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Ambulatory Blood Pressure Patterns in Children With Chronic Kidney Disease

Joshua SamuelsFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PADerek K. NgFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PAJoseph T. FlynnFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PAMark MitsnefesFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PATim PoffenbargerFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PABradley A. WaradyFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PASusan L. FurthFrom the University of Texas Health Science Center at Houston (J.S., T.P.), Houston, TX; Department of Epidemiology (D.N.), Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; Seattle Children's Hospital (J.T.F.), Seattle, WA; Cincinnati Children's Hospital Medical Center (M.M.), Cincinnati, OH; Children's Mercy Hospital (B.A.W.), Kansas City, MO; Children's Hospital of Philadelphia (S.F.), Philadelphia, PA
2012en
ABI

Аннотация

Ambulatory blood pressure (BP) monitoring (ABPM) is the best method of detecting abnormal BP in patients with chronic kidney disease (CKD), whose hypertension may be missed with casual BP measurements. We report ABPM findings in 332 children 1 year after entry in the Chronic Kidney Disease in Children cohort study. All of the subjects underwent casual and ambulatory BP measurement. BP was categorized based on casual and ABPM results into normal (42%), white-coat (4%), masked (35%), and ambulatory (14%) hypertension. Only half of the subjects had a normal ABPM. BP load was elevated (>25%) in 52% (n = 172), whereas mean BP was elevated in 32% (n = 105). In multivariate analysis, those using an angiotensin-converting enzyme inhibitor were 89% more likely to have a normal ABPM than those who did not report using an angiotensin-converting enzyme inhibitor (odds ratio, 1.89 [95% CI, 1.17-3.04]). For every 20% faster decline in annualized glomerular filtration rate change, the odds of an abnormal ABPM increased 26% (odds ratio, 1.26 [95% CI, 0.97-1.64]). A 2.25-fold increase in urine protein:creatinine ratio annualized change was associated with a 39% higher odds of an abnormal ABPM (odds ratio, 1.39 [95% CI, 1.06-1.82]). Abnormalities on ABPM are common in children with chronic kidney disease and are strongly associated with known risk factors for end-stage renal disease. Individuals on angiotensin-converting enzyme inhibitors were less likely to have abnormal ABPM, suggesting a possible therapeutic intervention. ABPM should be used to monitor risk and guide therapy in children with chronic kidney disease.

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