IMR-Heart Trasplant Study

The IMR-HT study is a multicenter, prospective observational study that will include post-HT stable patients undergoing coronary physiological assessment in the first three months and one year.

Assessment of IMR, coronary flow reserve (CFR) and fractional flow reserve (FFR) will be performed using the standard thermodilution technique. The left anterior descending coronary artery will be evaluated in all patients. Circumflex or right coronary artery could be additionally evaluated at operator's discretion. An intracoronary pressure and temperature sensor-tipped guidewire (Pressure Wire TM X guide- wire 0.014', Abbott, IL, USA) will be used to perform the measurements. The tip pressure sensor will be advanced into the mid-to-distal portion of the evaluated vessel. Baseline aortic pressure (Pa) and distal intracoronary pressure (Pd) will be obtained to calculate the resting index Pd/Pa. To measure the mean transit time (Tmn) under basal conditions, intracoronary administration of 3 mL of room-temperature saline will be manually injected three times in succession (3 mL/s). Then maximal hyperemia will be induced using adenosine iv (140 to 180 mg/kg/min) and three additional intracoronary room temperature saline boluses of 3 ml will be administered to determine the mean transit time at hyperemia (Tmnh). Finally, fractional flow reserve (FFR), coronary flow reserve (CFR) and IMR will be calculated using the software Coroventis Coroflow (Coroventis Abbott, Uppsala, Sweden).

Changes in HT patient management (number of EMBs, immunosuppressive therapy modifications) after knowing IMR values will also be assessed.

Based on previously published clinical data on IMR in heart transplant patients, a post-HT management algorithm is proposed:

• IMR < 15: The frequency of biopsies could be reduced or maintained as per protocol. No changes to immunosuppressive therapy would be required.
• IMR ≥ 15: Biopsies would be performed at the standard frequency according to protocol. Immunosuppressive therapy could be intensified or maintained the same.

Of note, given the observational characteristics of the study, clinical management decisions will be made at the discretion of the treating physician, taking into account the patient's clinical condition and other complementary tests.

Both groups (IMR<15 vs IMR≥15) will be compared in terms of cardiac events occurrence.

Clinical conditions, laboratory findings and clinical events will be assessed at one month and one year. Follow up will be extended for up to five years. Data will be included in an online database specifically designed for the study on platform REDCap (Research Electronic Data Capture).

A number will be assigned to each patient; their identity will not be disclosed in any case. All shared information will be anonymized. The principal investigator at each center will be responsible for keeping the data anonymized.Data will be processed in accordance with the protection legislation in force (Spanish Personal Data Protection and Guarantee of Digital Rights Act 3/2018, and Regulation (EU) 2016/679).

Our aim will be to assess IMR values in heart transplant patients within one year and evaluate changes in management after knowing of IMR values. We believe it is important to move forward in AAR surveillance and reduce the number of endomyocardial biopsies. In addition to assessing their diagnostic capabilities, IMR should also be assessed based on clinical outcomes. Therefore, we are convinced the results of this trial will be very important for our HT patient population.

Inclusion criteria

• Heart transplant patients >18 years.
• Patients who have received and signed informed consent.

Exclusion criteria

• Patients with hemodynamic instability after HT, including cardiogenic shock or severe coagulopathy.
• Patients with acute cellular rejection before intracoronary physiological assessment.
• Patients with bronchial asthma or bronchopathy with a positive bronchodilation test, which contraindicates the use of adenosine.
• Patients with epicardial coronary lesions with a resting physiological index ≤0.89 or ≤0.80 at hyperemia.
• Patients unlikely to cooperate or with inability or unwillingness to give informed consent.