The Hypertensive Disorders of Pregnancy: A Focus on Definitions for Clinical Nephrologists

About 5–10% of pregnancies are complicated by one of the hypertensive disorders of pregnancy. The women who experience these disorders have a greater risk of having or developing kidney diseases than women with normotensive pregnancies. While international guidelines do not provide clear indications for a nephrology work-up after pregnancy, this is increasingly being advised by nephrology societies. The definitions of the hypertensive disorders of pregnancy have changed greatly in recent years. The objective of this short review is to gather and comment upon the main definitions of the hypertensive disorders of pregnancy as a support for nephrologists, who are increasingly involved in the short- and long-term management of women with these disorders.


Introduction
The hypertensive disorders of pregnancy (HDP) are no longer seen as "transitory diseases cured by delivery", but as windows into the future that allow us to predict a woman's future cardiovascular and kidney health.
This paradigm shift has led to an increased need for integrated care for women who experience a hypertensive disorder during pregnancy, involving specialists that can oversee and coordinate treatment, and, whenever possible, work to identify risk factors and correct them [1,2].
Definitions of the hypertensive disorders of pregnancy have changed greatly in recent years. The objective of this article is to briefly review their main definitions and epidemiology as a support for nephrologists, who are increasingly involved in the management of HDP in the short and long term. In order to accomplish our task, we reviewed the available guidelines and the relevant literature. Chronic HTN with at least one of the following: -resistant HTN -new-onset or worsening of proteinuria -one or more "adverse conditions" (e.g., PE) -one or more "severe complications" (e.g., PE) The different conditions will be discussed in detail in the pages that follow.

Hypertension in Pregnancy
Gestational or pregnancy-induced hypertension, which affects up to 10% of pregnant women, is recognized by all societies as new-onset blood pressure (BP) ≥ 140/90 mmHg at or after 20 gestational weeks. The risk of progression to PE is estimated as 17.1-25% [7][8][9][10][11][12][13]. About 50% of patients with gestational hypertension continue to have high BP levels after delivery. Conversely, about 10% of the women who are normotensive during pregnancy may develop hypertension up to 6 weeks postpartum [14]. In the latter case, the patients have the same risk of short-and long-term cardiovascular complications as women affected by hypertension during gestation [15].
While the prevalence of chronic hypertension increases with age, it can affect all patients of childbearing age, both in its idiopathic and secondary forms, and is estimated to be present in 1-2% of pregnancies [16]. Apart from the specific susceptibility of women of Afro-American ethnicity, the prevalence of chronic hypertension in pregnancy is rising, as shown by a population-based cross-sectional study of more than 150 million hospital deliveries in the United States, where the increase in chronic hypertension was closely related to increased maternal age and body mass index (BMI) [17]. The clinical relevance of chronic hypertension in pregnancy is high, as it is associated with a higher rate of maternal and neonatal complications, including the need for cesarean section (41%), smallfor-gestational-age (SGA) newborns (17%), preterm delivery (28%), the need for a neonatal intensive care unit (NICU) (21%), and perinatal death (4%) [18]. In addition, hypertension is an independent risk factor for "superimposed" PE (relative risk (RR), 5.1; 95% CI, 4.0-6.5) [16,[19][20][21], defined by the development of proteinuria or end-organ damage in hypertensive patients after 20 gestational weeks.
Several issues are not yet clear: the blood pressure target is still a matter of discussion and, while reaching lower targets was not associated with an improvement in maternal and fetal health, the presence of known chronic kidney disease (CKD) is acknowledged as a reason for trying to reach lower BP targets ( Table 2). Things are not as simple as they may seem, considering that CKD is probably the most common cause of secondary hypertension in a non-obese, non-diabetic young woman, and that many forms of CKD are not detected unless specifically searched for using both biochemical assessment and renal imaging [22,23].
Overall, the current guidelines on hypertension in pregnancy recommend treating all cases of severe hypertension (>160/110 mmHg) and suggest starting antihypertensive treatment in milder cases (BP between 140-159/90-109 mmHg) only in the presence of cardiovascular diseases, diabetes, CKD or acknowledged risk factors for cardiovascular diseases ( Table 2). Once more, nephrologists often have a different view of the situation, as is suggested by the best-practice guidelines of the Italian Society of Nephrology, which, while acknowledging the risks of hypotension in pregnancy, recommend the correction of hypertension, as in the case of young patients outside the context of pregnancy (target BP ≤ 130/80 mmHg), under strict clinical surveillance [24]. The main risks to be avoided are seen as those related to hypercorrection, since hypotension can cause placental hypoperfusion, with detrimental effects on the fetus. Careful follow-up is needed to allow optimal blood pressure to be reached [24]. The issue is similar to those problems that may arise in attempting to control diabetes, where hypercorrection and frequent hypoglycemia can have negative effects on pregnancy outcomes [25]. When setting BP goals in pregnancy, we should keep in mind that outside the context of pregnancy, the results for CKD patients under tight hypertension control in the recent ACCORD BP trial demonstrated that the benefits obtained in reducing cardiovascular events and mortality were offset by a higher risk of adverse kidney outcomes, which are mainly represented by AKI [26]. No such data are available for pregnancy. Table 2. Indications for starting antihypertensive medication in pregnancy, and blood pressure goals in the hypertensive disorders of pregnancy in national and international guidelines.

Guideline
Recommended

Preeclampsia
PE is a multisystem disease, generally defined as a condition in which the onset of arterial hypertension after 20 weeks of gestation is accompanied by at least one sign of renal, hepatic, central nervous system, or hematologic impairment [7][8][9][10][11][12] (Figure 1). Proteinuria levels ≥0.3 g/24 h or a protein-to-creatinine ratio (PCR) ≥ 0.3 g/g is present in about 75% of the cases defined as PE. While, in the past, proteinuria was required for a PE diagnosis, international boards now consider it to be of the same importance as other symptoms and signs [7][8][9][10][11][12]. In this regard, the new guidelines underline the central role of kidney involvement, basing a diagnosis not only on proteinuria but also on a reduction in kidney function from the baseline pre-gestational level [7][8][9][10][11][12]. Other "new" features of the definition of PE are laboratory findings regarding liver involvement, with an increase in aminotransferases (alanine aminotransferase and/or aspartate aminotransferase at >40 IU/L, whether or not this is accompanied by rightupper quadrant or epigastric abdominal pain), thrombocytopenia (platelets at <10 9 /L), disseminated intravascular coagulation (DIC), and hemolysis. In this regard, the more extensive PE definition merges with the definition of HELLP syndrome, indirectly alluding to a univocal definition of HDPs.
Symptoms reported by patients range from severe headaches, persistent visual scotomata, or blindness to alterations in mental state and complications such as clonus, eclampsia, and stroke. The Society of Obstetricians and Gynaecologists of Canada (SOGC) and the Society of Obstetric Medicine of Australia and New Zealand (SOMANZ) also include cardiac and/or pulmonary involvement in the diagnostic criteria for PE [7][8][9][10][11][12]. Moreover, except for the American College of Obstetrics and Gynecologists (ACOG), all other societies include signs of uteroplacental dysfunction, such as fetal growth restriction, an abnormal umbilical artery Doppler wave, and stillbirth as being diagnostic criteria of PE [7][8][9][10]12]. Once more, this choice reflects the view that all HDPs are interlinked, even though they do not necessarily occur with the same severity ( Figure 2).
A recent retrospective cohort study of 22,094 pregnancies, followed up at Monash Health in Australia, showed that the wider criteria for defining PE, such as those adopted by the International Society for the Study of Hypertension in Pregnancy (ISSHP) in 2018, made it possible to classify a further 14.8% of women, who in the past would have been excluded from consideration by the ISSHP's 2018 or ACOG's 2018 guidelines, as having experienced PE [7,11,33]. The ISSPH's 2018 guidelines highlighted that among the signs included for the diagnosis of PE, FGR, thrombocytopenia, proteinuria, AKI, or liver impairment had the strongest association with the risks of severe adverse maternal-fetal outcomes [33].
This acknowledgment of the high heterogeneity of PE, in parallel with the proposal to unify the pathogenesis of PE and other hypertensive disorders of pregnancy, has led to an attempt to stratify PE, based on a variety of elements from severity to the period of onset and pathogenic mechanisms (Table 3) [34]. While none of these has proved to be sufficient to clearly distinguish between phenotypes and, above all, to be invariably correlated with maternal-fetal short-and long-term outcomes, these approaches are the basis of a better description of the phenotype of PE, which, albeit with wide overlaps, can enable clinicians to perform a prognostic evaluation of individual cases. In fact, even though late-onset PE may be life-threatening for both mother and fetus, early-onset PE is more often "placental", severe, and associated with profound angiogenic-antiangiogenic imbalance, and, at least according to some studies, has a higher risk of recurrence in subsequent pregnancies [35][36][37].

Small for Gestational Age, Intrauterine Growth Restriction, Fetal Growth Restriction (FGR), and Intrauterine Death
The hypertensive disorders of pregnancy have been related to defective placentation, which may be severe enough to impair the physiologic development of the fetus during pregnancy. These include babies that are small for gestational age (SGA), intrauterine growth restriction (IUGR) or its synonymous fetal growth restriction (FGR), and an increased risk of pre-term delivery, which is usually classified as very early pre-term (<28 gestational weeks), early pre-term (28-34 weeks or, presently, more often, 28-32 gestational weeks) and late pre-term (according to the previous definitions: 32-37 or 34-37 gestational weeks), or intrauterine death [7][8][9][10][11][12]. In this scenario, FGR, newborns that are small for gestational age, and intrauterine death, are part of the spectrum of the hypertensive disorders of pregnancy; while they can occur in association with hypertension or full-blown PE, they may also be isolated and without other PE features [7][8][9][10][11][12].
FGR is defined by the fetal weight, or an abdominal circumference estimated using ultrasounds, showing growth between the 3rd and 10th percentile for gestational age (moderate fetal growth restriction) or less than the 3rd percentile (the severe form) [38]. However, other studies set the cut-off points at the 10th and 5th percentile. The definition of FGR is also dynamic and may need to be raised when there is a flattening of the growth curve [38], to distinguish between low-birth-weight babies with harmonic growth, for genetic (or pathological) reasons, and babies whose normal growth was impaired at some point in their intrauterine life. Considering that FGR can also be the result of fetal diseases, a genetic evaluation should be proposed by the obstetric team, in cases of early recognition (<32 gestational weeks) or when in association with polyhydramnios or, more obviously, of fetal malformations [38].
Conversely, the definition of small for gestational age (SGA) usually applies if the effective birth weight is less than the 10th percentile of the expected adjusted figure for gestational age, according to local growth curves; once more, the definition is not homogeneous, and the cut-off point of less than the 5th percentile is also used [38].
The International Society of Ultrasound in Obstetrics and Gynecology (ISUOG) guidelines distinguish between FGR and SGA, as follows: FGR is defined as the fetus failing to reach its genetically predetermined growth potential, while SGA is diagnosed when the fetus size falls below a predefined threshold for its gestational age (usually the 10th percentile) [39]. In addition, these guidelines specify that an SGA fetus may be small but not at increased risk of adverse perinatal outcomes, while a fetus with a size above the 10th percentile may still be considered FGR and at increased risk of adverse perinatal and long-term outcomes [39].
Intrauterine death is distinguished from miscarriage, which is defined as fetal loss before 20 gestational weeks in the United States, while the British guidelines still set the cut-off point at 24 weeks, which was previously the agreed point. The anticipation of the definition is due to current improvements in allowing viability in very preterm babies, as the definition of intrauterine death usually applies to gestational ages compatible with survival [40][41][42].
According to the US fetal mortality rate, in 2013, "early" intrauterine death was estimated as occurring in 3.01 per 1000 births before 28 gestational weeks, while "late" cases (after 28 weeks) occurred in 2.97 per 1000 births [43]. Over 30% of these fetuses were SGA, often without a causal diagnosis [44].
The relevance for nephrologists of the inclusion of FGR in the context of the hypertensive disorders of pregnancy is high. Including these conditions increases the number of cases that, at least according to the Italian Society of Nephrology (to date, the only group to have published a specific statement on follow-up after preeclampsia), should undergo a basic nephrology evaluation to exclude the presence of CKD [45].
The probability that PE is associated with pre-existing CKD is high, as has also been reported by the Mayo clinic, and it is probably present in at least 20% of the women who experience a PE episode [22,45,46].
The second element of interest is that being born small for gestational age and/or with a low birth weight is, in turn, associated with the risk of developing CKD, hypertension, diabetes, and metabolic syndrome in adulthood and, for females, with developing preeclampsia once pregnant, thus generating a vicious circle of diseases reappearing over generations, not necessarily with a genetic basis [47][48][49][50]. Despite the fact that the relationship between low birth weight and prematurity and subsequent disorders during pregnancy has been described for decades, the message that the risk of preeclampsia in the mother decreases with increased gestational age has not been fully integrated into clinical practice, and no specific surveillance programs have been set up for such high-risk pregnancies (the odds ratio (OR) of developing PE was about 4 for mothers born earlier than 34 gestational weeks, and is even higher for those born under 4.5 lb, about 2 kg) [47].
Among the numerous subsequent studies on this important issue, the recent large population study by Gjerde and co-workers deserves mention: considering over two million individuals, after a mean follow-up period of 26 years, low birth weight was associated with an odds ratio of 1.72 for CKD, 1.79 for SGA, and 1.48 for preterm birth (95% CI, 1.33 to 1.66) [51].

HELLP Syndrome
The position of the HELLP syndrome in the context of the hypertensive disorders of pregnancy is still debated, although this severe condition is currently included in most guidelines regarding HDP [7][8][9][10][11][12]. Currently, there are two different approaches: one that considers HELLP syndrome a severe variant of PE (Figure 3), and one that sees it as a distinct disease, while acknowledging that there is a shared pathogenesis and risk factors as well as an interplay between all these disorders [34]. Along with hemolysis, thrombocytopenia, and liver impairment, other typical features are hypertension, present in 82-88% of pregnant women, and proteinuria, which is found in 86-100% of pregnant women, according to the cohorts evaluated [52].
Conversely, an interesting "unifying" approach includes HELLP syndrome, together with pregnancy-induced thrombotic microangiopathies (TMAs), mainly because they share patterns of endothelial cell injury (primarily affecting the kidneys and the cardiovascular and central nervous systems, with a hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, and catastrophic antiphospholipid syndrome) [53]. Laboratory findings, including peripheral thrombocytopenia, mechanical hemolytic anemia (defined by hemoglobin levels of ≤10 g/dL, lactate dehydrogenase (LDH) at the upper limit of normal, undetectable haptoglobin, and the presence of schistocytes on the blood smear), as well as signs of impaired organ function, such as a rise in serum creatinine or transaminases, can be present in PE and HELLP as well as in TMAs [53]. Although this interpretation is not universally accepted, it offers a change in perspective, making it possible for us to see the hypertensive disorders of pregnancy not only as "transient" alterations due to gestation but also as endothelial disorders that may recur in subsequent pregnancies or evolve into long term endothelial dysfunction and, in turn, CKD.

Acute Kidney Injury in Pregnancy
The definition of acute kidney injury (AKI) in pregnancy, in the absence of agreed formulae for calculating the kidney function, is usually based on serum creatinine (the definition of AKI usually corresponds to an increase in serum creatinine of at least 0.3 mg/dL over baseline) [54]. However, the physiological reduction in serum creatinine during physiological pregnancies should be considered. In this context, two recent systematic reviews suggest that a normal serum creatinine value in pregnancy should correspond to less than 80% of the pre-pregnancy normal one [55,56]. However, since serum creatinine assessment is not part of the work-up of physiological pregnancies, the interpretation of a serum creatinine level that is still in the normal range in pregnancy may be difficult, if not impossible. This limitation, and the importance accorded to kidney function in pregnancy, are a further indication of the need for including at least serum creatinine in the routine control tests in pregnancy [57,58].
Moreover, we should consider that renal damage may be induced by causes other than the hypertensive disorders of pregnancy, such as hypovolemia, ischemia (e.g., severe postpartum hemorrhage), or sepsis, which can cause acute tubular necrosis or cortical necrosis with adverse outcomes for maternal renal function, both immediately and in the long term [34,59].

The Hypertensive Disorders of Pregnancy and the Future Risk of CKD and End-Stage Renal Disease (ESRD)
If, on the one hand, HDPs may reveal the presence of an underlying disease or predisposition, on the other hand, PE may act as a hit, often in the context of the multiple-hit pathogenesis of cardiovascular, renal, and metabolic disorders [60][61][62][63][64][65]. While a discussion of the cardiovascular effects of PE is beyond the scope of this review, its effects on kidney function deserve mention. After Viske's pivotal study on the Norway registry, highlighting the risk of end-stage kidney disease after PE (an OR of about 4.7), attention has increasingly been focused on these issues: subsequent studies showed a close association between an episode of PE and the need for a kidney biopsy later in life, suggesting that hypertensive disorder may be either a trigger for or an early marker of renal dysfunction [60,66,67].
A large meta-analysis evaluating trials with at least 20 preeclampsia patients, with a follow-up of ≥4 years, involving 110,803 PE cases and 2,680,929 controls, quantified the OR of developing ESRD after preeclampsia at 6.35; however, it also suggested a knowledge gap regarding the "intermediate" phases of CKD, thus indicating the need for prospective follow-up after PE, to better clarify the natural history of CKD after PE [68]. Of note, the baseline CKD risk is probably significant, as shown by the different risk curves observed in Norway (low incidence of CKD) and Taiwan (high incidence of CKD) [69].
Moreover, the best way to manage patients after an episode of pregnancy-related AKI remains undefined [1,34,70]. The hypertensive disorders of pregnancy, in particular PE and HELLP, can further exert a negative effect on kidney health via the development of AKI; once more, the baseline renal conditions matter, and especially in developing countries, the difference between AKI and AKI associated with CKD may be difficult to distinguish, but it is relevant to the future of renal function, i.e., 7-29% of the women needing dialysis in pregnancy fail to fully recover [71][72][73][74].

Risk Factors for PE and HDP
A long-standing misconception is that PE more frequently, or even almost exclusively, affects first pregnancies. Things are not so simple; the incidence of PE in subsequent pregnancies is an example of conditioned probability. In fact, as reported in a classic study on a large cohort, conducted by Hernandez Diaz and co-workers in Sweden in 2009, the risk of PE was found to be 4.1% in first pregnancies, while the incidence of PE was 1.7% in the subsequent gestations of patients without a history of PE, and PE in the first pregnancy was associated with a 14.7% risk of its recurrence in the second gestation and a risk of up to 31.9% after two PE episodes [75]. While these figures hold true for singleton pregnancies, the risk of a first PE episode is higher in multiple pregnancies, where the probability of developing PE was estimated to be 12% in the Swedish study [74], but, interestingly, without significantly increasing the risk of recurrent PE in subsequent singleton pregnancies. The phenotype of PE also seems to modulate the risk of recurrence and, according to the same study, the risk of recurrence was much higher in early-onset PE (up to 60% in a second pregnancy and up to 90% after two early PE episodes) [75].
However, the data on the risk of recurrence varies widely: a population-based recordlinkage cohort study in Australia found much lower cumulative rates of recurrence of PE in the subsequent pregnancy after a first early PE episode. Comparing early PE (<28 weeks) to PE at 28-33 weeks, the first group was found to be more likely to deliver preterm (38.8% and 28.7%, respectively) and to experience perinatal death (4.3% vs. 1.2%) during a subsequent gestation [76]. Overall, 33.8% of women who experienced an episode of early PE during the first pregnancy developed PE in a subsequent singleton pregnancy [76]. Other smaller cohort studies report a variable recurrence rate of preeclampsia, ranging from 25 to 65% [77][78][79][80].
A recent meta-analysis of 92 studies, involving 25,356,688 gestations, identified further maternal predisposing conditions for the onset of PE [19]. Interestingly, apart from having experienced a hypertensive disorder and/or placental dysfunction during pregnancy, a familial history of PE in a first-degree relative represented a significant risk factor (RR 2.90, 95% CI 1.70-4.93) [19].
Besides multiple pregnancies (with a relative risk estimated here of 2.9), the adoption of medically assisted reproduction should be considered the criterion for more rigorous follow-up in gestation (RR 1.8); once more, the risks of medically assisted reproduction are modulated by the type of intervention, with the greatest risk being associated with egg donation, possibly influenced by generally higher maternal age and, often, reduced baseline kidney function [82].
The elements defining high-risk and moderate-risk factors for PE in the different guidelines are summarized in Table 4. Table 4. PE risk factors, according to international boards.

WHO (2011) [83]
High risk factors: previous episode of PE multiple gestations chronic HTA pre-existing diabetes renal disease autoimmune disease SOMANZ (2014) [9] No distinction between high or moderate risk factors:

Follow-Up Outside the Context of Pregnancy
Despite the increasing evidence of long-term risks to kidney health after PE, the only indication included in gynecological international guidelines regards the need for yearly screening of blood pressure, lipids, fasting blood sugar, and body mass index for women with prior preeclampsia that was preterm (<37 weeks) or recurrent [11,12].
The American Heart Association (AHA) has included a history of PE or gestational hypertension as a major risk factor for cardiovascular disease since 2011 [85,86] and, in a 2017 meta-analysis, Wu and colleagues confirmed that PE was independently associated with an increased risk of future heart failure (RR 4.19), coronary heart disease (RR 2.50), global cardiovascular disease-related death (RR 2.21), and stroke (RR 1.81) [87].
As for nephrology guidelines, in 2017, those of the Italian Society of Nephrology included a best-practice statement for the prevention and follow-up of PE [45]. After the first episode of a hypertensive disorder of pregnancy, a multidisciplinary basic pre-gestational screening is deemed desirable, to identify undisclosed maternal diseases and/or to make possible the timely treatment of predisposing factors, such as hormonal imbalance, obesity, and nutritional deficits [56]. It is also suggested that if recurrent or severe PE occurs in a woman with acknowledged risk factors, she should be referred to a tertiary care center in the case of subsequent gestation [45].
While this may be difficult to put into practice, given a lack of dedicated resources, the expert agreement reported in the best practice holds that a woman should be monitored by a nephrologist for at least 6 months after a PE episode (monthly, until the normalization of proteinuria and hypertension, and at least once for 2 to 3 months afterward) to identify unresolved hypertension, kidney function impairment or persistent proteinuria. In these cases, the consensus statement holds that women should be monitored according to local indications for CKD, while yearly follow-ups should be offered to other women, especially those who express the wish for a new pregnancy. Screening should include blood pressure control and the assessment of proteinuria or albuminuria, as well as kidney function. The appearance of hypertension or proteinuria should prompt additional testing to determine its cause and to guarantee an early treatment start [45].

Follow-Ups in Subsequent Pregnancies
While the correction of pre-gestational BMI and other potentially reversible predisposing factors has not been demonstrated to completely offset the increased risk of PE recurrence, it appears to mitigate the risk of adverse pregnancy-related events [56]. Dietary management before and during pregnancy should be considered in both overweight and underweight patients, as well as screening for vitamin status, in particular for the vitamin D axis, which appears to be related to PE onset [56,88,89].
Self-monitoring of blood pressure, possibly integrated as needed with 24-h blood pressure measurement, is part of the management recommended for women classified as being at high risk of PE. Similarly, starting from the 20th to the 24th week, frequent checking of the proteinuria/creatinuria ratio on spot urine (for instance, every 1-2 weeks, according to clinical condition) can allow the early identification of incipient proteinuria; monitoring the sFLT1/PIGF ratio, starting at the 20th week, can make it possible to have the elements available to anticipate placental distress [90]. Moreover, the sFlt-1 to PlGF ratio may help in differentiating between the different causes of increasing proteinuria, especially in CKD patients: a low ratio (<30), in fact, is usually associated with CKD, while a ratio of >150 is not compatible with CKD alone and is highly suggestive of preeclampsia [91]. This information may help clinicians in the management of pregnancy, prolonging gestation in the case of CKD, or intensifying care or anticipating the delivery in the presence of preeclampsia.
Low-dose acetylsalicylate (ASA) is considered to be the most promising drug for reducing the risk of PE and FGR, as well as preterm birth and perinatal mortality in women classified as being at high risk of PE [92][93][94]. According to the ASPRE trial, in fact, women taking low-dose ASA during their pregnancies had a 0.38 odds ratio of experiencing PE compared to controls [95]. There is still a lack of universal consensus on ASA dose (current recommendations range from 75 to 150 mg), and the timing of treatment start, although the idea of "the earlier the better" is widespread (Table 5) [96].

Conclusions
Research on the hypertensive disorders of pregnancy over the past 20 years has led to the recognition of these ailments as possible "signs" of an underlying disease and as "precursors" of future health problems involving the kidney.
Although pregnancy can reveal future or existing kidney disorders, which are difficult to diagnose if they are not known about and searched for, the key message of the usefulness of nephrological surveillance has not yet been standardized in common clinical practice.
Even more "neglected" than the mother is the offspring, although it is known that children with a low birth weight, which is frequently related to hypertensive disorders during the mother's pregnancy, have a greater risk of developing chronic kidney disease and a greater risk, for girls, of future preeclampsia. Identification and correction, where possible, of the risk factors for both these disorders and for potential future health problems, early counseling, and long-term nephrological follow-up could help improve the management of the health of women and their offspring.
Prospective longitudinal studies with large cohorts are necessary to support the key role of the kidney, and clearly define the need for clinical evaluation by a nephrologist during and after an episode of a hypertensive disorder in pregnancy.