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1.
Transfusion ; 57(12): 2836-2844, 2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-28880362

RESUMEN

BACKGROUND: Laboratory and clinical evidence suggest that cold-stored platelets (CS-PLTs) might be preferable to room temperature platelets (RT-PLTs) for active bleeding. Ease of prehospital use plus potential hemostatic superiority led our facility to pursue approval of CS-PLTs for actively bleeding trauma patients. STUDY DESIGN AND METHODS: From November 18, 2013, through October 8, 2015, correspondence was exchanged between our facility, the AABB, and the US Food and Drug Administration (FDA). An initial AABB variance request was for 5-day CS-PLTs without agitation. The AABB deferred its decision pending FDA approval to use our platelet (PLT) bags for CS-PLTs. On March 27, 2015, the FDA approved 3-day CS-PLTs without agitation. On October 8, 2015, the AABB approved 3-day CS-PLTs without agitation and without bacterial testing for actively bleeding trauma patients. Our facility's goal is to carry CS-PLTs on air ambulances. RESULTS: CS-PLTs have been used for trauma patients at our facility since October 2015. As of August 2016, a total of 21 (19.1%) of 119 CS-PLTs have been transfused. The short 3-day storage period combined with the formation of clots in plasma-rich CS-PLTs during storage have been the major causes of a high (80.9%) discard rate. CONCLUSION: In the future, pathogen-reduced (PR), PLT additive solution (PAS) CS-PLTs seem more practical due to low risks of bacterial contamination and storage-related clotting. This should make longer storage of CS-PLTs feasible (e.g., 10 days or more). With a longer shelf life, PR PAS CS-PLTs could potentially be used in a wider range of patient populations.


Asunto(s)
Plaquetas , Frío , Transfusión de Plaquetas/métodos , Heridas y Lesiones/terapia , Ambulancias Aéreas , Hemostasis , Humanos , Transfusión de Plaquetas/normas , Refrigeración , Factores de Tiempo , Estudios de Validación como Asunto
2.
Clin Leadersh Manag Rev ; 18(6): 361-3, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15597559

RESUMEN

This article describes our journey for quality in the Department of Laboratory Medicine and Pathology (DLMP) at Mayo Clinic. It provides the background of the department and the process for the development and implementation of the quality program. In addition, a quality conference and the development of a quality school are outlined. Throughout the course of this process, valuable lessons were learned and are discussed. We are pleased with the success of the quality journey. However, we realize that the quest has just begun. We look forward to the future and the challenges that lie ahead.


Asunto(s)
Instituciones de Atención Ambulatoria/normas , Laboratorios/normas , Patología Clínica , Garantía de la Calidad de Atención de Salud/organización & administración , Estudios de Casos Organizacionales , Objetivos Organizacionales , Evaluación de Resultado en la Atención de Salud , Estados Unidos
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