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相关概念视频

Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

327
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
327
Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

179
Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
179
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

157
Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
157
Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

266
Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
266
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

189
Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
189
Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

199
Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into...
199

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Improving IV Insulin Administration in a Community Hospital
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胰岛素水与格拉吉因相关

Jessica Wood1, Varun Samji1, Francesco S Celi2

  • 1Division of Endocrinology, Diabetes and Metabolism, Virginia Commonwealth University Health, Richmond, VA 23298, USA.

JCEM case reports
|December 20, 2023
PubMed
概括

胰岛素,胰岛素治疗的罕见并发症,可以导致显著的液体保留. 切换胰岛素类型,就像在1型糖尿病病例中看到的那样,有效地解决了腿部胀和体重增加.

科学领域:

  • 内分泌学 在内分泌学.
  • 药理学 药理学是指药理学的学科.

背景情况:

  • 胰岛素是胰岛素治疗的罕见并发症,影响1型和2型糖尿病患者.
  • 它通常在开始或加强胰岛素治疗后表现出来,特别是在新诊断或控制不良的情况下.

研究的目的:

  • 在患有1型糖尿病的年轻患者中呈现胰岛素的情况.
  • 为了突出诊断挑战和胰岛素的管理.
  • 为了强调考虑胰岛素胀的重要性,作为在胰岛素治疗期间出现不明原因的胀的患者排除的诊断.

主要方法:

  • 一个病例报告,一名20岁的男性被诊断患有1型糖尿病.
  • 最初的治疗包括胰岛素glargine和lispro,导致双边腿的发展和显著的体重增加.
  • 胰岛素的诊断是在排除其他可能导致的原因之后确立的.
  • 管理涉及从胰岛素格拉吉因切换到胰岛素脱.

主要成果:

  • 患者在开始胰岛素治疗后的几天内出现了显著的双边腿和体重增加.
  • 排除了其他系统性的原因.
  • 切换到胰岛素脱代克导致胀在三天内完全消失.
  • 这表明特定胰岛素配方在胰岛素的发展或解决中可能发挥作用.
关键词:
edemema edemema 胀 胀 在 胀 胀这是一个很好的方法. glargine在这种情况下,胰岛素胰岛素.2型糖尿病是什么?

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结论:

  • 胰岛素是胰岛素治疗的罕见但显著并发症,需要排除诊断.
  • 该案例表明,切换胰岛素配方可以有效地管理和解决胰岛素.
  • 临床医生应该保持对胰岛素的认识,因为胰岛素治疗可能是副作用,特别是在新诊断或控制不良的糖尿病患者中.