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Continuous-flow left ventricular assist device therapy in patients with preoperative hepatic failure: are we pushing the limits too far?
- Source :
-
Artificial organs [Artif Organs] 2015 Apr; Vol. 39 (4), pp. 336-42. Date of Electronic Publication: 2014 Oct 27. - Publication Year :
- 2015
-
Abstract
- The purpose of this study was to evaluate the effects and outcome of continuous-flow left ventricular assist device (cf-LVAD) therapy in patients with preoperative acute hepatic failure. The study design was a retrospective review of prospectively collected data. Included were 42 patients who underwent cf-LVAD implantation (64.3% HeartMate II, 35.7% HeartWare) between July 2007 and May 2013 with preoperative hepatic failure defined as elevation of greater than or equal to two liver function parameters above twice the upper normal range. Mean patient age was 35 ± 12.5 years, comprising 23.8% females. Dilated cardiomyopathy was present in 92.9% of patients (left ventricular ejection fraction 17.3 ± 5.9%). Mean support duration was 511 ± 512 days (range: 2-1996 days). Mean preoperative laboratory parameters for blood urea nitrogen, serum creatinine, total bilirubin, and alanine aminotransferase were 9.5 ± 5.4 mg/dL, 110.3 ± 42.8 μmol/L, 51.7 ± 38.3 mmol/L, and 242.1 ± 268.6 U/L, respectively. All parameters decreased significantly 1 month postoperatively. The mean preoperative modified Model for Endstage Liver Disease excluding international normalized ratio score was 16.03 ± 5.57, which improved significantly after cf-LVAD implantation to 10.62 ± 5.66 (P < 0.001) at 7 days and 5.83 ± 4.98 (P < 0.001) at 30 days postoperatively. One-year and 5-year survival was 75.9 and 48.1%, respectively. 21.4% of the patients underwent LVAD explantation for myocardial recovery, 16.7% were successfully transplanted, and 7.1% underwent LVAD exchange for device failure over the follow-up period. Patients with preexisting acute hepatic failure are reasonable candidates for cf-LVAD implantation, with excellent rates of recovery and survival, suggesting that cf-LVAD therapy should not be denied to patients merely on grounds of "preoperative elevated liver enzymes/hepatopathy."<br /> (Copyright © 2014 International Center for Artificial Organs and Transplantation and Wiley Periodicals, Inc.)
- Subjects :
- Adult
Device Removal
Female
Heart Failure complications
Heart Failure diagnosis
Heart Failure mortality
Heart Failure physiopathology
Heart Transplantation
Humans
Kaplan-Meier Estimate
Liver Failure, Acute diagnosis
Liver Failure, Acute mortality
Liver Failure, Acute physiopathology
Liver Function Tests
Male
Middle Aged
Patient Selection
Predictive Value of Tests
Prosthesis Design
Recovery of Function
Retrospective Studies
Risk Factors
Stroke Volume
Time Factors
Treatment Outcome
Ventricular Dysfunction, Left complications
Ventricular Dysfunction, Left diagnosis
Ventricular Dysfunction, Left mortality
Ventricular Dysfunction, Left physiopathology
Young Adult
Heart Failure therapy
Heart-Assist Devices
Liver Failure, Acute complications
Ventricular Dysfunction, Left therapy
Ventricular Function, Left
Subjects
Details
- Language :
- English
- ISSN :
- 1525-1594
- Volume :
- 39
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Artificial organs
- Publication Type :
- Academic Journal
- Accession number :
- 25345547
- Full Text :
- https://doi.org/10.1111/aor.12375