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...
Saved in:
Published in | Critical care (London, England) Vol. 23; no. 1; pp. 300 - 13 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
04.09.2019
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
Cover
Loading…
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 |
Author_xml | – sequence: 1 givenname: Hangyong orcidid: 0000-0001-9972-0929 surname: He fullname: He, Hangyong – sequence: 2 givenname: Bing surname: Sun fullname: Sun, Bing – sequence: 3 givenname: Lirong surname: Liang fullname: Liang, Lirong – sequence: 4 givenname: Yanming surname: Li fullname: Li, Yanming – sequence: 5 givenname: He surname: Wang fullname: Wang, He – sequence: 6 givenname: Luqing surname: Wei fullname: Wei, Luqing – sequence: 7 givenname: Guofeng surname: Li fullname: Li, Guofeng – sequence: 8 givenname: Shuliang surname: Guo fullname: Guo, Shuliang – sequence: 9 givenname: Jun surname: Duan fullname: Duan, Jun – sequence: 10 givenname: Yuping surname: Li fullname: Li, Yuping – sequence: 11 givenname: Ying surname: Zhou fullname: Zhou, Ying – sequence: 12 givenname: Yusheng surname: Chen fullname: Chen, Yusheng – sequence: 13 givenname: Hongru surname: Li fullname: Li, Hongru – sequence: 14 givenname: Jingping surname: Yang fullname: Yang, Jingping – sequence: 15 givenname: Xiyuan surname: Xu fullname: Xu, Xiyuan – sequence: 16 givenname: Liqiang surname: Song fullname: Song, Liqiang – sequence: 17 givenname: Jie surname: Chen fullname: Chen, Jie – sequence: 18 givenname: Yong surname: Bao fullname: Bao, Yong – sequence: 19 givenname: Feng surname: Chen fullname: Chen, Feng – sequence: 20 givenname: Ping surname: Wang fullname: Wang, Ping – sequence: 21 givenname: Lixi surname: Ji fullname: Ji, Lixi – sequence: 22 givenname: Yongxiang surname: Zhang fullname: Zhang, Yongxiang – sequence: 23 givenname: Yanyan surname: Ding fullname: Ding, Yanyan – sequence: 24 givenname: Liangan surname: Chen fullname: Chen, Liangan – sequence: 25 givenname: Ying surname: Wang fullname: Wang, Ying – sequence: 26 givenname: Lan surname: Yang fullname: Yang, Lan – sequence: 27 givenname: Tian surname: Yang fullname: Yang, Tian – sequence: 28 givenname: Heng surname: Weng fullname: Weng, Heng – sequence: 29 givenname: Hongyan surname: Li fullname: Li, Hongyan – sequence: 30 givenname: Daoxin surname: Wang fullname: Wang, Daoxin – sequence: 31 givenname: Jin surname: Tong fullname: Tong, Jin – sequence: 32 givenname: Yongchang surname: Sun fullname: Sun, Yongchang – sequence: 33 givenname: Ran surname: Li fullname: Li, Ran – sequence: 34 givenname: Faguang surname: Jin fullname: Jin, Faguang – sequence: 35 givenname: Chunmei surname: Li fullname: Li, Chunmei – sequence: 36 givenname: Bei surname: He fullname: He, Bei – sequence: 37 givenname: Lina surname: Sun fullname: Sun, Lina – sequence: 38 givenname: Changzheng surname: Wang fullname: Wang, Changzheng – sequence: 39 givenname: Mingdong surname: Hu fullname: Hu, Mingdong – sequence: 40 givenname: Xiaohong surname: Yang fullname: Yang, Xiaohong – sequence: 41 givenname: Qin surname: Luo fullname: Luo, Qin – sequence: 42 givenname: Jin surname: Zhang fullname: Zhang, Jin – sequence: 43 givenname: Hai surname: Tan fullname: Tan, Hai – sequence: 44 givenname: Chen surname: Wang fullname: Wang, Chen |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31484582$$D View this record in MEDLINE/PubMed |
BookMark | eNp1UstqGzEUFSWlSdx-QDdF0E03k-o9M5tCMH0EAoWSroVGuuPKzEiuNGPw30e2kzYOLRLocc85l3M5l-gsxAAIvaXkitJGfcyUEykqQtuKyVpW6gW6oFyJqpFcnj25n6PLnNeE0LpR_BU651Q0QjbsAm2u8TgPk7cQJkj4x_IOxx6XPj5sTfZbwNtS8YOZfAzYB7wJMI-lbCof3GzBYTBp2OHRDw4bO0-AE-SNT2aKaYedz1N5Z5x3waU4wmv0sjdDhjcP5wL9_PL5bvmtuv3-9WZ5fVtZxdRUgas7blqroDZOdLyWDReG1463THXFl2070TfOMtc4A1R1zMpW9FR2QnGgfIFujroumrXeJD-atNPReH34iGmlTSq-B9CcQt-C6ETXCSEkN4JaRUAZaoywPSlan45am7kbwe1nlcxwInpaCf6XXsWtVjWredkL9OFBIMXfM-RJjz5bGAYTIM5ZM9ZISgQ9QN8_g67jnEIZVUG1rBZKSvoXtTLFgA99LH3tXlRfK0IYo0o0BXX1D1RZDkZvS5Z6X_5PCO-eGv3j8DEvBVAfATbFnBP02vrpkI2i7AdNid4nUx-TqUsy9T6ZWhUmfcZ8FP8_5x4yUuZn |
CitedBy_id | crossref_primary_10_1007_s11845_022_03116_5 crossref_primary_10_1177_1753466620914220 crossref_primary_10_1007_s00134_023_07050_7 crossref_primary_10_1001_jama_2024_25906 crossref_primary_10_1186_s40560_021_00539_7 crossref_primary_10_3389_fmed_2022_1068327 crossref_primary_10_1097_CCM_0000000000004819 crossref_primary_10_1002_hsr2_1757 crossref_primary_10_1001_jama_2020_9524 crossref_primary_10_1016_j_jointm_2025_01_001 crossref_primary_10_1016_j_chest_2022_05_018 crossref_primary_10_1016_j_ejim_2022_04_012 crossref_primary_10_1097_CM9_0000000000001832 crossref_primary_10_1055_a_2148_3323 crossref_primary_10_1016_j_cjca_2020_04_010 crossref_primary_10_1186_s13054_020_2738_5 crossref_primary_10_1186_s40560_022_00615_6 crossref_primary_10_1136_bmjresp_2021_001149 crossref_primary_10_3390_jcm9072116 crossref_primary_10_1177_17407745231151842 crossref_primary_10_1186_s13054_021_03835_8 crossref_primary_10_1186_s40981_022_00525_4 crossref_primary_10_17816_EID101092 crossref_primary_10_1016_j_ijnurstu_2021_103924 crossref_primary_10_1186_s40001_022_00972_w crossref_primary_10_3904_kjm_2023_98_5_212 crossref_primary_10_1186_s13054_023_04370_4 crossref_primary_10_1016_j_chest_2023_04_022 crossref_primary_10_1055_s_0041_1731433 crossref_primary_10_7759_cureus_32013 crossref_primary_10_1136_bmjopen_2020_040580 crossref_primary_10_1186_s13054_019_2666_4 crossref_primary_10_4037_ajcc2024663 crossref_primary_10_1016_j_bja_2021_02_027 crossref_primary_10_15407_internalmed2020_02_054 crossref_primary_10_1007_s10753_022_01726_w crossref_primary_10_1183_13993003_00396_2024 crossref_primary_10_1007_s11739_020_02548_0 crossref_primary_10_1186_s13613_024_01389_w crossref_primary_10_1016_j_jointm_2024_12_003 crossref_primary_10_1007_s00134_021_06459_2 crossref_primary_10_3389_fphys_2021_728243 crossref_primary_10_1016_j_resinv_2022_05_003 crossref_primary_10_1186_s13613_024_01367_2 crossref_primary_10_5005_jp_journals_10071_G23186 crossref_primary_10_1016_j_accpm_2021_100897 crossref_primary_10_3389_fmed_2023_1088709 |
Cites_doi | 10.1186/cc11247 10.1001/jama.2015.12402 10.1007/s00134-016-4601-3 10.1007/s00134-003-2136-x 10.1001/jama.2010.218 10.1056/NEJMoa1503326 10.1097/01.CCM.0000251821.44259.F3 10.1186/1471-2466-14-19 10.1001/jama.2016.6338 10.1186/cc13103 10.1001/jama.293.5.589 10.1183/09031936.03.00010203 10.1164/rccm.200301-072OC 10.1007/s00134-006-0324-1 10.1183/13993003.02426-2016 10.1001/jama.2016.0291 10.1164/rccm.201610-2138ED 10.1164/rccm.201606-1306OC 10.1097/CCM.0b013e318236ec4f 10.1097/CCM.0000000000001379 10.1164/rccm.201605-1081CP 10.1097/CCM.0000000000002361 10.1097/CCM.0b013e318232d75e 10.1097/00003246-200211000-00008 10.1097/00003246-200006000-00015 10.1001/jama.284.18.2352 10.1097/CCM.0b013e31828a3d99 10.1007/s00134-014-3325-5 10.1007/s00134-012-2475-6 |
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 |
Contributor_xml | – sequence: 1 givenname: Hangyong surname: He fullname: He, Hangyong – sequence: 2 givenname: Bing surname: Sun fullname: Sun, Bing – sequence: 3 givenname: Lirong surname: Liang fullname: Liang, Lirong – sequence: 4 givenname: Yanming surname: Li fullname: Li, Yanming – sequence: 5 givenname: He surname: Wang fullname: Wang, He – sequence: 6 givenname: Luqing surname: Wei fullname: Wei, Luqing – sequence: 7 givenname: Guofeng surname: Li fullname: Li, Guofeng – sequence: 8 givenname: Bin surname: Liu fullname: Liu, Bin – sequence: 9 givenname: Shuliang surname: Guo fullname: Guo, Shuliang – sequence: 10 givenname: Jun surname: Duan fullname: Duan, Jun – sequence: 11 givenname: Yuping surname: Li fullname: Li, Yuping – sequence: 12 givenname: Ying surname: Zhou fullname: Zhou, Ying – sequence: 13 givenname: Yusheng surname: Chen fullname: Chen, Yusheng – sequence: 14 givenname: Hongru surname: Li fullname: Li, Hongru – sequence: 15 givenname: Rujun surname: Hong fullname: Hong, Rujun – sequence: 16 givenname: Xiujuan surname: Yao fullname: Yao, Xiujuan – sequence: 17 givenname: Fengfeng surname: Lu fullname: Lu, Fengfeng – sequence: 18 givenname: Jingping surname: Yang fullname: Yang, Jingping – sequence: 19 givenname: Xiyuan surname: Xu fullname: Xu, Xiyuan – sequence: 20 givenname: Hui surname: Wang fullname: Wang, Hui – sequence: 21 givenname: Ling surname: Wang fullname: Wang, Ling – sequence: 22 givenname: Hongjun surname: Tian fullname: Tian, Hongjun – sequence: 23 givenname: Liqiang surname: Song fullname: Song, Liqiang – sequence: 24 givenname: Jie surname: Chen fullname: Chen, Jie – sequence: 25 givenname: Yunfu surname: Wu fullname: Wu, Yunfu – sequence: 26 givenname: Yong surname: Bao fullname: Bao, Yong – sequence: 27 givenname: Feng surname: Chen fullname: Chen, Feng – sequence: 28 givenname: Ping surname: Wang fullname: Wang, Ping – sequence: 29 givenname: Lixi surname: Ji fullname: Ji, Lixi – sequence: 30 givenname: Xiaofang surname: Huang fullname: Huang, Xiaofang – sequence: 31 givenname: Min surname: Sun fullname: Sun, Min – sequence: 32 givenname: Yongxiang surname: Zhang fullname: Zhang, Yongxiang – sequence: 33 givenname: Yanyan surname: Ding fullname: Ding, Yanyan – sequence: 34 givenname: Liangan surname: Chen fullname: Chen, Liangan – sequence: 35 givenname: Ying surname: Wang fullname: Wang, Ying – sequence: 36 givenname: Zhixin surname: Liang fullname: Liang, Zhixin – sequence: 37 givenname: Lan surname: Yang fullname: Yang, Lan – sequence: 38 givenname: Tian surname: Yang fullname: Yang, Tian – sequence: 39 givenname: Heng surname: Weng fullname: Weng, Heng – sequence: 40 givenname: Hongyan surname: Li fullname: Li, Hongyan – sequence: 41 givenname: Xu surname: Lin fullname: Lin, Xu – sequence: 42 givenname: Daoxin surname: Wang fullname: Wang, Daoxin – sequence: 43 givenname: Jin surname: Tong fullname: Tong, Jin – sequence: 44 givenname: Wang surname: Deng fullname: Deng, Wang – sequence: 45 givenname: Yongchang surname: Sun fullname: Sun, Yongchang – sequence: 46 givenname: Ran surname: Li fullname: Li, Ran – sequence: 47 givenname: Jie surname: Xu fullname: Xu, Jie – sequence: 48 givenname: Faguang surname: Jin fullname: Jin, Faguang – sequence: 49 givenname: Yandong surname: Nan fullname: Nan, Yandong – sequence: 50 givenname: Chunmei surname: Li fullname: Li, Chunmei – sequence: 51 givenname: Bei surname: He fullname: He, Bei – sequence: 52 givenname: Ning surname: Shen fullname: Shen, Ning – sequence: 53 givenname: Lina surname: Sun fullname: Sun, Lina – sequence: 54 givenname: Changzheng surname: Wang fullname: Wang, Changzheng – sequence: 55 givenname: Mingdong surname: Hu fullname: Hu, Mingdong – sequence: 56 givenname: Xiaohong surname: Yang fullname: Yang, Xiaohong – sequence: 57 givenname: Qin surname: Luo fullname: Luo, Qin – sequence: 58 givenname: Mei surname: Li fullname: Li, Mei – sequence: 59 givenname: Jin surname: Zhang fullname: Zhang, Jin – sequence: 60 givenname: Hai surname: Tan fullname: Tan, Hai – sequence: 61 givenname: Chen surname: Wang fullname: Wang, Chen |
Copyright | COPYRIGHT 2019 BioMed Central Ltd. 2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. The Author(s). 2019 |
Copyright_xml | – notice: COPYRIGHT 2019 BioMed Central Ltd. – notice: 2019. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: The Author(s). 2019 |
CorporateAuthor | for the ENIVA Study Group ENIVA Study Group |
CorporateAuthor_xml | – name: for the ENIVA Study Group – name: ENIVA Study Group |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7X7 7XB 88E 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH K9. M0S M1P PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI 7X8 5PM DOA |
DOI | 10.1186/s13054-019-2575-6 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central ProQuest One ProQuest Central Proquest Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Health & Medical Complete (Alumni) ProQuest Health & Medical Collection Medical Database ProQuest Central Premium ProQuest One Academic (New) ProQuest Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journal Collection |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest One Academic Eastern Edition ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Hospital Collection (Alumni) ProQuest Central ProQuest Health & Medical Complete Health Research Premium Collection ProQuest Medical Library ProQuest One Academic UKI Edition Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection ProQuest Central (New) ProQuest One Academic ProQuest One Academic (New) ProQuest Medical Library (Alumni) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic Publicly Available Content Database |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journal Collection url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 4 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1364-8535 1466-609X 1366-609X |
EndPage | 13 |
ExternalDocumentID | oai_doaj_org_article_31ef9e4b4bb44453a41c60e6a1aa4cf0 PMC6727327 A600221648 31484582 10_1186_s13054_019_2575_6 |
Genre | Randomized Controlled Trial Multicenter Study Journal Article |
GeographicLocations | China |
GeographicLocations_xml | – name: China |
GrantInformation_xml | – fundername: National Natural Science Foundation of China grantid: 81490534 – fundername: National Science and Technology Pillar Program During the 12th Five-year Plan grantid: 2012BAI05B02 – fundername: ; grantid: 81490534 – fundername: ; grantid: 2012BAI05B02 |
GroupedDBID | --- 0R~ 29F 2WC 4.4 53G 5GY 5VS 6J9 6PF 7X7 88E 8FI 8FJ AAFWJ AAJSJ AASML AAWTL AAYXX ABUWG ACGFS ACJQM ADBBV ADUKV AEGXH AENEX AFKRA AFPKN AHBYD AHMBA AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIAM AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C6C CCPQU CITATION CS3 DIK E3Z EBD EBLON EBS EMOBN F5P FYUFA GROUPED_DOAJ GX1 HMCUK HYE IAO IHR INH INR ITC KQ8 M1P OK1 PHGZM PHGZT PIMPY PQQKQ PROAC PSQYO RBZ ROL RPM RSV SJN SMD SOJ SV3 TR2 U2A UKHRP WOQ YOC -5E -5G -BR 3V. ACRMQ ADINQ C24 CGR CUY CVF ECM EIF NPM PMFND 7XB 8FK AZQEC DWQXO EJD K9. PJZUB PKEHL PPXIY PQEST PQUKI 7X8 5PM PUEGO |
ID | FETCH-LOGICAL-c626t-ed7b3a9c6e7ad4b375834a37d3926b364c9b4f8dc2d8dae16b2c594f15b463e13 |
IEDL.DBID | 7X7 |
ISSN | 1364-8535 1466-609X |
IngestDate | Wed Aug 27 01:21:40 EDT 2025 Thu Aug 21 18:28:39 EDT 2025 Fri Jul 11 08:22:30 EDT 2025 Fri Jul 25 05:56:56 EDT 2025 Tue Jun 17 21:25:18 EDT 2025 Tue Jun 10 20:18:10 EDT 2025 Thu Jan 02 22:59:20 EST 2025 Tue Jul 01 03:54:48 EDT 2025 Thu Apr 24 23:07:20 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | Acute respiratory distress syndrome (ARDS) Pneumonia Noninvasive ventilation (NIV) |
Language | English |
License | Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c626t-ed7b3a9c6e7ad4b375834a37d3926b364c9b4f8dc2d8dae16b2c594f15b463e13 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 14 ObjectType-Feature-3 ObjectType-Evidence Based Healthcare-1 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
ORCID | 0000-0001-9972-0929 |
OpenAccessLink | https://www.proquest.com/docview/2292746551?pq-origsite=%requestingapplication% |
PMID | 31484582 |
PQID | 2292746551 |
PQPubID | 44362 |
PageCount | 13 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_31ef9e4b4bb44453a41c60e6a1aa4cf0 pubmedcentral_primary_oai_pubmedcentral_nih_gov_6727327 proquest_miscellaneous_2285104127 proquest_journals_2292746551 gale_infotracmisc_A600221648 gale_infotracacademiconefile_A600221648 pubmed_primary_31484582 crossref_citationtrail_10_1186_s13054_019_2575_6 crossref_primary_10_1186_s13054_019_2575_6 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-09-04 |
PublicationDateYYYYMMDD | 2019-09-04 |
PublicationDate_xml | – month: 09 year: 2019 text: 2019-09-04 day: 04 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | Critical care (London, England) |
PublicationTitleAlternate | Crit Care |
PublicationYear | 2019 |
Publisher | BioMed Central Ltd BioMed Central BMC |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central – name: BMC |
References | Q Zhan (2575_CR13) 2012; 40 BK Patel (2575_CR21) 2016; 315 G Carteaux (2575_CR25) 2016; 44 AM Brambilla (2575_CR2) 2014; 40 M Ferrer (2575_CR19) 2003; 168 G Prinianakis (2575_CR23) 2004; 23 J Duan (2575_CR28) 2017; 43 XP Xu (2575_CR4) 2017; 45 AW Thille (2575_CR7) 2013; 17 B Rochwerg (2575_CR11) 2017; 50 L Brochard (2575_CR26) 2017; 195 M Briel (2575_CR18) 2010; 303 V Squadrone (2575_CR3) 2005; 293 E Ozyilmaz (2575_CR27) 2014; 14 M Kojicic (2575_CR29) 2012; 16 P Navalesi (2575_CR22) 2000; 28 A Carrillo (2575_CR6) 2012; 38 A Demoule (2575_CR8) 2006; 32 G Hilbert (2575_CR14) 2012; 40 JP Frat (2575_CR24) 2015; 372 G Bellani (2575_CR1) 2016; 315 C Delclaux (2575_CR15) 2000; 284 V Lemiale (2575_CR20) 2015; 314 JE Levitt (2575_CR16) 2013; 41 G Bellani (2575_CR10) 2017; 195 M Antonelli (2575_CR5) 2007; 35 C Brun-Buisson (2575_CR12) 2004; 30 NS Hill (2575_CR9) 2017; 195 E Estenssoro (2575_CR17) 2002; 30 31730002 - Crit Care. 2019 Nov 15;23(1):358 |
References_xml | – volume: 16 start-page: R46 issue: 2 year: 2012 ident: 2575_CR29 publication-title: Crit Care doi: 10.1186/cc11247 – volume: 314 start-page: 1711 issue: 16 year: 2015 ident: 2575_CR20 publication-title: JAMA doi: 10.1001/jama.2015.12402 – volume: 43 start-page: 192 issue: 2 year: 2017 ident: 2575_CR28 publication-title: Intensive Care Med doi: 10.1007/s00134-016-4601-3 – volume: 30 start-page: 524 issue: 3 year: 2004 ident: 2575_CR12 publication-title: Intens Care Med doi: 10.1007/s00134-003-2136-x – volume: 303 start-page: 865 issue: 9 year: 2010 ident: 2575_CR18 publication-title: JAMA doi: 10.1001/jama.2010.218 – volume: 372 start-page: 2185 issue: 23 year: 2015 ident: 2575_CR24 publication-title: N Engl J Med doi: 10.1056/NEJMoa1503326 – volume: 35 start-page: 18 issue: 1 year: 2007 ident: 2575_CR5 publication-title: Crit Care Med doi: 10.1097/01.CCM.0000251821.44259.F3 – volume: 14 start-page: 19 year: 2014 ident: 2575_CR27 publication-title: BMC Pulm Med doi: 10.1186/1471-2466-14-19 – volume: 315 start-page: 2435 issue: 22 year: 2016 ident: 2575_CR21 publication-title: JAMA doi: 10.1001/jama.2016.6338 – volume: 17 start-page: R269 issue: 6 year: 2013 ident: 2575_CR7 publication-title: Crit Care doi: 10.1186/cc13103 – volume: 293 start-page: 589 issue: 5 year: 2005 ident: 2575_CR3 publication-title: JAMA doi: 10.1001/jama.293.5.589 – volume: 23 start-page: 314 issue: 2 year: 2004 ident: 2575_CR23 publication-title: Eur Respir J doi: 10.1183/09031936.03.00010203 – volume: 168 start-page: 1438 issue: 12 year: 2003 ident: 2575_CR19 publication-title: Am J Respir Crit Care Med doi: 10.1164/rccm.200301-072OC – volume: 32 start-page: 1756 issue: 11 year: 2006 ident: 2575_CR8 publication-title: Intensive Care Med doi: 10.1007/s00134-006-0324-1 – volume: 50 start-page: 1602426 issue: 2 year: 2017 ident: 2575_CR11 publication-title: Eur Respir J doi: 10.1183/13993003.02426-2016 – volume: 315 start-page: 788 issue: 8 year: 2016 ident: 2575_CR1 publication-title: JAMA doi: 10.1001/jama.2016.0291 – volume: 195 start-page: 9 issue: 1 year: 2017 ident: 2575_CR9 publication-title: Am J Respir Crit Care Med doi: 10.1164/rccm.201610-2138ED – volume: 195 start-page: 67 issue: 1 year: 2017 ident: 2575_CR10 publication-title: Am J Respir Crit Care Med doi: 10.1164/rccm.201606-1306OC – volume: 40 start-page: 669 issue: 2 year: 2012 ident: 2575_CR14 publication-title: Crit Care Med doi: 10.1097/CCM.0b013e318236ec4f – volume: 44 start-page: 282 issue: 2 year: 2016 ident: 2575_CR25 publication-title: Crit Care Med doi: 10.1097/CCM.0000000000001379 – volume: 195 start-page: 438 issue: 4 year: 2017 ident: 2575_CR26 publication-title: Am J Respir Crit Care Med doi: 10.1164/rccm.201605-1081CP – volume: 45 start-page: e727 issue: 7 year: 2017 ident: 2575_CR4 publication-title: Crit Care Med doi: 10.1097/CCM.0000000000002361 – volume: 40 start-page: 455 issue: 2 year: 2012 ident: 2575_CR13 publication-title: Crit Care Med doi: 10.1097/CCM.0b013e318232d75e – volume: 30 start-page: 2450 issue: 11 year: 2002 ident: 2575_CR17 publication-title: Crit Care Med doi: 10.1097/00003246-200211000-00008 – volume: 28 start-page: 1785 issue: 6 year: 2000 ident: 2575_CR22 publication-title: Crit Care Med doi: 10.1097/00003246-200006000-00015 – volume: 284 start-page: 2352 issue: 18 year: 2000 ident: 2575_CR15 publication-title: JAMA doi: 10.1001/jama.284.18.2352 – volume: 41 start-page: 1929 issue: 8 year: 2013 ident: 2575_CR16 publication-title: Crit Care Med doi: 10.1097/CCM.0b013e31828a3d99 – volume: 40 start-page: 942 issue: 7 year: 2014 ident: 2575_CR2 publication-title: Intensive Care Med doi: 10.1007/s00134-014-3325-5 – volume: 38 start-page: 458 issue: 3 year: 2012 ident: 2575_CR6 publication-title: Intensive Care Med doi: 10.1007/s00134-012-2475-6 – reference: 31730002 - Crit Care. 2019 Nov 15;23(1):358 |
SSID | ssj0017863 |
Score | 2.5154672 |
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... |
SourceID | doaj pubmedcentral proquest gale pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
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 |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journal Collection dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYlh9JL6btu0qJAoVAQsS15JB-3oSEE0kNJIDehl6khdZbNbn9_ZmTvdk2hvfRqSUbSjKT5NDOfGPtYGbrAL6VQoQOhYkPJyiqJUIZoau0QdFBy8uU3OL9WFzfNzd5TXxQTNtIDjxN3IqvUtUl55b1SqpFOVQHKBK5yDv-f0TqeeVswNfkPtAE5-TArAyf3uFM3FG3RClTRRsDsFMpk_X9uyXtn0jxecu8AOnvGnk6WI1-MPX7OHqXhBXt8OfnGX7LlgufoQGqeVvz76RW_6_hA162_HAWp8xzaOMa-8X7gyyFtUAl7JxCXo4QjT8R2zH_2t5G7sFknvvrtiOexH_NK-Jbk4BW7Pvt6dXoupvcUREDYshYpai9dGyBpF5WXCBWkclJHtJHAS1Ch9aozMdTRRJcq8HVoWtVVjVcgUyVfswPsdXrLeILWlAaLyOQzAHSV5F3buabrQDtXsHI7vzZMZOP05sWtzaDDgB1FYlEklkRioWCfd02WI9PG3yp_IaHtKhJJdv6AqmMn1bH_Up2CfSKRW1rK2LngpowEHCKRYtkF-SxrxJOmYEezmrgEw7x4qzR22gLubV23iPgBLdKCHe-KqSWFtQ3pbkN10OAlxjNdsDejju2GJBGoklOzYHqmfbMxz0uG_kcmCCfvuqz1u_8xSYfsSU3rJvvQjtjBerVJ79EOW_sPeck9AJDfMLQ priority: 102 providerName: Directory of Open Access Journals |
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 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1ba9swFBZbC2MvY_d564IGg8FA1LZkWX4aSWkpg5YRWgh7Ebp5DXROlst-_86RlbRm0Jc8RBJIPjedi75DyOdCYQA_50y4VjLhK3ysLAJzufOqrA04Hfg4-eJSnl-L77NqlgJu61RWudOJUVH7hcMY-XFZNuBASTDw35Z_GHaNwuxqaqHxmBwidBmWdNWzvcNV1Cp2Uiu4FAzMUpWymoWSx2vQ3RXWXzQMmLZicmCXInz__0r6npUaVlDeM0lnz8mzdJek4574L8ij0L0kTy5StvwVWY5prBfE5WFFpydXdNHSDgOwfw2WrdNY7NhXw9F5R5dd2MI554aBpw409zQg_jH9Pb_11LjtJtDVXWqe-nn_0oTuYA9ek-uz06uTc5Y6LDAHjsyGBV9bbhonQ228sBycBy4Mrz3cmqSFz-YaK1rlXemVN6GQtnRVI9qiskLyUPA35AB2Hd4RGmSjcgVDeAlUUmJwyZqmNVXbytqYjOS776tdgh_HLhi3OrohSuqeJBpIopEkWmbk637JssfeeGjyBIm2n4iw2fGPxeqXTlKoeRHaJggrrBVCVNyIwsk8SFMYA8yaZ-QLklyjcMPmnElvFOCICJOlx5jFLMHDVBk5GswEoXTD4R3T6KQU1vqOhTPyaT-MK7HQrQuLLc6BKzBioNUZedvz2P5IHFxXTHNmpB5w3-DMw5FufhMhwzHfzsv6_cPb-kCeligRMV92RA42q234CHeujR1FwRqRw8np5Y_pKEYu4Hc6-fkP33QtDg |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR3batRA9FC3oL6Id6NVR1AEITTJTCbJg8i2tmxtd5HSQt-mk5mJBmp23YviT_mNnpPLtkHoW18zM2Fmzn3ODeBtmNIDfsB9YQrpCxtTsrJwvgmMTaNEo9FBycnjiRydii9n8dkG_O1yYSissuOJNaO2U0Nv5NtRlKEBJVHAf5r99KlrFHlXuxYaDVocuj-_0WRbfDz4jPB9F0X7eye7I7_tKuAbVN6XvrNJznVmpEu0FTlHhZkLzROLmoLMuRQmy0WRWhPZ1GoXyjwycSaKMM6F5C7k-N9bsCk4mjID2NzZm3w9XvstkrTu3Rbib3wUhHHrRw1Tub1AaRFTxEfmI5nEvuxJwrphwP9i4Ypc7MdsXhGC-_fhXqu9smGDbg9gw1UP4fa49c8_gtmQ1RGKtNzN2fHuCZsWrKIn31-aAuVZHV7ZxN-xsmKzyq3wZkvtl5VFLLPMUcVl9qO8sEyb1dKx-WUwALNlk9vCukILj-H0Rm7_CQxw1-4ZMCezNEhxiNTOVEp6zsp1Vui4KGSitQdBd7_KtAXPqe_GhaoNn1SqBiQKQaIIJEp68GG9ZNZU-7hu8g4BbT2RCnXXH6bzb6qle8VDV2RO5CLPhRAx1yI0MnBSh1ojeQQevCeQK2InuDmj26wIPCIV5lJD8ptGaNOmHmz1ZiIbMP3hDmlUy4YW6pJoPHizHqaVFFpXuemK5qDSTVXXEg-eNji2PhJHY5kcqx4kPezrnbk_UpXf6yLl5OHnUfL8-m29hjujk_GROjqYHL6AuxFRR-2t24LBcr5yL1HjW-avWjJjcH7TlP0Pi55oTQ |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+multicenter+RCT+of+noninvasive+ventilation+in+pneumonia-induced+early+mild+acute+respiratory+distress+syndrome&rft.jtitle=Critical+care+%28London%2C+England%29&rft.au=He%2C+Hangyong&rft.au=Sun%2C+Bing&rft.au=Liang%2C+Lirong&rft.au=Li%2C+Yanming&rft.date=2019-09-04&rft.pub=BioMed+Central&rft.issn=1364-8535&rft.eissn=1466-609X&rft.volume=23&rft_id=info:doi/10.1186%2Fs13054-019-2575-6&rft_id=info%3Apmid%2F31484582&rft.externalDocID=PMC6727327 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1364-8535&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1364-8535&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1364-8535&client=summon |