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Updated: Jan 23, 2026

Protocol and Guidelines for Point-of-Care Lung Ultrasound in Diagnosing Neonatal Pulmonary Diseases Based on International Expert Consensus
Published on: March 6, 2019
Implementation study reporting diagnostic accuracy, outcomes and costs in a multicentre randomised controlled trial
Kylie Baker1,2, Stephen Brierley1, Frances Kinnear2,3
1Department of Emergency Medicine, Ipswich General Hospital, Ipswich, Queensland, Australia.
Background:
Lung ultrasound experts claim that 'B line' artefacts herald pulmonary oedema, but links between early recognition and improved outcome are unconfirmed, particularly for non-expert clinicians.
Objective:
Assess individual and system impacts of early, non-expert lung ultrasound (LUS) in breathless older patients.
Methods:
Prospective single-blinded randomised controlled trial of point of care LUS by non-expert clinicians, augmenting ED assessment of patients over 60 years, presenting with dyspnoea. After brief training, clinicians at three hospitals used computer-generated block randomisation envelopes to allocate a convenience sample of consenting presenters to conventional or LUS-augmented management. ED provisional diagnosis was compared to a post-discharge chart audit diagnosis, blinded to ultrasound findings. Secondary outcomes were the length of stay in ED and hospital, costs and discharge destinations.
Results:
From three sites, 224 controls were compared with 218 interventions. LUS improved diagnostic accuracy, with a small effect size in favour of LUS (risk difference: 6.5%, 95% CI 0.9-12) and a number needed to scan of 16 (95% CI 8-107). With LUS, ED and hospital stay increased non-significantly, while discharge destination trends improved. No harm ensued.
Conclusions:
Non-expert LUS augmenting dyspnoea workup may improve diagnostic accuracy, but did not significantly alter costs or outcomes in the ED or the hospital.
Trial Registration:
Australia and New Zealand Clinical Trials Registry (ACTRN12613001023741).
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