Physical Compatibility Between Intravenous Magnesium Sulfate and Potassium or Sodium Phosphate in a Pediatric Intensive Care Unit

IF 0.8 Q4 PHARMACOLOGY & PHARMACY Hospital Pharmacy Pub Date : 2024-04-15 DOI:10.1177/00185787241247133
Susana Clemente Bautista, I. Jiménez Lozano, Laura Castellote Belles, C. Parramón-Teixidó, Carme Garcia Esquerda, A. Puertas Sanjuan, Carla Daina Noves, Vanessa Segura Encinas, Maria Josep Cabañas Poy
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Abstract

Objective:To evaluate the physical compatibility between intravenous magnesium sulfate and potassium and sodium phosphate, a common electrolyte intravenous supplementation in pediatric intensive care units. Study design: Magnesium sulfate was mixed separately with potassium phosphate and sodium phosphate at ratios of 1:1, 1:4, and 4:1. Binary mixtures were prepared, in triplicate and under sterile conditions, by permuting the order of addition. The undiluted pure drugs were used as controls for possible sequence effects. Visual changes, turbidity, and pH were assessed immediately after mixing (baseline) and at 4 and 24 hours. Two observers performed visual changes by naked-eye visual inspection in order to search visible haze, particulate matter, gas formation, or color change. Turbidity was measured by nephelometry and incompatibility was defined as an increase of ≥0.5 nephelometric turbidity units (NTU) from baseline. pH was measured using a portable pH meter and incompatibility was defined as a variation of >1 pH unit during the observation period. Results: None of the admixtures exhibited visual changes or significant variations in turbidity (increases of ≥0.5 in nephelometric turbidity units) or pH (changes of >1 unit) during the observation period and neither compared with baseline. Conclusion: In this study, no visual changes were observed, and turbidity and pH evaluated by instrumental methods remained within acceptable limits and showed no significant variations from baseline, therefore no physical incompatibility between magnesium sulfate and potassium or sodium phosphate was found.
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儿科重症监护室静脉注射硫酸镁与磷酸二氢钾或磷酸二氢钠之间的物理兼容性
目的:评估儿科重症监护室静脉注射硫酸镁与钾和磷酸钠(儿科重症监护室常用的电解质静脉补充剂)之间的物理相容性。研究设计:按 1:1、1:4 和 4:1 的比例将硫酸镁分别与磷酸二氢钾和磷酸二氢钠混合。在无菌条件下,通过改变添加顺序制备一式三份的二元混合物。未稀释的纯药物用作对照,以防可能出现的顺序效应。混合后(基线)、4 小时和 24 小时后立即评估视觉变化、浑浊度和 pH 值。两名观察者通过肉眼目测视觉变化,以寻找可见的雾度、颗粒物、气体形成或颜色变化。浊度用浊度计测量,与基线相比浊度增加≥0.5 个浊度单位(NTU)即为不相容;pH 值用便携式 pH 计测量,观察期间 pH 值变化大于 1 个单位即为不相容。结果在观察期间,没有一种混合物的浊度(浊度单位增加≥0.5)或 pH 值(变化大于 1 个单位)与基线相比有视觉变化或显著变化。结论在这项研究中,没有观察到视觉变化,用仪器方法评估的浊度和 pH 值保持在可接受的范围内,与基线相比也没有显著变化,因此没有发现硫酸镁与磷酸二氢钾或磷酸二氢钠之间存在物理不相容性。
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来源期刊
Hospital Pharmacy
Hospital Pharmacy PHARMACOLOGY & PHARMACY-
CiteScore
1.70
自引率
0.00%
发文量
63
期刊介绍: Hospital Pharmacy is a monthly peer-reviewed journal that is read by pharmacists and other providers practicing in the inpatient and outpatient setting within hospitals, long-term care facilities, home care, and other health-system settings The Hospital Pharmacy Assistant Editor, Michael R. Cohen, RPh, MS, DSc, FASHP, is author of a Medication Error Report Analysis and founder of The Institute for Safe Medication Practices (ISMP), a nonprofit organization that provides education about adverse drug events and their prevention.
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