Managing pregnancy in chronic kidney disease: improving outcomes for mother and baby
Authors Fitzpatrick A, Mohammadi F, Jesudason S
Received 15 February 2016
Accepted for publication 20 April 2016
Published 14 July 2016 Volume 2016:8 Pages 273—285
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Professor Elie Al-Chaer
Alyssa Fitzpatrick,1 Fadak Mohammadi,2 Shilpanjali Jesudason1–3
1Women’s and Babies Division, Women’s and Children’s Hospital, 2Central and Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, 3Department of Medicine, University of Adelaide, Adelaide, South Australia, Australia
Abstract: Parenthood is a central focus for women with chronic kidney disease, but raises important fears and uncertainties about risks to their own and their baby’s health. Pregnancy in women with background kidney disease, women receiving dialysis, or those with a functioning kidney transplant poses a challenging clinical scenario, associated with high maternal–fetal morbidity and potential impact on maternal renal health. Improvements in care over recent decades have led to a paradigm shift with cautious optimism and growing interest regarding pregnancies in women with chronic kidney disease. In this review, we discuss obstetric and renal outcomes, and practical aspects of management of pregnancy in this complex cohort.
Keywords: renal, obstetric, fetal, transplant, drugs
Pregnancy and the kidney
The prevalence of chronic kidney disease (CKD) is rising, and may affect 3% of women in their childbearing years.1 Preexisting CKD of any stage impacts upon maternal and perinatal outcomes. The challenging nature of these pregnancies underscores the need for careful prepregnancy planning in known CKD patients, early identification of new-onset maternal CKD, management of pregnancy with shared decision making, and a patient-centered approach, in an integrated specialized obstetric and nephrology service. This review provides an overview of key issues in clinical management for women with CKD and their infants and discusses strategies for preconception counseling for those planning pregnancy.
Physiological changes in pregnancy
Pregnancy increases renal workload due to marked anatomical and physiological changes occurring from early gestation. The glomerular filtration rate (GFR) increases by ~50%, with commensurate fall in serum creatinine secondary to plasma volume expansion, renal vasodilation, hyperfiltration, and heightened glomerular basement membrane permeability. Renal adaptations in pregnancy have been explored comprehensively by Odutayo and Hladunewich,2 and will not be further described.
Of importance, the physiological changes of pregnancy may unmask or worsen preexisting renal disease. Failure of serum creatinine to fall during pregnancy may indicate underlying renal disease – indeed, levels of creatinine >90 μmol/L should be considered pathological in pregnancy.3 Proteinuria is a hallmark feature of renal disease, but urine protein excretion of up to 300 mg/day may be observed in normal pregnancy.4
Defining CKD in pregnancy
Due to these physiological shifts in the typical markers of CKD (serum creatinine and urine protein), defining CKD in pregnancy is difficult. In the nonpregnant state, the widely used Kidney Disease Outcomes Quality Initiative staging system (Table 1) broadly defines CKD. Commonly used formulae to estimate creatinine clearance or estimated GFR (eGFR) are inaccurate in pregnancy. This includes the Cockroft–Gault and Modification of Diet in Renal Disease formulae. The Cockroft–Gault overestimates GFR, while in preeclampsia, the Modification of Diet in Renal Disease formula underestimates GFR compared with 24-hour creatinine clearance.5 Twenty-four-hour urine collections for inulin or creatinine clearance remain the gold standard for GFR measurement, but are clinically impractical and rarely needed, hence our ongoing reliance on serum creatinine.6 The heterogeneous classification of CKD in pregnancy studies contributes to underrecognition and uncertainties around diagnosis.
Table 1 Staging of CKD (KDOQI)
Renal biopsy is reserved for situations where accurate histological diagnosis will substantially change clinical management during pregnancy. A synthesis of studies containing 197 biopsies in total (for diverse indications including preeclampsia) revealed major and minor complications in 2% and 5% of cases, respectively, peaking in later pregnancy (after 25 weeks).7 Therefore, biopsy should be used judiciously and is rarely indicated to differentiate preeclampsia and renal disease.
Epidemiology of CKD in pregnant populations
Few studies have explored the population prevalence of CKD in pregnancy. A Norwegian population study provides the best data, suggesting CKD affects 3.3% of pregnancies, with the prevalence of CKD stages 1, 2, and 3 being 2.4%, 0.8%, and 0.1%, respectively.1 Early stage CKD can be difficult to define in pregnancy, and robust prevalence data are lacking.8 Advanced CKD (stage 3–5) is estimated to affect 1:150 women of reproductive age and 1:750 pregnancies.3,9 Population incidence rates for dialysis and transplant pregnancies vary between countries and are mostly derived from historical registry data, where there may be reporting bias especially with poor capture of early pregnancy losses. The most contemporaneous data are available from the Australian and New Zealand Dialysis and Transplant Registry (ANZDATA). The reported pregnancy rate in chronically dialyzed patients was 3.1/1,000 patient-years at risk during 1966–2000 and rose to 8.4/1,000 in 2001–2011 with a live birth rate of 1.26/1,000 patient-years.10 Other studies have reported a conception rate of 0.3/100 patient-years in Belgium,11 3.4% on hemodialysis in Japan,12 2.4% on hemodialysis, and 1.1% on peritoneal dialysis in the USA.13 In ANZDATA, the pregnancy rate in female transplant recipients during 1966–2005 was 20/1,000 patient-years, with a live birth rate of 16/1,000 patient-years.14,15 In the USA, the pregnancy rate in the first 3 years posttransplant between 1990 and 2003 was 33/1,000 women; the live birth rate was 19/1,000 women.16 The differences in pregnancy and live birth rates between dialyzed and transplanted women underscore the effects of CKD on fertility and markedly improved fertility and permissiveness toward pregnancy following renal transplantation.
CKD stage and pregnancy outcomes
Numerous studies exist describing pregnancy and renal outcomes in women with CKD. Importantly, interpretation and comparison of outcomes between studies is limited by small numbers, restricted clinical data, historical cohorts from different eras of medical care, heterogeneous cohorts with variable primary disease and clinical features, variable definitions of CKD, and lack of preconception GFR data. Nevertheless, it is clinically useful to broadly recognize that any maternal CKD increases the likelihood of adverse maternal–fetal outcomes, with risks compounded by advancing CKD stage, hypertension, proteinuria, and comorbidities.17–24 It is also important to note some women have uncomplicated pregnancies, and the discussion of medical risks may heighten anxiety around conception and pregnancy.25 This issue is discussed further in “Patient perspectives and shared decision making” section.
Two recent large studies by Kendrick et al26 (reporting outcomes for 778 American women with renal disease identified retrospectively by a variety of methods), and Piccoli et al20 (reporting outcomes for a prospectively recruited cohort), again highlight that CKD pregnancies (compared with low risk or healthy controls) have excess maternal risk of preeclampsia and cesarean section, and fetal risk of preterm birth, poor growth, low birth weight, and need for neonatal intensive care admission. The rate of pregnancy and perinatal complications (principally driven by preeclampsia) increases with worsening severity of CKD, and may occur even in women with normal eGFR without other comorbidities.17,20,27 Pregnancies in women with stage 4–5 CKD are most challenging, with hypertensive disorders and preterm birth affecting the majority. Reassuringly, while pregnancy loss is increased in women with CKD, neonatal and maternal death is rare in developed countries.18
Pregnancy and progression of CKD
The risk of renal deterioration during pregnancy remains a concern. Current evidence is conflicting. A meta-analysis by Zhang et al21 revealed no association between pregnancy and deterioration of renal function, irrespective of etiology or baseline stage, although few included studies had advanced CKD patients. Piccoli et al20 observed 7.6% of women with CKD stage 1 experienced a shift in CKD stage or start of renal replacement therapy with pregnancy, rising to 20% for women with CKD stage 4–5. Jones and Hayslett24 observed renal function in women with moderate-to-severe CKD (creatinine >124 μmol/L) during pregnancy and postpartum, reporting transient deterioration in 43% and permanent deterioration in 31% of cases. Similarly, a small but widely noted study by Imbasciati et al22 found prepregnancy eGFR <40 mL/min/1.73 m2 with proteinuria >1 g/24 hours predicted renal decline after pregnancy. Preconception graft function is similarly the key predictor of decline in kidney transplant recipients.28 Therefore, evidence that pregnancy accelerates early CKD is limited, but deterioration is more likely in women with more advanced renal disease.
Primary renal diagnosis and outcomes
CKD etiology has less influence on outcomes than CKD stage, proteinuria, hypertension, and preeclampsia. An exception is systemic lupus erythematosus (SLE) nephritis: outcomes are poorer than for women with comparable renal impairment from other causes, particularly if associated with antiphospholipid antibodies.29 A recent meta-analysis identified risks of SLE flare (25.6%), hypertension (16.3%), preeclampsia (7.6%), premature birth (39.4%), and intrauterine growth restriction (12.7%) in 37 studies of 2,751 pregnancies.29 Differentiating preeclampsia from SLE nephritis is difficult. Key differentiating features include the typical rash, arthritis, hematuria, low complement levels in SLE, or the presence of antiphospholipid antibodies, while abnormal liver function tests suggest preeclampsia rather than SLE flare.30,31 Overall, the prognosis for women with SLE nephritis has improved since the 1960s, with fetal loss rates decreasing from 40% in 1960 to 17% in 2000.30
Women with autosomal dominant polycystic kidney disease have an increased risk of preeclampsia and urinary tract infection.19,32 Hepatic cysts may enlarge in the estrogenic environment, and known cerebral aneurysms should be assessed prior to labor.33,34 There is also a risk of intracystic hemorrhage during labor, and large renal cysts should be monitored prior to and following delivery.35
Outcomes in other common nephropathies including IgA nephropathy do not consistently differ from same-stage CKD of other etiology,23 although robust comparative data between primary diseases remain limited. Diabetic patients (particularly if poorly controlled) have increased rates of preeclampsia, fetal abnormalities, and fetal loss; proteinuric diabetic nephropathy may worsen in pregnancy, and the combination of diabetes, proteinuria, renal impairment, and hypertension is particularly difficult.36 These risks may be elevated in women with “overt” diabetic nephropathy compared with those with early stage disease.37 Establishing good glycemic control and lowering the hemoglobin A1c preconception is important to improve maternal and neonatal outcomes, including reducing the risk of fetal malformation. There is some evidence that the risk of congenital abnormalities in diabetic women may be increased in the presence of nephropathy,38 underscoring the need for optimized glycemic control.
Management of pregnancy in women with CKD
An algorithm for approaching pregnancy care in women with CKD is proposed in Figure 1, and specific management points are discussed here.
Given the high rate of associated morbidity, women with CKD should have prepregnancy counseling early in their disease course. Contraceptive options should be explored if a delay in pregnancy is desirable, with clear explanation of the benefits of careful pregnancy planning. Key areas for discussion include an exploration of risks and outcomes as described above, assessment of relevant risk factors; optimizing modifiable factors including control of primary renal disease and blood pressure (BP); implementation of drug changes; decisions regarding timing of conception; and development of a comprehensive pregnancy management plan. Genetic counseling should be offered to women with inheritable renal disease. As for all pregnant women, preconception and first trimester folic acid supplementation is recommended. In dialyzed women, 3–5 mg/day may be required, due to losses during dialysis.
Pregnant women with CKD benefit from specialized (tertiary or quaternary) multidisciplinary team management including obstetricians, obstetric physicians/nephrologists, anesthetists, dietetic, and midwifery input.39,40 While the overall risk of pregnancy problems is increased in women with CKD, many women will have uncomplicated pregnancies and excellent outcomes, but still require frequent antenatal review, particularly monitoring maternal renal function and BP, and fetal growth and well-being.
Management of primary disease
Women with glomerulonephritis including lupus nephritis require quiescent disease and stable immunosuppression for at least 6 months prior to conception. Immunosuppression should be adjusted and continued throughout pregnancy to abrogate risk of disease flare (Table 2), with recent reports of successful use of tacrolimus for SLE nephritis in pregnancy.41 Women with SLE should have testing for anti-Ro and anti-La antibodies, which are associated with neonatal lupus and congenital heart block, and markers of antiphospholipid antibody syndrome, which may necessitate specific management in pregnancy.29,31 Hydroxychloroquine should be continued through pregnancy in Ro+/La+ women. Stanhope et al31 provide an excellent algorithm for the management of lupus nephritis in pregnancy.
Table 2 Recommendations for immunosuppressant medications in pregnancy
Comorbid conditions require specific attention. Good diabetic control is important preconception and during pregnancy, and is associated with better outcomes.36 Urine surveillance should occur regularly, with aggressive treatment of asymptomatic bacteriuria, particularly in women with reflux nephropathy, autosomal dominant polycystic kidney disease, and immunosuppression. Prophylactic antibiotics should be considered for the remainder of the pregnancy after a first episode of urinary tract infection, although this is not universally implemented.3,42
Diagnosis of pregnancy
Renal excretion of β-human chorionic gonadotropin (β-hCG) produced by somatic cells is reduced in CKD. Urine pregnancy tests may be falsely positive. Serial blood β-hCG testing and pelvic ultrasound are useful to confirm pregnancy and determine accurate gestational age, rather than date of last menstrual cycle, as irregular cycles and anovulation are common in advanced CKD.
Women with CKD should be offered standard antenatal screening as per local practice, but interpreted cautiously. First trimester screening for aneuploidies involves ultrasound nuchal translucency measurement and serum-free β-hCG and pregnancy-associated plasma protein A (PAPP-A).43,44 In the second trimester, free β-hCG, unconjugated estradiol, α-fetoprotein, and inhibin A is measured. Impaired renal clearance of free β-hCG may affect test validity. Benachi et al45 investigated free and total β-hCG in the second trimester to determine those “at risk” of Down syndrome (defined as risk of >1:250). A significantly higher number of women with CKD met “at risk” criteria using free β-hCG (48% vs 12% of controls), whereas total hCG gave a nonsignificant difference (25% vs 15%). Levels of α-fetoprotein, utilized in screening for neural tube defects, are not affected by renal disease.46 PAPP-A is a risk marker for small-for-gestational-age (SGA) babies. PAPP-A has been studied as a biomarker in CKD generally. While still interpretable in early stage CKD in pregnancy, PAPP-A is unreliable in late CKD including dialysis47 and falsely elevated in women receiving heparin.48 Unconjugated estriol is cleared by dialysis, unlike α-fetoprotein and β-hCG.46 No data exist regarding noninvasive renal testing using cell-free placental DNA in CKD cohorts. Further studies are required to improve interpretation of screening tests in CKD patients.
Controlling hypertension before and during pregnancy is essential. A meta-analysis by Bramham et al49 of nearly 800,000 pregnancies in non-CKD chronic hypertensive women demonstrated markedly increased risks of superimposed preeclampsia, cesarean section, preterm delivery, intensive care admission, and perinatal death. Hypertension is an additive risk factor at all stages of CKD. Piccoli et al20 reported threefold higher odds for preterm birth in hypertensive women versus normotensive women with stage 1 CKD.20 A similar additive effect was reported by Munkhaugen et al,1 with a combined odds of preeclampsia, preterm birth, or SGA of 1.18 versus 4.24 in normotensive women versus hypertensive women with eGFR <90 mL/min/1.73 m2 compared to those with higher eGFR.
There is insufficient evidence regarding BP targets and treatment-related modification of outcomes in hypertensive CKD pregnancies,50 although the National Institute for Health and Care Excellence guidelines recommend maintaining BP <140/90 mmHg in hypertensive women with CKD. Concerns regarding effects of lower BP on fetal growth51 were addressed in the CHIPS trial, where tighter control of diastolic BP reduced severe maternal hypertension with no significant fetal impact.52 However, caution should be used in extrapolating these findings to women with CKD owing to potential differences in vascular disease burden or placentation.
First-line medications commonly used for pregnancy hypertension include methyldopa, labetalol, and nifedipine. Antihypertensive management in pregnancy has been recently comprehensively summarized in international guidelines.53–55
Angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers are contraindicated due to intrauterine growth restriction, renal dysplasia, oligohydramnios, and fetal death.56 Cooper et al56 suggested a > twofold increased risk of congenital malformations associated with first trimester usage, notably cardiac and central nervous system abnormalities, but could not adjust for the confounder of maternal diabetes. More recent studies suggest that congenital defects are related to hypertension and comorbidities, not ACE inhibitors themselves.49,57 Given the anti-proteinuric benefits of renin–angiotensin–aldosterone system blockade, continuing these drugs until conception is confirmed may be considered acceptable in proteinuric patients.58
Preeclampsia prophylaxis and diagnosis
Studies of aspirin for preeclampsia risk reduction in the CKD pregnant cohort are limited, and management recommendations are extrapolated from studies in low-risk cohorts. The National Institute for Health and Care Excellence guidelines currently support low-dose aspirin (75 mg/day) for women with CKD from 12 weeks until delivery.59 A Cochrane review of aspirin for preeclampsia prevention identified a significant 5.2% decrease in the absolute risk of preeclampsia among high-risk women in 59 trials.60 Therefore, aspirin is recommended in women with hypertension and CKD, particularly women with SLE.30
Diagnosing preeclampsia in women with CKD presents a specific diagnostic challenge. The clinical features of worsening hypertension, proteinuria, or biochemical parameters may be a manifestation of underlying renal disease affected by pregnancy, or may represent preeclampsia. Nonrenal parameters such as liver enzymes and platelet count are most useful. Renal biopsy is rarely indicated. Preliminary studies suggest assays of soluble fms-like tyrosine kinase (sFLT-1), placental growth factor, and serum placental protein 13 may assist in differentiating preeclampsia from CKD, and predicting preeclampsia in high-risk populations, including women with CKD.61,62 Although not widely available, these biomarkers are being validated in CKD patients and may significantly influence future management.63
Management, including timing of delivery, for women with CKD and superimposed preeclampsia should be according to local practices for non-CKD preeclampsia, with focus on controlling BP and monitoring renal function peripartum and on an ongoing basis postpartum.
Proteinuria and nephrotic syndrome
Proteinuria is an important parameter for risk stratification of maternal CKD. The sensitivity and specificity of the spot protein/creatinine ratio is adequate to exclude significant proteinuria, and enable monitoring of existing proteinuria. However, in many centers, 24-hour urine collections remain the preferred test. Proteinuria is more likely to commence or worsen in pregnancy as CKD stage advances, and is probably independently associated with adverse pregnancy outcome.17,20 In women with diagnosed pregnancy hypertension or preeclampsia, the severity of proteinuria has not been shown to consistently predict maternal or fetal outcomes.64
Little data are available regarding prophylaxis against venous thromboembolism in women who develop nephrotic-range proteinuria or nephrotic syndrome in pregnancy. Given the prothrombotic risks of nephrotic syndrome and pregnancy, along with other risk factors including obesity and immobility, it may be appropriate to commence prophylaxis with low-molecular-weight heparin. Doses should be corrected for renal function in advanced CKD. If underlying glomerulonephritis is suspected, immunosuppression may be appropriate. Substantial edema may be managed with diuretics, with monitoring for oligohydramnios. Albumin infusion has also been used; however, the supporting evidence is insufficient and proteinuria may be paradoxically increased.58
Pregnancy in dialyzed women
Despite reduced fertility in women with advanced (stage 4–5) CKD undergoing dialysis, pregnancies still occur, presenting significant clinical challenges. Historically, high rates of fetal loss (>50%) and generally poor outcomes reinforced clinical pessimism. However, since the late 1990s, with recognition that increased dialysis intensity improves outcomes, successful birth rates have risen to 70%–90%, although pregnancies remained complicated by hypertension (50%–70%), preeclampsia (18%–67%), polyhydramnios (up to 40%), intrauterine growth restriction (17%–77%), and prematurity and low birth weight (50%–100%).8,10,13,22,65–67 Saliem et al66 compared obstetric outcomes in dialyzed women with transplanted women, and found that many complications including hypertensive disorders and preterm birth occurred with equal frequency; however, dialyzed mothers were more likely to have growth-restricted babies, placental abruption, blood transfusions, and intrauterine fetal death.
Improvements in live birth, gestational age, and birth weight have been observed with intensive hemodialysis regimens, achieved via daily (or near-daily) treatments, longer treatment hours, or nocturnal dialysis.65,68–73 Piccoli et al74 recently demonstrated a relationship between greater number of hours of dialysis and the reduced risk of preterm delivery or SGA neonate in a metaregression. Intensive hemodialysis is now the standard model of care for women receiving dialysis in pregnancy, particularly if residual renal function is minimal. The Italian Study Group of the Kidney and Pregnancy suggests daily nocturnal dialysis for women without residual renal clearance, aiming for at least 36 hours per week.68 Hladunewich et al69 have recently demonstrated substantially improved outcomes in 22 Canadian women treated with intensive dialysis compared with an American registry cohort. Long-hours dialysis achieves lower maternal urea levels, reducing fetal-osmotic diuresis and polyhydramnios, and avoiding rapid fluid shifts, uteroplacental hypoperfusion, and fetal distress. Treatment should aim for predialysis blood urea nitrogen levels <50 mg/dL (17.9 mmol/L) or urea levels <100 mg/dL (16.6 mmol/L); women with residual renal function may require less intense dialysis to achieve these targets.68–70 Hemodialysis management considerations include attention to predialysis biochemical parameters, frequent review of ideal weight, BP control, anticoagulation, diet modifications, and anemia management. Detailed management is beyond the scope of this review, and recent expert recommendations have been published.68,70
Data regarding pregnancy outcomes in women receiving peritoneal dialysis are limited to individual case reports, an Australian series of five patients,75 and minimal representation in registry data. ANZDATA registry data suggest lower conception rates in women receiving peritoneal dialysis,10,14 possibly due to hypertonic fluid and adhesions disturbing implantation.42 The dialysis prescription may require adjustment to limit abdominal fullness, with more frequent exchanges and smaller volumes, and vigilance for peritonitis. Evidence favoring initiation of peritoneal dialysis over hemodialysis in advanced CKD pregnancies is limited. In the ANZDATA cohort, most women switched from peritoneal dialysis to hemodialysis in pregnancy.10 In maintenance dialysis patients, continuing an intensified version of the established dialysis is reasonable in pregnancy, providing that good dialysis efficiency is achieved.68
Timing of conception in dialyzed women
The timing of initiating dialysis has prognostic significance because residual renal function is an important determinant of outcome.10,65 Data from the ANZDATA registry demonstrated superior live birth rates (91% vs 63%), but no difference in gestational age or birth weight, in women with advanced CKD who commence chronic dialysis (predominantly hemodialysis) during pregnancy, compared with women already receiving chronic dialysis at conception.10 Those women commencing dialysis after conception had higher eGFR at dialysis initiation than the chronic cohort. While there is no evidence regarding the optimal time to initiate dialysis in women with advanced CKD in pregnancy, most clinicians would consider a lower threshold than in the nonpregnant patient, usually once serum urea is >20 mmol/L.
Pregnancy in transplant recipients
Fertility is significantly increased after kidney transplantation, and the chances of successful birth are markedly increased compared with the dialysis cohort.67 The ANZDATA registry has reported an overall live birth rate of 76% (97.8% for pregnancies reaching >20 weeks gestation), with most pregnancy losses occurring in the first trimester, and the rate of elective termination falling over time from 25% in the 1970s to 3% in the 2000s.15,76,77 Although rare, successful pregnancies utilizing assisted reproduction technology including in vitro fertilization have also been reported for the transplant cohort.76,78 The results of these studies should be interpreted with caution, as there may be selection bias, and there may be risks of hormonal conditioning in transplant patients.
The American Society of Transplantation first published guidelines for the management of kidney transplant pregnancies in 2005,79 with further recommendations by the National Kidney Foundation KDIGO group in 2009.80 Since that time, there has been an explosion of data with numerous registry and cohort studies, systematic reviews, and a meta-analysis reporting kidney transplant pregnancy outcomes.16,66,67,76–78,81–87 The universal finding is that even in successfully transplanted women, substantial rates of important obstetric complications are observed. In particular, preeclampsia occurs in 25%–35% of pregnancies, and growth restriction or preterm birth in 30%–50%; rates have been shown to be similar between transplanted and dialyzed women.66 The ANZDATA registry analyses demonstrated a difference in mean gestational age of 3.5 weeks and birth weight of 873 g for babies of transplanted women compared with the Australian birth cohort, a difference that has clinical relevance for those babies.76 Women who are transplanted as children have similar pregnancy outcomes compared with women transplanted as adults, despite longer exposure to kidney failure and immunosuppression.77
For women with stable and good allograft function, pregnancy does not appear to adversely impact long-term graft function or patient survival, although some women will have transient graft dysfunction or failure of creatinine to fall during pregnancy.15,28,84,85 Surprisingly low rates of acute rejection have been reported during pregnancy, <6% in most studies.83,84 In addition, the risk of de novo allosensitization after pregnancy in a transplanted women is also <6%.88 Risk factors for inferior perinatal outcomes and decline in maternal graft function are likely similar to those observed in CKD cohorts, with preconception graft function shown to be a key determinant.84,87 More data are required regarding long-term graft and infant outcomes and methods of risk stratification. Of particular concern are those women with borderline preconception allograft function; the long-term impact of pregnancy is much less defined in this cohort.
Clinical management is largely similar to the CKD pregnancy cohort. Issues specific to transplanted women include determining appropriate timing of conception posttransplant, adjustment of immunosuppression, surveillance of allograft function, and vigilant monitoring for preeclampsia, rejection, and infection in the immunocompromised recipient (Figure 1). As in women with CKD, distinguishing preeclampsia from chronic hypertension or graft rejection can present a diagnostic dilemma.
The optimal timing of pregnancy is not conclusively established by the available data, but must be balanced against the window of opportunity for childbearing. Effective contraception should be strongly recommended peri-transplantation;80 contraceptive options require careful consideration based on comorbidities and individual factors, however, intrauterine devices or combined barrier/hormonal methods are considered the safest option.89,90 Pregnancy occurring within 1 year from transplantation may be safe,91 but other studies suggest a longer time posttransplant is favorable.16,76 The recommended interval of transplantation to pregnancy is 1–2 years, provided graft function is stable, hypertension controlled, and the immunological environment favorable with low risk of rejection or infection.83,89,90 Reported average transplant pregnancy intervals in Australia and New Zealand are in fact much longer (3–5 years).76 Infections such as cytomegalovirus are much less common by this time, but status should be checked prepregnancy.
Immunosuppressive therapy must be adjusted preconception in transplant and nontransplant patients. Table 2 summarizes general recommendations. Graft function should be monitored for at least 3 months following immunosuppression changes, with reassessment of donor-specific antibodies in sensitized recipients. Most studies report a large number of immunosuppression combinations used in pregnancy, making subanalysis of immunosuppression and pregnancy outcomes difficult. Calcineurin inhibitors (tacrolimus or cyclosporine), prednis(ol)one, and azathioprine are most commonly used, and considered reasonably safe, without increased risk of congenital defects above the background population rate.83,89,92 During pregnancy, blood levels of tacrolimus and cyclosporine may fall, necessitating surveillance and dose adjustment.92 Tacrolimus pharmacokinetics alter in pregnancy with increased unbound active fraction, although this is not routinely measured.93 Tacrolimus and prednis(ol)one have been associated with diabetes mellitus, but evidence for increased rates of gestational diabetes in the kidney transplant cohort is inconclusive.15,84,85 Mycophenolate mofetil is known to increase early pregnancy loss and birth defects, and should be ceased preconception.94 More data are needed to explore the safety of mammalian targets of rapamycin inhibitors in pregnancy, with some evidence of effect on fetal metabolism and growth;95 therefore, avoidance is preferable.
Decisions regarding the timing of delivery depend on maternal and fetal well-being, balanced against the gestational age. Fetal surveillance should be conducted by experienced sonographers ideally with materno–fetal medicine obstetricians. Ultrasound assessment of fetal growth, amniotic fluid volume, and Doppler assessment of uterine, umbilical, and fetal cerebral vessels, and ductus venosus provide important information regarding fetal well-being, and should be performed fortnightly from 28 to 30 weeks. The value of each parameter alters depending on gestational age.96 Changes in the umbilical artery such as absent flow or reversed end-diastolic flow reflect increased placental vascular resistance and precede alterations in middle cerebral artery blood flow and brain sparing, which reflect late fetal compromise.96,97 Polyhydramnios is common in the setting of maternal diabetes or high serum urea. Cardiotocography may be used after 28 weeks to assess fetal condition, especially in women receiving dialysis. Surveillance for intrauterine growth restriction or other fetal compromise is imperative as this is often the primary precipitant for early delivery.
Timing and type of delivery
No data are available in the CKD population regarding optimal timing; however, rapidly worsening maternal or fetal parameters usually warrant delivery. Local practices for women with chronic hypertension or preeclampsia should be followed. The HYPITAT-II trial regarding induction of labor versus expectant management for women with nonsevere hypertensive disorders between 34 and 37 weeks did not support routine immediate delivery, as the nonsignificant reduction in maternal complications was outweighed by the significantly elevated risk of neonatal respiratory distress.98 Delivery should be conducted as per usual local practice. There is no specific indication for cesarean section in women with renal impairment, including women with transplants, although cesarean section rates are significantly higher in renal cohorts, likely driven by emergency deliveries.19,20 The location of the transplant, ureter, and vessels should be reviewed with the obstetric team, in liaison with the transplant surgical team, if required.
The benefits of breastfeeding (particularly for preterm infants) may outweigh theoretical risks of adverse effects on infants; therefore, breastfeeding options should be considered well before delivery. All hypertensive medications used antenatally are suitable for breastfeeding, in addition to enalapril, captopril, and quinapril.53 Data remain limited for many immunosuppressants, but breast milk exposure is likely minimal.99 Glucocorticoids and azathioprine are relatively safe. Recent data regarding tacrolimus and cyclosporine suggest minimal fetal exposure via breast milk, and as such patients should not be discouraged from breastfeeding.93,99–101 Breastfeeding cannot be safely recommended while taking mycophenolate or mammalian targets of rapamycin inhibitors due to lack of data. It should be noted that current counseling practices differ between centers.
Given the increased morbidity of unplanned pregnancy where medical issues are not optimized, contraceptive counseling is essential at all CKD stages, even where fertility may be severely reduced by CKD or age.39 Contraceptive choices must be individualized by comorbidity, and potentially serious side effects balanced against risks of pregnancy. Contraceptive options for women with CKD broadly involve barrier methods, hormonal methods, and intrauterine devices; however, there are little data on efficacy and failure rates in women with kidney disease.90,102,103 Barrier methods alone are insufficient to deliver the highly effective contraception required in this cohort. Surgical sterilization should be considered if the family is completed. The UK Royal College of Obstetricians and Gynaecologists provides an excellent guide for contraceptive risk–benefit decision making in women with hypertension and other comorbidities, although not specifically renal disease (Table 3).104
Table 3 Summary of RCOG guidance on contraceptive use in hypertension, diabetes, and SLE104
Oral contraceptive pills (OCPs) containing estrogen are generally contraindicated in women with cardiovascular disease, a history of thromboembolism, and smokers >35 years of age, and relatively contraindicated in hypertension, diabetes mellitus, or SLE.102 A low-dose OCP is preferred. However, given the availability of safer alternatives, other contraceptive methods are more appropriate in women with hypertension.
Progesterone-only contraceptives may be an effective and safer option, including the progesterone-only OCP, subdermal implants or intrauterine devices, and injectable medroxyprogesterone (Table 3). Among the choices for progesterone-only OCPs, desogestrel-containing pills have the advantage of a longer window of action. Potential benefits of progesterone-only contraceptives include amenorrhea, which may assist with the management of iron deficiency anemia.90 Nonhormonal (copper) intrauterine devices overcome some limitations of hormonal methods, although some have had concerns regarding efficacy in immunosuppressed women.102
Emergency contraception is likely safe in this cohort. Medical abortion with mifepristone or misoprostol has been reported in women with CKD, without complications, but should be used cautiously due to lack of data.105
Patient perspectives and shared decision making
Few studies have examined patients’ perspectives of pregnancy and CKD, which is of importance in guiding clinical approaches to preconception counseling. Our group undertook a systematic review and thematic synthesis of 15 qualitative studies including 257 women with renal disease, identifying themes including a strong desire for fulfilling motherhood, guilt at failure to meet societal expectations, fear of birth defects and fetal harm, emotional conflict in decision making, fears of exacerbating disease, and issues around control and determination.106 Our subsequent study explored pregnancy experiences in 41 Australian women from two centers with CKD stages 3b–525 and highlighted the complexities of navigating parenthood with CKD. Major themes identified included a sense of physical failure and fragility due to CKD, feelings of loss when denied motherhood, guilt in relation to disappointing partners and family, guilt at gambling with their health, and rationalizing the health risks of pregnancy in order to pursue motherhood. Women who chose to prioritize survival described strategies for coping with loss of motherhood by reorienting focus toward positive elements of their lives. A key concern was distress at clinician focus on negative outcomes, perceived discouragement and judgment by medical professionals, and a lack of ownership in the decision-making process. Significant hope was provided by a positive attitude from clinicians. A recent cross-sectional analysis of the perspectives of 179 British women with CKD receiving counseling within a multidisciplinary renal-focused obstetric clinic found that preconception counseling aided decision making for 92% of participants, with only 17% intimidated by the process.40 The findings highlighted the crucial value of preconception counseling to women with CKD and their partners for shared decision making with clinicians, in a way that acknowledges the women’s goals and priorities, and is adapted to the differing needs of this high-risk cohort.
Maternal CKD in pregnancy presents a number of challenges to women and clinicians, even at early stages of disease, with escalating obstetric and perinatal risks according to disease stage and comorbidity. Preconception counseling is essential to support women in making informed, autonomous decisions, and to maximize opportunities to modify medical care to optimize outcomes if pregnancy occurs. A multidisciplinary specialized team approach is integral to the care of these women and their babies.
The authors thank Dr Kevin Chen for his contribution to the literature review.
The authors report no conflicts of interest in this work.
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