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. 2021 Feb 19;42:43–48. doi: 10.1016/j.prrv.2021.02.001

Table 2.

Roll out process.

  • Clinicians provided a suitability and priority list of patients.

  • Child allocated suitable spirometer based on technique by the physiologist*.

  • Called parents to explain sending them a device and check they have a smart phone/table; and to confirm address.

  • Sent out in post spirometer with instructions for set up with a covering letter; and additional information including the child’s latest height, weight and ethnicity according to GLI reference ranges.

  • On receiving spirometer, patients and parents asked to set up and perform a spirometry session.

  • One of the devices had an automatic platform through which we received the data. The other one required parents to create a pdf from the accompanying app and email to us.

  • Once results received, physiologist checked acceptability/reproducibility in line with ATS/ERS criteria.

  • If satisfactory, results were uploaded to the patient’s electronic record so clinicians could access them.

  • Contacted patients if acceptability criteria not met and offered video call for further instruction. There was no time to offer video call routinely although this would have been preferable.

*

At first one of the spirometers did not give a flow volume loop so these were used for children we knew had reproducible technique; this was soon rectified.