This registry follows patients undergoing two methods of aortic heart valve replacement in adults aged 18-60, the Ross procedure or conventional aortic valve replacement using a biologic or mechanical heart valve. The Ross procedure replaces a patient's diseased aortic valve with his/her own pulmonary valve and uses a donor valve in the pulmonary position which receives less stress than the aortic valve. Mechanical valves tend to form blood clots so they need long-term blood thinners that increase risk of bleeding and lower quality of life. Animal tissue valves reduce clotting and bleeding risks but wear out sooner and shorten patient life-span. The REVIVAL Registry will run in parallel with the REVIVAL randomized trial.
Heart valves help control blood flow through the heart and, if diseased, may need to be replaced. After having a heart valve replaced, patients have a higher risk of death than people who have not had a valve replaced. In young adult patients, replacing the aortic heart valve with a mechanical valve halves their life-span compared to other people their age. Mechanical valves tend to form blood clots so they need long-term blood thinners that increase risk of bleeding and lower quality of life. Animal tissue valves reduce clotting and bleeding risks but wear out sooner and shorten patient life-span. An operation, called the Ross procedure, replaces a patient's diseased aortic valve with his/her own pulmonary valve and uses a donor valve in the pulmonary position which receives less stress than the aortic valve. The Ross procedure aims to improve valve durability with less clotting, avoiding use of blood thinners. Patients and physicians need a large, high-quality study comparing the Ross procedure and standard valve replacement to know if either approach is better. In parallel to the REVIVAL Registry, a REVIVAL Randomized Trial will also take place. Patients included in randomized trials often systematically differ from those who are not. By creating a registry of patients who are eligible for but not recruited into the REVIVAL trial, the investigators will better understand: 1) the reasons for not including these patients; 2) how those patients differ in terms of baseline characteristics from the trial cohort; 3) whether the outcomes of registry participants differ from those in the trial, assessed by treatment group. The registry will aid in understanding the generalizability of the results that the trial produces.
Study Type
OBSERVATIONAL
Enrollment
62
Hamilton General Hospital
Hamilton, Ontario, Canada
Evaluation of systematic differences between registry and trial patients
The primary outcome of the REVIVAL registry is to examine for systematic differences between the demographics and outcomes of patients enrolled in the REVIVAL trial and patients not enrolled in the trial. We will use descriptive statistics including mean (standard deviation), median (interquartile range), and count (proportion) to describe the REVIVAL registry cohort.
Time frame: Through REVIVAL Trial completion, estimated to be 10 years
Evaluate the number of patients meeting eligibility criteria for the REVIVAL trial per month who are not enrolled into the trial.
To determine the number of eligible patients and reasons why they were not enrolled into the REVIVAL trial.
Time frame: Through completion of the pilot trial, estimated to be 3 years
Evaluate the proportion of Ross procedures compared to conventional aortic valve replacement.
Measure the proportions of type of mechanical valve versus biological valves versus Ross procedure in the REVIVAL registry participants.
Time frame: Through completion of the pilot trial, estimated to be 3 years
The rate of survival free of a composite of life-threatening valve-related complications (major bleeding, stroke or systemic thromboembolism, valve thrombosis, and operated-on valve reintervention)
Evaluate the frequency of REVIVAL trial outcomes among registry participants. The primary outcome is the rate of survival free of life-threatening valve-related complications (major bleeding, stroke or systemic thromboembolism, valve thrombosis, and operated-on valve reintervention) over duration of follow-up. Assessment of this composite over time is particularly important, as the Ross procedure may show initial benefit secondary to thromboembolic and bleeding reduction, however should the technique show high late rates of reoperation as suggested in some observational literature, the effect magnitude may change significantly over time.
Time frame: Through trial completion, estimated to be 10 years
The rate of perioperative and non-perioperative major bleeding over the duration of patient follow-up.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Perioperative (index surgery only) Intraoperative: After administration of protamine, delay of chest closure for bleeding \> 500 mL/hr requiring packing and transfusion of more than 3 units red blood cells /whole blood. Upon leaving OR to 48hrs postop (modified BARC type 4) Intracranial bleeding within 48hrs Reoperation after sternum closure for purpose of controlling bleeding or relief of tamponade Transfusion of ≥ 5 units packed red blood cells /whole blood in the 48hr period Chest tube output ≥ 2L in the first 24hr Non-perioperative Per the International Society of Thrombosis and Hemostasis (ISTH) major bleeding definition.
Time frame: Through trial completion, estimated to be 10 years
The rate of stroke or systemic thromboembolism over the duration of patient follow-up.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Stroke is acute focal brain dysfunction due to a vascular cause lasting ≥ 24 hrs in the absence of brain imaging or requires evidence of acute stroke on brain imaging. Stroke is divided into 3 types: ischemic stroke, hemorrhagic stroke, and undetermined stroke. If death occurs within 24 hours, the neurological deficit must persist up to the time of death. Systemic arterial embolism is an abrupt vascular insufficiency associated with evidence of arterial occlusion in the absence of other likely mechanisms. Clinical signs/symptoms must be consistent with embolic arterial occlusion, there must be clear evidence of abrupt occlusion of a systemic artery, with at least one type of supporting evidence (surgical report indicating evidence of arterial embolism, pathological specimens related to embolism removal, imaging evidence consistent with arterial embolism, or autopsy report).
Time frame: Through trial completion, estimated to be 10 years
The rate of valve thrombosis per VARC criteria over the duration of patient follow-up.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Valve thrombosis is defined as any thrombus not caused by infection attached to or near an operated valve that occludes part of the blood flow path, interferes with valve function, or is large enough to warrant treatment. Valve thrombus found at autopsy in a patient whose cause of death was not valve related or found at operation for and unrelated indication is to be counted as valve thrombosis.
Time frame: Through trial completion, estimated to be 10 years
The rate of operated-on valve reintervention over the duration of patient follow-up.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Rate of valve reintervention Any surgical or percutaneous procedure that repairs, or otherwise alters or adjusts, or replaces a previously implanted prosthesis or valve.
Time frame: Through trial completion, estimated to be 10 years
Rate of mortality within 30 days post-operatively.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants.
Time frame: 30 days
Measure health related quality of life using the 36-Item Short Form Survey (SF-36) questionnaire over the duration of patient follow-up
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. The 36-Item Short Form Survey (SF-36) is a health related quality of life questionnaire that measure eight health domains and each survey provides psychometrically-based physical component summary (PCS) and mental component summary (MCS) scores. The domains are physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. The questionnaire is calibrated such that scored values of 50 represent the norm and higher scored values according to the scoring key represent a more favourable health state. A baseline score will be obtained prior to the patient's surgery and the SF-36 will be administered annually thereafter over the duration of patient follow-up.
Time frame: Through trial completion, estimated to be 10 years
The rate of operated-valve endocarditis over the duration of patient follow-up
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Defined as any infection involving a valve on which an operation has been performed. The diagnosis is based on one or more of the following: 1) reoperation with evidence of abscess, paravalvular leak, pus, or vegetation confirmed as secondary to infection by histologic or bacteriologic studies; 2) autopsy findings of abscess, pus, or vegetation involving an operated-on valve; or 3) the meeting of Duke criteria for endocarditis.
Time frame: Through trial completion, estimated to be 10 years
The rate of aortic valve re-intervention over the duration of patient follow-up.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants Any surgical or percutaneous procedure that repairs, or otherwise alters or adjusts, or replaces a previously implanted prosthesis or valve in the aortic position.
Time frame: Through trial completion, estimated to be 10 years
The rate of pulmonary valve re-intervention over the duration of patient follow-up.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants Any surgical or percutaneous procedure that repairs, or otherwise alters or adjusts, or replaces a previously implanted prosthesis or valve in the pulmonary position.
Time frame: Through trial completion, estimated to be 10 years
Mean aortic valve gradient.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Measured through echocardiography
Time frame: Through trial completion, estimated to be 10 years
Mean pulmonic valve gradient
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Measured through echocardiography
Time frame: Through trial completion, estimated to be 10 years
Severity of aortic valve regurgitation.
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Measured through echocardiography, categorized as mild, moderate, or severe
Time frame: Through trial completion, estimated to be 10 years
Severity of pulmonic valve regurgitation
Evaluate the frequency of REVIVAL trial outcomes among REVIVAL registry participants. Measured through echocardiography, categorized as mild, moderate, or severe
Time frame: Through trial completion, estimated to be 10 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.