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Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis
in
Arteritis
/ Clinical trials
/ Drug therapy
/ Inflammation
/ Leflunomide
/ Meta-analysis
/ Monoclonal antibodies
/ Placebos
/ Positron emission tomography
/ Prednisolone
/ Rheumatology
/ Systematic review
/ Takayasu's disease
/ Tumor necrosis factor
/ Tumors
/ Vein & artery diseases
2021
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Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis
by
in
Arteritis
/ Clinical trials
/ Drug therapy
/ Inflammation
/ Leflunomide
/ Meta-analysis
/ Monoclonal antibodies
/ Placebos
/ Positron emission tomography
/ Prednisolone
/ Rheumatology
/ Systematic review
/ Takayasu's disease
/ Tumor necrosis factor
/ Tumors
/ Vein & artery diseases
2021
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis
in
Arteritis
/ Clinical trials
/ Drug therapy
/ Inflammation
/ Leflunomide
/ Meta-analysis
/ Monoclonal antibodies
/ Placebos
/ Positron emission tomography
/ Prednisolone
/ Rheumatology
/ Systematic review
/ Takayasu's disease
/ Tumor necrosis factor
/ Tumors
/ Vein & artery diseases
2021
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Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis
Journal Article
Disease-modifying anti-rheumatic drugs for the management of Takayasu arteritis—a systematic review and meta-analysis
2021
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Overview
The pharmacotherapy of Takayasu arteritis (TAK) with disease-modifying anti-rheumatic drugs (DMARDs) is an evolving area. A systematic review of Scopus, Web of Science, Pubmed Central, clinical trial databases and recent international rheumatology conferences for interventional and observational studies reporting the effectiveness of DMARDs in TAK identified four randomized controlled trials (RCTs, with another longer-term follow-up of one RCT) and 63 observational studies. The identified trials had some concern or high risk of bias. Most observational studies were downgraded on the Newcastle-Ottawa scale due to lack of appropriate comparator groups. Studies used heterogenous outcomes of clinical responses, angiographic stabilization, normalization of inflammatory markers, reduction in vascular uptake on positron emission tomography, reduction in prednisolone doses and relapses. Tocilizumab showed benefit in a RCT compared to placebo in a secondary per-protocol analysis but not the primary intention-to-treat analysis. Abatacept failed to demonstrate benefit compared to placebo for preventing relapses in another RCT. Pooled data from uncontrolled observational studies demonstrated beneficial clinical responses and angiographic stabilization in nearly 80% patients treated with tumour necrosis factor alpha inhibitors, tocilizumab or leflunomide. Certainty of evidence for outcomes from RCTs ranged from moderate to very low and was low to very low for all observational studies. There is a paucity of high-quality evidence to guide the pharmacotherapy of TAK. Future observational studies should attempt to include appropriate comparator arms. Multicentric, adequately powered RCTs assessing both clinical and angiographic responses are necessary in TAK.
Publisher
Springer Nature B.V
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