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Thrombocytopenia and platelet transfusions in ICU patients: an international inception cohort study (PLOT-ICU)

  • Carl Thomas Anthon
  • , Frédéric Pène
  • , Anders Perner
  • , Elie Azoulay
  • , Kathryn Puxty
  • , Andry Van De Louw
  • , Andreas Barratt-Due
  • , Sanjay Chawla
  • , Pedro Castro
  • , Pedro Póvoa
  • , Luis Coelho
  • , Victoria Metaxa
  • , Matthias Kochanek
  • , Tobias Liebregts
  • , Thomas Kander
  • , Johanna Hästbacka
  • , Jo Bønding Andreasen
  • , Edwige Péju
  • , Lene Bjerregaard Nielsen
  • , Christine Lodberg Hvas
  • Etienne Dufranc, Emmanuel Canet, Linda Lundqvist, Christopher John Wright, Lene Russell*, The PLOT-ICU Collaborators and the Nine-I Study Group
*Corresponding author for this work
  • Rigshospitalet
  • Hospital Cochin
  • University of Copenhagen
  • Paris Hospitals and Paris Descartes University
  • Glasgow Royal Infirmary
  • The Pennsylvania State University
  • Oslo University Hospital
  • Memorial Sloan-Kettering Cancer Center
  • Weill Cornell Medicine
  • University of Barcelona
  • San Francisco Xavier Hospital
  • NOVA University Lisbon
  • King's College London
  • University Hospital Cologne
  • Essen University Hospital
  • Lund University
  • Skåne University Hospital
  • University of Helsinki
  • Tampere University Hospital
  • Aalborg University Hospital
  • Aarhus University Hospital
  • Hospital Henri Mondor
  • University Hospital of Nantes
  • the Queen Elisabeth University Hospital
  • Copenhagen University Hospital

Research output: Contribution to journal › Journal article › Research › peer-review

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Abstract

Purpose: Thrombocytopenia (platelet count < 150 × 109/L) is common in intensive care unit (ICU) patients and is likely associated with worse outcomes. In this study we present international contemporary data on thrombocytopenia in ICU patients. Methods: We conducted a prospective cohort study in adult ICU patients in 52 ICUs across 10 countries. We assessed frequencies of thrombocytopenia, use of platelet transfusions and clinical outcomes including mortality. We evaluated pre-selected potential risk factors for the development of thrombocytopenia during ICU stay and associations between thrombocytopenia at ICU admission and 90-day mortality using pre-specified logistic regression analyses. Results: We analysed 1166 ICU patients; the median age was 63 years and 39.5% were female. Overall, 43.2% (95% confidence interval (CI) 40.4–46.1) had thrombocytopenia; 23.4% (20–26) had thrombocytopenia at ICU admission, and 19.8% (17.6–22.2) developed thrombocytopenia during their ICU stay. Absence of acquired immune deficiency syndrome (AIDS), non-cancer-related immune deficiency, liver failure, male sex, septic shock, and bleeding at ICU admission were associated with the development of thrombocytopenia during ICU stay. Among patients with thrombocytopenia, 22.6% received platelet transfusion(s), and 64.3% of in-ICU transfusions were prophylactic. Patients with thrombocytopenia had higher occurrences of bleeding and death, fewer days alive without the use of life-support, and fewer days alive and out of hospital. Thrombocytopenia at ICU admission was associated with 90-day mortality (adjusted odds ratio 1.7; 95% CI 1.19–2.42). Conclusion: Thrombocytopenia occurred in 43% of critically ill patients and was associated with worse outcomes including increased mortality. Platelet transfusions were given to 23% of patients with thrombocytopenia and most were prophylactic.

Original languageEnglish
JournalIntensive Care Medicine
Volume49
Issue number11
Pages (from-to)1327-1338
ISSN0342-4642
DOIs
Publication statusPublished - Nov 2023

Funding

Open access funding provided by Royal Library, Copenhagen University Library. This study was funded by the Research Council of Rigshospitalet, the Ehrenreich’s Foundation, and the Dagmar Marshalls Foundation. The Memorial Sloan Kettering Cancer Center part of the study was supported by the Core Grant, Grant/Award Number: P30CA008748; Department of Anaesthesiology & Critical Care Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States of America. None of the funders had any influence on the design, conduct or reporting of the study. The Department of Intensive Care at Rigshospitalet (CTA, AG, MHM, AP, LR) has received funding for other projects from the Novo Nordisk Foundation, Sygeforsikringen ‘danmark’, and Pfizer and has conducted contract research for AM-Pharma. FP has received honoraria for consulting and lectures from Gilead and an institutional grant from Alexion Pharma. AP has received honoraria from Novartis for participation in an advisory board. EA has received research grants from MSD Avenir and Alexion and honoraria for lectures from Alexion, Sanofi and Pfizer. . AVDL has received honoraria from Sanofi for participation in an advisory board. PC has received consulting fees from Sanofi, Gilead, Alexion and Janssen and honoraria for lectures from Merck Sharp & Dohme, Gilead, Alexion and Pfizer. PP has received consulting fees from Sanofi and Gilead and honoraria from Merck Sharp & Dohme, Gilead, Mundipharma and Pfizer for academic and educational work. JH has received consulting fees from Paion and honoraria for lectures from the Finnish Medical Association, Laboratory Medicine and Duodecim. EC received fees for lectures and conference talks and had travel and accommodation expenses related to attending scientific meetings covered by Gilead, Shionogi B.V. and Sanofi-Genzyme. ARH has received honoraria from Pfizer for lectures. MHB has received consulting fees from AM-pharma and Inotrem. Full disclosure forms from all authors are available on the publisher’s website.

Keywords

  • Bleeding
  • Critical illness
  • Intensive care unit
  • Platelet transfusion
  • Thrombocytopenia
  • Thrombosis
  • Hemorrhage/etiology
  • Intensive Care Units
  • Prospective Studies
  • Humans
  • Middle Aged
  • Male
  • Thrombocytopenia/epidemiology
  • Adult
  • Female
  • Retrospective Studies
  • Platelet Transfusion/adverse effects
  • Cohort Studies

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  • Correction: Thrombocytopenia and platelet transfusions in ICU patients: an international inception cohort study (PLOT-ICU)

    Anthon, C. T., Pène, F., Perner, A., Azoulay, E., Puxty, K., Van De Louw, A., Barratt-Due, A., Chawla, S., Castro, P., Póvoa, P., Coelho, L., Metaxa, V., Kochanek, M., Liebregts, T., Kander, T., Hästbacka, J., Andreasen, J. B., Péju, E., Nielsen, L. B. & Hvas, C. L. & 31 others, Dufranc, E., Canet, E., Lundqvist, L., Wright, C. J., Schmidt, J., Uhel, F., Ait-Oufella, H., Krag, M., Cos Badia, E., Díaz-Lagares, C., Menat, S., Voiriot, G., Clausen, N. E., Lorentzen, K., Kvåle, R., Hildebrandt, T., Holten, A. R., Strand, K., Tzalavras, A., Bestle, M. H., Klepstad, P., Fernandez, S., Vimpere, D., Paulino, C., Graça, C., Lueck, C., Juhl, C. S., Costa, C., Bådstøløkken, P. M., Miranda, T. & the PLOT-ICU Collaborators and the Nine-I Study Group, Jan 2024, In: Intensive Care Medicine. 50, 1, p. 154-155

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