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Curr Pediatr Res 2016; 20 (1&2): 7-10 ISSN 0971-9032
www.currentpediatrics.com
Curr Pediatr Res 2016 Volume 20 Issue 1 & 27
The normal range of heart rate at birth in a healthy term neonate: a critical
review of the evidence.
David J R Hutchon
Darlington Memoiral Hospital, Obstetrics, Darlington, UK.
Introduction
The heart rate or pulse is one of the most fundamental
measures of life and health. During labour the normal range
of heart rate of a healthy term fetus is well established
and has been validated by hundreds of thousands of well
documented recordings of the fetal heart using either
Doppler ultrasound or a fetal electrocardiogram (ECG) [1].
The normal range extends from 110 bpm to 160 bpm. Subtle
patterns within this normal range can also be recognized,
indicating a healthy or unhealthy fetus. With the fetus in
utero and obscured from view, the heart rate is the only
physiological parameter which can be readily measured.
Probably for this reason the ability to measure and
document in real-time the fetal heart during routine clinical
care has advanced well beyond the ability to measure and
document the neonatal heart rate immediately after birth.
After birth other parameters of health such as the regularity
of breathing, crying, muscle tone and movements of the
baby, and the colour of the skin are available to assess the
health of the neonate. During transition however the heart
rate remains a most important parameter especially in the
neonate that is not obviously breathing well or crying. At
birth major changes in the circulation have to take place
while the fetus transitions from placental respiration to the
pulmonary respiration of the neonate. This transition takes
place over a few minutes.
Transition at birth
The transition from placental to pulmonary respiration is
not instantaneous but takes place over a few minutes after
birth [2]. This involves aeration of the lungs and a marked
increase in the pulmonary circulation while at the same
time a gradual closure of the placental circulation initiated
by constriction of the two umbilical arteries. Transition
is completed when the umbilical vein closes followed
finally by closure of the ductus venosus, foramen ovale
and ductus arteriousus. The parallel output of the two sides
of the fetal heart is now converted into the serial output
of the neonatal heart. The changes in breathing, crying
and colour may be obvious but are less objective than the
heart rate and, in routine clinical practice, much less easily
documented in real-time. A normal heart rate is evidence
of good circulation, so as long as we can be confident that
the heart rate is within the normal range there is unlikely to
be a need for immediate assistance with positive pressure
ventilation (PPV) of the lungs in the apparently apnoeic
neonate. If the neonate is not breathing during the first
minute or so after birth but there is a good circulation, the
neonate is likely to be sufficiently oxygenated from the
placental circulation [3]. However this decision requires
that the heart rate is confidently measured. It also needs
to be properly documented for subsequent audit and for
medico-legal purposes. What is the normal range of heart
rate in a healthy term neonate during the first few minutes
after birth?
Physiological range of the neonatal heart rate
The normal range of heart rate in a healthy neonate during
transition to pulmonary respiration over the first few
minutes after birth is not well agreed and published ranges
over the past 30 years can have striking disagreement [4].
For the past five years the most commonly used defined
reference range [5] does not begin until the first minute
after birth. This was established using oximetry which
does not usually register for the first minute. In healthy
term infants, needing no medical intervention, the 10th
and
The heart rate of a neonate at birth is used to determine whether or not resuscitation is required.
The normal healthy range of heart rate is not well established and the method for determining
the heart rate is often unreliable and undocumented in the first minute or so after birth. The
reasons for the poorly established heart rate norms are discussed and the solution for reliable
measurement and documentation of the neonatal heart rate immediately after birth is presented.
Abstract
Keywords: Neonatal heart rate, Auscultation, Stethoscope, ECG, Doppler ultrasound, Resuscitation.
Accepted February 05, 2016
The normal range of heart rate at birth in a healthy term neonate: a critical review of the evidence.
Curr Pediatr Res 2016 Volume 20 Issue 1 & 2
8
90th
percentiles are from 68 to 107 bpm one minute after
birth. At two minutes the values are from 102 to 173 bpm
and at five minutes from 153 to 179 bpm. More recently a
further series of healthy babies [6] with routine midwifery
care showed the heart rate at one minute, determined by
oximetry, was from 38 to 171 bpm, from 54 to 179 bpm
at two minutes and from 126 to 169 bpm at five minutes.
The ECG is an effective method of measuring the heart rate
during the first minute [7]. This method was used in 1962
by Brady and James [8]. In their small series they found
that immediate clamping of the umbilical cord before the
onset of respirations was followed by a rapid and profound
bradycardia. Even when the cord was clamped as early
as 30 seconds the heart rate did not fall below 100 bpm
provided they had breathed spontaneously by that time.
Electrical Cardiometry measures impedance across the
chest. The impedance changes as the vessels in the chest
fill and empty with each heart cycle and can therefore
measure cardiac output, heart rate and stroke volume. A
small series of healthy term neonates [9] showed that the
heart rate (standard deviation) for these neonates at the
first minute after birth was (175.9 (15.3), 170.7 (20.4) at
two minutes and 168.2 (20.0) at 5 minutes.
Resuscitation
Between 1% and 3% of term babies require assistance
[10,11], but how do carers make the decision to intervene
to assist the baby who is failing to transition successfully
within the first few minutes after birth? Unnecessary
intervention to assist breathing with PPV is not without
risk of damage to the lungs [12] while delaying such
intervention in an already hypoxic neonate may lead to
hypoxic injury to the heart or irreversible brain damage
[13]. The precise interval before irreversible brain injury
occurs depends on the level of hypoxia and acidemia but
can never be determined with any accuracy when the
information is needed at the moment of birth.
Accuratemeasurementoftheheartrateisthemostimportant
measure of health in an apnoeic newborn. The neonatal
2010 International Liaison Committee on Resuscitation
(ILCOR) recommendations state that the primary vital
sign to judge the need for resuscitation and positive
pressure ventilation should remain the heart rate and the
heart rate should also provide evidence of the efficacy of
the resuscitation.Assessment of the heart rate should be by
auscultation of the precordium. The committee considered
that there is a high likelihood of underestimating the
heart rate with palpation of the umbilical pulse, but this is
preferable to other palpation locations [14]. In the ILCOR
algorithm the first measurement of the heart rate should
take place by 30 seconds after birth. Based on expert
opinion, ILCOR recommend that PPV should be initiated
if the heart rate is under 100 bpm.
Method of heart rate measurement
The ECG is considered the gold standard for determining
the heart rate although it has to be born in mind that
an electrical signal does not guarantee any cardiac
output. Pulse oximetry provides evidence of both heart
rate and significant peripheral circulation as well as
oxygen saturation. The equipment allows the output to
be documented in real time and would be the ideal but
it is unreliable during the first minute after birth when
decisions need to be made. Ausculation with a stethoscope
is recommended by ILCOR. Stethoscopes are readily
available but often not practical especially in assisted
vaginal births and at caesarean births when sterility is
essential. Midwives do not routinely wear a stethoscope
around their neck at birth and its accuracy depends on
counting the heart sounds over a timed interval. This
only provides a rough measure of the heart rate. It does
not provide any real-time documentation. Palpation of the
umbilical cord is still the commonest method of initially
determining the heart rate in a depressed neonate, and
as with auscultation it is not very accurate and provides
no real-time documentation. Doppler ultrasound, used
during labour to measure and document the fetal heart
rate, also works well in the neonate and has the additional
advantages of providing an accurate result from the
moment of birth, of being low cost, is easily documented.
It generates an audible signal which correlates with the
strength of cardiac contractions [15,16].
Discussion
The current standard reference range of heart rate at
birth was established on neonates who were considered
to require no intervention to assist transition, but they all
had the umbilical cord clamped soon after birth. This was
standard practice at the time of the study. It is notable that
there is a marked disparity between the normal healthy
range of the fetus and the neonate in the first few minutes
after birth. In view of the finding of Brady and James
there was concern that the marked bradycardia shown in
the standard reference range may be the result of early
cord clamping. Early cord clamping before the onset of
respiration was shown to cause a marked bradycardia and
fall in cardiac output in lambs and the authors state that if
there is a long delay between UCC and lung aeration, the
infant will be exposed to a hypoxic episode superimposed
on top of a period of severely restricted cardiac function.
The combined effects of these two adverse events are
potentially catastrophic, leading to a severe hypoxic/
ischemic event [17].
In the recent study of normal midwifery births where the
cord was left intact and the baby placed skin to skin on
the mother’s chest, the range was very similar to that of
the standard reference range [6]. Indeed the bradycardia
in the first few minutes was more marked. The babies did
however show a significantly better oxygen saturation
than those in the standard reference range. The authors
attributed the bradycardia to a calming effect of skin to
skin on the mother’s body. This does not explain why
the upper range was still well over 160 bpm. Were these
Hutchon
Curr Pediatr Res 2016 Volume 20 Issue 1 & 29
babies also calmed? Why should the neonatal heart rate in
some babies fall so low. The cardiac output in the fetus is
highly dependent upon the heart rate so with a heart rate
of only 38, the cardiac output must fall to at least one third
of the normal.
In the small series using electrical cardiometry, no
bradycardia was found. These babies not only had a
continuing placental circulation with an intact cord, they
remained 10 to 20 cm below the level of the mother’s
introitus which is likely to have enhanced the rate of
redistribution of blood from the placenta into the neonate,
and ensure that the preload of the heart is optimized.
Althoughthetotalvolumeoftheplacentaltransfusionisnot
affected by placing the neonate on the mother’s abdomen
immediately after birth, it does reduce the pressure gradient
between the placental and the neonatal compartments of
the circulation. Elevation onto the mother’s abdomen will
therefore slow down the rate of redistribution of blood
into the baby [18]. With a slower redistribution, preload
of the neonate’s heart will be reduced during these first
few minutes. This could account for a bradycardia in some
babies. Rapid redistribution may be critical if there has
been any degree of cord compression just before birth [19].
Placing the baby immediately onto the mother’s abdomen
by the midwife could be considered an intervention [20].
In a natural birth with the mother squatting or on all fours,
she would be able to pick up her newborn baby herself
when she was ready. This brief pause is long enough to
ensure that all babies have optimal opportunity for the
redistribution of blood from the placental transfusion. This
may explain why Katheria [9] did not find any bradycardia
in the babies who remained 10 to 20 cm below the introitus,
lying on the soft warm surface (mimicking skin to skin) of
the LifeStart trolley [21] for a few minutes after birth.
Virginia Apgar, an obstetrical anaesthetist first recognised
the importance of measuring the condition of the neonate
at birth to determine which babies required ventilatory
assistance [22]. Her scoring system allowed this to be
readily documented and is still used universally to this
day. Without real-time documentation of a heart rate,
subsequent audit provides only the APGAR score which
incorporates the precise heart rate into the very broad
categories of below 60 bpm, 60 to 100 bpm and above
100 bpm. All the parameters measured by the Apgar
score are dependent upon the circulation, which is largely
dependent upon the heart rate. While there have been
potentially millions of fetal heart rate records with known
short term outcomes made over the last 30 years, this is
not the case for neonatal heart rates shortly after birth
because the neonatal heart rate has been obscured and
only documented within the APGAR score. Thus a cohort
study of case notes can never be used to define the normal
physiological range of neonatal heart rate or outcomes
directly related to heart rate alone.
There is thus considerable uncertainly about the normal
range of heart rate at birth in a healthy term neonate.
With modern electronics there is an opportunity for
this to be established with more accuracy. We are not
calling for the introduction of yet more technology in
normal low risk births. In breathing, crying, baby with
good tone and colour, the heart rate is largely academic.
However we should be prepared at all births to be able
to accurately measure and document the heart rate in
a baby that is not breathing and in whom resuscitation
intervention is anticipated. For high risk births accurate
measurement and documentation is essential and a real-
time record of the heart rate should always be made.
The marked bradycardia found in some apparently healthy
normal physiological births should be investigated further
to determine if immediate elevation onto the mother’s
abdomen is the underlying cause. This should encourage
a normal physiological range of heart rate at birth to be
confidently established.
References
1.	 Alfirevic Z, Devane D, Gyte GML. Continuous
cardiotocography (CTG) as a form of electronic fetal
monitoring (EFM) for fetal assessment during labour.
Cochrane Database of Systematic Reviews 2013.
2.	 Hutchon DJR. Ventilation before umbilical cord clamping
improves physiological transition at birth or “Umbilical
cord clamping before ventilation is established destabilizes
physiological transition at birth”. Front Pediatr 2015; 3: 29.
3.	 Wiberg N, Kallen K, Olofsson P. Delayed umbilical cord
clamping at birth has effects on arterial and venous blood
gases and lactate concentrations. BJOG 2008; 115: 697-703.
4.	 Fleming S, Thompson M, Heneghan C, Plüddemann
A, Maconochie I, et al. Normal ranges of heart rate and
respiratory rate in children from birth to 18 years of age:
A systematic review of observational studies. Lancet 2011;
377(9770):1011-1018.
5.	 Dawson JA, Kamlin CO, Wong C, te Pas AB, Vento M, et al.
Changes in heart rate in the first minutes after birth. Arch Dis
Child Fetal Neonatal Ed 2010; 95: F177-181.
6.	 Smit M, Dawson J A, Ganzeboom A, Hooper SB, van
Roosmalen J, te Pas AB. Pulse oximetry in newborns with
delayed cord clamping and immediate skin-to-skin contact.
Arch Dis Child Fetal Neonatal Ed 2014; 10: F1-F6.
7.	 Katheria A, Rich W, Finer N. Pediatrics Electrocardiogram
Provides a Continuous Heart Rate Faster Than Oximetry
during Neonatal Resuscitation. Pediatrics 2012; 130: e1177.
8.	 Brady JP, James LS. Heart rate changes in the fetus and
newborn infant during labor, delivery, and the immediate
neonatal period. Am J Obstet Gynecol 1962; 84: 1e12.
9.	 Katheria, Wozniak M, et al. Measuring cardiac changes
using electrical impedance during delayed cord clamping:
a feasibility trial. Maternal Health, Neonatology, and
Perinatology 2015; 1: 15.
10.	Palme-Kilander C. Methods of resuscitation in low-Apgar-
score newborn infants-a national survey. Acta Paediatr 1992;
81: 739-744.
The normal range of heart rate at birth in a healthy term neonate: a critical review of the evidence.
Curr Pediatr Res 2016 Volume 20 Issue 1 & 2
10
11.	Wyllie J, Bruinenbergb J, Roehrd C, et al., European
Resuscitation Council Guidelines for Resuscitation 2015
Section 7. Resuscitation and support of transition of babies
at birth. Resuscitation 2015; 95: 249–263.
12.	Schmölzer GM, te Pas AB, Davis PG, Morley CJ. Reducing
lung injury during neonatal resuscitation of preterm infants.
J Pediatr 2008; 153: 741-745.
13.	Hutchon DJR, Wepster B. The Estimated Cost of Cord
Clamping at Birth within Europe. International Journal of
Childbirth 2014; 4: 250-256.
14.	Perlman JM, Wyllie J, Kattwinkel J, Atkins DL, Chameides
L, Goldsmith JP, et al. Part 11: Neonatal resuscitation: 2010
International Consensus on Cardiopulmonary Resuscitation
and Emergency Cardiovascular Care Science With Treatment
Recommendations. Circulation 2010; 122: S516e38.
15.	Hutchon DJR. Technological Developments in Neonatal
Care at Birth. J Nurs Care 2014; 3: 218.
16.	Goenka S, Khan M, Koppel RI, Heiman HS. Precordial
Doppler Ultrasound Achieves Earlier and More Accurate
Newborn Heart Rates in the Delivery Room. Pediatric
Academic Societies andAsian Society for Pediatric Research
2014; 590p.
17.	Hooper SB, Polglase GR, te Pas AB. A physiological
approach to the timing of umbilical cord clamping at birth.
Arch Dis Child Fetal Neonatal Ed 2014; 0: F1-F6.
18.	Vain NE, Satragno DS, Gorenstein AN, et al. Effect of
gravity on volume of placental transfusion: a multicentre,
randomised, non-inferiority trial. Lancet.
19.	Uwins C, Hutchon DJR. Delayed umbilical cord clamping
after child birth: potential benefits to baby's health. Pediatric
Health, Medicine and Therapeutics 2014; 5: 161-171.
20.	Malloy ME. Waiting to Inhale: How to Unhurry the Moment
of Birth. The Journal of Perinatal Education 2011; 20: 8-13.
21.	Hutchon D. Evolution of neonatal resuscitation with intact
placental circulation. INFANT 2014; 10: 58-61.
22.	Clark DA, Hakanson DO. The inaccuracy of Apgar scoring.
J Perinatol 1988; 8: 203-205.
Correspondence to:
David J R Hutchon
Darlington Memorial Hospital
Obstetrics
Hollyhurst Road
Darlington, DL3 6HX
United Kingdom.
Tel: +44 1325253278
E-mail:djrhutchon@hotmail.co.uk

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The normal-range-of-heart-rate-at-birth-in-a-healthy-term-neonate-a-critical-review-of-the-evidence

  • 1. Curr Pediatr Res 2016; 20 (1&2): 7-10 ISSN 0971-9032 www.currentpediatrics.com Curr Pediatr Res 2016 Volume 20 Issue 1 & 27 The normal range of heart rate at birth in a healthy term neonate: a critical review of the evidence. David J R Hutchon Darlington Memoiral Hospital, Obstetrics, Darlington, UK. Introduction The heart rate or pulse is one of the most fundamental measures of life and health. During labour the normal range of heart rate of a healthy term fetus is well established and has been validated by hundreds of thousands of well documented recordings of the fetal heart using either Doppler ultrasound or a fetal electrocardiogram (ECG) [1]. The normal range extends from 110 bpm to 160 bpm. Subtle patterns within this normal range can also be recognized, indicating a healthy or unhealthy fetus. With the fetus in utero and obscured from view, the heart rate is the only physiological parameter which can be readily measured. Probably for this reason the ability to measure and document in real-time the fetal heart during routine clinical care has advanced well beyond the ability to measure and document the neonatal heart rate immediately after birth. After birth other parameters of health such as the regularity of breathing, crying, muscle tone and movements of the baby, and the colour of the skin are available to assess the health of the neonate. During transition however the heart rate remains a most important parameter especially in the neonate that is not obviously breathing well or crying. At birth major changes in the circulation have to take place while the fetus transitions from placental respiration to the pulmonary respiration of the neonate. This transition takes place over a few minutes. Transition at birth The transition from placental to pulmonary respiration is not instantaneous but takes place over a few minutes after birth [2]. This involves aeration of the lungs and a marked increase in the pulmonary circulation while at the same time a gradual closure of the placental circulation initiated by constriction of the two umbilical arteries. Transition is completed when the umbilical vein closes followed finally by closure of the ductus venosus, foramen ovale and ductus arteriousus. The parallel output of the two sides of the fetal heart is now converted into the serial output of the neonatal heart. The changes in breathing, crying and colour may be obvious but are less objective than the heart rate and, in routine clinical practice, much less easily documented in real-time. A normal heart rate is evidence of good circulation, so as long as we can be confident that the heart rate is within the normal range there is unlikely to be a need for immediate assistance with positive pressure ventilation (PPV) of the lungs in the apparently apnoeic neonate. If the neonate is not breathing during the first minute or so after birth but there is a good circulation, the neonate is likely to be sufficiently oxygenated from the placental circulation [3]. However this decision requires that the heart rate is confidently measured. It also needs to be properly documented for subsequent audit and for medico-legal purposes. What is the normal range of heart rate in a healthy term neonate during the first few minutes after birth? Physiological range of the neonatal heart rate The normal range of heart rate in a healthy neonate during transition to pulmonary respiration over the first few minutes after birth is not well agreed and published ranges over the past 30 years can have striking disagreement [4]. For the past five years the most commonly used defined reference range [5] does not begin until the first minute after birth. This was established using oximetry which does not usually register for the first minute. In healthy term infants, needing no medical intervention, the 10th and The heart rate of a neonate at birth is used to determine whether or not resuscitation is required. The normal healthy range of heart rate is not well established and the method for determining the heart rate is often unreliable and undocumented in the first minute or so after birth. The reasons for the poorly established heart rate norms are discussed and the solution for reliable measurement and documentation of the neonatal heart rate immediately after birth is presented. Abstract Keywords: Neonatal heart rate, Auscultation, Stethoscope, ECG, Doppler ultrasound, Resuscitation. Accepted February 05, 2016
  • 2. The normal range of heart rate at birth in a healthy term neonate: a critical review of the evidence. Curr Pediatr Res 2016 Volume 20 Issue 1 & 2 8 90th percentiles are from 68 to 107 bpm one minute after birth. At two minutes the values are from 102 to 173 bpm and at five minutes from 153 to 179 bpm. More recently a further series of healthy babies [6] with routine midwifery care showed the heart rate at one minute, determined by oximetry, was from 38 to 171 bpm, from 54 to 179 bpm at two minutes and from 126 to 169 bpm at five minutes. The ECG is an effective method of measuring the heart rate during the first minute [7]. This method was used in 1962 by Brady and James [8]. In their small series they found that immediate clamping of the umbilical cord before the onset of respirations was followed by a rapid and profound bradycardia. Even when the cord was clamped as early as 30 seconds the heart rate did not fall below 100 bpm provided they had breathed spontaneously by that time. Electrical Cardiometry measures impedance across the chest. The impedance changes as the vessels in the chest fill and empty with each heart cycle and can therefore measure cardiac output, heart rate and stroke volume. A small series of healthy term neonates [9] showed that the heart rate (standard deviation) for these neonates at the first minute after birth was (175.9 (15.3), 170.7 (20.4) at two minutes and 168.2 (20.0) at 5 minutes. Resuscitation Between 1% and 3% of term babies require assistance [10,11], but how do carers make the decision to intervene to assist the baby who is failing to transition successfully within the first few minutes after birth? Unnecessary intervention to assist breathing with PPV is not without risk of damage to the lungs [12] while delaying such intervention in an already hypoxic neonate may lead to hypoxic injury to the heart or irreversible brain damage [13]. The precise interval before irreversible brain injury occurs depends on the level of hypoxia and acidemia but can never be determined with any accuracy when the information is needed at the moment of birth. Accuratemeasurementoftheheartrateisthemostimportant measure of health in an apnoeic newborn. The neonatal 2010 International Liaison Committee on Resuscitation (ILCOR) recommendations state that the primary vital sign to judge the need for resuscitation and positive pressure ventilation should remain the heart rate and the heart rate should also provide evidence of the efficacy of the resuscitation.Assessment of the heart rate should be by auscultation of the precordium. The committee considered that there is a high likelihood of underestimating the heart rate with palpation of the umbilical pulse, but this is preferable to other palpation locations [14]. In the ILCOR algorithm the first measurement of the heart rate should take place by 30 seconds after birth. Based on expert opinion, ILCOR recommend that PPV should be initiated if the heart rate is under 100 bpm. Method of heart rate measurement The ECG is considered the gold standard for determining the heart rate although it has to be born in mind that an electrical signal does not guarantee any cardiac output. Pulse oximetry provides evidence of both heart rate and significant peripheral circulation as well as oxygen saturation. The equipment allows the output to be documented in real time and would be the ideal but it is unreliable during the first minute after birth when decisions need to be made. Ausculation with a stethoscope is recommended by ILCOR. Stethoscopes are readily available but often not practical especially in assisted vaginal births and at caesarean births when sterility is essential. Midwives do not routinely wear a stethoscope around their neck at birth and its accuracy depends on counting the heart sounds over a timed interval. This only provides a rough measure of the heart rate. It does not provide any real-time documentation. Palpation of the umbilical cord is still the commonest method of initially determining the heart rate in a depressed neonate, and as with auscultation it is not very accurate and provides no real-time documentation. Doppler ultrasound, used during labour to measure and document the fetal heart rate, also works well in the neonate and has the additional advantages of providing an accurate result from the moment of birth, of being low cost, is easily documented. It generates an audible signal which correlates with the strength of cardiac contractions [15,16]. Discussion The current standard reference range of heart rate at birth was established on neonates who were considered to require no intervention to assist transition, but they all had the umbilical cord clamped soon after birth. This was standard practice at the time of the study. It is notable that there is a marked disparity between the normal healthy range of the fetus and the neonate in the first few minutes after birth. In view of the finding of Brady and James there was concern that the marked bradycardia shown in the standard reference range may be the result of early cord clamping. Early cord clamping before the onset of respiration was shown to cause a marked bradycardia and fall in cardiac output in lambs and the authors state that if there is a long delay between UCC and lung aeration, the infant will be exposed to a hypoxic episode superimposed on top of a period of severely restricted cardiac function. The combined effects of these two adverse events are potentially catastrophic, leading to a severe hypoxic/ ischemic event [17]. In the recent study of normal midwifery births where the cord was left intact and the baby placed skin to skin on the mother’s chest, the range was very similar to that of the standard reference range [6]. Indeed the bradycardia in the first few minutes was more marked. The babies did however show a significantly better oxygen saturation than those in the standard reference range. The authors attributed the bradycardia to a calming effect of skin to skin on the mother’s body. This does not explain why the upper range was still well over 160 bpm. Were these
  • 3. Hutchon Curr Pediatr Res 2016 Volume 20 Issue 1 & 29 babies also calmed? Why should the neonatal heart rate in some babies fall so low. The cardiac output in the fetus is highly dependent upon the heart rate so with a heart rate of only 38, the cardiac output must fall to at least one third of the normal. In the small series using electrical cardiometry, no bradycardia was found. These babies not only had a continuing placental circulation with an intact cord, they remained 10 to 20 cm below the level of the mother’s introitus which is likely to have enhanced the rate of redistribution of blood from the placenta into the neonate, and ensure that the preload of the heart is optimized. Althoughthetotalvolumeoftheplacentaltransfusionisnot affected by placing the neonate on the mother’s abdomen immediately after birth, it does reduce the pressure gradient between the placental and the neonatal compartments of the circulation. Elevation onto the mother’s abdomen will therefore slow down the rate of redistribution of blood into the baby [18]. With a slower redistribution, preload of the neonate’s heart will be reduced during these first few minutes. This could account for a bradycardia in some babies. Rapid redistribution may be critical if there has been any degree of cord compression just before birth [19]. Placing the baby immediately onto the mother’s abdomen by the midwife could be considered an intervention [20]. In a natural birth with the mother squatting or on all fours, she would be able to pick up her newborn baby herself when she was ready. This brief pause is long enough to ensure that all babies have optimal opportunity for the redistribution of blood from the placental transfusion. This may explain why Katheria [9] did not find any bradycardia in the babies who remained 10 to 20 cm below the introitus, lying on the soft warm surface (mimicking skin to skin) of the LifeStart trolley [21] for a few minutes after birth. Virginia Apgar, an obstetrical anaesthetist first recognised the importance of measuring the condition of the neonate at birth to determine which babies required ventilatory assistance [22]. Her scoring system allowed this to be readily documented and is still used universally to this day. Without real-time documentation of a heart rate, subsequent audit provides only the APGAR score which incorporates the precise heart rate into the very broad categories of below 60 bpm, 60 to 100 bpm and above 100 bpm. All the parameters measured by the Apgar score are dependent upon the circulation, which is largely dependent upon the heart rate. While there have been potentially millions of fetal heart rate records with known short term outcomes made over the last 30 years, this is not the case for neonatal heart rates shortly after birth because the neonatal heart rate has been obscured and only documented within the APGAR score. Thus a cohort study of case notes can never be used to define the normal physiological range of neonatal heart rate or outcomes directly related to heart rate alone. There is thus considerable uncertainly about the normal range of heart rate at birth in a healthy term neonate. With modern electronics there is an opportunity for this to be established with more accuracy. We are not calling for the introduction of yet more technology in normal low risk births. In breathing, crying, baby with good tone and colour, the heart rate is largely academic. However we should be prepared at all births to be able to accurately measure and document the heart rate in a baby that is not breathing and in whom resuscitation intervention is anticipated. For high risk births accurate measurement and documentation is essential and a real- time record of the heart rate should always be made. The marked bradycardia found in some apparently healthy normal physiological births should be investigated further to determine if immediate elevation onto the mother’s abdomen is the underlying cause. This should encourage a normal physiological range of heart rate at birth to be confidently established. References 1. Alfirevic Z, Devane D, Gyte GML. Continuous cardiotocography (CTG) as a form of electronic fetal monitoring (EFM) for fetal assessment during labour. Cochrane Database of Systematic Reviews 2013. 2. Hutchon DJR. Ventilation before umbilical cord clamping improves physiological transition at birth or “Umbilical cord clamping before ventilation is established destabilizes physiological transition at birth”. Front Pediatr 2015; 3: 29. 3. Wiberg N, Kallen K, Olofsson P. Delayed umbilical cord clamping at birth has effects on arterial and venous blood gases and lactate concentrations. BJOG 2008; 115: 697-703. 4. Fleming S, Thompson M, Heneghan C, Plüddemann A, Maconochie I, et al. Normal ranges of heart rate and respiratory rate in children from birth to 18 years of age: A systematic review of observational studies. Lancet 2011; 377(9770):1011-1018. 5. Dawson JA, Kamlin CO, Wong C, te Pas AB, Vento M, et al. Changes in heart rate in the first minutes after birth. Arch Dis Child Fetal Neonatal Ed 2010; 95: F177-181. 6. Smit M, Dawson J A, Ganzeboom A, Hooper SB, van Roosmalen J, te Pas AB. Pulse oximetry in newborns with delayed cord clamping and immediate skin-to-skin contact. Arch Dis Child Fetal Neonatal Ed 2014; 10: F1-F6. 7. Katheria A, Rich W, Finer N. Pediatrics Electrocardiogram Provides a Continuous Heart Rate Faster Than Oximetry during Neonatal Resuscitation. Pediatrics 2012; 130: e1177. 8. Brady JP, James LS. Heart rate changes in the fetus and newborn infant during labor, delivery, and the immediate neonatal period. Am J Obstet Gynecol 1962; 84: 1e12. 9. Katheria, Wozniak M, et al. Measuring cardiac changes using electrical impedance during delayed cord clamping: a feasibility trial. Maternal Health, Neonatology, and Perinatology 2015; 1: 15. 10. Palme-Kilander C. Methods of resuscitation in low-Apgar- score newborn infants-a national survey. Acta Paediatr 1992; 81: 739-744.
  • 4. The normal range of heart rate at birth in a healthy term neonate: a critical review of the evidence. Curr Pediatr Res 2016 Volume 20 Issue 1 & 2 10 11. Wyllie J, Bruinenbergb J, Roehrd C, et al., European Resuscitation Council Guidelines for Resuscitation 2015 Section 7. Resuscitation and support of transition of babies at birth. Resuscitation 2015; 95: 249–263. 12. Schmölzer GM, te Pas AB, Davis PG, Morley CJ. Reducing lung injury during neonatal resuscitation of preterm infants. J Pediatr 2008; 153: 741-745. 13. Hutchon DJR, Wepster B. The Estimated Cost of Cord Clamping at Birth within Europe. International Journal of Childbirth 2014; 4: 250-256. 14. Perlman JM, Wyllie J, Kattwinkel J, Atkins DL, Chameides L, Goldsmith JP, et al. Part 11: Neonatal resuscitation: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations. Circulation 2010; 122: S516e38. 15. Hutchon DJR. Technological Developments in Neonatal Care at Birth. J Nurs Care 2014; 3: 218. 16. Goenka S, Khan M, Koppel RI, Heiman HS. Precordial Doppler Ultrasound Achieves Earlier and More Accurate Newborn Heart Rates in the Delivery Room. Pediatric Academic Societies andAsian Society for Pediatric Research 2014; 590p. 17. Hooper SB, Polglase GR, te Pas AB. A physiological approach to the timing of umbilical cord clamping at birth. Arch Dis Child Fetal Neonatal Ed 2014; 0: F1-F6. 18. Vain NE, Satragno DS, Gorenstein AN, et al. Effect of gravity on volume of placental transfusion: a multicentre, randomised, non-inferiority trial. Lancet. 19. Uwins C, Hutchon DJR. Delayed umbilical cord clamping after child birth: potential benefits to baby's health. Pediatric Health, Medicine and Therapeutics 2014; 5: 161-171. 20. Malloy ME. Waiting to Inhale: How to Unhurry the Moment of Birth. The Journal of Perinatal Education 2011; 20: 8-13. 21. Hutchon D. Evolution of neonatal resuscitation with intact placental circulation. INFANT 2014; 10: 58-61. 22. Clark DA, Hakanson DO. The inaccuracy of Apgar scoring. J Perinatol 1988; 8: 203-205. Correspondence to: David J R Hutchon Darlington Memorial Hospital Obstetrics Hollyhurst Road Darlington, DL3 6HX United Kingdom. Tel: +44 1325253278 E-mail:djrhutchon@hotmail.co.uk