A Journal Article-Based Approach to Understanding the Clinical Aspects of Hypertension
Volume 2 Issue 2
 February 2017
Context and Study Objective
The optimal additional medication in resistant hypertension (persistent hypertension despite 3 agents including an appropriately dosed diuretic) is unknown. This study sought to determine whether spironolactone, bisoprolol, or doxazosin was the most effective agent; the primary endpoint was change in home systolic blood pressure (BP). 

Design, Setting, and Participants
In a double blind fashion, patients received spironolactone (25-50 mg/d), bisoprolol (10mg/d), doxazosin (8 mg/HS), or placebo for 12 weeks in a random but consecutive fashion (no washout period). Inclusion criteria: office systolic pressure >140 mm Hg and home >130 mm Hg despite maximally tolerated doses of an ACE/ARB, a CCB, and thiazide. Exclusion criteria: GFR < 45 cc/min 1.73 m2 or a potassium "outside the normal range." The study sponsor had no role in the trial.
Results
-335 patients were randomized, 230 completed the  study. Mean age 61, 70% male. Ethnicity data not provided, home 148/84 mm Hg, office 157/90 mm Hg,  K 4.1 mEq/L, Cr 1.0 mg/dL, 24hr urine Na 137 mEq.  Baseline ACE/ARB, CCB, thiazide agent/dose were not specified. 
-Figure: All agents resulted in statistically significant reductions in systolic pressure compared to placebo; spironolactone resulted in larger reductions than any other agent (p<0.05).
-Upon trial completion, K was 4.4 mEq/L in the spironolactone arm (unchanged with other agents), Cr 1.1 mg/dL in all groups.
-Discontinuation rates related to gynecomastia/sexual dysfunction, renal impairment, or hyperkalemia were no higher in the spironolactone group. 
Clinical Perspective
-My own experience is compatible with this trial's conclusions. I find 25mg/day of spironolactone has excellent anti-hypertensive efficacy and I've yet to see sexual side effects/gynecomastia at this dose. It's also highly effective in those with metabolic syndrome. My editorial in the Lancet accompanies this article. 
-In those with advanced kidney disease or a baseline K above 4.5 mEq/L, I start at 12.5 mg if I feel the benefits outweigh the risk.  I  monitor elderly patients for evidence of volume depletion given the hemodynamic effects of ACE/ARB, diuretic, and spironolactone triple therapy.
-Because this is the first randomized, placebo-controlled trial for resistant hypertension, I believe it is a landmark study. It enshrines spironolactone as the agent of choice among those already on a diuretic, calcium channel blocker, and ACEi/ARB.
.-The use of home BP readings ensured the presence of resistant hypertension by excluding a white coat effect; the (expected) marked difference between office and home readings reinforces this phenomenon. 
-Limitations: While rates of creatinine elevation and hyperkalemia were insignificant, those with GFR < 45 cc/ mL 1.73 m2 or  elevated pre-trial K  were excluded. It is unclear what thiazide/dose was used; the number of black patients was not specified. 
-Disclosures: None to declare. 
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Creator & Author: Hillel Sternlicht, MD
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