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2013 ESH/ESC Guidelines for the management of arterial hypertension: the Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC).2013年欧洲高血压学会(ESH)和欧洲心脏病学会(ESC)动脉高血压管理指南:欧洲高血压学会(ESH)和欧洲心脏病学会(ESC)动脉高血压管理特别工作组
J Hypertens. 2013 Jul;31(7):1281-357. doi: 10.1097/01.hjh.0000431740.32696.cc.
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Control of hypertension among adults--National Health and Nutrition Examination Survey, United States, 2005-2008.美国2005 - 2008年国家健康与营养检查调查:成年人高血压控制情况
MMWR Suppl. 2012 Jun 15;61(2):19-25.
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Suitability of measures of self-reported medication adherence for routine clinical use: a systematic review.自我报告药物依从性测量在常规临床应用中的适宜性:系统评价。
BMC Med Res Methodol. 2011 Nov 3;11:149. doi: 10.1186/1471-2288-11-149.
4
Modelling of blood pressure and total cardiovascular risk outcomes after second-line valsartan therapy: the BSCORE study.二线缬沙坦治疗后的血压和总体心血管风险结局建模:BSCORE 研究。
Arch Cardiovasc Dis. 2011 Aug;104(8-9):428-34. doi: 10.1016/j.acvd.2010.12.005. Epub 2011 Feb 22.
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Epidemiology of resistant hypertension.耐药性高血压的流行病学。
J Clin Hypertens (Greenwich). 2011 Jul;13(7):523-8. doi: 10.1111/j.1751-7176.2011.00445.x. Epub 2011 Mar 28.
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Effectiveness of amlodipine-valsartan single-pill combinations: hierarchical modeling of blood pressure and total cardiovascular disease risk outcomes (the EXCELLENT study).氨氯地平-缬沙坦单片复方制剂的疗效:血压和总体心血管疾病风险结局的分层模型分析(EXCELLENT 研究)。
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Real-world effectiveness of valsartan on hypertension and total cardiovascular risk: review and implications of a translational research program.缬沙坦对高血压和总体心血管风险的真实世界疗效:一项转化研究计划的综述与启示
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Medication adherence: WHO cares?药物依从性:谁在乎?
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Selection of a validated scale for measuring medication adherence.选择经过验证的量表来测量药物依从性。
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The psychometric properties and practicability of self-report instruments to identify medication nonadherence in adult transplant patients: a systematic review.自评工具识别成年器官移植患者药物不依从性的心理测量特性和实用性:系统评价。
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使用医生单项目测量法预测血压结果:比利时观察性研究的回顾性汇总分析

Predicting blood pressure outcomes using single-item physician-administered measures: a retrospective pooled analysis of observational studies in Belgium.

作者信息

Villa Lorenzo, Sun Diana, Denhaerynck Kris, Vancayzeele Stefaan, Brié Heidi, Hermans Christine, Aerts Ann, Levengood Michael, MacDonald Karen, Abraham Ivo

机构信息

Faculty of Pharmacy, University of Concepción, Concepción, Chile.

Center for Health Outcomes & PharmacoEconomic Research, College of Pharmacy, The University of Arizona, Tucson, AZ, US.

出版信息

Br J Gen Pract. 2015 Jan;65(630):e9-15. doi: 10.3399/bjgp15X683101.

DOI:10.3399/bjgp15X683101
PMID:25548319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4276010/
Abstract

BACKGROUND

Patient adherence is often not monitored because existing methods of evaluating adherence are either burdensome or do not accurately predict treatment outcomes.

AIM

To examine whether two simple, single-item physician-administered measures of patient adherence to antihypertensive medication are predictive of blood pressure outcomes.

DESIGN AND SETTING

Retrospective database analysis of patients with hypertension treated in Belgian primary care.

METHOD

Using pooled data from five observational studies, a sample was identified of 9725 patients who were assessed using two single-item physician-administered measures of adherence to antihypertensive medication: the first item of the Basel Assessment of Adherence Scale (BAAS) and the Visual Analogue Scale (VAS). These two assessment tools were administered by GPs during regular appointments with patients. Systolic blood pressure (SBP), diastolic blood pressure (DBP), and combined SBP/DBP were measured at baseline and at 90 days.

RESULTS

BAAS-identified adherent patients achieved lower mean SBP and DBP compared with non-adherent patients at 90 days (P<0.001), and had odds ratios of achieving blood pressure control of 0.66 (95% confidence intervals (CI) = 0.61 to 0.73, P<0.001) for SBP, 0.69 (95% CI = 0.62 to 0.76, P<0.001) for DBP, and 0.65 (95% CI = 0.59 to 0.72, P<0.001) for combined SBP/DBP. For VAS-identified adherent patients, the odds ratios of achieving blood pressure control were 0.93 (95% CI = 0.86 to 1.00, P<0.001) for SBP, 0.79 (95% CI = 0.73 to 0.85, P<0.001) for DBP, and 0.91 (95% CI = 0.84 to 0.99, P<0.001) for combined SBP/DBP.

CONCLUSIONS

The first item of the BAAS and the VAS are independent predictors of blood pressure control. These methods can be integrated seamlessly into routine clinical practice by allowing GPs to quickly evaluate a patient's adherence and tailor treatment recommendations accordingly.

摘要

背景

患者依从性通常未得到监测,因为现有的评估依从性的方法要么繁琐,要么无法准确预测治疗结果。

目的

研究两种由医生进行的简单单项患者抗高血压药物依从性测量方法是否能预测血压结果。

设计与背景

对比利时初级保健中治疗的高血压患者进行回顾性数据库分析。

方法

使用来自五项观察性研究的汇总数据,确定了9725例患者的样本,这些患者使用两种由医生进行的单项抗高血压药物依从性测量方法进行评估:巴塞尔依从性评估量表(BAAS)的第一项和视觉模拟量表(VAS)。这两种评估工具由全科医生在与患者的定期预约中使用。在基线和90天时测量收缩压(SBP)、舒张压(DBP)以及综合SBP/DBP。

结果

在90天时,与非依从患者相比,经BAAS确定为依从的患者平均SBP和DBP更低(P<0.001),SBP达到血压控制的比值比为0.66(95%置信区间(CI)=0.61至0.73,P<0.001),DBP为0.69(95%CI = 0.62至0.76,P<0.001),综合SBP/DBP为0.65(95%CI = 0.59至0.72,P<0.001)。对于经VAS确定为依从的患者,SBP达到血压控制的比值比为0.93(95%CI = 0.86至1.00,P<0.001),DBP为0.79(95%CI = 0.73至0.85,P<0.001),综合SBP/DBP为0.91(95%CI = 0.84至0.99,P<0.001)。

结论

BAAS的第一项和VAS是血压控制的独立预测因素。通过让全科医生快速评估患者的依从性并据此调整治疗建议,这些方法可以无缝整合到常规临床实践中。