Sodium-glucose cotransporter-2 inhibitor use in patients with a Fontan circulation

被引:0
|
作者
Gaydos, Stephanie S. [1 ]
Mchugh, Kimberly E. [1 ]
Woodard, Frances K. [1 ]
Judd, Rochelle N. [2 ]
Brenzel, Thomas J. [3 ]
Henderson, Heather T. [1 ]
Savage, Andrew J. [1 ]
Atz, Andrew M. [1 ]
Gregg, David [2 ]
机构
[1] Med Univ South Carolina, Dept Pediat, Div Pediat Cardiol, Charleston, SC USA
[2] Med Univ South Carolina, Dept Med, Div Cardiol, Charleston, SC 29425 USA
[3] Med Univ South Carolina, Dept Internal Med, Charleston, SC USA
关键词
Fontan; sodium-glucose cotransporter-2 inhibitors; heart failure; sodium-glucose cotransporter-2;
D O I
10.1017/S1047951125000514
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Sodium-glucose cotransporter-2 inhibitors reduce cardiovascular outcomes in patients with congestive heart failure and a biventricular circulation. Congestive heart failure in Fontan univentricular circulation is distinctly different. Experience with sodium-glucose cotransporter-2 inhibitors in this group has not yet been well described. Objectives: This work describes safety and tolerability of sodium-glucose cotransporter-2 inhibitors in patients with Fontan circulation. Methods: Single-centre review of patients with Fontan circulation prescribed a sodium-glucose cotransporter-2 inhibitors for congestive heart failure. Primary outcome was tolerability or need for discontinuation. Secondary outcomes were changes in New York Heart Association class, congestive heart failure hospitalisation, ventricular function, exercise performance, and laboratory values. Results: We identified 25 patients with Fontan circulation prescribed an sodium-glucose cotransporter-2 inhibitors, most with a systemic right ventricle. Over a third of subjects had at least moderately reduced baseline ventricular function. Baseline catheterisation showed a mean Fontan pressure of 17.1 +/- 3.7 mmHg and pulmonary capillary wedge pressure 11.7 +/- 3.2 mmHg at rest; 59% had occult diastolic dysfunction with abnormal pulmonary capillary wedge pressure elevation following volume expansion. Most were on congestive heart failure medications and/or a pulmonary vasodilator prior to sodium-glucose cotransporter-2 inhibitors addition, and three had a congestive heart failure hospitalisation within the previous year. All reported good medication tolerance except one patient was nonadherent to medications and two discontinued sodium-glucose cotransporter-2 inhibitors for perceived side effects. There were no significant differences in secondary outcomes. There was, however, a downward trend of serum brain natriuretic peptide (n = 13) and improved peak VO2 (n = 6), though neither statistically significant (p > 0.05). Conclusion: This series, the largest published to date, suggests that sodium-glucose cotransporter-2 inhibitors are safe and tolerable congestive heart failure therapy in Fontan circulation. Further research is warranted to explore therapy in this unique population.
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页数:3
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