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| ???org.dspace.app.webui.jsptag.ItemTag.dcfield??? | Value | Language |
|---|---|---|
| dc.contributor.advisor | 賴美淑(Mei-Shu Lai) | |
| dc.contributor.author | Yen-Chieh Lee | en |
| dc.contributor.author | 李彥潔 | zh_TW |
| dc.date.accessioned | 2021-06-08T04:22:02Z | - |
| dc.date.copyright | 2010-09-09 | |
| dc.date.issued | 2010 | |
| dc.date.submitted | 2010-07-07 | |
| dc.identifier.citation | 1.Longstreth GF. Epidemiology of hospitalization for acute upper gastrointestinal hemorrhage: a population-based study. Am J Gastroenterol. Feb 1995;90(2):206-210.
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Risk of serious upper gastrointestinal events with concurrent use of NSAIDs and SSRIs: a case-control study in the general population. Eur J Clin Pharmacol. Apr 2007;63(4):403-408. 12.Opatrny L, Delaney JA, Suissa S. Gastro-intestinal haemorrhage risks of selective serotonin receptor antagonist therapy: a new look. Br J Clin Pharmacol. Jul 2008;66(1):76-81. 13.Lewis JD, Strom BL, Localio AR, et al. Moderate and high affinity serotonin reuptake inhibitors increase the risk of upper gastrointestinal toxicity. Pharmacoepidemiol Drug Saf. Apr 2008;17(4):328-335. 14.Vidal X, Ibanez L, Vendrell L, Conforti A, Laporte JR. Risk of upper gastrointestinal bleeding and the degree of serotonin reuptake inhibition by antidepressants: a case-control study. Drug Saf. 2008;31(2):159-168. 15.de Abajo FJ, Garcia-Rodriguez LA. Risk of upper gastrointestinal tract bleeding associated with selective serotonin reuptake inhibitors and venlafaxine therapy: interaction with nonsteroidal anti-inflammatory drugs and effect of acid-suppressing agents. Arch Gen Psychiatry. Jul 2008;65(7):795-803. 16.Targownik LE, Bolton JM, Metge CJ, Leung S, Sareen J. Selective serotonin reuptake inhibitors are associated with a modest increase in the risk of upper gastrointestinal bleeding. Am J Gastroenterol. Jun 2009;104(6):1475-1482. 17.Dall M, Schaffalitzky de Muckadell OB, Lassen AT, Hansen JM, Hallas J. An association between selective serotonin reuptake inhibitor use and serious upper gastrointestinal bleeding. Clin Gastroenterol Hepatol. Dec 2009;7(12):1314-1321. 18.http://www.whocc.no/atc_ddd_index/. 19.Tatsumi M, Groshan K, Blakely RD, Richelson E. Pharmacological profile of antidepressants and related compounds at human monoamine transporters. Eur J Pharmacol. Dec 11 1997;340(2-3):249-258. 20.Caplan L, Pittman CB, Zeringue AL, et al. An observational study of musculoskeletal pain among patients receiving bisphosphonate therapy. Mayo Clin Proc. Apr 2010;85(4):341-348. 21.Bharmal MF, Weiner M, Sands LP, Xu H, Craig BA, Thomas J, 3rd. Impact of patient selection criteria on prevalence estimates and prevalence of diagnosed dementia in a Medicaid population. Alzheimer Dis Assoc Disord. Apr-Jun 2007;21(2):92-100. 22.Garvey Wilson AL, Messer SC, Hoge CW. U.S. military mental health care utilization and attrition prior to the wars in Iraq and Afghanistan. Soc Psychiatry Psychiatr Epidemiol. Jun 2009;44(6):473-481. 23.Hoge CW, Lesikar SE, Guevara R, et al. Mental disorders among U.S. military personnel in the 1990s: association with high levels of health care utilization and early military attrition. Am J Psychiatry. Sep 2002;159(9):1576-1583. 24.Sturmer T, Joshi M, Glynn RJ, Avorn J, Rothman KJ, Schneeweiss S. A review of the application of propensity score methods yielded increasing use, advantages in specific settings, but not substantially different estimates compared with conventional multivariable methods. J Clin Epidemiol. May 2006;59(5):437-447. 25.Parsons LS. Reducing Bias in a Propensity Score-Matched Pair Sample Using Greedy Matching Techniques Ovation Research Group, Seattle,WA;2001. 26.Moore M, Yuen HM, Dunn N, Mullee MA, Maskell J, Kendrick T. Explaining the rise in antidepressant prescribing: a descriptive study using the general practice research database. BMJ. 2009;339:b3999. 27.Olfson M, Marcus SC. National patterns in antidepressant medication treatment. Arch Gen Psychiatry. Aug 2009;66(8):848-856. 28.de Abajo FJ, Montero D, Rodriguez LA, Madurga M. Antidepressants and risk of upper gastrointestinal bleeding. Basic Clin Pharmacol Toxicol. Mar 2006;98(3):304-310. 29.Dalton SO, Sorensen HT, Johansen C. SSRIs and upper gastrointestinal bleeding: what is known and how should it influence prescribing? CNS Drugs. 2006;20(2):143-151. 30.Wagner B, Schneider B, Blochl-Daum B, et al. Effect of ritanserin, a 5-hydroxytryptamine2-receptor antagonist, on platelet function and thrombin generation at the site of plug formation in vivo. Clin Pharmacol Ther. Oct 1990;48(4):419-423. 31.Baumann P. Care of depression in the elderly: comparative pharmacokinetics of SSRIs. Int Clin Psychopharmacol. Sep 1998;13 Suppl 5:S35-43. 32.Dome P, Lazary J, Kalapos MP, Rihmer Z. Smoking, nicotine and neuropsychiatric disorders. Neurosci Biobehav Rev. Mar 2010;34(3):295-342. 33.Lynskey MT. The comorbidity of alcohol dependence and affective disorders: treatment implications. Drug Alcohol Depend. Nov 1 1998;52(3):201-209. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/22603 | - |
| dc.description.abstract | 過去許多觀察性研究發現,選擇性血清素回收抑制劑 (selective serotonin reuptake inhibitors, SSRI)的使用,會增加上消化道出血住院之風險,其研究多侷限於西方國家,對於相關藥物(如非類固醇類抗發炎藥物NSAID/Coxib:選擇性或非選擇性,胃酸抑制劑PPI/H2RA)之交互作用亦未有一致定論。
本研究利用全民健保資料庫執行一回朔性世代研究,研究族群為2005-2006年同時合併精神科共病之抗憂鬱劑新使用者,依抗憂鬱劑之使用分類為三組:高、中、及低親和性抗憂鬱劑使用者,以使用低血清素親和性抗憂鬱劑之病患做為基準,分別於高和中血清素親和性抗憂鬱組別中配對propensity score相近者,成功於兩組中找到配對者即與其配對者一起納入配對後世代做結果分析;族群觀察始於藥物使用日,若發生上消化道出血住院,停藥,換別組藥物或研究結束日(2006-12-31)則觀察終止。 配對後世代各組各包含65133名抗憂鬱劑之新使用者,研究期間共有526例上消化道出血病例,分別占三組比例為0.34%、0.24%及0.23%,使用高及中親和性血清素抗憂鬱劑,對照於低血清素親和性使用者分別造成1.32(1.07-1.63) 及 1.13(0.90-1.41)之相對風險,且隨著血清素親和性的增加,隨著趨勢性上升(p=0.0081),於敏感度分析(sensitivity analysis)中亦有相似結論,在次族群分析中,發現老年人及有上消化道出血病史之病患對高血清素親和性之抗憂鬱劑有較高之易感性,在藥物交互作用方面,則未見NSAID/Coxib或H2RA/PPI有風險調控之效果。 隨著對血清素親和性的增加,抗憂鬱劑之使用亦趨勢性增加上消化道出血之風險,臨床上開立處方應考量相關危險因子做個別評估,在本篇研究中未能發現胃酸抑制劑有風險調控之效益。 | zh_TW |
| dc.description.abstract | Background
Previous studies have shown that use of selective serotonin reuptake inhibitions(SRIs) was associated with increased risk for upper gastrointestinal bleeding (UGIB). Our study aims to examine the association of UGIB with use of antidepressants with different serotonin affinity in psychiatric patients Material and Method We conducted a retrospective cohort study using the Taiwan National Health Insurance claims database. We identified 304,789 adults who initiated antidepressants during 2005-2006 and had a diagnosis of psychiatric diseases. Antidepressants were classified into 3 groups according to affinity to serotonin transporters (High, Intermediate and Low affinity_SRIs, HA_SRIs, IA_SRIs, LA_SRIs). Patients in LA_SRIs groups were matched in 1:1 fashion respectively to those in HA_SRIs and IA_SRIs groups with similar propensity score based on patients’ demographic, co-morbidities and medical utilization characteristics. Those successfully matched in 3 groups were followed from date of antidepressants initiation to first hospitalization for UGIB, drug discontinuation, shift of antidepressants from one group to another, or study end. We estimated crude and adjusted hazard ratios with a Cox proportional hazards model. Result In the propensity score matched cohort, 526 patients had experienced their first episode of hospitalization for UGIB, which accounts for 0.34, 0.24 and 0.23% in HA_SRIs, IA_SRIs and LA_SRIs group respectively. Use of HA_SRIs and IA_SRIs was associated with a HR of 1.32(1.07-1.63) and 1.13(0.90-1.41) for UGIB. Elderly and those with a history of upper GI bleeding were more susceptible. No effect modification was noticed with NSAID and acid suppressing agents Conclusion Use of high affinity serotonin reuptake inhibitors ,as compared with antidepressants with low serotonin transporter affinity, was associated with increased risk for admission for UGIB in psychiatric patients. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-08T04:22:02Z (GMT). No. of bitstreams: 1 ntu-99-R96846006-1.pdf: 603099 bytes, checksum: e0fdf60b03a2599a73a28bb1bcb5db3d (MD5) Previous issue date: 2010 | en |
| dc.description.tableofcontents | 第一章 前言 1
第一節 研究背景 1 第二節 研究目的 2 第二章 文獻探討 3 第一節 SSRI類抗憂鬱劑使用與上消化道出血之相關性 3 第二節 SSRI 與主要併用藥品與上消化道出血之研究 7 1. 非類固醇抗發炎藥物 (NSAID/Coxib): 7 2. 胃酸抑制劑 (H2RA/PPI): 8 第三章 研究材料與方法 19 第一節 研究設計與資料來源 19 第二節 研究假說 19 第三節 研究架構與主要變項 19 第四節 相關變項定義 22 第五節 分析步驟 25 第六節 統計方法 28 第四章 研究結果 29 第一節 研究族群之建立 29 第二節 暴露模式(exposure model, propensity score model)之分析結果 32 第三節 血清素親和性抗憂鬱藥物造成上消化道出血危險比值之分析結果 39 第四節 敏感度分析(sensitivity analysis) 40 第五節 Secondary analysis 40 第六節 與上消化道出血相關藥品併用之相關分析 44 第五章 討論 46 參考文獻 | |
| dc.language.iso | zh-TW | |
| dc.subject | 世代研究 | zh_TW |
| dc.subject | 血清素 | zh_TW |
| dc.subject | 上消化道出血 | zh_TW |
| dc.subject | 抗憂鬱劑 | zh_TW |
| dc.subject | serotonin | en |
| dc.subject | cohort study | en |
| dc.subject | upper gastrointestinal bleeding | en |
| dc.subject | selective serotonin reuptake inhibitors | en |
| dc.subject | antidepressants | en |
| dc.title | 不同血清素親和性抗憂鬱劑與上消化道出血之相關性研究 | zh_TW |
| dc.title | Variability of serotonin reuptake inhibition of antidepressants and the risk of upper gastrointestinal bleeding : retrospective cohort study | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 98-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 林敏雄,劉仁沛,張家勳(Chia-Hsuin Chang),邵文逸(Wen-Yi Shau) | |
| dc.subject.keyword | 抗憂鬱劑,上消化道出血,世代研究,血清素, | zh_TW |
| dc.subject.keyword | antidepressants,selective serotonin reuptake inhibitors,upper gastrointestinal bleeding,cohort study,serotonin, | en |
| dc.relation.page | 53 | |
| dc.rights.note | 未授權 | |
| dc.date.accepted | 2010-07-07 | |
| dc.contributor.author-college | 公共衛生學院 | zh_TW |
| dc.contributor.author-dept | 預防醫學研究所 | zh_TW |
| Appears in Collections: | 流行病學與預防醫學研究所 | |
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