概括
糖共运输体2 (SGLT2) 抑制剂可以导致外科手术期间的糖尿病酸性酸症 (DKA),这可能是euglycemic或hyperglycemic. 对于在服用SGLT2抑制剂时接受手术的患者来说,及时诊断和管理至关重要.
科学领域:
- 内分泌学 在内分泌学.
- 腎臟病學 (nephrology) 是一種醫學專業.
- 心脏病学 心脏病学
背景情况:
- 糖共运输体2 (SGLT2) 抑制剂越来越多地用于糖尿病,心力衰竭和慢性病.
- 在外科手术期间使用SGLT2抑制剂存在糖尿病酸症 (DKA) 的风险.
研究的目的:
- 为了说明与SGLT2抑制剂相关的外术期DKA的频谱.
- 突出SGLT2抑制剂相关的DKA的诊断和管理挑战.
主要方法:
- 在服用SGLT2抑制剂时经历了术后DKA的四名患者的病例系列介绍.
- 详细描述患者的人口统计,手术程序和DKA特征 (euglycaemic与hyperglycaemic).
主要成果:
- 介绍了与使用SGLT2抑制剂相关的四例外科期DKA病例.
- DKA发生在euglycemic和hyperglycemic形式.
- 一个病例表明,在恢复SGLT2抑制剂治疗后,DKA的复发.
结论:
- 术后使用SGLT2抑制剂带有DKA的风险,这可能是难以诊断的.
- 在接受手术的SGLT2抑制剂患者中,保持对DKA的高度临床怀疑至关重要.
- 对于与SGLT2抑制剂相关的术后DKA,及时治疗至关重要.
相关概念视频
Oral Hypoglycemic Agents: Glinides
747
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...
747
Diabetes Mellitus: Type 2 and Gestational
5.2K
Type 2 diabetes, characterized by insulin resistance, arises when the insulin receptors on cells lose responsiveness to insulin, diminishing the cell's capacity to take up glucose, resulting in elevated blood glucose levels. To receive a diagnosis of Type 2 diabetes, a series of blood glucose tests are necessary to assess whether the blood glucose falls within normal parameters. If the result is out of the normal range, a patient may be diagnosed as prediabetic or diabetic, depending on the...
5.2K
Oral Hypoglycemic Agents: Biguanides and Glitazones
721
Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
721
Dipeptidyl Peptidase 4 Inhibitors
770
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...
770
Hypoglycemia and Glucagon
1.1K
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...
1.1K
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
650
α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
Acarbose and miglitol are...
650


