Medical Treatment to Prevent Transient Ischemic Attacks and Ischemic Stroke



Medical Treatment to Prevent Transient Ischemic Attacks and Ischemic Stroke



Ido Weinberg and Michael R. Jaff


The distinction between a transient ischemic attack (TIA) and stroke is made by duration of symptoms: The duration of a TIA is less than 24 hours. A TIA is a harbinger of stroke in up to 17% of patients, most often during the first week after the event. Ischemic stroke accounts for 88% of all strokes. Classic subtypes of stroke have been well defined (Box 1). More than 75% of strokes are first events, allowing an opportunity for meaningful intervention.




Modification of Risk Factors


The risk for stroke and TIA is affected by various modifiable and nonmodifiable risk factors (Box 2). Treatment recommendations have been established (Table 1).





Hypertension


Hypertension is related to stroke in a graded, continuous manner, and stroke risk is increased even when blood pressure levels are considered normal by current guidelines. Patients with prehypertension should be encouraged to control their pressure with nonpharmacologic lifestyle measures. The Joint National Committee (JNC) 7 guidelines for the classification and treatment of hypertension have been published (Table 2).



TABLE 2


Classification and Treatment of Blood Pressure



































Classification Systolic Blood Pressure (mm Hg) Diastolic Blood Pressure (mm Hg) No Compelling Indication With Compelling Indication
Normal <120 <80 No antihypertensive drug No antihypertensive drug
Prehypertension 120–139 80–89 No antihypertensive drug Drugs for compelling indication
Stage I hypertension 140–159 90–99 Thiazide-type diuretic for most; may consider ACEI, ARB, CCB, BB, or combination Drugs for compelling indication, other drugs as needed
Stage II hypertension ≥160 ≥100 Two-drug combination for most, usually a thiazide diuretic and a choice of ACEI, ARB, CCB, or BB Drugs for compelling indication, other drugs as needed


image


ACEI, Angiotensin converting enzyme inhibitor; ARB, angiotensin receptor blocker; BB, β-blocker; CCB, calcium channel blocker.


Lifestyle modifications are encouraged for all and include weight reduction for overweight patients, limitation of ethanol intake, increased aerobic physical activity (30–45 minutes daily), reduction of sodium intake (2.34 g), maintenance of adequate dietary potassium (120 mmol/day), smoking cessation, and DASH diet (rich in fruits, vegetables, and low-fat dairy products and reduced in saturated and total fat).


From Goldstein LB, Bushnell CD, Adams RJ, et al: Guidelines for the primary prevention of stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association, Stroke 42:517–584, 2011. Used with permission. ©2011 American Heart Association, Inc.


A meta-analysis of 29 trials including 162,341 patients concluded that stroke risk is effectively reduced by lowering pressure (23%; 95% confidence interval [CI], 5%–37%). Most of the effect was not a direct result of the chosen pharmacologic regimen but rather was secondary to absolute reduction of blood pressure. Calcium channel blocker–based regimens showed a trend toward better efficacy when compared with β-blocker, diuretic-based (7%; CI, 1%–14%), or angiotensin converting enzyme (ACE) inhibitor–based regimens (12%; CI, 1%–25%). Current guidelines suggest that blood pressure should be maintained below 140/90 mm Hg in asymptomatic patients with extracranial carotid or vertebral artery atherosclerosis.




Diabetes Mellitus


Diabetes mellitus (DM) increases the risk of ischemic stroke. Three large-scale trials—ACCORD (Action to Control Cardiovascular Risk in Diabetes), ADVANCE (Action in Diabetes and Vascular Disease), and VADT (Veterans Affairs Diabetes Trial)—have failed to show a protective effect for intensive glucose control to near-normal hemoglobin A1c levels in patients with type 2 DM. Ten-year follow-up of the UKPDS (United Kingdom Prospective Diabetes Study) also failed to show a reduction in stroke risk with less-intensive glucose control compared with conventional therapy. The STENO-2 trial was a small but elegant trial in which 160 patients with type 2 DM were assigned to intensive or conventional therapy. Intensive therapy targeted glycosylated hemoglobin, fasting lipids, and blood pressure and included ACE inhibitors for patients with microalbuminuria and aspirin for primary prevention. Though no statistical significance was reported after over 13 years of surveillance, there were six stroke events in the intensive treatment group and 30 in the conventional group. Furthermore, there was an overall reduction in cardiovascular death (p = .04) and cardiovascular events (p < 0.001).


EDIC (Epidemiology of Diabetes Interventions and Complications), the long-term follow-up of the DCCT (Diabetes Control and Complications Trial) examined the long-term effects of intensive glycemic control in patients with type 1 DM. Intensive treatment was administered as part of the DCCT over 6.5 years, and in EDIC patients were all treated in a similar, intensive, fashion. After 11 years of follow-up, patients who had received prior intensive treatment had a 57% reduced combined cardiovascular event rate including myocardial infarction, stroke, and death from a cardiovascular cause. In addition to controlling diabetes, other cardiovascular risk factors should be managed aggressively in diabetic patients (see Table 1). Antiplatelet agents have not been consistently shown to be of value for primary prevention of stroke in patients with diabetes and are discussed in more detail later.

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Aug 25, 2016 | Posted by in CARDIOLOGY | Comments Off on Medical Treatment to Prevent Transient Ischemic Attacks and Ischemic Stroke

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