TY - JOUR
T1 - Bedtime dosing of antihypertensive medications
T2 - systematic review and consensus statement: International Society of Hypertension position paper endorsed by World Hypertension League and European Society of Hypertension
AU - Stergiou, George
AU - Brunström, Mattias
AU - MacDonald, Thomas
AU - Kyriakoulis, Konstantinos G.
AU - Bursztyn, Michael
AU - Khan, Nadia
AU - Bakris, George
AU - Kollias, Anastasios
AU - Menti, Ariadni
AU - Muntner, Paul
AU - Orias, Marcelo
AU - Poulter, Neil
AU - Shimbo, Daichi
AU - Williams, Bryan
AU - Adeoye, Abiodun Moshood
AU - Damasceno, Albertino
AU - Korostovtseva, Lyudmila
AU - Li, Yan
AU - Muxfeldt, Elizabeth
AU - Zhang, Yuqing
AU - Mancia, Giuseppe
AU - Kreutz, Reinhold
AU - Tomaszewski, Maciej
N1 - Funding Information:
The authors would like to thank the support from National Natural Science Foundation of China (Grant No. 51976028), the Education Department of Jilin Province (Grant Nos. JJKH20220102CY and JJKH20190698KJ), and Jilin Science and Technology Bureau (Grant No. 20190104142).
Publisher Copyright:
© 2022 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2022/10
Y1 - 2022/10
N2 - Antihypertensive drug therapy is one of the most efficient medical interventions for preventing disability and death globally. Most of the evidence supporting its benefits has been derived from outcome trials with morning dosing of medications. Accumulating evidence suggests an adverse prognosis associated with night-time hypertension, nondipping blood pressure (BP) profile and morning BP surge, with increased incidence of cardiovascular events during the first few morning hours. These observations provide justification for complete 24-h BP control as being the primary goal of antihypertensive treatment. Bedtime administration of antihypertensive drugs has also been proposed as a potentially more effective treatment strategy than morning administration. This Position Paper by the International Society of Hypertension reviewed the published evidence on the clinical relevance of the diurnal variation in BP and the timing of antihypertensive drug treatment, aiming to provide consensus recommendations for clinical practice. Eight published outcome hypertension studies involved bedtime dosing of antihypertensive drugs, and all had major methodological and/or other flaws and a high risk of bias in testing the impact of bedtime compared to morning treatment. Three ongoing, well designed, prospective, randomized controlled outcome trials are expected to provide high-quality data on the efficacy and safety of evening or bedtime versus morning drug dosing. Until that information is available, preferred use of bedtime drug dosing of antihypertensive drugs should not be routinely recommended in clinical practice. Complete 24-h control of BP should be targeted using readily available, long-acting antihypertensive medications as monotherapy or combinations administered in a single morning dose.
AB - Antihypertensive drug therapy is one of the most efficient medical interventions for preventing disability and death globally. Most of the evidence supporting its benefits has been derived from outcome trials with morning dosing of medications. Accumulating evidence suggests an adverse prognosis associated with night-time hypertension, nondipping blood pressure (BP) profile and morning BP surge, with increased incidence of cardiovascular events during the first few morning hours. These observations provide justification for complete 24-h BP control as being the primary goal of antihypertensive treatment. Bedtime administration of antihypertensive drugs has also been proposed as a potentially more effective treatment strategy than morning administration. This Position Paper by the International Society of Hypertension reviewed the published evidence on the clinical relevance of the diurnal variation in BP and the timing of antihypertensive drug treatment, aiming to provide consensus recommendations for clinical practice. Eight published outcome hypertension studies involved bedtime dosing of antihypertensive drugs, and all had major methodological and/or other flaws and a high risk of bias in testing the impact of bedtime compared to morning treatment. Three ongoing, well designed, prospective, randomized controlled outcome trials are expected to provide high-quality data on the efficacy and safety of evening or bedtime versus morning drug dosing. Until that information is available, preferred use of bedtime drug dosing of antihypertensive drugs should not be routinely recommended in clinical practice. Complete 24-h control of BP should be targeted using readily available, long-acting antihypertensive medications as monotherapy or combinations administered in a single morning dose.
KW - ambulatory blood pressure monitoring
KW - antihypertensive drugs
KW - bedtime administration
KW - chronotherapy
KW - dipper
KW - nocturnal blood pressure
KW - ambulatory blood pressure
KW - blood pressure
KW - chronic kidney disease
KW - Controlled Onset Verapamil Investigation of Cardiovascular End Points
KW - Hellenic-Anglo Research into Morning or Night Antihypertensive Drug Delivery
KW - major adverse cardiovascular events
KW - obstructive sleep apnoea
KW - Medication-event monitoring system
KW - Treatment In Morning vs. Evening
KW - Prospective Open-label Blinded-endpoint
KW - Preferred Reporting Items for Systematic reviews and Meta-Analyses
KW - systematic review
UR - http://www.scopus.com/inward/record.url?scp=85137137234&partnerID=8YFLogxK
U2 - 10.1097/HJH.0000000000003240
DO - 10.1097/HJH.0000000000003240
M3 - Article
C2 - 35983870
SN - 0263-6352
VL - 40
SP - 1847
EP - 1858
JO - Journal of Hypertension
JF - Journal of Hypertension
IS - 10
ER -