Background/Aims: A prolonged QT interval is frequent in chronic liver disease and its aetiology remains unsettled. The study's aim was to assess the role of portal hypertension in the pathogenesis of QT prolongation. Methods: We measured the QT interval in: (1) 10 patients with non-cirrhotic portal hypertension (NCPH) and preserved liver function; (2) 19 cirrhotic patients before, 1-3 and 6-9 months after transjugular intrahepatic portosystemic shunt (TIPS) insertion. Results: Baseline corrected maximum QT interval (QTcmax) was prolonged (>440 ms) in eight NCPH and 16 cirrhotic patients, and its value did not differ between the two groups (453 ± 8 vs. 465 ± 6 ms, P = NS). No patients showed an abnormal baseline QT dispersion. In cirrhotic individuals, QTcmax further increased 1-3 months after TIPS (P = 0.042), thereafter remaining steadily elevated. QT dispersion only increased at the second post-TIPS determination (P = 0.030). Such changes occurred despite no deterioration of liver function, plasma electrolytes and haemoglobin. Conclusions: QT interval is frequently prolonged in patient with both non-cirrhotic and cirrhotic portal hypertension and portal decompression by TIPS worsens this abnormality. These results suggest that the portosystemic shunting is responsible for the altered ventricular repolarisation possibly through a dumping into the systemic circulation of splanchnic-derived cardioactive substances. © 2003 European Association for the Study of the Liver. Published by Elsevier Science B.V. All rights reserved.

QT interval in patients with non-cirrhotic portal hypertension and in cirrhotic patients treated with transjugular intrahepatic portosystemic shunt / Trevisani F.; Merli M.; Savelli F.; Valeriano V.; Zambruni A.; Riggio O.; Caraceni P.; Domenicali M.; Bernardi M.. - In: JOURNAL OF HEPATOLOGY. - ISSN 0168-8278. - ELETTRONICO. - 38:4(2003), pp. 461-467. [10.1016/S0168-8278(03)00057-6]

QT interval in patients with non-cirrhotic portal hypertension and in cirrhotic patients treated with transjugular intrahepatic portosystemic shunt

Trevisani F.;Zambruni A.;Caraceni P.;Domenicali M.;Bernardi M.
2003

Abstract

Background/Aims: A prolonged QT interval is frequent in chronic liver disease and its aetiology remains unsettled. The study's aim was to assess the role of portal hypertension in the pathogenesis of QT prolongation. Methods: We measured the QT interval in: (1) 10 patients with non-cirrhotic portal hypertension (NCPH) and preserved liver function; (2) 19 cirrhotic patients before, 1-3 and 6-9 months after transjugular intrahepatic portosystemic shunt (TIPS) insertion. Results: Baseline corrected maximum QT interval (QTcmax) was prolonged (>440 ms) in eight NCPH and 16 cirrhotic patients, and its value did not differ between the two groups (453 ± 8 vs. 465 ± 6 ms, P = NS). No patients showed an abnormal baseline QT dispersion. In cirrhotic individuals, QTcmax further increased 1-3 months after TIPS (P = 0.042), thereafter remaining steadily elevated. QT dispersion only increased at the second post-TIPS determination (P = 0.030). Such changes occurred despite no deterioration of liver function, plasma electrolytes and haemoglobin. Conclusions: QT interval is frequently prolonged in patient with both non-cirrhotic and cirrhotic portal hypertension and portal decompression by TIPS worsens this abnormality. These results suggest that the portosystemic shunting is responsible for the altered ventricular repolarisation possibly through a dumping into the systemic circulation of splanchnic-derived cardioactive substances. © 2003 European Association for the Study of the Liver. Published by Elsevier Science B.V. All rights reserved.
2003
QT interval in patients with non-cirrhotic portal hypertension and in cirrhotic patients treated with transjugular intrahepatic portosystemic shunt / Trevisani F.; Merli M.; Savelli F.; Valeriano V.; Zambruni A.; Riggio O.; Caraceni P.; Domenicali M.; Bernardi M.. - In: JOURNAL OF HEPATOLOGY. - ISSN 0168-8278. - ELETTRONICO. - 38:4(2003), pp. 461-467. [10.1016/S0168-8278(03)00057-6]
Trevisani F.; Merli M.; Savelli F.; Valeriano V.; Zambruni A.; Riggio O.; Caraceni P.; Domenicali M.; Bernardi M.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/961847
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