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Preferences for Antihypertensive Prescribing in Older Adults: A Discrete Choice Experiment
Edel O'Hagan1, Ann Livingstone2, Thomas Gadsden3
1Westmead Applied Research Centre, Faculty of Medicine and Health, The University of Sydney, Westmead, New South Wales, Australia.
Background:
Understanding which attributes influence blood pressure (BP) prescribing, and the magnitude of their effects, could inform strategies to reduce clinical inertia in older adults.
Objectives:
The purpose of this study was to examine doctors' preferences and trade-offs when deciding to intensify antihypertensive treatment in adults aged ≥65 years with uncontrolled BP.
Methods:
We conducted a discrete choice experiment with Australian doctors, presenting hypothetical patient profiles varying by age, frailty, fall history, residual cardiovascular risk, and availability of digital health monitoring. Doctors chose between 2 systolic BP targets: intensive (≤130 mm Hg) or standard (131-150 mm Hg). A mixed multinomial logit model was used to estimate attribute effects, and latent class analysis to explore heterogeneity in preferences.
Results:
Overall, doctors favored the intensive treatment target (OR: 2.70; 95% CI: 1.84-9.96) but this preference decreased with increasing patient age (eg, age 80; OR: 0.05; 95% CI: 0.03-0.07), recent falls (OR: 0.22; 95% CI: 0.16-0.29), and moderate frailty (OR: 0.24; 95% CI: 0.12-0.46). Higher residual cardiovascular risk reduced the likelihood of intensive treatment, whereas digital health availability increased it (OR: 1.50; 95% CI: 1.05-2.15). Latent class analysis identified 2 groups: risk tolerant, digitally engaged (64%), who preferred intensive treatment and were responsive to digital data, and risk-averse (36%), with no overall preference and were unaffected by digital information.
Conclusions:
Clinicians' decisions to intensify antihypertensive treatment in older adults are influenced by age, falls, frailty, perceived benefit, and access to digital monitoring data. Use of digital health interventions may reduce clinical inertia and should be evaluated in clinical trials.
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