Updated: Sep 26, 2007
The ulnar collateral ligament (UCL) of the elbow is critical for valgus stability of the elbow and is the primary elbow stabilizer.1,2 As such, the UCL plays an important role in most throwing sports, including baseball and javelin, as well as racquet sports and ice hockey.
Elbow injuries in young athletes are generally chronic, with persistent pain and instability from repetitive overhead activities. In the athlete, ligamentous injury can also be heralded by an acute traumatic event such as an elbow dislocation. This can then lead to chronic pain and valgus instability. An understanding of the anatomy and biomechanics of the elbow in throwing sports is essential to the correct diagnosis and treatment of this potentially disabling injury.3
The UCL originates at the posterior distal aspect of the medial epicondyle and inserts into the base of the coronoid process. At 90 º of flexion, it provides 55% of the resistance to valgus stress at the elbow. In full extension, the UCL, bony architecture, and anterior capsule equally maintain valgus stability.
The UCL is composed of 3 bands: anterior, posterior, and transverse. The anterior band, which arises from the anteroinferior surface of the medial epicondyle and inserts on the sublime tubercle of the ulna, provides the major contribution to valgus stability.
The acceleration phase of the overhead throw causes the greatest amount of valgus stress to the elbow.4 Extension occurs at a rate of up to 2500 º per second and continues to 20 º of flexion. During this phase, the forearm lags behind the upper arm and generates valgus stress while the elbow is primarily dependent on the anterior band of the UCL for stability. During the acceleration phase, valgus stress can exceed 60 Newton meters (Nm), which is significantly higher than the measured strength of the UCL in cadavers. The valgus force can, therefore, overcome the tensile strength of the UCL and cause either chronic microscopic tears or acute rupture.
Elbow and Forearm Overuse Injuries
Little League Elbow Syndrome
Medial Condylar Fracture of the Elbow
Medial Epicondylitis
Flexor pronator muscle tear/tendinitis
Ulnar neuritis/ulnar nerve entrapment
Medial epicondylar fracture
Valgus extension overload
Generally, 3-6 months of conservative therapy with rest, nonsteroidal anti-inflammatory drugs (NSAIDs), and local physical therapy for ROM are necessary for recovery.
When pain and swelling completely resolve and the athlete has returned to a premorbid ROM (usually not before 3 months of treatment), progressive return to activity with increasing velocity and duration of training may be attempted.
Surgery may be considered in several situations. Surgical repair is generally indicated for acute tears in competitive athletes, when chronic instability exists, and when the patient has recurring pain and laxity after 2 or more attempts at conservative therapy.
Direct repair of the ligament is generally not indicated. Reconstruction of the UCL (eg, repair of the anterior bundle) is the more common approach to surgical treatment, with use of a palmaris longus tendon autograft. The graft is pulled through bone tunnels in the medial epicondyle of the humerus and the sublime tubercle of the ulna in a figure-8 pattern. Ulnar nerve transposition may be undertaken at the time of surgery, if indicated.
Consultation with an orthopedic surgeon, preferably a sports or upper-extremity specialist, is indicated when surgical intervention is contemplated.
Steroid injection is not recommended for UCL injuries.
After surgery, the elbow is immobilized in a posterior splint for 10 days in 90° of flexion. The wrist is maintained free, and a soft rubber ball is given to the patient for squeezing to maintain grip strength. Active ROM is initiated after removal of the posterior splint. A hinged brace that prevents valgus stress should be used.
At approximately 1 month after surgery, isometric strengthening exercises should be initiated. Limited progressive strengthening can be initiated at 8 weeks and plyometrics at 12 weeks. Shoulder and elbow exercises should be instituted as soon as feasible, but valgus stress of the elbow should be avoided for at least 4-6 months until the graft has had sufficient time to incorporate.
After 4-6 months, throwing may be resumed with a training program that is designed to return the patient to competitive throwing by 9-12 months after surgery.
Both transient and permanent ulnar neuropathy may occur after reconstruction, occasionally requiring ulnar nerve transposition or revision of transposition. Flexion contracture (generally <5°) may also occur in 25-30% of patients.
Ulnar nerve transposition (or revision of transposition) may be required for persistent postoperative ulnar neuropathy.
Flexibility and strength training of the elbow are useful in the maintenance phase to prevent recurrent injury.
During the maintenance phase, particular attention to the patient's throwing technique is essential to prevent recurrence of injury.
Long-term complications may include chronic pain with throwing and chronic instability of the elbow.
NSAIDs are the cornerstone of therapy for the control of pain that is associated with UCL injuries.
Pain control is essential to patient care.
DOC for treating mild to moderate pain if no contraindications exist. Inhibits inflammatory reactions and pain by decreasing the activity of the enzyme COX and thereby inhibiting production of prostaglandins.
400 mg PO q4-6h, 600 mg q6h, or 800 mg q8h PO while symptoms persist; not to exceed 3.2 g/d
<6 months: Not established
6 months to 12 years: 20-40 mg/kg/d PO divided tid/qid
>12 years: Administer as in adults
Probenecid may increase the concentrations and, possibly, the toxicity of NSAIDs; ibuprofen may decrease the effect of loop diuretics; PT duration may increase when ibuprofen is administered with anticoagulants; monitor PT and observe for bleeding; ibuprofen and other NSAIDs may increase serum lithium levels and the risk of methotrexate toxicity
Documented hypersensitivity; aspirin-, iodide-, or other NSAID-induced hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Use with caution in patients with congestive heart failure, hypertension, and decreased renal and hepatic function.
DOC for treating mild pain in patients with documented hypersensitivity to aspirin or NSAIDs, those diagnosed with upper GI disease, or those who take PO anticoagulants.
325-650 mg PO q4-6h or 1000 mg tid/qid; not to exceed 4 g/d
Alternative, 1000 mg tid/qid; not to exceed 4 g/d
<12 years: 10-15 mg/kg/dose PO q4-6h prn; not to exceed 2.6 g/d
>12 years: 325-650 mg PO q4h; not to exceed 5 doses/d
Rifampin can reduce the analgesic effects of APAP; barbiturates, carbamazepine, hydantoins, and isoniazid may increase liver toxicity.
Documented hypersensitivity; G6PD deficiency
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Hepatotoxicity can occur in patients with long-term alcoholism.
Used for relief of mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing the activity of the enzyme COX and thereby inhibiting production of prostaglandins.
500 mg PO followed by 250 mg q6-8h; not to exceed 1.25 g/d; may increase to 1.5 g/d for limited periods
<2 years: Not established
>2 years: 2.5 mg/kg/dose PO; not to exceed 10 mg/kg/d
Probenecid and lithium may increase the concentrations and, possibly, the toxicity of NSAIDs; effect of loop diuretics may decrease when coadministered with this drug; PT duration may increase when naproxen is coadministered with anticoagulants; monitor PT and watch for bleeding; coadministration with phenytoin may increase serum phenytoin levels, resulting in an increase in the pharmacologic and toxic effects of phenytoin
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Acute renal insufficiency, hyperkalemia, hyponatremia, interstitial nephritis, and renal papillary necrosis may occur; increases risk of acute renal failure in patients with preexisting renal disease or compromised renal perfusion; low WBC counts (rare) usually return to the reference range in ongoing therapy; discontinuing therapy may be necessary if persistent leukopenia, granulocytopenia, or thrombocytopenia occurs; perform ophthalmologic studies in patients who develop eye symptoms during therapy; discontinue therapy if changes are noted; changes may include blurred or diminished vision, corneal deposits and retinal disturbances, scotomata, changes in color vision, and macular degeneration
Used to relieve mild to moderate pain and inflammation. Initially administer small dosages to patients with a small body size, elderly patients, and those with renal or liver disease. Doses >75 mg do not increase therapeutic effects. Administer high doses with caution, and closely observe patients for response.
25-50 mg PO q6-8h prn; not to exceed 300 mg/d
<3 months: Not established
3 months to 12 years: 0.1-1 mg/kg PO q6-8h
>12 years: Administer as in adults
Probenecid and lithium may increase the concentrations and, possibly, the toxicity of NSAIDs; effect of loop diuretics may decrease when coadministered; PT duration may increase when ketoprofen is coadministered with anticoagulants; monitor PT closely and watch for bleeding; coadministration with phenytoin may increase serum phenytoin levels, resulting in an increase in the pharmacologic and toxic effects of phenytoin
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Avoid use in patients diagnosed with GI disease, cardiovascular disease, or renal or hepatic impairment and in patients receiving anticoagulants.
Drug combination indicated for treatment of mild to moderate pain.
Based on codeine dose: 30-60 mg/dose PO q4-6h or 1-2 tab PO q4h; not to exceed 12 tabs/d
Based on codeine dose: 0.5-1 mg/kg/dose PO
Based on acetaminophen dose: 10-15 mg/kg/dose PO q4h; not to exceed 2.6 g/d of acetaminophen
Toxicity increases when coadministered with CNS depressants or tricyclic antidepressants
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Administer with caution in patients who are dependent on opiates because this substitution may result in acute opiate withdrawal symptoms; exercise caution when patients have severe renal or hepatic dysfunction.
Drug combination indicated to relieve moderate to severe pain. DOC for aspirin-hypersensitive patients.
1-2 tab or cap PO q4-6h prn
0.05-0.15 mg/kg/dose of oxycodone PO; not to exceed 5 mg/dose of oxycodone PO q4-6h prn
Phenothiazines may decrease analgesic effects of this medication; toxicity increases with coadministration of either CNS depressants or tricyclic antidepressants
Documented hypersensitivity
C - Safety for use during pregnancy has not been established.
Duration of action may increase in elderly patients; be aware of the patient's total daily dose of acetaminophen; doses higher than the maximum (4000 mg/d) may cause liver toxicity
Drug combination indicated to relieve moderate to severe pain.
1-2 tab or cap PO q4-6h prn
<12 years: 10-15 mg/kg/dose acetaminophen PO q4-6h prn; not to exceed 2.6 g/d of acetaminophen or 5 mg of hydrocodone bitartrate per dose
>12 years: 650 mg acetaminophen PO q4h; not to exceed 4 g/d acetaminophen or 10 mg of hydrocodone bitartrate per dose
Phenothiazines may decrease analgesic effects; toxicity of this drug increases when coadministered with CNS depressants or tricyclic antidepressants
Documented hypersensitivity; elevated intracranial pressure
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Tabs contain metabisulfite, which may cause allergic reactions; administer with caution in patients who are dependent on opiates because this substitution may result in acute opiate withdrawal symptoms; exercise caution when patients have severe renal or hepatic dysfunction.
Competition may be resumed when the following criteria are met:
Injuries to the UCL are best prevented by ensuring proper throwing biomechanics. Coaches are essential to assessing the proper throwing techniques in the athlete. Thorough warm-up and flexibility exercises also play an essential role in preventing UCL injuries.
Return to competitive throwing by the patient is possible after successful rehabilitation and reconstruction, when indicated.
Proper throwing technique is essential to preventing UCL injuries; therefore, athlete education is critical. Analysis of the athlete's throwing technique and constructive criticism by coaches may be helpful.
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medial collateral ligament injury, little leaguer's elbow, UCL injury, elbow injury/trauma, elbow pain, valgus elbow instability
Robert F Kacprowicz, MD, Program Director, San Antonio Uniformed Services Health Education Consortium Residency in Emergency Medicine
Robert F Kacprowicz, MD is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
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Eric Chumbley, MD, Consulting Staff, Department of Sports Medicine, Trover Clinic
Eric Chumbley, MD is a member of the following medical societies: American Academy of Family Physicians, American College of Sports Medicine, and Uniformed Services Academy of Family Physicians
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Craig C Young, MD, Associate Professor, Departments of Orthopedic Surgery and Community and Family Medicine, Medical Director of Sports Medicine, Sports Medicine Fellowship Director, Medical College of Wisconsin
Craig C Young, MD is a member of the following medical societies: American Academy of Family Physicians, American College of Sports Medicine, American Medical Society for Sports Medicine, Phi Beta Kappa, and Wilderness Medical Society
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Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
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Henry T Goitz, MD, Chief, Sports Medicine, Associate Professor, Department of Orthopaedic Surgery, Medical College of Ohio
Henry T Goitz, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons and American Orthopaedic Society for Sports Medicine
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Jon B Whitehurst, MD, Clinical Instructor of Surgery, University of Illinois College of Medicine; Partner and Executive Board Member, Rockford Orthopedic Associates; Orthopedic Chairman, Rockford Memorial Hospital
Jon B Whitehurst, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Orthopaedic Society for Sports Medicine, and Arthroscopy Association of North America
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Sherwin SW Ho, MD, Associate Professor, Department of Surgery, Section of Orthopedic Surgery and Rehabilitation Medicine, University of Chicago
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