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Synergy between health technology assessments and clinical guidelines for multiple sclerosis.
Hogervorst, Milou A; Vreman, Rick A; Zawada, Anna; Zielinska, Magdalena; Dawoud, Dalia M; de Jong, Brigit A; Mantel-Teeuwisse, Aukje K; Goettsch, Wim G.
Afiliação
  • Hogervorst MA; Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands.
  • Vreman RA; National Health Care Institute (ZIN), Diemen, The Netherlands.
  • Zawada A; Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands.
  • Zielinska M; National Health Care Institute (ZIN), Diemen, The Netherlands.
  • Dawoud DM; Department of Pharmacoeconomics, Medical University of Warsaw, Warsaw, Poland.
  • de Jong BA; Department of Pharmacoeconomics, Medical University of Warsaw, Warsaw, Poland.
  • Mantel-Teeuwisse AK; National Institute for Health and Care Excellence (NICE), London, UK.
  • Goettsch WG; Faculty of Pharmacy, Clinical Pharmacy Department, Cairo University, Cairo, Egypt.
Clin Transl Sci ; 16(5): 835-849, 2023 05.
Article em En | MEDLINE | ID: mdl-36855929
ABSTRACT
Decision-making for reimbursement and clinical guidelines (CGs) serves different purposes although the decision-criteria and required evidence largely overlap. This study aimed to assess similarities and discrepancies between health technology assessment (HTA) reports as compared to CGs for multiple sclerosis (MS) medicines. All HTA reports and corresponding CGs for MS from the UK, France, Germany, the Netherlands, Poland, Sweden, and the European Union were assessed to identify synergies in recommendations for MS medicines (approved 1995-2020). A content analysis of HTA reports and CGs was performed to identify similarities and discrepancies in wording of treatment recommendations across documents. We assessed 132 HTA reports and 9 CGs for 16 MS treatments. Final recommendations for reimbursement and inclusion in CGs were mostly similar (90%), albeit with considerable differences in treatment lines and subindications. Since 2010, HTA reports refer to the use of CGs in 42% (55/132) and to consultations with clinicians in 43% (57/132) of cases. Six of nine CGs referred to HTA reports and two referred to HTA consultations, in one case having a formal relation to the HTA organization. CGs referenced pharmacoeconomic studies (4/9) for costs and cost-effectiveness. To date, not all new HTA recommendations for MS treatments are included in CGs. Some synergy exists between treatment recommendations in HTA reports and CGs, although discrepancies were seen in timelines and in recommended treatment lines and subindications. More stakeholder dialogue and/or consultation of each other's publications may further improve synergy, facilitate transparency, and enhance patient access.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Avaliação da Tecnologia Biomédica / Esclerose Múltipla Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Avaliação da Tecnologia Biomédica / Esclerose Múltipla Idioma: En Ano de publicação: 2023 Tipo de documento: Article