White River Health System, Batesville, AR, USA.
J Investig Med High Impact Case Rep. 2020 Jan-Dec;8:2324709620982440. doi: 10.1177/2324709620982440.
Bartter syndrome is a rare disorder that is characterized by weakness and fatigue with laboratory findings of hypokalemia and metabolic alkalosis with increased aldosterone and angiotensin. It specifically acts on the ascending loop of Henle, characterized by miscoded proteins affecting NaCl transports and channels. Patients will require replacement of potassium and sometimes magnesium due to the kidneys' inability to reabsorb these ions. So what happens when the body's other primary mechanism of absorption of these elements are taken out? In this article, we present the case of a 47-year-old woman with Bartter syndrome on oral potassium 40 mg BID (twice a day) and magnesium oxide 800 TID (thrice a day), who recently had a small bowel resection that required intravenous potassium and magnesium throughout her hospital admission. Significant questions arose as to how her electrolytes should be managed, given her unusual presentation with rare underlying disorder. We discuss the implications of her bowel resection in the context of Bartter syndrome and our views on her future course based on available literature.
巴特综合征是一种罕见的疾病,其特征是乏力和疲劳,实验室检查发现低钾血症和代谢性碱中毒,醛固酮和血管紧张素增加。它主要作用于亨利氏上升襻,特征是编码错误的蛋白质影响 NaCl 的转运和通道。由于肾脏无法重吸收这些离子,患者将需要补充钾,有时还需要补充镁。那么,当身体吸收这些元素的其他主要机制被去除时会发生什么呢?在本文中,我们介绍了一位 47 岁的女性患者的病例,她患有巴特综合征,口服钾 40mgbid(每天两次)和氧化镁 800tid(每天三次),最近因小肠切除而需要在整个住院期间静脉补充钾和镁。由于她的罕见基础疾病表现异常,出现了如何管理她的电解质的重大问题。我们根据现有文献讨论了她的肠切除术在巴特综合征中的意义,以及我们对她未来病程的看法。