OLECRANON BURSITIS

OLECRANON BURSITIS

Olecranon bursitis is inflammation of the bursa overlying the olecranon process at the proximal aspect of the ulna.

 

The bursa is located between the ulna and the skin at the posterior tip of the elbow.

PATHOPHYSIOLOGY

Normally, the olecranon bursa prevents tissue tears by providing a mechanism with which the skin can glide freely over the olecranon process.

Bursal inflammation may be caused by a variety of mechanisms. Owing to its superficial location, this bursa is susceptible to inflammation from either acute or repetitive (cumulative) trauma.

Less commonly, inflammation may result from infection (septic bursitis).

MORTALITY/MORBIDITY

AGE

This condition occurs in children and adults. In patients on long-term hemodialysis treatment, uremia or a mechanical factor (such as resting the posterior elbow during hemodialysis treatment) is thought possibly to cause the inflammation.

CLINICAL

HISTORY

PHYSICAL

CAUSES

DIAGNOSIS

LABORATORY STUDIES

IMAGING STUDIES

PROCEDURES

TREATMENT

PHYSICAL THERAPY

In general, physical and occupational therapy are not needed for this condition.

In some cases of nonseptic bursitis, however, the physician may recommend a course of physical or occupational therapy to speed recovery time.

Individuals who exhibit olecranon bursitis often are advised to apply the RICE (rest, ice, compression, elevation) method of treatment.

Physical therapy modalities (eg, phonophoresis, electrical stimulation) also may be helpful in further reducing pain and inflammation, although these modalities are not necessary for most patients with this condition.

The therapist can also complete patient education and present compensatory strategies for resting the involved upper extremity while healing takes place. If the patient's condition becomes severe and does not respond to conservative treatment, surgery may be indicated.

For the patient who undergoes bursal excision (bursectomy), physical therapy may be recommended postoperatively for regaining or maintaining the elbow's ROM and strength.

COMPLICATIONS

SURGICAL INTERVENTION

Usually, no surgical intervention is required; however, very severe cases of recalcitrant bursitis may require bursectomy.

OTHER TREATMENT

MEDICATION

For this musculoskeletal condition, medications are used primarily to decrease pain and inflammation.

Thus, the most commonly used medications are oral NSAIDs and focal corticosteroid injection in conjunction with the rest of the rehabilitation plan.

NONSTEROIDAL ANTI-INFLAMMATORY DRUGS

Can help to decrease pain and inflammation. Various oral NSAIDs can be used. The choice of NSAID is largely a matter of the adverse effect profile, as well as convenience (how frequently doses must be taken to achieve adequate analgesic and anti-inflammatory effects), patient preferences, and cost. 

IBUPROFEN (Motrin, Advil, Nuprin, Rufen)

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

Adult: 200-800 mg PO tid/qid

Pediatric:

<6 months: Not established

6 months to 12 years: 4-10 mg/kg/dose PO tid/qid

>12 years: Administer as in adults

Pregnancy

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

Precautions

Minimize risks of adverse effects by not taking multiple NSAIDs concurrently; caution in patients on anticoagulants or systemic corticosteroids and with bleeding disorders or significant alcohol use; caution in aspirin/NSAID-induced asthma; hypertension, CHF, and advanced age 

NAPROXEN (Anaprox, Naprelan, Naprosyn)

For relief of mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing activity of cyclooxygenase, which is responsible for prostaglandin synthesis.

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

Pediatric:

<2 years: Not established

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

Pregnancy

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

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 warrant further evaluation and may require discontinuation of drug 

KETOPROFEN (Oruvail, Orudis, Actron)

For relief of mild to moderate pain and inflammation.

Small doses are indicated initially in patients with small body size, elderly patients, and those with renal or liver disease.

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

Doses >75 mg do not increase therapeutic effects; administer high doses with caution and closely observe patient for response

Pediatric:

<3 months: Not established

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

>12 years: Administer as in adults

Pregnancy

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

Precautions

Caution in CHF, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy

CYCLOOXYGENASE-2 (COX-2) INHIBITORS

Although increased cost can be a negative factor, the incidence of costly and potentially fatal gastrointestinal (GI) bleeds is clearly less with cyclooxygenase-2 (COX-2) inhibitors than with traditional NSAIDs.

Ongoing analysis of cost avoidance of GI bleeds will further define the populations that will find COX-2 inhibitors the most beneficial. 

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 of celecoxib for each patient.

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

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

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

CORTICOSTEROIDS

In contrast to the widespread systemic distribution of an oral anti-inflammatory drug, a local corticosteroid injection can achieve focal placement of a potent anti-inflammatory agent at the site of maximal tenderness or inflammation.

A variety of corticosteroid preparations are available for injection. Commonly, the corticosteroid is mixed with a local anesthetic agent prior to injection. Various local anesthetic agents also are available. 

METHYLPREDNISOLONE (Solu-Medrol, Medrol, Adlone)

Corticosteroids, such as methylprednisolone, are commonly used for local injections of bursae or joints to provide a local anti-inflammatory effect while minimizing some of the GI and other risks of systemic medications.

Adult: 40 mg (1 mL) intralesionally is common for injection at many sites, often mixed with a few mL of a local anesthetic, such as 1% lidocaine.