Adverse events (AE) costs assessed in Poland based on existing Drug Programs – methodology of the project
DOI:
https://doi.org/10.12923/j.2084-980X/26.4/a.16Słowa kluczowe:
costs, adverse events, treatmentAbstrakt
The Drug Programs, Pharmaceutical Care and Pharmaceutical Law section (DPPCPL) within Polish Pharmacoeconomical Society decided to perform a research on the impact of the adverse events treatment costs incurred by National Health Fund (NHF) and by the public payer. The aim of the project is to develop a list of costs associated to different disease areas of adverse events treatment. The project consists of different phases. Firstly, a review of the drug programs financed by NHF will allow identifying the drugs used in the programs in Poland. It will be followed by a review of the SPCs of the identified drugs regarding the AEs occurrence. For the most common AEs treatment, Polish clinical guidelines will be searched. Additionally expert opinion on treatment patterns in Poland will be collected using an excel tool allowing for further costs calculations. Costs to identified resources used will be allocated using NHF and public payer perspective. The final report will describe the identified adverse events based on the list of drugs used in the Drug Programs in Poland, the results of clinical guidelines search, treatment patterns and related costs. The project will address an important issue related to the costs generated within the Drug Programs, being helpful for further calculations in pharmaco-economic analysis.
Bibliografia
1. Agency for Health Technology Assessment: Guidelines for conducting Health Technology Assessment (HTA), Warsaw, April 2009. http://www.aotm.gov.pl/assets/files/wytyczne_hta/2009/Guidelines_HTA_eng_MS_29062009.pdf (access 18.10.2013)
2. Busse R., Orvain J. Velasco M. et al: Best practice in undertaking and reporting health technology assessments. Intl. J. Of Technology Assessment In Health Care 18:2, 2002, 361 – 422, http://www.inahta.org/upload/HTA_resources/AboutHTA_Best_Practice_in_Undertaking_and_Reporting_HTAs.pdf (access 6.11.2013)
3. Guidelines for conducting Health Technology Assessment (HTA), version 2.1, April 2009; http://www.aotm.gov.pl/index.php?id=13 (access 26.09.2013)
4. National Institute for Health Research: An Evaluation of Methods of Eliciting Expert Opinion in Health Technology Assessment. http://clahrc-peninsula.nihr.ac.uk/an-evaluation-of-methods-of-eliciting-expert-opinion-in-health-technology-assessment.php (access 30.10.2013)
5. Note of the meetings the Polish ISPOR Chapter there is Drug Programs, Pharmaceutical Care and Pharmaceutical Law section http://www.farmakoekonomika.pl/cms/index.php/pl/sekcja-programow-terapeutycznych-i-opieki-farmaceutycznej (access 26.09.2013)
6. Rozporządzenie Ministra Zdrowia z dnia 2 kwietnia 2012 r. w sprawie minimalnych wymagań, jakie muszą spełniać analizy uwzględnione we wnioskach o objęcie refundacją i ustalenie urzędowej ceny zbytu oraz o podwyższenie urzędowej ceny zbytu leku, środka spożywczego specjalnego przeznaczenia żywieniowego, wyrobu medycznego, które nie mają odpowiednika refundowanego w danym wskazaniu. Dz.U.2012 nr 0 poz. 388.
7. Ustawa z dnia 27 sierpnia 2004 r. o świadczeniach opieki zdrowotnej finansowanych ze środków publicznych. Dz. U. 2004 nr 210 poz. 2135
Pobrania
Opublikowane
Numer
Dział
Licencja
Prawa autorskie (c) 2013 Autorzy

Praca jest udostępniana na licencji Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 Unported License.