W3: COVID & TB Flashcards

1
Q

pathogenesis and transmission of SARS-CoV-2.

A
  1. BETA CORONAVIRUS, DROPLETS + FOMITES -> ACE2 R CELLS (PREDOM. RESP SYSTEM)
  2. CELL DEATH + RELEASE OF MEDIATORS
  3. MACROPHAGE + DC RECRUITMENT => CYT T CELLS = > MILD SYMPTOMS
  4. HYPERINFLAMM: failure to contain => STORM
  5. MULTI ORGAN FAILURE
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2
Q

terms epidemic, pandemic, endemic and outbreak.

A
  1. EPIDEMIC rapid increase in cases in area population
  2. PANDEMIC epidemic spread over countries/continents, large no. of ppl
  3. ENDEMIC constant prevalence in pop in area
  4. OUTBREAK epidemic limited highly localised area
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3
Q

common clinical presentations of COVID-19 disease and proression + detection

A

-malaise, cough, flu-like, sore throat, fever

MYOCARDITIS, CLOT DYREG, CONFUSION, EPILEPSY

-CXR: pneumonia, ARDS: white patchy lungs d/t alveolar fluid

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4
Q

clinical management of COVID-19 including general supportive measures.

A
  1. ANTI-PYRETIC
  2. STEROIDS: 6mg of DEXAMETHASONE/day/10d
  3. FLUIDS, O2 THERAPY NC.
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5
Q

role of infection control practitioners in the management of COVID-19

A

Identifying incubation period, R number. Public health. Infection control in 2ºcare, isolation, PPE

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6
Q

Understand the concept of herd immunity in relation to population vaccination.

A

Containing spread/outbreak by protecting large majority + protecting most vulnerable. ↓transmission ↓mortality

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7
Q

global distribution of tuberculosis and its impact on tuberculosis in the UK.

A

High TB Burden countries, developing

UK: major city clusters + immigrant communities. deprivation: vulnerable groups

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8
Q

Granuloma formation in TB

A
  1. macrophage ingest pathogen via TH1 activation and IFN-g recruitment => EPITHELOID CELL
  2. EPITHELOID CELL => LANGERHAN’S GIANT CELLS
  3. Accum => Granuloma
  4. CENTRAL CASEATING NECROSIS: granuloma centre necrosis d/t insufficient support
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9
Q

TB Pres and. diagnostics

A
▲ FEVER NIGHT SWEAT WT LOSS
-sputum
- bronchoscopy BAL
lumbar puncture
-urine
- culture => sensitivity
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10
Q

PRIMARY TB

A

usually asymptomatic,
no preceding exposure = RESULT IN IMMUNITY
hilar lymph, lymphadeenopathy, pleural effusion

initial lesion => 1º COMPLEX @ LYMPH NODE => GHON FOCUS (calcification) + COMPLEX

  • GHON calcification is rare (15%)
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11
Q

POST-PRIMARY TB

A

most common, if not cleared.
=LATENT, balance

  • XR: apex, fluffy
  • lymphadenopathy, cavitation RARE
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12
Q

PROGRESSIVE TB

A
TB BRONCHOPNEUMONIA
- cavitation
- lobar collapse d/t enlarged lymph
- discharge to bronchus
= POOR PROG

MILIARY TB

  • haematogenous spread
  • XR: fine mottling, widespread small granulomas
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13
Q

TB MGMT

A
H - IONIAZID (hepatitis)
Z - PYRANIZAMIDE (gout)
R - RIFAMPICIN (hepatitis)
E - ETHAMBUTOL (optic neuropathy)
(at least 6mos)

4:2m or 2:4m (R/H)
12 tablets/day
+Vit B6 (neuropathy), Steroids

LEGAL NOTIFICATION

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14
Q

AAFB smear

A

+ve: pulmonary TB or Laryngeal TB

False -ves!

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15
Q

Oxygen Therapy Masks & Flows

A

NC, 1-6L

Simple face mask 5-10L

Resevoir 15L

Nasal high Flow O2 70L (severe, overwhelm hospital supply)

CPAP, 15L (severe, tolerance?)

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