James L Cook1, Caleb C Hudson, Keiichi Kuroki. 1. Comparative Orthopaedic Laboratory, University of Missouri, 900 E Campus Dr, Columbia, MO 65211, USA. cookjl@missouri.edu
Abstract
OBJECTIVE: To develop and assess clinical outcomes for osteochondral autografting for treatment of stifle osteochondrosis (OC) in dogs. STUDY DESIGN: Retrospective case series. ANIMALS: Dogs with stifle OC (n=10). METHODS: Osteochondral autografting was developed and optimized in canine cadavers and purpose-bred research dogs using the Osteochondral Autograft Transfer System (OATS). Dogs with stifle OC (n=10 dogs, 12 stifles) were then treated using the OATS system. Outcomes were assessed by radiography (n=12), magnetic resonance imaging (1), second-look arthroscopy (9), lameness scoring (12), and telephone survey of owners (10 clients, 12 stifles) 6-15 months after surgery. RESULTS: Complications were documented in 4 of the 12 stifles treated and included peri-incisional seromas (3) and marked stifle effusion (1). Subjective assessment of follow-up radiographs revealed evidence of integration of the grafts with maintenance of subchondral bone surface architecture. Subjective assessment of follow-up MRI in 1 stifle revealed evidence for incorporation of grafts with restoration of articular surface contour. Second-look arthroscopy 6-30 weeks after surgery revealed maintenance of articular cartilage at the graft site. Dogs were significantly (P<.001) less lame at follow-up compared with preoperative scores. Based on follow-up owner surveys, only 2 dogs had no pain or lameness; the other dogs were judged to have mild pain and/or lameness. All owners noticed improvement in the dogs' quality of life after surgery. CONCLUSION: Osteochondral autografting deserves consideration and further evaluation as a primary treatment option for stifle OC in dogs. CLINICAL RELEVANCE: Osteochondral autografting for treatment of lateral femoral condylar OC lesions in dogs using OATS instrumentation is safe and results in improved function and quality of life based on owners' perception 6-15 months after treatment.
OBJECTIVE: To develop and assess clinical outcomes for osteochondral autografting for treatment of stifle osteochondrosis (OC) in dogs. STUDY DESIGN: Retrospective case series. ANIMALS: Dogs with stifle OC (n=10). METHODS: Osteochondral autografting was developed and optimized in canine cadavers and purpose-bred research dogs using the Osteochondral Autograft Transfer System (OATS). Dogs with stifle OC (n=10 dogs, 12 stifles) were then treated using the OATS system. Outcomes were assessed by radiography (n=12), magnetic resonance imaging (1), second-look arthroscopy (9), lameness scoring (12), and telephone survey of owners (10 clients, 12 stifles) 6-15 months after surgery. RESULTS: Complications were documented in 4 of the 12 stifles treated and included peri-incisional seromas (3) and marked stifle effusion (1). Subjective assessment of follow-up radiographs revealed evidence of integration of the grafts with maintenance of subchondral bone surface architecture. Subjective assessment of follow-up MRI in 1 stifle revealed evidence for incorporation of grafts with restoration of articular surface contour. Second-look arthroscopy 6-30 weeks after surgery revealed maintenance of articular cartilage at the graft site. Dogs were significantly (P<.001) less lame at follow-up compared with preoperative scores. Based on follow-up owner surveys, only 2 dogs had no pain or lameness; the other dogs were judged to have mild pain and/or lameness. All owners noticed improvement in the dogs' quality of life after surgery. CONCLUSION: Osteochondral autografting deserves consideration and further evaluation as a primary treatment option for stifle OC in dogs. CLINICAL RELEVANCE: Osteochondral autografting for treatment of lateral femoral condylar OC lesions in dogs using OATS instrumentation is safe and results in improved function and quality of life based on owners' perception 6-15 months after treatment.
Authors: Kenneth W Ng; Eric G Lima; Liming Bian; Christopher J O'Conor; Prakash S Jayabalan; Aaron M Stoker; Keiichi Kuroki; Cristi R Cook; Gerard A Ateshian; James L Cook; Clark T Hung Journal: Tissue Eng Part A Date: 2010-03 Impact factor: 3.845
Authors: Samuel P Franklin; Aaron M Stoker; Sean M Murphy; Michael P Kowaleski; Mitchell Gillick; Stanley E Kim; Michael Karlin; Alan Cross; James L Cook Journal: Front Vet Sci Date: 2021-12-24
Authors: J L Cook; C T Hung; K Kuroki; A M Stoker; C R Cook; F M Pfeiffer; S L Sherman; J P Stannard Journal: Bone Joint Res Date: 2014-04-02 Impact factor: 5.853