MSK - Level 1 Flashcards
Description of septic arthritis?
- Infection producing inflammation in native/prosthetic joint or more than one joint
- Medical emergency and can destroy joint or develop sepsis <24 hour
- Reaches via bloodstream, adjacent osteomyelitis or external skin puncture wounds
Epidemiology of septic arthritis?
- Knee in >50% cases, followed by hip, shoulder, ankle and wrists
- 1-2% incidence
Risk Factors of septic arthritis?
o Age>80 o Rheumatoid arthritis/Gout o DM o Immunosuppresion o Renal failure o Prosthetic joints/Recent surgery o IVDU
Causative organisms of septic arthritis?
o S.aureus (most common) o Streptococcus o N.gonorrhoea o TB o Salmonella o Coagulase neg staph – prosthetic joints
Symptoms and signs of septic arthritis?
o Monoarticular
o Red, painful, swollen joint developing acutely
o Pain on active and passive movement and often held in position of most comfort (slightly flexed)
o May be fever, rigors, shaking, vomiting
- Signs may be less marked in elderly, IVDU, immunocompromised
Investigations needed in septic arthritis?
- Bloods
o FBC, ESR, CRP, blood cultures - Joint aspiration
o Send for leukocyte count, Gram staining, microscopy and culture, ?AAFB
o Infectious aspiration – yellow, turbid, purulent, >10000 cells, neutrophils, Gram stain and culture +ve
o Normal aspiration – colourless/pale yellow, clear, 200-1000 cells, mononuclear cells, Gram stain and culture -ve - X-rays
o Normal or soft tissue swelling with displacement of capsular fat planes and swelling of soft tissue
o Later, bone destruction occurs - CT/MRI scan reserved for difficult cases
Initial Management of septic arthritis? Orthopaedic management after referral?
o Analgesia
o IV Flucloxacillin for 2 weeks then oral switch for 4 weeks
If penicillin allergic - Clindamycin
If MRSA – Vancomycin
If gonococcal – cefotaxime
Empirical and start after aspiration
o Refer to Orthopaedic team for Joint irrigation/drainage, Analgesia, Splinting (In position of function, once infection under control then mobilisation will promote healing)
Management of osteomyelitis/septic arthritis?
- Flucloxacillin for 6 weeks
o Consider adding fusidic acid or rifampicin for 1st 2 weeks
o If penicillin allergic – clindamycin
o If MRSA – vancomycin
Prognosis of septic arthritis?
o Mortality is 10-20%
o Around half regain baseline joint function after treatment
Description of giant cell arteritis?
- Chronic immune-mediated vasculitis characterised by granulomatous inflammation in walls of medium and large arteries
- Preferentially extracranial branches of carotid artery and branches of ophthalmic artery
- GCA and polymyalgia rheumatica often occur together in 50%
Epidemiology of giant cell arteritis?
- Incidence rare before 50 and peaks at 70
- White people 7x more common
- 3x more common in women
Symptoms of giant cell arteritis?
Headache Unilateral over temporal region Temporal artery and scalp tenderness When combing hair Jaw claudication Pain while eating Amaurosis fugax Sudden blindness in eye Diplopia Fever, fatigue, anorexia Other – Neuropathy, morning stiffness
Signs of giant cell arteritis?
o Ischaemic disease on fundoscopy
o Temporal arteries – prominent, beaded, tender and pulseless
o Bruits may be heard over carotid
Suspect giant cell arteritis if..?
- Suspect if >50 and:
o New onset localised headache, unilateral in temporal area
o Temporal artery – tender, thickened, nodular, red, pulseless
When to refer people with suspected giant cell arteritis?
- Refer all people for temporal artery biopsy
o If visual impairment – same-day ophthalmology assessment
o If no visual impairment – urgent rheumatology assessment (biopsy within 7 days)
What bloods tests to order in giant cell arteritis?
o ESR, CRP raised
o FBC – normochromic normocytic anaemia, elevated platelets
o LFT – mildly elevated
Initial drug treatment of giant cell arteritis?
Immediate Prednisolone 60mg/d PO
Assess response over 1st 48 hours – if poor seek specialist advice
If develop visual symptoms – seek same-day assessment for IV methylprednisolone
Treatment reduced slowly and required for 1-2 years
Aspirin 75mg OD
Omeprazole 20mg OD
Ongoing management of giant cell arteritis?
o If symptoms controlled – reduce dose of prednisolone slowly
60mg until ESR/CRP normal, then reduce by 10mg every 2 weeks until 20mg daily, then reduce 2.5mg every 2-4 weeks until on 10mg daily, then 1mg evert 1-2 months
o Review a week after dose change and every 3 months for 1st year then 3-6 monthly
Do ESR, CRP, BP and glucose
o Assess fracture risk and whether need bisphosphonates
Managing a relapse of giant cell arteritis?
o If visual disturbance – increase to 60mg prednisolone & same-day assessment with ophthalmologist
o If jaw claudication – increase to 60mg daily &seek specialist advice
o If headaches, or PMR – increase dose and seek specialist advice
Prognosis of giant cell arteritis?
o Relapses common – especially when steroid treatment reduced or withdrawn too quickly
o Exacerbations occur in 30-50% of people during first 2 years
Complications of giant cell arteritis?
o Visual Loss – total or partial o Aortic aneurysm, aortic dissection, large artery stenosis and aortic regurgitation o CVD o Peripheral neuropathy o Confusion and encephalopathy
Description of spinal cord compression?
- Acute spinal cord compression is a neurosurgical emergency
- Cancers leading to MSCC – breast, bronchus, prostate, myeloma/lymphoma but can occur with any tumour
- Caused by tumour or metastases in vertebral body or paraspinal region pressing on spinal cord
Epidemiology of spinal cord compression?
- 2/3 in thoracic region
- Occurs in 20% of patients with spinal metastases
Aetiology of spinal cord compression?
o Metastases (breast, lung, prostate, thyroid, kidney)
o Cancer
o Trauma
o Cervical disc prolapse
Symptoms of spinal cord compression?
o Back pain/nerve root pain
Either unilateral/bilateral, aggravated by movement, coughing or lying flat
o Motor weakness – strength changes
o Subjective sensory disturbances
o Bladder/Bowel dysfunction generally occurs late
Signs of spinal cord compression?
o Weakness/Paraparesis/Paraplegia
o Changes in sensation below level of compression
o Hyperreflexia
o Clonus and painless bladder distension
o Can lead to paraparesis, paraplegia and incontinence
Red flags in spinal cord compression?
o Leg Weakness o Sensory Loss o Thoracic back pain o Constant pain o Urinary retention/incontinence o Saddle Anaesthesia & loss of anal tone
Management if suspected metastatic spinal cord compression?
o Contact MSCC coordinator urgently if:
Pain in thoracic or cervical spine, progressive lumbar spine, severe unremitting lower spinal pain, aggrevated by straining, local tenderness, nocturnal spinal pain
o Contact MSCC coordinator immediately if signs of MSCC
Initial management of spinal cord compression?
Initial Management
Nurse flat with neutral spine
Offer graduated compression/anti-embolism stockings
Catheterise in bladder incontinent
Medical
Urgent dexamethasone 16mg PO daily commenced at suspicion
PPI cover needed
Imaging
Urgent Whole Spine MRI
Definitive management of spinal cord compression?
Surgery • Should have before they cannot walk • Postoperative radiotherapy Radiotherapy • Urgent if surgery not suitable • Fractionated radiotherapy if epidural tumour without neurological involvement, pain or spinal instability
Prognosis of spinal cord compression?
- Outcomes correlate with level of function at the time of treatment
- If treated within 24 hours, 57% will walk again
- Complete paralysis, present for several days, is almost never reversible
What diseases have a positive rheumatoid factor?
Rheumatoid arthritis Sjogrens syndrome Felty’s syndrome Infection SLE, sclerosis
What diseases have a positive anti-CCP antibody?
Rheumatoid arthritis
What diseases have a positive antinuclear antibody?
SLE Autoimmune hepatitis Sjogren’s syndrome Systemic sclerosis Rheumatoid arthritis
What diseases have a positive anti-double stranded DNA (dsDNA) & positive anti-Sm & positive anti-RNP??
SLE
What diseases have a positive antihistone antibody?
Drug-induced SLE
What diseases have a positive antiphospholipid antibody (anti-cardiolipin)?
Antiphospholipid syndrome
SLE
What diseases have a positive anti-Ro?
• SLE, Sjogren’s syndrome, systemic sclerosis
What diseases have a positive anti-La?
• Sjogren’s syndrome, SLE
What diseases have a positive anti-Jo-1 & anti-mi-2?
• Polymyositis, dermatomyositis
What diseases have a positive anti-Scl70?
• Diffuse systemic sclerosis
What diseases have a positive antimitochondrial antibodies (AMA)?
Primary biliary cirrhosis
Autoimmune hepatitis
Idiopathic cirrhosis
What diseases have a positive anti-smooth muscle antibodies (SMA)?
Autoimmune hepatitis
Primary biliary cirrhosis
What diseases have a positive gastric parietal antibodies?
Pernicious anaemia
Atrophic gastritis
What diseases have a positive intrinsic factor antibodies?
Pernicious anaemia
What diseases have a positive anti-tissue transglutaminase & anti-endomysial antibodies?
Coeliac disease
What diseases have a positive thyroid peroxidase antibodies?
Hashimoto’s thyroiditis
Graves’ disease
What diseases have a positive islet cells Ab & glutamic acid decarboxylase?
T1DM
What diseases have a positive anti-GBM?
Goodpasture’s disease
What diseases have a positive antineutrophil cytoplasmic antibodies (ANCA) - cytoplasmic - specific for serine proteinase 3?
- Granulomatosis with polyangiitis (Wegeners)
- Microscopic polyangiitis
- Polyarteritis nodosa
What diseases have a positive antineutrophil cytoplasmic antibodies (ANCA) - perinuclear - specific for myeloperoxidase?
- Microscopic polyangiitis
* Churg-Strauss disease
What diseases also have a positive ANCA?
ANCA also positive in Crohn’s, UC, sclerosing cholangitis, autoimmune hepatitis, Felty’s, SLE, RA, drugs (antithyroid, allopurinol, ciprofloxacin)
What diseases have a positive acetylcholine receptor antibodies?
Myasthenia gravis
What diseases have a positive anti-voltage gated Ca-channel antibodies?
Lambert Eaton Syndrome