The prevalence of chronic kidney disease (CKD) is slightly higher in women than men. Women of childbearing age make up a small, yet important portion of this population (1, 2). Asking women in this age group about their future family plans can prevent unplanned pregnancies, provide timely education and intervention, and decrease adverse fetal and maternal outcomes associated with CKD. Still, for some women or for some nephrologists, speaking about pregnancy may be an uncomfortable and unfamiliar topic of conversation during an office visit. Discussed below are pertinent topics of conversation that can allow nephrologists to start an impactful conversation with their patients (Table 1).
Components of preconception counseling


Timing of pregnancy should be discussed so that pregnancies can be planned. This can be dependent on numerous factors, such as remission or relapse of their underlying glomerular disease, control of hypertension, rate of progression of their current kidney disease, age, and their status for kidney transplantation. If glomerular disease is in remission for 6 months to 1 year, it may be an ideal time to try to conceive. If the rate of kidney function decline is rapid, then pregnancy should be postponed, as CKD progression may accelerate. Ideally, if kidney transplantation is possible, then postponing pregnancy until 1–2 years post-transplantation would be preferred. Still, post-transplantation pregnancies carry their own maternal and fetal risks, including preterm deliveries, cesarean sections, preeclampsia, gestational diabetes, and pregnancy-induced hypertension (3). Likewise, if age permits, pregnancy can be postponed until the patient is well optimized.
For women who are not planning pregnancy, conversations regarding contraception should be initiated, and these can be followed up with more detail provided by a gynecologist. Individual preference, timing of conception, adherence to medications, along with underlying comorbid conditions, such as hypertension, thrombogenic conditions, and CKD, should be taken into consideration when discussing risks and benefits of certain contraceptive methods (4). Different methods of contraception are provided in Table 2.
Types of contraception


Fertility is an important topic to consider in women with CKD. This is of particular concern with past use of medications, such as cyclophosphamide, or even living with CKD, which can impact fertility potential. When treating women of childbearing age, nephrologists need to be mindful of what the woman's future family plans are so that fertility can be preserved as much as possible. If a woman chooses the use of assisted reproductive technologies (ARTs) to aid infertility, similar preconception counseling and assessment should be performed before beginning any ART. ART comes with inherent risks to the mother and fetus, which are likely similar to those for CKD yet not completely understood (5). ART increases risk of hypertensive disorders of pregnancy, including preeclampsia, preterm deliveries, and low birth-weight infants (6).
Laboratory testing to help prognosticate kidney outcome, as well as maternal and fetal outcomes, should be appropriately performed. Pre-pregnancy, 24-hour urine for proteinuria, creatinine clearance, and serum creatinine levels can all help with counseling. Checking hemoglobin A1c levels will be helpful for those with diabetes mellitus. Assessing autoimmune activity in patients with lupus vasculitis, for example, should be performed. Since challenges of performing a kidney biopsy during pregnancy exist in women with proteinuria of undetermined etiology, performing a kidney biopsy pre-pregnancy may be indicated to ensure there is a pre-pregnancy glomerular diagnosis so that appropriate therapy can be initiated during pregnancy if indicated. Likewise, in women with advanced CKD, performing a kidney biopsy may help prognosticate their post-pregnancy kidney outcome, as well as offer treatment if the disease progresses during pregnancy.
Based on lab assessment, it is important to discuss risk with these women. Some women may be oblivious to the risks that their kidney disease poses on a pregnancy. Risks of relapse, progression of their underlying kidney disease or proteinuria during pregnancy, and adverse outcomes of CKD to the mother and fetus should all be discussed. Women with CKD have a higher likelihood for preterm deliveries, gestational hypertension, preeclampsia or eclampsia, and cesarean sections (7). Adverse fetal outcomes include small gestational-age and lower birth-weight infants and increased admissions to neonatal intensive care units (8).
Appropriate medication adjustments should be made before conception. In women treated with immunosuppressive agents, such as mycophenolate mofetil, whether for post-transplantation or for the treatment of glomerular disease, pregnancy should ideally be postponed until teratogenic medications are successfully removed for a reasonable amount of time or substituted for non-teratogenic agents. Similarly, women who are being treated with anti-hypertensive agents that are teratogenic, such as angiotensin-converting enzyme inhibitors or angiotensin II receptor blockers, should be switched to other, safer alternatives, such as labetalol, hydralazine, calcium channel antagonists (e.g., nifedipine), or methyldopa. Blood pressure should be followed up to ensure optimal control preconception. Sodium-glucose cotransporter-2 inhibitors have been shown to affect kidney development in animal studies, especially in the second and third trimesters; hence, these medications should be avoided until more is known about their use in pregnancy. Diuretics should be used with caution to prevent volume depletion. Since CKD is a risk factor for preeclampsia, low-dose aspirin is ideally initiated before 16 weeks gestation to decrease risk (9).
One nephrology office visit can suffice to initiate and discuss most issues that encompass preconception counseling. Follow-up on the recommendations from this visit are still recommended. Referral to a high-risk obstetrician and other subspecialists in a timely manner can further supplement appropriate preconception counseling and stratification.
References
- 1.↑
US Renal Data System (USRDS); National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH). CKD in the general population. https://usrds-adr.niddk.nih.gov/2022/chronic-kidney-disease/1-ckd-in-the-general-population
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Coresh J, et al. Prevalence of chronic kidney disease in the United States. JAMA 2007; 298:2038–2047. doi: 10.1001/jama.298.17.2038
- 3.↑
Shah S, et al. Pregnancy outcomes in women with kidney transplant: Metaanalysis and systematic review. BMC Nephrol 2019; 20:24. doi: 10.1186/s12882-019-1213-5
- 4.↑
Burgner A, Hladunewich MA. Contraception and CKD. Clin J Am Soc Nephrol 2020; 15:563–565. doi: 10.2215/CJN.09770819
- 5.↑
Ahmed S, et al. Fertility, contraception, and novel reproductive technologies in chronic kidney disease. Semin Nephrol 2017; 37:327–336. doi: 10.1016/j.semnephrol.2017.05.004
- 6.↑
Bhaduri M, et al. Systemic review of pregnancy and renal outcomes for women with chronic kidney disease receiving assisted reproductive therapy. J Nephrol 2022; 35:2227–2236. doi: 10.1007/s40620-022-01510-x
- 7.↑
Piccoli GB, et al. Pregnancy and chronic kidney disease: A challenge in all CKD stages. Clin J Am Soc Nephrol 2010; 5:844–855. doi: 10.2215/CJN.07911109
- 8.↑
Hladunewich MA. Chronic kidney disease and pregnancy. Semin Nephrol 2017; 37:337–346. doi: 10.1016/j.semnephrol.2017.05.005
- 9.↑
Henderson JT, et al. Aspirin use to prevent preeclampsia and related morbidity and mortality: Updated evidence report and systematic review for the US Preventive Services Task Force. JAMA 2021; 326:1192. doi: 10.1001/jama.2021.8551