Continuous positive airway pressure versus high-flow nasal cannula oxygen therapy for acute hypoxemic respiratory failure: A randomized controlled trial.

acute hypoxemic respiratory failure continuous positive airway pressure high-flow nasal cannula oxygen therapy

Journal

Respirology (Carlton, Vic.)
ISSN: 1440-1843
Titre abrégé: Respirology
Pays: Australia
ID NLM: 9616368

Informations de publication

Date de publication:
30 Aug 2023
Historique:
received: 01 02 2023
accepted: 16 08 2023
medline: 31 8 2023
pubmed: 31 8 2023
entrez: 30 8 2023
Statut: aheadofprint

Résumé

The relative effectiveness of initial non-invasive respiratory strategies for acute respiratory failure using continuous positive airway pressure (CPAP) or high-flow nasal cannula (HFNC) is unclear. We conducted a multicenter, open-label, parallel-group randomized controlled trial to compare the efficacy of CPAP and HFNC on reducing the risk of meeting the prespecified criteria for intubation and improving clinical outcomes of acute hypoxemic respiratory failure. The primary endpoint was the time taken to meet the prespecified criteria for intubation within 28 days. Eighty-five patients were randomly assigned to the CPAP or HFNC group. Eleven (28.9%) in the CPAP group and twenty (42.6%) in the HFNC group met the criteria for intubation within 28 days. Compared with HFNC, CPAP reduced the risk of meeting the intubation criteria (hazard ratio [HR], 0.327; 95% CI, 0.148-0.724; p = 0.006). There were no significant between-group differences in the intubation rates, in-hospital and 28-day mortality rates, ventilator-free days, duration of the need for respiratory support, or duration of hospitalization for respiratory illness. Pulmonary oxygenation was significantly better in the CPAP group, with significantly lower pH and higher partial pressure of carbon dioxide, but there were no differences in the respiratory rate between groups. CPAP and HFNC were associated with few possibly causal adverse events. CPAP is more effective than HFNC at reducing the risk of meeting the intubation criteria in patients with acute hypoxemic respiratory failure.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
The relative effectiveness of initial non-invasive respiratory strategies for acute respiratory failure using continuous positive airway pressure (CPAP) or high-flow nasal cannula (HFNC) is unclear.
METHODS METHODS
We conducted a multicenter, open-label, parallel-group randomized controlled trial to compare the efficacy of CPAP and HFNC on reducing the risk of meeting the prespecified criteria for intubation and improving clinical outcomes of acute hypoxemic respiratory failure. The primary endpoint was the time taken to meet the prespecified criteria for intubation within 28 days.
RESULTS RESULTS
Eighty-five patients were randomly assigned to the CPAP or HFNC group. Eleven (28.9%) in the CPAP group and twenty (42.6%) in the HFNC group met the criteria for intubation within 28 days. Compared with HFNC, CPAP reduced the risk of meeting the intubation criteria (hazard ratio [HR], 0.327; 95% CI, 0.148-0.724; p = 0.006). There were no significant between-group differences in the intubation rates, in-hospital and 28-day mortality rates, ventilator-free days, duration of the need for respiratory support, or duration of hospitalization for respiratory illness. Pulmonary oxygenation was significantly better in the CPAP group, with significantly lower pH and higher partial pressure of carbon dioxide, but there were no differences in the respiratory rate between groups. CPAP and HFNC were associated with few possibly causal adverse events.
CONCLUSION CONCLUSIONS
CPAP is more effective than HFNC at reducing the risk of meeting the intubation criteria in patients with acute hypoxemic respiratory failure.

Identifiants

pubmed: 37648252
doi: 10.1111/resp.14588
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Philips Japan Limited

Informations de copyright

© 2023 Asian Pacific Society of Respirology.

Références

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Auteurs

Kazuma Nagata (K)

Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Toshiki Yokoyama (T)

Department of Respiratory Medicine and Allergy, Tosei General Hospital, Seto, Aichi, Japan.

Ryosuke Tsugitomi (R)

Department of Pulmonary Medicine, Thoracic Center, St. Luke's International Hospital, Chuo City, Tokyo, Japan.

Harunori Nakashima (H)

Department of Respiratory Medicine, Ogaki Municipal Hospital, Ogaki, Gifu, Japan.

Hiroshi Kuraishi (H)

Department of Pulmonary Medicine, Nagano Red Cross Hospital, Nagano, Nagano, Japan.

Shinichiro Ohshimo (S)

Department of Emergency and Critical Care Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima, Japan.

Yoshihiro Mori (Y)

Department of Respiratory Medicine, KKR Takamatsu Hospital, Takamatsu, Kagawa, Japan.

Masaaki Sakuraya (M)

Department of Emergency and Intensive Care Medicine, JA Hiroshima General Hospital, Hiroshima, Hiroshima, Japan.

Ryogo Kagami (R)

Department of Pulmonary Medicine, National Hospital Organization Himeji Medical Center, Himeji, Hyogo, Japan.

Motoaki Tanigawa (M)

Department of Respiratory Medicine, Japanese Red Cross Ise Hospital, Ise, Mie, Japan.

Kazunori Tobino (K)

Department of Respiratory Medicine, Iizuka Hospital, Iizuka, Fukuoka, Japan.

Tetsuro Kamo (T)

Department of Respiratory Medicine, Saiseikai Utsunomiya Hospital, Utsunomiya, Tochigi, Japan.

Toru Kadowaki (T)

Department of Pulmonary Medicine, National Hospital Organization Matsue Medical Center, Matsue, Shimane, Japan.

Yasutaka Koga (Y)

Advanced Medical Emergency and Critical Care Center, Yamaguchi University Hospital, Ube, Yamaguchi, Japan.

Yoshitaka Ogata (Y)

Department of Critical Care Medicine, Yao Tokushukai General Hospital, Yao, Osaka, Japan.

Naoki Nishimura (N)

Department of Pulmonary Medicine, Thoracic Center, St. Luke's International Hospital, Chuo City, Tokyo, Japan.

Yasuhiro Kondoh (Y)

Department of Respiratory Medicine and Allergy, Tosei General Hospital, Seto, Aichi, Japan.

Satsuki Taniuchi (S)

Department of Medical Statistics, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Osaka, Japan.

Ayumi Shintani (A)

Department of Medical Statistics, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Osaka, Japan.

Keisuke Tomii (K)

Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Hyogo, Japan.

Classifications MeSH