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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 藥學專業學院
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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/79083
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor王繼娟zh_TW
dc.contributor.advisorChi-Chuan Wangen
dc.contributor.author李幸蓉zh_TW
dc.contributor.authorHsing-Jung Lien
dc.date.accessioned2021-07-11T15:42:35Z-
dc.date.available2024-02-28-
dc.date.copyright2018-10-11-
dc.date.issued2018-
dc.date.submitted2002-01-01-
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20. Chiang CE, Wu TJ, Ueng KC, et al. 2016 Guidelines of the Taiwan Heart Rhythm Society and the Taiwan Society of Cardiology for the management of atrial fibrillation. J Formos Med Assoc. 2016;115(11):893-952.
21. Ganesan AN, Chew DP, Hartshorne T, et al. The impact of atrial fibrillation type on the risk of thromboembolism, mortality, and bleeding: a systematic review and meta-analysis. Eur Heart J. 2016;37(20):1591-1602.
22. Link MS, Giugliano RP, Ruff CT, et al. Stroke and Mortality Risk in Patients With Various Patterns of Atrial Fibrillation: Results From the ENGAGE AF-TIMI 48 Trial (Effective Anticoagulation With Factor Xa Next Generation in Atrial Fibrillation-Thrombolysis in Myocardial Infarction 48). Circulation Arrhythmia and electrophysiology. 2017;10(1).
23. Takabayashi K, Hamatani Y, Yamashita Y, et al. Incidence of Stroke or Systemic Embolism in Paroxysmal Versus Sustained Atrial Fibrillation: The Fushimi Atrial Fibrillation Registry. Stroke. 2015;46(12):3354-3361.
24. Violi F, Pastori D, Pignatelli P. Mechanisms And Management Of Thrombo-Embolism In Atrial Fibrillation. Journal of atrial fibrillation. 2014;7(3):1112.
25. Fuster V, Ryden LE, Cannom DS, et al. 2011 ACCF/AHA/HRS focused updates incorporated into the ACC/AHA/ESC 2006 guidelines for the management of patients with atrial fibrillation: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. Circulation. 2011;123(10):e269-367.
26. Lip GY, Nieuwlaat R, Pisters R, Lane DA, Crijns HJ. Refining clinical risk stratification for predicting stroke and thromboembolism in atrial fibrillation using a novel risk factor-based approach: the euro heart survey on atrial fibrillation. Chest. 2010;137(2):263-272.
27. Zeng YI, Sun R, Li X, Liu M, Chen S, Zhang P. Pathophysiology of valvular heart disease. Exp Ther Med. 2016;11(4):1184-1188.
28. Hollenberg SM. Valvular Heart Disease in Adults: Etiologies, Classification, and Diagnosis. FP essentials. 2017;457:11-16.
29. Kunchakarra S, Puthumana J, Maganti K. Valvular Heart Disease: Introduction, Clinical Pathogenesis, and Management. In: Jagadeesh G, Balakumar P, Maung-U K, eds. Pathophysiology and Pharmacotherapy of Cardiovascular Disease. Cham: Springer International Publishing; 2015:1151-1185.
30. Lip GYH, Collet JP, Caterina R, et al. Antithrombotic therapy in atrial fibrillation associated with valvular heart disease: a joint consensus document from the European Heart Rhythm Association (EHRA) and European Society of Cardiology Working Group on Thrombosis, endorsed by the ESC Working Group on Valvular Heart Disease, Cardiac Arrhythmia Society of Southern Africa (CASSA), Heart Rhythm Society (HRS), Asia Pacific Heart Rhythm Society (APHRS), South African Heart (SA Heart) Association and Sociedad Latinoamericana de Estimulacion Cardiaca y Electrofisiologia (SOLEACE). Europace. 2017;19(11):1757-1758.
31. Darby AE, Dimarco JP. Management of atrial fibrillation in patients with structural heart disease. Circulation. 2012;125(7):945-957.
32. Baumgartner H, Falk V, Bax JJ, et al. 2017 ESC/EACTS Guidelines for the management of valvular heart disease. Eur Heart J. 2017;38(36):2739-2791.
33. Di Biase L. Use of Direct Oral Anticoagulants in Patients With Atrial Fibrillation and Valvular Heart Lesions. J Am Heart Assoc. 2016;5(2).
34. Eikelboom JW, Connolly SJ, Brueckmann M, et al. Dabigatran versus warfarin in patients with mechanical heart valves. N Engl J Med. 2013;369(13):1206-1214.
35. Pan KL, Singer DE, Ovbiagele B, Wu YL, Ahmed MA, Lee M. Effects of Non-Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Atrial Fibrillation and Valvular Heart Disease: A Systematic Review and Meta-Analysis. J Am Heart Assoc. 2017;6(7).
36. Noseworthy PA, Yao X, Shah ND, Gersh BJ. Comparative effectiveness and safety of non-vitamin K antagonist oral anticoagulants versus warfarin in patients with atrial fibrillation and valvular heart disease. International journal of cardiology. 2016;209:181-183.
37. National Health Insurance Administration, Ministry of Health and Welfare, Taiwan, R.O.C. National Health Insurance Annual Report 2016-2017.
38. Quan H, Sundararajan V, Halfon P, et al. Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Medical care. 2005;43(11):1130-1139.
39. AbuDagga A, Stephenson JJ, Fu AC, Kwong WJ, Tan H, Weintraub WS. Characteristics affecting oral anticoagulant therapy choice among patients with non-valvular atrial fibrillation: a retrospective claims analysis. BMC health services research. 2014;14:310.
40. National Health Insurance Administration, Ministry of Health and Welfare
https://www.nhi.gov.tw/.
41. Suissa S, Moodie EE, Dell'Aniello S. Prevalent new-user cohort designs for comparative drug effect studies by time-conditional propensity scores. Pharmacoepidemiology and drug safety. 2017;26(4):459-468.
42. Liang K. ZS. Longitudinal Data Analysis Using Generalized Linear Models. Biometrika. 1986;73(1):13-22.
43. Timp JF, Braekkan SK, Versteeg HH, Cannegieter SC. Epidemiology of cancer-associated venous thrombosis. Blood. 2013;122(10):1712-1723.
44. Chan KE, Giugliano RP, Patel MR, et al. Nonvitamin K Anticoagulant Agents in Patients With Advanced Chronic Kidney Disease or on Dialysis With AF. J Am Coll Cardiol. 2016;67(24):2888-2899.
45. Di Minno A, Frigerio B, Spadarella G, et al. Old and new oral anticoagulants: Food, herbal medicines and drug interactions. Blood Rev. 2017;31(4):193-203.
46. Lauffenburger JC, Farley JF, Gehi AK, Rhoney DH, Brookhart MA, Fang G. Factors driving anticoagulant selection in patients with atrial fibrillation in the United States. Am J Cardiol. 2015;115(8):1095-1101.
47. Lane DA, Lip GY. Use of the CHA(2)DS(2)-VASc and HAS-BLED scores to aid decision making for thromboprophylaxis in nonvalvular atrial fibrillation. Circulation. 2012;126(7):860-865.
48. Pisters R, Lane DA, Nieuwlaat R, de Vos CB, Crijns HJ, Lip GY. A novel user-friendly score (HAS-BLED) to assess 1-year risk of major bleeding in patients with atrial fibrillation: the Euro Heart Survey. Chest. 2010;138(5):1093-1100.
49. Austin PC. Optimal caliper widths for propensity-score matching when estimating differences in means and differences in proportions in observational studies. Pharmaceutical statistics. 2011;10(2):150-161.
50. Austin PC. Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples. Statistics in medicine. 2009;28(25):3083-3107.
51. Austin PC. Using the Standardized Difference to Compare the Prevalence of a Binary Variable Between Two Groups in Observational Research. Communications in Statistics - Simulation and Computation. 2009;38(6):1228-1234.
52. Burn J, Dennis M, Bamford J, Sandercock P, Wade D, Warlow C. Long-term risk of recurrent stroke after a first-ever stroke. The Oxfordshire Community Stroke Project. Stroke. 1994;25(2):333-337.
53. Shen AY, Yao JF, Brar SS, Jorgensen MB, Chen W. Racial/ethnic differences in the risk of intracranial hemorrhage among patients with atrial fibrillation. J Am Coll Cardiol. 2007;50(4):309-315.
54. Renda G, Ricci F, Giugliano RP, De Caterina R. Non-Vitamin K Antagonist Oral Anticoagulants in Patients With Atrial Fibrillation and Valvular Heart Disease. J Am Coll Cardiol. 2017;69(11):1363-1371.
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/79083-
dc.description.abstract背景
瓣膜性心臟病的病人通常伴隨著心房顫動,但新型口服抗凝血劑用於此類病患之療效尚未明確,因此本研究的目標是探討同時患有瓣膜性心臟病及心房顫動的病人,使用新型抗凝血劑(Dabigatran, Rivaroxaban, Apixaban)與傳統口服抗凝血劑(Warfarin)的處方現況比較及成效分析。

方法
本研究為一回溯性研究,以「衛生福利部衛生福利資料科學中心」之全人口檔進行分析,首先篩選出同時有心房顫動及瓣膜性心臟病,且有任何一筆口服抗凝血劑處方的病人,以傾向分數配對法校正新型及傳統口服抗凝血劑的使用族群間差異,並利用Cox比例風險模式評估兩個族群發生事件的風險。

結果
本研究共納入21,280人。相較於warfarin,新型抗凝血劑有較低的靜脈栓塞(HR: 0.40, 95% CI: 0.23-0.69)、綜合出血(HR: 0.81, 95% CI: 0.74-0,89)及顱內出血(HR: 0.50, 95% CI: 0.40-0.62)風險。但是在嚴重瓣膜心臟病的病人,新型抗凝血劑有較高的栓塞風險(HR: 1.89, 95% CI: 1.18-3.01),尤其是經歷瓣膜手術的病人(HR: 2.96, 95% CI: 1.49-5.88)。而在不同的新型抗凝血劑之間,dabigatran及rivaroxaban有較低的顱內出血風險;在綜合出血的表現上,dabigatran更勝一籌(HR: 0.77, 95% CI: 0.68-0.87)。

結論
新型口服抗凝血劑相較於傳統口服抗凝血劑對同時患有心房顫動及瓣膜性心臟病的病人來說是個更安全的選擇。然而在不同的新型口服抗凝血劑之中,dabigatran及rivaroxaban相對於warfarin有較低的顱內出血風險。針對嚴重瓣膜性心臟病,尤其是做過瓣膜手術的病人則不建議使用新型抗凝血劑。
zh_TW
dc.description.abstractBackground
Although valvular heart disease (VHD) was often escorted by atrial fibrillation (AF), the outcome of non-vitamin K anticoagulants (NOAC) use in this population was unclear. The goal of our research was to investigate the effectiveness and safety of NOACs compared to warfarin in Asians with AF and VHD.

Methods
A retrospective cohort study using Health and Welfare Data in Taiwan was performed. Patients with AF and VHD, and prescribed with either NOACs (dabigatran, rivaroxaban, apixaban) or warfarin were included. Propensity score matching was used to balance baseline characteristics. Cox proportional hazards models were applied to evaluate the relationship between the medication and outcome of interests.

Results
There were 21,280 patients included in this study. Compared to warfarin, NOACs had a lower risk of venous thromboembolism (HR: 0.40, 95% CI: 0.23-0.69), composite bleeding (HR: 0.81, 95% CI: 0.74-0.89) and intracranial hemorrhage (HR: 0.50, 95% CI: 0.40-0.62). Severe VHD patients, however, possessed a higher stroke risk with NOAC use (HR: 1.89, 95% CI: 1.18-3.01). This phenomenon was even apparent among patients with previous valve surgery (HR: 2.96, 95% CI: 1.49-5.88). Among NOACs, dabigatran and rivaroxaban had a lower risk of intracranial hemorrhage. Significant decreased overall bleeding risk was also found in dabigatran (HR: 0.77, 95% CI: 0.68-0.87).

Conclusions
NOACs versus warfarin were safer choices for patients with comorbid AF and VHD. Among NOACs, dabigatran and rivaroxaban versus warfarin were associated with a lower risk of intracranial hemorrhage. However, among patients with severe VHD, especially those with previous valve surgery, NOACs were not recommended.
en
dc.description.provenanceMade available in DSpace on 2021-07-11T15:42:35Z (GMT). No. of bitstreams: 1
ntu-107-R04423038-1.pdf: 3138662 bytes, checksum: 1b5aa781c2afbed23c14980e3b2341a7 (MD5)
Previous issue date: 2018
en
dc.description.tableofcontents致謝 I
摘要 II
ABSTRACT III
TABLE OF CONTENTS IV
LIST OF FIGURES VII
LIST OF TABLES VIII

CHAPTER 1: INTRODUCTION 1
1.1 Atrial Fibrillation 2
1.1.1 Epidemiology 2
1.1.2 Pathophysiology 2
1.1.3 Risk factors 2
1.1.4 Clinical subtypes 3
1.1.5 Thromboembolic risk 3
1.2 Valvular Heart Disease 5
1.2.1 Epidemiology 5
1.2.2 Pathophysiology 5
1.2.3 Risk factors 5
1.2.4 Clinical subtypes 6
1.2.5 Thromboembolic risk 6
1.3 Oral Anticoagulants 7
1.3.1 Vitamin K antagonist 7
1.3.2 Non-Vitamin K antagonists 7
1.4 Findings from Previous Studies 9
1.4.1 Experimental studies (including meta-analysis) 9
1.4.2 Observational studies 11
1.5 Knowledge Gap and Study Objectives 12

CHAPTER 2: METHOD 13
2.1 Data Source 13
2.2 Study Design 14
2.2.1 Study population 15
2.2.2 Exposure assessment 18
2.2.3 Follow-up period 19
2.2.4 Outcome assessment 19
2.3 Covariates 21
2.4 Statistical Analysis 24
2.5 Sensitivity Analysis 25

CHAPTER 3: RESULTS 26
3.1 Study population 26
3.2 Prescription patterns (Aim 1) 27
3.2.1 Prescription level 27
3.2.2 Patient level 27
3.2.3 Dose at transition (warfarin-experienced NOAC group) 28
3.3 Main analysis (Aim 2) 29
3.3.1 Baseline characteristics 29
3.3.2 Outcome assessment 30
3.4 Subgroup analysis: classified by NOACs (Aim 3) 32
3.4.1 Baseline characteristics 32
3.4.2 Outcome assessment 32
3.5 Subgroup analysis: classified by VHD types (Aim 3) 34
3.5.1 Baseline characteristics 34
3.5.2 Outcome assessment 35
3.6 Sensitivity analysis 37

CHAPTER 4: DISCUSSION 39
4.1 Prescription patterns (Aim 1) 39
4.2 Main analysis (Aim 2) 41
4.2.1 Baseline characteristics 41
4.2.2 Outcome assessment 41
4.3 Subgroup analysis: by individual NOACs (Aim 3) 44
4.3.1 Baseline characteristics 44
4.3.2 Outcome assessment 44
4.4 Subgroup analysis: by VHD types (Aim 4) 46
4.4.1 Baseline characteristics 46
4.4.2 Outcome assessment 46
4.5 Strengths and Limitations 48
4.5.1 Strengths 48
4.5.2 Limitations 48

CHAPTER 5: CONCLUSION 49
FIGURES 51
TABLES 55
REFERENCES 139
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dc.language.isoen-
dc.title新型抗凝血劑用於同時患有心房顫動及瓣膜性心臟病病人的處方現況及成效分析zh_TW
dc.titlePatterns and Outcomes of Non-Vitamin K Anticoagulants Use among Patients with Atrial Fibrillation and Valvular Heart Disease in the Real-World Settingsen
dc.typeThesis-
dc.date.schoolyear106-2-
dc.description.degree碩士-
dc.contributor.oralexamcommittee林芳如;林欣儀;洪啟盛zh_TW
dc.contributor.oralexamcommitteeFang-Ju Lin;Shin-Yi Lin;Chi-Sheng Hungen
dc.subject.keyword瓣膜性心臟病,心房顫動,新型口服抗凝血劑,dabigatran,rivaroxaban,apixaban,warfarin,zh_TW
dc.subject.keywordnon-vitamin K anticoagulants,valvular heart disease,atrial fibrillation,dabigatran,rivaroxaban,apixaban,warfarin,en
dc.relation.page143-
dc.identifier.doi10.6342/NTU201802648-
dc.rights.note未授權-
dc.date.accepted2018-08-13-
dc.contributor.author-college醫學院-
dc.contributor.author-dept藥學研究所-
dc.date.embargo-lift2023-10-11-
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