eMedicine Specialties > Pediatrics: General Medicine > Rheumatology

Costochondritis: Treatment & Medication

Author: Joseph P Garry, MD, Director of Sports Medicine and Sports Medicine Fellowship, Associate Professor of Family Medicine and Exercise & Sport Science, Department of Family Medicine, East Carolina University Brody School of Medicine
Coauthor(s): Barry L Myones, MD, Associate Professor, Departments of Pediatrics and Immunology, Pediatric Rheumatology Section, Baylor College of Medicine; Director of Research, Pediatric Rheumatology Center, Texas Children's Hospital
Contributor Information and Disclosures

Updated: Nov 8, 2007

Treatment

Medical Care

  • Reassure patients diagnosed with costochondritis that the cause of their chest pain is neither cardiac nor malignant in origin.
  • Treatment involves conservative local care with judicious use of nonsteroidal anti-inflammatory drugs (NSAIDs) or analgesics, as necessary. Cough suppressants may be beneficial if cough is an aggravating factor.
  • Liberal use of ice is recommended for 20-minute intervals.
  • Advise relative rest for the patient's upper extremities and avoidance of possible precipitating or exacerbating activities.

Consultations

Occasional refractory cases may require consultation with the following specialists:

  • Primary care sports medicine physician
  • Rheumatologist

Activity

  • Activity restrictions include relative rest. Instruct the patient to avoid activities that exacerbate symptoms. Collision or contact sports may be limited until the patient can perform activity-specific movements without pain.
  • Applying ice after activity usually helps alleviate a significant amount of pain or discomfort.
  • Resumption of aggravating activities prior to resolution may cause relapse.

Medication

NSAIDs provide analgesia for mild-to-moderate chest pain and may modulate the presumed inflammatory process. Purely analgesic drugs (eg, acetaminophen, tramadol hydrochloride) may suffice.

Nonsteroidal anti-inflammatory drugs

These provide analgesia and may play a role in controlling inflammation.


Ibuprofen (Motrin, Advil, Ibuprin)

Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis.

Adult

400-800 mg PO q6-8h prn

Pediatric

5-10 mg/kg PO q6-8h prn

Avoid concomitant use of aspirin; may increase bleeding with anticoagulants, increase toxicity of methotrexate, and increase serum lithium levels; may decrease effects of furosemide or thiazide diuretics

Documented hypersensitivity, known hypersensitivity to aspirin or other NSAIDs; active GI bleeding, active ulcer

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

History of upper GI disease, peptic ulcer, gastric ulcer; impaired renal or hepatic function; edema, hypertension; bleeding disorder; diabetes; dehydration; pregnancy category D at third trimester


Naproxen (Aleve)

Available as OTC preparation and in prescription form; OTC preparation has faster onset of action, though limited duration of action. Prescription form is available in both pill and elixir forms and has a convenient bid-dosing schedule.

Adult

200-500 mg PO bid prn

Pediatric

<2 years: Not established
>2 years: 2.5-5 mg/kg PO q8-12h prn; not to exceed 20 mg/kg/d or 1 g/d

Avoid concomitant aspirin; may potentiate protein-bound drugs (eg, hydantoins, sulfonamides, sulfonylureas); monitor PO anticoagulants; may antagonize diuretics, beta-blockers, other antihypertensives; increased renal toxicity with ACE inhibitors; reduces methotrexate excretion; increases serum lithium levels

Documented hypersensitivity, known hypersensitivity to aspirin or other NSAIDs; active GI bleeding, active ulcer

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

Active peptic ulcer; history of GI disease; impaired renal or hepatic function; heart failure; edema; hypertension; monitor blood, hepatic, renal, and ocular function with long-term use; pregnancy category D at third trimester

Analgesics

These may be used to relieve mild-to-moderate pain.


Acetaminophen (Tylenol)

May be used to relieve mild-to-moderate pain. Inhibits prostaglandin synthetase in the CNS by inhibiting cyclooxygenase.

Adult

650-1000 mg PO q6-8h prn; not to exceed 4 g/d

Pediatric

10-15 mg/kg PO q6-8h prn; not to exceed 2.6 g/d

Rifampin can interact to reduce analgesic effects; conversely, barbiturates, carbamazepine, hydantoins, isoniazid, may increase hepatotoxicity

Documented hypersensitivity; G-6-PD deficiency

Pregnancy

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

Precautions

Hepatotoxicity reported with high or chronic dosing; severe or recurrent pain or high or continued fever may indicate a serious illness; contained in many OTC products and combined use with these products may result in cumulative doses exceeding recommended maximum dose


Tramadol hydrochloride (Ultram)

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

Adult

Gradually titrate upward over 3 d to 50-100 mg PO q4-6h; not to exceed 400 mg/d

Pediatric

<16 years: Not recommended
>16 years: Administer as in adults

Do not use concomitantly with MAOIs; may potentiate seizure risk with use of MAOIs, SSRIs, tricyclics, neuroleptics, and opioids; use caution when administering with other depressants; may potentiate digoxin activity; may be potentiated with concomitant use of CYP2D6 inhibitors (eg, quinidine, fluoxetine, paroxetine, amitriptyline)

Documented hypersensitivity; acute intoxication with alcohol; hypnotics, analgesics, opioids, or psychotropic drugs dependence

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

Initiate dose gradually to minimize nausea and vomiting; can cause dizziness, nausea, constipation, sweating, pruritus; additive sedation with alcohol and TCAs; abrupt discontinuation can precipitate opioid withdrawal symptoms; adjust dose in liver disease, myxedema, hypothyroidism, hypoadrenalism; pregnancy, breastfeeding; seizure; development of tolerance or dependency with extended use

More on Costochondritis

Overview: Costochondritis
Differential Diagnoses & Workup: Costochondritis
Treatment & Medication: Costochondritis
Follow-up: Costochondritis
References

References

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  3. Aspegren D, Hyde T, Miller M. Conservative treatment of a female collegiate volleyball player with costochondritis. J Manipulative Physiol Ther. May 2007;30(4):321-5. [Medline].

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Further Reading

Keywords

chest wall syndrome, costochondral syndrome, costosternal chondrodynia, Tietze syndrome, chest pain, costal chondritis, costochondral joint, costochondritis, costochondral cartilage, crepitus

Contributor Information and Disclosures

Author

Joseph P Garry, MD, Director of Sports Medicine and Sports Medicine Fellowship, Associate Professor of Family Medicine and Exercise & Sport Science, Department of Family Medicine, 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)

Barry L Myones, MD, Associate Professor, Departments of Pediatrics and Immunology, Pediatric Rheumatology Section, Baylor College of Medicine; Director of Research, Pediatric Rheumatology Center, Texas Children's Hospital
Barry L Myones, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American College of Rheumatology, American Heart Association, American Society for Microbiology, Clinical Immunology Society, and Texas Medical Association
Disclosure: Nothing to disclose.

Medical Editor

James M Oleske, MD, MPH, François-Xavier Bagnoud Professor of Pediatrics, Director, Division of Pulmonary, Allergy, Immunology and Infectious Diseases, Department of Pediatrics, New Jersey Medical School
James M Oleske, MD, MPH is a member of the following medical societies: Academy of Medicine of New Jersey, American Academy of Pediatrics, American Public Health Association, American Society for Microbiology, Infectious Diseases Society of America, and Pediatric Infectious Diseases Society
Disclosure: "no financial interest" None None

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc
Disclosure: Nothing to disclose.

Managing Editor

David D Sherry, MD, Professor of Pediatrics, Division of Rheumatology, University of Pennsylvania; Director of Clinical Rheumatology, Children's Hospital of Philadelphia
David D Sherry, MD is a member of the following medical societies: American College of Rheumatology and American Pain Society
Disclosure: Nothing to disclose.

CME Editor

Daniel Rauch, MD, FAAP, Director, Pediatric Hospitalist Program, Associate Professor, Department of Pediatrics, New York University School of Medicine
Daniel Rauch, MD, FAAP is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, and Society of Hospital Medicine
Disclosure: Nothing to disclose.

Chief Editor

Barry L Myones, MD, Associate Professor, Departments of Pediatrics and Immunology, Pediatric Rheumatology Section, Baylor College of Medicine; Director of Research, Pediatric Rheumatology Center, Texas Children's Hospital
Barry L Myones, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American College of Rheumatology, American Heart Association, American Society for Microbiology, Clinical Immunology Society, and Texas Medical Association
Disclosure: Nothing to disclose.

 
 
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