eMedicine Specialties > Orthopedic Surgery > Systemic Diseases

Septic Arthritis

Author: Gabriel Munoz, MD, Consulting Staff, Department of Emergency Medicine, Decatur Memorial Hospital
Coauthor(s): Edmund W Raycraft, MD, Consulting Staff, Raycraft & Jones Orthopedics
Contributor Information and Disclosures

Updated: Jul 14, 2009

Introduction

Septic arthritis is inflammation of a synovial membrane with purulent effusion into the joint capsule, usually due to bacterial infection. This disease entity also is referred to in the literature as bacterial, suppurative, purulent, or infectious arthritis.1,2,3,4,5

Septic arthritis is a rather rare but important disease that typically affects monoarticular joints. The age range of those affected is broad, from the neonatal period to advanced age.6,7,8,9,10 Treatment consists of a combined medical and surgical approach.1,11,12,13 Septic arthritis usually is divided into gonococcal and nongonococcal arthritis, as clinical and treatment regimens differ.14 In adults, septic arthritis most commonly affects the knee; in children, infection into the hip joint predominates.8,15,16,17

Despite advances in diagnostic studies, powerful antibiotics, and early drainage, significant joint destruction commonly occurs.

Recent studies

A retrospective comparison by Sammer and Shin of 36 patients (40 wrists) with septic arthritis of the wrist treated between 1997 and 2007 with either open or arthroscopic irrigation and debridement showed that arthroscopic irrigation and debridement is an effective treatment for patients with isolated septic arthritis of the wrist. Patients treated arthroscopically had fewer operations and a shorter hospital stay than patients who received open treatment; however, these benefits were not seen in patients with multiple sites of infection. The 90-day perioperative mortality rate was 18% (3 patients) in the open-treatment group and 21% (4 patients) in the arthroscopy group.18

Collins et al found that synovial fluid TREM-1 (triggering receptor expressed on myeloid cells-1) expression is increased in septic arthritis and rheumatoid arthritis. According to the authors, in patients with acute inflammatory arthritis, elevated synovial fluid sTREM 1 levels may help point to a diagnosis of septic arthritis or rheumatoid arthritis, and in patients with rheumatoid arthritis, targeting TREM-1 may provide therapeutic benefit by reducing local proinflammatory cytokine and chemokine release.19

Pessler et al, in an analysis of the synovium in patients with chronic pyogenic arthritis, identified extensive neovascularization and cell proliferation, persistent bacterial colonization, and heterogeneous inflammatory infiltrates rich in CD15+ neutrophils.20

Problem

Septic arthritis can quickly destroy a joint and can cause many complications, including osteomyelitis, bony erosions, fibrous ankylosis, sepsis, and even death.

Barriers to successful management include lack of clinical suspicion in the early phase of presentation, delay in definitive diagnostic needle aspiration, and failure to provide adequate drainage of the joint.

In addition, septic arthritis in neonates and infants can be especially treacherous as a result of blunted inflammatory signals and/or confounding infection at a distant site (eg, ear, umbilical catheter site).

Frequency

Of all the forms of arthritis, septic arthritis is the most aggressive at quickly destroying a joint. The frequency of septic arthritis is approximately 2-10 cases per 100,000 in the general population.

In patients with immunologic disorders (eg, rheumatoid arthritis, systemic lupus erythematosus), the occurrence is approximately 30-70 cases per 100,000.21 The incidence in patients with joint prosthesis is similar to that of patients with immunologic disorders.

In gonococcal arthritis, women are approximately 3 times as likely as men to develop this disease.

Etiology

Most septic arthritis cases are caused by Staphylococcus aureus and streptococci. In all age groups, 80% of cases are caused by Gram-positive aerobes (60% S aureus; 15% beta-hemolytic streptococci; 5% Streptococcus pneumoniae), and approximately 20% of cases are caused by Gram-negative anaerobes.22

In neonates and infants younger than 6 months, S aureus and Gram-negative anaerobes comprise the majority of infections. The incidence of Haemophilus influenzae has decreased dramatically owing to widespread use of the H influenzae vaccine.

In children aged 6 months to 2 years, S aureus and, to a lesser degree, H influenzae are the major organisms of infection. In patients older than 2 years, S aureus becomes the principle culprit. As sexual activity begins in the teen years, Neisseria gonorrhoeae should be suspected.

Pathophysiology

Various sources of infection exist for the joint space. Bacteria may enter the joint directly, as with trauma. Infection may enter hematogenously (eg, intravenous [IV] drug injection). Infection may enter from osteomyelitis that is adjacent to the capsule. Infection also may enter from soft-tissue infections (eg, cellulitis, abscess, bursitis, tenosynovitis). The knee accounts for approximately 40-50% of joint infections, and the hip accounts for 20-25% of joint infections. However, in infants and very young children, hip involvement is most common. Shoulders, ankles, and elbows account for approximately 10-15% of infections. Finally, septic arthritis of the wrist occurs in 10% of cases.4,8,15,23,24

Presentation

Septic arthritis can be difficult to diagnose in the early stages of progression. Once purulence has developed and a bulging effusion is noted, diagnosis is made easily. Typically, the patient presents with fever and a joint that is hot, red, painful, distended, and has a markedly decreased range of motion. Restriction of movement occurs to active and passive attempts.7,8,25,26,27

In young, sexually active patients with fever, tenosynovitis, migratory polyarthralgia, and dermatitis, suspect N gonorrhoeae. The rash may appear as papules over the trunk and extensor surfaces of distal extremities that eventually can turn into hemorrhagic pustules. Women are more likely to develop gonococcal arthritis than are men.

In patients with a history of intravenous drug use (IVDU), suspect Pseudomonas.

In infants and children, diagnosis can be very difficult. Neonates and infants often have blunted inflammatory signals. Symptoms such as fever, decreased appetite, and irritability without obvious joint involvement can easily lead to an incorrect diagnosis. Aside from obvious open fractures, foreign object, and trauma, searching for distant infections is very important. Clinical presentation in the older child will be similar to that in the adult. However, the child may not allow the affected joint to be touched and, sometimes, may not even allow the affected joint to be seen. Additional confounding symptoms may be present, including nausea, vomiting, headache, sore throat, and abdominal pain. Ear infections are the most common source of bacteria leading to septic arthritis in children.

Distinguishing transient synovitis from septic arthritis is an area of particular concern.28 In 1 study of children, 4 independent variables have been found useful as clinical predictors for septic arthritis, including the following:

  • History of fever
  • Nonweightbearing
  • Erythrocyte sedimentation rate higher than 40 mm/h
  • WBC count higher than 12,000/µL

Indications

If rapid improvement is not achieved with needle aspiration, open drainage and lavage (arthroscopically or via arthrotomy) is strongly recommended.

Contraindications

Generally, few contraindications to arthrocentesis exist. One caveat to consider is to avoid aspirating from an area that has an established overlying soft-tissue infection. This may introduce bacteria into an otherwise noninfected joint.

Patients with bleeding disorders and those who are on anticoagulatory medications pose a difficult challenge, and risks must be weighed against benefits on an individual basis.

More on Septic Arthritis

Overview: Septic Arthritis
Workup: Septic Arthritis
Treatment: Septic Arthritis
Follow-up: Septic Arthritis
Multimedia: Septic Arthritis
References
Further Reading

References

  1. Donatto KC. Orthopedic management of septic arthritis. Rheum Dis Clin North Am. May 1998;24(2):275-86. [Medline].

  2. Metzger AL, Morris RI. Rheumatoid arthritis. In: Primary Practice. Lippincott. Jan-Feb 1988;2(1):52-65.

  3. Thaler SJ, Maguire JH. Acute bacterial arthritis. In: Harrison's Online. 1999. 1999:324.

  4. Vigorita VJ. Septic arthritis. In: Orthopedic Pathology. 1999:241-7, 523-5.

  5. Williams KD. Infectious arthritis. In: Campbell's Operative Orthopaedics. 1998;1 (15):601-7.

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

  7. Bettin D, Schul B, Schwering L. Diagnosis and treatment of joint infections in elderly patients. Acta Orthop Belg. Jun 1998;64(2):131-5. [Medline].

  8. 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].

  9. Nowbar S, Ridout E, Chan ED. A 60-year-old man with septic arthritis and hypotension after a fall. Chest. Mar 1999;115(3):883-5. [Medline].

  10. Dessì A, Crisafulli M, Accossu S, Setzu V, Fanos V. Osteo-articular infections in newborns: diagnosis and treatment. J Chemother. Oct 2008;20(5):542-50. [Medline].

  11. Kim HK, Alman B, Cole WG. A shortened course of parenteral antibiotic therapy in the management of acute septic arthritis of the hip. J Pediatr Orthop. Jan-Feb 2000;20(1):44-7. [Medline].

  12. Aslam S, Darouiche RO. Antimicrobial therapy for bone and joint infections. Curr Infect Dis Rep. Jan 2009;11(1):7-13. [Medline].

  13. Saphyakhajon P, Joshi AY, Huskins WC, Henry NK, Boyce TG. Empiric antibiotic therapy for acute osteoarticular infections with suspected methicillin-resistant Staphylococcus aureus or Kingella. Pediatr Infect Dis J. Aug 2008;27(8):765-7. [Medline].

  14. Cucurull E, Espinoza LR. Gonococcal arthritis. Rheum Dis Clin North Am. May 1998;24(2):305-22. [Medline].

  15. Simon RR, Koenigsknecht SJ. Septic arthritis of the hip joint. In: Emergency Orthopedics: The Extremities. 2001:404-6.

  16. Williams RJ, Laurencin CT, Warren RF. Septic arthritis after arthroscopic anterior cruciate ligament reconstruction. Diagnosis and management. Am J Sports Med. Mar-Apr 1997;25(2):261-7. [Medline].

  17. Rutz E, Brunner R. Septic arthritis of the hip - current concepts. Hip Int. Jan-Mar 2009;19 Suppl 6:S9-12. [Medline].

  18. Sammer DM, Shin AY. Comparison of arthroscopic and open treatment of septic arthritis of the wrist. J Bone Joint Surg Am. Jun 2009;91(6):1387-93. [Medline].

  19. Collins CE, La DT, Yang HT, Massin F, Gibot S, Faure G, et al. Elevated synovial expression of triggering receptor expressed on myeloid cells-1 (TREM-1) in patients with septic arthritis or rheumatoid arthritis. Ann Rheum Dis. Dec 3 2008;[Medline].

  20. Pessler F, Dai L, Diaz-Torne C, Ogdie A, Gomez-Vaquero C, Paessler ME, et al. Increased angiogenesis and cellular proliferation as hallmarks of the synovium in chronic septic arthritis. Arthritis Rheum. Aug 15 2008;59(8):1137-46. [Medline].

  21. Favero M, Schiavon F, Riato L, Carraro V, Punzi L. Rheumatoid arthritis is the major risk factor for septic arthritis in rheumatological settings. Autoimmun Rev. Oct 2008;8(1):59-61. [Medline].

  22. Schattner A, Vosti KL. 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). Mar 1998;77(2):122-39. [Medline].

  23. Lossos IS, Yossepowitch O, Kandel L, Yardeni D, Arber N. Septic arthritis of the glenohumeral joint. A report of 11 cases and review of the literature. Medicine (Baltimore). May 1998;77(3):177-87. [Medline].

  24. Kirchhoff C, Braunstein V, Paul J, Imhoff AB, Hinterwimmer S. Septic arthritis as a severe complication of elective arthroscopy:clinical management strategies. Patient Saf Surg. Mar 31 2009;3(1):6. [Medline].

  25. Craig JG. Infection: ultrasound-guided procedures. Radiol Clin North Am. Jul 1999;37(4):669-78. [Medline].

  26. Onadeko OO, Parsh B, Scott J, Wilson D. Index of suspicion. Case 3. Diagnosis: septic arthritis. Pediatr Rev. Feb 2000;21(2):67, 70-1. [Medline].

  27. van der Heijden IM, Wilbrink B, Vije AE. Detection of bacterial DNA in serial synovial samples obtained during antibiotic treatment from patients with septic arthritis. Arthritis Rheum. Oct 1999;42(10):2198-203. [Medline].

  28. Simon RR, Koenigsknecht SJ. Transient synovitis. In: Emergency Orthopedics: The Extremities. 2001:89-90.

  29. Peltola H, Pääkkönen M, Kallio P, Kallio MJ. Prospective, randomized trial of 10 days versus 30 days of antimicrobial treatment, including a short-term course of parenteral therapy, for childhood septic arthritis. Clin Infect Dis. May 1 2009;48(9):1201-10. [Medline].

  30. Kaandorp CJ, Krijnen P, Moens HJ. The outcome of bacterial arthritis: a prospective community-based study. Arthritis Rheum. May 1997;40(5):884-92. [Medline].

  31. Pioro MH, Mandell BF. Septic arthritis. Rheum Dis Clin North Am. May 1997;23(2):239-58. [Medline].

  32. Jonsson IM, Lindholm C, Luong TT, Lee CY, Tarkowski A. mgrA regulates staphylococcal virulence important for induction and progression of septic arthritis and sepsis. Microbes Infect. Oct 2008;10(12-13):1229-35. [Medline].

Keywords

septic arthritis, bacterial arthritis, suppurative arthritis, purulent arthritis, infectious arthritis

Contributor Information and Disclosures

Author

Gabriel Munoz, MD, Consulting Staff, Department of Emergency Medicine, Decatur Memorial Hospital
Gabriel Munoz, MD is a member of the following medical societies: American College of Emergency Physicians and American Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Edmund W Raycraft, MD, Consulting Staff, Raycraft & Jones Orthopedics
Edmund W Raycraft, MD is a member of the following medical societies: American College of Surgeons
Disclosure: Nothing to disclose.

Medical Editor

Jegan Krishnan, MBBS, FRACS, PhD, Professor, Chair, Department of Orthopedic Surgery, Flinders University of South Australia; Senior Clinical Director of Orthopedic Surgery, Repatriation General Hospital; Private Practice, Orthopaedics SA, Ashford Specialist Centre
Jegan Krishnan, MBBS, FRACS, PhD is a member of the following medical societies: Australian Medical Association, Australian Orthopaedic Association, and Royal Australasian College of Surgeons
Disclosure: Nothing to disclose.

Pharmacy Editor

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

Managing Editor

Jerome D Wiedel, MD, Chair, Professor, Department of Orthopedics, University of Colorado Health Sciences Center
Disclosure: Nothing to disclose.

CME Editor

Dinesh Patel, MD, FACS, Associate Clinical Professor of Orthopedic Surgery, Harvard Medical School; Chief of Arthroscopic Surgery, Department of Orthopedic Surgery, Massachusetts General Hospital
Dinesh Patel, MD, FACS is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Association of Physicians of Indian Origin, American College of International Physicians, and American College of Surgeons
Disclosure: Nothing to disclose.

Chief Editor

Harris Gellman, MD, Consulting Surgeon, Broward Hand Center; Voluntary Clinical Professor of Orthopedic Surgery and Plastic Surgery, Departments of Orthopedic Surgery and Surgery, University of Miami School of Medicine
Harris Gellman, MD is a member of the following medical societies: American Academy of Medical Acupuncture, American Academy of Orthopaedic Surgeons, American Orthopaedic Association, American Society for Surgery of the Hand, and Arkansas Medical Society
Disclosure: Nothing to disclose.

 
 
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