Study Methods
* Population of study: Patients who have a clinical indication for long term VKA.
* Study location: Aswan Heart Center.
* Inclusion criteria: Adult patients above 18 years who are indicated for long term VKA and has been on VKA for more than 6 months.
* Exclusion criteria:
1\. Refusal to join the study. 2. History of life-threatening bleeding or thrombo-embolic events. 3. Illiterate patients with no caregivers living at the same home.
* Patient informed consent:
Individual informed consent will be taken from every candidate for the study. The candidates will have the right to withdraw from the study at any time without any changes in the clinical service provided to them.
\- Methodology in details:
A-Medical history including:
Age, gender, indication of VKA. Data about valve surgery including date, location and type of valve. Past history of any chronic medical conditions, thrombo-embolic or bleeding events. Past history of blood transfusion.
B-Social history including:
Marital status, occupation, level of education and self-care capability.
C- Clinical examination including:
Assessment of body weight, height and body mass index calculation. Vital signs including blood pressure measurement using standard technique, assessment of the pulse, respiratory rate and temperature.
C- Blood sample and chemistry:
Blood tests will be done for all participants initially and at the end of the study. Laboratory workup will include complete blood count, liver, kidney function tests and electrolytes.
F- Electrocardiography (ECG):
12-lead ECG will be done for all participants initially and the end of the study to confirm rhythm.
H- Echocardiography:
* Trans-thoracic echocardiography will be done for all patients to assess valve function, leaflet excursion, peak and mean pressure gradients across the valve.
* In case of abnormally elevated pressure gradients, abnormal leaflet motion or suspected prosthesis-related mass, trans-oesophageal echocardiography will be done to confirm or exclude MVP malfunction.
I. Randomization:
* Patients will be randomized with the ratio of 1:1 to undergo self-management of INR versus standard management in the anticoagulation clinic using a randomization table.
* Self-management arm:
• All participants will receive full education class of minimum one-hour time and training about how to interpret INR levels and adjust their medication dose according to a pre-determined dose-INR schedule.
• A registered nurse will be responsible for education and training. Another registered nurse would be responsible to check the participant feedback and well-understanding.
• The participant will receive a chart to record INR results, test dates and dose modifications for the upcoming 6 months.
• The participant will be educated about bleeding events, how to grade and when to seek medical attention immediately.
• The participant will be educated about early manifestations of thrombo-embolism including shortness of breath, focal neurological deficits or lower limb pain.
• If INR exceeds 8 at any time, the participant will be instructed to urgently contact the center and seek medical advice, he/she will be withdrawn from the trial and switched to the standard monitoring care.
• If major bleeding or thrombotic event occurred, the participant will be instructed to contact us urgently and will be withdrawn from the trial and switched to the standard monitoring care.
* Standard monitoring arm:
* This group will be managed according to the local protocol of INR monitoring in a dedicated anticoagulation clinic. A registered nurse (supervised by a physician) would be responsible for medication dose adjustment, scheduling tests and recording any thrombo-embolic or bleeding events.
K. Follow-up:
Standard monitoring group will be reviewed on monthly basis or less according to INR test results. Self-management group will be reviewed 6 months after randomization, with the following data to be obtained:
1. All-cause death.
2. Bleeding events will be graded according to BARC classification
* Minor bleeding Type 1: self-controlled bleeding that doesn't need seeking medical advice.
* Major bleeding Type 2: Overt bleeding that requires medical intervention or hospitalization. Type 3a: Bleeding with Hb drop (3-5 gm/dL), or requiring blood transfusion. Type 3b: Bleeding with Hb drop 5 gm/dL or more, or requiring surgical intervention.
Type 4: Coronary artery bypass graft-related bleeding. Type 5: Fatal bleeding. 4. Thrombo-embolic event: defined as mechanical valve thrombosis confirmed by trans-oesophageal echocardiography (prosthesis-related mass, elevated gradients, stuck leaflet motion), cerebrovascular stroke, peripheral embolism causing acute limb ischemia.
5\. Time and proportion of tests in therapeutic range will be calculated using Rosendaal method.
6\. Frequency of tests will be recorded.
In case of mortality, data will be collected about the date and cause of mortality, and any reported clinical events before mortality.
Data will be presented and used without inference to the name or personal data of the patients. All patient records will be handled in accordance to hospital and national confidentiality protocols.
