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Vancomycin Prescribing Practices and Therapeutic Drug Monitoring for Critically Ill Neonatal and Pediatric Patients: A Survey of Physicians and Pharmacists in Hong Kong

机译:批判性新生儿和儿科患者的万古霉素处方和治疗药物监测:香港医师和药剂师的调查

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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.
机译:背景:由于推荐的剂量算法不一致,来自最佳万古霉素给药的偏差可能发生在新生儿和儿科群中。本研究旨在收集香港12主要医疗中心新生儿或儿科重症监护单位(Nicu / Picus)的临床医生的专家意见。方法:这是一个多中心的横截面研究。符合条件的医师和药剂师完成了一个结构化问卷,以确定选择最初间歇性万古霉素给药时它们遇到的挑战。他们还回答了关于万古霉素治疗监测服务(TDM)的问题,包括施用于复杂和简单的感染的经验万古霉素方案的靶向槽水平。结果:共23名医生和43名药剂师完成了调查。报告的最重要的临床参数对于确定初始万古霉素给药的最重要的是肾功能(90.9%),月经/产后年龄(81.8%),体重(66.7%)和可疑/记录病原体(53.0%)。受访者报告了确定目标水平最佳初始剂量(53.0%),给药参考(43.9%)之间不一致的困难等挑战(43.9%)和缺乏明确的医院指南(27.3%)。有一半的药剂师(48.8%)报告说,他们有助于解释TDM结果并推荐VIKOMYCIN剂量调整> 75%的病例。对于耐甲氧西林耐金黄色葡萄球菌感染,医生和药剂师分别报道了靶槽水平分别为〜10-15和15-20 mg / L.对于疑似中/简并复杂的革兰氏阳性感染,医生倾向于更喜欢5-10mg / L的低谷范围,而药剂师优选的范围为10-15mg / L。结论:我们的结果表明,临床医生在其实践中使用不同的万古霉素给药指导方针。通过建立标准化的给药指南并实施一个结构良好的证据的服务协议,可以进一步提高香港的多学科TDM服务。未来的工作包括进行药物利用研究,以评估现实世界的抗菌使用模式和对有形临床结果的影响,以及在批判性新生儿和儿科患者中开发用于抗微生物的药代动力学引导剂量计算器。

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