Investigations
CXR is a key investigation in
respiratory disease. It will give you informa-tion about lung volume (e.g.
hyperinflation in asthma), signs of chronic in-flammation (e.g. peribronchial
cuffing), and evidence of congenitial lesions (e.g. lung cysts). However, it is
an investigation that can be overused. It should not replace a thorough
clinical examination, and think hard before requesting repeat studies.
A CXR is used to glean more
clinical evidence about what the child’s underlying problem is. So, in each
presentation consider why you have requested the test. Here are some examples.
A CXR is not needed every time a
patient presents with ‘asthma’. However, if that child has never had an X-ray,
or there is something atypical about the history, consider other possibilities:
·
Suspected foreign body inhalation:
i.e. inspiratory and expiratory
film (object often radiolucent).
·
Suspected gastro-oesophageal
reflux with aspiration, or aspiration from abnormal swallowing: i.e. looking for different lobes
affected at different times.
·
Monophonic wheeze: i.e. looking for hilar lymph nodes
compressing on the right main-stem
bronchus, or a large left atrium compressing the left main-stem bronchus, or
mediastinal mass.
Suspected tracheal lesion around
the thoracic inlet.
·
Suspected
typical and atypical pneumonia, or empyema.
·
Suspected
bronchiectasis.
·
Suspected
pulmonary parenchymal disease.
·
Pneumothorax.
·
Suspected
heart disease, e.g. heart failure.
Suspected
cardiopulmonary disease or cor pul-monale from chronic upper airway
obstruction.
Four tests are frequently
performed at the bedside or in the laboratory are lung function testing, sweat
test, and arterial blood sampling.
Spirometry can be achieved in
5-yr-olds, but measurements are easier in >=7 year olds. Peak expiratory
flow rate (PEFR) monitoring is useful in asthma. Other measurements include:
·FEV1/FVC: the forced expired volume in 1s as
a fraction of forced vital capacity.
·Exercise testing.
·Bronchodilator responsiveness
(i.e. reversibility).
This test is used in the diagnosis
of cystic fibrosis. Sweating is induced in an area of the forearm using
pilocarpine, and a capillary tube is used to collect the sweat. A minimum of
15µL (and preferably >30µL) of sweat should be collected. In cystic fibrosis
abnormal function of the sweat glands results in higher concentrations of
chloride in the sweat:
·Suspicious:
>40mmol/L (>30mmol/L in
newborn screened babies).
·Diagnostic:
>60mmol/L.
Assessment of
oxygen saturation (SpO2) using a pulse oximeter is a non-invasive way of assessing a child’s oxygenation
using a probe attached to a finger or toe.
Assessment of
blood O2, CO2, and acid–base are impor-tant in critically
ill children, or in those where you suspect significant lung disease.
Sometimes more detailed
investigations are needed before you can select the best treatment for your
patient. These include the following:
·Chest
computed tomography: useful
for assessing abnormalities in airways
as well as abnormalities in parenchymal tissue density.
·Thoracic
MRI: useful for looking
at airway–blood interface, and vascular and
mediastinal anatomy.
·Nuclear
imaging: useful for
assessing regional ventilation (V) and perfusion
(Q), as well as V/Q matching.
Flexible
bronchoscopy: used
to assess directly the airway from nose to
distal bronchus; used to lavage the lung for microscopy and culture
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