TY - JOUR
T1 - Incidence, kinetics, and clinical impact of thrombocytopenia in venovenous ECMO
T2 - insights from the multicenter observational PROTECMO study
AU - PROTECMO Study group
AU - Buchtele, Nina
AU - Tanaka, Kenichi
AU - Tuzzolino, Fabio
AU - Agerstrand, Cara
AU - Ait Hssain, Ali
AU - Riera, Jordi
AU - Schellongowski, Peter
AU - Schmidt, Matthieu
AU - Ramanan, Raj
AU - Balik, Martin
AU - Broman, Lars Mikael
AU - Rizzitello, Nicolo
AU - Szułdrzyński, Konstanty
AU - Gannon, Whitney D.
AU - Fanelli, Vito
AU - Trethowan, Brian
AU - Buscher, Hergen
AU - Alfoudri, Huda
AU - Giani, Marco
AU - Combes, Alain
AU - Grasselli, Giacomo
AU - Lorusso, Roberto
AU - Arcadipane, Antonio
AU - Brodie, Daniel
AU - Martucci, Gennaro
AU - Maclaren, Graeme
AU - Ramanathan, Kollengode
AU - Hara, Yoshitaka
AU - Hoshino, Kota
AU - Aliudin, Jeffrey
AU - Villanueva, Joy Ann
AU - Sallam, Hend
AU - Kwan, Ming Chit
AU - Jeon, Kyeongman
AU - Buabbas, Sarah
AU - Cho, Young Jae
AU - Subramanian, Harikesh
AU - Rivosecchi, Ryan
AU - Cheplic, Collette
AU - Nunez, Jose
AU - Grandin, Wilson E.
AU - Rice, Todd W.
AU - Galvagno, Samuel
AU - Menaker, Jay
AU - Tabatabai, Ali
AU - Cavayas, Yiorgos Alexandros
AU - Abrams, Darryl
AU - Serra, Alexis
AU - Holsworth, Tyler
AU - Rizzo, Monica
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Background: Thrombocytopenia is a recognized risk factor for bleeding during extracorporeal membrane oxygenation (ECMO). This study determines the incidence, risk factors, and clinical relevance of thrombocytopenia and platelet transfusions during venovenous (VV) ECMO. Methods: The multicenter, prospective observational PROTECMO study included 652 adult patients who received VV ECMO for respiratory failure. Thrombocytopenia was classified as mild (100–149·109/L), moderate (50–99·109/L), or severe (< 50·109/L). Bleeding events were evaluated using a modified Bleeding Academy Research Consortium score. Cox proportional hazards and logistic regression analyses were done to identify predictors, and quantify the association between platelet counts and bleeding risk. Results: A total of 182 patients (27.9%) had thrombocytopenia at baseline (mild in 14.7%, moderate in 8.7%, and severe in 4.4%). Thrombocytopenia during ECMO, at least once in 80.2% of patients, was mild in 21.3% of cases, moderate in 32.2%, and severe in 26.7%. A 10·109/L decrease in platelet count was associated with a 3.7% (95% CI: 2.4–5.0%) increase in risk of bleeding. There was no strong evidence of nonlinear relationship within the platelet count range between 25,000 and 300,000. This relation remained consistent across all ECMO weeks. Mild thrombocytopenia increased the risk of experiencing a bleeding event by 61% (hazard ratio (HR) 1.611, 95% CI 1.230–2.109, p = 0.0005), while moderate and severe thrombocytopenia increased the risk by roughly 90% (moderate: HR 1.944 (CI 1.484–2.545), p < 0.0001; severe: HR 1.876 (CI 1.275–2.7680), p = 0.0014). The risk for thrombocytopenia < 100·109/L during ECMO significantly increased with ICU days prior to ECMO start, postoperative admission, immunocompromised state, renal replacement therapy, septic shock, low hemoglobin, and circuit exchange. Conclusions: Thrombocytopenia is highly prevalent in VV ECMO, and associated with a significant increase in the risk of bleeding, and a reduction in 6-month survival, particularly at platelet counts below 100·109/L. Further research is needed to better define the outcomes associated with specific thresholds for transfusion of platelets.
AB - Background: Thrombocytopenia is a recognized risk factor for bleeding during extracorporeal membrane oxygenation (ECMO). This study determines the incidence, risk factors, and clinical relevance of thrombocytopenia and platelet transfusions during venovenous (VV) ECMO. Methods: The multicenter, prospective observational PROTECMO study included 652 adult patients who received VV ECMO for respiratory failure. Thrombocytopenia was classified as mild (100–149·109/L), moderate (50–99·109/L), or severe (< 50·109/L). Bleeding events were evaluated using a modified Bleeding Academy Research Consortium score. Cox proportional hazards and logistic regression analyses were done to identify predictors, and quantify the association between platelet counts and bleeding risk. Results: A total of 182 patients (27.9%) had thrombocytopenia at baseline (mild in 14.7%, moderate in 8.7%, and severe in 4.4%). Thrombocytopenia during ECMO, at least once in 80.2% of patients, was mild in 21.3% of cases, moderate in 32.2%, and severe in 26.7%. A 10·109/L decrease in platelet count was associated with a 3.7% (95% CI: 2.4–5.0%) increase in risk of bleeding. There was no strong evidence of nonlinear relationship within the platelet count range between 25,000 and 300,000. This relation remained consistent across all ECMO weeks. Mild thrombocytopenia increased the risk of experiencing a bleeding event by 61% (hazard ratio (HR) 1.611, 95% CI 1.230–2.109, p = 0.0005), while moderate and severe thrombocytopenia increased the risk by roughly 90% (moderate: HR 1.944 (CI 1.484–2.545), p < 0.0001; severe: HR 1.876 (CI 1.275–2.7680), p = 0.0014). The risk for thrombocytopenia < 100·109/L during ECMO significantly increased with ICU days prior to ECMO start, postoperative admission, immunocompromised state, renal replacement therapy, septic shock, low hemoglobin, and circuit exchange. Conclusions: Thrombocytopenia is highly prevalent in VV ECMO, and associated with a significant increase in the risk of bleeding, and a reduction in 6-month survival, particularly at platelet counts below 100·109/L. Further research is needed to better define the outcomes associated with specific thresholds for transfusion of platelets.
KW - Anticoagulation
KW - Bleeding
KW - Intensive care
KW - Platelet kinetics
KW - Predictors
KW - Thrombocytopenia
KW - VV ECMO
UR - https://www.scopus.com/pages/publications/105013239175
U2 - 10.1186/s13054-025-05569-3
DO - 10.1186/s13054-025-05569-3
M3 - Article
C2 - 40775790
AN - SCOPUS:105013239175
SN - 1364-8535
VL - 29
JO - Critical Care
JF - Critical Care
IS - 1
M1 - 349
ER -