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High‐Flow Nasal Cannula Versus Conventional Oxygen Therapy in Emergency Department Patients With Cardiogenic Pulmonary Edema: A Randomized Controlled Trial

Onlak Makdee, A. Monsomboon, Usapan Surabenjawong, Nattakarn Praphruetkit, Wansiri Chaisirin, T. Chakorn, C. Permpikul, Phakphoom Thiravit et al.

Annals of Emergency Medicine, 2017

128 participants · 132 citations

Abstract

Study objective: High‐flow nasal cannula is a new method for delivering high‐flow supplemental oxygen for victims of respiratory failure. This randomized controlled trial compares high‐flow nasal cannula with conventional oxygen therapy in emergency department (ED) patients with cardiogenic pulmonary edema. Methods: We conducted an open‐label randomized controlled trial in the ED of Siriraj Hospital, Bangkok, Thailand. Patients aged 18 years or older with cardiogenic pulmonary edema were randomly assigned to receive either conventional oxygen therapy or high‐flow nasal cannula. The primary outcome was the respiratory rate 60 minutes postintervention. Results: We enrolled 128 participants (65 in the conventional oxygen therapy and 63 in the high‐flow nasal cannula groups). Baseline high‐flow nasal cannula and conventional oxygen therapy mean respiratory rates were 28.7 breaths/min (SD 3.2) and 28.6 breaths/min (SD 3.5). Mean respiratory rates at 60 minutes postintervention were lower in the high‐flow nasal cannula group (21.8 versus 25.1 breaths/min; difference 3.3; 95% confidence interval 1.9 to 4.6). No significant differences were found in the admission rate, ED and hospital lengths of stay, noninvasive ventilation, intubation, or mortality. Conclusion: In patients with cardiogenic pulmonary edema in the ED, high‐flow nasal cannula therapy may decrease the severity of dyspnea during the first hour of treatment.

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 128 participants or records.

How the five levels of evidence work. The level is assigned automatically from the abstract and can be wrong, so check the paper.

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