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A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair

BACKGROUND: Hip abductor tendon (HAT) tearing is commonly implicated in greater trochanteric pain syndrome. Studies reporting surgical outcomes are often on small cohorts and with limited information on functional improvement. PURPOSE: To report the 2-year clinical and functional outcomes in a serie...

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Autores principales: Ebert, Jay R., Brogan, Kit, Janes, Gregory C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977235/
https://www.ncbi.nlm.nih.gov/pubmed/32030347
http://dx.doi.org/10.1177/2325967119897881
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author Ebert, Jay R.
Brogan, Kit
Janes, Gregory C.
author_facet Ebert, Jay R.
Brogan, Kit
Janes, Gregory C.
author_sort Ebert, Jay R.
collection PubMed
description BACKGROUND: Hip abductor tendon (HAT) tearing is commonly implicated in greater trochanteric pain syndrome. Studies reporting surgical outcomes are often on small cohorts and with limited information on functional improvement. PURPOSE: To report the 2-year clinical and functional outcomes in a series of patients undergoing HAT repair augmented with a ligament augmentation and reconstruction system (LARS) ligament. STUDY DESIGN: Case series; Level of evidence, 4. METHODS: Between October 2012 and December 2016, a total of 142 patients with symptomatic HAT tears underwent open bursectomy, V-Y lengthening, and reattachment of the tendon with suture anchors augmented with a LARS ligament. This included 132 women (93%) with a mean age of 64.3 years (range, 43-84 years), a mean body mass index of 28.2 kg/m(2) (range, 20.0-41.3 kg/m(2)), and an average duration of symptoms of 4.0 years (range, 6 months-20 years). Following surgery, patients underwent a graduated rehabilitation program consisting of hydrotherapy and land-based exercises. Patient-reported outcome measures (PROMs) were evaluated preoperatively and at 3, 6, 12, and 24 months postoperatively with the Harris Hip Score, Oxford Hip Score, 12-item Short Form Health Survey, and visual analog scale (VAS) for pain. Hip range of motion, hip abduction strength, 30-s single-leg stance (SLS), and 6-minute walk test (6MWT) capacity were evaluated. Patient satisfaction and perceived global rating of change were evaluated postsurgery. Analysis of variance was employed to evaluate clinical improvement over time. RESULTS: A significant improvement (P < .05) was demonstrated up to 24 months in all PROMs and clinical scores, including hip range of motion in all planes, hip abductor strength limb symmetry indices (mean ± SD; presurgery, 90.1% ± 42.5%; 24 months, 102.6% ± 15.0%), and the 6MWT (presurgery, 421.8 ± 91.9 m; 24 months, 509.7 ± 105.1 m). Furthermore, several variables, including pain (VAS and pain scores during the 6MWT and 30-s SLS) and patient-perceived improvement (global rating of change), continued to improve from 12 to 24 months. At 24 months, 95.7% of patients were satisfied with their surgical outcome (excluding 3 patients who underwent reoperation within the 24-month period). There was a 5.6% (n = 8) failure rate over the study period. CONCLUSION: HAT repair augmented with a synthetic ligament demonstrated significantly improved clinical and functional outcomes, high levels of patient satisfaction, and a relatively low failure rate up to 24 months postsurgery. REGISTRATION: ACTRN12616001655437 (Australian New Zealand Clinical Trials Registry).
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spelling pubmed-69772352020-02-06 A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair Ebert, Jay R. Brogan, Kit Janes, Gregory C. Orthop J Sports Med Article BACKGROUND: Hip abductor tendon (HAT) tearing is commonly implicated in greater trochanteric pain syndrome. Studies reporting surgical outcomes are often on small cohorts and with limited information on functional improvement. PURPOSE: To report the 2-year clinical and functional outcomes in a series of patients undergoing HAT repair augmented with a ligament augmentation and reconstruction system (LARS) ligament. STUDY DESIGN: Case series; Level of evidence, 4. METHODS: Between October 2012 and December 2016, a total of 142 patients with symptomatic HAT tears underwent open bursectomy, V-Y lengthening, and reattachment of the tendon with suture anchors augmented with a LARS ligament. This included 132 women (93%) with a mean age of 64.3 years (range, 43-84 years), a mean body mass index of 28.2 kg/m(2) (range, 20.0-41.3 kg/m(2)), and an average duration of symptoms of 4.0 years (range, 6 months-20 years). Following surgery, patients underwent a graduated rehabilitation program consisting of hydrotherapy and land-based exercises. Patient-reported outcome measures (PROMs) were evaluated preoperatively and at 3, 6, 12, and 24 months postoperatively with the Harris Hip Score, Oxford Hip Score, 12-item Short Form Health Survey, and visual analog scale (VAS) for pain. Hip range of motion, hip abduction strength, 30-s single-leg stance (SLS), and 6-minute walk test (6MWT) capacity were evaluated. Patient satisfaction and perceived global rating of change were evaluated postsurgery. Analysis of variance was employed to evaluate clinical improvement over time. RESULTS: A significant improvement (P < .05) was demonstrated up to 24 months in all PROMs and clinical scores, including hip range of motion in all planes, hip abductor strength limb symmetry indices (mean ± SD; presurgery, 90.1% ± 42.5%; 24 months, 102.6% ± 15.0%), and the 6MWT (presurgery, 421.8 ± 91.9 m; 24 months, 509.7 ± 105.1 m). Furthermore, several variables, including pain (VAS and pain scores during the 6MWT and 30-s SLS) and patient-perceived improvement (global rating of change), continued to improve from 12 to 24 months. At 24 months, 95.7% of patients were satisfied with their surgical outcome (excluding 3 patients who underwent reoperation within the 24-month period). There was a 5.6% (n = 8) failure rate over the study period. CONCLUSION: HAT repair augmented with a synthetic ligament demonstrated significantly improved clinical and functional outcomes, high levels of patient satisfaction, and a relatively low failure rate up to 24 months postsurgery. REGISTRATION: ACTRN12616001655437 (Australian New Zealand Clinical Trials Registry). SAGE Publications 2020-01-22 /pmc/articles/PMC6977235/ /pubmed/32030347 http://dx.doi.org/10.1177/2325967119897881 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc-nd/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (https://creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article
Ebert, Jay R.
Brogan, Kit
Janes, Gregory C.
A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair
title A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair
title_full A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair
title_fullStr A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair
title_full_unstemmed A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair
title_short A Prospective 2-Year Clinical Evaluation of Augmented Hip Abductor Tendon Repair
title_sort prospective 2-year clinical evaluation of augmented hip abductor tendon repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977235/
https://www.ncbi.nlm.nih.gov/pubmed/32030347
http://dx.doi.org/10.1177/2325967119897881
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