MSK Flashcards

(89 cards)

1
Q

Osteoarthritis

A

Described as Wear & Tear in the joints.

It occurs in the synovial joints & results from genetic factors, overuse & injury.

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2
Q

Osteoarthritis Pathology

A

Thought to result from an imbalance between the cartilage wearing down & the Chondrocytes repairing it → leading to Structural issues in the joint.

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3
Q

Osteoarthritis Risks

A
  • Obesity
  • Age
  • Occupation
  • Trauma
  • Female
  • Family Hx
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4
Q

Osteoarthritis affected joints

A
  • Hips
  • knees
  • Sacroiliac joints
  • Distal - interphalangeal joints in the hands
  • Carpometacarpal joint at the base of the thumb
  • Wrist
  • Cervical spine (cervical Spondylosis)
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5
Q

Osteoarthritis Diagnosis

A
  • Diagnose without Ix if patient over 45, has typical pain, no morning stiffness.
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6
Q

Osteoarthritis X-ray changes

A
L = Loss of joint space
O = Osteophytes (bone spurs)
S = Subarticular sclerosis 
S = Subchondral cysts (fluid- filled holes in bone)
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7
Q

Ostoearthritis symptoms

A
  • Joint enlargement & bone swelling in fingers (Heberden & Bouchard)
  • Restricted range of motion - Stiffness on rest
  • Crepitus on movement
  • Effusions (fluid) around joint
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8
Q

Osteoarthritis Signs

A

In Hands:

→ Heberden’s nodes (in DIP joints)
→ Bouchard’s nodes (in PIP joints)
→ Weak grip
→ Squaring at base of the thumb (at carpometacarpal joint)

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9
Q

1Osteoarthritis Management

A
  1. Oral paracetamol & topical NSAIDs
  2. Analgesics
  3. Intra-articular Steroid injection - methylprednisolone
  4. Joint replacement
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10
Q

Rheumatoid arthritis.

A

Autoimmune condition that causes Chronic inflammation of the synovial lining (synovitis) of the joints, tendon sheaths & bursa.
RA is symmetrical & affects multiple joints (symmetrical polyarthritis).

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11
Q

Rheumatoid Arthritis Risks

A

Gene:
→ HLA DR4
→HLA DR1

  • Female
  • Develops in middle age
  • Family risk
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12
Q

Rheumatoid Arthritis Pathology

A

Anti - CCP antibodies - indicate that R.A. will form.

Rheumatoid Factor → autoantibody.
Targets the Fc portion of the lgG antibody → causes activation of the immune system against the Patients own lgG causing systemic inflammation,

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13
Q

Rheumatoid Arthritis Symptoms

A

Symmetrical Distal Polyarthropathy

  • Pain
  • Swelling
  • Morning Stiffness
    Deformities of the hand:
    → Ulnar deviation
    → Swan neck
    → Boutenniere deformities
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14
Q

Osteoarthritis VS Rheumatoid Arthritis Diff.

A

R.A = Pain is worse after rest but improves with activity.

Osteoarthritis = Pain worse after activity but improves with rest.

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15
Q

Extra- articular manifestations of Rheumatoid Arthritis

A
→ Pulmonary fibrosis with nodules
→ Bronchiolitis obliterans 
→ Felty's syndrome (RA, neutropenia, & splenomegaly) 
→ Secondary Sjogren's Syndrome
→ Anaemia of chronic disease
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16
Q

Rheumatoid Arthritis Investigations

A

Bloods:

  • Check Rheumatoid Factor
  • anti-CCP Antibodies
  • Check inflammatory markers - CRP & ESR
  • X-Ray of hands & feet
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17
Q

Rheumatoid Arthritis X-Ray changes

A
L = Loss of joint space
0 = Osteopenia
E = Erosion of bone
S = Swelling of soft tissue
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18
Q

Rheumatoid Arthritis Management

A
- Methotrexate + Folate
(DMARDs)
- Hydroxychloroquine
- TNF blocker (Infliximab)
- B-cell inhibitors (Rituximab)
- NSAIDs for pain
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19
Q

Main TNF inhibitors for R. A.

A
  • Adalimumab
  • Infliximab
  • Etanercept
  • Rituximab
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20
Q

Side Effects:

→ Methotrexate

→ Leflunomide

→ Sulfasalazine

→ Hydroxychloroquine

→ Anti-TNF medications

→ Rituximab

A

→ Methotrexate = Bone marrow suppression & Leukopenia & highly teratogenic.

→ Leflunomide = Hypertension & Peripheral neuropathy

→ Sulfasalazine = Male infertility (low sperm count)

→ Hydroxychloroquine = Nightmares & reduced visual acuity

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21
Q

Osteoporosis

A

Reduction in the density & mass of the bones & micro- architectural deterioration.

→ more fragility prone to fractures.

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22
Q

Risk factors for Osteoporosis

A
  • Old age
  • Female - especially post- menopausal
  • Reduced mobility
  • low BMI
  • Rheum. Arthritis
  • Alcohol & Smoking
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23
Q

Osteoporosis Investigations

A
  • FRAX Tool - gives risk of a fragility fracture over next 10 yrs.
  • Bone mineral density measured using a DEXA scan (Dual- Energy X-Ray absorptiometry) → check T score at the hip.
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24
Q

Osteoporosis Management

A
  • 1st Line = Bisphosphonates (e.g. Alendronate, Zoledronic, Risedronate)
    → Reduce osteoclast activity preventing reabsorption of bone.
  • Denosumab (monoclonal antibody) used if Bisphosphonates is contraindicated.
  • Hormone Replacement Therapy
  • Calcium supplementation with Vitamin D
    (Calcichew - D3 + ColecalciferoI)
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25
Giant Cell Arteritis (Temporal)
Systemic vasculitis of the medium & large arteries.
26
Giant Cell Arteritis Symptoms
Main is severe unilateral headache around temple & forehead - Scalp tenderness - Jaw claudication - Blurred or Double vision - Irreversible painless complete sight loss → Fever → Muscle aches & weight loss → Fatigue → Peripheral oedema
27
Giant Cell Arteritis Diagnosis
- Temporal artery biopsy (find multinucleated giant cells) - Bloods (Raised ESR & CRP levels) - LFT (raised alkaline phosphatase)
28
Giant Cell Arteritis Management
→ Steroids 40-60mg Prednisolone → Aspirin → PPIs (Omeprazole) ``` DON'T = Don't stop taking steroids abruptly → Risk of adrenal crisis S = Sick day rules T = Treatment Card O = Osteoporosis - Bisphosphonates with Calcium & VitD p = PPI for gastric protection ```
29
Giant Cell Arteritis Complications
→ vision loss → Cerebrovascular accident (stroke) → Relapse of condition → Aortitis leads to aortic aneurysm & aortic dissection
30
Osteoporosis Causes
- Endocrine (Cushing's & Parathyroid) - Haematology (Myeloma) - GI (Malabsorption) → Iatrogenic (Steroid use)
31
Systemic Lupus Erythematosus (SLE)
Inflammatory multisystem autoimmune disorder with arthralgia (joint pain) & rashes. Type III hypersensitivity. - Female - 20-40 yrs
32
SLE Presentation
- Joint pain - Skin - Malar butterfly rash, discoid rash, Photosensitive rash - Serositis - Scleritis, Pericarditis, Pleuritis, Oral ulcers - kidneys - Glomerulonephritis with proteinuria - GNS - Depressions, Psychosis
33
SLE Diagnosis
- Bloods - ESR/ CRP | - ANA, Anti-dsDNA, Serum C3 & C4
34
SLE Treatment
- NSAIDs - Hydroxychloroquine - Steroids
35
Antiphospholipid
Antibody - mediated acquired thrombophilia characterised by thrombosis &/ recurrent miscarriages.
36
Antiphospholipid Signs & Symptoms
- Coagulation defects - Livedo reticularis - Obstetric issues - Thrombocytopenia
37
Antiphospholipid Diagnosis
Clinical criteria : Vascular thrombosis, Pregnancy morbidity Lab Criteria : Anticardiolipin antibody, Lupus anticoagulant, Anti-Beta 2 Glycoprotein 1 antibody
38
Antiphospholipid Treatment
- Blood clots (anticoagulate with heparin) - Chronix (Warfarin) - Pregnancy (Heparin with aspirin) Prevent CVS issues → Quit smoking, More exercise
39
Sjogren's Syndrome
Chronic inflammatory autoimmune disorder. - Immunologically mediated destruction of epithelial exocrine glands especially the lacrimal & salivary glands.
40
Sjogren's Signs & Symptoms
- Dry eyes, mouth, Parotid gland enlargement - Joint pain - Raynauds - Systemic features Associated with RA, SLE, PBC & Scleroderma
41
Sjogren's Diagnosis
Schirmer Tear Test - Rose Bengal staining & sit lamp exam Rheumatoid Factors, Anti Nuclear Antibody, Anti - Ro, Anti-La
42
Sjogren's Treatment
NSAID Hydroxychloroquine M3 agonist - Pilocarpine Lifestyle: Humidifier, Eye-drops, Mouth wash
43
Poly / Dermato myositis
Polymyositis = Rare muscle disorder where there's inflammation & necrosis of skeletal muscle fibres. Dermatomyositis = Poly + skin involvement
44
Poly | Dermato myositis
Polymyositis: Symmetrical progressive muscle weakness & wasting affecting the proximal muscles of the shoulder & pelvic girdle. Dermatomyositis: Heliotrope (purple) discolouration of eyelids. Scaly erythematous plaques over the knuckles. - Arthralgia, Dysphagia
45
Poly/ Dermato myositis Diagnosis
- Muscle biopsy - Bloods: Raised Serum creatine kinase, Aminotransferases, Lactate dehydrogenase & Aldolase - Immunology - ANA, Anti jo1, Anti mi2
46
Poly | Dermato myositis Management
- IV prednisolone - Stronger Immunosuppressants - Symptomatic treatment of skin disease
47
Septic Arthritis Causes
- IV Drug Use - Immunocompromised - Intra-articular injections
48
Septic Arthritis Risks
``` Common Bugs: → Staphylococcus Aureus → Neisseria Gonorrhoea → Gram -ve Bacteria (E. Coli) → Haemophilus Influenza ```
49
Septic Arthritis Treatment
→ Flucloxacillin → Penicillin or Clindamycin → If MRSA give Vancomycin Or Telcoplanin → If Gram -ve, Cefotaxime Or Ceftriaxone
50
Uric Acid Formation & Pathology
Cell breakdown → Hypoxanthine → Xanthine → Uric Acid + Diet (Xanthine Oxidase) Build-up of uric acid → Uric acid crystals → Deposits in joint spaces causing inflammation
51
Hyperuricaemia Types
Pseudogout = + ve Birefringent Ca Pyrophosphate. Gout = - ve Birefringent Monosodium Urate
52
Stages of Gout progression
High Uric acid levels Acute Gout Intercritical Gout Chronic Gout
53
Hyperuricaemia
> 420umol / L (Male) > 360umol / L (Female) Asymptomatic
54
Hyperuricaemia Causes
Diuretics - Thiazides High insulin levels High fructose intake Dysfunction of URAT-1 transporter
55
Hyperuricaemia Symptoms
- Red, Hot joint - Painful - Swollen - Acute onset → Mainly affects Big toe, Midfoot, Ankle, Knee, Wrist
56
Hyperuricaemia Investigations
1St Line = Bloods Gold = Joint aspiration U+E + eGFR - Renal family history Uric acid levels
57
Hyperuricaemia Management
ACUTE: 1st Line = NSAIDs or Colchicine 2nd line = Intra - articular Steroid injection CHRONIC: 1st Line = Allopurinol - inhibit Xanthine Oxidase 2nd Line = Febuxostat
58
Osteomyelitis
``` Infection of bone marrow. Ways of entry: → Haematogenously → Open wound → Contiguously = Skin into blood ```
59
Osteomyelitis formation
Acute inflammation → Subperiosteal abscess → Sequestrum → Involcrum → Cloacae
60
Osteomyelitis Diagnosis
Labs: High CRP, ESR, WBC Imaging: X- Ray, CT, MRI, Bone scan Bone biopsy Bone culture
61
Osteomyelitis Management
Antibiotic - Penicillin or Clindamycin Amoxicillin Cefotaxime
62
Ankylosing Spondylitis
Inflammation of sacroiliac joints. Loss of spinal movements
63
Ankylosing Spondylitis Investigations
- Bloods = HLA B27 | - X Ray = Bamboo spine
64
Ankylosing Spondylitis X- Ray changes
- Bamboo spine due to fusion - Sacroiliac joints - eroded & Sclerotic - Unclear margin between rims - Bone spurs aka syndesmophytes
65
Reactive Arthritis
Mainly due to infection
66
Reactive Arthritis Symptoms
- Can't see - Uveitis - Can't pee - Urethritis - Entheritis → Keratoma Blennorhagica → Circinate Balanitis
67
Reactive Arthritis Investigations
Bloods: Inflammatory markers High ESR, CRP, ANA, Rheumatoid factor Imaging
68
Psoriatic Arthritis Signs & Symptoms
``` Painful Swollen Stiff joints Psoriatic plaques Dactylitis ```
69
Ankylosing Spondylitis Treatment
- Supportive - Pain management : NSAIDs or Corticosteroids - Biological therapy - Infliximab
70
Lower Back pain Management
``` Analgesia ladder Paracetamol NSAIDs Weak opiates Neuropathic Pain Tx - Gabapentin / Tricyclic ```
71
Fibromyalgia
Chronic widespread Pain
72
Fibromyalgia Investigations
Exclude all other differentials with bloods & imaging
73
Fibromyalgia Treatment
Neuropathic pain relief → Tricyclic Acid (TCA) → Gabapentin → Pregabalin Opiates
74
Scleroderma
Disease characterised by fibrosis across multiple organ systems. - Most common in women aged 30-50 - Due to increased production of collagen in tissues.
75
Scleroderma Investigations
``` Usually in fingers: → skin becomes tight → fingers become stiff & inflexible → Symptoms of Raynauds → Joint & Muscle pain ```
76
Scleroderma Management
→ Immunosuppressants (e.g. Cyclophosphamide) → Physiotherapy / Occupational Therapy Symptomatic Treatment: - Analgesia - Calcium Channel blocker - Topic skin emollients - PPI & antacids (Oesophageal reflux) - Treating Pulmonary Artery Hypertension ( Bosentan, Sildenafil, Iloprost )
77
Bone Tumours Types
→ Osteosarcoma = Primary bone malignancy, metaphysis of long bones → Ewing Sarcoma = From mesenchymal cells originating from long bones → Osteochondroma = (Benign) Overproduction of bone which deposits on metaphysis
78
Secondary Bone Tumours Metastasis
``` P = Prostate B = Breast k = Kidneys T = Thyroid L = Lungs ```
79
Bone Tumour Investigations
Bloods: FBC, U&E, ALP, PSA Imaging X-Ray - Lytic lesions CT Scan - metastases
80
Bone Tumours Management
- Pain Management - Bisphosphonates - Radiotherapy - Chemotherapy
81
Paget's Disease
Disorder of excessive bone turnover due to excessive activity of both Osteoblasts & clasts Leads to patchy areas of sclerosis & lysis. Mainly affects axial skeleton
82
Paget's Disease Sx
- Bone pain - Bone deformity - Fractures - Bone enlargement
83
Paget's Disease Ix
- Osteoporosis circumscripta (less dense) - Cotton wool appearance of Skull - V-shaped defects in Long bones - Raised alkaline phosphatase
84
Paget's Disease Tx
Bisphosphonates NSAIDs Calcium & Vit. D
85
Septic Arthritis Sx Common Bac.
Infection occurs in joint. Sx: Hot, red, swollen painful joint Stiffness Fever Staphylococcus Aureus Neisseria Gonorrhoea Strep. pyogenes E. coli
86
Septic Arthritis Tx
Joint aspiration Flucloxacillin + Rifampicin Vancomycin + Rifampicin (penicillin allergy) Clindamysin
87
Gout Risks Joint's
High blood uric acid levels. Risk: High purine diet, Diuretics, Obesity Joints: Metatarsophalangeal joint, Wrists, Carpometacarpal joints, knee, Ankle
88
Gout Ix Tx
Aspiration of fluid: No bac. growth Needle shaped urate crystals -ve Birefringent of Polarised light Joint X-ray: Lytic lesions, Punched out erosions ``` Tx NSAIDS Colchicine Steroids Allopurinol - Xanthine Oxidase inhibitor ```
89
Pseudogout Sx Ix Tx
Caused by calcium pyrophosphate crystals. Sx: hot, swollen, Stiff, Painful knee Ix: Aspirated fluid = Rhomboid crystals, +ve Birefringent of Polarised light Tx: NSAIDS, Colchicine, joint aspiration, steroids