Predictors of revision, prosthetic joint infection and mortality following total hip or total knee arthroplasty in patients with rheumatoid arthritis: A nationwide cohort study using Danish healthcare registers
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Predictors of revision, prosthetic joint infection and mortality following total hip or total knee arthroplasty in patients with rheumatoid arthritis : A nationwide cohort study using Danish healthcare registers. / Cordtz, Rene Lindholm; Zobbe, Kristian; Højgaard, Pil; Kristensen, Lars Erik; Overgaard, Søren; Odgaard, Anders; Lindegaard, Hanne; Dreyer, Lene.
In: Annals of the Rheumatic Diseases, Vol. 77, No. 2, 01.02.2018, p. 281-288.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Predictors of revision, prosthetic joint infection and mortality following total hip or total knee arthroplasty in patients with rheumatoid arthritis
T2 - A nationwide cohort study using Danish healthcare registers
AU - Cordtz, Rene Lindholm
AU - Zobbe, Kristian
AU - Højgaard, Pil
AU - Kristensen, Lars Erik
AU - Overgaard, Søren
AU - Odgaard, Anders
AU - Lindegaard, Hanne
AU - Dreyer, Lene
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Objectives: To investigate predictors of 10-year risk of revision and 1-year risk of prosthetic joint infection (PJI) and death following total hip/total knee arthroplasty (THA/TKA) in (1) patients with rheumatoid arthritis (RA) compared with patients with osteoarthritis (OA); and (2) patients with RA treated with biological diseasemodifying antirheumatic drugs (bDMARD) within 90 days preceding surgery compared with non-treated. Methods: Register-based cohort study using the Danish National Patient Register, the DANBIO rheumatology register (RA-specific confounders and treatment episodes) and the Danish Hip and Knee Arthroplasty Registers. Survival analyses were used to calculate confounder-adjusted sub-HRs (SHR) and HRs. Results: In total, 3913 patients with RA with THA/ TKA were compared with 120 499 patients with OA. Patients with RA had decreased risk of revision (SHR 0.71 (0.57-0.89)), but increased risk of PJI (SHR=1.46 (1.13-1.88)) and death (HR=1.25 (1.01-1.55)). In DANBIO, 345 of 1946 patients with RA with THA/ TKA had received bDMARD treatment within 90 days preceding surgery. bDMARD-treated patients did not have a statistically significant increased risk of revision (SHR=1.49 (0.65-3.40)), PJI (SHR=1.61 (0.70-3.69)) nor death (HR=0.75 (0.24-2.33)) compared with nontreated. Glucocorticoid exposure (HR=2.87 (1.12-7.34)) and increasing DAS28 (HR=1.49 (1.01-2.20)) were risk factors for mortality. Conclusion: Patients with RA had a decreased 10- year risk of revision while the risk of death and PJI was increased compared with patients with OA following THA/TKA. bDMARD exposure was not associated with statistically significant increased risk of neither PJI nor death in this study. Glucocorticoid exposure and increased disease activity were associated with an increased risk of death.
AB - Objectives: To investigate predictors of 10-year risk of revision and 1-year risk of prosthetic joint infection (PJI) and death following total hip/total knee arthroplasty (THA/TKA) in (1) patients with rheumatoid arthritis (RA) compared with patients with osteoarthritis (OA); and (2) patients with RA treated with biological diseasemodifying antirheumatic drugs (bDMARD) within 90 days preceding surgery compared with non-treated. Methods: Register-based cohort study using the Danish National Patient Register, the DANBIO rheumatology register (RA-specific confounders and treatment episodes) and the Danish Hip and Knee Arthroplasty Registers. Survival analyses were used to calculate confounder-adjusted sub-HRs (SHR) and HRs. Results: In total, 3913 patients with RA with THA/ TKA were compared with 120 499 patients with OA. Patients with RA had decreased risk of revision (SHR 0.71 (0.57-0.89)), but increased risk of PJI (SHR=1.46 (1.13-1.88)) and death (HR=1.25 (1.01-1.55)). In DANBIO, 345 of 1946 patients with RA with THA/ TKA had received bDMARD treatment within 90 days preceding surgery. bDMARD-treated patients did not have a statistically significant increased risk of revision (SHR=1.49 (0.65-3.40)), PJI (SHR=1.61 (0.70-3.69)) nor death (HR=0.75 (0.24-2.33)) compared with nontreated. Glucocorticoid exposure (HR=2.87 (1.12-7.34)) and increasing DAS28 (HR=1.49 (1.01-2.20)) were risk factors for mortality. Conclusion: Patients with RA had a decreased 10- year risk of revision while the risk of death and PJI was increased compared with patients with OA following THA/TKA. bDMARD exposure was not associated with statistically significant increased risk of neither PJI nor death in this study. Glucocorticoid exposure and increased disease activity were associated with an increased risk of death.
UR - http://www.scopus.com/inward/record.url?scp=85041526465&partnerID=8YFLogxK
U2 - 10.1136/annrheumdis-2017-212339
DO - 10.1136/annrheumdis-2017-212339
M3 - Journal article
C2 - 29097373
AN - SCOPUS:85041526465
VL - 77
SP - 281
EP - 288
JO - Annals of the Rheumatic Diseases
JF - Annals of the Rheumatic Diseases
SN - 0003-4967
IS - 2
ER -
ID: 199378300