Bone and Joint Infections Flashcards
1
Q
Osteomyelitis - Pathogenesis

A
- A progressive infectious process resulting in inflammatory destruction, bone necrosis and new bone formation
- Pathogenesis requires high innocula, trauma or foreign material
- 3 types:
- Haematogenous
- Contiguous
- Diabetic
- May be acute or chronic (relapsing)
2
Q
Osteomyelitis - Haematogenous
A
- Following bacteraemia
- Escpecially in children
- Affects metaphyseal area of long bones
3
Q
Osteomyelitis - Contiguous
A
- After trauma/surgery or overlying soft-tissue infection
- Due to direct spread on infection
- Affects any ages
- Affects any bones
- May be associated with foreign bodies:
- Prostheses
- Pins
- Plates
4
Q
Osteomyelitis - Diabetic
A
- A consequence of:
- Reduced vascularity
- Neuropathic skin changes
- Decreased local immunity
- Metabolic disturbance
- Often associated with foot ulcers
- Assume osteomyelitis if bone is evident at the base of an ulcer
- Very hard to treat
- Progressive spread mans often results in amputation
5
Q
Osteomyelitis - Signs and Symptoms
A
- Possible acute symptoms
- Pain
- Swelling
- Overlying inflammation
- Infants may have few localising signs
- May be evidence of surgery or trauma
- Possible chronic signs
- May be minimal
- Often a sinus (communiation with skin)
- Old scars
- May be acutely inflammed
- On X-ray
- Periosteal thickening/elevation
- Lysis and sclerosis
6
Q
Osteomyelitis - Investigations
A
- Investigate
- Blood cultures
- FBC
- CRP
- Deep tissue swabs from theatres
- Wound swabs? - may be heavily colonised with skin flora
- Sinus swabs - NO due to contamination with skin flora
- Imaging
- Don’t initate antibiotics until necessary samples are taken
7
Q
Osteomyelitis - Pathogens
A
- Most common is Staphlococcus aureus
- **Adhesin **receptors bind
- Bone matrix
- Cartilage - collagen-binding
- Foreign material - fibronectin-binding
- **Adhesin **receptors bind
- Infants
- Group B Streptococci
- Staphlococcus aureus
- E. Coli
-
Children 1-6 years
- Staphlococcus aureus
- Streptococcus pyogenes
- H.influenzae
-
Adults
- Staphlococcus aureus
- Staphlococcus epidermis
- Pseudomonas aeruginosa
- Gram negatives e.g. E.coli
8
Q
Septic Arthritis

A
- Infection of joint space
- Haematogenous
- Contiguous
- Most commonly hip or knee
- Usually monoarticular
- Predisposed to if existing:
- Rhematoid arthritis
- Joint disease
9
Q
Septic Arthritis - Pathogenesis
A
- Synovial membrane is highly vascular
- Local polymorphonuclear response –>
- Release of proteolytic enzymes and bacterial toxins
- Rapid cartilage destruction + joint effusion
- Drecreased blood supply due to compression of vasculature
10
Q
Septic Arthritis - Signs and Symptoms
A
11
Q
Septic Arthritis - Pathogens
A
- Most commonly *Staphylococcus aureus *or Streptococcus species
- *Haemophilus influenzae *if much less common since HiB vaccine
- *Neisseria gonorrhoea *in young adults - !
- Less commonly Gram-negative infection e.g. Pseudomonas in IVDU
- 10% of infections are polymicrobial
12
Q
Reactive Arthritis

A
- May occur following infectious diarrhoea:
- Salmonella
- Campylobacter
- Yersinia
- Shigella
-
Following STIs = ‘Reiter’s syndrome’ (+ conjunctivitis, arthritis +/- rash)
- Chlamydia
- Gonorrhoea
- Also may be due to Hepatitis B
- Bacteria will not be cultured from the joint as arthritis is an inflammatory reaction to infection elsewhere
- Investigate to confirm diagnosis with:
- Serology
- Stool cultures
- GU swabs
13
Q
Prosthetic Joint Infection

A
- Septic arthritis in a prosthetic joint
- May follow joint replacement
- Months-years after surgery = late infection
- Follows 0.5-2% of all joint replacements
- Symptoms may be mild - joint pain/discomfort
14
Q
Prosthetic Joint Infection - Pathogenesis
A
- Early infection usually due to direct inoculation - skin type flora
- Late infection usually haematogenous
- Often multiple organisms
- Leads to a biofilm on the foreign material
- Thought to be involved in most infections now
- Compled communities of surface-associated cells in an extracellular matrix
- Provided physical protection against antibiotics
- Cells may change phenotype making them less susceptible to treatment
- Sometimes bacteria stop dividing and become dormant - resistant to abx targeting division
15
Q
Prosthetic Joint Infection - Diagnosis
A
- Often difficult
- Hx & examination
- Chronic infection fewer signs than acute
- ESR
- CRP
- Isotope scans
- MC&S of joint aspirate
- Bacteriological diagnosis important
- Gram stain of joint fluid has poor sensitivity - culture better
16
Q
Prosthetic Joint Infection - Conservative Treatment
A
- Conservative
- Joint retained
- Drainage, washout and debridement of joint
- 6 weeks of antibiotics
- Risk of missing adherent bacteria to cement/prosthesis if only rely on aspiration for diagnosis
- Success rate approximately 20% - better in:
- Early post-op cases when treatment is intiated promptly
- >80% failure rate if debrided >2 days after symptoms present
- Avirulent organisms i.e. not Staphylococcus aureus
- Early post-op cases when treatment is intiated promptly
- Lifelong suppresive therapy if unfit for surgery
- 30-60% of patients retain useful joint function
- Do nothing if elderly or comorbidites and symptoms do not impact on quality of life
17
Q
Prosthetic Joint Infection - Radical Treatment
A
- Involves removal of prosthesis
- 1 stage replacement
- Removal and replacement in same operation
- Uses antibiotic loaded cement
- 70-80% success
- May be suitable for patients unfit for 2 operations
- Removal and replacement in same operation
- 2 stage replacement
- Removal followed by 6 weeks abx (+/- cement spacer impregnated with abx)
- Then re-implantation
- 90-95% success rate
- May require plastic sugery and skin/muscle flaps
- Removal followed by 6 weeks abx (+/- cement spacer impregnated with abx)
- 1 stage replacement
18
Q
Treatment - Bone/Joint Infections
A
- Seek advice dependent on culture results
- Combination theapy recommended for PJI and often osteomyelitis
- Abx course:
- 2-3 weeks for septic arthritis
- 4 weeks for paediatric osteomyelitis
- 6-8+ weeks for adult osteomyelitis and PJI - may need to continue for:
- Months if prosthesis remains in place
- Years if infection is persistant and can’t be cured
- Drainage of effusion/pus is essential
- Also povides specimen for diagnosis
- Debridedment of all infected bone material essential in osteomyelitis (except paediatric)
- Removal of prosthetic joint usually required to clear infection
- NB - rarely necessary to start antibiotics immediately in patients with PJI or chronic osteomyelitis - get appropriate samples for cultures first
19
Q
Treatment - Bone/Joint Infections: Antibiotics
A
- Sensitivities:
- *Staphlococcus aureus - **flucloxacillin + rifampicin *or fusidic acid or gentamycin
- MRSA - vancomycin + rifampicin or fusidic acid
- Streptococci - benzypenicillin **or **cefuroxime
- *Coliforms - *consider ciprofloxacin
- *Pseudomonas - ciprofloxacin/ceftazidime + gentamycin *initially -** ! **check sensitivities
- IV vs oral
- Possible to use oral antibiotics for switch therapy
- Some e.g. clindamycin or ciprofloxacin can be used as part of combination therapy for long-term treatment
- **! **- advice important
- Some oral abx are poorly absorbed from gut e.g. penicillin
- Some penetrate bone poorly e.g. some cephalosporins
20
Q
Reducing Contamination of Operative Site
A
- Main sources of contamination
- Patient skin flora
- Hands of surgical team
- Pre-existing infection
- Airborne from:
- Skin
- Mucous membranes
- Clothing of patient/surgical team