Perinatal, neonatal + newborn Flashcards

1
Q

When to evaluate the APGAR score?

A

At minute 1, then minute 5. Every 5 minutes thereafter as long as resuscitation is continuing.

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2
Q

APGAR score definition

A

Not predictive of long-term outcome, but an improvement system for det first minutes of life.
0-4: poor
5-7: fair
8-10: good

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3
Q

How low should the bradycardia be, before starting CPR?

A

Hart rate drops <60/minute after five effective inflation breaths and 30 seconds of effective ventilation

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4
Q

How to calculate APGAR score?

A

Appearance: 0 - blue, 1 - cyanotic/pale, 2 - pink
Pulse: 0 - absent, 1 - <100/min, 2 - >100/min
Grimace (reflex): 0 - absent, 1 - facial grimace, 2 - active withdrawal
Activity (tone): 0 - absent, 1 - weak/passive/flexion, 2 - active
Respiration: 0 - absent, 1 - irregular, shallow, 2 - crying

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5
Q

TTN (transient tachypnoea of the newborn)

A
  • Most common cause of respiratory distress in term infants
  • Caused by delay in the resorption of lung liquid
  • More common in C-section
  • Symptoms: grunting
  • Dx: X-ray may show fluid
  • Tx: PPV
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6
Q

Ventilation breath ration

A

3:1

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7
Q

Asymmetrical growth restriction

A
  • When the weight or abdominal circumference lies on a lower gentile that that of the head.
  • Cause by placenta fails to provide adequate nutrition late in pregnancy, but head is relative spared at the expense of liver glycogen and skin fat
  • Dx: Uteroplacental dysfunction secondary to;
    1. Maternal pre-eclampsia
    2. Multiple pregnancies
    3. Maternal smoking
    4. Ideopathic
  • Increased risk of obesity and DM2 later in life
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8
Q

Symmetrical growth restriction

A
  • Head circumference is equally reduced with the rest of the body
  • Caused by prolonged period of poor intrauterine growth starting in early pregnancy
  • Dx
    1. Small but normal fetus
    2. Fetal chromsome disorder or syndrome
    3. Congenital infection
    4. Maternal drug and alcohol abuse
    5. Maternal chronic medical condition or malnutrition
  • Infants more likely to remain small permanently
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9
Q

After birth, a growth-restricted infant are liable to:

A
  • Hypothermia
  • Hypoglycemia (poor fat an glycogen stores)
  • Hypocalcemia
  • Polycythemia
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10
Q

Vitamin given right after birth?

A

Vitamin K

- To prevent hemorrhagic disease of the newborn

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11
Q

How to test for DDH (developmental dysplasia of the hip)?

A
  • Barlow manoeuvre = hip is held flexed and the femoral head is adducted and pushed downwards. If hip is dislocated, femoral head will be pushed posteriorly out of the acetabulum
  • Ortolani manoeuvre = to see if the hip can be returned from its dislocated position back into the acetabulum.
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12
Q

Risk factors of DDH

A
  • Girls (6-fold increase)
  • Positive family history (20% of affected infants)
  • Breech birth
  • Neuromuscular disorder
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13
Q

A tense fontanelle may be due to:

A
  • Baby is crying
  • Hydrocephalus
  • Late sign of meningitis
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14
Q

Abnormal pulse pressure in femoral pulses, can indicate:

A
  • Reduced
  • Coarctation of the aorta (confirmed by measuring BP in arms and legs)
  • Increased
  • Patent ductus arteriosus
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15
Q

Primitive reflexes

A
  • Moro: sudden extension of head causes symmetrical extension, then flexion of arms
  • Grasp
  • Rooting: head turns to stimulus when touched near the mouth
  • Stepping response
  • Asymmetrical tonic neck reflex: infant adopts an outstretched arm to the side to which the head is turned
  • Sucking reflex
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16
Q

Port wine stain

A
  • Present from birth, usually grows with infant
  • Due to vascular malformation of the capillaries in the dermis
  • Unilateral, distribution of the trigeminal nerve
  • Can be associated with Sturge-Weber syndrome
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17
Q

Immediate effects after hypoxic-ischemic encephalopathy

A
  • Hypoxemia –> Hypercarbia –> Respiratory acidosis

- Low CO –> Decreased tissue perfusion –> Ischemia –> Metabolic acidosis –> Capillary leak, edema

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18
Q

HIE, multi-organ failure

A
  • Encephalopathy: abnormal neuralgic signs, seizures
  • Respiratory failure: persisten pulmonary HTN
  • Myocaridal dysfunction: Hypotension
  • Metabolic: Hypoglycemia, Hypocalcemia, Hyponatremia
  • Renal failure
  • DIC
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19
Q

Erb palsy

A

Upper nerve root (C5 and C6 injury

Usually resolves completely

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20
Q

Other causes of surfactant deficiency than preterm

A
  • Infants of diabetic mothers

- Genetic mutations in the surfactant genes

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21
Q

The benefits of giving clucocorticoides antenatally in expected preterm deliveries

A
  • Reduces RDS
  • Reduces bronchopulmonary dysplasia
  • Reduces intraventricular hemorrhage (IVH)
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22
Q

RDS definition

A
  • Also called hyaline membrane disease

- Deficiency of surfactant –> lowers surface tension –> widespread alveolar collapse and inadequate gas exchange

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23
Q

RDS symptoms, Dx, and Tx

A
Symptoms:
- Tachypnoea >60 breaths/minute
- Laboured breathing with chest wall recession (particularly sternal and subcostal indrawing)
- Nasal flaring
- Expiratory grunting - try to create positive pressure
- Cyanosis - if severe
Dx:
- Chest x-ray: Hypoexpanded, atelectasis, granular or "ground glass" appearance. 
Tx:
- Surfactant directly into the lungs
- NIV - CPAP
- Intubation
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24
Q

Patent ductus arteriosus

A
  • Normal: close within first week of life
  • Shunting: left to right
  • Most common in preterm with RDS
  • Associated with maternal Rubella infection
  • Symptoms: Asymptomatic or apnea, bradycardia, increased oxygen requirement
  • Increased pulse pressure, “bounding”pulses
  • Systolic murmur may be audible - “machinery”
  • If symptomatic –> Indomethacin (PGE synthesis inhibitor) or Ibuprofen
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25
Q

Preterm fluid requirement

A

60-90 ml/kg 1s day of life, then increased by 20-30 ml/kg per day until reached 150-180 ml/kg (about day 5 of life)

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26
Q

Preterm nutritional supplements

A
  • Phosphates
  • Calcium
  • Vitamin D
  • Iron
  • Prebiotics and probiotics for preventing necrotizing enterocolitis
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27
Q

Symptoms of necrotizing enterocolitis

A
  • Feed intolerance
  • Vomiting (may be bile stained)
  • Distended abdomen
  • Fresh blood in stool
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28
Q

X-ray features for necrotizing enterocolitis

A
  • Distended loops of bowel
  • Thickening of the bowel wall with intramural gas (pneumatosis intestinal = pathognomonic)
  • May be gas in the portal venous tract
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29
Q

Tx of necrotizing enterocolitis

A
  • Stop oral feeding
  • Broad spectrum antibiotics
  • Parenteral nutrition
  • Sometimes mechanical ventilation and circulatory support
  • Surgery if bowel perforation
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30
Q

IVH (intraventricular hemorrhages)

A
  • Happens because highly vascularization lining the ventricles
  • Typically occur in the germinal matrix above the caudate nucleus
  • Most occur within the first 72h of life
  • More common following perinatal asphyxia and in infants with severe RDS
  • Antenatal glucocorticoids reduce incidence
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31
Q

Periventricular leukomalacia (PVL)

A
  • Bilateral multiple cysts within the brain parenchyma –> definitive loss of white matter.
  • Following brain ischemia or inflammation
  • 80-90% risk of spastic diplegia, often with cognitive impairment
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32
Q

Cause and Tx of retinopathy in prematurity

A
  • Vascular proliferation –> may progress to retinal detachment, fibrosis and blindness
    Tx:
  • Laser therapy
  • Intravitreal anti-VEFG (anti-vascular endothelial growth factor)
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33
Q

Definiton of Bronchopulmonary Dysplasia (BPD)

A
  • Infants who still have an oxygen requirement at a postmenstrual age of 36 weeks
  • Damage from
    1. Delay in lung maturation
    2. Pressure and volume trauma from artificial ventilation
    3. Oxygen toxicity
    4. Infection
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34
Q

Problems in preterm infants

A
  • Respiratory: RDS, Pneumothorax, BPD, Apnea, Desaturation,
  • Circulation: Hypotension, Patent Ductus Arteriosus
  • Temperature control
  • Nutrition: Nasogastric tube feeding, Feeding intolerance
  • Infection: Main problem is nosocomial infection
  • GI: Necrotizing enterocolitis
  • Metabolic: Hypoglycemia, Electrolyte disturbances, Osteopenia of prematurity
  • Eyes: Retinopathy
  • CNS: IVH, Hydrocephalus, Periventricular leukomalacia
  • Other: Jaundice, Anemia, Hearing
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35
Q

Physiology of newborn jaundice

A
  1. Marked physiological release of Hb from the breakdown of RBC because of high Hb concentration at birth
  2. RBC lifespan is short (70 days)
  3. Hepatic bilirubin metabolism is less efficient in the first few days of life
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36
Q

What is Kernicterus?

A
  • Encephalopathy resulting from the deposition of unconjugated bilirubin in the basal ganglia and brainstem nuclei
  • Occur when the level of unconjugated bilirubin exceeds the albumin-binding capacity of bilirubin
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37
Q

Manifestations of kernicterus

A
  • Acute manifestations:
  • Lethargy
  • Poor feeding
  • ‘High-pitched cry’
  • Severe cases:
  • Meningismus
  • Irritability
  • The baby lies with an arched back (opisthotonos)
  • Hypotonia
  • Seizures
  • Coma
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38
Q

At which level does babies become clinically jaundiced?

A

Bilirubin >80 micromol/l

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39
Q

Rhesus haemolytic disease

A

Cause of jaundice: Indirect, Coombs (+)

  • Anemia
  • Hydrops
  • Hepatosplenomegaly
  • Rapidly developing severe jaundice
40
Q

Triggers of jaundice in G6PD

A
  • Oxidant (ASA, Sulfa drugs, Antimalarias, Fava beans)

- Infection and severe illness

41
Q

Causes of jaundice appearing <24h of age

A
  • Haemolytic disorders:
  • Rhesus incompatibility
  • ABO incompatibility
  • G6PD deficiency
  • Spherocytosis
  • Pyruvate kinase deficiency
42
Q

Causes of jaundice appearing >24h of age - 2 weeks of age

A
  • Physiologic jaundice
  • Breast milk fed
  • Dehydration
  • Infection
  • Haemolysis
  • Crigler-Najjar syndrome (Glucuronyl transferase deficiency)
  • Gilbert syndrome
43
Q

Causes of prolonged (>2 weeks / >3 weeks in preterm) unconjugated hyperbilirubinaemia

A
  • “Brest milk jaundice” = most common cause
  • Infection
  • Congenital hypothyroidism
44
Q

Value and signs of conjugated hyperbilirubinaemia

A
>25 micromol/l
Signs:
* Baby passing dark urine
* Unpigmented pale stool
* Hepatomegaly
* Poor weight gain
45
Q

Causes of conjugated (direct) hyperbilirubinaemia

A

Direct - always pathological!

  • Neonatal hepatitis syndrome
  • Sepsis
  • TORCH
  • Hypothyroidism
  • Galactosemia
  • Choledochal cyst
  • Biliary atresia
46
Q

Complications of meconium aspiration

A
  • Mechanical obstruction
  • Chemical pneumonitis
  • Infection
  • Air leak –> pneumothorax and pneumomediastinum
  • May develop persistent pulmonary hypertension of the newborn
47
Q

Conditions leading to persistent pulmonary hypertension

A
  • Birth asphyxia
  • Meconium aspiration
  • Septicaemia
  • RDS
48
Q

Clinical features of neonatal sepsis

A
  • Fever or tmp instability or hypothermia
  • Poor feeding
  • Vomiting
  • Apnea and bradycardia
  • Respiratory distress
  • Abdominal distension
  • Jaundice
  • Neutropenia
  • Hypo/hyperglycemia
  • Shock
  • Irritability
  • Seizures
  • Lethargy, drowsiness
49
Q

Most common source of infection in NICU

A

Indwelling central venous catheter, invasive procedures that break the protective barrier of the skin, and tracheal tubes.

50
Q

Most common pathogen causing nosocomially acquired infections

A

Staph. epidermidis (coagulase-negative

51
Q

Most common organisms causing neonatal sepsis (up to 3 months of age)

A
  1. Group B Streptococcus (S. Agalactiae)
  2. E. coli
  3. Listeria monocytogenes
52
Q

Complications of neonatal meningitis

A
  • Cerebral abscess
  • Ventriculitis
  • Hydrocephalus
  • Hearing loss
  • Neurodevelopmental impairment
53
Q

Conjuctivitis

A

Purulent discharge with conjunctival injection and swelling of the eyelids

  • Within 48h of life: Gonococcal infection
  • At 1-2 weeks of age: Chlamydia trachomatis (Tx. oral erythromycin for 2 weeks)
54
Q

Risk factors for hypoglycemia in first 24h of life

A
  • IUGR (poor glycogen stores)
  • Preterm (poor glycogen stores)
  • Born to mothers with DM (hyperplasia of islet cells –> high insulin levels)
  • Large-for-dates
  • Hypothermic
  • Polycythaemic
  • Ill for any reason
55
Q

Symptoms of hypoglycemia

A
  • Jitteriness
  • Irritability
  • Apnea
  • Lethargy
  • Drowsiness
  • Seizures
56
Q

Aiming level of blood glucose

A

2,6 mmol/L

57
Q

Typical features of neonatal seizures

A
  • Repetetive, rhythmic (clonic) movements of limbs that persist despite restraint
  • Eye movements
  • Changes in respiration
58
Q

What causes need to ble excluded first in neonatal seizures?

A
  • Hypoglycemia

- Meningitis

59
Q

Causes of neonatal seizures

A
  • HIE (hypoxic-ischemic encephalopathy)
  • Cerebral infarction
  • Septicemia/meningitis
  • Metabolic:
  • Hypoglycemia
  • Hypo/hypernatremia
  • Hypocalcemia
  • Hypomagnesemia
  • Intracranial haemorrhage
  • Cerebral malformations
  • Drug withdrawal, e.g. maternal opiates
  • Congenital infections
  • Kernicterus
60
Q

Most common cause of perinatal stroke

A

Ischemia of middle cerebral artery

- Mechanism = thrombotic, either thromboembolism from placental vessels or sometimes secondary to inherited thombophilia

61
Q

When to do surgical repair of cleft lip and cleft palate?

A

Cleft lip: at 3 months of age

Cleft palate: 6-12 months of age

62
Q

What are the features in Pierre Robin sequence?

A
  • Mirognathia
  • Posterior displacement of the tongue (glossoptosis/retroglossia)
  • Midline cleft or the soft palate
63
Q

Clinical presentation of esophageal atresia

A
  • Persistent salivation
  • Drooling from the mouth
  • Later:
  • Cough and choke when fed –> cyanotic episodes
  • May be aspiration of saliva from mouth and acid from stomach into lungs
64
Q

VACTERL association

A
V - vertebral defects
A - anal atresia
C - cardiac defects (VSD)
TE - tracheo-esophageal fistula
R - renal defects
L - limb defects (radial)
65
Q

Small bowel obstruction symptoms

A
  • Persisten vomiting (bile stained unless above ampulla of Vater)
  • Delayed or absent meconium passage
  • Abdominal distension (more prominent the more distal the obstruction)
  • High lesion –> present soon after birth
  • Lower lesions –> may not present for some days
66
Q

Small bowel obstruction causes

A
  • Atresia or stenosis of the duodenum (1/3 have Down’s)
  • “Double bubble” on x-ray
  • Atresia or stenosis of the jejunum or ileum
  • Malrotation with volvulus
  • Meconium ileus (almost all affected have CF)
  • Meconium plug
67
Q

Large bowel obstruction causes

A
  • Hirschsprung disease

- Rectal atresia

68
Q

Pathophysiology of Hirschsprung disease

A
  • Absence of the myenteric nerve plexus in the rectum, which may extend along the colon
  • More common in boys and Down’s
69
Q

Exomphalos (omphalocele)

A

Abdominal contents protrude through the umbilical ring, covered with a transparent sac formed by the amniotic membrane and peritoneum

70
Q

Gastrochisis

A

Bowel protrudes through a defect in the anterior abdominal wall adjacent to the umbilicus, no covering sac

71
Q

The 4 major problems in preterm infants

A
  1. RDS –> BPD (bronchopulmonary dysplasia)
  2. ROP (retinopathy)
  3. IVH (intraventricular haemorrhage)
  4. NEC (necrotizing enterocolitis)
72
Q

What are the risk of smoking during pregnancy?

A
  • Low birth weight
  • Increased risk of miscarriage and stillbirth
  • Risk of sudden infant death syndrome
73
Q

What are the benefits for pre-pregnancy folic acid supplements?

A
  • Reduce the risk of neural tube defects
  • Low-dose recommended for all women
  • High-dose recommended for high risk women: previous family history, DM or using anticonvulsants
74
Q

What are the benefits of glucocorticoid therapy perinatally?

A
  • Given before preterm delivery (at lest 24h before delivery)
  • Accelerates lung maturity and surfactant production - reduces incidence of RDS
  • Reduces incidence of intraventricular hemorrhage
  • Reduces incidence of neonatal mortality
75
Q

What can the fetus develop if rhesus isoimmunization?

A
  • Hydrops fetalis
  • Edema
  • Ascitis
76
Q

What defects in the fetus can oligohydramnios cause?

A
  • Pulmonary hypoplasia

- Limb and facial deformities from pressure in on the fetus (feks. Potter syndrome)

77
Q

What is polyhydramnios associated with?

A
  • Maternal diabetes

- Structural GI abnormalities (e.g. atresia in the fetus)

78
Q

What are the risk factors for preterm delivery?

A
  • Previous preterm infant
  • Short inter-pregnancy interval (<6 months)
  • Maternal age (<20 or >35)
  • Obesity
  • Ethnicity
  • Multiple births
  • Maternal infection
  • Smoking and substance misuse
  • Maternal psychological or social stress
79
Q

What are the fetal associations with maternal diabetes?

A
  1. Congenital malformations (6% risk)
    - Increased incidence of cardiac malformations, sacral agenesis, hypoplastic left colon
  2. IUGR
  3. Macrosomia (25% have a birthweight >4kg)
  4. Neonatal hypoglycemia
  5. RDS
  6. Hypertrophic cardiomyopathy - of cardiac septum
  7. Polycythemia - infant look plethoric (florid, red-faced)
80
Q

Clinical features of neonates with hyperthyroid

A
  • Irritability
  • Weight loss
  • Tachycardia
  • HF
  • Diarrhea
  • Exophthalmos
81
Q

What are maternal use of SSRIs associated with?

A

Persisten pulmonary hypertension of the newborn

82
Q

Clinical features of fetal alcohol syndrome

A
  • Growth restriction
  • Characteristic face
  • Saddle-shaped nose
  • Maxillary hypoplasia
  • Absent philtrum
  • Short, thin upper lip
  • Developmental delay
  • Cardiac defects
83
Q

Drugs that should be avoided during pregnancy

A
  • Anticonvulsants
  • Cytotoxic agents
  • Iodides/propylthiouracil
  • Lithium
  • SSRIs
  • Tetracycline
  • Thalidomide
  • Vitamin A and retinoids
  • Warfarinq
84
Q

Clinical features of drug withdrawal in neonate

A
  • Jitteriness
  • Sneezing
  • Yawning
  • Poor feeding
  • Vomiting
  • Diarrhea
  • Weight loss
  • Seizures
85
Q

TORCH infections

A
T - Toxoplasma gondii
O - Other (Syphilis, Varicella zoster)
R - Rubella
C - CMV
H - Herpes
86
Q

Congenital Rubella

A
  1. Cataracts
  2. Deafness
  3. Congenital heart defects (PDA)
  4. Rash: Blueberry muffin spots
87
Q

What is the most common congenital infection?

A

CMV

88
Q

Clinical features in congenital CMV

A
  1. Microcephaly with periventricular calcifications
  2. Petechia with thrombocytopenia
  3. Other:
    - Hepatosplenomegaly
    - Hearing loss
    - Cerebral palsy
    - Epilepsy
    - Cognitive impairment
89
Q

Clinical features of toxoplasmosis

A
  • Retinopathy, chorioretinitis
  • General cerebral calcifications
  • Hydrocephalus
90
Q

When is the infant susceptible to maternal varicella infection?

A

Within 5 days before or 5 days after delivery.

Infant then need protection - zoster Ig, Aciclovir if any development of infection.

91
Q

Clinical features of syphilis

A
  • Characteristic rash of palms and soles of the feet
  • Osteochondritis
  • Periostitis
92
Q

What are the fetal oxygen saturation?

A
  • 65% of upper body

- 35% of lower body

93
Q

What factors initiate breathing at birth?

A
  1. Thermal (cold)
  2. Tactile
  3. Hormonal (increase in catecholamine levels)
    * Catecholamine levels also stimulate reabsorption of alveolar fluid
94
Q

What is the mean time to establish regular breathing?

A

30 seconds

- On average, the first breath occurs 6 seconds after delivery

95
Q

After delivery, when should chest compressions be given?

A

If heart rate dops below 60 beats/minute after 5 effective inflation breaths and 30 second of effective ventilation, compressions should be given