Abstract
Neonatal resuscitation is a coordinated, team-based series of timed sequential steps that focuses on a transitional physiology to improve perinatal and neonatal outcomes. The practice of neonatal resuscitation has evolved over time and continues to be shaped by emerging evidence as well as key opinions. We present the revised Neonatal Resuscitation Guidelines for Singapore 2021. The recommendations from the International Liaison Committee on Resuscitation Neonatal Task Force Consensus on Science and Treatment Recommendations (2020) and guidelines from the American Heart Association and European Resuscitation Council were compared with existing guidelines. The recommendations of the Neonatal Subgroup of the Singapore Resuscitation and First Aid Council were derived after the work group discussed and appraised the current available evidence and their applicability to local clinical practice.
Keywords: neonatal resuscitation, newborn resuscitation, Singapore Resuscitation and First Aid Council (SRFAC) guidelines for resuscitation 2021
BACKGROUND AND INTRODUCTION
Resuscitation at birth requires a team of providers with different skill sets to communicate, collaborate and perform the necessary steps efficiently, guided by a standardised protocol and uniform practice guidelines. The majority of preterm newborns require some form of resuscitation and/or stabilisation during transition to extrauterine life. In comparison, about 10% of term newborns require stimulation to initiate breathing, 5% require positive pressure ventilation (PPV) before spontaneous breathing is established, 2% require intubation for longer respiratory support, 0.1% require cardiac compressions and 0.05% require adrenaline.(1-4)
This review by the Neonatal Subgroup of the Singapore Resuscitation and First Aid Council (SRFAC) is an update of the previous Singapore Neonatal Resuscitation Guidelines (2016)(5) and draws from the International Liaison Committee on Resuscitation (ILCOR) 2020 Consensus on Science with Treatment Recommendations (CoSTR), the American Heart Association guidelines for cardiopulmonary resuscitation and emergency cardiovascular care and the European Resuscitation Council newborn life support (2021) recommendations.(6-8) This guideline applies to newborns transitioning to extrauterine life irrespective of their place of birth and neonates who have completed newborn transition and require resuscitation during the initial hospitalisation. The key highlights are presented in Box 1 and in the discussion on treatment recommendations and practice guidelines, which are organised in alignment with the newborn resuscitation algorithm (Fig. 1).
Box 1.
Key take-home messages for neonatal resuscitation:
Fig. 1.
Flowchart shows the newborn resuscitation algorithm. CPAP: continuous positive airway pressure; CPR: cardiopulmonary resuscitation; ECG: electrocardiography; ETT: endotracheal tube; HR: heart rate; IV: intravenous; LMA: laryngeal mask airway; O2: oxygen; PPV: positive pressure ventilation; SpO2: oxygen saturation
ANTICIPATION AND PREPARATION FOR RESUSCITATION
Identification of antepartum and intrapartum risk factors (Box 2) helps to anticipate the need for resuscitation at birth. Resuscitation may not be anticipated at all times; hence, it is important to be able to mobilise a team capable of advanced resuscitation at short notice. The topic on prediction of respiratory support in the delivery room was reviewed in 2020.(6) There was no new evidence to support a change in the recommendations from the 2010 ILCOR guidelines.(9,10)
Box 2.
Common risk factors that may predict the need for neonatal resuscitation:
Recommendations on anticipation and preparation
Anticipate resuscitation needs and prepare in advance.
The environment should be warm, well-lit and draught-free, and should have a designated resuscitation area with an overhead warmer and equipment for monitoring.
Equipment may be grouped by thermoregulation, ventilation and circulatory support, and kept well maintained and ready for use.
Providers of newborn resuscitation should be trained in basic neonatal life support at the minimum.
A team of advanced skilled providers trained in all steps of resuscitation should attend to high-risk deliveries.
UMBILICAL CORD MANAGEMENT
Delayed cord clamping
Delayed cord clamping (DCC) by at least 30 seconds in term newborns increases haematocrit and reduces iron deficiency at the age of 3–6 months.(11) However, there is no proven benefit in terms of reduction of mortality or longer-term neurodevelopmental outcome.
In vigorous preterm newborns, there is unequivocal evidence that DCC for 30–60 seconds reduces transfusions, necrotising enterocolitis (NEC) and all grades of intraventricular haemorrhage (IVH).(12-14) However, evidence is unclear regarding the true benefit of DCC for preventing neurodevelopmental impairment in the early years, chronic lung disease (CLD), periventricular leukomalacia (PVL), late-onset sepsis and retinopathy of prematurity (ROP).(13-15) For the critical outcome of in-hospital mortality after birth, accumulated evidence tends to favour DCC in babies born before 37 weeks. The relative risks of mortality in two large systematic reviews were 0.68, 95% confidence interval (CI) 0.52–0.90 (n = 2,834), and 0.73, 95% CI 0.54–0.98 (n = 2,680).(13,14) However, the benefits of DCC among 2,988 babies born at less than 34 weeks of gestation were equivocal, with a survival risk ratio (RR) of 1.02, 95% CI 1.00–1.04.(16)
Umbilical cord milking
Umbilical cord milking (UCM) has been performed with intact cord (i.e. intact-cord milking; ICM) or after cutting the cord (cut-cord milking). ICM has not been shown to provide survival advantage or lower morbidity over early cord clamping or DCC in preterms.(16) Previous studies have shown increased risk of severe IVH with UCM among very premature newborns (< 28 weeks).(17,18)
Recommendations on cord management
DCC for 30–60 seconds is recommended for both stable term and preterm newborns who do not require resuscitation at birth.
DCC takes precedence over cord blood banking.
DCC should not delay resuscitation in babies who require immediate resuscitation.
DCC is contraindicated in settings of monochorionic twins or when placental circulation is compromised (e.g. abruption, bleeding placenta praevia, cord avulsion).
Cord milking is not recommended in preterm deliveries other than in research settings.
THERMOREGULATION AND INITIAL STEPS
Thermoregulation
A low admission temperature among non-asphyxiated term or preterm newborns is a strong predictor of mortality and morbidity.(19,20) Hence, the earlier recommendation on recording an admission temperature is strengthened.(5-8,21,22) Premature and very-low-birth-weight babies are at risk of hypothermia and require additional thermoregulatory interventions (e.g. overhead warmers, polyethylene wrap, exothermic mattress, warm humidified gas for ventilation).(20,23-30) For newborns who are unintentionally hypothermic (temperature < 36°C) on admission, current evidence does not support rapid (≥ 0.5°C/hr) over slow rewarming (< 0.5°C/hr).(31-34) Their body temperature should be monitored during rewarming to avoid hyperthermia.
Recommendations on temperature measurement and goals
Measure and record temperature after birth and upon admission.
Skin, axillary or rectal temperature measurements are acceptable.
Maintain temperature of non-asphyxiated newborns between 36.5°C and 37.5°C.
Prevent hypothermia (< 36°C) among non-asphyxiated newborns, and hyperthermia (> 38°C).
Recommendations to prevent hypothermia
Maintain ambient environment of the delivery room at 23°C–25°C.
For preterm newborns at < 33 weeks of gestation, an ambient temperature ≥ 25°C is preferred.
Healthy term and preterm newborns with gestational age ≥ 33 weeks who do not require resuscitation can be placed for skin-to-skin contact with the mother, both covered with a warm blanket for improvement of breastfeeding, temperature maintenance and glucose stability.
Term and preterm babies with gestational age ≥ 33 weeks who require resuscitative intervention should be placed under a radiant warmer and dried with warmed towels.
Preterms with gestational age < 33 weeks should be placed without drying in a polyethylene wrap or bag, under a radiant warmer. Iatrogenic hyperthermia should be avoided when multiple thermoregulatory interventions are simultaneously used.
Thermoregulation should be maintained during the transfer of the newborn.
Initial steps
During the first 60 seconds of life, the ‘golden minute’, providers support the newborn transition to extrauterine life, and critical assessments are conducted to determine the need for resuscitation.(5-8,21,22) Thermoregulatory steps mentioned previously are implemented during this phase. Most newborns, including preterms, initiate spontaneous breathing if they are adequately positioned with an open airway.(35) Newborns with primary apnoea or irregular breathing may require gentle stimulation to attain regular breathing. Routine oropharyngeal or nasopharyngeal suctioning can be harmful, as it may precipitate apnoea and bradycardia, leading to hypoxaemia, longer time to normoxia, impaired cerebral blood flow and raised intracranial pressure.(36-44)
Recommendations on initial steps
Ensure warmth.
Gently rub the soles of the feet or back to stimulate breathing.
Maintain an open airway by placing the newborn supine over a flat surface, with the neck in a neutral, sniffing position.
Avoid routine suctioning. If the airway is obstructed, use a bulb sucker or suction catheter with a suction pressure of 80–100 mmHg to provide gentle and brief (< 10 seconds) suctioning.
Assess the adequacy of breathing and stability of the heart rate (HR) by the end of the golden minute to determine the need for further resuscitation.
Management of babies born through meconium-stained liquor
In utero passage of meconium is indicative of fetal stress and associated with fetal hypoxia-ischaemia. 5%–15% of all deliveries may be complicated by in utero passage of meconium, and up to 5% of babies born through meconium-stained liquor develop meconium aspiration syndrome (MAS).(45-47) In 449 non-vigorous babies born through meconium-stained liquor, immediate laryngoscopy with or without tracheal suction showed no survival advantage compared with immediate resuscitation without laryngoscopy (RR 0.99, 95% CI 0.93–1.06).(47) There was no difference in the outcomes of MAS, pulmonary hypertension, hypoxic ischaemic encephalopathy (HIE) or initial resuscitation requirements. Recent systematic reviews further support this finding.(48-52)
Recommendations on management of babies born through meconium-stained liquor
Intrapartum suction of nose or mouth is contraindicated.
In both vigorous and non-vigorous babies born through meconium-stained amniotic fluid, routine oropharyngeal or nasopharyngeal suctioning is not required. Bulb suctioning or suctioning using ≥ 10-Fr size catheter may be required under direct vision if upper airways are suspected to be obstructed.
Follow usual resuscitation steps in a non-vigorous baby to establish regular respiration. If PPV and ventilation correction steps do not result in lung inflation, the possibility of proximal lower airway obstruction by meconium may be considered, and tracheal suction may be attempted using an endotracheal tube (ETT) and meconium aspirator.
ASSESSMENT OF THE NEWBORN
During the initial steps, the provider needs to determine the transition needs of the newborn through assessment of breathing, tone and HR. Pallor, cyanosis, poor tone, weak cry in a term newborn, shallow or gasping breathing and bradycardia (HR < 100/min) are important clues that indicate a need for further resuscitation.
Assessment of heart rate
An increase in the HR is the most important indicator of effective resuscitation. Auscultation remains the easiest method for the initial assessment of HR, while pulse oximetry and three-lead electrocardiography (ECG) provide continuous and reliable HR assessment.(7) ECG may be faster and more reliable than pulse oximetry or auscultation in providing accurate HR assessment, with no technical difficulties in applying the leads.(6,7,53) A study from a local neonatal unit showed that not only was it faster to apply the ECG leads than a pulse oximetry probe (27 seconds vs. 33.5 seconds, p < 0.001), but reliable data acquisition was also faster with ECG (10 seconds vs. 30.5 seconds, p < 0.001).(54) However, ECG cannot replace the need for pulse oximetry to assess oxygenation and perfusion.
Recommendations on assessment of heart rate and oxygen saturation
Auscultation is the preferred method for the initial assessment of HR. If a stethoscope is not available, umbilical cord palpation may be used.
Use of ECG should be considered when advanced resuscitation is anticipated.
Pulse oximetry should be used to evaluate oxygen saturation during resuscitation.
POSITIVE PRESSURE VENTILATION
Inspiratory and expiratory pressures for providing positive pressure ventilation
Effective PPV is the most important step for successful resuscitation in newborns with apnoea or bradycardia.(22) The majority of non-vigorous newborns respond to the initial steps and PPV, with the risk of death or prolonged admission increasing by 16% for every 30-second delay in initiating PPV.(7,55)
Inflation pressures up to 30 cm H2O in term newborns and up to 25 cm H2O in preterms are sufficient to inflate the lungs. High tidal volumes are associated with lung injury, impaired gas exchange and reduced lung compliance in immature animals, and severe IVH in preterm newborns.(22,56)
During PPV, use of positive end-expiratory pressure (PEEP) helps to maintain alveolar recruitment, resulting in lower intubation rates, lower inspiratory pressure, shorter duration of PPV and higher number of infants resuscitated in room air.(57-60) Use of PEEP is associated with increased survival to discharge without CLD, severe IVH or PVL (odds ratio 1.38, 95% CI 1.06–1.80).(61)
Recommendations on pressure for providing PPV
PPV should be initiated within 60 seconds (the ‘golden minute’) after birth in newborns who remain apnoeic, gasping or bradycardic (HR < 100/min) despite the initial steps.
Initiate PPV with an inspiratory pressure of 20–25 cm H2O. Adjust inflation pressure to achieve optimal chest rise.
In preterm infants with gestational age < 33 weeks who require PPV, a PEEP of 5 cm H2O is suggested. In newborns with gestational age ≥ 33 weeks, provision of PEEP may be beneficial.
Rate and inspiratory time during PPV
A short inspiratory time of < 1 second while providing PPV matches the natural breathing pattern in newborns.(62) Sustained lung inflation (SLI) with an inspiratory time > 5 seconds has shown a decreased requirement for mechanical ventilation compared with conventional PPV or continuous positive airway pressure (CPAP).(63-69) However, a recent systematic review showed no difference in the primary outcome of death before discharge (RR 1.09, 95% CI 0.83–1.43) as well as other pre-specified critical outcomes.(70-72) A large randomised controlled trial was terminated early owing to increased early death in newborns with gestational age < 29 weeks who were randomised to SLI (RR 2.42, 95% CI 1.15–5.09).(73)
Recommendations on rate and inspiratory time during PPV
In term and preterm newborns requiring PPV, it is reasonable to initiate PPV with an inspiratory time ≤ 1 second, at a rate of 40–60 breaths per minute.
In preterm newborns, we do not recommend routine initial SLI for > 5 seconds to initiate resuscitation. SLI may be considered only in research settings.
OXYGEN ADMINISTRATION
Term and preterm newborns administered high oxygen concentrations are vulnerable to free radical formation and tissue injury. Oxygen use in newborns was reviewed by the NLS task force and published as a meta-analysis as well as an ILCOR CoSTR statement.(74,75) Among newborns with a gestational age ≥ 35 weeks who were receiving respiratory support at birth, 40 fewer deaths out of 1,000 deaths were observed with 21% vs. 100% oxygen, with no difference in HIE and long-term neurodevelopmental impairment. For preterm newborns with a gestational age < 35 weeks, a comparison of lower (≤ 50%) vs. higher (> 50%) initial oxygen concentration showed no effect on short- or long-term morbidity or mortality.
The European Resuscitation Council (2021) has supported a recent European consensus statement recommending a gestational age-dependant graded use for the starting fraction of inspired oxygen (FiO2). 30% oxygen was recommended for newborns with gestational age < 28 weeks, 21%–30% for 28–31 weeks and 21% for > 31 weeks.(8,76)
Recommendations on use of supplemental oxygen
For preterm newborns with gestational age < 33 weeks, resuscitation should be initiated at 21%–30% oxygen. If an oxygen blender is unavailable, a self-inflating bag without a reservoir that is connected to pure oxygen delivers about 40% oxygen and may be an acceptable alternative.
For newborns with gestational age ≥ 33 weeks, resuscitation should be commenced at 21% oxygen.
Supplemental oxygen should be titrated in accordance with target preductal (right hand) minute specific oxygen saturation ranges (Fig. 1).
CONTINUOUS POSITIVE AIRWAY PRESSURE
In spontaneously breathing preterm newborns with respiratory distress at birth, application of CPAP reduces the risk of death or bronchopulmonary dysplasia at 36 weeks (number needed to treat = 25) compared with intubation or mechanical ventilation, with no differences in pneumothorax rates, IVH, NEC and ROP.(76-81) The optimal PEEP during CPAP is unclear. A randomised controlled trial comparing higher (6–8 cm H2O) vs. lower (3–5 cm H2O) PEEP during neonatal resuscitation until the first 120 hours of life is currently under way.(82)
Recommendation on the use of CPAP
· Support spontaneously breathing preterm newborns in respiratory distress at birth with CPAP (PEEP of 5–6 cm H2O).
ENDOTRACHEAL INTUBATION AND LARYNGEAL MASK AIRWAY
Endotracheal intubation
Tracheal intubation may be considered at several time points during neonatal resuscitation. The size and depth of the ETT are calculated using several methods (Table I).(83-87) The position of the ETT is confirmed by observing chest rise, auscultation for equal breath sounds and prompt increase in HR. Capnography or colorimetric detection of carbon dioxide may be used to ensure appropriate tracheal placement of the ETT, especially during the transport of an intubated newborn.(88-90)
Table I.
Endotracheal tube (ETT) size and depth of tube placement for oral intubation.*
Recommendations for endotracheal intubation
Consider intubation with ETT if mask ventilation is ineffective, chest compressions are initiated, there is a prolonged need for ventilation, there is requirement of tracheal toileting for presumed airway obstruction, and in special circumstances (e.g. diaphragmatic hernia).
Use of capnography or colorimetric detection of carbon dioxide to confirm endotracheal (ET) intubation is suggested.
Laryngeal mask airway
A recent systematic review reported that respiratory management with laryngeal mask airway (LMA) is feasible for a defined subgroup of newborns (gestational age ≥ 34 weeks, weight > 1,500 g), although current evidence is insufficient to recommend the LMA instead of face mask ventilation in the delivery room.(91)
Recommendation for laryngeal mask airway
LMA may be used as an airway device when intubation is not successful or feasible in late preterm and term newborns.
CHEST COMPRESSION
Based on expert opinion, newborns whose HR remains < 60/min despite 30 seconds of effective ventilation require circulatory support to supply oxygenated blood to the brain and vital organs. Previous recommendations on neonatal cardiopulmonary resuscitation (CPR) remain unchanged,(5-8,21,22) with synchronised compression to ventilation at a ratio of 3:1. Animal studies that compared this with alternate ratios did not show any advantage with respect to return of circulation or survival.(92-96) The two-thumb-encircling hands technique of chest compression is associated with improved blood pressure and less provider fatigue compared with the two-finger technique.(97,98) Chest compressions can be performed from the side or from above the head-end once the airway is secured, to facilitate placement of an umbilical venous (UV) catheter.
Recommendations on chest compressions
Chest compressions should be commenced if the HR remains < 60/min after at least 30 seconds of effective PPV.
When chest compressions are initiated, increase inspired oxygen to 100% and titrate to target, based on pulse oximetry.
The two-thumb, hands-encircling-chest technique is recommended. Thumbs (overlapping thumb in a small newborn) are placed over the lower third of the sternum.
Depress the sternum about one-third of the anteroposterior diameter of the chest and release to allow chest recoil and ventilation.
Chest compressions should be coordinated with ventilation at a 3:1 ratio, providing 90 compressions and 30 inflations (120 events) per minute.
Reassess HR, oxygen saturation and return of spontaneous breathing after every 60 seconds of coordinated chest compression and ventilation.
MEDICATIONS
Intravascular access
In circumstances where circulation fails to return with synchronised PPV and chest compressions, medications and/or volume expanders are recommended to maintain circulation. UV catheterisation is a safe and easy vascular access.(7,99) If this is not feasible or fails, medications and fluids may be delivered via the intraosseous (IO) route.(22,99-101) Case reports of tibial fractures, compartment syndrome from extravasation of fluid and medications, and amputation have been reported from IO access, particularly in preterm newborns.(100,102-106)
Recommendations on intravascular access
UV catheterisation remains the standard method of vascular access in delivery room resuscitation.
If UV access is not feasible, the IO route may be used with caution, especially in preterm newborns.
Adrenaline
Adrenaline, with its vasoconstrictive effect, increases blood flow to the coronary vessels, improving cardiac contractility and return of spontaneous circulation (ROSC). Studies comparing the efficacy of intravenous (IV) versus ET adrenaline in newborns demonstrate no significant difference in efficacy between initial ET and initial IV dose.(107,108) However, most newborns require at least one dose of IV adrenaline before ROSC.(4,109) An animal study showed faster and higher rates of ROSC with 0.3 mL/kg of IV adrenaline compared with 1 mL/kg of ET adrenaline.(110) Use of saline flush following intravenous administration improves medication delivery.(111,112)
Recommendations on use of adrenaline
If HR remains < 60/min after one minute of CPR, IV adrenaline (1 in 10,000; 0.1 mg/mL) is recommended at a dose of 0.1–0.3 mL/kg (0.01–0.03 mg/kg), administered rapidly followed by a 3-mL saline flush.
Continue CPR after adrenaline and assess response after 60 seconds. Repeat adrenaline every 3–5 minutes if HR remains < 60/min.
If the IV route is not immediately available, administer ET adrenaline (1 in 10,000; 0.1 mg/mL) at 0.5–1 mL/kg. Administer IV adrenaline once intravascular access is obtained.
Volume replacement
Newborns who do not respond to advanced resuscitation may have hypovolaemia and occult blood loss; hence, a trial of volume administration may be considered.(9,10) Both animal and human studies support the use of crystalloids over albumin as the first choice for volume expansion.(113-117)
Recommendations on volume replacement
Early volume replacement in newborns is recommended following non-response to advanced resuscitation, even if blood loss is not apparent.
10 mL/kg of 0.9% saline administered over 5–10 minutes is the first choice.
Uncross-matched O, Rh-negative blood is recommended when blood loss or anaemia is suspected.
Use of sodium bicarbonate in resuscitation
Severe metabolic acidosis during prolonged resuscitation may depress myocardial contractility. This forms the basis of considering sodium bicarbonate administration. There is, however, no role for its use during brief resuscitation.(9,10)
Recommendation on use of sodium bicarbonate
Consider sodium bicarbonate (2–4 mL/kg of 4.2% sodium bicarbonate) only in prolonged cardiac arrest unresponsive to adequate ventilation synchronised with chest compression, adrenaline and/or volume expansion.
POST-RESUSCITATION CARE
Newborns may continue to have substantial dysregulation of their metabolic and homeostatic adaptation following successful resuscitation. Hence, close monitoring and anticipatory care are required.
Glucose control
Newborns requiring resuscitation are prone to hypoglycaemia and impaired glucose homeostasis, which predispose them to adverse neurodevelopmental outcomes.(118-121)
Recommendations on glucose control
Monitor blood glucose following resuscitation at appropriate intervals.
Avoid hypoglycaemia, hyperglycaemia and wide fluctuations in blood glucose.
Early institution of glucose infusion or parenteral nutrition is recommended for newborns at risk of hypoglycaemia.
Therapeutic hypothermia
Need for advanced resuscitation is highly predictive of HIE.(109,122-126) A Cochrane review conclusively demonstrated that therapeutic hypothermia (TH) significantly reduces the risk of death or major neurodisability at 18 months in term and near-term newborns with moderate to severe perinatal asphyxia (RR 0.75, 95% CI 0.68–0.83).(127) Current evidence is insufficient to recommend a change in practice for newborns with gestational age < 36 weeks. There is insufficient evidence to recommend TH in the setting of mild HIE, delayed initiation for > 6 hours, TH beyond 72 hours or target temperature below 33°C.(128-130)
Recommendations on therapeutic hypothermia
TH should be offered to infants with gestational age ≥ 36 weeks with moderate to severe HIE within six hours of life.
TH should be performed as per established protocols, and core temperature should be maintained between 33°C and 34°C for 72 hours. Rewarming to 36.5°C should be achieved slowly in no less than four hours.
Newborns requiring TH should be managed in centres that have the appropriate expertise and support, including the provision of longitudinal follow-up care.
WITHHOLDING RESUSCITATION AND DISCONTINUING RESUSCITATIVE EFFORTS
Options of withholding or discontinuing resuscitative efforts are best discussed with parents in the framework of shared decision-making.(131-135) Both options are ethically equivalent.(136)
Withholding resuscitation
When a newborn faces certain early death or there is high anticipated burden in the event of survival owing to resuscitative measures, withholding resuscitation may be reasonable. A coordinated approach and communication between the parents and different stakeholders from the neonatal and obstetric teams ensure consistency in management.(137-139) Maximal resuscitation should be provided until the parents have been consulted.(131)
Recommendations on withholding resuscitation
Resuscitation of newborns with gestational age < 23 weeks is not recommended.
It may be reasonable to attempt resuscitation in newborns with gestational age ranging from 23+0 to 23+6 weeks if the parents express a strong wish for resuscitation. Decisions must be additionally guided by the certainty of gestation and other risk factors, condition at birth and response to initial resuscitation measures.
At 24+0 to 24+6 weeks, it would be normal practice to offer full resuscitation unless the parents and clinicians make a shared decision against it based on the baby’s clinical condition and best interest principles.
When antenatally identified conditions are associated with almost certain early death or unacceptably poor outcomes among survivors (e.g. anencephaly), resuscitation should not be offered.
Discontinuing resuscitation
There is no evidence that any specific duration of resuscitation is universally predictive of mortality or adverse neurodevelopmental outcomes.(140) Recent reports reveal a small but definite possibility of ROSC and acceptable outcome despite an Apgar score of 0 at ten minutes.(123,141) Response to resuscitation may not be apparent until all steps of resuscitation are performed and reversible causes are treated; this may take longer than ten minutes.(142)
Recommendations on discontinuing resuscitation
If 20 minutes of optimal resuscitation and correction of all reversible causes do not result in ROSC or cardiac activity, resuscitation may be discontinued.
The decision to continue or discontinue resuscitative efforts must be individualised and discussed with the parents.
OUT-OF-HOSPITAL RESUSCITATION OF NEWBORN INFANTS
Emergency services dealing with unexpected births in the community should have trained personnel who are expected to carry the appropriate equipment. Out-of-hospital deliveries should ideally be attended by two personnel, one of whom should be competent in PPV and chest compression.(8)
Recommendations on out-of-hospital resuscitation of newborns
First responders are recommended to follow the neonatal resuscitation algorithm, with a focus on supporting transition, temperature maintenance and breathing with bag-mask ventilation, if required.
ECG may be used to monitor the HR, or a portable pulse oximeter may be used to monitor HR and oxygen saturation at resuscitation and during transit.
Information about gestation, number of babies, presence of recognised risk factors and need for resuscitation should be communicated early and clearly to the receiving hospital.
BRIEFING AND DEBRIEFING
Implementation of video-assisted, performance-focused debriefings improved neonatal resuscitation skills, adherence to best practice guidelines and team performance.(143) The use of pre-briefing and debriefing checklists during neonatal resuscitation was helpful in improving communication.(144,145)
Recommendations on briefing and debriefing
Briefing before delivery should be conducted where possible.
In a multi-member team, a team leader should assign roles and responsibilities to team members, anticipate interventions and provide a short briefing if time permits.
Debriefing after neonatal resuscitation is encouraged.
TRAINING FREQUENCY
Several studies have shown that providers who received frequent refresher training and booster simulations showed better procedural skills and teamwork behaviours, with potential impact on neonatal outcomes.(146-148)
Recommendation on retraining of providers
It is recommended that individual providers attend regular focused retraining of skills and knowledge at two-yearly intervals or more frequently, where possible.
INFECTION PREVENTION AND CONTROL
The 2003 severe acute respiratory syndrome outbreak and COVID-19 pandemic have led us to refocus our attention on ensuring appropriate infection prevention and control (IPC) measures during all neonatal resuscitation standbys. Specific recommendations relating to newborn resuscitation in COVID-19 for Singapore have recently been published.(149,150) Additional institution-specific workflows pertaining to enhanced transmission-based precautions may be developed in collaboration with the individual IPC teams. Simulation training can facilitate safe neonatal resuscitation practices during specific IPC situations.
Recommendations on IPC
Standard precautions should be observed for all neonatal deliveries.
Transmission-based precautions are required in situations dealing with unique infections. Additional considerations on processes, preparation, site of delivery, personal protective equipment and personnel will ensure the safety of the patients and healthcare workers alike.
CONCLUSION
The 2020 guidelines from ILCOR, AHA and ERC 2021 are a testament to the extensive appraisal of information that has emerged since the 2015 review. While the 2015 resuscitation algorithm remains unchanged, many of the existing recommendations were reaffirmed. Some received stronger support (e.g. no routine tracheal suctioning of newborns delivered in the setting of meconium-stained liquor), while for others, caution was raised from emerging safety data (e.g. harm in preterm newborns following SLI). Still, many questions remain for future reviews (e.g. the optimal initial FiO2 for preterm newborns). The Singapore Neonatal Resuscitation Guidelines 2021 represent the consensus view of a workgroup of neonatologists who reviewed the current evidence and developed recommendations that are relevant for local practice.
ACKNOWLEDGEMENTS
The authors thank Prof Lim Swee Han, Chairman, SRFAC, and Senior Consultant, Department of Emergency Medicine, Singapore General Hospital; all the instructors of the Singapore Neonatal Resuscitation Course for their contributions in training and education; and Dr Dimple Rajgor for helping with the formatting and submission of this manuscript for publication.
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