eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease

Arthritis, Septic: Differential Diagnoses & Workup

Author: Richard J Scarfone, MD, Associate Professor, Department of Pediatrics, University of Pennsylvania School of Medicine; Attending Physician and Director of Emergency Preparedness, Division of Emergency Medicine, The Children's Hospital of Philadelphia
Contributor Information and Disclosures

Updated: Apr 29, 2009

Differential Diagnoses

Juvenile Rheumatoid Arthritis
Kawasaki Disease
Lyme Disease
Rheumatic Fever
Serum Sickness
Transient Synovitis

Other Problems to Be Considered

The differential diagnosis of a painful monoarthritis is rather extensive, and includes the following:

  • In contrast to children with septic arthritis (SA), children with transient synovitis appear well and are usually afebrile with just a mild limp.6 The American College of Radiology has established guidelines for the assessment of a limping child.7
  • In adolescents, a slipped capital femoral epiphysis may manifest as a painful hip, thigh, or knee. Most patients are afebrile and the onset of pain may be preceded by minor trauma.
  • Legg-Calve-Perthes disease, which is most common in boys, afflicts children aged 4-8 years. In contrast to septic arthritis, the pain is subacute with a more indolent onset, and these children do not have fever. 
  • One study demonstrated that children with septic arthritis were less likely to have knee involvement, a history of a tick bite, or a fever than children with Lyme disease.5 Additionally, median values of inflammatory markers were higher among those with septic arthritis; however, a large overlap was noted between the groups. 
  • Aside from gonococcal arthritis or septic arthritis in the neonate, polyarthritis is not typically caused by bacteria within the joints. The differential for polyarthritis in children is broad and includes Lyme disease, acute rheumatic fever, serum sickness, Kawasaki disease, systemic lupus erythematosus, and Henoch-Schönlein purpura.

Workup

Laboratory Studies

Diagnosis of septic arthritis (SA) is established by a combination of clinical findings and results of synovial fluid analysis.

  • When septic arthritis is suspected, synovial fluid should be obtained for CBC count, glucose, Gram stain, and culture. Synovial culture has poor sensitivity (60-70%), and the data that establish the typical characteristics of synovial fluid in septic arthritis were collected in the era of widespread H influenzae type B infection. How these characteristics will change in the current era remains to be seen. Similarly, although blood cultures should be obtained, they have relatively low yields.
  • A synovial fluid WBC count of more than 50,000/mL suggests SA, especially if the count exceeds 100,000/mL or if a predominance of polymorphonuclear cells is observed. Still, counts are often lower, and high counts may be associated with other conditions.
  • The synovial fluid glucose concentration averages 30% of that in the serum, a finding unique to septic arthritis.
  • Erythrocyte sedimentation rate is typically elevated, but in one series, fewer than one half of children with septic arthritis had peripheral WBC counts above 15,000 cells/μ L.
  • Although often elevated, a peripheral WBC count within the reference range does not rule out septic arthritis.
  • The C-reactive protein (CRP) is a more sensitive marker for septic arthritis than is the peripheral WBC count. In one study, a CRP of more than 2 mg/dL was found to be a strong independent risk factor for septic arthritis of the hip among children presenting with hip pain.2

Imaging Studies

  • Radiography
    • Although plain radiography may reveal an effusion as widening of the joint space with displacement of fat planes, it is insensitive in the diagnosis of septic arthritis.
    • Radiography may be most helpful in screening for etiologies other than septic arthritis as a cause of joint pain. For example, it may reveal bony changes suggestive of osteomyelitis, bony tumors or fractures as the source of swelling, and Legg-Perthes disease or a slipped capital femoral epiphysis, which are diagnostic considerations in a child with an irritable hip.
  • Ultrasonography
    • Ultrasonography is a simple, sensitive, and relatively inexpensive technique for detecting a hip effusion.
    • This test has a greater sensitivity than plain radiography and is becoming the modality of choice to reveal hip effusions. Ultrasonography is also used to guide the aspiration needle if an effusion is detected.
    • In a study of 96 children suspected to have septic arthritis of the hip, 40 had normal ultrasonography findings and no septic arthritis.
    • Ultrasonography has several advantages over CT in this setting, including eliminating radiation exposure and guiding the aspiration of deep joints such as the hip.
  • Scintigraphy: This has a limited role in most cases but may be helpful if multifocal disease is suspected in neonates. It also assists with the detection of an associated osteomyelitis.

Procedures

  • Clinicians should have a low threshold for performing an arthrocentesis, especially for children with a painful monoarthritis, significantly limited range of motion, and no plausible noninfectious explanation.
  • Emergency department physicians are usually adept at performing arthrocentesis of most joints. The knee joint, for example, can usually be entered fairly easily using either a medial or superolateral approach. However, aspiration of fluid from the hip typically requires the involvement of a radiologist and an orthopedic surgeon.
  • General practices that help to ensure the safety and success of arthrocentesis include liberal use of sedatives and analgesics, joint immobilization, sterile technique, and local anesthesia. Use of a needle large enough (18-20 gauge) to aspirate the viscous synovial fluid is necessary.

More on Arthritis, Septic

Overview: Arthritis, Septic
Differential Diagnoses & Workup: Arthritis, Septic
Treatment & Medication: Arthritis, Septic
Follow-up: Arthritis, Septic
Multimedia: Arthritis, Septic
References

References

  1. Kocher MS, Zurakowski D, Kasser JR. Differentiating between septic arthritis and transient synovitis of the hip in children: an evidence-based clinical prediction algorithm. J Bone Joint Surg Am. Dec 1999;81(12):1662-70. [Medline].

  2. Caird MS, Flynn JM, Leung YL, et al. Factors distinguishing septic arthritis from transient synovitis of the hip in children. A prospective study. J Bone Joint Surg Am. Jun 2006;88(6):1251-7. [Medline].

  3. Kaplan SL. Challenges in the evaluation and management of bone and joint infections and the role of new antibiotics for gram positive infections. Adv Exp Med Biol. 2009;634:111-20. [Medline].

  4. Welkon CJ, Long SS, Fisher MC, Alburger PD. Pyogenic arthritis in infants and children: a review of 95 cases. Pediatr Infect Dis. Nov-Dec 1986;5(6):669-76. [Medline].

  5. Thompson A, Mannix R, Bachur R. Acute pediatric monoarticular arthritis: distinguishing lyme arthritis from other etiologies. Pediatrics. Mar 2009;123(3):959-65. [Medline].

  6. Taekema HC, Landham PR, Maconochie I. Towards evidence based medicine for paediatricians. Distinguishing between transient synovitis and septic arthritis in the limping child: how useful are clinical prediction tools?. Arch Dis Child. Feb 2009;94(2):167-8. [Medline].

  7. Fordham L, Gunderman R, Blatt ER, et al. Limping child--ages 0-5 years. American College of Radiology (ACR). 2007;5.

  8. Dagan R. Management of acute hematogenous osteomyelitis and septic arthritis in the pediatric patient. Pediatr Infect Dis J. Jan 1993;12(1):88-92. [Medline].

  9. Frank G, Mahoney HM, Eppes SC. Musculoskeletal infections in children. Pediatr Clin North Am. Aug 2005;52(4):1083-106, ix. [Medline].

  10. Kratz A, Greenberg D, Barki Y, et al. Pantoea agglomerans as a cause of septic arthritis after palm tree thorn injury; case report and literature review. Arch Dis Child. Jun 2003;88(6):542-4. [Medline].

  11. Shetty AK, Gedalia A. Septic arthritis in children. Rheum Dis Clin North Am. May 1998;24(2):287-304. [Medline].

Further Reading

Keywords

septic arthritis, SA, bacterial arthritis, infectious arthritis, pyogenic arthritis, suppurative arthritis, purulent synovitis, pyarthrosis, suppurative synovitis, osteomyelitis, pressure necrosis, avascular necrosis, Haemophilus influenzae type B, community-acquired methicillin-resistant Staphylococcus aureus, MRSA-CA, hemophilia, hemarthrosis, sickle cell anemia, human immunodeficiency virus, HIV, chronic arthritis, joint pain, polyarticular disease, pseudoparalysis, arthralgia, transient synovitus, reactive arthritis, Escherichia coli, varicella-zoster virus, Salmonella, diagnosis, treatment

Contributor Information and Disclosures

Author

Richard J Scarfone, MD, Associate Professor, Department of Pediatrics, University of Pennsylvania School of Medicine; Attending Physician and Director of Emergency Preparedness, Division of Emergency Medicine, The Children's Hospital of Philadelphia
Richard J Scarfone, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Pediatrics
Disclosure: Nothing to disclose.

Medical Editor

Itzhak Brook, MD, MSc, Professor, Department of Pediatrics, Georgetown University School of Medicine
Itzhak Brook, MD, MSc is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians-American Society of Internal Medicine, American Federation for Clinical Research, American Medical Association, American Society for Microbiology, Armed Forces Infectious Diseases Society, Association of Military Surgeons of the US, Infectious Diseases Society of America, International Immunocompromised Host Society, International Society for Infectious Diseases, Medical Society of the District of Columbia, New York Academy of Sciences, Pediatric Infectious Diseases Society, Society for Ear, Nose and Throat Advances in Children, Society for Experimental Biology and Medicine, Society for Pediatric Research, Southern Medical Association, and Surgical Infection Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Joseph Domachowske, MD, Professor of Pediatrics, Microbiology and Immunology, Department of Pediatrics, Division of Infectious Diseases, State University of New York-Upstate Medical University
Joseph Domachowske, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American Society for Microbiology, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Phi Beta Kappa
Disclosure: Nothing to disclose.

CME Editor

Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine
Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility
Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; sanofi pasteur Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching

Chief Editor

Russell W Steele, MD, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine
Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association
Disclosure: None None None

 
 
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