Peter Davies Senior Pharmacist Venous thromboembolic prevention is a DH patient safety priority NICE clinical guideline venous thromboembolism reducing the risk CQUIN The NHS standard contract for acute services and VTE prevention VTE risk assessment audit Clinical incident/Pharmacy intervention monitoring Healthcare record audit Root cause analysis of hospital acquired thrombosis Rivaroxaban use in elective THR and TKR Audit data since June 2008 Data collected from the front of the drug administration and record chart 3 monthly data until May 2010 now monthly CQUIN requirements VTE risk assessment at Salisbury Hospital 2008-2010 100 90 Percentage (%) risk assessed 80 70 60 50 40 30 20 10 0 Reporting forms adapted to include fields to record incidents and interventions relating to VTE prevention and prophylaxis Report generated by clinical risk and sent monthly to the thrombosis committee Data provided by individual wards Audit of 5 sets of healthcare records Record data on whether risk assessment and thromboprophylaxis is appropriate on an electronic data collection form Data collated by clinical audit and forwarded to the Thrombosis committee Hospital acquired thrombosis detected by DVT/Anticoagulant clinic Coding Diagnostics Autopsies Subjected to a root cause analysis Reviewed by the Thrombosis committee For elective Primary THR or TKR First dose 30 hours post surgery 14 days for TKR and 35 days for THR Contra-indicated e-GFR <30ml/min Not used if on long term anticoagulant Documented bleeding episodes resulting in rivaroxaban being stopped/omitted Wound oozing/bleeding Number of episodes 4 GI bleed 2 Haematuria in catheterised patient 1 Bleed from drain 2 Off-label use of rivaroxaban Number of patients Revision of TKR 3 Revision of THR 3 Patella resurfacing 2 Hip resurfacing 2 Uni-compartment knee replacement 2 Fractured neck of Femur leading to THR 1