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Relevant bibliographies by topics / Long Qt Interval

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Academic literature on the topic 'Long Qt Interval'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Long Qt Interval"

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Avilova, A. A., Ye I. Kirichenko, and O. V. Rodionova. "Long QT interval syndrome." Public health of the Far East Peer-reviewed scientific and practical journal 2, no. 88 (2021): 44–48. http://dx.doi.org/10.33454/1728-1261-2021-2-44-48.

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The article provides an analysis of modern literature on the problem of diagnosing the long QT syndrome. The diagnostic criteria of this syndrome, features of rare congenital and acquired forms of the disease are described in the article. Risk factors for the development and diagnostic criteria of this disease are presented.

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MICHALOUDIS, D., and TH BISHINIOTIS. "Long QT interval syndrome with increased QT dispersion." Acta Anaesthesiologica Scandinavica 41, no. 4 (1997): 541–44. http://dx.doi.org/10.1111/j.1399-6576.1997.tb04739.x.

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Lewin, Mark B., Randall M. Bryant, Arnold L. Fenrich, and Ronald G. Grifka. "Cisapride-induced long QT interval." Journal of Pediatrics 128, no. 2 (1996): 279–81. http://dx.doi.org/10.1016/s0022-3476(96)70409-2.

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Surawicz, Borys. "Encountering a long QT interval." ACC Current Journal Review 5, no. 2 (1996): 71–73. http://dx.doi.org/10.1016/1062-1458(96)82290-2.

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Czuriga, Dániel, Andrea Szegedi, Ferenc Győry, et al. "Transient Long QT Development in a Patient with Takotsubo Cardiomyopathy." Journal Of Cardiovascular Emergencies 2, no. 2 (2016): 81–84. http://dx.doi.org/10.1515/jce-2016-0013.

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Abstract QT interval prolongation on the electrocardiogram is considered a precursory sign for imminent, potentially lethal ventricular arrhythmias. Beside the inherited condition of long QT syndrome, numerous drugs, certain electrolyte disturbances and early transmural ischemia have been identified to induce reversible prolongation of the QT interval, collectively called as acquired long QT syndrome. Herein we describe a case of a patient with transient QT prolongation and Takotsubo cardiomyopathy, a rather infrequent cause of long QT development. Serial changes of the repolarization pattern

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Savic, Natasa, and Ljiljana Gojkovic-Bukarica. "Long QT syndrome: Genetic implications and drug influence." Vojnosanitetski pregled 65, no. 4 (2008): 308–12. http://dx.doi.org/10.2298/vsp0804308s.

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<zakljucak> Produzeni QT interval predstavlja problem u klinickoj praksi kome se posvecuje sve veca paznja i koji je oblast intenzivnog istrazivanja. Genetske studije kod pojedinaca koji imaju klinicki izrazene simptome produzenog QT intervala i/ili pozitivnu porodicnu anamnezu za iznenadnu srcanu smrt, mogu za pocetak da budu ogranicene na KCNQ1, HERG i SCN5A gene sa verovatnocom otkrivanja mutacije od 65%. Predstojece studije tek treba da objasne znacaj polimorfizma odredjenih gena za pojavu produzenja QT intervala.

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Diamant, Ulla-Britt, Annica Winbo, Annika Rydberg, Eva-Lena Stattin, Milos Kesek, and Steen Jensen. "Vectorcardiographic recordings of QT interval predicts long QT syndrome." Journal of Electrocardiology 40, no. 4 (2007): S63—S64. http://dx.doi.org/10.1016/j.jelectrocard.2007.03.061.

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Komoliatova, V. N., L. M. Makarov, A. G. Akopyan, A. N. Komarov, N. V. Aksenova, and D. A. Besportochny. "Handgrip strength test for the diagnosis of long QT syndrome." Russian Journal of Cardiology 29, no. 2S (2024): 5762. http://dx.doi.org/10.15829/1560-4071-2024-5762.

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Long QT syndrome (LQTS) assessment is based on the QT/ÖRR equation (the so-called Bazett's formula) and calculating the corrected QT (QTc). However, this formula reliably estimates the QT interval in the heart rate range (HR) of 60-90 bpm, which makes it difficult to diagnose LQTS in patients with sinus bradycardia, typical of this disease.Aim. To improve the LQTS diagnosis in patients with sinus bradycardia using the handgrip strength test.Material and methods. A total of 188 patients aged 5-53 years (16 [13;17]) were examined: group I — 40 healthy children aged 9-17 years (14 [12;16]); group

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Yunisova, A. S., and A. V. Smolensky. "Acquired long QT interval in athletes." Sports medicine: research and practice 11, no. 4 (2022): 17–25. http://dx.doi.org/10.47529/2223-2524.2021.4.3.

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Long QT syndrome (LQTS) is a common disorder that leads to dramatic patient outcomes, chief among which is sudden cardiac death. This review provides detailed data on the diagnosis, prevalence, classification, etiology. The variety of causes leading to LQTS creates difficulties in the differential diagnosis of this condition and, as a result, LQTS often remains outside the attention of physicians who monitor the health of athletes. Particular attention is paid to the acquired forms of LQTS, particularly, the drug-induced form. The results of studies aimed at studying the prevalence of LQTS and

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Nakagawa, Mikiko, Tetsu Iwao, Shuji Ishida, et al. "Dynamics of QT Interval in a Patient With Long QT Syndrome and a Normal QT Interval." Japanese Circulation Journal 62, no. 3 (1998): 215–18. http://dx.doi.org/10.1253/jcj.62.215.

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Dissertations / Theses on the topic "Long Qt Interval"

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Kijtawornrat, Anusak. "Potential mechanisms for drug-induced prolongation of QT interval and genesis of torsades de pointes evaluated in the failing rabbit heart." Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1165467926.

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Crotti, Lia. "An investigation of the clinical profile and extent of Long QT Syndrome (LQTS) associated with the KCNQ1-A341V mutation in South Africa and with the KCNH2-A1116V mutation in an Italian family and the role that autonomic nervous system (ANS) activity and genetics play in clinical variability." Thesis, Stellenbosch : University of Stellenbosch, 2007. http://hdl.handle.net/10019.1/1417.

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Thesis (DMed (Medicine. Internal Medicine))--University of Stellenbosch, 2007.<br>Background Although great progress has been made in defining genes conferring the majority of genetic risk in Long QT Syndrome (LQTS) patients, there remains a substantial challenge to explain the widely observed variability in disease expression and phenotype severity, even among family members, sharing the same mutation. Identifying clinical and genetic variables capable of influencing/predicting the clinical phenotype of LQTS patients would allow a more accurate risk stratification, important for determi

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Meyer, Olivier. "Application des méthodes automatiques de mesure électrocardiographique continues pour l'évaluation des risques torsadogènes lors des essais cliniques : Une alternative fiable aux méthodes conventionnelles ?" Phd thesis, Université de Strasbourg, 2013. http://tel.archives-ouvertes.fr/tel-00967563.

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Les médicaments qui provoquent un allongement de la repolarisation cardiaque, mesuré sur l'électrocardiogramme (ECG) par la prolongation de l'intervalle QT, ont été associés à une augmentation du risque pro-arythmique, et plus particulièrement à la survenue de Torsades de pointes, une tachycardie ventriculaire polymorphe potentiellement mortelle. Les méthodes d'analyse du QT conventionnelles se restreignent à l'extraction de quelques complexes ECG. Cette pratique se traduit par de nombreuses limitations. L'inclusion de tous les battements enregistrés sur 24h et mesurés par des méthodes automat

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Fernandes, Fl?via Evelyn Medeiros. "Uso de medicamentos e prolongamento do intervalo QTc em uma Unidade de Terapia Intensiva adulto." PROGRAMA DE P?S-GRADUA??O EM CI?NCIAS FARMAC?UTICAS, 2017. https://repositorio.ufrn.br/jspui/handle/123456789/23841.

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Vesna, Mijatović. "Procena kardiološke bezbednosti pri primeni metadona u supstitucionoj terapiji zavisnika od opijata." Phd thesis, Univerzitet u Novom Sadu, Medicinski fakultet u Novom Sadu, 2014. http://www.cris.uns.ac.rs/record.jsf?recordId=87273&source=NDLTD&language=en.

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Metadon je sintetski agonist opijatnih receptora koji se primenjuje u sklopu supstitucione terapije opijatnih zavisnika metadonom (STM) i u terapiji hroničnog bola. Dugoročna primena STM je praćena blagim, uglavnom prolaznim, neželjenim delovanjima. Međutim, metadon pripada grupi lekova koji mogu da prouzrokuju prolongaciju korigovanog QT intervala (QTc) u elektrokardiogramu (EKG-u) i povećaju rizik za nastanak potencijalno fatalnih aritmija tipa torsades de pointes. Opijatni zavisnici metadon najče&scaron;će koriste u kombinaciji sa benzodiazepinima, i ova kombinacija lekova predstavlja fakto

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Berman, Catherine. "Prolonged QT interval: accuracy of the '' rule of thumb'' method for measuring the QT interval in the elderly attending geriatric clinical practices." Thesis, 2017. https://hdl.handle.net/10539/26872.

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Background Long QT syndrome (LQTS) is characterized by a prolonged QT interval on the electrocardiogram (ECG), a risk for sudden cardiac death. A simple 'rule of thumb' method states that if a patient's heart rate is between 60-100 bpm, the QT interval should not be more than half the R-R interval. The clinical accuracy of this method has not been tested in the elderly. Objectives To determine if the 'rule of thumb' to calculate QT interval prolongation, is accurate, compared to the corrected QT interval calculated using Bazett's formula. Secondary objectives include the prevalence of long

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Putnikovic, Marijana. "Use of Electrocardiogram Monitoring in Adult Patients Taking High-Risk QT Interval Prolonging Drugs in Clinical Practice: A Systematic Review." Thesis, 2022. https://hdl.handle.net/2440/136628.

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Drugs with the potential to cause QT prolongation belong to a wide spectrum of therapeutic classes and their use is expected in all types of clinical practice settings. QT prolongation can lead to serious arrythmias including torsades de pointes (TdP) which can be fatal. Detection and mitigation of QT prolongation involves use of electrocardiographic (ECG) monitoring, which remains a fundamental strategy to support quality use of high-risk QT interval prolonging drugs and to reduce patient harm, in all areas of clinical practice. The objective of this review was to summarise the best available

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Mecová, Marie. "Hodnocení dynamiky tepové frekvence a QTc intervalu v zotavení v závislosti na poloze těla." Master's thesis, 2020. http://www.nusl.cz/ntk/nusl-435719.

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At present, doctors are not consistent in the way they set the QTc interval in the recovery phase. The main goal of this study was to screen healthy subjects in the two different exercise stress tests and to compare the obtained data from both tests. We wanted to explore whether the heart rate and the QTc interval differs from each other when performed in two different body positions during the recovery phase. The main purpose was to present evidence that would prove or disprove a hypothesis that the figures differ in the different body positions. In the theoretical part we submitted the main

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Hreiche, Raymond. "Implication des interactions médicamenteuses, des transporteurs membranaires, du sexe et du diabète dans les mécanismes de survenue du syndrome du QT long médicamenteux." Thèse, 2008. http://hdl.handle.net/1866/6690.

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Silva, Vera Andreia Ribeiro Passos da. "Alterações do intervalo QT no eletrocardiograma: Síndrome do QT longo e Síndrome do QT curto." Master's thesis, 2014. https://repositorio-aberto.up.pt/handle/10216/75866.

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Book chapters on the topic "Long Qt Interval"

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Hajimolahoseini, Habib, Damian Redfearn, and Andrew Krahn. "A Deep Learning Approach for Diagnosing Long QT Syndrome Without Measuring QT Interval." In Advances in Artificial Intelligence. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-18305-9_42.

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Shah, Rashmi R. "Drug-Induced QT Interval Prolongation-Regulatory Guidance and Perspectives on hERG Channel Studies." In The hERG Cardiac Potassium Channel: Structure, Function and Long QT Syndrome. John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/047002142x.ch19.

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Locati, Emanuela H., and Giuseppe Bagliani. "Heart Rate Dependency of QT-Interval in Congenital and Acquired Prolonged Ventricular Repolarization: Long-Term Analysis by Holter Monitoring." In Advances in Noninvasive Electrocardiographic Monitoring Techniques. Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4090-4_14.

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Mitchell, L. Brent. "Polymorphic ventricular tachycardias including torsade de pointes." In ESC CardioMed, edited by Brian Olshansky. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0541.

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Polymorphic ventricular tachycardia (PMVT) is a rapid ventricular tachycardia in which the QRS complexes vary in coupling interval, morphology, and axis on a beat-to-beat basis. PMVT occurs in two distinct forms: PMVT without QT interval prolongation and PMVT with QT interval prolongation. The two types differ in important ways with respect to their differential diagnosis and treatment. PMVT without QT interval prolongation usually emerges in the setting of an unstable structural heart disorder, such as acute ischaemia or decompensated heart failure. Treatment is directed at the underlying hea

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Mitchell, L. Brent. "Polymorphic ventricular tachycardias including torsade de pointes." In ESC CardioMed, edited by Brian Olshansky. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0541_update_001.

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Polymorphic ventricular tachycardia (PMVT) is a rapid ventricular tachycardia in which the QRS complexes vary in coupling interval, morphology, and axis on a beat-to-beat basis. PMVT occurs in two distinct forms: PMVT without QT interval prolongation and PMVT with QT interval prolongation. The two types differ in important ways with respect to their differential diagnosis and treatment. PMVT without QT interval prolongation usually emerges in the setting of an unstable structural heart disorder, such as acute ischaemia or decompensated heart failure. Treatment is directed at the underlying hea

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Ferguson, Kris, and Peter Papapetrou. "Prolonged QT Syndrome." In Advanced Anesthesia Review, edited by Alaa Abd-Elsayed. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/med/9780197584521.003.0038.

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Abstract Long QT syndrome is an uncommon condition and, if left untreated, can be a life-threatening condition. Patient presentation can range from asymptomatic to sudden death. The typical presentation is in younger patients, with symptoms ranging from asymptomatic to mild palpitations to cardiac arrest. Treatment is proportional to symptomatology. Outpatient medication management is directed toward minimizing factors that increase sympathetic output and β-blockade. More invasive management such as with defibrillators are life-saving for severe symptomatic disease. Anesthesia management is di

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Yamaguchi Izumi, Fujita Hideo, and Ohe Kazuhiko. "Early Detection of QT Interval Prolongation from the ECG Database System." In Studies in Health Technology and Informatics. IOS Press, 2013. https://doi.org/10.3233/978-1-61499-289-9-1043.

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To prevent unexpected sudden cardiac patient death due to drug-induced Long QT syndrome (LQTS), we seek to build a computerized early detection and warning system of QTc interval increase tendency. We built an ECG database system that holds the digital waveform data and related information of the ECGs performed in out hospital, and developed an experimental detection system of QTc increase tendency. Despite the several problems about the accuracy of detection, we succeeded in extracting a patient who seemed to be drug-induced LQTS. A combination of such a detection system with more accuracy an

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Srivastava, Ankur, and James E. Littlejohn. "QTc Prolongation and Torsades de Pointes." In Cardiothoracic Critical Care. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190082482.003.0013.

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This chapter looks at QTc prolongation and torsades de pointes (Tdp). In cases of recurrent polymorphic ventricular tachycardia, Tdp should be an immediate consideration. Tdp appears like a “twisting of points” of the cardiac axis, which is most often due to acquired QTc prolongation. The QT interval is inversely related to heart rate; therefore, it is corrected (QTc) using formulas such as Bazett's, Fridericia, and Framingham. There are several congenital and acquired causes of QTc prolongation. The congenital long QT syndrome, Romano-Ward syndrome, and Jervell and Lange-Nielsen syndrome are

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Mazzanti, Andrea, and Silvia G. Priori. "Personalized therapies for cardiac channelopathies." In ESC CardioMed, edited by Paulus Kirchhof. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0729.

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The new target for treatment of patients with long QT syndrome (LQTS) and catecholaminergic polymorphic ventricular tachycardia (CPVT) is represented by the correction of the arrhythmogenic substrate underlying the disorders, in order to restore a physiological duration of ventricular repolarization in LQTS and a normal intracellular calcium handling in CPVT. This chapter reviews how conventional drugs, such as sodium channel blockers, may be suitable to treat the type 3 LQTS, both reverting the prolongation of QT interval and reducing arrhythmic events caused by abnormalities in the cardiac s

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Li, Jie Jack. "Cardiovascular Drugs: From Nitroglycerin to Lipitor." In Laughing Gas, Viagra, and Lipitor. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780195300994.003.0008.

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Cardiovascular diseases are the leading cause of death worldwide and are projected to remain in the lead through 2025. Heart-related diseases include angina, arrhythmia, atrial fibrillation, congestive heart failure, hypertension, atherosclerosis, myocardial infarction (heart attack), and sudden cardiac death. More than 300,000 Americans suffer sudden heart attacks each year. In addition, one of the more important recently identified drug-induced cardiac events, which has occasionally resulted in drugs being withdrawn, is drug-induced torsade des pointes. This is a rare, fatal arrhythmia that

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Conference papers on the topic "Long Qt Interval"

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Rodrigues, António Filipe Pinto, and Bruno Tiago Madeira Morais Valentim. "Acquired long QT Syndrome: Case report." In III SEVEN INTERNATIONAL MULTIDISCIPLINARY CONGRESS. Seven Congress, 2023. http://dx.doi.org/10.56238/seveniiimulti2023-107.

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Long QT syndrome, whether genetic or acquired, is closely associated with arrhythmogenic potential and consequently with syncope or even sudden death. This case report concerns a 77-year-old female who attended the emergency department for right-sided hemiparesis, diagnosed with ischemic stroke. She underwent Holter monitoring for paroxysmal atrial fibrillation, where an increase in the QT interval was found, which triggered a Torsades de Pointes by R on T phenomenon. After investigating the cause, it was found that the origin of the increase in the QT interval was iatrogenic. The drug that wa

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Pukkila, "Teemu, Matti Molkkari, Jiyeong Kim, and Esa Rasanen." "Reduced RR Interval Correlations of Long QT Syndrome Patients." In 2022 Computing in Cardiology Conference. Computing in Cardiology, 2022. http://dx.doi.org/10.22489/cinc.2022.284.

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Bari, Vlasta, Jose F. Valencia, Montserrat Vallverdu, et al. "Refined multiscale entropy analysis of heart period and QT interval variabilities in long QT syndrome type-1 patients." In 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2013. http://dx.doi.org/10.1109/embc.2013.6610808.

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Furuya, Masaki, Yuta Masuda, Kei Sato, Toshihiro Nishibe, Kazuo Yana, and Takuya Ono. "Long and short term QT-RR interval co-variability in type 2 diabetes." In 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2014. http://dx.doi.org/10.1109/embc.2014.6943523.

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Kanniainen, Matias, Teemu Pukkila, Matti Molkkari, and Esa Rasanen. "Effect of Diurnal Rhythm on RR Interval Correlations of Long QT Syndrome Patients." In 2023 Computing in Cardiology Conference. Computing in Cardiology, 2023. http://dx.doi.org/10.22489/cinc.2023.287.

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Bari, Vlasta, Beatrice De Maria, Giulia Girardengo, et al. "Multiscale Complexity Analysis of Short QT Interval Variability Series Stratifies the Arrhythmic Risk of Long QT Syndrome Type 1 Patients." In 2018 Computing in Cardiology Conference. Computing in Cardiology, 2018. http://dx.doi.org/10.22489/cinc.2018.053.

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Bari, Vlasta, Giulia Girardengo, Beatrice De Maria, et al. "Frequency Domain Heart Period and QT Interval Variability Markers Are Linked to Arrhythmic Risk in Long QT Syndrome Type 2." In 2020 Computing in Cardiology Conference. Computing in Cardiology, 2020. http://dx.doi.org/10.22489/cinc.2020.065.

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Lakhwani, B., D. Ranganathan, S. Singh, J. Galvin, and C. McGorrian. "44 Which correction method? The usefuless of qt interval measure as a screening tool for cascade testing in asymptomatic patients at risk of long QT syndrome." In Irish Cardiac Society Annual Scientific Meeting & AGM, October 17th – 19th 2024, Europa Hotel, Belfast. BMJ Publishing Group Ltd and British Cardiovascular Society, 2024. http://dx.doi.org/10.1136/heartjnl-2024-ics.45.

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Kim, "Jiyeong, Matias Kanniainen, Ilya Potapov, and Esa Rasanen." "Transfer Entropy between RR and QT Intervals in Long QT Syndrome." In 2022 Computing in Cardiology Conference. Computing in Cardiology, 2022. http://dx.doi.org/10.22489/cinc.2022.273.

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"METHADONE WITHDRAWAL PSYCHOSIS: A CLINICAL CASE." In 23° Congreso de la Sociedad Española de Patología Dual (SEPD) 2021. SEPD, 2021. http://dx.doi.org/10.17579/sepd2021p132v.

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The purpose of this article is, through a clinical case, to review the literature on psychosis secondary to methadone withdrawal. Observation of the patient and consultation of the clinical file. Non-systematic literature review on methadone use, methadone discontinuation and dual pathology. A 47-year-old male, history of opioid and cannabinoid use disorder, currently in abstinence and under opioid substitution therapy with methadone. After abrupt discontinuation of methadone, he began presenting delusional ideas of jealousy and persecution with multiple delusional interpretations. A diagnosis

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