The overall objective of compiling this registry is to obtain a complete collection of data, in a dedicated database, on all patients who have undergone transplantation at our Center in order to assess the main causes of mortality, hospitalization, and morbidity.

Secondary objective: the information acquired will enable us to review more appropriate outpatient management of these patients and redefine our internal management protocols in order to reduce morbidity, hospitalization, and mortality in these patients.

Inclusion Criteria:

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To be included in the study the patient must:

• Give written informed consent to participate for the prospective evaluations
• Be a heart transplanted patient
• Be aged 18 years and over

Exclusion Criteria:

• Withdrawn of the consent

The objective of the registry is to have an up-to-date, high quality and exhaustive data collection for the evaluation of the overall survival in the population of heart transplanted recipients and the incidence of hearth, kidney, infectious complications over the last thirty years and their determinants.