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Hypertension. 2014 May ; 63(5): 1116–1135. doi:10.1161/HYP.0000000000000007.
Update: Ambulatory Blood Pressure Monitoring in Children and

Adolescents:
A Scientific Statement From the American Heart Association
Joseph T. Flynn, MD, MS [Chair], Stephen R. Daniels, MD, PhD, FAHA, Laura L. Hayman,
PhD, MSN, FAHA, David M. Maahs, MD, PhD, Brian W. McCrindle, MD, MPH, FAHA, Mark
Mitsnefes, MD, MS, Justin P. Zachariah, MD, MPH, and Elaine M. Urbina, MD, MS, FAHA on
behalf of the American Heart Association Atherosclerosis, Hypertension and Obesity in
Youth Committee of the Council on Cardiovascular Disease in the Young
Keywords
AHA Scientific Statements; adolescents; ambulatory blood pressure monitoring; blood pressure;
high; child; guideline; hypertension
Ambulatory blood pressure monitoring (ABPM) has established roles in the evaluation and
management of hypertension in adults but has only been applied to children and adolescents
more recently.1 In 2008, the American Heart Association (AHA) issued the first set of
consensus recommendations for performance and interpretation of ABPM in pediatrics.
Since then, ABPM has found increasing use in children and adolescents, as recently
summarized.2 The present document updates the 2008 AHA statement on the use of ABPM
in the pediatric population3 with additional data published since the release of that report
and also presents a revised interpretation schema. Because no outcome studies are yet
available relating ABPM levels in children to outcomes such as myocardial infarction or
stroke, these guidelines are largely driven by expert opinion, although they are also informed
by available pediatric data on ABPM and surrogate markers of cardiovascular disease.
Cardiovascular Risk in the Pediatric Population

Epidemiology of Hypertension
High blood pressure (BP) is the leading risk factor–related cause of death throughout the
world, accounting for 12.8% of all deaths, including 51% of stroke deaths and 45% of
coronary heart disease deaths.4 In the United States, 33.0% of adults >20 years of age have
© 2014 American Heart Association, Inc.

The American Heart Association makes every effort to avoid any actual or potential conflicts of interest that may arise as a result of an
outside relationship or a personal, professional, or business interest of a member of the writing panel. Specifically, all members of the
writing group are required to complete and submit a Disclosure Questionnaire showing all such relationships that might be perceived
as real or potential conflicts of interest.
This statement was approved by the American Heart Association Science Advisory and Coordinating Committee on December 20,
2013. A copy of the document is available at http://my.americanheart.org/statements by selecting either the “By Topic” link or the “By
Publication Date” link. To purchase additional reprints, call 843-216-2533 or kelle.ramsay@wolterskluwer.com.
The online-only Data Supplement is available with this article at http://hyper.ahajournals.org/lookup/suppl/doi:10.1161/HYP.
0000000000000007/-/DC1.
Flynn et al. Page 2
hypertension.5 As our population continues to age, this will only increase, because 90% of
people with normal BP at age 55 years will go on to develop hypertension in their lifetimes.6
The prevalence of hypertension in youths is also on the rise. US National Health and
Nutrition Examination Survey (NHANES) data from 1963 to 2002 showed a 2.3% increase
in prehypertension and a 1% increase in hypertension from 1988 to 1999, with higher rates
in non-Hispanic blacks and Mexican Americans.7 In fact, the entire distribution of childhood
BP has shifted upward in the United States by 1.4 mm Hg for systolic BP (SBP) and 3.3 mm
Hg for diastolic BP (DBP).8 However, adjustment of the NHANES data for body mass
index (BMI) attenuated the increase in SBP by 29% and DBP by 12%, which suggests that
some of the increase may be related to the obesity epidemic.8 This is supported by studies of
the effect of the westernization of primitive societies, in which BMI has the most substantial
effect on the age-related increase in BP compared with all other risk factors.9 A cross-
sectional pediatric study conducted in Canada found that obese adolescents had 7.6 mm Hg
higher SBP than normal-weight youths, with BMI exerting the strongest effect on BP.10 The
increased prevalence of prehypertension and sustained hypertension with increasing BMI
was confirmed in a school-based study in Texas.11 Furthermore, longitudinal evaluation of
the National High Blood Pressure Education Program childhood BP database confirmed that
a higher BMI increases the rate of progression from prehypertension to hypertension.12
However, an obesity-related increase in BP has not been documented in all studies. In the
Bogalusa Heart Study, which used the mean of 6 resting BP measurements instead of 2 or 3
measurements, there was a significant increase in the prevalence of obesity from 1974 to
1993, yet there were only small changes in BP levels.13 Therefore, despite methodological
differences that make cross-population estimates of hypertension difficult to interpret,14
most investigators believe obesity-related hypertension is on the rise.
The rise in prevalence of hypertension in the young is especially worrisome, because

autopsy studies such as the Bogalusa Heart Study and the Pathobiological Determinates of
Atherosclerosis in Youth study have demonstrated increased atherosclerosis at higher BP
levels in youths.15,16 Therefore, accurate assessment of BP and treatment of hypertension in
children and adolescents are essential for the prevention of future heart disease.17 Emerging
data suggest that ABPM may be superior to clinic BP in predicting cardiovascular morbidity
and mortality in adults.18 For this reason, ABPM is being increasingly used in the evaluation
for hypertension and risk of end-organ damage in youths.
BP and Risk for Target-Organ Damage

Substantial data exist that link elevated BP levels measured in childhood and future target-
organ damage. Pooled data from longitudinal epidemiological studies of cardiovascular risk
factors in youths from the International Childhood Cardiovascular Cohort (i3C) Consortium
demonstrated that higher BP measured at as young as 12 years of age predicted increased
adult carotid intima-media thickness (cIMT).19 Similarly, childhood hypertension was
related to higher adult pulse-wave velocity in the Cardiovascular Risk in Young Finns
Study,20 which indicates increased arterial stiffness, and the Bogalusa Heart Study found
that the cumulative burden of SBP from childhood to adulthood was a significant predictor
of adult left ventricular mass (LVM).21

Flynn et al. Page 3
BP levels have also been related to target-organ damage measured in childhood. SBP has
been demonstrated to independently determine cIMT in both children22 and adolescents.23
Alterations of vascular function also occur at higher levels of childhood BP, including
reduced brachial artery distensibility,24,25 higher pulse-wave velocity,26,27 and increased

augmentation index,28 all of which indicate increasing arterial stiffness. This is relevant to
future cardiovascular disease, because increased vascular thickness29 and stiffness30 are
associated with higher LVM in adolescents, a risk factor for future adult cardiovascular
disease.31 Therefore, it is not surprising that hypertensive youths may demonstrate left
ventricular hypertrophy (LVH),32,33 but what is even more worrisome is the observation that
adolescents with prehypertension already have higher LVM values than normotensive
control subjects.28,34 Furthermore, hypertension may also have neurovascular consequences,
because untreated hypertensive children had lower cerebral artery reactivity than
normotensive control subjects,35 which may explain the lower scores on cognitive tests
found in children with elevated BP.36
ABPM may be superior to casual (office) BP measurement in its ability to distinguish

patients at the highest risk for target-organ damage. In adults, ABPM correlates more
strongly with LVM than casual BP.37 In children in a hypertension clinic, no correlation was
found between LVM and casual BP, yet a strong relationship existed with ABPM
parameters.38 In fact, when hypertension was confirmed by 24-hour ABPM, the odds for
LVH were 7.23 compared with only 4.13 when hypertension was diagnosed with casual BP
levels.39 Another study found APBM parameters were superior to both casual and home BP
in predicting LVM.40 Most other pediatric studies, with 1 notable exception,41 have
confirmed the strong relationship between hypertension diagnosed with ABPM and elevated
LVM.34,42–44 The 1 study that found no association between ABPM and LVM was missing
echocardiograms on 24% of subjects (possible selection bias) and used oscillometric devices
to measure casual BP (possible measurement bias).41
Increased cIMT, a risk factor for stroke in adults,45 is similarly correlated with high BP on
ABPM,46,47 with the relationship independent of casual BP.48 In hypertensive children,
thicker cIMT is found with higher ABPM levels,49–51 even when the children are matched
by BMI.52 The only study that found no relationship between ABPM levels and cIMT was a
small study of children who had received a renal transplant, in whom other serious disease
processes or medication use may have confounded the relationship.53 New data are now
available relating BP measured with ABPM and arterial stiffness. The ambulatory arterial
stiffness index (AASI), which correlates with pulse-wave velocity, is calculated as 1 minus
the regression slope of DBP plotted against SBP from ABPM. Using this technique,
Simonetti et al54 found that hypertensive children had higher AASI values than
normotensive control subjects. This has been replicated in youths with type 1 diabetes
mellitus and hypertension.55 Using direct measurements, when BP was evaluated with
ABPM, youths categorized as either prehypertensive or truly hypertensive had increased
pulse-wave velocity compared with normotensive subjects.56 In obese youths, higher ABPM
(but not casual BP) was found to be associated with higher carotid stiffness and reduced
endothelial function.57 Similarly, decreased carotid distensibility was associated with higher
daytime ambulatory SBP load in pediatric renal transplant recipients.58

Flynn et al. Page 4
Usefulness of ABPM to Classify BP

White Coat Hypertension
White coat hypertension (WCH) is defined as casual/office BP levels that are ≥95th
percentile but normal outside of a clinical setting. It has been suggested that high BP
variability, perhaps caused by transient, stress-induced elevation of BP, may contribute to
clinical misclassification of hypertension.59 However, WCH may not be entirely benign. In
adults with normal ABPM, BP variability increases with increasing BP and is associated
with target-organ damage and cardiovascular events.60 In fact, WCH may represent an
intermediate pathophysiological stage between normotension and hypertension.61 Target-
organ damage, such as increased LVM,32,51,62,63 increased cIMT,51,63 abnormalities in BP
and heart rate rhythmicity,64 and impaired cerebral vascular reactivity,65 may develop in
youths with WCH.
A wide range of WCH prevalence has been reported in the literature. A study of 18 male
adolescent athletes reported 88% had WCH,66 whereas a study of 1071 Icelandic children 9
to 10 years of age found sustained hypertension in 2.5% and WCH in just 0.6%.67 Other
pediatric studies have reported the prevalence of WCH to be in the range of 22% to 32%.68
Of note, Sorof et al69 have suggested that the use of ABPM to rule out WCH should be
limited to patients with borderline or mild clinical hypertension, because patients with
higher office BP levels are more likely to be truly hypertensive.
Masked Hypertension
ABPM may also detect masked hypertension (MH), defined as a normal clinic BP but
elevated ambulatory levels. MH is difficult to detect but may be suspected with previous
reports of elevated clinical BP from other providers, or if the clinical presentation (ie, LVH)
appears inconsistent with the clinic BP. Estimates of the prevalence of MH range from 7.6%
in 592 unselected children70 to 9.4% in 85 youths referred for hypertension evaluation71 to
15% in Brazilian youths.72 In 1 study, rates of MH did not appear to differ by age (older or
younger than 15 years),73 but MH may be more common in obese youths (19%), especially
if they display a nondipper pattern (32.3%; P≤0.001).74 A meta-analysis reported a 7%
prevalence of MH in children and 19% in adults, with an overall average of 16.8%.75 This
report also found that LVM in patients with MH was higher than in normotensive people
and similar to that in people with sustained hypertension, which suggests that MH imparts a
similar cardiovascular risk as sustained hypertension.75 In pediatric patients, data also
suggest that MH predicts target-organ damage.70,71 Unfortunately, determining the true
prevalence of MH would require the use of ABPM in large unselected populations.
Other situations in which ABPM may be especially helpful in “unmasking” hypertension

include pediatric dialysis patients, whose BP may be normal after dialysis but hypertensive
at other times.76 Similarly, after aortic coarctation repair, MH was associated with abnormal
left ventricular structure and function.77 The prevalence of MH was reported at 9.5% in
youths with type 1 diabetes mellitus.68

Flynn et al. Page 5
Prehypertension and Progression to Sustained (Ambulatory) Hypertension

Prehypertension is now recognized as a condition that requires careful evaluation and
follow-up. Pediatric patients with casual prehypertension may demonstrate abnormalities on

ABPM intermediate between normotensive and truly hypertensive people,78 and some
studies have demonstrated subtle signs of target-organ damage in patients with
prehypertension, including LVM values similar to youths with sustained hypertension,34
lower glomerular filtration rate, and increased urine protein excretion,79 as well as higher
cIMT than normotensive patients.80 Patients with prehypertension may also be at higher risk
of progressing to sustained hypertension.12 Although no longitudinal ABPM studies have
been performed to evaluate the risk of progression of prehypertension, such studies could
clarify the importance of prehypertension by providing more careful phenotyping of the BP
patterns that produce the highest risk of progression to sustained hypertension.
Determinants of Ambulatory BP
Several determinants that influence ambulatory BP must be adjusted for in the establishment
of normalized values in pediatric patients. In the pediatric population, age is independently
correlated with 24-hour SBP81 and BP variability.82,83 Birth weight has been shown to be
associated with ambulatory BP. Most but not all studies84 find an inverse association
between birth weight and daytime SBP after controlling for covariates.85–89 Ethnicity is
known to influence ambulatory BP in children and youths, an effect that may be attributable
to racial differences in the relationship of body size to BP90,91 or racial differences in the
effect of psychosocial stress on BP.92 Ambulatory BP is also affected by sex, with male
youths having higher ambulatory BP than their female counterparts, irrespective of
ethnicity.93,94 Obesity, possibly through the restriction of sodium excretion,95 is associated
with increased ambulatory BP.95,96
Other proposed determinants of ambulatory BP include autonomic tone,97–99

adiponectin,100,101 and serum uric acid.102 Lower plasma renin activity was independently
associated with lower 24-hour SBP in obese adolescents.103 However, blood aldosterone-to-
renin ratio was not found to be associated with ambulatory BP in healthy children, although
it did correlate with LVM.104 Finally, elevation of several ambulatory BP parameters has
been associated with stimulant use in pediatric patients, including stimulants used for
attention deficit/hyperactivity disorder105,106 and caffeine.107
Normative Data for ABPM

Data on normal ambulatory BP ranges in pediatric patients are required for the effective
application of this assessment tool to this population. Once normal reference values are
established, clinically relevant ABPM abnormalities can be differentiated and quantified as
important deviations from the population-based distributions. Reference data must be
derived from studies of healthy populations with sufficiently large samples that are
proportionally representative of the larger pediatric population. Ideally, samples should be
free of confounders that may alter BP measurement, including concurrent medication use
and comorbidities such as obesity. Normative data should allow calculation of standardized
values, particularly z scores and percentiles. Particularly in pediatric patients, assessment

Flynn et al. Page 6
should be adjusted for various determinants of BP, such as age, sex, body size, race, and
ethnicity. Established normative ambulatory BP ranges should also be validated by
determination of associations with clinically relevant outcomes in the reference population,
for example, end-organ damage and cardiovascular mortality/ morbidity.108 Although these
associations have been determined in adults on the basis of a growing body of evidence,
outcomes are largely preclinical in the pediatric population, and necessary longitudinal data
are lacking; hence, the definitions are based on population-based distributions.
ABPM values differ substantially from casual measurements; therefore, comparisons to

normative casual BP values such as those in the Fourth Report on the Diagnosis, Evaluation,
and Treatment of High Blood Pressure in Children and Adolescents101a or the more recent
integrated pediatric cardiovascular risk reduction guidelines17 may result in mis-
classification of BP category.109,110 Reference values provided by the German Working
Group on Pediatric Hypertension are currently considered the best available data for
pediatric ABPM.81,111 Of several ABPM studies in healthy control subjects, this study alone
has established percentiles normalized for the nongaussian distribution of 24-hour BP in
children according to age and sex, using the LMS analysis method.81 However, as
highlighted by Flynn,112 this data set has several limitations. First, it includes only central
European white children, which limits its generalizability given that normal ABPM ranges
appear to vary with ethnicity.113 Furthermore, relatively few shorter children (<140 cm in
height) were included, which may limit the applicability of the results to children with
certain health conditions, specifically chronic kidney disease (CKD).112 Finally, the data set
demonstrated a striking lack of variability in ambulatory DBP values (Figure); resting DBP
is known to vary by age and height, whereas at least 1 study has shown that ambulatory
DBP varies with age.112,114 Thus, the normative values provided by the German Working
Group on Pediatric Hypertension may not be representative of the normal ambulatory DBP
in all pediatric patients.
Beyond these data, other groups have measured ABPM in healthy populations, although
none have provided useful normative values. O’Sullivan et al115 studied ambulatory BP in
1121 healthy school-aged children, reporting mean SBP and DBP during time at school, at
home, and asleep. Ambulatory SBP was found to have a wide range in normal children, and
no important differences were noted between school and home hours. Another study by
Lurbe et al116 assessed ABPM values in 241 healthy children aged 6 to 16 years and
reported BP as systolic and diastolic means and percentiles, circadian variability, and
pressure load. Some ABPM data have also been collected from very young healthy children;
Varda et al117 studied the applicability of ABPM in 97 healthy infants and toddlers,
reporting mean daytime, nighttime, and 24-hour SBP and DBP. Similarly, Gellermann et
al118 reported mean daytime and nighttime SBP and DBP for healthy children aged 3 to 6
years. Still, despite this research, there is a critical need for expanded normative data for
pediatric ABPM; specifically, normal values for ambulatory DBP are needed, because they
may not be appropriately represented by the currently available data.

Flynn et al. Page 7
Methods for Performance of ABPM

Nursing Implications
Nurses and other healthcare personnel involved in ABPM should follow a standardized
approach to ABPM to maintain the functionality of the equipment, minimize measurement
errors, and obtain valid, reliable, and reproducible BP data.3 Care of the equipment may
include yearly calibration (by either the institution’s biomedical engineering department or
the manufacturer), depending on the manufacturer’s recommendation; cleaning the hardware
with disinfecting wipes; and laundering the reusable cloth covers for the BP cuffs between
patients. The nurse or other appropriately trained staff should review the patient’s history for
any contraindications to ABPM (severe clotting disorders or rhythm disturbances, and for
some brands of equipment, latex allergy). Serious adverse events such as arm vein
thrombosis have not been reported in children, although mild sleep disturbances have been
documented.119,120 Although some investigators do not believe these alterations in sleep
substantially alter ABPM results,121 1 study did find higher 48-hour ABPM in white but not
black adolescents who had shortened actigraphy-assessed sleep time.122
Care should be taken in selection of the appropriate size cuff according to published
guidelines.101a Although casual BP is usually taken in the dominant arm, ABPM should be
applied to the child’s nondominant arm to avoid interference with school work, unless the
child has arterial surgery on that side, such as repair of coarctation of the aorta or creation of
an arteriovenous fistula.101a After application, the ambulatory BP should be measured and
compared with resting, clinic BP by use of the same technique as the ABPM (auscultatory or
oscillometric). If the average of 3 values is >5 mm Hg higher or lower, cuff placement
should be adjusted or the device checked for calibration.
Successful ABPM is possible in most patients even during sleep,124 and comprehensive,
standardized patient/parent education will reduce the failure rate in obtaining accurate
ABPM.125 Patients and their parents need to be instructed how to stop a reading if there is
excessive discomfort. This may signal kinked tubing. They should also be told to keep the
arm still during readings. This is essential. Continuing with normal activities of daily living
is encouraged, but monitors should not be allowed to get wet during swimming or damaged
during contact sports. Removal of the monitor is not recommended, but if absolutely
necessary, the device should be removed immediately after a reading to reduce the number
of missed readings and reapplied as soon as possible. Finally, children should maintain a
diary that indicates sleep and wake times, as well as activities that may influence BP
measurements, including stressful situations or exercise, and timing of anti-hypertensive
medications. Symptoms such as dizziness should also be recorded, because up to 91% of
children with a history of syncope demonstrate postural hypotension on ABPM.126
After the ABPM data have been downloaded, the readings should be scanned briefly to
assess the quality of the study. If BP dipping is seen at times other than the sleep time noted
in the patient log, clarification with the patient of actual sleep/ wake times may be needed.
Common reasons for missing data include the patient disconnecting the device at night,
suspension of a reading by use of the cancellation button, turning the monitor off, dead
batteries, movement artifact, or kinks in the tubing. Obtaining additional information from

Flynn et al. Page 8
the patient will help determine whether missing data are patient or device related. Because
ABPM studies as short as 6 hours’ duration have been found to correlate with 24-hour
results in 1 recent pediatric study,127 many physicians will still interpret and accept the
results of shortened monitoring periods for routine clinical care.
Equipment
For more detail on equipment used in ABPM, refer to the 2008 AHA scientific statement.3
Briefly, both oscillometric and auscultatory monitors are available for use in pediatric
ABPM.111,115 Many monitors are available and have been evaluated with use of the
Association for the Advancement of Medical Instrumentation US national standard or the
British Hypertension Society standard.128,129 A comprehensive list noting validation status
is available online at www.dableducational.org. Unfortunately, monitors that have not
undergone validation testing or US Food and Drug Administration clearance can be sold in
the United States, and few have been formally validated in children.130 Child-specific issues
include the need for lightweight devices appropriate for smaller bodies, proper cuff sizing to
ensure that the cuff width is ≈40% of the midarm circumference, and device tolerance of
excessive motion.101a For auscultatory devices, users should ascertain whether the fourth or
fifth Korotkoff sound is being used to estimate DBP and should be aware that no normative
data are available for auscultatory ABPM.131,132 Although oscillometric devices may be
easier to use and have fewer erroneous readings, oscillometric BP measurement also has
inherent limitations, as reflected in the generally lower ratings on British Hypertension
Society protocol evaluation.108 Nevertheless, most centers that perform ABPM in children
and adolescents use oscillometric devices. These issues are summarized in Table 1.
Frequency of Measurement and Accounting for Activity

Expert opinion in pediatric ABPM recommends that at least 1 or 2 valid readings should be
obtained per hour over the entire 24 hours (including during sleep) to consider an ABPM
study to be adequate/interpretable. In routine clinical practice, it may be acceptable to
consider as “interpretable” some ABPM studies that do not meet this high standard. Ideally,
monitors should be programmed to obtain readings every 15 to 20 minutes, although some
decrease in frequency during sleep is acceptable. Patient diaries are critical tools in the
proper use of ABPM and should at minimum record the sleep times, nap times, and periods
of physical activity.133,134
Interpretation software allows for customization of diurnal patterns and exclusion of selected
readings gleaned ideally from accurate diary entries. Without specific day/night notation,
automatic nighttime divisions may be set that range anywhere from a 9 PM to midnight start
time and from a 6 to 9 AM wake time, with some algorithms excluding the readings
obtained during these “buffer” periods.111 The use of inappropriate day/night divisions can
lead to substantial mis-classification.133 Alternatively, patient-independent activity monitor–
derived notation of diurnal cycles may be superior to patient notation.135 Activity period
BPs are shown to be captured reliably on ABPM in general, although some specialists
recommend avoidance of contact sports or vigorous exercise during ABPM.134,136 One
study found that for each 1-unit increase in physical activity recorded by wrist actigraph,
there were increases in SBP, DBP, and heart rate on ABPM of 0.02 mm Hg, 0.01 mm Hg,

Flynn et al. Page 9
and 0.02 bpm, respectively.137 Recording on a school day may also be helpful, because
weekend days may produce lower ABPM results.138
Editing Data and Calculations

Interpretation of ABPM studies is usually based on a combination of criteria, including
mean SBP or DBP and BP loads. First, outlier data are filtered out by various automated
approaches to minimize the observer bias inherent in users selecting particular
measurements139,140; however, these automated filters may not be appropriate for young
children, so caution is advised. Then, mean SBP and DBP are calculated for the entire 24-
hour period, as well as the wake and sleep periods, with software that allows the user to
define the diurnal transitions.141 BP load is then calculated as the proportion of readings
above a threshold (usually the pediatric 95th percentile). Dipping is defined as the
percentage drop from mean daytime to mean nighttime levels.
More complicated calculations of circadian BP rhythms have also been attempted in

pediatric patients. One group used Fourier analysis to define circadian (24-hour) and
ultradian (6-, 8- and 12-hour) BP rhythms in 938 healthy school children aged 5 to 18
years.142 When these methods were applied to children and adolescents with stage 2 to 4
CKD, a lower amplitude of circadian and all ultradian BP and heart rate rhythms (P<0.01)
was found than in the healthy cohort.143 BP variability can also be calculated. Compared
with mean BP values, BP variance over long- and short-term periods may be a better
reflection of consequential biological dysfunction in BP regulatory mechanisms, such as
alterations in the sympathetic nervous system.144 The standard deviation of BP during a 24-
hour ABPM provides an account of short-term BP variability, whereas visit-to-visit BP
variation is posited to reflect long-term variability.145–147 More long-term variability
predicts LVH and cardiovascular events such as stroke,60,147 whereas short-term BP
variability is associated with LVH in children.148 Another parameter calculated from ABPM
is the AASI (see preceding section on target-organ damage). In adults, the AASI correlates
with arterial stiffness (pulse-wave velocity)149 and predicts cardiovascular mortality.150 In
children, the AASI was found to be elevated in hypertensive children.54,151 Although
interesting, these advanced calculations remain feasible only in a research setting.
Interpretation
The standard parameters of mean BP level, load, and dipping are compared against
normative pediatric values to determine normal or elevated BP. The smoothed age- and sex-
specific 95th percentiles of Wühl et al,81 which were calculated from the original data from
Soergel et al,111 are the preferred reference data (Appendix Tables A1 through A4).
Differences in normative standards can lead to variability in diagnosis.108,133,152 BP loads in
excess of 25% are generally considered abnormal, with increased loads associated with
LVH.38,153 The circadian BP decline from day to night, termed dipping, should be ≥10%.154
Reproducibility
Although few studies of reproducibility of ABPM have been conducted in pediatric
patients,155–157 most experts agree there is a moderate to strong correlation seen in serial
ABPM measurement.158 Furthermore, ABPM is superior to casual BP measurement both in

Flynn et al. Page 10
identifying children with target-organ damage and in determining adequate antihypertensive

therapy, thus supporting the superiority of an ABPM-derived assignment of hypertension
compared with casual BP in children, as in adults.34,41,148,157,159–164 However, outcome
data linking ABPM in childhood or adolescence to cardiovascular disease in adulthood are

not yet available.
Recommendations for Standard Application of ABPM in Pediatrics

The preceding sections have outlined the advantages of ABPM in specific clinical situations
in the evaluation and management of pediatric hypertension, as well as the rationale for
modification of the prior recommendations for interpretation of ABPM studies in children
and adolescents. Although there remain some uncertainties with respect to ABPM in
pediatrics,112 its benefits likely outweigh the uncertainties in most patients, particularly for
initial diagnosis. Additionally, there are clearly disease states in which ABPM has been
shown to be particularly useful, as summarized in Table 2 and discussed further in the
online-only Data Supplement.
What follows is a synthesis of our recommendations for pediatric ABPM in list form, which
we hope will prove useful to clinicians who obtain ABPM studies in children and
adolescents.
• Indications for routine performance of ABPM include the following:
– To confirm the diagnosis of hypertension in a patient with hypertension

according to casual BP measurements
♦ Determine whether sustained hypertension or WCH exists
– To evaluate for the presence of MH when there is a clinical suspicion of

hypertension but normal or prehypertensive casual measurements
– To assess BP patterns in high-risk patients
♦ Assess for abnormal circadian variation in BP, such as

blunted dipping or isolated sleep hypertension in patients
with diabetes mellitus, CKD, solid organ transplants, and
severe obesity with or without sleep-disordered breathing.
♦ Assess the severity and persistence of BP elevation in

patients at high risk for hypertensive target-organ damage.
– To evaluate effectiveness of drug therapy for hypertension
♦ Confirm BP control in treated patients, especially those with

secondary forms of hypertension.
♦ Evaluate for apparent drug-resistant hypertension.
♦ Determine whether symptoms can be attributed to drug-

related hypotension.
• An ABPM device suitable for use in children should be selected.

– Only devices that have been validated according to Association for the
Advancement of Medical Instrumentation or British Hypertension Society
standards should be used.
– An oscillometric or auscultatory technique can be used.
– Appropriate cuff sizes as recommended in the Fourth Report on the

Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children
and Adolescents101a must be available for the device selected.
• A standard approach to obtaining ABPM readings should be used.
– ABPM should only be performed by personnel with specific training in

the application of the device and interpretation of ABPM data in pediatric
patients.
– Monitors should be applied to the nondominant arm unless contraindicated

(presence of a permanent dialysis access), or if a significant BP
discrepancy between the extremities exists, the monitor should be placed
on the arm with the higher BP.
– Devices should be programmed to record BP every 15 to 20 minutes

during waking hours and every 20 to 30 minutes during sleep.
– After application, BP measured with the device should be compared with

resting, clinic BP by the same technique used by the ambulatory device
(auscultatory or oscillometric).
– Patients should be instructed to record antihypertensive medication

administration, activity, sleep, and wake times in a diary.
• A sufficient number of valid BP recordings are needed for a study to be considered

interpretable.
– Minimum of 1 reading per hour, including during sleep
– At least 40 to 50 readings for a full 24-hour report
– 65% to 75% of all possible BP readings for a partial day report (depends
on frequency of recording programmed into the monitor)
• ABPM recordings should be edited for outlying values.
– Data should be inspected visually for gross inconsistencies that fall

considerably outside the normal ranges for awake or asleep BP and heart
rate for the patient’s age.
– Values that fall outside of the following range should be discarded:
♦ SBP 60 to 220 mm Hg
♦ DBP 35 to 120 mm Hg
♦ Heart rate 40 to 180 bpm
♦ Pulse pressure 40 to 120 mm Hg

– Ideally, the above limits should be programmed into the ABPM software
to minimize subjective editing of ABPM data.
– Any resting BP measurements made with the ABPM device immediately

after application of the device should also be edited out.
• Standard calculations should be reported.
– Mean ambulatory SBP and DBP during the entire 24-hour awake and
sleep periods.
– BP load (percentage of readings above the ambulatory 95th percentile) for

both SBP and DBP during the entire 24-hour awake and sleep periods.
– Dipping (percent day/night difference) should be determined ([mean

awake BP-mean sleep BP]/mean awake BP×100) for both SBP and DBP.
• ABPM levels should be interpreted with appropriate pediatric normative data.
– ABPM values should be compared with sex- and height-specific data

obtained in large pediatric populations using similar techniques3 and not
with resting BP levels.
– A suggested schema for staging ABPM is included in Table 3. These are

consensus rather than evidence-based recommendations because of a lack
of pediatric cardiovascular outcome data based on ABPM.
Interpretation of ABPM Studies

Building on an earlier proposed classification scheme by Lurbe et al,108 the 2008 AHA
statement issued suggested criteria for classification of children as normotensive, white coat
hypertensive, prehypertensive, masked hypertensive, and hypertensive.3 These
recommended classifications incorporated the office BP reading and the mean ambulatory
SBP. Of note, this scheme is different from that used to analyze ABPM studies in adults,
which uses fixed BP levels as normal/abnormal, does not include a prehypertension
category, and considers a slightly higher BP load of 30% to be abnormal.165
Since publication of the AHA statement in 2008, the field of pediatric ABPM has continued
to advance rapidly, and several issues have arisen with respect to the suggested classification
scheme in that document. Some of these issues have been raised formally through peer-
reviewed publications in the pediatric hypertension literature, and some have become
apparent as practitioners have attempted to apply the classification scheme clinically. These
issues and potential solutions will be addressed in the following sections.
Prehypertension
Several concerns have been raised regarding the definition of prehypertension in the 2008
AHA statement. First, the definition mistakenly states that the office BP cut point for
prehypertension is a BP >95th percentile, but the actual definition by the National High
Blood Pressure Education Program is that prehypertension is office BP ≥90th percentile and
<95th percentile, or >120/80 mm Hg.101a Thus, we have changed the definition of

prehypertension in the classification scheme to office BP ≥90th percentile or >120/80 mm

Hg, mean ambulatory BP <95th percentile but elevated BP loads.
The second concern with prehypertension as defined in the 2008 AHA statement is the lack
of clinical evidence as to whether this actually corresponds to prehypertension as defined by
the National High Blood Pressure Education Program. Only 1 recent study has examined
ambulatory BP in pediatric patients with prehypertension based on office BP.78 Although
the investigators demonstrated that prehypertensive patients had higher ambulatory BP than
normotensive patients, they did not use the 2008 AHA criteria to classify the ambulatory BP
studies and did not report whether the mean ambulatory BP values of the prehypertensive
patients were <95th percentile according to pediatric ambulatory BP criteria. Interestingly,
some of the patients with office prehypertension were indeed hypertensive by ABPM, a
finding that would actually classify them as having MH.
Finally, as noted above, there is no corresponding concept of prehypertension when it comes

to ABPM in adults. This may be related to the lack of incorporation of BP load into the
analysis of ambulatory BP studies in adults in the more recent AHA recommendations for
BP measurement.166 However, many pediatric hypertension experts believe that
prehypertension on casual BP recordings with elevated load, despite normal means, may
represent a higher-risk pattern. Therefore, we have decided to keep this category in the
revised classification scheme.
Diastolic Hypertension
The classification scheme outlined in the 2008 AHA statement suggests that children
undergoing ABPM should be classified on the basis of clinic and ambulatory SBP. Yet in
routine clinical use of ABPM, it is apparent that some children have isolated diastolic
hypertension. The frequency and significance of this are unknown; however, in at least 1
study, diastolic hypertension on ABPM has been shown to potentially signal the presence of
underlying secondary causes of hypertension.167 This would be consistent with single-center
studies that used office BP measurements, which have shown that children with primary
hypertension tend to have isolated SBP elevation,168,169 and with a recent multicenter study
that showed a high prevalence of DBP elevation in younger children with secondary
hypertension.170 These data suggest that diastolic hypertension is important to identify from
a diagnostic standpoint and suggest that DBP elevation should also be incorporated into the
classification.
However, there are some issues related to ambulatory DBP that should be considered. Many
ambulatory BP devices use the oscillometric technique, which has been shown to be less
accurate in measuring DBP than SBP.171,172 Although this may not be true for all devices, it
may in fact be responsible for the remarkable lack of DBP variation that was seen in the
German pediatric ambulatory BP database (Figure).112 On the other hand, all indirect
methods of BP measurement have inaccuracies for both SBP and DBP compared with direct
intra-arterial measurements,173 so perhaps the widely held belief that automated devices are
less accurate for DBP than SBP is erroneous.

One additional issue is that the DBP values found in the German pediatric ambulatory
databases are fairly high: ≈80 to 81 mm Hg for the awake 90th percentile and 82 to 84 mm
Hg for the awake 95th percentile (these are similar for boys and girls and, as noted above,
are similar regardless of height).3 For younger children especially, sustained DBP above this
value would almost certainly be considered hypertensive by most clinicians, and if one
believes that the actual normative values should be lower than this for younger children, one
would potentially miss patients with hypertension if DBP elevation were not included in the
classification scheme. Thus, we have incorporated DBP into the revised ambulatory BP
classification scheme.
Nocturnal Hypertension
Nocturnal hypertension has significant prognostic implications in certain patient
populations, including adults and children with CKD and diabetes mellitus.80,174–178 It has
also been cited as the most significant predictor of cardiovascular outcome in hypertensive
adults.179 Furthermore, isolated nocturnal hypertension occurs commonly in other clinical
situations in which ABPM has proven useful, particularly in solid organ transplantation.180
It is clear from these data that nocturnal hypertension is an important variable that should be
incorporated into any ambulatory BP classification scheme. Thus, we believe that even
patients with isolated abnormalities of sleep BP on ABPM should be considered as having
MH and that abnormalities of sleep BP should be given the same weight as abnormalities of
awake BP.
Mean Arterial Pressure

The majority of devices used to perform ABPM use the oscillometric technique, which
directly measures mean arterial pressure (MAP) and back-calculates SBP and DBP by use of
manufacturer-specific software algorithms. The resultant calculated SBP and DBP values
have been shown to vary significantly compared with SBP and DBP values obtained by
auscultation.173,181 It may be more appropriate to use MAP to classify the results of ABP
studies, because this is the one BP parameter that is measured directly by most devices used
to perform ABPM in children. Furthermore, treatment guided by ambulatory MAP has been
shown to reduce the rate of progression of CKD in the recently published Effect of Strict
Blood Pressure Control and ACE Inhibition on the Progression of CRF in Pediatric Patients
(ESCAPE) trial,182 which further highlights the importance of this ambulatory BP

parameter.
However, additional evidence would likely be needed before MAP could be adopted as the
standard for classifying ambulatory BP studies. Most recent publications on ABPM and
outcomes have reported their results based on ambulatory SBP and DBP. We have included
the full German data set, including MAP values (Appendix Tables A1 through A4). We
encourage investigators to begin examining the relationship between ambulatory MAP and
both intermediate and long-term outcomes so that sufficient evidence can be generated to
fully evaluate the possibility of incorporating MAP into the classification scheme.

Severe Ambulatory Hypertension

This diagnosis should be evaluated in the context of the mean ambulatory BP level. For
instance, a subject with a mean BP level that is mildly elevated (eg, consistently at the 96th
percentile) may have an increased load of >50%, but this may not represent as high a risk as
the subject with load >50% and mean BP at significantly higher than the 95th percentile (eg,
in the 99th percentile) or with “spikes” of BP to extremely high levels.
Uncategorized Patients
The classification scheme in the 2008 AHA statement does not provide guidance on how to
categorize patients with 2 related patterns on ABPM: (1) office BP ≥95th percentile, normal
mean ambulatory BP, and elevated BP loads; and (2) normal office BP (<90th percentile),
normal mean ambulatory BP, but elevated ambulatory BP loads. Should these children be
considered normotensive or masked hypertensive?
How to approach such “unclassified patients” probably depends on whether or not one
agrees that the concept of BP load is a valid parameter to consider. BP load was initially
adopted enthusiastically as a predictor of hypertensive target-organ damage,183 but more
recent studies have not relied on BP load, and the most recent AHA guidelines for analysis
of ABPM studies in adults do not incorporate BP load.166
Interestingly, the investigators of the Chronic Kidney Disease in Children study have
decided to classify these children as having MH,178,184 which may be justifiable in patients
with CKD, but further study is needed to validate this approach in other populations. We
would recommend approaching such patients on a case-by-case basis, taking into account
the presence or absence of underlying secondary causes of hypertension or specific
cardiovascular risk factors.
Revised ABPM Classification

Although further study is needed to answer some of the above questions, we do believe that
the classification scheme in the 2008 AHA statement can be simply modified to address
some of the more obvious issues, including what to do about DBP, isolated nocturnal BP
elevation, and the correct identification of children with prehypertension. We have
summarized these modifications in Table 3.
Conclusions and Future Directions

Although much experience with pediatric ABPM has been gained since publication of the
2008 AHA scientific statement, much more work needs to be done. Specifically, there is an
urgent need for more comprehensive normative ABPM data across sex, race, and age.
Devices that can measure DBP more accurately may be useful in determining the true
increase in DBP over age, because current norms indicate a flat DBP curve (Figure).112
Better data linking ABPM patterns to target-organ damage are also needed to improve our
characterization of BP, because children with abnormal load, dipping, or a circadian pattern
may be at risk for cardiovascular disease despite normal ABPM mean levels. Finally,

additional data evaluating the efficacy of ABPM in measuring the effect of interventions and
effectiveness of ABPM-driven BP control in reversing target-organ damage are needed.
Supplementary Material
Refer to Web version on PubMed Central for supplementary material.
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Appendix
Table A1
Normal Values for Ambulatory BP (mm Hg) for Healthy Boys by Height
Height, cm
BP Percentile 120 125 130 135 140 145 150 155 160 165 170 175 180 185
24-h SBP
50th 104.5 105.3 106.2 107.2 108.3 109.5 110.9 112.5 114.2 116.1 118.0 119.7 121.5 123.2
75th 109.2 110.1 111.1 112.1 113.3 114.6 116.1 117.7 119.5 121.4 123.2 125.0 126.6 128.2
90th 113.8 114.8 115.9 116.9 118.2 119.5 121.0 122.6 124.4 126.3 128.1 129.8 131.3 132.8
95th 116.8 117.8 118.9 120.0 121.2 122.5 124.0 125.7 127.4 129.3 131.1 132.6 134.1 135.5
99th 122.9 123.9 125.0 126.1 127.3 128.6 130.1 131.7 133.4 135.2 136.8 138.2 139.4 140.5
Daytime SBP
50th 110.8 111.1 111.5 112.0 112.7 113.7 115.1 116.8 118.6 120.6 122.6 124.4 126.2 128.0
75th 116.2 116.5 116.9 117.4 118.0 119.0 120.4 122.1 124.2 126.4 128.4 130.3 132.2 134.1
90th 121.7 121.9 122.2 122.5 123.0 123.9 125.3 127.1 129.4 131.9 134.1 136.1 138.0 139.9
95th 125.2 125.3 125.5 125.7 126.0 126.9 128.3 130.2 132.7 135.3 137.6 139.6 141.6 143.5
99th 132.6 132.4 132.2 132.0 132.1 132.8 134.2 136.3 139.1 142.2 144.7 146.8 148.6 150.5
Nighttime SBP
50th 93.6 94.6 95.6 96.7 97.9 99.0 100.1 101.3 102.6 104.1 105.6 107.2 108.7 110.2
75th 98.6 99.8 101.0 102.3 103.6 104.7 105.9 107.1 108.4 109.9 111.5 113.1 114.6 116.1
90th 103.3 104.8 106.3 107.8 109.3 110.6 111.8 113.0 114.3 115.7 117.2 118.8 120.3 121.8
95th 106.3 107.9 109.7 111.4 113.0 114.4 115.7 116.8 118.1 119.4 120.9 122.4 123.9 125.3
99th 112.1 114.2 116.5 118.7 120.8 122.5 123.8 124.9 126.0 127.1 128.4 129.6 131.0 132.2
24-h DBP
50th 65.6 65.9 66.1 66.4 66.6 66.9 67.1 67.2 67.3 67.5 67.6 67.8 68.0 68.2
75th 69.7 69.9 70.2 70.4 70.6 70.8 71.0 71.1 71.2 71.3 71.5 71.7 71.8 71.9

Height, cm
BP Percentile 120 125 130 135 140 145 150 155 160 165 170 175 180 185
90th 73.9 74.1 74.2 74.4 74.5 74.7 74.8 74.8 74.9 75.1 75.3 75.4 75.5 75.6
95th 76.7 76.8 76.9 76.9 77.0 77.1 77.1 77.2 77.3 77.5 77.7 77.8 77.9 78.0
99th 82.7 82.5 82.3 82.1 81.9 81.8 81.8 81.8 81.9 82.2 82.5 82.7 82.9 83.0
Daytime DBP
50th 72.3 72.3 72.2 72.1 72.1 72.1 72.1 72.1 72.2 72.3 72.6 72.8 73.1 73.4
75th 76.5 76.4 76.3 76.2 76.0 76.0 75.9 75.9 76.0 76.2 76.5 76.8 77.2 77.5
90th 80.2 80.1 79.9 79.7 79.5 79.4 79.3 79.3 79.4 79.7 80.0 80.5 80.9 81.3
95th 82.4 82.2 82.0 81.8 81.5 81.4 81.2 81.2 81.3 81.7 82.1 82.6 83.1 83.6
99th 86.5 86.2 85.9 85.6 85.2 85.0 84.8 84.8 85.0 85.4 86.0 86.6 87.3 87.9
Nighttime DBP
50th 54.3 54.8 55.1 55.5 55.8 56.0 56.2 56.2 56.3 56.5 56.7 56.9 57.1 57.3
75th 57.6 58.2 58.8 59.2 59.6 59.9 60.1 60.2 60.2 60.3 60.5 60.6 60.8 60.9
90th 60.7 61.4 62.1 62.7 63.2 63.5 63.7 63.8 63.8 63.9 63.9 64.0 64.1 64.2
95th 62.6 63.4 64.2 64.8 65.4 65.8 66.0 66.0 66.0 66.0 66.1 66.1 66.1 66.2
99th 66.2 67.2 68.2 69.0 69.7 70.1 70.4 70.4 70.3 70.3 70.2 70.1 70.0 69.9
24-h MAP
50th 77.5 78.1 78.7 79.3 79.9 80.5 81.1 81.7 82.3 83.1 83.9 84.7 85.5 86.3
75th 81.8 82.4 83.0 83.5 84.1 84.6 85.2 85.9 86.6 87.3 88.1 89.0 89.8 90.7
90th 86.3 86.7 87.2 87.6 88.0 88.5 89.1 89.7 90.3 91.1 91.9 92.7 93.5 94.3
95th 89.3 89.6 89.9 90.2 90.5 90.9 91.4 91.9 92.6 93.3 94.0 94.8 95.6 96.4
99th 95.9 95.7 95.5 95.4 95.4 95.6 95.9 96.3 96.7 97.4 98.0 98.7 99.4 100.1
Daytime MAP
50th 83.8 84.1 84.3 84.5 84.7 85.0 85.4 85.8 86.4 87.1 88.0 89.0 90.0 91.0
75th 88.5 88.7 88.9 89.0 89.1 89.4 89.6 90.1 90.7 91.6 92.6 93.7 94.9 96.1
90th 92.9 93.0 93.1 93.1 93.1 93.2 93.4 93.8 94.5 95.4 96.5 97.7 99.0 100.3
95th 95.6 95.6 95.6 95.5 95.5 95.5 95.7 96.0 96.7 97.7 98.8 100.1 101.4 102.8
99th 101.0 100.7 100.5 100.2 99.9 99.7 99.8 100.1 100.8 101.7 102.9 104.3 105.7 107.1
Nighttime MAP
50th 66.8 67.6 68.3 69.0 69.6 70.1 70.6 71.2 71.9 72.7 73.6 74.5 75.4 76.2
75th 71.0 71.9 72.7 73.4 73.9 74.4 74.9 75.4 76.0 76.8 77.6 78.3 79.1 79.8
90th 75.9 76.6 77.3 77.9 78.3 78.6 78.9 79.2 79.7 80.3 80.9 81.5 82.1 82.7
95th 79.5 80.0 80.5 80.9 81.2 81.3 81.4 81.5 81.9 82.3 82.8 83.3 83.8 84.3
99th 88.4 88.1 87.8 87.6 87.2 86.7 86.3 86.0 86.0 86.1 86.3 86.5 86.8 87.0
BP indicates blood pressure; DBP, diastolic blood pressure; MAP, mean arterial pressure; and SBP, systolic blood pressure.
Modified from Wuhl et al81 with permission of the publisher. Copyright © 2002, Lippincott Williams & Wilkins, Inc.
Table A2
Normal Values for Ambulatory BP (mm Hg) for Healthy Girls by Height
Height, cm
BP Percentile 120 125 130 135 140 145 150 155 160 165 170 175
24-h SBP

Height, cm
BP Percentile 120 125 130 135 140 145 150 155 160 165 170 175
50th 104.0 105.0 106.0 106.8 107.6 108.7 109.9 111.2 112.4 113.7 115.0 116.4
75th 108.2 109.3 110.3 111.2 112.1 113.2 114.6 115.9 117.0 118.0 119.2 120.4
90th 112.0 113.2 114.3 115.3 116.2 117.4 118.7 120.0 121.0 121.8 122.8 123.8
95th 114.3 115.6 116.7 117.7 118.7 119.9 121.2 122.5 123.3 124.1 124.9 125.8
99th 118.8 120.1 121.3 122.4 123.4 124.6 126.0 127.1 127.7 128.2 128.8 129.3
Daytime SBP
50th 110.0 110.5 111.0 111.6 112.2 113.1 114.3 115.6 117.0 118.3 119.8 121.2
75th 114.4 115.0 115.7 116.3 117.0 118.1 119.4 120.7 121.9 123.1 124.2 125.3
90th 118.2 119.0 119.7 120.4 121.3 122.5 123.9 125.2 126.4 127.3 128.1 128.9
95th 120.4 121.3 122.1 122.9 123.8 125.1 126.5 127.9 129.1 129.8 130.5 131.0
99th 124.5 125.5 126.4 127.4 128.5 129.9 131.5 133.0 134.0 134.5 134.8 135.0
Nighttime SBP
50th 95.0 95.7 96.4 96.9 97.5 98.1 98.9 100.0 101.1 102.2 103.4 104.6
75th 99.4 100.3 101.2 101.9 102.6 103.4 104.4 105.5 106.4 107.3 108.2 109.2
90th 103.3 104.4 105.5 106.5 107.5 108.5 109.5 110.5 111.2 111.8 112.4 113.1
95th 105.6 106.9 108.1 109.3 110.4 111.6 112.7 113.6 114.1 114.4 114.8 115.3
99th 109.8 111.5 113.1 114.7 116.2 117.7 118.9 119.5 119.6 119.4 119.3 119.4
24-h DBP
50th 65.9 65.9 66.0 66.1 66.2 66.3 66.5 66.7 67.0 67.4 68.0 68.6
75th 68.6 68.9 69.2 69.5 69.8 70.1 70.4 70.6 70.7 71.0 71.3 71.6
90th 70.9 71.4 71.9 72.4 72.9 73.4 73.8 74.0 74.1 74.2 74.4 74.5
95th 72.2 72.8 73.4 74.1 74.7 75.3 75.7 76.0 76.1 76.2 76.2 76.2
99th 74.6 75.3 76.2 77.1 77.9 78.7 79.3 79.7 79.9 79.9 79.9 79.7
Daytime DBP
50th 73.2 72.8 72.4 72.1 71.8 71.7 71.8 72.0 72.4 73.1 73.9 74.8
75th 76.9 76.6 76.4 76.2 76.1 76.1 76.1 76.2 76.4 76.8 77.3 77.8
90th 80.1 79.9 79.8 79.8 79.7 79.8 79.9 79.9 79.9 80.0 80.2 80.5
95th 81.9 81.8 81.8 81.8 81.9 82.0 82.0 82.0 82.0 81.9 82.0 82.0
99th 85.3 85.3 85.4 85.6 85.8 85.9 86.0 85.9 85.7 85.4 85.2 84.9
Nighttime DBP
50th 55.4 55.3 55.1 54.8 54.6 54.4 54.3 54.4 54.6 54.9 55.1 55.4
75th 59.5 59.5 59.4 59.3 59.1 58.9 58.8 58.7 58.8 58.9 61.0 59.3
90th 63.1 63.3 63.4 63.4 63.3 63.1 63.0 62.9 62.9 62.9 66.9 63.1
95th 65.2 65.5 65.7 65.8 65.8 65.7 65.6 65.5 65.5 65.5 70.8 65.5
99th 69.1 69.6 70.1 70.4 70.6 70.8 70.8 70.7 70.7 70.6 79.0 70.4
24-h MAP
50th 77.2 77.8 78.3 78.7 79.2 79.7 80.2 80.8 81.5 82.3 83.1 84.0
75th 80.6 81.2 81.8 82.4 82.9 83.5 84.1 84.7 85.3 85.9 86.6 87.4
90th 83.6 84.2 84.9 85.5 86.1 86.7 87.3 87.9 88.4 88.9 89.5 90.1
95th 85.3 86.0 86.7 87.4 88.0 88.6 89.2 89.7 90.2 90.6 91.1 91.7
99th 88.5 89.2 89.9 90.6 91.3 91.9 92.5 93.0 93.3 93.6 94.0 94.5

Height, cm
BP Percentile 120 125 130 135 140 145 150 155 160 165 170 175
Daytime MAP
50th 83.3 83.7 84.0 84.1 84.3 84.5 84.9 85.5 86.2 87.0 88.0 88.9
75th 87.4 87.9 88.2 88.5 88.7 88.9 89.3 89.8 90.3 90.9 91.6 92.2
90th 90.9 91.5 91.9 92.2 92.4 92.7 93.0 93.4 93.7 94.1 94.5 94.9
95th 92.9 93.6 94.0 94.4 94.6 94.9 95.1 95.4 95.6 95.8 96.1 96.4
99th 96.6 97.4 97.9 98.3 98.6 98.8 99.0 99.0 99.0 99.0 99.0 99.1
Nighttime MAP
50th 68.0 68.2 68.4 68.5 68.7 69.0 69.3 69.8 70.4 71.2 72.0 72.8
75th 72.6 72.7 72.9 73.0 73.2 73.5 73.9 74.3 74.8 75.4 76.1 76.9
90th 76.8 76.9 77.0 77.2 77.4 77.7 78.0 78.3 78.6 79.1 79.6 80.3
95th 79.5 79.4 79.6 79.7 79.9 80.2 80.4 80.6 80.8 81.2 81.6 82.2
99th 84.6 84.4 84.5 84.6 84.8 85.0 85.0 85.0 85.0 85.0 85.3 85.6
Table A3
Normal Values for Ambulatory BP (mm Hg) for Healthy Boys by Age
Age, y
BP Percentile 5 6 7 8 9 10 11 12 13 14 15 16
24-h SBP
50th 104.6 105.5 106.3 107.0 107.7 108.8 110.4 112.6 115.1 117.8 120.6 123.4
75th 109.0 110.0 111.0 111.9 112.8 114.1 115.9 118.2 120.9 123.7 126.5 129.4
90th 113.4 114.7 115.8 116.8 117.9 119.2 121.2 123.7 126.4 129.3 132.1 134.9
95th 116.4 117.7 118.9 120.0 121.1 122.5 124.6 127.1 129.9 132.7 135.5 138.2
99th 122.7 124.1 125.4 126.6 127.7 129.2 131.4 134.0 136.9 139.5 142.0 144.5
Daytime SBP
50th 111.1 111.5 111.9 112.2 112.6 113.4 114.9 117.0 119.5 122.3 125.3 128.2
75th 115.7 116.3 116.8 117.3 117.9 118.8 120.5 122.9 125.6 128.5 131.5 134.6
90th 120.1 120.9 121.6 122.2 122.9 124.0 125.9 128.4 131.2 134.2 137.3 140.4
95th 122.9 123.8 124.6 125.3 126.1 127.3 129.3 131.8 134.7 137.7 140.8 143.9
99th 128.5 129.6 130.6 131.5 132.3 133.7 135.8 138.6 141.5 144.4 147.4 150.4
Nighttime SBP
50th 95.0 95.5 96.1 96.7 97.3 98.1 99.4 101.2 103.4 105.8 108.3 110.9
75th 99.2 100.2 101.1 102.0 102.9 103.9 105.3 107.1 109.3 111.9 114.4 116.9
90th 103.4 104.9 106.2 107.5 108.5 109.6 111.0 112.8 115.0 117.5 120.0 122.5
95th 106.3 108.0 109.6 111.0 112.1 113.2 114.6 116.3 118.6 121.0 123.4 125.9
99th 112.3 114.6 116.7 118.4 119.6 120.7 121.9 123.4 125.5 127.8 130.1 132.3
24-h DBP
50th 65.3 65.7 66.1 66.3 66.5 66.6 66.9 67.2 67.4 67.7 68.1 68.6
75th 68.8 69.3 69.6 69.9 70.0 70.2 70.5 70.8 71.0 71.4 71.8 72.3
90th 72.2 72.6 73.0 73.2 73.3 73.4 73.7 74.0 74.3 74.6 75.1 75.6

Age, y
BP Percentile 5 6 7 8 9 10 11 12 13 14 15 16
95th 74.4 74.8 75.1 75.2 75.3 75.4 75.7 75.9 76.2 76.6 77.0 77.5
99th 78.9 79.0 79.1 79.1 79.1 79.1 79.3 79.6 79.9 80.2 80.7 81.3
Daytime DBP
50th 72.2 72.4 72.5 72.5 72.3 72.1 72.0 72.0 72.2 72.5 73.0 73.5
75th 75.9 76.1 76.3 76.4 76.2 76.0 76.0 76.0 76.2 76.5 77.0 77.6
90th 79.1 79.3 79.7 79.8 79.7 79.5 79.5 79.5 79.7 80.0 80.6 81.3
95th 81.0 81.3 81.6 81.8 81.7 81.5 81.5 81.6 81.7 82.1 82.8 83.5
99th 84.5 84.8 85.2 85.5 85.4 85.3 85.3 85.4 85.6 86.1 86.8 87.7
Nighttime DBP
50th 55.0 55.3 55.5 55.7 55.8 55.8 55.9 56.0 56.3 56.5 56.8 57.1
75th 58.5 59.1 59.5 59.8 60.0 60.0 60.0 60.1 60.3 60.5 60.7 60.9
90th 62.3 63.2 63.8 64.2 64.3 64.2 64.1 64.1 64.1 64.2 64.3 64.3
95th 65.1 66.1 66.8 67.1 67.1 66.9 66.7 66.5 66.5 66.5 66.4 66.4
99th 71.6 72.7 73.5 73.5 73.2 72.6 71.9 71.4 71.1 70.8 70.6 70.3
24-h MAP
50th 77.4 77.9 78.7 79.3 79.7 80.2 80.8 81.7 82.7 83.8 85.1 86.4
75th 81.4 81.9 82.7 83.4 83.8 84.3 85.0 85.9 86.9 88.0 89.3 90.5
90th 85.5 86.0 86.8 87.4 87.9 88.3 88.9 89.7 90.6 91.6 92.7 93.9
95th 88.3 88.7 89.5 90.0 90.4 90.8 91.3 91.9 92.7 93.7 94.7 95.7
99th 94.3 94.6 95.1 95.4 95.6 95.7 95.8 96.2 96.7 97.3 98.1 98.9
Daytime MAP
50th 83.5 84.1 84.5 84.8 84.9 85.0 85.3 85.9 86.8 88.0 89.4 90.8
75th 87.5 88.2 88.8 89.2 89.4 89.5 89.9 90.6 91.5 92.7 94.2 95.7
90th 91.3 92.1 92.8 93.3 93.5 93.7 94.0 94.7 95.6 96.8 98.3 99.8
95th 93.6 94.5 95.3 95.8 96.1 96.2 96.5 97.1 98.0 99.2 100.6 102.1
99th 98.2 99.2 100.1 100.7 101.0 101.0 101.2 101.6 102.4 103.4 104.7 106.1
Nighttime MAP
50th 66.7 67.7 68.6 69.2 69.7 70.0 70.5 71.2 72.1 73.1 74.0 74.9
75th 70.5 71.7 72.8 73.5 74.1 74.5 75.0 75.6 76.4 77.2 78.0 78.6
90th 74.7 76.0 77.2 78.1 78.6 78.9 79.3 79.7 80.3 80.8 81.3 81.7
95th 77.6 79.0 80.2 81.1 81.6 81.8 82.0 82.3 82.6 82.9 83.2 83.4
99th 84.1 85.7 86.9 87.6 87.8 87.7 87.4 87.1 86.9 86.8 86.6 86.4
Table A4
Normal Values for Ambulatory BP (mm Hg) for Healthy Girls by Age
Age, y
BP Percentile 5 6 7 8 9 10 11 12 13 14 15 16
24-h SBP
50th 102.8 104.1 105.3 106.5 107.6 108.7 109.7 110.7 111.8 112.8 113.8 114.8

Age, y
BP Percentile 5 6 7 8 9 10 11 12 13 14 15 16
75th 107.8 109.1 110.4 111.5 112.6 113.6 114.7 115.7 116.7 117.6 118.4 119.2
90th 112.3 113.7 115.0 116.1 117.2 118.2 119.2 120.2 121.2 121.9 122.6 123.2
95th 114.9 116.4 117.7 118.9 120.0 121.1 122.1 123.0 123.9 124.5 125.0 125.6
99th 119.9 121.5 123.0 124.3 125.5 126.5 127.5 128.4 129.0 129.5 129.7 130.0
Daytime SBP
50th 108.4 109.5 110.6 111.5 112.4 113.3 114.2 115.3 116.4 117.5 118.6 119.6
75th 113.8 114.9 115.9 116.8 117.6 118.5 119.5 120.6 121.7 122.6 123.5 124.3
90th 118.3 119.5 120.6 121.5 122.4 123.3 124.3 125.3 126.4 127.2 127.9 128.5
95th 120.9 122.2 123.3 124.3 125.2 126.2 127.2 128.2 129.2 129.9 130.4 130.9
99th 125.6 127.1 128.4 129.6 130.6 131.7 132.7 133.7 134.5 135.0 135.2 135.4
Nighttime SBP
50th 94.8 95.6 96.2 96.8 97.5 98.2 99.0 99.7 100.5 101.3 102.0 102.9
75th 100.2 101.1 101.8 102.5 103.2 104.0 104.7 105.2 105.8 106.3 106.8 107.3
90th 105.3 106.3 107.2 108.0 108.8 109.5 110.1 110.4 110.7 110.9 111.0 111.2
95th 108.4 109.6 110.6 111.5 112.3 113.0 113.5 113.6 113.7 113.6 113.5 113.5
99th 114.5 116.0 117.3 118.4 119.3 119.9 120.1 119.8 119.4 118.8 118.2 117.8
24-h DBP
50th 65.5 65.6 65.8 65.9 66.0 66.2 66.4 66.6 67.0 67.2 67.5 67.7
75th 68.9 69.1 69.2 69.3 69.5 69.8 70.0 70.4 70.8 71.1 71.2 71.4
90th 72.1 72.2 72.3 72.4 72.6 72.9 73.2 73.7 74.1 74.4 74.6 74.7
95th 74.0 74.1 74.2 74.2 74.4 74.7 75.1 75.6 76.1 76.4 76.6 76.7
99th 77.6 77.6 77.6 77.6 77.7 78.0 78.4 79.1 79.7 80.1 80.4 80.5
Daytime DBP
50th 72.6 72.6 72.4 72.2 72.0 71.8 71.8 72.1 72.4 72.8 73.2 73.5
75th 76.7 76.6 76.5 76.3 76.0 75.9 75.9 76.2 76.5 76.8 77.0 77.2
90th 80.2 80.2 80.0 79.8 79.5 79.3 79.4 79.6 80.0 80.2 80.3 80.3
95th 82.3 82.2 82.1 81.8 81.5 81.3 81.4 81.6 82.0 82.2 82.2 82.1
99th 86.1 86.0 85.8 85.5 85.2 85.0 85.0 85.3 85.6 85.7 85.6 85.4
Nighttime DBP
50th 56.4 55.9 55.5 55.1 54.8 54.6 54.3 54.2 54.3 54.5 54.9 55.3
75th 61.1 60.6 60.1 59.7 59.4 59.2 58.9 58.7 58.7 58.7 58.8 59.1
90th 65.6 65.1 64.6 64.1 63.8 63.7 63.4 63.1 62.9 62.8 62.8 62.8
95th 68.5 67.9 67.4 66.9 66.6 66.5 66.2 65.9 65.6 65.4 65.3 65.2
99th 74.2 73.6 72.9 72.4 72.2 72.0 71.8 71.4 71.1 70.7 70.3 70.0
24-h MAP
50th 77.5 78.0 78.4 78.8 79.2 79.6 80.2 80.9 81.5 82.2 82.7 83.0
75th 81.2 81.7 82.1 82.5 82.9 83.3 84.0 84.7 85.4 86.0 86.5 86.8
90th 84.6 85.0 85.4 85.7 86.1 86.5 87.1 87.9 88.6 89.2 89.7 89.9
95th 86.6 87.0 87.3 87.6 87.9 88.3 88.9 89.7 90.5 91.0 91.5 91.7
99th 90.5 90.8 90.9 91.0 91.2 91.6 92.2 93.0 93.7 94.2 94.6 94.8
Daytime MAP

Age, y
BP Percentile 5 6 7 8 9 10 11 12 13 14 15 16
50th 83.7 83.9 84.0 84.1 84.2 84.4 84.7 85.2 85.9 86.5 87.1 87.7
75th 88.2 88.3 88.4 88.4 88.4 88.5 88.9 89.4 90.1 90.8 91.4 91.9
90th 92.2 92.2 92.2 92.1 92.0 92.1 92.4 93.0 93.6 94.3 94.8 95.4
95th 94.6 94.5 94.4 94.2 94.1 94.2 94.4 95.0 95.6 96.2 96.8 97.3
99th 99.0 98.7 98.5 98.2 97.9 97.9 98.1 98.6 99.2 99.7 100.2 100.7
Nighttime MAP
50th 68.7 68.8 68.8 68.8 68.9 69.1 69.3 69.6 70.1 70.6 71.2 71.8
75th 73.0 73.1 73.1 73.2 73.4 73.6 73.8 74.1 74.5 74.9 75.4 75.9
90th 76.9 77.0 77.1 77.2 77.4 77.6 77.8 78.0 78.3 78.6 78.9 79.3
95th 79.2 79.4 79.6 79.7 79.8 80.1 80.2 80.3 80.5 80.7 80.9 81.2
99th 83.8 84.1 84.2 84.3 84.5 84.6 84.7 84.6 84.6 84.6 84.6 84.7
Disclosures
Writing Group Disclosures
Writing Other Speakers’ Consultant/

Group Research Research Bureau/ Expert Ownership Advisory
Member Employment Grant Support Honoraria Witness Interest Board Other
Joseph T. Flynn Seattle Children’s Hospital None None None None None None None
Stephen R. Daniels University of Colorado None None None None None None None
Laura L. Hayman University of Massachusetts None None None None None None None
David M. Maahs University of Colorado, Denver Abbott None None None None None None
Diabetes
Care†; Eli
Lilly &
Co†
Brian W. McCrindle The Hospital for Sick Children None None None None None None None
Mark Mitsnefes Cincinnati Children’s Hospital None None None None None None None
Elaine M. Urbina Cincinnati Children’s Hospital NHLBI† None None None None None None
Justin P. Zachariah Boston’s Children’s Hospital None None None None None None None
Heart Foundation/Harvard
Medical School
This table represents the relationships of writing group members that may be perceived as actual or reasonably perceived
conflicts of interest as reported on the Disclosure Questionnaire, which all members of the writing group are required to
complete and submit. A relationship is considered to be “significant” if (1) the person receives $10 000 or more during any
12-month period, or 5% or more of the person’s gross income; or (2) the person owns 5% or more of the voting stock or
share of the entity, or owns $10 000 or more of the fair market value of the entity. A relationship is considered to be
“modest” if it is less than “significant” under the preceding definition.
†
Significant.
Reviewer Disclosures
Speakers’ Consultant/
Research Other Research Bureau/ Expert Ownership Advisory
Reviewer Employment Grant Support Honoraria Witness Interest Board Other
Rae-Ellen W. Kavey University of Rochester None None None None None None None
Karen L. Redwine Arkansas Children’s Hospital UAMS Translational Research None None None None None None
Institute

Speakers’ Consultant/
Research Other Research Bureau/ Expert Ownership Advisory
Reviewer Employment Grant Support Honoraria Witness Interest Board Other

(KL2RR029883/1UL1RR029884)
†
Joshua Samuels University of Texas Health None None None None None None None
Science Center at Houston
This table represents the relationships of reviewers that may be perceived as actual or reasonably perceived conflicts of
interest as reported on the Disclosure Questionnaire, which all reviewers are required to complete and submit. A
relationship is considered to be “significant” if (1) the person receives $10 000 or more during any 12-month period, or 5%
or more of the person’s gross income; or (2) the person owns 5% or more of the voting stock or share of the entity, or owns
$10 000 or more of the fair market value of the entity. A relationship is considered to be “modest” if it is less than
“significant” under the preceding definition.
†
Significant.

Figure.
Graph of mean daytime diastolic ambulatory blood pressure (BP) for girls according to
height in the Central European pediatric ambulatory blood pressure monitoring database.
DBP indicates diastolic blood pressure. Modified from Wühl et al81 with permission of the
publisher. Copyright © 2002, Lippincott Williams & Wilkins, Inc.


Table 1
Pros and Cons of Oscillometric Versus Auscultatory Ambulatory BP Devices

Oscillometric Auscultative
Pros: Pros:
• Easier to use • Diastolic BP may be defined as 4th or 5th Korotkoff sound
• Fewer erroneous readings • Systolic and diastolic pressures are measured in a similar fashion to resting,
casual BP
Cons: Cons:
• Systolic and diastolic pressures are • No normative data available
calculated, not measured
• More difficult to use
• Calculation formulas are proprietary
• Fewer machines to choose
• No consensus on lower age at which Korotkoff sounds are audible or
accurate
BP indicates blood pressure.


Table 2
Conditions in Which ABPM May Be Particularly Helpful*

Condition Relevance of ABPM

Secondary hypertension Elevated load, abnormal dipping and variability
Chronic kidney disease Prevalence of hypertension, masked hypertension, association with target- organ changes and disease
progression
Types 1 and 2 diabetes mellitus Abnormal circadian variation, association with microalbuminuria and vascular changes
Obesity Masked hypertension, correlation between BMI and hypertension severity, abnormal dipping, association
with target-organ damage
Sleep apnea Hypertension severity, abnormal circadian variation
Genetic syndromes Abnormal BP patterns indicating secondary cause of hypertension, especially renal artery stenosis and
Neurofibromatosis type 1 aortic coarctation
Turner syndrome
Williams syndrome
Treated patients with hypertension Response to antihypertensive medications and/or lifestyle changes
Hypertension research Reduction in subject number in drug trials
ABPM indicates ambulatory blood pressure monitoring; BMI, body mass index; and BP, blood pressure.
*
For a detailed discussion and references, see the online-only Data Supplement.

Table 3
Suggested Revised Schema for Staging of Ambulatory BP Levels in Children

Mean Ambulatory SBP or SBP or DBP Load,

Classification Office BP* DBP†,‡ %‡,§
Normal BP <90th %tile <95th %tile <25
White coat hypertension ≥95th %tile <95th %tile <25
Prehypertension ≥90th %tile or >120/80 mm <95th %tile ≥25
Hg
Masked hypertension <95th %tile >95th %tile ≥25
Ambulatory hypertension|| >95th %tile >95th %tile 25–50
Severe ambulatory hypertension (at risk for end- >95th %tile >95th %tile >50
organ damage)
%tile indicates percentile; BP, blood pressure; DBP, diastolic blood pressure; and SBP, systolic blood pressure.
*
Based on National High Blood Pressure Education Program Task Force normative data.101a
†
Based on normative pediatric ABPM values in Appendix Tables A1 through A4.
‡
For either the wake or sleep period of the study, or both.
§
For patients with elevated load but normal mean ambulatory BP and office BP that is either normal (<90th percentile) or hypertensive (≥95th
percentile), no specific ambulatory BP classification can be assigned based on current evidence and expert consensus. These “unclassified” patients
should be evaluated on a case-by-case basis, taking into account the presence of secondary hypertensiona or multiple cardiovascular risk factors.
||
Some clinicians may prefer the term sustained hypertension rather than ambulatory hypertension.

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Hypertension. 2014 May ; 63(5): 1116–1135. doi:10.1161/HYP.0000000000000007.

Update: Ambulatory Blood Pressure Monitoring in Children and

Cardiovascular Risk in the Pediatric Population

© 2014 American Heart Association, Inc.

a higher BMI increases the rate of progression from prehypertension to hypertension.12

The rise in prevalence of hypertension in the young is especially worrisome, because

for hypertension and risk of end-organ damage in youths.

BP and Risk for Target-Organ Damage

Hypertension. Author manuscript; available in PMC 2015 May 01.

reduced brachial artery distensibility,24,25 higher pulse-wave velocity,26,27 and increased

ABPM may be superior to casual (office) BP measurement in its ability to distinguish

Hypertension. Author manuscript; available in PMC 2015 May 01.

Usefulness of ABPM to Classify BP

Other situations in which ABPM may be especially helpful in “unmasking” hypertension

Hypertension. Author manuscript; available in PMC 2015 May 01.

Prehypertension and Progression to Sustained (Ambulatory) Hypertension

follow-up. Pediatric patients with casual prehypertension may demonstrate abnormalities on

Other proposed determinants of ambulatory BP include autonomic tone,97–99

Normative Data for ABPM

Hypertension. Author manuscript; available in PMC 2015 May 01.

ABPM values differ substantially from casual measurements; therefore, comparisons to

Hypertension. Author manuscript; available in PMC 2015 May 01.

Methods for Performance of ABPM

Hypertension. Author manuscript; available in PMC 2015 May 01.

results of shortened monitoring periods for routine clinical care.

Frequency of Measurement and Accounting for Activity

Hypertension. Author manuscript; available in PMC 2015 May 01.

Editing Data and Calculations

More complicated calculations of circadian BP rhythms have also been attempted in

Hypertension. Author manuscript; available in PMC 2015 May 01.

identifying children with target-organ damage and in determining adequate antihypertensive

data linking ABPM in childhood or adolescence to cardiovascular disease in adulthood are

Recommendations for Standard Application of ABPM in Pediatrics

• Indications for routine performance of ABPM include the following:

– To confirm the diagnosis of hypertension in a patient with hypertension

♦ Determine whether sustained hypertension or WCH exists

– To evaluate for the presence of MH when there is a clinical suspicion of

– To assess BP patterns in high-risk patients

♦ Assess for abnormal circadian variation in BP, such as

♦ Assess the severity and persistence of BP elevation in

– To evaluate effectiveness of drug therapy for hypertension

♦ Confirm BP control in treated patients, especially those with

♦ Evaluate for apparent drug-resistant hypertension.

♦ Determine whether symptoms can be attributed to drug-

• An ABPM device suitable for use in children should be selected.

Hypertension. Author manuscript; available in PMC 2015 May 01.

– An oscillometric or auscultatory technique can be used.

– Appropriate cuff sizes as recommended in the Fourth Report on the

• A standard approach to obtaining ABPM readings should be used.

– ABPM should only be performed by personnel with specific training in

– Monitors should be applied to the nondominant arm unless contraindicated

– Devices should be programmed to record BP every 15 to 20 minutes

– After application, BP measured with the device should be compared with

– Patients should be instructed to record antihypertensive medication

• A sufficient number of valid BP recordings are needed for a study to be considered

– Minimum of 1 reading per hour, including during sleep

– At least 40 to 50 readings for a full 24-hour report

• ABPM recordings should be edited for outlying values.

– Data should be inspected visually for gross inconsistencies that fall