BRONCHOSPASM
DEFINITION
Reversible constriction of the small air passages of the lower
respiratory tract.
TOXIC CAUSES
Beta adrenergic blocking drugs
Dust
Hydrocarbon aspiration
Irritant gases: Ammonia
Chlorine
Fluorine
Hydrochloric acid fumes
Nitrogen dioxide
Ozone
Phosgene
Sulphur dioxide
Metal fumes ("metal fume fever")
Organophosphates
Smoke
NON-TOXIC CAUSES
Anaphylaxis
Asthma
CLINICAL FEATURES
Dyspnoea, wheezing, cyanosis and cough are the presenting features.
The patient may also be too breathless to speak. There may be a
'silent' chest. There is usually a tachycardia. In severe cases,
"pulsus paradoxus" may be evident.
DIFFERENTIAL DIAGNOSIS
Airways obstruction due to increased bronchial secretions
Chronic obstructive airways disease
Hyperventilation
Left ventricular failure (cardiac asthma)
Pulmonary thromboembolism
Pneumonia
Pneumothorax
Respiratory compensation for metabolic acidosis
Upper airway obstruction
RELEVANT INVESTIGATIONS
Arterial blood gases (in severely ill patients)
Chest X-ray
Peak Expiratory Flow Rate (PEFR)
Forced Expiratory volume in one second (FEV1).
TREATMENT
Administer supplemental oxygen.
In the first instance, give a beta-adrenergic agonist such as
salbutamol as an aerosol using a nebulizer (2ml of 0.5% salbutamol
respirator solution contains 10mg of salbutamol). The dose may be
repeated at 20 minute intervals or even continuously. Salbutamol
may also be given intravenously, starting with an infusion of a
solution containing 5 mg in 500 ml (10 mcg/mL) at a rate of 3 to 20
mcg/minute.
If there is no satisfactory response to 2 to 3 administered doses of
salbutamol, give hydrocortisone 300mg, intravenously stat and 200mg
intravenously every four hours thereafter until the patient is better.
Oral prednisolone 40mg/day may be started at the same time as
intravenous corticosteroids.
In severe cases, aminophylline may be added (a loading dose of
5 mg/kg infused over 60 minutes, and 0.5 to 0.9 mg/kg each hour
thereafter, aiming to obtain a serum concentration between 8 and
20 mg/L).
If the patient's clinical condition and arterial blood gases
deteriorate despite the above measures, intermittent positive pressure
ventilation (IPPV) may be necessary. Ventilation however is rarely
necessary for bronchospasm following toxic exposures.
CLINICAL COURSE AND MONITORING
Unless the patient is an asthmatic, improvement is generally rapid.
Fatalities are rare. The patient should be carefully monitored until
improvement occurs.
LONG-TERM COMPLICATIONS
None from the bronchospasm itself.
Sensitization to a toxic substance may result in reactive airways
disease.
AUTHOR(S)/REVIEWERS
Author: Dr Ravindra Fernando
National Poisons Information Centre
Faculty of Medicine
Kynsey Road
Colombo 8
Sri Lanka
Tel: +94 1 686142
Fax: +94 1 691581
Reviewers: Rio de Janeiro 9/97: J.N. Bernstein, E. Birtanov,
R. Fernando, H. Hentschel, T.J. Meredith, Y. Ostapenko,
P. Pelclova, C.P. Snook, J. Szajewski.
London 3/98: T. Della Puppa, T.J. Meredith, L. Murray,
A. Nantel.