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Characteristics and outcome of pregnancy-related acute kidney injury in a teaching hospital in a low-resource setting: a five-year retrospective review

Abstract

Background

Pregnancy-related kidney injury contributes to a high burden of acute kidney injury in low-resource settings and causes maternal and perinatal morbidity and mortality. Few studies have examined the impact of acute kidney injury in resource-limited countries, with very limited research on pregnancy-specific disorders in Ethiopia. This study aimed to determine the characteristics of pregnancy-related acute kidney injury, outcomes and associated factors.

Methods

A retrospective study was conducted to evaluate the clinical profile and maternal-fetal outcome of pregnancy-related acute kidney injury at Ayder Comprehensive Specialized Hospital in Tigray, Ethiopia, from January 1, 2017, to December 31, 2021. Maternal and fetal outcomes were analyzed using descriptive statistics. Multivariate logistic regression was used to determine the association between the dependent and independent variables.

Results

Of 27,350 mothers who delivered at Ayder Comprehensive Specialized Hospital between January 1, 2017, and December 31, 2021, a total of 187 women developed pregnancy-related acute kidney injury, a prevalence rate of 68 per 100,000 births. Preeclampsia, sepsis and pre-renal causes due to dehydration and hemorrhage were the most common causes of pregnancy-related acute kidney injury in this study. Hemodialysis was needed in 8.6% (n = 16) of patients. Of the 187 pregnancy-related acute kidney injuries, 143 (76.5%) recovered completely and 30 (16%) partially. The mortality rate was 7.5%. Preexisting chronic kidney disease (AOR = 30.13; 95% CI: 2.92, 310.84), use of vasoactive agents (AOR = 5.77; 95% CI: 1.47, 22.67), increase in creatinine per unit (AOR = 1.65; 95% CI: 1.11, 2.45) and complications related to acute kidney injury (AOR = 5.26; 95% CI: 1.73, 16.00) were determinants of the composite endpoints (partial renal recovery and death).

Conclusions

This study emphasizes acute kidney injury in resource-limited settings is a significant cause of maternal and fetal morbidity and mortality. The vast majority of patients with pregnancy-related acute kidney injury recovered completely from kidney injury. The main causes of pregnancy-related acute kidney injury were preeclampsia, sepsis and pre-renal associated with hemorrhage and dehydration. Preexisting renal disease, use of vasopressors, increase in creatinine per unit and complications associated with acute kidney injury were determining factors for concomitant fetomaternal mortality. Appropriate preventive strategies during prenatal care and prompt treatment are needed for pregnancy-related acute kidney injury.

Peer Review reports

Introduction

Pregnancy-related acute kidney injury (PR-AKI) is a heterogeneous disorder that encompasses all causes of acute renal impairment from early pregnancy to 3 months postpartum [1]. It is an important obstetric complication associated with significant maternal and fetal morbidity and mortality [2]. Although the incidence of PR-AKI has decreased significantly in developed countries due to improved general health care, it remains a serious public health problem in developing countries [3]. A recent meta-analysis found an overall prevalence rate of 2% [4], and 3–5% of all AKI cases in developing countries such as India are due to PR-AKI [5]. Acute kidney injury (AKI) in sub-Saharan Africa is a major challenge due to the late presentation of patients to health facilities and the lack of resources to care for patients with established AKI [6]. In Africa, PR-AKI is the second most common cause of AKI [7]. In Ethiopia, among patients with AKI requiring dialysis, 18.5% of AKI is attributed to pregnancy-related causes [8].

The etiology and presentation of AKI differ between high-income and low-income countries [9]. In Africa, the most commonly reported causes are infections, nephrotoxins, and obstetric and surgical complications [10]. The main conditions associated with AKI in the antenatal and postpartum period are preeclampsia/eclampsia, obstetric hemorrhage, HELLP syndrome and postpartum sepsis [11]. During the first trimester of pregnancy, AKI is commonly reported, secondary to pre-renal AKI due to dehydration from hyper emesis gravidarum and septic shock associated with sepsis [12]. In the third trimester and immediate Puerperium, it is associated with preeclampsia/eclampsia, ante partum hemorrhage (APH), postpartum hemorrhage (PPH), puerperal sepsis, hemolytic uremic syndrome (HUS) and HELLP syndrome [13].

Regarding the outcome of this disease, complete renal recovery is usually achieved if these patients are treated appropriately and promptly. However, pregnancy-related AKI has high impact on morbidity and mortality in both maternal and fetal outcomes. Inadequate initial resuscitation, late initiation of antibiotics, prolonged intervals until an appropriate clinical setting is reached and consequently significantly delayed initiation of dialysis are the main reasons for poor outcomes [14]. The maternal mortality rate (MMR) increases with increasing severity of pregnancy-related complications and can range from 13 to 24% in developing countries due to PR-AKI [15]. In Ethiopia, maternal mortality has changed significantly in recent decades. MMR decreased from 871 per 100,000 in 2000 to 401 per 100,000 in 2017, which corresponds to the death of approximately 12,000 mothers per year. Direct obstetric complications are responsible for 85% of these deaths [16]. In addition, fetal, neonatal and perinatal mortality is particularly high in newborns born to mothers with pregnancy-related AKI [17]. Therefore, pregnancy-related AKI leads to serious complications and higher maternal and fetal mortality [18]. Although low- and middle-income countries (LMICS) suffer the most from PR-AKI, few studies have investigated its prevalence and impact in obstetric patients. Therefore, this study sought to examine the prevalence, causes and outcomes of pregnancy-related AKI at Ayder Comprehensive Specialized Hospital, a tertiary medical center in northern Ethiopia.

Methods

Study design

A facility based retrospective study design was conducted at Ayder Comprehensive Specialized Hospital, Tigray, Ethiopia, to assess pregnancy-related AKI causes, outcomes and determine factors associated with severe maternal outcomes.

Study period

The medical charts of all women who were diagnosed with pregnancy-related AKI between January 1, 2017, and December 31, 2021, were reviewed.

Study setting

The study was carried out at ACSH, a tertiary care and teaching hospital located in the Tigray region of northern Ethiopia. It is the largest referral center in the Tigray region, with a catchment area of more than 8 million people from the Tigray region and neighboring districts of the Afar and Amhara regions. There are 500 inpatient beds. The hospital’s services include obstetrics and gynecology which is run by 20 consultants and 150 midwives. There are separate antenatal care clinics for low- and high-risk patients. The number of deliveries is increasing annually, and the hospital currently records an average of 5000 deliveries per year. Ayder Hospital’s hemodialysis center was established under a public-private partnership model. It is equipped with 12 modern B-Braun Dialog plus hemodialysis machines and is the only dialysis center in the region available for patients with acute kidney injury and chronic kidney disease, with the number of annual registrations for the dialysis unit increasing. The unit is staffed by 11 dialysis nurses and two adult nephrologists and has cared for almost 600 patients with kidney disease requiring dialysis since it was established in 2013.

Study population

The records of all women who developed AKI and needed dialysis during pregnancy, childbirth, the post-abortion period and/or the Puerperium during the study period were included.

Sample size and power

The charts of all women who were diagnosed with pregnancy-related AKI between January 1, 2017 and December 31, 2021 were reviewed. The list of mothers was compiled from the maternity delivery logbook, the operating theater logbook, the emergency logbook, and the ICU admission registers. Due to the rarity of pregnancy-related AKI, all cases were collected consecutively rather than employing a sampling technique. We computed the statistical power for a cohort comprising 187 mothers consecutively diagnosed with pregnancy-related AKI. Using the single population proportion formula, a significance level of α = 0.05, and a minimum effect size of 0.2, the calculated power was 0.87.

Data collection tool and procedures

Initially, we identified AKI cases by cross-referencing medical record numbers with a separate logbook dedicated to near misses. Subsequently, we obtained and analyzed 187 AKI charts, using a questionnaire developed based on existing literature. A pilot test was then conducted to assess the tool’s usability and identify potential problems, leading to subsequent refinements. Open Data Kit (ODK) tool was utilized for data collection. Data extraction from patient records encompassed various aspects including, Sociodemographic characteristics, obstetric profile, Comorbidity, clinical presentation, investigation, management, and outcomes of women with pregnancy-related AKI. Trained medical doctors were responsible for collecting the data. Study participants were enrolled if they had [1] Absolute serum creatinine ≥ 1.2 mg/dl; [2] elevation of serum creatinine by 0.3 mg/dl within 48 h from their baseline; [3] decreased urine output for ≥ 6 h; and [4] the need for dialysis.

To guarantee the quality of the data, medical doctors involved in data collection underwent one-week training. Moreover, throughout the data collection process, investigators conducted daily supervision to ensure data completeness, accuracy, and validity.

Measurement

AKI

AKI was defined according to the Kidney Disease Improving Global Outcomes (KDIGO) 2012 criteria as the increase in the absolute value of the SCr by 0.3 mg/dl within 48 h or an increase > 50% compared to the baseline values within 7 days, or a urine output < 0.5 mL/kg/h ≥ 6-hour [19].

Pregnancy-related AKI (PR-AKI)

all causes of acute renal function impairment from early pregnancy to three months postpartum [20].

Complete renal recovery

Serum creatinine at day 7 returned to baseline creatinine or to < 1.5x baseline [21] or returned to within 50% above baseline serum creatinine [22].

Partial renal recovery

No need for renal replacement therapy (RRT) but did not meet the criteria for complete renal recovery or creatinine persistently ≥ 1.5 mg/dL at day 7.

CKD

abnormalities of kidney structure or functional abnormalities with GFR ≤ 60 mL/min/1.73 m2 that is present for more than three months [23].

Composite endpoint

Creatinine persistently > 1.5 mg/dl indicating partial renal recovery at day 7 or death attributed to PR-AKI.

Data analysis

We entered the data into the Open Data Kit Tool (ODK); the data were then transferred to the statistical software Stata version 16 and analyzed. Descriptive statistics are presented in the form of frequencies and percentages. After we checked the normal distribution of the data, the measures of central tendency and dispersion were reported using the mean with its standard deviation (SD) or the median with its interquartile range (IQR). The chi-square test or Fisher’s exact test was used to compare categorical variables, depending on the expected cell count. The difference between continuous variables was compared using an independent t-test.

Bivariate analysis was performed to examine the association between the independent variables and the composite endpoint outcome (creatinine > 1.5 mg/dl (partial renal recovery) or death). Variables that showed an association with the composite endpoint (with a p-value of < 0.25) were analyzed using multivariate logistic regression to assess whether there was a significant association between each independent variable. Independent variables that were associated with the outcome variable at a P value of < 0.05 were considered statistically significant. Multicolinearity diagnostics were performed, and collinear variables were excluded from the final model. The fit of the final model was tested using the Hosmer‒Lemeshow goodness-of-fit model. A receiver operating characteristic (ROC) analysis was also performed to estimate the predictive power of the final fitted model.

Ethical clearance

This is a secondary analysis of data for a study on maternal near misses. Ethical approval was granted by the Institutional Review Board (IRB) of Mekelle University, University of Health Sciences, with ethical approval number MU-IRB 1950/2022. We were unable to obtain informed consent from the study participants, as the study was a retrospective design. However, a letter of support was obtained from the hospital’s medical director’s office, and patient profiles and data were granted full anonymity. The IRB also waived the requirement to obtain informed consent after reviewing the protocol for this study.

Results

Demographic and clinical characteristics

In the five years in which the hospital hosted 27,350 deliveries, 187 developed AKI. The median age of the participants was 27 years (IQR = 5) years. Most (51.3%) of the participants were rural dwellers. A total of 78 (41.7%) of the mothers were gravid one (range, 0–10). More than half (73.3%) had antenatal care follow-ups; 44 (23.5%) ended their pregnancy with spontaneous abortions. Regarding pregnancy outcomes, 100 (53.5%) mothers delivered vaginally. The median systolic and diastolic blood pressures at diagnosis were 140 (IQR = 40) and 90 (IQR = 30), respectively (Table 1).

Table 1 Demographic and clinical characteristics of the study participants, Ayder Comprehensive Specialized Hospital, Mekelle, Northern Ethiopia, 2017–2021 (n = 187)

Causes and co morbidities of pregnancy-related acute kidney injury

Hypertensive disorders of pregnancy 141(75.4%), sepsis 92(49.2%) and pre renal AKI 76(40.6%) attributed to hemorrhage and dehydration are the major causes associated with pregnancy-related AKI. Co morbidities were present in 44 (23.5%) of those with PR-AKI and the predominant ones identified are chronic liver disease in 15 (8%), pre existing chronic kidney disease in 11 (5.9%) and heart disease in 9 (4.8%) (Table 2).

Table 2 Causes and co-morbidities of pregnancy related acute kidney injury (PR-AKI), Ayder Comprehensive Specialized Hospital, Mekelle, Northern Ethiopia, 2017–2021 (n = 187)

Laboratory findings of the pregnancy-related AKI patients

Creatinine levels above or equal to 1.2 were observed in almost all 180 patients (96.3%). The maximum creatinine level for those with composite endpoints was 3.8 mg/dl. Positive dipstick albuminuria was observed in 107(69.5%) patients. Of the 97 participants whose urine output was monitored, 78(80.4%) had non-oliguric AKI. One-third of the patients had leukocytosis, and half of the patients had anemia (Table 3).

Table 3 Laboratory findings of the study participants, Ayder Comprehensive Specialized Hospital, Mekelle, Northern Ethiopia, 2017–2021 (n = 187)

Process of care and outcomes of the pregnancy-related AKI patients

Nearly one-third of patients with pregnancy-related AKI were admitted to the intensive care unit, and almost half of the patients needed mechanical ventilation. Vasoactive agents and parenteral antibiotics were used in 26(14%) and 109(58.3%) patients, respectively. Hemodialysis was offered in 16 (8.6%) patients with obstetric AKI. Of those who had pregnancy-related AKI 165 (88.2%) of them had recovery of their serial serum creatinine values to less than 1.5times of their baseline at around day 7. One-third of the patients had AKI-related complications. Anemia, impaired consciousness and hypertension were the predominant complications noted in 45 (71.4%), 26 (41.3%) and 19 (30.2%) patients, respectively. Live birth occurred in more than half of the mothers, while stillbirth and IUFD occurred in 33(17.7%) and 20(10.7%) mothers, respectively (Table 4).

Table 4 Outcome of the study participants, Ayder Comprehensive Specialized Hospital, Mekelle, Northern Ethiopia, 2017–2021 (n = 187)

Factors associated with the composite endpoint (partial renal recovery and death)

A total of 14 (7.5%) patients with pregnancy-related AKI died, and 30 (16.0%) were discharged with a creatinine level above 1.5 mg/dl, yielding a total of 44 (23.5%) patients with a composite endpoint. Table 5 summarizes the factors that were associated with the composite endpoint. In the multivariable analysis, patients with preexisting CKD had a higher risk of developing the composite endpoint than their counterparts (AOR = 30.13; 95% CI: 2.92, 310.84). For every one-unit increase in creatinine, the odds of reaching the composite endpoint increased by 65% (AOR = 1.65; 95% CI: 1.11, 2.45). Similarly, patients taking vasoactive agents were six times more likely to either die or be discharged with a creatinine above 1.5 mg/dl (AOR = 5.77; 95% CI: 1.47, 22.67). Patients with AKI-related complications were also highly likely to reach the composite endpoint (AOR = 5.26; 95% CI: 1.73, 16.00) (Table 5).

Table 5 Factors associated with the composite endpoint, Ayder Comprehensive Specialized Hospital, Mekelle, Northern Ethiopia, 2017–2021 (n = 187)

As Fig. 1 clearly shows, of the women with PR-AKI (n = 187), 76.5% had achieved a complete renal recovery that was a cure from their AKI.

Fig. 1
figure 1

Maternal outcome among pregnancy related acute kidney injury patients. Ayder Comprehensive Specialized Hospital, Mekelle, Northern Ethiopia, 2017–2021 (n = 187)

Discussions

Among 27,350 parturient mothers hospitalized in the Department of Obstetrics in a tertiary hospital in northern Ethiopia, the incidence of AKI during pregnancy and puerperium was 0.68%. In the present study, the main causes of PR-AKI were hypertensive disorders of pregnancy, sepsis and pre renal AKI resulting from APH/PPH and dehydration. In more than two-thirds of the patients with PR-AKI, the kidneys recovered completely. Sixteen women (8.6%) received renal replacement therapy. The mortality rate among women with pregnancy-related AKI due to renal injury and its complications was 7.5%. The presence of preexisting CKD, increment of creatinine per unit above normal, vasoactive drug use and AKI-related complications were associated with increased mortality in these patients. Most complications were preventable with appropriate prenatal care.

The incidence of pregnancy-related AKI in the present study was 0.68%, i.e., 68 per 10,000 deliveries. Although PR-AKI is a rare occurrence in high-income countries, its incidence has recently increased [28,29,30,31]. For example, the incidence of pregnancy-related AKI in the USA has recently increased from 0.04% in 2006 to 0.12% in 2015, with an overall rate of 0.08% [32]. The rising incidence of pregnancy-related AKI is attributed to higher detection rates, higher hospital delivery rates, an increase in high-risk pregnancies, and higher rates of comorbidities due to advanced maternal age [33]. The overall rate of PR-AKI is decreasing worldwide, indicating an improvement in awareness of antenatal care. The significant improvement in obstetric care and reduction in septic abortions in recent decades may have contributed to the decrease in the burden of this problem worldwide [26]. The incidence of PR-AKI in our study is lower than reports from low- and middle-income countries (4-26%) and from some high-income countries (1-2.8%) [34,35,36]. Studies from India have shown that the incidence of AKI in pregnancy has decreased in relation to the total number of AKI cases over the last 30 years [37, 38]. Out of 4741 pregnant women, PR-AKI was detected in 132 (2.78%) during the third trimester and postpartum period [25]. The main reasons for the persistently high incidence of PR-AKI in developing countries are septic abortions, overall poor postnatal care, lack of medical facilities in rural areas, and relatively late referral of patients with these conditions. The lower incidence of PR-AKI reflected in our studies may be due to a lack of detection measures, limited available screening tests, and a poor understanding of the disease in low-income countries [39].

The most common causes of PR-AKI in the present study were hypertensive disorders of pregnancy, sepsis and pre-renal AKI due to dehydration and hemorrhage. This is consistent with several studies from developed and developing countries where hypertensive disorders of pregnancy, sepsis and hemorrhage accounted for > 50% of cases of PR-AKI [40, 41]. In our study most of the pregnant mothers at diagnosis of pregnancy-related AKI were in their third trimester, 92 (83%) where the above three are recognized as main causes of PR-AKI in the late third trimester. Early detection and treatment of preeclampsia, sepsis and hemorrhage are limited in low-income countries, including Ethiopia. Timely and aggressive management of obstetric hemorrhage and puerperal sepsis is needed to reduce the burden of such treatable and preventable etiologies of PR-AKI in developing countries.

In low-income countries, inadequate perinatal care and inappropriate treatment of pregnancy-related complications are still the main causes of PR-AKI [35, 42]. In the present study, preeclampsia was the leading obstetric comorbidity in patients with pregnancy-related AKI, occurring in more than two-thirds (71.1%), which is consistent with the fact that preeclampsia is the leading cause of severe PR-AKI and typically occurs in the third trimester and postpartum period [43]. In the same study, a higher burden of preeclampsia was found [43]. The effect of preeclampsia on endothelial damage and vasoconstriction contributes to long-term renal dysfunction and persistent impairment of the glomerular filtration rate [44], as seen in our study, in which partial renal recovery was observed in 16% of cases. In the past, AKI was also considered a completely reversible syndrome, but in recent years, several studies have indicated that AKI may increase the risk of developing CKD, i.e., further damage to the kidneys [44, 45].

HEELP syndrome, considered a continuum of preeclampsia, is a serious disorder in pregnancy and contributor of pregnancy-related AKI. It accounted for 26.7% of PR-AKI in our study, which is consistent with the literature accounting for 15–40% of all cases of PR-AKI [46]. As pre-eclampsia was seen in more than two- thirds (71%) of mothers with PR-AKI, the rate of HELLP syndrome is also expected to be higher than non pre-eclamptic pregnant mothers. HELLP syndrome is also associated with increased maternal morbidity and mortality [47].

Acute kidney injury in pregnancy (PR-AKI) deserves special attention as it poses a risk to two lives (mother and fetus). Maternal and fetal outcomes of concern related to pregnancy-related AKI include permanent renal injury, maternal survival, rate of renal recovery, dialysis dependency, rate of live births, stillbirths, and intrauterine death. In our study, AKI during pregnancy was associated with a higher risk of maternal death [44]. The mortality rate among women with PR-AKI in our study was 7.5%, higher than in developed countries, which range from 2.7 to 4.3% [48], but lower than reports from developing countries, which range from 23 to 33% [27, 49]. However, this result is similar to studies from India, where the reported maternal mortality rate was 6% [50]. The results of this study show that PR- AKI remains an alarming source of morbidity in low-income countries. This calls for a concerted effort by health workers for early detection and prompt treatment of mothers at high risk of AKI and its associated complications.

The majority of women with AKI did not require renal replacement therapy and were treated conservatively. Hemodialysis was needed in 8.6% of patients, which is comparable to studies from China and Nepal (6% and 8%, respectively) [25, 51] but lower than the Moroccan study (16.2%) [52]. In previous studies, a higher percentage (16% in South Africa and 33.3% in Turkey) of pregnant women with AKI needed dialysis treatment [53, 54]. However, in these studies, a higher serum creatinine value was used to confirm the diagnosis of AKI. This could be a possible explanation for the high mortality rates and high dialysis rates in the earlier studies.

The recovery rate of renal function in women with PR- AKI is satisfactory. In our study, 75.6% and 16% of PR-AKI patients had complete and partial recovery of renal function, respectively. The results of our study are consistent with other research findings, which found complete recovery of renal function in 68-89% [5, 25, 55,56,57]. Early detection and treatment of PR-AKI should favor good outcomes. However, outcome studies suggest that PR-AKI is associated with residual renal dysfunction [34].

In the present study, fetal survival was found in only almost half (56%) of cases with AKI, while IUFD, stillbirth and early neonatal death (ENND) occurred in 10.7%, 17% and 1.6% of cases, respectively. This high fetal mortality rate is consistent with a study from India and China in which stillbirth and perinatal mortality associated with AKI were reported to be 23.5% and 30%, respectively [47, 58]. A more recent study from a tertiary care hospital in Somaliland also revealed high maternal and fetal mortality rates [9.68%; 95% CI, 22.49–27.51] and [58.6%; 95% CI, 1.45–1.99], respectively [59].

Admission to the ICU was 26.7% in our study and was higher in mothers with composite outcomes (52% vs. 19%). This is consistent with studies from Somaliland on PR-AKI, where the need for ICU admission was 26% [59]. Admission to the ICU increases maternal mortality.

The determinants of mortality in PR-AKI were the use of vasoactive agents, preexisting CKD, AKI-related complications and high serum creatinine levels. This finding is consistent with a study from Brazil [60] in which norepinephrine use, hemodialysis therapy, and KDIGO stage 3 were independently associated with higher maternal mortality in patients with PR-AKI.

Conclusions

Although acute kidney injury is a rare complication of pregnancy, it is associated with high maternal morbidity and mortality. The most common causes of PR-AKI include pregnancy-induced hypertension, dehydration, hemorrhage and sepsis. The prevalence of complete renal recovery in pregnant patients with acute kidney injury was similar to that in other studies. Timely and aggressive treatment of obstetric hemorrhage and puerperal sepsis is needed to reduce the burden of PR-AKI. In developing countries, antenatal care should be emphasized in public health care to prevent septic abortion-related sepsis and pregnancy-induced hypertension [57].

The provision of health facilities with appropriately trained staff and the implementation of prevention strategies will be of great value in reducing the scale of the problem [7]. Our analysis also serves as a stimulus for future studies to investigate improvements in antenatal care and early referral to nephrologists to prevent AKI and mitigate its associated consequences.

Limitations of the study

To determine the prevalence of PR- AKI in facilities with inadequate resources, this study examined five years of data. Our study has several limitations. First, key Sociodemographic variables were missing from the patient charts. Demographic variables such as marital status, education level, and occupation were not routinely recorded in the medical charts. Second, neonatal status was not routinely recorded in patient notes during postnatal follow-up. The neonatal mortality recorded in this study mainly reflects neonatal death until the mother is discharged from the hospital. Both neonatal and maternal status is routinely recorded in the discharge letter. Some inherent disadvantages of a retrospective cohort should also be noted, such as missing information when using existing records (information bias) or selection bias, as individuals are selected after the outcome has occurred, so the presence of both conditions (exposure and outcome) at the time of data collection may have influenced our study. Using KDIGO definitions for pregnancy-related AKI is reasonable but has limitations as creatinine naturally decreases during mid-pregnancy and there is actually no real consensus on the definition of AKI in pregnancy. Moreover, creatinine tends to rise transiently after delivery in normal pregnancy. This study did not assess CKD risks among those with episodes of PR-AKI as the three months follow up was not available or complete from the registries. Finally, reporting OR in a cohort study is a limitation as it shows association and not causality.

Data availability

The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.

Abbreviations

ACE I:

Angiotensin-converting enzyme inhibitors

ACSH:

Ayder Comprehensive Specialized Hospital

AFLP:

Acute fatty liver of pregnancy

AKI:

Acute kidney injury

ALT:

Alanine transaminase

APGAR:

Appearance, pulse, grimace, activity, and respiration

APH:

Antepartum hemorrhage

AOR:

Adjusted odd ratio

AST:

Aspartate transaminase

CKD:

Chronic kidney disease

CLD:

Chronic liver disease

DBP:

Diastolic blood pressure

ENND:

Early neonatal death

GA:

Gestational age

HUS:

Hemolytic uremic syndrome

HELLP:

Hemolysis Elevated Liver enzymes and Low Platelets

ICU:

Intensive Care Unit

IQR:

Interquartile range

IRB:

Institutional Review Board

IUFD:

Intrauterine fetal death

KDIGO:

Kidney Disease Improving Global Outcomes

LMICs:

Low- and middle-income countries

MMR:

Maternal mortality rate

MU:

Mekelle University

NSAID:

Non-steroidal anti-inflammatory drug

PR AKI:

Pregnancy-related acute kidney injury

PPH:

Postpartum hemorrhage

PR:

Pulse rate

RRT:

Renal Replacement Therapy

SBP:

Systolic blood pressure

TTP:

Thrombotic thrombocytopenic purpura

References

  1. Acharya A, Santos J, Linde B, Anis K. Acute kidney injury in pregnancy-current status. Adv Chronic Kidney Dis. 2013;20(3):215–22. https://doi.org/10.1053/j.ackd.2013.02.002.

    Article  PubMed  Google Scholar 

  2. Vinturache A, Popoola J, Watt-Coote I. The changing Landscape of Acute kidney Injury in pregnancy from an Obstetrics Perspective. J Clin Med. 2019;8(9):1396. https://doi.org/10.3390/jcm8091396).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Aggarwal RS, Mishra VV, Jasani AF, Gumber M. Acute renal failure in pregnancy: our experience. Saudi J Kidney Dis Transpl. 2014;25:450–5.

    Article  PubMed  Google Scholar 

  4. Prakash J, Prakash S, Ganiger VC. Changing epidemiology of acute kidney injury in pregnancy: a journey of four decades from a developing country. Saudi J Kidney Dis Transpl 2019 Sep-Oct;30(5):1118–30. https://doi.org/10.4103/1319-2442.270268.

  5. Trakarnvanich T, Ngamvichchukorn T, Susantitaphong P. Incidence of acute kidney injury during pregnancy and its prognostic value for adverse clinical outcomes: a systematic review and meta-analysis. Med (Baltim). 2022;101(30):e29563. https://doi.org/10.1097/MD.0000000000029563.).

    Article  CAS  Google Scholar 

  6. Naicker S, Aboud O, Gharbi MB. Epidemiology of acute kidney injury in Africa. Semin Nephrol. 2008;28:348–53. https://doi.org/10.1016/j.semnephrol.2008.04.003.

    Article  PubMed  Google Scholar 

  7. Shalaby AS, Shemies RS. Pregnancy-related acute kidney injury in the African continent: where do we stand? A systematic review. J Nephrol. 2022;35(9):2175–89. https://doi.org/10.1007/s40620-022-01349-2).

    Article  PubMed  PubMed Central  Google Scholar 

  8. Ibrahim A, Ahmed MM, Kedir S, Bekele D. Clinical profile and outcome of patients with acute kidney injury requiring dialysis-an experience from a hemodialysis unit in a developing country. BMC Nephrol. 2016;17(1):91. https://doi.org/10.1186/s12882-016-0313-8.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Lameire NH, Cruz D, et al. Acute kidney injury: an increasing global concern. Lancet. 2013;382:170–9. https://doi.org/10.1016/S0140-6736(13)60647-9.

    Article  PubMed  Google Scholar 

  10. Kahindo CK, Mukuku O, Wembonyama SO, Tsongo ZK. Prevalence and factors associated with acute kidney injury in sub-saharan African adults: a review of the current literature. Int J Nephrol. 2022;20225621665. https://doi.org/10.1155/2022/5621665.

  11. Piccoli GB, Zakharova E, Attini R, Ibarra Hernandez M, Covella B, Alrukhaimi M, Liu ZH, Ashuntantang G, Orozco Guillen A, Cabiddu G, Li PKT, Garcia-Garcia G, Levin A. Acute kidney Injury in pregnancy: the need for higher awareness. A pragmatic review focused on what could be improved in the Prevention and Care of pregnancy-related AKI, in the year dedicated to women and kidney diseases. J Clin Med. 2018;7(10):318. https://doi.org/10.3390/jcm7100318.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Shah S, Verma P. Pregnancy-related acute kidney Injury: do we know what to do? Nephron. 2023;147(1):35–8. https://doi.org/10.1159/000525492.

    Article  PubMed  Google Scholar 

  13. Incidence, Cooke WR, Hemmila UK, Craik AL, et al. BMC Nephrol. 2018;19:25.

    Article  Google Scholar 

  14. Acute renal failure in pregnancy: tertiary center experience from north Indian population, Patel ML, Sachan R. Radheshyam Radheshyam, Sachan P. Niger Med J 2013;54:191–195.).

  15. Bokhari SRA, Inayat F, Jabeen M, Sardar Z, Saeed S, Malik AM, Nasir S, Zareen A, Ahmad HI. Characteristics and Outcome of Obstetric Acute Kidney Injury in Pakistan: a single-center prospective observational study. Cureus. 2018;10(9):e3362. https://doi.org/10.7759/cureus.3362.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Overview of maternal health in Ethiopia. MoH. https://www.moh.gov.et/site/initiatives-4-col/Maternal_Health. Accessed on May 19, 2023).

  17. Maternal, Gul A, Aslan H, Cebeci A, Polat I, Ulusoy S, Ceylan Y. Ren Fail. 2004;26:557–62.

    Article  Google Scholar 

  18. Liu Y, Ma X, Zheng J, et al. Pregnancy outcomes in patients with acute kidney injury during pregnancy: a systematic review and meta-analysis. BMC Pregnancy Childbirth. 2017;17:235. https://doi.org/10.1186/s12884-017-1402-9.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Kidney Disease Improving Global Outcomes (KDIGO). Acute Kidney Injury Work Group. KDIGO Clinical Practice Guideline for Acute Kidney Injury. 2012.

  20. Van Hook JW. Acute kidney injury during pregnancy. Clin Obstet Gynecol. 2014;57:851–61.

    Article  PubMed  Google Scholar 

  21. Palevsky PM, Zhang JH, O’Connor TZ, Chertow GM, Crowley ST, Choudhury D, et al. Intensity of renal support in critically ill patients with acute kidney injury. N Engl J Med. 2008;359(1):7–20.

    Article  CAS  PubMed  Google Scholar 

  22. Bellomo R, Ronco C, Kellum JA, Mehta RL, Palevsky P. Acute Dialysis quality initiative w. acute renal failure - definition, outcome measures, animal models, fluid therapy and information technology needs the second international consensus conference of the acute Dialysis Quality Initiative (ADQI) group. Crit Care. 2004;8(4): R204–12).

  23. Levin A, Stevens PE. Summary of KDIGO 2012 CKD guideline: behind the scenes, need for guidance, and a framework for moving forward. Kidney Int. 2014;85(1):49–61. https://doi.org/10.1038/ki.2013.444.

    Article  PubMed  Google Scholar 

  24. Prakash J, Ganiger VC. Acute kidney Injury in pregnancy-specific disorders. Indian J Nephrol. 2017 Jul-Aug;27(4):258–70. https://doi.org/10.4103/0971-4065.202406.

  25. Prakash J, Ganiger VC, Prakash S, Iqbal M, Kar DP, Singh U, Verma A. Acute kidney injury in pregnancy with special reference to pregnancy-specific disorders: a hospital-based study (2014–2016). J Nephrol. 2018;31(1):79–85. https://doi.org/10.1007/s40620-017-0466-y.).

    Article  CAS  PubMed  Google Scholar 

  26. Prakash J, Kumar H, Sinha DK, Kedalaya PG, Pandey LK, Srivastava PK, et al. Acute renal failure in pregnancy in a developing country: twenty years of experience. Ren Fail. 2006;28(4):309–13.

    Article  PubMed  Google Scholar 

  27. Najar MS, Shah AR, Wani IA, et al. Pregnancy-related acute kidney injury: a single center experience from the Kashmir Valley. Indian J Nephrol. 2008;18:159–61.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Taber-Hight E, Shah S. Acute kidney injury in pregnancy. Adv Chronic Kidney Dis. 2020;27(6):455–60.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Mehrabadi A, Liu S, Bartholomew S, Hutcheon JA, Magee LA, Kramer MS et al. (2014) Hypertensive disorders of pregnancy and the recent increase in obstetric acute renal failure in Canada: population-based retrospective cohort study. BMJ 2014;349: g4731.

  30. Szczepanski J, Griffin A, Novotny S, Wallace K. (2020) Acute kidney injury in pregnancies complicated with preeclampsia or HELLP syndrome. Front Med 7(22).

  31. Karimi Z, Malekmakan L, Farshadi M. The prevalence of pregnancy-related acute renal failure in Asia: a systematic review. Saudi J Kidney Dis Transpl. 2017;28:1–8.

    Article  PubMed  Google Scholar 

  32. Shah S, Meganathan K, Christianson AL, Harrison K, Leonard AC, Thakar CV. Pregnancy-related acute kidney Injury in the United States: clinical outcomes and Health Care utilization. Am J Nephrol. 2020;51(3):216–26. https://doi.org/10.1159/000505894.

    Article  PubMed  Google Scholar 

  33. Taber-Hight E, Shah S. Acute kidney Injury in pregnancy. Adv Chronic Kidney Dis. 2020;27(6):455–60. https://doi.org/10.1053/j.ackd.2020.06.002.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Davidson B, Bajpai D, Shah S, Jones E, Okyere P, Wearne N, Gumber R, Saxena N, Osafo C. Pregnancy-Associated Acute kidney Injury in Low-Resource settings: Progress over the last decade. Semin Nephrol. 2023;42(5):151317. https://doi.org/10.1016/j.semnephrol.2023.151317.

    Article  PubMed Central  Google Scholar 

  35. Piccoli GB, Zakharova E, Attini R, Ibarra Hernandez M, Covella B, Alrukhaimi M, et al. Acute kidney injury in pregnancy: the need for higher awareness. A pragmatic review focused on what could be improved in the prevention and care of pregnancy-related AKI in the year dedicated to women and kidney diseases. J Clin Med. 2018;7(10):318.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Gaber TZ, Shemies RS, Baiomy AA, Aladle DA, Mosbah A, Abdel-Hady ES et al. (2021) Acute kidney injury during pregnancy and puerperium: an Egyptian hospital-based study. J Nephrol.

  37. Prakash J. The kidney in pregnancy: a journey of three decades. Indian J Nephrol. 2012;22(3):159–67. https://doi.org/10.4103/0971-4065.98750.).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Prakash J, Pant P, Prakash S, Sivasankar M, Vohra R, Doley PK, Pandey LK, Singh U. Changing picture of acute kidney injury in pregnancy: study of 259 cases over 33 years. Indian J Nephrol. 2016 Jul-Aug;26(4):262–7. https://doi.org/10.4103/0971-4065.161018).

  39. Mehta RL, Burdmann EA, Cerda J. Recognition and management of acute kidney injury in the International Society of Nephrology 0by25 Global Snapshot: a multinational cross-sectional study. Lancet. 2016;387:2017–25.

    Article  PubMed  Google Scholar 

  40. Gopalakrishnan N, Dhanapriya J, Muthukumar P, et al. Acute kidney injury in pregnancy—a single center experience. Ren Fail. 2015;37:1476–80.

    Article  PubMed  Google Scholar 

  41. Prakash J, Kumar H, Sinha DK et al. Acute renal failure in pregnancy in a developing country: twenty years of experience. Ren Fail. 2006; 28:309–13) (Prakash J, Vohra R, Wani IA, .

  42. Liu Y, Ma X, Zheng J, Liu X, Yan T. Pregnancy outcomes in patients with acute kidney injury during pregnancy: a systematic review and meta-analysis. BMC PregnancyChildb. 2017;17(1):235.

    Google Scholar 

  43. Teka H, Yemane A, Abraha HE, Berhe E, Tadesse H, et al. Clinical presentation, maternal-fetal, and neonatal outcomes of early-onset versus late-onset preeclampsia-eclampsia syndrome in a teaching hospital in a low-resource setting: a retrospective cohort study. PLoS ONE. 2023;18(2):e0281952. https://doi.org/10.1371/journal.pone.0281952.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Vikse BE, Irgens LM, Leivestad T, Skjaerven R, Iversen BM. Preeclampsia and the risk of end-stage renal disease. N Engl J Med. 2008;359:800–9. https://doi.org/10.1056/NEJMoa0706790.

    Article  CAS  PubMed  Google Scholar 

  45. Goplani K, Shah P, Gera D, Gumber M, Dabhi M, Feroz A, et al. Pregnancy-related acute renal failure: a single-center experience. Indian J Nephrol. 2008;18:17–21. https://doi.org/10.4103/0971-4065.41283.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Liu Y, Ma X, Zheng J, Liu X, Yan T. Pregnancy outcomes in patients with acute kidney injury during pregnancy: a systematic review and meta-analysis. BMC Pregnancy Childbirth. 2017;17:235. https://doi.org/10.1186/s12884-017-1402-9.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Liu YM, Bao HD, Jiang ZZ, et al. Pregnancy-related acute kidney injury and a review of the literature in China. Intern Med. 2015;54:1695–703.

    Article  PubMed  Google Scholar 

  48. Wallace K, Harris S, Addison A, Bean C. HELLP syndrome: pathophysiology and current therapies. Curr Pharmaceut Biotechnol. 2018;19:816–26. https://doi.org/10.2174/1389201019666180712115215.

    Article  CAS  Google Scholar 

  49. Munnur U, Karnad DR, Bandi VD, et al. Critically ill obstetric patients in an American and an Indian public hospital: comparison of case-mix, organ dysfunction, intensive care requirements, and outcomes. Intensive Care Med. 2005;31:1087–94.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Patel ML, Sachan R, Radheshyam Sachan P, et al. Acute renal failure in pregnancy: tertiary center experience from north Indian population. Niger Med J. 2013;54:191–5.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Huang C, Chen S. Acute kidney injury during pregnancy and puerperium: a retrospective study in a single center. BMC Nephrol. 2017;18:146.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Bhansakarya R, Baral G, Shrestha S, Subedi S, Ghimire S, Shrestha P, Nath Chaudhary A. Complete recovery of renal function among obstetric patients with acute kidney Injury at a Tertiary Care Hospital: a descriptive cross-sectional study. JNMA J Nepal Med Assoc. 2021;59(244):1289–92. https://doi.org/10.31729/jnma.7135.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Arrayhani M, El Youbi R, Sqalli T. Pregnancy-related acute kidney injury: experience of the nephrology unit at the University Hospital of Fez, Morocco. ISRN Nephrol. 2012;2013:109034. https://doi.org/10.5402/2013/109034.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Randeree IG, Czarnocki A, Moodley J, Seedat YK, Naiker IP. Acute renal failure in pregnancy in South Africa. Ren Fail. 1995;17(2):147–53. https://doi.org/10.3109/08860229509026251).

    Article  CAS  PubMed  Google Scholar 

  55. Erdemoğlu M, Kuyumcuoğlu U, Kale A, Akdeniz N. Pregnancy-related acute renal failure in the southeast region of Turkey: analysis of 75 cases. Clin Exp Obstet Gynecol. 2010;37(2):148–9.

    PubMed  Google Scholar 

  56. Wang F, Xing T, Wang N, Huang Y. A clinical study of pregnancy-associated renal insufficiency. Kidney Blood Press Res. 2011;34(1):34–40. https://doi.org/10.1159/00032211.

    Article  PubMed  Google Scholar 

  57. Goplani KR, Shah PR, Gera DN, Gumber M, Dabhi M, Feroz A, et al. Pregnancy-related acute renal failure: a single-center experience. Indian J Nephrol. 2008;18(1):17–21. https://doi.org/10.4103/0971-4065.41283.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Arora N, Mahajan K, Jana N, Taraphder A. Pregnancy-related acute renal failure in eastern India. Int J Gynecol Obstet. 2010;111(3):213–6.

    Article  Google Scholar 

  59. Rage HI, Kumar Jha P, Hashi HA, Abdillahi NI, Pregnancy-Related AKI. A Tertiary Care Hospital experience in Somaliland. Kidney Int Rep. 2023;8(3):388–91. https://doi.org/10.1016/j.ekir.2023.01.021.

    Article  PubMed  PubMed Central  Google Scholar 

  60. Ferreira DP, Amorim FF, Matsuura AJ, de Sousa JL, Santana AR, de Souza JA, Imoto AM. Pregnancy-related acute kidney injury: mortality and survival of patients treated at a maternal intensive care unit. J Nephrol. 2020;33(6):1361–7. https://doi.org/10.1007/s40620-020-00711-6.

    Article  PubMed  Google Scholar 

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Acknowledgements

All of the authors are grateful for the support received from Ayder comprehensive specialized hospital.

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There is no any source of funding that was solicited for this study.

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E.B. and H.T; Made conceptualization of the study, E.B., H.T., B.T.A., M.A.G., T.G., M.Y., B.A., Hb.T., H.G., F.T., M.M.E., R.K. and A.Y.; involved in data entry, E. B., H.E.A. and H.T.; involved in data cleaning E.B., H.E.A. and M.M.E; made data analysis, E.B. and H.T.; wrote the main manuscript All authors reviewed the manuscript. All authors have read and approved the final version of the manuscript. They have agreed both to be personally accountable for the author’s contributions and to ensure that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and the resolution documented in the literature.

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Correspondence to Ephrem Berhe.

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was granted by the Institutional Review Board of Mekelle University, University of Health Sciences, with ethical approval number MU-IRB 1950/2022. All methods were performed in accordance with relevant guidelines and regulations. We were not able to obtain informed consent from the study participants, as the study was a retrospective design. However, a letter of support was obtained from the hospital’s medical director’s office, and full anonymity was granted for the patient profile and patient data. The Institutional Review Board of Mekelle University, University of Health Sciences, also waived informed consent after reviewing the protocol for this study.

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Berhe, E., Teka, H., Abraha, H.E. et al. Characteristics and outcome of pregnancy-related acute kidney injury in a teaching hospital in a low-resource setting: a five-year retrospective review. BMC Nephrol 25, 182 (2024). https://doi.org/10.1186/s12882-024-03616-9

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