危重儿科患者静脉药物稀释度的标准化和特征。

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Laura Torralba-Fernández, Marta García-Palomo, Miguel López de Abechuco-Ruiz, Natalia Ramos-Sánchez, Clara Jiménez-Méndez, Rocío Prieto-Galindo, María Carmen Lorenzo-Lozano, Pablo Aguado-Barroso
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引用次数: 0

摘要

目的:规范儿科重症监护室静脉给药的药物稀释度,并根据其pH值、渗透压和发泡剂性质对这些稀释度进行表征。目的是指导选择最合适的血管通路装置,尽量减少相关并发症,并保留患者的静脉资本。方法:通过药房和儿科部门之间的共识,选择儿科重症监护病房最常用的静脉注射药物。为每种药物建立两种不同的稀释度,然后测定其各自的渗透压和pH值。根据Clark等人提出的分类对每种药物的泡腾性进行评估。此外,血管通路装置的选择由Manrique等人提出的算法指导,该算法考虑了药物的性质、静脉治疗的持续时间和患者的静脉资本状态。结果:共分析了抗菌药(56%)、抗癫痫药(13%)、镇静剂(7%)、利尿剂(7%)、抗炎镇痛药(7%)和其他(10%)30种药物对应的60种稀释度。25%的稀释液至少表现出一种静脉炎的高风险因素(渗透压bbb600 mOsm/L或pH  9),而35%被归类为中等风险(渗透压450-600 mOsm/L或pH 4-5或 > 7.5-9)。只有10%的分析药物被归类为泡腾剂(阿昔洛韦、苯妥英和万古霉素)。9种不同药物的17种稀释度被确定为不应通过外周静脉导管施用,即使是在短期治疗中。其中,15人有引起静脉炎的高风险,2人有中等风险。结论:药物的理化性质(渗透压、pH)和泡沫性是导致小儿危重症患者静脉炎发生的关键因素。药物稀释度的标准化和特征化将有助于选择最合适的血管通路装置,提高静脉治疗的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Standarization and characterization of intravenous drug dilutions in critically ill pediatric patients.

Objective: To standardize the drug dilutions administered intravenously in a Pediatric Intensive Care Unit and to characterize these dilutions based on their pH, osmolarity, and vesicant nature. This aims to guide the selection of the most appropriate vascular access device, minimizing associated complications, and preserving the patient's venous capital.

Methods: Through a consensus between Pharmacy and Pediatric Services, the most frequently administered intravenous drugs in the Pediatric Intensive Care Unit were selected. Two different dilutions were established for each drug, followed by the determination of their respective osmolarity and pH values. The vesicant nature of each drug was assessed according to the classification proposed by Clark et al. Additionally, vascular access device selection was guided by the algorithm proposed by Manrique et al., which considers the drug's properties, the duration of intravenous therapy, and the patient's venous capital status.

Results: A total of 60 dilutions corresponding to 30 drugs from the following therapeutic groups were analyzed: antimicrobials (56%), antiepileptics (13%), sedatives (7%), diuretics (7%), anti-inflammatory and analgesics (7%), and others (10%). Twenty-five percent of the dilutions exhibited at least one high-risk factor for phlebitis (osmolarity >600 mOsm/L or pH < 4 or > 9), while 35% were classified as intermediate risk (osmolarity 450-600 mOsm/L or pH 4-5 or > 7.5-9). Only 10% of the analyzed drugs were classified as vesicants (acyclovir, phenytoin, and vancomycin). Seventeen dilutions of nine different drugs were identified that should not be administered through a peripheral venous catheter, even in short-term treatments. Of these, 15 had a high risk of causing phlebitis, while 2 had an intermediate risk.

Conclusions: The physicochemical properties (osmolarity and pH) and vesicant nature of drugs are key factors contributing to the development of phlebitis in critically ill pediatric patients. Standardizing and characterizing drug dilutions will facilitate the selection of the most appropriate vascular access device, improving the safety and effectiveness of intravenous therapy.

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来源期刊
FARMACIA HOSPITALARIA
FARMACIA HOSPITALARIA PHARMACOLOGY & PHARMACY-
CiteScore
1.90
自引率
21.40%
发文量
46
审稿时长
37 days
期刊介绍: Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.
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