| Outcome |
---|---|
Primary | 1. Patients with a history of peptic ulcer who have been prescribed a non-selective non-steroidal anti-inflammatory drug without co-prescription of a proton-pump inhibitor |
2. Patients with asthma who have been prescribed a β blocker | |
Secondary | 3. Patients aged 75Â years and older who have been prescribed an angiotensin converting enzyme inhibitor or a loop diuretic long-term who have not had a computer-recorded check of their renal function and electrolytes in the previous 15Â months |
2a.Patients with asthma (and no history of coronary heart disease) who had been prescribed a β blocker | |
4. Proportions of women with a past medical history of venous or arterial thrombosis who had been prescribed the combined oral contraceptive pill | |
5. Patients receiving methotrexate for at least 3Â months who had not had a full blood count recorded 5a or liver function test 5b in the previous 3Â months | |
6. Patients receiving warfarin for at least 3Â months who had not had a recorded check of their international normalised ratio in the previous 12Â weeks | |
7. Patients receiving lithium for at least 3Â months who had not had a recorded check of their lithium concentrations in the previous 3Â months | |
8. Patients receiving amiodarone for at least 6Â months who had not had a thyroid function test in the previous 6Â months | |
9. Patients receiving prescriptions of methotrexate without instructions that the drug should be taken every week | |
10. Patients receiving prescriptions of amiodarone for at least 1Â month who are receiving a dose of more than 200Â mg per day Composite secondary outcome measures | |
Composite secondary outcome measures | 11. Patients with at least one prescription problem (a combination of outcome measures 1, 2, or 4) |
12. Patients with at least one monitoring problem (a combination of outcome measures 3, 5, 6, 7, and 8) In the trial protocol |