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7th Brazilian Guideline of Arterial Hypertension: Chapter 10 - Hypertension in Children and Adolescents

M V B Malachias, V Koch, Colombo Colombo, Silva Silva, I C B Guimarães, P K Nogueira.   

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Year:  2016        PMID: 27819389      PMCID: PMC5319464          DOI: 10.5935/abc.20160160

Source DB:  PubMed          Journal:  Arq Bras Cardiol        ISSN: 0066-782X            Impact factor:   2.000


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Epidemiological context and importance of hypertension in pediatrics

Arterial hypertension was identified as the major source of combined mortality and morbidity, representing 7% of global disability-adjusted life years.[1] The adoption of the BP definitions and normalization of the "National High Blood Pressure Education Program" (NHBPEP) 2004[2] has standardized the BP classification in the pediatric population. The percentage of children and adolescents diagnosed with AH is estimated to have doubled in the past two decades. The current prevalence of AH in the pediatric population is around 3% to 5%,[3-5] while that of PH reaches 10% to 15%,[3,4,6,7] and such values are mainly attributed to the large increase in childhood obesity.[8] The etiology of pediatric AH can be either secondary, most often associated with nephropathies, or primary, attributed to genetic causes with environmental influence, predominating in adolescents. Pediatric AH is usually asymptomatic, but as many as 40% of hypertensive children have LVH at the initial diagnosis of AH. Although oligosymptomatic in childhood, LVH is a precursor of arrhythmias and HF in adults.[9] In addition, pediatric AH is associated with the development of other changes in target organs, such as increased carotid IMT, arterial compliance reduction, and retinal arteriolar narrowing. Early diagnosis and treatment of childhood AH are associated with a lower risk for AH and for increased carotid atheromatosis in adult life.[10] Therefore, periodical BP measurements in children and adolescents are recommended, even contradicting the U.S. Preventive Services Task Force's suggestion, which considers the evidence of benefits of primary AH screening in asymptomatic children and adolescents insufficient to prevent CVD in childhood or adulthood.[11]

Definitions and diagnosis

Definition and etiology

Children and adolescents are considered hypertensive when SBP and/or DBP are greater than or equal to the 95th percentile for age, sex and height percentile, on at least three different occasions.[2] Prehypertension in children is defined as SBP/DBP ≥ the 90th percentile < the 95th percentile, and in adolescents as BP levels ≥ 120/80 mm Hg and < the 95th percentile. Stage 1 AH is considered for readings between the 95th percentile and the 99th percentile plus 5 mm Hg, while stage 2 AH, for readings > stage 1. The height percentiles can be obtained by using Centers for Disease Control and Prevention's (CDC) growth charts.[12] In addition, normal and high BP levels for children and adolescents are available in mobile apps, such as PA Kids and Ped(z). In the pediatric population, WCH and MH can be diagnosed based on established normality criteria for ABPM.[13] After a detailed clinical history and physical examination, children and adolescents considered hypertensive should undergo investigation. The younger the child, the greater the chance of secondary AH. Parenchymal, renovascular and obstructive nephropathies account for approximately 60-90% of the cases, and can affect all age groups (infants, children and adolescents), being more prevalent in younger children with higher BP elevations. Endocrine disorders, such as excessive mineralocorticoid, corticoid or catecholamine secretion, thyroid diseases and hypercalcemia associated with hyperparathyroidism, account for approximately 5% of secondary AH cases. Coarctation of the aorta is diagnosed in 2% of the cases, and 5% of secondary AH cases are attributed to other etiologies, such as adverse effects of vasoactive and immunosuppressive drugs, steroid abuse, central nervous system changes, and increased intracranial pressure. Primary AH is more prevalent in overweight or obese children and adolescents with family history of AH. Currently, primary AH seems to be the most common form of AH in adolescence, being, however, a diagnosis of exclusion, and, in that population, secondary causes should be investigated whenever possible.

Diagnosis

Method for BP measurement

Measuring BP in children is recommended at every clinical assessment after the age of 3 years, abiding by the standards for BP measurement.[2] Children under the age of 3 years should have their BP assessed on specific situations.[2,14] For BP measurement, children should be calm and sitting for at least 5 minutes, with back supported and feet on the floor, having refrained from consuming stimulant foods and beverages. The BP should be taken at heart level on the right arm, because of the possibility of coarctation of the aorta. Table 1 shows the specific recommendations for auscultatory BP measurement in children and adolescents. Whenever BP is high on the upper limbs, SBP should be assessed on the lower limbs. Such assessment can be performed with the patient lying down, with the cuff placed on the calf, covering at least two-thirds of the knee-ankle distance. The SBP reading on the leg can be higher than that on the arm because of the distal pulse amplification phenomenon. A lower SBP reading on the leg as compared to that on the arm suggests coarctation of the aorta.
Table 1

Specific recommendations for BP measurement in children and adolescents

• Auscultatory method.
• Use 1st Korotkoff sound for SBP, and 5th Korotkoff sound for DBP.
• When using the oscillometric device, it requires validation.
• Detection of AH by use of the oscillometric device requires confirmation with auscultation.
• Use appropriate cuff size; air bag width: 40% of arm circumference in the middle point between the acromion and olecranon, and air bag length: 80-100% of arm circumference.
• Conditions under which children < 3 years old should have BP measured: neonatal intensive care; congenital heart diseases, kidney diseases, treatment with drugs known to raise BP, and evidence of increased intracranial pressure.
Specific recommendations for BP measurement in children and adolescents Tables 2 and 3 show the BP percentiles by sex, age and height percentile. Figures 1 and 2 show BP values for boys and girls, respectively, from birth to the age of 1 year based on data from the Report of the Second Task Force on Blood Pressure Control in Children - 1987.[15]
Table 2

Blood pressure levels for boys by age and height percentile[2]

 BPSBP (mm Hg)DBP (mm Hg)
Agepercentile ← Percentile of Height → ← Percentile of Height →
(Year) 5th10th25th50th75th90th95th5th10th25th50th75th90th95th
150th8081838587888934353637383939
 90th9495979910010210349505152535354
 95th9899101-10310410610654545556575858
 99th10510610811011211311461626364656666
250th8485878890929239404142434444
 90th979910010210410510654555657585859
 95th10110210410610810911059596061626363
 99th10911011111311511711766676869707171
350th8687899193949544444546474848
 90th10010110310510710810959596061626363
 95th10410510710911011211363636465666767
 99th11111211411611811912071717273747575
450th8889919395969747484950515152
 90th10210310510710911011162636465666667
 95th10610710911111211411566676869707171
 99th11311411611812012112274757677787879
550th9091939596989850515253545555
 90th10410510610811011111265666768696970
 95th10810911011211411511669707172737474
 99th11511611812012112312377787980818182
650th91929496989910053535455565757
 90th10510610811011111311368686970717272
 95th10911011211411511711772727374757676
 99th11611711912112312412580808182838484
750th929495979910010155555657585959
 90th10610710911111311411570707172737474
 95th11011111311511711811974747576777878
 99th11711812012212412512682828384858686
850th9495979910010210256575859606061
 90th10710911011211411511671727273747576
 95th11111211411611811912075767778797980
 99th11912012212312512712783848586878788
950th95969810010210310457585960616162
 90th10911011211411511711872737475767677
 95th11311411611811912112176777879808181
 99th12012112312512712812984858687888889
1050th979810010210310510658596061616263
 90th11111211411511711911973737475767778
 95th11511611711912112212377787980818182
 99th12212312512712813013085868688888990
1150th9910010210410510710759596061626363
 90th113114115J1711912012174747576777878
 95th11711811912112312412578787980818282
 99th12412512712913013213286868788899090
1250th10110210410610810911059606162636364
 90th11511611812012112312374757576777879
 95th11912012212312512712778798081828283
 99th12612712913113313413586878889909091
1350th10410510610811011111260606162636464
 90th11711812012212412512675757677787979
 95th12112212412612812913079798081828383
 99th12813013113313513613787878889909191
1450th10610710911111311411560616263646565
 90th12012112312512612812875767778797980
 95th12412512712813013213280808182838484
 99th13113213413613813914087888990919292
1550th10911011211311511711761626364656666
 90th12212412512712913013176777879808081
 95th12612712913113313413581818283848585
 99th13413513613814014214288899091929393
1650th11111211411611811912063636465666767
 90th12512612813013113313478787980818282
 95th12913013213413513713782838384858687
 99th13613713914114314414590909192939494
1750th11411511611812012112265666667686970
 90th12712813013213413513680808182838484
 95th13113213413613813914084858687878889
 99th13914014114314514614792939394959697
Table 3

Blood pressure levels for girls by age and height percentile2

 BP  SBP (mm Hg)    DBP (mm Hg)  
AgePercentile ← Percentile of Height → ← Percentile of Height →
(Year) 5th10th25th50th75th90th95th5th10th25th50th75th90th95th
150th8384858688899038393940414142
 90th97979810010110210352535354555556
 95th10010110210410510610756575758595960
 99th10810810911111211311464646565666767
250th8585878889919143444445464647
 90th989910010110310410557585859606161
 95th10210310410510710810961626263646565
 99th10911011111211411511669697070717272
350th8687888991929347484849505051
 90th10010010210310410610661626263646465
 95th10410410510710810911065666667686869
 99th11111111311411511611773737474757676
450th8888909192949450505152525354
 90th10110210310410610710864646566676768
 95th10510610710811011111268686970717172
 99th11211311411511711811976767677787979
550th8990919394959652535354555556
 90th10310310510610710910966676768696970
 95th10710710811011111211370717172737374
 99th11411411611711812012078787979808181
650th9192939496979854545556565758
 90th10410510610810911011168686970707172
 95th10810911011111311411572727374747576
 99th11511611711912012112280808081828383
750th9393959697999955565657585859
 90th10610710810911111211369707071727273
 95th11011111211311511611673747475767677
 99th11711811912012212312481818282838484
850th959596989910010157575758596060
 90th10810911011111311411471717172737474
 95th11211211411511611811875757576777878
 99th11912012112212312512582828383848586
950th96979810010110210358585859606161
 90th11011011211311411611672727273747575
 95th11411411511711811912076767677787979
 99th12112112312412512712783838484858687
1050th989910010210310410559595960616262
 90th11211211411511611811873737374757676
 95th11611611711912012112277777778798080
 99th12312312512612712912984848586868788
1150th10010110210310510610760606061626363
 90th11411411611711811912074747475767777
 95th118118119 -12112212312478787879808181
 99th12512512612812913013185858687878889
1250th10210310410510710810961616162636464
 90th11611611711912012112275757576777878
 95th11912012112312412512679797980818282
 99th12712712813013113213386868788888990
1350th10410510610710911011062626263646565
 90th11711811912112212312476767677787979
 95th12112212312412612712880808081828383
 99th12812913013213313413587878889899091
1450th10610610710911011111263636364656666
 90th11912012112212412512577777778798080
 95th12312312512612712912981818182838484
 99th13013113213313513613688888990909192
1550th10710810911011111311364646465666767
 90th12012112212312512612778787879808181
 95th12412512612712913013182828283848585
 99th13113213313413613713889899091919293
1650th10810811011111211411464646566666768
 90th12112212312412612712878787980818182
 95th12512612712813013113282828384858586
 99th13213313413513713813990909091929393
1750th10810911011111311411564656566676768
 90th12212212312512612712878797980818182
 95th12512612712913013113282838384858586
 99th13313313413613713813990909191929393
Figure 1

Blood pressure levels for boys, from birth to the age of 1 year97

Figure 2

Blood pressure levels for girls, from birth to the age of 1 year97

Blood pressure levels for boys by age and height percentile[2] Blood pressure levels for girls by age and height percentile2 Blood pressure levels for boys, from birth to the age of 1 year97 Blood pressure levels for girls, from birth to the age of 1 year97 Note: Adolescents with BP ≥ 120/80 mm Hg should be considered prehypertensive, even if the 90th percentile value is greater than that. This can occur for SBP in patients older than 12 years, and for DBP in patients older than 16 years. For children/adolescents, ABPM is indicated to investigate WCH and MH, and to follow prehypertensive or hypertensive patients up.[13] The prevalence of WCH has been reported as between 22% and 32%. The use of ABPM should be restricted to patients with borderline or mild AH, because patients with high office BP readings are more likely to be hypertensive.[16]

Anamnesis

A careful recollection of data on birth, growth and development, personal antecedents, and renal, urological, endocrine, cardiac and neurological diseases should be performed. The following patterns should be characterized: physical activity; dietary intake; smoking habit and alcohol consumption; use of steroids, amphetamines, sympathomimetic drugs, tricyclic antidepressants, contraceptives and illicit substances; and sleep history, because sleep disorders are associated with AH, overweight and obesity. In addition, family antecedents for AH, kidney diseases and other CVRF should be carefully assessed.

Physical examination

On physical examination, BMI should be calculated.[17] Growth delay might suggest chronic disease, and persistent tachycardia might suggest hyperthyroidism or pheochromocytoma. Pulse decrease on the lower limbs leads to the suspicion of coarctation of the aorta. Adenoid hypertrophy is associated with sleep disorders. Acantosis nigricans suggests insulin resistance and DM. Abdominal fremitus and murmurs can indicate renovascular disease.[18]

Complementary tests

Laboratory and imaging tests are aimed at defining the etiology of AH (primary or secondary) and detecting TOD and CVRF associated with AH (Tables 4 and 5).[2,14]
Table 4

Initial investigation of children and adolescents with AH

Complete blood count
Renal function and electrolytes (including calcium, phosphorus and magnesium)
Fasting lipid panel
Plasma uric acid levels
Fasting glucose
Urinalysis and urine culture
Retinal exam
Chest X ray
ECG / Doppler echocardiography
Renal US with Doppler of renal arteries
Table 5

Complementary tests to confirm the etiology ofsecondary AH in children and adolescents

Measurement of urine electrolytes, proteinuria and urine creatinine
Plasma levels of renin (or plasma renin activity) and aldosterone, salivary cortisol test, PTH, TSH, free T4 and T3
Hemoglobin electrophoresis
Specific auto-antibodies: FAN, anti DNA, ANCA p, ANCA c
Urine catecholamines and metanephrines (or plasma metanephrine) and MIBG scintigraphy

MIBG: metaiodobenzylguanidine

Initial investigation of children and adolescents with AH Complementary tests to confirm the etiology ofsecondary AH in children and adolescents MIBG: metaiodobenzylguanidine Target-organ assessment should be performed in all children and adolescents with stage 1 and 2 AH. Sleep study by use of polysomnography or home respiratory polygraphy is indicated for children and adolescents with sleep disorders detected on anamnesis.[2] To investigate secondary AH, see Chapter 12. Table 5 shows some tests for children and adolescents suspected of having secondary AH.

Therapeutic aspects

In children and adolescents with confirmed AH, therapeutic management is guided by the AH etiology definition, CV risk assessment, and TOD characterization.

Nonpharmacological management

Nonpharmacological management should be introduced to all pediatric patients with BP levels above the 90th percentile.[2] (GR: IIa; LE: C). It includes body weight loss, a physical exercise program, and dietary intervention.[2] Body weight reduction yields good results in the treatment of obese hypertensive children,[19] similarly to physical exercise, which has better effect on SBP levels.[19] Regular aerobic activity is recommended as follows: moderate-intensity physical exercise, 30-60 minutes/day, if possible, every day. Children with AH can practice resistance or localized training, except for weight lifting. Competitive sports are not recommended for patients with uncontrolled stage 2 AH.[20] Dietary intervention can comprise sodium restriction,[21] and potassium and calcium supplementation; the efficacy in that population, however, is yet to be proven.[22]

Pharmacological management

Pharmacological therapy should be initiated for children with symptomatic AH, secondary AH, presence of TOD, types 1 and 2 DM, CKD and persistent AH nonresponsive to nonpharmacological therapy.[2] (GR: IIa; LE: B). The treatment is aimed at BP reduction below the 95th percentile in non-complicated AH, and BP reduction below the 90th percentile in both complicated AH, characterized by TOD and comorbidities (DM, CKD), and secondary AH.[2] (GR: IIa; LE: C). The treatment should begin with a first-line antihypertensive agent, whose dose should be optimized, and, if target BP level is not attained, other pharmacological groups should be added in sequence. A recent systematic review[23] has identified neither a randomized study assessing the efficacy of antihypertensive drugs on TOD, nor any consistent dose-response relationship with any drug class assessed. The adverse events associated with the use of antihypertensive agents for children and adolescents have been usually of mild intensity, such as headache, dizziness, and upper respiratory tract infections. All classes of antihypertensive drugs seem safe, at least in the short run.[23] The only randomized, double-blind, controlled study, by Schaefer et al., comparing the efficacy and safety of drugs of parallel groups and assessing hypertensive children on enalapril or valsartan, has shown comparable results regarding the efficacy and safety of both drugs.[24] In secondary AH, the antihypertensive drug choice should be in consonance with the pathophysiological principle involved, considering the comorbidities present. For example, non-cardioselective BBs should be avoided in individuals with upper airway reactivity, because of the risk for bronchospasm.[25] In pregnancy, ACEIs and ARBs are contraindicated, because of their potential for fetal malformation.[26] The use of those drugs for childbearing-age girls should be always accompanied by contraceptive guidance.[26,27] For renovascular AH, of ACEIs or ARBs are indicated in association with vasodilators and DIUs. In cases of coarctation of the aorta, in the preoperative period, the initial drug is usually a BB. If the AH persists postoperatively, the BB can be maintained, replaced or associated with an ACEI or ARB. For AH associated with DM and CKD, an ACEI or ARB is initially used. The use of ACEI and ARB relaxes the efferent arteriole, reducing the glomerular capillary hydrostatic pressure, and posing a risk for AKI in situations of hypovolemia. Similarly, those drugs are contraindicated for patients with bilateral renal artery stenosis.[26-29] For obese adults, ACEIs, ARBs, CCBs, BBs and DIUs are effective in reducing BP.[30] In adults, ACEIs and ARBs seem to reduce the risk of developing DM and to increase insulin sensitivity.[31-33] Table 6 shows the updated pediatric doses of the most frequently prescribed hypotensive agents to treat CAH.[2,27,28]
Table 6

Most frequently used oral drugs for management of pediatric chronic arterial hypertension2

DrugInitial dose (mg/kg/dose)  Maximum dose (mg/kg/day)Interval
Amlodipine (6-17 years)0.10.524h
Nifedipine XL0.25-0.53 (max:120 mg/day)12-24h
Captopril
Children0.3-0.568h
Neonate0.03-0.1528-24h
Enalapril0.080.612-24h
Losartan0.7 (max: 50 mg/day)1.4 (max: 100 mg/day)24h
Propranolol1-24 (max: 640 mg/day)8-12h
Atenolol0.5-12 (max: 100 mg/day)12-24h
Furosemide0.5-264-12h
Hydrochlorothiazide13 (max: 50 mg/day)12h
Spironolactone13.3 (max: 100 mg/day)6-12h
Clonidine( ≥12 years)0.2 mg/day2.4 mg/day12h
Prazosin0.05-0.10.58h
Hydralazine0.757.5 (max: 200 mg/day)6h
Minoxidil   
< 12 years0.250 mg/day6-8h
≥ 12 years5 mg/day 100 mg/day  

max: maximum; h: hour.

Most frequently used oral drugs for management of pediatric chronic arterial hypertension2 max: maximum; h: hour.

Hypertensive crisis

Hypertensive emergency is characterized by acute BP elevation associated with TOD, which can comprise neurological, renal, ocular and hepatic impairment or myocardial failure, and manifests as encephalopathy, convulsions, visual changes, abnormal electrocardiographic or echocardiographic findings, and renal or hepatic failure.[34] Hypertensive urgency is described as BP elevation above the 99th percentile plus 5 mm Hg (stage 2), associated with less severe symptoms, in a patient at risk for progressive TOD, with no evidence of recent impairment. Oral drugs are suggested, under monitoring, with BP reduction in 24-48 hours.[2] In HE, the BP reduction should occur slowly and progressively: 30% reduction in the programed amount in 6-12 hours, 30% in 24 hours, and final adjustment in 2-4 days.[35] Very rapid BP reduction is contraindicated, because it leads to hypotension, failure of self-regulating mechanisms, and likelihood of cerebral and visceral ischemia.[36] The HE should be treated exclusively with parenteral drugs. In Brazil, the most frequently used drug for that purpose is SNP, which is metabolized into cyanide, which can cause metabolic acidosis, mental confusion, and clinical deterioration. Thus, SNP administration for more than 24 hours requires monitoring of serum cyanide levels, especially in patients with renal failure.[35,36] After patient's stabilization with SNP, an oral antihypertensive agent should be initiated, so that the SNP dose can be reduced. The use of SNP should be avoided in pregnant adolescents and patients with central nervous system hypoperfusion. Special clinical conditions can be managed with more specific hypotensive agents for the underlying disease. Patients with catecholamine-producing tumors can be initially alpha-blocked with phenoxybenzamine, or prazosin if the former is not available, followed by the careful addition of a BB. After BP control and in the absence of kidney or heart dysfunction, a sodium-rich diet is suggested to expand blood volume, usually reduced by the excess of catecholamines, favoring postoperative BP management and reducing the chance of hypotension. An IV short-acting antihypertensive drug should be used for intraoperative BP control. Furosemide is the first-choice drug for HC caused by fluid overload, for example, in patients with kidney disease, such as acute glomerulonephritis. In case of oliguria/anuria, other antihypertensive drugs can be used concomitantly, and dialysis might be necessary for blood volume control. Arterial hypertension associated with the use of cocaine or amphetamines can be treated with lorazepam or other benzodiazepine, which is usually effective to control restlessness and AH. In the presence of a HE, phentolamine, if available, is the drug of choice, and should be used in combination with lorazepam.[37] Table 7 shows the most frequently used drugs in pediatric HE.[38,39]
Table 7

Major pediatric drugs and doses used to control hypertensive emergency[2],95,96

DrugRouteDoseAction beginningDuration
Sodium nitroprussideIV0.5-10µg/kg/minSecondsOnly during infusion
LabetalolIV0.25-3 mg/kg/h or Bolus: 0.2-1 mg/kg followed by infusion: 0.25-3 mg/kg/h2-5 min2-4 h
NicardipineIV1-3µg/kg/min2-5 min30 min-4 h, the greater, the longer the use
HydralazineIVIMBolus: 0.2-0.6 mg/kg IV,  IM, max = 20 mg10-30 min4-12 h
EsmololIVAttack: 100-500µg/kg followed by infusion: 50-300µg/kg/minSeconds10-30 min
PhentolamineIVBolus: 0.05-0.1 mg/kg, max = 5 mg/doseSeconds15-30 min

IV: intravenous; IM: intramuscular; min: minute; h: hour.

Major pediatric drugs and doses used to control hypertensive emergency[2],95,96 IV: intravenous; IM: intramuscular; min: minute; h: hour.

90th percentile

SBP87101106106106106106106106106106106106
DBP68666363636666676868696969
Height (cm)51596366687072737476777880
Weight (kg)44556789910101111

Source: Report of the Second Task Force on Blood Pressure Control in Children - 1987. Task Force on Blood Pressure Control in Children. National Heart, Lung and Blood Institute, Bethesda, Maryland. Pediatrics 1987;79(1):1-25.

90th percentile

SBP7696101104105106106106106106106106106
DBP68666464656666666667676767
Height (cm)54565656616366687072747577
Weight (kg)4445567899101011

Source: Report of the Second Task Force on Blood Pressure Control in Children - 1987. Task Force on Blood Pressure Control in Children. National Heart, Lung and Blood Institute, Bethesda, Maryland. Pediatrics 1987;79(1):1-25.

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1.  The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents.

Authors: 
Journal:  Pediatrics       Date:  2004-08       Impact factor: 7.124

2.  Blood pressure response to potassium supplementation in normotensive adults and children.

Authors:  J Z Miller; M H Weinberger; J C Christian
Journal:  Hypertension       Date:  1987-10       Impact factor: 10.190

3.  Does it matter how blood pressure is lowered in patients with metabolic risk factors?

Authors:  Arya M Sharma
Journal:  J Am Soc Hypertens       Date:  2008 Jul-Aug

4.  Efficacy and safety of valsartan compared to enalapril in hypertensive children: a 12-week, randomized, double-blind, parallel-group study.

Authors:  Franz Schaefer; Mieczyslaw Litwin; Jacek Zachwieja; Aleksandra Zurowska; Sandor Turi; Amie Grosso; Nicole Pezous; Mahomed Kadwa
Journal:  J Hypertens       Date:  2011-12       Impact factor: 4.844

5.  Athletic participation by children and adolescents who have systemic hypertension.

Authors:  Teri M McCambridge; Holly J Benjamin; Joel S Brenner; Charles T Cappetta; Rebecca A Demorest; Andrew J M Gregory; Mark Halstead; Chris G Koutures; Cynthia R LaBella; Stephanie Martin; Stephen G Rice
Journal:  Pediatrics       Date:  2010-05-31       Impact factor: 7.124

6.  Report of the Second Task Force on Blood Pressure Control in Children--1987. Task Force on Blood Pressure Control in Children. National Heart, Lung, and Blood Institute, Bethesda, Maryland.

Authors: 
Journal:  Pediatrics       Date:  1987-01       Impact factor: 7.124

7.  Trends in blood pressure among children and adolescents.

Authors:  Paul Muntner; Jiang He; Jeffrey A Cutler; Rachel P Wildman; Paul K Whelton
Journal:  JAMA       Date:  2004-05-05       Impact factor: 56.272

8.  Prevalence of hypertension and pre-hypertension among adolescents.

Authors:  Karen L McNiece; Timothy S Poffenbarger; Jennifer L Turner; Kathy D Franco; Jonathan M Sorof; Ronald J Portman
Journal:  J Pediatr       Date:  2007-06       Impact factor: 4.406

9.  The effects of telmisartan treatment on the abdominal fat depot in patients with metabolic syndrome and essential hypertension: Abdominal fat Depot Intervention Program of Okayama (ADIPO).

Authors:  Kazutoshi Murakami; Jun Wada; Daisuke Ogawa; Chikage Sato Horiguchi; Tomoko Miyoshi; Motofumi Sasaki; Haruhito A Uchida; Yoshio Nakamura; Hirofumi Makino
Journal:  Diab Vasc Dis Res       Date:  2012-05-04       Impact factor: 3.291

10.  First-attack pediatric hypertensive crisis presenting to the pediatric emergency department.

Authors:  Wen-Chieh Yang; Lu-Lu Zhao; Chun-Yu Chen; Yung-Kang Wu; Yu-Jun Chang; Han-Ping Wu
Journal:  BMC Pediatr       Date:  2012-12-31       Impact factor: 2.125

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1.  Metabolic risk associated with liver enzymes, uric acid, and hemoglobin in adolescents.

Authors:  Sonimar de Souza; Cézane P Reuter; Lars B Andersen; Rodrigo A Lima; Karin A Pfeiffer; Elza D de Mello; Anelise R Gaya; Silvia I R Franke; Jane D P Renner
Journal:  Pediatr Res       Date:  2020-03-14       Impact factor: 3.756

2.  Brazilian pediatricians need to use national blood pressure reference values for their adolescents.

Authors:  Tomáš Seeman; Terezie Šuláková
Journal:  J Pediatr (Rio J)       Date:  2019-06-15       Impact factor: 2.990

3.  Blood pressure reference values for Brazilian adolescents: data from the Study of Cardiovascular Risk in Adolescents (ERICA Study).

Authors:  Thiago Veiga Jardim; Bernard Rosner; Katia Vergetti Bloch; Maria Cristina Caetano Kuschnir; Moyses Szklo; Paulo César Veiga Jardim
Journal:  J Pediatr (Rio J)       Date:  2018-12-04       Impact factor: 2.990

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