roma Flashcards

1
Q

azathioprine adverse effects and interactions

A

-bone marrow suppression
-nausea-vomit
-pancreatitis
-increased risk for non-melanoma skin cancer
-interact with allopurinol

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2
Q

how does allopurinol cause interaction with azathioprine?

A

-cause severe bone marrow suppression-pancytopenia-low wbc-allow for cap/tonsillitis/pharyngitis
-allopurinol-xanthine oxidase inhibitor-metabolises 6-mp into active form=azathioprine

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3
Q

what is the next best step if temporal arteritis is suspected?

A

urgent high dose prednisolone before the temporal artery biopsy to prevent permanent vision loss

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4
Q

Treatment of Temporal Arteriti

A

Urgent High-Dose Glucocorticoids: Administered when suspected and before temporal artery biopsy
Visual Loss: IV methylprednisolone used if evolving visual loss; dramatic response expected
Urgent Ophthalmology Review: Visual damage is often irreversible
Other Treatments: Bisphosphonates for bone protection during steroid therapy, low-dose aspirin (evidence base weak)

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5
Q

Investigations for Temporal Arteritis

A

Raised Inflammatory Markers: ESR > 50 mm/hr (CRP may also be elevated)
Temporal Artery Biopsy: May show skip lesions
Creatine Kinase and EMG: Normal

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6
Q

Clinical Features of Temporal Arteritis

A

Age: Typically > 60 years old
Onset: Rapid (e.g., < 1 month)
Common Symptoms: Headache (85%), jaw claudication (65%)
Vision Testing: Key investigation; anterior ischemic optic neuropathy is a major complication
Ocular Complications: Swollen pale disc, blurred margins, amaurosis fugax, sudden permanent visual loss, diplopia
Physical Exam: Tender, palpable temporal artery

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7
Q

Temporal arteritis overlap with which other disease?

A

PMR=Overlap with Polymyalgia Rheumatica (PMR)
Definition: About 50% of temporal arteritis patients exhibit features of PMR.
PMR Features: Aching, morning stiffness in proximal limb muscles (not weakness), lethargy, depression, low-grade fever, anorexia, night sweats.

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8
Q

Lateral epicondylitis-tennis elbow-signs
Diagnostic
Management

A

worse on resisted wrist extension/suppination whilst elbow extended
X-ray usually normal/us-tendon thickening/mri-assess bone-cartilage-ligaments as well/cbc-rule out osteitis pubis
-rest.ice-nsaid-physio-steroid/lidocaine not directly into tendon-surgery if not better in 6 months
STEROID INJECTIONS AVOIDED IN INSERTIONAL tendinopathies-may cause TENDON RUPTURE

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9
Q

NORMAL IN PMR

A

CREATINE KINASE

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10
Q

SLE TX FIRST LINE

A

HYDROXYCHLOROQUINE

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11
Q

Methotrexate adverse effects

A

Pneumonitis
Pulm fibrosis
Liver fibrosis

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12
Q

Gout: management

A

Acute management
NSAIDs or colchicine are first-line
the maximum dose of NSAID should be prescribed until 1-2 days after the symptoms have settled
gastroprotection (e.g. a proton pump inhibitor) may also be indicated
colchicine
inhibits microtubule polymerization by binding to tubulin, interfering with mitosis. Also inhibits neutrophil motility and activity
has a slower onset of action
may be used with caution in renal impairment: the BNF advises to reduce the dose if eGFR is 10-50 ml/min and to avoid if eGFR < 10 ml/min BNF
the main side-effect is diarrhoea
oral steroids may be considered if NSAIDs and colchicine are contraindicated.
a dose of prednisolone 15mg/day is usually used
another option is intra-articular steroid injection
if the patient is already taking allopurinol it should be continued

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13
Q

Hydroxychloroquine side effects

A

Permanent bulls eye retinopathy

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14
Q

Cyclophosphamide side effect

A

Hemorrhagic cystatis

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15
Q

Pmr tx

A

Prednisolone

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16
Q

OA xr changes

A

Loss of joint space
Osteophytes forming at joint margins
Subchondral sclerosis
Subchondral cysts

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17
Q

APLS TX

A

primary thromboprophylaxis
low-dose aspirin
secondary thromboprophylaxis
initial venous thromboembolic events: lifelong warfarin with a target INR of 2-3
recurrent venous thromboembolic events: lifelong warfarin; if occurred whilst taking warfarin then consider adding low-dose aspirin, increase target INR to 3-4
arterial thrombosis should be treated with lifelong warfarin with target INR 2-3

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18
Q

DERMATOMYOSITIS SIGNS

A

Heliotrope rash-periorbital
Gottron’s papules-red papules over extensor surfaces of fingers
Gottron sign-violaceous macules, sometimes with associated oedema, over the knees and elbows. This is also associated with dermatomyositis

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19
Q

RA management for disease slowing

A

Methotrexate+short course prednisolone

choices for initial DMARD monotherapy:
methotrexate is the most widely used DMARD. Monitoring of FBC & LFTs is essential due to the risk of myelosuppression and liver cirrhosis. Other important side-effects include pneumonitis
sulfasalazine
leflunomide
hydroxychloroquine: should only be considered for initial therapy if mild or palindromic disease

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20
Q

Ra tx monitoring-scoring system

A

Crp monitoring
DAS28

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21
Q

ANKYLOSING SPONDYLITIS INITIAL MANAGEMENT

A

Exercise and nsaids

22
Q

What is the most sensitive antibody for sle

23
Q

No true weakness on examination of shoulder/pelvic girdle but there is pain. What is the condition?

A

Pmr-any weakness of muscle is due to pain/myalgia

24
Q

Rotator cuff injury presentation

A

Unilateral-pain on abduction of arm

25
Frozen shoulder presentation
Unilateral pain and stiffness First pain followed by stiffness
26
Pseudogout-joint fluid shows
positively birefringent rhomboid shaped crystals. Pseudogout, also known as calcium pyrophosphate deposition (CPPD) disease, is characterized by the presence of positively birefringent rhomboid shaped crystals in the joint fluid. These crystals are composed of calcium pyrophosphate dihydrate (CPPD) and can cause acute inflammation and pain in affected joint
27
Septic arthritis clinical features and diagnostic
Classic triad: fever/joint pain/restricted ROM Monoarticular usually Gonococcal arthritis is a variant Absence of fever not rule out SA Wbc count increased in synovial fluid analysis Arthrocentesis with synovial fluid analysis Xray of affected joint-might be normal
28
Reactive arthritis clinical features, diagnosis, tx
Postinfectious with chlamydia, ureaplasma, shigella, salmonella, campylobacter, yersinia 1-4 wks latency Oligoarthritis, asimetrik, acute onset Sacroilitis, enthesitis, dactylitis Conjunctivitis, urethritis, oral ulcers, aortic regurg, av block, pericarditis, diarrhea Dx: clinical diagnosis—stool culture, urethral swab, labs-cbc: wbc and platelets high, esr and crp high, gram stain and cultures might be negative but PCR would show for chylamydia and gonorrhea Tx: treat infection,nsaids first line-start high titrate down, steroids if nsaids contraindc, dmard if more than 6 months of ongoing symptoms-sulfasalazine/methotrexate
29
RA early xray feature
Juxtaarticular osteoporosis/osteopenia Swelling in small joints of hands
30
Ra xray changes
Early x-ray findings loss of joint space juxta-articular osteoporosis soft-tissue swelling periarticular erosions subluxation
31
Dexa -1 to -2.5=? >-2.5=?
T-score of -1.0 to -2.5 indicates osteopenia, and a T-score of -2.5 or lower indicates osteoporosis
32
AS schober test criteria
Schober's test <5cm is suggestive of ankylosing spondylitis. This is an indication of reduced lumbar flexion.
33
AS other features starts with A
Apical fibrosis Anterior uveitis Aortic regurgitation Achilles tendonitis AV node block Amyloidosis and cauda equina syndrome peripheral arthritis (25%, more common if female)
34
Osteoporosis in man-what hormone to check?
Testosterone Hypogonadism is a common cause of osteoporosis in men. It is classified either as hypergonadotropic (primary gonadal failure) or hypogonadotropic (secondary to a defect in the hypothalamic-pituitary axis) hypogonadism. The role of androgens on male bone metabolism is twofold. First, androgens stimulate bone formation during puberty. Second, androgens prevent bone resorption during and after puberty.
35
Gout tx including flares and long term
Acute management NSAIDs or colchicine are first-line the maximum dose of NSAID should be prescribed until 1-2 days after the symptoms have settled gastroprotection (e.g. a proton pump inhibitor) may also be indicated colchicine inhibits microtubule polymerization by binding to tubulin, interfering with mitosis. Also inhibits neutrophil motility and activity has a slower onset of action may be used with caution in renal impairment: the BNF advises to reduce the dose if eGFR is 10-50 ml/min and to avoid if eGFR < 10 ml/min BNF the main side-effect is diarrhoea oral steroids may be considered if NSAIDs and colchicine are contraindicated. a dose of prednisolone 15mg/day is usually used another option is intra-articular steroid injection if the patient is already taking allopurinol it should be continued Indications for urate-lowering therapy (ULT) the British Society of Rheumatology Guidelines now advocate offering urate-lowering therapy to all patients after their first attack of gout ULT is particularly recommended if: >= 2 attacks in 12 months tophi renal disease uric acid renal stones prophylaxis if on cytotoxics or diuretics ULT- allopurinol is first-line initial dose of 100 mg od, with the dose titrated every few weeks to aim for a serum uric acid of < 360 µmol/l CKS a lower target uric acid level below 300 µmol/L may be considered for patients who have tophi, chronic gouty arthritis or continue to have ongoing frequent flares despite having a uric acid below 360 µmol/L a lower initial dose of allopurinol should be given if the patient has a reduced eGFR colchicine cover should be considered when starting allopurinol. NSAIDs can be used if colchicine cannot be tolerated. The BSR guidelines suggest this may need to be continued for 6 months the second-line agent when allopurinol is not tolerated or ineffective is febuxostat (also a xanthine oxidase inhibitor) in refractory cases other agents may be tried: uricase (urate oxidase) is an enzyme that catalyzes the conversion of urate to the degradation product allantoin. It is present in certain mammals but not humans in patients who have persistent symptomatic and severe gout despite the adequate use of urate-lowering therapy, pegloticase (polyethylene glycol modified mammalian uricase) can achieve rapid control of hyperuricemia. It is given as an infusion once every two weeks
36
Fibromyalgia-how long should the symptoms be present before dx can be made
3 months
37
Raynaud-which medication help
Nifedipine
38
Ewing sarcoma=location, appearance
Ewing's sarcoma - malignant tumour that occurs most frequently in the diaphysis of the pelvis and long bones Onion skin appearance on xray Ews fli1 protein
39
Osteochondroma
most common benign bone tumour more in males, usually diagnosed in patients aged < 20 years cartilage-capped bony projection on the external surface of a bone
40
Osteosarcoma
most common primary malignant bone tumour seen mainly in children and adolescents occurs most frequently in the metaphyseal region of long bones prior to epiphyseal closure, with 40% occuring in the femur, 20% in the tibia, and 10% in the humerus x-ray shows Codman triangle (from periosteal elevation) and 'sunburst' pattern mutation of the Rb gene significantly increases risk of osteosarcoma (hence association with retinoblastoma) other predisposing factors include Paget's disease of the bone and radiotherapy
41
Chondrosarcoma
malignant tumour of cartilage most commonly affects the axial skeleton more common in middle-age
42
Osteoma
benign 'overgrowth' of bone, most typically occuring on the skull associated with Gardner's syndrome (a variant of familial adenomatous polyposis, FAP)
43
Giant cell tumor
tumour of multinucleated giant cells within a fibrous stroma peak incidence: 20-40 years occurs most frequently in the epiphyses of long bones X-ray shows a 'double bubble' or 'soap bubble' appearance
44
Which medications increase the risk of gout
pyrazinamide and ethambutol can increase uric acid levels.
45
Temporal arteritis visual pathology
Anterior ischemic optic neuropathy accounts for the majority of ocular complications in temporal arteritis
46
———— is a risk factor for pseudogout
Haemochromatosis is a risk factor for pseudogout Risk factors include haemochromatosis, hyperparathyroidism, hypophosphataemia, hypothyroidism and hypomagnesemia. Also old age is a big risk factor.
47
patients with Sjogren's syndrome have an increased risk of ———
patients with Sjogren's syndrome have an increased risk of lymphoid malignancies.
48
Pencil in cup
Psoriatic arthritis due to periarticular erosions and bone resorption
49
Which antibiotics have risk of severe bone marrow suppression if used with methotrexate
Trimethoprim and co-trimoxazole, anti-folate antibiotics, should be avoided concurrently with methotrexate due to the risk of bone marrow aplasia
50
Sle clinical features
General features fatigue fever mouth ulcers lymphadenopathy Skin malar (butterfly) rash: spares nasolabial folds discoid rash: scaly, erythematous, well demarcated rash in sun-exposed areas. Lesions may progress to become pigmented and hyperkeratotic before becoming atrophic photosensitivity Raynaud's phenomenon livedo reticularis non-scarring alopecia Musculoskeletal arthralgia non-erosive arthritis Cardiovascular pericarditis: the most common cardiac manifestation myocarditis Respiratory pleurisy fibrosing alveolitis Renal proteinuria glomerulonephritis (diffuse proliferative glomerulonephritis is the most common type) Neuropsychiatric anxiety and depression psychosis seizures
51
Pain improves with exercise
Ankylosing spondylitis