Acquired intermittent long QT syndrome might be challenging in substitution dosing in adult patient with Addison disease: case report after 3 years follow up

2019 ◽  
Author(s):  
Dragan Tesic ◽  
Dragica Andric ◽  
Dalibor Somer ◽  
Milena Mitrovic
Circulation ◽  
1999 ◽  
Vol 100 (24) ◽  
pp. 2431-2436 ◽  
Author(s):  
Parvin C. Dorostkar ◽  
Michael Eldar ◽  
Bernard Belhassen ◽  
Melvin M. Scheinman

Author(s):  
Irene De Biase ◽  
Neena Lorenzana Champaigne ◽  
Richard Schroer ◽  
Laura Malinda Pollard ◽  
Nicola Longo ◽  
...  

2011 ◽  
Vol 21 (12) ◽  
pp. 1265-1267 ◽  
Author(s):  
Banashree Mandal ◽  
Gurpreet Kaur ◽  
Yatindra K. Batra ◽  
Sachin Mahajan

2020 ◽  
Vol 11 ◽  
Author(s):  
Lu Han ◽  
Fuxiang Liu ◽  
Qing Li ◽  
Tao Qing ◽  
Zhenyu Zhai ◽  
...  

Long QT syndrome (LQTS) is an arrhythmic heart disease caused by congenital genetic mutations, and results in increased occurrence rates of polymorphic ventricular tachyarrhythmias and sudden cardiac death (SCD). Clinical evidence from numerous previous studies suggested that beta blockers (BBs), including atenolol, propranolol, metoprolol, and nadolol, exhibit different efficacies for reducing the risk of cardiac events (CEs), such as syncope, arrest cardiac arrest (ACA), and SCD, in patients with LQTS. In this study, we identified relevant studies in MEDLINE, PubMed, embase, and Cochrane databases and performed a meta-analysis to assess the relationship between the rate of CEs and LQTS individuals with confounding variables, including different gender, age, and QTc intervals. Moreover, a network meta-analysis was not only established to evaluate the effectiveness of different BBs, but also to provide the ranked efficacies of BBs treatment for preventing the recurrence of CEs in LQT1 and LQT2 patients. In conclusion, nadolol was recommended as a relatively effective strategy for LQT2 in order to improve the prognosis of patients during a long follow-up period.


2002 ◽  
Vol 22 (13) ◽  
pp. 1209-1212 ◽  
Author(s):  
Ing-Kuang Chang ◽  
Ming-Kwang Shyu ◽  
Chien-Nan Lee ◽  
Miau-Ling Kau ◽  
Yu-Hsueh Ko ◽  
...  

2019 ◽  
Vol 37 (03) ◽  
pp. 322-325
Author(s):  
Bethany D. Kaemingk ◽  
Timothy J. Ulrich ◽  
Man Li ◽  
William A. Carey ◽  
Marc A. Ellsworth

Objective Long QT syndrome (LQTS) is a known cause of unexpected death, leading some to recommend routine neonatal electrocardiographic (ECG) screening. We used continuous electronic heart rate corrected QT interval (QTc) monitoring to screen for interval prolongation in a cohort of hospitalized neonates to identify those at a risk of having LQTS. We hypothesized that this screening method would yield an acceptable positive predictive value (PPV). Study Design A cohort of 589 infants hospitalized in a level II neonatal intensive care unit were screened through continuous electronic QTc monitoring linked to an investigator-designed, computerized data sniffer. Screening was conducted from days-of-life 3 through 7 or until hospital discharge. The data sniffer alerted investigators for a 24-hour average QTc of ≥475 ms. Positively screened patients were further evaluated with 12-lead ECG. Results Positive screens were obtained in 5.6% of patients, all of whom had negative follow-up ECG testing (PPV = 0%). Furthermore, one-quarter of positively screened neonates underwent echocardiography based on ECG findings, none of which identified clinically relevant pathology. Conclusion Electronic monitoring of QTc in hospitalized neonates during the first week of life was not an efficient way to identify those at a risk of having LQTS. Conversely, screening triggered unnecessary testing.


2020 ◽  
Vol 22 (3) ◽  
pp. 125-127
Author(s):  
Yvan R. Persia-Paulino ◽  
Jose Rozado-Castano ◽  
Maria Vigil-Escalera-Diaz ◽  
Julian Rodriguez-Reguero ◽  
Daniel Garcia-Iglesias ◽  
...  

2013 ◽  
Vol 9 (1) ◽  
pp. E11-E15 ◽  
Author(s):  
Kristin M. Burns ◽  
E. Anne Greene

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