Cough and haemoptysis Flashcards

1
Q

Cough

A

Cough is a non-specific reaction to irritation anywhere in the respiratory tract from the pharynx to the alveol

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2
Q

Acute vs chronic cough

A
  • ‘Acute cough’ is defined as cough of 8 weeks it becomes a ‘chronic cough’ and subacute if somewhere in between.
  • As most viral upper respiratory tract infections will have resolved within 3 weeks, any cough lasting >8 weeks or >3 weeks with other symptoms warrants systematic investigation
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3
Q

Most common cause of acute cough

A

infections such as common cold or chest infections which usually clear within 3 weeks

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4
Q

Most common causes of chronic cough

A
Smoking 
ACE inhibitors - dry cough
Acid reflux 
Asthma
COPD
Cancer - Lung cancer, mesothilioma, secondary metastases, lymphoma
Atopy
Postnasal drip 
Environmental pollution, especially PM10 particulates (particles of 10 micrometres or fewer).
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5
Q

Features of smoking-related cough

A

Cigarette smoke is irritant to the lining of the airways, so being a smoker, or being around other people smoking (being a passive smoker) is a common cause of cough. Smoking-related coughs are usually dry - in other words you don’t cough anything up - and tend to be worst in the mornings

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6
Q

GORD cough

A
Heartburn (but may have no gastrointestinal symptoms).
Cough worse at night.
Cough when eating/talking.
Hoarseness.
Sour taste.
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7
Q

Asthma cough

A

History of atopy.
Nocturnal cough.
Wheeze.
Peak flow rate variable by >20% or reversible changes on spirometry (these ‘rule in’ asthma but their absence does not rule it out).

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8
Q

COPD cough

A

The cough of COPD usually comes with gradually worsening breathlessness when you do anything.

Colds often progress to coughs which turn into chest infections and linger. It is usually caused by many years of smoking.

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9
Q

Less common causes of chronic cough - cardiovascular

A

left ventricular failure, pulmonary emboli, aortic aneurysm

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10
Q

Cases where cause of cough is not found

A
  • Idiopathic cough. (Idiopathic means there is no cause to be found.)
  • Chronic refractory cough.
  • Cough hypersensitivity syndrome.
  • Neurogenic or psychogenic cough.
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11
Q

Cough reflex

A

The cough reflex is triggered by mechanical or inflammatory changes or irritants in the airways. The afferent pathway is via the vagus nerve to respiratory neurons termed the ‘cough centre’ in the brain stem. Higher cortical centres also control the cough.

Chronic cough tends to be inhibited during sleep.

Chronic cough is often associated with bronchial hyper-reactivity (bronchial hyper-responsiveness), which can persist in the absence of the initiating cough event.

Bronchial hyper-responsiveness is defined as a state of increased sensitivity to a wide variety of airway-narrowing stimuli - eg, exercise, dry or cold air and hypertonic or hypotonic aerosols. It occurs in asthma and chronic obstructive pulmonary disease (COPD) but also can occur in the absence of lung disease.

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12
Q

Less common causes of cough - chronic infections

A
  • Bronchiectasis, tuberculosis, cystic fibrosis, lung abscess.
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13
Q

Postinfectious cough

A
  • May be more likely following infection with Mycoplasma pneumoniae, chlamydial pneumonia and whooping cough.
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14
Q

Parenchymal lung diseases

A
  • interstitial lung fibrosis, emphysema, sarcoidosis.
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15
Q

Cancers that can cause cough

A

Lung cancer, metastatic carcinoma, lymphoma, mediastinal tumours, benign tumours

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16
Q

Upper airway causes of cough

A

chronic tonsil enlargement, obstructive sleep apnoea, chronic snoring, irritation of external auditory meatus.

Laryngeal problems are increasingly recognised as being part of chronic cough

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17
Q

Foriegn body obstruction - cough causes

A
  • recurrent aspiration, inhaled foreign body, endobronchial sutures.
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18
Q

Can cardiac arrhythmias cause cough

A

Yes but rarely

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19
Q

Cough only when supine indication

A
  • may be due to collapse of large airways
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20
Q

Red flag symptoms in chronic cough

A

Copious sputum production (bronchiectasis).

Systemic symptoms - fever, sweats, weight loss (tuberculosis, lymphoma, bronchial carcinoma).

Haemoptysis (tuberculosis, bronchial carcinoma).

Significant dyspnoea (heart failure, COPD, fibrotic lung disease).

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21
Q

Postnasal drip syndrome

A

Subjective symptoms - postnasal drip, having a recurrent need to clear the throat.

Persistent nasal blockage.

Persistent nasal discharge.

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22
Q

Green sputum

A

Indicative of longstanding respiratory infection (green from degenerative changes in cell debris) as in pneumonia, ruptured lung abscess, chronic infectious bronchitis, and infected bronchiectasis or cystic fibrosis.

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23
Q

Rust coloured sputum

A

Usually caused by pneumococcal bacteria (in pneumonia), pulmonary embolism, lung cancer or pulmonary tuberculosis.

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24
Q

Brown sputum

A

chronic bronchitis (greenish/yellowish/brown); chronic pneumonia (whitish-brown); tuberculosis; lung cancer.

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25
Q

Yellow sputum

A

containing pus. “The sputum color of patients with acute cough and no underlying chronic lung disease does not imply therapeutic consequences such as prescription of antibiotics.”
The color can provide hints as to effective treatment in chronic bronchitis patients:
A yellow-greenish (mucopurulent) color suggests that treatment with antibiotics can reduce symptoms. The green color is caused by degenerating neutrophil verdoperoxidase.

26
Q

Foamy white sputum

A
  • May come from earlier-phase pulmonary edema.
27
Q

Frothy pink sputum

A
  • May indicate more severe pulmonary edema. Antibiotics may not be necessary at this time.
28
Q

Clear sputum

A
  • Pulmonary embolism (clear to frothy); COPD chronic obstructive pulmonary disease (clear to gray); viral respiratory infection (clear to whitish and sometimes a hint of yellow); asthma (thick and white to yellowish).
29
Q

Initial investigation and management for smokers with cough

A

For smokers, initial investigations are CXR and spirometry, with advice to stop smoking.

If smoking is the cause, cough should improve within eight weeks of smoking cessation.

30
Q

Initial investigation and management for non-smokers with cough

A

For non-smokers, if taking an ACE inhibitor, trial of stopping/replacing this drug.

ACE inhibitor-induced cough should improve within four weeks of stopping the drug.

Then consider CXR and spirometry (or serial peak flow measurements, if spirometry is unavailable).

31
Q

GORD management

A

Trial of high-dose proton pump inhibitors (may require up to 12 weeks for improvement).

32
Q

Postnasal drip syndrome management

A

Trial of antihistamines or nasal steroids.

33
Q

What is postnasal drip syndrome

A

Post-nasal drip (PND) occurs when excessive mucus is produced by the nasal mucosa.

The excess mucus accumulates in the back of the nose and eventually the throat once it drips down the back of the throat.

It can be caused by rhinitis, sinusitis, gastroesophageal reflux disease (GERD / GORD), or by a disorder of swallowing (such as an esophageal motility disorder).

Other causes can be allergy, cold, flu, and side effects from medications

34
Q

Cough - blood tests

A

FBC (infection, eosinophilia), ESR/CRP (infection, malignancy, connective tissue disorders)

35
Q

Cough - contributing factors

A

reflux disease, rhinitis, occupation (there may be more than one factor causing chronic cough). Try treating these (or removing the cause, if occupational) for a limited period to observe response

36
Q

Cough - imaging investigations besides cxr

A

Bronchial provocation testing (methacholine or histamine)

  • positive result supports diagnosis of asthma but cough may be steroid-responsive even if negative.
  • Assess for eosinophilic airway inflammation - by induced sputum analysis or trial of steroids (prednisolone 30 mg daily for two weeks).
  • Bronchoscopy - if inhalation of a foreign body is suspected, or where common causes have been excluded.
  • Echocardiogram or other cardiac investigations - if a cardiac cause is suspected clinically.
  • 24-hour ambulatory oesophageal pH testing and/or oesophageal manometry.
  • Radiology of sinuses - eg, CT or MRI scanning.
  • High-resolution CT scan of thorax - however, there is low diagnostic yield in this scenario.
37
Q

Assessment of cough

A

May use a cough assessment tool such as the cough visual analogue scale or the Leicester Cough Questionnaire

38
Q

Cough management

A

Treat the underlying cause(s), if possible

A ‘trial of treatment’ strategy is often appropriate, ensuring that each treatment is used for a sufficient time - eg, eight weeks for inhaled steroids, 12 weeks for anti-reflux treatment

Smoking cessation; avoid exposure to irritants.
If initial management is unsuccessful, referral to secondary care may be required.

This may involve a chest physician, ENT specialist and/or gastroenterologist, depending on the individual context

39
Q

Codeine in cough management

A

Codeine may be effective but can cause dependence. Dextromethorphan and pholcodine have fewer side-effects.

40
Q

Sedating antihistamines in cough management

A

Sedating antihistamines are used as the cough suppressant component of many compound cough preparations on sale to the public

41
Q

Usage of morphine in cough management

A

Morphine or diamorphine at higher doses may be used for severe, distressing cough in palliative care.

42
Q

Mucolytics in cough management

A

Mucolytics (eg, carbocisteine or erdosteine) are prescribed to facilitate expectoration by reducing sputum viscosity.

In some patients with COPD and a chronic productive cough, mucolytics can reduce exacerbations. Mucolytic therapy should be stopped if there is no benefit after a four-week trial.

Steam inhalation with postural drainage is effective in bronchiectasis and in some cases of chronic bronchitis.

43
Q

Demulcent substances in cough management

A

Demulcent cough preparations contain soothing substances such as syrup or glycerol and may be used to relieve a dry irritating cough.

Preparations such as simple linctus have the advantage of being harmless and inexpensive.

44
Q

What is pseudohaemoptysis

A

Where a cough reflex is stimulated by blood not derived from the lungs or bronchial tubes.

This may be from the oral cavity or nasopharynx (eg, following an epistaxis) or following aspiration of haematemesis into the lungs.

45
Q

Causes of haemoptysis - trachea or bronchus

A

Malignancy:

Bronchogenic carcinoma.
Endobronchial metastatic tumour.
Kaposi’s sarcoma.
Carcinoid tumour.

Bronchitis.
Bronchiectasis.
Airway trauma.
Foreign body.

46
Q

Causes of haemoptysis - lung parenchyma

A
Lung abscess.
Pneumonia - bacterial (eg, Staphylococcus aureus, Pseudomonas aeruginosa) or viral (eg, influenza).
Tuberculosis (TB).
Fungal infection and mycetoma.
Hydatid cysts.
Goodpasture's syndrome.
Pulmonary haemosiderosis.
Wegener's granulomatosis.
Behçet disease.
Lupus pneumonitis.
Lung contusion.
'Crack' lung.
47
Q

Vascular causes of haemoptysis

A

Arteriovenous malformation.
Aortic aneurysm.
Pulmonary embolism (PE).
Mitral stenosis.
Other cause of pulmonary venous hypertension - eg, left ventricular failure (LVF).
Trauma.
Iatrogenic (eg, chest drain malposition, secondary to pulmonary artery catheter manipulation).

48
Q

Other causes of haemoptysis

A

Pulmonary endometriosis.
Congenital or acquired systemic coagulopathy - eg, leukaemia.
Anticoagulant or thrombolytic agents.
Factitious haemoptysis.

49
Q

Most common cause of haemoptysis

A

Haemoptysis is rare in children and often only presents where bleeding is substantial, as children tend to swallow rather than expectorate their sputum.

Respiratory tract infection is the most common cause.

Foreign body inhalation is the second most common cause (particularly with younger children) and congenital heart disease and bronchiectasis secondary to cystic fibrosis are other important causes.

50
Q

Features of haemoptysis

A
No nausea or vomiting
Concurrent lung disease	
Sputum is frothy	
Sputum has a liquid or clotted appearance	
Haemoptysis is bright red or pink	
Alkaline pH	
Mixed with macrophages and neutrophils
51
Q

Associated symptoms - haemoptysis

A

Abrupt-onset cough, fever with bloody and purulent sputum - suggestive of acute pneumonia or bronchitis.
Chronic productive cough - suggestive of chronic bronchitis or bronchiectasis.
Fevers, night sweats and weight loss - consider TB and other infections or malignancy.
Anorexia, weight loss and changing cough - think of possible bronchogenic carcinoma.
Dyspnoea, fatigue, orthopnoea, paroxysmal nocturnal dyspnoea, frothy pink sputum - suggestive of congestive heart failure.
Dyspnoea and pleuritic chest pain - consider a PE.

52
Q

Nasal cavity + oropharynx - Haemoptysis signs

A

Extrapulmonary causes (pseudohaemoptysis).
Signs of vasculitis.
Gingival thickening, mulberry gingivitis, saddle nose, and nasal perforation suggest Wegener’s granulomatosis.

53
Q

Cardiovascular examination signs - haemoptysis

A

The diastolic murmur of mitral stenosis.
Signs of LVF.
Tachypnoea, tachycardia, fixed split S2, pleural rub, and unilateral leg pain or swelling which may indicate thromboembolic disease.

54
Q

Resp examination signs - haemoptysis

A

Fine inspiratory rales (associated with alveolar blood).
Inspiratory and expiratory rhonchi (associated with airway secretions and blood).

Look for evidence of an exacerbation of chronic obstructive pulmonary disease or lower respiratory tract infection.

Unilateral wheeze and distal consolidation raise the suspicion of endobronchial tumour. Unilateral wheeze or stridor may also indicate the presence of a foreign body.

With apical dullness and cachexia, TB should be considered.

Digital clubbing can reflect chronic lung disease (lung cancer, bronchiectasis, lung abscess).

Supraclavicular lymphadenopathy, cachexia, hoarse voice, Cushing’s syndrome, hyperpigmentation, and Horner’s syndrome may be associated with malignancy.

55
Q

Haemoptysis investigations

A

Bronchoscopy combined with imaging technology usually identifies the bleeding site in the lungs.

Imaging - CXR +/- CT scan. About 30% of patients with haemoptysis have normal CXRs. A negative CXR warrants other investigations, usually including a bronchoscopy.

A CT scan is more sensitive than a CXR.

Computed tomography angiography (CTA) can play a crucial role in assessing the cause and origin of the haemoptysis and directing the interventional radiologist prior to treatment.

Fibreoptic bronchoscopy enables direct visualisation and is required where there is a mass on CXR, there are risk factors for cancer despite normal CXR, or where diagnosis remains open, particularly in instances of recurrent haemoptysis.

ECG +/- echocardiogram (ECHO) - if a cardiac cause or PE is suspected.

Other tests are dependent on the clinical setting but may include FBC, ESR, U&Es, coagulation studies, urinalysis, arterial blood gases, sputum cytology and culture, acid-fast bacillus (AFB) smear and culture, D-dimer testing, and HIV test.

56
Q

Management of minor haemoptysis

A

Effort should be concentrated on determining the origin of the haemoptysis, providing specific treatment where available and excluding serious underlying pathology.

Normal CXR, history consistent with bronchitis - oral antibiotic, advise smoking cessation and follow-up in a few weeks.
Consider chest CT scan and bronchoscopy where:
Haemoptysis lasts longer than two weeks.
There are recurrent episodes of haemoptysis.
The volume of haemoptysis is >30 ml per day.
The patient is a smoker and >40 years old.
There is suspected bronchiectasis.

All smokers or ex-smokers aged >40 years with persistent haemoptysis should urgently be referred to a chest physician under the two-week wait rules.

57
Q

Management of moderate haemoptysis

A

Moderate haemoptysis (30-50 ml in the previous 24 hours) requires hospitalisation for observation, due to increased risk of further heavy bleeding.

58
Q

Management of severe haemoptysis

A

This is a medical emergency with a high mortality rate. However, there are few large, good-quality, controlled trials looking at best management to guide practice - particularly in the medical versus surgical dilemma.

Resuscitate according to ‘ABC’ principles. Intubate where there are signs of acute respiratory failure. Selective intubation of the right or left main bronchus with a large single-lumen endotracheal tube or, alternatively, the use of a double lumen tube should be considered. Maintain oxygenation saturations with high flow oxygen and suction. Obtain IV access and give fluids/blood transfusion as appropriate. Correct any clotting abnormalities. The patient will require admission to intensive care.

Localisation of the bleeding site via radiology and early bronchoscopy. CXR and even CT scanning may not be helpful (due to the presence of aspirated blood). The use of rigid or flexible fibreoptic bronchoscopy remains controversial and tends to depend on local preference and expertise.

59
Q

Specific therapies to control bleeding in haemoptysis

A

Specific therapies to control bleeding:

Angiography and embolisation - endovascular embolisation is the most effective and minimally invasive technique for managing massive and recurrent haemoptysis.

Bronchoscopic therapy:
Iced saline lavage.
Topical agents - eg, use of thrombin or fibrinogen-thrombin glue.
Endobronchial balloon catheter tamponade.
Laser photocoagulation.
Surgical resection:
Segmentectomy.
Lobectomy.
Pneumonectomy.
Under emergency conditions, surgery is difficult, has a high risk of septic complications and a significant mortality rate. Surgery is usually only the treatment of choice in selected cases, such as chest trauma and iatrogenic pulmonary artery rupture. Emergency surgery should therefore be reserved for patients with persistent life-threatening haemoptysis.

Radiotherapy - may be used to treat aspergillomas and vascular tumours.

Antifibrinolytic therapy - although there is currently insufficient evidence to determine whether antifibrinolytics can be used to treat haemoptysis from any cause, there is limited evidence to suggest they may reduce the duration of bleeding

60
Q

Palliative care in haemoptysis

A

Given the bleak prognosis of a massive haemoptysis, active resuscitation may not be desired or appropriate. Under these circumstances, the emphasis should be on the relief of pain and of fear in the patient and supporting witnesses and family:

Nurse the patient lying on the side of the tumour.
Administer parenteral opioid and fast-acting benzodiazepine.
Mask blood with red or green towels.
In some, the likelihood of such a bleed can be predicted (based on the tumour site, earlier bleeds, etc) and it may be appropriate to discuss and plan for such an eventuality with the patient and their family.

Where active treatment is desired, management of a major bleed is as above. With more minor haemoptysis, additional palliative care measures may include:

Oral haemostatics - eg, tranexamic acid.
Cough suppression.
Anticoagulation (where PE).
Antibiotics (where infection).
Radiotherapy or laser treatment of the tumour site.
Therapeutic bronchoscopy with balloon tamponade and infusion of vasoactive agents such as adrenaline (epinephrine) may be successful. Bronchial angiography with bronchial artery embolisation can sometimes control haemoptysis.

61
Q

Haemoptysis prognosis

A

Haemoptysis may be a mild, self-limiting symptom or may herald serious underlying disease. Massive haemoptysis can directly cause death and has a bad prognosis, worse in some groups such as those with an underlying cancer.