Results 11 to 20 of about 222 (145)

Acquired long QT syndrome: as risky as congenital long QT syndrome? [PDF]

open access: yesEuropace, 2011
This editorial refers to ‘Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: A long-term follow-up’ by G. Monnig et al ., on page 396 Long QT syndrome (LQTS) describes a group of disorders characterized by QT interval prolongation secondary to delayed cardiac repolarization that may either be genetic ...
Leonie C H, Wong, Elijah R, Behr
openaire   +2 more sources

Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study

open access: yesHepatology, EarlyView., 2022
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel   +93 more
wiley   +1 more source

Case report of antiseizure medicine-induced long QT syndrome and a literature review

open access: yesActa Epileptologica, 2022
Background To realize the clinical characteristics of long QT syndrome (LQTS) caused by antiseizure medicines (ASMs), and to improve the prevention and management of ASM-acquired QT syndrome.
Xiongying Yu   +6 more
doaj   +1 more source

Long QT syndrome - causes and risk factors

open access: yesJournal of Education, Health and Sport, 2018
Sudden cardiac death is a major public health challenge, which can be caused by genetic or acquired structural or electrophysiological abnormalities. These abnormalities include channelopathies such as long QT, short QT and Brugada syndromes.
Erwin Ciechański   +3 more
doaj   +3 more sources

Selective acquired long QT syndrome (saLQTS) upon risperidone treatment

open access: yesBMC Psychiatry, 2012
Background Numerous structurally unrelated drugs, including antipsychotics, can prolong QT interval and trigger the acquired long QT syndrome (aLQTS). All of them are thought to act at the level of KCNH2, a subunit of the potassium channel.
Lazarczyk Maciej   +3 more
doaj   +1 more source

Mechanisms, Risk Factors, and Management of Acquired Long QT Syndrome: A Comprehensive Review

open access: yesThe Scientific World Journal, 2012
Long QT syndrome is characterized by prolongation of the corrected QT (QTc) interval on the surface electrocardiogram and is associated with precipitation of torsade de pointes (TdP), a polymorphic ventricular tachycardia that may cause sudden death ...
Eleftherios M. Kallergis   +4 more
doaj   +1 more source

Comparative Characteristics of Beta-Blockers in Patients with Congenital Long QT Syndrome

open access: yesРациональная фармакотерапия в кардиологии, 2021
Congenital long QT syndrome is a pathology that requires special attention and knowledge about the safety and effectiveness of various medications.
A. Yu. Proshlyakov   +2 more
doaj   +1 more source

Acquired long QT syndrome and Torsades de Poin

open access: yesThe Egyptian Heart Journal, 2016
Acetylcholinesterase inhibitors are group of drugs commonly used in Alzheimer disease and have beneficial effects on treatment. Although they have many known side effects, cardiovascular side effects are rarely seen.
Ahmet Seyfeddin Gurbuz   +7 more
doaj   +1 more source

Observation of acquired long QT syndrome

open access: yesПедиатрический вестник Южного Урала, 2022
Приобретённое удлинение интервала QT (ALQT) может провоцироваться назначением некоторых препаратов, нарушением электролитного баланса, брадикардией, воспалительной, ишемической и наследственной патологией миокарда, катастрофами центральной нервной системы в подавляющем большинстве случаев при генетической предрасположенности.
openaire   +1 more source

Torsades de pointes in the PACU after outpatient endoscopy: a case report

open access: yesBMC Anesthesiology, 2021
Background This case demonstrates the severe electrolyte derangements that may present after a common therapy such as a bowel preparation for an outpatient procedure and the rare yet potential detrimental outcomes of those abnormalities.
Andrew Schaar   +2 more
doaj   +1 more source

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