2.1 Fetal Lung Developnment Flashcards

1
Q

EXAM ?

Lung development

A
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2
Q

EXAM ?

explain the stages of lung development

Every premature child takes air

Embryonic

Psuedoglandular

Canalicular

Terminal sac

Alveolar

A
  • Embryonic
    • 0-6 week
    • bronchi
    • trachae
  • psuedoglandular
    • 7 - 16 weeks
    • bronchioles
    • lung circulation
    • terminal bronchioles
  • Canalicular
    • 17 - 24 weeks
    • primitive alveoli
    • respiratory bronchioles
    • about 22-24 weeks of pregnanc
  • terminal sac
    • 25 - 36 weeks
    • alveolar ducts
    • primitive alveoli
    • thin walled alveolar sacs
  • Alveolar
    • >37 weeks
    • definitive alveoli and mature type 2 cells
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3
Q

EXAM ?

Signs of respiratory distress

A
  • tachypaena
  • grunting - expiration
  • nasal flaring
  • use of accessory muscles. intercostal space
  • low O2 sats
  • change in colour
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4
Q

At what gestation does the fetus begin to produce surfactant

A
  • about 22-24 weeks of pregnancy.
  • If a baby is premature (born before 37 weeks of pregnancy), they may not have made enough surfactant yet
  • When there is not enough surfactant, the tiny alveoli collapse further with each breath.
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5
Q

EXAM ?

Explain the concept of respiratory distress and identify common respiratory diseases in the newborn period

A
  • grunting
  • nasal flaring
  • low o2 sats
  • poor tone
  • low hr <100
  • use of intracoastal muscles
  • common respiratory disease
    • TTN
    • meconium aspiration
    • RDS
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6
Q

Transition at Birth - what is the relevance to respiratory disorders?

A
  • transition is caused by
    • cooler environmental temperature
    • tactile stimulation
    • changes in partial pressures of O2 and carbon dioxide during birth
  • high pressures in the lungs in the uterus
  • for successful transition:
    • The initiation and sustained regular respiration
    • Fluid-filled air spaces cleared of excess fluid to air-filled for effective gas exchange,
    • Redirect blood flow towards the fetal lungs and close fetal shunts
  • Spontaneous labour triggers fetal catecholamines:
    • noradrenaline and adrenaline
    • facilitates the mobilisation of lung fluid
  • about ⅓ of total amniotic fluid volume maybe removed with the remains fluid slowly reasborbed;
    • by the lymphatic system
    • Pulmonary circulation
    • sodium channels drive by adrenaline released during labour
  • c-section deliveries may have a slower transition with th amniotic fluid shunted via the lymphatic systems
  • The release of catecholamines during spontaneous labour ensures an availability of surfactant for the preparation of respiration post birth
    *
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7
Q

EXAM ?

Meconium Aspiration Syndrome (MAS)

A
  • parasympathetic activity from fetal stress
  • Mainly affects term and post term infants
    • (rarely occurs in preterm infants less than 34 weeks)
  • Hypoxic event occurs before birth
    • stimulates the intestinal peristalsis
    • relaxes the anal sphincter
  • Respiration post birth is that meconium is draw into the major airway
  • Meconium visible in trachea
  • subsequently into the smaller airways
  • causing
    • Obstruction
    • atelectasis
    • air trapping
    • pneumothorax
    • chemical pneumonitis (meconium is a chemical irritant)
    • inactivation of the surfactant impairs gas exchange
  • In severe cases
    • leads to respiration distress
    • secondary persistent pulmonary hypertension due right to left ductal shunting due to increased pressure
    • patent ductus arteriosus
  • Risk factors
    • fetal distress
    • mec stained liquor
    • post dates
    • prolonged labour
    • gestational htn
    • cord compression
    • hypoxic event
    • SGA
    • cigarette smoking
  • management key
    • Ventilation may be required
    • O2 management
    • antibiotics
    • chest xray
    • maintenance of optimal thermal environment
      warmer
    • nurse baby upright
    • small frequent feeds
    • orogastric tube
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8
Q

EXAM ?

Apnoea

A
  • common occurrence in preterm infants
  • is cessation of breathing for 20 secs or longer
  • cessation of breathing for 10 sec with cyanosis or/and bradytcardia
  • types of apnoea
    • Central Apnoea
      • decreased central nervous system stimuli to respiratory muscles
    • Obstructive apnoea
      • pharyngeal instability
      • collapse
      • neck flexion
      • nasal obstruction
    • Mixed Apnoea
      • combination of both
      • persistence obstructive apnoea leads to CNS depression due to hypoxia and acidosis
  • Apnoea of prematurity
    • poorly positioned head and neck
    • drugs
    • gastrointestional
    • metabolic
    • CNS
    • Infection
    • cardiovascular
    • pain
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9
Q

EXAM ?

Transient Tachypnoea of the newborn (TTN)

A
  • delayed reabsorption of normal lung fluid
    • precipitous birth
    • c-section births
    • term or late gestation
    • prenatal exposure to methamphetamine
  • Onset usually two to six hours after birth
  • Respiratory distress is evident
    • Tachypnoea
    • mild retraction
    • grunting
    • nasal flaring
    • cyanosis may be present
  • Management
    • CPAP
    • HiFlow
    • ?treat with abx until cultures come back
  • Risk factors
    • term infant - c section
    • precip labour
    • me
    • bradycardic event during labour
    • reduced catacohmines
    • prenatal exposured to methampetine
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10
Q

EXAM ?

Describe the treatment and management of respiratory distress in the neonate

A

RDS:

  • Resp monitoring
  • Sats RR
  • HFNP/CPAP
  • prevention
    • administer antenatal corticosteroids

MAS

  • Ventilation may be required
  • O2 management
  • antibiotics
  • chest xray
  • maintenance of optimal thermal environment
  • warmer
  • nurse baby upright
  • small frequent feeds
  • orogasric tube
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11
Q

EXAM ?

Explain the term respiratory distress

A
  • progressive impairment of the lungs to exchange gas at the alveolar level
  • having to work harder to breath and getting enough oxygen,
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12
Q

EXAM ?

Respiratory distress syndrome (RDS)

A
  • RDS
    • consequence of immature lungs anatomy and physiology
    • Cannot support oxygenation ad ventilation
    • alveolar sacs are not developed
    • decreased surface area for gas exchange
    • volume of surfactant is insufficient to prevent collapse of unstable alveoli
    • Alveoli collapses with each breath
    • therefore Normal Functional residual capacity is not established
    • (very similar to spesis)
  • RISK factors
    • prematurity
    • size and gestation of neonate
    • maternal diabetes
    • c-section
  • Management
    • monitoring
    • HFNP/CPAP
    • administer of corticosteroids antenatal
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13
Q

Pneumonia

A

Early onset - within 3 days of birth

  • MAS
  • GBS positive (maternal long term PPROM)
  • genital herpes
  • chicken pox
  • Rubella
  • mumps
  • fungal infections
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14
Q

EXAM ?

Describe the role of PIPER

A
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15
Q

The following diagram illustrates the changes occurring within the fetal-placental circulation whereby circulation is re-routed via the lungs at birth.

A
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16
Q

EXAM ?

Discuss the principles regarding stabilisation and transfer of the unwell neonate prior to transfer

A
17
Q

Describe the physiology of the onset of breathing.

A
  • the inflation of the lungs encourages the intra-alveolar fluid to move into the surrounding interstitial
  • It is also absorbed by the body
  • the respiratory system in the medulla oblongata of the brain matches the respiratory effort to cellular metabolic needs
  • The medulla is influenced by chemoreceptors and stretch reflexes.
    • during its descent through the birth canal, the fetus experiences a reduction in oxygen (physiological hypoxia) and an accumulation of carbon dioxide. This Hypoxia and Hypercarbia is crucial to the establishment of a new respiratory drive with the medulla oblongata and contributes to more successful pulmonary ventilation.
    • the emptying of pulmonary fluid from the lung, expansion of the pulmonary vascular bed and pulmonary tissue creates a NEGATIVE PRESSURE which assists the first breath 3) elastic recoil of the rib cage at delivery increases the capacity and the infant is stimulated to inspire (at first inspiration, the diaphragm contracts strongly and the flexible ribs and sternum are pulled concave. Subsequent breaths require much less mechanical work).
18
Q

baby circulation right after birth

Umbilical veins - days

Ductus venosus - days

Foramen Ovale - minutes

Ductus Arteriosus - hours

umbilical artery -

A

Placenta is removed

  • low resistance to high resistance
  • Temp decreases the Wharton jelly - starts contracting
  • lungs take in air
  • deoxygenated blood flows from the umbilical arteries
    • into the IVC (and now remains deoxygenated)
    • into the SVC
    • into the right atrium
    • into the right ventricle
    • pumped out to the pulmonary arteries
    • towards the lung
  • alveoli are filled with fluid
  • air pushes the fluid out of the alveoli
  • fluid enters the capillaries
  • the rise in o2 sends a signal to the arterial to dilate
  • resistance has fallen (lungs previously have high resistance)
  • Iungs now have low resistance
  • deoxygenated blood goes into the lungs
  • Right side of heart lower in resistance
  • Temp decreases the Wharton jelly - starts contracting -
  • oxygenated blood going into the left atrium (higher pressure on the left side now)
  • foramen ovale (pressure right side low closes off) right side of heart has higher pressure now
  • lung goes from high to low pressure due to the closure of the ductus etc
  • Left ventricle
  • into the aorta (oxygenated blood)
  • ductus arteriosus (constriction - smooth muscle po2 levels are high will start to constriction) prostaglandin decrease
  • internal iliac artery toward the umb artery high levels of o2 and low prostaglandin
19
Q

Discuss the effects of the combined respiratory and circulatory changes at birth

A
  • when the baby takes its first breath the lungs inflate for the first time
  • increasing pulmonary blood flow.
  • Blood returning from the lungs increases the pressure in the left atrium,
  • closing the flap over the FORAMEN OVALE and preventing blood flow between the atria.
  • Blood entering the atrium is therefore diverted into the right ventricle and into the pulmonary circulation through the pulmonary arteries.
  • As pulmonary circulation is established, blood oxygen levels increase, causing constriction and closure of the ductus arteriosus
  • if these adaptations do not occur, they are evident as congenital abnormalities
20
Q

What type of cells produce surfactant

A

Type II alveolar cells

type 11 pneumocytes

21
Q

At what gestation is surfactant production able to sustain respiratory function

A

after 37 weeks

bethamethazone is used for preterm babies

22
Q

Pulmonary Surfactant

A
  • Alveolar fluid contains a substance known as SURFACTANT reduce surface tension
  • Pulmonary surfactant - secretes into the alveoli by Type II alveolar cells - or Type II pneumocytes
  • consists of
    • Phosphatidylcholine
    • Phosphatidylglycerol
    • Hydrophobic surfactant proteins
  • Surfactant becomes interspersed between molecules at the water-air interface
  • Reduces the hydrogen bonds between water molecules at the surface and reduces surface tension
  • change in pressure

about 22-24 weeks of pregnancy surfactant

  • 26 weeks neonate able to
  • lungs are stiff
  • give steriods
23
Q

Case study - mitchell

A

Baby Mitchell was admitted to the special care nursery because of prematurity and respiratory distress. The baby was born at 32 weeks and 6 days gestation by caesarean section for breech presentation, premature labour, and preterm premature rupture of membranes of approximately 2 hours duration. He weighed 1950 grams and was vigorous at birth with spontaneous respirations; Apgars were 7@1 & 8@5. Mitchell’s mum Marta is a 26 year old Gravida 1 Para 1 who had gestational hypertension which was managed with oral anti hypertensives for the past 4 weeks. Maternal blood group is O positive. GBS is unknown. Marta wishes to breastfeed. After a cuddle with Mum and Dad in the recovery room Mitchell was transferred to the Special care nursery for ongoing assessment and care. Shortly thereafter Mitchell’s work of breathing increased. On examination, Mitchell is non dysmorphic, skin colour is pale remains pink centrally. He has subcostal retractions, grunting, and nasal flaring. Auscultation reveals decreased air entry in the lung fields throughout. Vital signs: Temperature 36.5 degrees Celsius. Heart rate is 174 respiratory rate is 68 Oxygen saturation is 94% in room air. Mitchell requires further assessment and symptom management of his respiratory distress including a care plan.

24
Q

case study mitchell 2

A

Potential problems and complications

  • difficulty establishing sucks
  • NGT
  • Muscle development with extended stay in incubator
  • attachment with parents because of being on o2/ in isoletee for so long
  • difficulty bonding
  • Struggling to establish suck, swallow and breath. CNS undeveloped
  • Previous hx of resp distress
  • NEC
  • ongoing respiratory issue
  • infection due to stay in SCN
  • Thermoregulation difficulties

Goals of care

  • facilitating to life
  • BGL
  • RDS verses Sepsis
  • developmental care
  • BF
  • FBC
  • Second daily weight
  • nutritional needs BF/NGT/Oral feeds
  • educating parents on care required
  • encourage hand expressing
  • skin to skin
  • normalise to open cot

Midwifery interventions and rationale for Michell and Marta

  • mental health
  • cluster care for when parents visit
  • expressing plan
  • kangaroo care
  • thermoregulation
  • vital monitor

Evaluation of care

  • wean out of isoletee
  • extended periods of out of the cot s2s
  • monitor output FBC
    *