Pregnancy in Patients Receiving Home Dialysis
- PMID: 38285469
- PMCID: PMC11835159
- DOI: 10.2215/CJN.0000000000000437
Pregnancy in Patients Receiving Home Dialysis
Abstract
Pregnancy is an important goal for many women with CKD or kidney failure, but important barriers exist, particularly as CKD stage progresses. Women with advanced CKD often have a limited fertility window and may miss their opportunity for a pregnancy if advised to defer until after kidney transplantation. Pregnancy rates in women with advanced kidney failure or receiving dialysis remain low, and despite the improved outcomes in recent years, these pregnancies remain high risk for both mother and baby with high rates of preterm birth due to both maternal and fetal complications. However, with increased experience and advances in models of care, this paradigm may be changing. Intensive hemodialysis regimens have been shown to improve both fertility and live birth rates. Increasing dialysis intensity and individualizing dialysis prescription to residual renal function, to achieve highly efficient clearances, has resulted in improved live birth rates, longer gestations, and higher birth weights. Intensive hemodialysis regimens, particularly nocturnal and home-based dialysis, are therefore a potential option for women with kidney failure desiring pregnancy. Global initiatives for the promotion and uptake of home-based dialysis are gaining momentum and may have advantages in this unique patient population. In this article, we review the epidemiology and outcomes of pregnancy in hemodialysis and peritoneal dialysis recipients. We discuss the role home-based therapies may play in helping women achieve more successful pregnancies and outline the principles and practicalities of management of dialysis in pregnancy with a focus on delivery of home modalities. The experience and perspectives of a patient are also shared.
Copyright © 2024 by the American Society of Nephrology.
Conflict of interest statement
M.A. Hladunewich, funding from Roche to study Biomarkers of Preeclampsia. M.A. Hladunewich reports Research Funding: Calliditas Therapeutics, Chinook Pharmaceuticals, Ionis, and Pfizer; Honoraria: UpToDate; and Other Interests or Relationships: Medical Lead for Glomerular Disease Ontario Renal Network. N. Tangirala is supported by a Higher Degree Research Scholarship from the Women's and Childrens's Hospital Research Foundation, Adelaide, Australia. All remaining authors have nothing to disclose.
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