You are in: eMedicine Specialties > Sports Medicine > Lower Limb Slipped Capital Femoral EpiphysisArticle Last Updated: Jun 8, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Henry Marano, MD, Director, Department of Orthopedic Surgery, Associate Professor, St Joseph's Hospital, Albert Einstein College of Medicine Henry Marano is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Medical Association, and Medical Society of the State of New York Coauthor(s): David Y Lin, MD, Fellow, Department of Orthopedic Surgery, Section of Pediatrics, University of Tennessee Campbell Clinic; Evan Schwartz, MD, Director of Orthopedic Surgery, New York Medical College; Assistant Professor, St John's Queens Hospital, Department of Surgery, Albert Einstein School of Medicine Editors: Anthony J Saglimbeni, MD, Medical Director, Center for Sports Medicine, O'Connor Hospital; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Marlene DeMaio, MD, Consulting Staff, Department of Orthopedic Surgery, Assistant Professor, Bone & Joint/Sports Medicine Institute, Naval Medical Center; Jon Whitehurst, MD, Consulting Staff, Rockford Orthopedic Associates; Wylie D Lowery, Jr, MD, Department of Orthopedic Surgery, Associate Professor, George Washington University Author and Editor Disclosure Synonyms and related keywords: SCFE, hip disorder, slipped hip, adolescent hip disorder, femoral head displacement, Salter-Harris physeal fracture, Salter-Harris fracture, hip pain, hip joint pain INTRODUCTIONBackgroundSlipped capital femoral epiphysis (SCFE) persists as one of the most common adolescent hip disorders encountered in orthopedic practice. While the underlying defect may be multifactorial (eg, mechanical and constitutional factors), SCFE represents a unique type of instability of the proximal femoral growth plate. Clinically, the patient may report hip, medial thigh, and/or knee pain; an acute or insidious onset of a limp; and possible decreased range of motion. On x-ray films, the femoral head is seen displaced in varying degrees, posteriorly and inferiorly in relation to the femoral neck and within the confines of the acetabulum. Treatment is primarily operative internal fixation. FrequencyUnited StatesThe prevalence is approximately 0.7-10.8 cases per 100,000 persons. The male-to-female ratio is 2.4:1. SCFE occurs in boys aged 10-16 years and girls aged 12-14 years. In the general population, 25% of SCFE cases are bilateral. Of patients with known unilateral involvement, 60-80% develop SCFE in the contralateral hip. Children who are obese are at risk for this problem. Functional AnatomySCFE results from a Salter-Harris–type physeal fracture. In adolescents with SCFE, the epiphyseal growth plate is unusually widened, primarily due to expansion of the zone of hypertrophy. The hypertrophic zone, which constitutes 15-30% of the normal physis, accounts for up to 80% of the width of the physeal plate in affected patients. Histologically, abnormal cartilage maturation, endochondral ossification, and perichondral ring instability occur, leading to a disruption of the normal cartilaginous palisading architecture. Slippage occurs through this weakened area. In most affected patients, a variable period of prodromal symptoms or a sudden mechanical traumatic episode is reported. In addition, the position of the proximal physis normally changes from horizontal to oblique during preadolescence and adolescence, redirecting hip forces from compression forces to shear forces. Other concomitant findings in the hip include inflammatory synovitis and disorganized collagen fibrils with accumulations of proteoglycans and glycoproteins within the growth plate; however, whether these changes are a cause or a result of this disorder remains undetermined. CLINICALHistory
Physical
DIFFERENTIALSFemoral Head Avascular Necrosis Femoral Neck Fracture Femoral Neck Stress Fracture Femur Injuries and Fractures Groin Injury Osteitis Pubis
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| Drug Name | Acetaminophen (Tylenol, Feverall, Tempra) |
|---|---|
| Description | DOC for pain in patients with documented hypersensitivity to aspirin or NSAIDs, with upper GI disease, or who are taking oral anticoagulants. |
| Adult Dose | 650 mg PO q4h prn |
| Pediatric Dose | 10-15 mg/kg PO q4h prn |
| Contraindications | Documented hypersensitivity; known G-6-PD deficiency |
| Interactions | Rifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Hepatotoxicity possible in chronic alcoholism following various dose levels; severe or recurrent pain or high or continued fever may indicate a serious illness; acetaminophen is contained in many OTC products, and combined use with these products may result in cumulative doses exceeding recommended maximum dose |
| Drug Name | Hydrocodone and acetaminophen (Vicodin, Lorcet, Lortab) |
|---|---|
| Description | Drug combination for moderate to severe pain. |
| Adult Dose | 1-2 tab or cap PO q4-6h prn |
| Pediatric Dose | <12 years: 10-15 mg/kg/dose acetaminophen PO q4-6h prn; not to exceed 2.6 g/d acetaminophen >12 years: 750 mg acetaminophen PO q4h; not to exceed 10 mg hydrocodone bitartrate per dose or 5 doses/d |
| Contraindications | Documented hypersensitivity; HACE or elevated ICP |
| Interactions | Coadministration with phenothiazines may decrease analgesic effects; toxicity increases with CNS depressants or TCAs |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Tabs contain metabisulfite, which may cause hypersensitivity; caution in patients dependent on opiates because this substitution may result in acute opiate-withdrawal symptoms; caution in severe renal or hepatic dysfunction |
| Drug Name | Acetaminophen with codeine (Tylenol With Codeine [#2, #3, #4]) |
|---|---|
| Description | Indicated for mild to moderate pain. Opioid and analgesic. Acetaminophen and codeine content of Tylenol products is as follows: Tylenol #2: 300 mg acetaminophen/15 mg codeine Tylenol #3: 300 mg acetaminophen/30 mg codeine Tylenol #4: 300 mg acetaminophen/60 mg codeine |
| Adult Dose | 1-2 tab Tylenol #2 or #3 PO q4h prn 1 tab Tylenol #4 PO q4h prn |
| Pediatric Dose | Tylenol with codeine elix (120 mg acetaminophen and 12 mg codeine)/5 mL 3-6 years: 5 mL PO 3-4 times/d prn 7-12 years: 10 mL PO 3-4 times/d prn |
| Contraindications | Documented hypersensitivity |
| Interactions | Toxicity increases with CNS depressants or TCAs |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Head injury; increased ICP; acute abdomen; impaired renal, hepatic, thyroid, or adrenocortical function; prostatic hypertrophy or urethral stricture; asthma (tabs); drug abuse; elderly; debilitated; labor and delivery; pregnancy (category C); nursing mothers May cause dizziness, sedation, nausea, vomiting, constipation, urinary retention, rash, respiratory depression, hepatotoxicity (overdose) |
Have analgesic, anti-inflammatory, and antipyretic activities. Their mechanism of action is not known, but may inhibit cyclooxygenase activity and prostaglandin synthesis. Other mechanisms also may exist, such as leukotriene synthesis inhibition, lysosomal enzyme release, lipoxygenase activity, neutrophil aggregation, and various cell membrane functions.
| Drug Name | Ibuprofen (Motrin, Advil) |
|---|---|
| Description | DOC for mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis. |
| Adult Dose | 200-600 mg PO q8h prn |
| Pediatric Dose | 10 mg/kg PO q6-8h prn |
| Contraindications | Documented hypersensitivity; peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, or high risk of bleeding |
| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Category D in third trimester of pregnancy; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy |
| Drug Name | Ketoprofen (Orudis, Actron, Oruvail) |
|---|---|
| Description | Indicated for mild to moderate pain and inflammation. Small initial doses are indicated in small and elderly patients and in those with renal or liver disease. Doses >75 mg do not increase therapeutic effects. Administer high doses with caution and closely observe patient for response. |
| Adult Dose | 25-50 mg PO q6-8h prn; not to exceed 300 mg/d |
| Pediatric Dose | 3 months to 12 years: 0.1-1 mg/kg PO q6-8h >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Category D in third trimester of pregnancy; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy |
| Drug Name | Naproxen (Naprelan, Anaprox, Naprosyn) |
|---|---|
| Description | Indicated for mild to moderate pain; inhibits inflammatory reactions and pain by decreasing activity of cyclooxygenase, which results in a decrease of prostaglandin synthesis. |
| Adult Dose | 500 mg PO followed by 250 mg q6-8h; not to exceed 1.25 g/d |
| Pediatric Dose | <2 years: Not established >2 years: 2.5 mg/kg/dose PO; not to exceed 10 mg/kg/d |
| Contraindications | Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency |
| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Category D in third trimester of pregnancy; acute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia, and renal papillary necrosis may occur; patients with preexisting renal disease or compromised renal perfusion risk acute renal failure; leukopenia occurs rarely, is transient, and usually returns to normal during therapy; persistent leukopenia, granulocytopenia, or thrombocytopenia warrants further evaluation and may require discontinuation |
Following fixation, the patient is given crutches with protected weightbearing for 6-8 weeks. However, most patients are not compliant and discontinue the use of crutches after a few weeks once they have achieved an acceptable comfort level. Most children return to play once the pain has resolved. Radiographic follow-up is often continued until physeal closure is achieved to ensure the slippage has not progressed. Loss of fixation of the slip can occur but is rare.
AVN of the femoral head is thought to result from vascular damage during the time of the initial traumatic event but may result from forceful reduction during the time of surgery. The amount of energy, magnitude of epiphyseal damage and displacement, level of increased intra-articular pressure, and degree of vascular occlusion have been implicated in this process. The risk of AVN is approximately 20-50% with an attempted reduction versus less than 5% without reduction.
Chondrolysis is possible. The destruction of cartilage is believed to occur irrespective of the method of treatment. Intra-articular penetration of hardware and violation of the joint has been associated with chondrolysis. However, chondrolysis has occurred in patients who have not undergone treatment.
Leg length inequality may result from incomplete reduction, AVN, chondrolysis, or secondary coxa vara.
Osteoarthritis may result from AVN, chondrolysis, or alterations of the hip biomechanics following slippage and is a late complication.
Hardware failure, failure of epiphysiodesis, failure of slip progression, and/or infection may occur.
Most patients with SCFEs who are treated with in situ percutaneous pinning do well. However, in those cases with severe slippage and resultant deformity, long-term sequelae may result (eg, AVN, chondrolysis, leg length discrepancy, stiffness, osteoarthritis). While conservative modalities (eg, therapy, analgesics, orthotics, assistive aids) are used initially for symptomatic relief, operative intervention may be indicated. Young patients with unremitting pain, loss of motion, and stiffness secondary to chondrolysis, AVN, or osteoarthritis may require salvage hip arthrodeses. In hips that are incompletely damaged, proximal osteotomies may aid in redirecting joint forces to less damaged areas of the articular femoral head.
For excellent patient education resources, visit eMedicine's Foot, Ankle, Knee, and Hip Center and Sports Injury Center. Also, see eMedicine's patient education article Repetitive Motion Injuries.
| Media file 1: A Klein line is a line drawn along the superior border of the femoral neck that would normally pass through a portion of the femoral head. If not, slipped capital femoral epiphysis is diagnosed. | |
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| Media file 2: X-ray film of a hip following operative percutaneous fixation of a slipped capital femoral epiphysis | |
![]() | View Full Size Image | Media type: X-RAY |
Slipped Capital Femoral Epiphysis excerpt
Article Last Updated: Jun 8, 2006