The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure

Abstract In congenitally corrected transposition of the great arteries, the morphological right ventricle supports the systemic circulation. This chronic exposure to pressure overload ultimately leads to systemic right ventricular (sRV) dysfunction and heart failure. Pharmacological options for the...

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Main Authors: Anastasia D. Egorova, Marieke Nederend, Laurens F. Tops, Hubert W. Vliegen, Monique R.M. Jongbloed, Philippine Kiès
Format: Article
Language:English
Published: Wiley 2022-06-01
Series:ESC Heart Failure
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Online Access:https://doi.org/10.1002/ehf2.13871
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author Anastasia D. Egorova
Marieke Nederend
Laurens F. Tops
Hubert W. Vliegen
Monique R.M. Jongbloed
Philippine Kiès
author_facet Anastasia D. Egorova
Marieke Nederend
Laurens F. Tops
Hubert W. Vliegen
Monique R.M. Jongbloed
Philippine Kiès
author_sort Anastasia D. Egorova
collection DOAJ
description Abstract In congenitally corrected transposition of the great arteries, the morphological right ventricle supports the systemic circulation. This chronic exposure to pressure overload ultimately leads to systemic right ventricular (sRV) dysfunction and heart failure. Pharmacological options for the treatment of sRV failure are poorly defined and no solid recommendations are made in the most recent guidelines. Sodium‐glucose cotransporter 2 (SGLT‐2) inhibitors are a new class of antihyperglycaemic drugs that have been demonstrated to significantly reduce the risk of worsening heart failure and death from cardiovascular causes in patients with chronic heart failure with reduced left ventricular ejection fraction, yet no data are available in sRV patients. We report on the treatment and clinical follow‐up of a patient with advanced heart failure and poor sRV function in the context of congenitally corrected transposition of the great arteries, who did not tolerate sacubitril/valsartan and had a high burden of heart‐failure‐related hospitalizations. Treatment with dapagliflozin was well tolerated and resulted in (small) subjective and objective functional and echocardiographic improvement and a reduction in heart‐failure‐related hospitalizations.
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institution Kabale University
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series ESC Heart Failure
spelling doaj-art-202fa3d15fca4d448edea07800a84e432025-02-05T05:22:10ZengWileyESC Heart Failure2055-58222022-06-01932007201210.1002/ehf2.13871The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failureAnastasia D. Egorova0Marieke Nederend1Laurens F. Tops2Hubert W. Vliegen3Monique R.M. Jongbloed4Philippine Kiès5CAHAL, Center for Congenital Heart Disease Amsterdam Leiden Leiden University Medical Center Leiden The NetherlandsCAHAL, Center for Congenital Heart Disease Amsterdam Leiden Leiden University Medical Center Leiden The NetherlandsDepartment of Cardiology, Leiden Heart‐Lung Center Leiden University Medical Center Albinusdreef 2 Leiden 2333 ZA The NetherlandsCAHAL, Center for Congenital Heart Disease Amsterdam Leiden Leiden University Medical Center Leiden The NetherlandsCAHAL, Center for Congenital Heart Disease Amsterdam Leiden Leiden University Medical Center Leiden The NetherlandsCAHAL, Center for Congenital Heart Disease Amsterdam Leiden Leiden University Medical Center Leiden The NetherlandsAbstract In congenitally corrected transposition of the great arteries, the morphological right ventricle supports the systemic circulation. This chronic exposure to pressure overload ultimately leads to systemic right ventricular (sRV) dysfunction and heart failure. Pharmacological options for the treatment of sRV failure are poorly defined and no solid recommendations are made in the most recent guidelines. Sodium‐glucose cotransporter 2 (SGLT‐2) inhibitors are a new class of antihyperglycaemic drugs that have been demonstrated to significantly reduce the risk of worsening heart failure and death from cardiovascular causes in patients with chronic heart failure with reduced left ventricular ejection fraction, yet no data are available in sRV patients. We report on the treatment and clinical follow‐up of a patient with advanced heart failure and poor sRV function in the context of congenitally corrected transposition of the great arteries, who did not tolerate sacubitril/valsartan and had a high burden of heart‐failure‐related hospitalizations. Treatment with dapagliflozin was well tolerated and resulted in (small) subjective and objective functional and echocardiographic improvement and a reduction in heart‐failure‐related hospitalizations.https://doi.org/10.1002/ehf2.13871Systemic right ventricleHeart failureCongenital heart diseaseAdult congenital heart diseaseChronic heart failureSodium‐glucose cotransporter inhibitor
spellingShingle Anastasia D. Egorova
Marieke Nederend
Laurens F. Tops
Hubert W. Vliegen
Monique R.M. Jongbloed
Philippine Kiès
The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
ESC Heart Failure
Systemic right ventricle
Heart failure
Congenital heart disease
Adult congenital heart diseaseChronic heart failureSodium‐glucose cotransporter inhibitor
title The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
title_full The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
title_fullStr The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
title_full_unstemmed The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
title_short The first experience with sodium‐glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
title_sort first experience with sodium glucose cotransporter 2 inhibitor for the treatment of systemic right ventricular failure
topic Systemic right ventricle
Heart failure
Congenital heart disease
Adult congenital heart diseaseChronic heart failureSodium‐glucose cotransporter inhibitor
url https://doi.org/10.1002/ehf2.13871
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