scholarly journals 228 * SAFETY OF A NOVEL SURGICAL THERAPY FOR THE TREATMENT OF ADVANCED HEART FAILURE: REVIEW OF SURGICAL MORBIDITY AND MORTALITY OF ALGISYL-LVR FROM THE AUGMENT-HF TRIAL

2014 ◽  
Vol 19 (suppl 1) ◽  
pp. S68-S68
Author(s):  
L. Menicanti ◽  
I. Mocanu ◽  
F. Miraldi ◽  
S. Marasco ◽  
A. Hinson ◽  
...  
2003 ◽  
Vol 91 (9) ◽  
pp. 88-94 ◽  
Author(s):  
Ettore Vitali ◽  
Tiziano Colombo ◽  
Pasquale Fratto ◽  
Claudio Russo ◽  
Giuseppe Bruschi ◽  
...  

2005 ◽  
Vol 45 (7) ◽  
pp. 1064-1071 ◽  
Author(s):  
Paul A. Grayburn ◽  
Christopher P. Appleton ◽  
Anthony N. DeMaria ◽  
Barry Greenberg ◽  
Brian Lowes ◽  
...  

2003 ◽  
Vol 9 (5) ◽  
pp. S96
Author(s):  
Ioana Dumitru ◽  
Kevin J. Makati ◽  
Gregory A. Ewald ◽  
Edward M. Geltman ◽  
Joseph G. Rogers

PLoS ONE ◽  
2021 ◽  
Vol 16 (1) ◽  
pp. e0244453
Author(s):  
Waguih William IsHak ◽  
Samuel Korouri ◽  
Tarneem Darwish ◽  
Brigitte Vanle ◽  
Jonathan Dang ◽  
...  

Objectives Heart Failure is a chronic syndrome affecting over 5.7 million in the US and 26 million adults worldwide with nearly 50% experiencing depressive symptoms. The objective of the study is to compare the effects of two evidence-based treatment options for adult patients with depression and advanced heart failure, on depressive symptom severity, physical and mental health related quality of life (HRQoL), heart-failure specific quality of life, caregiver burden, morbidity, and mortality at 3, 6 and 12-months. Methods Trial design. Pragmatic, randomized, comparative effectiveness trial. Interventions. The treatment interventions are: (1) Behavioral Activation (BA), a patient-centered psychotherapy which emphasizes engagement in enjoyable and valued personalized activities as selected by the patient; or (2) Antidepressant Medication Management administered using the collaborative care model (MEDS). Participants. Adults aged 18 and over with advanced heart failure (defined as New York Heart Association (NYHA) Class II, III, and IV) and depression (defined as a score of 10 or above on the PHQ-9 and confirmed by the MINI International Neuropsychiatric Interview for the DSM-5) selected from all patients at Cedars-Sinai Medical Center who are admitted with heart failure and all patients presenting to the outpatient programs of the Smidt Heart Institute at Cedars-Sinai Medical Center. We plan to randomize 416 patients to BA or MEDS, with an estimated 28% loss to follow-up/inability to collect follow-up data. Thus, we plan to include 150 in each group for a total of 300 participants from which data after randomization will be collected and analyzed. Conclusions The current trial is the first to compare the impact of BA and MEDS on depressive symptoms, quality of life, caregiver burden, morbidity, and mortality in patients with depression and advanced heart failure. The trial will provide novel results that will be disseminated and implemented into a wide range of current practice settings. Registration ClinicalTrials.Gov Identifier: NCT03688100.


2020 ◽  
Vol 59 (2) ◽  
pp. 570
Author(s):  
Anirudh Rao ◽  
Sherry Gholami ◽  
Hasan Javed ◽  
Tankala Shantal Gupta ◽  
Mark Hofmeyer ◽  
...  

2003 ◽  
Vol 2 (1) ◽  
pp. 115-116
Author(s):  
J PARISSIS ◽  
S ADAMOPOULOS ◽  
K VENETSANOU ◽  
D MENTZIKOF ◽  
K KIRANAKOS ◽  
...  

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