1. Rate and Timing of Progression to Total Knee Arthroplasty After Anterior Cruciate Ligament Reconstruction in Patients With Systemic Inflammatory Disease: A Long-term Propensity-Matched Cohort Study.
- Author
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Pan X, Wang AS, Johnson QJ, Clark SC, Camp CL, Okoroha KR, Saris DBF, Tagliero AJ, Hevesi M, and Krych AJ
- Subjects
- Humans, Female, Male, Retrospective Studies, Adult, Middle Aged, Anterior Cruciate Ligament Injuries surgery, Young Adult, Anterior Cruciate Ligament Reconstruction, Arthroplasty, Replacement, Knee, Propensity Score
- Abstract
Background: Anterior cruciate ligament reconstruction (ACLR) is one of the most common orthopaedic procedures and one of the most well studied. Despite extensive research dedicated to ACLR, there is limited understanding of how chronic inflammatory systemic diseases (CIDs) such as rheumatoid arthritis and systemic lupus erythematosus affect outcomes., Purpose: To compare the outcomes of ACLR in cohorts of patients with and without CID., Study Design: Cohort study; Level of evidence, 3., Methods: A retrospective query of a regional data set was conducted for all patients who underwent ACLR from 1990 to 2021 for traumatic ACL rupture. All patients with CID were identified and propensity matched to non-CID controls. Baseline characteristics and clinical outcomes were identified through retrospective chart review, and patients were contacted for subjective outcomes., Results: A total of 30 patients with ACLR and a diagnosis of CID were identified. These patients were propensity matched to 120 non-CID controls. Baseline demographic and surgical characteristics demonstrated no statistical differences. Follow-up duration was similar between the CID and non-CID groups (mean, 14.6 vs 14.2 years; P = .868). The CID cohort had a higher arthrofibrosis rate (16.7% vs 4.3%; P = .031), higher osteoarthritis rate (33.3% vs 16.7%; P = .041), higher total knee arthroplasty (TKA) rate (16.7% vs 3.3%; P = .016), and earlier time to TKA (14.7 vs 23.5 years; P = .032). Knee range of motion, infection rate, retear rate, time to retear, and time to osteoarthritis were not statistically different between the cohorts. The CID cohort had higher visual analog scale pain scores (mean, 2.00 vs 1.20; P = .043) but slightly higher satisfaction (mean, 3.92 vs 3.39; P = .043). There were no differences in preinjury Tegner, postoperative Tegner, change in Tegner, or IKDC score. In a univariate Cox regression model, the CID cohort had a retear hazard ratio of 1.43 (95% CI, 0.46-4.51; P = .537). Kaplan-Meier survival revealed no significant differences in retear-free survival between the CID and non-CID cohorts at 25 years (85.7% vs 87.3%; P = .53). The CID cohort had a TKA hazard ratio of 3.94 (95% CI, 1.05-14.8; P = .042). Kaplan-Meier survival demonstrated significantly decreased TKA-free survival at 25 years in the CID cohort (64.9% vs 91.2%; P = .029)., Conclusion: CID increases the incidence of arthrofibrosis, osteoarthritis, and TKA in those undergoing ACLR. Patients with CID also undergo TKA significantly sooner than non-CID counterparts. Notably, the majority of patient-reported outcome measures are no worse in patients who have a CID diagnosis. Thus, ACLR constructs themselves may not necessarily fare worse in patients with CID. Nonetheless, these patients need to be cautiously counseled on the clinical outlook after their ACLR., Competing Interests: One or more of the authors has declared the following potential conflict of interest or source of funding: C.L.C. has received consulting fees and support for education from Arthrex. D.B.F.S. has received consulting fees from Smith & Nephew, Phoenix Kinetic, and Relive Biotechnologies; nonconsulting fees from Aesculap Biologics, LLC; and research support from JRF. K.R.O. has received consulting fees from Arthrex, Inc, Smith & Nephew, and Endo Pharmaceuticals; support for education from Gemini Medical, Smith & Nephew, Arthrex, Endo Pharmaceuticals, Pinnnacle, Inc, Foundation Medical, and Medwest Associates; speaking fees from Synthes GmbH; hospitality payments from Stryker, Wright Medical Technology, Medical Device Business Services, and Zimmer Biomet; and a grant from Arthrex. A.J.T. has received hospitality payments from Stryker, Arthrex, Medical Device Business Services, and Zimmer Biomet Holdings. M.H. has received education payments from Arthrex, Foundation Medical, Medwest Associates, and Smith & Nephew; honoraria from Encore Medical; hospitality payments from Orthalign, Stryker, and Medical Device Business Services; consulting fees from Vericel, DJO-Enovis, Moximed, and Vericel; support for education Smith & Nephew and Medwest Associates; and hospitality payments from Medical Device Business Services. A.J.K. has received consulting fees from Arthrex, Ceterix, Gemini Mountain Medical, Joint Restoration Foundation, Responsive Arthroscopy, and Smith & Nephew; royalties from Arthrex and Responsive Arthroscopy; a grant from DJO; honoraria from Joint Restoration Foundation and Musculoskeletal Transplant; and research support from Aesculap/B. Braun, Arthritis Foundation, Ceterix, and Histogenics. AOSSM checks author disclosures against the Open Payments Database (OPD). AOSSM has not conducted an independent investigation on the OPD and disclaims any liability or responsibility relating thereto.
- Published
- 2025
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