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Septic Arthritis Allison I. Martin, BSN, RN.

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Presentation on theme: "Septic Arthritis Allison I. Martin, BSN, RN."— Presentation transcript:

1 Septic Arthritis Allison I. Martin, BSN, RN

2 Diagnosis Septic arthritis is an infection in the joint cavity most often caused by bacteria, but also can be caused by fungi or mycobacteria Nongonococcal bacteria can lead to irreversible joint damage Gonococcal bacteria is far less destructive to joints Acute monoarticular arthritis Infectious and inflammatory

3 Mechanism of infection
Hematogenous spread Bacteremia IV drug abuse Immunocompromised state (Diabetes, HIV) Direct inoculation Recent joint surgery Prosthetic joint Steroid injections Trauma Spread from local infection Skin infection or ulcer Osteomyelitis Septic bursitis Abscess Contaminated joint prosthesis can cause an early or delayed joint infection up to 24 months after surgery. Late infection of a prosthesis is usually due to hematogenous seeding from dental work, skin infection, pneumonia, or UTI Hematogenous spread or seeding- spread from a remote site of infection, such as UTI, pneumonia, etc

4 Pathogenesis The synovial fluid within the joint cavity is normally sterile Synovial tissue has no limiting basement plate so bacteria quickly gain access Most common causative agents: Staphylococcus aureus Streptococcus species Gram-negative bacilli in immunocompromised and IV drug abusers Bacteria cause an acute inflammatory cell response in the synovial membrane with purulent effusion into the joint capsule Following onset, there is a marked hyperplasia of the lining cells in the synovial membrane within 7 days Inflammatory cells release cytokines and proteases that cause cartilage degradation and inhibit cartilage synthesis leading to rapid destruction of the joint Gram negative bacilli- E. coli, Proteus mirabilis, Klebsiella, and Enterobacter Gram negative cocci include Neisseria gonorrheae and Neisseria meningitidis (cause gonococcal arthritis, less destructive)

5 Risk Factors Advanced age (50% of patients are > 60 years)
Diabetes mellitus Rheumatoid arthritis Presence of prosthetic joint Recent joint surgery Skin infection Intravenous drug use, alcoholism Prior intraarticular corticosteroid injection Bacteremia is more likely to localize in a joint with preexisting arthritis because of damage—osteoarthritis and rheumatoid arthritis Patients with RA have additional risk factors of maintenance immunosuppressive medications and intraarticular steroid injections Risk may also be increased in crystal arthropathies

6 Clinical Manifestations
History Presentation Monoarticular acute joint swelling, pain, erythema, warmth, joint immobility; ROM is significantly restricted and very painful Infection in the knee is most common (> 50% of cases), but the hip, shoulder, ankle, elbow, and wrist can also be affected HPI – OLDCARTS Onset, location, associated symptoms, risk factors, concurrent illness Ask about injury or trauma, recent infections of skin or urinary tract Abrupt onset with fever and chills points to infectious cause History of skin lesions, vaginal or urethral discharge, exposure to gonorrhea, tick bites or exposure to ticks Polyarticular diseases may initially present with one acutely inflamed joint or with symptoms that are more pronounced in one joint Examples: RA, Reiter syndrome, ankylosing spondylitis, psoriatic arthritis, the arthritis of inflammatory bowel disease, and sarcoidosis Sternoclavicular and sacroiliac joint can be affected in injection drug users Infection of the hip can manifest as groin pain exacerbated by walking

7 Clinical Manifestations
ROS: General: fever and chills (common but are absent in up to 20% of cases), fatigue HEENT: drainage, mucosal ulcers, petechiae in eyes or mouth Cardiovascular: chest pain, syncope Respiratory: cough, shortness of breath, dyspnea GU: urinary symptoms, hematuria, discharge GI: bowel changes, N/V Skin: skin wound, lesion, ulcers, bites, petechiae Musculoskeletal: swelling, erythema, warmth, joint stiffness and immobility (mono-, oligo- or polyarticular)

8 Clinical Manifestations
PMH: Diabetes mellitus, rheumatoid arthritis, gout or pseudogout, prosthetic joint, osteoarthritis, prior intraarticular corticosteroid injections, immunosuppression, HIV infection, previous trauma PSH: Recent joint surgery (within 24 months), dental procedures Social history: IV drug abuse, alcoholism, sexual history and STDs (gonococcal arthritis) Medications: Immunosuppressive therapy, steroids, chemotherapy

9 Physical examination Vitals: Note temperature
Most patients with septic arthritis are febrile with high fever Patients with gout and rheumatoid arthritis may have low-grade fever HEENT: Examine eyes for conjunctivitis and iritis, fundi for signs of endocarditis, mouth for mucosal ulcers Cardiovascular: Auscultate for murmur Respiratory: Auscultate lungs Integumentary: Lesions, wounds, ulcers, track marks, tophi Genitalia: Check for signs of gonococcal urethritis and cervicitis Musculoskeletal: Examine all joints; assess involved joint for increased warmth, swelling, redness, effusion, and immobility; test active and passive ROM Differentiate inflammation of the joint space versus periarticular process (tendons, bursa, or skin) which may have preserved ROM despite pain Check spine ROM, restriction and tenderness can indicate spondylitis Bacterial arthritis can by the presenting sign of infective endocarditis, listen for murmurs of endocarditis Skin: also tophi, rheumatoid nodules, pitting of nails and other psoriatic manifestations, erythema nodosum, psoriasis

10 Diagnostic tests Synovial fluid aspiration is the definitive diagnostic test Gram stain: gram positive bacteria in about 80% of cases Culture: positive in 90% of cases with nongonococcal arthritis Leukocyte count with differential: exceeds 50,000/mcL and often > 100,000/mcL Crystal analysis Blood cultures should be obtained (positive in 50% of patients) CBC: elevated WBCs, common, but not specific C-reactive protein: 92% sensitive, not specific Erythrocyte sedimentation rate: 98% sensitive, not specific Radiographs obtained for baseline image, detect fracture, or underlying inflammatory arthritis MRI to detect effusions and inflammation in joints that are difficult to examine, including the hip and sacroiliac joints Ultrasound more sensitive for effusions of the hip Synovial fluid aspiration is the first choice if an effusion or other signs of inflammation are present CBC and ESR are moderately helpful in distinguishing inflammatory from noninflammatory when joint fluid cannot be obtained CRP and ESR are highly sensitive inflammatory markers in septic arthritis, 92% and 98% Radiographs of infected joint should be obtained to provide a baseline that is useful for comparison during or after treatment to evaluate response to therapy. Also in some cases osteomyelitis or concurrent joint disease may be present. Omar et al. (2014) – investigated leukocyte esterase and glucose reagent strips to rapidly test synovial fluid for bacterial infection

11 Categories of Synovial Fluid based upon Clinical and Lab Findings
Measure Normal Non-inflammatory Inflammatory Septic Volume, mL (knee) < 3.5 Often > 3.5 Clarity Transparent Translucent Translucent-opaque Opaque Color Clear Yellow Yellow to opalescent Yellow to green, frank pus Viscosity High Low Variable WBC, per mm3 < 200 0 to 2000 2000 to 100,000 15,000 to > 100,000 PMNs (%) < 25 >= 50 >= 75 Culture Negative Positive PMN= Polymorphonuclear leukocytes In gout and septic joints, the WBC count often exceeds 50,000/mm3 Prosthetic joints with WBCs > 1700/mm3 and neutrophils > 65% are highly sensitive and specific for infection if there is no underlying inflammatory joint disease Crystal examination under a polarizing lens is the gold standard test for diagnosing gout and pseudogout Adapted from

12 Differential diagnosis
Inflammatory Crystal-induced arthritis: Gout: uric acid crystals Pseudogout: calcium pyrophosphate crystals Rheumatoid arthritis Reactive arthritis Infectious Lyme disease Disseminated Gonorrhea Non-inflammatory Hemarthrosis Red flags Septic arthritis Emergency Immediate hospital admission required Significant joint destruction and other complications, including amputation, sepsis, and death Osteomyelitis Avascular necrosis RA-

13 treatment Treatment includes immediate hospitalization for antibiotics and joint drainage Early consult with orthopedics, rheumatology, and infectious disease Synovial fluid aspiration analysis, start empirical antibiotics according to gram stain, then tailor antibiotics to culture results Antibiotic therapy Gram positive cocci: Vancomycin (also 1st line for MRSA) Daptomycin, linezolid, and clindamycin are alternatives Gram negative bacilli: third-generation cephalosporin Ceftriaxone, cefotaxime, ceftazidime Pseudomonas aeruginosa (IV drug abusers) Ceftazidime and gentamicin Cephalosporin-allergic patients Ciprofloxacin and aminoglycoside Parenteral and oral antibiotic therapy produce adequate drug levels in joint fluid. Intraarticular antibiotics may induce an inflammatory response and are not recommended. The initial regimen should be tailored to culture and susceptibility results when available

14 Treatment Duration of therapy Joint drainage
Parenteral antibiotics for at least 14 days followed by oral therapy for an additional 14 days Parenteral antibiotics for 4-7 days followed by days of oral therapy Three to four weeks of IV therapy may be needed for arthritis caused by P. aeruginosa, Enterobacter spp., S. aureus, or in the setting of bacteremia Joint drainage Needle aspiration (arthrocentesis) Arthroscopic drainage Arthrotomy (open surgical drainage) Immobilization, elevation, ice packs Postpone anti-inflammatory medications for hours; can use analgesics without anti-inflammatories if pain is severe Early active range of motion as tolerated will speed recovery Duration of therapy varies and typically depends on the causative agent Joint drainage should be performed for septic arthritis because this condition represents a closed abscess Anti-inflammatories delayed so that cultures can grow and arthrocentesis can be repeated if the first result was nondiagnostic

15 Treatment Needle aspiration Arthroscopy Surgical drainage
Knee, perform until culture negative If not adequate for joint decompression after 3-5 days, then surgical drainage is required Arthroscopy Provides easy irrigation and better visualization Knee, shoulder, wrist Surgical drainage Hips, shoulders, and prosthetic joint infections Any joint not improving after serial needle aspiration or if needle drainage is inadequate

16 outcomes Prognosis dependent on prior health of the patient, the causative organism, and promptness of treatment S. aureus is associated with poor functional outcome in 46-50% of cases Overall mortality rates range from % Mortality rate increases to 30% for patients with polyarticular sepsis Morality is 50% if infection due to S. aureus or occurs in the presence of RA Morbidity occurs in one-third of patients with bacterial arthritis Amputation, arthrodesis, prosthetic surgery, severe functional deterioration Failure to initiate appropriate antibiotic therapy within 24 to 48 hours of onset can cause subchondral bone loss and permanent irreversible joint damage and dysfunction Prompt identification and referral for treatment are imperative Even with prompt referral and initiation of abx therapy—patient may suffer significant joint destruction Cormorbid conditions, such as older age, renal or cardiac disease, and concurrent immunosuppression lead to poorer outcome

17 Summary

18 References Evaluation of acute monoarticular arthritis (2014). In A. H. Goroll & A. G. Mulley (Ed.), Primary care medicine: Office evaluation and management of the adult patient (7th ed.). Philadelphia: Lippincott Williams & Wilkins. Goldenberg, D. L., & Sexton, D. J. (2016). Septic arthritis in adults. In Calderwood, S. B. (Ed.), UpToDate. Retrieved from Hellman, D. B., & Imboden, J. B. (2015). Nongocococcal acute bacterial (septic) arthritis. In M. A. Papadakis, S. J. McPhee, & M. W. Rabow (Eds.). Current medical diagnosis & treatment (54th ed., pp ). New York: McGraw-Hill Horowitz, D. L., Katzap, E., Horowitz, S., & Barilla-LaBarca, M. (2011). Approach to septic arthritis. American Family Physician. 84(6), Retrieved from Omar, M., Ettinger, M., Reichling, M., Petri, M., Lichtinghagen, R., Guenther, D.,…Krettek, C. (2014). Preliminary results of a new test for rapid diagnosis of septic arthritis with use of leukocyte esterase and glucose reagent strips. The Journal of Bone and Joint Surgery. American Volume, 96(24), doi: /JBJS.N.00173

19 Questions?


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