The results of our study reveal that AKI is common in ELBW infants and that hypotension, elevated mean airway pressure, and the use of cephalosporin are associated with the development of AKI in ELBW infants. We have also shown that ELBW infants with AKI have a high mortality, especially if their AKI is associated with oliguria. To the best of our knowledge, our case–control study is the largest reported study on AKI in ELBW infants.
There is no universally accepted definition for neonatal AKI. Serum creatinine levels and reduced urine output (oliguria <1 ml/kg/h) are the most commonly used markers to identify acute renal failure or AKI [7]. We and others have previously shown that serum creatinine in ELBW infants usually rises in the immediate neonatal period due to inherited maternal creatinine load, reaches a peak on the second day, and then decline to normal levels over the next 1–2 weeks [19, 20]. However, a raising or persistent high level of serum creatinine >1.5 mg/dl after 48–72 h of life has been used as a definition for AKI [7, 17, 21–23].
The reported incidence of AKI in newborn infants admitted to NICUs has been reported to vary between 3.4 and 24%, which is consistent with our findings [4–6]. In a study of 359 premature infants born at <37 weeks of GA, Csaicsich et al. found that the incidence of AKI was 4.5% among all premature infants and 6.4% among ELBW infants (n = 156) [6]. In our study, the incidence of AKI was 12.5% among our 472 ELBW infants. One possible explanation for the difference between the incidence of AKI in our study and that of Csaicsich et al. is that our case group consisted exclusively of ELBW infants who were relatively smaller; for example, the average weight of ELBW infants studied by Csaicsich et al. was 725 g (n = 10), whereas the mean weight of our patients was 615 g (n = 46).
In newborn infants, AKI is predominantly associated with oliguria. The reported incidence of AKI with oliguria has varied between 46 and 93%, which is consistent with our findings [5, 15, 16, 22]. In our study, 82.6% of our patients had AKI associated with oliguria, and a small proportion had a nonoliguric AKI. The incidence of nonoliguric AKI has been reported to be higher in full term infants. Approximately one-third of all acute renal failures in full term infants are nonoliguric and in asphyxiated infants in particular, two thirds of all acute renal failures are nonoliguric [5, 9, 24, 25].
Prenatal use of nephrotoxic medications has been associated with AKI in premature infants. For example, studies and case reports have shown that prenatal exposure to NSAIDs is associated with nephrotoxicity and AKI in newborn infants [10, 23, 26, 27]. Cataldi et al. reported an increase in prenatal use of nephrotoxic medications, mainly antibiotics and NSAIDs, in preterm infants with AKI [10]. In our study, we did not find prenatal exposure to different nephrotoxic medications, including NSAIDs, to be associated with AKI in our ELBW patients. Our findings may differ from those of others because of differences in medical management and practices. For instance, only 6% of our patients’ mothers were exposed to NSAIDs versus 37% in Cataldi et al.’s study [10].
Low Apgar scores of <7 at 5 min of life have been reported to be a risk factor for AKI in GA infants ≤36 weeks and ≥34 weeks. [10, 23, 28]. In a study of infants ≥ 34 weeks GA, Aggarwal et al. reported an increase in the incidence of AKI in infants who were asphyxiated with a low 5-min Apgar scores of <6 in comparison to their controls (56 vs. 4%, respectively)[28]. In our study, we did not find a significant difference in Apgar scores between our cases and controls, most probably because we had a small number of infants who had low Apgar scores at 5 min (less than 25% of our patients had an Apgar score ≤5, as shown in the interquartile range of the median Apgar scores at 5 min of life in our patients). In a large retrospective cohort study, the mean 5-min Apgar score reported in ELBW infants was 6.6 ± 2.1 [29], which is comparable to that of our patients.
A clinically significant PDA can be responsible for AKI, either as a result of a large left to right shunting and aortic run-off causing renal hypo-perfusion or as a result of an attempted medical closure with NSAIDs [10, 30]. In our series, the incidence of PDA was similar between the groups. In our patients, medical closure was attempted in a small number of patients, and surgical ligation was performed in the majority of our patients. It is possible that our practice of early surgical ligation of PDAs in ELBW infants during the study period contributed to our lower incidence of PDA-related renal failure. Alexander et al. reported similar findings: i.e., surgically treated PDA was associated with less renal dysfunction than indomethacin-treated PDA in ELBW infants [31].
In preterm infants, 50% of all acute renal failures have been attributed to postnatal drug exposure [7]. Cataldi et al. demonstrated that infants with AKI were subjected to long-term exposure to antibiotics, NSAIDs, and diuretics [10]. The use of several drugs has been associated with AKI; for example, the use of angiotensin-converting enzyme inhibitors has been associated with AKI in newborn infants [32], and the use of midazolam has been associated with hypotension and oliguria [33]. In our study, the bivariate analysis revealed that infants with AKI had a higher postnatal exposure to cefotaxime, benzodiazepines, diuretics and dopamine/dobutamine prior to the development of AKI. However, following adjustment to statistically significant and relevant confounders in a logistic regression model, cephalosporin remained the only drug that was associated with AKI.
It has been speculated that loop diuretics via prostaglandin-induced vasodilatation may improve vasomotor nephropathy-related AKI; however, the efficacy of this intervention has not been confirmed in adult studies [34]. It has also been suggested that patients who respond to diuretics might have less severe AKI [34]. In our study, and following adjustment to possible confounders, the use of diuretics was not associated with AKI in our patients.
The higher exposure to cephalosporin prior to the development of AKI seen in our study is consistent with previous reports [10]. The nephrotoxicity of cephalosporin depends on the intra-cortical concentration of the drug, which in turn depends on tubular transport mechanisms. Therefore, any alteration of tubular transportation can potentially lead to nephrotoxic drug levels [35]. Most cephalosporins are safe for use in newborn infants; however, at extremely high levels, third-generation cephalosporins, which are the most common drugs used to treat newborn infants, may cause renal damage [35]. Unfortunately, drug levels of cephalosporins are not routinely monitored at the bedside, and the potential to reach high drug concentrations in the setting of vasomotor nephropathy is possible and might have contributed to worsening renal failure in our infants, especially given the fact that our patients with AKI had a lower mean arterial blood pressure than their controls.
The vasomotor nephropathy-related prerenal failure seen in neonates with respiratory disorders is often induced/aggravated by positive airway pressure ventilation [4, 7, 9, 10]. In our study, infants with AKI had a higher mean airway pressure than their controls, suggesting that infants with AKI had more severe respiratory distress symptoms, which is consistent with the findings of previous studies [4, 10]. Higher mean airway pressures in our AKI patients might have impaired the systemic venous return, decreased cardiac output, and decreased systemic blood pressure, leading to a decrease in renal perfusion.
In our study, infants with AKI had significantly lower arterial blood pressures and higher intravenous fluid intakes (within 24 h of the development of their renal failure) than their controls, suggesting that our AKI patients remained hemodynamically unstable in the period that preceded their renal failure despite fluid resuscitation. This observation emphasizes the importance of pre-renal kidney failure as the most common cause of AKI in ELBW infants [4, 9, 10]. However, since daily infants’ weights were not available to review, it would be difficult to determine if infants with AKI had adequate fluid resuscitation or not and if their need for a higher mean airway pressure was not a response to treat pulmonary edema and fluid overload.
To adjust for possible confounders, we developed a binary logistic regression model to study potential risk factors associated with AKI in premature infants, similar to the approach adopted by Cataldi et al. in their study [10]. In their multivariate logistic regression analysis, Cataldi et al. found that a low Apgar score, a medullary hyperechogenicity, ampicillin, ceftazidime, and ibuprofen were risk factors; in contrast, we found that high mean airway pressure, low blood pressure, and cefotaxime were associated with AKI in premature infants. Our results may differ from those of Cataldi et al. for at least two reasons. Cataldi et al. studied a larger and less premature population, and they used a different definition for acute renal failure [10]. In their study of 71 premature infants (<38 weeks GA) with acute renal failure, the average GA and birth weight were 27.8 weeks and 1115.9 g, respectively; in comparison, the average GA and birth weight of our patients were 24.7 weeks and 614.6 g, respectively. Therefore, our study completes the aforementioned study by analyzing only ELBW premature infants who might differ from older premature infants. The definition of AKI in our study was also different. Cataldi et al. defined AKI in infants <33 weeks GA as a serum creatinine level >114.92 micromol/l (or 1.3 mg/dl) with and without oliguria after 60 h of life; in comparison, our definition of AKI was an oliguria of <1 ml/kg/h of urine output developing after 24 h of birth or an increasing serum creatinine level >1.5 mg/dl after 72 h of birth [10]. Few of our cases met the criteria of AKI based on oliguria alone and would have been missed under the serum creatinine criteria only.
Our renal ultrasound findings of infants with AKI are consistent with previous findings and reports [10]. In our study, all patients who had renal imaging studies available for review had normal renal anatomy, with the exception of one patient who had small kidneys and one patient who had mild pelviesctasis. Our predominant renal ultrasound finding was renal medullary hyperechogenicity, which is usually associated with a medical renal disease or an index of nonspecific renal stress, a finding that is consistent with previous reports [10]. Aortic thrombosis-related AKI has been reported as a complication of umbilical arterial lines [10, 36–38]. The number of umbilical arterial lines was similar between the groups in our study. However, we had one patient with AKI who had an abdominal aortic clot, although the clot did not extend to the level of the renal arteries. Overall, our patients’ renal ultrasound findings are most probably secondary to the AKI rather than being an associated risk factor.
Most acute renal failures in neonates are secondary, transient, and reversible with the resolution of the underlying conditions, with the exception of a few cases of congenital or primary renal conditions [9, 10, 39–41]. A high mortality rate has been reported in neonate with AKI (range 25– 80%), which is consistent with our findings (our mortality rate was 70% in patients with AKI) [8, 15, 16, 23].
In our study, at the time of discharge from the NICU, there were no differences in serum creatinine, serum BUN, or blood pressures in survivors of AKI and their controls. However, long-term follow-up is necessary since ELBW infants, even without evidence of AKI in the neonatal period, are subject to a decrease in their GFR and tubular phosphate transportation, probably as a consequence of an impaired postnatal nephrogenesis [13]. Abitbol et al. conducted a long-term follow-up study of 20 ELBW infants with a history of AKI in the neonatal period and found that proteinuria (urine protein/creatinine >0.6 mg/dl), elevated serum creatinine (serum creatinine >0.6 mg/dl at 1 year of age), and tendency to obesity (with body mass index >85th percentile) are prominent risk factors for long-term progressive renal disease. Based on these findings, the authors emphasized the need for long-term follow-up of renal function in this highly vulnerable population [42].
Our study has multiple limitations. It is a retrospective, small-sized, single-center study that reviewed the outcome of ELBW infants over an 8-year time span. The management of premature infants has evolved over the years, and it is possible that the management of our patients has changed during the study period. However, we attempted to counteract this potential problem by designing our study as a case–control study with contemporary controls. An attempt to identify perfect matches to our cases may also be a limitation to our study with the potential of an over-matching bias. Given the retrospective design of our analysis, we can only describe associations between variables and can only state that our risk factors are only associated risk factors with AKI in ELBW—only prospective studies have the potential to address causality. For example, to be able to confirm that cephalosporin is a risk factor, a prospective controlled study is needed. The use of cephalosporin by the treating physicians could have been related to factors that are undetected by our analysis. Since the majority of ELBW infants require frequent blood tests for the management of their fluid and electrolytes, we relied on our medical records to identify infants with AKI. However, one of the limitations of our retrospective review is that potential cases of AKI could have been missed since we did not have a universal serum creatinine screening of all infants or serial renal studies (such as fractional excretion of sodium and urea), and since there is no universal definition for AKI in ELBW infants. Another limitation of our study is related to our reliance on serum creatinine as one of the criteria for the diagnosis of AKI. However, serum creatinine may be a late marker of renal failure. In the future, relying on urinary biomarkers may be more helpful in identifying renal failures prior to the rise in serum creatinine.
Although we did not find a difference in outcome at discharge between patients who developed AKI and their controls, our study was not designed or powered to study the outcome of AKI in ELBW infants. Future prospective, long-term, multi-institutional studies are needed to determine the long-term outcome of AKI in ELBW.