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Erschienen in: Critical Care 1/2020

Open Access 10.07.2020 | COVID-19 | Research Letter

Classification of COVID-19 in intensive care patients

verfasst von: Xiaofan Lu, Yang Wang, Taige Chen, Jun Wang, Fangrong Yan

Erschienen in: Critical Care | Ausgabe 1/2020

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Xiaofan Lu, Yang Wang, Taige Chen and Jun Wang contributed equally to this work.

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Dear Editor,
Previous studies on coronavirus disease 2019 (COVID-19) mainly described patients’ general information [1]. We aimed to bridge the gap between disease classification and clinical outcome in intensive care patients, which could help in the individual evaluation and provide effective triage for treatment and management.
One hundred fifty-one intensive care patients with complete medical records were obtained from Tongji Hospital in Wuhan, China. Data on the day of admission were collected, including six data categories: demographic information of age and gender, symptoms ([> 10%] fever, fatigue, dry cough, anorexia, myalgia, dyspnea, expectoration, diarrhea), original comorbidities ([> 5%] hypertension, diabetes, cardiovascular disease [CVD], chronic obstructive pulmonary disease [COPD], malignancy), vital signs (respiratory rate, heart rate, blood pressure, SpO2, FiO2), blood routine tests (count of WBC, lymphocyte, neutrophil, platelet and monocyte, red cell distribution width [RDW]), and inflammatory marker measurements (high-sensitivity C-reactive protein [hs-CRP], interleukin-2 receptor [IL-2R], IL-6, IL-8, IL-10, TNF-α). Blood routine tests were also measured at days 3 and 5 since admission, and adjuvant corticosteroid therapy throughout the disease course was retrieved. Clinical outcome was 28-day mortality after admission. The Ethics Commission of Tongji Hospital approved this study, with a waiver of informed consent. We constructed a fully Bayesian latent variable model for integrative clustering of the six data categories [2]. The appropriate clustering number was determined by minimizing the Bayesian information criterion. Only features with high posterior probability (e.g., 0.8) were kept.
We identified four prognostic types of COVID-19 (Fig. 1). The characteristics of the four types were described below (Table 1). Type A: Extremely poor prognosis and elderly enriched; Dry cough, dyspnea, and fatigue were common symptoms; hypertension, diabetes, and CVD were common preexisting medical conditions. Patients presented severe respiratory failure, dramatically elevated counts of WBC and neutrophil, and lymphocyte depletion. Remarkably elevated cytokine occurred, accompanied by later development of ARDS and multiple organ failure. Type B: Poor prognosis and elderly enriched; dyspnea and cough with expectoration were common symptoms, accompanied by diarrhea and anorexia. Unfavorable respiratory condition and decreased lymphocyte count could be observed. Patients presented an imminent elevation of cytokine and a high risk of developing ARDS and multiple organ failure later after treatment. Type C: Intermediate prognosis; symptoms of dry cough and fatigue, and original comorbidity of hypertension were common. The respiratory condition was normal, and most laboratory tests were within normal or moderately elevated. Type D: Favorable prognosis and middle age enriched; primary symptom was cough with expectoration. Patients had stable breathing and most laboratory tests were in a normal range or slightly elevated.
Table 1
Presenting characteristics of four types of COVID-19 in intensive care patients (n = 151)
 
A (n = 37)
B (n = 45)
C (n = 27)
D (n = 42)
Age, years
77 (70–81)
62 (52–70)
65 (51–74)
53 (43–58)
Signs and symptoms
 Cough
26 (70)
45 (100)
12 (44)
34 (81)
 Dyspnea
24 (65)
41 (91)
14 (52)
13 (31)
 Fatigue
19 (51)
27 (60)
21 (78)
1 (2)
 Expectoration
6 (16)
40 (89)
1 (4)
16 (38)
 Diarrhea
5 (14)
20 (44)
7 (26)
9 (21)
 Anorexia
6 (16)
15 (33)
9 (33)
1 (2)
Original comorbidities
 Hypertension
20 (54)
15 (33)
17 (63)
8 (19)
 Diabetes
13 (35)
6 (13)
7 (26)
5 (12)
 CVD
15 (41)
0
6 (22)
2 (5)
Vital signs
 Respiratory rate, rpm
25 (20–32)
22 (20–26)
20 (20–23)
21 (20–25)
 SpO2/FiO2
99 (90–158)
222 (100–294)
297 (237–336)
298 (248–345)
Laboratory findings
Routine blood test
  WBCs, × 109/L
   Day 1
11.1 (8.0–15.5)
7.4 (5.3–10.2)
5.6 (4.5–6.5)
5.2 (3.5–7.2)
   Day 3
12.5 (9.2–17.4)
10.5 (8.3–12.9)
8.3 (5.5–9.3)
6.6 (3.9–8.3)
   Day 5
11.1 (7.4–12.7)
11.5 (7.7–14.6)
6.6 (4.5–7.2)
7.2 (5.1–10.3)
  Absolute lymphocytes, × 109/L
   Day 1
0.5 (0.3–0.7)
0.7 (0.5–1.0)
0.8 (0.7–1.2)
1.0 (0.7–1.4)
   Day 3
0.4 (0.3–0.7)
0.6 (0.4–0.8)
0.8 (0.6–1.7)
0.9 (0.6–1.0)
   Day 5
0.4 (0.3–0.6)
0.8 (0.5–1.3)
0.8 (0.5–1.3)
1.3 (0.8–2.2)
  Absolute neutrophils, ×109/L
   Day 1
9.5 (7.1–15.0)
5.5 (4.3–9.1)
4.2 (3.0–5.1)
3.1 (2.2–5.0)
   Day 3
12.0 (8.2–15.8)
9.5 (7.2–12.0)
5.7 (4.3–8.8)
4.6 (2.5–7.1)
   Day 5
10.2 (6.5–11.8)
10.0 (6.1–13.4)
4.6 (2.7–6.1)
4.7 (3.1–7.2)
  RDW-CV
13.4 (12.8–14.1)
12.2 (11.9–12.8)
12.6 (11.8–13.0)
12.2 (11.8–12.7)
Inflammatory marker
  hs-CRP, mg/L
126 (76–190)
80 (42–109)
19 (5–49)
28 (10–70)
  IL-2R, U/ml
1341 (940–1809)
1038 (678–1185)
701 (430–813)
685 (439–928)
  IL-6, pg/ml
68 (37–137)
43 (21–79)
10 (2–20)
14 (5–30)
  IL-8, pg/ml
42 (21–95)
21 (13–40)
12 (7–24)
15 (10–21)
  IL-10, pg/ml
15 (9–24)
7 (3–11)
3 (3–6)
3 (3–9)
  TNF-α, pg/ml
15 (10–23)
9 (8–11)
7 (5–9)
8 (7–10)
Corticosteroid therapy
28 (76)
38 (84)
13 (48)
27 (64)
Continuous variables were described as median (IQR) while categorical variables were expressed as frequencies (%). All records were measured at admission to intensive care wards unless otherwise indicated. Multiple group comparison was done with Kruskal–Wallis test; proportions for categorical variables were compared using Fisher’s exact test. All calculated P values were less than or equal to 0.001 except for respiratory rate (P = 0.004), absolute lymphocytes at day 3 since admission (P = 0.013), and corticosteroid therapy (P = 0.013)
Abbreviations: CVD cardiovascular disease, rpm breaths per minute, SpO2 peripheral oxygen saturation, FiO2 fraction of inspired oxygen, WBC white blood cell, RDW red cell distribution width
This report, to our knowledge, is the first attempt of dealing with the classification of COVID-19 in intensive care patients. The four prognostic types present a stepwise distribution in age, respiratory condition, and inflammatory markers, suggesting their prognostic efficacy. The specificity of symptoms does not appear to be strong, but gastrointestinal response (e.g., diarrhea) needs vigilance [3]. Unexpectedly, hypertension is more evenly distributed, which contradicts previous study indicating hypertensive with COVID-19 was more likely to be in a high risk of mortality [4]. Notably, types A and B always showed higher content of WBCs and neutrophils, no matter on days 1, 3, or 5 since admission, while types C and D had relatively higher lymphocyte counts compared to other types; such trend seemed not to be affected by corticosteroids even though more patients in types A and B received adjuvant corticosteroids therapy than C and D. Investigations in larger cohorts are required to provide more evidence. The study is limited by ignoring the potential treatment effect. However, such classification could help in better triage, allowing for a more rational allocation of scarce medical resources in a resource-constrained environment.

Acknowledgements

We would like to thank all the hospital staff members for their efforts in collecting the information that was used in this study, and all the patients who consented to donate their data for analysis and the medical staff members who are on the front line of caring for patients.
Ethical approval was waived by the Ethics Committee of Tongji Hospital (Wuhan, China) in view of the retrospective and observational nature of the study, and all the procedures being performed were part of the routine care.
The informed consents of patients were waived by the Ethics Commission of Tongji Hospital (Wuhan, China) for the rapid emergence of this epidemic.

Competing interests

The authors declare that they have no competing interests.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​. 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 in a credit line to the data.

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Metadaten
Titel
Classification of COVID-19 in intensive care patients
verfasst von
Xiaofan Lu
Yang Wang
Taige Chen
Jun Wang
Fangrong Yan
Publikationsdatum
10.07.2020
Verlag
BioMed Central
Schlagwort
COVID-19
Erschienen in
Critical Care / Ausgabe 1/2020
Elektronische ISSN: 1364-8535
DOI
https://doi.org/10.1186/s13054-020-03127-7

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