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Non-Operative and Operative Rehabilitation of an Overhead Athlete with a SLAP Lesion

Activity Details
  • Credit Amounts:
    • CME: 2.00
    • BOC: 1.75
  • Cost: $25.00
  • Release: Nov 1, 2015
  • Expires: Dec 31, 2017
  • Estimated Time to Complete:
    2 Hour(s)
  • System Requirements:
  • Average User Rating:
    (2 Ratings)


Timothy L.  Uhl Timothy L. Uhl, PhD, PT, ATC
Director of Musculoskeletal Laboratory
Professor, Athletic Training
College of Health Sciences
University of Kentucky
Lexington, KY

Needs Statement

Surgical management of Superior Labral Anterior-Posterior (SLAP) Tears has been on an unprecedented upswing in surgical case reported at the board examination for orthopedic surgeons. The surgical cases presented are three times greater the likely incidence of SLAP Tears.  Unfortunately, the return to play following surgery in overhead athlete is only averaging 63% return rate. At the same time there is only 3 published articles in the English literature that have investigated the benefit on non-operative management of SLAP lesion. There is a relative dearth of information on what is the best way to manage these patients from both non-operatively and post-operatively perspective. This very common diagnose requires further investigation so that athletic trainers understand what challenge their athletes are faced with when diagnosed with a SLAP lesion. This presentation will help educate clinicians about their patients’ prognosis of both non-operative and operative outcomes for SLAP lesions and describe key elements in designing an effective rehabilitation intervention.

Target Audience

This activity is designed for athletic trainers, physical therapists, sports medicine physicians, physical medicine and rehabilitation physicians, and  physician assistants. 


At the conclusion of the session, attendees will be able to:
1. Describe how to integrate a non-operative rehabilitation program into their clinical management of SLAP lesions.
2. Educate their patients on the prognosis of both non-operative and operative outcomes for SLAP lesions.
3. Recall a post-operative rehabilitation program for type 2 SLAP tears


This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of the University of Kentucky College of Medicine, and UK College of Health Science. The University of Kentucky College of Medicine is accredited by the ACCME to provide continuing medical education for physicians.

The University of Kentucky College of Medicine designates this enduring material for a maximum of 2.00 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

The University of Kentucky College of Medicine presents this activity for educational purposes only. Participants are expected to utilize their own expertise and judgment while engaged in the practice of medicine. The content of the presentations is provided solely by presenters who have been selected for presentations because of recognized expertise in their field.

ACGME Competencies

  • Patient care
  • Medical knowledge
  • Practice-based learning and improvement

NATABOC The University of Kentucky is recognized by the Board of Certification, Inc. to offer continuing education for Certified Athletic Trainers. This program has been approved for a maximum of 1.75 hours of EBP Category continuing education. Certified Athletic Trainers are responsible for claiming only those hours actually spent participating in the continuing education activity.

BOC Approved EBP Provider Number: P2382-5

Faculty Disclosure

Timothy L. Uhl, PhD, PT, ATC (Speaker) has relevant financial relationships with commercial interests as follows:
New Option Sports, Inc - Inventor - Royalties
Patterson Medical Supply, Inc - Independent Contractor - Research Grant

No (other) speakers or planners have any relevant financial relationships to disclose.

The material presented in this course represents information obtained from the scientific literature as well as the clinical experiences of the speakers. In some cases, the presentations might include discussion of investigational agents and/or off-label indications for various agents used in clinical practice. Speakers will inform the audience when they are discussing investigational and/or off-label uses.

Content review confirmed that the content was developed in a fair, balanced manner free from commercial bias. Disclosure of a relationship is not intended to suggest or condone commercial bias in any presentation, but it is made to provide participants with information that might be of potential importance to their evaluation of a presentation.


This activity is jointly provided by the University of Kentucky and UK College of Health Science.

CE Content Concerns


Concerns or complaints related to ACPE or ACCME standards may be submitted in writing to the Director of UK HealthCare CECentral by fax to 859-323-2920, or by mail to 2365 Harrodsburg Road, Ste B475, Lexington, KY 40504


  • The Director or his/her designee will review, investigate, forward and/or respond to complaints and will put forth a best effort to adjudicate the issue(s), along with CECentral staff members, within two (2) weeks of receipt of the grievance or complaint.
  • If needed, concerns, complaints, or grievances will be brought before the UK HealthCare CECentral Advisory Board.
  • Issues regarding activity content also will be reviewed and addressed by the Activity Director.
  • A written decision will be issued in a timely manner by the Director of UK HealthCare CECentral or his/herdesignee.
  • Grievances will be considered when planning future activities.

Appeal Procedure

  • Persons who wish to appeal a decision should address the appeal by email, fax or in writing to the Director of UK HealthCare CECentral within two (2) weeks of receipt of the response.
  • The Director will bring the appeal to the UK HealthCare CECentral Advisory Board.
  • The results of the appeal will be sent to the participant no later than two (2) weeks following the meeting of the board.