{"title":"Transformative potential of artificial intelligence in global health policy.","authors":"Ridwan Islam Sifat, Upali Bhattacharya","doi":"10.1080/20016689.2023.2230660","DOIUrl":"https://doi.org/10.1080/20016689.2023.2230660","url":null,"abstract":"ChatGPT is an extraordinary example of how far artificial intelligence has come regarding conversational interfaces. Its exceptional ability to mimic human interaction by utilizing advanced natural language processing techniques has completely transformed how people interact with technology today [1,2]. It offers a highly immersive experience for users; their conversations feel natural and realistic as if they are interacting with another human being [3]. What distinguishes ChatGPT from other chatbots or virtual assistants is its incredible aptitude: when answering questions, it acknowledges user assumptions and challenges them using sophisticated algorithms. This feature significantly contributes to creating valuable insights and enhancing overall learning experiences for the users who engage with ChatGPT [4,5]. Overall, through its remarkable features, powerful machine learning models, and capacity to improve throughout interactions, ChatGPT represents one of the most innovative technologies available currently and continues to evolve every day, thus transforming communication [6]. Its ability to generate accurate responses without additional user input has made it a valuable resource beyond simple inquiries, with users relying on it for academic papers and essays due to its capability to provide supporting references upon request. However, it is important to acknowledge that these references may contain errors, as noted by researchers [7,8]. The remarkable transformation of artificial intelligence technology has revolutionized multiple fields, particularly public policy. Artificial intelligence systems are indispensable tools in policymaking due to their proficiencies in recognizing patterns in vast amounts of information [9]. With these capabilities, policymakers can make more informed decisions precisely based on insights rather than relying entirely on intuition or assumptions. The potential for AI’s continued evolution is immense and wildly anticipated to facilitate unparalleled advancements that could change how we shape our policies. ChatGPT is a promising AI technology that can revolutionize global health policy. It can facilitate communication between humans and machines, enabling vital contributions to complex decision-making processes at all levels of government agencies. However, whether ChatGPT will significantly impact governance regarding efficiency improvements or transparency development within society is unclear. 2. Advantages of integrating ChatGPT in global health policy","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2230660"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/eb/fa/ZJMA_11_2230660.PMC10316731.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10195134","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bérengère Macabeo, Liam Wilson, Jianwei Xuan, Ruichen Guo, Petar Atanasov, Linda Zheng, Clement François, Philippe Laramée
{"title":"Access to innovative drugs and the National Reimbursement Drug List in China: Changing dynamics and future trends in pricing and reimbursement.","authors":"Bérengère Macabeo, Liam Wilson, Jianwei Xuan, Ruichen Guo, Petar Atanasov, Linda Zheng, Clement François, Philippe Laramée","doi":"10.1080/20016689.2023.2218633","DOIUrl":"https://doi.org/10.1080/20016689.2023.2218633","url":null,"abstract":"<p><strong>Background and objectives: </strong>Multiple reforms aimed at improving the Chinese population's health have been introduced in recent years, including several designed to improve access to innovative drugs. We sought to review current factors affecting access to innovative drugs in China and to anticipate future trends.</p><p><strong>Methods: </strong>Targeted reviews of published literature and statistics on the Chinese healthcare system, medical insurance and reimbursement processes were conducted, as well as interviews with five Chinese experts involved in the reimbursement of innovative drugs.</p><p><strong>Results: </strong>Drug reimbursement in China is becoming increasingly centralized due to the removal of provincial pathways, the establishment of the National Healthcare Security Administration and the implementation of the National Reimbursement Drug List (NRDL), which is now the main route for drug reimbursement in China. There is also an increasing number of other channels via which patients may access innovative treatments, including various types of commercial insurance and special access. Health technology assessment (HTA) and health economic evidence are becoming pivotal elements of the NRDL decision-making process. Alongside the optimization of HTA decision making, innovative risk-sharing agreements are anticipated to be increasingly leveraged in the future to optimize access to highly specialized technologies and encourage innovation while safeguarding limited healthcare funds.</p><p><strong>Conclusions: </strong>Drug public reimbursement in China continues to align more closely with approaches widely used in Europe in terms of HTA, health economics and pricing. Centralization of decision-making processes for public reimbursement of innovative drugs allows consistency in assessment and access, which optimizes the improvement of the Chinese population's health.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2218633"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/de/68/ZJMA_11_2218633.PMC10266112.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10545126","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Miyuki Ezura, Katsuhiko Sawada, Yusuke Takushima, Ataru Igarashi, Lida Teng
{"title":"A systematic review of the characteristics of data assessment tools to measure medical doctors' work-related quality of life.","authors":"Miyuki Ezura, Katsuhiko Sawada, Yusuke Takushima, Ataru Igarashi, Lida Teng","doi":"10.1080/20016689.2023.2234139","DOIUrl":"https://doi.org/10.1080/20016689.2023.2234139","url":null,"abstract":"<p><strong>Purpose: </strong>Remarkable progress in healthcare technology has recently been made alongside changes in concepts related to drugs and medical devices. It is speculated that this progress benefits not only patients but also healthcare professionals, such as medical doctors. We performed a systematic review of the characteristics of current data assessment tools to measure medical doctors' work-related quality of life (QOL).</p><p><strong>Methods: </strong>A literature search was conducted through PubMed and Ichushi-Web in 2020. The related search terms used were 'medical doctor,' 'quality of work life,' and 'questionnaire/interview.' Two reviewers independently screened the studies, and the characteristics of the QOL assessment tools used in the identified studies were qualitatively reviewed and summarized.</p><p><strong>Results: </strong>In total, 5,443 and 760 articles were retrieved from PubMed and Ichushi-Web, respectively, of which 82 studies were included in this review. Sixty-five (79%) studies used structured questionnaires, and 17 (21%) studies used semistructured questionnaires. In terms of the study purpose, the identified studies mainly included four: mental health, the work or labor situation, satisfaction, and QOL. Components used to measure work-related QOL included satisfaction, burnout, QOL, the work environment, stress, mental health, work-life balance, and others. None of the studies used an originally developed QOL questionnaire to assess the work-related benefits of medical doctors.</p><p><strong>Conclusion: </strong>This systematic review found that there is a lack of studies directly assessing the work-related QOL of medical doctors and a lack of effective data collection tools to assess all work-related QOL components.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2234139"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b4/71/ZJMA_11_2234139.PMC10367570.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10194366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Andrea Aiello, Elisa Elena Mariano, Mariangela Prada, Cristina Teruzzi, Nicoletta Martone, Stefano Capri, Giuseppe Carli, Sergio Siragusa
{"title":"Budget impact analysis for avatrombopag in the treatment of chronic primary immune thrombocytopenia in adult patients refractory to other treatments.","authors":"Andrea Aiello, Elisa Elena Mariano, Mariangela Prada, Cristina Teruzzi, Nicoletta Martone, Stefano Capri, Giuseppe Carli, Sergio Siragusa","doi":"10.1080/20016689.2023.2230663","DOIUrl":"https://doi.org/10.1080/20016689.2023.2230663","url":null,"abstract":"<p><p><b>Introduction:</b> Primary immune thrombocytopenia is a rare autoimmune disease characterised by a decreased platelet count resulting in an increased risk of bleeding events and even life-threatening haemorrhages. Thrombopoietin receptor agonists (TPO-RAs) are the standard of care second-line therapy for adult patients with chronic immune thrombocytopenia. The first TPO-RAs approved and reimbursed in Italy, eltrombopag and romiplostim, while effective, pose some issues in terms of safety (e.g., hepatotoxicity) or general management (e.g., dietary restrictions). Avatrombopag, an effective and well-tolerated TPO-RA, was recently granted reimbursement. <b>Methods:</b> A 3-year (2023-2025) budget impact analysis (BIA) was conducted to estimate its impact on the Italian National Health Service (NHS). Two scenarios were compared, of which one represents the current situation, without avatrombopag, and the other provides for an increasing market share of avatrombopag (up to 26.6%). <b>Results:</b> BIA shows that the increase in the use of avatrombopag correlates with savings for NHS: in the first year, saving would be €1,300,564, increasing to €2,774,210 in the third year, for a total of €6,083,231 over the 3-year period. The sensitivity analysis confirmed these savings in the scenario with avatrombopag. <b>Conclusions:</b> Based on this BIA, the introduction and reimbursement of avatrombopag is an efficient and advantageous choice for the Italian NHS.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2230663"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a1/4c/ZJMA_11_2230663.PMC10316730.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10195136","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alexa C Klimchak, Lauren E Sedita, Louise R Rodino-Klapac, Jerry R Mendell, Craig M McDonald, Katherine L Gooch, Daniel C Malone
{"title":"Assessing the value of delandistrogene moxeparvovec (SRP-9001) gene therapy in patients with Duchenne muscular dystrophy in the United States.","authors":"Alexa C Klimchak, Lauren E Sedita, Louise R Rodino-Klapac, Jerry R Mendell, Craig M McDonald, Katherine L Gooch, Daniel C Malone","doi":"10.1080/20016689.2023.2216518","DOIUrl":"https://doi.org/10.1080/20016689.2023.2216518","url":null,"abstract":"<p><p><b>Background</b>: Delandistrogene moxeparvovec (SRP-9001) is an investigational gene therapy that may delay progression of Duchenne muscular dystrophy (DMD), a severe, rare neuromuscular disease caused by <i>DMD</i> gene mutations. Early cost-effectiveness analyses are important to help contextualize the value of gene therapies for reimbursement decision making. <b>Objective</b>: To determine the potential value of delandistrogene moxeparvovec using a cost-effectiveness analysis. <b>Study design</b>: A simulation calculated lifetime costs and equal value of life years gained (evLYG). Inputs included extrapolated clinical trial results and published utilities/costs. As a market price for delandistrogene moxeparvovec has not been established, threshold analyses established maximum treatment costs as they align with value, including varying willingness-to-pay up to $500,000, accounting for severity/rarity. <b>Setting</b>: USA, healthcare system perspective <b>Patients</b>: Boys with DMD <b>Intervention</b>: Delandistrogene moxeparvovec plus standard of care (SoC; corticosteroids) versus SoC alone <b>Main outcome measure</b>: Maximum treatment costs at a given willingness-to-pay threshold <b>Results</b>: Delandistrogene moxeparvovec added 10.30 discounted (26.40 undiscounted) evLYs. The maximum treatment cost was approximately $5 M, assuming $500,000/evLYG. Varying the benefit discount rate to account for the single administration increased the estimated value to #$5M, assuming $500,000/evLYG. <b>Conclusion</b>: In this early economic model, delandistrogene moxeparvovec increases evLYs versus SoC and begins to inform its potential value from a healthcare perspective.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2216518"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/29/7e/ZJMA_11_2216518.PMC10228300.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10195653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Implementation of equity and access in Indian healthcare: current scenario and way forward.","authors":"Canna Ghia, Gautam Rambhad","doi":"10.1080/20016689.2023.2194507","DOIUrl":"https://doi.org/10.1080/20016689.2023.2194507","url":null,"abstract":"<p><strong>Introduction: </strong>The Indian healthcare system is evolving towards better healthcare implementation and coverage. However, even today, the health-care system faces several challenges, a few of which are yet to be addressed. The present review is aimed to delineate the past and present healthcare scenarios in India, health-care policies, and other initiatives for achieving universal health coverage (UHC).</p><p><strong>Methods: </strong>A literature search was done on various government databases, websites, and PubMed for obtaining data and statistics on healthcare funding, health insurance schemes, healthcare budget allocations, categories of medical expenses, government policies, and health technology assessment (HTA) in India.</p><p><strong>Results: </strong>The available data indicates 37.2% of the total population is covered by any health insurance of which 78% are covered by public insurance companies. Around 30% of the total health expenditure is borne by the public sector, and there is high out-of-pocket (OOP) expenditure on healthcare.</p><p><strong>Discussion: </strong>Several new health policies and schemes, an increase in 2021 budget for healthcare by 137%, vaccination drives, augmenting manufacturing of medical devices, special training packages, Artificial Intelligence/Machine Learning (AI/ML)-based standard treatment workflow systems to ensure proper treatment and clinical decision-making have been initiated by the government for improving healthcare funding, equity, and access.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2194507"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/43/34/ZJMA_11_2194507.PMC10044314.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9224173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Niamh Carey, Joy Leahy, Lea Trela-Larsen, Laura Mc Cullagh, Michael Barry
{"title":"Cost-utility and value of information analysis of tisagenlecleucel for relapsed/refractory diffuse large B-cell lymphoma in the Irish healthcare setting.","authors":"Niamh Carey, Joy Leahy, Lea Trela-Larsen, Laura Mc Cullagh, Michael Barry","doi":"10.1080/20016689.2023.2166375","DOIUrl":"https://doi.org/10.1080/20016689.2023.2166375","url":null,"abstract":"<p><strong>Background: </strong>The evidence base of tisagenlecleucel is uncertain.</p><p><strong>Objective: </strong>To evaluate the cost-effectiveness of tisagenlecleucel. To conduct expected value of perfect information (EVPI) and partial EVPI (EVPPI) analyses.</p><p><strong>Study design: </strong>A three-state partitioned survival model. A short-term decision tree partitioned patients in the tisagenlecleucel arm according to infusion status. Survival was extrapolated to 5 years; general population mortality with a standardised mortality ratio was then applied. EVPI and EVPPI were scaled up to population according to the incidence of the decision.</p><p><strong>Setting: </strong>Irish healthcare payer.</p><p><strong>Participants: </strong>Patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL).</p><p><strong>Interventions: </strong>Tisagenlecleucel versus Salvage Chemotherapy (with or without haematopoietic stem cell transplant).</p><p><strong>Main outcome measure: </strong>Incremental cost-effectiveness ratio (ICER). Population EVPI and EVPPI.</p><p><strong>Results: </strong>At list prices, the ICER was €119,509 per quality-adjusted life year (QALY) (incremental costs €218,092; incremental QALYs 1.82). Probability of cost-effectiveness, at a €45,000 per QALY threshold, was 0%. Population EVPI was €0.00. Population EVPI, at the price of tisagenlecleucel that reduced the ICER to €45,000 per QALY, was €3,989,438. Here, survival analysis had the highest population EVPPI (€1,128,053).</p><p><strong>Conclusion: </strong>Tisagenlecleucel is not cost-effective, versus salvage chemotherapy (with or without haematopoietic stem cell transplant), for R/R DLBCL in Ireland. At list prices, further research to decrease decision uncertainty may not be of value.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2166375"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/12/0c/ZJMA_11_2166375.PMC9858398.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10582070","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ana Teresa Paquete, Rui Martins, Mark P Connolly, Marie Meulle, Nítida Pastor, Grégoire Benoist, Patrick Tounian
{"title":"Cost-effectiveness of infant hypoallergenic formulas to manage cow's milk protein allergy in France.","authors":"Ana Teresa Paquete, Rui Martins, Mark P Connolly, Marie Meulle, Nítida Pastor, Grégoire Benoist, Patrick Tounian","doi":"10.1080/20016689.2022.2154418","DOIUrl":"https://doi.org/10.1080/20016689.2022.2154418","url":null,"abstract":"<p><strong>Background: </strong>Clinician's choice of hypoallergenic formulas in the first-line management of cow's milk protein allergy (CMPA) should be informed by evidence on clinical efficacy and cost-effectiveness.</p><p><strong>Objective: </strong>We compare the cost-effectiveness of amino acid-based formula (AAF), extensively hydrolyzed casein formula with Lactobacillus rhamnosus Gorbach Goldin (EHCF+LGG), extensively hydrolyzed whey formula (EHWF), and rice hydrolyzed formula (RHF) in non-breastfed children in France.</p><p><strong>Methods: </strong>Immunotolerance and atopic manifestations' prevalence were based on a prospective non-randomized study with a 36-month follow-up. Resource utilization was sourced from a survey of French clinicians, and unit costs were based on national data. Costs and health consequences were discounted at 2.5% annually. Results were reported using the Collective and French National Health Insurance perspectives.</p><p><strong>Results: </strong>Children receiving EHCF+LGG were predicted to require less healthcare resources, given their reduced prevalence of CMPA symptoms at 3 years. In the base case, EHCF+LGG led to savings of at least €674 per child compared to AAF, EHWF, and RHF at 3 years, from both perspectives. Nutrition had the highest economic burden in CMPA, driven by hypoallergenic formulas and dietetic replacements costs. Results were robust to one-way and probabilistic sensitivity analyses.</p><p><strong>Conclusions: </strong>EHCF+LGG was associated with more symptom-free time, higher immune tolerance, and lower costs.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2154418"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/01/05/ZJMA_11_2154418.PMC9744214.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10367222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lauren Van Haesendonck, Jörg Ruof, Thomas Desmet, Walter Van Dyck, Steven Simoens, Isabelle Huys, Rosa Giuliani, Mondher Toumi, Christian Dierks, Juliana Dierks, Antonella Cardone, Francois Houÿez, Mira Pavlovic, Michael Berntgen, Peter G M Mol, Anja Schiel, Wim Goettsch, Fabrizio Gianfrate, Stefano Capri, James Ryan, Pierre Ducournau, Oriol Solà-Morales, Elaine Julian
{"title":"The role of stakeholder involvement in the evolving EU HTA process: <i>Insights generated through the European Access Academy's multi-stakeholder pre-convention questionnaire</i>.","authors":"Lauren Van Haesendonck, Jörg Ruof, Thomas Desmet, Walter Van Dyck, Steven Simoens, Isabelle Huys, Rosa Giuliani, Mondher Toumi, Christian Dierks, Juliana Dierks, Antonella Cardone, Francois Houÿez, Mira Pavlovic, Michael Berntgen, Peter G M Mol, Anja Schiel, Wim Goettsch, Fabrizio Gianfrate, Stefano Capri, James Ryan, Pierre Ducournau, Oriol Solà-Morales, Elaine Julian","doi":"10.1080/20016689.2023.2217543","DOIUrl":"https://doi.org/10.1080/20016689.2023.2217543","url":null,"abstract":"<p><p>Involvement of all relevant stakeholders will be of utmost importance for the success of the developing EU HTA harmonization process. A multi-step procedure was applied to develop a survey across stakeholders/collaborators within the EU HTA framework to assess their current level of involvement, determine their suggested future role, identify challenges to contribution, and highlight efficient ways to fulfilling their role. The 'key' stakeholder groups identified and covered by this research included: patients', clinicians', regulatory, and Health Technology Developer representatives. The survey was circulated to a wide expert audience including all relevant stakeholder groups in order to determine self-perception by the 'key' stakeholders regarding involvement in the HTA process (self-rating), and in a second, slightly modified version of the questionnaire, to determine the perception of 'key' stakeholder involvement by HTA bodies, payers, and policymakers (external rating). Predefined analyses were conducted on the submitted responses. Fifty-four responses were received (patients 9; clinicians: 8; regulators: 4; HTDs 14; HTA bodies: 7; Payers: 5; policymakers 3; others 4). The mean self-perceived involvement score was consistently lower for each of the 'key' stakeholder groups than the respective external ratings. Based on the qualitative insights generated in the survey, a RACI Chart (Responsible/Accountable/Consulted/Informed) was developed for each of the stakeholder groups to determine their roles and involvement in the current EU HTA process. Our findings suggest extensive effort and a distinct research agenda are required to ensure adequate involvement of the key stakeholder groups in the evolving EU HTA process.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2217543"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f6/b6/ZJMA_11_2217543.PMC10240997.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10196142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Pharmaceutical pricing and reimbursement policies in Algeria, Morocco, and Tunisia: comparative analysis.","authors":"Hajer Dahmani, Ines Fradi, Leila Achour, Mondher Toumi","doi":"10.1080/20016689.2023.2244304","DOIUrl":"https://doi.org/10.1080/20016689.2023.2244304","url":null,"abstract":"<p><strong>Objectives: </strong>In this paper, we outline and compare pharmaceutical pricing and reimbursement policies for in-patent prescription medicines in three Maghreb countries, Algeria, Morocco, and Tunisia, and explore possible improvements in their pricing and reimbursement systems.</p><p><strong>Methods: </strong>The evidence informing this study comes from both an extensive literature review and a primary data collection from experts in the three studied countries.</p><p><strong>Key findings: </strong>Twenty-six local experts where interviewed Intervieweesincluded ministry officials, representatives of national regulatory authorities, health insurance organizations, pharmaceutical procurement departments and agencies, academics, private pharmaceutical-sector actors, and associations. Results show that External Reference Pricing (ERP) is the dominant pricing method for in-patent medicines in the studied countries. Value-based pricing through Health Technology Assessment (HTA) is a new concept, recently used in Tunisia to help the reimbursement decision of some in-patent medicines but not yet used in the pricing of innovative medicines in the studied countries. Reimbursement decision is mainly based on negotiations set on Internal Reference Pricing (IRP).</p><p><strong>Conclusion: </strong>Whereas each country has its specific regulations, there are many similarities in the pricing and reimbursement policies of in-patent medicines in Algeria, Morocco, and Tunisia. The ERP was found to be the dominant method to inform pricing and reimbursement decisions of in-patent medicines. Countries in the region can focus on the development of explicit value assessment systems and minimize their dependence on ERP over the longer-term. In this context, HTA will rely on local assessment of the evidence.</p>","PeriodicalId":73811,"journal":{"name":"Journal of market access & health policy","volume":"11 1","pages":"2244304"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ea/01/ZJMA_11_2244304.PMC10443953.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10197219","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}