When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

  1. Newborn resuscitation requires anticipation and preparation by providers who train individually and as teams.

  2. Most newly born infants do not require immediate cord clamping or resuscitation and can be evaluated and monitored during skin-to-skin contact with their mothers after birth.

  3. Inflation and ventilation of the lungs are the priority in newly born infants who need support after birth.

  4. A rise in heart rate is the most important indicator of effective ventilation and response to resuscitative interventions.

  5. Pulse oximetry is used to guide oxygen therapy and meet oxygen saturation goals.

  6. Chest compressions are provided if there is a poor heart rate response to ventilation after appropriate ventilation corrective steps, which preferably include endotracheal intubation.

  7. The heart rate response to chest compressions and medications should be monitored electrocardiographically.

  8. If the response to chest compressions is poor, it may be reasonable to provide epinephrine, preferably via the intravenous route.

  9. Failure to respond to epinephrine in a newborn with history or examination consistent with blood loss may require volume expansion.

  10. If all these steps of resuscitation are effectively completed and there is no heart rate response by 20 minutes, redirection of care should be discussed with the team and family.

It is estimated that approximately 10% of newly born infants need help to begin breathing at birth,1–3 and approximately 1% need intensive resuscitative measures to restore cardiorespiratory function.4,5 The neonatal mortality rate in the United States and Canada has fallen from almost 20 per 1000 live births6,7 in the 1960s to the current rate of approximately 4 per 1000 live births. The inability of newly born infants to establish and sustain adequate or spontaneous respiration contributes significantly to these early deaths and to the burden of adverse neurodevelopmental outcome among survivors. Effective and timely resuscitation at birth could therefore improve neonatal outcomes further.

Successful neonatal resuscitation efforts depend on critical actions that must occur in rapid succession to maximize the chances of survival. The International Liaison Committee on Resuscitation (ILCOR) Formula for Survival emphasizes 3 essential components for good resuscitation outcomes: guidelines based on sound resuscitation science, effective education of resuscitation providers, and implementation of effective and timely resuscitation.8 The 2020 neonatal guidelines contain recommendations, based on the best available resuscitation science, for the most impactful steps to perform in the birthing room and in the neonatal period. In addition, specific recommendations about the training of resuscitation providers and systems of care are provided in their respective guideline Parts.9,10

Introduction

Scope of Guideline

This guideline is designed for North American healthcare providers who are looking for an up-to-date summary for clinical care, as well as for those who are seeking more in-depth information on resuscitation science and gaps in current knowledge. The science of neonatal resuscitation applies to newly born infants transitioning from the fluid-filled environment of the womb to the air-filled environment of the birthing room and to newborns in the days after birth. In circumstances of altered or impaired transition, effective neonatal resuscitation reduces the risk of mortality and morbidity. Even healthy babies who breathe well after birth benefit from facilitation of normal transition, including appropriate cord management and thermal protection with skin-to-skin care.

The 2015 Neonatal Resuscitation Algorithm and the major concepts based on sections of the algorithm continue to be relevant in 2020 (Figure). The following sections are worth special attention.

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Figure. Neonatal Resuscitation Algorithm. CPAP indicates continuous positive airway pressure; ECG, electrocardiographic; ETT, endotracheal tube; HR, heart rate; IV, intravenous; O2, oxygen; Spo2, oxygen saturation; and UVC, umbilical venous catheter.

  • Positive-pressure ventilation (PPV) remains the main intervention in neonatal resuscitation. While the science and practices surrounding monitoring and other aspects of neonatal resuscitation continue to evolve, the development of skills and practice surrounding PPV should be emphasized.

  • Supplemental oxygen should be used judiciously, guided by pulse oximetry.

  • Prevention of hypothermia continues to be an important focus for neonatal resuscitation. The importance of skin-to-skin care in healthy babies is reinforced as a means of promoting parental bonding, breast feeding, and normothermia.

  • Team training remains an important aspect of neonatal resuscitation, including anticipation, preparation, briefing, and debriefing. Rapid and effective response and performance are critical to good newborn outcomes.

  • Delayed umbilical cord clamping was recommended for both term and preterm neonates in 2015. This guideline affirms the previous recommendations.

  • The 2015 American Heart Association (AHA) Guidelines Update for Cardiopulmonary Resuscitation (CPR) and Emergency Cardiovascular Care (ECC) recommended against routine endotracheal suctioning for both vigorous and nonvigorous infants born with meconium-stained amniotic fluid (MSAF). This guideline reinforces initial steps and PPV as priorities.

It is important to recognize that there are several significant gaps in knowledge relating to neonatal resuscitation. Many current recommendations are based on weak evidence with a lack of well-designed human studies. This is partly due to the challenges of performing large randomized controlled trials (RCTs) in the delivery room. The current guideline, therefore, concludes with a summary of current gaps in neonatal research and some potential strategies to address these gaps.

COVID-19 Guidance

Together with other professional societies, the AHA has provided interim guidance for basic and advanced life support in adults, children, and neonates with suspected or confirmed coronavirus disease 2019 (COVID-19) infection. Because evidence and guidance are evolving with the COVID-19 situation, this interim guidance is maintained separately from the ECC guidelines. Readers are directed to the AHA website for the most recent guidance.12

Evidence Evaluation and Guidelines Development

The following sections briefly describe the process of evidence review and guideline development. See “Part 2: Evidence Evaluation and Guidelines Development” for more details on this process.11

Organization of the Writing Committee

The Neonatal Life Support Writing Group includes neonatal physicians and nurses with backgrounds in clinical medicine, education, research, and public health. Volunteers with recognized expertise in resuscitation are nominated by the writing group chair and selected by the AHA ECC Committee. The AHA has rigorous conflict of interest policies and procedures to minimize the risk of bias or improper influence during development of the guidelines.13 Before appointment, writing group members and peer reviewers disclosed all commercial relationships and other potential (including intellectual) conflicts. Disclosure information for writing group members is listed in Appendix 1.

Methodology and Evidence Review

These 2020 AHA neonatal resuscitation guidelines are based on the extensive evidence evaluation performed in conjunction with the ILCOR and affiliated ILCOR member councils. Three different types of evidence reviews (systematic reviews, scoping reviews, and evidence updates) were used in the 2020 process. Each of these resulted in a description of the literature that facilitated guideline development.14–17

Class of Recommendation and Level of Evidence

Each AHA writing group reviewed all relevant and current AHA guidelines for CPR and ECC18–20 and all relevant 2020 ILCOR International Consensus on CPR and ECC Science With Treatment Recommendations evidence and recommendations21 to determine if current guidelines should be reaffirmed, revised, or retired, or if new recommendations were needed. The writing groups then drafted, reviewed, and approved recommendations, assigning to each a Level of Evidence (LOE; ie, quality) and Class of Recommendation (COR; ie, strength) (Table).11

This table defines the Classes of Recommendation (COR) and Levels of Evidence (LOE). COR indicates the strength the writing group assigns the recommendation, and the LOE is assigned based on the quality of the scientific evidence. The outcome or result of the intervention should be specified (an improved clinical outcome or increased diagnostic accuracy or incremental prognostic information).Classes of RecommendationCOR designations include Class 1, a strong recommendation for which the potential benefit greatly outweighs the risk; Class 2a, a moderate recommendation for which benefit most likely outweighs the risk; Class 2b, a weak recommendation for which it’s unknown whether benefit will outweigh the risk; Class 3: No Benefit, a moderate recommendation signifying that there is equal likelihood of benefit and risk; and Class 3: Harm, a strong recommendation for which the risk outweighs the potential benefit.Suggested phrases for writing Class 1 recommendations includeIs recommendedIs indicated/useful/effective/beneficialShould be performed/administered/otherComparative-effectiveness phrases include treatment/strategy A is recommended/indicated in preference to treatment B, and treatment A should be chosen over treatment B.Suggested phrases for writing Class 2a recommendations includeIs reasonableCan be useful/effective/beneficialComparative-effectiveness phrases include treatment/strategy A is probably recommended/indicated in preference to treatment B, and it is reasonable to choose treatment A over treatment B.For comparative-effectiveness recommendations (COR 1 and 2a; LOE A and B only), studies that support the use of comparator verbs should involve direct comparisons of the treatments or strategies being evaluated.Suggested phrases for writing Class 2b recommendations includeMay/might be reasonableMay/might be consideredUsefulness/effectiveness is unknown/unclear/uncertain or not well-establishedSuggested phrases for writing Class 3: No Benefit recommendations (generally, LOE A or B use only) includeIs not recommendedIs not indicated/useful/effective/beneficialShould not be performed/administered/otherSuggested phrases for writing Class 3: Harm recommendations includePotentially harmfulCauses harmAssociated with excess morbidity/mortalityShould not be performed/administered/otherLevels of EvidenceFor LOEs, the method of assessing quality is evolving, including the application of standardized, widely-used, and preferably validated evidence grading tools; and for systematic reviews, the incorporation of an Evidence Review Committee. LOE designations include Level A, Level B-R, Level B-NR, Level C-LD, and Level C-EO.Those categorized as Level A are derived fromHigh-quality evidence from more than 1 randomized clinical trial, or RCTMeta-analyses of high-quality RCTsOne or more RCTs corroborated by high-quality registry studiesThose categorized as Level B-R (randomized) are derived fromModerate-quality evidence from 1 or more RCTsMeta-analyses of moderate-quality RCTsThose categorized as Level B-NR (nonrandomized) are derived fromModerate-quality evidence from 1 or more well-designed, well-executed nonrandomized studies, observational studies, or registry studiesMeta-analyses of such studiesThose categorized as Level C-LD (limited data) are derived fromRandomized or nonrandomized observational or registry studies with limitations of design or executionMeta-analyses of such studiesPhysiological or mechanistic studies in human subjectsThose categorized as Level C-EO (expert opinion) are derived fromConsensus of expert opinion based on clinical experienceCOR and LOE are determined independently (any COR may be paired with any LOE).A recommendation with LOE C does not imply that the recommendation is weak. Many important clinical questions addressed in guidelines do not lend themselves to clinical trials. Although RCTs are unavailable, there may be a very clear clinical consensus that a particular test or therapy is useful or effective.

Table. Applying Class of Recommendation and Level of Evidence to Clinical Strategies, Interventions, Treatments, or Diagnostic Testing in Patient Care (Updated May 2019)*

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Guideline Structure

The 2020 guidelines are organized into “knowledge chunks,” grouped into discrete modules of information on specific topics or management issues.22 Each modular knowledge chunk includes a table of recommendations using standard AHA nomenclature of COR and LOE. A brief introduction or short synopsis is provided to put the recommendations into context with important background information and overarching management or treatment concepts. Recommendation-specific text clarifies the rationale and key study data supporting the recommendations. When appropriate, flow diagrams or additional tables are included. Hyperlinked references are provided to facilitate quick access and review.

Document Review and Approval

Each 2020 AHA Guidelines for CPR and ECC document was submitted for blinded peer review to 5 subject matter experts nominated by the AHA. Before appointment, all peer reviewers were required to disclose relationships with industry and any other potential conflicts of interest, and all disclosures were reviewed by AHA staff. Peer reviewer feedback was provided for guidelines in draft format and again in final format. All guidelines were reviewed and approved for publication by the AHA Science Advisory and Coordinating Committee and AHA Executive Committee. Disclosure information for peer reviewers is listed in Appendix 2.

References

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  • 3. Aziz K, Chadwick M, Baker M, Andrews W. Ante- and intra-partum factors that predict increased need for neonatal resuscitation.Resuscitation. 2008; 79:444–452. doi: 10.1016/j.resuscitation.2008.08.004CrossrefMedlineGoogle Scholar
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Major Concepts

These guidelines apply primarily to the “newly born” baby who is transitioning from the fluid-filled womb to the air-filled room. The “newly born” period extends from birth to the end of resuscitation and stabilization in the delivery area. However, the concepts in these guidelines may be applied to newborns during the neonatal period (birth to 28 days).

The primary goal of neonatal care at birth is to facilitate transition. The most important priority for newborn survival is the establishment of adequate lung inflation and ventilation after birth. Consequently, all newly born babies should be attended to by at least 1 person skilled and equipped to provide PPV. Other important goals include establishment and maintenance of cardiovascular and temperature stability as well as the promotion of mother-infant bonding and breast feeding, recognizing that healthy babies transition naturally.

The Neonatal Resuscitation Algorithm remains unchanged from 2015 and is the organizing framework for major concepts that reflect the needs of the baby, the family, and the surrounding team of perinatal caregivers.

Anticipation and Preparation

Every healthy newly born baby should have a trained and equipped person assigned to facilitate transition. Identification of risk factors for resuscitation may indicate the need for additional personnel and equipment. Effective team behaviors, such as anticipation, communication, briefing, equipment checks, and assignment of roles, result in improved team performance and neonatal outcome.

Cord Management

After an uncomplicated term or late preterm birth, it is reasonable to delay cord clamping until after the baby is placed on the mother, dried, and assessed for breathing, tone, and activity. In other situations, clamping and cutting of the cord may also be deferred while respiratory, cardiovascular, and thermal transition is evaluated and initial steps are undertaken. In preterm birth, there are also potential advantages from delaying cord clamping.

Initial Actions

When possible, healthy term babies should be managed skin-to-skin with their mothers. After birth, the baby should be dried and placed directly skin-to-skin with attention to warm coverings and maintenance of normal temperature. There should be ongoing evaluation of the baby for normal respiratory transition. Radiant warmers and other warming adjuncts are suggested for babies who require resuscitation at birth, especially very preterm and very low-birth-weight babies.

Stimulation may be provided to facilitate respiratory effort. Suctioning may be considered for suspected airway obstruction.

Assessment of Heart Rate

Heart rate is assessed initially by auscultation and/or palpation. Oximetry and electrocardiography are important adjuncts in babies requiring resuscitation.

Positive-Pressure Ventilation

PPV remains the primary method for providing support for newborns who are apneic, bradycardic, or demonstrate inadequate respiratory effort. Most babies will respond to this intervention. An improvement in heart rate and establishment of breathing or crying are all signs of effective PPV.

Oxygen Therapy

PPV may be initiated with air (21% oxygen) in term and late preterm babies, and up to 30% oxygen in preterm babies. Oximetry is used to target the natural range of oxygen saturation levels that occur in term babies.

Chest Compressions

If the heart rate remains less than 60/min despite 30 seconds of adequate PPV, chest compressions should be provided. The suggested ratio is 3 chest compressions synchronized to 1 inflation (with 30 inflations per minute and 90 compressions per minute) using the 2 thumb–encircling hands technique for chest compressions.

Vascular Access

When vascular access is required in the newly born, the umbilical venous route is preferred. When intravenous access is not feasible, the intraosseous route may be considered.

Medications

If the heart rate remains less than 60/min despite 60 seconds of chest compressions and adequate PPV, epinephrine should be administered, ideally via the intravenous route.

Volume Expansion

When blood loss is known or suspected based on history and examination, and there is no response to epinephrine, volume expansion is indicated.

Withholding and Discontinuing Resuscitation

It may be possible to identify conditions in which withholding or discontinuation of resuscitative efforts may be reasonably considered by families and care providers. Appropriate and timely support should be provided to all involved.

Human Factors and Systems

Teams and individuals who provide neonatal resuscitation are faced with many challenges with respect to the knowledge, skills, and behaviors needed to perform effectively. Neonatal resuscitation teams may therefore benefit from ongoing booster training, briefing, and debriefing.

Abbreviations

AHAAmerican Heart Association
CORClass of Recommendation
CPAPcontinuous positive airway pressure
ECCemergency cardiovascular care
ECGelectrocardiogram/electrocardiographic
H2Owater
HIEhypoxic-ischemic encephalopathy
ILCORInternational Liaison Committee on Resuscitation
LOELevel of Evidence
MSAFmeconium-stained amniotic fluid
PEEPpositive end-expiratory pressure
PPVpositive pressure ventilation
RCTrandomized controlled trial
ROSCreturn of spontaneous circulation

Anticipation of Resuscitation Need

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Approximately 10% of newborns require assistance to breathe after birth.1–3,5,13 Newborn resuscitation requires training, preparation, and teamwork. When the need for resuscitation is not anticipated, delays in assisting a newborn who is not breathing may increase the risk of death.1,5,13 Therefore, every birth should be attended by at least 1 person whose primary responsibility is the newborn and who is trained to begin PPV without delay.2–4

A risk assessment tool that evaluates risk factors present during pregnancy and labor can identify newborns likely to require advanced resuscitation; in these cases, a team with more advanced skills should be mobilized and present at delivery.5,7 In the absence of risk stratification, up to half of babies requiring PPV may not be identified before delivery.6,13

A standardized equipment checklist is a comprehensive list of critical supplies and equipment needed in a given clinical setting. In the birth setting, a standardized checklist should be used before every birth to ensure that supplies and equipment for a complete resuscitation are present and functional.8,9,14,15

A predelivery team briefing should be completed to identify the leader, assign roles and responsibilities, and plan potential interventions. Team briefings promote effective teamwork and communication, and support patient safety.8,10–12

Recommendation-Specific Supportive Text

  1. A large observational study found that delaying PPV increases risk of death and prolonged hospitalization.1 A systematic review and meta-analysis showed neonatal resuscitation training reduced stillbirths and improved 7-day neonatal survival in low-resource countries.3 A retrospective cohort study demonstrated improved Apgar scores among high-risk newborns after neonatal resuscitation training.16

  2. A multicenter, case-control study identified 10 perinatal risk factors that predict the need for advanced neonatal resuscitation.7 An audit study done before the use of risk stratification showed that resuscitation was anticipated in less than half of births requiring PPV.6 A prospective cohort study showed that risk stratification based on perinatal risk factors increased the likelihood of skilled team attendance at high-risk births.5

  3. A multicenter quality improvement study demonstrated high staff compliance with the use of a neonatal resuscitation bundle that included briefing and an equipment checklist.8 A management bundle for preterm infants that included team briefing and equipment checks resulted in clear role assignments, consistent equipment checks, and improved thermoregulation and oxygen saturation.9

  4. A single-center RCT found that role confusion during simulated neonatal resuscitation was avoided and teamwork skills improved by conducting a team briefing.11 A statewide collaborative quality initiative demonstrated that team briefing improved team communication and clinical outcomes.10 A single-center study demonstrated that team briefing and an equipment checklist improved team communication but showed no improvement in equipment preparation.12

References

  • 1. 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 low-income countries: a prospective descriptive observational study.Resuscitation. 2012; 83:869–873. doi: 10.1016/j.resuscitation.2011.12.011CrossrefMedlineGoogle Scholar
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  • 5. Aziz K, Chadwick M, Baker M, Andrews W. Ante- and intra-partum factors that predict increased need for neonatal resuscitation.Resuscitation. 2008; 79:444–452. doi: 10.1016/j.resuscitation.2008.08.004CrossrefMedlineGoogle Scholar
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  • 10. Talati AJ, Scott TA, Barker B, Grubb PH; Tennessee Initiative for Perinatal Quality Care Golden Hour Project Team. Improving neonatal resuscitation in Tennessee: a large-scale, quality improvement project.J Perinatol. 2019; 39:1676–1683. doi: 10.1038/s41372-019-0461-3CrossrefMedlineGoogle Scholar
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Umbilical Cord Management

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

During an uncomplicated term or late preterm birth, it may be reasonable to defer cord clamping until after the infant is placed on the mother and assessed for breathing and activity. Early cord clamping (within 30 seconds) may interfere with healthy transition because it leaves fetal blood in the placenta rather than filling the newborn’s circulating volume. Delayed cord clamping is associated with higher hematocrit after birth and better iron levels in infancy.9–21 While developmental outcomes have not been adequately assessed, iron deficiency is associated with impaired motor and cognitive development.24–26 It is reasonable to delay cord clamping (longer than 30 seconds) in preterm babies because it reduces need for blood pressure support and transfusion and may improve survival.1–8

There are insufficient studies in babies requiring PPV before cord clamping to make a recommendation.22 Early cord clamping should be considered for cases when placental transfusion is unlikely to occur, such as maternal hemorrhage or hemodynamic instability, placental abruption, or placenta previa.27 There is no evidence of maternal harm from delayed cord clamping compared with early cord clamping.10–12,28–34 Cord milking is being studied as an alternative to delayed cord clamping but should be avoided in babies less than 28 weeks’ gestational age, because it is associated with brain injury.23

Recommendation-Specific Supportive Text

  1. Compared with preterm infants receiving early cord clamping, those receiving delayed cord clamping were less likely to receive medications for hypotension in a meta-analysis of 6 RCTs1–6 and receive transfusions in a meta-analysis of 5 RCTs.7 Among preterm infants not requiring resuscitation, delayed cord clamping may be associated with higher survival than early cord clamping is.8 Ten RCTs found no difference in postpartum hemorrhage rates with delayed cord clamping versus early cord clamping.10–12,28–34

  2. Compared with term infants receiving early cord clamping, term infants receiving delayed cord clamping had increased hemoglobin concentration within the first 24 hours and increased ferritin concentration in the first 3 to 6 months in meta-analyses of 12 and 6 RCTs,9–21 respectively. Compared with term and late preterm infants receiving early cord clamping, those receiving delayed cord clamping showed no significant difference in mortality, admission to the neonatal intensive care unit, or hyperbilirubinemia leading to phototherapy in meta-analyses of 4,10,13,29,35, 10,12,17,19,21,28,31,34,36,37 and 15 RCTs, respectively.9,12,14,18–21,28–30,32–34,38,39 Compared with term infants receiving early cord clamping, those receiving delayed cord clamping had increased polycythemia in meta-analyses of 1310,11,13,14,17,18,21,29,30,33,39–41 and 8 RCTs,9,10,13,19,20,28,30,34 respectively.

  3. For infants requiring PPV at birth, there is currently insufficient evidence to recommend delayed cord clamping versus early cord clamping.

  4. A large multicenter RCT found higher rates of intraventricular hemorrhage with cord milking in preterm babies born at less than 28 weeks’ gestational age.23

References

  • 1. Dong XY, Sun XF, Li MM, Yu ZB, Han SP. [Influence of delayed cord clamping on preterm infants with a gestational age of <32 weeks].Zhongguo Dang Dai Er Ke Za Zhi. 2016; 18:635–638.MedlineGoogle Scholar
  • 2. Gokmen Z, Ozkiraz S, Tarcan A, Kozanoglu I, Ozcimen EE, Ozbek N. Effects of delayed umbilical cord clamping on peripheral blood hematopoietic stem cells in premature neonates.J Perinat Med. 2011; 39:323–329. doi: 10.1515/jpm.2011.021CrossrefMedlineGoogle Scholar
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  • 22. Wyckoff MH, Aziz K, Escobedo MB, Kapadia VS, Kattwinkel J, Perlman JM, Simon WM, Weiner GM, Zaichkin JG. Part 13: Neonatal Resuscitation: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care (Reprint).Pediatrics. 2015; 136 Suppl 2:S196–S218. doi: 10.1542/peds.2015-3373GCrossrefMedlineGoogle Scholar
  • 23. Katheria A, Reister F, Essers J, Mendler M, Hummler H, Subramaniam A, Carlo W, Tita A, Truong G, Davis-Nelson S, Schmölzer G, Chari R, Kaempf J, Tomlinson M, Yanowitz T, Beck S, Simhan H, Dempsey E, O’Donoghue K, Bhat S, Hoffman M, Faksh A, Arnell K, Rich W, Finer N, Vaucher Y, Khanna P, Meyers M, Varner M, Allman P, Szychowski J, Cutter G. Association of Umbilical Cord Milking vs Delayed Umbilical Cord Clamping With Death or Severe Intraventricular Hemorrhage Among Preterm Infants.JAMA. 2019; 322:1877–1886. doi: 10.1001/jama.2019.16004CrossrefMedlineGoogle Scholar
  • 24. Gunnarsson BS, Thorsdottir I, Palsson G, Gretarsson SJ. Iron status at 1 and 6 years versus developmental scores at 6 years in a well-nourished affluent population.Acta Paediatr. 2007; 96:391–395. doi: 10.1111/j.1651-2227.2007.00086.xCrossrefMedlineGoogle Scholar
  • 25. Grantham-McGregor S, Ani C. A review of studies on the effect of iron deficiency on cognitive development in children.J Nutr. 2001; 1312S-2649S–666S; discussion 666S. doi: 10.1093/jn/131.2.649SCrossrefMedlineGoogle Scholar
  • 26. Lozoff B, Beard J, Connor J, Barbara F, Georgieff M, Schallert T. Long-lasting neural and behavioral effects of iron deficiency in infancy.Nutr Rev. 2006; 645 Pt 2S34–43; discussion S72. doi: 10.1301/nr.2006.may.s34-s43CrossrefMedlineGoogle Scholar
  • 27. Committee on Obstetric Practice. Committee opinion no. 684: delayed umbilical cord clamping after birth.Obstet Gynecol. 2017; 129:e5–e10. doi: 10.1097/aog.0000000000001860CrossrefMedlineGoogle Scholar
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  • 29. Backes CH, Huang H, Cua CL, Garg V, Smith CV, Yin H, Galantowicz M, Bauer JA, Hoffman TM. Early versus delayed umbilical cord clamping in infants with congenital heart disease: a pilot, randomized, controlled trial.J Perinatol. 2015; 35:826–831. doi: 10.1038/jp.2015.89CrossrefMedlineGoogle Scholar
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  • 32. Oxford Midwives Research Group. A study of the relationship between the delivery to cord clamping interval and the time of cord separation.Midwifery. 1991; 7:167–176. doi: 10.1016/s0266-6138(05)80195-0CrossrefMedlineGoogle Scholar
  • 33. van Rheenen P, de Moor L, Eschbach S, de Grooth H, Brabin B. Delayed cord clamping and haemoglobin levels in infancy: a randomised controlled trial in term babies.Trop Med Int Health. 2007; 12:603–616. doi: 10.1111/j.1365-3156.2007.01835.xCrossrefMedlineGoogle Scholar
  • 34. Withanathantrige M, Goonewardene I. Effects of early versus delayed umbilical cord clamping during antepartum lower segment caesarean section on placental delivery and postoperative haemorrhage: a randomised controlled trial.Ceylon Med J. 2017; 62:5–11. doi: 10.4038/cmj.v62i1.8425CrossrefMedlineGoogle Scholar
  • 35. Datta BV, Kumar A, Yadav R. A Randomized Controlled Trial to Evaluate the Role of Brief Delay in Cord Clamping in Preterm Neonates (34-36 weeks) on Short-term Neurobehavioural Outcome.J Trop Pediatr. 2017; 63:418–424. doi: 10.1093/tropej/fmx004CrossrefMedlineGoogle Scholar
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  • 40. Grajeda R, Pérez-Escamilla R, Dewey KG. Delayed clamping of the umbilical cord improves hematologic status of Guatemalan infants at 2 mo of age.Am J Clin Nutr. 1997; 65:425–431. doi: 10.1093/ajcn/65.2.425CrossrefMedlineGoogle Scholar
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Initial Actions

Temperature at Birth

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Temperature should be measured and recorded after birth and monitored as a measure of quality.1 The temperature of newly born babies should be maintained between 36.5°C and 37.5°C.2 Hypothermia (less than 36°C) should be prevented as it is associated with increased neonatal mortality and morbidity, especially in very preterm (less than 33 weeks) and very low-birth-weight babies (less than 1500 g), who are at increased risk for hypothermia.3–5,7 It is also reasonable to prevent hyperthermia as it may be associated with harm.4,6

Recommendation-Specific Supportive Text
  1. Hypothermia after birth is common worldwide, with a higher incidence in babies of lower gestational age and birth weight.3–5

  2. There are long-standing worldwide recommendations for routine temperature management for the newborn.2

  3. In observational studies in both preterm (less than 37 weeks) and low-birth-weight babies (less than 2500 g), the presence and degree of hypothermia after birth is strongly associated with increased neonatal mortality and morbidity.3–5

  4. Two observational studies found an association between hyperthermia and increased morbidity and mortality in very preterm (moderate quality) and very low-birth-weight neonates (very low quality).4,6

Temperature Management for Newly Born Infants

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Healthy babies should be skin-to-skin after birth.8 For preterm and low-birth-weight babies or babies requiring resuscitation, warming adjuncts (increased ambient temperature [greater than 23°C], skin-to-skin care, radiant warmers, plastic wraps or bags, hats, blankets, exothermic mattresses, and warmed humidified inspired gases)10,11,14 individually or in combination may reduce the risk of hypothermia. Exothermic mattresses have been reported to cause local heat injury and hyperthermia.15

When babies are born in out-of-hospital, resource-limited, or remote settings, it may be reasonable to prevent hypothermia by using a clean food-grade plastic bag13 as an alternative to skin-to-skin contact.8

Recommendation-Specific Supportive Text
  1. A systematic review (low to moderate certainty) of 6 RCTs showed that early skin-to-skin contact promotes normothermia in healthy neonates.8 Two meta-analyses reviewed RCTs and observational studies of extended skin-to-skin care after initial resuscitation and/or stabilization, some in resource-limited settings, showing reduced mortality, improved breastfeeding, shortened length of stay, and improved weight gain in preterm and low-birth-weight babies (moderate quality evidence).16,17

  2. Most RCTs in well-resourced settings would routinely manage at-risk babies under a radiant warmer.11

  3. RCTs and observational studies of warming adjuncts, alone and in combination, demonstrate reduced rates of hypothermia in very preterm and very low-birth-weight babies.10,11 However, meta-analysis of RCTs of interventions that reduce hypothermia in very preterm or very low-birth-weight babies (low certainty) show no impact on neonatal morbidity or mortality.11 Two RCTs and expert opinion support ambient temperatures of 23°C and above.2,14,18

  4. One moderate quality RCT found higher rates of hyperthermia with exothermic mattresses.15

  5. Numerous nonrandomized quality improvement (very low to low certainty) studies support the use of warming adjunct “bundles.”12

  6. One RCT in resource-limited settings found that plastic coverings reduced the incidence of hypothermia, but they were not directly compared with uninterrupted skin-to-skin care.13

Clearing the Airway and Tactile Stimulation in Newly Born Infants

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

The immediate care of newly born babies involves an initial assessment of gestation, breathing, and tone. Babies who are breathing well and/or crying are cared for skin-to-skin with their mothers and should not need interventions such as routine tactile stimulation or suctioning, even if the amniotic fluid is meconium stained.7,19 Avoiding unnecessary suctioning helps prevent the risk of induced bradycardia as a result of suctioning of the airway.

Recommendation-Specific Supportive Text
  1. A meta-analysis of 8 RCTs19 (low certainty of evidence) suggest no benefit from routine suctioning after birth.7 Subsequently, 2 additional studies supported this conclusion.7

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

If there is ineffective breathing effort or apnea after birth, tactile stimulation may stimulate breathing. Tactile stimulation should be limited to drying an infant and rubbing the back and soles of the feet.21,22 There may be some benefit from repeated tactile stimulation in preterm babies during or after providing PPV, but this requires further study.23 If, at initial assessment, there is visible fluid obstructing the airway or a concern about obstructed breathing, the mouth and nose may be suctioned. Suction should also be considered if there is evidence of airway obstruction during PPV.

Recommendation-Specific Supportive Text
  1. Limited observational studies suggest that tactile stimulation may improve respiratory effort. One RCT (low certainty of evidence) suggests improved oxygenation after resuscitation in preterm babies who received repeated tactile stimulation.23

  2. Suctioning for suspected airway obstruction during PPV is based on expert opinion.7

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Direct laryngoscopy and endotracheal suctioning are not routinely required for babies born through MSAF but can be beneficial in babies who have evidence of airway obstruction while receiving PPV.7

Recommendation-Specific Supportive Text
  1. Endotracheal suctioning for apparent airway obstruction with MSAF is based on expert opinion.

  2. A meta-analysis of 3 RCTs (low certainty of evidence) and a further single RCT suggest that nonvigorous newborns delivered through MSAF have the same outcomes (survival, need for respiratory support, or neurodevelopment) whether they are suctioned before or after the initiation of PPV.7

References

  • 1. Perlman JM, Wyllie J, Kattwinkel J, Wyckoff MH, Aziz K, Guinsburg R, Kim HS, Liley HG, Mildenhall L, Simon WM, et al.; on behalf of the Neonatal Resuscitation Chapter Collaborators. Part 7: neonatal resuscitation: 2015 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Circulation. 2015; 132(suppl 1):S204–S241. doi: 10.1161/CIR.0000000000000276LinkGoogle Scholar
  • 2. Department of Reproductive Health and Research (RHR) WHO. Thermal Protection of the Newborn: A Practical Guide (WHO/RHT/MSM/97.2). Geneva, Switzerland: World Health Organisation; 1997. https://apps.who.int/iris/bitstream/handle/10665/63986/WHO_RHT_MSM_97.2.pdf;jsessionid=9CF1FA8ABF2E8CE1955D96C1315D9799?sequence=1. Accessed March 1, 2020.Google Scholar
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  • 8. Moore ER, Bergman N, Anderson GC, Medley N. Early skin-to-skin contact for mothers and their healthy newborn infants.Cochrane Database Syst Rev. 2016; 11:CD003519. doi: 10.1002/14651858.CD003519.pub4MedlineGoogle Scholar
  • 9. Kattwinkel J, Perlman JM, Aziz K, Colby C, Fairchild K, Gallagher J, Hazinski MF, Halamek LP, Kumar P, Little G, et al.. Part 15: neonatal resuscitation: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Circulation. 2010; 122(suppl 3):S909–S919. doi: 10.1161/CIRCULATIONAHA.110.971119LinkGoogle Scholar
  • 10. Meyer MP, Owen LS, Te Pas AB. Use of Heated Humidified Gases for Early Stabilization of Preterm Infants: A Meta-Analysis.Front Pediatr. 2018; 6:319. doi: 10.3389/fped.2018.00319CrossrefMedlineGoogle Scholar
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  • 12. Donnellan D, Moore Z, Patton D, O’Connor T, Nugent L. The effect of thermoregulation quality improvement initiatives on the admission temperature of premature/very low birth-weight infants in neonatal intensive care units: a systematic review.J Spec Pediatr Nurs. 2020e12286. doi: 10.1111/jspn.12286MedlineGoogle Scholar
  • 13. Belsches TC, Tilly AE, Miller TR, Kambeyanda RH, Leadford A, Manasyan A, Chomba E, Ramani M, Ambalavanan N, Carlo WA. Randomized trial of plastic bags to prevent term neonatal hypothermia in a resource-poor setting.Pediatrics. 2013; 132:e656–e661. doi: 10.1542/peds.2013-0172CrossrefMedlineGoogle Scholar
  • 14. Duryea EL, Nelson DB, Wyckoff MH, Grant EN, Tao W, Sadana N, Chalak LF, McIntire DD, Leveno KJ. The impact of ambient operating room temperature on neonatal and maternal hypothermia and associated morbidities: a randomized controlled trial.Am J Obstet Gynecol. 2016; 214:505.e1–505.e7. doi: 10.1016/j.ajog.2016.01.190CrossrefGoogle Scholar
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  • 16. Boundy EO, Dastjerdi R, Spiegelman D, Fawzi WW, Missmer SA, Lieberman E, Kajeepeta S, Wall S, Chan GJ. Kangaroo mother care and neonatal outcomes: a meta-analysis.Pediatrics. 2016; 137: doi: 10.1542/peds.2015–2238CrossrefMedlineGoogle Scholar
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  • 18. Jia YS, Lin ZL, Lv H, Li YM, Green R, Lin J. Effect of delivery room temperature on the admission temperature of premature infants: a randomized controlled trial.J Perinatol. 2013; 33:264–267. doi: 10.1038/jp.2012.100CrossrefMedlineGoogle Scholar
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  • 20. 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 low-income countries: a prospective descriptive observational study.Resuscitation. 2012; 83:869–873. doi: 10.1016/j.resuscitation.2011.12.011CrossrefMedlineGoogle Scholar
  • 21. Lee AC, Cousens S, Wall SN, Niermeyer S, Darmstadt GL, Carlo WA, Keenan WJ, Bhutta ZA, Gill C, Lawn JE. Neonatal resuscitation and immediate newborn assessment and stimulation for the prevention of neonatal deaths: a systematic review, meta-analysis and Delphi estimation of mortality effect.BMC Public Health. 2011; 11(suppl 3):S12. doi: 10.1186/1471-2458-11-S3-S12CrossrefMedlineGoogle Scholar
  • 22. World Health Organization. Guidelines on Basic Newborn Resuscitation. Geneva, Switzerland: World Health Organization; 2012. https://apps.who.int/iris/bitstream/handle/10665/75157/9789241503693_eng.pdf;jsessionid=EA13BF490E4D349E12B4DAF16BA64A8D?sequence=1. Accessed March 1, 2020.Google Scholar
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Assessment of Heart Rate During Neonatal Resuscitation

After birth, the newborn’s heart rate is used to assess the effectiveness of spontaneous respiratory effort, the need for interventions, and the response to interventions. In addition, accurate, fast, and continuous heart rate assessment is necessary for newborns in whom chest compressions are initiated. Therefore, identifying a rapid and reliable method to measure the newborn’s heart rate is critically important during neonatal resuscitation.

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Auscultation of the precordium remains the preferred physical examination method for the initial assessment of the heart rate.9 Pulse oximetry and ECG remain important adjuncts to provide continuous heart rate assessment in babies needing resuscitation.

ECG provides the most rapid and accurate measurement of the newborn’s heart rate at birth and during resuscitation. Clinical assessment of heart rate by auscultation or palpation may be unreliable and inaccurate.1–4 Compared to ECG, pulse oximetry is both slower in detecting the heart rate and tends to be inaccurate during the first few minutes after birth.5,6,10–12 Underestimation of heart rate can lead to potentially unnecessary interventions. On the other hand, overestimation of heart rate when a newborn is bradycardic may delay necessary interventions. There are limited data comparing the different approaches to heart rate assessment during neonatal resuscitation on other neonatal outcomes. Use of ECG for heart rate detection does not replace the need for pulse oximetry to evaluate oxygen saturation or the need for supplemental oxygen.

Recommendation-Specific Supportive Text

  1. In one RCT and one observational study, there were no reports of technical difficulties with ECG monitoring during neonatal resuscitation, supporting its feasibility as a tool for monitoring heart rate during neonatal resuscitation.6,7

  2. One observational study compared neonatal outcomes before (historical cohort) and after implementation of ECG monitoring in the delivery room.8 Compared with the newborns in the historical cohort, newborns with the ECG monitoring had lower rates of endotracheal intubation and higher 5-minute Apgar scores. However, newborns with ECG monitoring also had higher odds of receiving chest compressions in the delivery room.

  3. Very low-quality evidence from 8 nonrandomized studies2,5,6,10,12–15 enrolling 615 newborns and 2 small RCTs7,16 suggests that at birth, ECG is faster and more accurate for newborn heart assessment compared with pulse oximetry.

  4. Very low-quality evidence from 2 nonrandomized studies and 1 randomized trial show that auscultation is not as accurate as ECG for heart rate assessment during newborn stabilization immediately after birth.2–4

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

When chest compressions are initiated, an ECG should be used to confirm heart rate. When ECG heart rate is greater than 60/min, a palpable pulse and/or audible heart rate rules out pulseless electric activity.17–21

Recommendation-Specific Supportive Text

  1. Given the evidence for ECG during initial steps of PPV, expert opinion is that ECG should be used when providing chest compressions.

References

  • 1. Chitkara R, Rajani AK, Oehlert JW, Lee HC, Epi MS, Halamek LP. The accuracy of human senses in the detection of neonatal heart rate during standardized simulated resuscitation: implications for delivery of care, training and technology design.Resuscitation. 2013; 84:369–372. doi: 10.1016/j.resuscitation.2012.07.035CrossrefMedlineGoogle Scholar
  • 2. Kamlin CO, O’Donnell CP, Everest NJ, Davis PG, Morley CJ. Accuracy of clinical assessment of infant heart rate in the delivery room.Resuscitation. 2006; 71:319–321. doi: 10.1016/j.resuscitation.2006.04.015CrossrefMedlineGoogle Scholar
  • 3. Owen CJ, Wyllie JP. Determination of heart rate in the baby at birth.Resuscitation. 2004; 60:213–217. doi: 10.1016/j.resuscitation.2003.10.002CrossrefMedlineGoogle Scholar
  • 4. Voogdt KG, Morrison AC, Wood FE, van Elburg RM, Wyllie JP. A randomised, simulated study assessing auscultation of heart rate at birth.Resuscitation. 2010; 81:1000–1003. doi: 10.1016/j.resuscitation.2010.03.021CrossrefMedlineGoogle Scholar
  • 5. Kamlin CO, Dawson JA, O’Donnell CP, Morley CJ, Donath SM, Sekhon J, Davis PG. Accuracy of pulse oximetry measurement of heart rate of newborn infants in the delivery room.J Pediatr. 2008; 152:756–760. doi: 10.1016/j.jpeds.2008.01.002CrossrefMedlineGoogle Scholar
  • 6. Katheria A, Rich W, Finer N. Electrocardiogram provides a continuous heart rate faster than oximetry during neonatal resuscitation.Pediatrics. 2012; 130:e1177–e1181. doi: 10.1542/peds.2012-0784CrossrefMedlineGoogle Scholar
  • 7. Katheria A, Arnell K, Brown M, Hassen K, Maldonado M, Rich W, Finer N. A pilot randomized controlled trial of EKG for neonatal resuscitation.PLoS One. 2017; 12:e0187730. doi: 10.1371/journal.pone.0187730CrossrefMedlineGoogle Scholar
  • 8. Shah BA, Wlodaver AG, Escobedo MB, Ahmed ST, Blunt MH, Anderson MP, Szyld EG. Impact of electronic cardiac (ECG) monitoring on delivery room resuscitation and neonatal outcomes.Resuscitation. 2019; 143:10–16. doi: 10.1016/j.resuscitation.2019.07.031CrossrefMedlineGoogle Scholar
  • 9. Wyckoff MH, Aziz K, Escobedo MB, Kapadia VS, Kattwinkel J, Perlman JM, Simon WM, Weiner GM, Zaichkin JG. Part 13: neonatal resuscitation: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Circulation. 2015; 132(suppl 2):S543–S560. doi: 10.1161/CIR.0000000000000267LinkGoogle Scholar
  • 10. Mizumoto H, Tomotaki S, Shibata H, Ueda K, Akashi R, Uchio H, Hata D. Electrocardiogram shows reliable heart rates much earlier than pulse oximetry during neonatal resuscitation.Pediatr Int. 2012; 54:205–207. doi: 10.1111/j.1442-200X.2011.03506.xCrossrefMedlineGoogle Scholar
  • 11. Narayen IC, Smit M, van Zwet EW, Dawson JA, Blom NA, te Pas AB. Low signal quality pulse oximetry measurements in newborn infants are reliable for oxygen saturation but underestimate heart rate.Acta Paediatr. 2015; 104:e158–e163. doi: 10.1111/apa.12932CrossrefMedlineGoogle Scholar
  • 12. van Vonderen JJ, Hooper SB, Kroese JK, Roest AA, Narayen IC, van Zwet EW, te Pas AB. Pulse oximetry measures a lower heart rate at birth compared with electrocardiography.J Pediatr. 2015; 166:49–53. doi: 10.1016/j.jpeds.2014.09.015CrossrefMedlineGoogle Scholar
  • 13. Dawson JA, Saraswat A, Simionato L, Thio M, Kamlin CO, Owen LS, Schmölzer GM, Davis PG. Comparison of heart rate and oxygen saturation measurements from Masimo and Nellcor pulse oximeters in newly born term infants.Acta Paediatr. 2013; 102:955–960. doi: 10.1111/apa.12329CrossrefMedlineGoogle Scholar
  • 14. Gulati R, Zayek M, Eyal F. Presetting ECG electrodes for earlier heart rate detection in the delivery room.Resuscitation. 2018; 128:83–87. doi: 10.1016/j.resuscitation.2018.03.038CrossrefMedlineGoogle Scholar
  • 15. Iglesias B, Rodrí Guez MAJ, Aleo E, Criado E, Martí Nez-Orgado J, Arruza L. 3-lead electrocardiogram is more reliable than pulse oximetry to detect bradycardia during stabilisation at birth of very preterm infants.Arch Dis Child Fetal Neonatal Ed. 2018; 103:F233–F237. doi: 10.1136/archdischild-2016-311492CrossrefMedlineGoogle Scholar
  • 16. Murphy MC, De Angelis L, McCarthy LK, O’Donnell CPF. Randomised study comparing heart rate measurement in newly born infants using a monitor incorporating electrocardiogram and pulse oximeter versus pulse oximeter alone.Arch Dis Child Fetal Neonatal Ed. 2019; 104:F547–F550. doi: 10.1136/archdischild-2017-314366CrossrefMedlineGoogle Scholar
  • 17. Luong D, Cheung PY, Barrington KJ, Davis PG, Unrau J, Dakshinamurti S, Schmölzer GM. Cardiac arrest with pulseless electrical activity rhythm in newborn infants: a case series.Arch Dis Child Fetal Neonatal Ed. 2019; 104:F572–F574. doi: 10.1136/archdischild-2018-316087CrossrefMedlineGoogle Scholar
  • 18. Luong DH, Cheung PY, O’Reilly M, Lee TF, Schmolzer GM. Electrocardiography vs. Auscultation to Assess Heart Rate During Cardiac Arrest With Pulseless Electrical Activity in Newborn Infants.Front Pediatr. 2018; 6:366. doi: 10.3389/fped.2018.00366CrossrefMedlineGoogle Scholar
  • 19. Patel S, Cheung PY, Solevåg AL, Barrington KJ, Kamlin COF, Davis PG, Schmölzer GM. Pulseless electrical activity: a misdiagnosed entity during asphyxia in newborn infants?Arch Dis Child Fetal Neonatal Ed. 2019; 104:F215–F217. doi: 10.1136/archdischild-2018-314907CrossrefMedlineGoogle Scholar
  • 20. Sillers L, Handley SC, James JR, Foglia EE. Pulseless Electrical Activity Complicating Neonatal Resuscitation.Neonatology. 2019; 115:95–98. doi: 10.1159/000493357CrossrefMedlineGoogle Scholar
  • 21. Solevåg AL, Luong D, Lee TF, O’Reilly M, Cheung PY, Schmölzer GM. Non-perfusing cardiac rhythms in asphyxiated newborn piglets.PLoS One. 2019; 14:e0214506. doi: 10.1371/journal.pone.0214506CrossrefMedlineGoogle Scholar

Ventilatory Support After Birth: PPV and Continuous Positive Airway Pressure

Initial Breaths (When and How to Provide PPV)

The vast majority of newborns breathe spontaneously within 30 to 60 seconds after birth, sometimes after drying and tactile stimulation.1 Newborns who do not breathe within the first 60 seconds after birth or are persistently bradycardic (heart rate less than 100/min) despite appropriate initial actions (including tactile stimulation) may receive PPV at a rate of 40 to 60/min.2,3 The order of resuscitative procedures in newborns differs from pediatric and adult resuscitation algorithms. On the basis of animal research, the progression from primary apnea to secondary apnea in newborns results in the cessation of respiratory activity before the onset of cardiac failure.4 This cycle of events differs from that of asphyxiated adults, who experience concurrent respiratory and cardiac failure. For this reason, neonatal resuscitation should begin with PPV rather than with chest compressions.2,3 Delays in initiating ventilatory support in newly born infants increase the risk of death.1

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

The adequacy of ventilation is measured by a rise in heart rate and, less reliably, chest expansion. Peak inflation pressures of up to 30 cm H2O in term newborns and 20 to 25 cm H2O in preterm newborns are usually sufficient to inflate the lungs.5–7,9,11–14 In some cases, however, higher inflation pressures are required.5,7–10 Peak inflation pressures or tidal volumes greater than what is required to increase heart rate and achieve chest expansion should be avoided.24,26–28

The lungs of sick or preterm infants tend to collapse because of immaturity and surfactant deficiency.15 PEEP provides low-pressure inflation of the lungs during expiration. PEEP has been shown to maintain lung volume during PPV in animal studies, thus improving lung function and oxygenation.16 PEEP may be beneficial during neonatal resuscitation, but the evidence from human studies is limited. Optimal PEEP has not been determined, because all human studies used a PEEP level of 5 cm H2O.18–22

Recommendation-Specific Supportive Text
  1. A large observational study showed that most nonvigorous newly born infants respond to stimulation and PPV. The same study demonstrated that the risk of death or prolonged admission increases 16% for every 30-second delay in initiating PPV.1

  2. Animal studies in newborn mammals show that heart rate decreases during asphyxia. Ventilation of the lungs results in a rapid increase in heart rate.3,4 Several case series found that most term newborns can be resuscitated using peak inflation pressures of 30 cm H2O, delivered without PEEP.5–8 Occasionally, higher peak pressures are required.5,7–10

  3. Case series in preterm infants have found that most preterm infants can be resuscitated using PPV inflation pressures in the range of 20 to 25 cm H2O,11–14 but higher pressures may be required.10,11

  4. An observational study including 1962 infants between 23 and 33 weeks’ gestational age reported lower rates of mortality and chronic lung disease when giving PPV with PEEP versus no PEEP.19

  5. Two randomized trials and 1 quasi-randomized trial (very low quality) including 312 infants compared PPV with a T-piece (with PEEP) versus a self-inflating bag (no PEEP) and reported similar rates of death and chronic lung disease.20–22 One trial (very low quality) compared PPV using a T-piece and PEEP of 5 cm H2O versus 0 cm H2O and reported similar rates of death and chronic lung disease.23

  6. Studies of newly born animals showed that PEEP facilitates lung aeration and accumulation of functional residual capacity, prevents distal airway collapse, increases lung surface area and compliance, decreases expiratory resistance, conserves surfactant, and reduces hyaline membrane formation, alveolar collapse, and the expression of proinflammatory mediators.16,18

  7. One observational study in newly born infants associated high tidal volumes during resuscitation with brain injury.25

  8. Several animal studies found that ventilation with high volumes caused lung injury, impaired gas exchange, and reduced lung compliance in immature animals.24,26–28

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

It is reasonable to initiate PPV at a rate of 40 to 60/min to newly born infants who have ineffective breathing, are apneic, or are persistently bradycardic (heart rate less than 100/min) despite appropriate initial actions (including tactile stimulation).1

To match the natural breathing pattern of both term and preterm newborns, the inspiratory time while delivering PPV should be 1 second or less. While there has been research to study the potential effectiveness of providing longer, sustained inflations, there may be potential harm in providing sustained inflations greater than 10 seconds for preterm newborns. The potential benefit or harm of sustained inflations between 1 and 10 seconds is uncertain.2,29

Recommendation-Specific Supportive Text
  1. Providing PPV at a rate of 40 to 60 inflations per minute is based on expert opinion.

  2. The ILCOR task force review, when comparing PPV with sustained inflation breaths, defined PPV to have an inspiratory time of 1 second or less, based on expert opinion. One observational study describes the initial pattern of breathing in term and preterm newly born infants to have an inspiratory time of around 0.3 seconds.2

  3. Two systematic reviews29,30 in preterm newborns (low to moderate certainty) found no significant benefit from sustained lung inflation over PPV; one review found a higher risk of death in the first 48 hours. One large RCT31 was stopped early when an increased rate of early mortality was identified in babies less than 28 weeks’ gestational age who received sustained inflations; no significant difference was found in the primary outcome of death or bronchopulmonary dysplasia.

Continuous Positive Airway Pressure Administration

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Newly born infants who breathe spontaneously need to establish a functional residual capacity after birth.8 Some newly born infants experience respiratory distress, which manifests as labored breathing or persistent cyanosis. CPAP, a form of respiratory support, helps newly born infants keep their lungs open. CPAP is helpful for preterm infants with breathing difficulty after birth or after resuscitation33 and may reduce the risk of bronchopulmonary dysplasia in very preterm infants when compared with endotracheal ventilation.34–36 CPAP is also a less invasive form of respiratory support than intubation and PPV are.

Recommendation-Specific Supportive Text
  1. Four RCTs and 1 meta-analysis32,34–37 (high quality) showed reduction in the combined outcome of death and bronchopulmonary dysplasia when starting treatment with CPAP compared with intubation and ventilation in very preterm infants (less than 30 weeks of gestation) with respiratory distress (the number needed to prevent was 25). The meta-analysis reported no differences in the individual outcomes of mortality, bronchopulmonary dysplasia, pneumothorax, interventricular hemorrhage, necrotizing enterocolitis, or retinopathy of prematurity.32

References

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  • 10. Upton CJ, Milner AD. Endotracheal resuscitation of neonates using a rebreathing bag.Arch Dis Child. 1991; 661 Spec No39–42. doi: 10.1136/adc.66.1_spec_no.39CrossrefMedlineGoogle Scholar
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  • 12. Hird MF, Greenough A, Gamsu HR. Inflating pressures for effective resuscitation of preterm infants.Early Hum Dev. 1991; 26:69–72. doi: 10.1016/0378-3782(91)90045-5CrossrefMedlineGoogle Scholar
  • 13. Lindner W, Vossbeck S, Hummler H, Pohlandt F. Delivery room management of extremely low birth weight infants: spontaneous breathing or intubation?Pediatrics. 1999; 1035 Pt 1961–967. doi: 10.1542/peds.103.5.961CrossrefMedlineGoogle Scholar
  • 14. Menakaya J, Andersen C, Chirla D, Wolfe R, Watkins A. A randomised comparison of resuscitation with an anaesthetic rebreathing circuit or an infant ventilator in very preterm infants.Arch Dis Child Fetal Neonatal Ed. 2004; 89:F494–F496. doi: 10.1136/adc.2003.033340CrossrefMedlineGoogle Scholar
  • 15. te Pas AB, Davis PG, Hooper SB, Morley CJ. From liquid to air: breathing after birth.J Pediatr. 2008; 152:607–611. doi: 10.1016/j.jpeds.2007.10.041CrossrefMedlineGoogle Scholar
  • 16. Siew ML, Te Pas AB, Wallace MJ, Kitchen MJ, Lewis RA, Fouras A, Morley CJ, Davis PG, Yagi N, Uesugi K, et al.. Positive end-expiratory pressure enhances development of a functional residual capacity in preterm rabbits ventilated from birth.J Appl Physiol (1985). 2009; 106:1487–1493. doi: 10.1152/japplphysiol.91591.2008CrossrefMedlineGoogle Scholar
  • 17. Wyckoff MH, Aziz K, Escobedo MB, Kapadia VS, Kattwinkel J, Perlman JM, Simon WM, Weiner GM, Zaichkin JG. Part 13: neonatal resuscitation: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Circulation. 2015; 132(suppl 2):S543–S560. doi: 10.1161/CIR.0000000000000267LinkGoogle Scholar
  • 18. Probyn ME, Hooper SB, Dargaville PA, McCallion N, Crossley K, Harding R, Morley CJ. Positive end expiratory pressure during resuscitation of premature lambs rapidly improves blood gases without adversely affecting arterial pressure.Pediatr Res. 2004; 56:198–204. doi: 10.1203/01.PDR.0000132752.94155.13CrossrefMedlineGoogle Scholar
  • 19. Guinsburg R, de Almeida MFB, de Castro JS, Gonçalves-Ferri WA, Marques PF, Caldas JPS, Krebs VLJ, Souza Rugolo LMS, de Almeida JHCL, Luz JH, Procianoy RS, Duarte JLMB, Penido MG, Ferreira DMLM, Alves Filho N, Diniz EMA, Santos JP, Acquesta AL, Santos CND, Gonzalez MRC, da Silva RPVC, Meneses J, Lopes JMA, Martinez FE. T-piece versus self-inflating bag ventilation in preterm neonates at birth.Arch Dis Child Fetal Neonatal Ed. 2018; 103:F49–F55. doi: 10.1136/archdischild-2016-312360CrossrefMedlineGoogle Scholar
  • 20. Dawson JA, Schmölzer GM, Kamlin CO, Te Pas AB, O’Donnell CP, Donath SM, Davis PG, Morley CJ. Oxygenation with T-piece versus self-inflating bag for ventilation of extremely preterm infants at birth: a randomized controlled trial.J Pediatr. 2011; 158:912–918.e1-2doi: 10.1016/j.jpeds.2010.12.003CrossrefMedlineGoogle Scholar
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  • 22. Thakur A, Saluja S, Modi M, Kler N, Garg P, Soni A, Kaur A, Chetri S. T-piece or self inflating bag for positive pressure ventilation during delivery room resuscitation: an RCT.Resuscitation. 2015; 90:21–24. doi: 10.1016/j.resuscitation.2015.01.021CrossrefMedlineGoogle Scholar
  • 23. Finer NN, Carlo WA, Duara S, Fanaroff AA, Donovan EF, Wright LL, Kandefer S, Poole WK; National Institute of Child Health and Human Development Neonatal Research Network. Delivery room continuous positive airway pressure/positive end-expiratory pressure in extremely low birth weight infants: a feasibility trial.Pediatrics. 2004; 114:651–657. doi: 10.1542/peds.2004-0394CrossrefMedlineGoogle Scholar
  • 24. Hillman NH, Moss TJ, Kallapur SG, Bachurski C, Pillow JJ, Polglase GR, Nitsos I, Kramer BW, Jobe AH. Brief, large tidal volume ventilation initiates lung injury and a systemic response in fetal sheep.Am J Respir Crit Care Med. 2007; 176:575–581. doi: 10.1164/rccm.200701-051OCCrossrefMedlineGoogle Scholar
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  • 29. Wyckoff MH, Wyllie J, Aziz K, de Almeida MF, Fabres J, Fawke J, Guinsburg R, Hosono S, Isayama T, Kapadia VS, et al.; on behalf of the Neonatal Life Support Collaborators. Neonatal life support: 2020 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Circulation. 2020 142(suppl 1):S185–S221. doi: 10.1161/CIR.0000000000000895LinkGoogle Scholar
  • 30. Foglia EE, Te Pas AB, Kirpalani H, Davis PG, Owen LS, van Kaam AH, Onland W, Keszler M, Schmölzer GM, Hummler H, et al.. Sustained inflation vs standard resuscitation for preterm infants: a systematic review and meta-analysis.JAMA Pediatr. 2020e195897. doi: 10.1001/jamapediatrics.2019.5897CrossrefMedlineGoogle Scholar
  • 31. Kirpalani H, Ratcliffe SJ, Keszler M, Davis PG, Foglia EE, Te Pas A, Fernando M, Chaudhary A, Localio R, van Kaam AH, Onland W, Owen LS, Schmölzer GM, Katheria A, Hummler H, Lista G, Abbasi S, Klotz D, Simma B, Nadkarni V, Poulain FR, Donn SM, Kim HS, Park WS, Cadet C, Kong JY, Smith A, Guillen U, Liley HG, Hopper AO, Tamura M; on behalf of the SAIL Site Investigators. Effect of Sustained Inflations vs Intermittent Positive Pressure Ventilation on Bronchopulmonary Dysplasia or Death Among Extremely Preterm Infants: The SAIL Randomized Clinical Trial.JAMA. 2019; 321:1165–1175. doi: 10.1001/jama.2019.1660CrossrefMedlineGoogle Scholar
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  • 33. Hooper SB, Polglase GR, Roehr CC. Cardiopulmonary changes with aeration of the newborn lung.Paediatr Respir Rev. 2015; 16:147–150. doi: 10.1016/j.prrv.2015.03.003MedlineGoogle Scholar
  • 34. Dunn MS, Kaempf J, de Klerk A, de Klerk R, Reilly M, Howard D, Ferrelli K, O’Conor J, Soll RF; Vermont Oxford Network DRM Study Group. Randomized trial comparing 3 approaches to the initial respiratory management of preterm neonates.Pediatrics. 2011; 128:e1069–e1076. doi: 10.1542/peds.2010-3848CrossrefMedlineGoogle Scholar
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  • 36. SUPPORT Study Group of the Eunice Kennedy Shriver NICHD Neonatal Research Network. Early CPAP versus surfactant in extremely preterm infants.N Engl J Med. 2010; 362:1970–1979. doi: 10.1056/NEJMoa0911783CrossrefMedlineGoogle Scholar
  • 37. Sandri F, Plavka R, Ancora G, Simeoni U, Stranak Z, Martinelli S, Mosca F, Nona J, Thomson M, Verder H, Fabbri L, Halliday H; CURPAP Study Group. Prophylactic or early selective surfactant combined with nCPAP in very preterm infants.Pediatrics. 2010; 125:e1402–e1409. doi: 10.1542/peds.2009-2131CrossrefMedlineGoogle Scholar

Oxygen Administration

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

During an uncomplicated delivery, the newborn transitions from the low oxygen environment of the womb to room air (21% oxygen) and blood oxygen levels rise over several minutes. During resuscitation, supplemental oxygen may be provided to prevent harm from inadequate oxygen supply to tissues (hypoxemia).4 However, overexposure to oxygen (hyperoxia) may be associated with harm.5

Term and late preterm newborns have lower short-term mortality when respiratory support during resuscitation is started with 21% oxygen (air) versus 100% oxygen.1 No difference was found in neurodevelopmental outcome of survivors.1 During resuscitation, pulse oximetry may be used to monitor oxygen saturation levels found in healthy term infants after vaginal birth at sea level.3

In more preterm newborns, there were no differences in mortality or other important outcomes when respiratory support was started with low (50% or less) versus high (greater than 50%) oxygen concentrations.2 Given the potential for harm from hyperoxia, it may be reasonable to start with 21% to 30% oxygen. Pulse oximetry with oxygen targeting is recommended in this population.3

Recommendation-Specific Supportive Text
  1. A meta-analysis of 5 randomized and quasi-randomized trials enrolling term and late preterm newborns showed no difference in rates of hypoxic-ischemic encephalopathy (HIE). Similarly, meta-analysis of 2 quasi-randomized trials showed no difference in moderate-to-severe neurodevelopmental impairment at 1 to 3 years of age1 for newborns administered 21% versus 100% oxygen.1

  2. Meta-analysis of 10 randomized trials enrolling preterm newborns, including subanalysis of 7 trials reporting outcomes for newborns 28 weeks’ gestational age or less, showed no difference in short-term mortality when respiratory support was started with low compared with high oxygen.2 In the included studies, low oxygen was generally 21% to 30% and high oxygen was always 60% to 100%. Furthermore, no differences were found in long-term mortality, neurodevelopmental outcome, retinopathy of prematurity, bronchopulmonary dysplasia, necrotizing enterocolitis, or major cerebral hemorrhage.2 In a systematic review of 8 trials that used oxygen saturation targeting as a cointervention, all preterm babies in whom respiratory support was initiated with 21% oxygen (air) required supplemental oxygen to achieve the predetermined oxygen saturation target.2 The recommendation to initiate respiratory support with a lower oxygen concentration reflects a preference to avoid exposing preterm newborns to additional oxygen (beyond what is necessary to achieve the predetermined oxygen saturation target) without evidence demonstrating a benefit for important outcomes.3

  3. Meta-analysis of 7 randomized and quasi-randomized trials enrolling term and late preterm newborns showed decreased short-term mortality when using 21% oxygen compared with 100% oxygen for delivery room resuscitation.1 No studies looked at starting with intermediate oxygen concentrations (ie, 22% to 99% oxygen).

References

  • 1. Welsford M, Nishiyama C, Shortt C, Isayama T, Dawson JA, Weiner G, Roehr CC, Wyckoff MH, Rabi Y; on behalf of the International Liaison Committee on Resuscitation Neonatal Life Support Task Force. Room air for initiating term newborn resuscitation: a systematic review with meta-analysis.Pediatrics. 2019; 143. doi: 10.1542/peds.2018-1825Google Scholar
  • 2. Welsford M, Nishiyama C, Shortt C, Weiner G, Roehr CC, Isayama T, Dawson JA, Wyckoff MH, Rabi Y; on behalf of the International Liaison Committee on Resuscitation Neonatal Life Support Task Force. Initial oxygen use for preterm newborn resuscitation: a systematic review with meta-analysis.Pediatrics. 2019; 143. doi: 10.1542/peds.2018-1828Google Scholar
  • 3. Escobedo MB, Aziz K, Kapadia VS, Lee HC, Niermeyer S, Schmölzer GM, Szyld E, Weiner GM, Wyckoff MH, Yamada NK, Zaichkin JG. 2019 American Heart Association Focused Update on Neonatal Resuscitation: An Update to the American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Circulation. 2019; 140:e922–e930. doi: 10.1161/CIR.0000000000000729LinkGoogle Scholar
  • 4. Saugstad OD. Resuscitation of newborn infants: from oxygen to room air.Lancet. 2010; 376:1970–1971. doi: 10.1016/S0140-6736(10)60543-0CrossrefMedlineGoogle Scholar
  • 5. Weinberger B, Laskin DL, Heck DE, Laskin JD. Oxygen toxicity in premature infants.Toxicol Appl Pharmacol. 2002; 181:60–67. doi: 10.1006/taap.2002.9387CrossrefMedlineGoogle Scholar

Chest Compressions

CPR Timing

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Most newborns who are apneic or have ineffective breathing at birth will respond to initial steps of newborn resuscitation (positioning to open the airway, clearing secretions, drying, and tactile stimulation) or to effective PPV with a rise in heart rate and improved breathing. If the heart rate remains less than 60/min despite these interventions, chest compressions can supply oxygenated blood to the brain until the heart rate rises. Ventilation should be optimized before starting chest compressions, with endotracheal intubation if possible. Chest compressions should be started if the heart rate remains less than 60/min after at least 30 seconds of adequate PPV.1

Oxygen is essential for organ function; however, excess inspired oxygen during resuscitation may be harmful. Although current guidelines recommend using 100% oxygen while providing chest compressions, no studies have confirmed a benefit of using 100% oxygen compared to any other oxygen concentration, including air (21%). However, it may be reasonable to increase inspired oxygen to 100% if there was no response to PPV with lower concentrations. Once return of spontaneous circulation (ROSC) is achieved, the supplemental oxygen concentration may be decreased to target a physiological level based on pulse oximetry to reduce the risks associated with hyperoxia.1,2

Recommendation-Specific Supportive Text
  1. The initiation of chest compressions in newborn babies with a heart rate less than 60/min is based on expert opinion because there are no clinical or physiological human studies addressing this question.

  2. A meta-analysis (very low quality) of 8 animal studies (n=323 animals) that compared air with 100% oxygen during chest compressions showed equivocal results.3 Two animal studies (very low quality) compared the tissue oxidative stress or damage between air (21%) and 100% oxygen and reported no difference in brain or lung inflammatory markers.3 The use of 100% oxygen during chest compressions is therefore expert opinion.

Compression-to-Ventilation Ratio and Techniques (Newborn)

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Chest compressions are a rare event in full-term newborns (approximately 0.1%) but are provided more frequently to preterm newborns.11 When providing chest compressions to a newborn, it may be reasonable to deliver 3 compressions before or after each inflation: providing 30 inflations and 90 compressions per minute (3:1 ratio for 120 total events per minute).

Alternative compression-to-ventilation ratios to 3:1, as well as asynchronous PPV (administration of inflations to a patient that are not coordinated with chest compressions), are routinely utilized outside the newborn period, but the preferred method in the newly born is 3:1 in synchrony. Newer methods of chest compression, using a sustained inflation that maintains lung inflation while providing chest compressions, are under investigation and cannot be recommended at this time outside research protocols.12,13

When providing chest compressions to a newborn, the 2 thumb–encircling hands technique may have benefit over the 2-finger technique with respect to blood pressure generation and provider fatigue. When providing chest compressions with the 2 thumb–encircling hands technique, the hands encircle the chest while the thumbs depress the sternum.1,2 The 2 thumb–encircling hands technique can be performed from the side of the infant or from above the head of the newborn.1 Performing chest compressions with the 2 thumb–encircling hands technique from above the head facilitates placement of an umbilical venous catheter.

Recommendation-Specific Supportive Text
  1. In animal studies (very low quality), the use of alterative compression-to-inflation ratios to 3:1 (eg, 2:1, 4:1, 5:1, 9:3, 15:2, and continuous chest compressions with asynchronous PPV) are associated with similar times to ROSC and mortality rates.4–8

  2. In a small number of newborns (n=2) with indwelling catheters, the 2 thumb–encircling hands technique generated higher systolic and mean blood pressures compared with the 2-finger technique.9

  3. One small manikin study (very low quality), compared the 2 thumb–encircling hands technique and 2-finger technique during 60 seconds of uninterrupted chest compressions. The 2 thumb–encircling hands technique achieved greater depth, less fatigue, and less variability with each compression compared with the 2-finger technique.10

References

  • 1. Wyckoff MH, Aziz K, Escobedo MB, Kapadia VS, Kattwinkel J, Perlman JM, Simon WM, Weiner GM, Zaichkin JG. Part 13: neonatal resuscitation: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Circulation. 2015; 132(suppl 2):S543–S560. doi: 10.1161/CIR.0000000000000267LinkGoogle Scholar
  • 2. Perlman JM, Wyllie J, Kattwinkel J, Wyckoff MH, Aziz K, Guinsburg R, Kim HS, Liley HG, Mildenhall L, Simon WM, et al.; on behalf of the Neonatal Resuscitation Chapter Collaborators. Part 7: neonatal resuscitation: 2015 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Circulation. 2015; 132(suppl 1):S204–S241. doi: 10.1161/CIR.0000000000000276LinkGoogle Scholar
  • 3. Garcia-Hidalgo C, Cheung PY, Solevåg AL, Vento M, O’Reilly M, Saugstad O, Schmölzer GM. A Review of Oxygen Use During Chest Compressions in Newborns-A Meta-Analysis of Animal Data.Front Pediatr. 2018; 6:400. doi: 10.3389/fped.2018.00400CrossrefMedlineGoogle Scholar
  • 4. Solevåg AL, Schmölzer GM, O’Reilly M, Lu M, Lee TF, Hornberger LK, Nakstad B, Cheung PY. Myocardial perfusion and oxidative stress after 21% vs. 100% oxygen ventilation and uninterrupted chest compressions in severely asphyxiated piglets.Resuscitation. 2016; 106:7–13. doi: 10.1016/j.resuscitation.2016.06.014CrossrefMedlineGoogle Scholar
  • 5. Schmölzer GM, O’Reilly M, Labossiere J, Lee TF, Cowan S, Nicoll J, Bigam DL, Cheung PY. 3:1 compression to ventilation ratio versus continuous chest compression with asynchronous ventilation in a porcine model of neonatal resuscitation.Resuscitation. 2014; 85:270–275. doi: 10.1016/j.resuscitation.2013.10.011CrossrefMedlineGoogle Scholar
  • 6. Solevåg AL, Dannevig I, Wyckoff M, Saugstad OD, Nakstad B. Extended series of cardiac compressions during CPR in a swine model of perinatal asphyxia.Resuscitation. 2010; 81:1571–1576. doi: 10.1016/j.resuscitation.2010.06.007CrossrefMedlineGoogle Scholar
  • 7. Solevag AL, Dannevig I, Wyckoff M, Saugstad OD, Nakstad B. Return of spontaneous circulation with a compression:ventilation ratio of 15:2 versus 3:1 in newborn pigs with cardiac arrest due to asphyxia.Arch Dis Child Fetal Neonatal Ed. 2011; 96:F417–F421. doi: 10.1136/adc.2010.200386CrossrefMedlineGoogle Scholar
  • 8. Pasquin MP, Cheung PY, Patel S, Lu M, Lee TF, Wagner M, O’Reilly M, Schmolzer GM. Comparison of Different Compression to Ventilation Ratios (2: 1, 3: 1, and 4: 1) during Cardiopulmonary Resuscitation in a Porcine Model of Neonatal Asphyxia.Neonatology. 2018; 114:37–45. doi: 10.1159/000487988CrossrefMedlineGoogle Scholar
  • 9. David R. Closed chest cardiac massage in the newborn infant.Pediatrics. 1988; 81:552–554.CrossrefMedlineGoogle Scholar
  • 10. Christman C, Hemway RJ, Wyckoff MH, Perlman JM. The two-thumb is superior to the two-finger method for administering chest compressions in a manikin model of neonatal resuscitation.Arch Dis Child Fetal Neonatal Ed. 2011; 96:F99–F101. doi: 10.1136/adc.2009.180406CrossrefMedlineGoogle Scholar
  • 11. Handley SC, Sun Y, Wyckoff MH, Lee HC. Outcomes of extremely preterm infants after delivery room cardiopulmonary resuscitation in a population-based cohort.J Perinatol. 2015; 35:379–383. doi: 10.1038/jp.2014.222CrossrefMedlineGoogle Scholar
  • 12. Schmölzer GM, M OR, Fray C, van Os S, Cheung PY. Chest compression during sustained inflation versus 3:1 chest compression:ventilation ratio during neonatal cardiopulmonary resuscitation: a randomised feasibility trial.Arch Dis Child Fetal Neonatal Ed. 2018; 103:F455–F460. doi: 10.1136/archdischild-2017–313037CrossrefMedlineGoogle Scholar
  • 13. Schmölzer GM, O’Reilly M, Labossiere J, Lee TF, Cowan S, Qin S, Bigam DL, Cheung PY. Cardiopulmonary resuscitation with chest compressions during sustained inflations: a new technique of neonatal resuscitation that improves recovery and survival in a neonatal porcine model.Circulation. 2013; 128:2495–2503. doi: 10.1161/circulationaha.113.002289LinkGoogle Scholar

Intravascular Access

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Babies who have failed to respond to PPV and chest compressions require vascular access to infuse epinephrine and/or volume expanders. In the delivery room setting, the primary method of vascular access is umbilical venous catheterization. Outside the delivery room, or if intravenous access is not feasible, the intraosseous route may be a reasonable alternative, determined by the local availability of equipment, training, and experience.

Recommendation-Specific Supportive Text

  1. Umbilical venous catheterization has been the accepted standard route in the delivery room for decades.2 There are no human neonatal studies to support one route over others.1

  2. There are 6 case reports indicating local complications of intraosseous needle placement.3–8

  3. Practitioners outside of the delivery room setting, and when umbilical venous catheterization is not feasible, may secure vascular access with the intraosseous route.

References

  • 1. Wyckoff MH, Wyllie J, Aziz K, de Almeida MF, Fabres J, Fawke J, Guinsburg R, Hosono S, Isayama T, Kapadia VS, et al.; on behalf of the Neonatal Life Support Collaborators. Neonatal life support: 2020 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Circulation. 2020 142(suppl 1):S185–S221. doi: 10.1161/CIR.0000000000000895LinkGoogle Scholar
  • 2. Niermeyer S, Kattwinkel J, Van Reempts P, Nadkarni V, Phillips B, Zideman D, Azzopardi D, Berg R, Boyle D, Boyle R, Burchfield D, Carlo W, Chameides L, Denson S, Fallat M, Gerardi M, Gunn A, Hazinski MF, Keenan W, Knaebel S, Milner A, Perlman J, Saugstad OD, Schleien C, Solimano A, Speer M, Toce S, Wiswell T, Zaritsky A. International Guidelines for Neonatal Resuscitation: An excerpt from the Guidelines 2000 for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care: International Consensus on Science. Contributors and Reviewers for the Neonatal Resuscitation Guidelines.Pediatrics. 2000; 106:E29. doi: 10.1542/peds.106.3.e29MedlineGoogle Scholar
  • 3. Vidal R, Kissoon N, Gayle M. Compartment syndrome following intraosseous infusion.Pediatrics. 1993; 91:1201–1202.CrossrefMedlineGoogle Scholar
  • 4. Katz DS, Wojtowycz AR. Tibial fracture: a complication of intraosseous infusion.Am J Emerg Med. 1994; 12:258–259. doi: 10.1016/0735-6757(94)90261-5CrossrefMedlineGoogle Scholar
  • 5. Ellemunter H, Simma B, Trawöger R, Maurer H. Intraosseous lines in preterm and full term neonates.Arch Dis Child Fetal Neonatal Ed. 1999; 80:F74–F75. doi: 10.1136/fn.80.1.f74CrossrefMedlineGoogle Scholar
  • 6. Carreras-González E, Brió-Sanagustín S, Guimerá I, Crespo C. Complication of the intraosseous route in a newborn infant [in Spanish].Med Intensiva. 2012; 36:233–234. doi: 10.1016/j.medin.2011.05.004MedlineGoogle Scholar
  • 7. Oesterlie GE, Petersen KK, Knudsen L, Henriksen TB. Crural amputation of a newborn as a consequence of intraosseous needle insertion and calcium infusion.Pediatr Emerg Care. 2014; 30:413–414. doi: 10.1097/PEC.0000000000000150CrossrefMedlineGoogle Scholar
  • 8. Suominen PK, Nurmi E, Lauerma K. Intraosseous access in neonates and infants: risk of severe complications - a case report.Acta Anaesthesiol Scand. 2015; 59:1389–1393. doi: 10.1111/aas.12602CrossrefMedlineGoogle Scholar

Medications (Epinephrine) IN Neonatal Resuscitation

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Medications are rarely needed in resuscitation of the newly born infant because low heart rate usually results from a very low oxygen level in the fetus or inadequate lung inflation after birth. Establishing ventilation is the most important step to correct low heart rate. However, if heart rate remains less than 60/min after ventilating with 100% oxygen (preferably through an endotracheal tube) and chest compressions, administration of epinephrine is indicated.

Administration of epinephrine via a low-lying umbilical venous catheter provides the most rapid and reliable medication delivery. The intravenous dose of epinephrine is 0.01 to 0.03 mg/kg, followed by a normal saline flush.4 If umbilical venous access has not yet been obtained, epinephrine may be given by the endotracheal route in a dose of 0.05 to 0.1 mg/kg. The dosage interval for epinephrine is every 3 to 5 minutes if the heart rate remains less than 60/min, although an intravenous dose may be given as soon as umbilical access is obtained if response to endotracheal epinephrine has been inadequate.

Recommendation-Specific Supportive Text

  1. The very limited observational evidence in human infants does not demonstrate greater efficacy of endotracheal or intravenous epinephrine; however, most babies received at least 1 intravenous dose before ROSC.1,2 In a perinatal model of cardiac arrest using term lambs undergoing transition with asphyxia-induced cardiopulmonary arrest, central venous epinephrine was associated with shorter time to ROSC and higher rates of ROSC than endotracheal epinephrine was.3 Intravenous epinephrine followed by a normal saline flush improves medication delivery.4

  2. One very limited observational study (human) showed 0.03 mg/kg to be an inadequate endotracheal dose.1 In the perinatal model of cardiac arrest, peak plasma epinephrine concentrations in animals were higher and were achieved sooner after central or low-lying umbilical venous administration compared with the endotracheal route, despite a lower intravenous dose (0.03 mg/kg intravenous versus 0.1 mg/kg endotracheal route).3

  3. In one very limited observational study, most infants who received an endotracheal dose achieved ROSC after a subsequent intravenous dose.2 Although the more rapid response to intravenous epinephrine warrants its immediate administration once umbilical access is obtained, repetitive endotracheal doses or higher intravenous doses may result in potentially harmful plasma levels that lead to associated hypertension and tachycardia.5–8

  4. In one very limited observational study, many infants received multiple doses of epinephrine before ROSC.2 The perinatal model of cardiac arrest documented peak plasma epinephrine concentrations at 1 minute after intravenous administration, but not until 5 minutes after endotracheal administration.3

References

  • 1. Barber CA, Wyckoff MH. Use and efficacy of endotracheal versus intravenous epinephrine during neonatal cardiopulmonary resuscitation in the delivery room.Pediatrics. 2006; 118:1028–1034. doi: 10.1542/peds.2006-0416CrossrefMedlineGoogle Scholar
  • 2. Halling C, Sparks JE, Christie L, Wyckoff MH. Efficacy of Intravenous and Endotracheal Epinephrine during Neonatal Cardiopulmonary Resuscitation in the Delivery Room.J Pediatr. 2017; 185:232–236. doi: 10.1016/j.jpeds.2017.02.024CrossrefMedlineGoogle Scholar
  • 3. Vali P, Chandrasekharan P, Rawat M, Gugino S, Koenigsknecht C, Helman J, Jusko WJ, Mathew B, Berkelhamer S, Nair J, et al.. Evaluation of timing and route of epinephrine in a neonatal model of asphyxial arrest.J Am Heart Assoc. 2017; 6:e004402. doi: 10.1161/JAHA.116.004402LinkGoogle Scholar
  • 4. Vali P, Sankaran D, Rawat M, Berkelhamer S, Lakshminrusimha S. Epinephrine in neonatal resuscitation.Children (Basel). 2019; 6:E51. doi: 10.3390/children6040051MedlineGoogle Scholar
  • 5. Perondi MB, Reis AG, Paiva EF, Nadkarni VM, Berg RA. A comparison of high-dose and standard-dose epinephrine in children with cardiac arrest.N Engl J Med. 2004; 350:1722–1730. doi: 10.1056/NEJMoa032440CrossrefMedlineGoogle Scholar
  • 6. Vandycke C, Martens P. High dose versus standard dose epinephrine in cardiac arrest - a meta-analysis.Resuscitation. 2000; 45:161–166. doi: 10.1016/s0300-9572(00)00188-xCrossrefMedlineGoogle Scholar
  • 7. Berg RA, Otto CW, Kern KB, Hilwig RW, Sanders AB, Henry CP, Ewy GA. A randomized, blinded trial of high-dose epinephrine versus standard-dose epinephrine in a swine model of pediatric asphyxial cardiac arrest.Crit Care Med. 1996; 24:1695–1700. doi: 10.1097/00003246-199610000-00016CrossrefMedlineGoogle Scholar
  • 8. Burchfield DJ, Preziosi MP, Lucas VW, Fan J. Effects of graded doses of epinephrine during asphxia-induced bradycardia in newborn lambs.Resuscitation. 1993; 25:235–244. doi: 10.1016/0300-9572(93)90120-fCrossrefMedlineGoogle Scholar

Volume Replacement

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

A newly born infant in shock from blood loss may respond poorly to the initial resuscitative efforts of ventilation, chest compressions, and/or epinephrine. History and physical examination findings suggestive of blood loss include a pale appearance, weak pulses, and persistent bradycardia (heart rate less than 60/min). Blood may be lost from the placenta into the mother’s circulation, from the cord, or from the infant.

When blood loss is suspected in a newly born infant who responds poorly to resuscitation (ventilation, chest compressions, and/or epinephrine), it may be reasonable to administer a volume expander without delay. Normal saline (0.9% sodium chloride) is the crystalloid fluid of choice. Uncrossmatched type O, Rh-negative blood (or crossmatched, if immediately available) is preferred when blood loss is substantial.4,5 An initial volume of 10 mL/kg over 5 to 10 minutes may be reasonable and may be repeated if there is inadequate response. The recommended route is intravenous, with the intraosseous route being an alternative.

Recommendation-Specific Supportive Text

  1. There is no evidence from randomized trials to support the use of volume resuscitation at delivery. One large retrospective review found that 0.04% of newborns received volume resuscitation in the delivery room, confirming that it is a relatively uncommon event.1 Those newborns who received volume resuscitation in the delivery room had lower blood pressure on admission to the neonatal intensive care unit compared with those who did not, indicating that factors other than blood loss may be important.1

  2. There is insufficient clinical evidence to determine what type of volume expander (crystalloid or blood) is more beneficial during neonatal resuscitation. Extrapolation from studies in hypotensive newborns shortly after birth6–8 and studies in animals (piglets) support the use of crystalloid over albumin expanders5 and blood over crystalloid solutions.4 One review discussed recommendations for the use of volume expanders.2

References

  • 1. Wyckoff MH, Perlman JM, Laptook AR. Use of volume expansion during delivery room resuscitation in near-term and term infants.Pediatrics. 2005; 115:950–955. doi: 10.1542/peds.2004-0913CrossrefMedlineGoogle Scholar
  • 2. Finn D, Roehr CC, Ryan CA, Dempsey EM. Optimising intravenous volume resuscitation of the newborn in the delivery room: practical considerations and gaps in knowledge.Neonatology. 2017; 112:163–171. doi: 10.1159/000475456CrossrefMedlineGoogle Scholar
  • 3. Conway-Orgel M. Management of hypotension in the very low-birth-weight infant during the golden hour.Adv Neonatal Care. 2010; 10:241–5; quiz 246. doi: 10.1097/ANC.0b013e3181f0891cCrossrefMedlineGoogle Scholar
  • 4. Mendler MR, Schwarz S, Hechenrieder L, Kurth S, Weber B, Hofler S, Kalbitz M, Mayer B, Hummler HD. Successful resuscitation in a model of asphyxia and hemorrhage to test different volume resuscitation strategies. a study in newborn piglets after transition.Front Pediatr. 2018; 6:192. doi: 10.3389/fped.2018.00192CrossrefMedlineGoogle Scholar
  • 5. Wyckoff M, Garcia D, Margraf L, Perlman J, Laptook A. Randomized trial of volume infusion during resuscitation of asphyxiated neonatal piglets.Pediatr Res. 2007; 61:415–420. doi: 10.1203/pdr.0b013e3180332c45CrossrefMedlineGoogle Scholar
  • 6. Niermeyer S. Volume resuscitation: crystalloid versus colloid.Clin Perinatol. 2006; 33:133–140. doi: 10.1016/j.clp.2005.12.002CrossrefMedlineGoogle Scholar
  • 7. Shalish W, Olivier F, Aly H, Sant’Anna G. Uses and misuses of albumin during resuscitation and in the neonatal intensive care unit.Semin Fetal Neonatal Med. 2017; 22:328–335. doi: 10.1016/j.siny.2017.07.009CrossrefMedlineGoogle Scholar
  • 8. Keir AK, Karam O, Hodyl N, Stark MJ, Liley HG, Shah PS, Stanworth SJ; NeoBolus Study Group. International, multicentre, observational study of fluid bolus therapy in neonates.J Paediatr Child Health. 2019; 55:632–639. doi: 10.1111/jpc.14260CrossrefMedlineGoogle Scholar

Postresuscitation Care

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Newly born infants who receive prolonged PPV or advanced resuscitation (eg, intubation, chest compressions ± epinephrine) should be closely monitored after stabilization in a neonatal intensive care unit or a monitored triage area because these infants are at risk for further deterioration.

Infants 36 weeks’ or greater estimated gestational age who receive advanced resuscitation should be examined for evidence of HIE to determine if they meet criteria for therapeutic hypothermia. Therapeutic hypothermia is provided under defined protocols similar to those used in published clinical trials and in facilities capable of multidisciplinary care and longitudinal follow-up. The impact of therapeutic hypothermia on infants less than 36 weeks’ gestational age with HIE is unclear and is a subject of ongoing research trials.

Hypoglycemia is common in infants who have received advanced resuscitation and is associated with poorer outcomes.8 These infants should be monitored for hypoglycemia and treated appropriately.

Infants with unintentional hypothermia (temperature less than 36°C) immediately after stabilization should be rewarmed to avoid complications associated with low body temperature (including increased mortality, brain injury, hypoglycemia, and respiratory distress). Evidence suggests that warming can be done rapidly (0.5°C/h) or slowly (less than 0.5°C/h) with no significant difference in outcomes.15–19 Caution should be taken to avoid overheating.

Recommendation-Specific Supportive Text

  1. In a meta-analysis of 8 RCTs involving 1344 term and late preterm infants with moderate-to-severe encephalopathy and evidence of intrapartum asphyxia, therapeutic hypothermia resulted in a significant reduction in the combined outcome of mortality or major neurodevelopmental disability to 18 months of age (odds ratio 0.75; 95% CI, 0.68–0.83).1

  2. Newly born infants who required advanced resuscitation are at significant risk of developing moderate-to-severe HIE2–4 and other morbidities.5–7

  3. Newly born infants with abnormal glucose levels (both low and high) are at increased risk for brain injury and adverse outcomes after a hypoxic-ischemic insult.8–14

  4. Two small RCTs16,19 and 4 observational studies15,17,18,20 of infants with hypothermia after delivery room stabilization found no difference between rapid or slow rewarming for outcomes of mortality,15,17 convulsions/seizures,19 intraventricular or pulmonary hemorrhage,15,17,19,20 hypoglycemia,16,17,19 or apnea.16,17,19 One observational study found less respiratory distress in infants who were slowly rewarmed,18 while a separate study found less respiratory distress syndrome in infants who were rapidly rewarmed.17

References

  • 1. Jacobs SE, Berg M, Hunt R, Tarnow-Mordi WO, Inder TE, Davis PG. Cooling for newborns with hypoxic ischaemic encephalopathy.Cochrane Database Syst Rev. 2013CD003311. doi: 10.1002/14651858.CD003311.pub3MedlineGoogle Scholar
  • 2. Laptook AR, Shankaran S, Ambalavanan N, Carlo WA, McDonald SA, Higgins RD, Das A; Hypothermia Subcommittee of the NICHD Neonatal Research Network. Outcome of term infants using apgar scores at 10 minutes following hypoxic-ischemic encephalopathy.Pediatrics. 2009; 124:1619–1626. doi: 10.1542/peds.2009-0934CrossrefMedlineGoogle Scholar
  • 3. Ayrapetyan M, Talekar K, Schwabenbauer K, Carola D, Solarin K, McElwee D, Adeniyi-Jones S, Greenspan J, Aghai ZH. Apgar scores at 10 minutes and outcomes in term and late preterm neonates with hypoxic-ischemic encephalopathy in the cooling era.Am J Perinatol. 2019; 36:545–554. doi: 10.1055/s-0038-1670637CrossrefMedlineGoogle Scholar
  • 4. Kasdorf E, Laptook A, Azzopardi D, Jacobs S, Perlman JM. Improving infant outcome with a 10 min Apgar of 0.Arch Dis Child Fetal Neonatal Ed. 2015; 100:F102–F105. doi: 10.1136/archdischild-2014-306687CrossrefMedlineGoogle Scholar
  • 5. Barber CA, Wyckoff MH. Use and efficacy of endotracheal versus intravenous epinephrine during neonatal cardiopulmonary resuscitation in the delivery room.Pediatrics. 2006; 118:1028–1034. doi: 10.1542/peds.2006-0416CrossrefMedlineGoogle Scholar
  • 6. 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; 196:463.e1–463.e5. doi: 10.1016/j.ajog.2006.10.877CrossrefGoogle Scholar
  • 7. Wyckoff MH, Salhab WA, Heyne RJ, Kendrick DE, Stoll BJ, Laptook AR; National Institute of Child Health and Human Development Neonatal Research Network. Outcome of extremely low birth weight infants who received delivery room cardiopulmonary resuscitation.J Pediatr. 2012; 160:239–244.e2. doi: 10.1016/j.jpeds.2011.07.041CrossrefMedlineGoogle Scholar
  • 8. Salhab WA, Wyckoff MH, Laptook AR, Perlman JM. Initial hypoglycemia and neonatal brain injury in term infants with severe fetal acidemia.Pediatrics. 2004; 114:361–366. doi: 10.1542/peds.114.2.361CrossrefMedlineGoogle Scholar
  • 9. Castrodale V, Rinehart S. The golden hour: improving the stabilization of the very low birth-weight infant.Adv Neonatal Care. 2014; 14:9–14; quiz 15. doi: 10.1097/ANC.0b013e31828d0289CrossrefMedlineGoogle Scholar
  • 10. Nadeem M, Murray DM, Boylan GB, Dempsey EM, Ryan CA. Early blood glucose profile and neurodevelopmental outcome at two years in neonatal hypoxic-ischaemic encephalopathy.BMC Pediatr. 2011; 11:10. doi: 10.1186/1471-2431-11-10CrossrefMedlineGoogle Scholar
  • 11. McKinlay CJ, Alsweiler JM, Ansell JM, Anstice NS, Chase JG, Gamble GD, Harris DL, Jacobs RJ, Jiang Y, Paudel N, Signal M, Thompson B, Wouldes TA, Yu TY, Harding JE; CHYLD Study Group. Neonatal Glycemia and Neurodevelopmental Outcomes at 2 Years.N Engl J Med. 2015; 373:1507–1518. doi: 10.1056/NEJMoa1504909CrossrefMedlineGoogle Scholar
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Withholding and Discontinuing Resuscitation

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Expert neonatal and bioethical committees have agreed that, in certain clinical conditions, it is reasonable not to initiate or to discontinue life-sustaining efforts while continuing to provide supportive care for babies and families.1,2,4

If the heart rate remains undetectable and all steps of resuscitation have been completed, it may be reasonable to redirect goals of care. Case series show small numbers of intact survivors after 20 minutes of no detectable heart rate. The decision to continue or discontinue resuscitative efforts should be individualized and should be considered at about 20 minutes after birth. Variables to be considered may include whether the resuscitation was considered optimal, availability of advanced neonatal care (such as therapeutic hypothermia), specific circumstances before delivery, and wishes expressed by the family.3,6

Some babies are so sick or immature at birth that survival is unlikely, even if neonatal resuscitation and intensive care are provided. In addition, some conditions are so severe that the burdens of the illness and treatment greatly outweigh the likelihood of survival or a healthy outcome. If it is possible to identify such conditions at or before birth, it is reasonable not to initiate resuscitative efforts. These situations benefit from expert consultation, parental involvement in decision-making, and, if indicated, a palliative care plan.1,2,4–6

Recommendation-Specific Supportive Text

  1. It is the expert opinion of national medical societies that conditions exist for which it is reasonable to not initiate resuscitation or to discontinue resuscitation once these conditions are identified.1,2,4,5

  2. Randomized controlled studies and observational studies in settings where therapeutic hypothermia is available (with very low certainty of evidence) describe variable rates of survival without moderate-to-severe disability in babies who achieve ROSC after 10 minutes or more despite continued resuscitation. None of these studies evaluate outcomes of resuscitation that extends beyond 20 minutes of age, by which time the likelihood of intact survival was very low. The studies were too heterogeneous to be amenable to meta-analysis.3

  3. Conditions in which noninitiation or discontinuation of resuscitation may be considered include extremely preterm birth and certain severe congenital anomalies. National guidelines recommend individualization of parent-informed decisions based on social, maternal, and fetal/neonatal factors.1,2,4 A systematic review showed that international guidelines variably described periviability between 22 and 24 weeks’ gestational age.7

References

  • 1. American Academy of Pediatrics Committee on Fetus and Newborn. Bell EF. Noninitiation or withdrawal of intensive care for high-risk newborns.Pediatrics. 2007; 119:401–403. doi: 10.1542/peds.2006–3180CrossrefMedlineGoogle Scholar
  • 2. Cummings J; and the Committee on Fetus and Newborn. Antenatal Counseling Regarding Resuscitation and Intensive Care Before 25 Weeks of Gestation.Pediatrics. 2015; 136:588–595. doi: 10.1542/peds.2015-2336CrossrefMedlineGoogle Scholar
  • 3. Wyckoff MH, Wyllie J, Aziz K, de Almeida MF, Fabres J, Fawke J, Guinsburg R, Hosono S, Isayama T, Kapadia VS, et al.; on behalf of the Neonatal Life Support Collaborators. Neonatal life support: 2020 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Circulation. 2020 142(suppl 1):S185–S221. doi: 10.1161/CIR.0000000000000895LinkGoogle Scholar
  • 4. American College of Obstetricians and Gynecologists; Society for Maternal-Fetal M. Obstetric Care Consensus No. 6: periviable birth.Obstet Gynecol. 2017; 130:e187–e199. doi: 10.1097/AOG.0000000000002352CrossrefMedlineGoogle Scholar
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  • 7. Guillén Ú, Weiss EM, Munson D, Maton P, Jefferies A, Norman M, Naulaers G, Mendes J, Justo da Silva L, Zoban P, Hansen TW, Hallman M, Delivoria-Papadopoulos M, Hosono S, Albersheim SG, Williams C, Boyle E, Lui K, Darlow B, Kirpalani H. Guidelines for the Management of Extremely Premature Deliveries: A Systematic Review.Pediatrics. 2015; 136:343–350. doi: 10.1542/peds.2015-0542CrossrefMedlineGoogle Scholar

Human and System Performance

Training Frequency

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

To perform neonatal resuscitation effectively, individual providers and teams need training in the required knowledge, skills, and behaviors. Historically, the repeat training has occurred every 2 years.6–9 However, adult, pediatric, and neonatal studies suggest that without practice, CPR knowledge and skills decay within 3 to 12 months10–12 after training. Short, frequent practice (booster training) has been shown to improve neonatal resuscitation outcomes.5 Educational programs and perinatal facilities should develop strategies to ensure that individual and team training is frequent enough to sustain knowledge and skills.

Recommendation-Specific Supportive Text
  1. In a randomized controlled simulation study, medical students who underwent booster training retained improved neonatal intubation skills over a 6-week period compared with medical students who did not receive booster training. There was no difference in neonatal intubation performance after weekly booster practice for 4 weeks compared with daily booster practice for 4 consecutive days.1

In a randomized controlled simulation study, pediatric and family practice residents who underwent booster training 9 months after an initial Neonatal Resuscitation Program course demonstrated better procedural skills and teamwork behaviors at a follow-up assessment at 16 months compared with residents who did not receive booster training.2

In a prospective cohort study, physicians and nurses trained in Helping Babies Breathe demonstrated a rapid loss of resuscitation skills by 1 month after training. Subjects who received monthly practice sessions were more likely to pass an objective structured clinical evaluation than those who practiced less frequently.3

In a prospective observational study, implementation of weekly, brief Helping Babies Breathe simulation training after a 1-day Helping Babies Breathe training course resulted in increased frequency of stimulation of newborns, decrease in bag-mask ventilation, and decreased neonatal mortality at 24 hours.4

References

  • 1. Ernst KD, Cline WL, Dannaway DC, Davis EM, Anderson MP, Atchley CB, Thompson BM. Weekly and consecutive day neonatal intubation training: comparable on a pediatrics clerkship.Acad Med. 2014; 89:505–510. doi: 10.1097/ACM.0000000000000150CrossrefMedlineGoogle Scholar
  • 2. Bender J, Kennally K, Shields R, Overly F. Does simulation booster impact retention of resuscitation procedural skills and teamwork?J Perinatol. 2014; 34:664–668. doi: 10.1038/jp.2014.72CrossrefMedlineGoogle Scholar
  • 3. Tabangin ME, Josyula S, Taylor KK, Vasquez JC, Kamath-Rayne BD. Resuscitation skills after Helping Babies Breathe training: a comparison of varying practice frequency and impact on retention of skills in different types of providers.Int Health. 2018; 10:163–171. doi: 10.1093/inthealth/ihy017CrossrefMedlineGoogle Scholar
  • 4. Mduma E, Ersdal H, Svensen E, Kidanto H, Auestad B, Perlman J. Frequent brief on-site simulation training and reduction in 24-h neonatal mortality–an educational intervention study.Resuscitation. 2015; 93:1–7. doi: 10.1016/j.resuscitation.2015.04.019CrossrefMedlineGoogle Scholar
  • 5. Reisman J, Arlington L, Jensen L, Louis H, Suarez-Rebling D, Nelson BD. Newborn resuscitation training in resource-limited settings: a systematic literature review.Pediatrics. 2016; 138:e20154490. doi: 10.1542/peds.2015–4490CrossrefMedlineGoogle Scholar
  • 6. American Academy of Pediatrics and American Heart Association. Textbook of Neonatal Resuscitation (NRP). 7th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2016.CrossrefGoogle Scholar
  • 7. American Heart Association. Basic Life Support Provider Manual. Dallas, TX: American Heart Association; 2016.Google Scholar
  • 8. American Heart Association. Pediatric Advanced Life Support Provider Manual. Dallas, TX: American Heart Association; 2016.Google Scholar
  • 9. American Heart Association. Advanced Cardiovascular Life Support Provider Manual. Dallas, TX: American Heart Association; 2016.Google Scholar
  • 10. Soar J, Mancini ME, Bhanji F, Billi JE, Dennett J, Finn J, Ma MH, Perkins GD, Rodgers DL, Hazinski MF, et al.; on behalf of the Education, Implementation, and Teams Chapter Collaborators. Part 12: education, implementation, and teams: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations.Resuscitation. 2010; 81(suppl 1):e288–e330. doi: 10.1016/j.resuscitation.2010.08.030CrossrefMedlineGoogle Scholar
  • 11. Bang A, Patel A, Bellad R, Gisore P, Goudar SS, Esamai F, Liechty EA, Meleth S, Goco N, Niermeyer S, Keenan W, Kamath-Rayne BD, Little GA, Clarke SB, Flanagan VA, Bucher S, Jain M, Mujawar N, Jain V, Rukunga J, Mahantshetti N, Dhaded S, Bhandankar M, McClure EM, Carlo WA, Wright LL, Hibberd PL. Helping Babies Breathe (HBB) training: What happens to knowledge and skills over time?BMC Pregnancy Childbirth. 2016; 16:364. doi: 10.1186/s12884-016-1141-3CrossrefMedlineGoogle Scholar
  • 12. Arlington L, Kairuki AK, Isangula KG, Meda RA, Thomas E, Temu A, Mponzi V, Bishanga D, Msemo G, Azayo M, et al.. Implementation of “Helping Babies Breathe”: a 3-year experience in Tanzania.Pediatrics. 2017; 139:e20162132. doi: 10.1542/peds.2016–2132CrossrefMedlineGoogle Scholar

Briefing and Debriefing

When coordinating PPV with chest compressions How long does it take to complete a cycle of 3 compressions and 1 breath NRP?

Synopsis

Briefing has been defined as “a discussion about an event that is yet to happen to prepare those who will be involved and thereby reduce the risk of failure or harm.”4Debriefing has been defined as “a discussion of actions and thought processes after an event to promote reflective learning and improve clinical performance”5 or “a facilitated discussion of a clinical event focused on learning and performance improvement.”6 Briefing and debriefing have been recommended for neonatal resuscitation training since 20107 and have been shown to improve a variety of educational and clinical outcomes in neonatal, pediatric, and adult simulation-based and clinical studies. The effect of briefing and debriefing on longer-term and critical outcomes remains uncertain.

Recommendation-Specific Supportive Text

Multiple clinical and simulation studies examining briefings or debriefings of resuscitation team performance have shown improved knowledge or skills.8–12

  1. In a prospective interventional clinical study, video-based debriefing of neonatal resuscitations was associated with improved preparation and adherence to the initial steps of the Neonatal Resuscitation Algorithm, improved quality of PPV, and improved team function and communication.1

In 2 pre–quality improvement/post–quality improvement initiatives, use of a team briefing, debriefing, and predelivery checklist was associated with an improvement in team communication in the delivery room and short-term clinical outcomes, such as decreased frequency of intubation in the delivery room and increased frequency of normothermia on admission to the neonatal intensive care unit. There was no significant effect on other in-hospital clinical outcomes such as bronchopulmonary dysplasia, necrotizing enterocolitis, retinopathy of prematurity, intraventricular hemorrhage, or length of stay.2,3

References

  • 1. Skåre C, Calisch TE, Saeter E, Rajka T, Boldingh AM, Nakstad B, Niles DE, Kramer-Johansen J, Olasveengen TM. Implementation and effectiveness of a video-based debriefing programme for neonatal resuscitation.Acta Anaesthesiol Scand. 2018; 62:394–403. doi: 10.1111/aas.13050CrossrefMedlineGoogle Scholar
  • 2. Sauer CW, Boutin MA, Fatayerji AN, Proudfoot JA, Fatayerji NI, Golembeski DJ. Delivery Room Quality Improvement Project Improved Compliance with Best Practices for a Community NICU.Sci Rep. 2016; 6:37397. doi: 10.1038/srep37397CrossrefMedlineGoogle Scholar
  • 3. Katheria A, Rich W, Finer N. Development of a strategic process using checklists to facilitate team preparation and improve communication during neonatal resuscitation.Resuscitation. 2013; 84:1552–1557. doi: 10.1016/j.resuscitation.2013.06.012CrossrefMedlineGoogle Scholar
  • 4. Halamek LP, Cady RAH, Sterling MR. Using briefing, simulation and debriefing to improve human and system performance.Semin Perinatol. 2019; 43:151178. doi: 10.1053/j.semperi.2019.08.007CrossrefMedlineGoogle Scholar
  • 5. Mullan PC, Kessler DO, Cheng A. Educational opportunities with postevent debriefing.JAMA. 2014; 312:2333–2334. doi: 10.1001/jama.2014.15741CrossrefMedlineGoogle Scholar
  • 6. Sawyer T, Loren D, Halamek LP. Post-event debriefings during neonatal care: why are we not doing them, and how can we start?J Perinatol. 2016; 36:415–419. doi: 10.1038/jp.2016.42CrossrefMedlineGoogle Scholar
  • 7. Kattwinkel J, Perlman JM, Aziz K, Colby C, Fairchild K, Gallagher J, Hazinski MF, Halamek LP, Kumar P, Little G, et al.. Part 15: neonatal resuscitation: 2010 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care.Circulation. 2010; 122(suppl 3):S909–S919. doi: 10.1161/CIRCULATIONAHA.110.971119LinkGoogle Scholar
  • 8. Savoldelli GL, Naik VN, Park J, Joo HS, Chow R, Hamstra SJ. Value of debriefing during simulated crisis management: oral versus video-assisted oral feedback.Anesthesiology. 2006; 105:279–285. doi: 10.1097/00000542-200608000-00010CrossrefMedlineGoogle Scholar
  • 9. Edelson DP, Litzinger B, Arora V, Walsh D, Kim S, Lauderdale DS, Vanden Hoek TL, Becker LB, Abella BS. Improving in-hospital cardiac arrest process and outcomes with performance debriefing.Arch Intern Med. 2008; 168:1063–1069. doi: 10.1001/archinte.168.10.1063CrossrefMedlineGoogle Scholar
  • 10. Morgan PJ, Tarshis J, LeBlanc V, Cleave-Hogg D, DeSousa S, Haley MF, Herold-McIlroy J, Law JA. Efficacy of high-fidelity simulation debriefing on the performance of practicing anaesthetists in simulated scenarios.Br J Anaesth. 2009; 103:531–537. doi: 10.1093/bja/aep222CrossrefMedlineGoogle Scholar
  • 11. Dine CJ, Gersh RE, Leary M, Riegel BJ, Bellini LM, Abella BS. Improving cardiopulmonary resuscitation quality and resuscitation training by combining audiovisual feedback and debriefing.Crit Care Med. 2008; 36:2817–2822. doi: 10.1097/CCM.0b013e318186fe37CrossrefMedlineGoogle Scholar
  • 12. Wolfe H, Zebuhr C, Topjian AA, Nishisaki A, Niles DE, Meaney PA, Boyle L, Giordano RT, Davis D, Priestley M, Apkon M, Berg RA, Nadkarni VM, Sutton RM. Interdisciplinary ICU cardiac arrest debriefing improves survival outcomes*.Crit Care Med. 2014; 42:1688–1695. doi: 10.1097/CCM.0000000000000327CrossrefMedlineGoogle Scholar

Knowledge Gaps

Neonatal resuscitation science has advanced significantly over the past 3 decades, with contributions by many researchers in laboratories, in the delivery room, and in other clinical settings. While this research has led to substantial improvements in the Neonatal Resuscitation Algorithm, it has also highlighted that we still have more to learn to optimize resuscitation for both preterm and term infants. With growing enthusiasm for clinical studies in neonatology, elements of the Neonatal Resuscitation Algorithm continue to evolve as new evidence emerges.

The current guidelines have focused on clinical activities described in the resuscitation algorithm, rather than on the most appropriate devices for each step. Reviews in 2021 and later will address choice of devices and aids, including those required for ventilation (T-piece, self-inflating bag, flow-inflating bag), ventilation interface (face mask, laryngeal mask), suction (bulb syringe, meconium aspirator), monitoring (respiratory function monitors, heart rate monitoring, near infrared spectroscopy), feedback, and documentation.

Review of the knowledge chunks during this update identified numerous questions and practices for which evidence was weak, uncertain, or absent. The following knowledge gaps require further research:

Resuscitation Preparedness

  • The frequency and format of booster training or refresher training that best supports retention of neonatal resuscitation knowledge, technical skills, and behavioral skills

  • The effects of briefing and debriefing on team performance

During and Just After Delivery

  • Optimal cord management strategies for various populations, including nonvigorous infants and those with congenital heart or lung disease

  • Optimal management of nonvigorous infants with MSAF

Early Resuscitation

  • The most effective device(s) and interface(s) for providing PPV

  • Impact of routine use of the ECG during neonatal resuscitation on resuscitation

  • Feasibility and effectiveness of new technologies for rapid heart rate measurement (such as electric, ultrasonic, or optical devices)

  • Optimal oxygen management during and after resuscitation

Advanced Resuscitation

  • Novel techniques for effective delivery of CPR, such as chest compressions accompanied by sustained inflation

  • Optimal timing, dosing, dose interval, and delivery routes for epinephrine or other vasoactive drugs, including earlier use in very depressed newly born infants

  • Indications for volume expansion, as well as optimal dosing, timing, and type of volume

  • The management of pulseless electric activity

Specific Populations

  • Management of the preterm newborn during and after resuscitation

  • Management of congenital anomalies of the heart and lungs during and after resuscitation

  • Resuscitation of newborns in the neonatal unit after the newly born period

  • Resuscitation of newborns in other settings up to 28 days of age

Postresuscitation Care

  • Optimal dose, route, and timing of surfactant in at-risk newborns, including less-invasive administration techniques

  • Indications for therapeutic hypothermia in babies with mild HIE and in those born at less than 36 weeks’ gestational age

  • Adjunctive therapies to therapeutic hypothermia

  • Optimal management of blood glucose

  • Optimal rewarming strategy for newly born infants with unintentional hypothermia

For all these gaps, it is important that we have information on outcomes considered critical or important by both healthcare providers and families of newborn infants.

The research community needs to address the paucity of educational studies that provide outcomes with a high level of certainty. Internal validity might be better addressed by clearly defined primary outcomes, appropriate sample sizes, relevant and timed interventions and controls, and time series analyses in implementation studies. External validity might be improved by studying the relevant learner or provider populations and by measuring the impact on critical patient and system outcomes rather than limiting study to learner outcomes.

Researchers studying these gaps may need to consider innovations in clinical trial design; examples include pragmatic study designs and novel consent processes. As mortality and severe morbidities decline with biomedical advancements and improvements in healthcare delivery, there is decreased ability to have adequate power for some clinical questions using traditional individual patient randomized trials. Another barrier is the difficulty in obtaining antenatal consent for clinical trials in the delivery room. Adaptive trials, comparative effectiveness designs, and those using cluster randomization may be suitable for some questions, such as the best approach for MSAF in nonvigorous infants. High-quality observational studies of large populations may also add to the evidence. When feasible, well-designed multicenter randomized clinical trials are still optimal to generate the highest-quality evidence.

Finally, we wish to reinforce the importance of addressing the values and preferences of our key stakeholders, the families and teams who are involved in the process of resuscitation. Gaps in this domain, whether perceived or real, should be addressed at every stage in our research, educational, and clinical activities.

Article Information

The American Heart Association requests that this document be cited as follows: Aziz K, Lee HC, Escobedo MB, Hoover AV, Kamath-Rayne BD, Kapadia VS, Magid DJ, Niermeyer S, Schmölzer GM, Szyld E, Weiner GM, Wyckoff MH, Yamada NK, Zaichkin J. Part 5: neonatal resuscitation: 2020 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation. 2020;142(suppl 2):S524–S550. doi: 10.1161/CIR.0000000000000902

This article has been copublished in Pediatrics.

Acknowledgment

We thank Dr Abhrajit Ganguly for assistance in manuscript preparation.

Appendix 1. Writing Group Disclosures

Writing Group MemberEmploymentResearch GrantOther Research SupportSpeakers’ Bureau/HonorariaExpert WitnessOwnership InterestConsultant/Advisory BoardOther
Khalid AzizUniversity of Alberta
Pediatrics
NoneNoneNoneNoneNoneNoneSalary: University of Alberta†
Henry C. LeeStanford UniversityNICHD (PI of R1 grant examining intensive care for infants born at extremely early gestational age)*NoneNoneNoneNoneNoneNone
Marilyn B EscobedoUniversity of Oklahoma Medical School
Pediatrics
NoneNoneNoneNoneNoneNoneNone
Amber V. HooverAmerican Heart AssociationNoneNoneNoneNoneNoneNoneNone
Beena D. Kamath-RayneAmerican Academy of PediatricsNoneNoneNoneNoneNoneNoneNone
Vishal S. KapadiaUT Southwestern
Pediatrics
NIH, NICHD†NoneNoneNoneNoneNoneNone
David J. MagidUniversity of ColoradoNIH†; NHLBI†; CMS†; AHA†NoneNoneNoneNoneNoneAmerican Heart Association (Senior Science Editor)†
Susan NiermeyerUniversity of Colorado
Pediatrics
NoneNoneNoneNoneNoneNoneNone
Georg M. SchmölzerUniversity of Alberta PediatricsHeart and Stroke Foundation Canada*; Canadian Institute of Health Research*; THRASHER Foundation*; Canadian Institute of Health Research*NoneNoneNoneOwner of RETAIN LABS Medical Inc*NoneNone
Edgardo SzyldUniversity of OklahomaNoneNoneNoneNoneNoneNoneNone
Gary M. WeinerUniversity of Michigan
Pediatrics-Neonatology
NoneNoneNoneNoneNoneNoneNone
Myra H. WyckoffUT Southwestern
Pediatrics
NoneNoneNoneNoneNoneNoneNone
Nicole K. YamadaStanford UniversityAHRQ†NoneNoneNoneNoneNoneNone
Jeanette ZaichkinSelf usedNoneNoneNoneNoneNoneAmerican Academy of Pediatrics Neonatal Resuscitation Program†None

Appendix 2. Reviewer Disclosures

ReviewerEmploymentResearch GrantOther Research SupportSpeakers’ Bureau/HonorariaExpert WitnessOwnership InterestConsultant/Advisory BoardOther
Christoph BührerCharité University Medical Center (Germany)NoneNoneUniversity of Tübingen*NoneNoneNoneNone
Praveen ChandrasekharanSUNY BuffaloNoneNoneNoneNoneNoneNoneNone
Krithika LingappanBaylor College of MedicineNoneNoneNoneNoneNoneNoneNone
Ju-Lee OeiRoyal Hospital for Women (Australia)NoneNoneNoneNoneNoneNoneNone
Birju A. ShahThe University of OklahomaNoneNoneNoneNoneNoneNoneNone