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首页> 外文期刊>藥學雜誌 >Necessity of Personalized Initial Loading Dose Calculation of Teicoplanin by Clinical Pharmacist -Examination of the Utility of Using Systemic Inflammatory Response Syndrome Score-
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Necessity of Personalized Initial Loading Dose Calculation of Teicoplanin by Clinical Pharmacist -Examination of the Utility of Using Systemic Inflammatory Response Syndrome Score-

机译:由临床药剂师个性化计算替考拉宁初始负荷剂量的必要性-检验使用全身性炎症反应综合征评分的效用-

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When teicoplanin (TEIC) is injected at the maintenance dose, a long period is required for achievement of the target plasma trough concentration because of its long elimination half-life. An initial loading dose is necessary for rapid achievement of an effective plasma trough concentration. Thus, we proposed that it is necessary for a pharmacist determine the initial loading dose of TEIC to reach an effective plasma trough concentration rapidly after its administration to a patient. In the present study, we evaluated the effectiveness of initial loading dose determination by pharmacists and physicians by comparing the achievement rate of target plasma trough concentrations (>15 mu g/mL) and expression of adverse effects. Among 61 patients, 34 were treated according to an initial loading dose determined by a pharmacist (pharmacist intervention) and 27 were treated according to the treating physician's discretion (non-pharmacist intervention). The achievement rate of target concentrations was 91.2% (plasma trough concentration 23.3 +/- 5.3 mu g/mL) in the pharmacist intervention group and 25.9% (plasma trough concentration 14.0 +/- 5.9 mu g/mL) in the non-pharmacist intervention group. There was no difference in the incidence of adverse effects between the two groups. Also, we found that systemic inflammatory response syndrome (SIRS) may have a correlation with plasma trough concentrations of TEIC. We suggest that the SIRS score could become a means way of determining initial loading dose. These findings suggest that it is potentially effective for a pharmacist to determine this initial dose in order to rapidly achieve the target plasma trough concentration of TEIC.
机译:当以维持剂量注射替考拉宁(TEIC)时,由于其消除半衰期长,因此需要较长时间才能达到目标血浆谷浓度。初始加载剂量对于快速达到有效血浆谷浓度是必需的。因此,我们建议药剂师有必要确定TEIC的初始加载剂量,以便在向患者给药后迅速达到有效血浆谷浓度。在本研究中,我们通过比较目标血浆谷浓度(> 15μg / mL)的达到率和不良反应的表达,评估了药剂师和医生确定初始负荷剂量的有效性。在61名患者中,有34名根据药剂师确定的初始负荷剂量进行治疗(药剂师干预),而27名根据主治医生的判断进行了治疗(非药剂师干预)。药剂师干预组的目标浓度达标率为91.2%(血浆谷浓度23.3 +/- 5.3μg / mL),非药剂师达到25.9%(血浆谷浓度14.0 +/- 5.9μg/ mL)干预组。两组之间不良反应的发生率没有差异。此外,我们发现全身性炎症反应综合征(SIRS)可能与TEIC的血浆谷浓度相关。我们建议SIRS评分可能成为确定初始负荷剂量的一种手段。这些发现表明,为了快速达到TEIC的目标血浆谷浓度,药剂师确定该初始剂量可能是有效的。

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