PMID- 35596611 OWN - NLM STAT- MEDLINE DCOM- 20221101 LR - 20230816 IS - 1525-1594 (Electronic) IS - 0160-564X (Linking) VI - 46 IP - 11 DP - 2022 Nov TI - Acquired platelet defects are responsible for nonsurgical bleeding in left ventricular assist device recipients. PG - 2244-2256 LID - 10.1111/aor.14319 [doi] AB - BACKGROUND: Left ventricular assist devices (LVADs) have been used as a standard treatment option for patients with advanced heart failure. However, these devices are prone to adverse events. Nonsurgical bleeding (NSB) is the most common complication in patients with continuous flow (CF) LVADs. The development of acquired von Willebrand syndrome (AVWS) in CF-LVAD recipients is thought to be a key factor. However, AVWS is seen across a majority of LVAD patients, not just those with NSB. The purpose of this study was to examine the link between acquired platelet defects and NSB in CF-LVAD patients. METHODS: Blood samples were collected from 62 CF-LVAD patients at pre- and 4 post-implantation timepoints. Reduced adhesion receptor expression (GPIbalpha and GPVI) and activation of platelets (GPIIb/IIIa activation) were used as markers for acquired platelet defects. RESULTS: Twenty-three patients experienced at least one NSB episode. Significantly higher levels of platelet activation and receptor reduction were seen in the postimplantation blood samples from bleeders compared with non-bleeders. All patients experienced the loss of high molecular weight monomers (HMWM) of von Willebrand Factor (vWF), but no difference was seen between the two groups. Multivariable logistic regression showed that biomarkers for reduced platelet receptor expression (GPIbalpha and GPVI) and activation (GPIIb/IIIa) have more predictive power for NSB, with the area under curve (AUC) values of 0.72, 0.68, and 0.62, respectively, than the loss of HMWM of vWF (AUC: 0.57). CONCLUSION: The data from this study indicated that the severity of acquired platelet defects has a direct link to NSB in CF-LVAD recipients. CI - (c) 2022 International Center for Artificial Organ and Transplantation (ICAOT) and Wiley Periodicals LLC. FAU - Arias, Katherin AU - Arias K AUID- ORCID: 0000-0003-0779-3405 AD - Fischell Department of Bioengineering, A. James Clark School of Engineering, University of Maryland, College Park, Maryland, USA. AD - Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA. FAU - Sun, Wenji AU - Sun W AD - Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA. FAU - Wang, Shigang AU - Wang S AD - Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA. FAU - Sorensen, Erik N AU - Sorensen EN AD - Division of Perioperative Services, University of Maryland Medical Center, Baltimore, Maryland, USA. FAU - Feller, Erika AU - Feller E AD - Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA. FAU - Kaczorowski, David AU - Kaczorowski D AD - Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA. FAU - Griffith, Bartley AU - Griffith B AD - Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA. FAU - Wu, Zhongjun J AU - Wu ZJ AUID- ORCID: 0000-0003-0807-7195 AD - Fischell Department of Bioengineering, A. James Clark School of Engineering, University of Maryland, College Park, Maryland, USA. AD - Department of Surgery, University of Maryland School of Medicine, Baltimore, Maryland, USA. LA - eng GR - R01 HL124170/HL/NHLBI NIH HHS/United States GR - R01 HL118372/HL/NHLBI NIH HHS/United States GR - R01HL124170/HL/NHLBI NIH HHS/United States GR - R01HL118372/HL/NHLBI NIH HHS/United States GR - R01HL141817/HL/NHLBI NIH HHS/United States PT - Journal Article DEP - 20220530 PL - United States TA - Artif Organs JT - Artificial organs JID - 7802778 RN - 0 (von Willebrand Factor) SB - IM MH - Humans MH - *Heart-Assist Devices/adverse effects MH - von Willebrand Factor MH - Hemorrhage/therapy/complications MH - *von Willebrand Diseases/etiology MH - Platelet Activation MH - *Heart Failure/surgery OTO - NOTNLM OT - acquired platelet defects OT - heart failure OT - left ventricular assist devices OT - mechanical circulatory support OT - nonsurgical bleeding EDAT- 2022/05/22 06:00 MHDA- 2022/11/02 06:00 CRDT- 2022/05/21 04:02 PHST- 2022/04/02 00:00 [revised] PHST- 2021/09/15 00:00 [received] PHST- 2022/05/13 00:00 [accepted] PHST- 2022/05/22 06:00 [pubmed] PHST- 2022/11/02 06:00 [medline] PHST- 2022/05/21 04:02 [entrez] AID - 10.1111/aor.14319 [doi] PST - ppublish SO - Artif Organs. 2022 Nov;46(11):2244-2256. doi: 10.1111/aor.14319. Epub 2022 May 30.