TY - JOUR
T1 - Immature platelets as a novel biomarker for adverse cardiovascular events in patients after non-cardiac surgery
AU - Anetsberger, Aida
AU - Blobner, Manfred
AU - Haller, Bernhard
AU - Schmid, Sebastian
AU - Umgelter, Katrin
AU - Hager, Theresa
AU - Langgartner, Clemens
AU - Kochs, Eberhard F.
AU - Laugwitz, Karl Ludwig
AU - Jungwirth, Bettina
AU - Bernlochner, Isabell
N1 - Publisher Copyright:
© Schattauer 2017.
PY - 2017
Y1 - 2017
N2 - This study evaluates whether immature platelets (IPF) determined in the post anesthesia care unit (PACU) can predict major adverse cardiovascular events (MACE) or other thromboembolic events after intermediate and high-risk surgery. IPF are increased in patients with acute coronary syndrome and recently gained interest as novel biomarker for risk stratification. In this prospective observational trial 732 patients undergoing intermediate or high-risk non-cardiac surgery were enrolled (NCT02097602). IPF was measured preoperatively and postoperatively in the PACU. Primary outcome was a composite endpoint defined as MACE, deep vein thrombosis or pulmonary embolism during hospital stay (modMACE). A cut off for IPF identifying a threshold between a low and high risk for modMACE was calculated by logrank optimization. A multivariate Cox regression was calculated in a forward stepwise manner to assess the relation between this IPF cut off and modMACE as well as other established risk factors (inclusion if p<0.05). Preoperatively, there were no differences in IPF between patients with and without modMACE (3.1 % [2.2 % – 4.7 %](median [interquartile range]) vs. 2.8 % [1.9 % – 4.3 %]. Patients with modMACE (28 of 730 patients; 3.8 %) had higher IPF values in the PACU compared to patients without modMACE (3.6 % [2.6–6 %] vs. 2.9 % [2–4.4 %]; p=0.011). The optimal cut off of IPF > 5.4 % was associated with an increased risk for modMACE after adjustment for covariates (hazard ratio: 2.528; 95 % confidence interval: 1.156 to 5.528, p=0.02). In conclusion, IPF is an independent predictor of modMACE after surgery and might improve risk stratification of surgical patients.
AB - This study evaluates whether immature platelets (IPF) determined in the post anesthesia care unit (PACU) can predict major adverse cardiovascular events (MACE) or other thromboembolic events after intermediate and high-risk surgery. IPF are increased in patients with acute coronary syndrome and recently gained interest as novel biomarker for risk stratification. In this prospective observational trial 732 patients undergoing intermediate or high-risk non-cardiac surgery were enrolled (NCT02097602). IPF was measured preoperatively and postoperatively in the PACU. Primary outcome was a composite endpoint defined as MACE, deep vein thrombosis or pulmonary embolism during hospital stay (modMACE). A cut off for IPF identifying a threshold between a low and high risk for modMACE was calculated by logrank optimization. A multivariate Cox regression was calculated in a forward stepwise manner to assess the relation between this IPF cut off and modMACE as well as other established risk factors (inclusion if p<0.05). Preoperatively, there were no differences in IPF between patients with and without modMACE (3.1 % [2.2 % – 4.7 %](median [interquartile range]) vs. 2.8 % [1.9 % – 4.3 %]. Patients with modMACE (28 of 730 patients; 3.8 %) had higher IPF values in the PACU compared to patients without modMACE (3.6 % [2.6–6 %] vs. 2.9 % [2–4.4 %]; p=0.011). The optimal cut off of IPF > 5.4 % was associated with an increased risk for modMACE after adjustment for covariates (hazard ratio: 2.528; 95 % confidence interval: 1.156 to 5.528, p=0.02). In conclusion, IPF is an independent predictor of modMACE after surgery and might improve risk stratification of surgical patients.
KW - Immature platelet fraction
KW - Major adverse events
KW - Non-cardiac surgery
KW - Reticulated platelets
KW - Thrombotic events
UR - http://www.scopus.com/inward/record.url?scp=85031085994&partnerID=8YFLogxK
U2 - 10.1160/TH16-10-0804
DO - 10.1160/TH16-10-0804
M3 - Article
C2 - 28796275
AN - SCOPUS:85031085994
SN - 0340-6245
VL - 117
SP - 1887
EP - 1895
JO - Thrombosis and Haemostasis
JF - Thrombosis and Haemostasis
IS - 10
ER -