Cardiac Ultrasound Imaging in Heart Failure: Recent Advances

2012 ◽  
Vol 9 (2) ◽  
pp. 154-161 ◽  
Author(s):  
Umar A. Khan ◽  
Gerard P. Aurigemma
2017 ◽  
Vol 23 (10) ◽  
pp. S12
Author(s):  
Shinro Matsuo ◽  
Kenichi Nakajima ◽  
Masakazu Yamagishi

Circulation ◽  
2008 ◽  
Vol 118 (suppl_18) ◽  
Author(s):  
Yoshikazu Yazaki ◽  
Mitsuaki Horigome ◽  
Kazunori Aizawa ◽  
Takeshi Tomita ◽  
Hiroki Kasai ◽  
...  

Background : We previously described severity of heart failure and ventricular tachycardia (VT) as independent predictors of mortality in patients with cardiac sarcoidosis (CS). Medical treatment for chronic heart failure has been established over the last few decades. Prophylactic use of implantable cardioverter defibrillator (ICD) and cardiac resynchronization therapy (CRT or CRT-D) have been introduced in patients with severe heart failure. We therefore hypothesized that the prognosis of CS improves due to such advances in the management of heart failure and VT. Methods : To confirm our hypothesis, we analyzed 43 CS patients diagnosed between 1988 and 2006 and treated with corticosteroids. We classified two sequential referral patients diagnosed between 1988 and 1997 (n=19) and between 1998 and 2006 (n=24), and compared treatment and prognosis between the two cohorts. Results : Left ventricular ejection fraction (LVEF) and dimensions were similar between the two cohorts. Although age in the 1988–1997 referral cohort was significantly younger than that in the 1998–2006 referral cohort (54±14years versus 62±10years, p<0.05), survival in the earlier cohort was significantly worse (log-rank=4.41, p<0.05). The 1- and 5-year mortality rates were 88% and 71% in the 1988–1997 referral cohort, and 96% and 92% in the 1998–2006 referral cohort, respectively. The 1998–2006 referral cohort showed significantly higher incidence of ICD or CRT-D implantation (29% versus 6%, p<0.05), β-blocker use (46% versus 6%, p<0.01) and addition of methotrexate (21% versus 0%, p<0.05), and increased maintenance dose (7.0±1.9mg/day versus 5.0±0.9mg/day, p<0.01) compared to the 1988–1997 referral cohort. Multivariate analysis including age, LVEF, and sustained ventricular tachycardia (sVT) identified diagnosis between 1988 and 1997 (hazard ratio [HR]: 19.8, p<0.01) and LVEF (HR: 0.83/1% increase, p<0.01) as independent predictors of mortality. Conclusions : Survival in the recent CS patients is significantly better than previously described. Recent advances in the device therapies and medical treatments including modified immunosuppression alter the clinical outcome in patients with CS.


2019 ◽  
Vol 6 (6) ◽  
pp. 1140-1148 ◽  
Author(s):  
Markus S. Anker ◽  
Sara Hadzibegovic ◽  
Alessia Lena ◽  
Yury Belenkov ◽  
Jutta Bergler‐Klein ◽  
...  

2013 ◽  
Vol 115 (6) ◽  
pp. 819-832 ◽  
Author(s):  
Juliana Marotti ◽  
Stefan Heger ◽  
Joachim Tinschert ◽  
Pedro Tortamano ◽  
Fabrice Chuembou ◽  
...  

1998 ◽  
Vol 74 (877) ◽  
pp. 658-661 ◽  
Author(s):  
F. A. McAlister ◽  
K. K. Teo

2015 ◽  
Vol 9s2 ◽  
pp. CMC.S32652
Author(s):  
Anthony Szema ◽  
Allison McLarty ◽  
Hal Skopicki ◽  
Michelle Bloom ◽  
Rita Jermyn

2019 ◽  
Vol 20 (19) ◽  
pp. 4714 ◽  
Author(s):  
Nadine Wehbe ◽  
Suzanne Nasser ◽  
Gianfranco Pintus ◽  
Adnan Badran ◽  
Ali Eid ◽  
...  

Like other organs, the heart undergoes normal adaptive remodeling, such as cardiac hypertrophy, with age. This remodeling, however, is intensified under stress and pathological conditions. Cardiac remodeling could be beneficial for a short period of time, to maintain a normal cardiac output in times of need; however, chronic cardiac hypertrophy may lead to heart failure and death. MicroRNAs (miRNAs) are known to have a role in the regulation of cardiac hypertrophy. This paper reviews recent advances in the field of miRNAs and cardiac hypertrophy, highlighting the latest findings for targeted genes and involved signaling pathways. By targeting pro-hypertrophic genes and signaling pathways, some of these miRNAs alleviate cardiac hypertrophy, while others enhance it. Therefore, miRNAs represent very promising potential pharmacotherapeutic targets for the management and treatment of cardiac hypertrophy.


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