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

Summary 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...

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Veröffentlicht in:The lancet. Diabetes & endocrinology 2016-09, Vol.4 (9), p.739-746
Hauptverfasser: Dekkers, Tanja, MD, Prejbisz, Aleksander, MD, Kool, Leo J Schultze, Prof, Groenewoud, Hans J M M, MSc, Velema, Marieke, MD, Spiering, Wilko, MD, Kołodziejczyk-Kruk, Sylwia, MD, Arntz, Mark, MD, Kądziela, Jacek, MD, Langenhuijsen, Johannes F, MD, Kerstens, Michiel N, MD, van den Meiracker, Anton H, MD, van den Born, Bert-Jan, MD, Sweep, Fred C G J, Prof, Hermus, Ad R M M, Prof, Januszewicz, Andrzej, Prof, Ligthart-Naber, Alike F, MD, Makai, Peter, PhD, van der Wilt, Gert-Jan, Prof, Lenders, Jacques W M, Prof, Deinum, Jaap, Dr
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Zusammenfassung:Summary 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 advan
ISSN:2213-8587
2213-8595
DOI:10.1016/S2213-8587(16)30100-0