eMedicine Specialties > Sports Medicine > Hip

Snapping Hip Syndrome: Treatment & Medication

Author: Joseph P Garry, MD, Director of Sports Medicine and Sports Medicine Fellowship, Department of Family Medicine, Associate Professor of Family Medicine and Exercise & Sport Science, East Carolina University Brody School of Medicine
Coauthor(s): Walter L Jenkins, MS, PT, ATC, Interim Chair, Department of Physical Therapy, Clinical Professor, East Carolina University
Contributor Information and Disclosures

Updated: Jun 15, 2006

Treatment

Acute Phase

Rehabilitation Program

Physical Therapy

Treatment for a patient with snapping hip syndrome begins with a thorough examination. During the subjective evaluation, the clinician must question the patient to determine which actions exacerbate symptoms during daily activities and athletics. The objective examination is designed to determine the severity of pathology and to perform a biomechanical assessment. Included in the objective portion of the examination are the standard muscle-tendon unit and joint assessments. The information gathered in this portion of the examination can be used to guide specific elements of the treatment program. Muscle-tendon length and strength, joint mobility testing, and palpation of the injured area are key to a proper examination.

Biomechanical assessment of the patient includes both static (posture) and dynamic (gait/functional movement) elements. Inspect the entire lower extremity while it is static. Particular areas of attention during this portion of the examination include observation of genu recurvatum, knee flexion contracture, overpronation of the foot, hip flexion contracture, and the amount of internal or external rotation present in the lower extremity during static stance. Also take note of leg length. Gait analysis allows the clinician to confirm the findings of static examination and to observe if a movement dysfunction is present. Functional movements (eg, squatting, stair ascent/descent) may further demonstrate to the clinician the severity of the movement dysfunction. During examination, the clinician must be aware that even minor deviations in posture, gait, or functional movement can contribute to pathology.

Treatment during the acute phase consists of standard anti-inflammatory care and elimination of activities that exacerbate symptoms. Physical therapy modalities (eg, ice, ultrasound, phonophoresis, electrical stimulation, iontophoresis) may be used during this time. Activity modification depends on the severity of the pathology. Crutches may be used in severe cases, while decreasing the time and intensity of the aggravating activity is commonly used in less severe cases.

Medical Issues/Complications

In most cases, an acute event related to the onset of symptoms is not identified. During the acute phase of treatment for patients with pain associated with snapping hip syndrome, the initiation of relative rest, the application of ice, and a short course (eg, 7-14 d) of nonsteroidal anti-inflammatory drugs (NSAIDs), along with a physical therapy rehabilitation program, is the treatment of choice.

Surgical Intervention

In cases in which therapy is failing and a strong consideration remains for a possible labral tear, hip arthroscopy may be appropriate.

Recovery Phase

Rehabilitation Program

Physical Therapy

Perform this examination in a similar fashion to that described for the acute-phase examination (see Acute Phase, Physical Therapy). Again, the clinician emphasizes examination of the muscle-tendon units, joints of the lower extremity, and biomechanics of the lower extremity. Treatment programs are linked directly to examination findings. Patients are cautioned to eliminate repetitive motion activities (eg, running, cycling) until they are relatively asymptomatic. Premature return to repetitive motion activities may result in a resumption of symptoms.

External snapping hip syndrome

External snapping hip syndrome (iliotibial band, bursitis, or both) is commonly associated with physical therapy examination findings that include leg length difference (usually the long side is symptomatic), tightness in the iliotibial band on the involved side, weakness in hip abductors and external rotators, and poor lumbopelvic stability. Abnormal foot mechanics (eg, overpronation) leading to increased femoral internal rotation may also be a part of the clinical picture.

Muscle weakness, tightness, or both in the thigh or pelvis are addressed with a strengthening and stretching program. Overpronation may require a foot orthotic to assist with foot stabilization. Leg length deformities commonly require a lift in the shoe to assist with balancing the entire lower extremity (including the pelvis).

Internal snapping hip syndrome

Internal snapping hip syndrome (iliopsoas tendinitis, iliopsoas tendinosis, iliopsoas bursitis, or a combination) has a similar clinical picture. Commonly, the patient has an underlying mechanical problem in the lower extremity that eventually manifests in this region. The basis of physical therapy management is to treat the pathology with mechanical measures. Tightness, weakness, or both in the musculature of the hip and lumbopelvic region, leg length differences, and overpronation of the foot are common findings during the physical examination of patients with iliopsoas bursitis. Therapy consists of treating abnormalities identified during the physical examination.

Because the findings from the physical therapy examination are similar in iliopsoas and trochanteric bursitis, treatment of these pathologies is also similar. As described for trochanteric bursitis, every effort should be made to balance length and strength in musculature and to balance the biomechanics of the involved extremity to the uninvolved extremity. Lumbopelvic stability is particularly important in this patient population. Once treatment goals have been accomplished, restoration of normal movement patterns should decrease the mechanical stresses placed on the affected muscle, tendon, or bursa.

Medical Issues/Complications

During the rehabilitation treatment phase, the emphasis of treatment is physical therapy. Occasionally, patients may require intermittent NSAID therapy or simple analgesics as they progress in activities. A corticosteroid injection may be beneficial for those who have persistent pain despite an adequate therapy program.

Surgical Intervention

Several surgical interventions have been described for patients with persistent pain associated with a snapping hip that has failed to respond to an adequate trial of nonsurgical therapy. However, surgical intervention is rarely necessary in the management of this condition.

One of several common surgical approaches to external snapping hip syndrome can be used. The first is resection of the posterior half of the iliotibial tract at the insertion site of the gluteus maximus, with excision of the trochanteric bursa. Second, elliptical resection of a portion of the iliotibial band overlying the greater trochanter, with removal of the trochanteric bursa, can be performed. This procedure, described by Zoltan et al, was performed in 5 patients and repeated at 11 months on a single patient with a recurrence of symptoms. All patients had resolution of their snapping, were involved in sports, and self-reported significant improvement. Third, Z-plasty of the iliotibial band, resulting in lengthening of the tendon, is another option. Brignall and Stainsby described this technique in 6 patients. A single patient required a second, more extensive Z-plasty to obtain symptom resolution. In all patients, snapping was absent and pain relief was excellent.

Provencher et al reported that in 8 patients treated by Z-plasty, all but one had complete resolution of pain and 5 patients returned to activities such as daily running, hiking, or cycling. Finally, a step cut procedure involving the iliotibial tract over the greater trochanter was recently described by White et al in which 14 of 16 patients had resolution of pain and symptoms, though it was unclear at what level of activity they were able to return.

Several options are also available for surgical treatment of internal snapping hip syndrome. A lengthening procedure can be performed on the iliopsoas tendon, typically by partial release of the tendon. Jacobson and Allen described the results of this procedure after it was performed in 20 hips of 18 patients. At an average of 25 months of follow-up, 85% reported they were "much better." One patient reported no change in snapping and an increase in pain. Another 5 patients reported recurrence of snapping but with a reduced frequency and intensity of pain. Three patients reported subjective weakness in hip flexion; however, only a single patient had to modify his activity as a result of such weakness.

Gruen et al reported 73% of patients returned to previous athletic activities, with 45% also returning to their previous level of athletic participation following surgery. Hoskins et al reviewed their experience with surgical correction by iliopsoas tendon fractional lengthening in 92 cases. Complications were noted in one third of patients and mostly included persistent hip pain, sensory deficits, and hip flexor weakness.

Another option is resection of the bony prominence of the lesser trochanter. A third option is complete release of the iliopsoas tendon. In a case series of 14 patients (16 hips), this procedure resulted in resolution of snapping in 63%, occasional snapping in 31%, and no change in snapping in a single patient. Pain resolved in 75% and was improved in the remaining 25% of patients at an average follow-up of 18 months. Two patients reported subjective weakness of hip flexion higher than 90°, but they regarded this to be a minor inconvenience.

Dobbs et al recently reported outcomes for surgical fractional lengthening of the iliopsoas tendon in adolescents (mean age 15 y). At 4-year mean follow-up, all patients had returned to their preoperative level of activity without subjective weakness.

All procedures generally have good outcomes in terms of decreased snapping and pain at follow-up.

Consultations

Consider referring those patients who are not responding well to medical and physical therapy for either an injection (interventional radiologist or orthopedic surgeon) or potential surgical evaluation (orthopedic surgeon).

Other Treatment (Injection, manipulation, etc.)

Corticosteroid injection is indicated for patients with prolonged symptoms despite an adequate course of rehabilitation. The injection is administered under direct visualization via ultrasonic or bursographic guidance and consists of a combination of a corticosteroid (eg, betamethasone, triamcinolone) and local anesthetic (eg, lidocaine, bupivacaine). This combination may be injected either around the iliopsoas tendon or into the iliopsoas bursa.

Maintenance Phase

Rehabilitation Program

Physical Therapy

Once symptoms have decreased and the patient is able to return to daily and athletic activities, a maintenance program of stretching and strengthening can be initiated. Programs typically consist of light aerobic activity (warmup) followed by stretching and strengthening. Maintenance of the proper hamstring, hip flexor, hip adductor, and iliotibial band length is important for reducing recurrences. Likewise, recommend a maintenance-level strength-training program at least twice a week to assist with lumbopelvic and lower extremity stability. Patients are typically started on a home program during the later stages of the recovery phase. The same home program can be modified for the maintenance phase of rehabilitation.

Medication

NSAIDs are the drugs of choice for treating pain associated with snapping hip syndrome. This class of drugs provides good analgesia and possible anti-inflammatory effects for concomitant conditions.

Nonsteroidal anti-inflammatory drugs

These drugs have analgesic, anti-inflammatory, and antipyretic activities. Mechanism of action is not known, but NSAIDs may inhibit cyclooxygenase (COX) activity and prostaglandin synthesis. Other mechanisms may coexist, such as inhibition of leukotriene synthesis, lysosomal enzyme release, lipoxygenase activity, neutrophil aggregation, and various cell-membrane functions.


Ibuprofen (Ibuprin, Advil, Motrin)

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

Adult

600-800 mg PO q6-8h; not to exceed 3.2 g/d

Pediatric

10-20 mg/kg/d PO divided tid/qid

May decrease effects of loop diuretics with coadministration; coadministration with anticoagulants may increase PT (monitor and watch for signs of bleeding); may increase serum lithium levels and risk of methotrexate toxicity; probenecid may increase toxicity

Documented hypersensitivity to ibuprofen, other NSAIDs, or aspirin; peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, and high risk of bleeding

Pregnancy

B - Usually safe but benefits must outweigh the risks.

Precautions

Caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy; monitor blood, hepatic, renal, and ocular function with long-term use; discontinue if visual or liver dysfunction occurs


Naproxen (Anaprox, Naprelan, Naprosyn)

For relief of mild to moderate pain; inhibits inflammatory reactions and pain by decreasing activity of COX, which is responsible for prostaglandin synthesis. May demonstrate more analgesia compared to ibuprofen.

Adult

250-500 mg PO bid

Pediatric

<2 years: Not recommended
>2 years: 2.5-5 mg/kg/dose PO bid

Probenecid may increase toxicity; may decrease effects of loop diuretics with coadministration; coadministration with anticoagulants may prolong PT (watch for signs of bleeding); may increase serum lithium levels and risk of methotrexate toxicity (eg, stomatitis, bone marrow suppression, nephrotoxicity)

Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; third trimester of pregnancy

Pregnancy

B - Usually safe but benefits must outweigh the risks.

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 drug

Cyclooxygenase-2 inhibitors

Although increased cost can be a negative factor, the incidence of expensive and potentially fatal GI bleeds is clearly less with COX-2 inhibitors than with traditional NSAIDs. Ongoing analysis of cost avoidance of GI bleeds will further define populations that will benefit most from COX-2 inhibitors.


Celecoxib (Celebrex)

Inhibits primarily COX-2. COX-2 is considered an inducible isoenzyme, induced during pain and inflammatory stimuli. Inhibition of COX-1 may contribute to NSAID GI toxicity. At therapeutic concentrations, COX-1 isoenzyme is not inhibited, thus GI toxicity may be decreased. Seek lowest dose for patient.

Adult

100 mg PO bid or 200 mg PO qd

Pediatric

Not established

Caution with drugs that inhibit CYP2C9 (eg, fluconazole) or are metabolized by CYP2D6; may antagonize or increase risk of renal failure with ACE inhibitors or diuretics; increased risk of GI bleed with concomitant use of aspirin or corticosteroids; monitor warfarin because INR may be increased; may potentiate effects of lithium

Documented hypersensitivity to sulfonamides; third trimester of pregnancy

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Not recommended for patients with severe renal disease; discontinue if liver disease develops; monitor for GI ulcer/bleed in patients at high risk for GI ulcer, edema, or heart failure

Analgesic agents

Simple analgesics may be preferred for conditions in which NSAIDs are not advised or for which an underlying inflammatory process is doubtful.


Acetaminophen (Tylenol, Panadol, Aspirin-Free Anacin)

DOC for pain in patients with documented hypersensitivity to aspirin or NSAIDs or those diagnosed with upper GI disease or on oral anticoagulants.

Adult

650-1000 mg PO q6-8h

Pediatric

15 mg/kg/dose PO q6-8h

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

Caution with hepatic dysfunction, pregnancy, and nursing; hepatotoxicity can occur in chronic alcoholism at various dosages; severe or recurrent pain or high or continued fever may indicate a serious illness

More on Snapping Hip Syndrome

Overview: Snapping Hip Syndrome
Differential Diagnoses & Workup: Snapping Hip Syndrome
Treatment & Medication: Snapping Hip Syndrome
Follow-up: Snapping Hip Syndrome
References

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Further Reading

Keywords

iliotibial band subluxation, iliopsoas syndrome, external snapping hip syndrome, internal snapping hip syndrome, hip disorder, hip injury, snapping hip

Contributor Information and Disclosures

Author

Joseph P Garry, MD, Director of Sports Medicine and Sports Medicine Fellowship, Department of Family Medicine, Associate Professor of Family Medicine and Exercise & Sport Science, East Carolina University Brody School of Medicine
Joseph P Garry, MD is a member of the following medical societies: American Academy of Family Physicians, American College of Sports Medicine, American Heart Association, American Medical Society for Sports Medicine, North American Primary Care Research Group, and North Carolina Medical Society
Disclosure: Nothing to disclose.

Coauthor(s)

Walter L Jenkins, MS, PT, ATC, Interim Chair, Department of Physical Therapy, Clinical Professor, East Carolina University
Walter L Jenkins, MS, PT, ATC is a member of the following medical societies: American Orthopaedic Society for Sports Medicine
Disclosure: Nothing to disclose.

Medical Editor

Andrew D Perron, MD, Residency Director, Department of Emergency Medicine, Maine Medical Center
Andrew D Perron, MD is a member of the following medical societies: American College of Emergency Physicians, American College of Sports Medicine, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Russell D White, MD, Professor of Medicine, Department of Community and Family Medicine, University of Missouri-Kansas City School of Medicine, Truman Medical Center Lakewood
Disclosure: Nothing to disclose.

CME Editor

Jon Whitehurst, MD, Consulting Staff, Rockford Orthopedic Associates
Disclosure: Nothing to disclose.

Chief Editor

William Jay Bryan, MD, Clinical Professor, Department of Orthopedic Surgery, Baylor University College of Medicine
William Jay Bryan, MD is a member of the following medical societies: Texas Orthopaedic Association
Disclosure: Nothing to disclose.

 
 
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