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  1. NTU Theses and Dissertations Repository
  2. 公共衛生學院
  3. 公共衛生碩士學位學程
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/19175
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor楊銘欽
dc.contributor.authorJeong-Ting Hsiehen
dc.contributor.author謝炅廷zh_TW
dc.date.accessioned2021-06-08T01:47:37Z-
dc.date.copyright2016-08-26
dc.date.issued2016
dc.date.submitted2016-08-05
dc.identifier.citation1. Tandon R, Keshavan, MS and Nasrallah HA. Schizophrenia, “just the facts” what we know in 2008. 2. Epidemiology and etiology. Schizophr Res. 2008;102:1-18.
2. McGuffin P, Asherson P, Owen M, et al. The strength of the genetic effect. Is there room for an environmental influence in the aetiology of schizophrenia? Br J Psychiatry. 1994 May;164(5):593-9.
3. Jones P, Cannon M. The new epidemiology of schizophrenia. Psychiatr Clin North Am. 1998 Mar;21(1):1-25.
4. Schizophrenia, the epigenetic puzzle. Gottesman II & Shields J. Press Syndicate of the University of Cambridge. New Yourk, NY, USA. 1982.
5. Lichtenstein P, Yip BH, Björk C, Pawitan Y, et al. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet. 2009 Jan 17;373(9659):234-9.
6. European Network of Schizophrenia Networks for the Study of Gene-Environment Interactions. Schizophrenia aetiology: do gene-environment interactions hold the key? Schizophr Res. 2008;102:21-6.
7. Iritani S. Neuropathology of schizophrenia: a mini review. Neuropathology. 2007;27:604-8.
8. Kato T. Bridging pharmacology and neurodevelopment in schizophrenia. Int J Neuropsychopharmacol. 2007;10:713-6.
9. Laviolette SR. Dopamine modulation of emotional processing in cortical and subcortical neural circuits: evidence for a final common pathway in schizophrenia? Schizophr Bull. 2007;33:971-81.
10. Chen CK, Lin SK, Sham PC, et al. Pre-morbid characteristics and co-morbidity of methamphetamine users with and without psychosis. Psychol Med. 2003;33:1407-14.
11. Muller-Vahl KR and Emrich HM. Cannabis and schizophrenia: towards a cannabinoid hypothesis of schizophrenia. Expert Rev Neurother. 2008;8:1037-48.
12. Lieberman JA. Dopamine partial agonists: a new class of antipsychotic. CNS Drugs. 2004;18(4):251-67.
13. American Psychiatric Association. Practice Guideline for the Treatment of Patients With Schizophrenia. 2nd ed. Arlington, VA: APA; 2004. Available from URL: http://www.psych.org
14. Abi-Dargham A and Laruelle M. Mechanisms of action of second generation antipsychotic drugs in schizophrenia: insights from brain imaging studies. Eur Psychiatry. 2005;20:15-27.
15. Moore TA, Buchanan RW, Buckley PF, et al. The Texas Medication Algorithm Project antipsychotic algorithm for schizophrenia: 2006 update. J Clin Psychiatry. 2007 Nov;68(11):1751-62.
16. Informa Healthcare. The Maudsley Prescribing Guidelines. 10th ed. London, UK: Informa Healthcare; 2009.
17. Cassano GB, Fagiolini A, Lattanzi L, et al. Aripiprazole in the treatment of schizophrenia: a consensus report produced by schizophrenia experts in Italy. Clin Drug Invest. 2007;27(1):1-13.
18. Burris KD, Molski TF, Xu C, et al. Aripiprazole, a novel antipsychotic, is a high-affinity partial agonist at human dopamine D2 receptors. JPET. 2002;302:381-9.
19. Casey DE, Carson WH, Saha AR, et al. Switching patients to aripiprazole from other antipsychotic agents: a multicenter randomized study. Psychopharmacology. 2003;166:391-9.
20. Yokoi F, Grunder G, Biziere K, et al. Dopamine D2 and D3 receptor occupancy in normal humans treated with the antipsychotic drug aripiprazole (OPC 14597): a study using positron emission tomography and [11C]raclopride. Neuropsychopharmacology. 2002;27:248-59.
21. Grunder G, Fellows C, Janouschek H, et al. Brain and plasma pharmacokinetics of aripiprazole in patients with schizophrenia: an [18F] fallypride PET study. Am J Psychiatry. 2008;165:988-95.
22. Tandon R, Marcus RN, Stock EG, et al. A prospective, multicenter, randomized, parallel-group, open-label study of aripiprazole in the management of patients with schizophrenia or schizoaffective disorder in general psychiatric practice: Broad Effectiveness Trial with Aripiprazole (BETA). Schizophr Res. 2006;84(1):77-89.
23. Wolf J, Janssen F, Lublin H, et al. A prospective, multicentre, open-label study of aripiprazole in the management of patients with schizophrenia in psychiatric practice in Europe: Broad Effectiveness Trial with Aripiprazole in Europe (EU-BETA). Curr Med Res Opin. 2007;23(10):2313-23.
24. Hsieh MH, Lin WW, Chen ST, et al. A 64-week, multicenter, open-label study of aripiprazole effectiveness in the management of patients with schizophrenia or schizoaffective disorder in a general psychiatric outpatient setting. Ann Gen Psychiatry. 2010 S ep 17;9:35.
25. Taylor D, Hanssens L, Loze JY, et al. Preference of medicine and patient-reported quality of life in community-treated schizophrenic patients receiving aripiprazole vs standard of care: results from the STAR study. Eur Psychiatry. 2008 Aug;23(5):336-43.
26. Kolotkin RL, Corey-Lisle PK, Crosby RD, et al. Changes in weight and weight-related quality of life in a multicentre, randomized trial of aripiprazole versus standard of care. Eur Psychiatry. 2008 Dec;23(8):561-6.
27. Dieter Naber a, Karina Hansen b, et al. Qualify: a randomized head-to-head study of aripiprazole once-monthlyand paliperidone palmitate in the treatment of schizophrenia. Schizophrenia Research 168 (2015) 498–504
28. Colombo GL, Caruggi M, Di Matteo S, et al. An economic evaluation of aripiprazole vs olanzapine adapted to the Italian setting using outcomes of metabolic syndrome and risk for diabetes in patients with schizophrenia. Neuropsychiatr Dis Treat. 2008 Oct;4(5):967-76.
29. King D, Knapp M, Thomas P, et al. Cost-effectiveness analysis of aripiprazole vs standard-of-care in the management of community-treated patients with schizophrenia: STAR study. Curr Med Res Opin. 2011 Feb;27(2):365-74.
30. Leslie Citrome , Siddhesh A. Kamat , Christophe Sapin, et al. Cost-effectiveness of aripiprazole once-monthly compared with paliperidone palmitate once-monthly injectable for the treatmentof schizophrenia in the United States. Journal of Medical Economics 2014, 1–10
31. 全民健保研究資料庫非學術研究類 (編號:SI-101004).
32. Kane JM, Sanchez R, Perry PP, et al. Aripiprazole intramuscular depot as maintenance treatment in patients with schizophrenia: a 52-week, multicenter, randomized, double-blind, placebo-controlled study. J Clin Psychiatry 2012;73:617-24.
33. Gaebel W, Schreiner A, Bergmans P, et al. Relapse prevention in schizophrenia and schizoaffective disorder with risperidone long-acting injectable vs quetiapine: results of a long-term, open-label, randomized clinical trial. Neuropsychopharmacology 2010;35:2367-77.
34. Hough D, Gopal S, Vijapurkar U, Lim P, Morozova M, Eerdekens M. Paliperidone palmitate maintenance treatment in delaying the time-to-relapse in patients with schizophrenia: a randomized, double-blind, placebo-controlled study. Schizophr Res 2010;116:107-17.
35. Mahlich J, Nishi M, Saito Y. Modeling the budget impact of long-acting injectable paliperidone palmitate in the treatment of schizophrenia in Japan. Clinicoecon Outcomes Res 2015;7:267-72
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/19175-
dc.description.abstract研究目的
藉由實務實習計畫參與,了解在二代健保制度下,台灣新藥上市的藥價政策和未來趨勢、全民健康保險藥品核價原則及作業流程、藥品價格調整原則及作業流程、藥品與特殊材料費用有關之總額支付制度與藥物核價資訊、與健保新藥使用有關的醫療科技評估及成本效益分析,以及新藥上市可能對健保預算產生的財務衝擊預估等。
方法
本研究以一尚未在台灣上市的新一代抗精神病藥長效型針劑做研究標的,配合實習計畫的進度採用相關的研究方法:
一、在擬定給付價格的階段,將採內容分析法(content analysis),針對英國、澳洲及加拿大三國醫藥科技評估(HTA)的結果做探討,並分析健保署參照的世界先進十國藥品給付現況,提出台灣給付價格可行區間假設。
二、利用深度訪談(in-depth interview) 疾病治療與健保給付相關專家,了解台灣的流行病學資訊、本土的臨床照顧模式以及醫療利用情形,以便最佳化健保預算衝擊模型的考量因子。
三、在經濟效益評估的階段,利用回溯性世代(retrospective cohort) 分析2010-2013年健保資料庫百萬歸人檔中思覺失調症患者的相關處方用藥與其他醫療成本,將相關參數導入財務影響分析中(budget impact analysis),評估新的治療是否可以減少相關的健保支出;再利用基準情境(base-case scenario)與敏感度分析(sensitivity analysis),檢視如果改變重要假設(key assumptions)中的參數,會對分析結果產生的影響
結果
台灣針對本研究藥物給付區間可能落在新台幣7,665元至9,257元間,而此新藥定位為取代現有治療方式,本經濟評估採較保守的9,257元依健保署觀點、直接成本進行財務影響分析。基礎分析結果,以健保「藥費」預算觀點,第一年到第五年分別為新台幣0.6萬、-46萬、34萬、-40萬及-135萬元。同樣的分析方式下,以健保「藥費」預算觀點,第一年到第五年分別為新台幣-137萬、-509萬、-583萬、-873萬及-1,251萬元。情境分析顯示所測試的參數皆不改變節省健保支出之結論。
結論
本研究藥物與其他藥物相比,在療效、安全性與耐受性方面有相當或較優越的表現,此新一代長效針劑納入給付亦能為健保節省整體醫療支出,綜合各項分析,將此新藥列於健保給付治療選擇中,除了帶給醫師與病患新的選擇外,也能與國際接軌,讓台灣在思覺失調症治療能更進一步。
zh_TW
dc.description.abstractObjective
By means of practicum, we are capable of understanding the pricing and reimbursement policy for the new treatment launch Taiwan. A holistic economic evaluation, including Health Technology Assessment report, cost-effectiveness analysis, and budget impact analysis will bring comprehensive picture for the novel treatment.
Method
This study aims for a long-acting injectable antipsychotic which has not launched in Taiwan. Stepwise methods are applied according to the process:
1. Content analysis will be applied to HTA reports discussion issued by UK, Australia, and Canada. The assumption of possible reimbursed interval will come up after putting advanced 10 countries price into consideration.
2. Conduct in-depth interview with key opinion leaders to confirm the prevalence, clinic practice, and treatment algorithm for schizophrenia.
3. At economic evaluation phase, utilize retrospective cohort of Normalized Million People File from 2010 to 2013 (National Health Insurance Research Database) to analyze medication and other medical cost for schizophrenic patients. The parameters will be applied into budget impact analysis; meanwhile, base-case scenario and sensitivity analysis will be conduct to check the budget impact under different assumed circumstances.
Results
According to the policy, the possible reimbursed price interval of this novel long-acting injectable may fall between TWD 7,665 and TWD9,257. To be modest, we took TWD 9,257 as the assumed reimbursement price which is positioned to replace exited long-acting injectables. The economic evaluation is based on perspective of national health insurance and direct cost to conduct budget impact analysis. In base-case analysis, the novel long-acting injectable will save TWD 12.51 million in fifth-year after reimbursement, including 1.35 million in drug expenditure and 11.16 million in OPD and IPD cost. Whilst, in scenario analysis, the conclusion of cost saving remains the same no matter which parameter varies.
Conclusion
The novel long-acting injectable in this study is non-inferior or superior to the other existed long-acting injectable in efficacy, safety, and tolerability. From the perspective of economic evaluation, the reimbursement of this novel treatment will not only save drug expenditure but also all medical cost for national health care insurance.
en
dc.description.provenanceMade available in DSpace on 2021-06-08T01:47:37Z (GMT). No. of bitstreams: 1
ntu-105-R03847028-1.pdf: 1961965 bytes, checksum: 0489f6655d3856b6206836ba604509d7 (MD5)
Previous issue date: 2016
en
dc.description.tableofcontents第一章 導論 1
第二章 研究方法 7
第三章 研究結果與討論 9
第四章 結論 41
參考文獻 42
附錄 45
一、專家深度訪談問卷 45
二、專家深度訪談摘要 51
三、IMS資料統計 61
四、健保資料庫分析 62
dc.language.isozh-TW
dc.title新一代抗精神病藥長效型針劑之訂價與給付策略探討zh_TW
dc.titlePricing and Reimbursement Strategy for A Novel Long Acting Injectable Antipsychoticen
dc.typeThesis
dc.date.schoolyear104-2
dc.description.degree碩士
dc.contributor.oralexamcommittee郎慧珠,周楷沛
dc.subject.keyword思覺失調症,長效針劑,財務影響分析,基礎分析,情境分析,zh_TW
dc.subject.keywordschizophrenia,long-acting injectable,budget impact analysis,base case scenario,sensitivity analysis,en
dc.relation.page63
dc.identifier.doi10.6342/NTU201601957
dc.rights.note未授權
dc.date.accepted2016-08-05
dc.contributor.author-college公共衛生學院zh_TW
dc.contributor.author-dept公共衛生碩士學位學程zh_TW
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