Key result
Uncontrolled BP in resistant hypertension is linked to ~8% higher MACE+ risk.
Why the study?
Patients with apparent treatment-resistant hypertension are at increased risk of end-organ damage and cardiovascular events, but little is known about the effects of blood pressure control in this population.
Does uncontrolled blood pressure increase the risk of MACE+ in adults with apparent treatment-resistant hypertension?
Cohort (n=33,760)
Yes
Does uncontrolled blood pressure increase the risk of MACE+ in adults with apparent treatment-resistant hypertension?
Suboptimal blood pressure control in apparent treatment-resistant hypertension is associated with significantly increased risks of major adverse cardiovascular events and end-stage renal disease.
Answers are grounded in this paper and cite their sources.
May warrant closer monitoring in apparent resistant hypertension; leaves open whether intensification reduces MACE+ in trials.
Patients with apparent treatment-resistant hypertension (aTRH) are at increased risk of end-organ damage and cardiovascular events. Little is known about the effects of blood pressure (BP) control in this population. Using a national claims database integrated with electronic medical records, the authors evaluated the relationships between uncontrolled BP (UBP; ≥130/80 mmHg) or controlled BP (CBP; <130/80 mmHg) and risk of major adverse cardiovascular events plus (MACE+; stroke, myocardial infarction, heart failure requiring hospitalization) and end-stage renal disease (ESRD) in adult patients with aTRH (taking ≥3 antihypertensive medication classes concurrently within 30 days between January 1, 2015 and June 30, 2021). MACE+ components were also evaluated separately. Multivariable regression models were used to adjust for baseline differences in demographic and clinical characteristics, and sensitivity analyses using CBP <140/90 mmHg were conducted. Patients with UBP (n = 22 333) were younger and had fewer comorbidities at baseline than those with CBP (n = 11 427). In the primary analysis, which adjusted for these baseline differences, UBP versus CBP patients were at an 8% increased risk of MACE+ (driven by a 31% increased risk of stroke) and a 53% increased risk of ESRD after 2.7 years of follow-up. Greater MACE+ (22%) and ESRD (98%) risk increases with UBP versus CBP were seen in the sensitivity analysis. These real-world data showed an association between suboptimal BP control in patients with aTRH and higher incidence of MACE+ and ESRD linked with UBP despite the use of multidrug regimens. Thus, there remains a need for improved aTRH management.
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Bakris et al. (2023) conducted a cohort in Apparent treatment-resistant hypertension (aTRH) (n=33,760). Uncontrolled blood pressure (≥130/80 mmHg) vs. Controlled blood pressure (<130/80 mmHg) was evaluated on Major adverse cardiovascular events plus (MACE+; stroke, myocardial infarction, heart failure requiring hospitalization) (8% increased risk (adjusted)). Uncontrolled blood pressure in patients with apparent treatment-resistant hypertension was associated with an adjusted 8% increased risk of MACE+ compared to controlled blood pressure.
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