Nursing Research Division, Department of Nursing, Mayo Clinic, Rochester, MN, USA.
Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN, USA.
J Intensive Care Med. 2021 Nov;36(11):1281-1285. doi: 10.1177/0885066620946303. Epub 2020 Jul 31.
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.
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.
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.
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.
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.
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。
(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。
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。
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。
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。