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2014 | nr 2 | 64--75
Tytuł artykułu

Can We Determine The Optimal Cycle Length for Which Half-Cycle Correction Should Always Be Applied?

Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The aim of the study is to measure the influence of cycle length and progression rates on differences between final results obtained using different approaches concerning time of transition to another state in Markov models (at the beginning, at the end of the cycle or half-cycle correction - HCC) and to estimate an optimal cycle length for which HCC should always be applied. A hypothetical, two-state Markov model was built. Assuming different progression rates, four methods concerning time of transition were compared. For each rate, the threshold values were determined, i.e. the maximal cycle length for which the difference between HCC/ 'life-table' (LT) method and 'beginning'/'end' methods were not greater than 5%. Cycles longer than the estimated threshold are assumed to imply the application of HCC/LT. Under few assumptions, the threshold cycle length for annual progression of 0.05 was 1 year or 2 years, for 5% and 0% discount rate, respectively. The threshold cycle lengths became shorter for lower progression rates (2 weeks for 0.90 rate). The results obtained for single intervention cannot be easily repeated for incremental outcomes; however, some general relationships can be determined(original abstract)
Słowa kluczowe
Rocznik
Numer
Strony
64--75
Opis fizyczny
Twórcy
  • HTA Consulting, Krakow, Poland
  • HTA Consulting, Krakow, Poland
autor
  • University of Liverpool Management School, United Kingdom
  • HTA Consulting, Krakow, Poland
  • HTA Consulting, Krakow, Poland
Bibliografia
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  • Wisløff T., Hagen G., Rand-Hendriksen K. Half-Cycle Correction and Simpson's Method Tested in Real Health Economic Models - Does it Matter Which Method We Use? 2011
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  • Taylor M., Lewis L. The Half-Cycle "Correction": How Much of a Correction is it? ISPOR 15th Annual European Congress. 2012 Nov, Berlin, Germany; Available from: http://www.ispor.org/research_pdfs/42/pdffiles/PRM48.pdf
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  • Pharmaceutical Benefits Advisory Committee. Guidelines for preparing submissions to the Pharmaceutical Benefits Advisory Committee. Version. 4.4. 2013; Available from: http://www.pbac.pbs.gov.au/content/information/printable-files/pbacg-book.pdf
  • Agency for Health Technology Assessment. Guidelines for conducting Health Technology Assessment (HTA). Version 2.1. Warsaw 2009; Available from: http://www.aotm.gov.pl/www/assets/files/wytyczne_hta/2009/Guidelines_HTA_eng_MS_29062009.pdf
  • Pharmaceutical Management Agency. Prescription for Pharmacoeconomic Analysis. Methods for cost-utility analysis. Version 2.1. New Zealand; 2012; Available from: http://www.pharmac.health.nz/assets/pfpa-final.pdf
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  • NICE technology appraisal guidance 242. Cetuximab, bevacizumab and panitumumab for the treatment of metastatic colorectal cancer after first-line chemotherapy. 2012. Available from: http://www.nice.org.uk/guidance/ta242\
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Typ dokumentu
Bibliografia
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Identyfikator YADDA
bwmeta1.element.ekon-element-000171464845

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