eMedicine Specialties > Sports Medicine > Spine

Thoracic Discogenic Pain Syndrome: Treatment & Medication

Author: Gerard A Malanga, MD, Founder and Director, New Jersey Sports Medicine Institute; Director of Pain Management, Overlook Hospital; Director of Sports Medicine, Sports Medicine Fellowship Director, Mountainside Hospital; Clinical Chief, Rehabilitation Medicine and Electrodiagnosis, St Michael's Medical Center; Medical Director, Consultant, Horizon Healthcare Worker's Compensation Services, Blue Cross and Blue Shield Worker's Compensation
Coauthor(s): James P McLean, MD, Staff Physician, Department of Physical Medicine and Rehabilitation, Kessler Institute for Rehabilitation, University of Medicine and Dentistry of New Jersey; Irfan Alladin, MD, Staff Physician, Department of Physical Medicine and Rehabilitation, University of Medicine and Dentistry at New Jersey; Qing Tai, MD, PhD, Staff Physician, Department of Physical Medicine and Rehabilitation, University of Medicine and Dentistry of New Jersey; Stephen G Andrus, MD, Sports Medicine Fellow, Department of Physical Medicine and Rehabilitation, Kessler Institute for Rehabilitation, University of Medicine and Dentistry of New Jersey; Rachael Smith, DO, Consulting Staff, Mid-Atlantic Pain Institute, PC
Contributor Information and Disclosures

Updated: Jan 8, 2009

Treatment

Acute Phase

Rehabilitation Program

Physical Therapy

During the acute phase of a rehabilitation program for thoracic disc herniations, the focus of treatment is reducing pain symptoms. Instruction in posture and body mechanics in activities of daily living is aimed at protecting injured structures, reducing symptoms, and preventing further injury. Educate patients to avoid positions that increase intradiscal pressure, such as sitting, bending, and lifting.

A short course of bed rest of 2 days or shorter may provide some beneficial effects secondary to pain modulation and reduction of intradiscal pressure. However, longer courses of bed rest may have detrimental effects on bones, connective tissue, muscle, and cardiovascular fitness. Emphasis on activity modification, rather than strict bed rest, is recommended to avoid the unwanted effects of immobilization.

Modalities such as electrical stimulation should be limited to the initial stages of treatment so that patients can progress quickly to more active treatment that addresses restoration of motion and strengthening.

Surgical Intervention

Surgery for removal of a herniated thoracic disc is often a technically difficult procedure. The limited space available for spinal cord manipulation and the relatively tenuous blood supply increase the susceptibility of the spinal cord to injury during decompression. However, in the hands of a competent surgeon, carefully selected patients have had good outcomes.
 
No strict evidence-based indications have been developed for surgical thoracic discectomy; however, general guidelines have been determined. The general agreement is that surgery is indicated when myelopathic signs are present. These patients may benefit from early surgery because the rate of recovery diminishes when more advanced neurologic deficits are present.  Surgical indications in cases of radiculopathy are less clear, because many patients' conditions respond to conservative management. However, surgery is a viable option for patients with radicular symptoms who have not had a satisfactory response to conservative care. Patients with purely discogenic or axial pain are not generally treated surgically.10    
 
Many approaches can be used to remove herniated thoracic discs. The earliest surgical approach, used in the early 1900s, was a posterior laminectomy. That technique was used for many years until numerous studies demonstrated it produces poor results and has an unacceptable complication rate. In current practice, many other surgical options are available for thoracic disc herniations, all of which are modifications of 3 basic approaches.
 
The 3 approaches are the anterolateral, the lateral, and the posterolateral. The anterolateral approaches include transthoracic, trans-sternal, and thoracoscopic. The lateral approaches include costotransversectomy, lateral extracavitary, and parascapular. The posterolateral approaches are a transpedicular or transfacet pedicle-sparing procedure.
 
The decision regarding the most appropriate surgical approach is individualized and based on the consistency of the compressive disc, the level of herniation, its relationship to the spinal cord, and the likelihood of dural involvement. The surgeon’s familiarity with the particular approach must also be taken into consideration.

Consultations

The presence of significant myelopathic signs or progressive neurologic deficit is an absolute indication for immediate consultation with and intervention by a neurosurgeon. 

Other Treatment

Thoracic epidural steroid injections should be reserved for patients with an unacceptable level of pain that has not responded to other conservative treatments. No rationale exists for performing a series of injections.

Recovery Phase

Rehabilitation Program

Physical Therapy

Physical therapy should emphasize extension-based strengthening exercises, postural training, and education in proper posture and body mechanics. Pain during this phase should be judiciously managed with nonsteroidal anti-inflammatory drugs (NSAIDs), acetaminophen, or other oral agents to allow the patient to adequately participate in therapy.

With the progression of therapy and control of painful symptoms, a spine stabilization program should follow. With spine stabilization exercises, the goal is to teach the patient how to find and maintain a neutral spine during everyday activities. The neutral spine position is specific to the individual and is determined by the pelvic and spine posture that places the least stress on the elements of the spine and supporting structures. In classic discogenic pain, the neutral spine has an extension bias.

In classic posterior element pain and spinal stenosis, both of which may result from the ongoing degenerative cascade initiated by disc degeneration, the neutral spine may have a mild flexion bias. Dynamic spinal stabilization may be used with the McKenzie approach to provide dynamic muscular control and to protect the spine from biomechanical stresses, including tension, compression, torsion, and shear. Spinal stabilization emphasizes the synergistic activation of the trunk and spinal musculature in the midrange position.

Strengthening of the abdominal and gluteal muscle groups is emphasized, because these muscles attach to the thoracolumbar fascial support system, one of the potential spine stabilizing structures. The overall goals of this comprehensive exercise program are to reduce pain, to develop the muscular support of the trunk and spine, and, ultimately, to diminish the overall stress to the intervertebral disc and other static stabilizers of the spine.

Surgical Intervention

See Surgical Intervention under Acute Phase.

Maintenance Phase

Rehabilitation Program

Physical Therapy

The maintenance phase represents the final phase of the rehabilitation process following thoracic disc herniation or thoracic discogenic pain syndrome. Eccentric muscle strengthening exercises, including more dynamic conditioning exercises, are added to the program. In addition, sport-specific training should be incorporated so that the athlete can maintain a neutral spine in all recreational activities.

The goals of a comprehensive spine rehabilitation program are met when the individual no longer demonstrates the original symptoms and when (1) full range of motion of the spine, (2) normal strength and flexibility, and (3) normal sport-specific mechanics are demonstrated.

Medication

Various medications can be used in the treatment of thoracic disc herniations, including acetaminophen, NSAIDs, muscle relaxants, opioid analgesics, oral corticosteroids, and antidepressants. Before prescribing these medications, the physician should be aware of the contraindications, common adverse effects, and mode of action of each agent.

Nonsteroidal Anti-inflammatory Drugs (NSAIDs)

Acetaminophen is used for its anti-inflammatory effects. The dose needed to produce anti-inflammatory effects substantially differs from that for analgesic effects. Most NSAIDs achieve only analgesic effects because the dosage prescribed is too small and too infrequent to produce an anti-inflammatory effect.

The risks associated with NSAIDs are particularly pertinent in elderly persons and patients with a history of peptic ulcer diseases, hypertension, or renal insufficiency. Newer-generation NSAIDs selectively interact with the cyclooxygenase-2 (COX-2) receptors and have a lower gastrointestinal risk. Prolonged use of these medications generally is not recommended for most low back problems.

Related eMedicine topics:
Abdominal Pain in Elderly Persons
Toxicity, Nonsteroidal Anti-inflammatory Agents


Ibuprofen (Motrin, Ibuprin)

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

Adult

400-600 mg PO q6h with food

Pediatric

Not established

Coadministration with aspirin increases the risk of serious NSAID-related adverse effects; probenecid may increase the concentrations and, possibly, the toxicity of NSAIDs; 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; aspirin/NSAID-induced asthma; bleeding disorders; concurrent warfarin therapy; history of GI bleeding

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

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in patients with a history of nasal polyps, CHF, hypertension, and GI upset


Celecoxib (Celebrex)

Inhibits primarily COX-2. COX-2 is considered an inducible isoenzyme, one induced with 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 the lowest dose for each patient.

Adult

200 mg/d PO qd; alternatively, 100 mg PO bid

Pediatric

Not established

Coadministration with fluconazole may cause an increase in celecoxib plasma concentrations because of inhibition of celecoxib metabolism; coadministration with rifampin may decrease celecoxib plasma concentrations.

Pregnancy

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

Precautions

May cause fluid retention and peripheral edema; caution in patients with compromised cardiac function, hypertension, and conditions predisposing to fluid retention; caution in the presence of severe heart failure and hyponatremia because circulatory hemodynamics may deteriorate; NSAIDs may mask the usual signs of infection (caution in the presence of existing controlled infections); evaluate symptoms and signs that suggest liver dysfunction or in the presence of abnormal liver laboratory test results

Analgesics

Use of opioids should be limited to pain that is unresponsive to alternative medication. Opioids can be prescribed for acute disc herniation to facilitate participation in an active rehabilitation program. These agents should be used on a defined dosing schedule and not on an as-needed basis. An adequate baseline dose should be established to achieve analgesia. Use of nonopioid analgesics, such as tramadol, is also an option.

Related eMedicine topics:
Opioid Abuse
Toxicity, Narcotics


Oxycodone (OxyContin)

Analgesic with multiple actions similar to those of morphine; may produce less constipation, smooth muscle spasm, and depression of cough reflex than similar analgesic doses of morphine.

Adult

10 mg PO bid initially

Pediatric

Not established; adjust for weight

Phenothiazines may antagonize analgesic effects; MAOIs, general anesthesia, CNS depressants, and TCAs may increase toxicity.

Patients with a significant history of respiratory depression whose respiratory functions are not being monitored closely; severe bronchial asthma; patients with hypocarbia; paralytic ileus

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 the presence of COPD, emphysema, and renal insufficiency


Tramadol (Ultram)

Inhibits ascending pain pathways, altering perception of and response to pain. Also inhibits reuptake of norepinephrine and serotonin.

Adult

50-100 mg PO q4-6h; not to exceed 400 mg/d

Pediatric

Not established

Significantly decreases carbamazepine effects; cimetidine increases toxicity; risk of serotonin syndrome with the coadministration of antidepressants

Documented hypersensitivity; opioid-dependent patients; concurrent use of MAOIs or within 14 d; use of SSRIs, TCAs, or opioids; acute alcohol intoxication

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

Can cause dizziness, nausea, constipation, sweating, and pruritus; caution in additive sedation with alcohol or TCAs, pregnancy, breastfeeding, or seizures; abrupt discontinuation can precipitate opioid withdrawal symptoms; adjust the dose in the presence of liver disease, myxedema, hypothyroidism, and hypoadrenalism; tolerance or dependency may develop with extended use

Muscle Relaxants

Medications categorized as muscle relaxants may be helpful in some patients with low back pain; these agents seem to have additional beneficial effects when used in conjunction with NSAIDs. Muscle relaxants can be used as short-term adjunctive medications, and they should be taken at bedtime to take advantage of their sedating effects.


Cyclobenzaprine (Flexeril)

Skeletal muscle relaxant that acts centrally and reduces the motor activity of tonic somatic origins that influence both alpha and gamma motor neurons. Structurally related to TCAs and, thus, has some of the same liabilities.

Adult

10 mg PO tid initially; not to exceed 60 mg/d

Pediatric

Not established

Coadministration with MAOIs and TCAs may increase toxicity; may have an additive effect when used concurrently with anticholinergics; effects of alcohol, CNS depressants, and barbiturates may be enhanced

Acute recovery phase of MI; history of arrhythmia; heart block; conduction disturbances; hyperthyroidism

Pregnancy

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

Precautions

Caution in patients with angle-closure glaucoma and urinary hesitance


Metaxalone (Skelaxin)

Prescribed for use as a muscle relaxant. The mechanism of action not firmly established, but it may act as a CNS depressant and direct pain reliever. No direct action on contractile mechanism of striated muscle. Can be used as an adjunct pain reliever for the short term in situations of severe myofascial strain.

Adult

800 mg (2 tab) PO tid/qid

Pediatric

<12 years: Not recommended

>12 years: Administer as in adults.

Documented hypersensitivity; known tendency to drug-induced hemolytic anemia or other anemias; significantly impaired renal or hepatic function

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in patients with hepatic impairment

Corticosteroids

Corticosteroids are potent anti-inflammatory medications, and they represent a theoretically useful agent in the treatment of patients with radiculopathy due to local inflammation that results from disc injury or herniation.

Related eMedicine topics:
Corticosteroid-Induced Myopathy
Corticosteroid Injections of Joints and Soft Tissues


Prednisone (Deltasone, Orasone, Meticorten)

Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability.

Adult

60-80 mg/d PO qd or divided bid initially; taper over 8-10 d

Pediatric

Not established

Coadministration with digoxin may increase digitalis toxicity secondary to hypokalemia; estrogens may increase levels; phenobarbital, phenytoin, and rifampin may decrease levels (adjust dose); monitor for hypokalemia in patients concurrently taking diuretics

Documented hypersensitivity; viral, fungal, or tubercular skin infections

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

Hyperglycemia, edema, osteonecrosis, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, growth suppression, myopathy, and infections are possible complications of glucocorticoid use.

More on Thoracic Discogenic Pain Syndrome

Overview: Thoracic Discogenic Pain Syndrome
Differential Diagnoses & Workup: Thoracic Discogenic Pain Syndrome
Treatment & Medication: Thoracic Discogenic Pain Syndrome
Follow-up: Thoracic Discogenic Pain Syndrome
Multimedia: Thoracic Discogenic Pain Syndrome
References

References

  1. Epstein NE, Epstein JA, Rosenthal AD. Thoracic disc disease. In: Dee R, ed. Principles of Orthopedic Practice. Vol 2. New York , NY: McGraw-Hill, Inc; 1989:991-7.

  2. Mirkovic S, Cybulski GR. Thoracic disc herniations. In: Garfin SR, Vaccaro AR, eds. Orthopaedic Knowledge Update V. Rosemont, Ill: American Academy of Orthopaedic Surgeons; 1996.

  3. Awwad EE, Martin DS, Smith KR Jr, Baker BK. Asymptomatic versus symptomatic herniated thoracic discs: their frequency and characteristics as detected by computed tomography after myelography. Neurosurgery. Feb 1991;28(2):180-6. [Medline].

  4. Wood KB, Garvey TA, Gundry C, Heithoff KB. Magnetic resonance imaging of the thoracic spine. Evaluation of asymptomatic individuals. J Bone Joint Surg Am. Nov 1995;77(11):1631-8. [Medline][Full Text].

  5. Schellhas KP, Pollei SR, Dorwart RH. Thoracic discography. A safe and reliable technique. Spine. Sep 15 1994;19(18):2103-9. [Medline].

  6. Nannapaneni R, Marks SM. Posterolateral thoracic disc disease: clinical presentation and surgical experience with a modified approach. Br J Neurosurg. Oct 2004;18(5):467-70. [Medline].

  7. Brown CW, Deffer PA Jr, Akmakjian J, Donaldson DH, Brugman JL. The natural history of thoracic disc herniation. Spine. Jun 1992;17(6 suppl):S97-102. [Medline].

  8. Kaplan PA, Helms CA, Dussault R, Anderson MW, Major NM. Musculoskeletal MRI. Philadelphia, Pa: WB Saunders Company; 2001:279-332.

  9. Wood KB, Schellhas KP, Garvey TA, Aeppli D. Thoracic discography in healthy individuals. A controlled prospective study of magnetic resonance imaging and discography in asymptomatic and symptomatic individuals. Spine. Aug 1 1999;24(15):1548-55. [Medline].

  10. Boswell MV, Trescot AM, Datta S, et al, for the American Society of Interventional Pain Physicians. Interventional techniques: evidence-based practice guidelines in the management of chronic spinal pain. Pain Physician. Jan 2007;10(1):7-111. [Medline][Full Text].

  11. Albrand OW, Corkill G. Thoracic disc herniation. Treatment and prognosis. Spine. Jan-Feb 1979;4(1):41-6. [Medline].

  12. Arce CA, Dohrmann GJ. Herniated thoracic disks. Neurol Clin. May 1985;3(2):383-92. [Medline].

  13. Bohlman HH, Zdeblick TA. Anterior excision of herniated thoracic discs. J Bone Joint Surg Am. Aug 1988;70(7):1038-47. [Medline][Full Text].

  14. Broc GG, Crawford NR, Sonntag VK, Dickman CA. Biomechanical effects of transthoracic microdiscectomy. Spine. Mar 15 1997;22(6):605-12. [Medline].

  15. Carson J, Gumpert J, Jefferson A. Diagnosis and treatment of thoracic intervertebral disc protrusions. J Neurol Neurosurg Psychiatry. Feb 1971;34(1):68-77. [Medline][Full Text].

  16. Derby R, Chen Y, Lee SH, Seo KS, Kim BJ. Non-surgical interventional treatment of cervical and thoracic radiculopathies. Pain Physician. Jul 2004;7(3):389-94. [Medline][Full Text].

  17. el-Kalliny M, Tew JM Jr, van Loveren H, Dunsker S. Surgical approaches to thoracic disc herniations. Acta Neurochir (Wien). 1991;111(1-2):22-32. [Medline].

  18. Haro H, Domoto T, Maekawa S, et al. Resorption of thoracic disc herniation. Report of 2 cases. J Neurosurg Spine. Mar 2008;8(3):300-4. [Medline].

  19. Hott JS, Feiz-Erfan I, Kenny K, Dickman CA. Surgical management of giant herniated thoracic discs: analysis of 20 cases. J Neurosurg Spine. Sep 2005;3(3):191-7. [Medline].

  20. Krauss WE, Edwards DA, Cohen-Gadol AA. Transthoracic discectomy without interbody fusion. Surg Neurol. May 2005;63(5):403-8; discussion 408-9. [Medline].

  21. Le Roux PD, Haglund MM, Harris AB. Thoracic disc disease: experience with the transpedicular approach in twenty consecutive patients. Neurosurgery. Jul 1993;33(1):58-66. [Medline].

  22. Lesoin F, Rousseaux M, Autricque A, et al. Thoracic disc herniations: evolution in the approach and indications. Acta Neurochir (Wien). 1986;80(1-2):30-4. [Medline].

  23. Maiman DJ, Larson SJ, Luck E, El-Ghatit A. Lateral extracavitary approach to the spine for thoracic disc herniation: report of 23 cases. Neurosurgery. Feb 1984;14(2):178-82. [Medline].

  24. Mulier S, Debois V. Thoracic disc herniations: transthoracic, lateral, or posterolateral approach? A review. Surg Neurol. Jun 1998;49(6):599-606; discussion 606-8. [Medline].

  25. Ohnishi K, Miyamoto K, Kanamori Y, Kodama H, Hosoe H, Shimizu K. Anterior decompression and fusion for multiple thoracic disc herniation. J Bone Joint Surg Br. Mar 2005;87(3):356-60. [Medline][Full Text].

  26. Patterson RH Jr, Arbit E. A surgical approach through the pedicle to protruded thoracic discs. J Neurosurg. May 1978;48(5):768-72. [Medline].

  27. Perez-Cruet MJ, Kim BS, Sandhu F, Samartzis D, Fessler RG. Thoracic microendoscopic discectomy. J Neurosurg Spine. Jul 2004;1(1):58-63. [Medline].

  28. Perot PL Jr, Munro DD. Transthoracic removal of midline thoracic disc protrusions causing spinal cord compression. J Neurosurg. Oct 1969;31(4):452-8. [Medline].

  29. Ransohoff J, Spencer F, Siew F, Gage L Jr. Transthoracic removal of thoracic disc. Report of three cases. J Neurosurg. Oct 1969;31(4):459-61. [Medline].

  30. Regan JJ, Ben-Yishay A, Mack MJ. Video-assisted thoracoscopic excision of herniated thoracic disc: description of technique and preliminary experience in the first 29 cases. J Spinal Disord. Jun 1998;11(3):183-91. [Medline].

  31. Rosenthal D, Rosenthal R, de Simone A. Removal of a protruded thoracic disc using microsurgical endoscopy. A new technique. Spine. May 1 1994;19(9):1087-91. [Medline].

  32. Simpson JM, Silveri CP, Simeone FA, Balderston RA, An HS. Thoracic disc herniation. Re-evaluation of the posterior approach using a modified costotransversectomy. Spine. Oct 1 1993;18(13):1872-7. [Medline].

  33. Stillerman CB, Chen TC, Couldwell WT, Zhang W, Weiss MH. Experience in the surgical management of 82 symptomatic herniated thoracic discs and review of the literature. J Neurosurg. Apr 1998;88(4):623-33. [Medline].

  34. Stillerman CB, Weiss MH. Management of thoracic disc disease. Clin Neurosurg. 1992;38:325-52. [Medline].

  35. Ulivieri S, Oliveri G, Petrini C, Voltolini L, Gotti G. Transmanubrial osteomuscolar sparing approach for T1-T2 thoracic disc herniation. Minerva Chir. Oct 2008;63(5):421-3. [Medline].

  36. Wakefield AE, Steinmetz MP, Benzel EC. Biomechanics of thoracic discectomy. Neurosurg Focus. Sep 15 2001;11(3):E6. [Medline].

  37. Wenger DR, Frick SL. Scheuermann kyphosis. Spine. Dec 15 1999;24(24):2630-9. [Medline].

  38. Williams MP, Cherryman GR, Husband JE. Significance of thoracic disc herniation demonstrated by MR imaging. J Comput Assist Tomogr. Mar-Apr 1989;13(2):211-4. [Medline].

  39. Wood KB, Blair JM, Aepple DM, et al. The natural history of asymptomatic thoracic disc herniations. Spine. Mar 1 1997;22(5):525-9; discussion 529-30. [Medline].

Further Reading

Keywords

thoracic discogenic pain syndrome, thoracic disc herniation, thoracic disk herniation, thoracic degenerative disc disease, thoracic degenerative disk disease, TDH, back pain, mid back pain, midback pain, TDPS, TDP syndrome, thoracic pain, thoracic disc injuries

Contributor Information and Disclosures

Author

Gerard A Malanga, MD, Founder and Director, New Jersey Sports Medicine Institute; Director of Pain Management, Overlook Hospital; Director of Sports Medicine, Sports Medicine Fellowship Director, Mountainside Hospital; Clinical Chief, Rehabilitation Medicine and Electrodiagnosis, St Michael's Medical Center; Medical Director, Consultant, Horizon Healthcare Worker's Compensation Services, Blue Cross and Blue Shield Worker's Compensation
Gerard A Malanga, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Physical Medicine and Rehabilitation, American College of Sports Medicine, North American Spine Society, and Physiatric Association of Spine, Sports and Occupational Rehabilitation
Disclosure: Nothing to disclose.

Coauthor(s)

James P McLean, MD, Staff Physician, Department of Physical Medicine and Rehabilitation, Kessler Institute for Rehabilitation, University of Medicine and Dentistry of New Jersey
Disclosure: Nothing to disclose.

Irfan Alladin, MD, Staff Physician, Department of Physical Medicine and Rehabilitation, University of Medicine and Dentistry at New Jersey
Irfan Alladin, MD is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation
Disclosure: Nothing to disclose.

Qing Tai, MD, PhD, Staff Physician, Department of Physical Medicine and Rehabilitation, University of Medicine and Dentistry of New Jersey
Qing Tai, MD, PhD is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American Paraplegia Society, and Society for Neuroscience
Disclosure: Nothing to disclose.

Stephen G Andrus, MD, Sports Medicine Fellow, Department of Physical Medicine and Rehabilitation, Kessler Institute for Rehabilitation, University of Medicine and Dentistry of New Jersey
Stephen G Andrus, MD is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American College of Sports Medicine, American Medical Association, and Physiatric Association of Spine, Sports and Occupational Rehabilitation
Disclosure: Nothing to disclose.

Rachael Smith, DO, Consulting Staff, Mid-Atlantic Pain Institute, PC
Rachael Smith, DO is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation, American Osteopathic Association, Association of Academic Physiatrists, and Physiatric Association of Spine, Sports and Occupational Rehabilitation
Disclosure: Nothing to disclose.

Medical 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, Phi Beta Kappa, and Wilderness Medical Society
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 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

Sherwin SW Ho, MD, Associate Professor, Department of Surgery, Section of Orthopedic Surgery and Rehabilitation Medicine, University of Chicago
Sherwin SW Ho, 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.

 
 
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