Department of Surgery, Section of Endocrine Surgery, University of Chicago, Chicago, IL.
Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX.
Surgery. 2019 Jan;165(1):221-227. doi: 10.1016/j.surg.2018.05.085. Epub 2018 Nov 8.
Primary aldosteronism is a common but underdiagnosed cause of hypertension. Patients with this disorder have worse morbidity compared with those with essential hypertension, but with timely diagnosis and appropriate intervention these patients are potentially cured and may have reversal of target organ damage. The goal of this study was to determine if hypertensive patients considered high risk were checked for primary aldosteronism.
We reviewed electronic health records to identify patients age 18 years or older with coexisting hypertension and hypokalemia or hypertension and sleep apnea, then determined if they had been investigated with measurement of aldosterone or renin. We built regression models to identify explanatory variables for screening in these 2 high-risk groups.
Of nearly 37,000 patients with hypertension and hypokalemia, only 2.7% were ever screened for primary aldosteronism. Most opportunities for case detection were during inpatient hospitalizations, yet in this setting, patients were less likely than clinic patients be screened. Similarly, 3.0% of hypertensive patients with sleep apnea were screened since the inclusion of this group in case detection recommendations.
Uptake of practice guidelines by hospital physicians, fueled by support from their specialty societies, may help to identify many more patients with unrecognized primary aldosteronism.
原发性醛固酮增多症是一种常见但未被充分诊断的高血压病因。与原发性高血压患者相比,患有这种疾病的患者发病率更高,但如果及时诊断和适当干预,这些患者有可能被治愈,并且可能逆转靶器官损伤。本研究的目的是确定是否对被认为患有高血压高危的患者进行原发性醛固酮增多症筛查。
我们回顾了电子健康记录,以确定同时患有高血压和低钾血症或高血压和睡眠呼吸暂停的年龄在 18 岁或以上的患者,然后确定他们是否接受过醛固酮或肾素的测量以进行检查。我们建立了回归模型,以确定这 2 个高危人群筛查的解释变量。
在近 37000 名患有高血压和低钾血症的患者中,仅有 2.7%的患者接受过原发性醛固酮增多症筛查。大多数病例检测机会发生在住院期间,但在这种情况下,与门诊患者相比,患者接受筛查的可能性更小。同样,自从将该组纳入病例检测建议以来,仅 3.0%的患有睡眠呼吸暂停的高血压患者接受了筛查。
医院医生采用的实践指南,在其专业协会的支持下,可能有助于发现更多未被识别的原发性醛固酮增多症患者。