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Adverse events in apheresis: An update of the WAA registry data

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F16%3A10331717" target="_blank" >RIV/00179906:_____/16:10331717 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/16:10331717 RIV/00843989:_____/16:E0105401

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.transci.2016.01.003" target="_blank" >http://dx.doi.org/10.1016/j.transci.2016.01.003</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.transci.2016.01.003" target="_blank" >10.1016/j.transci.2016.01.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Adverse events in apheresis: An update of the WAA registry data

  • Original language description

    Apheresis with different procedures and devices are used for a variety of indications that may have different adverse events (AEs). The aim of this study was to clarify the extent and possible reasons of various side effects based on data from a multinational registry. The WAA-apheresis registry data focus on adverse events in a total of 50846 procedures in 7142 patients (42% women). AEs were graded as mild, moderate (need for medication), severe (interruption due to the AE) or death (due to AE). More AEs occurred during the first procedures versus subsequent (8.4 and 5.5%, respectively). AEs were mild in 2.4% (due to access 54%, device 7%, hypotension 15%, tingling 8%), moderate in 3% (tingling 58%, urticaria 15%, hypotension 10%, nausea 3%), and severe in 0.4% of procedures (syncope/hypotension 32%, urticaria 17%, chills/fever 8%, arrhythmia/asystole 4.5%, nausea/vomiting 4%). Hypotension was most common if albumin was used as the replacement fluid, and urticaria when plasma was used. Arrhythmia occurred to similar extents when using plasma or albumin as replacement. In 64% of procedures with bronchospasm, plasma was part of the replacement fluid used. Severe AEs are rare. Although most reactions are mild and moderate, several side effects may be critical for the patient. We present side effects in relation to the procedures and suggest that safety is increased by regular vital sign measurements, cardiac monitoring and by having emergency equipment nearby.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Transfusion and Apheresis Science

  • ISSN

    1473-0502

  • e-ISSN

  • Volume of the periodical

    54

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    14

  • Pages from-to

    2-15

  • UT code for WoS article

    000374614700002

  • EID of the result in the Scopus database

    2-s2.0-84954304755