Abstract

Background: Deviations from the optimal vancomycin dosing may occur in the neonatal and pediatric population due to inconsistencies in the recommended dosing algorithms. This study aims to collect the expert opinions of clinicians who practice in the neonatal or pediatric intensive care units (NICU/PICUs) of 12 major medical centers in Hong Kong.Methods: This was a multicenter, cross-sectional study. Eligible physicians and pharmacists completed a structured questionnaire to identify the challenges they encountered when selecting the initial intermittent vancomycin dosing. They also answered questions concerning therapeutic monitoring services (TDM) for vancomycin, including the targeted trough levels for empirical vancomycin regimens administered for complicated and uncomplicated infections.Results: A total of 23 physicians and 43 pharmacists completed the survey. The top clinical parameters reported as most important for determining the initial vancomycin dosing were renal function (90.9%), post-menstrual/postnatal age (81.8%), body weight (66.7%), and suspected/documented pathogen (53.0%). Respondents reported challenges such as difficulties in determining the optimal initial dose for a targeted level (53.0%), inconsistencies between dosing references (43.9%) and a lack of clear hospital guidelines (27.3%). Half of the pharmacists (48.8%) reported that they had helped to interpret the TDM results and recommend vancomycin dose adjustments in >75% of cases. For methicillin-resistant Staphylococcus aureus infection, physicians, and pharmacists reported target trough levels of ~10–15 and 15–20 mg/L, respectively. For suspected moderate/uncomplicated Gram-positive infections physicians tended to prefer a lower trough range of 5–10 mg/L, while pharmacists preferred a range of 10–15 mg/L.Conclusions: Our results demonstrate that clinicians used varying vancomycin dosing guidelines in their practices. The multidisciplinary TDM service in Hong Kong can be improved further by establishing a standardized dosing guideline and implementing a well-structured, evidence-based service protocol. Future work includes conducting drug utilization studies to evaluate real-world antimicrobial usage patterns and the impact on tangible clinical outcomes, and developing pharmacokinetic-guided dose calculator for antimicrobials in critically ill neonates and pediatric patients.

Highlights

  • Ill neonatal and pediatric patients face a higher risk of nosocomial infection due to a combination of immature humoral and cellular immunity and the use of invasive techniques such as central venous catheterization and endotracheal intubation

  • This study aims to collect the expert opinions of clinicians who practice in the neonatal or pediatric intensive care units (NICU/PICUs) of 12 major medical centers in Hong Kong

  • Our results demonstrate that clinicians used varying vancomycin dosing guidelines in their practices

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Summary

Introduction

Ill neonatal and pediatric patients face a higher risk of nosocomial infection due to a combination of immature humoral and cellular immunity and the use of invasive techniques such as central venous catheterization and endotracheal intubation. Selection of antimicrobial therapy for a critically ill patient may vary based on the nature of treatment (empirical or directed), source of infection and/or likely pathogen(s) and susceptibility. The incidence of neonatal sepsis has increased over time in developed countries among very low-birthweight (VLBW) infants, and CoNS has emerged as a major pathogen in this context [2, 3]. In a NICU/PICU setting, empirical vancomycin therapy is commonly initiated in a patient with suspected staphylococcal infections until the susceptibility pattern of the pathogen is confirmed. This study aims to collect the expert opinions of clinicians who practice in the neonatal or pediatric intensive care units (NICU/PICUs) of 12 major medical centers in Hong Kong

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