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Erschienen in: BMC Pulmonary Medicine 1/2024

Open Access 01.12.2024 | Research

Incidence of noninvasive ventilation failure and mortality in patients with acute respiratory distress syndrome: a systematic review and proportion meta-analysis

verfasst von: Jie Wang, Jun Duan, Ling Zhou

Erschienen in: BMC Pulmonary Medicine | Ausgabe 1/2024

Abstract

Background

Noninvasive ventilation (NIV) is commonly used in patients with acute respiratory distress syndrome (ARDS). However, the incidence and distribution of treatment failure are unclear.

Methods

A comprehensive online search was conducted to select potentially eligible studies with reports of the rate of NIV failure in patients with ARDS. A manual search was also performed to identify additional studies. Data were extracted to calculate the pooled incidences of NIV failure and mortality. Based on oxygenation, the severity of the disease was classified as mild, moderate, or severe ARDS. Based on etiologies, ARDS was defined as being of pulmonary origin or extrapulmonary origin.

Results

We enrolled 90 studies in this meta-analysis, involving 98 study arms. The pooled incidence of NIV failure was 48% (n = 5847, 95% confidence interval [CI]: 43–52%). The pooled incidence of ICU mortality was 29% (n = 2363, 95%CI: 22–36%), and that of hospital mortality was 33% (n = 2927, 95%CI: 27–40%). In patients with mild, moderate, and severe ARDS, the pooled incidence of NIV failure was 30% (n = 819, 95%CI: 21–39%), 51% (n = 1332, 95%CI: 43–60%), and 71% (n = 525, 95%CI: 62–79%), respectively. In patients with pulmonary ARDS, it was 45% (n = 2687, 95%CI: 39–51%). However, it was 30% (n = 802, 95%CI: 21–38%) in those with extrapulmonary ARDS. In patients with immunosuppression, the incidence of NIV failure was 62% (n = 806, 95%CI: 50–74%). However, it was 46% (n = 5041, 95%CI: 41–50%) in those without immunosuppression.

Conclusions

Nearly half of patients with ARDS experience NIV failure. The incidence of NIV failure increases with increasing ARDS severity. Pulmonary ARDS seems to have a higher rate of NIV failure than extrapulmonary ARDS. ARDS patients with immunosuppression have the highest rate of NIV failure.
Hinweise

Supplementary Information

The online version contains supplementary material available at https://​doi.​org/​10.​1186/​s12890-024-02839-8.
Jun Duan and Ling Zhou are joint corresponding authors.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
NA
Not available
NIV
Noninvasive ventilation
BiPAP
Bi-level positive airway pressure
CPAP
Continuous positive airway pressure
ARDS
Acute respiratory distress syndrome
CI
Confidence interval
P-SILI
Patient self-inflicted lung injury

Introduction

Acute respiratory distress syndrome (ARDS) was first described by Ashbaugh et al. in 1967 [1]. Its features are acute onset of hypoxemia, bilateral opacities not fully explained by effusions, lobar/lung collapse or nodules, respiratory failure not fully explained by cardiac failure or fluid overload, and PaO2/FiO2 less than 300 mmHg [2]. The etiologies of ARDS include pneumonia, pancreatitis, abdominal infection, blood transfusion, and trauma [3, 4]. ARDS is classified as pulmonary or extrapulmonary according to its cause. Based on oxygenation, it can be classified as mild, moderate, or severe [5]. To relieve respiratory distress, respiratory support is commonly used in ARDS patients.
Physiological studies have shown that noninvasive ventilation (NIV) decreases the work of breathing and improves oxygenation in patients with ARDS [6]. In contrast with invasive mechanical ventilation, NIV preserves the ability to swallow, cough, and communicate verbally; avoids intubation-associated complications; and reduces the likelihood of nosocomial pneumonia. Therefore, NIV has been commonly used in patients with ARDS [7]. However, the incidence and distribution of NIV failure in ARDS population are unclear. Here, we report the incidence of NIV failure in ARDS patients and further clarify the distributions of NIV failure in different subgroups.

Methods

This article reports the results of a systematic review and meta-analysis of NIV failure and mortality, focusing on patients with ARDS. It was performed in conformity with Preferred Reporting Items for Systematic Reviews and Meta-analysis statement [8].

Search techniques and selection criteria

We searched PubMed, Web of Science, the Cochrane library, and some Chinese databases (CBM, Wanfang Data, and CNKI), without any language limitation, for pertinent research published before September 30, 2022. We also performed manual searches of the reference lists of the identified articles and pertinent reviews to identify additional relevant articles. The search used the following key words: (“noninvasive ventilation” OR “noninvasive mechanical ventilation” OR “noninvasive positive pressure ventilation” OR “NIV” OR “NPPV” OR “NIPPV” OR “continuous positive airway pressure” OR “CPAP” OR “noninvasive pressure support ventilation” OR “noninvasive oxygen” OR “noninvasive oxygenation” OR “mask ventilation” OR “nasal ventilation” OR “helmet ventilation”) and (“ARDS” OR “acute respiratory distress syndrome” OR “ALI” OR “acute lung injury” OR “acute respiratory failure” OR “acute hypoxemic respiratory failure” OR “hypoxemic respiratory failure”).
Studies were enrolled based on the following inclusion criteria: ARDS or ALI was diagnosed, adult patients were involved, and NIV was used as a first-line intervention. The following works were excluded: reviews, case reports, editorials, letters, and conference abstracts; articles with no available data for NIV failure; studies that used NIV as preoxygenation before intubation; and studies that used NIV as a ventilator weaning strategy.

Data extraction and quality assessment

All studies were independently selected by two investigators (JW and JD). Any discrepancies were resolved by consensus. If the researchers failed to reach consensus, a third investigator (LZ) reviewed the data and made a determination. We extracted the data as follows: first author’s name, country, publication year, proportion of male patients, proportion of immunosuppressed patients, age, PaO2/FiO2, number of total patients, number of patients with ARDS, number of NIV failures in patients with ARDS, number of deaths in patients with ARDS, NIV mode, NIV interface, causes of ARDS, and the proportion of mild, moderate, and severe ARDS. NIV failure and mortality data were also collected.
We intended to report the incidence of treatment failure and mortality in ARDS patients who received NIV; thus, the quality of enrolled studies was assessed using Murad’s tool for non-comparative studies [9, 10]. This method includes five questions: (1) did the patients represent all of the cases seen by the medical center, (2) was the diagnosis correctly made, (3) were other important diagnosis excluded, (4) were all important data cited in the report, and (5) was the outcome correctly ascertained? Each question was assigned 1 (yes) or 0 (no) points. The quality of an enrolled study was classified as high, moderate, or low if the total scores were 5, 4, or ≤ 3, respectively.

Statistical analysis

The data were analyzed using R (version 4.2.2). The Shapiro-Wilk test of normality was used to analyze the distribution of the incidence of NIV failure and mortality among the included studies. Values of p more than 0.05 were taken to indicate that the rate of the relevant event was normally distributed. If it was abnormally distributed, the data were transferred to normally distributed data using logarithmic transformation, sine transformation, or arc sine transformation. I2 was used to describe heterogeneity, where I2 ≥ 50% represents significant heterogeneity. A random-effects model was used to pool the data, and a subgroup analysis was performed to explore potential heterogeneity. If no heterogeneity was observed, a common-effects model (also known as a fixed-effects model) was used.
The mean-pooled incidences of treatment failure and mortality were estimated. The corresponding confidence intervals (95% CIs) were also estimated. Egger’s test was used to assess the possibility of publication bias [11]. A funnel plot (plot of treatment effect against trial precision) was created to visualize publication bias.

Results

Characteristics of the included studies

In all, 2219 studies were obtained using the search strategy, and 23 studies were identified from other sources (Fig. 1). After screening the titles and abstracts and reviewing full papers, we enrolled 90 studies involving 98 study arms. These studies were published between 1999 and 2022 (Table 1). Egger’s test (p = 0.69) and a funnel plot showed that there was no publication bias (Supplementary Fig. 1). The quality of most of the studies was high or moderate (Supplementary Fig. 2).
Table 1
Characteristics of the included studies
Author
Year
Country
Design
COVID-19
Male
(%)
Immunosuppression
(%)
Age
PaO2/FiO2
Definition of NIV failure
Patients with ARDS
NIV interface
NIV mode
NIV failure
ICU mortality
Hospital mortality
Rocker
1999
Canada
Observational
No
30%
NA
47 ± 23
102 ± 57
Intubation or death
10
Oronasal
BiPAP
5
3
3
Antonelli
2000
Italy
RCT
No
65%
100%
45 ± 19
129 ± 30
Intubation
8
Oronasal
BiPAP
3
3
NA
Hilbert
2000
France
Observational
No
55%
100%
45 ± 16
128 ± 32
Intubation
64
Oronasal
CPAP
48
44
NA
Delclaux
2000
France
RCT
No
61%
NA
56 (19–85)#
140 (59–228)#
Intubation
40
Oronasal
CPAP
15
9
12
Antonelli
2001
Italy
Observational
No
64%
10%
Success: 58 (16–96)$
Failure: 60 (13–86)$
Success: 119 ± 35
Failure: 120 ± 40
Intubation
86
Oronasal
BiPAP
44
26
NA
Confalonieri
2002
Italy
Observational
No
NA
100%
37 ± 9
122 ± 44
Intubation
24
Oronasal
BiPAP
8
6
NA
Ferrer
2003
Spain
RCT
No
55%
18%
61 ± 17
102 ± 21
Intubation
7
Oronasal
BiPAP
6
5
NA
Zhi
2003
China
Observational
No
42%
NA
40 ± 3
Success: 144 ± 15
Failure: 111 ± 8
Intubation or death
12
Oronasal or nasal
BiPAP
4
NA
4
Xu
2003
China
Observational
No
57%
NA
59 ± 12
Pul*: 147 ± 28
Extrapul*: 163 ± 46
Intubation
23
Oronasal
BiPAP
6
NA
NA
Rai
2004
India
Observational
No
64%
NA
68 (29–82)$
NA
Intubation
4
Oronasal
BiPAP
2
NA
NA
Li
2005
China
Observational
No
72%
NA
Pul*: 38 ± 12
Extrapul*: 34 ± 15
Pul*: 138 ± 29
Extrapul*: 141 ± 33
Intubation
18
Oronasal
BiPAP
8
NA
6
Gu
2005
China
Observational
No
69%
NA
43 (29–84)$
PaO2 51 ± 5
Intubation
29
Oronasal or nasal
BiPAP
4
NA
4
Rana
2006
USA
Observational
No
61%
43%
Success: 60 (46–84)
Failure: 64 (55–73)
Success: 147 (118–209)
Failure: 112 (70–157)
Intubation
54
Oronasal
BiPAP or CPAP
38
NA
26
Antonelli
2007
Italy
Observational
No
63%
15%
Success: 53 (35–64)
Failure: 60 (51–68)
Success: 116 ± 38
Failure: 105 ± 33
Intubation
147
Oronasal or helmet
BiPAP
68
41
53
Adda
2008
France
Observational
No
68%
100%
Success: 59 (47–66)
Failure: 57 (47–67)
PaO2 success: 44 (38–51)
PaO2 failure: 54 (41–59)
Intubation
32
Oronasal
BiPAP
31
NA
NA
Yoshida
2008
Japan
Observational
No
72%
NA
Success: 68 ± 12
Failure: 70 ± 10
Success: 122 ± 43
Failure: 125 ± 51
Intubation
47
Oronasal
BiPAP or CPAP
14
9
13
Domenighetti
2008
Switzerland
Observational
No
42%
NA
66 ± 8
104 ± 42
Intubation
12
Oronasal
BiPAP
4
5
NA
Agarwal
2009
India
Observational
No
43%
43%
42 ± 24
131 ± 46
Intubation
21
Oronasal
BiPAP
12
7
NA
Ding
2009
China
Observational
No
74%
42%
49 ± 17
123 ± 32
Intubation, death or withdrawal of therapy
31
Oronasal
BiPAP or CPAP
8
NA
NA
Zan
2009
China
Observational
No
68%
NA
58 (32–79)$
151 ± 19
Intubation
22
Oronasal
BiPAP
10
NA
9
Wang
2009
China
Observational
No
53%
NA
28 ± 2
229 ± 5
Intubation
21
Oronasal
BiPAP
6
NA
2
Gu
2010
China
Observational
No
65%
NA
38 (28–64)$
PaO2 55 ± 4
Intubation or tracheotomy
40
Oronasal or nasal
BiPAP
9
0
0
Uçgun
2010
Turkey
Observational
No
90%
NA
45 ± 20
NA
Intubation
10
Oronasal
BiPAP
6
3
NA
Gristina
2011
Italy
Observational
No
59%
100%
60 ± 16
NA
NA
89
Oronasal or helmet
BiPAP
53
52
56
Bhadade
2011
India
Observational
No
74%
NA
NA
NA
Intubation
17
Oronasal
NA
11
NA
NA
Bai
2011
China
Observational
No
61%
12%
46 (34–60)
244 (211–290)
Intubation or death
24
NA
NA
11
9
NA
Kirakli
2011
Turkey
Observational
No
44%
NA
39 (24–52)
Survivor: 150 (98–232)
Nonsurvivor: 67 (60–100)
Intubation
10
NA
NA
7
NA
6
Kikuchi
2011a
Japan
Observational
No
70%
NA
69 ± 17
PaO2 79 ± 27
Intubation
17
Oronasal or nasal
BiPAP or CPAP
4
NA
NA
Kikuchi
2011b
Japan
Observational
No
51%
NA
58 ± 23
PaO2 81 ± 43
Intubation
18
Oronasal or nasal
BiPAP or CPAP
6
NA
NA
Carrillo
2012a
Spain
Observational
No
59%
NA
62 ± 18
127 ± 34
Intubation or death
35
Oronasal or nasal
BiPAP
25
NA
13
Carrillo
2012b
Spain
Observational
No
77%
NA
72 ± 11
136 ± 37
Intubation or death
15
Oronasal or nasal
BiPAP
9
NA
7
Sharma
2012
India
Observational
No
52%
NA
48 ± 18
125 ± 78
Intubation
12
Oronasal
BiPAP
9
NA
NA
Zhan
2012
China
RCT
No
76%
24%
44 ± 14
225 ± 17
Intubation
21
Oronasal
BiPAP
1
1
1
Jin
2012
China
Observational
No
37%
NA
Yushu earthquake:
33 ± 20
Wenchuan earthquake:
52 ± 19
NA
Intubation
19
Oronasal
BiPAP
6
NA
NA
Zhi
2012
China
RCT
No
73%
NA
48 ± 17
139 ± 49
Intubation
15
Oronasal
BiPAP or CPAP
5
1
NA
Türkoğlu
2013
Turkey
Observational
No
69%
100%
45 (28–57)
104 (74–165)
Intubation
46
Oronasal
BiPAP
36
34
35
Wang
2013
China
Observational
No
54%
NA
Success: 70 (59–82)
Failure: 60 (47–75)
Success: 192 ± 50
Failure: 170 ± 51
Intubation
24
Oronasal or nasal
NA
20
NA
NA
Thille
2013
France
Observational
No
66%
44%
Success: 58 ± 17
Failure: 63 ± 14
Success: 211 ± 86
Failure: 163 ± 92
Intubation
82
Oronasal
BiPAP
50
24
NA
Zhang
2014a
China
Observational
No
41%
NA
49 ± 10
127 ± 22
NIV intolerance or requirement of intubation or death
17
Oronasal
BiPAP
10
NA
NA
Zhang
2014b
China
Observational
No
53%
NA
48 ± 9
125 ± 24
17
Oronasal
BiPAP
7
NA
NA
Zhang
2014c
China
Observational
No
41%
NA
53 ± 9
132 ± 22
17
Oronasal
BiPAP
4
NA
NA
Verma
2014
India
Observational
No
52%
NA
NA
NA
Intubation
6
Oronasal
BiPAP
6
4
NA
Yu
2014
China
Observational
No
97%
NA
61 ± 7
126 ± 32
Intubation
64
Oronasal
NA
32
NA
2
Tsushima
2014
Japan
Observational
No
77%
NA
Survivor: 71 ± 14
Nonsurvivor: 81 ± 5
Survivor: 143 ± 62
Nonsurvivor: 122 ± 84
Intubation
47
Oronasal
BiPAP
17
NA
12
Sehgal
2015
India
Observational
No
34%
NA
27 (23–36)
180 (166–232)
Intubation
41
Oronasal
BiPAP
23
NA
19
Frat
2015
France
Observational
No
71%
36%
61 (49–68)
192 (158–251)
Intubation
23
Oronasal
BiPAP
8
NA
NA
Chawla
2016
India
Observational
No
62%
NA
49 ± 15
192 ± 51
Intubation
96
Oronasal
BiPAP
42
29
NA
Korkmaz
2016
Turkey
Observational
No
54%
71%
63 ± 16
145 ± 50
Intubation
28
Oronasal
BiPAP
17
NA
NA
Patel
2016a
USA
RCT
No
54%
36%
61 (56–71)
144 (90–223)
Intubation
39
Oronasal
BiPAP
24
NA
19
Patel
2016b
USA
RCT
No
55%
34%
58 (50–68)
118 (93–170)
Intubation
44
Helmet
BiPAP
8
NA
12
Meeder
2016
Netherlands
Observational
No
53%
11%
Success: 73 (28–87)$
Failure: 72 (41–88)$
Success: 296 (211–369)
Failure: 207 (146–296)
Intubation
11
NA
NA
5
NA
NA
Ye
2016
China
Observational
No
60%
NA
54 ± 19
130 ± 46
Intubation
43
Oronasal
BiPAP
17
NA
22
Zhao
2016
China
Observational
No
60%
NA
47 ± 13
NA
Intubation
127
Oronasal or nasal
BiPAP
24
NA
9
Zeng
2016
China
Observational
No
57%
NA
Success: 58 ± 17
Failure: 65 ± 19
Success: 156 ± 12
Failure: 104 ± 10
Intubation
103
Oronasal
BiPAP
34
22
NA
Bellani
2017
Italy
Observational
No
60%
22%
Success: 67 (52–78)
Failure: 63 (53–74)
Success: 171 ± 65
Failure: 145 ± 60
Intubation
349
NA
BiPAP or CPAP
131
79
94
Duan
2017a
China
Observational
No
70%
NA
Success: 65 ± 17
Failure: 66 ± 17
Success: 179 ± 83
Failure: 137 ± 65
Intubation
85
Oronasal
BiPAP or CPAP
61
NA
NA
Duan
2017b
China
Observational
No
62%
NA
Success: 65 ± 17
Failure: 67 ± 17
Success: 165 ± 63
Failure: 146 ± 68
Intubation
45
Oronasal
BiPAP or CPAP
27
NA
NA
Liu
2017
China
Observational
No
71%
100%
Success: 42 ± 10
Failure: 44 ± 11
Success: 114 ± 33
Failure: 111 ± 45
Intubation, death, or withdrawal of therapy
17
NA
BiPAP
8
NA
NA
Neuschwander
2017
France
Observational
No
64%
100%
57 (46–67)
NA
Intubation
387
Oronasal or nasal
NA
276
171
213
Liu
2017
Canada
Observational
No
60%
100%
56 ± 14
PaO2 73 ± 38
Intubation or change to palliative care
41
Oronasal
BiPAP or CPAP
28
NA
NA
Kumar
2018
India
Observational
No
49%
NA
40 ± 3
197 ± 74
Intubation
35
Oronasal
NA
15
7
NA
Hong
2018
China
Observational
No
74%
NA
77 ± 7
141 ± 60
Intubation
64
Oronasal
BiPAP
46
NA
33
Briones-Claudett
2018
Ecuador
Observational
No
65%
NA
68 ± 22
PaO2 77 ± 11
Intubation
38
Oronasal
BiPAP
13
11
NA
Wang
2018
China
Observational
No
68%
NA
68 ± 12
Success: 198 ± 74
Failure: 168 ± 63
Intubation
56
Oronasal
BiPAP or CPAP
20
NA
14
He
2019
China
RCT
No
67%
9%
53 ± 18
232 ± 35
Intubation
102
Oronasal
BiPAP
9
7
7
Bajaj
2019
India
Observational
No
46%
NA
53 ± 17
143 ± 94
Intubation
27
Oronasal
BiPAP
11
7
NA
Paternoster
2020
Italy
Observational
No
36%
NA
62 ± 10
108 ± 21
Intubation
11
Helmet
CPAP
3
NA
2
Satou
2020
Japan
Observational
No
75%
NA
68 ± 19
Success: 137 ± 69
Failure: 126 ± 67
Intubation or death
68
Oronasal
BiPAP or CPAP
16
NA
13
Liengswangwong
2020
Thailand
Observational
No
49%
NA
Success: 75 ± 13
Failure: 73 ± 14
PaO2 success: 122 ± 38
PaO2 Failure: 125 ± 60
Intubation
5
NA
NA
5
NA
NA
Ding
2020
China
Observational
No
65%
NA
Success: 47 ± 9
Failure: 54 ± 11
Success: 125 ± 41
Failure: 119 ± 19
Intubation
20
Oronasal
BiPAP or CPAP
9
1
1
Menzella
2020
Italy
Observational
Yes
71%
NA
67 ± 11
120 ± 42
Intubation
79
Oronasal
BiPAP
41
NA
30
Carrillo
2020
Spain
Observational
No
52%
NA
67 ± 17
141 ± 36
Intubation or death
262
Oronasal
BiPAP
184
NA
NA
Pagano
2020
Italy
Observational
Yes
72%
NA
Success: 70 ± 11
Failure: 68 ± 14
Success: 143 ± 91
Failure: 167 ± 72
Intubation
18
NA
CPAP
8
NA
11
Shen
2020
China
Observational
No
44%
100%
Success: 39 (27–55)
Failure: 41 (30–54)
Success: 146 (114–204)
Failure: 153 (103–228)
Intubation
70
Oronasal
BiPAP
44
39
NA
Duca
2020a
Italy
Observational
Yes
86%
NA
70 (62–79)
131 (97–190)
Intubation or death
71
Helmet
CPAP
65
NA
54
Duca
2020b
Italy
Observational
Yes
71%
NA
75 (59–80)
87 (53–120)
Intubation or death
7
Helmet
BiPAP
4
NA
4
Tonelli
2020
Italy
Observational
No
67%
NA
71 (66–81)
125 (101–170)
Intubation or death
15
Oronasal
BiPAP
7
NA
NA
Liu
2020
China
Observational
No
53%
40%
58 ± 12
65 ± 19
Intubation
15
Oronasal
BiPAP
10
NA
NA
Wang
2020
China
Observational
Yes
69%
NA
64 ± 7
268 ± 6
Intubation
32
NA
BiPAP
6
NA
8
Simioli
2021
Italy
Observational
Yes
86%
NA
64 ± 23
95 ± 57
Intubation
29
Oronasal or helmet
BiPAP or CPAP
3
3
NA
Drescher
2021
USA
Observational
No
51%
13%
Success: 65 (49–71)
Failure: 67 (57–75)
Success: 198 (149–298)
Failure: 187 (106–235)
Intubation
18
Oronasal
BiPAP
15
NA
NA
Koga
2021
Japan
Observational
No
68%
NA
78 (69–84)
141 (97–186)
Intubation, death or crossover to HFNC
10
Oronasal
BiPAP or CPAP
7
NA
NA
Carpagnano
2021
Italy
Observational
Yes
73%
NA
Survivor: 64 ± 14
Nonsurvivor: 75 ± 13
Survivor: 226 ± 76
Nonsurvivor: 137 ± 54
Death
61
NA
BiPAP or CPAP
25
25
NA
Menzella
2021
Italy
Observational
Yes
71%
NA
67 ± 11
120 ± 42
Intubation or death
79
Oronasal
BiPAP
41
20
NA
Briones
2021
Ecuador
Observational
No
66%
NA
71 ± 19
192 ± 40
Intubation
5
Oronasal
BiPAP
2
NA
1
Zhao
2021
China
Observational
Yes
75%
NA
68 (62–76)
NA
Meet the criteria of intubation
24
Oronasal
NA
16
NA
14
Zhu
2021
China
Observational
No
62%
NA
Success: 57 ± 13
Failure: 63 ± 15
Success: 145 ± 23
Failure: 122 ± 20
Intubation or death
180
NA
NA
27
NA
NA
Ramirez
2022
Italy
Observational
Yes
80%
5%
61 (53–71)
98 (74–137)
Intubation or death
90
Oronasal
CPAP
35
NA
17
Lazzeri
2022
Italy
Observational
Yes
75%
NA
Success: 60 ± 13
Failure: 70 ± 13
Success: 123 (110–145)
Failure: 82 (66–103)
Intubation
75
Oronasal
BiPAP
31
NA
23
Sun
2022
China
Observational
No
64%
NA
Success: 66 (59–76)
Failure: 65 (57–77)
Success: 236 ± 53
Failure: 194 ± 78
Meet the criteria of intubation
131
Oronasal
BiPAP or CPAP
64
NA
NA
Chiumello
2022
Italy
Observational
Yes
77%
NA
58 (52–64)
264 (204–301)
NA
104
Oronasal or helmet
BiPAP or CPAP
20
NA
13
Duan
2022a
China
Observational
No
69%
8%
Success: 63 ± 16
Failure: 64 ± 16
Success: 178 ± 74
Failure: 153 ± 60
Need for intubation
311
Oronasal or nasal
BiPAP or CPAP
153
NA
NA
Duan
2022b
China
Observational
No
67%
19%
Success: 61 ± 17
Failure: 61 ± 16
Success: 147 ± 104
Failure: 137 ± 85
Need for intubation
143
Oronasal or nasal
BiPAP or CPAP
86
NA
NA
Jurjević
2022
Croatia
Observational
Yes
57%
NA
66 ± 11
137 ± 57
Intubation
58
Oronasal
BiPAP or CPAP
15
NA
NA
Chacko
2022
India
Observational
Yes
84%
NA
53 ± 12
161 ± 80
Intubation or death
209
Oronasal
BiPAP
91
NA
NA
Isaac
2022
India
Observational
Yes
83%
NA
54 ± 12
NA
Intubation or death
168
Oronasal
BiPAP or CPAP
39
28
NA
Tetaj
2022
Italy
Observational
Yes
65%
NA
60 (48–73)
NA
Intubation or death
224
Oronasal or helmet
BiPAP or CPAP
64
NA
43
Yaroshetskiy
2022
Russia
Observational
Yes
56%
NA
72 (62–80)
Success: 131 (92–230)
Failure: 90 (70–120)
Meet the criteria of intubation
80
Oronasal
BiPAP
57
NA
57
NA = not available, NIV = noninvasive ventilation, BiPAP = bi-level positive airway pressure, CPAP = continuous positive airway pressure, RCT = randomized control trial
#Data are reported as medians and 5th to 95th percentiles
$Data are reported as medians and ranges
*Pul; pulmonary; Extrapul: extrapulmonary

NIV failure and mortality in ARDS patients

In total, 5847 ARDS patients were enrolled in studies reporting NIV failure (Fig. 2). Significant heterogeneity was found between studies (I2 = 95%). Therefore, a random-effects model was selected. The pooled incidence of NIV failure was 48% (95%CI: 43–52%). In all, 2363 ARDS patients were enrolled in studies reporting ICU mortality (Fig. 3). The pooled incidence of ICU mortality was 29% (95%CI: 22–36%). In total, 2927 ARDS patients were enrolled in studies reporting hospital mortality (Fig. 4). The pooled incidence of hospital mortality was 33% (95%CI: 27–40%).

NIV failure in different subgroups

In all, 24, 20, and 17 study arms reported the rate of NIV failure in patients with mild, moderate, and severe ARDS, respectively (Fig. 5). The pooled incidence of NIV failure was 30% (95%CI: 21–39%), 51% (95%CI: 43–60%), and 71% (95%CI: 62–79%) in these ARDS groups, respectively.
There were 46 study arms that involved 2687 patients with pulmonary ARDS that reported NIV failure (Supplementary Fig. 3), and 19 study arms that involved 802 patients with extrapulmonary ARDS that reported NIV failure (Supplementary Fig. 4). The pooled incidence of NIV failure was 45% (95%CI: 39–51%) and 30% (21–38%) in patients with pulmonary and extrapulmonary ARDS, respectively (Fig. 6A). For pulmonary ARDS in particular, the pooled incidence of NIV failure was 42% (95%CI: 31–52%) and 47% (95%CI: 41–54%) in patients with and without COVID-19, respectively (Fig. 6B, supplementary Figs. 5 and 6).
The pooled incidence of NIV failure was 62% (95%CI: 50–74%) and 46% (95%CI: 41–50%) in patients with and without immunosuppression, respectively (Fig. 6C, supplementary Figs. 7 and 8). NIV failure was 49% (95%CI: 44–53%) in observational studies and 34% (95%CI: 16–53%) in randomized control trials (Fig. 6D, supplementary Figs. 9 and 10). In patients who were ventilated using BiPAP, the NIV failure was 48%, the same as in those ventilated via CPAP (Fig. 6E, supplementary Figs. 11 and 12).
The pooled incidence of NIV failure was 44% (95%CI: 32–57%) before 2005 (Fig. 7). Between 2006 and 2010, it was 47% (33–62%). However, this did not change after 2010 when patients with COVID-19 were excluded (52% for 2011–2015, 49% for 2016–2020, and 52% for 2021 and 2022).

Discussion

This meta-analysis shows that the incidence of NIV failure was high in patients with ARDS. A gradual increase in NIV failure was found in ARDS patients with an increase in disease severity. Patients with pulmonary ARDS had a higher rate of NIV failure than those with extrapulmonary ARDS. ARDS patients with immunosuppression had the highest failure rate.
An international, multicenter, prospective cohort study reported that 15.5% of patients with ARDS had received NIV [6]. This indicates that the use of NIV in patients with ARDS is not rare. However, ARDS is a risk factor for NIV failure in patients who have acute respiratory failure [1214]. In our analyses, nearly half of the ARDS patients experienced NIV failure. ARDS patients commonly developed excessive inspiratory effort and high transpulmonary pressures; this can lead the patient to self-inflicted lung injury (P-SILI) [15, 16]. Therefore, P-SILI greatly contributes to the high rate of NIV failure in ARDS patients. Esophageal pressure monitoring can detect the risk for P-SILI, which can help identify NIV failure early [17].
This meta-analysis shows that pulmonary ARDS leads to a higher rate of NIV failure than extrapulmonary ARDS, in line with a previous study [18]. Pulmonary ARDS is mainly caused by pneumonia, and extrapulmonary ARDS is mainly caused by sepsis [19, 20]. In patients with pulmonary ARDS, consolidation in chest CT scans is greater, and the response to the lung recruitment maneuver is worse than that in patients with extrapulmonary ARDS [21, 22]. This may be the reason for the lower NIV failure rate in patients with extrapulmonary ARDS. However, our study was a meta-analysis and the demographic information between two groups could not be comparable. Studies are required to further clarify this issue.
It is challenging to avoid intubation in immunocompromised patients with acute respiratory failure [23]. Patients with immunosuppression were more likely to receive NIV as a first-line therapy [24]. Relative to conventional oxygen therapy, use of NIV reduces the rate of intubation in patients with immunosuppression [25]. However, in our analyses, the pooled incidence of NIV failure in the immunocompromised group was 62%, the highest of all subgroups. Patients who experienced NIV failure had a higher likelihood of death in hospital than those who directly received intubation [26]. Therefore, the early identification of high-risk patients followed by the early application of intubation would be an alternative solution to reduce mortality.
This study had several limitations. First, there were various definitions of NIV failure among the studies considered. Some studies defined it as intubation, whereas others defined it as intubation, death, or crossover to a high-flow nasal cannula. However, because it was commonly defined as intubation, the incidence of NIV failure may have been overestimated. Second, only four study arms, involving 133 patients, could be used to pool the incidence of helmet NIV failure. As helmet NIV shows much more favorable outcomes than oronasal NIV, the pooled incidence of helmet NIV failure may be overestimated [27]. Third, the incidence of NIV failure was high in the ARDS population. This does not imply that patients with ARDS cannot obtain benefits from NIV. In the future, randomized controlled trials should be performed to further investigate this issue.

Conclusions

Nearly half of ARDS patients experience NIV failure. With increasing ARDS severity, the pooled incidence of NIV failure increased. Patients with pulmonary ARDS seem to experience more NIV failure than those with extrapulmonary ARDS. ARDS patients with immunosuppression may be at highest risk for NIV failure.

Declarations

Not applicable.
Not applicable.

Competing interests

The authors declare no competing interests.
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Metadaten
Titel
Incidence of noninvasive ventilation failure and mortality in patients with acute respiratory distress syndrome: a systematic review and proportion meta-analysis
verfasst von
Jie Wang
Jun Duan
Ling Zhou
Publikationsdatum
01.12.2024
Verlag
BioMed Central
Erschienen in
BMC Pulmonary Medicine / Ausgabe 1/2024
Elektronische ISSN: 1471-2466
DOI
https://doi.org/10.1186/s12890-024-02839-8

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