Michael Doherty

Prof. Michael Doherty

orcid

Research Focus & Metrics

Academic Career Length

47Years (1980-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2008 in Osteoarthritis and Cartilage
Verified
Journal Article
Closed access
WZW. Zhang
W. Zhang
RMR.W. Moskowitz
R.W. Moskowitz
GNG. Nuki
G. Nuki
SAS. Abramson
S. Abramson
RAR.D. Altman
R.D. Altman
PTPeter Tugwell
Peter Tugwell

1 January 2017 in Annals of the Rheumatic Diseases
Verified
Journal Article
Open access
PDF file
PRPascal Richette
Pascal Richette
MDMichael Doherty
Michael Doherty
EPE Pascual
E Pascual
VBV Barskova
V Barskova
Fabio BecceFabio Becce
Fabio Becce
TBThomas Bardin
Thomas Bardin
Background New drugs and new evidence concerning the use of established treatments have become available since the publication of the first European League Against Rheumatism (EULAR) recommendations for the management of gout, in 2006. This situation has prompted a systematic review and update of the 2006 recommendations. Methods The EULAR task force consisted of 15 rheumatologists, 1 radiologist, 2 general practitioners, 1 research fellow, 2 patients and 3 experts in epidemiology/methodology from 12 European countries. A systematic review of the literature concerning all aspects of gout treatments was performed. Subsequently, recommendations were formulated by use of a Delphi consensus approach. Results Three overarching principles and 11 key recommendations were generated. For the treatment of flare, colchicine, non-steroidal anti-inflammatory drugs (NSAIDs), oral or intra-articular steroids or a combination are recommended. In patients with frequent flare and contraindications to colchicine, NSAIDs and corticosteroids, an interleukin-1 blocker should be considered. In addition to education and a non-pharmacological management approach, urate-lowering therapy (ULT) should be considered from the first presentation of the disease, and serum uric acid (SUA) levels should be maintained at<6 mg/dL (360 µmol/L) and <5 mg/dL (300 µmol/L) in those with severe gout. Allopurinol is recommended as first-line ULT and its dosage should be adjusted according to renal function. If the SUA target cannot be achieved with allopurinol, then febuxostat, a uricosuric or combining a xanthine oxidase inhibitor with a uricosuric should be considered. For patients with refractory gout, pegloticase is recommended. Conclusions These recommendations aim to inform physicians and patients about the non-pharmacological and pharmacological treatments for gout and to provide the best strategies to achieve the predefined urate target to cure the disease.

1 April 2010 in Osteoarthritis and Cartilage
Verified
Journal Article
Closed access
WZW. Zhang
W. Zhang
GNG. Nuki
G. Nuki
RMR.W. Moskowitz
R.W. Moskowitz
SAS. Abramson
S. Abramson
RAR.D. Altman
R.D. Altman
PTPeter Tugwell
Peter Tugwell

1 July 2013 in Annals of the Rheumatic Diseases
Verified
Journal Article
Closed access
LFLinda Fernandes
Linda Fernandes
KHKåre B Hagen
Kåre B Hagen
JBJohannes W J Bijlsma
Johannes W J Bijlsma
OAOyvor Andreassen
Oyvor Andreassen
PCPia Christensen
Pia Christensen
TVThea Vlieland
Thea Vlieland

7 July 2015 in Nature Reviews Rheumatology
Verified
Journal Article
Closed access
CKChang-Fu Kuo
Chang-Fu Kuo
MGMatthew J. Grainge
Matthew J. Grainge
WZWeiya Zhang
Weiya Zhang
MDMichael Doherty
Michael Doherty

1 October 2006 in Annals of the Rheumatic Diseases
Verified
Journal Article
Open access
PDF file
WZW Zhang
W Zhang
MDMichael Doherty
Michael Doherty
TBT Bardin
T Bardin
EPE Pascual
E Pascual
VBV Barskova
V Barskova
IZI Zimmermann-Gòrska
I Zimmermann-Gòrska
Objective: To develop evidence based recommendations for the management of gout. Methods: The multidisciplinary guideline development group comprised 19 rheumatologists and one evidence based medicine expert representing 13 European countries. Key propositions on management were generated using a Delphi consensus approach. Research evidence was searched systematically for each proposition. Where possible, effect size (ES), number needed to treat, relative risk, odds ratio, and incremental cost-effectiveness ratio were calculated. The quality of evidence was categorised according to the level of evidence. The strength of recommendation (SOR) was assessed using the EULAR visual analogue and ordinal scales. Results: 12 key propositions were generated after three Delphi rounds. Propositions included both non-pharmacological and pharmacological treatments and addressed symptomatic control of acute gout, urate lowering therapy (ULT), and prophylaxis of acute attacks. The importance of patient education, modification of adverse lifestyle (weight loss if obese; reduced alcohol consumption; low animal purine diet) and treatment of associated comorbidity and risk factors were emphasised. Recommended drugs for acute attacks were oral non-steroidal anti-inflammatory drugs (NSAIDs), oral colchicine (ES = 0.87 (95% confidence interval, 0.25 to 1.50)), or joint aspiration and injection of corticosteroid. ULT is indicated in patients with recurrent acute attacks, arthropathy, tophi, or radiographic changes of gout. Allopurinol was confirmed as effective long term ULT (ES = 1.39 (0.78 to 2.01)). If allopurinol toxicity occurs, options include other xanthine oxidase inhibitors, allopurinol desensitisation, or a uricosuric. The uricosuric benzbromarone is more effective than allopurinol (ES = 1.50 (0.76 to 2.24)) and can be used in patients with mild to moderate renal insufficiency but may be hepatotoxic. When gout is associated with the use of diuretics, the diuretic should be stopped if possible. For prophylaxis against acute attacks, either colchicine 0.5–1 mg daily or an NSAID (with gastroprotection if indicated) are recommended. Conclusions: 12 key recommendations for management of gout were developed, using a combination of research based evidence and expert consensus. The evidence was evaluated and the SOR provided for each proposition.