Clinical Pharmacology of Antihypertensive Therapy for the Treatment of Hypertension in CKD
dc.contributor.author | Sinha, Arjun D. | |
dc.contributor.author | Agarwal, Rajiv | |
dc.contributor.department | Medicine, School of Medicine | en_US |
dc.date.accessioned | 2020-07-31T11:35:29Z | |
dc.date.available | 2020-07-31T11:35:29Z | |
dc.date.issued | 2019-05-07 | |
dc.description.abstract | CKD is common and frequently complicated with hypertension both predialysis and in ESKD. As a major modifiable risk factor for cardiovascular disease in this high-risk population, treatment of hypertension in CKD is important. We review the mechanisms and indications for the major classes of antihypertensive drugs, including angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, β-adrenergic blocking agents, dihydropyridine calcium channel blockers, thiazide diuretics, loop diuretics, mineralocorticoid receptor blockers, direct vasodilators, and centrally acting α-agonists. Recent evidence suggests that β-adrenergic blocking agents may have a greater role in patients on dialysis and that thiazide diuretics may have a greater role in patients with advanced CKD. We conclude with sharing our general prescribing algorithm for both patients with predialysis CKD and patients with ESKD on dialysis. | en_US |
dc.eprint.version | Final published version | en_US |
dc.identifier.citation | Sinha, A. D., & Agarwal, R. (2019). Clinical Pharmacology of Antihypertensive Therapy for the Treatment of Hypertension in CKD. Clinical journal of the American Society of Nephrology : CJASN, 14(5), 757–764. https://doi.org/10.2215/CJN.04330418 | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/23467 | |
dc.language.iso | en_US | en_US |
dc.publisher | American Society of Nephrology | en_US |
dc.relation.isversionof | 10.2215/CJN.04330418 | en_US |
dc.relation.journal | Clinical Journal of the American Society of Nephrology | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | PMC | en_US |
dc.subject | Antihypertensive Agents | en_US |
dc.subject | Sodium Chloride Symporter Inhibitors | en_US |
dc.subject | Angiotensin-Converting Enzyme Inhibitors | en_US |
dc.subject | Sodium Potassium Chloride Symporter Inhibitors | en_US |
dc.subject | Calcium Channel Blockers | en_US |
dc.subject | NR3C2 protein | en_US |
dc.subject | Human | en_US |
dc.subject | Receptors | en_US |
dc.subject | Mineralocorticoid | en_US |
dc.subject | Vasodilator Agents | en_US |
dc.subject | Risk factors | en_US |
dc.subject | Pharmacology | en_US |
dc.subject | Clinical | en_US |
dc.subject | Renal dialysis | en_US |
dc.subject | Adrenergic beta-Antagonists | en_US |
dc.subject | Kidney Failure | en_US |
dc.subject | Chronic | en_US |
dc.subject | Hypertension | en_US |
dc.subject | Angiotensin Receptor Antagonists | en_US |
dc.subject | Algorithms | en_US |
dc.subject | Dihydropyridines | en_US |
dc.title | Clinical Pharmacology of Antihypertensive Therapy for the Treatment of Hypertension in CKD | en_US |
dc.type | Article | en_US |
ul.alternative.fulltext | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500954/ | en_US |
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