2. Meconium aspiration occurs due to
combination of meconium stained amniotic
fluid and gasping by the fetus or newly born.
3. EPIDEMIOLOGY
Meconium stained amniotic fluid complicates approximately 10% to 15% of
deliveries
The incidence of MSAF in preterm is very low.
Most babies with MSAF are 37 weeks or older and many meconium stained
infants are post mature or SGA.
Incidence has decreased in developed coumtries due to better perinatal care
but remains high in developing countries.
4. MECONIUM
Sterile, thick, black-green, odorless material that results from accumulation
of debries in fetal intestine stating in 3rd month of gestation
5. COMPOSITION OF MECONIUM
Water
Desquamated cells
GI mucin
Lanugo hair cells
Bile
Amniotic fluid
6. CAUSES
Passage of meconium in utero
Normally passage of meconium from fetus to amnion is prevented by lack of
peristalsis i.e low motilin levels, tonic contraction of Anal spincter.
Post term fetus has high motilin levels.
Vagal stimulation by chord or head compression or in utero fetal stress
causing relaxation of Anal spincter.
7. RISK FACTORS
Maternal Hypertension
Maternal DM
Maternal heavy cigarette smoking
Maternal chronic respiratory or cardiovascular disorder
Post term pregnancy
Pre-eclampsia/eclampsia
Oligohydramnios
IUGR
Abnormal fetal HR pattern
9. PATHOPHYSIOLOGY
Chemical pneumonitis
Surfactant inactivation
When aspirated into lungs, meconium may stimulate release of cytokines and
vasoactive substances that result in cardiovascular and inflammatory response
in fetus and newborn .
Meconium causes mechanical obstruction leading to atelectasis and ball valve
effect with resultant air trapping.
Aspirated meconium inhibits surfactant function.
Enzymatic and sterol component of meconium disrupts the surfactant
phospholipids and limit the ability of surfactant to to lower surface tension.
10.
11. PATHOPHYSIOLOGY
Pulmonary hypertension
Aspirated meconium leads to vasospasm,hypertrophy of pulmonary
vasculature and pulmonary hypertension
About one-third infants with MAS develop persistant pulmonary hypertension
of newborn, which contribute to mortality associated with the syndrome,
12. SEVERITY
MAS is considered mild in infants requiring <40% oxygen foe <48 hours and
moderate in infants requiring >40% oxygen for >48 hours without air leak.
It is considered severe in infants who require assisted ventilation and/or CPAP
and is often associated with PPHN.
13. CLINICAL FEATURES
Infants with MAS must have a history of MSAF.
They often are term or post term.
IUGR
14.
15. CLINICAL FEATURES
Physical examination
Evidence of post maturity:peeling skin, long fingernails etc.
The vernix,umbilical chord and nails may be meconium stained,depending
upon how long the infant has been exposed in utero.
17. DIAGNOSIS
A chest radiograph may help determine those infants who are most likely to
develop respiratory distress.
Significant number of asymptomatic infants will have an abnormal appearing
chest film.
Classic findings are diffuse, asymmetric patchy infiltrates, areas of
consolidation, often worse on right and hyperventilation.
Monitoring of oxygen saturation during this period aids assessment of the
severity of the infant`s condition and avoids hypoxemia.
18. PREVENTION OF MAS
Prevention of passage of meconium in utero
Amnioinfusion
Timing and Mode of delivery
Womens at risk which includes those with eclampsia, preeclampsia,
hypertensive, IUGR should be carefully monitored during pregnancy.
Associated with improvement in perinatal outcome.
It is not clear whether the benefits are due to dilution of meconium or relief
of oligohydramnios.
Induction as early as 41 weeks can prevent MAS.
Mode of delivery does not affect the risk of aspiration.
19. MANAGEMENT OF INFANTS DELIVERED
THROUGH MECONIUM STAINED FLUID
Oropharyngeal and nasopharyngeal suctioning on perineum and routine
tracheal intubation and aspiration of meconium in vigorous infants are not
effective in preventing MAS.
Although it was earlkier recommended in nonvigorous infants.
According to 2015 Neonatal Resuscitation Guidelines, emphasis should be
placed on appropriate interventions to support ventilation and oxygenation.
If an infant does not improve with intubation and positive-pressure ventilation
trachea should be suctioned using a suction catheter inserted through the ET
tube or directly suctioned through the tube using meconium aspirator.
Recommended suction pressure should be less than 80 to 100 mmHg.
20. MANAGEMENT OF MAS
A. OBSERVATION
1. chest x-ray
2. monitoring of oxygen saturation
B. CARE FOR NEONATE WITH MAS
1. infant should be maintained in neutral thermal environment.
2. blood glucose and calcium levels should be assessed and managed if
necessary.
3. therapy for hypotension and poor cardiac output, including cardiotonic
medications such as dopamine.
4.circulatory support with NS or packed RBC in patients with marginal
oxygenation, in infants with substantial oxygenation and ventilator requirements
we maintain Hb concentration above 15g.
5. monitor renal functions.
21. C. OXYGEN THERAPY
management of hypoxemia should be accomplished by increasing the
inspired oxygen concentration and by monitoring blood gases and pH.
D. ASSISTED VENTILATION
1. CPAP – if FiO2 requirement exceeds 0.40.
2. MECHANICAL VENTILATION - indicated for excessive CO2 retention
(PaCO2 >60 mmhg) or for persistant hypoxemia (PaO2 <50 mmhg) .
peak inspiratory pressure should be limited to pressures resulting in
gentle chest movement and tidal volume 5 to 6 ml/kg; PEEP should depend on
individual`s response.adequate expiratory time should be permitted to
prevent air trapping behind partly obstructed airways.
useful starting points are inspiratory time of 0.4 seconds at a rate of 30 to
40 breths per minute.
3. INHALED NITRIC OXIDE AND EXTRACORPOREAL MEMBRANE
OXYGENATION- in refractory respiratory failure
22. E. MEDICATIONS
1. Antibiotics
use of broad spectrum antibiotics (e.g. ampicillin and gentamycin ) is usually indicated in
infants when an infiltrate is seen on chest radioghaph.
blood cultures should be obtained to identify the bacterial disease, if present and to
determine duration of antibiotic course.
2. Surfactant
surfactant replacement improves oxygenation and reduces need for EMCO and is
recommended by committee on Fetus and Newborn of the American Academy of Pediatrics.
BAL with dilute surfactant might be beneficial.
3. Corticosteroids
not recommended routinely.
this approach has been proposed to minimize prostaglandin-mediated pulmonary
vasoconstriction.
4. Sedatives
in infants who require mechanical ventilation.
5.Antioxidants
N-acetylcystein and recombinant human superoxide dismutase to mitigate reactive oxygen
species(ROS) –induced lung injuryin MAS.
23. COMPLICATIONS
1. AIR LEAK
pneumothorax or pneumomediastinum occurs in approximately 15% to 33% of patients with
MAS.
occurs more commonly with mechanical ventilation, especially in setting of air trapping
2. PPHN
seen in approximately one-third of cases and contributes to mortality associated with this
syndrome.
depending on the extent of hypoxemia, echocardiography should be performed to
ascertain the degree to which the right and left shunt is contributing to infant`s overall
hypoxemia and exclude congenital heart disease.
3. Pulmonary sequelae
approximately 5% of survivors require supplemental oxygen at 1 month and a substantial
proportion may have an abnormal pulmonary function including increased functional residual
capacity and a higher incidence of pneumonia.