Online Supplementary Appendices Table of Contents Figure S1. Gastrointestinal Bleeding Source by Cohort Figure S2. Diagnostic Procedure Identifying Bleeding Source by Cohort Appendix S1. Considerations with Post-operative Assessment Echocardiographic Assessment Post-operative transthoracic echocardiograms (TTE) were assessed when available for all patients after placement of continuous-flow left ventricular assist device (CF-LVAD). TTE performed between 2 and 6 months after LVAD were eligible for assessment with preference given to the earliest TTE during this post-operative time period. Those patients who did not have a qualifying TTE were not assessed. Pertinent data are presented in Table S1. Assessment of LVAD Function Markers of LVAD function including TTE assessment of aortic valve opening and pulsatility index (HeartMate II® only) were performed post-operatively. Aortic valve opening was assessed via review of the TTE as presented above. Relevant data are presented in Table S1. PI was assessed at two time points in the post-operative setting. The average PI over the 24 hours prior to discharge from index hospitalization was obtained. The average PI obtained from LVAD interrogation at the first post-operative clinic visit was also obtained when available. The mean of the pre-discharge and follow-up PI was calculated and is presented in Table S1. Table S1. Post-operative Echocardiographic and LVAD Function Parameters Control Severe RV Dysfunction (n = 175) (n = 37) p Value TAPSE* 1.03 0.28 0.98 0.34 0.49 Tei Index 0.47 0.20 0.53 0.25 0.14 RA Pressure 7.95 4.70 10.26 6.32 0.08 RVEDD 3.80 0.72 3.95 0.90 TR Severity 0.32 0.03 None 22 (14.0) 9 (26.5) Mild 104 (66.2) 14 (41.2) 2 (1.3) 0 (0) 17 (10.8) 6 (17.6) 0 (0) 1 (2.9) 12 (7.6) 4 (11.8) Pulsatility Index 4.97 0.71 4.95 0.92 0.93 Persistent AV Closure 104 (61.9) 24 (75) 0.38 Mild-Moderate Moderate Moderate-Severe Severe All values reported as number (%) or mean +/- SD. *TAPSE has been shown to be an unreliable marker of RV function post-LVAD. AV = aortic valve, RA = right atrial, RVEDD = right ventricular end diastolic diameter, TAPSE = tricuspid annular plane systolic excursion, TR = tricuspid regurgitation. Appendix S2. Validation Analyses CVP and GIB We performed an analysis assessing the relationship between post-operative CVP and GIB to validate our findings linking RV dysfunction and GIB. CVP is an easily measureable post-VAD clinical marker of RV dysfunction. We obtained the postoperative CVP on post-operative day 2 or 3 on all patients with available data. We identified 173 patients with available data and divided this group into terciles with a low CVP tercile with CVP < 10 (58 patients), a middle tercile with CVP 10-13 (58 patients) and a high CVP tercile with CVP ≥ 13 (57 patients). GIB was assessed over time, and a Kaplan-Meier analysis was performed to analyze event-free survival rates. The log-rank test was performed to determine clinical significance, and a p-value of 0.0315 was determined. Post-operative Inotrope Duration and GIB We sought to perform an analysis similar to our primary analysis using a clinical definition of RV dysfunction to further validate our findings. Accepted definitions of post-VAD clinical RV dysfunction include prolonged duration of inotropes (≥14 days) and need for RVAD support. Due to the markedly diminished survival and lack of follow-up data of our patients who required RVAD support, we felt that this group would confound our results. We opted instead to focus on duration of inotropes as a predictor of GIB. We identified 412 patients in an expanded cohort of all patients who have received a CF-LVAD at our institution from 2006-2014. Of this group, 112 patients required inotropic support ≥ 14 days and compared this group with 300 patients who required < 14 days of inotropes after LVAD implantation. GIB was assessed over time, and a Kaplan-Meier analysis was performed to analyze event-free survival rates. The Wilcoxon test was performed to determine clinical significance, and a p-value of 0.0309 was determined.