Skip to main content
Erschienen in: Critical Care 1/2020

Open Access 01.12.2020 | COVID-19 | Research Letter

Dynamic trajectory of platelet-related indicators and survival of severe COVID-19 patients

verfasst von: Jieyu He, Yongyue Wei, Jiao Chen, Feng Chen, Wei Gao, Xiang Lu

Erschienen in: Critical Care | Ausgabe 1/2020

download
DOWNLOAD
print
DRUCKEN
insite
SUCHEN
Hinweise
Jieyu He and Yongyue Wei contributed equally to the work.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Dear Editor,
Previous studies have found approximately a 30% cumulative incidence for thrombosis in critically unwell patients, almost all whom already present impaired platelets function and activity, with COVID-19 in the intensive care unit (ICU) [1, 2]. We aimed to explore the association between platelet-related laboratory indicators and prognosis in critically ill patients with COVID-19.
All the severe and critically ill COVID-19 patients (Table 1) diagnosed in Huangshi City, Hubei Province, China, till 6 March, 2020, were recruited in this study which were distributed in the three hospitals including Huangshi Central Hospital, Huangshi Hospital of Traditional Chinese Medicine, and Daye People’s Hospital. Laboratory examinations including routine blood tests, lymphocyte subsets, inflammatory or infection-related biomarkers, cardiac, renal, liver and coagulation function tests were obtained at admission and during hospitalization. The baseline laboratory measures with over 40% missing value were excluded from the analysis. Death in 28 days after admission to the hospital was the primary end point of this study. Patients discharge from hospital within 28 days or kept in hospitalization after 28 days were considered as censored outcome. Time-to-event outcome was defined for the following statistical models.
Table 1
Demographic and clinical characteristics at hospitalization of severe or critically ill COVID-19 patients
Characteristics
NMissing (%)
Total (n = 112)
Survived (n = 81)
Dead (n = 31)
Age [mean (SD)]
 
61.0 (14.9)
57.1 (13.8)
71.0 (13.0)
Male [n (%)]
 
73 (65.2)
54 (66.7)
19 (61.3)
Vital signs [mean (SD)]
 Temperature (°C)
2 (1.8)
37.3 (0.8)
37.3 (0.8)
37.2 (0.8)
 Heart rate (beats/min)
29 (25.9)
89.4 (17.7)
87.1 (16.7)
94.4 (19.0)
 Respiratory rate (Breaths/min)
5 (4.5)
24.8 (5.6)
25.1 (5.9)
24.1 (4.9)
Blood pressure (mm Hg)
 Diastolic
5 (4.5)
73.2 (13.7)
73.3 (14.7)
72.8 (11.0)
 Systolic
5 (4.5)
124.9 (17.3)
124.0 (18.0)
127.0 (15.7)
Symptoms [n (%)]
 Fever
 
91 (81.2)
67 (82.7)
24 (77.4)
 Cough
 
86 (76.8)
62 (76.5)
24 (77.4)
 Chest tightness
 
73 (65.2)
56 (69.1)
17 (54.8)
 Fatigue
 
65 (58.0)
54 (66.7)
11 (35.5)
 Shortness of breath
 
34 (30.4)
21 (25.9)
13 (41.9)
 Phlegm
 
28 (25.0)
20 (24.7)
8 (25.8)
 Dyspnea
 
25 (22.3)
14 (17.3)
11 (35.5)
 Diarrhea
 
19 (17.0)
15 (18.5)
4 (12.9)
 Headache
 
9 (8.0)
7 (8.6)
2 (6.5)
 Myalgia
 
6 (5.4)
5 (6.2)
1 (3.2)
 Sore throat
 
5 (4.5)
4 (4.9)
1 (3.2)
 Nausea and vomiting
 
5 (4.5)
2 (2.5)
3 (9.7)
Imaging abnormalitya
 
18 (16.1)
13 (16.0)
5 (16.1)
No. of symptoms [n (%)]
 0
 
2 (1.8)
 
2 (6.5)
 1
 
4 (3.6)
4 (4.9)
 
 2
 
15 (13.4)
10 (12.3)
5 (16.1)
 3
 
20 (17.9)
15 (18.5)
5 (16.1)
 4
 
30 (26.8)
23 (28.4)
7 (22.6)
 5
 
23 (20.5)
16 (19.8)
7 (22.6)
 6
 
12 (10.7)
8 (9.9)
4 (12.9)
 ≥ 7
 
6 (5.4)
5 (6.2)
1 (3.2)
Comorbidities [n (%)]
 Hypertension
 
40 (35.7)
26(32.1)
14 (45.2)
 Respiratory failure
 
27 (24.1)
16 (19.8)
11 (35.5)
 Cardiovascular disease
 
17 (15.2)
10 (12.3)
7 (22.6)
 Diabetes
 
21 (18.8)
15 (18.5)
6 (19.4)
 Acute lung injury
 
14 (12.5)
9 (11.1)
5 (16.1)
 COPDb
 
5 (4.5)
2 (2.5)
3 (9.7)
 Bacterial pneumonia
 
3 (2.7)
2 (2.5)
1 (3.2)
 Hepatic injury
 
3 (2.7)
3 (3.7)
 
 Septic shock
 
3 (2.7)
2 (2.5)
1 (3.2)
 Cerebral infarction
 
2 (1.8)
1 (1.2)
1 (3.2)
 Acute kidney injury
 
1 (0.9)
1 (1.2)
 
 Cerebral hemorrhage
 
1 (0.9)
1 (1.2)
 
 Sepsis
 
1 (0.9)
1 (1.2)
 
N of comorbidities [n (%)]
 0
 
46 (41.1)
36 (44.4)
10 (32.3)
 1
 
26 (23.2)
20 (24.7)
6 (19.4)
 2
 
19 (17.0)
13 (16.0)
6 (19.4)
 3
 
13 (11.6)
7 (8.6)
6 (19.4)
 4
 
4 (3.6)
2 (2.5)
2 (6.5)
 5
 
1 (0.9)
1 (1.2)
0 (0)
 ≥ 6
 
3 (2.7)
2 (2.5)
1 (3.2)
Worst severity in hospital
 Severe
 
63
63
0
 Critical illness [n (%)]
 
49
18
31
SD standard deviation
aIncluding chest radiography and computed tomography (CT)
bChronic obstructive pulmonary disease
The platelet-related indicators included platelet count (PLT), mean platelet volume (MPV), platelet distribution width (PDW), thrombocytocrit (PCT), and platelet large cell ratio (P-LCR). Baseline indicators were dichotomized by the median to low and high groups. For each platelet-related indicator with repeated examinations during hospitalization, trajectory analysis was performed to cluster the patients based on the dynamic time-series trend of the corresponding indicator, using R package traj [3]. According to the requirement of the method, patients during hospitalization with less than four observations of the specific indicator were classified as a separate cluster. Cox proportional hazards model with adjustment for age, gender, number of comorbidities were applied to test the association between dynamic trajectory of platelet-related indicators and overall survival of COVID-19 patients.
The patients at admission with high PLT (HR 0.28; 95% CI 0.11–0.69; P = 0.0057; Fig. 1a) were associated with the preferred survival; however, patients with high PDW (HR 2.52; 95% CI 1.17–5.44; P = 0.0185; Fig. 1b), high MPV (HR 3.73; 95% CI 1.55–9.02; P = 0.0034; Fig. 1c), or high P-LCR (HR 3.00; 95% CI 1.40–6.41; P = 0.0046; Fig. 1d) were significantly associated with the worse survival. On the other hand, dynamic trajectory of PLT couldn’t distinguish patients’ survival (Fig. 1e). However, a similar dynamic trajectory pattern with rapid acceleration in the first 2 weeks followed by a considerable deceleration, was identified for MPV, PLCR, and PDW; patients with such pattern were significantly associated with about 2 to 5 times increased death hazard (Fig. 1f–h). All the above results remained significant after false discovery rate (FDR) control.
The findings of this study were accordant with several evidences suggesting platelets as well as related indicators participating in inflammation and prothrombotic responses in many viral infections [4]. The damage to endothelial cells leads to activation, aggregation, and retention of platelets, and the formation of thrombus at the injured site, which may cause a depletion of platelets and megakaryocytes, resulting in decreased platelets production and increased consumption. In addition to their traditional role in thrombosis and hemostasis, platelets mediate key aspects of inflammatory and immune processes [5]. Platelets have been reported to express surface receptors able to mediate binding and entry of various viruses [6]. In brief, paying close attention to the dynamics of platelet-related indicators of COVID-19 patients will undoubtedly improve our knowledge on diseases progression, but could also bring the improvement in therapeutic options for severe or critically ill patients.

Acknowledgements

We would like to thank all the medical staff for their efforts in collecting the data used in this study, and all the patients who consented to donate their data for analysis and the all medical staff members who are on the front line of caring for patients.
The ethics committee of the hospitals (Huangshi Central Hospital, Huangshi Hospital of Traditional Chinese Medicine, and Daye People’s Hospital) waived the written informed consent from patients with COVID-19, and all the procedures being performed were part of the routine care.
The informed consents of patients were waived by the Ethics Commission of the hospitals (Huangshi Central Hospital, Huangshi Hospital of Traditional Chinese Medicine, and Daye People’s Hospital) for the rapid emergence of this epidemic.

Competing interests

The authors declare no competing financial 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.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Literatur
1.
Zurück zum Zitat Klok FA, Kruip M, van der Meer NJM, Arbous MS, Gommers D, Kant KM, Kaptein FHJ, van Paassen J, Stals MAM, Huisman MV, et al. Incidence of thrombotic complications in critically ill ICU patients with COVID-19. Thromb Res. 2020;191:145–7.CrossRefPubMed Klok FA, Kruip M, van der Meer NJM, Arbous MS, Gommers D, Kant KM, Kaptein FHJ, van Paassen J, Stals MAM, Huisman MV, et al. Incidence of thrombotic complications in critically ill ICU patients with COVID-19. Thromb Res. 2020;191:145–7.CrossRefPubMed
2.
Zurück zum Zitat Thomas W, Varley J, Johnston A, Symington E, Robinson M, Sheares K, Lavinio A, Besser M. Thrombotic complications of patients admitted to intensive care with COVID-19 at a teaching hospital in the United Kingdom. Thromb Res. 2020;191:76–7.CrossRefPubMed Thomas W, Varley J, Johnston A, Symington E, Robinson M, Sheares K, Lavinio A, Besser M. Thrombotic complications of patients admitted to intensive care with COVID-19 at a teaching hospital in the United Kingdom. Thromb Res. 2020;191:76–7.CrossRefPubMed
3.
Zurück zum Zitat Leffondré K, Abrahamowicz M, Regeasse A, Hawker GA, Badley EM, Belzile E. Statistical measures were proposed for identifying longitudinal patterns of change in quantitative health indicators. J Clin Epidemiol. 2004;57(10):1049–62.CrossRef Leffondré K, Abrahamowicz M, Regeasse A, Hawker GA, Badley EM, Belzile E. Statistical measures were proposed for identifying longitudinal patterns of change in quantitative health indicators. J Clin Epidemiol. 2004;57(10):1049–62.CrossRef
4.
Zurück zum Zitat Hottz ED, Bozza FA, Bozza PT. Platelets in immune response to virus and immunopathology of viral infections. Front Med (Lausanne). 2018;5:121.CrossRefPubMed Hottz ED, Bozza FA, Bozza PT. Platelets in immune response to virus and immunopathology of viral infections. Front Med (Lausanne). 2018;5:121.CrossRefPubMed
5.
Zurück zum Zitat Guo L, Rondina MT. The era of thromboinflammation: platelets are dynamic sensors and effector cells during infectious diseases. Front Immunol. 2019;10:2204.CrossRefPubMed Guo L, Rondina MT. The era of thromboinflammation: platelets are dynamic sensors and effector cells during infectious diseases. Front Immunol. 2019;10:2204.CrossRefPubMed
6.
Zurück zum Zitat Chabert A, Hamzeh-Cognasse H, Pozzetto B, Cognasse F, Schattner M, Gomez RM, Garraud O. Human platelets and their capacity of binding viruses: meaning and challenges? BMC Immunol. 2015;16:26.CrossRefPubMed Chabert A, Hamzeh-Cognasse H, Pozzetto B, Cognasse F, Schattner M, Gomez RM, Garraud O. Human platelets and their capacity of binding viruses: meaning and challenges? BMC Immunol. 2015;16:26.CrossRefPubMed
Metadaten
Titel
Dynamic trajectory of platelet-related indicators and survival of severe COVID-19 patients
verfasst von
Jieyu He
Yongyue Wei
Jiao Chen
Feng Chen
Wei Gao
Xiang Lu
Publikationsdatum
01.12.2020
Verlag
BioMed Central
Schlagwort
COVID-19
Erschienen in
Critical Care / Ausgabe 1/2020
Elektronische ISSN: 1364-8535
DOI
https://doi.org/10.1186/s13054-020-03339-x

Weitere Artikel der Ausgabe 1/2020

Critical Care 1/2020 Zur Ausgabe

Update AINS

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.