Introduction
Compared to the general population and to renal transplant patients, women with end-stage renal disease (ESRD) undergoing dialysis are at greater risk of infertility, fetal death in early pregnancy period, and premature birth [
1]. However, renal transplantation is difficult to access in Japan because of the limited number of cadaveric organ donations. In 2016, the average waiting time for cadaveric renal transplantation was 15.5 years [
2]. The number of occurrences of living and cadaveric renal transplantation were 1471 and 177, respectively [
3] (only 4.0% of total ESRD patients), whereas 39,344 patients started hemodialysis or peritoneal dialysis in the same year [
4]. According to the Dialysis Outcomes and Practice Patterns Study, around the year 2000, the mean number of years on dialysis was 7.4 years in Japan, 5.1 years in Europe, and 3.4 years in the USA [
5]. In Japan, the health insurance system covers most of the cost of dialysis treatment, which has enabled intensive treatment. As dialysis access and vintage are much greater in Japan than in other countries, the Japanese situation provides a unique opportunity to study pregnancy under long-term dialysis.
The first ever description of conception and successful delivery in a woman with ESRD was reported in 1971 [
6]. In Japan, the first successful delivery was achieved in 1977 [
7]. A nationwide survey by Toma et al. in 1996 reported that the frequency of pregnancy in Japanese dialysis patients was 3.4% and the live birth rate, excluding cases with elective abortion and unknown outcome, was 66.7% [
8]. A retrospective study at a single Japanese dialysis unit in 2009 reported a similar live birth rate of 64.3% [
9]. According to recent surveys in other countries, higher live birth rates in hemodialysis patients are associated with decreased blood urea nitrogen (BUN) levels caused by high frequency dialysis [
9‐
11]. Since 1996, there had been no nationwide survey about pregnancy in women with ESRD undergoing dialysis in Japan. Therefore, we undertook a survey 21 years later to update the information on the dialysis settings and outcomes. Furthermore, we collected blood pressure (BP) and biochemical data during each trimester for women undergoing dialysis, something that had not been well described in previous reports. These findings may help to improve the outcomes of pregnancy and delivery among women under dialysis. This study was carried out under the name of the Tsubasa Project, as one of the studies on gender led by young Japanese female doctors and supported by The Japanese Society for Dialysis Therapy (JSDT).
Discussion
In the present survey of the Tsubasa Project, among 1992 Japanese women with ESRD aged 15–44 years, 25 pregnancies (1.26%/5 years) were reported for 20 women receiving hemodialysis. Detailed information about 19 pregnancies was collected for 15 women. Compared to the previous survey in 1996 [
8], when cases with elective abortion and unknown outcome were excluded, the live birth rate elevated from 66.7 to 77.8% (but not significantly,
P = 0.38). Among 14 pregnancies resulting in surviving infants, 5 mothers had undergone dialysis for more than 10 years, and 11 maternal and 3 neonatal complications occurred. Age at conception ≥ 38 years tended to have an increased association with maternal complications compared to ≤ 37 years, but neonatal complications developed in mothers whose ages were 32, 33 and 39 years. Furthermore, malnutrition suggested by sAlb ≤ 3.2 mg/dL in the first trimester appears to be a common risk for both maternal and neonatal complications [
16,
17]. These complex findings are in line with a previous report by Villar et al. which proposed that preeclampsia (as a maternal complication) and FGR (as a neonatal complication) may have distinct etiologies among obstetric disorders [
18].
In our study, the cutoff for neonatal and maternal complications was set at sAlb 3.2 mg/dL (Fig. S2). Since sAlb decreases gradually as pregnancy progresses (Table
2) [
19], different cutoffs may apply to women in different settings. This study examined pregnancies among women on dialysis undergoing regular blood tests. However, for most women not receiving dialysis, obtaining biochemistry data in the first trimester may not be practical, as they are not necessarily recommended by guidelines to undergo such testing [
20].
Table 2
Comparison of biochemistry, anthropometry findings and dialysis prescription in each trimester between preterm and full-term deliveries
Number | 9 | 5 | | 9 | 5 | | 5 | 5 | |
Age (years) | 36.7 ± 3.5 | 33.6 ± 4.5 | 0.18 | | | | | | |
Dialysis vintage (years) | 10.5 ± 7.7 | 7.6 ± 4.9 | 0.47 | | | | | | |
Biochemical parameters | | | | | | | | | |
Timing of examination (weeks)a | 13 ± 1 | 12 ± 3 | 0.49 | 21 ± 1 | 21 ± 1 | 0.35 | 33 ± 2 | 32 ± 2 | 0.70 |
Blood urea nitrogen (mg/dL) | 45 ± 22 | 56 ± 11 | 0.29 | 38 ± 7 | 50 ± 14 | 0.053 | 34 ± 16 | 24 ± 10 | 0.26 |
Creatinine (mg/dL) | 8.7 ± 2.5 | 9.7 ± 1.9 | 0.44 | 7.4 ± 1.0 | 9.0 ± 2.6 | 0.12 | 6.4 ± 2.7 | 5.8 ± 1.9 | 0.69 |
Albumin (g/dL) | 3.3 ± 0.2 | 3.6 ± 0.3 | 0.09 | 3.1 ± 0.4 | 3.3 ± 0.2 | 0.18 | 2.7 ± 0.4 | 2.9 ± 0.1 | 0.37 |
Potassium (mEq/L) | 4.3 ± 0.6 | 4.6 ± 0.9 | 0.50 | 4.1 ± 0.4 | 4.5 ± 0.6 | 0.18 | 3.9 ± 0.6 | 3.9 ± 0.7 | 0.88 |
Calcium (mg/dL) | 8.8 ± 0.6 | 9.1 ± 0.6 | 0.41 | 9.1 ± 0.5 | 9.2 ± 0.2 | 0.54 | 8.7 ± 0.7 | 9.1 ± 0.6 | 0.29 |
Phosphate (mg/dL) | 4.5 ± 1.8 | 5.2 ± 1.4 | 0.43 | 4.2 ± 1.0 | 3.9 ± 0.8 | 0.33 | 3.8 ± 1.5 | 3.6 ± 1.0 | 0.88 |
Hemoglobin (g/dL) | 9.7 ± 0.9 | 10.0 ± 0.8 | 0.48 | 9.8 ± 1.7 | 10.0 ± 1.5 | 0.71 | 11.0 ± 1.5 | 9.8 ± 0.4 | 0.12 |
Blood pressure and dry weight | | | | | | | | | |
Timing of examination (weeks)a | 13 ± 1 | 12 ± 3 | 0.49 | 20 ± 3 | 21 ± 1 | 0.33 | 33 ± 2 | 32 ± 2 | 0.70 |
Systolic blood pressure (mmHg) | 128 ± 32 | 122 ± 26 | 0.71 | 136 ± 29 | 117 ± 17 | 0.21 | 141 ± 21 | 115 ± 15 | 0.0496 |
Diastolic blood pressure (mmHg) | 75 ± 16 | 72 ± 20 | 0.71 | 79 ± 21 | 69 ± 10 | 0.36 | 90 ± 12 | 68 ± 10 | 0.013 |
Dry weight (kg) | 58.6 ± 10.8 | 60.6 ± 12.0 | 0.76 | 60.3 ± 11.4 | 62.0 ± 11.7 | 0.80 | 63.3 ± 12.8 | 65.6 ± 11.9 | 0.78 |
Dialysis prescription | | | | | | | | | |
Dialysis time (hour/week) | 19.8 ± 4.9 | 20.5 ± 9.9 | 0.86 | 22.5 ± 3.7 | 22.9 ± 8.7 | 0.91 | 24.8 ± 5.0 | 27.8 ± 5.2 | 0.38 |
Frequency (times/week) | 4.2 ± 0.8 | 4.4 ± 1.3 | 0.76 | 5.1 ± 0.9 | 4.8 ± 1.3 | 0.67 | 5.4 ± 0.5 | 5.8 ± 0.4 | 0.24 |
Neonatal complications occurred in 2 of 3 infants with extremely preterm delivery and in 1 of the 4 FGR infants. Despite having repeated HDP and FGR, Case 6 had second and third deliveries without neonatal complications at 37 and 36 weeks, respectively, after taking a low dose of aspirin (presumably following expert recommendations [
21]) and increasing both the dialysis blood flow and the size of the dialysis membrane. Three pregnancies which occurred among women who began dialysis between the ages of 12 to 17 resulted in two extremely preterm deliveries and one delivery with placental abruption and severe fetal complications. These observations raise the possibility that kidney disease onset, immunosuppressive treatment and dialysis initiation during adolescence adversely affected the functional maturation of the uterus. Indeed, adolescent pregnancy in general is reported to be associated with maternal and neonatal complications [
22].
The present study also provides some hints about the relationship between the cause of ESRD and pregnancy outcomes. A previous study indicated that ESRD due to glomerulonephritis was associated with increased live birth rates, while diabetes was associated with decreased live birth rates [
23]. On the other hand, in a Canadian study by Hladunewich et al. among 17 women on dialysis, extremely preterm deliveries of 360 g and 980 g infants occurred in mothers who had ESRD due to IgA nephropathy [
10]. Hoffman et al. reported that ESRD due to diabetes or lupus was associated with neonatal morbidity [
24]. In our study, mean age at dialysis initiation among 4 mothers who had ESRD due to diabetic nephropathy (33.5 ± 3.9 years, range 29–38) was much older than that of the other 11 mothers (23.6 ± 7.4 years, range 12–39,
P = 0.03). Our findings suggest that dialysis initiation at a relatively young age reduces the probability of developing ESRD due to diabetic nephropathy.
In our study, HDP (52.6%) and preterm delivery (64.3%) were frequent during pregnancy in women on dialysis (Table
1). In pregnancy in the general population, these factors are tightly linked, and are associated with increased risk for neonatal morbidity and mortality [
18]. In our study, there were 3 women who did not have chronic hypertension at pregnancy start but developed HDP and preterm labor later (Table
1). Importantly, ideal BP target for hypertensive mothers is controversial [
25,
26]. A recent study reported that initiating tight (versus less-tight) control of BP at < 24 weeks significantly reduced severe maternal hypertension and preterm birth (without a significant effect on maternal death). However, this effect was counterbalanced by an increased incidence of mildly small for gestational age, such that there was no overall effect on neonatal morbidity or death [
27]. On the other hand, a randomized clinical trial in the general population revealed that aggressive treatment of mild to moderate hypertension in the third trimester reduced premature delivery and neonatal respiratory distress requiring intensive care compared to placebo treatment [
28]. Taken together, the above findings suggest that the timing to potentiate antihypertensive treatment is an important consideration for pregnancy both in general and under conditions of dialysis.
It is well established that low BUN is associated with favorable maternal and neonatal outcomes in pregnancy with ESRD [
9‐
11,
29]. However, BUN may not be a simple surrogate of uremic toxin accumulation [
10]. Frequent, long-time dialysis should not only efficiently remove uremic toxins but also reduce the amount and speed of water removal during the dialysis session, which should be helpful for stabilizing maternal and fetal circulation. In that sense, BUN seems to be a reliable surrogate for dialysis performance. In a single-center, core facility report from Brazil [
30], favorable fetal outcomes were obtained when midweek BUN was < 35 mg/dL. Our study consistently found that mean BUN at the beginning of the week in the third trimester was 34 mg/dL and 24 mg/dL (
P = 0.26) in the preterm and full-term cases, respectively (Table
2). When women on dialysis become pregnant, it is recommended that they increase protein and total calorie intake from the second trimester to compensate for fetal growth and intensified dialysis-induced protein loss [
31], but information about actual or recommended protein intake was not collected in our study. It is interesting to note that, in the second trimester, Case 6 showed phosphate levels of 5.2 ± 0.5 mg/dL in three pregnancies (6P1–6P3), which were higher than the overall mean level of 4.1 mg/dL among 14 pregnancies. This might have been caused by increased protein intake to maintain sAlb, by poor compliance in taking phosphate binders by the patient, or by the use of low efficiency dialysis to cope with dialysis difficulty, for instance, by intradialytic hypotension. Therefore, we have to point out there is the possibility that higher BUN level may not be a cause of poor pregnancy outcomes, but a result of difficult dialysis. This view is supported by a study by Luders et al. of pregnancy in women with ESRD [
32]. In their study, the adverse fetal outcome group had higher BUN levels than the favorable fetal outcome group, but the dialysis doses were similar between the groups, indicating that low efficiency dialysis was not the cause of the poor outcomes.
In our survey, the live birth rate was 77.8%, and preterm delivery was predominant among these live births. However, there was no occurrence of maternal death or of congenital abnormalities. Importantly, although the live birth rate in women on dialysis is much lower than that in the general population (see below) [
1,
29], a recent, large-scale, meta-analysis reported that ESRD patients have a maternal perinatal mortality rate of only 0.4% and the same congenital abnormality rate as the general population (2%) [
11].
We further compared the results of the survey in 1996 [
8] and this survey in 2017 (Table S3). The response rate in 1996 was 1.8-fold higher than that in 2017. It was difficult to compare the frequency of pregnancy (3.4% versus 0.25%/year), because the 1996 study did not specify the time period covered. Moreover, in the 2017 study, there were tendencies that mean gestational age was longer, the preterm delivery rate was lower, and the birth weight was higher, despite the fact that the mothers were older and the duration of dialysis prior to pregnancy was longer. The frequency of major neonatal complications in surviving infants, which were tightly associated with lower gestational age and birth weight (Fig.
1), decreased from 41.7 to 21.4% (
P = 0.18). In addition, mean dialysis time before delivery increased from 22.0 to 24.9 h per week and mean dialysis frequency increased from 4.5 to 5.6 times per week (Table S3).
The tendency toward improved pregnancy outcomes over 21 years may have been caused by longer and more frequent dialysis [
10,
11,
29], good anemia control (Table
2) [
9], and technical progress in pregnancy and neonate care. Indeed, the rate of neonatal death in the Japanese general population improved from 2.0 per 1000 live born babies in 1996 [
33] to 0.9 in 2016 [
34].
We also compared the outcomes of pregnancy on dialysis among nationwide surveys in other countries published in 1998 or later (Table
3). The mean dialysis vintage of 8.4 years in our study was almost double that of the longest dialysis vintages previously reported for other countries [
23,
35]. Our study found that the frequency of pregnancy was 2.5 per 1000 patient-years (PTPY) and the live birth rate was 78%. This fit within the ranges of 2.1–5.5 PTPY and 40–83% in studies from Belgium [
36], the USA [
10,
37], Australia [
23], New Zealand [
23] and Canada [
10]. These findings are also consistent with a systematic review of 10 surveys published between 2000 and 2008 reporting that the mean live birth rate was 76% [
38].
Table 3
Nationwide surveys concerning pregnancy on dialysis
| Okundaye | USA | 1992–1995 | 6230 HD + PD | 14–44 | ND | 1 to 5 | 135/ND | > 5.5 | 40 |
| Bagon | Beigium | 1975–1996 | 1472 HD + PD | 18–44 | 28.0 ± 3.2 | 3.0 | 15/14 | 3.3 | 50 |
| Shahir | AU/NZ | 1966–2008 | 7796 HD + PD | 15–49 | 30.7 | 4.0 | 49/ND | 2.1 | 79 |
| Hladunewich | USA | 1990–2011 | ND, HD | ND | 27 ± 6 | 1.5 | 70/ND | ND | 53 |
| Hladunewich | Canada | 2000–2013 | ND, HD | ND | 34 ± 4 | 3.4 | 22/17 | ND | 83 |
| Shah | USA | 2005–2013 | 47,555 HD + PD | 15–44 | 29 ± 6 | < 1 | 2352b/ND | 17.8c | 39 |
| Oliverio | USA | 2002–2015 | 12,382 HD | 18–44 | 30.6 | 4.4 | ND/664b | (2.1–3.6)d | ND |
Tsubasa | Hirano | Japan | 2012–2016 | 1992 HD | 15–44 | 34.6 ± 5.7 | 8.4 | 25/20 | 2.5e | 78 |
Recently, a study in the USA using administrative claim data instead of survey data found that the delivery rate (but not pregnancy rate) in women undergoing hemodialysis increased from 2.1 to 3.6 PTPY, during the years 2002 to 2015 [
35]. Another claim-based report in the USA covering 2005 to 2013 indicated that the pregnancy rate was 17.8 PTPY and the live birth rate was 27% (39% when unknown outcomes were excluded), but mean dialysis vintage was recorded as less than a year, suggesting that there was a reporting bias [
39].
In our study, the incidence of live births was 1.4 PTPY among women on dialysis aged from 15 to 44 years (calculated as 14/1992/5), compared to 46.9 PTPY in the general Japanese population in 2016 (according to Vital Statistics collected by Ministry of Health, Labour and Welfare of Japan; 975,531 live births [
40] among 20,814,958 women aged 15–44 [
41]). A similar survey in Italy reported live birth rates of 0.7–1.1 PTPY for women on dialysis, and 72.5 PTPY for the general population aged 20–45 [
1].
Our survey has several limitations. The study design is limited by the fact that a survey was used to determine pregnancy rates and complications, and by its low response rate, both of which may have led to underreporting. Also, this study is a retrospective case series and has a small number of events, so the statistical power of this study is restricted, and we cannot establish cause/effect relationships. However, a strength in this study is that all of the pregnant women belonged to independent units, except for one pair of women, reflecting a multi-center feature of our analysis.
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