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毛细管微量采集体位能否促进危重症儿童头孢唑林临床药代动力学研究?

Can capillary microsampling facilitate a clinical pharmacokinetics study of cefazolin in critically ill children?

机构信息

UQ Centre for Clinical Research, The University of Queensland, Brisbane, QLD 4029, Australia.

Department of Paediatric Intensive Care, Queensland Children's Hospital, Brisbane, QLD 4101, Australia.

出版信息

Bioanalysis. 2024;16(16):873-881. doi: 10.1080/17576180.2024.2377912. Epub 2024 Jul 29.

Abstract

Pharmacokinetic studies in children are limited, in part due to challenges in blood sampling. We compare the use of capillary microsampling and conventional sampling techniques in pediatric patients to show results that can be used in the pharmacokinetic analysis of Cefazolin. Paired blood samples (n = 48) were collected from 12 patients (median age/weight 49 months/18 kg). The United States Federal Drug Administration incurred sample reanalysis acceptance criteria was used and identified 79% of paired samples achieved a difference of less than 20% in magnitude with a capillary microsampling bias of -10% (SD 20%). With exclusion of PK outliers, this rose to 88%. Capillary microsampling is reliable, meets acceptance criteria and can be used in pharmacokinetic studies. 12618001469202.

摘要

儿童药代动力学研究有限,部分原因是血液采样存在挑战。我们比较了毛细血管微采样和传统采样技术在儿科患者中的应用,以展示可用于头孢唑林药代动力学分析的结果。从 12 名患者(中位年龄/体重 49 个月/18 公斤)中采集配对血样(n=48)。采用美国食品和药物管理局规定的样本重新分析接受标准,确定 79%的配对样本的幅度差异小于 20%,毛细血管微采样偏差为-10%(SD 20%)。排除药代动力学异常值后,这一比例上升至 88%。毛细血管微采样可靠,符合接受标准,可用于药代动力学研究。12618001469202。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ea5/11457676/a7831d18b099/IBIO_A_2377912_F0001_B.jpg

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