Chiun-Fang Chiou
Amgen
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Publication
Featured researches published by Chiun-Fang Chiou.
Journal of the American Geriatrics Society | 2009
Peggy M. Cawthon; Kathleen M. Fox; Shravanthi R. Gandra; Matthew J. Delmonico; Chiun-Fang Chiou; Mary S. Anthony; Ase Sewall; Bret H. Goodpaster; Suzanne Satterfield; Steven R. Cummings; Tamara B. Harris
OBJECTIVES: To examine the association between strength, function, lean mass, muscle density, and risk of hospitalization.
Value in Health | 2008
Joel M. Gelfand; Alexa B. Kimball; Eliot N. Mostow; Chiun-Fang Chiou; Vaishali Patel; H. Amy Xia; Bruce Freundlich; Seth R. Stevens
OBJECTIVE The 24-week Etanercept Assessment of Safety and Effectiveness (EASE) study evaluated the effectiveness and tolerability of continuous versus interrupted etanercept treatment in patients with moderate to severe plaque psoriasis. The objective of this analysis was to assess patient-reported outcomes (PROs) and health-care resource utilization (HRU) data from the EASE study. METHODS Patients received open-label etanercept 50 mg twice weekly for 12 weeks and then received either continued or interrupted (single round of discontinuation and re-treatment with etanercept) etanercept 50 mg once weekly for the second 12 weeks. PROs included the following: 1) the patient global assessments of psoriasis, joint pain, and itching scores; 2) the Dermatology Life Quality Index; 3) the Medical Outcomes Study Short Form 36 vitality domain; 4) the Beck Depression Inventory; 5) the European Quality-of-Life Group Feeling Thermometer; and 6) a patient satisfaction survey. HRU was evaluated using the Economic Implications of Psoriasis patient questionnaire. RESULTS Continuous treatment with etanercept 50 mg twice weekly for 12 weeks followed by 50 mg once weekly for 12 weeks produced sustained and clinically important improvements in PROs and reductions in HRU. Reductions in some outcome measures after treatment discontinuation at week 12 were observed in the interrupted group; however, most changes did not revert to baseline levels, consistent with some residual clinical effect, and re-treatment produced improvements similar to week 12 levels. CONCLUSIONS Continuous etanercept treatment provided greater sustained improvements in PROs than interrupted therapy; however, interrupting etanercept therapy, if needed, has predictable and manageable effects.
Arthritis & Rheumatism | 2009
Patricia P. Katz; Edward H. Yelin; Vaishali Patel; Xing-Yue Huang; Chiun-Fang Chiou
OBJECTIVE To examine self-reported symptoms and functioning in a community-based sample of persons with rheumatoid arthritis who did and did not initiate treatment with biologic agents. METHODS Data were from annual telephone interviews (1998-2003) with an observational cohort identified through community rheumatologists. Self-reported function and symptoms of subjects who initiated biologic therapy (etanercept or infliximab) and reported consistent use at 2 annual interviews (continuous use; n = 64) were compared at 1 year prior to initiation of therapy (baseline), and years 1 and 2 of therapy to those with no biologic therapy (n = 183) and those who initiated biologic therapy but discontinued use (n = 42). RESULTS At baseline, subjects taking biologic agents reported significantly worse function and symptoms on all measures except fatigue and pain severity. After 2 years, significant differences in the Health Assessment Questionnaire scores remained, but there were no other significant differences between the nonuser group and the continuous use group. The discontinued use group exhibited significantly greater pain severity and more painful joints than nonusers. Improvements in the number of painful (33.4% versus 16.2%; P = 0.004), and swollen (38.4% versus 18.7%; P = 0.003) joints, and morning stiffness (27.3% versus 10.4%; P = 0.001) were more frequent in the continuous use group than in the nonuser group. CONCLUSION Results suggest that biologic treatment was initiated based on severe disease. Over approximately 17 months of treatment, differences in some but not all symptoms between the continuous use group and the nonuser group narrowed to statistical nonsignificance.
Journal of The American Academy of Dermatology | 2007
Elizabeth J. Horn; Kathleen M. Fox; Vaishali Patel; Chiun-Fang Chiou; Frank Dann; Mark Lebwohl
Journal of The American Academy of Dermatology | 2007
Elizabeth J. Horn; Kathleen M. Fox; Vaishali Patel; Chiun-Fang Chiou; Frank Dann; Mark Lebwohl
Journal of Drugs in Dermatology | 2007
Alexa B. Kimball; Jackson Jm; Jeffrey M. Sobell; Boh Ee; Grekin S; Pharmd Eb; Woolley Jm; Xia Ha; Chiun-Fang Chiou; Stevens
Clinical Journal of The American Society of Nephrology | 2010
Stephen L. Seliger; Kathleen M. Fox; Shravanthi R. Gandra; Brian D. Bradbury; Van Doren Hsu; Loreen Walker; Chiun-Fang Chiou; Jeffrey C. Fink
Archive | 2010
Gregory A. Nichols; Shravanthi R. Gandra; Chiun-Fang Chiou; Mary S. Anthony; Maria Alexander-Bridges; Jonathan B. Brown
/data/revues/01909622/v57i6/S0190962207011711/ | 2011
Elizabeth J. Horn; Kathleen M. Fox; Vaishali Patel; Chiun-Fang Chiou; Frank Dann; Mark Lebwohl
/data/revues/01909622/v57i6/S0190962207011711/ | 2011
Elizabeth J. Horn; Kathleen M. Fox; Vaishali Patel; Chiun-Fang Chiou; Frank Dann; Mark Lebwohl