| Literature DB >> 26664130 |
Joosup Kim1, Amanda G Thrift2, Mark R Nelson3, Christopher F Bladin4, Dominique A Cadilhac1.
Abstract
There are many recommended pharmacological and non-pharmacological therapies for the prevention of stroke, and an ongoing challenge is to improve their uptake. Personalized medicine is seen as a possible solution to this challenge. Although the use of genetic information to guide health care could be considered as the apex of personalized medicine, genetics is not yet routinely used to guide prevention of stroke. Currently personalized aspects of prevention of stroke include tailoring interventions based on global risk, the utilization of individualized management plans within a model of organized care, and patient education. In this review we discuss the progress made in these aspects of prevention of stroke and present a case study to illustrate the issues faced by health care providers and patients with stroke that could be overcome with a personalized approach to the prevention of stroke.Entities:
Keywords: education; personalized health care; prevention; stroke
Mesh:
Substances:
Year: 2015 PMID: 26664130 PMCID: PMC4671759 DOI: 10.2147/VHRM.S77571
Source DB: PubMed Journal: Vasc Health Risk Manag ISSN: 1176-6344
Issues with the prevention of stroke and their potential solutions
| Issues | Potential solutions |
|---|---|
| Knowledge gaps and misconceptions | Educational interventions |
| Poor adherence | Educational interventions |
| • Forgetfulness | Regular review |
| • Cost of therapy | |
| • Side effects | |
| Communication with health care providers and continuity of care | Individualized management programs with regular review |
Summary of meta analyses of antihypertensive, antiplatelet, anticoagulant, and cholesterol lowering drugs used for secondary prevention in patients with stroke and TIA
| Study, year | Type of patients | Primary outcome | Treatment | Control | RRR with treatment % (CI) |
|---|---|---|---|---|---|
| Lakhan and Sapko, 2009 | Stroke, TIA | Stroke, MI, VD | Blood pressure-lowering | Placebo | 31 (14–43) |
| Manktelow and Potter, 2009 | Stroke, TIA | Stroke | Statin | Placebo | 12 (0–23) |
| Algra and van Gijn, 1999 | Non-disabling stroke, TIA | Stroke, MI, VD | Aspirin | Placebo | 13 (6–19) |
| Halkes et al, 2008 | Ischemic stroke, TIA | Stroke, MI, VD | Aspirin + MR-DP | Aspirin | 18 (8–28) |
| Saxena and Koudstaal, 2004 | NRAF and minor ischemic stroke or TIA | Stroke, MI, VD | Warfarin | Aspirin | 33 (9–50) |
| Ntaios et al, 2012 | NRAF and stroke or TIA | Stroke, systemic embolism | NOACs | Warfarin | 15 (1–26) |
Abbreviations: TIA, transient ischemic attack; MI, myocardial infarction; VD, vascular death; NRAF, non-rheumatic atrial fibrillation; MR-DP, modified-release dipyridamole; RRR, relative risk reduction; CI, confidence interval; NOACs, new oral anticoagulants.
Randomized controlled trials of programs for risk management of patients with coronary heart disease involving general practitioners
| Study, year | n | Follow-up | Primary outcome measure | Significant primary outcome results |
|---|---|---|---|---|
| Murchie et al, 2003 | 1,343 | 5 years | – Improvements in prescription of secondary prevention therapies | – Improved pharmacological and lifestyle management |
| – Total mortality | – Decreased risk of mortality | |||
| – Coronary events | – Decreased risk of coronary events | |||
| Munoz et al, 2007 | 983 | 3 years | – Readmission for unstable angina, AMI, heart failure, arrhythmias, stroke, or coronary artery revascularization | – Nil |
| Khunti et al, 2007 | 1,316 | 1 year | – Prescription of β-blocker for patients with AMI | – More patients with AMI prescribed β-blocker |
| – Total cholesterol <5 mmol/L for patients with CHD | – More patients with CHD cholesterol <5 mmol/L | |||
| – Prescription of ACEI for patients with LVSD | ||||
| Wood et al, 2008 | 1,940 | 1 year | – Blood pressure | – Reduced blood pressure |
| – Blood lipids and glucose | – Reduced low-density lipoprotein levels | |||
| – Prescription of secondary prevention medications | – Increased prescriptions to statins | |||
| Murphy et al, 2009 | 903 | 18 months | – Target levels for blood pressure and cholesterol | – Decreased hospitalization |
| – Hospital admission | ||||
| – Changes in physical and mental health status |
Note:
Patients with coronary heart disease and chronic heart failure.
Abbreviations: AMI, acute myocardial infarction; CHD, coronary heart disease; LVSD, left ventricular systolic dysfunction; ACEI, ACE inhibitor.
Randomized controlled trials of programs for risk management of patients with stroke involving general practitioners
| Study, year | n | Follow-up | Primary outcome measure | Significant primary outcome results |
|---|---|---|---|---|
| Ellis et al, 2005 | 205 | 5 months | – Risk factors: SBP; DBP; total cholesterol; HbA1c | – Nil |
| – Combined risk factor control | ||||
| Joubert et al, 2009 | 186 | 1 year | – Blood pressure level | – Reduction in SBP |
| Allen et al, 2009 | 380 | 6 months | – Risk factor control: SBP >140 mmHg; DBP >90 mmHg; total cholesterol >180 mg/dL; HbA1c >6.5% | – Improved knowledge of stroke and behaviors for stroke risk reduction |
| – Proportion of participants on anticoagulants | ||||
| – Proportion of participants using method for medication compliance | ||||
| Wolfe et al, 2010 | 523 | 1 year | – Prescription of antihypertensive medication | – Nil |
| – Antiplatelet drug prescription | ||||
| – Smoking cessation | ||||
| Flemming et al, 2013 | 41 | 1 year | – Change in cardiovascular risk factors (SBP; LDL; HDL; triglycerides; HbA1c; BMI; Framingham cardiovascular risk score) | – Reduction in LDL, Framingham cardiovascular risk score, and SBP |
| – Achievement of targets for cardiovascular risk factors | ||||
| – Number of vascular events | ||||
| – Adherence to secondary prevention medication |
Abbreviations: SBP, systolic blood pressure; DBP, diastolic blood pressure; HbA1c, glycated hemoglobin; LDL, low-density lipoprotein; HDL, high-density lipoprotein; BMI, body mass index.