Australian recommendations on perioperative use of disease‐modifying anti‐rheumatic drugs in people with inflammatory arthritis undergoing elective surgery

Author:

Buchbinder Rachelle1ORCID,Glennon Vanessa1,Johnston Renea V.1,Brennan Sue E.1,Fong Chris2,Edward May Suzie3,O'Neill Sean4,Smitham Peter5,Trevena Lyndal6,Whittaker Glen7,Wluka Anita1,Whittle Samuel L.18

Affiliation:

1. School of Public Health and Preventive Medicine Monash University Victoria Melbourne Australia

2. Eastern Clinical Research Unit Eastern Health Box Hill Hospital and Monash University Victoria Melbourne Australia

3. Consumer Representative, Giving Voice Western Australia Perth Australia

4. Sydney Musculoskeletal Health Flagship University of Sydney Northern Clinical School and Royal North Shore Hospital New South Wales Sydney Australia

5. Orthopaedic & Trauma Department, Royal Adelaide Hospital & Discipline of Orthopaedics University of Adelaide South Australia Adelaide Australia

6. Faculty of Medicine and Health University of Sydney New South Wales Sydney Australia

7. Discipline of Podiatry, School of Allied Health, Human Services and Sport La Trobe University Victoria Melbourne Australia

8. Rheumatology Unit Queen Elizabeth Hospital South Australia Adelaide Australia

Abstract

AbstractDisease‐modifying anti‐rheumatic drugs (DMARDs) are effective treatments for inflammatory arthritis but carry an increased risk of infection. For patients undergoing surgery, there is a need to consider the trade‐off between a theoretical increased risk of infection with continuation of DMARDs perioperatively versus an increased risk of disease flare if they are temporarily withheld. We used the Grading of Recommendations Assessment, Development and Evaluation methodology to develop recommendations for perioperative use of DMARDs for people with inflammatory arthritis undergoing elective surgery. The recommendations form part of the National Health and Medical Research Council‐endorsed Australian Living Guideline for the Pharmacological Management of Inflammatory Arthritis. Conditional recommendations were made against routinely discontinuing conventional synthetic and biologic (b) DMARDs in the perioperative period but to consider temporary discontinuation of bDMARDs in individuals with a high risk of infection or where the impact of infection would be severe. A conditional recommendation was made in favour of temporary discontinuation of targeted synthetic DMARDs in the perioperative period.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Internal Medicine

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