TY - JOUR
T1 - A Subgroup Meta-Analysis Comparing the Renal Denervation Sham-Controlled Randomized Trials Among Those With Resistant and Nonresistant Hypertension
AU - Ahmed, Mohammad
AU - Nudy, Matthew
AU - Bussa, Rahul
AU - Naccarelli, Gerald V.
AU - Filippone, Edward J.
AU - Foy, Andrew J.
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/3/15
Y1 - 2023/3/15
N2 - Renal denervation (RD) has been investigated as an invasive blood pressure (BP) lowering treatment for hypertension (HTN). Resistant HTN (RHTN) has been defined as uncontrolled BP despite use of 3 antihypertensive medications of different classes, including a diuretic, at maximum tolerated doses. The impact of RD on RHTN remains under investigation. Ten sham-controlled trials testing RD were included in this trial-level analysis. A prespecified subgroup analysis was conducted to test whether efficacy of RD differed in patients with and without RHTN. The primary end points were change in 24-hour ambulatory systolic (SBP) and diastolic (DBP) using raw mean difference (RMD) between sham control and RD. Ten studies (6 RHTN and 4 nonresistant HTN) were identified that included 1,544 participants (1,001 RHTN and 543 essential HTN) with cumulative mean age (±SD) of 57 years (±3). Cochran risk of bias assessment showed 69% of the domains to be at low risk of bias. The RMD for 24-hour SBP between RD and sham control was statistically significant for nonresistant HTN trials (–4.19 mm Hg; 95% confidence interval [CI] –6.07 to –2.30) but was not statistically significant for RHTN trials (–1.86 mm Hg; 95% CI – 3.89 to 0.16). Despite the numerical difference in the subgroups, the interaction between subgroups failed to reach statistical significance (p = 0.10). The RMD for 24-hour DBP between RD and sham control was statistically significant for nonresistant HTN trials (–2.60 mm Hg; 95% CI –3.79 to –1.42) but was not statistically significant for RHTN trials (–0.67 mm Hg; 95% CI –1.84 to 0.50). The interaction between subgroups was statistically significant (p = 0.02). Our analysis indicates RD is a less effective intervention for patients with RHTN. These data may be beneficial for clinicians to consider when assessing patients with RHTN for RD.
AB - Renal denervation (RD) has been investigated as an invasive blood pressure (BP) lowering treatment for hypertension (HTN). Resistant HTN (RHTN) has been defined as uncontrolled BP despite use of 3 antihypertensive medications of different classes, including a diuretic, at maximum tolerated doses. The impact of RD on RHTN remains under investigation. Ten sham-controlled trials testing RD were included in this trial-level analysis. A prespecified subgroup analysis was conducted to test whether efficacy of RD differed in patients with and without RHTN. The primary end points were change in 24-hour ambulatory systolic (SBP) and diastolic (DBP) using raw mean difference (RMD) between sham control and RD. Ten studies (6 RHTN and 4 nonresistant HTN) were identified that included 1,544 participants (1,001 RHTN and 543 essential HTN) with cumulative mean age (±SD) of 57 years (±3). Cochran risk of bias assessment showed 69% of the domains to be at low risk of bias. The RMD for 24-hour SBP between RD and sham control was statistically significant for nonresistant HTN trials (–4.19 mm Hg; 95% confidence interval [CI] –6.07 to –2.30) but was not statistically significant for RHTN trials (–1.86 mm Hg; 95% CI – 3.89 to 0.16). Despite the numerical difference in the subgroups, the interaction between subgroups failed to reach statistical significance (p = 0.10). The RMD for 24-hour DBP between RD and sham control was statistically significant for nonresistant HTN trials (–2.60 mm Hg; 95% CI –3.79 to –1.42) but was not statistically significant for RHTN trials (–0.67 mm Hg; 95% CI –1.84 to 0.50). The interaction between subgroups was statistically significant (p = 0.02). Our analysis indicates RD is a less effective intervention for patients with RHTN. These data may be beneficial for clinicians to consider when assessing patients with RHTN for RD.
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U2 - 10.1016/j.amjcard.2022.12.032
DO - 10.1016/j.amjcard.2022.12.032
M3 - Review article
C2 - 36669381
AN - SCOPUS:85146461365
SN - 0002-9149
VL - 191
SP - 119
EP - 124
JO - American Journal of Cardiology
JF - American Journal of Cardiology
ER -