Home Hemodialysis during Pregnancy
Pregnancy, renal failure, home hemodialysis
We would like to report here the successful outcome of a pregnancy in a patient with end-stage kidney disease (ESKD) mainly managed with intensive home hemodialysis (HHD) throughout pregnancy.
Case ReportA 36-year-old patient, G2P1, with type 1 diabetes complicated with ESKD treated with HHD, was referred for a spontaneous pregnancy. In her medical history, she had a normal vaginal delivery at 36 weeks for preeclampsia before ESKD. The patient was informed of the need to increase the frequency and duration of the hemodialysis sessions and she opted to pursue it at home. She had 4-night sessions of 7 to 8 hours per week and after the second trimester onwards, she substituted one of those for a 4-hours session in the hospital. Antenatal care included blood tests, Doppler ultrasound, and multidisciplinary follow-up by nephrologist, endocrinologist and ophthalmologist. Aneuploidy was excluded. Diabetes was well controlled with glycated haemoglobin of around 6.8%. At 25 weeks, she had a weekly cardiotocogram; weekly HHD frequency was further increased to 6 nocturnal sessions/week. At 31 weeks gestation, she had preterm labour and was treated with progesterone tablets and nifedipine. She received a course of corticosteroids for fetal lung maturation. At 33 weeks gestation, she developed hypertension (174/84 mmHg) with legs oedemas. Proteinuria was not measured as the patient was anuric. She had no biological signs suggestive of preeclampsia. She was successfully treated with alpha-methyldopa 250 mg b.i.d., and nifedipine 30 mg b.i.d. At 35 weeks 2/7, liver enzymes started to increase and labour induction was initiated. After a course of vaginal prostaglandins followed by intravenous oxytocin, she delivered vaginally a girl weighing 3020g with an Apgar score of 10 at 5 and 10 minutes. The postpartum outcome was unremarkable for both mother and infant and they were discharged on day 4.
Pregnancy in women with ESKD and dialysis is a challenge requiring specific management [1-5]. Those patients have a decreased fertility and bad pregnancy outcome because of hypertension, preeclampsia, anemia, miscarriage, polyhydramnios, prematurity and intrauterine growth restriction . Antihypertensive therapy should be adapted, and anemia corrected with iron and erythropoietin. Aspirin 160 mg daily administration is also recommended [3, 5]. But more importantly, intensification of both length and frequency of hemodialysis to a minimum of 20 hours/week (ideally 36 hours/week) is necessary to reduce the risk of preterm delivery and low birth weight [1-3]. The aim of this dialysis intensification is to reach better clearances of urea and phosphate, to increase fluid removal (and lowering thus the risk of hypertension and cardiac hypertrophy), and to reduce the inflammation status, thereby improving endothelial function . To reach such an intensive hemodialysis programme, the most socially acceptable solution is to perform HHD, if possible, as illustrated in the present case. Amongst other recommendations, fetal and maternal monitoring (cardiotocogram, fetal echography and Doppler) should be done once weekly from 26 weeks onwards . For the delivery, planned induction is recommended around 37 weeks gestation and vaginal delivery is the preferred option. Short pre-induction dialysis should be performed without heparin to allow epidural anaesthesia and reduce postpartum hemorrhage risks .
Pregnancies under hemodialysis have a much better prognosis when intensification of the hemodialysis programme, both in duration and frequency, can be achieved. HHD, under the control of experienced multidisciplinary staff throughout pregnancy, can be a safe and feasible option more acceptable to the patient.
Article TypeLetter to the Editor
Publication historyReceived: Mon 24, May 2021
Accepted: Tue 08, Jun 2021
Published: Wed 23, Jun 2021
Copyright© 2023 Corinne Hubinont. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Hosting by Science Repository.
Corresponding AuthorCorinne Hubinont
Department of Obstetrics, Cliniques Universitaires Saint Luc, Brussels, Belgium
Figures & Tables
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