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NRP updates

2O2O
G Trinity Deepak,
Senior Resident, Dept. of Neonatology.
Learning Objectives
 Evidence relevant to Resuscitation
 NRP is not the scope
 Areas of interest for research-[ knowledge gaps.. ]
 Salient take home messages
Brief history
 NRP first published in 1987
Relevance…
85% initiate breathing spontaneously

10% after drying and stimulation

5% of term infants receive (PPV)

2% are intubated
0.1%0.05
receive
%
cardiac
recei
compressions
ve
com
press
ions
with
epine
Literature reviewed…
 Systematic review (SysRev)
 Scoping review (ScopRev)
 Evidence update (EvUp)
GRADE
LEVEL (QUALITY) OF
EVIDENCE
LEVEL A LEVEL B-NR (Nonrandomized)
High-quality evidence‡ from Moderate-quality evidence‡ from 1 or more well-designed, well-
more than 1 RCT executed nonrandomized studies, observational studies, or
Meta-analyses of high-quality registry studies
RCTs Meta-analyses of such studies
One or more RCTs corroborated
by high-quality registry studies LEVEL C-LD (Limited Data)
Randomized or nonrandomized observational or registry studies
with limitations of design or execution
Meta-analyses of such studies
LEVEL B-R (Randomized) Physiological or mechanistic studies in human subjects
Moderate-quality evidence‡ from
1 or more RCTs LEVEL C-EO (Expert Opinion)
Meta-analyses of moderate- Consensus of expert opinion based on clinical experience
quality RCTs
CLASS (STRENGTH) OF
RECOMMENDATION
CLASS 1 (STRONG) Benefit >>> Risk CLASS 2a (MODERATE) Benefit >> Risk
Suggested phrases for writing recommendations: Suggested phrases for writing
 Is recommended recommendations:
 Is indicated/useful/effective/beneficial  Is reasonable
 Should be performed/administered/other  Can be useful/effective/beneficial
 Comparative-Effectiveness Phrases†:  Comparative-Effectiveness Phrases†:
• Treatment/strategy A is • Treatment/strategy A is probably
recommended/indicated in preference to recommended/indicated in preference to
treatment B treatment B
• Treatment A should be chosen over • It is reasonable to choose treatment A
treatment B over treatment B
CLASS (STRENGTH) OF
RECOMMENDATION
CLASS 2b (WEAK) Benefit > Risk CLASS III: Harm (STRONG) Risk > Benefit
Suggested phrases for writing recommendations: Suggested phrases for writing
May/might be reasonable recommendations:
May/might be considered Potentially harmful
Usefulness/effectiveness is Causes harm
unknown/unclear/uncertain or not well established Associated with excess morbidity/mortality
CLASS 3: No Benefit (WEAK) Benefit = Risk Should not be performed/administered/other
Suggested phrases for writing recommendations:
Is not recommended
Is not indicated/useful/effective/beneficial
Should not be performed/administered/other
1. Anticipation and Preparation
2. Initial Assessment and Intervention
3. Physiological Monitoring and Feedback Devices
4. Ventilation and Oxygenation Circulatory Support
5. Drug and Fluid Administration
6. Prognostication During CPR
7. Postresuscitation Care
Anticipation and
Preparation
Prediction of need of respiratory
support in the delivery room
Effect of briefing/debriefing
following neonatal resuscitation
 New topic
 The ScopRev identified 1 RCT and 3 observational studies of
pre-intervention and post-intervention design.
 One study considered video debriefing
 1 considered the use of a checklist combined with video
debriefing
 1 considered the use of a checklist with a team prebrief/debrief
as the key element in a quality improvement bundle
Effect of briefing/debriefing
following neonatal resuscitation
Briefing or debriefing may improve short-term clinical and
performance outcomes for infants and staff.
The effects of briefing or debriefing on long-term clinical
and performance outcomes are uncertain.
Recommendations for Anticipating Resuscitation Need

COR LOE Recommendations


    1. Every birth should be attended by at least 1 person who can
    perform the initial steps of newborn resuscitation and
1 B-NR initiate PPV, and whose only responsibility is the care of the
newborn.1–4
    2. Before every birth, a standardized risk factors assessment tool
    should be used to assess perinatal risk and assemble a qualified
1 B-NR team on the basis of that risk.5–7
    3. Before every birth, a standardized equipment checklist should
    be used to ensure the presence and function of supplies and
1 C-LD equipment necessary for a complete resuscitation.8,9
    4. When anticipating a high-risk birth, a preresuscitation team
    briefing should be completed to identify potential interventions
1 C-LD and assign roles and responsibilities.8,10–12
Initial Assessment
and Intervention
Initial Temperature at birth
Recommendations for Temperature Management
COR LOE Recommendations
 1 B-NR 1. Admission temperature should be routinely recorded.1,2

1 C-EO 2. The temperature of newly born babies should be maintained


between 36.5°C and 37.5°C after birth through admission and
stabilization.2
1 B-NR 3. Hypothermia (temperature less than 36°C) should be prevented
due to an increased risk of adverse outcomes.3–5

2a B-NR 4. Prevention of hyperthermia (temperature greater than 38°C) is


reasonable due to an increased risk of adverse outcomes.4,6
Warming adjuncts
 Population: Preterm neonates less than 32  – Secondary:
weeks’ gestational age who are under radiant  Survival (critical)
warmers in the hospital delivery room  Morbidities associated with hypothermia
(important)
 Intervention: Increased room temperature,
 Hyperthermia and associated morbidities
thermal mattress, or another warming adjunct (important)
 Comparator: Compared with plastic wraps
alone

 Outcome:
 – Primary: Hypothermia (less than 36.0°C) on
admission to neonatal intensive care unit
(NICU)
Warming adjuncts
Additional Recommendations for Interventions to Maintain or Normalize Temperature
COR LOE Recommendations
    1. Placing healthy newborn infants who do not require resuscitation skin-to-skin after birth can be effective in
2a B-R improving breast- feeding, temperature control and blood glucose stability. 8

   2. It is reasonable to perform all resuscitation procedures, including endotracheal intubation, chest compressions,
2a C-LD and insertion of intravenous lines with temperature-controlling interventions in place. 9

    3. The use of radiant warmers, plastic bags and wraps (with a cap), increased room temperature, and warmed
2a   humidified inspired gases can be effective in preventing hypothermia in preterm babies in the delivery room. 10,11
B-R

    4. Exothermic mattresses may be effective in preventing hypothermia in preterm babies. 11


2b B-R
  5. Various combinations of warming strategies (or “bundles”) may be reasonable to prevent hypothermia in very
2b B-NR preterm babies.12

  6. In resource-limited settings, it may be reasonable to place newly born babies in a clean food-grade plastic bag
2b C-LD up to the level of the neck and swaddle them in order to prevent hypothermia. 13
Warming adjuncts
 Combination of interventions that may include environmental temperature
23°C to 25°C,
 Warm blankets,
 Plastic wrapping without drying,
 Cap, and
 Thermal mattress to reduce hypothermia (temperature less than 36.0°C)
on admission to NICU (weak recommendation, very low-certainty evidence).
 Hyperthermia (greater than 38.0°C) be avoided because it introduces
potential associated risks (weak recommendation, very low-certainty evidence).
Suctioning of clear fluid
 Population: Newborns delivered through  – Oxygen supplementation, use of PPV, intubation,
clear amniotic fluid CPR/medications, Apgar scores, time to reach heart
rate greater than 100/min (important)
 Intervention: Immediate routine suctioning  – Complications following procedure (desaturation,
(oropharyngeal or nasopharyngeal) delay in initiation of PPV, tissue injury, infection)
 – Respiratory complications (respiratory distress,
 Comparator: No suctioning or wiping tachypnea) (important)
 – Other inpatient morbidities (important)
 Outcome21:
 – Survival (critical)  Study design: RCTs and nonrandomized
 – Need for delivery room resuscitation and studies (non-RCTs, interrupted times series,
stabilization interventions (important) controlled before-and-after studies, cohort
studies) were eligible for inclusion
Suctioning of clear fluid
 Vagal-induced bradycardia as well as increased risk of infection.2
 Significant time to complete.
Routine intrapartum oropharyngeal and nasopharyngeal
Delay initiation
suctioning of ventilation
for newborn in non-breathing
infants with clear orinfants.
meconium-stained
amniotic fluidlower
Significantly is nooxygen
longersaturation
recommended.
through the first 6 minutes of
life and took longer to reach a normal saturation range.
 Irritation to mucous membranes, apnea, hypoxemia and arterial
oxygen desaturation, hypercapnia, impaired cerebral blood flow
regulation, increased intracranial pressure, and development of
subsequent neonatal brain injury.
Tracheal intubation / suction of non-
vigorous meconium-stained newborns
 Population: Non vigorous infants born at  Outcome21:
34 weeks’ or greater gestation delivered  – Primary
through meconium-stained amniotic fluid  Survival to hospital discharge (critical)
(of any consistency) at the start of  – Secondary
resuscitation (nonvigorous defined as heart  Neurodevelopmental impairment (critical)
rate less than 100/min, decreased muscle  MAS (critical)
tone, and/or depressed breathing at  Other respiratory outcomes (continuous positive
delivery) airway pressure or mechanical ventilation,
treatment of pulmonary hypertension with
 Intervention: Immediate laryngoscopy with inhaled nitric oxide, oral medications or
or without intubation and suctioning extracorporeal membrane oxygenation)
(important)
 Comparator: Immediate resuscitation
 Delivery room interventions (CPR/medications,
without direct laryngoscopy at the start of intubation for PPV) (important)
resuscitation  Length of hospitalization (important)
Tracheal intubation / suction of non-
vigorous meconium-stained newborns
For non-vigorous newborn infants delivered through meconium-
stained amniotic fluid, we suggest against routine immediate direct
laryngoscopy with or without tracheal suctioning compared with
immediate resuscitation without direct laryngoscopy (weak
recommendation, low-certainty evidence).
Tracheal intubation / suction of non-
vigorous meconium-stained newborns
 Additional RCTs are needed that focus on non-vigorous
infants in incidence of MAS is low, and in settings with
various levels of healthcare resources.
 Risks or benefits of intubation with tracheal suctioning
vary with any subgroup (gestational age, thickness of
meconium, operator experience)?
 Long-term outcomes are needed in future studies.
UMBILICAL CORD
MANAGEMENT
Recommendations for Umbilical Cord Management

COR LOE Recommendations


    1. For preterm infants who do not require resuscitation at birth, it
    is reasonable to delay cord clamping for longer than 30 s.1–8
2a B-R
    2. For term infants who do not require resuscitation at birth, it
    may be reasonable to delay cord clamping for longer than 30 s.9–21
2b C-LD
    3. For term and preterm infants who require resuscitation at birth,
    there is insufficient evidence to recommend early cord clamping
2b C-EO versus delayed cord clamping.22
    4. For infants born at less than 28 wk of gestation, cord milking is
3: No Benefit B-R not recommended.23
ABC?
Physiological
Monitoring and
Feedback Devices
Heart rate monitoring during
neonatal resuscitation
 Population: Newborns  New heart rate monitors,
requiring resuscitation digital stethoscopes,
 Intervention: ECG monitoring photoplethysmography
methods in addition to pulse
 Comparator: Oximetry or oximetry, and Doppler
auscultation ultrasonography methods with
 Outcome: Measurement of auditory or visual displays.
heart rate (speed and New interfaces for ECG
reliability) (important)21 monitoring include dry
electrode technology
Ventilation and
Oxygenation
Sustained inflation
 Population: Newborn infants who  – Secondary:
receive PPV due to bradycardia or  Death in the delivery room (critical)
 Death within first 48 hours (critical)
ineffective respirations at birth
 Need for mechanical ventilation during
 Intervention: Initiation of PPV with hospitalization (critical)
sustained inflation(s) more than 1  Air leaks
second  Bronchopulmonary dysplasia,)
 Intraventricular hemorrhage:
 Comparator: Initiation of PPV with
 Retinopathy of prematurity: Death by time of
intermittent inflations, lasting 1 second latest follow-up (critical)
or less per breath  Long-term neurodevelopmental or behavioral or
education outcomes (greater than18 months of
 Outcome21: corrected age; test used to assess
 – Primary: Death before discharge (critical) neurodevelopmental outcome should be of
adequate quality and validated) (critical)
Sustained inflation - Why?
Sustained inflation
Outcome Article With Total, n Certainty of RR (95% CI); Absolute Difference (95% CI)
Outcome of Interest
Evidence I2
Lindner, 200557;
Death before discharge Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1502 Low 1.09 (0.83–1.43); 10/1000 more patients died before discharge when PPV was initiated with sustained
Jiravisitkul, 2017 61;
Ngan, 201762;
El-Chimi, 201763; 42% inflation(s) >1 s compared with initiating PPV with intermittent inflations lasting ≤1 s per
El-Fattah, 201764;
Kirpalani, 201965;
La Verde, 201966 breath (18 fewer to 47 more per 1000)

2.82 (0.45–17.66); 4/1000 more patients died in the DR when PPV was initiated with sustained inflation(s) >1 s
Linder, 200557;
Death in the DR Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1076 Very low
Jiravisitkul, 2017 61;
Ngan, 201762; El-Chimi, 201763;
El-Fattah, 201764; 0% compared with initiating PPV with intermittent inflations lasting ≤1 s per breath (1 fewer to
LaVerde, 201966
33 more per 1000)
18/1000 more patients died within 48 h after birth when PPV was initiated with sustained
Linder, 200557;
Death within 48 h Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1502 Low 2.42 (1.15–5.09);
Jiravisitkul, 2017 61; Ngan, 201762;
El-Chimi, 201763;
El-Fattah, 201764; 8% inflation(s) >1 s compared with initiating PPV with intermittent inflations lasting ≤1 s per
Kirpalani, 201965;
La Verde, 201966
breath (2 more to 51 more per 1000). The number needed to harm is 55 (95% CI, 20–500).
Linder, 200557;
Bronchopulmonary Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1502 Low 0.93 (0.79–1.10); 19/1000 fewer patients developed bronchopulmonary dysplasia when PPV was initiated with
dysplasia Jiravisitkul, 2017 61;
Ngan, 201762;
El-Chimi, 201763; 8% sustained inflation(s) >1 s compared with initiating PPV with intermittent inflations lasting
El-Fattah, 201764;
Kirpalani, 201965;
La Verde, 201966 ≤1 s per breath (58 fewer to 27 more per 1000)
Linder, 200557;
Intraventricular Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1390 Low 0.88 (0.63–1.23); 11/1000 fewer developed intraventricular hemorrhage Grade 3 or 4 when PPV was initiated
hemorrhage Grade 3 or 4 Jiravisitkul, 2017 61;
Ngan, 201762;
El-Fattah, 201764; 0% with sustained inflation(s) >1 s compared with initiating PPV with intermittent inflations
Kirpalani, 201965;
La Verde, 201966
lasting ≤1 s per breath (35 fewer to 22 more per 1000)
Linder, 200557;
Retinopathy of prematurity Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1342 Low 0.83 (0.62–1.11); 22/1000 fewer patients developed retinopathy of prematurity Stage 3 or higher when PPV
Stage 3 or higher Jiravisitkul, 2017 61;
Ngan, 201762;
El-Fattah, 201764; 19% was initiated with sustained inflation(s) >1 s compared with initiating PPV with intermittent
Kirpalani, 201965;
La Verde, 201966
inflations lasting ≤1 s per breath (49 fewer to 14 more per 1000)
Lista, 2015 58;
Use of mechanical Mercadante, 2016 60;
Jiravisitkul, 2017 61;
El-Chimi, 201763;
813 Low 0.87 (0.74–1.02); 51/1000 fewer patients received mechanical ventilation during their hospitalization when
ventilation during El-Fattah, 201764;
La Verde, 201966
0% PPV was initiated with sustained inflation(s) >1 s compared with initiating PPV with
hospitalization intermittent inflations lasting ≤1 s per breath (103 fewer to 8 more per 1000)

9/1000 more patients developed airleak during their hospitalization when PPV was initiated
Linder, 200557;
Airleak during Lista, 2015 58;
Schwaberger, 2015 59;
Mercadante, 2016 60;
1076 Low 1.26 (0.72–2.21);
hospitalization Jiravisitkul, 2017 61;
Ngan, 201762;
El-Chimni, 201763; 17% with sustained inflation(s) >1 s compared with initiating PPV with intermittent inflations
El-Fattah, 201764;
La Verde, 201966
lasting ≤1 s per breath (9 fewer to 41 more per 1000)
Sustained inflation
 Preterm -PPV -suggest against the routine use of initial
sustained inflation(s) greater than 5 seconds (weak recommendation,
low-certainty evidence).

 Term or late preterm infants -PPV not possible to


recommend any specific duration for initial inflations due to
the very low confidence in effect estimates.
Sustained inflation
 How much of a role does glottis closure play in
determining the effectiveness of sustained inflation in
newborn infants of different gestational ages?
 What is the optimal duration, optimal inspiratory pressure,
and number of sustained inflation maneuvers that allow
establishment of functional residual capacity without
barotrauma?
Sustained inflation
 Studies comparing short duration sustained inflation (less than
5 seconds) with intermittent inflations (inspiratory time 1
second or less) are needed. This is an important knowledge
gap as the European Resuscitation Council currently
recommends using inflations of a 2- to 3-second duration for
the first 5 breaths in infants who are gasping or not breathing.
 Is there a role for sustained inflation for other situations in
resuscitation, such as during cardiac compressions? (For more
detail, see EvUp for NLS 895 CPR Ratios)
Positive end-expiratory pressure
(PEEP) versus no PEEP
 We suggest using PEEP for the initial ventilation of
premature newborn infants during delivery room
resuscitation (weak recommendation, low-quality
evidence).
 We cannot make any recommendation for term infants
because of insufficient data.
Continuous positive airway pressure
(CPAP) versus intermittent PPV
 CPAP is especially helpful for preterm newborn infants
with breathing difficulty after birth or after resuscitation.
 CPAP may also reduce the risk of death or
bronchopulmonary dysplasia in very preterm infants when
compared with endotracheal intubation and PPV
Continuous positive airway pressure
(CPAP) versus intermittent PPV
 Population: Spontaneously  – Bronchopulmonary dysplasia54
breathing preterm newborn (important)
infants with respiratory distress  – Air leak (important)
requiring respiratory support in  – Necrotizing enterocolitis
the delivery room (important)
 – Severe intraventricular
 Intervention: CPAP hemorrhage55(critical)
 Comparator: Intubation and  – Severe retinopathy of prematurity
intermittent PPV 56
(critical)
 Outcome21:
 – Death or bronchopulmonary
dysplasia (critical)
 – Death (critical)
Continuous positive airway pressure
(CPAP) versus intermittent PPV
For spontaneously breathing preterm newborn infants with
respiratory distress requiring respiratory support in the
delivery room,

suggest initial use of CPAP rather than intubation and
intermittent PPV (weak recommendation, moderate
certainly of evidence).
T-piece resuscitator versus self-
inflating bag for ventilation
 Population, Intervention,  – Survival to hospital discharge
Comparator, Outcome, Study (critical)
Design, and Time Frame  – Air leak (important)
 – Development of stable
 Population: Newborn infants
spontaneous breathing (no need for
receiving ventilation (PPV) intubation in delivery room)
during resuscitation (important)
 Intervention: T-piece resuscitator  – Bronchopulmonary dysplasia
(any) (important)
 Comparator: Self-inflating bag
 Outcome21:
T-piece resuscitator versus self-
inflating bag for ventilation
There is insufficient evidence regarding the use of T-piece
resuscitator or self-inflating bag for initial PPV at birth, so
the recommendation of one device over another would be
purely speculative because the confidence in effect
estimates is so low.
Oxygen for preterm resuscitation
 Preterm infants are vulnerable to oxidative stress as a result of
reduced antioxidant defenses and frequent exposure to
oxygen during stabilization in the delivery room.
 Bronchopulmonary dysplasia, retinopathy of prematurity and
intraventricular hemorrhage
Oxygen for preterm resuscitation
 Population: Preterm newborn infants  Long-term NDI (1–3 years) (critical)
(less than 35 weeks’ estimated  Retinopathy of prematurity (Stages III–V) 56
(critical)
gestational age) who receive  Necrotizing enterocolitis Stage II
respiratory support at birth (pneumatosis) or III (surgical)88 (important)
 Intervention: Lower initial oxygen  Bronchopulmonary dysplasia (moderate to
severe)54 (critical)
concentration (50% or less O2)  Major intraventricular hemorrhage (Grade
 Comparator: Higher initial oxygen III–IV)55 (critical)
 Time to heart rate more than 100/min
concentration (more than 50% O2) (important)
 Outcome21:
 – Primary: All-cause short-term mortality
(in hospital or 30 days) (critical)
 – Secondary:
 All-cause long-term mortality (1–3 years)
(critical)
Oxygen for preterm resuscitation
 For preterm newborn infants (less than 35 weeks’ gestation)
who receive respiratory support at birth, we suggest starting
with a lower oxygen concentration (21% to 30%) rather than
higher initial oxygen concentration (60% to 100%) (weak
recommendation, very low-certainty evidence).
 Subsequent titration of oxygen concentration using pulse
oximetry is advised (weak recommendation, very low-certainty evidence).
Oxygen for term resuscitation
 Population, Intervention,  – Primary: All-cause short-term
Comparator, Outcome, Study mortality (in hospital or 30 days)
Design, and Time Frame (critical)
 – Secondary: All-cause long-term
 Population: Newborn infants (35 mortality (1–3 years) (critical)
weeks’ or greater gestation) who  – Long-term NDI (1–3 years) (critical)
receive respiratory support at birth  – HIE (Sarnat Stage 2–3)90 (critical)
 Intervention: Lower initial oxygen
concentration (50% O2 or less)
 Comparator: Higher initial oxygen
concentration (greater than 50% O2)
 Outcome21:
Oxygen for term resuscitation
For newborn infants at 35 weeks’ or greater gestation
receiving respiratory support at birth, we suggest starting
with 21% oxygen (air)
(weak recommendation, low certainty of evidence).

We recommend against starting with 100% oxygen (strong


recommendation, low certainty of evidence).
Circulatory Support
CPR ratios for neonatal
resuscitation
 Population, Intervention,  – Time to ROSC (critical)
Comparator, Outcome, Study Design,  – Perfusion (important)
and Time Frame  – Gas exchange (important)
 Population: In newborn infants  – Tissue injury (important)
receiving cardiac compressions  – Compressor fatigue (important)

 Intervention: other ratios (5:1. 9:3, 15:2,  We suggest continued use of a 3:1
synchronous, etc) compression-to-ventilation ratio for
 Comparator: 3 compressions, 1
neonatal CPR
(weak recommendation, very low-quality evidence).
ventilation
 Outcome21:
 – Return of spontaneous circulation
(ROSC) (critical)
 – Survival (critical)
 – Neurodevelopmental impairment
CPR ratios for neonatal
resuscitation
 The NLS Task Force is aware of an ongoing study of a
new neonatal compression technique, with compressions
delivered while maintaining a sustained inflation
2-thumb versus 2-finger compressions
for neonatal resuscitation
 Population, Intervention,  – Neurodevelopmental impairment
Comparator, Outcome, Study (critical)
Design, and Time Frame  – Perfusion (important)
 – Gas exchange (important)
 Population: In newborn infants
 – Compressor fatigue (important)
receiving cardiac compressions
 Intervention: 2-thumb technique  We suggest that chest compressions
in the newborn infant should be
 Comparator: 2-finger technique delivered by the 2-thumb, hands-
 Outcome21: encircling-the-chest method as the
 – ROSC (critical) preferred option (weak
 – Survival (critical)
recommendation, very low-certainty
evidence).
Drug and Fluid
Administration
Epinephrine (Adrenaline) for
Neonatal Resuscitation
When the heart is hypoxic and depleted of energy substrate to the point of cardiac
arrest, providers must reestablish effective perfusion of the myocardium with
oxygenated blood.

Epinephrine (adrenaline) causes vasoconstriction,



which increases the amount of oxygenated blood entering the coronary arteries and
improves myocardial blood flow.
Perfusion of the myocardium with oxygenated blood facilitates the synthesis of ATP
within myocardial mitochondria, thus enhancing cell viability, contractility, and
ROSC
Epinephrine (Adrenaline) for
Neonatal Resuscitation
Outcome Study With Total, n Certainty of RR (95% CI); Absolute Difference (95% CI)
Outcome of Evidence I2
Interest
Mortality before Halling, 20177 50 Very low 1.03 (0.62– 17/1000 more neonates died when initial
hospital 1.71); NA endotracheal (0.05–0.1 mg/kg) versus initial IV
discharge (0.01–0.03 mg/kg) epinephrine was used (209
fewer–391 more per 1000)
Failure to Halling, 20177 97 Very low 0.97 (0.38– 7/1000 fewer failed to achieve ROSC when initial
achieve ROSC Barber, 200693 2.48); 0 endotracheal (0.05–0.1 mg/kg) versus initial IV
(0.01–0.03 mg/kg) epinephrine was used (135
fewer–322 more per 1000)
Time to ROSC Halling, 20177 50 Very low   ROSC was 2 min later when initial endotracheal
(minutes) (0.05–0.1 mg/kg) versus initial IV (0.01–0.03 mg/kg)
epinephrine was used (0.6 min earlier–4.6 min
later)
Epinephrine (Adrenaline) for
Neonatal Resuscitation
 Intravascular adrenaline (0.01–0.03 mg/kg) (weak recommendation, very
low-certainty evidence).

 If intravascular access is not yet available, we suggest


administering endotracheal adrenaline at a larger dose
(0.05–0.1 mg/kg) than the dose used for IV administration
(weak recommendation, very low-certainty evidence).

 The administration of endotracheal adrenaline should not


delay attempts to establish vascular access (weak recommendation, very
low-certainty evidence).
Epinephrine (Adrenaline) for
Neonatal Resuscitation
 We suggest the administration of further doses of
adrenaline every 3 to 5 minutes, preferably intravascularly,
if the heart rate remains less than 60/min (weak recommendation, very
low-certainty evidence).

 If the response to endotracheal (adrenaline) is inadequate,


we suggest that an intravascular dose be given as soon as
vascular access is obtained, regardless of the interval after
any initial endotracheal dose (weak recommendation, very low-certainty evidence).
Epinephrine (Adrenaline) for
Neonatal Resuscitation
 Optimal (heart rate) thresholds for administration of epinephrine (adrenaline)
 Optimal dose and interval of epinephrine (adrenaline)
 Optimal epinephrine dose and intervals specific to gestational age
 Optimal route and method of epinephrine (adrenaline) administration
 Potential harms of epinephrine (adrenaline) (single or multiple doses)
 Effect of vasoactive drugs other than epinephrine (adrenaline)
 Human factors approach to achieve the timely administration of epinephrine
(adrenaline)
 Neurodevelopmental outcomes after epinephrine (adrenaline) use
Intraosseous versus umbilical
vein for emergency access
Intraosseous versus umbilical
vein for emergency access
 Population, Intervention, Comparator,  – Long-term neurodevelopmental outcomes (critical)
Outcome, Study Design, and Time Frame  – ROSC: any signs of cardiac output with heart rate
60/min or greater, and time to ROSC (critical)
 Population: Newborn infants in any setting (in-
 – Brain injury (HIE Stage 2–3 Sarnat,90 [term only],
hospital or out-of-hospital) with cardiac arrest
(includes severe bradycardia and inadequate intraventricular hemorrhage Grades 3–4, 55
periventricular leukomalacia, preterm only) (critical)
perfusion requiring chest compressions)
 – Time to secure access (important)
 Intervention: Placement of an IO cannula with drug  – Morbidity related to IO (osteomyelitis, fracture,
administration through this IO site during cardiac epiphyseal plate injury, compartment syndrome) or to
arrest IV (extravasation, embolic phenomenon, phlebitis)
(important)
 Comparator: Placement of an IV cannula (umbilical
vein in newborn infants) and drug administration
through this IV during cardiac arrest

 Outcome21:
 – Death during event, within 24 hours and before
hospital discharge (critical)
Intraosseous versus umbilical
vein for emergency access
 We suggest umbilical venous catheterization as the primary
method of vascular access during newborn infant resuscitation
in the delivery room.
Feasible, the intraosseous route is a reasonable alternative for
vascular access during newborn resuscitation
(weak recommendation, very low-certainty evidence).
 Outside the delivery room setting, we suggest that either
umbilical venous access or the IO route may be used to
administer fluids and medications during newborn resuscitation
(weak recommendation, very low-certainty evidence).
Intraosseous versus umbilical
vein for emergency access
 Determination of time from start of CPR to achieving successful IO placement
 Determination time from start of CPR to achieving successful IV placement in umbilical vein
 Optimal IO device suitable for newborn infants
 Optimal site (head of humerus, proximal tibia, other) for successful IO access and drug and fluid
administration
 Short- and long-term safety of IO placement during newborn resuscitation
 Complications related to emergency umbilical venous catheterization
 Pharmacokinetics and plasma availability of drugs administered through IO compared with IV routes
 Optimal training for IO placement and IV umbilical vein placement during neonatal resuscitation
 How to best secure and maintain any emergency vascular access devices
 Optimal method to determine correct placement of any emergency vascular access device
 Whether results of studies in animal and simulation models apply to clinical practice
 IO access during neonatal resuscitation outside the delivery room
Volume infusion during neonatal
resuscitation
 Acute fetal-maternal hemorrhage,
 Bleeding vasa previa,
 Extensive vaginal bleeding,
 Placental laceration,
 Fetal trauma,
 Cord prolapse,
 Tight nuchal cord,
 Blood loss from the umbilical cord
Volume infusion during neonatal
resuscitation
 Early volume replacement with crystalloid or red cells is
indicated for newborn infants with blood loss who are not
responding to resuscitation.
 There is insufficient evidence to support the routine use of
volume administration in the newborn infant with no blood
loss who is refractory to ventilation, chest compressions,
and epinephrine.
Sodium bicarbonate during
neonatal resuscitation
 Population, Intervention, Comparator,  – HIE stage moderate to severe 90 (term infants
Outcome, Study Design, and Time Frame only) (critical)
 – Intraventricular hemorrhage Grades 3 to 4 55
 Population: Newborn infants who are (preterm only) (critical)
receiving resuscitation in the hospital  – Other morbidities in early infancy (eg,
 Intervention: Sodium bicarbonate necrotizing enterocolitis,92 retinopathy of
prematurity,56 bronchopulmonary dysplasia, 54
administration periventricular leukomalacia) (important)
 Comparator: No sodium bicarbonate  – Neurodevelopmental outcomes (critical)

 Outcome21:  Sodium bicarbonate is discouraged during


 – Survival (to hospital discharge or as defined by brief CPR but may be useful during
authors) (critical) prolonged arrests after adequate
 – ROSC (critical) ventilation is established and there is no
response to other therapies.
Prognostication
During CPR
Impact of duration of intensive
resuscitation
 Population: Newborn infants  – Survival (to any age) (critical)
presenting with at least 10  – Neurodevelopmental outcomes
minutes of asystole, bradycardia (critical)
(heart rate less than 60/min), or  – Composite of survival to any age
pulseless electric activity after without moderate or severe
birth for which CPR is indicated neurodisability (critical)
 Intervention: Ongoing CPR for
incremental time intervals
beyond 10 minutes after birth

 Comparator: CPR discontinued


at 10 minutes after birth
Impact of duration of intensive
resuscitation
Subgroup Studies Contributing
Infan Survival Assessed Survivors Composite:
ts, n to Last for NDI Assessed Survival
Follow- Without Without
up Moderate or Moderate or
Severe NDI Severe NDI
Casalaz, 1998104
Population Harrington, 2007103 131 13% 88% 60% (9/15) 7% (9/131)
level studies Jain, 1991106
Sproat, 2017111
Zhang, 2019117 (17/131) (15/17)
Therapeutic Ayerapetyan, 2019116
Kasdorf, 2015107
Natarajan, 2013108
206 60% 47% 37% (21/57) 20% (21/105)*
hypothermia Sarkar, 2010109
Shah, 2015110
Shibasaki, 2020112
(122/206) (57/122)
Sproat, 2017111
Zhang, 2019117
Zhong, 2019113

Gestational Ayerapetyan, 2019116


Casalaz, 1998104 286 51% 50% 32% (23/73) 14% (23/166)†
age ≥36 wk Harrington, 2007103
Kasdorf, 2015107
Natarajan, 2013108
Patel, 2004114
(146/286) (73/146)
Sarkar, 2010109
Shah, 2015110
Shibasaki, 2020112
Sproat, 2017111
Zhang, 2019117
Zhong, 2019113

Casalaz, 1998104
Gestational Harrington, 2007103 99 34% 24% 63% (5/8) 12% (5/42)‡
age <36 wk Shah, 2015110
Sproat, 2017111
Zhang, 2019117
Zhong, 2019113
(34/99) (8/34)
Impact of duration of intensive
resuscitation
 However, there is no evidence that any specific duration of
resuscitation consistently predicts mortality or moderate-to-severe
neurodevelopmental impairment.
 If, despite provision of all the recommended steps of resuscitation
and excluding reversible causes, a newborn infant requires
ongoing cardiopulmonary resuscitation (CPR) after birth, we
suggest discussion of discontinuing resuscitative efforts with the
clinical team and family. A reasonable time frame to consider this
change in goals of care is around 20 minutes after birth.
(Weak recommendation, very low-certainty evidence).
Postresuscitation
Care
Rewarming of hypothermic
newborns
 Population: Newborn infants who are hypothermic  – Need for respiratory support (important)
(less than 36.0°C) on admission  – Hypoglycemia (important)

 Intervention: Rapid rewarming  – Episodes of apnea (important)

 Comparator: Slow rewarming


 Outcome21:
 – Survival (to hospital discharge or as defined by
authors) (critical)  The confidence in effect estimates is so low that
 – Convulsions/seizures (critical)
 – Hemorrhage/pulmonary hemorrhage (critical) a recommendation for either rapid rewarming
(0.5°C/h or greater) or slow rewarming (0.5°C/h
or less) of unintentionally hypothermic newborn
infants (temperature less than 36°C) at hospital
admission would be speculative.
Recommendations for Postresuscitation Care
COR LOE Recommendations
 1 A 1. Newly born infants born at 36 wk or more estimated gestational age with evolving
moderate-to-severe HIE should be offered therapeutic hypothermia under clearly defined
protocols.1
 1 C-EO 2. Newly born infants who receive prolonged PPV or advanced resuscitation (intubation,
chest compressions, or epinephrine) should be maintained in
or transferred to an environment where close monitoring can be provided. 2–7
1 C-LD 3. Glucose levels should be monitored as soon as practical after advanced resuscitation, with
treatment as indicated.8–14

 2b C-LD 4. For newly born infants who are unintentionally hypothermic (temperature less than
36°C) after resuscitation, it may be reasonable to rewarm either rapidly (0.5°C/h) or slowly
(less than 0.5°C/h).15–19
Human and System performance
    For participants who have been trained in neonatal
    resuscitation, individual or team booster training should
    occur more frequently than every 2 yr at afrequency that
1 C-LD supports retention of knowledge, skills, and behaviors.1–5

    For neonatal resuscitation providers, it may be reasonable to


2b C-LD brief before delivery and debrief after
neonatalresuscitation.1–3
Topics Not Reviewed in 2020
 Term umbilical cord management (NLS 1551-SysRev in process)  Optimal peak inspiratory pressure (NLS New)

 Preterm umbilical cord management (NLS 787-Sys Rev in process)  Oxygen saturation target percentiles (NLS 1580)

 Babies born to mothers who are hypothermic or hyperthermic (NLS 804)  Use of feedback CPR devices for neonatal cardiac arrest (NLS 862)

 Stimulation for apneic newborns (NLS 1558)  Oxygen use post-ROSC for newborns (NLS 1569)

 Respiratory function monitoring in the delivery room (NLS 806)  Oxygen delivery during CPR (Neonatal) (NLS 738)

 Laryngeal mask for neonatal resuscitation (NLS 618)  Hypovolemia (risk factors for newborns) (NLS 1555)

 Less-invasive surfactant administration (New)  Effect of monitoring technology on team function (NLS 1559)

 CPAP versus increased oxygen for term infants in the delivery room (NLS

1579)
Take home messages…
 Newborn resuscitation requires anticipation and preparation by providers who train
individually and as teams.
 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.
 Inflation and ventilation of the lungs are the priority in newly born infants who
need support after birth.
 A rise in heart rate is the most important indicator of effective ventilation and
response to resuscitative interventions.
 Pulse oximetry is used to guide oxygen therapy and meet oxygen saturation goals.
Take home messages…
 Chest compressions are provided if there is a poor heart rate response to ventilation after
appropriate ventilation corrective steps, which preferably include endotracheal
intubation.
 The heart rate response to chest compressions and medications should be monitored
electrocardiographically.
 If the response to chest compressions is poor, it may be reasonable to provide
epinephrine, preferably via the intravenous route.
 Failure to respond to epinephrine in a newborn with history or examination consistent
with blood loss may require volume expansion.
 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.
THANK YOU

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