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Optimizing outcomes with incretin-based therapies: Practical information for nurse practitioners to share with patients

机译:优化基于Incetin的治疗方法:护士从业者与患者分享的实用信息

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Purpose: To introduce the role of incretin therapies and suggest strategies for nurse practitioners to implement them in practice. Data sources: PubMed, Medline, summary of product characteristics/package inserts. Conclusions: Incretin-based therapies offer a new alternative to currently available agents. They provide adequate levels of glycemic control and are associated with low incidence of hypoglycemia and weight gain. Dipeptidyl peptidase-4 inhibitors, for example sitagliptin, have a modest effect on Alc levels (-0.7%) as monotherapy; however, they reduce Alc to a greater extent when combined with metformin (appprox2.0%). Typical starting dose of sitagliptin is 100 mg; dose adjustments are required in subjects with renal complications. Glucagon-like peptide-1 receptor agonists, exenatide and liraglutide, reduce Alc levels (often in excess of 1.5%) and body weight. Exenatide has a starting dose of 5 mug and is not recommended for patients with hepatic impairment or severe/end-stage renal disease. Liraglutide has been found to benefit from a stepwise dose escalation (i.e., 0.6 mg weekly increments) until a 1.8-mg dose is reached. Unlike exenatide, dose adjustments in patients with renal and hepatic complications are not required. Implications for practice: Incretin-based therapies may help to overcome some of the drawbacks of current therapies used to treat type 2 diabetes.
机译:目的:介绍Incetin疗法的作用,并建议护士从业者在实践中实施它们的策略。数据源:PubMed,Medline,产品特性摘要/包装刀片。结论:基于Incetin的疗法为目前可用代理商提供新的替代品。它们提供足够的血糖控制水平,并且与低血糖发病率低和体重增加有关。二肽基肽酶-4抑制剂,例如SitaGlittin对ALC水平(-0.7%)作为单一疗法的效果。然而,当与二甲双胍(Appprox2.0%)结合时,它们在更大程度上减少ALC。典型的SitaGliptin起始剂量为100 mg;肾并发症的受试者需要调节剂量。胰高血糖素类肽-1受体激动剂,exenatide和Liraglutide,降低ALC水平(通常超过1.5%)和体重。艾森肽具有5杯的起始剂量,不推荐用于肝损伤或严重/终末期肾病的患者。已发现黎棱肽可从逐步剂量升级(即0.6mg每周增量)中受益,直至达到1.8mg剂量。与艾塞那肽不同,不需要肾和肝并发症患者的剂量调整。对实践的影响:基于Incetin的疗法可能有助于克服用于治疗2型糖尿病的当前疗法的一些缺点。

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