A multicenter RCT of noninvasive ventilation in pneumonia-induced early mild acute respiratory distress syndrome

Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO /FIO between 200 and 300). To evaluate whether early NIV ca...

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Published inCritical care (London, England) Vol. 23; no. 1; pp. 300 - 13
Main Authors He, Hangyong, Sun, Bing, Liang, Lirong, Li, Yanming, Wang, He, Wei, Luqing, Li, Guofeng, Guo, Shuliang, Duan, Jun, Li, Yuping, Zhou, Ying, Chen, Yusheng, Li, Hongru, Yang, Jingping, Xu, Xiyuan, Song, Liqiang, Chen, Jie, Bao, Yong, Chen, Feng, Wang, Ping, Ji, Lixi, Zhang, Yongxiang, Ding, Yanyan, Chen, Liangan, Wang, Ying, Yang, Lan, Yang, Tian, Weng, Heng, Li, Hongyan, Wang, Daoxin, Tong, Jin, Sun, Yongchang, Li, Ran, Jin, Faguang, Li, Chunmei, He, Bei, Sun, Lina, Wang, Changzheng, Hu, Mingdong, Yang, Xiaohong, Luo, Qin, Zhang, Jin, Tan, Hai, Wang, Chen
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 04.09.2019
BioMed Central
BMC
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Abstract Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO /FIO between 200 and 300). To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS. Prospective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria. Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO /FIO became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005-1.379], p = 0.043). Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO /FIO observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure. NCT01581229 . Registered 19 April 2012.
AbstractList Rationale Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO.sub.2/FIO.sub.2 between 200 and 300). Objectives To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS. Methods Prospective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria. Results Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO.sub.2/FIO.sub.2 became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005-1.379], p = 0.043). Conclusions Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO.sub.2/FIO.sub.2 observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure. Trial registration NCT01581229. Registered 19 April 2012 Keywords: Acute respiratory distress syndrome (ARDS), Noninvasive ventilation (NIV), Pneumonia
Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO /FIO between 200 and 300). To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS. Prospective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria. Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO /FIO became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005-1.379], p = 0.043). Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO /FIO observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure. NCT01581229 . Registered 19 April 2012.
Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO.sub.2/FIO.sub.2 between 200 and 300). To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS. Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO.sub.2/FIO.sub.2 became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005-1.379], p = 0.043). Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO.sub.2/FIO.sub.2 observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure.
Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO2/FIO2 between 200 and 300).RATIONALEOur pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with "early" stage of mild acute respiratory distress syndrome (ARDS, PaO2/FIO2 between 200 and 300).To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS.OBJECTIVESTo evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS.Prospective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria.METHODSProspective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria.Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO2/FIO2 became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005-1.379], p = 0.043).RESULTSTwo hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO2/FIO2 became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005-1.379], p = 0.043).Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO2/FIO2 observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure.CONCLUSIONSTreatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO2/FIO2 observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure.NCT01581229 . Registered 19 April 2012.TRIAL REGISTRATIONNCT01581229 . Registered 19 April 2012.
Rationale Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with “early” stage of mild acute respiratory distress syndrome (ARDS, PaO2/FIO2 between 200 and 300). Objectives To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS. Methods Prospective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria. Results Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO2/FIO2 became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005–1.379], p = 0.043). Conclusions Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO2/FIO2 observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure. Trial registration NCT01581229. Registered 19 April 2012
Abstract Rationale Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients with “early” stage of mild acute respiratory distress syndrome (ARDS, PaO2/FIO2 between 200 and 300). Objectives To evaluate whether early NIV can reduce the need for invasive ventilation in patients with pneumonia-induced early mild ARDS. Methods Prospective, multicenter, randomized controlled trial (RCT) of NIV compared with conventional administration of oxygen through a Venturi mask. Primary outcome included the numbers of patients who met the intubation criteria. Results Two hundred subjects were randomized to NIV (n = 102) or control (n = 98) groups from 21 centers. Baseline characteristics were similar in the two groups. In the NIV group, PaO2/FIO2 became significantly higher than in the control group at 2 h after randomization and remained stable for the first 72 h. NIV did not decrease the proportion of patients requiring intubation than in the control group (11/102 vs. 9/98, 10.8% vs. 9.2%, p = 0.706). The ICU mortality was similar in the two groups (7/102 vs. 7/98, 4.9% vs. 3.1%, p = 0.721). Multivariate analysis showed minute ventilation greater than 11 L/min at 48 h was the independent risk factor for NIV failure (OR, 1.176 [95% CI, 1.005–1.379], p = 0.043). Conclusions Treatment with NIV did not reduce the need for intubation among patients with pneumonia-induced early mild ARDS, despite the improved PaO2/FIO2 observed with NIV compared with standard oxygen therapy. High minute ventilation may predict NIV failure. Trial registration NCT01581229. Registered 19 April 2012
ArticleNumber 300
Audience Academic
Author Xu, Xiyuan
Wang, He
Guo, Shuliang
Li, Hongyan
Wang, Ying
Li, Chunmei
Ding, Yanyan
Yang, Lan
Li, Ran
Liang, Lirong
Yang, Tian
Chen, Liangan
Li, Guofeng
Jin, Faguang
Tan, Hai
Li, Yanming
Duan, Jun
Chen, Yusheng
Song, Liqiang
Zhang, Yongxiang
Bao, Yong
Ji, Lixi
He, Bei
Li, Yuping
Weng, Heng
Tong, Jin
Luo, Qin
Wang, Daoxin
Zhou, Ying
Chen, Jie
Wang, Ping
Li, Hongru
Zhang, Jin
Sun, Lina
Chen, Feng
He, Hangyong
Sun, Yongchang
Wang, Changzheng
Hu, Mingdong
Yang, Xiaohong
Wang, Chen
Wei, Luqing
Sun, Bing
Yang, Jingping
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/31484582$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Contributor Wang, He
Li, Hongyan
Lu, Fengfeng
Wang, Ying
Li, Chunmei
Ding, Yanyan
Yang, Lan
Li, Ran
Liang, Zhixin
Liu, Bin
Huang, Xiaofang
Li, Yanming
Duan, Jun
Song, Liqiang
Bao, Yong
Weng, Heng
Tong, Jin
Lin, Xu
Wang, Daoxin
Chen, Jie
Wang, Ping
Wang, Ling
Xu, Jie
Zhang, Jin
Sun, Lina
Nan, Yandong
He, Hangyong
Wu, Yunfu
Wang, Changzheng
Hu, Mingdong
Wei, Luqing
Hong, Rujun
Yang, Jingping
Xu, Xiyuan
Li, Mei
Guo, Shuliang
Liang, Lirong
Tian, Hongjun
Yang, Tian
Chen, Liangan
Li, Guofeng
Jin, Faguang
Tan, Hai
Chen, Yusheng
Deng, Wang
Zhang, Yongxiang
Ji, Lixi
He, Bei
Li, Yuping
Luo, Qin
Wang, Hui
Zhou, Ying
Li, Hongru
Shen, Ning
Chen, Feng
Sun, Min
Sun, Yongchang
Yang, Xiaohong
Wang, Chen
Sun, Bing
Yao, Xiujuan
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Issue 1
Keywords Acute respiratory distress syndrome (ARDS)
Pneumonia
Noninvasive ventilation (NIV)
Language English
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Snippet Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on patients...
Rationale Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of oxygen on...
Abstract Rationale Our pilot study suggested that noninvasive ventilation (NIV) reduced the need for intubation compared with conventional administration of...
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StartPage 300
SubjectTerms Acute respiratory distress syndrome (ARDS)
Adult
Adult respiratory distress syndrome
Aged
Care and treatment
Complications and side effects
Critical care
Evidence-based medicine
Female
Humans
Intubation
Male
Mechanical ventilation
Middle Aged
Mortality
Noninvasive ventilation (NIV)
Noninvasive Ventilation - adverse effects
Noninvasive Ventilation - methods
Patient outcomes
Pilot Projects
Pneumonia
Prospective Studies
Respiratory distress syndrome
Respiratory Distress Syndrome, Adult - complications
Respiratory therapy
Severity of Illness Index
Ventilation
Ventilator-Induced Lung Injury - etiology
Ventilator-Induced Lung Injury - therapy
Ventilators
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Title A multicenter RCT of noninvasive ventilation in pneumonia-induced early mild acute respiratory distress syndrome
URI https://www.ncbi.nlm.nih.gov/pubmed/31484582
https://www.proquest.com/docview/2292746551
https://www.proquest.com/docview/2285104127
https://pubmed.ncbi.nlm.nih.gov/PMC6727327
https://doaj.org/article/31ef9e4b4bb44453a41c60e6a1aa4cf0
Volume 23
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