Risk factors for acute kidney injury in critically ill patients receiving high intravenous doses of colistin methanesulfonate and/or other nephrotoxic antibiotics: a retrospective cohort study

Throughout the world, Acinetobacter baumannii, Pseudomonas aeruginosa and Klebsiella pneumonia have emerged as major causes of nosocomial infections [1], particularly in patients who are critically ill and/or immunocompromised. Concern has been raised by reports of a stepwise trend towards extensive drug-resistance in these organisms [1]. Infections caused by extensively drug-resistant (XDR) bacterial strains are associated with high mortality rates, especially in intensive care units (ICUs), where outbreaks are extremely difficult to control. The limited therapeutic options in these cases often lead clinicians to resort to salvage therapy with colistin methanesulfonate (CMS). This older polymyxin antibiotic, which is converted in vivo to colistin [2], was widely abandoned in the 1970s because of its unfavorable pharmacokinetic properties and frequent adverse effects, particularly nephrotoxicity.

The "modern polymyxin era" [3], which began in the late 1990s, is characterized by a variety of dosing schedules, but to date there is still a dearth of information on the clinical pharmacokinetics of CMS and colistin in critically ill patients [4]. Higher doses appear to be beneficial in these cases [5], but it is unclear whether the improved efficacy comes at a cost of increased toxicity. The aim of this retrospective cohort study was to evaluate the potential risk factors for acute kidney injury (AKI), as defined by the RIFLE (Risk of renal dysfunction, Injury to the kidney, Failure of kidney function, Loss of kidney function, End-stage kidney disease) classification system [6], in severely ill ICU patients without pre-existing renal disease who received high-dose intravenous CMS therapy for more than seven days.

This study was conducted in two large tertiary-care teaching hospitals in Rome, Italy (Policlinico Umberto I and the Policlinico Gemelli), and it involved retrospective analysis of prospectively collected data. Cases were identified through searches of the ICU patient databases, and data were collected from the patients' electronic medical records.

The study cohort consisted of adults (≥18 years) consecutively admitted to the general ICUs of the participating facilities between April 2009 and June 2011 (Figure 1). Inclusion criteria were: 1) no evidence on ICU admission - as well as at protocol admission - of chronic renal failure and normal estimated glomerular filtration rate (GFR) relative to serum creatinine (SCr) based on age, race and sex formula assuming a glomerular filtration rate of 75 mL/min/1.73 m², as recommended by the Acute Dialysis Quality Initiative (ADQI) Working Group [6]. Most ICU patients, in fact, have not a prior measure of renal function and a simplified modification of diet in renal disease (MDRD) formula provides a simple and precise estimation of baseline GFR and SCr 2) onset > 48 h after ICU admission of an XDR bacterial infection treated for seven or more days with intravenous (iv) CMS and/or other nephrotoxic antimicrobial agents (NAs, that is, aminoglycosides and glycopeptides).

Extensively drug-resistant (XDR) was defined as non-susceptibility to at least one agent in all but two or fewer antimicrobial categories (that is, bacterial isolates remain susceptible to only one or two categories) [7]. Patients were excluded if the antibiotic therapy described above had been started prior to ICU admission.

The primary end point of the study was to evaluate the potential risk factors for acute kidney injury (AKI) in severely ill ICU patients without pre-existing renal disease who received high-dose intravenous CMS therapy with or without other nephrotoxic antimicrobials.

For this purpose, patients were classified daily using the RIFLE criteria and AKI was defined using the serum creatinine compared to the baseline value of the SCr previously obtained from the MDRD equation.

A patient was considered to have AKI when he had an increase in SCr of at least 50% from baseline (defined as Risk) or if he doubled the SCr level from the baseline (defined as Injury) or had a three times increase in SCr (defined as Failure) [6, 8] (Figure 2).

For each patient included in the cohort, electronic hospital charts were reviewed, and the following collected data were recorded: demographic variables; Simplified Acute Physiology Score II (SAPS II); presence on admission of hypertension, diabetes mellitus, and/or congestive heart failure; reason for ICU admission; length of ICU stay; type and cause of infection; nephrotoxic drugs and iv iodate contrast used, immunocompromised status; albumin serum level, bilirubin serum level and, for CMS, duration of therapy and cumulative doses; presence of septic shock caused by the XDR infection; use of continuous renal replacement therapy (CRRT) during the ICU stay and ICU mortality.

Septic shock was diagnosed as a state of acute circulatory failure characterized by persistent arterial hypotension despite adequate fluid resuscitation or by tissue hypoperfusion in the presence of proven or suspected infection [9]. Bloodstream infection (BSI) was defined as at least one positive blood culture for a potential bacterium together with clinical features compatible with systemic inflammatory response syndrome; the clinical suspicion of pneumonia was based on either clinical criteria (new or progressive radiologic pulmonary infiltrate together with at least two of the following: temperature >38°C or <36°C, leukocytosis >12,000/mL or leucopoenia <4,000/mL, or purulent respiratory secretions) or a simplified Clinical Pulmonary Infectious Score greater than or equal to six points. The microbiologic evaluation included the collection of at least one lower respiratory airway sample by tracheobronchial aspirates, bronchoscopic or blind bronchoalveolar lavage, within the first 24 hours of the onset of symptoms. Microbiologic confirmation of pneumonia was defined by the presence of at least one potentially pathogenic microorganism in respiratory samples above predefined thresholds bronchoalveolar lavage >10⁴, and sputum or tracheobronchial aspirates >10⁵ colony-forming units/ml, respectively [10, 11].

This study was approved by our institutional review board that waived the need for informed consent, due to the retrospective design of this study.

Between April 2009 and June 2011, 1,474 adult patients were consecutively admitted to the two participating ICUs, and 279 (19%) of these met the criteria for inclusion in the study (Figure 1). Their characteristics are reported in Tables 1 and 2. The NAs patients were older, had a longer ICU stay and had a higher percentage immunocompromised than the other groups; the number of NAs patients treated with nonsteroidal anti-inflammatory drugs (NSAIDs) were statistically significant in respect to the CMS group (Table 1).

One hundred thirty-two of the patients received intravenous therapy with NAs alone (glycopeptides and aminoglycosides). Eight (6%) of these patients received two nephrotoxic antimicrobials.

CMS was administered as Colimicina^® (UCB Pharma SpA, Milan, Italy); 1 million UI per vial). All 147 patients received a loading dose of CMS (4 million IU) followed by a daily dose of 130,000 IU per kilogram of ideal body weight (IBW) (divided into three doses per day) [12]. For patients with creatinine clearance of less than 70 mL/min but more than 30 mL/min one-third of the normal daily dose twice a day (for example, 6 million IU divided into two doses per day for a 70 Kg patient); with a creatinine clearance <30 mL/min one-third of the normal daily dose once a day (for example, 3 million IU once a day for a 70 Kg patient); during CRRT we used one-third of the normal daily dose twice a day [13, 14].

The median length of CMS therapy was 11 days; the cumulative CMS dose was 93.999.975 IU, and there were no significant differences between the CMS and CMS + NA subgroups involving any of these variables (P = 0.26 and P = 0.37, respectively)

Normogram based on creatinine clearance (CLCr) was used for calculation of the vancomycin daily dosage administered by continuous infusion in order to target a steady state concentration (CSS) at 15 to 20 mg/L [15]. We, therefore, confirm our dosage monitoring the serum vancomicin concentration. Aminoglycoside were administered according to one daily dosing schedule of 20 mg/kg/day for Amikacin and 5 mg/kg/day for Gentamycin; dosage was confirmed by monitoring the serum concentration and was adjusted as a function of CLCr. The target trough (1 µg/mL) was easily achieved using a once daily dose [16]

A total of 116 (41%) of the patients died while they were in ICU (Table 1).

One hundred eleven (40%) of the 279 patients developed AKI during their stay in the ICU. In the NAs group, 10% the AKI cases were classified as Risk, 13% as Injury and 18% as Failure; in the CMS group, 6% of the cases were classified as Risk, 7% as Injury and 22% as Failure; and in the CMS + NAs group, 7% of the AKI cases classified as Risk, 12% as Injury and 26% as Failure. The median onset of AKI was 10 days (8 to 15) (25^th to 75^th) in the CMS group, 11 days (10 to 12) (25^th to 75^th) in the NAs group, 12 days (10 to 21) (25^th to 75^th) in the CMS + NAs group. Compared with the non-AKI subgroup, those who developed AKI were significantly older and had significantly higher SAPS II scores. In addition, septic shock rates and ICU mortality were roughly three times higher than those in the non-AKI group; in fact, in the AKI group, the ICU mortality and septic shock rates were 70% and 74%, respectively (Table 2). The vast majority of AKI patients had an albumin serum level less than 2 g/dL (Table 2). The vast majority of the infections considered in this study were ventilator-associated pneumonia (VAP) or catheter-related bloodstream infections (CRBSIs), and in almost half of all cases (46%), septic shock was present at infection onset.

We did not find any difference in the incidence of AKI in respect to the etiology of infections among the three groups studied. Nine out of 17 Failure patients who survived were discharged from ICU as Failure but without a dialysis prescription; 1 as Injury, 4 as Risk and 3 with a complete recovery of the renal function. Five out of 7 Injury patients who survived were discharged from ICU as Injury and 2 as Risk. Five out of 9 Risk patients who survived were discharged from ICU as Risk and 4 with a complete recovery of the renal function (Table 3).

The results of the logistic regression are shown in Tables 3, 4 and 5. In the complete study population (n = 279), the multivariate analysis showed that SAPS II scores and the presence of septic shock at infection onset were independently associated with AKI. The other significant variables at the univariate analysis were not included in the multivariate final logistic model using a stepwise procedure. A ROC curve analysis was performed to assess the accuracy of the final regression model showing AUC ± SE = 0.79 ± 0.03 with 95% C.I. 0.74 to 0.84; Chi Square statistics: P <0.001 (Table 4). In the 147 patients who received CMS (Table 5), the likelihood of developing AKI was not significantly different in the CMS and CMS + NA subgroups. In contrast, onset of AKI was two times more likely in patients with a SAPS II score ≥43 and six times more likely in those whose infections had presented with septic shock. A ROC curve analysis was performed to assess the accuracy of the final regression model showing AUC ± SE = 0.76 ± 0.04 with 95% CI 0.7 to 0.8; Chi-square statistics P <0.001.

A similar picture emerged when we analyzed the 222 patients who received CMS alone (n = 90) or NAs alone (n = 132) (Table 6). The only independent predictors of AKI in this group were SAPS II scores ≥44 and septic shock at infection onset. A ROC curve analysis was performed to assess the accuracy of the final regression model showing AUC = 0.8 ± 0.03 with 0.75 to 0.86 95% CI; Chi-square statistics: P <0.01.

These findings indicate that in ICU patients without pre-existing renal disease who require nephrotoxic antimicrobial drug therapy for XDR bacterial infections, the use of CMS - with or without NAs - does not significantly increase the risk for AKI over that associated with NAs therapy alone.

The cohort treated with high doses of CMS for nosocomial XDR infections in our study represented approximately 10% of the entire population admitted to the general ICUs during the two-year study period. The overall incidence of AKI in the 279 cases we analyzed was 40%, and there were no significant differences among rates observed in the CMS (34%), CMS+NAs (45%) and NAs subgroups (41%). These data are consistent with the results of the Nefroint study [8], a multicenter study conducted in Italian ICUs: in the subgroup of 133 patients without AKI at ICU admission, the incidence of AKI was 40% regardless of whether or not nephrotoxic drugs were administered. A recent meta-analysis [17] on six controlled studies comparing colistin vs other antibiotics for treatment of VAP in patients without cystic fibrosis suggested that colistin may be as safe as other standard antibiotics used for these drug-resistant infections. In particular, the nephrotoxicity rate for colistin was similar to that in the control group.

Our multivariate analysis revealed that SAPS II scores ≥43 and the presence of septic shock at infection onset were independently associated with AKI, but high-dose intravenous CMS therapy for more than seven days was not a risk factor for development of new onset AKI.

Since CMS's recent re-emergence as a last-resort treatment of infections caused by XDR pathogens (including Acinetobacter baumanii, Pseudomonas aeruginosa and Klebsiella pneumonia), many authors have investigated its adverse effects, in particular, its potential nephrotoxicity. Like aminoglycosides, the polymyxins cause damage to the kidneys at the level of the proximal tubules, where both classes of drugs are extensively reabsorbed via the endocytic receptor protein megalin [18]. Colistin was originally used in the 1960s to combat infections caused by gram-negative bacteria, but it was abandoned in the 1970s because of its reported association with high nephrotoxicity rates [13, 19] and because new, apparently less toxic antibiotics (for example, the aminoglycosides) were becoming available. Several studies published over the past decade, however, have demonstrated that CMS is not associated with serious adverse effects, and although nephrotoxicity incidence rates varied (0% to 32%) [20‐24], they were clearly lower than those reported in the 1960s and 1970s. The differences between older and more recent findings have been attributed to various factors, including the increased presence of chemical impurities in older colistin preparations, the variable definitions of acute renal impairment used in the various studies, closer monitoring and, last but not least, the improved maintenance of patient hydration by today's physicians [20].

Research endorsed by the Acute Dialysis Quality Initiative led to the publication of the RIFLE classification, with standardized criteria for various degrees of renal dysfunction [6]. The RIFLE approach can detect AKI with high sensitivity and high specificity. It can also be used to predict the prognosis of affected patients, and it provides a useful framework for comparing the results of different studies. Two recent studies that used the RIFLE criteria to investigate colistin-related nephrotoxicity [25, 26] documented high incidences of mild renal impairment (about 43%) in both cohorts (even though the two populations differed in terms of illness severity).

Indeed, in most recent studies, the colistin-treated populations have been heterogeneous in terms of baseline illness severity, baseline renal function and treatment variables, including daily doses and duration of treatment. Daily doses of CMS used in these studies ranged from 3 million to 11 million IU [21, 25, 27‐30]. To make matters worse, there is also wide variation involving the type of preparation used, that is, CMS (where 2 million IUs correspond to 160 mg of the drug) versus colistin base (where 2 million IUs equals 60 mg). The importance of universal dosing terminology has been emphasized by several investigators [19, 20].

This antibiotic is being used with increasing frequency to treat critically ill patients - despite the absence of clinical guidelines and dosing recommendations for this particular population. Multi-organ dysfunction and severe XDR infections can alter the pharmacokinetics of CMS and colistin in terms of half-life and rates of formation of colistin from CMS [30], and the larger volumes of distribution present in these critically ill septic patients can cause a lower concentration of the antibiotic [5]. Early and appropriate goal-directed fluid therapy is fundamental in acute resuscitation of these critically ill patients; however, it is almost always associated with a certain degree of fluid overload, especially in septic patients, which promotes tissue edema that could potentially contribute, itself, to progressive organ dysfunction. Both fluid balance and urine volume are independent predictors of mortality in adult critically ill patients with AKI [31].

Plachouras et al. [12] studied the pharmacokinetics of intravenously administered CMS in critically ill patients and concluded that a loading dose of at least 9 million IU of CMS is needed in these cases to produce plasma concentrations of the drug within the minimum inhibitory concentration (MIC) range indicative of susceptibility. Failure to achieve such concentrations can lead to the emergence of resistant strains, and it can also result in increased mortality.

In light of these findings, we decided to investigate the nephrotoxicity of high-dose CMS therapy, in terms of RIFLE-defined AKI, in patients with no AKI at baseline. Hartzell and collaborators [25] used a similar approach in a young and otherwise healthy population of patients on a general medicine ward. The patients had no other confounding comorbidity, but the mean duration of CMS therapy was longer than it was in our study. The authors found a significant association between the cumulative CMS dose and the risk of nephrotoxicity in patients receiving CMS for more than 14 days. This finding contrasts with the results of our logistic regression analysis, which showed that neither the cumulative CMS dose nor the duration of treatment was a risk factor for developing new-onset AKI in severely ill ICU patients. The median days of CMS treatment of our patients, however, was lower that than reported by Hartzell and collaborators and could probably justify the discordance with our results as well as the difference in severity of the two population studied. We agree, nevertheless, that creatinine levels need to be closely monitored in patients receiving prolonged treatment with CMS.

Pogue et al. [26] reported that CMS nephrotoxicity is related to the daily dose but not to cumulative exposure. However, the population they studied was heterogeneous in terms of pre-treatment renal function. Furthermore, although illness severity scores were not reported, their patients were probably not as critically ill as ours. Only 14% had septic shock, 15% were on vasopressors and only 62% were being mechanically ventilated. These are important differences because, as noted above, the pharmacokinetics of CMS and colistin are different in the critically ill [5, 29], and in our study a SAPS II score ≥43 was independently associated with AKI. Comparison of findings in ICU and non-ICU cohorts is also complicated by the fact that the former patients are likely to be more closely monitored and more rapidly treated than those being cared for on general wards.

Septic shock was the strongest predictor of AKI in our cohort. Many authors agree that the renal effects of sepsis, per se, should not be underestimated. Early AKI is common in septic shock [32], and it may potentiate the effects of colistin and other drugs on the kidney. The combination of septic shock and AKI had a consistently negative effect on survival. Among the patients with septic shock who did not receive CMS at all (that is, those who were treated with NAs alone), the incidence of AKI was 64% (45/70), which confirms the predominant role of septic shock in the kidney injury (Figure 1).

In conclusion, in ICU patients with normal baseline renal function who receive CMS and/or NAs, the incidence of AKI as defined by the RIFLE classification is clearly high - 40%. However, high-dose CMS therapy does not appear to be a risk factor for this outcome. Instead, the development of AKI was strongly correlated with the presence of septic shock and with the severity of the patients' underlying illness, as reflected by the SAPS II score. These findings suggest that renal protection measures, such as blood volume maintenance, are of utmost importance in critically ill patients with infections that require treatment with CMS.