Meconium Aspiration Syndrome (MAS) Flashcards

1
Q

What is meconium aspiration syndrome (MAS)?

A

Meconium Aspiration Syndrome (MAS) is the term used to describe a spectrum of disorders, marked by various degrees of respiratory distress in the new born infant. This follows the aspiration of meconium stained amniotic fluid (MSAF), which can happen either antenatally (2.8% of all pregnancies) or during birth (up to 23% of all pregnancies).

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2
Q

What is meconium?

A

Meconium is the dark green, sticky and lumpy faecal material produced during pregnancy. It is usually released from the bowels after birth.

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3
Q

Briefly differentiate between meconium aspiration syndrome (MAS) and aspiration of meconium stained amniotic fluid (MSAF)

A

Meconium is the dark green, sticky and lumpy faecal material produced during pregnancy. It is usually released from the bowels after birth, but in 8-25% of pregnancies, the baby can pass meconium in utero, leading to MSAF. Of these, 5-12% of babies can aspirate MSAF and develop MAS.

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4
Q

Why is MAS a problem?

A

MAS can cause the new born to develop respiratory distress which may be life threatening. It is still an important cause of morbidity and mortality amongst neonates. Also, MAS can lead or exacerbate other neonatal complications such as neonatal sepsis and ischaemic insults. MAS is highest amongst infants who are post term, had thick meconium at birth and suffered birth asphyxia.

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5
Q

Briefly descirbe the pathophysiology of MSAF

A

MSAF is the after-effect of in-utero peristalsis. In term or post term infants, where gastrointestinal maturation is appropriate, this movement leads to meconium passage. The peristalsis usually is the result of foetal hypoxic stress or vagal stimulation due to cord compression. There is also some evidence that chronic hypoxia may lead to it as well. These factors can also lead to fetal gasping which results in MAS.

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6
Q

Briefly describe the pathophysiology of MAS

A

The pathophysiology of MAS is complex. It depends not only on the meconium’s varied chemical composition (the inflammatory interactions of which are not fully understood) but other factors affecting the neonate’s health as well, such as fetal hypoxia andairway obstruction.

However, once aspirated, it can stimulate the release of many vasoactive and cytokine substances that activate inflammatory pathways, as well as triggering vasculature changes. It also inhibits the effect of surfactant in the lungs.

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7
Q

What are the common features of MAS-related respiratory distress in neonates?

A
  • Partial or total airway obstruction
  • Foetal hypoxia
  • Pulmonary inflammation
  • Infection
  • Surfactant inactivation
  • Persistent Pulmonary Hypertension (PPHN)
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8
Q

How can MAS lead to partial or total airway obstruction?

A

Due to its thick and sticky consistency, meconium can cause partial or total mechanical airway obstruction. This leads to a decrease in pulmonary ventilation of the small airways. This may lead to atelectasis and a “ball-valve” effect with air trapping. Currently, there is evidence that there is little correlation between the presence of meconium in the trachea and clinical signs of severe MAS. Once the airways are obstructed, the pulmonary pressure increases, leading to right-to-left shunt (through a patent ductus arteriosus or foramen ovale). This creates a V:Q mismatch, leading to a downward spiral of severe foetal hypoxia.

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9
Q

How can MAS lead to foetal hypoxia?

A

Foetal hypoxia results from a myriad of reasons in MAS: a V/Q mismatch, increase of pulmonary vascular pressures, mechanical obstruction, airway oedema and/or surfactant inactivation. All these can cause a decrease in gas exchange and a drop in foetal oxygen saturations. Although it is an important factor to consider in MAS (as it prompts the clinicians to react quicker to the patient) it is neither the cause nor the determinant factor in the severity of MAS in ¾ of the cases.

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10
Q

How can MAS lead to pulmonary inflammation?

A

Meconium contains many pro-inflammatory cytokines such as tumour necrosis factor (TNF) and interleukins that directly and indirectly contribute to lung tissue injury, surfactant inactivation and infection.

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11
Q

How can MAS lead to infection?

A

The inflammation process predisposes the foetal lung to an increased risk of infection and can cause a chemical pneumonitis. (N.B. even though both are usually considered sterile, meconium has been shown to be a good medium for microorganisms to grow in compared to clear amniotic fluid).

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12
Q

How can MAS lead to surfactant inactivation?

A

The inflammatory reaction caused by meconium deactivates surfactant which increases the surface tension of the alveoli. This reduces the efficiency of gas exchange and in turn further exacerbates foetal hypoxia.

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13
Q

How can MAS lead to Persistent Pulmonary Hypertension (PPHN)?

A

Persistent Pulmonary Hypertension (PPHN): PPHN results from remodelling of the pulmonary vascular bed in response to hypoxia, vasoactive mediators in the meconium and ventilation/perfusion mis-match. PPHN is one of the major causes of morbidity and mortality in MAS.

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14
Q

What are the risk factors for MAS?

A

The risk factors for MAS are not completely understood. It is though that conditions leading to foetal hypoxia and foetal gasping increase the risk of aspirating meconium in a term or post-term baby, they are as follows;

  • Gestational Age > 42 weeks
  • Foetal distress (tachycardia / bradycardia)
  • Intrapartum hypoxia secondary to placental insufficiency
  • Thick meconium particles
  • Apgar Score <7
  • Chorioamnionitis +/- Prolonged pre-rupture
  • Oligohydramnios
  • In utero growth restriction (IUGR)
  • Maternal hypertension, diabetes, pre-eclampsia or eclampsia, smoking and drug abuse
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15
Q

What are the clincal features of MAS?

A

A diagnosis of MAS is difficult given the non-specific presentation of respiratory distress on examination at birth (which often overlaps with other conditions). Having said this, it is still a clinical diagnosis. A full history of the risk factors, confirmed presence of meconium in the amniotic fluid and aspirated meconium (clinical signs of post-maturity and MSAF staining) are necessary to diagnose MAS in an infant presenting with respiratory distress where no other diagnosis can be confirmed ie. MAS is a diagnosis of exclusion.

On examination the newborn infant will show signs of respiratory distress:

  • Tachypnoea- a respiratory rate of >60 breaths per minute
  • Tachycardia- a heart rate of >160 beats per minute
  • Cyanosis- this requires immediate management
  • Grunting
  • Nasal flaring
  • Recessions- intercostal, supraclavicular, tracheal tug
  • Hypotension- systolic blood pressure of <70 mmHg
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16
Q

What investigations should be ordered for MAS?

A
  • Chest x-ray
  • FBC
  • CRP
  • Blood cultures
  • Arterial blood gas
  • Dual pulse oximetry
  • Echocardiography
  • Cranial ultrasound
17
Q

Why investigate using chest x-ray?

A

A plain radiograph will often show:

  • Increased lung volumes
  • Asymmetrical patchy pulmonary opacities
  • Pleural effusions
  • Pneumothorax or pneumomediastinum
  • Multifocal consolidation (due to chemical pneumonitis)
18
Q

Briefly describe what is shown on the chest x-ray

A

Chest x-ray showing bilateral asymmetric opacification of MAS.

19
Q

Why investigate using arterial blood gas?

A

This will allow reliable assessment of the neonate’s pH, Pa02, PaCO2 and any developing metabolic acidosis. A sample is usually taken from an indwelling umbilical artery catheter or peripheral arterial line. Arterial puncture could be used as a last resort.

20
Q

Why using dual pulse oximetry?

A

Oxygen saturations should be measured in the right upper limb and on and either lower limb (pre- and post-ductal) to determine hypoxia and assess any potential right-to-left shunts that may be present. A difference of 5-10% between the limbs is clinically significant of neonatal pathology.

21
Q

Why investigate using echocardiography?

A

Used to exclude any congenital heart abnormalities causing pulmonary hypertension e.g. PDA, PFO, tricuspid valve regurgitation.

22
Q

Why investigate using cranial ultrasound?

A

Used to assess for results of any hypoxic damage to the brain.

23
Q

Briefly describe the general principles of management of MAS

A

Management of MAS depends on the severity of respiratory distress the newborn is experiencing; while some patients born with MSAF may need no extra support, infants experiencing mild to severe respiratory distress will often require specialist ventilatory support, antibiotics and surfactant.

  • Observation
  • Routine care
  • Ventilation and oxygen therapy
  • Antibiotics
  • Surfactant
  • Inhaled nitric oxide (iNO)
  • Inhaled corticosteroids
24
Q

What is the role of observation in management of MAS?

A

Careful observation for respiratory distress needs to be taken with newborns born in MSAF, with particularly close watch over oxygen saturations.

Bedside care and decision-making been shown to be an important contributor to the child’s positive outcome.

25
Q

What is the role of routine care in management of MAS?

A

Newborns should be placed under an infant warmer, as hypothermia inhibits surfactant production

Continuous oxygen saturations should be monitored

Blood glucose, UE, FBC, CRP and calcium may need to be assessed and corrected if necessary to exclude other treatable pathologies.

Nutritional support should be commenced on day one in the form of IV fluids. The aim should be to switch to nasogastric and oral feeds when permitting.

26
Q

What is the role of ventilation and oxygen therapy in management of MAS?

A

Oxygen can be delivered in a variety of ways depending on the newborn’s requirements:

  • Via nasal cannula to achieve O2 saturations of 92-97%. This can be weaned if the baby is not showing signs of respiratory distress or is clinically improving.
  • Continuous Positive Airway Pressure (CPAP) should be started with nasal prongs in newborns with spontaneous breathing and good respiratory effort. CPAP has many side effects such as air trapping and so close monitoring via regular CXRs is advised.

If the above measures are not effective, infants can be intubated and mechanically ventilated. These infants should be managed in a Level 2 or greater NICU centre. If confirmed refractory pulmonary hypertension is seen, the child can be ventilated with inhaled Nitric Oxide (iNO).

27
Q

What is the role of antibiotics in management of MAS?

A

Antibiotics are usually indicated in infants born who have clinical suspicion of infection. Antibiotics can be stopped if the 48hr cultures and clinical examination findings are negative. The antibiotics usually prescribed are dependent on the unit’s local guideline. (I.e.: ampicillin IV 50-100mg/kg/day and gentamicin IV 4-5mg/kg/day). In MAS, the evidence shows that routine administration of antibiotics does not reduce its morbidity or mortality.

28
Q

What is the role of surfactant in management of MAS?

A

A bolus of surfactant may be administered in newborns with moderate MAS or if a pneumothorax is present. In severe cases a lung lavage with surfactant can be performed but this needs to be carried out by an experienced specialist and is very rarely required. It can decrease the need for extracorporeal membrane oxygenation therapy (ECMO) but does not reduce the mortality or morbidity of MAS.

29
Q

What is the role inhaled nitric oxide (iNO) in management of MAS?

A

In newborns requiring mechanical ventilation and surfactant there is often pulmonary hypertension also present which requires iNO. This should be given under close monitoring in a tertiary centre, and the patient should be investigated for right-to-left shunts e.g. dual-pulse oximetry, echocardiography etc.

30
Q

What is the role of corticosteroids in management of MAS?

A

The idea that steroids will reduce the inflammation on the lungs has been trialled with various successes. At present it is neither routine practice nor a recommended adjuvant.

31
Q

What are the complications of MAS?

A
  • Air leak
  • Persistent Pulmonary Hypertension (PPHN)
  • Cerebral Palsy (CP)
  • Chronic Lung Disease (CLD)
32
Q

Why is an air leak a complication of MAS?

A

Due to thick meconium sometimes causing a “ball-valve” effect, air leaks can occur due to alveolar hyperdistention leading to a pneumothorax or a pneumomediastinum. There needs to be a high index of suspicion in any MAS new born with compromised pulmonary or cardiac function. Prompt investigation and treatment, such as needle aspiration or continuous drainage, needs to be performed in order to stop further hypoxia and PPHN. Air leaks have a greater incidence when mechanical ventilation is used.

33
Q

Why is persistent pulmonary hypertension (PPHN) a complication of MAS?

A

PPHN can be either a result, complication or a differential diagnosis for MAS. Around 1/3rd of new born MAS patients have associated PPHN and it contributes significantly to the mortality of the condition. As previously stated, echocardiography for investigation and iNO for treatment should be performed.

34
Q

Why is cerebral palsy (CP) a complication of MAS?

A

MAS can lead to cerebral hypoxia resulting in cerebral palsy and other neurological conditions. Relevant brain imaging such as an MRI should be performed in these cases.

35
Q

Why is chronic lung disease (CLD) a complication of MAS?

A

CLD can develop from barotrauma and oxygen toxicity, amongst other things. Thus, MAS new-borns that have required mechanical ventilation with increased pressures and prolonged oxygen exposure are at high risk. Close monitoring of oxygen saturations and re-assessing the need for oxygen and potential to step down ventilatory measures can help reduce the likelihood of developing CLD.

36
Q

What differentials should be considered for MAS?

A
  • Transient tachypnoea of the newborn
  • Surfactant deficiency
  • Persistent pulmonary hypertension
37
Q

How does MAS and transient tachypnoea of the newborn differ?

A

This is a tachypnoea present in the newborn infant, which usually resolves after 24hr without any intervention. Neither hypoxia nor cyanosis are usually seen, but the child might need support on a neonatal unit if they are symptomatic. MSAF may or may not have been seen at delivery. CXR may show some perihilar markings and/or sail sign. Blood gases should be within normal values.

38
Q

How does MAS and surfactant deficiency differ?

A

Causes respiratory distress similar to MAS but more often seen in pre-term infants. The infant will likely need some ventilator and oxygen support. This may be differentiated from MAS if no MSAF was seen at delivery. Blood gases shows hypoxaemia and acidosis.

39
Q

How does MAS and persistent pulmonary hypertension differ?

A

This can be present on its own or in combination with MAS. The newborn has persistent hypoxaemia causing respiratory distress. Causes of PPHN need to be investigated e.g. PDA with pre-ductal and post-ductal oxygen saturations.