Neonatology Flashcards

1
Q

Gestational Age

A

Time from start of last period

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2
Q

Embryonic Age (Foetal Age)

A

Time from fertilisation (formation of zygote)
Estimated using ultrasound
- 1st trimester: crown rump length
- 2nd/3rd trimester: head circumference and femur length

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3
Q

Gestational Age (2)

A

Embryonic Age + 14 days

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4
Q

Which is more commonly use in clinical practice: Gestational Age or Embryonic Age?

A

Gestational Age

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5
Q

Stages of Ovulation (According to CM) (6)

A
  1. Follicular phase
  2. Dominant follicle development
  3. Lutenizing hormone surge
  4. Ovulation
  5. Corpus luteum formation
  6. Luteal phase
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6
Q

3 Stages of Gestation

A

Germinal stage
Embryonic stage
Foetal stage

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7
Q

Stages of Gestation - Germinal Stage

A

conception to implantation

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8
Q

Stages of Gestation - Embryonic Stage

A

To Approx. Week 9

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9
Q

Stages of Gestation - Foetal stage

A

Approx. Week 9 to Birth

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10
Q

Human Chorionic Gonadotropin (hCG)

A
  • hormone detected on pregnancy tests
  • syncytiotrophoblast releases the hormone hCG which enters the mother’s blood stream
  • stimulates the corpus luteum of the ovary to produce progesterone to maintain the pregnancy
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11
Q

Ectoderm fait (external)

A

Cells derived from the ectoderm ultimately give rise to the:
- Epidermis
- Central nervous system
- Peripheral nervous system
- Eyes
- Internal ears
- Many connective tissues of the head

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12
Q

Mesoderm fait (middle)

A

Cells derived from the mesoderm ultimately give rise to:
- Skeletal muscles
- Blood cells and blood vessel linings
- Cardiovascular system
- Excretory systems incl kidneys
- Reproductive organs
- Visceral smooth muscular coats
- Serosal linings of all body cavities, ducts and internal organs
( Excluding in the head and limbs, they are the source of connective tissues, cartilage, bones, tendons, ligaments and dermis )

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13
Q

Endoderm fait (internal)

A

Cells derived from the endoderm ultimately give rise to epithelial linings. This includes linings of:
- Full alimentary tract (GI tract)
- Respiratory system
- Glands opening onto the GI tract and glandular cells of associated organs such as the liver and pancreas

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14
Q

Clinical indications for Neonatal EEG (3)

A
  • Assess the severity of brain dysfunction and determine prognosis
  • Detect seizures and assess response to treatment
  • Assess cerebral maturation
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15
Q

Considerations for neonatal EEG (4)

A
  • Size and vulnerability
  • Myelination and sulcation
  • Skull thickness
  • State of baby (medication/sedation)
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16
Q

Recommended electrodes for neonatal (2)

A
  • self-adhesive wet gel with snap lead wire
  • self-adhesive wet gel with pre-attached lead wire
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17
Q

Disadvantage of cup/disc electrodes

A

impedance gel risks skin damage, pressure injury

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18
Q

Electrodes used in practice for clinical neonatal EEG

A

Disposable hydrogel electrodes

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19
Q

Extra-cerebral electrodes in neonatal EEG montage (7) + state what is key

A

Key: ECG & respiratory
Other: Left & right EOG, Left & Right EMG, Sp02

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20
Q

What area of the scalp is mainly missing electrodes in the limited montage and why?

A

Frontal lobe
- poorly developed
- lots of artefact

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21
Q

What is the benefit of EMG electrodes in the EEG montage?

A
  • To differentiate seizure types (myoclonic, tonic, spasms)
  • Can aid in lateralization
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22
Q

Limited EEG study
(Reasons why / benefits)

A
  • Therapeutic hypothermia protocol
  • Setups done out-of-hours
  • Prolonged recordings (>24 h)
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23
Q

Full head EEG study

A
  • Investigate seizures
  • Investigate neonatal epileptic encephalopathy
  • Better characterization of severely abnormal background in TH
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24
Q

Timebase of neonatal EEG

A

15mm/s

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25
Q

Information needed before starting neonatal EEG (5)

A

Age of baby
Time of birth
History of pregnancy issues
History of birth
Medication

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26
Q

What does APGAR score stand for?

A

Appearance (skin colour)
Pulse rate
Grimace
Activity (tone)
Respiratory effort

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27
Q

What is the purpose of APGAR score?

A

Used to help guide need for immediate treatment

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28
Q

When is APGAR done and how are the results interpreted?

A

Done: 1/5 mins
Results:
7+ normal
4-6 low
<= 3 critically low

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29
Q

Patient’s post menstrual age

A

Gestational age + chronological age

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30
Q
A
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31
Q
A
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31
Q
A
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32
Q
A
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33
Q
A
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34
Q
A
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35
Q

Parts of ECG Analysis (5)

A

Rate
- Fast (broad/ narrow)/slow
- Regular/ irregular
Rhythm
Axis
Intervals and voltages
Repolarisation

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36
Q

Normal Features in Paediatric ECG (7)

A

Sinus tachycardia when sick
Sinus arrhythmia
Isolated PACs + PVCs
Narrow QRS
2:1 Wenkebach during sleep
Notched T waves in V2/V3
Notched P waves V2/V3 in older children

37
Q

3 Key Features of Normal Sinus Rhythm

A

P before every QRS
QRS after every p
Normal p wave axis

38
Q

Congenital Heart Disease Death Incidence

A

0.8 per 1,000 births

39
Q

How does CHD present? (6)

A
  • Antenatal screening
  • Postnatal pulse oximetry screening
  • Cardiogenic shock- low output state
  • Incidental finding
  • Discharge exam
  • Cardiac failure
42
Q

Name the embryonic stage:
Primitive Gut Tube -> respiratory system

A

Early embryonic stage

43
Q

Name the embryonic stage:
Respiratory Diverticulum -> bifurcates in two buds = primary bronchi

44
Q

Name the embryonic stage:
Pseudoglandular Stage

(bronchopulmonary segment will become a specific portion of the lung - the lungs resemble the development of tubuloacinar glands)

A

Weeks 8-16

45
Q

Name the embryonic stage:
Canalicular Stage

(the respiratory bronchioles develop)

A

Weeks 16-26

46
Q

Name the embryonic stage:
Terminal Sac Stage

(Alveoli Develop)

A

> 26 Weeks

47
Q

4 Factors Affecting Breathing

A

Chemical (chemoreceptors in the carotid arteries and the aorta)

Mechanical (foetal chest compression during birth – reduces the negative pressure)

Thermal (skin thermoreceptors - change in temperature)

Sensory factors (tactile skin receptors)

48
Q

Surfactant

A

Naturally produced at end of 2nd & 3rd trimester
90%lipids 10%proteins
Purpose: Lowers the surface tension at the air-water interface in the alveoli

49
Q

Causes for resp complications of newborn (3)

A
  • Delayed adaptation (maladaptation)
  • Exiting conditions (surgical or congenital anomalies)
  • Acquired conditions
50
Q

Most common cause of respiratory distress in term newborns?

A

Transient Tachypnoea of Newborn (TTN)

51
Q

4 Term Newborn Resp Pathology

A

Transient Tachypnoea of Newborn (TTN)
Meconium Aspiration Syndrome (MAS)
Persistent Pulmonary Hypertension of the Newborn
(PPHN)
Pneumothorax

52
Q

2 Preterm Newborn Resp Pathology

A

Respiratory Distress Syndrome (RDS)
Chronic Lung Disease

53
Q

What is TTN and what effect does it have? (1,2)

A

Delay in clearance of lung fluid (after c-section)
- Low pressure on the thorax
- Low reabsorption of alveolar fluid via Na channels in the lung epithelium due to low circulating catecholamines

54
Q

How long does TTN usually take to settle?

55
Q

How can TTN be managed? (2)

A

O2 therapy
Respiratory support (HF, CPAP)

56
Q

What does TTN look like on an XRay? (2)

A

Fluid in the horizontal fissure
Streaky infiltrates with hyperinflation and peripheral haziness

57
Q

What does MAS look like on XRay? (3)

A

Hyperinflation
Course diffuse patchy consolidations on both sides.
Some subtle pleural fluid on both sides (arrowheads)

58
Q

What is involved in aspiration of meconium in MAS? (3)

A

Mechanical obstruction
Chemical pneumonitis
Inactivation of surfactant

59
Q

Who is at increased risk of MAS?

A

postdates newborns (>42 weeks)

60
Q

How can MAS be managed? (4)

A

O2 therapy
Respiratory Support
Surfactant therapy
NO therapy/ECMO

61
Q

What is PPHN?

A

Pulmonary hypertension leading to right-to-left shunt

62
Q

Causes of PPHN (5)

A

Birth asphyxia
Meconium aspiration
Sepsis
Diaphragmatic hernia
Primary disorder – less common

63
Q

Presentation of PPHN

A

cyanosis, difference in pre- and post-ductal saturations

64
Q

Management of PPHN (6)

A

O2 therapy
Mechanical ventilation support
Circulatory support
Surfactant therapy
NO therapy or sildenafil – pulmonary vasodilator
ECMO

65
Q

Diagnosis of PPHN (2)

A

XRay or Echo

66
Q

Management of pneumonia (2)

A

antibiotic treatment
respiratory support

67
Q

Most common cause of neonatal pneumonia

A

Group B streptococcal infection (GBS)

68
Q

Risk factors for neonatal pneumonia (4)

A

Prolonged rupture of the membranes (PROM)
Maternal infection
Fever
Chorioamnionitis

69
Q

What does pneumonia look like on XRay? (3)

A

Bilateral perihilar streaking
Atelectasis of the right middle lobe, probably due to mucus impaction of the bronchus
Position of the nasogastric catheter indicating mediastinal shift

70
Q

What is a pneumothorax?

A

Free air in pleural cavity

71
Q

How can a pneumothorax be managed? (3)

A

respiratory support (O2 therapy, mechanical ventilation)
spontaneous resolution
needle aspiration/chest drain

72
Q

Risk factors for respiratory distress syndrome (5)

A

Prematurity
Maternal diabetes mellitus
Sepsis
Hypoxemia and acidemia
Hypothermia

73
Q

Natural course of RDS? (2)

A

Getting worse over 24-72hrs Improvement with antenatal steroids

74
Q

How can RDS be managed? (4)

A

Antenatal steroids
Postnatal surfactant therapy (prophylaxis/rescue)
O2 therapy
Respiratory support (prevention of alveolar collapse): HF, CPAP, MV

75
Q

What is bronchopulmonary dysplasia?

A

Chronic lung disease

76
Q

bronchopulmonary dysplasia (definition)

A

O2 requirements at 28 days of life or at 36 weeks corrected

77
Q

Who is at risk of neonatal chronic lung disease?

A

low birthweight infants (20-30%)

78
Q

What is a major cause of mortality & morbidity in low birthweight infants?

A

Chronic lung disease

79
Q

How can neonatal chronic lung disease be managed? (5)

A

Respiratory support
Nutritional support
Corticosteroids
Diuretics
Sildenafil if PPHN

80
Q

Name 2 respiratory neonatal congenital anomalies and surgical conditions

A

Choanal Atresia
Congenital Diaphragmatic Hernia

81
Q

How can Congenital Diaphragmatic Hernia be managed? (4)

A

Intubate and ventilate from birth
Pass NG tube
Support for PPHN
Surgical repair

81
Q

How can Choanal Atresia be managed?

A

Oral airway
Surgical correction

82
Q

What is the best predictor of survival in PPHN?

A

Cardiac function

83
Q

Diagnosis of PPHN (6)

A

History and Physical Exam
Pre and post ductal saturation
Labile or profound hypoxaemia
Differential cyanosis
Chest XRay
ECHO

84
Q

TAPSE

A

tricuspid annular plane systolic excursion

Systolic longitudinal displacement of the lateral tricuspid annulus towards the apex, measured using M-mode echocardiography in the apical four-chamber view to assess right ventricular function

85
Q

General management for PPHN (5)

A
  • Normothermia
  • Noise and stress reduction
  • Sedation
  • Normalise pH
  • Ventilatory Management
86
Q

Therapeutic intervention for PPHN (6)

A
  • Optimise Ventilation
  • Oxygen
  • Surfactant
  • Nitric Oxide
  • Haemodyamic Considerations
  • Corticosteroids
87
Q

What are the 3 Functional Properties of Lungs Addressed by Routine PFTs?

A
  1. Airflow (inspiratory & expiratory)
  2. Lung Volumes & Capacities (TLC, RV, FRC)
  3. Alveolar-Capillary Gas Transfer (CO uptake over time)
88
Q

Abnormalities in these 3 functional properties of lungs addressed by routine PFTs?

A

1.Obstructive ventilatory
2. Restrictive ventilatory
3. Gas transfer limitations or impairments