L12 - therapies in interstitial lung diseases Flashcards

1
Q

IPD median survival

A

2-5 years from diagnosis

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2
Q

IPF cause

A

hypothesised it was a disease of inflammation leading to scarring so originally immunosuppression was the mainstay of treatment

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3
Q

IPF and immunosuppression drugs

A

actually increased mortality rate

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4
Q

Pirfenidone

A

IPF new treamtnet
targets fibroblasts by preventing TGFB and proliferation to increase apoptosis
three tablets three times daily

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5
Q

Pirfenidone side effects

A

photosensitivity, gastrointestinal upset and LFT abnormalities

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6
Q

Nintdanib

A

IPD treatment
licensed for cancer treatment
one tablet twice daily
works as an inhibitor of multiple tyrosine kinase receptors, fibroblast growth factor and vascular endothelial growth factor

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7
Q

Nintdanib side effects

A

mainly diarrhoea, but also LFT abnormalities and small increased risk of bleeding

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8
Q

Hypersensitivity pneumonitis

A

main treatment is exposure avoidance and identification, cause unidentified in up to 60% cases

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9
Q

HP treatment strategy

A

focused on inhibition of the adaptive immune system

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10
Q

HP treatments

A

corticosteroids commonly used as first line

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11
Q

Corticosteroids

A

derived from naturally occurring steroids produced by adrenal glands, decrease function of the lymphocyte and cytokine activity

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12
Q

Corticosteroids long term consequences

A

weight gain, GI tract problems, mental health and diabetes

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13
Q

Other immunosuppressants

A

methotrexate, azathioprine, mycophenylate motel, cyclophosphamide, rituximab

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14
Q

Methotraxate

A

inhibitors folate metabolism, reduces T cell ability to make proteins, can cause pneumonitis

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15
Q

Azathioprine

A

Prodrug converted to 6-mercaptopurine, inhibits purine synthesis and reduces T cell turnover.
Can cause hepatitis and bone marrow suppression

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16
Q

Mycophenylate

A

inhibits purine synthesis and reduces T cell turnover, immunosuppressive and susceptible to viral infection

17
Q

Rituximab

A

Depletion of CD20-positive B-lymphocytes, thereby inhibiting their differentiation into antibody-producing cells
inhibition of T cell co-stimulation

18
Q

Sarcoidosis treatment

A

not all patients require treatment, favoured in patients that are symptomatic, active inflammation, progressive organ damage and worsening pulmonary function

19
Q

Sarcoidosis and corticosteroids

A

first line therapy, initial doses of prolnisone

chances of relapse after therapy 14-74%

20
Q

Sarcoidosis and methotrexate

A

used as second line treatment in patients that are steroid-refractory, typically begin orally with gradually increasing dosing

21
Q

Lung transplantation

A

HP may recur in the allograft and impact clinical outcomes, vigilance for ongoing antigen exposure and disease recurrence, overall survival is good

22
Q

Palliative treatment

A

targeted at mitigating symptoms, opioids for breathlessness and pain, anxiolytics and supplementary oxygen

23
Q

Long term oxygen therapy

A

15+ hours a day
hypoxia at rest
often delivered by static air concentrator

24
Q

Ambulatory oxygen

A

enables greater exertion to be undertaken in patients with hypoxia on exercise