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Adrenal vein sampling versus CT scan to determine treatment in primary aldosteronism: an outcome-based randomised diagnostic trial

医学 原发性醛固酮增多症 肾上腺切除术 临床终点 腺瘤 盐皮质激素受体 泌尿科 螺内酯 血压 醛固酮 肾上腺腺瘤 醛固酮增多症 内科学 继发性高血压 人口 随机对照试验 环境卫生
作者
Tanja Dekkers,Aleksander Prejbisz,Leo J. Schultze Kool,Hans Groenewoud,Marieke Velema,Wilko Spiering,Sylwia Kołodziejczyk-Kruk,Mark Arntz,Jacek Kądziela,J.F. Langenhuijsen,Michiel N. Kerstens,Anton H. van den Meiracker,Bert‐Jan H. van den Born,Fred C.G.J. Sweep,A.R.M.M. Hermus,Andrzej Januszewicz,Alike F Ligthart-Naber,Péter Makai,Gert-Jan van der Wilt,Jacques W.M. Lenders,Jaap Deinum
出处
期刊:The Lancet Diabetes & Endocrinology [Elsevier]
卷期号:4 (9): 739-746 被引量:194
标识
DOI:10.1016/s2213-8587(16)30100-0
摘要

Background The distinction between unilateral aldosterone-producing adenoma or bilateral adrenal hyperplasia as causes of primary aldosteronism is usually made by adrenal CT or by adrenal vein sampling (AVS). Whether CT or AVS represents the best test for diagnosis remains unknown. We aimed to compare the outcome of CT-based management with AVS-based management for patients with primary aldosteronism. Methods In a randomised controlled trial, we randomly assigned patients with aldosteronism to undergo either adrenal CT or AVS to determine the presence of aldosterone-producing adenoma (with subsequent treatment consisting of adrenalectomy) or bilateral adrenal hyperplasia (subsequent treatment with mineralocorticoid receptor antagonists). The primary endpoint was the intensity of drug treatment for obtaining target blood pressure after 1 year of follow-up, in the intention-to-diagnose population. Intensity of drug treatment was expressed as daily defined doses. Key secondary endpoints included biochemical outcome in patients who received adrenalectomy, health-related quality of life, cost-effectiveness, and adverse events. This trial is registered with ClinicalTrials.gov, number NCT01096654. Findings We recruited 200 patients between July 6, 2010, and May 30, 2013. Of the 184 patients that completed follow-up, 92 received CT-based treatment (46 adrenalectomy and 46 mineralocorticoid receptor antagonist) and 92 received AVS-based treatment (46 adrenalectomy and 46 mineralocorticoid receptor antagonist). We found no differences in the intensity of antihypertensive medication required to control blood pressure between patients with CT-based treatment and those with AVS-based treatment (median daily defined doses 3·0 [IQR 1·0–5·0] vs 3·0 [1·1–5·9], p=0·52; median number of drugs 2 [IQR 1–3] vs 2 [1–3], p=0·87). Target blood pressure was reached in 39 (42%) patients and 41 (45%) patients, respectively (p=0·82). On secondary endpoints we found no differences in health-related quality of life (median RAND-36 physical scores 52·7 [IQR 43·9–56·8] vs 53·2 [44·0–56·8], p=0·83; RAND-36 mental scores 49·8 [43·1–54·6] vs 52·7 [44·9–55·5], p=0·17) for CT-based and AVS-based treatment. Biochemically, 37 (80%) of patients with CT-based adrenalectomy and 41 (89%) of those with AVS-based adrenalectomy had resolved hyperaldosteronism (p=0·25). A non-significant mean difference of 0·05 (95% CI −0·04 to 0·13) in quality-adjusted life-years (QALYs) was found to the advantage of the AVS group, associated with a significant increase in mean health-care costs of €2285 per patient (95% CI 1323–3248). At a willingness-to-pay value of €30 000 per QALY, the probability that AVS compared with CT constitutes an efficient use of health-care resources in the diagnostic work-up of patients with primary aldosteronism is less than 0·2. There was no difference in adverse events between groups (159 events of which nine were serious vs 187 events of which 12 were serious) for CT-based and AVS-based treatment. Interpretation Treatment of primary aldosteronism based on CT or AVS did not show significant differences in intensity of antihypertensive medication or clinical benefits for patients after 1 year of follow-up. This finding challenges the current recommendation to perform AVS in all patients with primary aldosteronism. Funding Netherlands Organisation for Health Research and Development–Medical Sciences, Institute of Cardiology, Warsaw.
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