Remboursement Xarelto 2,5 mg

We are delighted to announce that neurologists also have been recognised for the reimbursement of Xarelto 2.5mg in coronary artery disease (CAD) and peripheral artery disease PAD), since February 1, 2024.
Furthermore, the duration of acceptance has been changed, since the 3-year limit has been withdrawn.

 

Please find attached Bayer’s information letter: BE.XAR.VAE_Remboursement CADPAD_FR

Actilyse vials with latex plugs that could also contain traces of Gentamycine.

Dear members of the SB,

As part of the strategy to resolve the worldwide shortage of thrombolytic therapy, the BSC has been informed that Boehringer-Ingelheim will temporarily produce Actilyse vials with latex plugs that could also contain traces of Gentamycine. These vials could be encountered in your local hospital from the end of October onward (and will likely be produced for several months).

BI states that boxes containing vials with latex plugs and vials that could contain traces of Gentamycine will be clearly labeled by stickers (see photograph). These vials should never be administered to patients with a latex/rubber sensitivity or sensitivity to Gentamycine.

Joint Statement ESO and SAFE commemorate European Stroke Awareness Day 9 May 2023

Europe is failing to provide adequate stroke care and support
The scale of stroke care crisis is laid bare by new data release

New data collected as part of the Stroke Action Plan for Europe (SAP-E) Stroke Service Tracker reveals the
gross inequity of access to care and support for stroke patients and stroke survivors across Europe.

The SAP-E was launched in 2018 to provide a framework for European governments to improve stroke care
and support for all European citizens. As part of this plan, data from 36 countries across Europe, covering
12 key areas of improvement, has been collected in and is available via the SAP-E website.

SAP-E Joint Statement for ESAD 2023

UPDATE ON THROMBOLYTIC DRUG SHORTAGE

UPDATE ON THROMBOLYTIC DRUG SHORTAGE

UPDATE ON THROMBOLYTIC DRUG SHORTAGE

Thrombolytic drug shortage is expected to last until 2024. The manufacturing company is limiting supply to all countries worldwide. Currently, the impact on future drug delivery is still unclear. However, for the month October, drug delivery will be further restricted.
Additionally, the production of Actosolv, mainly used for IV cathether obstruction, has not yet been resumed and will likely become unavailable from January 2023.
With the help of Belgian experts, FAGG/AFMPS has released guidance for hospital pharmacists and medical doctors concerning the shortage of thrombolytic drugs. The guideline serves the purpose of making other medical specialities aware of the shortage and restricting the use of thrombolytics for non-urgent indications. Centralisation of hospital stock and monitoring of local usage is highly recommended. With regards to treatment of ischemic stroke, increased use of MRI or CT perfusion imaging is recommended to avoid treating stroke mimics as much as possible, avoiding off-label alteplase use and optimalisation of alteplase dosing using complete vials of 20 and 50mg, taking into account local availability of both dosages, is advised to avoid wastage.

Some guidelines for rational use of tPA:

Avoiding tPA wastage by limiting the use of 2x 50mg vials and rounding to full vial dosages. As a rule of thumb we suggest:

  • 60 kg: 1 x 50 mg
  • 70 kg: 3 x 20 mg
  • 80 kg: 1 x 20 mg + 1 x 50 mg
  • 90 kg: 4 x 20 mg
  • from 100 kg: 2 x 20 mg + 1 x 50 mg

Read also the FAGG recommendation here
Dutch: https://tinyurl.com/4hf5xvxp
French: https://tinyurl.com/c7av4k4c

See also additional guidance by the European Stroke Organization and the Advisory board Thrombolytics – Boehringer Ingelheim: