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  1. Article ; Online: Economic evaluation of cladribine tablets in high disease activity (HDA) relapsing multiple sclerosis (RMS) patients in Lebanon.

    Matni, Mirna / Yamout, Bassem / Koussa, Salam / Khamis, Chaker / Fleifel, Lora / Sharifi, Shahdak / Mohamed, Omneya

    Multiple sclerosis and related disorders

    2022  Volume 67, Page(s) 104169

    Abstract: Background: Cladribine tablets are a newly launched short course oral treatment approved for high disease activity (HDA) relapsing multiple sclerosis (RMS). The current analysis assessed the cost-utility and budgetary impact of introducing cladribine ... ...

    Abstract Background: Cladribine tablets are a newly launched short course oral treatment approved for high disease activity (HDA) relapsing multiple sclerosis (RMS). The current analysis assessed the cost-utility and budgetary impact of introducing cladribine tablets in HDA-RMS patients compared with other HDA-RMS therapies in Lebanon.
    Methods: The global cost-utility and budget impact models were adapted from Lebanese National Social Security Fund (NSSF) perspective. The data for the models' adaptation were retrieved from the literature and validated by Lebanese experts. The comparators considered in the cost-utility model were alemtuzumab, fingolimod, and natalizumab while budget impact analysis additionally considered dimethyl fumarate. A sensitivity analysis was also performed to assess the uncertainty in the analysis.
    Results: The cost-utility results showed that cladribine tablets are an economically dominant therapeutic strategy (i.e., less costly and better quality-adjusted life year [QALY]) compared to all comparators. The cost saving was driven by drug acquisition, administration, and monitoring costs; while incremental QALY gain was driven by differences in delayed Expanded Disability Status Scale progression. Sensitivity analysis showed that cladribine tablets have a high probability (99.3-100%) of being dominant at a threshold of 22,000 United States Dollars (approximately three times of gross domestic product) per QALY gained against different comparators. The budget impact analysis showed that the introduction of cladribine tablets would result in 5.0% to 21.5% savings in the overall budget over a period of five years.
    Conclusions: Cladribine tablets are a cost-effective and a budget-saving treatment option for the treatment of HDA-RMS patients in Lebanon from the NSSF perspective.
    MeSH term(s) Humans ; Cladribine/therapeutic use ; Cost-Benefit Analysis ; Multiple Sclerosis/drug therapy ; Multiple Sclerosis, Relapsing-Remitting/drug therapy ; Lebanon ; Immunosuppressive Agents/therapeutic use ; Recurrence ; Tablets
    Chemical Substances Cladribine (47M74X9YT5) ; Immunosuppressive Agents ; Tablets
    Language English
    Publishing date 2022-09-09
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2645330-7
    ISSN 2211-0356 ; 2211-0348
    ISSN (online) 2211-0356
    ISSN 2211-0348
    DOI 10.1016/j.msard.2022.104169
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Outcome-based reimbursement in Central-Eastern Europe and Middle-East.

    Ádám, Ildikó / Callenbach, Marcelien / Németh, Bertalan / Vreman, Rick A / Tollin, Cecilia / Pontén, Johan / Dawoud, Dalia / Elvidge, Jamie / Crabb, Nick / van Waalwijk van Doorn-Khosrovani, Sahar Barjesteh / Pisters-van Roy, Anke / Vincziczki, Áron / Almomani, Emad / Vajagic, Maja / Oner, Z Gulsen / Matni, Mirna / Fürst, Jurij / Kahveci, Rabia / Goettsch, Wim G /
    Kaló, Zoltán

    Frontiers in medicine

    2022  Volume 9, Page(s) 940886

    Abstract: Outcome-based reimbursement models can effectively reduce the financial risk to health care payers in cases when there is important uncertainty or heterogeneity regarding the clinical value of health technologies. Still, health care payers in lower ... ...

    Abstract Outcome-based reimbursement models can effectively reduce the financial risk to health care payers in cases when there is important uncertainty or heterogeneity regarding the clinical value of health technologies. Still, health care payers in lower income countries rely mainly on financial based agreements to manage uncertainties associated with new therapies. We performed a survey, an exploratory literature review and an iterative brainstorming in parallel about potential barriers and solutions to outcome-based agreements in Central and Eastern Europe (CEE) and in the Middle East (ME). A draft list of recommendations deriving from these steps was validated in a follow-up workshop with payer experts from these regions. 20 different barriers were identified in five groups, including transaction costs and administrative burden, measurement issues, information technology and data infrastructure, governance, and perverse policy outcomes. Though implementing outcome-based reimbursement models is challenging, especially in lower income countries, those challenges can be mitigated by conducting pilot agreements and preparing for predictable barriers. Our guidance paper provides an initial step in this process. The generalizability of our recommendations can be improved by monitoring experiences from pilot reimbursement models in CEE and ME countries and continuing the multistakeholder dialogue at national levels.
    Language English
    Publishing date 2022-09-23
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2022.940886
    Database MEDical Literature Analysis and Retrieval System OnLINE

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