Bilen O and Wenger NK. Hypertension management in older adults [version 1; peer review: 5 approved]. F1000Research 2020, 9(Faculty Rev):1003 (https://doi.org/10.12688/f1000research.20323.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
1Division of Cardiology, Department of Medicine, Emory University, Atlanta, GA, USA 2Emory Heart and Vascular Center, Atlanta, GA, USA 3Emory Women’s Heart Center, Atlanta, GA, USA
Ozlem Bilen
Roles:
Writing – Original Draft Preparation
Nanette K. Wenger
Roles:
Writing – Original Draft Preparation,
Writing – Review & Editing
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REVIEWER STATUS
Abstract
Vascular aging leads to arterial hypertension, which is the leading cause of cardiovascular mortality and morbidity in older adults. Blood pressure reduction is effective in reducing the cardiovascular risk and is safe in ambulatory older adults. It is important to note that blood pressure control in this group of patients is challenging because of comorbidities, polypharmacy, and frailty. Choice of pharmacotherapy is not simple and should be individualized.
What are the burden and mechanism of hypertension in older adults?
Vascular aging involves endothelial dysfunction and vascular remodeling. This process leads to an increase in large artery stiffness and isolated systolic hypertension, the predominant form of hypertension in older adults1,2, affecting more than 75% of people older than 75 years in the US2.
Hypertension is not a benign age-related phenomenon and indeed remains the leading cause of preventable cardiovascular mortality and morbidity3–6. The number of older patients continues to increase dramatically to be 8.5% of the world’s current population and this percentage is expected to reach about 17% by 20507. Hence, appropriate management of hypertension in this vulnerable population is crucial.
Do older adults benefit from blood pressure reduction?
Several randomized controlled trials have demonstrated that blood pressure (BP) lowering in systolic hypertension at an older age is effective in reducing the risk of fatal and non-fatal stroke, cardiovascular events, and death8–16.
One of the few interventions shown to reduce mortality risk in older individuals is BP reduction. One of the earlier hypertension trials in this group of individuals was the Hypertension in the Very Elderly Trial (HYVET). Individuals older than 80 years with an initial systolic BP (SBP) greater than 160 mm Hg were assigned to receive either treatment or placebo10. Reduction of BP significantly decreased the incidence of fatal stroke, all-cause mortality, any cardiovascular event, and heart failure. Another important study that included older individuals was the Systolic Blood Pressure Intervention Trial (SPRINT). Patients older than 50 years with SBP greater than 130 mm Hg and at least one additional cardiovascular risk factor (presence of clinical or subclinical cardiovascular disease other than stroke, chronic kidney disease, a Framingham Risk Score for 10-year cardiovascular disease risk of at least 15, or age greater than 75 years) were enrolled. Patients were randomly assigned to intensive SBP lowering (<120 mm Hg) or routine SBP management (<140 mm Hg). The trial was concluded early because of overwhelming evidence of benefit. There was significant reduction of the primary outcome (myocardial infarction, acute coronary syndrome, stroke, congestive heart failure, or cardiovascular death) (5.2% versus 6.8%, hazard ratio [HR] 0.75, 95% confidence interval [CI] 0.64–0.89; P <0.0001). Among patients at least 75 years of age (n = 2,636), primary outcomes for intensive versus routine BP management were 7.7% versus 11.2% (P <0.05). Rates of all-cause mortality were 5.5% versus 8.1%, respectively (P <0.05). There was a significantly increased risk of hypotensive events and metabolic derangements such as hyponatremia with intensive treatment. It is important to note that generalizability of results was limited as patients with diabetes mellitus, history of stroke, and heart failure within 6 months and residents of nursing homes were excluded and less than 40% of patients were female17. The SPRINT trial not only showed the clear benefit of hypertension treatment at an older age but also brought a new perspective to the intensive BP control controversy in this vulnerable population.
Another relevant clinical question when it comes to treating hypertension in older individuals is whether it is beneficial for cognitive function. Longitudinal observational data have shown a strong association between elevated BP and cognitive decline later in life18; indeed, midlife hypertension is considered to be a major risk factor for dementia19.
Whereas several trials demonstrated a lower incidence of dementia with anti-hypertensive treatment in older individuals9,20–22, others failed to show benefit and this was due in part to inadequate duration for follow-up23–25. A recently published sub-study of the SPRINT trial (SPRINT-MIND) did not show a significantly reduced risk of probable dementia with intensive BP control26. The study was terminated early and thus the cases of dementia were fewer than expected, and the study may have been underpowered for this endpoint. However, intensive BP control did significantly reduce the risk of mild cognitive impairment (14.6 versus 18.3 cases per 1000 person-years; HR 0.81, 95% CI 0.69–0.95) and the combined rate of mild cognitive impairment or probable dementia (20.2 versus 24.1 cases per 1000 person-years; HR 0.85, 95% CI 0.74–0.97), which were predefined secondary endpoints.
What is the optimal target blood pressure in older adults?
Although the benefit of hypertension treatment in older adults has been clearly demonstrated, several cross-sectional studies have raised questions about the risk of hypotension and related cerebrovascular accidents, falls, and kidney failure27,28; thus, the safety of BP reduction at an older age has been a controversial topic.
Recent US guidelines recommended initiation of anti-hypertensive drug therapy in older individuals with a BP greater than 130/80 mm Hg29, although the BP target for treatment differed in European guidelines30. This recommendation was based on several anti-hypertensive therapy trials that included large numbers of older individuals31–34. Some patients with mild frailty were also included but most of these patients were ambulatory and able to travel to a clinic. In these trials, cardiovascular morbidity and mortality were reduced during BP lowering with different BP targets, including when the SBP treatment goal was less than 120 mm Hg. However, the risk of adverse outcomes, including orthostatic hypotension or falls, did not increase9,10,12,35. Both HYVET and SPRINT included patients who were frail but still living independently in the community, and both were stopped early for benefit.
Thus, it is fair to say that BP control in ambulatory older patients seems to be safe. However, it is important to recognize that evidence-based recommendations for BP management are lacking in those who are very frail or institutionalized or those with cognitive impairment, several comorbidities, or polypharmacy. There is no evidence in the latter group that anti-hypertensive treatment reduces cardiovascular events or promotes established cognitive dysfunction36, and evidence suggests that such treatment may not be safe37. These individuals might be at risk for adverse consequences; thus, it is important for the clinician to pursue an individualized approach. Clinicians should carefully titrate BP lowering in persons with a high comorbidity burden37–39.
Another important consideration is initiation of anti-hypertensive therapy with two agents. These individuals need to be monitored carefully for orthostatic hypotension and history of falls. BP must be measured both sitting and standing. Older persons may present with neurogenic orthostatic hypotension. This is particularly common in neurodegenerative disorders such as Parkinson’s disease and hence should be taken into consideration.
What are the pharmacologic options for hypertension management in older adults?
Lifestyle measures are important in addition to pharmacotherapy. These include sodium restriction—Dietary Approaches to Stop Hypertension (DASH) diet—and physical activity40. BP control in older adults is challenging because of the presence of other comorbidities, polypharmacy, and frailty. Physicians should individualize management to weigh the benefits and potential harmful effects of such therapy.
Common anti-hypertensive drugs, including diuretics, angiotensin-converting enzyme (ACE) inhibitors, calcium channel blockers, and even beta-blockers, have been shown to be effective in older adults41–44.
It is important to note that each commonly used drug class has additional benefit in the presence of different comorbidities, such as ACE inhibitors in diabetes mellitus and beta-blockers in coronary disease. Decisions should be based on efficacy, tolerability, cost-effectiveness of each drug, and the presence of specific comorbidities and polypharmacy and thus drug interactions.
Beta-blockers should be used cautiously in older patients as these individuals are particularly sensitive to bradycardic effects. The main adverse effects of calcium channel blockers are related to edema and orthostatic hypotension. Also, constipation might be a significant limitation with diltiazem and verapamil. Nitrates are useful during hypertensive emergencies and angina; however, they are not preferred for long-term BP control at an older age. Owing to their side effect profile, peripheral agents such as hydralazine and minoxidil are not first-line agents. A centrally acting agent, clonidine, can be used for BP management. Owing to reflex hypertension when discontinued, oral clonidine is not advised; clonidine patch averts this problem. It has several side effects, including bradycardia and sedation, both of which are problematic in older and frail individuals. Diuretics should be used with caution as urinary incontinence can be a major concern in older adults.
Another important consideration in the management of hypertension in older individuals is to use ambulatory BP monitoring instead of relying on single office measurements. The development of isolated systolic hypertension (and thus wide pulse pressure), white coat effect, different measurements between ambulatory and clinical BP, prevalence of orthostatic hypotension, and medication interactions are among the reasons that necessitate ambulatory BP monitoring45.
Finally, another important consideration is de-escalation of anti-hypertensive medications in patients who are intolerant. The Discontinuation of Anti-hypertensive Treatment in Elderly people (DANTE) study showed that in older individuals with orthostatic hypotension, discontinuation of anti-hypertensives showed significant recovery from orthostasis46. Discontinuation of therapy might also be considered in older patients approaching the end of life, in whom the burden of therapy might exceed the purported benefit.
What are the future considerations?
Randomized clinical trials are needed in frail older individuals with hypertension residing in nursing homes to determine both the benefits and adverse effects of anti-hypertensive drug therapy in this vulnerable population.
Faculty Opinions recommended
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1
Division of Cardiology, Department of Medicine, Emory University, Atlanta, GA, USA 2
Emory Heart and Vascular Center, Atlanta, GA, USA 3
Emory Women’s Heart Center, Atlanta, GA, USA
Ozlem Bilen
Roles:
Writing – Original Draft Preparation
Nanette K. Wenger
Roles:
Writing – Original Draft Preparation,
Writing – Review & Editing
Bilen O and Wenger NK. Hypertension management in older adults [version 1; peer review: 5 approved]. F1000Research 2020, 9(Faculty Rev):1003 (https://doi.org/10.12688/f1000research.20323.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
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Faculty Reviews are commissioned and written by members of the prestigious Faculty Opinions Faculty, and are edited as a service to our readers. In order to make these reviews as comprehensive and accessible as possible, we seek the reviewers’ input before publication. The reviewers’ names and any additional comments they may have are published alongside the review, as is usual on F1000Research.
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Reviewer Report19 Aug 2020
Carl J Lavie,
Department of Cardiovascular Diseases, John Ochsner Heart and Vascular Institute, Ochsner Clinical School, University of Queensland School of Medicine, New Orleans, LA, USA
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Competing Interests: No competing interests were disclosed.
Faculty Reviews are commissioned and written by members of the prestigious Faculty Opinions Faculty, and are edited as a service to our readers. In order to make these reviews as comprehensive and accessible as possible, we seek the reviewers’ input before publication. The reviewers’ names and any additional comments they may have are published alongside the review, as is usual on F1000Research.
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Reviewer Report19 Aug 2020
Suzanne Oparil,
Vascular Biology and Hypertension Program, Division of Cardiovascular Disease, Department of Medicine, School of Medicine, The University of Alabama at Birmingham, Birmingham, AL, USA
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Competing Interests: No competing interests were disclosed.
Faculty Reviews are commissioned and written by members of the prestigious Faculty Opinions Faculty, and are edited as a service to our readers. In order to make these reviews as comprehensive and accessible as possible, we seek the reviewers’ input before publication. The reviewers’ names and any additional comments they may have are published alongside the review, as is usual on F1000Research.
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Reviewer Report19 Aug 2020
George Bakris,
Department of Medicine, Am. Heart Assoc. Comprehensive Hypertension Center, Section of Endocrinology, Diabetes and Metabolism, The University of Chicago Medicine, Chicago, IL, USA
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Competing Interests: No competing interests were disclosed.
Faculty Reviews are commissioned and written by members of the prestigious Faculty Opinions Faculty, and are edited as a service to our readers. In order to make these reviews as comprehensive and accessible as possible, we seek the reviewers’ input before publication. The reviewers’ names and any additional comments they may have are published alongside the review, as is usual on F1000Research.
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