Abstract 15794: Changes in Patient and Caregiver Depression and Anxiety Post-implantation of a Ventricular Assist Device

Circulation ◽  
2015 ◽  
Vol 132 (suppl_3) ◽  
Author(s):  
Julie T Bidwell ◽  
James O Mudd ◽  
Jill M Gelow ◽  
Karen S Lyons ◽  
Shirin O Hiatt ◽  
...  

Introduction: The impact of ventricular assist device (VAD) therapy on affective symptoms among patients with advanced heart failure (HF) and their informal caregivers is not well understood. Hypothesis: We hypothesized that patients’ affective symptoms would improve post-implant, while caregivers’ affective symptoms would worsen. Methods: Prospective, longitudinal data was collected on patients and their caregivers (n=25 dyads) prior to and at 30 and 90 days after VAD implantation. Depression was measured using the Patient Health Questionnaire-8 (PHQ-8; range 0-24, higher scores indicate worse depressive symptoms), and anxiety was measured using the Anxiety Scale of the Brief Symptom Inventory (BSI-ANX; range 0-4; higher scores indicate worse anxiety) in patients and their caregivers. Pre vs. post VAD comparisons in affective symptoms were examined using paired t-tests. Results: Patients requiring VAD implantation were 54.9±12.5 years of age and mostly male (84.0%), while caregivers were 53.9±11.1 years of age and mostly female (80.0%); a majority (72.0%) of dyads were spouses. Patient depression decreased significantly from pre-implant (9.3±5.6) to 30 days (6.9±5.4; t=2.2, p=0.04) and 90 days post-implant (3.6±3.6; t=5.3, p<0.01); patient anxiety also decreased from pre-implant (1.0±0.9) to 30 days (0.5±0.7; t=2.9, p<0.01) and 90 days post-implant (0.3±0.4; t=4.5, p<0.01). In contrast, there were no significant changes in caregiver depression from pre-implant (6.0±5.2) to 30 days (5.2±4.4; t=0.5, p=0.6) and 90 days post-implant (6.6±5.7; t=-0.4, p=0.7) or in caregiver anxiety from pre-implant (0.8±0.6) to 30 days (0.5±0.4; t=1.5, p=0.2) and 90 days post-implant (0.6±0.7; t=0.9, p=0.4). Conclusions: Although depression and anxiety improved dramatically for patients after VAD implantation, the pre-implant affective symptom burden of caregivers was substantially higher than national norms at baseline and was not ameliorated over time. As patient symptoms improve with VAD therapy, their caregivers may benefit from psychosocial interventions to address protracted symptoms of depression and anxiety.

2010 ◽  
Vol 140 (1) ◽  
pp. 169-173 ◽  
Author(s):  
David A. Bull ◽  
Bruce B. Reid ◽  
Craig H. Selzman ◽  
Rebecca Mesley ◽  
Stavros Drakos ◽  
...  

ASAIO Journal ◽  
2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Marc D. Samsky ◽  
Carmelo A. Milano ◽  
Salpy Pamboukian ◽  
Mark S. Slaughter ◽  
Emma Birks ◽  
...  

Open Heart ◽  
2020 ◽  
Vol 7 (2) ◽  
pp. e001385
Author(s):  
Sandra Haberkorn ◽  
Angelika Uwarow ◽  
Jean Haurand ◽  
Christian Jung ◽  
Malte Kelm ◽  
...  

ObjectivesThe aim of this study was to investigate the impact of acute left ventricular unloading by percutaneous left ventricular assist device on pulmonary congestion and pneumonia in patients with cardiogenic shock (CS).MethodsIn this retrospective study, we analysed patients with CS who received the Impella percutaneous left ventricular assist device (n=50) compared with those who received intra-aortic balloon pump (IABP) support (n=50). Pulmonary congestion was longitudinally assessed while on support by calculating characteristic findings on the chest X-ray using the Halperin score. The rate of pneumonia and early mortality were assessed as a secondary endpoint.ResultsThe groups (Impella vs IABP) did not differ in terms of age, Sequential Organ Failure Assessment (SOFA) score, Acute Physiology, Chronic Health Evaluation (APACHE) II score or serum lactate levels. Pulmonary congestion decreased in patient treated with Impella at each time point postimplantation. No change in congestion status was observed in patients supported with IABP. Multivariate analysis indicated Impella support as an independent predictor for pulmonary decongestion (OR 4.06, 95% CI 1.15 to 14.35, p=0.030). The rate of early pneumonia was lower in the Impella group compared with the IABP group (54% vs 74%, p=0.037). Failure of pulmonary decongestion during mechanical circulatory support independently predicted early pneumonia (OR 0.28, 95% CI 0.12 to 0.70, p=0.006).ConclusionPulmonary decongestion may facilitate treatment of pneumonia in patients with CS. Left ventricular unloading by Impella device might support pulmonary decongestion, although a larger prospective trial in this patient population is required.


2006 ◽  
Vol 25 (7) ◽  
pp. 820-824 ◽  
Author(s):  
Mohamad H. Yamani ◽  
Hsuan-Hung Chuang ◽  
Volkan Ozduran ◽  
Robin K. Avery ◽  
Steven D. Mawhorter ◽  
...  

ASAIO Journal ◽  
2019 ◽  
Vol 65 (8) ◽  
pp. 827-836 ◽  
Author(s):  
Daljeet Chahal ◽  
Amir A. Sepehry ◽  
Hamed Nazzari ◽  
Alissa Jade Wright ◽  
Mustafa Toma

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