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CHAPTER 4 Care at Birth
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89
who attended the delivery an opportunity to have a conversation and reflect on their care, teamwork, and communication. Debriefing
identifies aspects of the resuscitation that went well and those that could be improved, with the goal of practice and systems change for continuous improvement.
CARE OF THE FAMILY AND PERINATAL DECISION MAKING
Encouraging the presence of the father or another mature support person at birth is common obstetric practice and should not interfere with care after birth. Ideally, mem-
bers of the obstetric and neonatal resuscitation team should introduce themselves to the parents/ birth companion before the delivery. Parents
have a great deal of anxiety concerning pro­cedures performed on their newborn; a few moments spent describing routine procedures will help allay their fears and avoid misinter­pretation. When problems are anticipated, a calm,
professional explanation of neonatal assessment and life-support measures is necessary. Parental
awareness that the medical and nursing staff have anticipated and prepared for possible problems can partially relieve their anxieties.
Care must be taken, however, to avoid instilling undue alarm. Care providers should understand ethical principles and the impact of their personal moral and ethical beliefs on decisions made about resuscitation.
If an infant requires resuscitation or prolonged assessment and support, the attending staff ’s pri­mary obligation is to provide this care and com­municate with the parents. Parents should be
encouraged to have contact with their baby, but the presence of the father or a support person should not interfere with or delay the delivery of care. The pediatric staff should tell the parents what is happening at the earliest possible opportunity because a lack of com­munication prolongs anxiety for the parents.
A few brief statements to explain the status of the baby and procedures can relieve the anguish of silence. Especially when a difficult resuscita-
tion is anticipated, it is ideal to designate, in
40
advance, a team member who can keep parents informed.
When severe perinatal problems are suspected prenatally and confirmed after birth, such as extreme prematurity (gestational age less than 23 weeks, birth weight less than 400 g), anencephaly, or other potentially lethal anomalies, discussions
may be held in advance with obstetric care providers and the family about limiting the extent of resuscitative measures (see Chapter
40,60
32).
When problems are unanticipated, infor­mation is uncertain, or there has been no time for decision making before delivery, interven­tion in the delivery room may be warranted.22 This approach allows time for complete infor­mation to be gathered and discussed with the family. If appropriate, support measures can
be withdrawn later in the nursery. When an
infant fails to respond to intensive resuscitative measures in the delivery room, a decision, in consultation with the parents, must be made as to when to stop support. Survival is unlikely
if no heart rate has been obtained after 10 minutes.
15,38,49
Discontinuation of resuscita­tion may be appropriate if, after 10 minutes of full resuscitative effort, there is no return of spontaneous circulation. The data for infants
who have an inadequate response to resuscitation remain less clear. The probability of survival
diminishes and the probability of cerebral palsy increases with the length of time during which Apgar scores remain below 4. For
example, if the Apgar score remains below 4 at 20 minutes, the probability of cerebral palsy in surviving infants is greater than 50%.47 It is essen­tial to rapidly identify remediable causes of poor response to resuscitation.
Anticipation and recognition of fetal and neona­tal problems indicating delivery room resuscitation depend on a knowledgeable and prepared staff working as a team to effectively and efficiently communicate and respond in a critical situation. By applying current evidence in performing the skills necessary for neonatal resuscitation, evaluat­ing the infant’s response, and taking the time to discuss resuscitation options and outcomes with the parents and resuscitation team, successful deliv­ery room care and stabilization of the newborn is more likely.
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REFERENCES
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8. Aziz K, Chadwick M, Baker M, Andrews W. Ante- and intra-partum factors that predict increased need for neonatal resuscitation. Resuscitation. 2008;79(3):444.
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10. Bhat R, Vidyasagar D. Delivery room management of meconium-stained infant. Clin Perinatol. 2012;39(4):817.
11. Bhatt S, Alison BJ, Wallace EM, et al. Delaying cord clamping until ventilation onset improves cardiovascular function at birth in preterm lambs. J Physiol. 2013;591(8):2113.
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13. Blank DA, Badurdeen S, Kamlin CO, et al. Baby-directed umbilical cord clamping: a feasibility study. Resuscitation. 2018;131:1.
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16. Casey B, McIntire D, Leveno K. The continuing value of the Apgar score for the assessment of the newborn infant. N Engl J Med. 2001;344(7):467.
17. Dawes GS. Foetal and Neonatal Physiology. Chicago: Year Book Medical Publishers; 1968.
18. Dawson JA, Davis PG, O’Donnell CP, et al. Pulse oximetry for monitoring infants in the delivery room: a review. Arch Dis Child Fetal Neonat Ed. 2007;92(1):F4.
19. Dawson JA, Kamlin CO, Vento M, et al. Defining the reference range for oxygen saturation for infants after birth. Pediatrics. 2010;125(6):e1340.
20. Dawson JA, Schmolzer GM, Kamlin CO, et al. Oxygenation with T-piece versus self-inflating bag for ventilation of extremely preterm infants at birth: a randomized controlled trial. J Pediatr. 2011;158(6):912.
21. DeMauro SB, Douglas E, Kar p K, et al. Improving delivery room management for very preterm infants. Pediatrics. 2013;132(4):e1018.
22. Donohue PK, Boss RD, Shepard J, et al. Intervention at the border of viability: perspective over a decade. Arch Pediatr Adolesc Med. 2009;163(10):902.
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24. Ersdal HL, Mduma E, Svensen E, Perlman JM. Early initiation of basic resuscitation interventions including face mask ventilation may reduce birth asphyxia related mortality in low­income countries: a prospective descriptive observational study. Resuscitation. 2012;83(7):869.
25. Escrig R, Arruza L, Izquierdo I, et al. Achievement of targeted saturation values in extremely low gestational age neonates resuscitated with low or high oxygen concentrations: a prospective, randomized trial. Pediatrics. 2008;121(5):875.
26. Estol PC, Piriz H, Basalo S, et al. Oro-naso-pharyngeal suction at birth: effects on respiratory adaptation of normal term vaginally born infants. J Perinat Med. 1992;20(4):297.
27. Farrar D, Airey R, Law GR, et al. Measuring placental transfusion for term births: weighing babies with cord intact. Br J Obstet Gynaecol. 2011;118(1):70.
28. Finer NN, Rich W, Craft A, et al. Comparison of methods of bag and mask ventilation for neonatal resuscitation. Resuscitation. 2001;49(3):299.
29. Finer NN, Rich W, Halamek LP, et al. The delivery room of the future: the fetal and neonatal resuscitation and transition suite. Clin Perinatol. 2012;39(4):931.
30. Fogarty M, Osborn DA, Askie L, et al. Delayed vs early umbilical cord clamping for preterm infants: a systematic review and meta-analysis. Am J Obstetr Gynecol. 2018;218(1):1.
31. Garofalo M, Abenhaim HA. Early versus delayed cord clamping in term and preterm births: a review. J Obstet Gynaecol Can. 2012;34(6):525.
32. Geethanath RM, Ramji S, Thirupuram S, Rao YN. Effect of timing of cord clamping on the iron status of infants at 3 months. Indian Pediatr. 1997;34(2):103.
33. Goldberg RN, Chung D, Goldman SL, et al. The association of rapid volume expansion and intraventricular hemorrhage in the preterm infant. J Pediatr. 1980;96(6):1060.
34. Goldsmith JP. Delivery room resuscitation of the newborn: part
1. Overview and initial management. In: Martin RJ, Fanaroff AA, Walsh MC, eds. Fanaroff and Martin’s Neonatal-Perinatal Medicine. 9th ed. St. Louis: Elsevier Mosby; 2011.
35. Goudar SS, Somannavar MS, Clark R, et al. Stillbirth and newborn mortality in India after helping babies breathe training. Pediatrics. 2013;131(2):e344.
36. Gupta R, Ramji S. Effect of delayed cord clamping on iron stores in infants born to anemic mothers: a randomized controlled trial. Indian Pediatr. 2002;39(2):130.
37. Halamek LP. The simulated delivery-room environment as the future modality for acquiring and maintaining skills in fetal and neonatal resuscitation. Semin Fetal Neonat Med. 2008;13(6):448.
38. Harrington DJ, Redman CW, Moulden M, Greenwood CE. The long-term outcome in surviving infants with Apgar zero at 10 minutes: a systematic review of the literature and hospital-based cohort. Am J Obstet Gynecol. 2007;196(5):463.
39. Harris AP, Sendak MJ, Donham RT. Changes in arterial oxygen saturation immediately after birth in the human neonate. J Pediatr. 1986;109(1):117.
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40. Haward MF, Kirshenbaum NW, Campbell DE. Care at the edge of viability: medical and ethical issues. Clin Perinatol. 2011;38(3):471.
41. Hawkes CP, Ryan CA, Dempsey EM. Comparison of the T-piece resuscitator with other neonatal manual ventilation devices: a qualitative review. Resuscitation. 2012;83(7):797.
42. Hernandez JA, Fashaw LM, Evans R. Adaptation to extrauterine life and management during normal and abnormal transition. In: Thureen PJ, Deacon J, Hernandez JA, et al., eds. Assessment and Care of the Well Newborn. 2nd ed. Philadelphia: Saunders; 2005.
43. Hillman NH, Kallapur SG, Jobe AH. Physiology of transition from intrauterine to extrauterine life. Clin Perinatol. 2012;39(4):769.
44. Hutton EK, Hassan ES. Late vs early clamping of the umbilical cord in full-term neonates: systematic review and meta-analysis of controlled trials. J Am Med Assoc. 2007;297(11):1241.
45. Jobe AH, Hillman N, Polglase G, et al. Injury and inflammation from resuscitation of the preterm infant. Neonatology. 2008;94(3):190.
46. Kaempf JW, Tomlinson MW, Kaempf AJ, et al. Delayed umbilical cord clamping in premature neonates. Obstet Gynecol. 2012;120(2 Pt 1):325.
47. Kattwinkel J. Very difficult questions in neonatal resuscitation. NRP Instructor Update Suppl. 1996;5(3):1S.
48. Kattwinkel J, Chisholm CA, eds. Perinatal Continuing Education Program. 3rd ed. Elk Grove Village, IL: American Academy of Pediatrics; 2017.
49. Laptook AR, Shankaran S, Ambalavanan N, et al., Hypothermia Subcommittee of the NICHD Neonatal Research Network. Outcome of term infants using Apgar scores at 10 minutes following hypoxic-ischemic encephalopathy. Pediatrics. 2009;124(6):1619.
50. Lie KK, Groholt EK, Eskild A. Association of cerebral palsy with Apgar score in low and normal birthweight infants: population based cohort study. BMJ. 2010;341:e4900.
51. Lieberman E, Lang J, Richardson DK, et al. Intrapartum maternal fever and neonatal outcome. Pediatrics. 2000;105(1 Pt 1):8.
52. Linderkamp O. Placental transfusion: determinants and effects. Clin Perinatol. 1982;9(3):559.
53. Lou HC, Lassen NA, Friss-Hansen B. Impaired autoregulation of cerebral flow in the distressed newborn infant. J Pediatr. 1979;94(1):118.
54. McDonald SJ, Middleton P, Dowswell T, Morris PS. Effect of timing of umbilical cord clamping of term infants on maternal and neonatal outcomes. Cochrane Database Syst Rev. 2013;7:CD004074.
55. Mercer JS. Current best evidence: a review of the literature on umbilical cord clamping. J Midwife Women’s Health. 2001;46(6):402.
56. Morley CJ, Davis PG. Continuous positive airway pressure: scientific and clinical rationale. Curr Opin Pediatr. 2008;20(2):119.
57. Msemo G, Massawe A, Mmbando D, et al. Newborn mortality and fresh stillbirth rates in Tanzania after Helping Babies Breathe training. Pediatrics. 2013;131(2):e353.
58. Niermeyer S. A physiologic approach to cord clamping: clinical considerations. Matern Health Neonatol Perinatol. 2015;1:21.
59. O’Donnell CP, Schmolzer GM. Resuscitation of preterm infants: delivery room interventions and their effect on outcomes. Clin Perinatol. 2012;39(4):857.
60. Paulmichl K, Hattinger-Jurgenssen E, Maier B. Decision­making at the border of viability by means of values clarification: a case study to achieve distinct communication by ordinary language approach. J Perinat Med. 2011;39(5):595.
61. Perlman JM. Maternal fever and neonatal depression: preliminary observations. Clin Pediatr. 1999;38:287.
62. Perlman JM, Risser R. Cardiopulmonary resuscitation in the delivery room: associated clinical events. Arch Pediatr Adolesc Med. 1995;149(1):20.
63. Perlman JM, Wyllie J, Kattwinkel J, et al. Part 7: neonatal resuscitation: 2015 international consensus on cardiopulmonary resuscitation and emergency cardiovascular care science with treatment recommendations. Circulation. 2015;132(16 Suppl 1):S204.
64. Pfister RH, Soll RF. Initial respiratory support of preterm infants: the role of CPAP, the INSURE method, and noninvasive ventilation. Clin Perinatol. 2012;39(3):459.
65. Rabe H, Diaz-Rossello JL, Duley L, Dowswell T. Effect of timing of umbilical cord clamping and other strategies to influence placental transfusion at preterm birth on maternal and infant outcomes. Cochrane Database Syst Rev. 2012;8:CD003248.
66. Reddy VK, Holzman IR, Wedgwood JF. Pulse oximetry saturations in the first 6 hours of life in normal ter m infants. Clin Pediatr. 1999;38(2):87.
67. Rudiger M, Kuster H, Roehr CC. Pathophysiology of neonatal transition and meaningful measures for the initial stabilisation of extremely premature neonates. Z Geburtshilfe Neonatol. 2012;216(5):201.
68. Rudolph AM. High pulmonary vascular resistance after birth, I: pathophysiologic considerations and etiologic classification. Clin Pediatr. 1980;19(9):585.
69. Scarpelli EM. Perinatal lung mechanics and the first breath. Lung. 1984;162(2):61.
70. Schmolzer GM, Morley CJ, Wong C, et al. Respiratory function monitor guidance of mask ventilation in the delivery room: a feasibility study. J Pediatr. 2012;160(3):377.
71. Spector JM, Daga S. Preventing those so-called stillbirths. Bull World Health Organ. 2008;86(4):315.
72. Stenson BJ, Boyle DW, Szyld EG. Initial ventilation strategies during newborn resuscitation. Clin Perinatol. 2006;33(1):65.
73. Toth B, Becker A, Seelbach-Gobel B. Oxygen saturation in healthy newborn infants immediately after birth measured by pulse oximetry. Arch Gynecol Obstet. 2002;266(2):105.
74. Vain NE, Szyld EG, Prudent LM, et al. Oropharyngeal and nasopharyngeal suctioning of meconium-stained neonates before delivery of their shoulders: multicentre, randomised controlled trial. Lancet. 2004;l364(9434):597.
75. Vento M, Asensi M, Sastre J, et al. Resuscitation with room air instead of 100% oxygen prevents oxidative stress in moderately asphyxiated term neonates. Pediatrics. 2001;107(4):642.
76. Vento M, Moro M, Escrig R, et al. Preterm resuscitation with low oxygen causes less oxidative stress, inflammation, and chronic lung disease. Pediatrics. 2009;124(3):e439.
77. Vento M, Sastre J, Asensi M, et al. Oxidative stress in asphyxiated term infants resuscitated with 100% oxygen. J Pediatr. 2003;142(3):242.
78. Verder H, Bohlin K, Kamper J, et al. Nasal CPAP and surfactant for treatment of respiratory distress syndrome and prevention of bronchopulmonary dysplasia. Acta Paediatr. 2009;98(9):1400.
79. Wang CL, Anderson C, Leone TA, et al. Resuscitation of preterm neonates by using room air or 100% oxygen. Pediatrics. 2008;121(6):1083.
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80. Watkinson M. Temperature control of premature infants in the delivery room. Clin Perinatol. 2006;3(1):43.
81. Weiner GM, e d . Textbook of Neonatal Resuscitation. 7th ed. Elk Grove Village, IL: American Academy of Pediatrics and American Heart Association; 2016.
82. Weiner GM, Niermeyer S. Medications in neonatal resuscitation: epinephrine and the search for better alternative strategies. Clin Perinatol. 2012;39(4):843.
83. Weinstock P, Halamek LP. Teamwork during resuscitation. Pediatr Clin North Am. 2008;55(4):1011.
84. Winter J, Kattwinkel J, Chisholm C, et al. Ventilation of preterm infants during delayed cord clamping (VentFirst): a pilot study of feasibility and safety. Am J Perinatol. 2017;34(2):111.
85. Wood FE, Morley CJ, Dawson JA, et al. Assessing the effectiveness of two round neonatal resuscitation masks: study 1. Arch Dis Child Fetal Neonat Ed. 2008;93(3):F235.
86. Wood FE, Morley CJ, Dawson JA, et al. Improved techniques reduce face mask leak during simulated neonatal resuscitation: study 2. Arch Dis Child Fetal Neonat Ed. 2008;93(3):F230.
87. World Health Organization. Guideline. Delayed Umbilical Cord
Clamping for Improved Maternal and Infant Health and Nutrition Outcomes. Geneva: World Health Organization; 2014.
88. Wyckoff MH, Aziz K, Escobedo MB, et al. Part 13: neonatal resuscitation: 2015 American Heart Association guidelines update for cardiopulmonary resuscitation and emergency cardiovascular care. Pediatrics. 2015;136(Suppl 2):S196.
89. Wyllie J, Carlo WA. The role of carbon dioxide detectors for confirmation of endotracheal tube position. Clin Perinatol. 2006;33(1):111.
90. Yangthara B, Horrasith S, Paes B, Kitsommart R. Predictive factors for intensive birth resuscitation in a developing- country: a 5-year, single-center study. J Maternal-Fetal Neonatal Med.
2018. https://doi.org/10.1080/14767058.2018.1497602.
IMMEDIATE NEWBORN
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5
neonate must demonstrate a condition of well-being before being considered a normal,
A
low-risk infant. All neonatal intensive care
professionals must understand the normal neo­nate to care for the sick neonate. This chapter
discusses the initial assessment, transitional period, and gestational age characteristics that are funda­mental for providing quality initial care after.
Physical and physiologic changes occur so rap­idly after birth that the assessment of the newly born can be divided into four distinctive periods: delivery, transition, the first 24 hours of life, and discharge. Each of these assessments has a specific
purpose. These evaluations occur in relation to the age of the newborn infant (minutes, hours, days, and weeks) rather than the location of the mother and infant in the hospital or arbitrary nursery routines.
The evaluation at delivery is aimed at deter­mining the condition of the infant at the time of birth and at detecting potentially life-threat­ening emergencies. The examination during the
next few hours (transitional period) is used to
evaluate the infant’s adjustment to extrauterine life. The complete newborn examination by a qualified health care provider should ideally be delayed until after initiation of breastfeeding, but completed by 12 to 24 hours.8 It is the most
important examination, because many findings can be treated or complications can be avoided. Finally, the assessment/evaluation at discharge is of the utmost importance. Although it is not as detailed as the complete examination, it is aimed at establish-
ing the infant’s readiness to leave the hospital and to be cared for by the mother.
Both the initial complete examination and the discharge examination can be performed with parents present to demonstrate the baby’s
CARE AFTER BIRTH
SANDRA L. GARDNER AND SUSAN NIERMEYER
unique abilities and to answer the parents’ ques­tions. These are excellent opportunities to provide
support and encouragement as the parents begin to incorporate the new member into their family.
ASSESSMENT AND CARE AT
BIRTH
Before the birth, one should obtain pertinent facts
about the pregnancy, such as parity, gravidity, fetal losses, estimated birth weight (BW) and gestational age (GA) of the fetus, and, of course, any problems present in the current pregnancy. of prenatal screening tests should be available to the clinician at birth. Health care providers should note whether the mother was screened for group B streptococcus and whether she received any antibi­otic treatment.
During labor, one can observe the frequency
and duration of contractions and the maternal and fetal reaction to contractions. Fetal distress, passage of meconium, prolonged rupture of membranes, malodorous fluid, and other signs will alert the attendants to impending problems.
At birth, the most common way to assess the
infant’s condition is to use the Apgar scoring sys­tem.10 This score provides a comprehensive, objective measure of the state of an infant at given times after birth, traditionally at 1 and 5 minutes (see Chapter
4, Figure 4.7). The Apgar score standardizes ini-
tial newborn assessment and continues to be a predictor of neonatal survival.
score should not be used as the primary indicator for resuscitation because it is not normally assigned until 1 minute of age. Immediate assessment of respi-
ratory effort is paramount to begin resuscitative
8,44
116
10,146,182
The results
The Apgar
BLUE type highlights content that is particularly applicable to clinical settings.
93
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procedures if the infant is limp and not breathing
(see Chapter 4). If the baby is vigorous, the care pro- vider may place him or her on the mother’s abdo­men or in her arms; the first Apgar assessment can be done with the infant in skin-to-skin during the delay before umbilical cord clamping. Scoring is repeated at 5 minutes. Between the 1- and 5-minute Apgar
scores, one systematically evaluates the baby for potential or apparent medical emergencies.
Most infants are vigorous, cry at birth, and breathe easily thereafter. A healthy, vigorous infant generally does not even need suctioning after birth. With
appropriate ongoing monitoring, most infants can be given directly to the mother for skin-to-skin care after birth without compromising the infant.
Shortly after birth, a quick estimate of GA is done. Several tables, charts, and graphs have been developed over time to assist the clinician in performing this task. With practice and experience, the professional will be able to identify approximate GA from the physical appearance. Additional discussion on GA is presented later in this chapter. Immediately follow-
ing birth, a brief but complete initial examination should be performed on each newborn to assess the condition of the infant and to ensure that
there are no major anomalies or birth injuries, that the infant is pink, and that breathing is normal. The
entire body must be assessed, including overall size, proportionality and contour, respiratory pat­tern and presence of distress, posture, tone, and state of alertness. This usually allows the clinician to
reassure parents that their infant is well and appears normal. A more detailed evaluation/examination is described later.
The most severely ill neonates are usually apparent after birth. Most of them will have been identified prenatally (e.g., serious congenital
anomalies, extreme prematurity), their presence anticipated, and a management plan is made before delivery (see Chapter 4).
EVALUATION AND CARE DURING THE TRANSITIONAL PERIOD
Physiologic Changes and Clinical Stages
The initial evaluation, assessment, and management
of a newborn must be directed toward promoting
and facilitating normal adaptation to extrauterine life and early detection of significant health prob­lems so that they can be evaluated and treated promptly and appropriately.
The obligatory change of environment at birth necessitates adjustment to the extrauterine environment in a complex series of changes essential for survival. Every infant must com­plete this process of transition successfully to survive in the extrauterine environment. For a
small percentage of newborns, transition is never achieved; for a slightly larger number, transition is delayed or complicated. For most newborns, transi­tion is so smooth it appears uneventful.
With the first breath, all neonates begin the transition from intrauterine to extrauterine life.
Three major changes take place at birth. First, fluid in the alveoli is reabsorbed and air fills the alveoli, allowing for gas to diffuse into and out of the pul­monary blood vessels. Second, when the umbilical arteries and vein are clamped, the low-resistance placental circuit is gone and systemic blood pres­sure increases. Third, pulmonary vascular resistance decreases as a result of mechanical distention of the alveoli and increased alveolar oxygen content. Oxygen is a potent pulmonary vasodilator.
During the first few hours after birth, the normal newborn progresses through a fairly predictable sequence of events, recovering from the stress of birth and adapting to extrauterine life. Intrapartum and immediate neonatal events
result in sympathetic discharges reflected in changes in heart rate, color, respiration, motor activity, gas­trointestinal function, and temperature. Awake and
sleep states affect a neonate’s behavior and abil­ity to respond to the environment. A newborn
may go from one state to another quite frequently after birth and at home (see Critical Findings: Newborn States and Considerations for Caregiving in Chapter 13). Fig. 5.1 shows the classic descrip-
tion by Desmond of the transitional period, which includes the three stages shown in Box
5.1. Failure to establish this pattern of transition
requires careful observation and investigation.
91
Management of the Newborn during Transition
Traditionally, “normal newborn” care was based on
the optimistic assumption that most newborns have no difficulty with transition after birth and that
CHAPTER 5 Immediate Newborn Care After Birth
Minutes after birth Hours after birth
Respiration
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SD 1034 Apgar 9 Birth weight: 3586 g
Respiration rate (breaths/min) Heart rate (beats/min)
95
Color
Heart
sounds
Motor
activity
Brief cyanosis
Rales Flaring Grunting Retractions
Loud Forceful Irregular
First period
of reactivity
Alerting
PresentMucus
Sounds absent
Birth 5101530 1246810
Flushing with
cry
Barreling of chest
Regular
Sleep
Absent
Sounds presentBowel
Swift color changes
Labile
Second period
of reactivity
Variable
(gagging, arching)
Present
Meconium passage
100
80
60
40
200
180
160
140
120
100
80
Temperature (°C)
39
37
35
FIGURE 5.1 Critical findings: Neonatal transitional period. (From Desmond MM, Rudolph AJ, Phitaksphraiwan P, et al. The transitional
care nursery: a mechanism for preventive medicine in the newborn, Pediatr Clin North Am. 1966;13:651.)
term infants, in particular, do exceedingly well.91
Individualized newborn care recognizes the complexity of transitioning to extrauterine life, the need to support that transition, and the real­ity of serious disease, even in term newborns.
Newborn Should Be Treated as a Recovery Patient
SKILLED PROVIDERS SHOULD CARE FOR THE NEWBORN
Current standards of care8 require skilled health care providers (24 hours/day) to care
for newborns during the first minutes after birth (e.g., in the delivery room, at the birth center) and in the transitional period (e.g.,
in the birth room, mother-baby area, newborn nursery).91 All personnel caring for the newborn must be familiar with the transitional changes after birth and deviations from normal transition­al events. After a normal, low-risk pregnancy
and birth, primary evaluation and care of the newborn must be provided by nurses with neonatal-perinatal competencies who consult advanced practice nurses and/or physician(s) when appropriate.
8,91
BOX
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5.1
UNIT TWO Support of the Neonate96
TRANSITIONAL PERIOD
First Stage (0 to 30 Minutes) = First Period of Reactivity
• Rapid increase in heart rate to the range of 160 to 180 beats/min (0 to 15 min)
• Gradual decrease in heart rate over 30 minutes to baseline rate between 100 and 120 beats/min
• Irregular respirations (first 15 minutes), peak respiratory rates between 60 and 80 breaths/min
• Rales present on auscultation
• Grunting, flaring, and retractions may be noted, and brief periods of
apnea (<10 seconds in duration)
• Plethora
• Alert with spontaneous startle reactions, gustatory movements, trem-
ors, crying, and side-to-side head movements
• Decrease in body temperature
• Generalized increase in motor activity, with increased muscle tone
• Bowel sounds absent, and abdomen distended
• Production of saliva minimal
Second Stage (30 Minutes to 2 Hours) = Period of Decreased Responsiveness
• Newborn either sleeps or has a marked decrease in motor activity
• Muscle tone returns to normal, but responsiveness is diminished
• Fast, shallow, synchronous breathing (60 breaths/min) without dysp­nea occurs
• Newborn’s color is pale but pink with excellent perfusion and capillary refill
• Increase in anterior-posterior diameter (barreling) of the chest is usually present
• Heart rate decreases into the range of 100 to 120 beats/min or lower; the newborn is relatively less responsive to external stimuli
• Abdomen is rounded, and bowel sounds are audible; peristaltic waves may be visible, and meconium may be passed
• Oral mucus is absent
• Spontaneous jerks and twitches are common, but the newborn quickly returns to rest
Third Stage (2 to 8 Hours) = Second Period of Reactivity
• Return of and possible exaggeration of responsiveness
• Labile heart rate: periods of tachycardia
• Brief periods of rapid respirations: At 2 hours of age: median respiratory rates: 46 breaths/min; 95th percentile respiratory rates of 65 breaths/ min; 5th percentile: respiratory rates 30 to 32 breaths/min. higher when awake, rather than asleep, boys higher than girls, and after heavy meconium staining of amniotic fluid; no difference in rate between vaginal versus cesarean birth.
• Abrupt changes in tone, color, and bowel sounds
• Possible prominence of oral mucus; gagging and vomiting not unusual
• Possible clearing of meconium from the bowel
• Increased responsiveness to endogenous and exogenous stimuli
• Newborn hunger cues; quiet alert periods when maternal bonding is established
186
186
Rates
Modified from Hernandez JA, Thilo E. Routine care of the full-term newborn. In: Osborn LC, DeWitt TG, First LR, et al, eds. Pediatrics. St Louis, MO: Mosby; 2005.
STANDARDS FOR ROUTINE CARE AND PHYSIOLOGIC MONITORING DURING TRANSITION MUST BE MAINTAINED
Parent-infant bonding, skin-to-skin care, early breastfeeding, and careful neonatal monitor­ing during the transitional period should be addressed in delivery/birth room and other facility routines. After birth, the stable, pink new-
born whose Apgar score is greater than 7 at 5 min­utes can remain skin-to-skin with the mother.
Immediate skin-to-skin contact in the first hours after birth facilitates early initiation of breast­feeding in the setting of a stable neonate under continuous monitoring. After birth, at 15-min­ute intervals, every newborn must be assessed for general condition, respiratory effort, color, muscle tone, and temperature; all assessments must be documented.91 The mother and infant
should not be left alone in the first hours after birth.
Skin-to-skin care benefits parents, premature
neonates, and full-term neonates after vaginal, operative vaginal, and cesarean birth (see Table
5.1 and Fig. 5.2). Skin-to-skin care not only
prevents hypothermia26 but also is effective in treating hypothermia.
of skin-to-skin versus incubator care for rewarming
148
low-risk hypothermic neonates, skin-to-skin care
131
In a randomized study
was shown to be more effective (90%) than incuba­tor care (60%)51 (see Chapter 6).
Even newly born, low-birth-weight (LBW)
infants (1500 to 2500 g) transitioned by skin-to­skin care with their mothers have been shown to stabilize their cardiorespiratory function better than LBW infants cared for in incubators. This
randomized controlled trial (RCT) also found that
TABLE
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5.1
BENEFITS OF SKIN-TO-SKIN CARE FOR PARENTS AND NEWBORNS AFTER VAGINAL AND CESAREAN SECTION BIRTHS
BENEFITS AFTER VAGINAL BIRTH BENEFITS AFTER CESAREAN BIRTH
Psychological (Parental)
Promotes maternal and paternal infant bonding as a result of increased release of oxytocin Facilitates the process of becoming a parent; either restores or drains energy Increases positive activities with the newborn and growing infant
47,58,143,148
148
12,13
Psychological (Parental)
Enhances family bonding, attachment, and satisfaction Increases vocal interaction with newborn
Decreases expense because infant formula does not have to be purchased
174
192
Psychological (Maternal)
Enhances birth experience Increases confidence and competence Decreases postpartum cortisol levels, postpartum depression28 and
58
anxiety More positive maternal interactions at 1 week, 2 months, and 3 months
29
of age Decreases maternal pain during episiotomy repair
93
148
163
Psychological (Paternal)
Promotes parental role attainment Increases involvement and sensitivity toward newborn Exhibits more caring
191
Increases confidence and comforting behaviors toward neonate Facilitates more equal parenthood Decreases cortisol levels, stress, and anxiety Decreases relationship problems with mother of baby
164
and interactive behaviors
143
58,164
191
164
130
Physiologic (Maternal)
Decreases postpartum hemorrhage
58,157
secretion
with breastfeeding
Breastfeeding
Earlier initiation of breastfeeding
29,50,84,194
duration Assists in resolution of early breastfeeding problems such as latch-on Increases breastfeeding self-efficacy
Full Term Newborn
Novel bioactive substances in human colostrum may assist in postnatal adaptation related to thermoregulation, vascular adaptation, glucose metab­olism, lung function, and fluid homeostasis Breastfeeding within the first hour of life decreases neonatal mortality by 33% Higher breastfeeding rates
128,163
weeks,
1 month, More likely to breastfeed successfully during first feeding Enhances breastfeeding benefits: fewer postnatal infections (ear, gastroin­testinal, and respiratory); decreased incidence of SIDS and chronic illnesses (obesity, diabetes, cardiovascular) Dose-dependent relationship between the use of fentanyl administered by epidural and synthetic oxytocin and the inability of the newborn to initiate suckling in the first hour of life while skin-to-skin with mother.
157
as a result of increased oxytocin
50,84,88,114,193
153
and breastfeeding exclusivity at 6
115,128
4 months,
179
5,138
32
128
and 6 months of age.
Increases incidence and
180
167
128
128
34
Psychological (Maternal)
Enhances perception of own health, quality of life, and satisfaction with birth experience Decreases anxiety and pain; for anxiety and pain Rise in maternal salivary alpha-amylase directly after delivery when baby held skin-to-skin intraoperatively Decreases maternal oxidative stress Describes skin-to-skin care with father as the formation of the family Prefers father to provide skin-to-skin if mother unable, rather than newborn be alone on a radiant warmer
79
148,198
198
decreases administration of medications
107
207
78
78
Psychological (Paternal)
Increases conversation with mother Facilitates more equal parenthood enables the father to immediately and gradually change to “father” as he assumes the primary parenting responsibility and role with his newborn No influence on initiation of breastfeeding or exclusive breastfeeding rates at 3 or 6 months of age when compared to maternal skin-to-skin contact.
192
139
because togetherness with infant
70
Physiologic (Maternal)
Significant reduction in blood pressure and respiratory rate
Breastfeeding
Initiates earlier breastfeeding, infants were exclusively or predominantly breastfeeding at discharge, 3 months,
79,85
and 6 months of age.85
More likely still breastfeeding at 1 month and 4 months of age/more
128
successful
139
85
Continued
UNIT TWO Support of the Neonate98
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TABLE
5.1
BENEFITS OF SKIN-TO-SKIN CARE FOR PARENTS AND NEWBORNS AFTER VAGINAL AND CESAREAN SECTION BIRTHS—CONT’D
BENEFITS AFTER VAGINAL BIRTH BENEFITS AFTER CESAREAN BIRTH
Physiologic (Neonatal)
Full-Term Newborn
Decreases cortisol levels resulting from less birth stress decline in neurosteroid levels with more skin-to-skin contact Improves thermal stability: less hypothermia, improved ability to remain in thermal neutrality
140,164,172,193
Promotes earlier cardiopulmonary stabilization: slower heart rate combined with a slower increase in the first 3 minutes; Less tachycardia and more bradycardia in the first minutes after birth Improves blood glucose regulation; higher blood glucose levels. Nonpharmacologic intervention for neonatal pain resulting in less crying and lower pain scores
1,83,164
122,181
128,181
Higher Spo2 and
and a larger
122
166
128
Physiologic (Neonatal)
Full-Term Newborn
Decreases newborn stress of starting skin-to-skin care with father),71 calmer and better relax-
71,144,192
ation Reaches drowsy state sooner (within 60 minutes after birth) Prefeeding behaviors facilitated Initiates vocalization with parents (within 15 minutes of initiating skin-to­skin care), which further promotes bonding and attachment Thermal stability Lower transfer rates to NICU Fewer suspected neonatal infections
22,79
159
resulting in less crying (within 15 minutes
150,158
Premature Newborn
Improves physiologic stability: better temperatures, oxygen saturations, heart rate and blood glucose levels;
141
similar first body temperatures and blood glucose levels in moderately preterm infants (34–35 weeks gestational age) when compared to incubator care Nonpharmacologic intervention for neonatal pain
110
141,142
Decreases late preterm infant’s cortisol reactivity to handling, improves concordance between mother/infant salivary cortisol levels
130
Improves infant-to-parent bonding because of close proximity
71
71
192
150
LBW infants transitioned with skin-to-skin care had less need for respiratory support, intravenous fluids, and antibiotics during their hospitalization.49 Because of the extensive research evidence, the World Health Organization (WHO), American Academy
FIGURE 5.2 Skin-to-skin care and family bonding in the first hours after birth.
of Breastfeeding Medicine (ABM),2 American Academy of Pediatrics (AAP), Women’s Health, Obstetric and Neonatal Nurses (AWHONN).13 International Childbirth Education Association (ICEA),96 Neonatal Resuscitation
8,73
Association of