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Hypertension in Children and Adolescents

ACF  This article exemplifies the AAFP 2006 Annual Clinical Focus on caring for children and adolescents.

The development of a national database on normative blood pressure levels throughout childhood has contributed to the recognition of elevated blood pressure in children and adolescents. The epidemic of childhood obesity, the risk of developing left ventricular hypertrophy, and evidence of the early development of atherosclerosis in children would make the detection of and intervention in childhood hypertension important to reduce long-term health risks; however, supporting data are lacking. Secondary hypertension is more common in preadolescent children, with most cases caused by renal disease. Primary or essential hypertension is more common in adolescents and has multiple risk factors, including obesity and a family history of hypertension. Evaluation involves a thorough history and physical examination, laboratory tests, and specialized studies. Management is multifaceted. Nonpharmacologic treatments include weight reduction, exercise, and dietary modifications. Recommendations for pharmacologic treatment are based on symptomatic hypertension, evidence of endorgan damage, stage 2 hypertension, stage 1 hypertension unresponsive to lifestyle modifications, and hypertension with diabetes mellitus. (Am Fam Physician 2006;73:1158–68. Copyright İ 2006 American Academy of Family Physicians.)

The prevalence and rate of diagnosis of hypertension in children and adolescents appear to be increasing.1 This is due in part to the increasing prevalence of childhood obesity as well as growing awareness of this disease. There is evidence that childhood hypertension can lead to adult hypertension.2 Hypertension is a known risk factor for coronary artery disease (CAD) in adults, and the presence of childhood hypertension may contribute to the early development of CAD. Reports show that early development of atherosclerosis does exist in children and young adults and may be associated with childhood hypertension.3

Left ventricular hypertrophy (LVH) is the most prominent clinical evidence of end-organ damage in childhood hypertension. Data show that LVH can be seen in as many as 41 percent of patients with childhood hypertension.46 Patients with severe cases of childhood hypertension are also at increased risk of developing hypertensive encephalopathy, seizures, cerebrovascular accidents, and congestive heart failure. Based on these observations, early detection of and intervention in children with hypertension are potentially beneficial in preventing long-term complications of hypertension.

Data associating childhood hypertension with cardiovascular risk in adulthood are lacking. An update of recommendations for diagnosis, evaluation, and treatment of childhood hypertension is provided in the fourth report by the National High Blood Pressure Education Program (NHBPEP) Working Group on High Blood Pressure in Children and Adolescents.7

Epidemiology

Because body size is an essential determinant of blood pressure in children, it is necessary to include the child's height percentile to determine if blood pressure is normal. The revised childhood blood pressure tables include 50th, 90th, 95th, and 99th percentiles by sex, age, and height based on the 1999–2000 National Health and Nutrition Examination Survey data (Appendices 1 and 2)7.

Table 17 shows the classifications of hypertension for children one year of age or older and adolescents and the corresponding systolic and diastolic blood pressures. Blood pressure should be measured on three or more separate occasions before characterizing the type of hypertension.

TABLE 1
Classifications of Hypertension in Children One Year of Age and Older and Adolescents

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Reports have shown an association between blood pressure and body mass index (BMI),8,9 suggesting that obesity is a strong risk factor for developing childhood hypertension. There are insufficient data that define the role of race and ethnicity in childhood hypertension, although results of several studies1013 show black children having higher blood pressure than white children. Heritability of childhood hypertension is estimated at 50 percent.14 One report15 noted that 49 percent of patients with primary childhood hypertension had a relative with primary hypertension, and that 46 percent of patients with secondary childhood hypertension had a relative with secondary hypertension. Another report16 showed that in adolescents with primary hypertension there is an overall 86 percent positive family history of hypertension. There is evidence that shows breastfeeding in infancy may be associated with a lower blood pressure in childhood.1719

Blood Pressure Measurement

According to the NHBPEP recommendations, children three years of age or older should have their blood pressure measured when seen at a medical facility7; however, according to the U.S. Preventive Service Task Force (USPSTF), there is insufficient evidence to recommend for or against routine screening for childhood hypertension to reduce the risk of CAD.20

The preferred method for blood pressure measurement is auscultation. Aneroid manometers are used to measure blood pressure in children and are accurate when calibrated on a semiannual basis.21

Correct measurement of blood pressure in children requires use of a cuff that is appropriate to the size of the child's upper right arm. This is the preferred arm because of the possibility of decreased pressures in the left arm caused by coarctation of the aorta. By convention, an appropriate cuff size is one with an inflatable bladder width that is at least 40 percent of the arm circumference at a point midway between the olecranon and the acromion (Figure 1). The cuff bladder length should cover 80 to 100 percent of the circumference of the arm7(Figure 2). An oversized cuff can underestimate the blood pressure, whereas an undersized cuff can overestimate the measurement. Blood pressure should be measured in a controlled environment after five minutes of rest in the seated position with the right arm supported at heart level. If the blood pressure is greater than the 90th percentile, the blood pressure should be repeated twice at the same office visit to test the validity of the reading.



Ambulatory blood pressure monitoring (ABPM) requires a patient to wear a portable monitor that records blood pressure over a specified period. This allows measurements outside of the medical setting, where some patients may experience elevated blood pressure caused by anxiety (“white-coat hypertension”). Other uses for ABPM include episodic hypertension, autonomic dysfunction, and chronic kidney disease. ABPM also may have a role in differentiating primary from secondary hypertension and in identifying patients likely to have hypertension-induced end-organ damage.22 The USPSTF maintains that ABPM is subject to many of the same errors seen in the physician's office.20



Etiologies

Most childhood hypertension, particularly in preadolescents, is secondary to an underlying disorder (Table 27). Renal parenchymal disease is the most common (60 to 70 percent) cause of hypertension.23 Adolescents usually have primary or essential hypertension, making up 85 to 95 percent of cases.23 Table 32325 shows causes of childhood hypertension according to age.

Essential hypertension rarely is found in children younger than 10 years and is a diagnosis of exclusion. Significant risk factors for essential hypertension include family history and increasing BMI. Some sleep disorders and black race can be potential risk factors for essential hypertension. Essential hypertension often is linked to other risk factors that make up metabolic syndrome and can lead to cardiovascular disease. These risk factors for metabolic syndrome include low plasma high-density lipoprotein, elevated plasma triglycerides, abdominal obesity, and insulin resistance/hyperinsulinemia. The prevalence of metabolic syndrome among adolescents is between 4.2 and 8.4 percent.26

Secondary hypertension is more common in children than in adults. It can present in adolescents, especially if they have physical findings not typically seen with essential hypertension. Renal disease is the most common cause of secondary hypertension in children.2325 Other causes include endocrine disease (e.g., pheochromocytoma, hyperthyroidism) and pharmaceuticals (e.g., oral contraceptives, sympathomimetics, some over-the-counter preparations, dietary supplements). Transient rise in blood pressure, which can be mistaken for hypertension, is seen with caffeine use and certain psychological disorders (e.g., anxiety, stress).

TABLE 2
Physical Findings Indicative of a Secondary Cause for Childhood Hypertension
Physical examination finding Possible etiologies

Abdominal bruit

Renal artery stenosis

Abdominal mass

Polycystic kidney disease; hydronephrosis/obstructive renal lesions; neuroblastoma; Wilms' tumor

Acne

Cushing's syndrome

Adenotonsillar hypertrophy

Sleep disorder associated with hypertension

Decreased perfusion of lower extremities

Coarctation of the aorta

Diaphoresis

Pheochromocytoma

Flushing

Pheochromocytoma

Growth retardation

Chronic renal failure

Hirsutism

Cushing's syndrome

Joint swelling

Systemic lupus erythematosus

Malar rash

Systemic lupus erythematosus

Moon facies

Cushing's syndrome

Murmur

Coarctation of the aorta

Muscle weakness

Hyperaldosteronism

Obesity (general)

Association with primary hypertension

Obesity (of the face, neck, or trunk)

Cushing's syndrome

Tachycardia

Hyperthyroidism; pheochromocytoma; neuroblastoma

Thyromegaly

Hyperthyroidism


Adapted with permission from National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics 2004; 114(2 suppl 4th report):564.

Evaluation

Once hypertension has been confirmed, an extensive history and careful physical examination should be conducted to identify underlying causes of the elevated blood pressure and to detect any end-organ damage. With the appropriate information, unnecessary and often expensive laboratory and imaging studies can be avoided. The NHBPEP has developed an algorithm to help the physician navigate the diagnostic and management choices in childhood hypertension (Figure 3).7

HISTORY AND PHYSICAL EXAMINATION

As mentioned previously, the child with primary hypertension often has a positive family history of hypertension or cardiovascular disease. Other risk factors including metabolic syndrome and sleep-disordered breathing (from snoring to obstructive sleep apnea) also are associated with primary hypertension. A careful history will uncover these important elements. It is helpful to remember that secondary hypertension is more likely in a younger child with stage 2 hypertension, thus data about systemic conditions associated with elevated blood pressure should be elicited. Because most secondary hypertension is renovascular in origin, a focused review of that system may provide insight into the possible etiology. Table 47 is a summary of information in a patient's history that can help determine the causes of childhood hypertension. A medication history should include any use of over-the-counter, prescription, and illicit drugs because many medications and drugs can elevate blood pressure. The physician should also ask about the use of performance-enhancing substances, herbal supplements (e.g., ma huang), and tobacco use.

Physical examination should include calculation of BMI because of the strong association between obesity and hypertension. Obtaining blood pressure readings in the upper and lower extremities to rule out coarctation of the aorta also is recommended. Examination of the retina should be included to assess the effect of hypertension on an easily accessed end organ. In the majority of children with hypertension, however, the physical examination will be normal.

LABORATORY AND IMAGING TESTS

Laboratory testing and imaging on a child with hypertension should screen for identifiable causes, detect comorbid conditions, and evaluate end-organ damage (Table 57). Screening tests should be performed on all children with a confirmed diagnosis of hypertension. Decisions about additional testing are based on individual and family histories, the presence of risk factors, and the results of the screening tests. Young children, those with stage 2 hypertension, and those in whom a systemic condition is suspected require a more extensive evaluation because these children are more likely to have secondary hypertension. The child who is older or obese, with a family history of diabetes or other cardiovascular risk factors, will require further work-up for the metabolic abnormalities associated with primary hypertension.7

Hormone levels and 24-hour urine studies are readily available to most physicians, but more specialized tests such as renal angiography often require referral to a center with pediatric radiology, nephrology, and cardiology services. When renovascular disease is strongly suspected, conventional or intra-arterial digitally subtracted angiography are recommended. Scintography with or without angiotensin-converting enzyme (ACE) inhibition also can be used. These older imaging techniques are quite invasive. Data on newer studies such as magnetic resonance angiography and 3-dimensional or spiral computed tomography in children are limited, but documentation of their usefulness is increasing.7

In addition to the diagnostic tests already mentioned, an assessment of end-organ damage must be made. Retinopathy, microalbuminuria, and increased carotid artery thickness have all been reported in children with primary hypertension.4,5 Documenting LVH is an important component of the evaluation of children with hypertension.7 Because echocardiography is noninvasive, easily obtained, and more sensitive than electrocardiography,23 it should be part of the initial evaluation of all children with hypertension and may be repeated periodically.

Management

Managing childhood hypertension is directed at the cause of the elevated blood pressure and the alleviation of any symptoms. End-organ damage, comorbid conditions, and associated risk factors also influence decisions about therapy.

Nonpharmacologic and pharmacologic treatments are recommended based on the age of the child, the stage of hypertension, and response to treatment.

NONPHARMACOLOGIC TREATMENTS

For children and adolescents with prehypertension or stage 1 hypertension, therapeutic lifestyle changes are recommended. These include weight control, regular exercise, a low-fat and low-sodium diet, smoking cessation, and abstinence from alcohol use.

Obesity increases the occurrence of hypertension threefold while favoring the development of insulin resistance, hyperlipidemia, and salt sensitivity.24,27 Significant obesity also increases the likelihood of LVH independent of blood pressure level.27 Exercise has been shown to lower blood pressure in children but does not affect left ventricular function.28,29 Competitive sports are permitted for children with prehypertension, stage 1 hypertension, or controlled stage 2 hypertension in the absence of symptoms and end-organ damage.

TABLE 5
Laboratory Tests for the Child with Hypertension

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Data regarding dietary changes in children with hypertension are limited. Nevertheless, the NHBPEP has taken an aggressive stance on sodium restriction, recommending a sodium intake of 1,200 mg per day. A no-salt-added diet with more fresh fruits and vegetables combined with low-fat dairy and protein akin to the DASH (Dietary Approaches to Stop Hypertension) food plan30 may be successful in lowering blood pressure in children. Increased intake of potassium and calcium also have been suggested as nutritional strategies to lower blood pressure.31,32 Whatever lifestyle changes are recommended, a family-centered rather than patient-oriented approach usually is more effective.7

PHARMACOTHERAPY

Reasons to initiate antihypertensive medication in children and adolescents include symptomatic hypertension, end-organ damage (e.g., LVH, retinopathy, proteinuria), secondary hypertension, stage 1 hypertension that does not respond to lifestyle changes, and stage 2 hypertension.7 In the absence of end-organ damage or comorbid conditions, the goal is to reduce blood pressure to less than the 95th percentile for age, height, and sex. When end-organ damage or coexisting illness is present, a blood pressure goal of less than the 90th percentile is recommended. Drug therapy is always an adjunct to nonpharmacologic measures.

Information about long-term, untreated childhood hypertension and the impact of antihypertensive medications on growth and development is insubstantial. According to the NHBPEP, pharmacotherapy should follow a step-up plan, introducing one medication at a time at the lowest dose, then increasing the dose until therapeutic effects are seen, side effects are seen, or the maximal dose is reached. Only then should a second agent, preferably one with a complementary mechanism of action, be initiated. Long-acting medication is useful in improving compliance, and predictable problems such as the effect of diuretic medications in young athletes should be avoided.7

TABLE 6
Antihypertensive Medications with FDA Approval for Use in Children

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The choice of initial drug therapy is largely at the discretion of the physician. Diuretics and beta blockers have documented safety and effectiveness in children. Preferential use of specific classes of medications for certain underlying or coexisting pathology has led to the prescribing of ACE inhibitors in children with diabetes or proteinuria and beta-adrenergic or calcium channel blockers for children with migraines.33  Becoming familiar with medications in each major class and with effective combinations of medications will facilitate treatment. Many medications have growing research to support their use. Those with approval from the U.S. Food and Drug Administration for use in children are listed inTable 6.7 As with any chronic health issue, medical follow-up and appropriate monitoring are key to long-term success.


The Authors

GREGORY B. LUMA, M.D., is an attending physician with the Mount Sinai School of Medicine/Jamaica Hospital Medical Center Family Medicine Residency Program and is a clinical instructor at both New York College of Osteopathic Medicine in New York, N.Y., and Mount Sinai School of Medicine in Queens, N.Y. He received his medical degree from Temple University School of Medicine, Philadelphia, Pa., and completed his residency in family medicine with the West Jersey–Memorial Hospital at Virtua Program in Voorhees, N.J. He also completed a pediatric residency with the Thomas Jefferson University/duPont Hospital for Children Program in Wilmington, Del.

ROSEANN T. SPIOTTA, M.D., is clinical assistant professor at N.Y. College of Osteopathic Medicine, clinical instructor at Mount Sinai School of Medicine, and medical director of the Jamaica Hospital's Family Practice Center in New York, N.Y. She received her medical degree from the State University of N.Y. Downstate Medical Center, Brooklyn, and completed her pediatric residency at Long Island Jewish Hillside Medical Center, New Hyde Park, N.Y.

Address correspondence to Gregory B. Luma, M.D., Department of Family Medicine, 89–06 135th Street, Suite 3C, Jamaica, NY 11418 (e-mail: gregory.luma@mssm.edu). Reprints are not available from the authors.

Author disclosure: Nothing to disclose.

Appendix 1. Blood Pressure Levels for Boys by Age and Height Percentile

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Appendix 2. Blood Pressure Levels for Girls by Age and Height Percentile

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REFERENCES

1. Sorof  JM, Lai  D, Turner  J, Poffenbarger  T, Portman  RJ.  Overweight, ethnicity, and the prevalence of hypertension in school-aged children.  Pediatrics.  2004;113(3 pt 1):475–82.

2. Lauer  RM, Clarke  WR.  Childhood risk factors for high adult blood pressure: the Muscatine Study.  Pediatrics.  1989;84:633–41.

3. Berenson  GS, Srinivasan  SR, Bao  W, Newman  WP  3rd, Tracy  RE, Wattigney  WA.  Association between multiple cardiovascular risk factors and atherosclerosis in children and young adults. The Bogalusa Heart Study.  N Engl J Med.  1998;338:1650–6.

4. Sorof  JM, Alexandrov  AV, Cardwell  G, Portman  RJ.  Carotid artery intimal-medial thickness and left ventricular hypertrophy in children with elevated blood pressure.  Pediatrics.  2003;111:61–6.

5. Belsha  CW, Wells  TG, McNiece  KL, Seib  PM, Plummer  JK, Berry  PL.  Influence of diurnal blood pressure variations on target organ abnormalities in adolescents with mild essential hypertension.  Am J Hypertens.  1998;11(4 pt 1):410–7.

6. Hanevold  C, Waller  J, Daniels  S, Portman  R, Sorof  J.  International Pediatric Hypertension Association. The effects of obesity, gender, and ethnic group on left ventricular hypertrophy and geometry in hypertensive children: a collaborative study of the International Pediatric Hypertension Association [published correction appears in Pediatrics 2005;115:1118]  Pediatrics.  2004;113:328–33.

7.  National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents.  Pediatrics.  2004;114(2 suppl 4th report):555–76.

8. Stabouli  S, Kotsis  V, Papamichael  C, Constantopoulos  A, Zakopoulos  N.  Adolescent obesity is associated with high ambulatory blood pressure and increased carotid intimalmedial thickness.  J Pediatr.  2005;147:651–6.

9. Muntner  P, He  J, Cutler  JA, Wildman  RP, Whelton  PK.  Trends in blood pressure among children and adolescents.  JAMA.  2004;291:2107–13.

10. Voors  AW, Foster  TA, Frerichs  RR, Webber  LS, Berenson  GS.  Studies of blood pressures in children, ages 5–14 years, in a total biracial community: the Bogalusa Heart Study.  Circulation.  1976;54:319–27.

11. Berenson  GS, Voors  AW, Webber  LS, Dalferes  ER  Jr, Harsha  DW.  Racial differences of parameters associated with blood pressure levels in children—the Bogalusa Heart Study.  Metabolism.  1979;28:1218–28.

12. Berenson  GS, Wattigney  WA, Webber  LS.  Epidemiology of hypertension from childhood to young adulthood in black, white, and Hispanic population samples.  Public Health Rep.  1996;111(suppl 2):3–6.

13. Dekkers  JC, Snieder  H, Van Den Oord  EJ, Treiber  FA.  Moderators of blood pressure development from childhood to adulthood: a 10-year longitudinal study.  J Pediatr.  2002;141:770–9.

14. Jung  FF, Ingelfinger  JR.  Hypertension in childhood and adolescence.  Pediatr Rev.  1993;14:169–79.

15. Robinson  RF, Batisky  DL, Hayes  JR, Nahata  MC, Mahan  JD.  Significance of heritability in primary and secondary pediatric hypertension.  Am J Hypertens.  2005;18:917–21.

16. Flynn  JT, Alderman  MH.  Characteristics of children with primary hypertension seen at a referral center.  Pediatr Nephrol.  2005;20:961–6.

17. Martin  RM, Ness  AR, Gunnell  D, Emmett  P, Davey Smith  G.  ALSPAC Study Team. Does breast-feeding in infancy lower blood pressure in childhood? The Avon Longitudinal Study of Parents and Children (ALSPAC)  Circulation.  2004;109:1259–66.

18. Wilson  AC, Forsyth  JS, Greene  SA, Irvine  L, Hau  C, Howie  PW.  Relation of infant diet to childhood health: seven year follow up of cohort of children in Dundee infant feeding study.  BMJ.  1998;316:21–5.

19. Lawlor  DA, Najman  JM, Sterne  J, Williams  GM, Ebrahim  S, Davey Smith  G.  Associations of parental, birth, and early life characteristics with systolic blood pressure at 5 years of age: findings from the Mater-University study of pregnancy and its outcomes.  Circulation.  2004;110:2417–23.

20. U.S. Preventive Services Task Force. Screening for high blood pressure: recommendations and rationale. Rockville, Md.: Agency for Healthcare Research and Quality, 2003. Accessed online February 2, 2006, at: http://www.ahrq.gov/clinic/3rduspstf/highbloodsc/hibloodrr.htm.

21. Canzanello  VJ, Jensen  PL, Schwartz  GL.  Are aneroid sphygmomanometers accurate in hospital and clinic settings?  Arch Intern Med.  2001;161:729–31.

22. Flynn  JT.  Differentiation between primary and secondary hypertension in children using ambulatory blood pressure monitoring.  Pediatrics.  2002;110(1 pt 1):89–93.

23. Flynn  JT.  Evaluation and management of hypertension in childhood.  Prog Pediatr Cardiol.  2001;12:177–88.

24. Bartosh  SM, Aronson  AJ.  Childhood hypertension. An update on etiology, diagnosis, and treatment.  Pediatr Clin North Am.  1999;46:235–52.

25. Flynn  JT.  Hypertension in adolescents.  Adolesc Med Clin.  2005;16:11–29.

26. Goodman  E, Daniels  SR, Morrison  JA, Huang  B, Dolan  LM.  Contrasting prevalence of and demographic disparities in the World Health Organization and National Cholesterol Education Program Adult Treatment Panel III definitions of metabolic syndrome among adolescents.  J Pediatr.  2004;145:445–51.

27. Freedman  DS, Dietz  WH, Srinivasan  SR, Berenson  GS.  The relation of overweight to cardiovascular risk factors among children and adolescents: the Bogalusa Heart Study.  Pediatrics.  1999;103(6 pt 1):1175–82.

28. Daniels  SR, Loggie  JM, Khoury  P, Kimball  TR.  Left ventricular geometry and severe left ventricular hypertrophy in children and adolescents with essential hypertension.  Circulation.  1998;97:1907–11.

29. Mitchell  BM, Gutin  B, Kapuku  G, Barbeau  P, Humphries  MC, Owens  S, et al.  Left ventricular structure and function in obese adolescents: relations to cardiovascular fitness, percent body fat, and visceral adiposity, and effects of physical training.  Pediatrics.  2002;109:E73–3.

30. Sacks  FM, Svetkey  LP, Vollmer  WM, Appel  LJ, Bray  GA, Harsha  D, et al.  DASH-Sodium Collaborative Research Group. Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet.  N Engl J Med.  2001;344:3–10.

31. Kawano  Y, Minami  J, Takishita  S, Omae  T.  Effects of potassium supplementation on office, home, and 24-h blood pressure in patients with essential hypertension.  Am J Hypertens.  1998;11:1141–6.

32. Gillman  MW, Hood  MY, Moore  LL, Nguyen  US, Singer  MR, Andon  MB.  Effect of calcium supplementation on blood pressure in children.  J Pediatr.  1995;127:186–92.

33. Chobanian  AV, Bakris  GL, Black  HR, Cushman  WC, Green  LA, Izzo  JL  Jr, et al.  National Heart, Lung, and Blood Institutes Joint National Committee on Prevention, Detection Evaluation, and Treatment of High Blood Pressure, National High Blood Pressure Education Program Coordination Committee. The seventh report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure: The JNC 7 Report [published correction in appears in JAMA 2003;290:197]  JAMA.  2003;289:2560–72.

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