Connective tissue 2 Flashcards

1
Q

Arthralgia

A

Joint pains

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2
Q

Arthritis

A

Joint inflammation

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3
Q

What are symtoms of autoimmune disease?

A
Arthralgia/arthiritis
Fatigue
Myalgia,muscle weakness
Sicca symptoms
Raynaud's phenomenon
Alopecia
Mucosal ulcers
Unprovoked thrombosis/pregnancy losses/difficult pregnancy history
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4
Q

Female to male ratio is 9:1 T/F

A

T

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5
Q

What is APS characterised by?

A

Venous or arterial thrombosis and/or adverse pregnancy outcomes in the presence of persistent lab evidence on aPL
Can be primary or secondary
Antibodies to phospholipid binding proteins

Presence of Anti cardiolipin antibody. Lupus

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6
Q

What are the core clinical problems around CTD

A
Abnormal blood test results
Cold extermities
Joint pain/swelling
Muscle pain
Painful or uncomfortable mouth
Rash
Red/painful eyes
Shortness of breath
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7
Q

When would you suspect APS?

A

Occurrence of one or more otherwise unexplained venous or arterial events, esp in young patients

Foetal death after 10 weeks, premature brith due to severe pre-eclampsia or placental insufficiency or multiple embryonic losses ( less than 10 weeks gestation)

Otherwise unexplained thrombocytopenia or prolonged Aptt

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8
Q

What antibodies are important in APS?

A

IgM or IgG anticardiolipin
Lupus anticoagulants
IgM or IgG beta 2 glycoproteins
2 positive tests more than 12 weeks apart- confirmatory
1-5% of healthy individuals can have these antibodies

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9
Q

Treatment for APS

A

Lifelong anticoagulation for thrombosis
Aspirin/heparin to prevent pregnancy complications
Hydroxychloroquine

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10
Q

What is Sjogren’s syndrome?

A

Chronic autoimmune inflamatory disorder characterised by diminished lacrimal and salivary gland function resulting in dry eyes, dry mouth
Can be primary or secondary
Most common in women in 50s and 60s
Extra-glandular involvement

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11
Q

What are the symptoms of Sjogren’s

A
Dry eyes-gritty feeling
Dry mouth
Dry throat
Vaginal dryness
Bilateral parotid gland enlargement
Joint pains
Fatigue
Unexplained increase in dental caries
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12
Q

What antibodies are important in Sjogrens?

A
Anti-Ro
Anti-La
also watch out for IgG,ESR and rheumatoid factor
Other tests:
-Salivary gland US
-Labial gland biopsy
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13
Q

What treatments can be used for Sjogrens?

A
Artificial tear supplements
Ciclosporin eye dros
Punctal plugs
Saliva supplements
Pilocarpine
Hydroxychloroquine
Immunosuppression with methotrexate, leflunomide, B cell depletes etc if major organ involvement
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14
Q

What can systemic sclerosis be split into?

A

FIbrosis

Vacular endothelial changes

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15
Q

Diffuse cutaneous systemic sclerosis

A

Skin involvement proximal to forearms and involving torso
Rapid skin changes
Early organ involvement
Intestitial lung disease more common than pulmonary hypertension
Renal crisis can occur
Anti-topoisomerase or anti SCL-70 or anti RNA III polymerase antibody

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16
Q

Systemic sclerosis

A

Limited SSc
Skin involvement distal to elbows and not involving torso
Used to be called CREST
Calcinosis, Raynaud’s,Eoseophageal dysmotility,Sclerodactylt,Telangiectasia
Raynaud’s hypertension is a common complication
Small intestinal bacterial overgrowth
Anti centromere antibody

17
Q

How do you treat systemic sclerosis

A

Raynaud’s - CCB, phosphodiester inhibitors
If digital ulcers- iloprost infusions
Lung disease- Immunosuppression
Pulmonary Hypertension- CCB,Endothelin receptor antagonists, prostacyclin, home O2
Reflux- PPI, H2 receptor antagnosist
Tight control of BP
Antibodies for small intestinal bacterial overgrowth

18
Q

In mixed connective tissue disease what antibody is positive?

A

Anti RNP

19
Q

monitoring for autoimmune diseases

A
Clinical examination, history
Bloods- cell counts, serum complements
Uranalysis
Pulmonary function tests/CXR/Chest CT scan
ECHO
20
Q

If joint involvement what is used as treatment?

A

Methotrexate
DMARDs
Short course of steroids

21
Q

What treatments are used if there is organ involvement?

A

High dose steroids and immunosuppression