Division of Nephrology, Department of Medicine, The Chester County Hospital/University of Pennsylvania Health System, Philadelphia, Pennsylvania.
Division of Nephrology, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland.
Kidney360. 2020 Jul 23;1(10):1148-1156. doi: 10.34067/KID.0000922020. eCollection 2020 Oct 29.
Nearly seven decades have elapsed since the clinical and biochemical features of primary hyperaldosteronism (PA) were described by Conn. PA is now widely recognized as the most common form of secondary hypertension. PA has a strong correlation with cardiovascular disease and failure to recognize and/or properly diagnose this condition has profound health consequences. With proper identification and management, PA has the potential to be surgically cured in a proportion of affected individuals. The diagnostic pursuit for PA is not a simplistic endeavor, particularly because an enhanced understanding of the disease process is continually redefining the diagnostic and treatment algorithm. These new concepts have emerged in all areas of this clinical condition, including identification, diagnosis, and treatment. Here, we review the recent advances in this field and summarize the effect these advances have on both diagnostic and therapeutic modalities.
原发性醛固酮增多症(PA)的临床和生化特征由 Conn 描述以来,已经过去了近 70 年。PA 现在被广泛认为是继发性高血压最常见的形式。PA 与心血管疾病密切相关,如果未能识别和/或正确诊断这种疾病,将会产生严重的健康后果。通过适当的识别和管理,PA 有可能在一定比例的受影响个体中通过手术治愈。PA 的诊断并不是一项简单的任务,特别是因为对疾病过程的理解不断深化,正在重新定义诊断和治疗算法。这些新概念出现在这种临床情况的所有领域,包括识别、诊断和治疗。在这里,我们回顾了该领域的最新进展,并总结了这些进展对诊断和治疗方式的影响。