Regional and temporal variation in the treatment of rheumatoid arthritis across the UK: a descriptive register-based cohort study.
Regional and temporal variation in the treatment of rheumatoid arthritis across the UK: a descriptive register-based cohort study.
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DOI:
10.1136/bmjopen-2012-001603
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发表时间:
2012
期刊:
影响因子:
2.9
通讯作者:
Arden NK
中科院分区:
文献类型:
--
作者:
Edwards CJ;Campbell J;van Staa T;Arden NK
To describe current disease-modifying antirheumatic drugs (DMARDs) prescription in rheumatoid arthritis (RA) with reference to best practice and to identify temporal and regional trends in the UK. Descriptive, register-based cohort study. Permanently registered patients aged ≥18 years with a recorded diagnosis of RA between 1 January 1995 and 31 March 2010 and matched controls. Participants with RA were identified through screening of all patients in the General Practice Research Database (GPRD) with a clinical or referral record for RA and at least 1 day of follow-up. 639 general practices in the UK supplying data to the GPRD. Medication prescribing between 3 and 12 months of RA diagnosis by region and time period (1995–1999, 2000–2005 and 2006–April 2010). Of the 35 911 patients in the full RA cohort, 15 259 patients (42%) had incident RA. Analysis of prescribing in incident RA patients demonstrated that between 1995 (baseline) and 2010 there was a substantial increase in DMARD, and specifically methotrexate, prescribing across all regions with a less marked increase in combination DMARD prescribing. Taking 12-month prescribing as a snapshot: DMARD prescribing was 19–49% at baseline increasing to 45–74% by 2006–April 2010; methotrexate prescribing was 4–16% at baseline increasing to 32–60%; combination DMARD prescribing was 0–8% at baseline increasing to 3–17%. However, there was marked regional variation in the proportion of RA patients receiving DMARD regardless of time period. There has been a substantial increase in prescribing of DMARDs for RA since 1995; however, regional variation persists across the UK with relative undertreatment, according to established best practice. Improved implementation of evidence-based best clinical practice to facilitate removal of treatment variation is warranted. This may occur as a result of the implementation of published national guidance.
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影响因子:
5.5
作者:
Edwards, CJ;Arden, NK;Cooper, C
通讯作者:
Cooper, C
影响因子:
27.4
作者:
Smolen JS;Landewé R;Breedveld FC;Dougados M;Emery P;Gaujoux-Viala C;Gorter S;Knevel R;Nam J;Schoels M;Aletaha D;Buch M;Gossec L;Huizinga T;Bijlsma JW;Burmester G;Combe B;Cutolo M;Gabay C;Gomez-Reino J;Kouloumas M;Kvien TK;Martin-Mola E;McInnes I;Pavelka K;van Riel P;Scholte M;Scott DL;Sokka T;Valesini G;van Vollenhoven R;Winthrop KL;Wong J;Zink A;van der Heijde D
通讯作者:
van der Heijde D
DOI:
10.1093/pubmed/21.3.299
发表时间:
1999-09-01
期刊:
JOURNAL OF PUBLIC HEALTH MEDICINE
影响因子:
--
作者:
Lawrenson, R;Williams, T;Farmer, R
通讯作者:
Farmer, R
影响因子:
--
作者:
Graudal, Niels;Jurgens, Gesche
通讯作者:
Jurgens, Gesche
影响因子:
3.4
作者:
Ovayolu, Nimet;Ovayolu, Ozlem;Karadag, Guelendam
通讯作者:
Karadag, Guelendam