Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5885
Title: The efficacy and safety of etanercept in patients with rheumatoid arthritis and spondyloarthropathy on hemodialysis
Authors: Senel, S.
Kisacik, B.
Ugan, Y.
Kasifoglu, T.
Tunc, E.
Çobankara, Veli
Keywords: Ankylosing spondylitis
Anti-TNF
Etanercept
Hemodialysis
Rheumatoid arthritis
Spondyloarthropathy
C reactive protein
corticosteroid
etanercept
hydroxychloroquine
methotrexate
nonsteroid antiinflammatory agent
salazosulfapyridine
tumor necrosis factor antibody
adult
aged
amyloidosis
analgesic nephropathy
article
bacterial arthritis
Bath Ankylosing Spondylitis Disease Activity
clinical article
Disease Activity Score 28
disease duration
drug efficacy
drug safety
drug tolerability
drug withdrawal
erythrocyte sedimentation rate
female
follow up
hemodialysis
hemodialysis patient
human
immune deficiency
infection risk
kidney failure
long term care
male
nephrolithiasis
priority journal
retrospective study
rheumatoid arthritis
scoring system
spondyloarthropathy
Adult
Aged
Antirheumatic Agents
Arthritis, Rheumatoid
Female
Humans
Immunoglobulin G
Kidney Failure, Chronic
Male
Middle Aged
Receptors, Tumor Necrosis Factor
Renal Dialysis
Retrospective Studies
Spondylarthropathies
Treatment Outcome
Young Adult
Abstract: We aimed to evaluate the efficacy and safety of long-term use of etanercept therapy in patients with spondyloarthropathy (SpA) and rheumatoid arthritis (RA) on hemodialysis (HD). Selected RA or SpA patients treated with etanercept under HD were retrospectively evaluated. Etanercept-related adverse events were closely recorded for all patients. At the follow-up, erythrocyte sedimentation rate and C-reactive protein levels were monitored. Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) for SpA patients and Disease Activity Score (DAS28) for RA patients were measured at every 3 or 6 months. In total five end-stage renal disease (ESRD) patients were enrolled to the study. The causes of ESRD in the study subjects were amyloidosis (n?=?2), analgesic nephropathy (n?=?2), and nephrolithiasis (n?=?1). Three were diagnosed as SpA and two were RA. All patients used etanercept. The median age was 39 years (range 22-72 years). The median disease duration was 12 years (range 2-20 years). The median follow-up after etanercept therapy was 18 months (range 5-33 months). DAS28 score decreased after the treatment and did not increase during follow-up in RA patients. BASDAI score decreased after the treatment during follow-up in three patients with SpA. At the follow-up, only one patient was diagnosed with septic arthritis. As a result of our study, etanercept treatment in RA and SpA patients on HD seems to be safe, well tolerated, and effective in most of the patients. Above all, due to impaired host defense in patients with ESRD, enhanced risk of infections should be kept in mind during follow-up period and larger trials are needed to prove the safety of etanercept in HD patients. © 2011 Clinical Rheumatology.
URI: https://hdl.handle.net/11499/5885
https://doi.org/10.1007/s10067-011-1782-6
ISSN: 0770-3198
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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