Included will be patients on antithrombotics (unfractionated heparin (UFH), low-molecular weight heparin (LMWH), VKA or NOAC.
Conditions
Interventions
The intervention consists of the S-team, consisting of a specialized thrombosis nurse as casemanager,
haematologist, medical leader Thrombosis Service, hospital pharmacist/clinical pharmacologist, car
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: Included will be patients on antithrombotics (unfractionated heparin (UFH), low-molecular weight heparin (LMWH), VKA or NOAC.
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Composite endpoint: proportion of patients with equal or greater than 1 bleeding or equal or greater than 1 arterial/venous thrombotic events during and after hospitalization. | — |
Secondary
| Measure | Time frame |
|---|---|
| Each of the components of the primary endpoint separately (bleeding, thrombosis), severity of bleeding complication, length of hospital stay, patient related outcomes (quality of life, belief in medicines questionnaire [8], adherence; patient satisfaction), healthcare costs (labour costs versus costs for bleeding/thrombotic events (including use of antidotes), and cost-effectiveness analysis. | — |
Contacts
Public ContactP.M.L.A. Bemt, van den
Erasmus MC Hospital Pharmacy P.O. Box 2040
Outcome results
None listed