I50
Conditions
Interventions
Group 1: This retrospective study includes all patients who underwent LVAD implantation at the Department of Cardiac Surgery at the University Hospital Düsseldorf between 2010 and 2017
Sponsors
Klinik für Herzchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All adult patients (aged 18 years or older) who have successfully undergone LVAD implantation (e.g., HeartMate 3, HeartWare HVAD) as a bridge-to-transplant or destination therapy.
Exclusion criteria
Exclusion criteria: Pediatric cases, temporary RVAD/BiVAD, incomplete laboratory data
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| In-hospital mortality: Death during the index hospital stay following LVAD implantation 1-year all-cause mortality: Death within 365 days after surgery, regardless of cause | — |
Secondary
| Measure | Time frame |
|---|---|
| Intensive Care Unit (ICU) length of stay: Days from surgery to transfer to a general ward Hospital length of stay: Days from surgery to discharge Reoperations: All invasive revisions within 30 days (bleeding, tamponade, infection) Right ventricular failure (RVF): According to the INTERMACS definition—need for RVAD, NO/inotropes >14 days, or ECHO criteria (RVSP >50 mmHg, TAPSE <10 mm) Major bleeding (BARC =3): According to Bleeding Academic Research Consortium (BARC) classification, types 3–5 Renal replacement therapy (RRT): CVVH/CVVHD/dialysis =1 time during hospitalization | — |
Countries
Germany
Contacts
Public ContactHannan Dalyanoglu
Klinik für Herzchirurgie
Outcome results
None listed