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Haemovigilance in Czech Republic

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F27283933%3A_____%2F17%3A00005436" target="_blank" >RIV/27283933:_____/17:00005436 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Haemovigilance in Czech Republic

  • Original language description

    Haemovigilance is a system of processes, comprissing detection, summary and analysis of information concerning severe adverse effects and events on the part of transfusion donors and recipients and epidemiological monitoring of blood donors, The wider definition of haemovigilance includes clinical section, which means transfusion indication criteria, their control and good practise in the course of transfusion administration. A system of reporting of adverse effects of transfusion is of key importance. Thelegislative standard for the European Union member states is Directive No.2002/98/EC, which provides quality and safety standards for production of blood components, it does not solve the clinical section of problems. The basic recommendations for clinical practice can be found in the Guide to the Preparation, Use and Quality Assurance of Blood Components. The detailed instructions in guidelines of British Society for Hemstology and the recommendations for haemovigilance in ISBT standards. In the Czech Republic, the field of production of blood products is handled by the Medicine Act and Degree of Blood. These legal standards alsso scontain basic provision for haemovigilance especially for traceability of blood components and producing reports of serious transfusion reactions and events. The main institution is the State INstitute for Drug Control(SIDC), which issues a manufacturing authorization for transfusion services and the Ministry of Health. The Society for Transfusion Medicine has issued professional standards for key areas of transfusion service including national standard for the administration of blood components. In CR serious transfusion reactions and events are reported to SIDC. All reactions are reported to blood banks in hospitals. Medical faculties have begun pregraduate education in transfusiology and the textbooks od transfusion medicine have been published, However, the situation is not optimal. Most significantly national guidelines for the use blood components are missing.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30230 - Other clinical medicine subjects

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů