Meconium-stained Liquor

Authored by , Reviewed by Dr Colin Tidy | Last edited | Meets Patient’s editorial guidelines

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Treatment of almost all medical conditions has been affected by the COVID-19 pandemic. NICE has issued rapid update guidelines in relation to many of these. This guidance is changing frequently. Please visit https://www.nice.org.uk/covid-19 to see if there is temporary guidance issued by NICE in relation to the management of this condition, which may vary from the information given below.

Meconium is a dark green liquid normally passed by the newborn baby, containing mucus, bile and epithelial cells.

However, in some cases the meconium is passed while in utero, staining the amniotic fluid. This can vary from light to heavy staining. It is considered significant if dark green or black, with a thick, tenacious appearance.

Components of the meconium, especially the bile salts and enzymes, can cause serious complications if they are inhaled by the fetus at any stage of labour. This can result in meconium aspiration syndrome (MAS). There are several pathological mechanisms participating in MAS, including antenatal infection/inflammation and activation of the inflammatory cascade, mechanical airway obstruction, inactivation of surfactant and persistent pulmonary hypertension[1].

Meconium staining often occurs in conjunction with other causes of fetal distress. It is rare in babies born at <34 weeks of gestation.

The figure quoted for low-risk infants born with meconium-stained liquor is around 12% at term[2].

Deliveries complicated with meconium-stained amniotic fluid are associated with increased frequency of operative delivery, birth asphyxia, neonatal sepsis, and neonatal intensive care unit admissions compared to clear amniotic fluid[3].

Risk factors include:

These recommendations are from the National Institute for Health and Care Excellence (NICE) guidance, 2014 which was updated in 2017[4].

Intrapartum

  • If significant meconium staining is noted in labour, there should be continuous electronic fetal monitoring.
  • This is defined as dark green or black amniotic fluid that is thick or tenacious, or any amniotic fluid that contains lumps of meconium.
  • Transfer mother to obstetric-led care, if it is safe to do so and delivery is not imminent.
  • If there are signs of fetal distress, a fetal blood sample should be obtained. If pH is <7.21, there should be emergency delivery.
  • Ensure that the advanced resuscitation unit and appropriately trained staff are available.
  • There should be no suction prior to delivery.

At delivery - healthy neonate

  • If the baby is in good condition (Apgar score >5, based on colour, tone, heart rate and breathing), there should be no suction[5].
  • The baby should be observed for signs of respiratory distress in the first hour of life, in the second hour and then two-hourly until 12 hours old.
  • If there is blood or if there are lumps of meconium in the oropharynx, suction should be used in the upper airways.
  • Endotracheal intubation at birth in otherwise healthy, term meconium-stained babies, is no longer recommended.

At delivery - sick neonate

See the separate Meconium Aspiration article for further information. 

Infant respiratory distress syndrome[6]

  • Respiratory distress that usually occurs within four hours of birth and becomes persistently worse for 48 to 72 hours is known as infant respiratory distress syndrome. If not fatal, it resolves by 72 hours.
  • A deficiency of surfactant produces high alveolar surface tension. The baby must re-inflate the collapsed alveoli with every breath. Thus, every breath takes a lot of effort for relatively poor expansion.
  • Surfactant replacement therapy has shortened the duration of the disease and significantly reduced mortality. It is treated with administration of synthetic or animal surfactant.

Persistent pulmonary hypertension of the newborn

  • Babies may have persistent pulmonary hypertension of the newborn, as a consequence.
  • This occurs where the fetal circulation persists with blood being shunted away from the lungs through the foramen ovale and a patent ductus arteriosus.
  • It is a consequence of raised pulmonary vascular resistance. Clinical features include cyanosis, tachypnoea and the murmur of patent ductus arteriosus.

Treatment[7]
This includes:

  • Supportive measures, including ventilation.
  • Prostacyclin infusion.
  • Extracorporeal membrane oxygenation (ECMO).
  • Inhaled nitric oxide (iNO), which is well documented for treatment of PPHN, but 30% fail to respond.
  • Other current treatment options - these could be sildenafil, milrinone, prostaglandin analogues and bosentan.

Chronic lung disease

  • Children with meconium aspiration may develop chronic lung disease as a result of intense pulmonary intervention.
  • Infants with meconium aspiration have a slightly increased incidence of infections in the first year of life because the lungs are still in recovery.
  • Around 2% to 10% of babies born through amniotic fluid stained with meconium develop meconium aspiration syndrome (MAS)[8].
  • Late term fetuses have higher risk of developing respiratory complications[2].
  • Nearly all infants with MAS have complete recovery of pulmonary function.
  • Initial hypoxic events may cause the infant to have long-term neurological problems, including seizures, general learning disability and cerebral palsy.

Elective induction of labour for pregnancies at or beyond 41 weeks but before 42 weeks may be beneficial in preventing meconium staining and aspiration but is associated with several other adverse outcomes[9].

Amnioinfusion is associated with improved outcomes only in settings with reduced capability for perinatal surveillance[10].

Further reading and references

  • Gandhi CK; Management of Meconium-Stained Newborns in the Delivery Room. Neonatal Netw. 2018 May 137(3):141-148. doi: 10.1891/0730-0832.37.3.141.

  • Kelly LE, Shivananda S, Murthy P, et al; Antibiotics for neonates born through meconium-stained amniotic fluid. Cochrane Database Syst Rev. 2017 Jun 286:CD006183. doi: 10.1002/14651858.CD006183.pub2.

  1. Monfredini C, Cavallin F, Villani PE, et al; Meconium Aspiration Syndrome: A Narrative Review. Children (Basel). 2021 Mar 178(3). pii: children8030230. doi: 10.3390/children8030230.

  2. Hiersch L, Krispin E, Linder N, et al; Meconium-Stained Amniotic Fluid and Neonatal Morbidity in Low-Risk Pregnancies at Term: The Effect of Gestational Age. Am J Perinatol. 2017 Jan34(2):183-190. doi: 10.1055/s-0036-1585056. Epub 2016 Jul 1.

  3. Tolu LB, Birara M, Teshome T, et al; Perinatal outcome of meconium stained amniotic fluid among labouring mothers at teaching referral hospital in urban Ethiopia. PLoS One. 2020 Nov 1315(11):e0242025. doi: 10.1371/journal.pone.0242025. eCollection 2020.

  4. Intrapartum care for healthy women and babies; NICE Guideline (Dec 2014, updated Feb 2017)

  5. Kumar A, Kumar P, Basu S; Endotracheal suctioning for prevention of meconium aspiration syndrome: a randomized controlled trial. Eur J Pediatr. 2019 Dec178(12):1825-1832. doi: 10.1007/s00431-019-03463-z. Epub 2019 Oct 7.

  6. Chowdhury N, Giles BL, Dell SD; Full-Term Neonatal Respiratory Distress and Chronic Lung Disease. Pediatr Ann. 2019 Apr 148(4):e175-e181. doi: 10.3928/19382359-20190328-01.

  7. Pedersen J, Hedegaard ER, Simonsen U, et al; Current and Future Treatments for Persistent Pulmonary Hypertension in the Newborn. Basic Clin Pharmacol Toxicol. 2018 Oct123(4):392-406. doi: 10.1111/bcpt.13051. Epub 2018 Jul 19.

  8. Sayad E, Silva-Carmona M; Meconium Aspiration

  9. Rydahl E, Eriksen L, Juhl M; Effects of induction of labor prior to post-term in low-risk pregnancies: a systematic review. JBI Database System Rev Implement Rep. 2019 Feb17(2):170-208. doi: 10.11124/JBISRIR-2017-003587.

  10. Hofmeyr GJ, Xu H, Eke AC; Amnioinfusion for meconium-stained liquor in labour. Cochrane Database Syst Rev. 2014 Jan 23(1):CD000014. doi: 10.1002/14651858.CD000014.pub4.

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