Cystic Fibrosis, TB, Bronchitis Flashcards

1
Q

S+S of bronchitis

A

Cough with or without sputum

Resolves in 1-3 weeks

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2
Q

Causes of bronchitis

A

Resp virus

Rarely bacteria - bordetella pertussis, mycoplasma pneumonia, chlamydia pneumonia

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3
Q

Management of bronchitis

A

Supportive

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4
Q

What are transudate pleural effusions caused by?

A

Imbalances in hydrostatic + oncotic pressures in the chest

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5
Q

What causes exudative pleural effusions?

A
Infection
Malignancy 
Immunological responses 
Lymphatic abnormalities 
Noninfectious inflammation 
Trauma
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6
Q

What are Lights criteria?

A

If 1 of 3 is present, fluid is exudate:
Pleural fluid protein
Pleural fluid LDH/ serum LDH ratio >0.6
Pleural fluid LDH >2/3 the upper limit of normal serum LDH

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7
Q

What measurements can be done with pleural fluid?

A
Cholesterol 
Triglycerides 
Amylase
Creatinine 
pH
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8
Q

What does pleural fluid cytology assess?

A

Malignancy

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9
Q

Pathology of cystic fibrosis

A

Mutations in CFTR gene

Deranged chloride transport leads to thick, viscous secretions in lungs, liver, pancreas, intestine + reproductive tract

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10
Q

Diagnosis of CF

A

Clinical + evidence of CFTR dysfunction (elevated sweat chloride, presence of 2 disease causing mutations, abnormal nasal potential difference)
Sweat chloride test is diagnostic

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11
Q

What should be done following a positive sweat chloride test?

A

DNA analysis

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12
Q

What pathogens are common in CF?

A

Staph aureus + pseudomonas aeruginosa

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13
Q

Management of p. aeruginosa

A
Piperacillin-tazobactam 
Ceftazidime 
Imipenem-cilastatin 
Meropenem 
PLUS:
A fluoroquinolone
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14
Q

What bacteria causes TB?

A

Mycobacterium tuberculosis

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15
Q

What is active vs latent TB?

A
Active = symptomatic or progressive 
Latent = no clinically active TB
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16
Q

RF for TB

A

Born in high prevalance areas
children
Immunosuppression

17
Q

S+S of TB

A

Weight loss, fever, night sweats, anorexia or malaise

Persistent productive cough, SOB, haemoptysis

18
Q

Investigations for ?TB + results of CXR

A

CXR + sputum sample + early morning urine, + biopsy

Shows upper lobe cavitation, pleural effusion + miliary appearance

19
Q

Management of TB

A

Rifampicin, isoniazid, pyrazinamide, ethambutol for 2 months
Rifampicin + isoniazid for 4 months

20
Q

SE of TB drugs

A

Hepato, neuro + opth toxicity

21
Q

S+S of CF

A
Nasal polyps 
Steatorrhea 
Infertility 
Osteoporosis 
Repeated pneumonia 
chronic sinusitis 
Bronchiectasis
Pancreatic insufficiency
22
Q

What is non classic CF?

A

Milder mutation that only causes impairment in 1 organ

Have some CFTR expression

23
Q

What happens to sperm in CF?

A

Obstructive azoospermia due to blocked vas deferens

24
Q

What is DIOS?

A

Distal infective obstruction syndrome
Unique to CF
Changes in gut lead to accumulation of mucus which form mucofaeculant impactions

25
Q

Management of DIOS

A
Surgical review 
1) Laxatives (lactulose + senna) 
2) Oral gastrograffin 
3) Klean-prep (surgical decompression 2nd line) 
Compliance with pancreatic enzymes 
Avoid opiates + loperamide
26
Q

Future of CF

A

Modulator therapy that targets mutations