eMedicine Specialties > Rheumatology > Infectious Arthritis

Gonococcal Arthritis: Treatment & Medication

Author: Michael P Keith, MD, FACP, Chief of Rheumatology, National Naval Medical Center; Assistant Professor of Medicine, Uniformed Services University of the Health Sciences
Coauthor(s): Robert John Oglesby, MD, Chief of Rheumatology Service, Department of Medicine, Walter Reed Army Medical Center; Associate Professor of Medicine, Uniformed Services University of the Health Sciences
Contributor Information and Disclosures

Updated: Jul 27, 2009

Treatment

Medical Care

The management of acute septic arthritis is discussed in the eMedicine article Septic Arthritis. When septic arthritis is suspected, empiric antibiotics directed against likely pathogens should be used until confirmatory laboratory data are available. Antibiotic coverage in healthy hosts should initially include gram-positive organisms, which account for approximately 80% of nongonococcal monoarthritis cases. S aureus accounts for 60%, non–group A Streptococcus species cause 15%, and Streptococcus pneumoniae cause 3%. Gram-negative organisms, accounting for another 18%, should be covered in patients who are immunocompromised, elderly, or otherwise at risk.

Additional management considerations for gonococcal arthritis include the following:

  • Most patients with suspected acute infectious arthritis, including gonococcal arthritis, should be hospitalized to establish a diagnosis and to monitor for improvement or complications. Daily synovial fluid drainage is recommended for purulent effusions associated with gonococcal arthritis. Surgical drainage is needed when arthrocentesis is ineffective. The transition to oral antibiotics can usually be made 24-48 hours after clinical improvement.
  • A thorough travel history for the patient and any sexual partners is important in selecting initial therapy for gonococcal infections. Quinolone-resistant N gonorrhoeae (QRNG) is common in the Pacific and parts of Asia and is increasing in the United States, particularly on the West Coast.4 For this reason, the Centers for Disease Control (CDC) no longer recommends quinolones for the treatment of gonococcal infections.11
  • According to 2006 CDC guidelines, the initial treatment of choice for gonococcal arthritis or disseminated gonococcal infection (DGI) in adults is ceftriaxone 1 g IM or IV every 24 hours.12 Alternatives include ceftizoxime 1 g IV q8h or cefotaxime 1 g IV q8h.12 In patients intolerant of cephalosporins, spectinomycin 2 g IM every 12 hours is another option12 ; however, this antibiotic may not be readily available.13
  • The April 2007 update of CDC guidelines states that fluoroquinolones are no longer recommended in the treatment of gonococcal infections in the United States.11 The recommendation was based on analysis of new data from the CDC's Gonococcal Isolate Surveillance Project (GISP), which showed the proportion of fluoroquinolone-resistant (QRNG) gonorrhea cases in heterosexual men reached 6.7% in the first half of 2006, an 11-fold increase from 0.6% in 2001.11 This effectively limits treatment of gonorrhea to drugs in the cephalosporin class (see above).
  • Fluoroquinolones may be considered as alternative agents for DGI in patients unable to take cephalosporins if antimicrobial susceptibility can be documented with culture results. Fluoroquinolone regimens include ciprofloxacin (400 mg IV q12h; 400 mg PO bid), ofloxacin (400 mg IV/PO q12h) or levofloxacin (250 mg/d IV; 500 mg/d PO).
  • Oral regimens that can be started 24-48 hours after initial improvement include the following:
    • Cefixime 400 mg PO bid14 (once again available in the United States via Lupin Pharmaceuticals, Inc., of Baltimore, MD)
    • Cefixime suspension 500 mg PO bid
    • Cefpodoxime 400 mg PO bid13 (clinical study ongoing)
  • Patients should continue oral antibiotics for at least 1 week.
  • Special situations include pregnant and pediatric patients (<8 y). These patients should not be treated with quinolones or tetracyclines. Pregnant patients with gonococcal infections should be treated with a recommended cephalosporin.12 Spectinomycin is indicated for patients who cannot tolerate a cephalosporin. Pediatric patients can be treated with ceftriaxone 50 mg/kg/d IV or IM for 7 days. Data are insufficient to support the use of oral cephalosporins for DGI or arthritis in children.
  • Examine patients with DGI for clinical evidence of endocarditis and meningitis. These patients require ceftriaxone 1-2 g IV every 12 hours.12 Patients with endocarditis require much longer courses of antibiotics (4-6 wk) and may require surgical intervention.
  • Patients with confirmed diagnosis of a localized gonococcal infection can probably be discharged with outpatient medications if they are considered reliable for follow-up care. Synovial effusions may require a longer duration of antibiotics, but open drainage is rarely required. Intra-articular antibiotics have no known benefit.
  • Because 30%-50% of patients are co-infected with Chlamydia, test all patients and treat with azithromycin (1 g PO as a single dose) or doxycycline (100 mg PO bid for 7 d).12 Alternatives for pregnant patients include erythromycin (500 mg PO qid for 7 d) or amoxicillin (500 mg tid for 7 d). Regimens for the treatment of chlamydial infection in children include the following:12
    • Children who weigh less than 45 kg - Erythromycin base or ethylsuccinate 50 mg/kg PO divided qid for 14 days
    • Children who weigh more than 45 kg but who are younger than 8 years - Azithromycin 1 g PO as a single dose
    • Children older than 8 years - Azithromycin 1 g PO in a single dose or doxycycline 100 mg PO bid for 7 days
  • Patients should be advised to refer their sexual partners for evaluation and treatment.

Surgical Care

Open drainage or arthroscopy of infected joints is needed when arthrocentesis is insufficient. However, joint effusions in gonococcal arthritis rarely result in permanent damage.

Consultations

  • Consider consulting a rheumatologist for assistance in the evaluation and management of septic joints.
  • Consider consulting an infectious disease specialist for management of DGI cases and determination of optimal antibiotic therapy later in the course of the disease.
  • Consider consulting a cardiologist if acute endocarditis is suspected.
  • Consulting an orthopedist may be required for arthroscopic or surgical drainage of an inaccessible joint (eg, hip) or for failure of nonsurgical management (daily aspiration).

Activity

Bedrest during inpatient status and brief immobilization of the septic joint aid in decreasing pain, especially when nonsteroidal anti-inflammatory drugs (NSAIDs) are not used.

Medication

The goals of pharmacotherapy are to eradicate the infection, to reduce morbidity, and to prevent complications.

See Medical Care.

Antibiotics

These agents are indicated to treat gonococcal infection. Agents effective against chlamydial infection are included because of the significant co-infection rate.


Ceftriaxone (Rocephin)

Ceftriaxone is the DOC for disseminated gonococcal infection (DGI) or gonococcal arthritis, according to CDC guidelines. Bactericidal action is through inhibition of cell wall synthesis. No activity against Chlamydia.

Adult

DGI or gonococcal arthritis: 1g IM or IV q24h

Pediatric

50 mg/kg IV q24h

Probenecid and loop diuretics may increase cephalosporin levels; coadministration with aminoglycosides may increase nephrotoxicity

Pregnancy

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

Precautions

Adjust dose in renal impairment; caution in breastfeeding patients; cross-allergenicity with penicillins possible (caution in patients with known penicillin allergy)


Cefotaxime (Claforan)

An alternative third-generation cephalosporin to ceftriaxone for DGI or gonococcal arthritis. Bactericidal action is through inhibition of cell wall synthesis. No activity against Chlamydia.

Adult

DGI or gonococcal arthritis: 1 g IV q8h

Pediatric

Not specified in CDC guidelines
<50 kg: 50-180 mg/kg IV/IM divided q4-6h
>50 kg: Administer as in adults; not to exceed 12 g; dose increased in patients with meningitis

Probenecid and loop diuretics may increase cephalosporin levels; coadministration with aminoglycosides may increase nephrotoxicity

Pregnancy

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

Precautions

Adjust dose in renal impairment; caution in breastfeeding patients; cross-allergenicity with penicillins possible (caution in patients with known penicillin allergy)


Ceftizoxime (Cefizox)

Third-generation cephalosporin with broad-spectrum, gram-negative activity. May be used as an alternative to ceftriaxone for gonococcal arthritis or DGI. Lower efficacy against gram-positive organisms. Higher efficacy against resistant organisms. Arrests bacterial growth by binding to one or more penicillin-binding proteins.

Adult

1-2 g IV q8-12h

Pediatric

<6 months: Not established
>6 months: 50 mg/kg PO q6-8h

Coadministration of aminoglycosides increases nephrotoxicity; probenecid may increase effects

Pregnancy

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

Precautions

Adjust dose in renal impairment; transaminitis, anemia, leukopenia, thrombocytopenia, transient elevations in BUN/creatinine levels, or GI adverse effects may occur


Cefixime (Suprax)

By binding to one or more of the penicillin-binding proteins, it arrests bacterial cell wall synthesis and inhibits bacterial growth. In 2008, Morbidity and Mortality Weekly Report reported that manufacture of this medication resumed in the United States.14 It is the only oral cephalosporin that the CDC recommends for use in patients with DGI or gonococcal arthritis.

Adult

400 mg PO qd

Pediatric

<6 years: Not established
>6 years: 8 mg/kg/d of susp PO

Coadministration of aminoglycosides increases nephrotoxicity; probenecid may increase effects of cefixime

Pregnancy

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

Precautions

Adjust dose in renal impairment; GI adverse effects, hepatotoxicity, headaches, dizziness, thrombocytopenia, and leukopenia may occur


Doxycycline (Vibramycin)

Commonly used as a cotreatment for suspected Chlamydia infection. May be used in complicated cases of gonococcal urethritis but not recommended for septic arthritis from gonococcus or a disseminated infection. Bacteriostatic by inhibiting bacterial protein synthesis.

Adult

100 mg PO bid for 7 d

Pediatric

<8 years: Not recommended
>8 years: 100 mg PO bid for 7d

Bioavailability decreases with antacids that contain aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of PO contraceptives, causing breakthrough bleeding and increased risk of pregnancy

Documented hypersensitivity; severe hepatic dysfunction

Pregnancy

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

Precautions

Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (<8 y) can cause permanent discoloration of teeth; Fanconi-like syndrome may occur with outdated tetracyclines; drink fluids to reduce risk of esophageal irritation


Azithromycin (Zithromax)

Alternative to doxycycline as cotreatment aimed at Chlamydia infection. Ideal for the noncompliant patient because may be given as a one-time dose. Not a cited DOC for gonococcal arthritis or DGI.

Adult

1 g PO once

Pediatric

<45 kg: Not recommended
>45 kg but <8 years: 1 g PO once
>8 years: 1 g PO once

May increase toxicity of theophylline, warfarin, and digoxin; effects are reduced with coadministration of aluminum and/or magnesium antacids; increases cyclosporine levels, increasing risk of toxicity; increases effect of warfarin and triazolam, carbamazepine, hexobarbital, and phenytoin

Documented hypersensitivity; hepatic impairment; administration with pimozide

Pregnancy

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

Precautions

Site reactions can occur with IV route; bacterial or fungal overgrowth may result with prolonged antibiotic use; may increase hepatic enzymes and cholestatic jaundice; caution in patients with impaired hepatic function, prolonged QT intervals, or pneumonia; caution in patients who are hospitalized, geriatric, or debilitated; although rare, reports of allergic reactions (including anaphylaxis), Stevens-Johnson syndrome, and toxic epidermal necrolysis complicating therapy exist; adverse effects include nausea, vomiting, diarrhea, and abdominal pain


Erythromycin (E-mycin)

Alternative to doxycycline for Chlamydia infection. Medication used to cotreat Chlamydia infection in pregnancy. Not a cited DOC for treatment of gonococcal arthritis or DGI. Acts through inhibition of bacterial protein synthesis.

Adult

500 mg PO qid for 7 days

Pediatric

50 mg/kg/d PO divided q6h for 14 days

Coadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis; reported antagonism between clindamycin and erythromycin; may result in ergot toxicity when used concomitantly with ergotamines; may increase the effect of various benzodiazepines through decreased clearance

Documented hypersensitivity; hepatic impairment

Pregnancy

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

Precautions

Reports of severe allergic reactions include SJS and toxic epidermal necrolysis; reports of hepatic dysfunction, including increased liver enzymes and hepatocellular and/or cholestatic hepatitis; monitor creatine kinase and serum transaminase levels in patients receiving concomitant lovastatin and erythromycin; may exacerbate symptoms of weakness in myasthenia gravis; adverse effects include nausea, vomiting, diarrhea, abdominal pain, and loss of appetite; reports of transient reversible hearing loss (in patients with renal dysfunction)


Amoxicillin (Amoxil, Biomox, Trimox)

According to CDC guidelines, amoxicillin may be used for the treatment of chlamydia in pregnant women. Not a cited DOC for DGI or gonococcal arthritis.

Adult

500 mg PO tid for 7 d

Pediatric

Not established

Coadministration with warfarin or heparin increases risk of bleeding; probenecid decreases renal tubular secretion of amoxicillin; may reduce efficacy of PO contraceptives; may increase incidence of rashes in patients on allopurinol

Pregnancy

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

Precautions

Caution in patients with history of multiple medication allergies, hepatic dysfunction, and breastfeeding women (excreted in breast milk); pseudomembranous colitis, bone marrow suppression, or CNS effects may occur


Spectinomycin (Trobicin)

Inhibits protein synthesis in bacterial cells. Site of action is 30S ribosomal subunit and is structurally different from related aminoglycosides. Recommended by the CDC as an option in patients intolerant of cephalosporin antibiotics12 ; however, this medication is not currently manufactured in the United States and may not be available.15

Adult

2 g IM q12h

Pediatric

Not established

Pregnancy

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

Precautions

Benzyl alcohol used as a diluent is associated with fatal gasping syndrome in infants; antibiotics may mask or delay symptoms of incubating syphilis; perform a serologic test for syphilis in all patients with gonorrhea at time of diagnosis followed by additional test after 3 mo; monitor clinical effectiveness to detect resistance by N gonorrhoeae; fever, nausea, and urticaria following injection, anaphylaxis, anemia, or transiently reduced CrCl may occur


Levofloxacin (Levaquin)

Used to treat complicated and uncomplicated skin and skin structure infections. Fluoroquinolones should be used empirically in patients likely to develop exacerbation due to organisms resistant to other antibiotics. This is the L stereoisomer of the D/L parent compound ofloxacin, the D form being inactive. Good monotherapy with extended coverage against Pseudomonas species, as well as excellent activity against pneumococcus. Agent acts by inhibition of DNA gyrase activity. Oral form has a reported bioavailability of 99%. New CDC guidelines no longer recommend fluoroquinolones because of resistance. May be used as alternative for DGI in patients unable to take cephalosporins if culture shows sensitivity to fluoroquinolones.

Adult

Complicated skin infection: 750 mg/d PO/IV for 7-14 d
Uncomplicated skin infection: 500 mg/d PO for 7-14 d

Pediatric

<18 years: Not recommended
>18 years: Administer as in adults

Concomitant use of theophylline may be associated with cardiac arrest, seizure, status epilepticus, and respiratory failure; antacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; ciprofloxacin reduces therapeutic effects of phenytoin; probenecid may increase ciprofloxacin serum concentrations; may increase toxicity of caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT)

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

In prolonged therapy, periodically evaluate organ system functions (eg, renal, hepatic, hematopoietic); adjust dose in patients with renal impairment; superinfections may occur with prolonged or repeated antibiotic therapy; associated with various CNS effects, including dizziness, psychosis, depression, increased intracranial pressure, convulsions, and suicidal ideation; caution in patients with known CNS disease, illness, or medications that may predispose to seizures; phototoxicity has been reported (avoid excessive sunlight), arthralgias and tendinopathies may occur, including tendon rupture; levofloxacin is also excreted in breast mild and should not be used in nursing mothers


Ciprofloxacin (Cipro)

Useful for initial therapy when given intravenously and for oral therapy after initial response to intravenous therapy. Also effective against Chlamydia. Can be used to treat patients who are penicillin allergic. Do not use in pregnant or pediatric persons. New CDC guidelines no longer recommend fluoroquinolones because of resistance. May be used as alternative for DGI in patients unable to take cephalosporins if culture shows sensitivity to fluoroquinolones.

Adult

DGI or gonococcal arthritis: 400 mg q12h IV or 500 mg q12h PO

Pediatric

<18 years: Not recommended
>18 years: Administer as in adults

Concomitant use of theophylline may be associated with cardiac arrest, seizure, status epilepticus, and respiratory failure; antacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; ciprofloxacin reduces therapeutic effects of phenytoin; probenecid may increase ciprofloxacin serum concentrations; may increase toxicity of caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT)

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

In prolonged therapy, periodically evaluate organ system functions (eg, renal, hepatic, hematopoietic); adjust dose in renal impairment; superinfections may occur with prolonged or repeated antibiotic therapy; associated with various CNS effects, including dizziness, psychosis, depression, increased intracranial pressure, convulsions, and suicidal ideation; caution in patients with known CNS disease, illness, or medications that may predispose to seizures; phototoxicity has been reported (avoid excessive sunlight), arthralgias and tendinopathies may occur, including tendon rupture; not for use in breastfeeding mothers


Ofloxacin (Floxin)

Useful medication for initial therapy when given IV and for oral therapy after an initial response to IV therapy. Also effective against Chlamydia and can be used to treat patients who are penicillin allergic. Do not use in pregnant or pediatric population. New CDC guidelines no longer recommend fluoroquinolones because of resistance. May be used as alternative for DGI in patients unable to take cephalosporins if culture shows sensitivity to fluoroquinolones.

Adult

DGI or gonococcal arthritis: 400 mg IV or PO q12h

Pediatric

<18 years: Not recommended
>18 years: Administer as in adults

Concomitant use of theophylline may be associated with cardiac arrest, seizure, status epilepticus, and respiratory failure; antacids, iron salts, and zinc salts may reduce serum levels; administer antacids 2-4 h before or after fluoroquinolones; cimetidine may interfere with metabolism of fluoroquinolones; ciprofloxacin reduces therapeutic effects of phenytoin; probenecid may increase ciprofloxacin serum concentrations; may increase toxicity of caffeine, cyclosporine, and digoxin (monitor digoxin levels); may increase effects of anticoagulants (monitor PT)

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

In prolonged therapy, periodically evaluate organ system functions (eg, renal, hepatic, hematopoietic); adjust dose in patients with renal impairment; superinfections may occur with prolonged or repeated antibiotic therapy; associated with various CNS effects, including dizziness, psychosis, depression, increased intracranial pressure, convulsions, and suicidal ideation; caution in patients with known CNS disease, illness, or medications that may predispose to seizures; phototoxicity has been reported (avoid excessive sunlight), arthralgias and tendinopathies may occur, including tendon rupture; ofloxacin is also excreted in breast milk and should not be used in nursing mothers

More on Gonococcal Arthritis

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

References

  1. Dalla Vestra M, Rettore C, Sartore P, Velo E, Sasset L, Chiesa G, et al. Acute septic arthritis: remember gonorrhea. Rheumatol Int. Nov 2008;29(1):81-5. [Medline].

  2. Bardin T. Gonococcal arthritis. Best Pract Res Clin Rheumatol. Apr 2003;17(2):201-8. [Medline].

  3. Rice PA. Gonococcal arthritis (disseminated gonococcal infection). Infect Dis Clin North Am. Dec 2005;19(4):853-61. [Medline].

  4. Centers for Disease Control and Prevention. Sexually transmitted disease surveillance 2005 supplement, gonococcal isolate surveillance project (GISP) Annual Report 2005. Atlanta, GA. US Department of Health and Human Services, Centers for Disease Control and Prevention, January 2007. Available at http://www.cdc.gov.std.gisp2005/. Accessed May 12, 2009.

  5. World Health Organization Fact Sheet Number 110. Available at http://www.who.int/mediacentre/factsheets/fs110/en/index.html. Accessed May 12, 2009.

  6. Marker-Hermann E. Septic arthritis, osteomyelitis, gonococcal and syphilitic arthritis. In: Hochberg MC, Silman AJ, Smolen JS, Weinblatt ME, Weisman MH, eds. Rheumatology. 4th ed. Philadelphia, PA: Mosby Elsevier; 2008:1013-28.

  7. Davis BT, Pasternack MS. Case records of the Massachusetts General Hospital. Case 19-2007 - a 19-year-old college student with fever and joint pain. N Engl J Med. Jun 21 2007;356(25):2631-7. [Medline].

  8. Liebling MR, Arkfeld DG, Michelini GA, Nishio MJ, Eng BJ, Jin T, et al. Identification of Neisseria gonorrhoeae in synovial fluid using the polymerase chain reaction. Arthritis Rheum. May 1994;37(5):702-9. [Medline].

  9. Read P, Abbott R, Pantelidis P, Peters BS, White JA. Disseminated gonococcal infection in a homosexual man diagnosed by nucleic acid amplification testing from a skin lesion swab. Sex Transm Infect. Oct 2008;84(5):348-9. [Medline].

  10. Kimmitt PT, Kirby A, Perera N, Nicholson KG, Schober PC, Rajakumar K, et al. Identification of Neisseria gonorrhoeae as the causative agent in a case of culture-negative dermatitis-arthritis syndrome using real-time PCR. J Travel Med. Sep-Oct 2008;15(5):369-71. [Medline].

  11. Update to CDC's Sexually Transmitted Diseases Treatment Guidelines 2006: Fluoroquinolones no longer recommended for treatment of gonococcal infections. Available at http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5614a3.htm. Accessed May 1, 2009.

  12. [Guideline] Centers for Disease Control and Prevention. Sexually transmitted diseases treatment guidelines, 2006. MMWR. 2006;55(No. RR-11):42-49.

  13. Newman LM, Moran JS, Workowski KA. Update on the management of gonorrhea in adults in the United States. Clin Infect Dis. Apr 1 2007;44 Suppl 3:S84-101. [Medline].

  14. MMWR. Availability of Cefixime 400 mg tablets---United States, April 2008. Available at http://www.cdc.gov.mmwr/preview/mmwrhtml/mm5716a5.htm. Accessed May 1, 2009.

  15. Centers for Disease Control and Prevention. Notice to readers: discontinuation of spectinomycin. MMWR. 2006;55:370.

Further Reading

Keywords

gonococcal arthritis, acute septic arthritis, Neisseria gonorrhoeae, N gonorrhoeae, disseminated gonococcal infection, DGI, arthritis-dermatitis syndrome, localized septic arthritis, dermatitis, tenosynovitis, migratory polyarthritis, migratory arthralgia, migratory arthritis, Fitz-Hugh and Curtis syndrome, gonococcal perihepatitis, Waterhouse-Friderichsen syndrome, gonococcal endocarditis, gonococcal meningitis

Contributor Information and Disclosures

Author

Michael P Keith, MD, FACP, Chief of Rheumatology, National Naval Medical Center; Assistant Professor of Medicine, Uniformed Services University of the Health Sciences
Michael P Keith, MD, FACP is a member of the following medical societies: American College of Physicians, American College of Rheumatology, and Clinical Immunology Society
Disclosure: Nothing to disclose.

Coauthor(s)

Robert John Oglesby, MD, Chief of Rheumatology Service, Department of Medicine, Walter Reed Army Medical Center; Associate Professor of Medicine, Uniformed Services University of the Health Sciences
Robert John Oglesby, MD is a member of the following medical societies: American College of Physicians, American College of Rheumatology, and Arthritis Foundation
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Lawrence H Brent, MD, Associate Professor of Medicine, Thomas Jefferson University; Chair, Program Director, Department of Medicine, Division of Rheumatology, Albert Einstein Medical Center
Lawrence H Brent, MD is a member of the following medical societies: American Association of Immunologists, American College of Physicians, and American College of Rheumatology
Disclosure: Genentech Honoraria Speaking and teaching; Genentech Grant/research funds Other; Amgen Honoraria Speaking and teaching; Wyeth Honoraria Speaking and teaching; Abbott Immunology Honoraria Speaking and teaching

CME Editor

Alex J Mechaber, MD, FACP, Associate Dean for Undergraduate Medical Education, Associate Professor of Medicine, University of Miami Miller School of Medicine
Alex J Mechaber, MD, FACP is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians-American Society of Internal Medicine, and Society of General Internal Medicine
Disclosure: Nothing to disclose.

Chief Editor

Herbert S Diamond, MD, Professor of Medicine, Temple University School of Medicine; Chairman Emeritus, Department of Internal Medicine, Western Pennsylvania Hospital
Herbert S Diamond, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Physicians, American College of Rheumatology, American Medical Association, and Phi Beta Kappa
Disclosure: medifocus Honoraria Review panel membership; health dialogs Honoraria Consulting; West Penn Allegheny Health System None Board membership

RELATED MEDSCAPE ARTICLES
Articles
 
 
HONcode

We subscribe to the
HONcode principles of the
Health On the Net Foundation

All material on this website is protected by copyright, Copyright© 1994- by Medscape.
This website also contains material copyrighted by 3rd parties.

DISCLAIMER: The content of this Website is not influenced by sponsors. The site is designed primarily for use by qualified physicians and other medical professionals. The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The information provided here is for educational and informational purposes only. In no way should it be considered as offering medical advice. Please check with a physician if you suspect you are ill.