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Asthma
Asthma is a clinical syndrome characterized by variable airflow obstruction secondary to inflammation of the airways. An acute asthmatic episode is usually the result of exposure to a trigger agent which may be either specific (pollen, animal dander, viral infection) or non specific. Typical symptoms include dyspnoea, wheeze, chest tightness and cough. They vary from being almost undetectable to severe, unremitting and sometimes life threatening.
The aims of hospital management are:
- To prevent death.
- To restore the patient's clinical condition and lung function.
- To maintain optimum lung function and prevent early relapse.
The assessment of the severity of an acute attack of asthma and the immediate treatment occur in parallel.
The severity of asthmatic episodes is frequently underestimated by both the patient and doctor. It is therefore essential to measure severity objectively so that rational decisions regarding investigation and immediate treatment can be made.
All patients should have the following measured:
- PEFR/spirometry.
- Respiratory rate.
- Pulse, blood pressure, temperature.
- Pulse oximetry. ABG in moderate or severe asthma.
At Christchurch Hospital the Asthma Admission Form should be used for ALL admissions.
Guidelines for Assessing the Severity of Acute Asthma
Individual features should not be interpreted in isolation. An overall assessment of severity should be made using clinical judgement and the following guidelines:
Severity Assessment in Acute Asthma
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Severity Assessment in Acute Asthma
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Mild
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Moderate
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Severe
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Speech
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Sentences
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Phrases
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Words
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PEFR (% of predicted or previous best)
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>60%
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40-60%
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Less than 40% or less than 150 L/min if best peak flow unknown
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FEV1 (% Predicted)
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>60%
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40-60%
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<40% or absolute value less than 1 L
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Respiratory rate
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Normal
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18-25
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>25 or <10
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Pulse rate
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<100
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100-120
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>120
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Oximetry
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>94%
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90-94%
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<90%
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PaO2
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Test not necessary
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<80 mm Hg
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<60 mm Hg
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PaCO2
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Test not necessary
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<40 mm Hg
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≥40 mm Hg
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DANGER SIGNS: Exhaustion, confusion, cyanosis, bradycardia, unconsciousness, silent chest on auscultation, signs of respiratory muscle fatigue (indrawing of lower costal margin, paradoxical breathing). See Life-Threatening Asthma.
Management of Asthma
Specific treatment is dependent on severity. All patients should be treated with a bronchodilator in the first instance. Other therapy is added depending on the response and reassessment of severity. Nebulizer treatment should be changed to an inhaler with spacer as soon as practicable.
Immediate Management of Asthma
Immediate Management of Asthma
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MILD Asthma: Management
- Repeated doses of salbutamol inhaler with a spacer device, or nebulized salbutamol 5 mg q4h + prn (1). Prednisone 40 mg orally stat then daily.
Monitoring:
- PEFR after initial treatment then QID. Pulse, respiratory rate QID.
MODERATE Asthma: Management
- Nebulized salbutamol 5 mg q4h + prn (1). Prednisone 40 mg orally stat then daily.
- Add oxygen to maintain sat.O2 >95% (usually 2 L/min by nasal cannulae).
- Contact Medical Registrar if not improving.
- Perform CXR (2) if condition deteriorates or evidence of a complication.
Monitoring:
- PEFR 2-4 hourly. Pulse oximetry (3). Pulse, respiratory rate, BP QID. Monitor for hypokalaemia which may be exacerbated by beta-agonist therapy.
SEVERE Asthma: Management
- Increase nebulized salbutamol 5 mg up to 2 hourly. Nebulized ipratropium 0.5 mg q4h. Oxygen 8 L/min by Hudson mask. Adjust to maintain sat.O2 >95%.
- Add intravenous access. Prednisone 40 mg orally stat then daily. If unable to take orally, give IV hydrocortisone 200 mg stat then q6h (for 24 hours). Fluids - sodium chloride 0.9% 1 L 6 hourly initially. IV bronchodilator if not responding to nebulized bronchodilator.
- Contact Respiratory Physician.
- Perform CXR (2) in all cases.
Monitoring:
- ICU or high dependency unit. Pulse oximetry/ABG.
- Continuous ECG. Pulse, respiratory rate, BP 2 hourly. Special nurse.
Serum potassium 12 hourly.
LIFE-THREATENING Asthma: Management
Clinical
- FEVl or PEFR <33% predicted (or of usual best).
- Silent chest, cyanosis, or feeble respiratory effort (4).
- Bradycardia or hypotension.
- Exhaustion, confusion or coma.
Management
- High flow oxygen (40-60%).
- Salbutamol + ipratropium via oxygen driven nebulizer (initially continuous).
- Loading dose IV salbutamol 250 microgram with subsequent infusion (5 mg/5 mL salbutamol made up to 100 mL with 5% glucose , infuse at 10-30 mL/hr).
- CXR to exclude pneumothorax.
- ICU or Respiratory team review.
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- It is essential that all nebulized bronchodilators are given with oxygen 6-8 L/min.
- Patients with life-threatening asthma, or severe asthma not responding to initial treatment, and patients in whom there is any suspicion of a complication require a CXR. Complications include pneumothorax, surgical emphysema, atelectasis and consolidation. All CXRs should be done at the bedside unless the patient is accompanied to X-ray by a nurse or doctor.
- Pulse oximetry is very useful in assessing the adequacy of tissue oxygenation in patients with asthma. It does not reflect the adequacy of ventilation. An initial ABG measurement should be made in all patients admitted to hospital unless severity assessed as mild.
- Patients with life-threatening asthma sometimes may not appear distressed.
Note: There is some evidence that IV magnesium may be helpful in severe asthma refractory to standard treatment. Seek Specialist advice. Nebulized magnesium is not recommended.
Note: A normal CO2 in an asthma attack is a marker of severe disease.
Note: IV aminophylline has not demonstrated improved outcomes when compared to IV salbutamol in the treatment of acute asthma, and is associated with significantly more frequent side effects.
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Subsequent Management of Acute Asthma Episode
Depends on the severity of the attack and the patient's response to initial treatment.
- General Measures
- Observation: Close observation should continue in patients with severe asthma until there is objective evidence of sustained improvement.
- Positioning: Recommend sitting upright and/or leaning forward.
- Continue Treatment
- Oxygen - according to arterial blood gases/oximetry.
- Beta2 agonist - if condition improving continue to give 4 hourly.
- Monitoring: Repeat PEFR (or FEV1) 15-30 minutes after starting treatment then as required depending on severity. Arterial blood gases should be repeated within two hours of starting treatment in the following circumstances:
- The initial PaO2 <60 mm Hg.
- The initial PaCO2 high normal or raised.
- The patient's condition deteriorates.
Measure and record heart rate and respiratory rate, at least QID.
- Investigations in hospital
All patients admitted to hospital should have:
- CBC + diff.
- Na, K, glucose, creatinine.
- ECG - in patients over 40 years of age.
- Indications for CXR
- Severe or life-threatening asthma attack - during resuscitation.
- Moderate to severe attack not responding to initial treatment.
- Patient suspected of having developed a complication or in whom another condition/diagnosis is suspected (see below).
- Failure to Improve
- Worsening asthma - check the adequacy of treatment e.g., check drugs given, dosage and adequacy of drug delivery.
Therapeutic options:
- Increase the dose/frequency of beta2 agonist.
- Add ipratropium bromide 0.5 mg q6h via a nebulizer.
- Consider using an intravenous bronchodilator.
- Consider the possibility of a complication or an alternative diagnosis:
- Pneumonia.
- Pneumothorax.
- Cardiac arrhythmia.
- Left ventricular failure.
- Laryngeal or tracheal obstruction.
- Acute Respiratory Distress Syndrome (ARDS).
- Pulmonary embolism.
- Post transfusion acute lung injury.
All patients who fail to improve or deteriorate despite initial treatment, must be monitored closely and discussed with the appropriate Consultant or the Respiratory Physician on call.
Management During Recovery and Following Discharge
Once the acute episode has been brought under control, attention must be directed towards:
- Interval asthma control.
- Severity assessment - what is the risk of severe asthma recurring?
- Self-management skills.
- Smoking status.
Interval Asthma Control
- Interval asthma control should be assessed by specific questioning directed at the following features:
- Nocturnal waking and morning chest tightness.
- Interference with exercise.
- Use of rescue bronchodilator.
- Peak flow values.
- Days off work or school.
- Use of corticosteroids and nebulizer for exacerbations.
- Compliance with preventer therapy.
Note: These features are itemized on the Asthma Admission Form used at Christchurch Hospital. Copies are available from the Department of General Medicine or Respiratory Ward 25.
Note: Patients with unstable features or poor compliance should be referred to a Respiratory Physician, preferably while in hospital.
Severity Assessment
- The risk of a severe or fatal asthma attack is higher when any of the following features are present:
- Hospital admission for asthma in the last 12 months.
- Previous severe asthma requiring ventilation or ICU admission.
- Frequent attendances to the emergency department.
- Nocturnal symptoms.
- Precipitous asthma episodes in the past - severe episodes coming on over less than 3 hours.
- Frequent requirement for courses of oral steroids.
- Poor self-management skills.
- Poor social circumstances.
- Psychological impairment.
Asthma Self-Management Skills
Smoking Status
- Give nicotine replacement and smoking cessation advice and support if required. Current smoking is associated with reduced effectiveness of inhaled corticosteroids. See Nicotine Dependent Patients.
Options for Ongoing Education as an Outpatient
- Respiratory Physician.
- Clinical Nurse Specialist - Respiratory Outpatient Unit.
- General Practitioner/Practice Nurse.
- Respiratory Educators/Health Promoters - Asthma Canterbury, 275 Cashel Street, PO Box 13 091, Christchurch. Email office@asthmacanty.org.nz.
(03) 366 5235, fax (03) 366 5209.
Treatment on Discharge
- This will obviously vary from case to case but usually the patient will receive:
- Inhaled corticosteroid - beclometasone or budesonide 800-2000 microgram daily or fluticasone 500-1000 microgram daily. This high dose must be reviewed on follow-up.
- Prednisone 40 mg mane for 1 week then 20 mg mane for 1 week (longer courses may be required for chronic severe asthma).
- A long acting beta2 agonist (e.g., salmeterol) may be appropriate in some patients, but is best started once they have recovered from an acute attack. It should be considered in patients with frequent daytime and nocturnal symptoms. Long-acting beta2 agonists should be added only in patients who are already taking inhaled steroids.
- Short acting beta2 agonist inhaler to use as required (NOT regularly).
- Advice regarding common side effects of these medications:
- Short acting beta2 agonists: palpitations, anxiety, cramps.
- Inhaled steroids: dysphonia, thrush - use mouth rinsing and a spacer.
- Prednisone (short courses): euphoria or dysphoria, hypertension, hyperglycaemia, indigestion, insomnia.
Note: Patients prescribed inhaled aerosolized corticosteroids should be encouraged to use a large volume spacer device.
Single Inhaler Therapy for Asthma
'Single inhaler therapy' (otherwise known as single maintenance and reliever therapy or SMART™) is the use of a combination inhaled steroid / beta2 agonist preparation as a preventer and a reliever. The only products able to be used in this way in New Zealand currently are those containing formoterol and budesonide (Symbicort™ and Vannair™). Seretide™ (salmeterol / fluticasone) should not be used in single inhaler therapy, because of the slower onset of action of salmeterol. For more information about the use of single inhaler therapy, see http://ndhadeliver.natlib.govt.nz/delivery/DeliveryManagerServlet?dps_pid=IE768736&dps_custom_att_1=ilsdb .
There is no evidence available to guide the decision when to restart single inhaler therapy following an exacerbation. Pragmatically it seems sensible to restart single inhaler therapy close to discharge, but to remind the patient to seek early medical advice if they are using more than 8 puffs of their combination product daily, or if symptoms are not improving.
Exhaled Nitric Oxide
Exhaled nitric oxide is a new breath test for detection of eosinophilic airway inflammation, usually in the context of asthma. High levels predict increased likelihood of response to inhaled steroids. Exhaled nitric oxide is useful for diagnosis of asthma, and for titrating steroid treatment. There may be a role for assessment of compliance with inhaled steroid treatment. Exhaled nitric oxide assessment can be ordered via the Respiratory Physiology Laboratory. For help interpreting the result, please contact the Acute Respiratory Physician on call.
Topic Code: 1643