Objective Infections with multidrug-resistant organisms (MDROs) such as Gram-negative bacteria have high morbidity and mortality with limited treatment options. Colistin, an antibiotic active against MDRO, was rarely used due to frequent adverse effects, but its use has now been recommended among adults. In this study, we determined the efficacy of colistin for the treatment of sepsis in neonates.
Design/setting/patients/outcomes We conducted a retrospective record review of all neonates admitted to the neonatal intensive care unit of Aga Khan University Hospital, Karachi, Pakistan, between June 2015 and June 2018, who had sepsis and received colistin by intravenous, inhalation and/or intrathecal routes. Predictors of colistin efficacy, for neonatal survival and microbial clearance, were assessed using multiple logistic regression.
Results 153 neonates received colistin; 120 had culture-proven sepsis; and 93 had MDR-GNB (84 colistin-sensitive). 111 (72.5%) neonates survived and were discharged from hospital; 82.6% had microbial clearance. Neonates with colistin-sensitive bacteria (adjusted OR (AOR)=3.2, 95% CI 2.8 to 4.0), and those in which colistin therapy started early (AOR=7.2, 95% CI 3.5 to 13.6) were more likely to survive. Neonates with increased gestational age (AOR=1.9, 95% CI 1.5 to 3.0), higher weight (AOR=5.4, 95% CI 3.3 to 11.8) and later onset of sepsis (AOR=4.3, 95% CI 2.0 to 9.0) had higher survival. Adverse events included nephrotoxicity in 5.2%; 13.7% developed seizures and 18.3% had electrolyte imbalance.
Conclusions Colistin therapy was associated with survival among neonates suffering from MDR-GNB sepsis. The frequency of side effects was moderate.
- infectious diseases
- intensive care
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What is already known on this topic?
Multidrug-resistant Gram-negative bacteria (MDR-GNB) are a big challenge in the neonatal population in Pakistan.
The number of MDR-GNB infections is increasing in neonates.
Colistin is considered a therapeutic option after the failure of carbapenem use.
What this study adds?
Predictors of response to colistin and significant association with neonatal survival with earlier microbial clearance.
Starting colistin within 1–2 hours of the onset of severe sepsis or septic shock may improve the survival of neonates with colistin-sensitive MDR-GNB infections.
Intrathecal colistin may improve the survival of neonates with MDR-GNB meningitis and ventriculitis.
Infection with multidrug-resistant Gram-negative-bacteria (MDR-GNB) is associated with high morbidity and mortality,1 2 and often these infections are nosocomial. The incidence of neonatal nosocomial infections has been reported between 7% and 24% in South Asia.1 3 Acinetobacter baumannii, Klebsiella pneumoniae, Pseudomonas aeruginosa and Echerichia coli are the most frequent Gram-negative-bacteria (GNB) in South Asia with a high rate of multidrug resistance.4 5 In one study, 89% of Acinetobacter species were MDR.4 Furthermore, carbapenem-resistant organisms (CROs) are among multidrug-resistant organisms (MDROs) which pose the greatest challenge with mortality ranging from 12% to 50% among neonates.5–7
Colistimethate sodium (CMS) is an inactive prodrug administered parenterally. It is then hydrolysed into its active metabolite colistin, which is a potent antimicrobial agent; CMS use was abandoned earlier due to frequent side effects. However, more recently, CMS has been recommended for adults with MDR-GNB infections.8 9 CMS treatment is particularly recommended when carbapenem resistance is reported. Cefiderocol is another therapeutic agent effective against MDRO like CROs.10 11 However, cefiderocol and similar agents are expensive with limited availability in low-income and middle-income countries (LMICs). Colistin is available in LMICs and is used for most of the susceptible CROs.12 Colistin can cause a high rate of neurotoxicity and nephrotoxicity if administered in high doses intramuscularly, although toxicities are negligible when given intravenously.13 Colistin has been used widely among adults with cancer, burns and in intensive care units.14 15 There are very few studies describing colistin use among children and neonates.9 16 Determining the safety of colistin use among neonates admitted to ICU is difficult due to the presence of other contributing comorbid conditions, including prematurity and use of other antibiotics. Thus, the safety and efficacy of colistin among neonates remain unclear, particularly in LMIC settings.17 18
The purpose of this study was to evaluate the use of colistin in a neonatal intensive care unit (NICU) setting in Pakistan. We investigated the efficacy and safety of colistin in the neonatal population considering coexisting clinical conditions and concomitant medicinal use.
Study design, participants’ eligibility and data sources
This was a retrospective review of medical records from a tertiary care hospital in Karachi, Pakistan. Infants admitted to NICU and the step-down unit, between June 2015 and June 2018, receiving colistin by any route (intravenous, nebuliser or intrathecal) for sepsis, were included in the study. Patients with seizures, acute kidney injury (AKI) or congenital abnormalities of the urinary tract were excluded.
Information was extracted from hospital electronic records. This included information on clinical characteristics and route, dose and duration of colistin therapy. Laboratory parameters like serum creatinine, blood urea nitrogen, serum electrolytes at baseline; days 1, 3 and 7, and then weekly until the end of colistin therapy were also recorded. We recorded concomitant use of other nephrotoxic drugs/antibiotics (within 7 days of colistin therapy) and the occurrence of seizures. In addition, data for culture and sensitivity, organism eradication period and survival/death was also retrieved.
Clinical sepsis and nosocomial infection were defined as per standard definitions from the Centers for Disease Control and Prevention.19 Neonates who had sepsis associated with any organ dysfunction, hypotension or on vasopressors were classified as having septic shock.19 Neonate with a clinical presentation of septicaemia, meningitis or pneumonia, along with pathogen isolation in control cultures of blood, cerebrospinal fluid (CSF), endotracheal aspirate or urine were defined as culture-positive sepsis. Treatment failure was considered when the same condition persisted or got worse over the period of 48–72 hours or new infection occurred or signs of worsening on radiology.20
We used the modified Kidney Disease Improving Global Outcomes definition for AKI.21 AKI assessed by changes in serum level creatinine (before, during and after the treatment) and defined as an increase in serum creatinine (at least 0.3 mg/dL within 48 hours or 150%–200% increase from baseline trough value).21 Neurotoxicity was defined as an episode of seizure or change in consciousness level at any time during colistin therapy. We defined microbiological response as no bacterial growth in cultures of CSF, blood or urine, at least 72 hours after starting colistin therapy. Cultures were collected and evaluated every 48 hours until microbial clearance. MDRO was defined as an isolate non-susceptible to at least one agent of ≥3 antimicrobial categories.22 Hypomagnesaemia was defined as serum magnesium concentration of <1.6 mg/dL23 and hypokalaemia as serum potassium concentrations of <3.5 mEq/L.24 The efficacy of colistin as an outcome measure was evaluated based on the microbiological clearance of cultures and patient survival with colistin therapy.
Baseline and subsequent cultures during therapy were taken from venous blood, endotracheal aspirate, CSF, urine, wound/tissue/pus or central venous catheter. These culture samples were inoculated on routine culture media (blood/chocolate/MacConkey agar). Pathogens were identified through Vitek-2 compact system and biochemical tests. Colistin susceptibility of isolated pathogens was confirmed by performing a broth microdilution test. Isolated pathogens with minimum inhibitory concentration (MIC) of ≤2 mg/dL were documented as colistin-sensitive using Clinical Laboratory Standards Institute (CLSI) guidelines.25
Institutional antibiotic guidelines were followed for the treatment of neonatal sepsis. First-line therapy included intravenous ampicillin and gentamicin or cefotaxime and amikacin. Second-line therapy was carbapenem with vancomycin. Colistin was reserved as a third-line antibiotic, mostly administered with meropenem. Colistin therapy was started; 1. after culture sensitivity reports; 2. as antimicrobial escalation for failure of first and second-line antibiotics; 3. in cases of severe sepsis/septic shock within 1–2 hours empirically with carbapenem based on our NICU antimicrobial susceptibility patterns.4 5 26 Since colistin is considered a controlled medication, approval from an infectious disease consultant was needed in non-culture proven sepsis when therapy continued for more than 72 hours.
Colistin (base) was administered intravenously at a dose of 2.5–5.0 mg (75 000–150 000 units)/kg/day in two to four divided doses, 4 mg/kg/dose twice daily via nebulisation and 0.16–0.24 mg/kg as a single daily dose via intrathecal/intraventricular route. Doses were adjusted in patients with reduced renal function.27–29 All intravenous and intrathecal doses were dispensed in prefilled ready to administer form in normal saline and infused over 30 min.
Outcome measures and statistical analysis
Primary outcome measures were microbiological clearance and patient survival during treatment. Colistin-associated adverse effects, such as nephrotoxicity, neurotoxicity and electrolyte imbalance, were evaluated as secondary outcomes.
Data were analysed using IBM SPSS V.20. Descriptive statistics were provided according to those neonates who survived and died. At the univariate level, each independent variable was analysed to see the association of survival and microbial clearance using binary logistic regression. Those variables with significance of ≤0.20 or biologically plausible (parameters related to antenatal care and neonatal clinical parameters) at univariate level were considered for multivariable analysis.
A total of 153 patients with sepsis who underwent colistin therapy were included in this study (see table 1). Most were male (n=102), preterm (n=118) and low birth weight (n=110). Bacteraemia was the most common diagnosis (n=108) followed by pneumonia (n=34) and meningitis (n=15); 120 were culture-proven cases, while the rest were diagnosed on clinical grounds K. pneumonia and A. baumannii were the most frequent organisms isolated. Multiple comorbid conditions were present among neonates. Nearly three quarters (72.5%) of neonates survived.
Colistin-sensitive organisms were found in 64 surviving and 20 neonates who died, while colistin-resistant organisms were found in 1 and 8 neonates who survived and died respectively. Concomitant use of carbapenem was 91.0% in those who survived and 90.5% in those who died. There was no difference in the mean duration of colistin therapy in those who survived versus those who died (table 1). The median life span of those neonates who died was 23 days (range 5–45 days). Adverse events associated with colistin use included AKI (n=8, 5.2%), seizures (n=21, 13.7%) and electrolyte imbalance (n=28,18.3%).
Table 2 describes the adjusted OR (AOR) for factors associated with survival among neonates with colistin use. Neonates with a positive culture and colistin-sensitive organisms were more likely to survive (AOR=3.2, 95% CI 2.8 to 4.0). Early initiation of colistin after the onset of severe sepsis/septic shock (AOR=7.2, 95% CI 3.5 to 13.6) led to a higher survival rate. Microbial clearance (AOR=5.2, 95% CI 2.2 to 13.2) was more likely to be associated with a higher survival rate. Other factors associated with improved survival included later onset of sepsis in the hospital, increased gestational age (GA), higher birth weight and absence of deteriorating signs.
Table 3 describes the AOR for factors associated with microbial clearance in neonates with colistin use. Colistin administered within 1–2 hours of the onset of sepsis/septic shock had much higher microbial clearance (AOR=32.9, 95% CI 15.4 to 58.5). Simultaneous use of carbapenem had no advantage for microbial clearance. Neonates with colistin-sensitive organisms were more likely to have microbial clearance (AOR=2.1, 95% CI 1.0 to 3.7). Later onset of sepsis in the hospital (AOR=2.0, 95% CI 1.0 to 1.5) and higher birth weight were associated with higher microbial clearance. However, the absence of deteriorating signs and GA had no association with microbial clearance.
Despite the reintroduction of colistin and its wide use among adults for MDR-GNB infections, there is very little evidence of colistin use in neonates. Few studies have reported intravenous use of colistin.27 30 31 This is one of the few studies with a reasonable sample size to determine the effectiveness and adverse effects of colistin in the critically ill neonatal population. Our study found that colistin use was associated with 72.5% survival among neonates with sepsis. Alan et al reported 4/21 deaths in neonates treated with colistin; however, their study was limited in size and deaths within 72 hours of birth were not included.18 Serafettin Tekgunduz et al reported a 50% mortality among neonates with culture-proven sepsis treated with colistin.31
The study also evaluated the predictors of survival and microbial clearance among neonates given colistin therapy. As expected, small for GA and low birthweight babies had higher mortality. These findings are consistent with several other studies globally.27 32 The absence of deteriorating clinical signs and laboratory parameters was significantly associated with survival, findings which are consistent and biologically plausible.33 Nonetheless, the duration of colistin therapy, the type of organism treated and the site of infection had no association with survival and microbial clearance. On the other hand, the presence of colistin-sensitive GNB and early initiation of colistin therapy after the onset of sepsis (especially administration of first intravenous dose within 1–2 hours of the onset of severe sepsis/septic shock) were associated with increased survival of the neonates and microbial clearance. To the best of our knowledge, this is the first study of its kind which has looked at the association of these factors in a neonatal population.
The concomitant use of other antimicrobial agents had no association with survival or microbial clearance. Studies have shown that long-term use of colistin leads to microbial resistance; however, the duration of therapy was short in our study and none showed subsequent resistance.34
To the best of our knowledge, this is the first study to report the use of intrathecal colistin for meningitis in neonates. In our study, 15 patients had meningitis, 7 received intrathecal colistin (5 of whom also received intravenous colistin); the other 8 patients with meningitis received only intravenous colistin. All neonates with meningitis who received both intravenous and intrathecal colistin survived, but none of those given intravenous colistin alone survived. Furthermore, two neonates who received only intrathecal colistin; one survived and one died. This suggests that the appropriate route of colistin has a significant impact on clinical outcomes, especially in neonates with ventriculitis and meningitis with colistin-sensitive GNB. However, these results should be interpreted with caution, as there was a small number of neonates in these categories. We recommend further studies in this regard.
Nephrotoxicity is the major side effect related to colistin use reported in the literature.9 Though we followed the definition for AKI used in previous neonatal studies, the rate of nephrotoxicity was much lower in our study.8 35–37 A study of very low birth weight (VLBW) neonates given a similar dose of colistin (5 mg/kg/day)27 found AKI in 4/28 (14%) VLBW neonates. This might be related to a shorter duration of colistin in our study compared with other studies with a higher prevalence of AKI.8 9 38 39 Bartter-like syndrome was reported in a neonate with 26 days of therapy.18 In our study, colistin was continued in AKI patients with dose adjustment according to weight and serum creatinine. The concomitant use of nephrotoxic medications did not seem to affect AKI development.
Overall, 28 (18.3%) patients in our study experienced reversible hyponatraemia, hypokalaemia, hypomagnesaemia and hypocalcaemia. These adverse effects were lower (16.2%) among patients who survived than those who died (23.8%). Colistin therapy was not discontinued in these cases who were managed with supportive care.18 40 The need for supplemental electrolytes in our study was lower than the previous VLBW neonatal study, which reported 78.6% and 53.6% neonates needing magnesium and potassium supplementations, respectively.27
In the present study, seizures were observed in 14 (12.6%) who survived and 7 (16.7%) of those who died.8 Of these 21 neonates, 3 had meningomyelocele, 1 each had brainstem bleed, an external ventricular drain/ventriculoperitoneal shunt, 5 had perinatal asphyxia, 2 had hydrocephalus, 4 had intraventricular haemorrhage (IVH), and 3 had IVH and hydrocephalus. A total of 8/21 had meningitis. It was not possible to directly correlate the neurological side effects with colistin therapy, given the comorbidities, clinical circumstances and other medications in these sick neonates.8 18 Overall, the number of patients in each category was too small to deduce any meaningful conclusions.
Our study is the largest reported study of neonatal colistin use, and we found successful colistin therapy via inhalation, intrathecal and intravenous routes with tolerable adverse effects. A few limitations must be considered. This was a single-centre retrospectively designed study. Also, some of the positive isolates in urine and tracheal aspirate could be colonising species rather than causative pathogens. Further prospective studies need to be conducted to confirm our findings.
In conclusion, this study suggests that colistin may be safe and effective for treating MDR-GNB infections in critically ill neonates. However, it remains the last resort for MDR-GNB after the failure of carbapenems. Moreover, for the optimal neonatal doses through different routes of administration, further pharmacodynamics and pharmacokinetic studies are required.
We would like to acknowledge the technical and editing assistance by Abdul Moiz Hussain and Dr Imran Nisar.
Correction notice This paper has been corrected since it was published online. There was a data error in table 1 in the row 'Diagnosis/site of infection', for meningitis and pneumonia.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Not required.
Ethics approval Ethical approval was obtained before starting this study from the Ethical Review Committee (ERC) of Aga Khan University, Karachi, Pakistan (ERC # 2018-0233-137).
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available upon reasonable request.
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