Bedside mixing of calcium gels for dermal hydrofluoric acid treatment leads to precipitate formation and loss of dissolved calcium.

IF 3.3
Colleen P Cowdery, Steve C Kazmierczak, John A Thompson
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Abstract

Introduction: Hydrofluoric acid is a weak acid with the potential for local and systemic fluoride toxicity. Standard care for dermal exposures includes the application of a topical calcium gel. If a commercially produced 2.5% calcium gel is not available, bedside mixing of one is recommended. We sought to determine whether bedside mixing of a calcium gel can reliably produce a suitable product for the treatment of this exposure.

Methods: A survey was sent to the medical directors of America's Poison Centers® to collect information on current treatment recommendations for dermal hydrofluoric acid exposures. Following this, bedside mixing of a 2.5% calcium gel was attempted with seven brands of water-based gels and one brand of petroleum-based gel. Each brand of gel was mixed in a 3:1 mL ratio with 10% calcium salt solutions (calcium gluconate or calcium chloride) in an attempt to create a 2.5% calcium gel solution. Mixtures were photographed and assessed visually for viscosity and precipitations and were analyzed for final calcium concentration.

Results: Five of seven water-based gels exhibited a rapid loss of gel-like viscosity and immediate development of gross precipitates upon mixing with calcium-containing salts. The mean calcium concentrations in these non-viscous, precipitate-containing mixtures were lower than the expected 2.5% for both calcium gluconate and calcium chloride mixtures. The petroleum-based gel failed to produce a usable mixture when combined with water-based calcium salt solutions.

Discussion: For the majority of gel brands tested in this study, the recommended practice of mixing a 2.5% calcium gel using 10% calcium salt solutions and water-based gels resulted in immediate precipitate formation, loss of gel viscosity, and a reduction in dissolved calcium concentration.

Conclusions: The standard recommendation of mixing a calcium gel at the bedside may result in the production of a non-viscous mixture with a calcium concentration lower than the expected 2.5%.

床边混合用于皮肤氢氟酸治疗的钙凝胶会导致沉淀形成和溶解钙的损失。
简介:氢氟酸是一种弱酸,有可能引起局部和全身氟化物中毒。皮肤暴露的标准护理包括局部应用钙凝胶。如果没有商业生产的2.5%钙凝胶,建议床边混合一种。我们试图确定床边混合钙凝胶是否可以可靠地产生适合治疗这种暴露的产品。方法:向美国中毒中心®的医学主任发送了一份调查,以收集有关皮肤氢氟酸暴露的当前治疗建议的信息。在此之后,将2.5%的钙凝胶与七个品牌的水基凝胶和一个品牌的石油基凝胶进行床边混合。每个牌子的凝胶以3:1 mL的比例与10%的钙盐溶液(葡萄糖酸钙或氯化钙)混合,试图得到2.5%的钙凝胶溶液。对混合物进行拍照,目测粘度和沉淀物,并分析最终钙浓度。结果:七种水基凝胶中有五种在与含钙盐混合后表现出凝胶样粘度的快速损失和立即发展的总沉淀物。在这些无粘性、含有沉淀的混合物中,平均钙浓度低于预期的葡萄糖酸钙和氯化钙混合物的2.5%。当与水基钙盐溶液结合时,石油基凝胶不能产生可用的混合物。讨论:对于本研究中测试的大多数凝胶品牌,推荐的做法是将2.5%钙凝胶与10%钙盐溶液和水基凝胶混合,导致立即形成沉淀,凝胶粘度降低,溶解钙浓度降低。结论:在床边混合钙凝胶的标准建议可能导致钙浓度低于预期的2.5%的无粘性混合物的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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