eMedicine Specialties > Sports Medicine > Lower Limb

Slipped Capital Femoral Epiphysis: Treatment & Medication

Author: Kevin D Walter, MD, FAAP, Assistant Professor, Department of Pediatric Orthopaedics and Department of Pediatrics, Medical College of Wisconsin; Member of Children's Specialty Group of Children's Hospital of Wisconsin; Program Director, Children's Hospital of Wisconsin Pediatric and Adolescent Primary Care Sports Medicine
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
Contributor Information and Disclosures

Updated: Dec 17, 2009

Treatment

Acute Phase

Medical Issues/Complications

Treatment of slipped capital femoral epiphysis (SCFE) is emergent; therefore, early and accurate diagnosis is paramount. There is no role for observation or attempts at closed reduction.

Classification schemes are as follows:

  • Determine whether the SCFE is acute (<3 weeks), chronic (3+ weeks), or acute on chronic (3+ weeks of symptoms with acute exacerbation or change).
  • Determine whether the SCFE stable (able to bear weight) or unstable (non-weight bearing). This determination has become more important than acute versus chronic due to the fact that unstable patients have been found to have a high complication rate.
  • Determine the radiographic classification. This is determined by the percentage of displacement of the hip in relation to the neck. Type I is less than 33% displacement, type II is 33-50% displacement, and type III is greater than 50% displacement.

Prophylactic treatment of the asymptomatic hip remains controversial. In Europe, the majority of patients receive prophylactic fixation of the contralateral hip. Each case should be approached individually, and the benefits and risks should be weighed when contemplating surgery on the unaffected hip.

In a review of the literature, prophylactic treatment may be considered in patients younger than 10 years or patients affected by various endocrinopathies because these individuals have higher relative risks for bilateral involvement. Prophylactic treatment should also be considered in a patient or family that is unreliable. In a typical patient who presents with unilateral SCFE, the parents should be warned of possible sequential bilateral involvement. The need for close follow-up and early operative intervention if the other hip becomes symptomatic must be understood by the family.

Delays in diagnosis or treatment can be very detrimental to the patient's outcome. The slip may progress, and increased severity of SCFE leads to early degenerative arthritis. With a diagnostic or treatment delay, stable slips may become unstable, which leads to higher rates of AVN.

Surgical Intervention

At this time, immediate internal fixation in-situ using a single cannulated screw is the treatment of choice of SCFE. Fixation allows early stabilization of the slippage, enhancement of physeal closure, prevention of further slippage, and amelioration of symptoms with minimal morbidity.24,25 Unstable or grade III slips may require gentle repositioning to improve alignment. Revision of the screw fixation may be needed if the child "outgrows" the screw, placing the child at risk for a repeat slip.

Prophylactic fixation of the unaffected hip in unilateral SCFE remains controversial.3,26 Each case should be approached individually. However, stronger consideration for the prophylactic fixation should be given to patients with endocrinologic or metabolic comorbidities, or patients who fall outside of the usual age range (10-16 y).

There is evidence that if surgical intervention occurs within 24 hours of SCFE onset, there is significantly less complications (7% AVN). However, if surgical intervention occurs between 24 and 48 hours, the AVN rate dramatically increases (87.5%). This risk decreases to 32% if the procedure is done after 48 hours. True cause and effect among onset, diagnosis, and intervention cannot be truly ascertained, thus, urgency with surgical intervention is still the unquestioned rule.

Osteotomy of the proximal femur is not indicated as the primary procedure for SCFE. However, it may be needed as a secondary procedure for repositioning of the femoral head to improve functional range of motion, or as a primary procedure for patients with severe morphologic displacement.

Bone-graft epiphysiodesis in combination with internal fixation or casting is advocated by some surgeons, but the procedure is associated with a high learning curve, a high prevalence of AVN and chondrolysis, poor initial fixation, prolonged operative time, increased intraoperative blood loss, and loss of epiphyseal position.27

Historically, spica casts were used28 ; however, because of the high morbidity (eg, AVN, chondrolysis) and difficulty in applying and maintaining these casts, especially in patients who are obese, spica casts have fallen out of favor.

Recently, 2 techniques to correct moderate and/or severe SCFE were evaluated29,30 :
 
Witbreuk et al performed epiphysiodesis combined with early Imhauser intertrochanteric osteotomy in 28 patients (32 hips) to downgrade moderate and severe SCFE to diminish mechanical impingement and prevent osteoarthritis.29 At a median follow-up of 8 years (range, 2-25 y), the patients were performing well clinically, functionally, and socially. In addition, there were no radiologic signs of chondrolysis or avascular necrosis, and greater than 80% of the patients did not have signs of osteoarthritis.29

Lawane et al retrospectively evaluated the Dunn procedure in adolescents aged 10-15 years with severe SCFE (epiphyseal slippage of 60-90 degrees) with regard to avascular necrosis of the femoral head.30 Of the 25 cases, 15 achieved good clinical and radiologic results, but 10 had immediate or late complications, for a 40% complication rate. Of the 8 immediate complications (32%), 4 were necroses (16%), 2 of which resulted in arthritis; 3 were chondrolyses, all of which progressed to arthritis; and 1 was mechanical.30 Before 10-year follow-up, 2 arthrodeses and 3 hip replacements were performed. At long-term follow-up, an additional 2 late deteriorations occurred despite initial favorable clinical and radiologic outcomes.

The investigators concluded that although the Dunn procedure limits the vascular risk of surgical correction of the SCFE displacement, there are issues of concern, including "tricky" technical aspects of the procedure and the risk of necrotic complication, at rates up to 17% in other reported series.30 Lawane et al reported a necrosis rate of 16%, which they found unacceptable in view of the immediate loss of joint function in the adolescent patients. Their preferred approach to severe SCFE is arthrotomy followed by a direct approach to the displacement with associated anterior cuneiform neck resection.30

Consultations

Orthopedic surgery consultation should be immediate in cases of SCFE.

Endocrinology consultation may be indicated for patients presenting earlier than age 10 years of or later than age 16 years. Also, if there are any concerns for endocrinopathy found on history or physical examination, consultation may be necessary to help evaluate for a potential disorder.

Medication

No medical therapy is available for the treatment of slipped capital femoral epiphysis (SCFE) except symptomatic pain relief. Medications may include acetaminophen, nonsteroidal anti-inflammatory drugs, or narcotics, depending on the physician's preference.

Analgesics/Antipyretics

Pain control is essential to quality patient care. Analgesics ensure patient comfort and have sedating properties, which are beneficial for patients who have sustained trauma or who have sustained injuries.


Acetaminophen (Tylenol, Feverall, Tempra)

DOC for pain in patients with documented hypersensitivity to aspirin or NSAIDs, with upper GI disease, or who are taking oral anticoagulants.

Adult

650 mg PO q4h prn

Pediatric

10-15 mg/kg PO q4h prn

Rifampin can reduce the analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity.

Documented hypersensitivity; known G6PD deficiency

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Hepatotoxicity is 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 that exceed the recommended maximum dose.


Hydrocodone and acetaminophen (Vicodin, Lorcet, Lortab)

Drug combination for moderate to severe pain.

Adult

1-2 tab or cap PO q4-6h prn

Pediatric

<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

Coadministration with phenothiazines may decrease the analgesic effects; the toxicity increases with CNS depressants or TCAs

Documented hypersensitivity; HACE or elevated ICP

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

The tables contain metabisulfite, which may cause hypersensitivity; caution in patients who are dependent on opiates because this substitution may result in acute opiate-withdrawal symptoms; caution in the presence of severe renal or hepatic dysfunction


Acetaminophen with codeine (Tylenol With Codeine [# 2, # 3, # 4])

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

1-2 tab Tylenol #2 or #3 PO q4h prn

1 tab Tylenol #4 PO q4h prn

Pediatric

Tylenol with codeine elix (120 mg acetaminophen and 12 mg codeine)/5 mL

<3 years: Not established

3-6 years: 5 mL PO 3-4 times/d prn

7-12 years: 10 mL PO 3-4 times/d prn

>12 years: Administer as in adults

Toxicity increases with CNS depressants or TCAs

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

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; nursing mothers

May cause dizziness, sedation, nausea, vomiting, constipation, urinary retention, rash, respiratory depression, hepatotoxicity (overdose)

Nonsteroidal Anti-inflammatory Drugs (NSAIDs)

NSAIDs have analgesic, anti-inflammatory, and antipyretic activities, which make these ideal agents for treating ankle injuries. The mechanism of action of NSAIDs is not known, but they may inhibit cyclooxygenase activity and prostaglandin synthesis. Other mechanisms may exist as well, such as inhibition of leukotriene synthesis, lysosomal enzyme release, lipoxygenase activity, neutrophil aggregation and various cell membrane functions.


Ibuprofen (Motrin, Advil)

DOC for mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis.

Adult

200-600 mg PO q8h prn

Pediatric

10 mg/kg PO q6-8h prn

Coadministration with aspirin increases the risk of inducing serious NSAID-related adverse effects; probenecid may increase the concentrations and, possibly, the toxicity; may decrease the effect of hydralazine, captopril, and beta-blockers; may decrease the diuretic effects of furosemide and thiazides; may increase PT duration when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase the risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

Documented hypersensitivity; peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, or high risk of bleeding

Pregnancy

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

Precautions

Caution in patients with congestive heart failure, hypertension, and decreased renal and hepatic function; caution in the presence of anticoagulation abnormalities or during anticoagulant therapy.


Ketoprofen (Orudis, Actron, Oruvail)

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 the therapeutic effects. Administer high doses with caution, and closely observe the patient for the response.

Adult

25-50 mg PO q6-8h prn; not to exceed 300 mg/d

Pediatric

<3 months: Not established

3 months to 12 years: 0.1-1 mg/kg PO q6-8h

>12 years: Administer as in adults

Coadministration with aspirin increases the risk of inducing serious NSAID-related adverse effects; probenecid may increase the concentrations and, possibly, the toxicity; may decrease the effect of hydralazine, captopril, and beta-blockers; may decrease the diuretic effects of furosemide and thiazides; may increase PT duration when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase the risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

Pregnancy

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

Precautions

Caution in patients with congestive heart failure, hypertension, and decreased renal and hepatic function; caution in the presence of anticoagulation abnormalities or during anticoagulant therapy


Naproxen (Naprelan, Anaprox, Naprosyn)

Indicated for mild to moderate pain; inhibits inflammatory reactions and pain by decreasing the activity of cyclooxygenase, which results in a decrease of prostaglandin synthesis.

Adult

500 mg PO followed by 250 mg q6-8h; not to exceed 1.25 g/d

Pediatric

<2 years: Not established

>2 years: 2.5 mg/kg/dose PO; not to exceed 10 mg/kg/d

Coadministration with aspirin increases the risk of inducing serious NSAID-related adverse effects; probenecid may increase the concentrations and, possibly, the toxicity; may decrease the effect of hydralazine, captopril, and beta-blockers; may decrease the diuretic effects of furosemide and thiazides; may increase PT duration when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase the risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency

Pregnancy

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

Precautions

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 of the drug.

More on Slipped Capital Femoral Epiphysis

Overview: Slipped Capital Femoral Epiphysis
Differential Diagnoses & Workup: Slipped Capital Femoral Epiphysis
Treatment & Medication: Slipped Capital Femoral Epiphysis
Follow-up: Slipped Capital Femoral Epiphysis
Multimedia: Slipped Capital Femoral Epiphysis
References
Further Reading

References

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  2. Katz DA. Slipped capital femoral epiphysis: the importance of early diagnosis. Pediatr Ann. Feb 2006;35(2):102-11. [Medline].

  3. Loder RT. Controversies in slipped capital femoral epiphysis. Orthop Clin North Am. Apr 2006;37(2):211-21, vii. [Medline].

  4. Frick SL. Evaluation of the child who has hip pain. Orthop Clin North Am. Apr 2006;37(2):133-40, v. [Medline].

  5. Peterson MD, Weiner DS, Green NE, Terry CL. Acute slipped capital femoral epiphysis: the value and safety of urgent manipulative reduction. J Pediatr Orthop. Sep-Oct 1997;17(5):648-54. [Medline].

  6. Loder RT, Richards BS, Shapiro PS, Reznick LR, Aronson DD. Acute slipped capital femoral epiphysis: the importance of physeal stability. J Bone Joint Surg Am. Aug 1993;75(8):1134-40. [Medline][Full Text].

  7. Klein A, Joplin RJ, Reidy JA, Hanelin J. Roentgenographic features of slipped capital femoral epiphysis. Am J Roentgenol Radium Ther Nucl Med. Sep 1951;66(3):361-74. [Medline].

  8. Uglow MG, Clarke NM. The management of slipped capital femoral epiphysis. J Bone Joint Surg Br. Jul 2004;86(5):631-5. [Medline].

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  11. Lehmann CL, Arons RR, Loder RT, Vitale MG. The epidemiology of slipped capital femoral epiphysis: an update. J Pediatr Orthop. May-Jun 2006;26(3):286-90. [Medline].

  12. Kelsey JL, Keggi KJ, Southwick WO. The incidence and distribution of slipped capital femoral epiphysis in Connecticut and Southwestern United States. J Bone Joint Surg Am. Sep 1970;52(6):1203-16. [Medline][Full Text].

  13. Azzopardi T, Sharma S, Bennet GC. Slipped capital femoral epiphysis in children aged less than 10 years. J Pediatr Orthop B. Jan 2010;19(1):13-8. [Medline].

  14. Riad J, Bajelidze G, Gabos PG. Bilateral slipped capital femoral epiphysis: predictive factors for contralateral slip. J Pediatr Orthop. Jun 2007;27(4):411-4. [Medline].

  15. Hagglund G, Hansson LI, Ordeberg G, Sandstrom S. Bilaterality in slipped upper femoral epiphysis. J Bone Joint Surg Br. Mar 1988;70(2):179-81. [Medline][Full Text].

  16. Benson EC, Miller M, Bosch P, Szalay EA. A new look at the incidence of slipped capital femoral epiphysis in new Mexico. J Pediatr Orthop. Jul-Aug 2008;28(5):529-33. [Medline].

  17. Zupanc O, Krizancic M, Daniel M, et al. Shear stress in epiphyseal growth plate is a risk factor for slipped capital femoral epiphysis. J Pediatr Orthop. Jun 2008;28(4):444-51. [Medline].

  18. Brenkel IJ, Dias JJ, Davies TG, Iqbal SJ, Gregg PJ. Hormone status in patients with slipped capital femoral epiphysis. J Bone Joint Surg Br. Jan 1989;71(1):33-8. [Medline][Full Text].

  19. Pritchett JW, Perdue KD. Mechanical factors in slipped capital femoral epiphysis. J Pediatr Orthop. Jul-Aug 1988;8(4):385-8. [Medline].

  20. Wells D, King JD, Roe TF, Kaufman FR. Review of slipped capital femoral epiphysis associated with endocrine disease. J Pediatr Orthop. Sep-Oct 1993;13(5):610-4. [Medline].

  21. Zubrow AB, Lane JM, Parks JS. Slipped capital femoral epiphysis occurring during treatment for hypothyroidism. J Bone Joint Surg Am. Mar 1978;60(2):256-8. [Medline][Full Text].

  22. Dwek JR. The hip: MR imaging of uniquely pediatric disorders. Magn Reson Imaging Clin N Am. Aug 2009;17(3):509-20, vi. [Medline].

  23. Tins B, Cassar-Pullicino V, McCall I. The role of pre-treatment MRI in established cases of slipped capital femoral epiphysis. Eur J Radiol. Apr 23 2008;epub ahead of print. [Medline].

  24. Aronson DD, Carlson WE. Slipped capital femoral epiphysis. A prospective study of fixation with a single screw. J Bone Joint Surg Am. Jul 1992;74(6):810-9. [Medline][Full Text].

  25. Ward WT, Stefko J, Wood KB, Stanitski CL. Fixation with a single screw for slipped capital femoral epiphysis. J Bone Joint Surg Am. Jul 1992;74(6):799-809. [Medline][Full Text].

  26. Kocher MS, Bishop JA, Hresko MT, et al. Prophylactic pinning of the contralateral hip after unilateral slipped capital femoral epiphysis. J Bone Joint Surg Am. Dec 2004;86-A(12):2658-65. [Medline][Full Text].

  27. Weiner DS, Weiner S, Melby A, Hoyt WA Jr. A 30-year experience with bone graft epiphysiodesis in the treatment of slipped capital femoral epiphysis. J Pediatr Orthop. Mar 1984;4(2):145-52. [Medline].

  28. Betz RR, Steel HH, Emper WD, Huss GK, Clancy M. Treatment of slipped capital femoral epiphysis. Spica-cast immobilization. J Bone Joint Surg Am. Apr 1990;72(4):587-600. [Medline][Full Text].

  29. Witbreuk MM, Bolkenbaas M, Mullender MG, Sierevelt IN, Besselaar PP. The results of downgrading moderate and severe slipped capital femoral epiphysis by an early Imhauser femur osteotomy. J Child Orthop. Sep 26 2009;epub ahead of print. [Medline][Full Text].

  30. Lawane M, Belouadah M, Lefort G. Severe slipped capital femoral epiphysis: The Dunn's operation. Orthop Traumatol Surg Res. Nov 18 2009;epub ahead of print. [Medline].

  31. Castaneda P, Macias C, Rocha A, Harfush A, Cassis N. Functional outcome of stable grade III slipped capital femoral epiphysis treated with in situ pinning. J Pediatr Orthop. Jul-Aug 2009;29(5):454-8. [Medline].

  32. Krahn TH, Canale ST, Beaty JH, Warner WC, LourenCo P. Long-term follow-up of patients with avascular necrosis after treatment of slipped capital femoral epiphysis. J Pediatr Orthop. Mar-Apr 1993;13(2):154-8. [Medline].

  33. Larson AN, Yu EM, Melton LJ 3rd, Peterson HA, Stans AA. Incidence of slipped capital femoral epiphysis: a population-based study. J Pediatr Orthop B. Jan 2010;19(1):9-12. [Medline].

Further Reading

Related eMedicine Topics

Clinical Trials

Clinical Guidelines

Keywords

slipped capital femoral epiphysis, hip pain, pain in hip, hip joint pain, SCFE, slipped epiphysis, femoral pain, hip disorder, slipped hip, adolescent hip disorder, femoral head displacement, Salter-Harris physeal fracture, Salter-Harris fracture, femoral head avascular necrosis

Contributor Information and Disclosures

Author

Kevin D Walter, MD, FAAP, Assistant Professor, Department of Pediatric Orthopaedics and Department of Pediatrics, Medical College of Wisconsin; Member of Children's Specialty Group of Children's Hospital of Wisconsin; Program Director, Children's Hospital of Wisconsin Pediatric and Adolescent Primary Care Sports Medicine
Kevin D Walter, MD, FAAP is a member of the following medical societies: American Academy of Pediatrics and American Medical Society for Sports Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

David Y Lin, MD, Fellow, Department of Orthopedic Surgery, Section of Pediatrics, University of Tennessee Campbell Clinic
David Y Lin, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons
Disclosure: Nothing to disclose.

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
Evan Schwartz, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons and American Orthopaedic Society for Sports Medicine
Disclosure: Nothing to disclose.

Medical Editor

Anthony J Saglimbeni, MD, Staff Physician, Family Practice Residency, President, South Bay Sports and Preventive Medicine Associates; Private Practice; Team Internist, San Francisco Giants; Team Internist, West Valley College; Team Physician, Bellarmine College Prep; Team Physician, Presentation High School
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

CME Editor

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
Disclosure: Nothing to disclose.

Chief Editor

Craig C Young, MD, 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, and Phi Beta Kappa
Disclosure: Nothing to disclose.

 
 
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