2019
DOI: 10.1186/s41927-019-0097-0
|View full text |Cite
|
Sign up to set email alerts
|

Factors that influence rheumatologists’ anti-tumor necrosis factor alpha prescribing decisions: a qualitative study

Abstract: BackgroundTreatment decisions for any disease are usually informed by reference to published clinical guidelines or recommendations. These recommendations can be developed to improve the relative cost-effectiveness of health care and to reduce regional variation in clinical practice. Anti-tumor necrosis factor alpha (anti-TNF) treatments are prescribed for people with rheumatoid arthritis according to specific recommendations by the National Institute for Health and Care Excellence in England. Evidence of regi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
4
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
3
1

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(4 citation statements)
references
References 32 publications
(33 reference statements)
0
4
0
Order By: Relevance
“…As newer drugs, JAKi do not have the evidence-base that biologics do, particularly from clinician and patient perspectives [ 15 17 ]. Although there are recent studies comparing the real-world effectiveness of JAKi with biologics, through registry data analysis of patients with RA [ 18 , 19 ], there is currently a lack of published literature on what clinicians and IA patients think about the awareness, prescription and use of JAKi; how they compare with biologics; and, relevant to current times, how the COVID-19 pandemic has affected JAKi use and prescription.…”
Section: Introductionmentioning
confidence: 99%
“…As newer drugs, JAKi do not have the evidence-base that biologics do, particularly from clinician and patient perspectives [ 15 17 ]. Although there are recent studies comparing the real-world effectiveness of JAKi with biologics, through registry data analysis of patients with RA [ 18 , 19 ], there is currently a lack of published literature on what clinicians and IA patients think about the awareness, prescription and use of JAKi; how they compare with biologics; and, relevant to current times, how the COVID-19 pandemic has affected JAKi use and prescription.…”
Section: Introductionmentioning
confidence: 99%
“…As newer drugs, JAKi do not have the evidence-base that biologics do, particularly from clinician and patient perspectives [15][16][17]. Although there are recent studies comparing the real-world effectiveness of JAKi with biologics, through registry data analysis of patients with RA [18,19], there is currently a lack of published literature on what clinicians and IA patients think about the awareness, prescription and use of JAKi; how they compare with biologics; and, relevant to current times, how the COVID-19 pandemic has affected JAKi use and prescription.…”
Section: Introductionmentioning
confidence: 99%
“…This led to the UK Medical Health and Regulatory Authority (MHRA) issuing a warning to limit the use of tofacitinib and, with uncertainty as to whether this was a class effect, the US Food and Drug Administration putting black box warnings on all licensed JAKi used for the treatment of IA in the USA in late 2021 [12,13]. In early 2022, The European Medicines Agency (EMA) started a safety review on all JAKi used in IA [14].As newer drugs, JAKi don't have the evidence-base that biologics do, particularly from clinician and patient perspectives [15][16][17]. Although there are recent studies comparing the real-world effectiveness of JAKi with biologics, through registry data analysis of patients with RA [18,19], there is currently a lack of published literature on what clinicians and IA patients think about the awareness, prescription and use of JAKi; how they compare with biologics; and, relevant to current times, how the COVID-19 pandemic has affected JAKi use and prescription.…”
mentioning
confidence: 99%
“…Biologic (b-) and targeted synthetic (ts-) disease-modifying anti-rheumatic drugs (DMARDs) represent a major therapeutic advance in rheumatology. However, response rates to b/tsDMARDs are variable ( 1 ); the evidence-base for directing switching from one agent to another is limited with most switches being empirical ( 2 , 3 ); and, responses to b/tsDMARDs regardless of the mechanism of action are generally similar ( 4 ). Furthermore, the overall rates of sustained remission and improvement in function are relatively modest ( 5 ), owing to several potential factors including lack of established criteria to direct initial or subsequent choice of one b/tsDMARD over another with a different MoA, following failure or inadequate response.…”
Section: Introductionmentioning
confidence: 99%