دورية أكاديمية

Experience With Pre-procedural Hemostatic Medications versus Platelet Transfusion in Patients With Platelet Storage Pool Deficiency.

التفاصيل البيبلوغرافية
العنوان: Experience With Pre-procedural Hemostatic Medications versus Platelet Transfusion in Patients With Platelet Storage Pool Deficiency.
المؤلفون: Lundy, Katharine A., Rabatin, Abigail, Davidson, Erica R., Li, Junan, Snider, Melissa J., Kraut, Eric H.
المصدر: Journal of Pharmacy Practice; Dec2023, Vol. 36 Issue 6, p1412-1418, 7p
مصطلحات موضوعية: PREOPERATIVE care, RESEARCH, RETROSPECTIVE studies, TREATMENT effectiveness, BLOOD platelet transfusion, DESCRIPTIVE statistics, BLOOD platelet disorders, HEMOSTATICS, HEMORRHAGE, LONGITUDINAL method, DISEASE complications
مستخلص: Background: Storage pool deficiency (SPD) is a rare bleeding disorder characterized by reduction in the number of delta granules within platelets, interfering with hemostasis. Current literature lacks well-designed studies from which to draw concrete conclusions regarding pre-procedural management of bleeding complications. Objective: The purpose of this study is to describe bleeding and safety outcomes of SPD patients receiving either pre-procedural platelet transfusions or platelet-sparing regimens. Methods: An exploratory retrospective cohort study was conducted among SPD patients, comparing major bleeding events between those who received platelet transfusion and those who received desmopressin, tranexamic acid, and/or aminocaproic acid within 24 hours prior to procedure. Results: Rates of major bleeding were not found to be higher among patients who received a platelet-sparing regimen [platelet-sparing: 2/25 (8%); platelet transfusion: 2/29 (6.9%); P =.99]. Incidence of non-major bleeding was higher in the platelet transfusion group, but this was not statistically significant [platelet-sparing: 0/25 (0%); platelet transfusion: 3/29 (10.3%); P =.24]. Treatment-related adverse effects were observed following 8 of 54 procedures (14.8%). Conclusion: Use of a platelet-sparing regimen was not associated with a significantly higher incidence of major or non-major bleeding events. Future prospective trials are recommended to compare outcomes between therapies. [ABSTRACT FROM AUTHOR]
Copyright of Journal of Pharmacy Practice is the property of Sage Publications Inc. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:08971900
DOI:10.1177/08971900221119167