Respiratory for history taking Flashcards

1
Q

DVT

A

Two level wells score:
Risk of DVT likely if ≥2
Risk of DVT unlikely if ≤1

  • Calf swelling by more than 3 cm compared with the asymptomatic leg (measured 10 cm below the tibial tuberosity).
  • Localised tenderness alonog deep venous distribution
  • Immobilization of the legs.
  • Pitting oedema (greater than on the asymptomatic leg).
  • Surgery in last 12 weeks
  • Collateral superficial veins (non-varicose).
  • Active cancer (treatment ongoing, within the last 6 months, or palliative).
  • Previously documented DVT.
  • Entire leg is swollen.

Likely: US scan within 4 hours/ treat
Unlikely D dimer
- if negative excluded
- if positive proceed to US

Exception:
US directly if pregnant/ delivered in last 2 weeks

Treatment: DOAC first line. provoked 3 months, unprovoked 6.

Investigations:

  • examine and basic bloods FBC, UsE, LFTs, clotting. only ix for cancer if concerns
  • thrombophilia screen if not for lifelong anticoagulant

Thrombophilia screen:

  • Antithrombin
  • Protein C
  • Protein S
  • APCR (screening test for Factor V Leiden)
  • Prothrombin (PT) gene mutation
  • antiphosophlipid antibody
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2
Q

PE

A

-PERC score to exclude

  • Two level wells score for PE
    Likely > 4
    Unlikely <= 4

Likely:

  • CTPA
  • if delay LMWH

Unlikely:
- D dimer

Massive PE= hypotension <90
Thrombolysis 50mg alteplase

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3
Q

PE/DVT RF

A
Immobilisation (>3 days)
Recent surgery (past 4 weeks)
Previous DVT/PE or family history
Malignancy in last 6 months
OCP/ oestrogen meds
Travel >4 hours (past 4 weeks)
Smoker
Pregnancy/ postpartum
Obesity
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4
Q

NIV indications and CI

A
Indications:
After 1 hour optimal treatment:
pH <7.35
pCO2 >6.5
 RR >23
OR in NM disease RR >20 if usual VC <1L
Contraindicaitons:
Facial deformity
Facial burns
Fixed upper airway obstruction
pH <7.15
GCS <8
Confusion/agitation
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5
Q

Bronchiectasis symptoms

Bronchiectasis clinical signs

A
  • persistent cough
  • purulent sputum
  • repeated infections
  • clubbing
  • coarse inspiratory creps
  • localised wheeze
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6
Q

Bronchiectasis next steps

Imaging findings

A
1- Full set of observations including sats and RR
2- sputum culture +/- AFB
3- CXR
4- HRCT chest
\+/-  spirometry

Think about causes for specific ix.

Imaging findings:

  • CXR tramlines and ring shadows
  • CT signet ring appearance
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7
Q

Kartagener

A

Primary ciliary dyskinesia
Autosomal recessive

Triad:

  • dextrocardia/ situs inverts
  • bronchiectasis/ recurrent sinusitis
  • sub fertility
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8
Q

Youngs syndrome

A

Abnormality of mucus- increased viscosity

Autosomal recessive
Infertility

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9
Q

Bronchiectasis treatment

A

Postural drainage
Prophylactic ab if 3x exacerbations per year (ECG prior for QTc)

Bronchodilators may help
Surgery if localised/ haemoptysis

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10
Q

Bronchiectasis causes

A

1- infection

  • recurrent childhood
  • TB
  • ABPA
  • immunodeficiencies
  • aspiration

2- congenital

  • CF
  • primary ciliary dyskinesia
  • Youngs
  • alpha 1 antitrypsin

3- CTD

  • RA
  • SLE

4- Idiopathic

5- traction bronchiectasis

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11
Q

Cystic fibrosis

A

Autosomal recessive defect in CFTR gene= altered viscosity of mucus

Symptoms:

  • respiratory- bronchiectasis, sinusitis, polyps
  • Pancreatic insufficiency - steatorrhoea and DM
  • meconium ileus + SBO
  • Infertility- no vas deferent

Investigations:
High sweat sodium
Genetic testing

Treatment:

  • physio
  • orkambi for delta F508
  • abs
  • mucolytics
  • beta agonists
  • transplant

infections:
burkholderia cepacia worst prognosis + CI to transplant

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