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  1. NTU Theses and Dissertations Repository
  2. 公共衛生學院
  3. 職業醫學與工業衛生研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/27528
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dc.contributor.advisor陳保中
dc.contributor.authorYu-Tse Tsanen
dc.contributor.author詹毓哲zh_TW
dc.date.accessioned2021-06-12T18:08:28Z-
dc.date.available2008-02-19
dc.date.copyright2008-02-19
dc.date.issued2007
dc.date.submitted2007-12-11
dc.identifier.citation1. Mellinger GD, Balter MB, Uhlenhuth EH. Insomnia and its treatment. Prevalence and correlates. Arch Gen Psychiatry 1985;42(3):225-32.
2. Terzano MG, Rossi M, Palomba V, Smerieri A, Parrino L. New drugs for insomnia: comparative tolerability of zopiclone, zolpidem and zaleplon. Drug Saf 2003;26(4):261-82.
3. Silber MH. Clinical practice. Chronic insomnia. N Engl J Med 2005;353(8):803-10.
4. Glass J, Lanctot KL, Herrmann N, Sproule BA, Busto UE. Sedative hypnotics in older people with insomnia: meta-analysis of risks and benefits. Bmj 2005;331(7526):1169.
5. Greenblatt DS, RI. Benzodiazepines N Engl J Med 1974;291:1011-1015.
6. Larrey D. Epidemiology and individual susceptibility to adverse drug reactions affecting the liver. Semin Liver Dis 2002;22(2):145-55.
7. Sgro C, Clinard F, Ouazir K, Chanay H, Allard C, Guilleminet C, et al. Incidence of drug-induced hepatic injuries: a French population-based study. Hepatology 2002;36(2):451-5.
8. Lee WM. Drug-induced hepatotoxicity. N Engl J Med 2003;349(5):474-85.
9. Larrey D. Drug-induced liver diseases. J Hepatol 2000;32(1 Suppl):77-88.
10. Garnier R, Guerault E, Muzard D, Azoyan P, Chaumet-Riffaud AE, Efthymiou ML. Acute zolpidem poisoning--analysis of 344 cases. J Toxicol Clin Toxicol 1994;32(4):391-404.
11. Karsenti D, Blanc P, Bacq Y, Metman EH. Hepatotoxicity associated with zolpidem treatment. Bmj 1999;318(7192):1179.
12. Brun JP. Zopiclone, a cyclopyrrolone hypnotic: review of properties. Pharmacol Biochem Behav 1988;29(4):831-2.
13. Maclure M. The case-crossover design: a method for studying transient effects on the risk of acute events. Am J Epidemiol 1991;133(2):144-53.
14. Navidi W. Bidirectional case-crossover designs for exposures with time trends. Biometrics 1998;54(2):596-605.
15. Donnan PT, Wang J. The case-crossover and case-time-control designs in pharmacoepidemiology. Pharmacoepidemiol Drug Saf 2001;10(3):259-62.
16. Benichou C. Criteria of drug-induced liver disorders. Report of an international consensus meeting. J Hepatol 1990;11(2):272-6.
17. Roy-Byrne P, Vittone BJ, Uhde TW. Alprazolam-related hepatotoxicity. Lancet 1983;2(8353):786-7.
18. Pickering D. Hepatic necrosis after chlordiazepoxide therapy. . N Engl J Med 1966;274:1449.
19. Hooshmand H. Intractable seizures. Treatment with a new benzodiazepine anticonvulsant. Arch Neurol 1972;27(3):205-8.
20. Tedesco FJ, Mills LR. Diazepam (Valium) hepatitis. Dig Dis Sci 1982;27(5):470-2.
21. Lawrence JM, Edwards JE, Briggs GS, Jones IH. A controlled clinical trial of a new antianxiety agent lorazepam (Ativan). Med J Aust 1974;2(18):660-1.
22. Kawar P, Briggs LP, Bahar M, McIlroy PD, Dundee JW, Merrett JD, et al. Liver enzyme studies with disoprofol (ICI 35,868) and midazolam. Anaesthesia 1982;37(3):305-8.
23. Parker JL. Potassium clorazepate (Tranxene)-induced jaundice. Postgrad Med J 1979;55(654):908-10.
24. Reynolds R, Lloyd DA, Slinger RP. Cholestatic jaundice induced by flurazepam hydrochloride. Can Med Assoc J 1981;124(7):893-4.
25. MICROMEDEX® Healthcare Series: Vol. 127 GV, Colorado (Edition expires [3/2006]).
26. Abboud G, Kaplowitz N. Drug-induced liver injury. Drug Saf 2007;30(4):277-94.
27. Kelly WN, Arellano FM, Barnes J, Bergman U, Edwards IR, Fernandez AM, et al. Guidelines for submitting adverse event reports for publication. Pharmacoepidemiol Drug Saf 2007;16(5):581-7.
28. Department of Health. Health and national health insurance annual statistics in Taiwan. Available at: http://www.doh.gov.tw/statistic/index.htm accessed 27 July 2007.
29. Larrey D, Pageaux GP. Genetic predisposition to drug-induced hepatotoxicity. J Hepatol 1997;26 Suppl 2:12-21.
30. Andrade RJ, Lucena MI, Aguilar J, Lazo MD, Camargo R, Moreno P, et al. Chronic liver injury related to use of bentazepam: an unusual instance of benzodiazepine hepatotoxicity. Dig Dis Sci 2000;45(7):1400-4.
31. Robin MA, Le Roy M, Descatoire V, Pessayre D. Plasma membrane cytochromes P450 as neoantigens and autoimmune targets in drug-induced hepatitis. J Hepatol 1997;26 Suppl 1:23-30.
32. Lin CY, Tsai MC, Huang CT, Hsu CW, Tseng SC, Tsai IF, et al. Liver injury is associated with enhanced regulatory T-cell activity in patients with chronic hepatitis B. J Viral Hepat 2007;14(7):503-11.
33. Della Bella S, Crosignani A, Riva A, Presicce P, Benetti A, Longhi R, et al. Decrease and dysfunction of dendritic cells correlate with impaired hepatitis C virus-specific CD4+ T-cell proliferation in patients with hepatitis C virus infection. Immunology 2007;121(2):283-92.
34. Belkaid Y, Rouse BT. Natural regulatory T cells in infectious disease. Nat Immunol 2005;6(4):353-60.
35. DeVane CL, Ware MR, Lydiard RB. Pharmacokinetics, pharmacodynamics, and treatment issues of benzodiazepines: alprazolam, adinazolam, and clonazepam. Psychopharmacol Bull 1991;27(4):463-73.
36. Greenblatt DJ, Harmatz JS, Shader RI. Clinical pharmacokinetics of anxiolytics and hypnotics in the elderly. Therapeutic considerations (Part II). Clin Pharmacokinet 1991;21(4):262-73.
37. Maddrey WC. Drug-induced hepatotoxicity: 2005. J Clin Gastroenterol 2005;39(4 Suppl 2):S83-9.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/27528-
dc.description.abstract簡介:隨著安眠藥於全世界廣泛使用,其安全性備受重視,除常見中樞神經副作用外,安眠藥引起的肝毒性亦不容忽視。大部分安眠藥需經過肝臟代謝,而安眠藥引起之肝毒性均為病例報告,沒有大型流行病學研究。因此,我們研究目的試圖驗證苯二酚和新一代安眠藥與急性肝炎住院間的關聯。
方法:從1997年至2004年的健保資料庫連結,依研究定義找出個案與前後各兩組對照組,然後去分析不同暴露時段,同時將個案分成乙型、丙型、酒精、非病毒非酒精性肝炎等組別,接著利用個案交叉研究方法算出因急性肝炎住院的勝算比。
結果:45,626個案因急性肝炎住院,連結門診檔分析後發現於急性肝炎住院前一週接受Zolpidem處方之勝算比為2.4 (95%信賴區間 1.9, 3.0)。而Zopiclone位第一週暴露時間,其勝算比為1.5 (95%信賴區間 1.0, 2.4)。對於傳統苯二酚,亦以住院前一週勝算比最明顯。此外,根據調整過之勝算比趨勢,另一高峰呈現於前三至六週。
討論:Zolpidem、zopiclone還有傳統苯二酚安眠藥處方時,會增加急性肝炎住院的風險應特別注意,且常見反應為非特異性與非線性劑量。臨床醫師使用這類潛在風險之安眠藥時,需定期監測肝功能。
zh_TW
dc.description.abstractIntroduction: With extensive use of hypnosedatives worldwide, in addition to the most commonly reported side effects of sedation, liver injury induced by benzodiazepines (BZDs) has been reported and should be monitored. BZDs, zolpidem and zopiclone all undergo hepatic metabolism. Hepatoxicity has been suspected so the aim of this study was to determine the association between the use of BZDs, zolpidem, zopiclone and the risk of hospitalization related to acute hepatitis.
Methods: The study cohort dataset was obtained from the National Health Insurance (NHI) research database in Taiwan from 1997-2004. We separated the groups of patients diagnosed before selected admission of outpatient visits or hospitalization as viral hepatitis B, C, non-viral, non-alcoholic hepatitis, alcoholic hepatitis. Since there were so many determinants, or potential confounders for acute hepatitis, we applied case-crossover design as a means of controlling factors within subjects.
Results: 45,626 cases of hospitalization relating to acute hepatitis were obtained. The odds ratio for the first week was the largest and most significant for these medicines. Conditional logistic regression analysis showed a significant adjusted odds ratio of 2.4 (95% confidence interval 1.9, 3.0) for zolpidem during the 7-day risk period. The adjusted odds ratio of zopiclone was 1.5 (95% confidence interval 1.0, 2.4) during the 7-day exposure period. In BZDs, the results were similar to the previous two drugs. In addition, based on the trend of the adjusted odds ratios, another peak was found during the 3 to 6-week period.
Discussion: There is an increased risk of hospitalization for acute hepatitis in patients treated with zolpidem, zopiclone and benzodiazepines, and most severe drug induced liver injuries can be idiosyncratic and dose-independent. Thus, physicians and clinical pharmacists should take such potential into consideration and monitor the liver function of patients taking hypnosedatives suspected to be hepatotoxic.
en
dc.description.provenanceMade available in DSpace on 2021-06-12T18:08:28Z (GMT). No. of bitstreams: 1
ntu-96-R93841001-1.pdf: 440322 bytes, checksum: ab6d437e0cc5e0030c982903f410104c (MD5)
Previous issue date: 2007
en
dc.description.tableofcontentsTable of Contents
摘要 5
Abstract 6
Introduction 8
Introduction of benzodiazepines, zolpidem and zopiclone 8
Liver injury induced by zolpidem, zopiclone and BZDs 8
With and without pre-existing liver diseases 9
Methods 11
Data Sources 11
Study Subjects 11
Case-crossover Design 13
Case and Control Exposure Windows and Washout Periods 14
Covariates for Adjustment 16
Statistical Analysis 16
Results 18
Demographic results 18
Increased risk of hospitalization for acute hepatitis in patients treated with zolpidem, zopiclone, BZDs 18
The risks of hospitalization for acute hepatitis in patients treated with zolpidem, zopiclone, BZDs between different hepatitis groups 19
The risks of hospitalization for acute hepatitis treated with zolpidem, zopiclone, BZDs by age, sex and dose 20
Discussion 21
Increased risk of hospitalization for acute hepatitis in patients treated with zolpidem, zopiclone, BZDs 21
The advantage of National Health Insurance in Taiwan 22
Increased risk of hospitalization for acute hepatitis in an individual hypnosedative 22
The risks of hospitalization for acute hepatitis in patients treated with zolpidem, zopiclone, BZDs between different hepatitis groups 23
The risks of hospitalization for acute hepatitis treated with zolpidem, zopiclone, BZDs by age, sex and dose 25
Potential limitations 26
Conclusion 28
Reference 29
Figure 1. Subjects selection process. 32
Figure 2. Timeline of the risk and four control periods 33
Table 1. Characteristics of study subjects with initial admission diagnosis of acute hepatitis, 1997-2004 34
Table 2. Odds ratios between hospitalizations and zolpidem, zopiclone, BZDs, by first week and 3 to 6-week risk periods in hepatitis groups 35
Table 3. Odds ratios between hospitalizations and zolpidem, zopiclone, BZDs, by risk period, age, sex and dose in hepatitis groups. 36
Appendix 1. Comparison the latency time and dosage between sedative hypnotics induced liver injury in Micromedex® and NHI databases 37
Appendix 2 Comparison between case reports of sedative hypnotics induced liver injury 39
Appendix 3. Hepatoxic Drugs (Generic Name) Identified in the Micromedex® Database 54
Appendix 4. The trend of adjusted odds ratio between hospitalizations and zolpidem, zopiclone, BZDs by the 1,2,3,4,5,6,7,8,9,10,11,12,13-weeks weekly exposure periods, and acute hepatitis groups. 56
Appendix 5. Categories of acute hepatitis according to the International Classification of Diseases, 9th Revision (ICD-9) code. 66
Appendix 6. Odds ratios of symmetrical bi-directional versus uni-directional cross-over design between hospitalizations and zolpidem, zopiclone, BZDs, by 3 to 6-week risk period in hepatitis groups 68
dc.language.isoen
dc.title新一代非苯二酚安眠藥造成急性肝炎住院之危險因子分析:以台灣健保資料庫連結研究zh_TW
dc.titleRisk of hospitalization for acute hepatitis in patients treated with non-benzodiazepine hypnosedatives: case-crossover study from the National Health Insurance in Taiwanen
dc.typeThesis
dc.date.schoolyear96-1
dc.description.degree碩士
dc.contributor.oralexamcommittee王榮德,陳健弘,洪東榮
dc.subject.keyword藥物流行病學,健保資料庫,苯二酚,安眠藥,zh_TW
dc.subject.keywordpharmacoepidemialogy, National Health Insurance File and NHI Major Disease File,benzodiazepine,zolpidem,zopiclone,hepatotoxicity,hypnosedative.,en
dc.relation.page68
dc.rights.note有償授權
dc.date.accepted2007-12-13
dc.contributor.author-college公共衛生學院zh_TW
dc.contributor.author-dept職業醫學與工業衛生研究所zh_TW
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