Respiratory for history taking Flashcards
DVT
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
PE
-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
PE/DVT RF
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
NIV indications and CI
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
Bronchiectasis symptoms
Bronchiectasis clinical signs
- persistent cough
- purulent sputum
- repeated infections
- clubbing
- coarse inspiratory creps
- localised wheeze
Bronchiectasis next steps
Imaging findings
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
Kartagener
Primary ciliary dyskinesia
Autosomal recessive
Triad:
- dextrocardia/ situs inverts
- bronchiectasis/ recurrent sinusitis
- sub fertility
Youngs syndrome
Abnormality of mucus- increased viscosity
Autosomal recessive
Infertility
Bronchiectasis treatment
Postural drainage
Prophylactic ab if 3x exacerbations per year (ECG prior for QTc)
Bronchodilators may help
Surgery if localised/ haemoptysis
Bronchiectasis causes
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
Cystic fibrosis
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