{"title":"Optimal Time to Administer Once-Daily Oral Cardiovascular Agents: Evidence Based on Randomized Clinical Trials in the Last Ten Years","authors":"Zhou Shu-yi, Zhu Ling-ling, Z. Quan","doi":"10.23937/2469-5858/1510057","DOIUrl":null,"url":null,"abstract":"Background: Sporadic studies have investigated the influence of administration time (morning versus evening) on the efficacy and safety of once-daily medications. It is necessary to let clinicians know the developments during the last ten years. Methods: Focusing on chronotherapeutic topic, a literature search on randomized controlled trials (RCTs) of oral oncedaily cardiovascular agents was conducted using PubMed, Cochrane Library, Scopus and Web of Science from Jan 01, 2008 to Sept 30, 2018. Results: Forty-seven RCTs investigated cardiovascular agents. Thirty-five RCTs showed the advantages of evening or bedtime dosing, only one RCT showed the superiority of morning dosing (perindopril for patients with obstructive sleep apnoea and hypertension), and 11 RCTs showed no relationship between dosing time and therapeutic outcomes. Two RCTs reported the difference in occurrence of actual side effects following morning versus evening administration (significantly lower incidence of edema following bedtime dosing of nifedipine rather than morning dosing, significantly lower rate of CKD event following bedtime dosing of ≥ 1 hypertension medications rather than therapy with all medications upon awakening). Rivaroxaban and amlodipine were cases of exhibiting chronopharmacokinetic feature. Factors determining whether to exhibit administration timedependent effects may include disease characteristics, gender, drug combination, treatment course, types of medications, dose, pharmaceutical dosage forms, and outcome measures. Conclusion: Chronotherapy intervention may be considered to improve medication therapy management before attempting to increase dose or add more drugs. Clinicians should educate patients about optimal administration time to take oral oncedaily medications. More RCTs are needed to explore the possibility of optimal dosing time because relevant descriptions are unavailable in prescribing information for many once-daily oral cardiovascular medications.","PeriodicalId":91314,"journal":{"name":"Journal of geriatric medicine and gerontology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of geriatric medicine and gerontology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23937/2469-5858/1510057","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Background: Sporadic studies have investigated the influence of administration time (morning versus evening) on the efficacy and safety of once-daily medications. It is necessary to let clinicians know the developments during the last ten years. Methods: Focusing on chronotherapeutic topic, a literature search on randomized controlled trials (RCTs) of oral oncedaily cardiovascular agents was conducted using PubMed, Cochrane Library, Scopus and Web of Science from Jan 01, 2008 to Sept 30, 2018. Results: Forty-seven RCTs investigated cardiovascular agents. Thirty-five RCTs showed the advantages of evening or bedtime dosing, only one RCT showed the superiority of morning dosing (perindopril for patients with obstructive sleep apnoea and hypertension), and 11 RCTs showed no relationship between dosing time and therapeutic outcomes. Two RCTs reported the difference in occurrence of actual side effects following morning versus evening administration (significantly lower incidence of edema following bedtime dosing of nifedipine rather than morning dosing, significantly lower rate of CKD event following bedtime dosing of ≥ 1 hypertension medications rather than therapy with all medications upon awakening). Rivaroxaban and amlodipine were cases of exhibiting chronopharmacokinetic feature. Factors determining whether to exhibit administration timedependent effects may include disease characteristics, gender, drug combination, treatment course, types of medications, dose, pharmaceutical dosage forms, and outcome measures. Conclusion: Chronotherapy intervention may be considered to improve medication therapy management before attempting to increase dose or add more drugs. Clinicians should educate patients about optimal administration time to take oral oncedaily medications. More RCTs are needed to explore the possibility of optimal dosing time because relevant descriptions are unavailable in prescribing information for many once-daily oral cardiovascular medications.
背景:零星的研究调查了给药时间(早上和晚上)对每日一次药物的疗效和安全性的影响。有必要让临床医生了解过去十年的发展情况。方法:2008年1月1日至2018年9月30日,围绕时间治疗主题,使用PubMed、Cochrane Library、Scopus和Web of Science对每日一次口服心血管药物的随机对照试验(RCT)进行文献检索。结果:47项随机对照试验调查了心血管药物。35项随机对照试验显示了晚上或睡前给药的优势,只有一项随机对照研究显示了早上给药的优越性(培哚普利用于阻塞性睡眠呼吸暂停和高血压患者),11项随机对照实验显示给药时间与治疗结果之间没有关系。两项随机对照试验报告了早晚给药后实际副作用发生率的差异(睡前给药硝苯地平后水肿发生率显著低于早晨给药,睡前给药≥1种高血压药物后CKD事件发生率显著降低,而不是在醒来时用所有药物治疗)。利伐沙班和氨氯地平是表现出时间药代动力学特征的病例。决定是否表现出给药时间依赖性影响的因素可能包括疾病特征、性别、药物组合、疗程、药物类型、剂量、药物剂型和结果指标。结论:在尝试增加剂量或添加更多药物之前,可以考虑采用时间治疗干预来改善药物治疗管理。临床医生应教育患者最佳给药时间,以便每天口服一次药物。需要更多的随机对照试验来探索最佳给药时间的可能性,因为许多每日一次的口服心血管药物的处方信息中没有相关描述。