Sandbox:septic arthritis

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Overview

Septic arthritis is a an important consideration in adults presenting with monoarticular arthritis in 80 to 90% of patients. It can involve any joint, but most commonly involves knee > hip > shoulder > ankle.[1] Other joints such as sacroiliac joint, sternoclacicular or costoclavicular joints may be involved in patient with history of intravenous drug abuse (IVDA), penetrating trauma, animal or human bites and local steroid injections.

Defintion

Historical perspective

Classification

Classification Based on the Etiology

Septic arthritis can be classified into 2 types based on the etiology:[2]

  • Gonococcal septic arthritis
  • Non gonococcal septic arthritis

Classification Based on the Presentation

Septic arthritis can be classified into 2 types based on the involvement of number of joints involved during presentation:[3]

  • Mono articular septic arthritis (MASA)
    • Most common type of presentation
  • Poly articular septic arthritis (PASA)
    • Less common presentation (~15% of total septic arthritis cases)
    • commonly caused by staphylococcus aureus and other non gonococcal infections such as streptococci and gram negative bacteria.

Causes

Septic arthritis is due to intra articular seeding of living microorganisms.[3] The most common etiological agent of all nongonococcal causes of septic arthritis in the United States is Staphylococcus aureus.[4] Gram-negative bacilli account for 10 to 20% of septic arthritis causes.[4] ~10% of patients with nongonococcal septic arthritis are due to polymicrobial cause of infections. Anaerobes are also can cause septic arthritis in few cases.

Most common cause of septic arthritis in children age < 2 years are Haemophilus influenzae (in immunized children), Staph. aureus, group A Streptococcal infections and Kingella kingae.[5]

Pathophysiology

Hematogenous spread: Septic arthritis most commonly develop as a result of hematogenous spreading bacteria into the vascular synovial membrane.[6]

Direct inoculation: Direct inoculation of microorganisms may occur during joint surgery, particularly in association with knee and hip arthroplasties.

Contiguous spread: Bone infection can spread by breaking through its outer cortex and then into the intracapsular region that lead to joint infection. This kind of spread is more common in children as the small capillaries can cross the epiphyseal growth plate and permit extension of infection into the epiphysis and joint space.[1][7]

Risk Factors

Common Risk Factors

Common risk factors that predespose septic arthritis are as follows:[8][9][10][11]

  • Age >60 years
  • Recent history of bacteremia
  • Degenerative joint diseases such as rheumatoid arthritis ( Prosthetic joint > Rheumatoid arthritis > Osteoarthritis)[9]
  • Corticosteroid therapy
  • Diabetes mellitus
  • Leukemia
  • Cirrhosis
  • Granulomatous diseases
  • Hypogammaglobulinemia
  • Intravenous substance abuse
  • Chronic kidney disease
  • Cytotoxic chemotherapy
Microorganism Associated risk factors
Staphylococcus aureus
  • Rheumatioid arthritis[12]
  • Diabetes mellitus[13]
  • HIV patients[14]
Streptococcus pyogenes

Streptococcal pneumonia

  • Autoimmune diseases[10]
  • Chronic skin infections[13]
  • Trauma
Groups B Streptococcal infection
  • Immunocompromised patients[15]
  • Diabetes mellitus
  • Malignancy
  • Severe genitourinary or gastrointestinal infections
Neisseria gonorrhoeae
  • Complement deficiency
  • Systemic lupus erythematosus
  • Male homosexuality
  • low socioeconomic status
Gram-negative bacilli

Most common gram-negative organisms are Pseudomonas aeruginosa

and Escherichia coli.

  • History of intravenous drug abuse[4]
  • Extremes of age
  • Immunocompromised patients
Haemophilus influenzae
  • Unimmunized children[16]
Anaerobes
  • Diabetes mellitus
  • Patients with prosthetic joints



  • Recent history of joint aspiration or local corticosteroid joint injection.[17][6]
  • History of Rhematoid arthritis[12]
  • History of diabetes mellitus[10]

Epidemiology and Demographics

Females are more at risk in getting gonorrheal arthritis and four fold risk compared to men, due to the asymptomatic nature of gonorrheal infection in women.

In children hip is most commonly involved.

PASA is more common in men when compared to women.[3]

Diagnosis

History and Symptoms

Phaysical Examination

Appearance of the Patient

Patient with septic arthritis usually appears toxic and with joint pain that involved

Vital Signs

  • Low grade fever
  • Hyperthermia over the joint involved
  • Tachycardia
  • Tachypnea

Skin

  • Warm over the joint
  • Erythema over the around the joint that involved

HEENT

Neck

Lungs

Heart

Abdomen

Back

Genitourinary

Extremities

Most commonly involves knee > hip > shoulder > ankle.[1] Other joints such as sacroiliac joint, sternoclacicular or costoclavicular joints may be involved in patient with history of intravenous drug abuse (IVDA), penetrating trauma, animal or human bites and local steroid injections.

  • Swelling of the joint that involved
  • Decreased range of motion

Neuromuscular

Laboratory Tests

Diagnosis of septic arthritis depends maily on the arthrocentesis and isolation of the pathogen from aspirated joint fluid.[18]

Prognosis

Prognosis of septic arthritis depends on several factors.

Poor prognostic factors include age >50 years, history of rheumatoid arthritis as an underlying disease, staph. aureus is the causative agent.

References

  1. 1.0 1.1 1.2 Barton LL, Dunkle LM, Habib FH (1987) Septic arthritis in childhood. A 13-year review. Am J Dis Child 141 (8):898-900. PMID: 3498362
  2. Shirtliff ME, Mader JT (2002) Acute septic arthritis. Clin Microbiol Rev 15 (4):527-44. PMID: 12364368
  3. 3.0 3.1 3.2 Dubost JJ, Fis I, Denis P, Lopitaux R, Soubrier M, Ristori JM et al. (1993) Polyarticular septic arthritis. Medicine (Baltimore) 72 (5):296-310. PMID: 8412643
  4. 4.0 4.1 4.2 Deesomchok U, Tumrasvin T (1990) Clinical study of culture-proven cases of non-gonococcal arthritis. J Med Assoc Thai 73 (11):615-23. PMID: 2283490
  5. Yagupsky P, Bar-Ziv Y, Howard CB, Dagan R (1995) Epidemiology, etiology, and clinical features of septic arthritis in children younger than 24 months. Arch Pediatr Adolesc Med 149 (5):537-40. PMID: 7735407
  6. 6.0 6.1 Klein RS (1988) Joint infection, with consideration of underlying disease and sources of bacteremia in hematogenous infection. Clin Geriatr Med 4 (2):375-94. PMID: 3288326
  7. Buckholz JM (1987) The surgical management of osteomyelitis: with special reference to a surgical classification. J Foot Surg 26 (1 Suppl):S17-24. PMID: 3559051
  8. Dickie AS (1986) Current concepts in the management of infections in bones and joints. Drugs 32 (5):458-75. PMID: 3792229
  9. 9.0 9.1 Kaandorp CJ, Van Schaardenburg D, Krijnen P, Habbema JD, van de Laar MA (1995) Risk factors for septic arthritis in patients with joint disease. A prospective study. Arthritis Rheum 38 (12):1819-25. PMID: 8849354
  10. 10.0 10.1 10.2 Morgan DS, Fisher D, Merianos A, Currie BJ (1996) An 18 year clinical review of septic arthritis from tropical Australia. Epidemiol Infect 117 (3):423-8. PMID: 8972665
  11. Rozadilla A, Nolla JM, Mateo L, del Blanco J, Valverde J, Roig D (1992) [Septic arthritis induced by pyogenic germs in patients without parenteral drug addiction. Analysis of 44 cases.] Med Clin (Barc) 98 (14):527-30. PMID: 1602850
  12. 12.0 12.1 Goldenberg DL, Cohen AS (1976) Acute infectious arthritis. A review of patients with nongonococcal joint infections (with emphasis on therapy and prognosis). Am J Med 60 (3):369-77. PMID: 769545
  13. 13.0 13.1 Le Dantec L, Maury F, Flipo RM, Laskri S, Cortet B, Duquesnoy B et al. (1996) Peripheral pyogenic arthritis. A study of one hundred seventy-nine cases. Rev Rhum Engl Ed 63 (2):103-10. PMID: 8689280
  14. Vassilopoulos D, Chalasani P, Jurado RL, Workowski K, Agudelo CA (1997) Musculoskeletal infections in patients with human immunodeficiency virus infection. Medicine (Baltimore) 76 (4):284-94. PMID: 9279334
  15. Schattner A, Vosti KL (1998) Bacterial arthritis due to beta-hemolytic streptococci of serogroups A, B, C, F, and G. Analysis of 23 cases and a review of the literature. Medicine (Baltimore) 77 (2):122-39. PMID: 9556703
  16. De Jonghe M, Glaesener G (1995) [Type B Haemophilus influenzae infections. Experience at the Pediatric Hospital of Luxembourg.] Bull Soc Sci Med Grand Duche Luxemb 132 (2):17-20. PMID: 7497542
  17. Hunter JA, Blyth TH (1999) A risk-benefit assessment of intra-articular corticosteroids in rheumatic disorders. Drug Saf 21 (5):353-65. PMID: 10554051
  18. Bayer AS (1980) Gonococcal arthritis syndromes: an update on diagnosis and management. Postgrad Med 67 (3):200-4, 207-8. PMID: 7355135