Septic arthritis is an infection of one or more joints.
Bacterial infection is by far the most common cause of septic arthritis with staphylococcus aureus most frequently isolated. It normally presents with pain and swelling of the affected joint with signs of systemic infection. The condition may be categorised as:
Septic arthritis requires prompt recognition and management. Untreated it can lead to articular destruction and an overwhelming sepsis. This note focuses on the condition in adult patients.
Septic arthritis is rare, it has an estimated incidence of 4-10 per 100,000 patient years in Western Europe.
It most commonly affects the extremes of age (children and the elderly). It is also more common in those with immunodeficiency or IV drug use.
The rate of prosthetic joint infection varies depending on the joint. The two most common joint replacements in the UK are the knee and hip. Knee arthroplasty (approx 0.5-2%) is more commonly affected by septic arthritis than the hip (approx 0.5-1%)
Identifying the underlying organism and resistance pattern is key to the management of septic arthritis.
Bacteria are by far the most common pathogen responsible for septic arthritis. The causative organisms vary depending on age, though staphylococcus aureus is the most common cause in all groups above the age of 2.
Staphylococcus aureus is a gram-positive cocci and the most common cause of septic arthritis in adults (accounting for 35-56% of cases) and children above the age of 2. There is increasing incidence of methicillin resistance (MRSA) particularly in the IVDU and elderly populations.
Streptococcal species (gram-positive cocci) are the second most commonly isolated organisms in most series. Includes streptococcus pyogenes and group B streptococci.
Neisseria gonorrhoeae, a gram-negative diplococci, is a common cause of septic arthritis, particularly in young, sexually active individuals. Neisseria meningitidis another gram-negative diplococci may also cause the disease.
Gram-negative rods including E.coli and Klebsiella may be isolated. Pseudomonas aeruginosa is most commonly seen in IVDU.
Septic arthritis arises when bacteria (or other pathogens) enters the synovium.
Haematogenous spread is the most common mechanism by which bacteria infects the joint. Bacteria in the blood stream seed into a jointand infection results.
Direct inoculation occurs during surgery, secondary to animal bites, wounds or rarely joint injection. Spread may also be occur due to the spread from neighbouring infective foci.
The synovium is a specialised membrane that is well vascularised and lacks a basement membrane. The lack of a limiting basement membrane makes it susceptible to infection.
Bacteria colonise the synovial fluid and a inflammatory response is generated. In immunocompetent patients the immune response may eliminate the pathogen and clear the infection. If infection continues inflammation leads to worsening joint effusion with a resulting rise in the intra-articular pressure impairing the vascular supply. If untreated infection becomes systemic and joint destruction occurs.
Prosthetic joint infection (PJI) represents an uncommon but serious complication of surgery.
PJI occurs in around 0.5-1% of hip replacements and 0.5-2% of knee replacements. If it occurs it commits the patient to long courses of antibiotics, further surgical intervention and hospital stays.
The presence of foreign material enhances certain bacterias ability to form a biofilm. This protective layer causes a significant reduction in the chance of successful elimination of infection with antibiotics alone.
The timing of infection can give an indication to the causative pathogen and mechanism of infection:
Septic arthritis is more frequently seen in elderly diabetic patients.
A high index of suspicion should be had for any patient presenting with acute atraumatic joint pain.
Patients present with an acutely swollen, warm and painful joint - signs of systemic infection may be present. Septic arthritis is normally monoarticular - though uncommonly polyarticular disease is seen.
Some will present with more subtle and insidious features - in these patients pain and swelling may be mild and signs of systemic infection absent.
A number of conditions may present with a similar clinical picture. Excluding septic arthritis is essential.
Joint aspiration is key and should be obtained prior to antibiotics (whenever possible).
Blood tests will normally show an elevated CRP and white cell count indicative of inflammation and infection - though this is non-specific and seen in other infections and gout. Observations frequently show pyrexia that may be accompanied by a tachycardia, on occasion haemodynamic instability is present.
Joint aspiration is the gold-standard for diagnosis - where possible taken prior to antibiotic therapy. Imaging, particularly MRI, can be supportive for a diagnosis of septic arthritis.
All patients with suspected neutropenic sepsis should be managed with the sepsis six care bundle.
The sepsis six bundle is a protocol by which a patient may be investigated and treated for sepsis. It is by no means exhaustive but incorporates key investigation and treatment points. The bundle should be initiated and completed within one hour of recognition of the signs.
Patients with haemodynamic instability, a lactate greater than 2 or evidence of end-organ dysfunction should receive urgent review by a senior clinician and a MET/Peri-arrest call if indicated.
It is imperative, (where possible) in the case of suspected septic arthritis, that joint aspirations are obtained prior to antibiotics.
Patients should receive high flow oxygen to achieve appropriate target saturations. A target of 94-98% is appropriate for the majority of patients. Those at risk of carbon dioxide retention (COPD) should have a target of 88-92%. IV fluids should be started, often 500ml of crystalloid over 15 minutes with reference the patient's haemodynamic status and co-morbidities. Antibiotics are key and should be given without delay, NICE recommend empirical treatment with piperacillin/tazobactam (tazocin).
A minimum of two sets of blood cultures should be taken. Ideally, this should happen prior to administration of antibiotics though they should not be a cause for delay. A serum lactate should be obtained normally via a blood gas (arterial or venous) to help assess the patient's status. Urine output should be measured ideally with a catheter with a careful fluid balance recorded.
Patients with septic arthritis should be referred to and managed by orthopaedics or rheumatology.
Antibiotic management should be guided by patient factors, the suspected organism and culture results. Liaise with microbiology early. Typical courses last six weeks, with at least two weeks of intravenous therapy.
Gram negative bacteria are more common in the elderly and those suffering with recurrent UTIs. MRSA should be considered in patient with risk factors such as known MRSA colonisation or long lines (e.g. CVC).
There is no single set of antimicrobial guidelines, clinicians should refer to their local protocols. Flucloxacillin is frequently first line therapy (clindamycin if penicillin allergic). Vancomycin or teicoplanin are used in cases of suspected MRSA and ceftriaxone for gonococcal arthritis or suspected gram negative infections.
Patients with PJI require joint specialist input from orthopaedic surgery and microbiology. IVDU, immunosuppressed and ITU patients should be treated with close coordinations with microbiology.
The septic joint should be aspirated too dryness, this may be repeated if required.
Arthroscopic drainage and washout should be considered. Complex interventions may be required for patients with a prosthesis, this should be determined by senior orthopaedic surgeons.
The mortality from septic arthritis is estimated to be around 11%.
Joint destruction is thought to result in loss of function in around 40% of patients - this is dependent on the pathogen and period between onset and treatment.
As a relatively rare condition a great deal of variety is seen in the published figures. Mortality is higher in IV drug users and those with significant co-morbidities.
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