The global numbers of confirmed cases and deceased critically ill patients with COVID-19 are increasing. However, the clinical course, and the 60-day mortality and its predictors in critically ill patients have not been fully elucidated. The aim of this study is to identify the clinical course, and 60-day mortality and its predictors in critically ill patients with COVID-19.
Methods
Critically ill adult patients admitted to intensive care units (ICUs) from 3 hospitals in Wuhan, China, were included. Data on demographic information, preexisting comorbidities, laboratory findings at ICU admission, treatments, clinical outcomes, and results of SARS-CoV-2 RNA tests and of serum SARS-CoV-2 IgM were collected including the duration between symptom onset and negative conversion of SARS-CoV-2 RNA.
Results
Of 1748 patients with COVID-19, 239 (13.7%) critically ill patients were included. Complications included acute respiratory distress syndrome (ARDS) in 164 (68.6%) patients, coagulopathy in 150 (62.7%) patients, acute cardiac injury in 103 (43.1%) patients, and acute kidney injury (AKI) in 119 (49.8%) patients, which occurred 15.5 days, 17 days, 18.5 days, and 19 days after the symptom onset, respectively. The median duration of the negative conversion of SARS-CoV-2 RNA was 30 (range 6–81) days in 49 critically ill survivors that were identified. A total of 147 (61.5%) patients deceased by 60 days after ICU admission. The median duration between ICU admission and decease was 12 (range 3–36). Cox proportional-hazards regression analysis revealed that age older than 65 years, thrombocytopenia at ICU admission, ARDS, and AKI independently predicted the 60-day mortality.
Conclusions
Severe complications are common and the 60-day mortality of critically ill patients with COVID-19 is considerably high. The duration of the negative conversion of SARS-CoV-2 RNA and its association with the severity of critically ill patients with COVID-19 should be seriously considered and further studied.
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Abkürzungen
AKI
Acute kidney injury
ALT
Alanine aminotransferase
APACHE II
Acute Physiology and Chronic Health Evaluation II
APTT
Activated partial thromboplastin time
ARDS
Acute respiratory distress syndrome
AST
Aspartate aminotransferase
COVID-19
Novel coronavirus disease 2019
ICUs
Intensive care units
ECMO
Extracorporeal membrane oxygenation
FiO2
Fraction of inspired oxygen
hsTNI
Hypersensitive troponin I
IQR
Interquartile range
IL-6
Interleukin 6
pO2
Partial pressure of oxygen
pCO2
Partial pressure of carbon dioxide
PT
Prothrombin time
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
Background
The epidemic of novel coronavirus disease 2019 (COVID-19) struck Wuhan in late December 2019. As of June 8, 2020, the global number of confirmed cases has reached 6,931,000, with 400,857 deaths [1]. Although most patients recovered from COVID-19, critically ill patients need long-term hospitalizations and have a considerable risk of death. Our previous small sample-sized study showed that approximately 7% of inpatients with COVID-19 developed critical complications. Among the critically ill patients, by 28-day after admission to an intensive care unit (ICU), 61.5% deceased, and 60% of the survivors were still in hospital [2]. The long-term prognosis of all survivors is unknown.
Critically ill patients with COVID-19 are characterized by progressive respiratory failure due to lung infection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) [3]. Recent evidence suggested that SARS-CoV-2 might directly dysregulate the normal functions of the kidney, liver, and peripheral blood components, which increases the risk of multiple organ failure [3‐5]. To our knowledge, some potential high-risk factors of death were speculated in small sample-sized studies on COVID-19 [2, 4, 6]. In another study exploring the risk factors of death, only 11 (8%) were treated in ICUs and only 3 (2%) received mechanical ventilation during hospitalization in the survivor group, and severe complications during the progression of COVID-19, including acute respiratory syndrome (ARDS), acute cardiac injury, acute kidney injury (AKI), and liver dysfunction, were not considered at all [7].
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Here, for this WHO-declared pandemic [8], we intended to report our findings on clinical course and the 60-day mortality in 239 critically ill patients with COVID-19 from Wuhan, China.
Methods
Study design and participants
We aimed to retrospectively study critically ill adult patients with COVID-19 admitted into ICUs from Wuhan Union Hospital, Jinyintan Hospital, and Wuhan Third Hospital, from January 12 to February 3, 2020. As previously described, SARS-CoV-2 infections were confirmed by a positive result on a reverse transcriptase-polymerase chain reaction (RT-PCR) assay of specimens from the respiratory tract according to guidelines released by National Health Commission of the People’s Republic of China [9]. Critically ill patients were defined to be individuals admitted to ICU, who required mechanical ventilation or had a fraction of inspired oxygen (FiO2) concentration greater than or equal to 60% as described in previous reports [2, 8, 10, 11]. Critically ill patients who deceased within 48 h after ICU admission were excluded, because their durations in ICUs were too short to reveal the effectiveness of treatments received in ICUs and to eliminate the bias on data collection of organ function or complications. Research approval (KY-2020-23.01) was granted by the ethics board of Jin Yin-tan Hospital as the central coordinating center. The need for informed consent was waived.
Criteria for ICU admission and treatment
The ICU admission criteria and treatment decisions for all patients, including determination of the need for intubation and respiratory support, were made at the discretion of the treating physicians and were not standardized. In general, the goal is to ascertain adequate oxygenation to maintain SpO2 ≥ 90% through high-flow nasal cannula (HFNC) and noninvasive ventilation (NIV) [12‐14]. If the respiratory failure progressively deteriorated, the patients were considered to be eligible for noninvasive or invasive mechanical ventilation when PaO2/FiO2 ≤ 200 mmHg. Where available, in patients with refractory hypoxemia (PaO2/FiO2 < 80 or 60 mmHg) veno-venous extracorporeal membrane oxygenation (ECMO) might serve as a therapeutic option to stabilize gas exchange [13, 14].
Data collection
Patient identification in the three hospitals was achieved by reviewing admission logs from available medical records. After several cycles of feedback and pilot testing, modified case report forms referencing the case record form shared by the International Severe Acute Respiratory and Emerging Infection Consortium for SARS-CoV-2 infection. Data were extracted from local servers by experienced research physicians at each center.
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Demographic data, preexisting comorbidities, vital signs at ICU admission, laboratory values at ICU admission, complications, treatments, and test result of SARS-CoV-2 RNA on samples from the respiratory tract and of serum SARS-CoV-2 IgM were collected. For patients discharged, phone calls were made by April 5, 2020, to record their living status.
Outcomes and definitions
The primary outcome was 60-day mortality and its predictors. ARDS were defined according to the Berlin Definition [15]. AKI was diagnosed according to KDIGO clinical practice guidelines based on the serum creatinine levels [16]. Acute cardiac injury was diagnosed if the serum concentration of hsTNI was measured in the laboratory above the upper limit of the reference range (> 28 pg/mL) [2]. Liver dysfunction was diagnosed if serum ALT > 50 U/L or AST > 40 U/L during disease progression [5]. Coagulopathy was defined if PT > 13.5 s or APTT > 37 s. Negative conversion of SARS-CoV-2 RNA was defined as the last time when SARS-CoV-2 RNA was tested positive on samples from the respiratory tract. Hospital-acquired infection was diagnosed if the patients had a positive culture of a new pathogen obtained from lower respiratory tract specimens (bacterial pneumonia), blood samples (bacteremia), or urine (urinary tract infection) taken ≥ 48 h after ICU admission [17].
Statistical analysis
No hypothesis was made for the present study, so sample size estimation was unavailable. Data were expressed as mean ± standard deviation, median [interquartile range], or median (range) for continuous variables and number (%) for categorical variables. Differences between survivors and non-survivors were explored using two-sample t test for parametric variables, Wilcoxon rank-sum test for non-parametric variables, and Fisher’s exact test for categorical variables. Kaplan-Meier plot was used for survival data. Age was dichotomized at 65 years. Lymphocyte counts at ICU admission were dichotomized at 1.1 × 109/L, the lower limit of normal range, and at 0.55 × 109/L and platelet counts at 125 × 109/L. Dichotomized age, lymphocyte counts and platelet counts, and comorbidities and dichotomous complications showing a p value < 0.2 in univariate analysis were included for Cox proportional-hazards regression analysis.
All statistical tests were 2-tailed with significance set at p value less than 0.05. The Stata/IC 15.1 software (StataCorp, College Station, TX, USA) was applied for all analyses.
Results
Demographic data and comorbidities of included patients
From January 12 to February 3, 2020, a total of 1748 patients with confirmed COVID-19 from the three study centers were screened, and 258 (14.8%) critically ill patients were identified. After excluding 19 patients who deceased within 48 h after ICU admission, 239 patients were included (Fig. 1). The three most common symptoms were fever (218 patients, 91.2%), cough (178 patients, 74.5%), and dyspnea (119 patients, 49.79%) (Supplementary table 1) Their mean age was 62.5 ± 13.3 years, including 112 (46.9%) patients over 65 years old (Table 1). One hundred sixty-two (67.8%) patients had one or more coexisting conditions, including hypertension in 105 (43.9%) patients, chronic cardiac disease in 35 (14.6%) patients, chronic pulmonary disease in 12 (5.0%) patients, cerebrovascular disease in 13 (5.4%) patients, chronic hepatic disease in 20 (8.4%) patients, malignancy in 13 (5.4%) patients, and diabetes mellitus in 44 (18.4%) patients.
Fig. 1
Flowchart of study of the included patients with COVID-2019. COVID-19, coronavirus disease 2019; MV, mechanical ventilation; DNR, do-not-resuscitate
Table 1
Demographic data and preexisting comorbidities in 239 critically ill patients with COVID-19
Characteristics
All patients (n = 239)
Non-survivors (n = 147)
Survivors (n = 92)
p value, survivors vs non-survivors
Age, mean ± SD, years
62.5 ± 13.3
65.7 ± 12.2
57.5 ± 13.5
< 0.001
Age ≥ 65 years
112 (46.9%)
82 (55.8%)
30 (32.6%)
< 0.001
Male
143 (59.8%)
90 (61.2%)
53 (57.6%)
0.337
APACHE II, median [IQR]a
15 [13–17]
15 [13–17]
13 [11–15]
0.006
SOFA scorea
6 [5–7]
6 [5–7]
5 [5–6]
0.0163
Preexisting comorbidities
Hypertension
105 (43.9%)
64 (43.5%)
41 (44.6%)
0.491
Chronic cardiac disease
35 (14.6%)
21 (14.3%)
14 (15.2%)
0.492
Chronic pulmonary disease
12 (5.0%)
9 (6.1%)
3 (3.3%)
0.253
Cerebrovascular disease
13 (5.4%)
9 (6.1%)
4 (4.3%)
0.392
Chronic liver disease
20 (8.4%)
13 (9.4%)
7 (8.4%)
0.511
Malignancy
13 (5.4%)
11 (7.5%)
2 (2.2%)
0.066
Diabetes
44 (18.4%)
24 (17.7%)
18 (19.6%)
0.420
COVID-19 coronavirus disease 2019, SD standard deviation, APACHE II Acute Physiology and Chronic Health Evaluation II, IQR interquartile range
Data were expressed as count (%) unless otherwise
aAPACHE II scores at ICU admission were available in 165 patients, because arterial blood gas analysis was conducted in 101 non-survivors and 64 survivors
×
Laboratory tests at ICU admission
The laboratory findings of all critically ill patients on ICU admission were summarized in Table 2. At ICU admission, 219 (91.6%) patients had lymphocyte counts less than 1.1 × 109/L and 103 (43.1%) had lymphocyte counts less than 0.55 × 109/L. A total of 59 (24.7%) patients had platelet count less than 125 × 109/L. Among 165 patients with an analysis of arterial blood gas, their partial pressure of oxygen divided by fraction of inspired oxygen was 91.3 [IQR, 66.6–133.5] mmHg.
Table 2
Laboratory tests at ICU admission in 239 critically ill patients with COVID-19
Laboratory tests at ICU admission
All patients (n = 239)
Non-survivors (n = 147)
Survivors (n = 92)
p value, survivors vs non-survivors
Hemoglobin, g/L
124.9 ± 17.9
124.8 ± 17.3
124.9 ± 19.0
0.966
White blood cell count, × 109/L
7.9 [5.2–10.7]
8.2 [5.1–11.0]
7.2 [5.2–10.4]
0.444
Neutrophil count, × 109/L
6.9 [4.0–19.7]
7.2 [4.0–9.7]
6.5 [4.0–9.3]
0.485
Lymphocytes, × 109/L
0.6 [0. 5–0.8]
0.6 [0.4–0.8]
0.7 [0.50–0.9]
0.008
Lymphocyte count < 1.1 × 109/L†
219 (91.6%)
139 (94.6%)
80 (87.0%)
0.036
Lymphocyte count < 0.55 × 109/L
103 (43.1%)
73 (50.0%)
30 (32.6%)
0.007
Platelets, × 109 /L
175 [125–219]
160 [110–206]
186 [148–232]
< 0.001
Platelet count < 125 × 109 /L‡
59 (24.7%)
48 (32.7%)
11 (12.0%)
< 0.001
PT, s
11.9 ± 1.7
12.0 ± 1.8
11.6 ± 1.4
0.079
APTT, s
29.3 ± 9.0
29.3 ± 8.9
29.4 ± 10.9
0.988
Total bilirubin, μmol/L
12.5 [10.3–16.8]
13.0 [10.8–18.7]
11.7 [9.5–15.8]
0.029
ALT, U/L
36 [22–56]
35 [21–54]
39 [26–59]
0.210
AST, U/L
41 [33–62]
45 [35–64]
38 [31–61]
0.051
Serum creatinine, U/L
72.1 [58–85.3]
73.2 [59.7–92.5]
70.2 [54.1–81.8]
0.018
hsTNI, pg/mL
85.5 [35.5–133.5]
91.0 [44.0–134.0]
80.0 [30.0–32.0]
0.410
Myoglobin, ng/mL
105.0 [54.0–155.0]
100.0 [54.0–150.0]
110.5 [56.0–162.5]
0.454
IL-6, pg/mL‖
9.1 [6.7–12.0]
9.1 [7.1–12.9]
9.1 [6.2–11.7]
0.385
Elevated IL-6 level¶
185 (77.4%)
119 (81.0%)
66 (71.7%)
0.068
Arterial blood gas analysis*
pH
7.46 ± 0.07
7.46 ± 0.08
7.45 ± 0.05
0.496
pO2/FiO2, mm Hg
91.3 [66.6–133.5]
82.4 [61.6–120.4]
109.0 [77.5–155.6]
0.005
pCO2, mmHg
35.1 ± 10.8
35.6 ± 12.9
34.4 ± 6.0
0.477
HCO3−, mmol/L
24.4 ± 4.0
24.3 ± 4.4
24.5 ± 3.3
0.839
COVID-19 coronavirus disease 2019, ICU intensive care unit, PT prothrombin time, APTT activated partial thromboplastin time, ALT alanine aminotransferase, AST aspartate aminotransferase, hsTNI hypersensitive troponin I, IL-6 interleukin 6, pO2 partial pressure of oxygen, FiO2 fraction of inspired oxygen, pCO2 partial pressure of carbon dioxide
Data were expressed median [interquartile range] or as mean ± standard deviation
†The lower limit of normal range of lymphocyte count was 1.1 × 109/L
‡The lower limit of normal range of platelet count was 125 × 109/L
‖IL-6 analysis was conducted in 114 non-survivors and 67 survivors
¶The upper limit of normal range was 7 pg/ml
*Arterial blood gas analysis was conducted in 101 non-survivors and 64 survivors
Complications, treatments, and medications
Complications of 239 critically ill patients included ARDS in 164 (68.6%) patients, acute cardiac injury in 103 (43.1%) patients, liver dysfunction in 191 (79.9%) patients, AKI in 119 (49.8%) patients, coagulopathy in 150 (62.7%) patients, bacterial pneumonia in 25 (10.5%) patients, and bacteremia 10 (4.2%) patients (Table 3). Chronologically, liver dysfunction, ARDS, coagulopathy, acute cardiac injury, and AKI occurred 13.5 days, 15.5 days, 17 days, 18.5 days, and 19 days after the symptom onset, respectively (Fig. 2).
Table 3
Complications, treatments, and medications in 239 critically ill patients with COVID-19
Characteristics
All patients (n = 239)
Non-survivors (n = 147)
Survivors (n = 92)
p value, survivors vs non-survivors
Complications
ARDS
164 (68.6%)
118 (80.3%)
46 (50.0%)
< 0.001
Acute cardiac injury
103 (43.1%)
81 (55.1%)
22 (23.9%)
< 0.001
AKI
119 (49.8%)
99 (67.4%)
20 (21.7%)
< 0.001
Liver dysfunction
191 (79.9%)
127 (86.4%)
64 (69.6%)
< 0.001
Coagulopathy
150 (62.7%)
111 (75.5%)
39 (42.4%)
< 0.001
Hospital-acquired infection
Bacterial pneumonia
25 (10.5%)
16 (10.9%)
9 (9.8%)
0.484
Bacteremia
10 (4.2%)
8 (5.4%)
2 (2.2%)
0.187
Urinary tract infection
5 (2.1%)
4 (2.7%)
1 (1.1%)
0.652
Treatments
Mechanical ventilation
165 (69.0%)
119 (81.0%)
46 (50.0)
< 0.001
Invasive
79 (33.1%)
71 (48.3%)
8 (8.7%)
< 0.001
Noninvasive
136 (56.1%)
95 (64.6%)
41 (43.6%)
0.002
Noninvasive + invasive
50 (20.9%)
47 (32.0%)
3 (3.3%)
< 0.001
Extracorporeal membrane oxygenation
9 (3.8%)
9 (6.1%)
0 (0.0%)
0.011
Renal replacement therapy
12 (5.0%)
11 (7.5%)
1 (1.1%)
0.022
Medications
Antiviral agents
132 (55.2%)
82 (55.8%)
50 (54.5%)
0.466
Arbidol
77 (32.2%)
46 (31.3%)
31 (33.7%)
0.776
Interferon alpha
91 (38.1%)
56 (38.1%)
35 (38.0%)
1.000
Oseltamivir
59 (24.7%)
32 (21.8%)
27 (29.4%)
0.218
Lopinavir/ritonavir
38 (15.9%)
24 (16.3%)
14 (15.2%)
0.858
Ribavirin
13 (5.4%)
6 (4.1%)
7 (7.6%)
0.255
Ganciclovir
41 (17.2%)
21 (14.3%)
20 (21.7%)
0.159
Antibacterial agents
229 (95.8%)
144 (98.0%)
85 (92.4%)
0.041
Methylprednisolon
189 (79.1%)
118 (80.3%)
71 (77.2%)
0.339
Commutative dosages, median [IQR], mg
360 [200–580]
370 [160–640]
320 [240–580]
0.517
Dose, methylprednisolon equivalent/days, mg
60.9 ± 21.7
64.6 ± 23.0
54.7 ± 17.9
0.0021
Duration of methylprednisolon, days
6 [4–10]
6 [3–10]
7 [5–11]
0.0345
Immunoglobulin
138 (57.7%)
94 (64.0%)
44 (47.8%)
0.010
Thymosin α1
103 (43.10)
67 (45.6%)
36 (39.1%)
0.199
Length of ICU stay, median [IQR], days
17 [10–26]
12 [8–18]
26.5 [19–46.5]
< 0.001
ARDS acute respiratory distress syndrome, AKI acute kidney injury, IQR interquartile range
In 49 patients with data on negative conversion of SARS-CoV-2 RNA, the median duration since symptom onset was 30 (range 6–81) days. Among these patients, 20 (40.8%) patients tested positive for SARS-CoV-2 IgM (Fig. 3).
Fig. 3
Durations of negative conversion of SARS-CoV-2 RNA in 49 critically ill survivors. Each bar indicates one survivor and the height of bars indicates duration between symptom onset and the day of last positive test for SARS-CoV-2 RNA. The red plus markers indicate the last positive tests of SARS-CoV-2 IgM. SARS-CoV-2, severe acute respiratory coronavirus 2; COVID-19, coronavirus disease 2019
×
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One hundred and sixty-five (69.0%) patients received mechanical ventilation (MV). Of these patients, 29 (17.6%) patients only received invasive ventilation (IMV), 86 (52.1%) patients only received noninvasive ventilation (NIV), and the remaining 50 (30.3%) patients received both, including only 1 patient receiving NIV after removal of endotracheal tube.
Of all patients, 9 (3.8%) patients with refractory hypoxemia received salvage therapy of extracorporeal membrane oxygenation (ECMO), while 12 (5.0%) patients received renal replacement therapy.
Antimicrobial and antiviral agents were given to 229 (95.8%) and 132 (55.2%) patients, respectively. The different antiviral therapy was summarized in Table 3. Methylprednisolone, the only type of glucocorticoids used, was given to 189 (79.1%) patients, with a median commutative dosage of 360 [IQR, 200–560] mg, and the mean daily dose of methylprednisolone was 60.9 ± 21.7 mg.
Mortality at 60 days and its predictors
One hundred and forty-seven (61.5%) patients deceased by 60 days after ICU admission. Twenty-eight patients deceased before receiving MV, comprising 2 patients with do-not-resuscitate, and 26 patients due to extra-respiratory causes. For 112 patients aged 65 years or older, 82 (73.2%) deceased, and for 127 patients under 65 years old, 65 (51.2%) deceased (Fig. 4). The mean duration between symptom onset and decease was 24.5 days (Fig. 2). The median duration between ICU admission and decease was 12 (range 3–36).
Fig. 4
Survival curves of 239 critically ill patients with COVID-19. The number of patients ≥ 65 years and patients < 65 years was 112 and 127, respectively. COVID-19, coronavirus disease 2019
×
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Of all critically ill patients, by April 5th, 2020, 85 (35.6%) patients had been discharged, including 5 patients on oxygen therapy using common nasal cannula at home. Seven patients were still being hospitalized, and their oxygen therapy comprised common nasal cannula in 5 patients, high-flow nasal cannula in 1 patient, and invasive ventilator in 1 patient.
In univariate analysis, in comparison with survivors, non-survivors were older (65.7 ± 12.2 years vs 57.5 ± 13.5 years, p < 0.001) with more patients older than 65 years (55.8% vs 32.6%, p < 0.001) (Table 1), higher APACHE II scores (15 [IQR, 13–17] in 90 patients vs 13 [IQR, 11–15] in 74 patients, p = 0.006) (Table 1), higher SOFA scores (5 [IQR, 5–7] in 90 patients vs 5 [IQR, 5–6] in 74 patients, p = 0.0163) (Table 1), less counts of lymphocytes (0.6 [IQR, 0.4–0.8] × 109/L vs 0.67 [IQR, 0.5–0.9] × 109/L, p = 0.008) with more patients with lymphocyte count less than 1.1 × 109/L (94.6% vs 87.0%, p = 0.036) and more with lymphocyte count less than 0.55 × 109/L (50.0% vs 32.6%, p = 0.007), less counts of platelets (160 [IQR, 110–206] vs 186 [IQR, 148–232], p < 0.001) with more patients with platelet count less than 125 × 109/L (32.7% vs 12.0%, p < 0.001). Compared with survivors, more non-survivors developed ARDS (80.3% % vs 50.0%, p < 0.001), acute cardiac injury (55.1% vs 23.9%, p < 0.001), AKI (67.4% vs 21.7%, p < 0.001), liver dysfunction (86.4% vs 69.6%, p < 0.001), and coagulopathy (75.5% vs 42.4%, p < 0.001). No significant difference between the two groups was identified in pharmacological therapies, except immunoglobulin (94 (64.0%) in survivors vs 44 (47.8%) in non-survivors, p = 0.010) (Table 3). Survivors had significantly longer length of ICU stay than non-survivors (26.5 [19–46.5] days vs 12 [8‐18] days, p < 0.001) (Table 3).
The unviable analysis result (columns 2–4 in Table 4) shows the risk effect in survival time solely determined by a predictor, without considering its relation with other risk factors. The multivariable Cox model result can be interpreted, and when multiple risk factors present simultaneously, some factors may be able to delegate the other factors’ risk effects. Cox proportional-hazards regression analysis stratified by study center revealed that age older than 65 years (hazards ratio (HR), 1.57 (95% CI 1.12–2.19), P = 0.009), platelet count less than 125 × 109/L at ICU admission (HR 2.01, (95%CI, 1.39–2.91), p < 0.001), ARDS (HR 1.67 (95%CI, 1.05–2.64), P = 0.029), and AKI (HR 2.06, (CI, 1.36 to 3.10), p = 0.001) were independent predictors of 60-day mortality (Table 4).
Table 4
Predictors of 60-day mortality in 239 critically ill patients with COVID-19 identified using Cox proportional-hazards model
Characteristics
Non-survivors (n = 147)
Survivors (n = 92)
p value
Cox proportional-hazards model
Hazard ratio (95% confidence interval)
p value
Age ≥ 65
82 (55.8%)
30 (32.6%)
< 0.001
1.57 (1.12–2.19)
0.009
Malignancy
11 (7.5%)
2 (2.2%)
0.066
1.62 (0.84–3.14)
0.149
Lymphocyte count < 0.55 × 109/L†
73 (50.0%)
30 (32.6%)
0.007
1.23 (0.88–1.73)
0.226
Platelet count < 125 × 109 /L‡
48 (32.7%)
11 (12.0%)
< 0.001
2.01 (1.39–2.91)
< 0.001
ARDS
118 (80.3%)
46 (50.0%)
< 0.001
1.67 (1.05–2.64)
0.029
Acute cardiac injury
81 (55.1%)
22 (23.9%)
< 0.001
0.88 (0.57–1.34)
0.542
AKI
99 (67.4%)
20 (21.7%)
< 0.001
2.06 (1.36–3.10)
0.001
Liver dysfunction
127 (86.4%)
64 (69.6%)
< 0.001
1.40 (0.77–2.55)
0.264
Coagulopathy
111 (75.5%)
39 (42.4%)
< 0.001
1.40 (0.88–2.21)
0.156
ARDS acute respiratory distress syndrome, AKI acute kidney injury
Data were expressed as count (%) unless otherwise
†The low limit of normal range of lymphocyte count was 1.1 × 109/L.
‡The low limit of normal range of platelet count was 125 × 109/L
Discussion
In this multicenter retrospective study on critically ill patients with COVID-19, the main findings include that the critically ill patients requiring ICU admission and mechanical ventilation or oxygen therapy with FiO2 greater than or equal to 60% had a considerable 60-day mortality and that age older than 65 years, thrombocytopenia at ICU admission, ARDS, and AKI were independent predictors of 60-day mortality of these patients.
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After excluding all the patients included in the previous study and incorporating two more centers, the mortality we found in the present study was similar to our previous study [2]. Compared to the present study, the previous study was a preliminary casualty report with a smaller sample size. On February 17th, the Chinese CDC stated that of 2087 critically ill patients with COVID-19, the case fatality rate was 49.0% [18]. The study was somewhat cross-sectional. It is impossible that 51.0% of patients in the denominator had been treated more than 60 days or discharged alive, so it is reasonable that the mortality rate of critically ill patients should be higher than 49.0%. According to the official guidelines, critically ill patients were those who need mechanical ventilator support, are in shock, or need supports for other dysfunctional organs [18]. The mortality of critically ill patients with COVID-19 reported in studies outside China was also high. In the first series of critically ill patients with COVID-19 in Washington, USA, the mortality was 67% [19]. In a study of 1591 critically ill patients from Lombardy Region, Italy, 26% deceased and 58% were still in ICU [20]. In another study, 282 (88.1%) of 320 patients who received mechanical ventilation deceased [21].
Advanced age, ARDS, and AKI influenced the mortality of critically ill patients with COVID-19 in an intertwined way. There were debates on whether COVID-19 caused typical ARDS, mainly because some patients were with preserved lung compliance [22]. But a recent postmortem study showed that the fundamental pathological characteristics of pulmonary infection caused by SARS-CoV-2 in critically ill patients were diffuse alveolar damage, which was also the typical pathological finding of severe acute respiratory syndrome and Middle East respiratory syndrome [23]. We believe alveolar damage occurs at early the stage of severe COVID-19, and some of these patients recovered gradually, some deceased in a short time, and the rest deteriorated with alveolar damage progressing, fulfilling the diagnostic criteria of ARDS at some point. Like in critically ill patients with SARS and MERS [24‐26], older critically ill patients with COVID-19 had a higher mortality [2]. In older patients, both the incidence and mortality of ARDS were higher [27‐30]. Both mild-moderate and severe ARDS are associated with a substantial increase in mortality in patients with AKI [31].
Besides the general association among advanced age, ARDS, and AKI, SARS-CoV-2 induces complications by binding to the angiotensin-converting enzyme 2 (ACE2) receptor [5, 32]. Angiotensin-converting enzyme 2 (ACE2), the same cell entry receptor for both SARS-CoV and SARS-CoV-2, plays an important role in organ damages in patients infected by either virus [32‐34]. The primary target organ of SARS-CoV is the lung [35]. In the respiratory tract, angiotensin-converting enzyme 2 (ACE2) is widely expressed on the epithelial cells and macrophages of alveoli, which facilitates the progression of ARDS, and thereafter causes death [3, 34, 36]. As a surface molecule, ACE2 also diffusely locates on epithelial cells of the renal tubules [37]. SARS-CoV particles have been detected in the cytoplasm of these cells in postmortem studies, which explains negative conversion of SARS-CoV in urine [38]. Recently, negative conversion of SARS-CoV-2 RNA in urine has also been confirmed [4]. The destruction of epithelial cells in the renal tubules leads to acute tubular necrosis, the most common form of AKI [37]. In a previous study, advanced age and ARDS are identified as independent risk factors for development of AKI, and AKI was known as an important indicator for death in patients with SARS [39].
The mechanisms of thrombocytopenia in patients with COVID-19 are not clear right now [40]. Mechanisms of SARS-CoV-2-induced thrombocytopenia have been suggested [41, 42]. On one hand, SARS-CoV-2 infects bone marrow cells, thereby causing abnormal hematopoiesis. On the other hand, the lung tissue damages with SARS-CoV-2 infection also cause platelet aggregation and consumption of platelets. The latter has been demonstrated by the findings of hemorrhagic necrosis in pathological examination of lungs from critically ill patients with COVID-19 [43].
In the process of diagnosing and treating patients with COVID, qualitative evaluations (positive or negative) of samples from the respiratory tract are widely used [44, 45]. In some studies, quantitative evaluations are mainly used in exploratory studies, showing that a high load of SARS-CoV-2 may be an indicator of the severity of infection [46, 47]. A median (range) duration of 30 (6–81) days between symptom onset and negative conversion of SARS-CoV-2 RNA in some critically ill survivors is surprising. The inability to clear off the virus in a short time may lead to a prolonged period of critical condition in these patients. But whether they can still spread the virus needs further study [48]. Studies on antibody responses against SARS-CoV-2 are also needed.
Our previous study showed that compared with survivors, non-survivors were more likely to have preexisting comorbidities, which were not identified in the present study, except malignancy in univariate analysis [2]. The major reason was the exclusion of patients who deceased within 48 h after ICU admission. This is one limitation of the present study. In a study of patients with COVID-19 including 137 survivors and 54 non-survivors, Zhou et al. conducted a multivariable logistic regression analysis to identify risk factors of death without including severe complications after hospital admission [7]. We conducted the present study to explore the treating effect of critical care deeply by excluding the dying patients who deceased in 48 h after ICU admission. Different predicting effects of preexisting comorbidities will be identified due to different study designs [49]. The second limitation was that some important information was not available, especially PO2/FiO2, which caused a failure to include APACH II score into the Cox proportional-hazards regression model. Third, 80% of included patients were from Jin-yintan Hospital, and all included patients from Jin-yintan Hospital were transferred from other hospitals. The details of treatment before admission to Jin-yintan Hospital were unavailable. But treating patients in designated hospitals was one paramount measure in dealing with the COVID-19 epidemic [50]. And we conducted Cox proportional-hazards regression stratified by study centers. Fourth, the sample size is not large enough, and other variables remain to be explored. We are expecting further studies.
Conclusion
The mortality of critically ill patients with COVID-19 is considerably high and age older than 65 years, thrombocytopenia at ICU admission, ARDS, and AKI are independent predictors of 60-day mortality. The duration between symptom onset and negative conversion of SARS-CoV-2 RNA and its association with the severity of critically ill patients should be seriously considered in treating patients with COVID-19 and needs to be studied.
We thank all patients and their families involved in the study. We thank Yuwen Li, MD, PhD, Assistant Professor of Pediatrics and Assistant Director of Molecular Genetics and Cytogenetics, Hayward Genetics Center, Tulane University School of Medicine, for language editing and valuable suggestions.
Ethics approval and consent to participate
The case series was approved by Ethics Committee of Jin Yin-tan Hospital (KY-2020-23.01). Written informed consent was waived owing to the rapid emergence of this infectious disease.
Consent for publication
Written informed consent for publication was obtained from all authors.
Competing interests
All the authors state that there are no conflicts of interest related to this study.
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Clinical course and predictors of 60-day mortality in 239 critically ill patients with COVID-19: a multicenter retrospective study from Wuhan, China
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