Evidence map›Paper›PMID 40456934›Full record

ArticleScientific reports2025

Management of COVID-19 associated coagulopathy in critically ill patients and the risk of acquired von willebrand syndrome.

Hiroyasu Ishikura, Yuhei Irie, Maiko Nakashio, Junichi Maruyama, Yoshihiko Nakamura, Takahiro Yamagaito, Maho Yoshida, Hiroki Hatomoto, Shintaro Yamasaki, Kota Hoshino

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Hiroyasu IshikuraEmergency and Critical Care Center, Rakuwakai Otowa Hospital, 2 Otowachinji-cho, Yamashina-ku, Kyoto, 607-8062, Japan. ishikurah@fukuoka-u.ac.jp.ORCID http://orcid.org/0000-0002-4862-5646
Yuhei IrieEmergency and Critical Care Center, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan- ku, Fukuoka, 814-0180, Japan.
Maiko NakashioEmergency and Critical Care Center, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan- ku, Fukuoka, 814-0180, Japan.
Junichi MaruyamaEmergency and Critical Care Center, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan- ku, Fukuoka, 814-0180, Japan.
Yoshihiko NakamuraEmergency and Critical Care Center, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan- ku, Fukuoka, 814-0180, Japan.
Takahiro YamagaitoSysmex Product Marketing, 1-2-2 Osaki, Shinagawa-ku, Tokyo, 141-0032, Japan.
Maho YoshidaSysmex Scientific Affairs, 1-3-2 Murotani, Nishi-ku, Kobe, 651-241, Japan.
Hiroki HatomotoDepartment of Clinical Engineer Center, Fukuoka University Hospital, Fukuoka, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Shintaro YamasakiDepartment of Clinical Engineer Center, Fukuoka University Hospital, Fukuoka, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180, Japan.
Kota HoshinoEmergency and Critical Care Center, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan- ku, Fukuoka, 814-0180, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the interplay between thrombosis and hemorrhage in critically ill COVID-19 patients, particularly those on extracorporeal membrane oxygenation (ECMO). Forty-three mechanically ventilated patients were divided into ECMO (n = 22) and non-ECMO (n = 21) groups. Thrombotic events occurred similarly in both groups (22.7% in ECMO, 28.6% in non-ECMO), both higher than the approximately 5% observed in patients hospitalized with viral respiratory illnesses other than COVID-19. However, bleeding events were significantly more frequent in the ECMO group (72.7%) compared to the non-ECMO group (14.3%) (P < 0.01). ECMO patients showed decreased platelet counts, fibrinogen, von Willebrand factor (VWF) activity using a ristocetin cofactor (VWF: RCo) assay, and developed acquired von Willebrand syndrome (AvWS) (VWF: RCo/VWF antigen (Ag) ratio < 0.7), along with increased D-dimer and lower high-molecular-weight VWF multimers. In contrast, the non-ECMO group showed no significant changes in platelet counts, fibrinogen, VWF: RCo, or D-dimer. Over time, both VWF: Ag and VWF: RCo increased significantly in both groups, but the VWF: RCo/VWF: Ag ratio remained above 0.7, and high-molecular-weight VWF multimers did not change significantly. These findings emphasize the need for vigilance regarding thrombotic and hemorrhagic complications, particularly in ECMO patients, where ECMO-induced shear stress may lead to AvWS, necessitating monitoring of VWF: Ag and VWF: RCo.

Indexed as

COVID-19von Willebrand DiseasesAdultAgedCritical IllnessExtracorporeal Membrane OxygenationFemaleFibrin Fibrinogen Degradation ProductsFibrinogenHemorrhageHumansMaleMiddle AgedPlatelet CountRespiration, ArtificialSARS-CoV-2Fibrin Fibrinogen Degradation ProductsFibrinogenvon Willebrand FactorAcquired von Willebrand syndromeCoagulopathyCOVID-19HemorrhageThrombosis

Identifiers

PMID40456934
PMCPMC12130217

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.