Improvement in the survival rates of extracorporeal membrane oxygenation-supported respiratory failure patients: a multicenter retrospective study in Korean patients
verfasst von:
Moon Seong Baek, Sang-Min Lee, Chi Ryang Chung, Woo Hyun Cho, Young-Jae Cho, Sunghoon Park, So-My Koo, Jae-Seung Jung, Seung Yong Park, Youjin Chang, Byung Ju Kang, Jung-Hyun Kim, Jin Young Oh, So Hee Park, Jung-Wan Yoo, Yun Su Sim, Sang-Bum Hong
Although the utilization of extracorporeal membrane oxygenation (ECMO) is increasing and its technology is evolving, only a few epidemiologic reports have described the uses and outcomes of ECMO. The aim of this study was to investigate the changes in utilization and survival rate in patients supported with ECMO for severe respiratory failure in Korea.
Methods
This was a multicenter study on consecutive patients who underwent ECMO across 16 hospitals in Korea. The records of all patients who required ECMO for acute respiratory failure between 2012 and 2015 were retrospectively reviewed, and the utilization of ECMO was analyzed over time.
Results
During the study period, 5552 patients received ECMO in Korea as a whole, and a total of 2472 patients received ECMO at the participating 16 hospitals. We analyzed 487 (19.7%) patients who received ECMO for respiratory failure. The number of ECMO procedures provided for respiratory failure increased from 104 to 153 during the study period. The in-hospital survival rate increased from 30.8% to 35.9%. The use of prone positioning increased from 6.8% to 49.0% (p < 0.001), and the use of neuromuscular blockers also increased from 28.2% to 58.2% (p < 0.001). Multiple regression analysis showed that old age (OR 1.038 (95% CI 1.022, 1.054)), use of corticosteroid (OR 2.251 (95% CI 1.153, 4.397)), continuous renal replacement therapy (OR 2.196 (95% CI 1.135, 4.247)), driving pressure (OR 1.072 (95% CI 1.031, 1.114)), and prolonged ECMO duration (OR 1.020 (95% CI 1.003, 1.038)) were associated with increased odds of mortality.
Conclusions
Utilization of ECMO and survival rates of patients who received ECMO for respiratory failure increased over time in Korea. The use of pre-ECMO prone positioning and neuromuscular blockers also increased during the same period.
Hinweise
Moon Seong Baek and Sang-Min Lee contributed equally to this work.
Abkürzungen
APACHE
Acute Physiology and Chronic Health Evaluation
ARDS
Acute respiratory distress syndrome
CNS
Central nervous system
CRRT
Continuous renal replacement therapy
ECMO
Extracorporeal membrane oxygenation
ELSO
Extracorporeal Life Support Organization
ICU
Intensive care unit
IQR
Interquartile range
OR
Odds ratio
SOFA
Sequential Organ Failure Assessment
Background
Extracorporeal membrane oxygenation (ECMO), which provides respiratory and/or cardiac support, allows treatment of patients with refractory gas-exchange abnormalities [1]. The use of ECMO to support patients with respiratory failure is increasing worldwide following the use of ECMO for severe acute respiratory failure during the 2009 influenza A pandemic [2‐5]. Recently, the EOLIA trial reported that in patients with severe acute respiratory distress syndrome (ARDS) there was no significant difference in 60-day mortality between patients who received early ECMO and those who received conventional mechanical ventilation that included ECMO as rescue therapy [6]. However, crossover to ECMO occurred in 28% of patients in the conventional group, who showed a high mortality rate of 57%. This suggests that ECMO can be used in severe ARDS patients who do not benefit from conventional treatment.
Survival of patients who received ECMO is also gradually increasing over time [7]. A recent epidemiologic report in Germany showed that ECMO utilization for severe respiratory failure significantly increased from 2007 until 2012, and in-hospital survival increased over time as well [8]. Sauer et al. [9] reported that the annual rates of ECMO cases increased by 433% from 2006 to 2011 in the United States, and that, albeit not statistically significant, there was an improving trend in the survival rate as well. In a single-center study in Korea, the survival rates associated with the ECMO procedure increased between 2009 and 2011 [10]. However, as we have previously reported, there was a discrepancy in the survival rate between those of the Extracorporeal Life Support Organization (ELSO) registry and Korean ECMO patients [11]. The in-hospital survival rate of ECMO-treated patients with acute respiratory failure was 46% from 2014 to 2015 in Korea, whereas the survival rate was 58% in the ELSO registry patients [7]. Also, we have suggested that age is an important factor in the survival of patients who received ECMO. Therefore, we sought to determine whether there has been an improvement in the survival rate of patients who received ECMO support for acute respiratory failure in Korea. Specifically, we evaluated the changes over time in the survival rates of patients supported with ECMO for severe respiratory failure and the factors associated with the survival rate.
Anzeige
Methods
Study design
This was a multicenter study of consecutive patients who received ECMO at 16 hospitals in Korea. The records of all patients who required ECMO for acute respiratory failure between 2012 and 2015 were retrospectively reviewed and the utilization of ECMO was analyzed over time. The decision to use ECMO was made at the discretion of the attending physicians at each center without standardization. The study protocol was approved by the institutional review board of Asan Medical Center, and by the local institutional review boards of all other participating centers. The requirement for informed consent was waived due to the retrospective design of the study.
Data collection
Data were collected from electronic medical records of patients older than 19 years who received ECMO support. Included variables were as follows: demographic information, Acute Physiology and Chronic Health Evaluation (APACHE) II and Sequential Organ Failure Assessment (SOFA) scores at intensive care unit (ICU) admission, etiology of respiratory failure, cardiac arrest, immunocompromised status, central nervous system (CNS) dysfunction, pre-ECMO hemodynamic data, mechanical ventilation parameters, and arterial blood gas data. Immunocompromised status and CNS dysfunction were defined according to the RESP study [12]. Immunocompromised status included hematological malignancies, solid tumors, solid-organ transplantation, high-dose or long-term corticosteroid and/or immunosuppressant use, and human immunodeficiency virus infection. CNS dysfunction included diagnoses of neurotrauma, stroke, encephalopathy, cerebral embolism, seizure, and epileptic syndrome. We collected information on adjunctive therapy such as the use of vasopressors, steroids, continuous renal replacement therapy (CRRT), prone positioning, nitric oxide, bicarbonate infusion, and neuromuscular blockers. We also collected data such as the ECMO mode, ECMO duration, duration of mechanical ventilation to ECMO initiation, hospital stay, and tracheotomy. The ECMO mode was categorized as veno-venous, veno-arterial, and veno-arteriovenous. Outcome variables of the study were survival at discharge and ECMO weaning (survival within 48 h after weaning from ECMO).
Statistical analysis
Demographics, pre-ECMO parameters, and outcomes were compared between 2012 and 2015. Differences with p < 0.05 were considered statistically significant. Categorical variables are expressed as the number (percentage). Continuous variables are expressed as the median (interquartile range). Pearson’s chi-square test or Fisher’s exact test was used to compare categorical data. The Kruskal–Wallis test was used to compare medians between groups.
Multiple logistic regression analysis using the backward elimination method was performed to identify the factors associated with survival at discharge. Candidate variables for inclusion in the multiple logistic regression model were chosen from the univariate analysis; variables with p < 0.1 in the univariate analyses were included in the multivariate analysis, and collinearity was assessed before the multivariate analysis. Calibrations of the models were evaluated with the Hosmer–Lemeshow goodness-of-fit test. Statistical analyses were performed using the Statistical Package for the Social Sciences (SPSS) version 22.0 (IBM Corporation, Armonk, NY, USA).
Anzeige
Results
Baseline characteristics of the study population
During the study period (2012–2015), 5552 patients received ECMO support in Korea. ECMO support was given to 2472 patients in the participating 16 hospitals. We analyzed 487 (19.7%) patients who received ECMO specifically for respiratory failure. The annual number of ECMO cases at 16 institutions varied widely: eight centers had fewer than 20 cases per year and the other eight centers had more than 30 cases per year, with two of those centers having had more than 120 cases per year.
The patients’ median age was 58 years (range 45–66 years), and the median body mass index was 22.2 kg/m2 (range 20.6–23.2 kg/m2). Pre-ECMO mechanical ventilation was provided in 92.2% of patients and corticosteroid therapy was used in 16.8% of patients. Prone positioning was applied in 29.5% of patients and neuromuscular blockers were used in 45.4% of patients. The majority of patients were initially supported with veno-venous ECMO (88.1%), and the median duration of support was 8 days (interquartile range (IQR) 4, 18 days). Survival and weaning rates were 38.8% and 57.1%, respectively (Table 1).
Table 1
Baseline characteristics of patients supported with ECMO for respiratory failure
Variable
Total (n = 487)
Age (years)
58 (45, 66)
Male
321 (65.9)
Body mass index (kg/m2)
22.2 (20.6, 23.2)
APACHE II score
21 (15, 28)
SOFA score
8 (5, 12)
PRESERVE score
5 (4, 6)
RESP score
0 (−2, 2)
Etiology of ARF
Viral pneumonia
47 (9.7)
Bacterial pneumonia
127 (26.1)
COPD and asthma
8 (1.6)
Trauma and burn
25 (5.1)
Asphyxia
13 (2.7)
Acute exacerbation of ILD
61 (12.5)
Chronic respiratory failure
24 (4.9)
ARDS
44 (9.0)
Airway obstruction
28 (5.7)
Other respiratory failure
110 (22.6)
Immunocompromiseda
122 (25.2)
CNS dysfunctionb
24 (5.0)
Vasopressor
301 (63.0)
Corticosteroid
82 (16.8)
Cardiac arrest
74 (15.2)
CRRT
83 (17.0)
Mechanical ventilation
449 (92.2)
Prone positioning
143 (29.5)
Pre-ECMO rescue therapy
Nitric oxide
127 (26.2)
Bicarbonate infusion
53 (11.0)
Neuromuscular blocker
230 (45.4)
Vital signs
MAP (mmHg)
70 (58, 84)
Heart rate (/min)
112 (95, 128)
Respiratory rate (/min)
22 (18, 28)
ECMO type
Veno-venous
429 (88.1)
Veno-arterial
42 (8.6)
Veno-arteriovenous
14 (2.9)
Other
2 (0.4)
Arterial blood gases
pH
7.28 (7.17, 7.38)
PaO2 (mmHg)
61 (51, 76)
PaCO2 (mmHg)
51 (39, 65)
HCO3− (mEq/L)
23 (19, 29)
SaO2 (%)
88 (79, 93)
Ventilation parameters
PaO2/FiO2
65 (53, 90)
FiO2
100 (90, 100)
PEEP (cmH2O)
10 (6, 12)
PIP (cmH2O)
28 (24, 32)
Tidal volume (ml/kg)
7 (6, 9)
Driving pressure (cmH2O)
18 (15, 24)
Minute ventilation (L/min)
9.6 (7.4, 12.4)
Interval MV–ECMO (days)
1 (0, 5)
ECMO duration (days)
8 (4, 18)
Hospital stay (days)
35 (18, 61)
Tracheostomy
199 (41.8)
Weaning rate
278 (57.1)
Survival rate
189 (38.8)
Values expressed as median (interquartile range) or n (%)
ECMO extracorporeal membrane oxygenation, APACHE Acute Physiology and Chronic Health Evaluation, SOFA Sequential Organ Failure Assessment, PRESERVE Predicting Death for Severe Acute Respiratory Distress Syndrome on Veno-venous ECMO, RESP Respiratory Extracorporeal Membrane Oxygenation Survival Prediction, ARF acute respiratory failure, ARDS acute respiratory distress syndrome, COPD chronic obstructive pulmonary disease, ILD interstitial lung disease, CNS central nervous system, CRRT continuous renal replacement therapy, MAP mean arterial pressure, PaO2 partial pressure of arterial oxygen, PaCO2 partial pressure of arterial carbon dioxide, HCO3− bicarbonate, SaO2 oxygen saturation, FiO2 fraction of inspired oxygen, PEEP positive end-expiratory pressure, PIP peak inspiratory pressure, MV mechanical ventilation
a“Immunocompromised” included hematological malignancies, solid tumors, solid-organ transplantation, high-dose or long-term corticosteroid and/or immunosuppressant use, and human immunodeficiency virus infection
b“CNS dysfunction” included diagnoses of neurotrauma, stroke, encephalopathy, cerebral embolism, seizure, and epileptic syndrome
Demographics, pre-ECMO parameters, and outcomes over time
The number of ECMO procedures for respiratory failure increased from 104 to 153 during the study period (Fig. 1). There were no significant differences in age, sex, APACHE II score, SOFA score, immunocompromised status, CNS dysfunction, cardiac arrest, CRRT, use of nitric oxide and bicarbonate infusion, PaO2/FiO2 ratio, ECMO duration, and duration of mechanical ventilation to ECMO initiation between groups. Use of prone positioning increased from 6.8% to 49.0% (p < 0.001) and the use of neuromuscular blockers also increased from 28.2% to 58.2% (p < 0.001; Table 2). Although the survival rate remained relatively low, it increased over time from 30.8% to 35.9% (p = 0.005; Table 3). Post-hoc analysis showed that the survival rate in 2014 was significantly higher than the rates in 2012 and 2015.
Fig. 1
Number of ECMO procedures and weaning and survival rates of patients who received ECMO for acute respiratory failure. ECMO extracorporeal membrane oxygenation
Table 2
Demographic features of survivors and nonsurvivors supported with ECMO for respiratory failure
Variable
2012 (n = 104)
2013 (n = 100)
2014 (n = 130)
2015 (n = 153)
p value
Age (years)
59 (49, 69)
60 (45, 68)
58 (43, 66)
57 (45, 63)
0.199
Male
69 (66.3)
71 (71.0)
93 (71.5)
88 (57.5)
0.050
Body mass index (kg/m2)
22.6 (20.4, 24.6)
22.9 (19.7, 25.0)
22.1 (21.0, 22.9)
22.0 (20.5, 22.9)
0.073
APACHE II score
21 (16, 27)
22 (16, 29)
21 (15, 30)
19 (14, 26)
0.162
SOFA score
8 (5, 12)
8 (5, 11)
8 (5, 12)
8 (6, 12)
0.842
PRESERVE score
5 (4, 7)
6 (4, 7)
5 (3, 6)
5 (3, 6)
0.245
RESP score
0 (−2, 2)
0 (−2, 2)
0 (−2, 2)
1(−1, 3)
0.497
Etiology of ARF
0.001
Viral pneumonia
7 (6.7)
8 (8.0)
11 (8.5)
21 (13.7)
Bacterial pneumonia
33 (31.7)
16 (16.0)
37 (28.5)
41 (26.8)
COPD and asthma
1 (1.0)
2 (2.0)
4 (3.1)
1 (0.7)
Trauma and burn
1 (1.0)
4 (4.0)
10 (7.7)
10 (6.5)
Asphyxia
0 (0.0)
3 (3.0)
8 (6.2)
2 (1.3)
Acute exacerbation of ILD
8 (7.7)
17 (17.0)
13 (10.0)
23 (15.0)
Chronic respiratory failure
11 (10.6)
4 (4.0)
6 (4.6)
3 (2.0)
ARDS
13 (12.5)
14 (14.0)
7 (5.4)
10 (6.5)
Airway obstruction
10 (9.6)
6 (6.0)
4 (3.1)
8 (5.2)
Other respiratory failure
20 (19.2)
26 (26.0)
30 (23.1)
34 (22.2)
Immunocompromiseda
26 (25.2)
21 (21.4)
34 (26.2)
41 (26.8)
0.799
CNS dysfunctionb
3 (2.9)
3 (3.1)
8 (6.2)
10 (6.5)
0.413
Vasopressor
48 (46.2)
59 (59.0)
96 (75.6)
98 (66.7)
< 0.001
Corticosteroid
22 (21.2)
21 (21.0)
23 (17.7)
16 (10.5)
0.068
Cardiac arrest
8 (7.7)
19 (19.0)
24 (18.5)
23 (15.0)
0.080
CRRT
20 (19.2)
19 (19.0)
20 (15.4)
24 (15.7)
0.783
Mechanical ventilation
94 (90.4)
83 (83.0)
125 (96.2)
147 (96.1)
< 0.001
Prone positioning
7 (6.8)
3 (3.1)
58 (44.6)
75 (49.0)
< 0.001
Pre-ECMO rescue therapy
Nitric oxide
29 (28.2)
22 (22.4)
42 (32.3)
34 (22.2)
0.197
Bicarbonate infusion
11 (10.7)
12 (12.2)
14 (10.8)
16 (10.5)
0.975
Neuromuscular blocker
29 (28.2)
32 (32.7)
80 (61.5)
89 (58.2)
< 0.001
Values expressed as median (interquartile range), mean ± standard deviation, or n (%)
ECMO extracorporeal membrane oxygenation, APACHE Acute Physiology and Chronic Health Evaluation, SOFA Sequential Organ Failure Assessment, PRESERVE Predicting Death for Severe Acute Respiratory Distress Syndrome on Veno-venous ECMO, RESP Respiratory Extracorporeal Membrane Oxygenation Survival Prediction, ARF acute respiratory failure, COPD chronic obstructive pulmonary disease, ILD interstitial lung disease, ARDS acute respiratory distress syndrome, CNS central nervous system, CRRT continuous renal replacement therapy
a“Immunocompromised” included hematological malignancies, solid tumors, solid-organ transplantation, high-dose or long-term corticosteroid and/or immunosuppressant use, and human immunodeficiency virus infection
b“CNS dysfunction” included diagnoses of neurotrauma, stroke, encephalopathy, cerebral embolism, seizure, and epileptic syndrome
Table 3
Pre-ECMO parameters of patients supported with ECMO for respiratory failure
Variable
2012 (n = 104)
2013 (n = 100)
2014 (n = 130)
2015 (n = 153)
p value
Vital signs
MAP (mmHg)
74 (62, 89)
72 (59, 86)
63 (56, 72)
70 (57, 84)
0.001
Heart rate (/min)
112 (98, 125)
116 (101, 131)
107 (94, 125)
112 (94, 129)
0.462
Respiratory rate (/min)
26 (20, 30)
24 (20, 30)
20 (16, 26)
20 (16, 26)
< 0.001
ECMO type
0.003
Veno-venous
96 (92.3)
95 (95.0)
113 (86.9)
125 (81.7)
Veno-arterial
4 (3.8)
2 (2.0)
11 (8.5)
25 (16.3)
Veno-arteriovenous
3 (2.9)
2 (2.0)
6 (4.6)
3 (2.0)
Other
1 (1.0)
1 (1.0)
0 (0.0)
0 (0.0)
Arterial blood gases
pH
7.31 (7.17, 7.43)
7.25 (7.17, 7.36)
7.26 (7.15, 7.37)
7.29 (7.18, 7.38)
0.081
PaO2 (mmHg)
60 (52, 74)
66 (56, 79)
62 (50, 75)
61 (46, 76)
0.211
PaCO2 (mmHg)
52 (40, 62)
56 (41, 72)
51 (39, 71)
47 (36, 59)
0.013
HCO3− (mEq/L)
24.3 (21.1, 31.0)
24.1 (19.9, 29.5)
22.4 (18.1, 27.9)
22.0 (18.2, 25.5)
0.003
SaO2 (%)
88 (83, 92)
89 (85, 94)
88 (79, 93)
87 (75, 93)
0.243
Ventilation parameters
PaO2/FiO2
62 (53, 80)
72 (59, 96)
65 (53, 90)
65 (48, 97)
0.131
FiO2
100 (100, 100)
100 (90, 100)
100 (80, 100)
100 (80, 100)
0.069
PEEP (cmH2O)
10 (6, 12)
8 (5, 12)
10 (6, 10)
10 (7, 12)
0.119
PIP (cmH2O)
28 (24, 33)
30 (25, 34)
28 (23, 33)
28 (24, 31)
0.382
Tidal volume (ml/kg)
389 (298, 575)
420 (321, 513)
444 (340, 600)
428 (299, 518)
0.255
Driving pressure (cmH2O)
18 (14, 24)
20 (16, 25)
18 (15, 23)
18 (15, 21)
0.077
Minute ventilation (L/min)
10.9 (7.8, 14.6)
9.6 (7.7, 12.7)
9.5 (7.2, 12.2)
9.3 (6.8, 12.0)
0.035
Interval MV–ECMO (days)
2 (0, 7)
1 (0, 5)
1 (0, 5)
2 (0, 5)
0.090
ECMO duration (days)
7 (4, 14)
8 (5, 22)
8 (3, 13)
7 (4, 24)
0.305
Hospital stay (days)
32 (17, 47)
34 (19, 65)
39 (18, 73)
34 (17, 60)
0.318
Tracheostomy
32 (30.8)
38 (38.0)
61 (48.8)
68 (46.3)
0.023
Weaning rate
56 (53.8)
50 (50.0)
86 (66.2)
86 (56.2)
0.075
Survival rate
32 (30.8)
35 (35.0)
67 (51.5)
55 (35.9)
0.005
Values expressed as mean ± standard deviation, or n (%)
ECMO extracorporeal membrane oxygenation, MAP mean arterial pressure, PaO2 partial pressure of oxygen, PaCO2 partial pressure of carbon dioxide, HCO3− bicarbonate, SaO2 oxygen saturation, FiO2 fraction of inspired oxygen, PEEP positive end-expiratory pressure, PIP peak inspiratory pressure, MV mechanical ventilation
×
Factors associated with mortality in patients supported with ECMO
Multiple regression analysis was performed using age, sex, year, APACHE II score, SOFA score, immunocompromised status, CNS dysfunction, corticosteroid, CRRT, prone positioning, nitric oxide, neuromuscular blocker, PaCO2, peak inspiratory pressure, driving pressure, and ECMO duration. Old age (OR 1.038 (95% CI 1.022, 1.054)), use of corticosteroid (OR 2.251 (95% CI 1.153, 4.397)), CRRT (OR 2.196 (95% CI 1.135, 4.247)), driving pressure (OR 1.072 (95% CI 1.031, 1.114)), and prolonged ECMO duration (OR 1.020 (95% CI 1.003, 1.038)) were associated with increased odds of mortality (Table 4).
Table 4
Univariate and multivariate analyses for mortality of ECMO
Variable
OR (95% CI)
p value
OR (95% CI)
p value
Age (years)
1.043 (1.029, 1.056)
< 0.001
1.038 (1.022, 1.054)
< 0.001
Male
0.720 (0.487, 1.064)
0.099
Year
0.645 (0.444, 0.939)
0.022
Body mass index (kg/m2)
0.982 (0.927, 1.040)
0.527
APACHE II score
1.032 (1.010, 1.054)
0.004
SOFA score
1.020 (0.978. 1.065)
0.358
Immunocompromised
1.335 (0.868, 2.054)
0.188
CNS dysfunction
1.274 (0.534, 3.038)
0.585
Vasopressor
1.254 (0.857, 1.836)
0.243
Corticosteroid
1.914 (1.130, 3.242)
0.016
2.251 (1.153, 4.397)
0.018
Cardiac arrest
1.050 (0.630, 1.747)
0.852
CRRT
2.102 (1.233, 3.581)
0.006
2.196 (1.135, 4.247)
0.019
Prone positioning
1.054 (0.705, 1.575)
0.798
Nitric oxide
1.853 (1.194, 2.875)
0.006
Bicarbonate infusion
1.521 (0.820, 2.820)
0.183
Neuromuscular blocker
1.186 (0.821, 1.711)
0.363
VV ECMO mode
0.810 (0.456, 1.439)
0.472
pH
0.800 (0.244, 2.618)
0.712
PaO2 (mmHg)
0.998 (0.993, 1.003)
0.433
PaCO2 (mmHg)
1.007 (0.999, 1.015)
0.083
PaO2/FiO2
0.999 (0.996, 1.002)
0.447
PEEP (cmH2O)
0.968 (0.918, 1.020)
0.219
PIP (cmH2O)
1.070 (1.034, 1.107)
< 0.001
Tidal volume (ml/kg)
0.999 (0.998, 1.000)
0.175
Driving pressure (cmH2O)
1.078 (1.039, 1.118)
< 0.001
1.072 (1.031, 1.114)
< 0.001
Minute ventilation (L/min)
1.022 (0.969, 1.077)
0.428
Interval MV–ECMO (days)
1.024 (0.998, 1.050)
0.068
ECMO duration (days)
1.016 (1.003, 1.029)
0.017
1.020 (1.003, 1.038)
0.021
ECMO extracorporeal membrane oxygenation, OR odds ratio, CI confidence interval, APACHE Acute Physiology and Chronic Health Evaluation, SOFA Sequential Organ Failure Assessment, CNS central nervous system, CRRT continuous renal replacement therapy. VV veno-venous, PaO2 partial pressure of oxygen, PaCO2 partial pressure of carbon dioxide, FiO2 fraction of inspired oxygen, PEEP positive end-expiratory pressure, PIP peak inspiratory pressure, MV mechanical ventilation
The median age was older in the nonsurvivors (61 years; IQR 52, 69 years) than in survivors (51 years; IQR 37, 62 years) (p < 0.001). The survival rate decreased with age, with patients older than 60 years having a survival rate of 30.8% (Fig. 2). ECMO duration was significantly longer in the nonsurvivors (9 days; interquartile range (IQR) 4, 22 days) than in survivors (7 days; IQR 3, 13 days) (p = 0.002). Compared with the survival rate within 2 weeks of ECMO support, the overall survival rate after 2 weeks of ECMO support showed a significant decrease from 43.4% to 27.8% (p = 0.001).
Fig. 2
Survival rates of ECMO patients according to age (years) (p < 0.001) and ECMO duration (p = 0.001). ECMO extracorporeal membrane oxygenation
×
Discussion
This multicenter study was conducted to evaluate the change in survival rates of patients who received ECMO support for acute respiratory failure in Korea. Utilization of ECMO for respiratory failure increased over time, and the survival rate was improved with increasing use of adjunctive management. Also, patient age and the duration of ECMO were significantly associated with survival.
A notable change during the study period was that the administration of neuromuscular blockades and use of prone positioning before ECMO had significantly increased from 28.2% to 58.2% and from 6.8% to 49.0%, respectively. Papazian et al. [13] reported that early use of neuromuscular blockades in patients with severe ARDS may improve survival. In the ELSO registry-based RESP study, neuromuscular blockade agents before ECMO were independently associated with hospital survival [12]. In addition, in patients with severe ARDS, early application of prolonged prone positioning was significantly associated with improved survival [14]. Schmidt et al. [15] demonstrated that use of prone positioning before ECMO was also associated with survival. These results are in accordance with those in a recent systematic review and meta-analysis [16]. Moreover, for patients with severe ARDS, prone positioning before and during ECMO may be helpful for weaning from ECMO [17, 18]. Another distinctive finding was the change in pre-ECMO ventilator parameters. In recent years, the driving pressure was lower and minute ventilation was decreased. Therefore, improvement in hospital survival of ECMO-supported patients with respiratory failure might be the result of increasing experience with ECMO over time, including evolving adjuvant therapies and improved management of mechanical ventilation.
The results of this study showed that the number of ECMOs carried out for respiratory failure increased from 104 to 153 from 2012 to 2015, and that the in-hospital survival rate increased from 30.8% to 35.9% during the same period. The overall survival rate of 39% in ECMO-supported respiratory failure patients in Korea is lower than the reported rate of 58% in the ELSO registry [7]. Meanwhile, an ECMO epidemiologic study performed in Germany reported that from 2012 to 2014 the in-hospital survival had steadily increased and the rate of survival was approximately 40%, which is similar to our findings [8]. In addition, Sauer et al. [9] reported that in the United States the survival rate of the patients who received ECMO was approximately 40%. In the German study, approximately 80% of patients were older than 40 years and increasing numbers of older patients had received ECMO. In the US study, the mean age of the patients who received ECMO was 50 years, which is higher than that of the patients included in the ELSO registry. Taken together, the discrepancies in demographics between the patients of ECMO centers not included in the ELSO and those in the ELSO registry may explain the difference in survival rates. Also, another explanation for the relatively low survival rate of Korean ECMO patients could be the infrequent use of prone positioning. The use of prone positioning and use of neuromuscular blockers were low compared with those in the EOLIA trial [6], in which prone positioning was applied in 90% of patients in the conventional ventilator support group, who showed a 54% survival rate. The relatively low survival rate in Korean ECMO patients may be due to excessive use of ECMO in patients who may have shown good response to prone positioning. Accordingly, the use of prone positioning is gradually increasing in Korea.
Anzeige
Another interesting finding of our study was that the survival rate was associated with the ECMO duration. The survival rate of patients who required prolonged ECMO (longer than 14 days) was significantly lower than that of patients who had shorter ECMO duration (28% vs 43%, respectively, p = 0.001). Recently, Posluszny et al. [19] reported that ECMO duration was inversely correlated with the survival rate in ECMO-supported patients with respiratory failure; the survival rate in patients who had longer ECMO duration was 10% lower than that in those with shorter ECMO duration. Nonetheless, the investigators suggested that prolonged ECMO was not futile because there was a significant improvement in survival from 37% to 49% in recent years. On the other hand, the aforementioned German epidemiologic study reported that prolonged ECMO was associated with poorer outcome; that the survival rate rapidly declined to 20% within 10 days after ECMO initiation [8]. Therefore, further studies are needed to provide a more solid association between ECMO duration and the survival rate.
Our study has several limitations. This study was retrospective and had a relatively short study period. Because not all patients treated with ECMO for respiratory failure in Korea were included, selection bias is possible. In addition, long-term outcomes and quality of life could not be assessed, which warrants an extended observation period of our study populations or further epidemiologic studies. Despite such limitations, our current multicenter study, which is not based on the ELSO registry, provides information on the change in the survival rate of ECMO patients with respiratory failure and the factors associated with survival, and adds to the understanding of survival in patients who receive ECMO due to respiratory failure.
Conclusions
This multicenter study performed in Korea showed that utilization of ECMO for respiratory failure had increased over time, and that the survival rates of ECMO-supported respiratory failure patients had improved with increasing utilization of adjunctive management. Patient age and duration of ECMO were significantly associated with survival at discharge.
Acknowledgements
Not applicable.
Anzeige
Funding
This study was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute funded by the Ministry of Health & Welfare, Republic of Korea (HC15C1507).
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study protocol was approved by the institutional review boards of Medical Center, Seoul National University, Samsung Medical Center, Pusan National University Yangsan Hospital, Seoul National University Bundang Hospital, Hallym University Sacred Heart Hospital, Soonchunhyang University Hospital, Korea University Anam Hospital, Chonbuk National University Hospital, Chungbuk National University, Ulsan University Hospital, Bundang CHA Hospital, Kyung Hee University Hospital at Gangdong, Dongguk University Ilsan Hospital, Gyeongsang National University, and Hallym University Kangnam Sacred Heart Hospital. The need for informed consent was waived due to the retrospective design of the study.
Consent for publication
Not applicable.
Anzeige
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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.
Improvement in the survival rates of extracorporeal membrane oxygenation-supported respiratory failure patients: a multicenter retrospective study in Korean patients
verfasst von
Moon Seong Baek Sang-Min Lee Chi Ryang Chung Woo Hyun Cho Young-Jae Cho Sunghoon Park So-My Koo Jae-Seung Jung Seung Yong Park Youjin Chang Byung Ju Kang Jung-Hyun Kim Jin Young Oh So Hee Park Jung-Wan Yoo Yun Su Sim Sang-Bum Hong
Patienten, die von Ärztinnen behandelt werden, dürfen offenbar auf bessere Therapieergebnisse hoffen als Patienten von Ärzten. Besonders gilt das offenbar für weibliche Kranke, wie eine Studie zeigt.
Akuter Schwindel stellt oft eine diagnostische Herausforderung dar. Wie nützlich dabei eine MRT ist, hat eine Studie aus Finnland untersucht. Immerhin einer von sechs Patienten wurde mit akutem ischämischem Schlaganfall diagnostiziert.
Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.
Schmerzen im Unterbauch, aber sonst nicht viel, was auf eine Appendizitis hindeutete: Ein junger Mann hatte Glück, dass trotzdem eine Laparoskopie mit Appendektomie durchgeführt und der Wurmfortsatz histologisch untersucht wurde.
Update AINS
Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.
