| Literature DB >> 23097696 |
Sophie Testa1, Oriana Paoletti, Anke Zimmermann, Laura Bassi, Silvia Zambelli, Emilia Cancellieri.
Abstract
Anticoagulation Clinics (ACs) are services specialized in management of patients on anticoagulant treatment. At present, ACs manage patients chiefly on antivitamin K antagonists (AVKs), but patient population has already changed in the last few years, because of an increase of treatments with other anticoagulant drugs, which require different management systems. The strong increase in the number of patients at AC, mainly on long-term treatment, has determined the development of web management, through telemedicine systems, improving the quality of life and maintaining the same clinical quality levels. New oral anticoagulants (NOAs) have shown to be as effective as AVK antagonists in stroke prevention in atrial fibrillation and for treatment of venous thromboembolism in addition to VTE prophylaxis in orthopaedic surgery, when administered at a fixed dose, but patient adherence and compliance are crucial for good quality treatment. At present, lacking data from the real world, an oversimplification of treatment with NOAs could cause unjustified risks for patients and also a possible future underuse of good drugs. For these reasons the vigilance must be high and ACs can have a crucial role in defining which is the best management for NOA patients and how to do it, as it happened for AVKs.Entities:
Year: 2012 PMID: 23097696 PMCID: PMC3477769 DOI: 10.1155/2012/835356
Source DB: PubMed Journal: Thrombosis ISSN: 2090-1488
Principal characteristics of the four management models.
| RMC | AC | PSM | PST | |
|---|---|---|---|---|
| Clinical quality | + | ++++ | ++++ | ++++ |
| TTR | + | +++ | +++ | ++++ |
| Accessibility | ++++ | ++ | + | ++ |
| Costs | + | ++ | +++ | ++++ |
Principal characteristics of new oral anticoagulants ([18, 19], modified).
| Dabigatran | Rivaroxaban | Apixaban | Edoxaban | |
|---|---|---|---|---|
| Target | IIa | Xa | Xa | Xa |
| Prodrug | Yes | No | No | No |
| Hours to | 2 | 2–4 | 1–3 | 1.5 |
| Bioavailability | 7% | 80% | 66% | 50% |
| Half-life (hours) | 12–14 | 9–13 | 8–15 | 6–11 |
| CYP metabolism | No | Yes | Yes | Yes |
| Efflux transporter P-gp | Yes | Yes | Yes | Yes |
| Renal elimination | 80% | 66% (33% cleared unchanged) | 25% | 35% |
| Dosing | Bid | Od | Bid | Od |
Patients management: comparison between NOA and AVK clinical actions.
| AVK | NOA | |
|---|---|---|
| Visit (anamnesis, physical examination) | Yes | Yes |
| Prescription (clinical indication, posology) | Yes | Yes |
| Information/education | Yes | Yes |
| Frequent lab coagulation monitoring | Yes | No |
| Renal function control | No | Yes |
| Dosing adjustment | Yes | No |
| Adherence/compliance control | No (routinely evaluated) | Yes |
| Management in special situations (surgery/complications) | Yes | Yes |
| Clinical periodical control | No (routinely evaluated) | Yes |
| Lab testing to support clinical and therapeutical intervention in specific condition | Yes | Yes (under evaluation) |