Introduction: Noninvasive respiratory support (NIRS) using helmet devices is an emerging treatment for acute respiratory failure in patients with coronavirus disease 2019 (COVID-19). However, the comparative efficacy of helmet NIRS versus other strategies in this context remains elusive.
Methodology: A network meta-analysis was conducted to compare the efficacy of various NIRS strategies in randomized controlled trials (RCTs) involving COVID-19 patients with acute respiratory failure. Strategies assessed included high-flow nasal oxygen (HFNO), continuous positive airway pressure (CPAP), helmet bilevel positive airway pressure (BiPAP), and standard oxygen therapy (SOT). Relevant RCTs were identified via PubMed, Embase, and Cochrane Central Register of Controlled Trials. Outcomes of interest included intubation rate, mortality rate, length of intensive care unit (ICU) stay, and length of hospital stay.
Results: Five RCTs published between 2021 and 2022 were included. Helmet BiPAP was associated with a significantly lower intubation risk compared with HFNO (relative risk (RR): 0.37, 95% confidence interval (CI): 0.16-0.86) and SOT (RR: 0.24, 95% CI: 0.10-0.62). Additionally, helmet BiPAP was linked to shorter ICU stay compared with SOT (RR: 0.10, 95% CI: 0.02-0.67). However, no significant differences were identified in mortality or hospital stay length between SOT, HFNO, CPAP, and helmet BiPAP groups.
Conclusions: Helmet BiPAP is recommended over HFNO and SOT for moderate-to-severe COVID-19 patients with acute respiratory failure, due to its lower intubation risk and shorter ICU stay. No significant differences were noted in mortality or length of hospital stay among the NIRS strategies.
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http://dx.doi.org/10.3855/jidc.19065 | DOI Listing |
J Infect Dev Ctries
February 2025
Department of Nursing, Air Force Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China.
Introduction: Noninvasive respiratory support (NIRS) using helmet devices is an emerging treatment for acute respiratory failure in patients with coronavirus disease 2019 (COVID-19). However, the comparative efficacy of helmet NIRS versus other strategies in this context remains elusive.
Methodology: A network meta-analysis was conducted to compare the efficacy of various NIRS strategies in randomized controlled trials (RCTs) involving COVID-19 patients with acute respiratory failure.
Noninvasive ventilation (NIV), including bilevel positive airway pressure and continuous positive airway pressure, is a safe and important therapeutic option in the management of prehospital respiratory distress. NAEMSP recommends:NIV should be used in the management of prehospital patients with respiratory failure, such as those with chronic obstructive pulmonary disease, asthma, and pulmonary edema.NIV is a safe intervention for use by Emergency Medical Technicians.
View Article and Find Full Text PDFCan J Respir Ther
July 2020
Section of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Introduction: Noninvasive positive pressure ventilation (NIPPV) plays an important role in the management of respiratory failure. However, since the emergence of the COVID-19 pandemic, utilization of traditional face mask NIPPV has been curtailed in part due to risk of aerosolization of respiratory particles and subsequent health care worker exposure. A randomized clinical trial in 2016 reported that an alternative interface, helmet NIPPV, may be more effective than traditional NIPPV at preventing intubation and improving mortality.
View Article and Find Full Text PDFMed Intensiva
November 2011
Servicio de Medicina Intensiva, Hospital General Castellón, Castellón, España.
Objective: The use of noninvasive mechanical ventilation was evaluated in our series of patients admitted to our ICU with pneumonia due to influenza A virus H1N1, assessing the need for intubation, arterial blood gases and clinical improvement, the development of complications and ICU and hospital stay.
Design: Retrospective and observational study.
Setting: ICU of Castellón University General Hospital (Castellón, Spain).
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