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Thoracic Disc Injuries
Article Last Updated: Dec 21, 2007
AUTHOR AND EDITOR INFORMATION
Section 1 of 10
Author: Kambiz Hannani, MD, Consulting Staff, Department of Orthopedic Surgery, Citrus Valley Medical Center
Kambiz Hannani is a member of the following medical societies: Phi Beta Kappa
Editors: 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; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Henry T Goitz, MD, Chief, Sports Medicine, Associate Professor, Department of Orthopaedic Surgery, Medical College of Ohio; 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; Sherwin SW Ho, MD, Associate Professor, Department of Surgery, Section of Orthopedic Surgery and Rehabilitation Medicine, University of Chicago
Author and Editor Disclosure
Synonyms and related keywords:
thoracic disc/disk herniation, thoracic degenerative disc/disk disease, thoracic DDD, thoracic herniated nucleus pulposus, thoracic HNP, thoracic disk injuries
Background
Thoracic disc injury, first described in 1838, is an uncommon site of injury owing to the stabilizing effect of the rib cage.1 The similarity of symptoms to lumbar disc herniation makes the diagnosis of a thoracic disc injury difficult,2, 3, 4, 5, 6 but the process tends to be self-limiting and rarely requires surgical intervention.4
(See also the eMedicine articles Disk Herniation and Thoracic Spine, Trauma [in the Radiology section], Thoracic Discogenic Pain Syndrome [in the Sports Medicine section], Lumbar Disc Disease [in the Neurosurgery section], and Herniated Nucleus Pulposus [in the Orthopedic Surgery section], as well as Return to Contact Sports After Spinal Surgery and Thoracoscopic Spine Surgery for Decompression and Stabilization of the Anterolateral Thoracic and Lumbar Spine on Medscape.)
For excellent patient education resources, visit eMedicine's Bone Health Center, Back, Ribs, Neck, and Head Center, Back, Neck, and Head Injury Center, and Muscle Disorders Center. Also, see eMedicine's patient education articles Back Pain and Chronic Pain.
Frequency
United States
The incidence of thoracic disc injuries is 1 in 1 million persons per year, and these injuries account for 0.25-0.75% of all disc herniations.7
Functional Anatomy
The thoracic discs are unusually stable compared with the cervical and lumbar discs. The stability of the thoracic discs is secondary to the surrounding rib cage, with the stabilizing effect of the rib articulations. However, the blood supply of the thoracic spine is more tenuous than the cervical and lumbar spine, especially at the T4-T9 watershed area, which is more prone to ischemic injury.
Sport-Specific Biomechanics
The facet orientation in the thoracic spine is vertical, with a slight medial angulation. This orientation allows for easier lateral bending and rotation versus pure bending. Biomechanical studies have shown that intervertebral discs are at the highest risk of injury when combined with bending and torsional forces. Therefore, the thoracic spine discs are at a decreased risk of injury because of the decreased bending potential in this segment of the spine. The spinal cord-to-canal ratio (the ratio of the cross-sectional area of the cord to the cross-sectional area of the spinal canal) is 40% in the thoracic spine versus 25% in the cervical spine. The thoracic spine is also naturally kyphotic. These 2 facts make the thoracic spine more sensitive to cord compression from disc herniation.
History
Determine the location and type of the patient's pain. Is the pain mainly located in the thoracolumbar spine, and is it radicular or mechanical in nature? - Thoracic disc disease may emulate the symptoms of lumbar disc disease.
- Shooting pain down the legs implies nerve root irritation versus cord compression.
- Pain in the thoracic area signifies mechanical pain that is possibly secondary to fractures, degenerative disc disease, tumors, or infections. (See also the eMedicine articles Degenerative Disk Disease and Thoracic Spine Fractures and Dislocations [in the Orthopedic Surgery section].)
- Night pain that wakes the patient is suggestive of infection or an oncologic process.
- Cord compression is present with myelopathy, which requires immediate attention.2 (See also the eMedicine articles Spinal Stenosis [in the Orthopedic Surgery section] and Spinal Cord, Topographical and Functional Anatomy [in the Neurology section].) Myelopathy is seen with the following:
- The presence of clonus or a positive Babinski reflex
- Bowel and bladder dysfunction (seen in up to 20% of symptomatic discs)
- High thoracic (T2-T5) herniation mimics cervical disc disease. (See also the eMedicine article Cervical Disc Disease.)
- Patients can present with upper extremity involvement, including Horner syndrome. (See also the eMedicine articles Horner Syndrome [in the Ophthalmology section] and Horner Syndrome [in the Oncology section].)
- If myelopathy is present, a negative result from the Hoffmann test makes cervical spine involvement unlikely. A positive result from the Hoffmann test is seen when the middle-finger metacarpophalangeal joint and the proximal interphalangeal joints are kept extended; a flexion reflex of the thumb is seen when the distal interphalangeal joint is flicked or suddenly extended. This is known as the Hoffmann sign.
- Radicular symptoms include pain/paresthesias or dysesthesias in a dermatomal distribution. Dermatome T10 is usually involved.
Physical
The physical examination for thoracic disc injuries includes the following: palpation over the thoracic spine; range-of-motion (ROM) examination of the hips, knees, and ankles; straight leg-raise test; motor and sensory examination; and reflex examination. - Palpation
- Palpate the entire region of the thoracic spine.
- Muscle spasms can be identified by palpation.
- ROM examination
- Assess the patient's ROM throughout the hips, knees, and ankles.
- A ROM examination, especially of the hip, can confirm the presence of radiculopathy versus referred pain from hip/knee pathology (eg, arthritis). (See also the Arthritis Resource Center on Medscape.)
- ROM in the thoracic spine can be affected by the type of pathology. Arthritic changes that cause mechanical pain usually limit extension; radiculopathy that is seen with disc herniation generally causes increasing pain with flexion.
- Bilateral straight leg-raise tests should be completed, and the patient's available ROM and symptoms should be noted and documented.
- Motor examination of all the lumbar roots, including L2-L4 (knee extension), L4 (inversion), L5 (dorsiflexion), and S1 (eversion and plantar flexion) is helpful for evaluating nerve root involvement in the lumbar spine and cord compression in the thoracic spine.
- Sensory examination
- Sensory examination of the dermatomes, especially in the thoracoabdominal region, can help the clinician identify the level of involvement.
- The nipple is innervated by T4; the xiphoid, T7; the umbilicus, T10; and the inguinal region, T12.
- Reflex testing
- The knee (L4) and ankle (S1) reflexes should be tested.
- The abdominal reflexes and cremasteric reflex (check for symmetry and presence) can help the clinician identify myelopathy and cord compression.
- Vascular examination of the dorsalis pedis artery, posterior tibial artery, and femoral artery can rule out other causes of the patient's symptoms.
Causes
The progressive wear and tear that is noted with degenerative disc disease increases the risk of injury via trauma. Contributing factors to disc injury include the following:
- Age
- Trauma
- Smoking
- Obesity
- Sedentary lifestyle
- Poor physical fitness
Brachial Plexus Injury
Lumbosacral Radiculopathy
Shoulder Impingement Syndrome
Thoracic Outlet Syndrome
Other Problems to Be Considered
Fractures, Rib
Herpes Zoster (in the Infectious Diseases section) (See also the eMedicine articles Postherpetic Neuralgia [in the Neurology section], Herpes Zoster [in the Emergency Medicine section], and Herpes Zoster [in the Dermatology section].)
Intrathoracic conditions - Cardiovascular, pulmonary, and mediastinal processes
Intra-abdominal causes - Hepatobiliary and gastrointestinal fibromyalgia
Osteoporosis (See also the eMedicine articles Osteoporosis (Primary), Osteoporosis (Secondary), and Osteoporosis and Spinal Cord Injury [in the Physical Medicine and Rehabilitation section], as well as Osteoporosis Resource Center and MORES May Help Identify Men at Risk for Osteoporosis on Medscape.)
Scoliosis (See also the eMedicine article Scoliosis, Idiopathic [in the Radiology section], as well as The Effect of Scoliosis Fusion on Spinal Motion: a Comparison of Fused and Nonfused Patients With Idiopathic Scoliosis, A Prospective Study of Brace Treatment Versus Observation Alone in Adolescent Idiopathic Scoliosis: a Follow-up Mean of 16 Years After Maturity, and Natural History of Progressive Adult Scoliosis on Medscape.)
Spinal causes - Infectious, neoplastic
Lab Studies
- Laboratory testing is helpful in screening for the differential diagnosis.
- Serology
Imaging Studies
Imaging studies are essential for making a diagnosis of disc injury.4, 8, 9
- Radiography
- Should be the initial examination that is ordered
- Unable to distinguish actual disc herniation
- May identify disc calcification (seen with degenerative disease in older patients)
- May help to identify infectious or oncologic causes for the patient's pain
- Magnetic resonance imaging (MRI)
- Both T1- and T2-weighted imaging are needed.10
- Sensitive for identification of disc herniation
- T2-weighted images exaggerate findings.
- Identifies calcification by low signal in T1- and T2-weighted images.
- Can identify the bony inflammation that is seen with tumors/infection
- Computed (CT) myelogram11
- Has improved bony visualization compared with MRI
- Not as sensitive for disc sequestration/migration
- Invasive relative to MRI
- Discogram
- Controversial
- Used for provocative testing for the level of involvement before surgery
Acute Phase
Rehabilitation Program
Physical Therapy
For the acute phase of a thoracic disc injury, the focus of physical therapy is to decrease the patient's symptoms with cold/heat therapy, ultrasound, and rest. Mild ROM exercises and very low-impact exercises that do not worsen the patient's symptoms are acceptable.
Medical Issues/Complications
Activity modification to minimize the patient's symptoms is important. Proper posture can help to prevent further disc injury. If oral drug usage fails to alleviate the patient's symptoms, consider steroid injection for intercostal nerve blocks. An orthosis (ie, brace) is initially acceptable for pain control but causes deconditioning over time. Thus, long-term bracing should be avoided.
Surgical Intervention
Surgical decompression is indicated in patients with myelopathy (unless improving), progressive neurologic symptoms, and worsening symptoms12, 13, 14 or lack of improvement in the patient's symptoms by 4-6 weeks of conservative management.10
Consultations
Myelopathy and progressive neurologic symptoms require emergent neurosurgical/orthopedic consultation.
Recovery Phase
Rehabilitation Program
Physical Therapy
When the patient's acute symptoms have resolved, general cardiovascular conditioning and abdominal muscle strengthening with ROM may be introduced.15
Maintenance Phase
Rehabilitation Program
Physical Therapy
Home exercises for abdominal and paraspinal muscle strengthening and cardiovascular conditioning is helpful in preventing recurrences.15
Medications are used to minimize pain and inflammation. In the early phase of a disc herniation, nonsteroidal anti-inflammatory drugs (NSAIDs) are recommended. If NSAIDs are not effective, a tapering course of steroids, such as with methylprednisolone, can be used to try to minimize the inflammatory process. In cases of severe pain, narcotics can be used in the acute phases; if pain has become a chronic problem, narcotics then become the primary modality for pain control. Muscle relaxants can be utilized to potentiate the effectiveness of NSAIDs, narcotics, or steroids.
Drug Category: Nonsteroidal anti-inflammatory drugs
NSAIDs are used to decrease the inflammatory process that is involved in disc herniation and nerve root irritation; furthermore, NSAIDs can help to decrease the pain that is associated with disc herniation.
| Drug Name | Ibuprofen (Motrin, Ibuprin) |
| Description | Drug of choice (DOC) for patients with mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis. |
| Adult Dose | 200-400 mg PO q4-6h while symptoms persist; not to exceed 3.2 g/d |
| Pediatric Dose | <6 months: Not established 6 months to 12 years: 4-10 mg/kg/dose PO tid/qid >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding |
| Interactions | Coadministration with aspirin increases the risk of inducing 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 |
| 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 |
| Drug Name | Naproxen (Naprosyn, Anaprox, Naprelan) |
| Description | For relief of mild to moderate pain; inhibits inflammatory reactions and pain by decreasing the activity of cyclooxygenase, which is responsible for prostaglandin synthesis. |
| Adult Dose | 250-500 mg PO bid; may increase to 1.5 g/d for limited periods |
| 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 the risk of inducing 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 |
| 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; increases the risk of acute renal failure in patients with preexisting renal disease or compromised renal perfusion; 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 |
| Drug Name | Diclofenac (Voltaren) |
| Description | Inhibits prostaglandin synthesis by decreasing the activity of the enzyme cyclooxygenase, which, in turn, decreases formation of prostaglandin precursors. |
| Adult Dose | 25 mg PO bid/tid; if well tolerated, increase by 25 or 50 mg qwk until satisfactory response obtained or total daily dose of 150-200 mg reached; higher doses generally do not increase effectiveness |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; do not administer into the CNS or give to patients with peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, and those with a high risk of bleeding |
| Interactions | Coadministration with aspirin increases the risk of inducing 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 |
| 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, hyperkalemia, hyponatremia, interstitial nephritis, and renal papillary necrosis may occur; increases the risk of acute renal failure in patients with preexisting renal disease or compromised renal perfusion; low white blood cell counts occur rarely, and usually return to normal in ongoing therapy; discontinuation of therapy may be necessary if there is persistent leukopenia, granulocytopenia, or thrombocytopenia |
| Drug Name | Celecoxib (Celebrex) |
| Description | Inhibits primarily COX-2. COX-2 is considered an inducible isoenzyme; it is 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 the lowest dose of celecoxib for each patient. |
| Adult Dose | 200 mg/d PO qd; alternatively, 100 mg PO bid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Coadministration with fluconazole may cause an increase in celecoxib plasma concentrations because of inhibition of celecoxib metabolism; coadministration of celecoxib 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 that predispose 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 the symptoms and signs that suggest liver dysfunction or in cases in which there are abnormal liver laboratory results |
Drug Category: Corticosteroids
Corticosteroids are potent anti-inflammatory agents that are used to relieve inflammation of the nerve roots and surrounding tissue.
| Drug Name | Prednisone (Deltasone, Meticorten, Orasone) |
| Description | May decrease inflammation by reversing increased capillary permeability and suppressing polymorphonuclear leukocyte activity. |
| Adult Dose | 5-60 mg/d PO qd or divided bid/qid; taper over 2 wk, as symptoms resolve |
| Pediatric Dose | 4-5 mg/m2/d PO; alternatively, 0.05-2 mg/kg PO divided bid/qid; taper over 2 wk, as symptoms resolve |
| Contraindications | Documented hypersensitivity; viral infection; peptic ulcer disease; hepatic dysfunction; connective tissue infections; fungal or tubercular skin infections; GI disease |
| Interactions | Coadministration with estrogens may decrease the clearance of prednisone; concurrent use with digoxin may cause digitalis toxicity secondary to hypokalemia; phenobarbital, phenytoin, and rifampin may increase the metabolism of glucocorticoids (consider increasing the maintenance dose); monitor for hypokalemia with the coadministration of diuretics. |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
|
| Precautions | Abrupt discontinuation of glucocorticoids may cause adrenal crisis; hyperglycemia, edema, osteonecrosis, myopathy, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, myasthenia gravis, growth suppression, and infections may occur with glucocorticoid use. |
| Drug Name | Methylprednisolone (Medrol, Solu-Medrol, Depo-Medrol) |
| Description | Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability. |
| Adult Dose | 2-60 mg/d PO in 1-4 divided doses, followed by a gradual reduction to the lowest level that will maintain clinical response |
| Pediatric Dose | 0.5-1.7 mg/kg/d or 5-25 mg/m2/d PO/IV/IM divided q6-12h |
| Contraindications | Documented hypersensitivity; viral, fungal, or tubercular skin infections |
| Interactions | Coadministration with digoxin may increase digitalis toxicity secondary to hypokalemia; estrogens may increase the levels of methylprednisolone; phenobarbital, phenytoin, and rifampin may decrease the levels of methylprednisolone (adjust the dose); monitor patients for hypokalemia when they are concurrently taking medication with diuretics. |
| 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. |
Drug Category: Muscle relaxants
Muscle relaxants reduce muscle spasms in the paraspinal muscles.
| Drug Name | Carisoprodol (Soma) |
| Description | Short-acting medication that may have depressant effects at the spinal cord level. |
| Adult Dose | 350 mg PO tid/qid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; acute intermittent porphyria |
| Interactions | Increases the toxicity of alcohol, CNS depressants, MAOIs, clindamycin, and phenothiazines |
| 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 | Caution in patients with renal and hepatic impairment |
| Drug Name | Cyclobenzaprine (Flexeril) |
| Description | 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 tricyclic antidepressants and, thus, carries some of their same risks. |
| Adult Dose | 20-40 mg/d PO divided bid/qid; not to exceed 60 mg/d |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; patients who have taken MAOIs within the last 14 d |
| Interactions | Coadministration with MAOIs and tricyclic antidepressants may increase toxicity; may have an additive effect when used concurrently with anticholinergics; effects of alcohol, CNS depressants, and barbiturates may be enhanced with cyclobenzaprine |
| 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 | Caution in patients with angle-closure glaucoma and those with urinary hesitance |
Drug Category: Narcotic analgesics
Narcotic analgesics are used for short-term pain control.
| Drug Name | Hydrocodone and acetaminophen (Vicodin, Lortab, Norcet) |
| Description | Drug combination indicated for short-term (<10 d) relief of moderate to severe acute pain. |
| Adult Dose | 1-2 tab PO q4-6h prn; not to exceed 5 tab/d |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; third trimester of pregnancy |
| Interactions | Coadministration with aspirin increases the risk of inducing 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; monitor PT duration closely (instruct patients to watch for signs of bleeding); may increase the risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
| 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 | Caution in individuals with impaired renal function, peptic ulcer disease, impaired thyroid function, asthma, hypertension, edema, heart failure, increased intracranial pressure, and erosive gastritis; duration of action may increase in elderly patients. |
| Drug Name | Oxycodone and acetaminophen (Percocet, Roxicet, Roxilox, Tylox) |
| Description | Drug combination indicated for the relief of moderate to severe pain. |
| Adult Dose | 1-2 tab or cap PO q4-6h prn |
| Pediatric Dose | 0.05-0.15 mg/kg/dose PO of oxycodone; not to exceed 5 mg/dose of oxycodone q4-6h prn |
| Contraindications | Documented hypersensitivity |
| Interactions | Phenothiazines may decrease the analgesic effects of this medication; toxicity increases with the coadministration of either CNS depressants or tricyclic antidepressants |
| 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 | Duration of action may increase in elderly patients; be aware of the total daily dose of acetaminophen that the patient is receiving; do not exceed 4,000 mg/24h of acetaminophen; higher doses may cause liver toxicity. |
Return to Play
Thoracic disc disease is usually self-limiting; return to play depends on the success of conservative management in controlling the pain/radiculopathy that is associated with the disc herniation.
Complications
The most serious but rare complication of thoracic disc disease is myelopathy. Myelopathic features, including hyperreflexia, weakness, and bowel/bladder dysfunction, may not improve after surgical decompression. Worsening myelopathic findings are an absolute indication for surgical decompression.
Prevention
Exercises, including cardiovascular training and abdominal/lumbar muscle training, are the primary preventive measure for thoracic disc disease.
Prognosis
Thoracic disc disease is essentially self-limiting and rarely requires surgical intervention. Most cases resolve within the first 4-6 weeks following onset.
Medical/Legal Pitfalls
- Failure to consider an alternative diagnosis such as intrathoracic lesions
- Failure to inform patients of the potential dangers of the diagnosis, including myelopathy with bowel or bladder dysfunction
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Thoracic Disc Injuries excerpt Article Last Updated: Dec 21, 2007
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