The edition · Pulmonology
AI sleep apnoea screening looks excellent in pooled data and unpredictable in any one clinic
Sixty studies, pooled sensitivity 0.94 at an apnoea-hypopnoea index of 5 - and a prediction interval for specificity running from 0.30 to 0.96. Plus synchronised non-invasive ventilation in preterm infants, and a symptom endpoint from MARIPOSA.
The edition in brief
Today's pulmonology desk is about the difference between a pooled estimate and what a test will do in your clinic. A meta-analysis of 60 studies of artificial-intelligence screening tools for obstructive sleep apnoea, 47 contributing to the pooled analysis, reports sensitivities of 0.94, 0.87 and 0.83 at apnoea-hypopnoea index thresholds of 5, 15 and 30 events per hour, with specificities of 0.77, 0.81 and 0.91. The summary areas under the curve run from 0.907 to 0.943. The prediction intervals tell a different story: specificity at a threshold of 5 has a 95% prediction interval from 0.30 to 0.96. Certainty of evidence was rated low or very low, and the authors call for prospective validation before routine use. A systematic review of 49 studies and 2864 preterm infants found that synchronising nasal intermittent positive pressure ventilation reduced extubation failure compared with nasal CPAP (risk ratio 0.38, 95% CI 0.17 to 0.85), with consistent reductions in breathing effort and patient-ventilator asynchrony. Neurally adjusted ventilatory assist achieved the best synchronisation, with trigger delay around 35 ms. In MARIPOSA, median time to symptomatic progression was 43.6 months with amivantamab plus lazertinib against 29.3 months with osimertinib (hazard ratio 0.69, 95% CI 0.57 to 0.83). A supplement to the intravitreal dexamethasone implant application has been approved, contents unspecified.
AI sleep apnoea screening: read the prediction interval, not the confidence interval
Ask for the prediction interval and local validation data before adopting any AI sleep apnoea screening tool; the pooled figures do not predict your clinic's performance.
Synchronising non-invasive ventilation in preterm infants cut extubation failure
Prefer synchronised nasal ventilation where the equipment allows, but do not expect the long-term outcome evidence to support it yet.
A supplement approved on the intravitreal dexamethasone implant, contents unstated
Nothing to act on: a licence supplement with unspecified contents and no respiratory relevance.
Ask the bed partner, then ask who else is in the room
Ask who shares the sleeping space and whether anyone has moved out because of the snoring; it is a better screen than most questionnaires.
A symptom endpoint from MARIPOSA: 43.6 months against 29.3 before things get worse
When discussing first-line options in EGFR-mutant lung cancer, quote time to symptomatic progression - 43.6 against 29.3 months - rather than radiographic progression.
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