Characterizing Day 1 Area Under the Curve Following Vancomycin Loading Dose Administration in Adult Hospitalized Patients Using Non-Trapezoidal Linear Pharmacokinetic Equations: A Retrospective Observational Study.

IF 4.7 3区 医学 Q1 INFECTIOUS DISEASES
Infectious Diseases and Therapy Pub Date : 2024-08-01 Epub Date: 2024-06-26 DOI:10.1007/s40121-024-01004-2
Abdulwhab Shremo Msdi, Jacinda C Abdul-Mutakabbir, Karen K Tan
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引用次数: 0

Abstract

Introduction: Methicillin-resistant Staphylococcus aureus (MRSA) infections are a serious threat to public health. Vancomycin (VAN) remains the primary treatment for these infections, and achieving the recommended area under the curve (AUC) target has been linked to improved clinical outcomes. The current VAN therapeutic monitoring guidelines recommend a loading dose (LD) of 20-35 mg/kg to rapidly attain targeted VAN exposures within 24 h of therapy. However, there is a paucity of data describing the impact of VAN LD on day 1 area under the curve (AUC0-24). This study aims to employ pharmacokinetic (PK) equations to calculate and describe the AUC0-24 following a VAN LD of 20 mg/kg.

Methods: This was a retrospective study of adult patients who were loaded with VAN 20 mg/kg, received ≥ 48 h of treatment, and had two consecutive serum VAN levels collected within 24 h. Linear, non-trapezoidal PK equations and two post-infusion VAN levels were used to calculate AUC0-24. Therapeutic AUC0-24 was defined as 400-600 mg/l*h.

Results: Among 123 included patients, the median age was 46 years (IQR 36, 62), 54% (67/123) of the patients had a body mass index (BMI) ≥ 30 kg/m2 and 27% (33/123) were admitted to the intensive care unit (ICU). Following a LD of 20 mg/kg, 50% (61/123) of the patients met the therapeutic AUC0-24, while 22% (27/123) of the patients were subtherapeutic, and 28% (35/123) were supratherapeutic. Compared with patients who achieved therapeutic AUC0-24, patients with subtherapeutic AUC0-24 were more likely to be younger (44 vs. 37 years old) and have a BMI ≥ 30 kg/m2 (67 vs. 52%). In contrast, patients with supratherapeutic AUC0-24 were more likely to be older (64 vs. 44 years old) and to have chronic kidney disease diagnosis (23 vs. 7%) when compared to patients who achieved a therapeutic AUC0-24. CONCLUSIONS: Only 50% of patients achieve the target AUC0-24 following a VAN 20 mg/kg LD, with younger, heavier patients underexposed and older patients with renal impairment overexposed, suggesting that different dosing strategies are needed for these populations.

Abstract Image

使用非梯形线性药代动力学方程描述成人住院患者万古霉素负荷剂量给药后第 1 天的曲线下面积:一项回顾性观察研究。
导言:耐甲氧西林金黄色葡萄球菌(MRSA)感染是对公共卫生的严重威胁。万古霉素(VAN)仍是治疗这类感染的主要药物,达到推荐的曲线下面积(AUC)目标值与临床疗效的改善有关。目前的万古霉素治疗监测指南建议使用 20-35 毫克/千克的负荷剂量 (LD),以便在治疗 24 小时内迅速达到目标万古霉素暴露量。然而,描述 VAN LD 对第 1 天曲线下面积(AUC0-24)影响的数据却很少。本研究旨在采用药代动力学(PK)方程来计算和描述 VAN LD 为 20 mg/kg 后的 AUC0-24:这是一项回顾性研究,研究对象为注射 VAN 20 mg/kg、接受治疗时间≥ 48 小时、在 24 小时内连续采集两次血清 VAN 水平的成年患者。治疗用 AUC0-24 的定义为 400-600 mg/l*h:在纳入的 123 名患者中,中位年龄为 46 岁(IQR 36,62),54%(67/123)的患者体重指数(BMI)≥ 30 kg/m2,27%(33/123)的患者住进了重症监护室(ICU)。LD 为 20 毫克/千克后,50% 的患者(61/123)达到了治疗 AUC0-24,22% 的患者(27/123)处于亚治疗状态,28% 的患者(35/123)处于超治疗状态。与达到治疗量 AUC0-24 的患者相比,治疗量 AUC0-24 以下的患者更年轻(44 岁对 37 岁),体重指数≥ 30 kg/m2 的比例更高(67% 对 52%)。相反,与达到治疗AUC0-24的患者相比,获得超治疗AUC0-24的患者更有可能年龄较大(64岁对44岁),而且更有可能确诊患有慢性肾病(23%对7%)。结论:只有 50% 的患者在服用 VAN 20 mg/kg LD 后达到目标 AUC0-24,年轻、体重较重的患者暴露不足,而有肾功能损害的老年患者则暴露过度,这表明需要针对这些人群采取不同的给药策略。
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来源期刊
Infectious Diseases and Therapy
Infectious Diseases and Therapy Medicine-Microbiology (medical)
CiteScore
8.60
自引率
1.90%
发文量
136
审稿时长
6 weeks
期刊介绍: Infectious Diseases and Therapy is an international, open access, peer-reviewed, rapid publication journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of infectious disease therapies and interventions, including vaccines and devices. Studies relating to diagnostic products and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to, bacterial and fungal infections, viral infections (including HIV/AIDS and hepatitis), parasitological diseases, tuberculosis and other mycobacterial diseases, vaccinations and other interventions, and drug-resistance, chronic infections, epidemiology and tropical, emergent, pediatric, dermal and sexually-transmitted diseases.
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