Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes.

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Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes. / Hansen, Stig; Møller, Søren; Bendtsen, Flemming; Jensen, Gorm; Henriksen, Jens H; Hansen, Stig; Møller, Søren; Bendtsen, Flemming; Jensen, Gorm; Henriksen, Jens H.

I: Journal of Hepatology, Bind 47, Nr. 3, 2007, s. 373-80.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hansen, S, Møller, S, Bendtsen, F, Jensen, G, Henriksen, JH, Hansen, S, Møller, S, Bendtsen, F, Jensen, G & Henriksen, JH 2007, 'Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes.', Journal of Hepatology, bind 47, nr. 3, s. 373-80. https://doi.org/10.1016/j.jhep.2007.03.013, https://doi.org/10.1016/j.jhep.2007.03.013

APA

Hansen, S., Møller, S., Bendtsen, F., Jensen, G., Henriksen, J. H., Hansen, S., Møller, S., Bendtsen, F., Jensen, G., & Henriksen, J. H. (2007). Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes. Journal of Hepatology, 47(3), 373-80. https://doi.org/10.1016/j.jhep.2007.03.013, https://doi.org/10.1016/j.jhep.2007.03.013

Vancouver

Hansen S, Møller S, Bendtsen F, Jensen G, Henriksen JH, Hansen S o.a. Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes. Journal of Hepatology. 2007;47(3):373-80. https://doi.org/10.1016/j.jhep.2007.03.013, https://doi.org/10.1016/j.jhep.2007.03.013

Author

Hansen, Stig ; Møller, Søren ; Bendtsen, Flemming ; Jensen, Gorm ; Henriksen, Jens H ; Hansen, Stig ; Møller, Søren ; Bendtsen, Flemming ; Jensen, Gorm ; Henriksen, Jens H. / Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes. I: Journal of Hepatology. 2007 ; Bind 47, Nr. 3. s. 373-80.

Bibtex

@article{27d286b01ba011df8ed1000ea68e967b,
title = "Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes.",
abstract = "BACKGROUND/AIMS: A long QT(C) interval has been described in a substantial fraction of patients with cirrhosis, but information on QT variation and dispersion is sparse. The aim was to determine QT variation with time and QT dispersion (QT(disp)). METHODS: The study population comprised 23 patients with cirrhosis, undergoing a haemodynamic investigation. 24-h 12 lead Holter monitoring provided information on QT and heart rate variability. RESULTS: Mean QT(C) was above upper normal limit (440 ms(1/2)) in eleven patients (47%) and significantly higher than in controls (441 vs 400 ms(1/2), p<0.01). The minimum value of QT(C) (but not the maximum value) showed a significant diurnal variation both in cirrhosis and controls. QT(disp) in cirrhosis and controls was similar (33 vs 36 ms, ns), but related to indicators of liver dysfunction, central circulation time, and arterial blood pressure (r=0.44-0.58, p=0.03-0.001). No diurnal variation of QT(disp) was found in cirrhosis. Heart rate variability was reduced with a significant relation to central hypovolaemia (r=0.55, p=0.01). CONCLUSIONS: Twenty-four hours QT(C) is prolonged in a substantial fraction of patients with cirrhosis, but with normal diurnal variation. The combination of long QT(C) and normal QT(disp) suggests delayed myocyte repolarisation on the cellular level, rather than temporal and spatial heterogeneity in the myocardial wall.",
author = "Stig Hansen and S{\o}ren M{\o}ller and Flemming Bendtsen and Gorm Jensen and Henriksen, {Jens H} and Stig Hansen and S{\o}ren M{\o}ller and Flemming Bendtsen and Gorm Jensen and Henriksen, {Jens H}",
note = "Keywords: Aged; Blood Circulation; Blood Pressure; Blood Volume; Circadian Rhythm; Electrocardiography; Electrophysiology; Female; Heart; Heart Rate; Humans; Hypovolemia; Liver; Liver Cirrhosis; Long QT Syndrome; Male; Middle Aged; Myocardium; Time Factors",
year = "2007",
doi = "10.1016/j.jhep.2007.03.013",
language = "English",
volume = "47",
pages = "373--80",
journal = "Journal of Hepatology, Supplement",
issn = "0169-5185",
publisher = "Elsevier",
number = "3",

}

RIS

TY - JOUR

T1 - Diurnal variation and dispersion in QT interval in cirrhosis: relation to haemodynamic changes.

AU - Hansen, Stig

AU - Møller, Søren

AU - Bendtsen, Flemming

AU - Jensen, Gorm

AU - Henriksen, Jens H

AU - Hansen, Stig

AU - Møller, Søren

AU - Bendtsen, Flemming

AU - Jensen, Gorm

AU - Henriksen, Jens H

N1 - Keywords: Aged; Blood Circulation; Blood Pressure; Blood Volume; Circadian Rhythm; Electrocardiography; Electrophysiology; Female; Heart; Heart Rate; Humans; Hypovolemia; Liver; Liver Cirrhosis; Long QT Syndrome; Male; Middle Aged; Myocardium; Time Factors

PY - 2007

Y1 - 2007

N2 - BACKGROUND/AIMS: A long QT(C) interval has been described in a substantial fraction of patients with cirrhosis, but information on QT variation and dispersion is sparse. The aim was to determine QT variation with time and QT dispersion (QT(disp)). METHODS: The study population comprised 23 patients with cirrhosis, undergoing a haemodynamic investigation. 24-h 12 lead Holter monitoring provided information on QT and heart rate variability. RESULTS: Mean QT(C) was above upper normal limit (440 ms(1/2)) in eleven patients (47%) and significantly higher than in controls (441 vs 400 ms(1/2), p<0.01). The minimum value of QT(C) (but not the maximum value) showed a significant diurnal variation both in cirrhosis and controls. QT(disp) in cirrhosis and controls was similar (33 vs 36 ms, ns), but related to indicators of liver dysfunction, central circulation time, and arterial blood pressure (r=0.44-0.58, p=0.03-0.001). No diurnal variation of QT(disp) was found in cirrhosis. Heart rate variability was reduced with a significant relation to central hypovolaemia (r=0.55, p=0.01). CONCLUSIONS: Twenty-four hours QT(C) is prolonged in a substantial fraction of patients with cirrhosis, but with normal diurnal variation. The combination of long QT(C) and normal QT(disp) suggests delayed myocyte repolarisation on the cellular level, rather than temporal and spatial heterogeneity in the myocardial wall.

AB - BACKGROUND/AIMS: A long QT(C) interval has been described in a substantial fraction of patients with cirrhosis, but information on QT variation and dispersion is sparse. The aim was to determine QT variation with time and QT dispersion (QT(disp)). METHODS: The study population comprised 23 patients with cirrhosis, undergoing a haemodynamic investigation. 24-h 12 lead Holter monitoring provided information on QT and heart rate variability. RESULTS: Mean QT(C) was above upper normal limit (440 ms(1/2)) in eleven patients (47%) and significantly higher than in controls (441 vs 400 ms(1/2), p<0.01). The minimum value of QT(C) (but not the maximum value) showed a significant diurnal variation both in cirrhosis and controls. QT(disp) in cirrhosis and controls was similar (33 vs 36 ms, ns), but related to indicators of liver dysfunction, central circulation time, and arterial blood pressure (r=0.44-0.58, p=0.03-0.001). No diurnal variation of QT(disp) was found in cirrhosis. Heart rate variability was reduced with a significant relation to central hypovolaemia (r=0.55, p=0.01). CONCLUSIONS: Twenty-four hours QT(C) is prolonged in a substantial fraction of patients with cirrhosis, but with normal diurnal variation. The combination of long QT(C) and normal QT(disp) suggests delayed myocyte repolarisation on the cellular level, rather than temporal and spatial heterogeneity in the myocardial wall.

U2 - 10.1016/j.jhep.2007.03.013

DO - 10.1016/j.jhep.2007.03.013

M3 - Journal article

C2 - 17459513

VL - 47

SP - 373

EP - 380

JO - Journal of Hepatology, Supplement

JF - Journal of Hepatology, Supplement

SN - 0169-5185

IS - 3

ER -

ID: 18049734