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. 2020 Nov 13;39(4):759–765. doi: 10.1097/HJH.0000000000002708

TABLE 2.

Outcomes at 6 months, observed values (n = 28) and after imputations for missing values (n = 30)

Needle type
Umbrella-shaped (N = 25) Single needle (N = 5) Total (N = 30)
Primary outcome
n successb/N total (%) [95% CI] 13/24 (54.2%) [32.8–74.4%] 1/4 (25.0%) [0.6–80.6%] 14/28 (50.0%) [30.6–69.4%]
n successb/N totala (%) [95% CI] 13/25 (52.0%) [31.3–72.2%] 1/5 (20.0%) [0.5–71.6%] 14/30 (46.7%) [28.3–65.7%]
Secondary outcomes
 Potassium ≥3.6 mmol/l without potassium supplementation, n (%) [95% CI] 18/21 (85.7%) [63.7–97.0%] 0/2 (0%) [0–84.2%] 18/23 (78.3%) [56.3–92.5%]
 Potassium ≥3.6 mmol/l without potassium supplementationa, n (%) [95% CI] 21/25 (84.0%) [63.9–95.5%] 0/5 (0%) [0–52.2%] 21/30 (70.0%) [50.6–85.3%]
 Normalized aldosterone-to-renin ratio, n (%) [95% CI] 19/19 (100%) [82.4–100%] 0/2 (0%) [0–84.2%] 19/21 (90.5%) [69.6–98.8%]
 Normalized aldosterone-to-renin ratioa, n (%) [95% CI] 23/25 (92.0%) [74.0–99.0%] 0/5 (0%) [0–52.2%] 23/30 (76.7%) [57.7–90.1%]

CI, confidence interval.

a

After imputation of missing outcomes.

b

Successes are defined as daytime SBP/DBP less than 135/85 mmHg at 6 months measured by ABPM without antihypertensive treatment or a decrease in daytime SBP of 20 mmHg or of DBP of 10 mmHg between baseline and 6 months.