Administration of Direct Oral Anticoagulants Through Enteral Feeding Tubes

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacy Technology Pub Date : 2016-05-13 DOI:10.1177/8755122516646384
J. J. Peterson, J. Hoehns
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引用次数: 15

Abstract

Objective: To review literature regarding direct oral anticoagulants (DOACs) and determine their viability of administration in solution or via enteral tubes. Data Sources: MEDLINE literature searches identified articles published 2007-present using MeSH terms: factor Xa inhibitors, antithrombins, biological availability, and enteral nutrition. Package inserts were included. Manufacturers were asked to provide literature. Study Selection and Data Extraction: We included studies emphasizing bioavailability or enteral administration. Data Synthesis: Dabigatran and edoxaban package inserts recommend against altering the dosage form, and against enteral administration. One rivaroxaban study was identified. Given with food, enteral administration was comparable to the oral tablet. The mean AUC (0.889, 90% CI 86.12-91.84%) was within the equivalency margins; however Cmax (0.820, 90% CI 78.84-85.86%) was slightly below the 80% threshold. One apixaban study was identified. They showed bioequivalence between oral and enteral administration in different vehicles, but decreased bioavailability when crushed tablets were given along with nutritional support. AUC and Cmax were 32% and 19% lower, respectively, when apixaban solution was given via nasogastric (NG) tube with nutritional supplement versus oral administration of solution. Conclusions: Dabigatran capsules should not be altered, due to large variations in drug exposure. Rivaroxaban can be given as oral solution or via NG tube. Larger doses must be given with nutritional supplementation and enteral tubes must not be distal to the stomach. Apixaban can be given as oral solution or via nasogastric or gastric tube on an empty stomach. Food impairs bioavailability of the crushed tablets. There are insufficient data to recommend enteral administration of edoxaban and the package insert recommends against altering tablets.
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经肠内喂养管直接口服抗凝血剂的应用
目的:回顾有关直接口服抗凝剂(DOACs)的文献,并确定其在溶液或肠内管给药方面的可行性。数据来源:MEDLINE文献检索确定2007年至今发表的文章,使用MeSH术语:Xa因子抑制剂、抗凝血酶、生物利用度和肠内营养。包括包装说明书。制造商被要求提供文献资料。研究选择和数据提取:我们纳入了强调生物利用度或肠内给药的研究。资料综合:达比加群和依多沙班的说明书不建议改变剂型,也不建议肠内给药。一项利伐沙班研究被确认。与食物一起给药,肠内给药与口服片剂相当。平均AUC (0.889, 90% CI 86.12-91.84%)在等效范围内;Cmax (0.820, 90% CI 78.84 ~ 85.86%)略低于80%的阈值。一项阿哌沙班研究被确认。在不同的载体中口服和肠内给药表现出生物等效性,但当粉碎片剂与营养支持一起给药时,生物利用度降低。与口服阿哌沙班溶液相比,经鼻胃管加营养补充给予阿哌沙班溶液的AUC和Cmax分别降低32%和19%。结论:达比加群胶囊不应该改变,因为药物暴露有很大的变化。利伐沙班可口服或经胃管给药。必须在营养补充的同时给予更大剂量,肠内管不能离胃很远。阿哌沙班可作为口服溶液或通过鼻胃管或胃管在空腹给予。食物会损害压碎片剂的生物利用度。没有足够的数据来推荐肠内使用依多沙班,包装说明书也不建议更换片剂。
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来源期刊
Journal of Pharmacy Technology
Journal of Pharmacy Technology PHARMACOLOGY & PHARMACY-
CiteScore
1.50
自引率
0.00%
发文量
49
期刊介绍: For both pharmacists and technicians, jPT provides valuable information for those interested in the entire body of pharmacy practice. jPT covers new drugs, products, and equipment; therapeutic trends; organizational, legal, and educational activities; drug distribution and administration; and includes continuing education articles.
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