219 - Haemoptysis 2 (Pulmonary circulation) Flashcards

1
Q

what is haemoptysis and what can it be confused with?

A

coughing up of blood/bloody sputum from respiratory tract below the larynx (blood is bright red & acidic)
confused with haematemesis (blood from GIT usually coffee ground colour & acidic) & epistaxis (ENT source)

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2
Q

haemoptysis always warrants invesitgation, what tests should a GP organise?

A

CVR (mandatory), bloods (FBC, clotting screens & MC&S), ABGs, sputum (MC&S, AFB (acid fast bacilli) & cytology)

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3
Q

what can cause small and massive haemoptysis?

A
  • bronchitis in smokers, pneumonia (lobular usuallt streptococcus pneumonia), tuberculosis, bronchiectasis, lung cancer, heart failure, PE, anticoagulation
  • massive haemoptysis (>100ml emergency) - bronchiectasis, lung CA, TB, aspergilloma, vascular abnormalities, vasculitis
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4
Q

what can cause cavities and are prone to opportunistic infections?

A

TB, sarcoidosis, aspergilloma

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5
Q

what is bronchiectasis?

A

abnormal & permanent dilation of the proximal bronchioles due to inflammation leading to the destruction of elastic/muscular components of walls. Occurs after damage by resp infections/cystic fibrosis & bronchioles dilate with damaged cilia & mucous stasis. infections occur as a result and further damage - cycle

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6
Q

what are the signs and symptoms of bronchiectasis?

A
  • persistent productive cough with symptoms of chronic bronchial sepsis (foul smelling, purulent sputum)
  • dyspnoea, polyphonic wheeze, finger clubbing, coarse mid inspiratory crackles, haemoptysis
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7
Q

what are the inherited and acquired causes of bronchiectasis?

A
  • inherited - cystic fibrosis, immotile cilia syndromes (kartagener’s)
  • acquired - childhood pneumonia (pertusis, measles, TB), chronic bronchial obstruction, chronic aspiration, allergic bronchopulmonary Aspergillosis (ABPA), IG deficiency, HIV, RA, UC
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8
Q

what is aspergillosis?

A

mould (fungal) infection seen in asthmatics & Cystic fribrosis with fungus ball in cavity. S&S - flitting pulmonary consolidations, blood & sputum eosinophilia & ↑IgE and apergillus precipitins. Tests - skin prick test

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9
Q

what investigations can be done for suspected bronchiectasis?

A
  • sputum - MC&S, bloods

* imaging - CT/MRI - cygnet ring - large lilated bronchiloles next to arterioles

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10
Q

what treatment should be given for bronchiectasis?

A

abx to treat infection

  • physiotherapy
  • bronchodilatiors
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11
Q

what is the difference between a non massive and massive PE?

A
  • non-massive - px haemodynamically stable, small distal infarction causes pleuritic pain, SOB, fever, haemoptysis
  • massive - px haemodynamically unstable, PE at bifurcation of PAs with ↑RR, ↓O2, systolic BP<90 or 40mm drop, ↑JVP, AF
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12
Q

what is a paradoxical emboli?

A

caused by atrial septal defect causing systemic manifestation

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13
Q

what is virchow’s triad?

A

a presdisposition to thrombosis caused by:

  • venous stasis
  • injury to vessel wall
  • ↑blood coagulability
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14
Q

what are the risk factors for a PE?

A
  • prothrombotic states - post surgery, pregnancy, malignancy
  • immobility - fracture, paralysis, bed rest
  • previous VTE
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15
Q

how might a px with a PE present?

A
  • often asymptomatic

* chest signs - pleuritic pain, dyspnoea, haemoptysis (in s sign (calf pain on dorsiflexion)

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16
Q

how might you assess the risk of a PE in a px?

A

Wells score - high >6 mod 2-6

17
Q

what investigation can be carried out on a px with a suspected PE?

A
  • bloods - D-Dimer (breakdown of cross linked fibrin ↑in thromboembolism) - only excludes those with low prob as can also be due to trauma, post surgery, liver/renal disease, pregnancy, ca, heart disease. ABG low CO2 & ↑pH (hyperventilation. FBC & clotting screen
  • ECG - S1Q3T(inv)3, RIght ventricular strain (ST depress & T wave in rt side (V1-V,II, III, aVF)), New right bundle branch block
  • CT Pulmonary angiogram 1st line
  • bedside echo - show RV overloaded
18
Q

what treatment would you give for a PE?

A
  • O2 therapy
  • resuscitation + fluids
  • anticoagulant therapy - Low molecular weight heparin - stop when INR 2.5 then warfarin
  • Thrombolysis in haemodynamic instability. warfarin for 3m if clear cause, 6m if no clear cause
19
Q

what other causes are there for a PE?

A

fat embolism (long bone fracture), tumour emblism, septic embolism (iv drug users - usually strphylococci)

20
Q

what causes a cavitating mass?

A
  • carcinoma (Squamous cell)
  • lung abscess
  • rheumatoid nodule
  • embolus (septic)
  • vasculitis with granulomatosis - chronic ENT symptoms, systemic symptoms, renal failure, +ve cANCA, high ESR
  • bronchogenic cyst
  • hydratic cyst
21
Q

what can cause pulmonary arterial hyperternsion?

A

collagen vascular disease, pulmonary shunts, portal hypertension, drugs/toxins, HIV. mean PAP>25mmHg…needs R+LHC to confirm

22
Q

what can cause pulmonary venous hyperternsion?

A

L sides atrial or ventricular heart disease / valvular disease

23
Q

what can cause pulmonary hyperternsion with hypoxia?

A

COPD, instititial lung disease, OSA

24
Q

what can cause pulmonary hyperternsion due to chronic thromboembolic disease?

A

thromboembolic obstruction pf proximal/distal PA, tumor, foreign material