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心血管手术后入住重症监护病房患者的药物基因组学检测描述。

Description of Pharmacogenomic Testing Among Patients Admitted to the Intensive Care Unit After Cardiovascular Surgery.

机构信息

Nursing Research Division, Department of Nursing, Mayo Clinic, Rochester, MN, USA.

Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN, USA.

出版信息

J Intensive Care Med. 2021 Nov;36(11):1281-1285. doi: 10.1177/0885066620946303. Epub 2020 Jul 31.

Abstract

BACKGROUND

Pharmacogenomic (PGx) testing has the potential to provide information on specific drug-metabolizing enzymes that may lead to an absence, reduction, or increase in medication effect in patients. There is a paucity of prospective studies examining PGx testing in the intensive care unit (ICU) setting.

RESEARCH AIMS

To (1) obtain a PGx panel in a sample of cardiovascular (CV) surgical patients with a planned ICU stay and identify phenotypes, and (2) identify PGx variants that may inform treatment regimens and may warrant prescribing adjustments.

DESIGN AND METHODS

Descriptive, single cohort cross-sectional design. Adult (≥18 years) CV patients with an anticipated postoperative ICU stay were enrolled from a large Midwestern tertiary academic medical center. Eligible patients provided informed consent at the time of their CV clinic appointment; PGx testing was then ordered. Pharmacogenomic testing consisted of the Focused Pharmacogenomics panel which included 10 genes and 55 medications.

RESULTS

Of the 272 patients screened, 100 (68% male) patients completed PGx testing (mean age 66.2 ± 9.6 years, mean Acute Physiology, Age and Chronic Health Evaluation III score 76.1 ± standard deviation). Pharmacogenomic results were available in the medical record within a median of 52.4 hours (interquartile range: 33.4-80.3). Pharmacogenomic testing results identified 5 poor metabolizers, 26 rapid metabolizers, 5 ultrarapid metabolizers, 6 poor metabolizers, 5 poor to intermediate metabolizers, and 2 rapid metabolizers identified. Overall, 98% of patients had actionable or potentially actionable PGx results, including 82% for warfarin, 65% for propafenone, 65% for tramadol, 46% for oxycodone, 45% for metoprolol, 33% for clopidogrel, 32% for proton pump inhibitors, 25% for statins, and 12% for haloperidol.

CONCLUSIONS

A significant portion of patients had identified genetic variants that may warrant changes in medication management during and after CV-ICU stay. It remains to be seen if PGx testing leads to improvements in ICU patient outcomes.

摘要

背景

药物基因组学(PGx)检测有可能提供有关特定药物代谢酶的信息,这些酶可能导致患者的药物效果缺失、减少或增加。目前,关于重症监护病房(ICU)环境中 PGx 检测的前瞻性研究很少。

研究目的

(1)在计划入住 ICU 的心血管(CV)外科患者样本中获得 PGx 检测结果,并确定表型;(2)确定可能影响治疗方案并需要调整处方的 PGx 变异体。

设计和方法

描述性、单队列横断面设计。从一家大型中西部三级学术医疗中心的 CV 诊所招募了预计术后 ICU 入住的成年(≥18 岁)CV 患者。符合条件的患者在 CV 诊所预约时提供了知情同意;随后,PGx 检测被订购。PGx 检测包括 Focused Pharmacogenomics 检测面板,其中包含 10 个基因和 55 种药物。

结果

在筛查的 272 名患者中,100 名(68%为男性)患者完成了 PGx 检测(平均年龄 66.2 ± 9.6 岁,平均急性生理学、年龄和慢性健康评估 III 评分 76.1 ± 标准差)。PGx 检测结果在医疗记录中的中位时间为 52.4 小时(四分位距:33.4-80.3)。PGx 检测结果鉴定出 5 名慢代谢者、26 名快代谢者、5 名超快代谢者、6 名慢代谢者、5 名慢至中代谢者和 2 名快代谢者。总体而言,98%的患者有可操作或潜在可操作的 PGx 结果,包括 82%的华法林、65%的普罗帕酮、65%的曲马多、46%的羟考酮、45%的美托洛尔、33%的氯吡格雷、32%的质子泵抑制剂、25%的他汀类药物和 12%的氟哌啶醇。

结论

很大一部分患者确定了可能需要改变 CV-ICU 期间和之后药物管理的遗传变异体。PGx 检测是否能改善 ICU 患者的结局仍有待观察。

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