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Kidney transplantation in children with decreased left ventricular systolic function: a Midwest Pediatric Nephrology Consortium study

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Abstract

Background

Left ventricular (LV) systolic dysfunction is a relatively uncommon but serious complication of pediatric chronic kidney disease, and may be related to uremia and uncontrolled hypertension. There is limited information on the strategy for managing these children. In some cases, combined heart–kidney transplant may be considered or kidney transplant delayed until cardiac function improves. It is unknown whether these patients are at increased risk for poor outcomes after kidney transplantation.

Methods

We conducted a retrospective, multicenter study on the outcomes of children with severe and symptomatic cardiomyopathy who underwent kidney transplantation.

Results

Eleven patients receiving maintenance dialysis with systolic dysfunction underwent kidney transplantation without simultaneous heart transplant. Nine patients had congestive heart failure in the pre-transplant period. There were no identified complications post-transplant related to the underlying cardiac dysfunction. LV systolic function normalized in all patients and the mean shortening fraction increased from 19.0 ± 4.6 % to 32.0 ± 4.4 % (p < 0.0001).

Conclusions

Kidney transplantation should be considered for children receiving maintenance dialysis with severe LV dysfunction.

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Abbreviations

CKD:

Chronic kidney disease

EF:

Ejection fraction

ESRD:

End-stage renal disease

LV:

Left ventricular

LVEF:

Left ventricular ejection fraction

LVH:

Left ventricular hypertrophy

LVSF:

Left ventricular shortening fraction

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Acknowledgments

We would like to thank Dr. Ritu Sachdeva, MD, for her help with echocardiogram data.

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Correspondence to Sandeep K. Riar.

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Riar, S.K., Mitsnefes, M.M., Nehus, E.J. et al. Kidney transplantation in children with decreased left ventricular systolic function: a Midwest Pediatric Nephrology Consortium study. Pediatr Nephrol 30, 1343–1348 (2015). https://doi.org/10.1007/s00467-015-3066-x

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  • DOI: https://doi.org/10.1007/s00467-015-3066-x

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