Reversal strategy in antagonizing the P2Y12‐inhibitor ticagrelor. (23rd September 2013)
- Record Type:
- Journal Article
- Title:
- Reversal strategy in antagonizing the P2Y12‐inhibitor ticagrelor. (23rd September 2013)
- Main Title:
- Reversal strategy in antagonizing the P2Y12‐inhibitor ticagrelor
- Authors:
- Hobl, Eva‐Luise
Derhaschnig, Ulla
Firbas, Christa
Schoergenhofer, Christian
Schwameis, Michael
Jilma, Bernd - Abstract:
- <abstract abstract-type="main" id="eci12168-abs-0001"> <title>Abstract</title> <sec id="eci12168-sec-0001" sec-type="section"> <title>Background</title> <p>Patients on antiplatelet therapy have a higher incidence of bleeding complications. Reversal of antiplatelet drug effects is an important issue at trauma or emergency departments. For old and conventional anticoagulants, reversal strategies are established. While the effects of ticagrelor are reversible, developing a method to restore platelet function in patients is of importance due to its longer half‐life (approximately 8 h), compared with other P2Y<sub>12</sub>‐inhibitors.</p> </sec> <sec id="eci12168-sec-0002" sec-type="section"> <title>Materials and methods</title> <p>We report an <italic>ex vivo</italic> model to reverse the effects of the novel and highly effective P2Y<sub>12</sub>‐inhibitor ticagrelor in 20 healthy volunteers. To normalize platelet reactivity, we added increasing amounts of autologous platelet‐rich plasma (PRP) to whole blood which was obtained 3 h after the intake of 180 mg of ticagrelor. Platelet aggregation was assessed by whole blood multiple electrode aggregometry (MEA), which is based on impedance aggregometry.</p> </sec> <sec id="eci12168-sec-0003" sec-type="section"> <title>Results</title> <p>The basal ADP‐induced platelet aggregation averaged 71 ± 16 U (Units). Ticagrelor decreased ADP‐induced platelet aggregation to 16 ± 8 U. A clear dose‐response was obtained after spiking whole blood<abstract abstract-type="main" id="eci12168-abs-0001"> <title>Abstract</title> <sec id="eci12168-sec-0001" sec-type="section"> <title>Background</title> <p>Patients on antiplatelet therapy have a higher incidence of bleeding complications. Reversal of antiplatelet drug effects is an important issue at trauma or emergency departments. For old and conventional anticoagulants, reversal strategies are established. While the effects of ticagrelor are reversible, developing a method to restore platelet function in patients is of importance due to its longer half‐life (approximately 8 h), compared with other P2Y<sub>12</sub>‐inhibitors.</p> </sec> <sec id="eci12168-sec-0002" sec-type="section"> <title>Materials and methods</title> <p>We report an <italic>ex vivo</italic> model to reverse the effects of the novel and highly effective P2Y<sub>12</sub>‐inhibitor ticagrelor in 20 healthy volunteers. To normalize platelet reactivity, we added increasing amounts of autologous platelet‐rich plasma (PRP) to whole blood which was obtained 3 h after the intake of 180 mg of ticagrelor. Platelet aggregation was assessed by whole blood multiple electrode aggregometry (MEA), which is based on impedance aggregometry.</p> </sec> <sec id="eci12168-sec-0003" sec-type="section"> <title>Results</title> <p>The basal ADP‐induced platelet aggregation averaged 71 ± 16 U (Units). Ticagrelor decreased ADP‐induced platelet aggregation to 16 ± 8 U. A clear dose‐response was obtained after spiking whole blood with increasing amounts of PRP. It is estimated that ≥2 units of apheresis platelet concentrates will be necessary to completely restore baseline platelet aggregation in the majority of patients after ticagrelor.</p> </sec> <sec id="eci12168-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Platelets dose dependently improve <italic>ex vivo</italic> platelet aggregation of subjects after a loading dose of 180 mg of ticagrelor, making transfusion of platelet concentrates potentially useful in bleeding patients and those who need to undergo emergency surgery.</p> </sec> </abstract> … (more)
- Is Part Of:
- European journal of clinical investigation. Volume 43:Number 12(2013:Dec.)
- Journal:
- European journal of clinical investigation
- Issue:
- Volume 43:Number 12(2013:Dec.)
- Issue Display:
- Volume 43, Issue 12 (2013)
- Year:
- 2013
- Volume:
- 43
- Issue:
- 12
- Issue Sort Value:
- 2013-0043-0012-0000
- Page Start:
- 1258
- Page End:
- 1261
- Publication Date:
- 2013-09-23
- Subjects:
- Pathology -- Periodicals
Medical research -- Periodicals
616.075 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2362 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/eci.12168 ↗
- Languages:
- English
- ISSNs:
- 0014-2972
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.727100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3114.xml