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Publikováno v:
Research in Cardiovascular Medicine, Vol 9, Iss 3, Pp 72-74 (2020)
Long QT syndrome (LQTS) is a rare (1:2500–1:10,000) inherited disorder characterized by the onset of arrhythmogenic syncope, polymorphic ventricular tachycardia, and sudden cardiac death. The aim of this article was to describe an unexpected succes
Autor:
Saman Alilou, Farhad Jalili, Seifollah Abdi, Hosein Ali Basiri, Shirin Rafatnia, Omid Shafe, Hamidreza Pouraliakbar, Hooman Bakhshandeh, Ali Setayesh, Jamal Moosavi, Sara Yasini Ardakani, Parham Sadeghipour
Publikováno v:
Research in Cardiovascular Medicine, Vol 8, Iss 2, Pp 46-53 (2019)
Objectives: The endovascular treatment (EVT) of patients with critical limb ischemia (CLI) has received considerable interest in recent years and has significantly affected the associated amputation and survival rates. Nonetheless, that this manageme
Publikováno v:
Research in Cardiovascular Medicine, Vol 7, Iss 3, Pp 137-143 (2018)
Objectives: We investigated the effects of nesiritide (NES) on inflammatory response during cardiac surgery. Materials and Methods: Twenty-nine cardiac surgery patients were randomized to an infusion of NES at 0.01 mcg/kg/min for 48 h versus placebo
Autor:
Surendra Bahadur Mathur, NB Mathur
Publikováno v:
Research in Cardiovascular Medicine, Vol 6, Iss 4, Pp 1-7 (2017)
We tried to discuss the impact of early diagnosis on outcome of critical congenital heart diseases (CCHDs), current options, and their limitations in timely diagnosis, utility of pulse oximetry screening (POS), current recommendations for screening a
Publikováno v:
Research in Cardiovascular Medicine, Vol 7, Iss 1, Pp 46-48 (2018)
Primary aldosteronism is characterized by hypertension, suppressed plasma renin activity, increased aldosterone excretion, and hypokalemia with metabolic alkalosis. Ventricular arrhythmia is an uncommon finding. We report the case of a 46-year-old fe
Autor:
Ahmad Amin, Maryam Mohsenian, Negar Salehi, Mitra Chitsazan, Nima Babaali, Majid Maleki, Shokoufeh Hajsadeghi, Mandana Chitsazan, Seifollah Abdi
Publikováno v:
Research in Cardiovascular Medicine, Vol 5, Iss 1 (2015)
Research in Cardiovascular Medicine
Research in Cardiovascular Medicine, Vol 5, Iss 1, Pp 3-3 (2016)
Research in Cardiovascular Medicine
Research in Cardiovascular Medicine, Vol 5, Iss 1, Pp 3-3 (2016)
Background The crucial role of inflammation in the development and progression of atherosclerosis has been previously described. However, there is insufficient data available to demonstrate the changes in high sensitivity C-reactive protein (hs-CRP)
Publikováno v:
Research in Cardiovascular Medicine, Vol 6, Iss 1, Pp 10-10 (2017)
Introduction: Coronary-subclavian steal syndrome (CSSS) is not a common complication but it can cause recurrent angina following coronary artery bypass grafting(CABG). CSSS results from proximal subclavian artery stenosis causing reversal of blood fl
Autor:
Hannan Ebrahimi, Reza Pourbahador, Heidar Dadkhah Tirani, Rasool Hassanzadeh, Manouchehr Aghajanzadeh
Publikováno v:
Research in Cardiovascular Medicine, Vol 5, Iss 3, Pp 7-7 (2016)
Research in Cardiovascular Medicine
Research in Cardiovascular Medicine
Introduction: Giant coronary artery aneurysm is an extremely rare form of coronary artery disease. The most common cause of coronary artery aneurysms is atherosclerosis. Although it is usually asymptomatic, it may have various clinical presentations,
Influenza H1N1 infection leading to cardiac tamponade in a previously healthy patient: A case report
Publikováno v:
Research in Cardiovascular Medicine, Vol 5, Iss 3, Pp 6-6 (2016)
Research in Cardiovascular Medicine
Research in Cardiovascular Medicine
Introduction: The cardiac manifestations of influenza A are broad, ranging from self-limited pericarditis to fatal cardiomyopathy. The 2009 H1N1 influenza A (H1N1) strain is a rare cause of pericarditis, and its role in developing a pericardial effus
Publikováno v:
Research in Cardiovascular Medicine, Vol 5, Iss 2, Pp 7-7 (2016)
Research in Cardiovascular Medicine
Research in Cardiovascular Medicine
Introduction: In Turner syndrome, cardiovascular complications are the most important causes of early mortality. Congenital cardiovascular abnormalities are found in approximately one third of Turner syndrome patients. Developments in diagnosis and t