Platelet transfusion practice in the intensive care unit: the Nine-I international platelet transfusion survey
- PMID: 40627074
- PMCID: PMC12237844
- DOI: 10.1186/s13613-025-01494-4
Platelet transfusion practice in the intensive care unit: the Nine-I international platelet transfusion survey
Abstract
Background: Platelet transfusions are frequent in the Intensive Care Unit (ICU), either as prophylaxis against bleeding complications or as treatment for bleeding. The European Society of Intensive Care Medicine guidelines for ICU patients generally recommend not using prophylactic platelet transfusions unless the platelet count falls below 10 × 109 cells/L in non-bleeding patients and make no recommendation for platelet transfusion threshold in non-massively bleeding patients with thrombocytopenia. Therefore, the decision to transfuse platelets is often left to clinical assessment by the treating physician. This study aims to describe current platelet transfusion preferences among ICU physicians.
Methods: An online, anonymous survey consisting of 43 items was produced in two languages (French and English) and distributed by investigators in the Nine-I research network to ICU physicians in Europe and the United States of America. The survey evaluated platelet transfusion practices in ICU patients with and without bleeding, the presence of local guidelines, and factors influencing the decisions to transfuse platelets. Only completed surveys were analysed.
Results: We received 997 surveys completed by ICU physicians. Overall, there was large heterogeneity in platelet transfusion practices between and within countries. In non-bleeding, thrombocytopenic medical ICU patients, most would transfuse prophylactic platelets at a platelet count threshold of 10 × 109 cells/L. Thirty percent would change their strategy in patients with bone marrow failure and either be more liberal (60%; 95% Confidence Limits 0.54, 0.66), more restrictive (31%; 0.26,0.36) or seek assistance. Higher thresholds were preferred in surgical patients, prior to procedures and in patients with bleeding. Only 173 (17%; 0.15,0.19) responded that they were confident about the clinical indications every time they prescribed a platelet transfusion. As for existing guidelines, only 123 (12%; 0.10,0.15) responded that they always read them. Colleagues' attitudes and departmental culture were important influencers on transfusion practice.
Conclusion: Platelet transfusion practice in the ICU is heterogeneous, both between and within countries; guidelines are often not used, and there is often uncertainty about the clinical indication.
Keywords: Critically ill; Intensive care; Platelet transfusions; Thrombocytopenia.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: Participation in the survey was voluntary, and completion was regarded as informed consent; this information was given to all participants when they opened the electronic survey link. According to national legislation in the European Union and the UK, ethical permissions are not required when conducting surveys of this kind as no patient data were collected. In the USA, local IRB permission was acquired where necessary. No financial support was provided. We did not collect data on locations other than countries, so individual participants could not be traced. All collected data were anonymous and stored on a secure server owned by the Capital region of Copenhagen. Relevant permission from the Research and Innovation Department, Capital Region of Denmark, to store the data was obtained as required. Consent for publication: Not applicable. Competing interests: Dr. Kentish-Barnes’ institution received funding from the French Ministry of Health. Professor Azoulay’s institution received funding from Fisher & Paykel, MSD, Pfizer, Baxter, and Gilead, and he received funding from Gilead, Baxter, Alexion, Ablynx, and Pfizer. Professor Péne has received lecture and consulting fees from GILEAD outside of this work. Dr. Castro has received honoraria for scientific collaboration (Pfizer, MSD, Gilead, AbbVie) and advisory board (Alexion, Janssen, Sanofi, Gilead). Professor Povoa has received honoraria for lectures (Gilead, Pfizer, Mundipharma, MSD) and participation in advisory boards (Biocodex, Gilead). The rest of the authors have no competing interests.
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