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Right heart failure and “failure to thrive” after left ventricular assist device: Clinical predictors and outcomes

https://doi.org/10.1016/j.healun.2011.03.006Get rights and content

Background

This study determined predictors of early post-operative right heart failure (RHF) and its consequences, as well as predictors of those who clinically thrive longer term after insertion of a continuous-flow left ventricular assist device (LVAD).

Methods

Pre-operative and latest follow-up data were analyzed for 40 consecutive patients who received third-generation centrifugal-flow LVADs. RHF was defined using previously described criteria, including post-operative inotropes, pulmonary vasodilator use, or right-sided mechanical support. Patients were also categorized according to clinical outcomes after LVAD insertion.

Results

LVADs were implanted as a bridge to transplantation (BTT) in 33 patients and as destination therapy in 7. Before LVAD implant, 22 patients were Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) level 1, and 17 were at level 2. Temporary mechanical assistance was present in 50% of the cohort at LVAD implantation. The 6-month survival/progression to transplant was 92.5%. Average LVAD support time was 385 days (range, 21–1,011 days). RHF developed postoperatively in 13 of 40 patients (32.5%). RHF patients had more severe pre-operative tricuspid incompetence than non-RHF patients. The BTT patients with evidence of RHF had poorer survival to transplant (6 of 11 [54.5%]) than those without RHF (20 of 22 [90.9%]), p = 0.027). There were no other hemodynamic or echocardiographic predictors of short-term RHF. After LVAD, 22 of the 40 patients (55%) thrived clinically. For BTT patients, 20 of 21 (95%) of those who thrived progressed to transplant or were alive at latest follow-up vs 6 of 12 (50%) of those who failed to thrive (FTT; p < 0.005). The thrivers had lower New York Heart Association class (1.5 vs 2.9, p < 0.001), spent less time in the hospital, and had less ventricular tachycardia than the FTT patients. However, no differences were noted in pre-operative INTERMACS level, echocardiographic, hemodynamic, and biochemical indices, or in early post-operative RHF. Age was the only significant predictor: the thrivers were significantly younger (43.7 ± 15.9 vs 60.3 ± 12.6 years; p < 0.001). This age difference was unchanged after exclusion of destination strategy patients. RV function deteriorated in the FTT patients and remained stable in those who thrived.

Conclusions

Early post-operative RHF results in poorer survival/progression to transplantation for BTT patients and is predicted by greater pre-operative tricuspid incompetence. The most important predictor for those who will clinically thrive longer-term after LVAD insertion is younger age.

Section snippets

Methods

This study was approved by the Human Research Ethics Committee at St. Vincent's Hospital, Sydney.

Demographics

For the overall group, the average age at implant was 51.2 ± 16.6 years (range, 14–75 years), and mean LVAD support time was 385 ± 283 days (range, 21–1,011 days). Before LVAD implant, 22 patients were at Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) level 1, 17 were at level 2, and 1 was at level 3. At the time of LVAD implantation, 20 (50%) were receiving pre-operative support from an intra-aortic balloon pump, and 4 (10%) were receiving venoarterial ECMO.

Discussion

Excellent overall survival and outcomes were documented in this cohort of consecutive patients with centrifugal continuous-flow LVADs. However, not all patients who undergo LVAD implantation progress smoothly, due to early RHF and FTT, despite hemodynamic improvements. Pre-operative TR severity was the best predictor of early post-implant RHF in this study, but early RHF did not necessarily impair long-term outcomes. Long-term clinical outcomes were predicted mainly by patient age and were

Disclosure statement

P. Spratt owns stock in HeartWare Inc, but none of the other authors have a financial relationship with a commercial entity that has an interest in the subject of the presented manuscript or other conflicts of interest to disclose.

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