Perioperative Glucocorticoids in Patients With Rheumatoid Arthritis Having Total Joint Replacements: Help or Harm?

Tariq Chukir; Susan M Goodman; Haley Tornberg; Huong Do; Charlene Thomas; Alana Sigmund; Peter Sculco; Mark Figgie; Bella Mehta; Linda Russell; Emily Stein

doi:10.1002/acr2.11306

Perioperative Glucocorticoids in Patients With Rheumatoid Arthritis Having Total Joint Replacements: Help or Harm?

ACR Open Rheumatol. 2021 Sep;3(9):654-659. doi: 10.1002/acr2.11306. Epub 2021 Jul 20.

Authors

Affiliations

¹ Weill Cornell Medicine and New York Presbyterian Hospital, New York, and Weill Cornell Medicine-Qatar, Education City, Doha, Qatar.
² Hospital for Special Surgery, New York, New York.
³ Weill Cornell Medicine and New York Presbyterian Hospital, New York.
⁴ Weill Cornell Medicine and New York Presbyterian Hospital and Hospital for Special Surgery, New York.

Abstract

Objective: The optimal strategy for perioperative glucocorticoid (GC) management in patients with rheumatoid arthritis (RA) on chronic GCs is unknown. Although there is a concern for hypotension if inadequate doses are used, higher GC exposure may increase perioperative complications. We aimed to investigate the relationships between perioperative GCs with hemodynamic instability and short-term postoperative complications following total hip arthroplasty (THA) and total knee arthroplasty (TKA) in patients with RA.

Methods: This retrospective study included patients with RA who underwent THA and TKA. GC exposure was assessed by the total cumulative dose (in prednisone equivalents) during hospitalization. Perioperative complications and hypotension were assessed.

Results: Of 432 patients, 387 (90%) received supraphysiologic perioperative GC. Thirty percent of patients were using chronic GCs (mean daily dose, 7 ± 4 mg). Half (54%) underwent TKA. The median age was 65 years, and 79% were women. The median cumulative GC dose during hospitalization was 37 mg (interquartile range, 27-53.3). A lower cumulative dose of GC did not increase odds of hypotension during hospitalization (unadjusted odds ratio, 1.00 [95% confidence interval, 0.99-1.01]; P = 0.66)]. However, postoperative complications were higher among patients who received higher cumulative doses after adjustment for age, body mass index, home GC use, smoking, and Charlson Comorbidity Index. Risk of short-term complications increased by 8.4% (P = 0.017) for every 10-mg increase in GC dose.

Conclusion: A lower GC dose was not associated with increased hypotension. However, patients with higher GC exposure were more likely to have hyperglycemia and other complications. These findings suggest that harms may be associated with high perioperative GC doses. Further research is needed to determine the optimal perioperative regimen for patients with RA.