HFSA ePoster Library

EBV-seronegative Status In Recipients Worsens Post Heart Transplant Survival
HFSA ePoster Library. Gadela N. 09/10/21; 343388; 162
Naga Vaishnavi Gadela
Naga Vaishnavi Gadela
Login now to access Regular content available to all registered users.
Abstract
Discussion Forum (0)
Introduction: There is little evidence about the short-term outcomes of patients undergoing implantation of ventricular assist devices (VADs) who require initiation of chronic intermittent hemodialysis (IHD). Filling this knowledge gap may help anticipate potential complications and improve outcomes.
Methods: This is a chart review, retrospective study that included all patients who underwent VAD implantation followed by initiation of IHD at our center. Intermittent hemodialysis was defined as ≤6-hour sessions, 3-4 times weekly. Continuous renal replacement therapy (CRRT) did not meet this inclusion criteria. Continuous and categorical variables were expressed in means (standard deviation) and numbers (%), respectively.
Results: Among the 11 patients that met inclusion criteria, 6 (54.6%) were female, 6 (54.6%) were African American, 6 (54.6%) had non-ischemic cardiomyopathy, 6 were being bridged to HT, and 9 (81.8%) had chronic kidney disease. Home regimen was available for 10 patients, all of whom were taking loop diuretics, but only 7 (70%) and 3 (30%) of them had medical regimens with ACEIs or ARBs, and spironolactone, respectively. All patients received tunneled catheters, and in 2 of them AV fistulas were performed afterwards. At least 3 patients experienced asymptomatic hypotension (<60 mm Hg) during the first 10 IHD sessions, leading to finishing the session early in one of the cases. Another patient had catheter thrombosis leading to catheter exchange. No other major event was documented during the 10 initial IHD sessions. One patient started IHD outpatient without complications. Among the 10 (90.9%) patients who started IHD during index hospitalization, the length of hospital stay was 81.5 (±40.7) days, and their most relevant complications were death (1), stroke (1), infections (5), gastrointestinal bleeding (4), right ventricular failure (2), and tracheostomy (1). For those who started IHD during index hospitalization, time to first readmission was 44.6 (±36.3) days, with 4 (44.4%) patients being readmitted within 30 days, and 1 of them dying during the first readmission. Additional information is found in Table 1.
Conclusions: This study confirms feasibility of IHD initiation after VAD implantation, even as outpatient, but also proves a high burden of morbidity during index hospitalization and short-term follow up. Larger studies prospective studies with the newest VADs could provide valuable insight into this strategy for left ventricular and renal replacement therapies.
Table 1. Baseline characteristics and outcomes
PatientACEI/ARBVADVAD strategyYear of VAD implantationLOS, daysIHD initiation settingTime to 1st readmission, days - Reason
36 YO F with ICM, CKD3NoHM2BTT201165IP100 - Ruptured ovarian cyst
42 YO M with NICM, CKD3-HM2-201241IP9 - Subtherapeutic INR
54 YO F with ICMYesHVADDT2012166IP41 - Femoral fracture
59 YO F with NICM, CKD3YesHVADBTT201354IP31 - HF exacerbation, subtherapeutic INR
48 YO F with NICM, CKD2NoHM2BTT2013109IP6 - Fever, ICH
66 YO F with ICM, CKD3YesHM2BTT201435IP17 - Subarachnoid hemorrhage
51 YO F with NICM, CKD3YesHM2DT201466IP84 - Subtherapeutic INR
66 YO M with NICM, CKD3YesHM2DT201681IP89 - Subtherapeutic INR
60 YO M with ICM, CKD3NoHM2BTT201673IP26 - Tunneled catheter related infection
64 YO M with NICMYesHM3BTT2019125IPN/A (died during index hospitalization)
50 YO M with ICM, CKD3YesHM3DT201924OP378 - Liver biopsy for abnormal hepatic test
ACEI/ARB, angiotensin converting enzyme inhibitor or angiotensin receptor blocker; BT, bridge to transplant; CKD2, chronic kidney disease stage 2; CKD3, chronic kidney disease stage 3; DT, destination therapy; F, female; HF, heart failure; HM, HeartMate; ICH, intracranial hemorrhage; ICM, ischemic cardiomyopathy; IHD, intermittent hemodialysis; IP, inpatient; LOS, length of hospital stay; M, male; N/A, not applicable; NICM, non-ischemic cardiomyopathy; OP, outpatient; VAD, ventricular assist device; YO, year old
Introduction: There is little evidence about the short-term outcomes of patients undergoing implantation of ventricular assist devices (VADs) who require initiation of chronic intermittent hemodialysis (IHD). Filling this knowledge gap may help anticipate potential complications and improve outcomes.
Methods: This is a chart review, retrospective study that included all patients who underwent VAD implantation followed by initiation of IHD at our center. Intermittent hemodialysis was defined as ≤6-hour sessions, 3-4 times weekly. Continuous renal replacement therapy (CRRT) did not meet this inclusion criteria. Continuous and categorical variables were expressed in means (standard deviation) and numbers (%), respectively.
Results: Among the 11 patients that met inclusion criteria, 6 (54.6%) were female, 6 (54.6%) were African American, 6 (54.6%) had non-ischemic cardiomyopathy, 6 were being bridged to HT, and 9 (81.8%) had chronic kidney disease. Home regimen was available for 10 patients, all of whom were taking loop diuretics, but only 7 (70%) and 3 (30%) of them had medical regimens with ACEIs or ARBs, and spironolactone, respectively. All patients received tunneled catheters, and in 2 of them AV fistulas were performed afterwards. At least 3 patients experienced asymptomatic hypotension (<60 mm Hg) during the first 10 IHD sessions, leading to finishing the session early in one of the cases. Another patient had catheter thrombosis leading to catheter exchange. No other major event was documented during the 10 initial IHD sessions. One patient started IHD outpatient without complications. Among the 10 (90.9%) patients who started IHD during index hospitalization, the length of hospital stay was 81.5 (±40.7) days, and their most relevant complications were death (1), stroke (1), infections (5), gastrointestinal bleeding (4), right ventricular failure (2), and tracheostomy (1). For those who started IHD during index hospitalization, time to first readmission was 44.6 (±36.3) days, with 4 (44.4%) patients being readmitted within 30 days, and 1 of them dying during the first readmission. Additional information is found in Table 1.
Conclusions: This study confirms feasibility of IHD initiation after VAD implantation, even as outpatient, but also proves a high burden of morbidity during index hospitalization and short-term follow up. Larger studies prospective studies with the newest VADs could provide valuable insight into this strategy for left ventricular and renal replacement therapies.
Table 1. Baseline characteristics and outcomes
PatientACEI/ARBVADVAD strategyYear of VAD implantationLOS, daysIHD initiation settingTime to 1st readmission, days - Reason
36 YO F with ICM, CKD3NoHM2BTT201165IP100 - Ruptured ovarian cyst
42 YO M with NICM, CKD3-HM2-201241IP9 - Subtherapeutic INR
54 YO F with ICMYesHVADDT2012166IP41 - Femoral fracture
59 YO F with NICM, CKD3YesHVADBTT201354IP31 - HF exacerbation, subtherapeutic INR
48 YO F with NICM, CKD2NoHM2BTT2013109IP6 - Fever, ICH
66 YO F with ICM, CKD3YesHM2BTT201435IP17 - Subarachnoid hemorrhage
51 YO F with NICM, CKD3YesHM2DT201466IP84 - Subtherapeutic INR
66 YO M with NICM, CKD3YesHM2DT201681IP89 - Subtherapeutic INR
60 YO M with ICM, CKD3NoHM2BTT201673IP26 - Tunneled catheter related infection
64 YO M with NICMYesHM3BTT2019125IPN/A (died during index hospitalization)
50 YO M with ICM, CKD3YesHM3DT201924OP378 - Liver biopsy for abnormal hepatic test
ACEI/ARB, angiotensin converting enzyme inhibitor or angiotensin receptor blocker; BT, bridge to transplant; CKD2, chronic kidney disease stage 2; CKD3, chronic kidney disease stage 3; DT, destination therapy; F, female; HF, heart failure; HM, HeartMate; ICH, intracranial hemorrhage; ICM, ischemic cardiomyopathy; IHD, intermittent hemodialysis; IP, inpatient; LOS, length of hospital stay; M, male; N/A, not applicable; NICM, non-ischemic cardiomyopathy; OP, outpatient; VAD, ventricular assist device; YO, year old
Code of conduct/disclaimer available in General Terms & Conditions

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies