Optimal use of beta-blockers in high-risk hypertension: a guide to dosing equivalence. (41/205)

Hypertension is the number one diagnosis made by primary care physicians, placing them in a unique position to prescribe the antihypertensive agent best suited to the individual patient. In individuals with diabetes mellitus, blood pressure (BP) levels>130/80 mmHg confer an even higher risk for cardiovascular and renal disease, and these patients will benefit from aggressive antihypertensive treatment using a combination of agents. beta-blockers are playing an increasingly important role in the management of hypertension in high-risk patients. beta-blockers are a heterogeneous class of agents, and this review presents the differences between beta-blockers and provides evidence-based protocols to assist in understanding dose equivalence in the selection of an optimal regimen in patients with complex needs. The clinical benefits provided by beta-blockers are only effective if patients adhere to medication treatment long term. beta-blockers with proven efficacy, once-daily dosing, and lower side effect profiles may become instrumental in the treatment of hypertensive diabetic and nondiabetic patients.  (+info)

Quantifying antibiotic use in paediatrics: a proposal for neonatal DDDs. (42/205)

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Current dosing of low-molecular-weight heparins does not reflect licensed product labels: an international survey. (43/205)

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Does safe dosing of iodinated contrast prevent contrast-induced acute kidney injury? (44/205)

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Vancomycin pharmacokinetics and pharmacodynamics during short daily hemodialysis. (45/205)

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Safety, tolerability, and immunologic effects of a food allergy herbal formula in food allergic individuals: a randomized, double-blinded, placebo-controlled, dose escalation, phase 1 study. (46/205)

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Vancomycin dosing assessment in intensive care unit patients based on a population pharmacokinetic/pharmacodynamic simulation. (47/205)

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Prospective alpha allocation in the Clarification of Optimal Anticoagulation through Genetics (COAG) trial. (48/205)

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