 Australian dollars. Sensitivity analyses were conducted.ResultsUsing QIV instead of TIV over the period 2002–2012 would have prevented an estimated 68,271 additional influenza cases, 47,537 GP consultations, 3,522 hospitalisations and 683 deaths in the population at risk of influenza. These results translate into influenza-related societal costs avoided of
Value in Health | 2015
Bérengère Macabeo; Levent Akin; Zafer Çalişkan; Serdar Altinel; Ilhan Satman
46.5 million. The estimated impact of QIV was higher for young children and the elderly. The overall impact of QIV depended mainly on vaccine effectiveness and the influenza attack rate attributable to the mismatched B lineage.ConclusionThe broader protection offered by QIV would have reduced the number of influenza infections and its related complications, leading to substantial influenza-related costs avoided.