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. 2020 Oct 14;24:607. doi: 10.1186/s13054-020-03339-x

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© The Author(s) 2020

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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Fig. 1 — Platelet-related indicators and their dynamic changes that associated with prognosis of severe or critically ill COVID-19 patients. a association between baseline platelet count (PLT) and prognosis of patients; b association between baseline mean platelet volume (MPV) and prognosis of patients; c association between baseline platelet large cell ratio (P-LCR) and prognosis of patients; d association between baseline platelet distribution width (PDW) and prognosis of patients; e trajectory of PLT; f trajectory of MPV; g trajectory of P-LCR; h trajectory of PDW; i association between trajectory of PLT and prognosis of patients; j association between trajectory of MPV and prognosis of patients; k association between trajectory of P-LCR and prognosis of patients; l association between trajectory of PDW and prognosis of patients. Thrombocytocrit (PCT) was not significant after false discovery rate control (P = 0.0545), and the trajectory of PCT was not available because the majority of patients lacked follow-up nodes