Feldman JJ, Ostrander B, Ithurburn MP, Fleisig GS, Tatum R, Ochsner MG, Ryan MK, Rothermich MA, Emblom BA, Dugas JR, and Lyle Cain E
Background: The use of all-suture anchors for rotator cuff repair is increasing. Potential benefits include decreased bone loss and decreased damage to the chondral surface. Minimal evidence exists comparing outcomes among medial-row anchor fixation methods in double-row suture bridge rotator cuff repair., Purpose: To compare the clinical outcomes between all-suture and solid medial-row anchors in double-row suture bridge rotator cuff repair., Study Design: Case series; Level of evidence, 4., Methods: A total of 352 patients (mean age at surgery, 60.3 years) underwent double-row suture bridge rotator cuff repair at our institution. Patients were separated into 2 groups based on whether they underwent all-suture (n = 280) or solid (n = 72) anchor fixation for the medial row. Outcomes data were collected via an ongoing longitudinal data repository or through telephone calls (minimum follow-up time, 2.0 years; mean follow-up time, 3.0 years). Outcomes were evaluated using the American Shoulder and Elbow Surgeons (ASES) standardized shoulder assessment form and the visual analog scale (VAS). The same rehabilitation protocol was administered to all patients. The proportions of patients meeting previously published Patient Acceptable Symptom State (PASS) thresholds were calculated for the outcome measures, and outcome scores and the proportions of patients meeting PASS thresholds between groups were compared using linear and logistic regression, respectively., Results: The groups did not differ in terms of age at surgery, sex distribution, rotator cuff tear size, or number of medial-row anchors used. The solid anchor group had a longer follow-up time compared with the all-suture anchor group (3.6 ± 0.7 vs 2.8 ± 0.8 years, respectively; P < .01). After controlling for follow-up time, the solid and all-suture anchor groups did not differ in ASES scores (89.6 ± 17.8 vs 88.8 ± 16.7, respectively; P = .44) or VAS scores (1.1 ± 2.1 vs 1.2 ± 2.1, respectively; P = .37). Similarly, after controlling for follow-up time, the solid and all-suture anchor groups did not differ in the proportions of patients meeting PASS cutoffs for the ASES (84.7% vs 80.7%, respectively; P = .44) or the VAS (80.6% vs 75.0%, respectively; P = .83)., Conclusion: Double-row suture bridge rotator cuff repair using all-suture anchors for medial-row fixation demonstrated similar excellent clinical outcomes to rotator cuff repair using solid medial-row anchors., Competing Interests: One or more of the authors has declared the following potential conflict of interest or source of funding: This study was funded in part by Arthrex (grant US-00697). The funding agency had no role in the collection, analysis, or interpretation of the data presented herein. Additionally, the funding agency had no involvement in the writing of the article or the decision to submit the article for publication. J.J.F. has received hospitality payments from Smith + Nephew and education payments from Arthrex and Smith + Nephew. M.G.O. has received education payments from Arthrex and Smith + Nephew and hospitality payments from Team 1. M.K.R. has received grant support from Arthrex; education payments from Arthrex, DJO, Smith + Nephew, and Fones Marketing Management; hospitality payments from Linvatec, Arthrex, and Prime Surgical; consulting fees from Arthrex and Zimmer Biomet; speaking fees from Arthrex and Zimmer Biomet; and compensation for services other than consulting from Arthrex. M.A.R. has received education payments from Arthrex, Smith + Nephew, and Zimmer Biomet; hospitality payments from Arthrex and Smith + Nephew; and compensation for services other than consulting from Arthrex. B.A.E. has received consulting fees from Arthrex, compensation for services other than consulting from Arthrex, and royalties from Arthrex. J.R.D. has received consulting fees from Arthrex, Bioventus, DJO, Smith + Nephew, and Royal Biologics; compensation for services other than consulting from Arthrex; and royalties from Arthrex and In2Bones. E.L.C. has received education payments from Prime Surgical and Zimmer Biomet; consulting fees from Arthrex, DJO, Smith + Nephew, and Zimmer Biomet; compensation for services other than consulting from Arthrex, Medical Device Business Services, and Smith + Nephew; royalties from Arthrex; hospitality payments from Encore Medical; and compensation for serving as faculty or as a speaker for an accredited or certified continuing education program from Medical Device Business Services. 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. Ethical approval for this study was obtained from Sterling IRB (ref No. 18-004; 6280)., (© The Author(s) 2024.)