Please use this identifier to cite or link to this item: http://dulieuso.hmu.edu.vn/handle/hmu/2936
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dc.contributor.advisorNguyễn Thị Phương, Thủy-
dc.contributor.authorLưu Cảnh, Linh-
dc.date.accessioned2021-12-09T03:57:28Z-
dc.date.available2021-12-09T03:57:28Z-
dc.date.issued2021-12-07-
dc.identifier.urihttp://dulieuso.hmu.edu.vn/handle/hmu/2936-
dc.description.abstractABSTRACT Objectives: To describe clinical indications, treatment outcomes of down-titration and withdrawal the biologic agents in rheumatoid arthritis. Subjects and methods: An electronic search of PubMed and Cochrane Database of Systematic Review was last executed on 10th August 2021 and the results were limited to references published from January 2016 to December 2020 in the English language. The electronic search combined the term “rheumatoid arthritis” and a term for down-titration, i.e., rheumatoid arthritis and dose decreasing or dosage decreasing. Results: We included 27 studies in our scoping review. Most of studies used the DAS28-CRP or DAS28-ESR score to identify low disease activity (<3.2) or clinical remission (<2.6) or deep remission (<2.0) required for tapering and these studies design included patients who achieved low disease activity or clinical remission for at least 6 months. Dose-tapering is always associated with the risk of flare after a period of time, but most of relapsing patients regained sustainability of low disease activity or clinical remission after reinstating biologics with standard dose. Disease-activity-guided dose optimization results in large cost savings per patient per year and no or a small loss in QALYs. DAS28-CRP (ESR) cut-off at baseline, presence of RF or anti- CCP antibody, dosage of methotrexate… was used to predict success or failure of tapering. Keywords: Rheumatoid arthritis, dose-tapering, biologics, remission.vi_VN
dc.description.tableofcontentsTABLE OF CONTENTS LIST OF ABBREVIATION LIST OF TABLES AND FIGURES INTRODUCTION 1 CHAPTER 1: LITERATURE REVIEW 3 1. 1. Rheumatoid Arthiritis: Overview 3 1.1.1: Definition 3 1.1.2: Epidemiology 3 1.1.3: Clinical manifestations 4 1.1.4: Laboratory findings 7 1.1.5: Diagnosis 8 1.1.6: Treatment of RA 12 1.2: Remission in treatment 13 1.3: Biologic drugs in rheumatoid arthritis 14 1.4: Efficacy of biologics in RA 15 1.5: Reasons for discontinuing the biologics treatment 17 1.6. Scoping review: an overview 19 1.6.1. Purpose of a scoping review 19 1.6.2. Methodological framework of scoping reviews 20 CHAPTER 2: MATERIALS AND METHODS 22 2.1: Protocol 22 2.2. Searching strategy 23 2.3. Eligibility criteria 25 2.4. Assessment tools of the quality in included studies 25 2.5. Study extraction 25 CHAPTER 3: RESULTS 27 3.1. Included studies 27 3.2. Tapering strategy 40 3.2.1. Tapering eligibility criteria 40 3.2.2: Tapering regimens 41 3.3. Success of biologics tapering 45 3.3.1. Outcomes of adalimumab tapering 45 3.3.2. Outcomes of infliximab tapering 47 3.3.3. Outcomes of tocilizumab tapering 48 3.3.4. Outcomes of etanercept tapering 49 3.3.5. Studies reporting tapering outcomes for various biologics combined 50 3.4. Retreatment after relapse 53 3.5. Safety 56 3.6. Predictors for successful tapering in rheumatoid arthritis 56 CHAPTER 4: DISCUSSION 58 4.1. Evidence synthesis 58 4.1.1. Indications for tapering or stopping biologics 58 4.1.2. Tapering strategies 61 4.1.3. Success and flare in tapering strategies 64 4.1.4. Treatment after relapse 66 4.1.5. Adverse events and radiographic progression 67 4.1.6: Predictors for success or relapse 68 4.1.7: Effectiveness on costs 73 4.2. Weakness of this scoping review 75 4.3. Research gaps and future research 75 CONCLUSION AND RECOMMENDATION 77 REFERENCES APPENDIX  vi_VN
dc.language.isoenvi_VN
dc.subjectrheumatoid arthritisvi_VN
dc.subjectbiologic agentsvi_VN
dc.subjectremissionvi_VN
dc.subjectwithdrawalvi_VN
dc.subjectdown-titrationvi_VN
dc.subjectlow disease activityvi_VN
dc.titleDown-titration and withdrawal of the biologic agents in rheumatoid arthritis: a review of literaturevi_VN
dc.typeThesisvi_VN
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