Meconium aspiration syndrome
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
vigorous infant born through meconium-stained amniotic fluid, no respiratory distress
observation
Normal-term infants born through meconium-stained amniotic fluid without a history of maternal group B streptococcal infection or other infections, who are vigorous at birth and manifest no respiratory distress, can be allowed to stay with the mother as a normal newborn after routine delivery room care.[53]American College of Obstetricians and Gynecologists. Committee opinion no 689: delivery of a newborn with meconium-stained amniotic fluid. Obstet Gynecol. 2017 Mar;129(3):e33-4. https://journals.lww.com/greenjournal/Fulltext/2017/03000/Committee_Opinion_No_689__Delivery_of_a_Newborn.46.aspx http://www.ncbi.nlm.nih.gov/pubmed/28225424?tool=bestpractice.com
Preventive measures for babies born through meconium-stained amniotic fluid have been investigated. Such interventions include amnioinfusion, oropharyngeal suctioning of the baby at the perineum, tracheal suction, and gastric aspiration. None of these interventions has been shown to reduce the risk of MAS, and their routine use is not recommended.[29]Wiswell TE, Gannon CM, Jacob J, et al. Delivery room management of the apparently vigorous meconium-stained neonate: results of the multicenter, international collaborative trial. Pediatrics. 2000 Jan;105(1 Pt 1):1-7.
http://www.ncbi.nlm.nih.gov/pubmed/10617696?tool=bestpractice.com
[33]Fraser WD, Hofmeyr J, Lede R, et al; Amnioinfusion Trial Group. Amnioinfusion for the prevention of the meconium aspiration syndrome. N Engl J Med. 2005 Sep 1;353(9):909-17.
http://www.nejm.org/doi/full/10.1056/NEJMoa050223#t=article
http://www.ncbi.nlm.nih.gov/pubmed/16135835?tool=bestpractice.com
[34]Velaphi S, Vidyasagar D. The pros and cons of suctioning at the perineum (intrapartum) and post-delivery with and without meconium. Semin Fetal Neonatal Med. 2008 Dec;13(6):375-82.
http://www.ncbi.nlm.nih.gov/pubmed/18474453?tool=bestpractice.com
[35]Vain NE, Szyld EG, Prudent LM, et al. Oropharyngeal and nasopharyngeal suctioning of meconium-stained neonates before delivery of their shoulders: multicentre, randomised controlled trial. Lancet. 2004 Aug 14-20;364(9434):597-602.
http://www.ncbi.nlm.nih.gov/pubmed/15313360?tool=bestpractice.com
[36]Falciglia HS, Henderschott C, Potter P, et al. Does DeLee suction at the perineum prevent meconium aspiration syndrome? Am J Obstet Gynecol. 1992 Nov;167(5):1243-9.
http://www.ncbi.nlm.nih.gov/pubmed/1442972?tool=bestpractice.com
[37]Chettri S, Adhisivam B, Bhat BV. Endotracheal suction for nonvigorous neonates born through meconium stained amniotic fluid: a randomized controlled trial. J Pediatr. 2015;166:1208-1213.
http://www.ncbi.nlm.nih.gov/pubmed/25661412?tool=bestpractice.com
[38]Nangia S, Sunder S,Biswas R, et al. Endotracheal suction in term nonvigorous meconium stained neonates - a pilot study. Resuscitation. 2016;105:79-84.
http://www.ncbi.nlm.nih.gov/pubmed/27255954?tool=bestpractice.com
[39]Kiremitci S, Tuzun F, Yesilirmak DC, et al. Is gastric aspiration needed for newborn management in delivery room? Resuscitation. 2011 Jan;82(1):40-4.
http://www.ncbi.nlm.nih.gov/pubmed/20951491?tool=bestpractice.com
[40]Yadav SK, Venkatnarayan K, Adhikari KM, et al. Gastric lavage in babies born through meconium stained amniotic fluid in prevention of early feed intolerance: a randomized controlled trial. J Neonatal Perinatal Med. 2018;11(4):393-7.
http://www.ncbi.nlm.nih.gov/pubmed/30149474?tool=bestpractice.com
[41]Gidaganti S, Faridi MM, Narang M, et al. Effect of gastric lavage on meconium aspiration syndrome and feed intolerance in vigorous infants born with meconium stained amniotic fluid: a randomized control trial. Indian Pediatr. 2018 Mar 15;55(3):206-10.
http://www.ncbi.nlm.nih.gov/pubmed/29629694?tool=bestpractice.com
[ ]
What are the benefits and harms of amnioinfusion for meconium‐stained liquor during labor in settings with standard peripartum surveillance?/cca.html?targetUrl=https://www.cochranelibrary.com/cca/doi/10.1002/cca.2208/fullShow me the answer
Treatment with antibiotics is not indicated if no risk factors or laboratory findings suggestive of infection are present (e.g., chorioamnionitis, prolonged rupture of membranes, oligohydramnios, fetal heart rate abnormalities, post-maturity).
observation plus antibiotics
Antibiotics are indicated in the presence of risk factors or laboratory findings suggestive of infection (e.g., chorioamnionitis, prolonged rupture of membranes, oligohydramnios, fetal heart rate abnormalities, post-maturity). Broad-spectrum antibiotics used include ampicillin and gentamicin.[54]Puopolo KM, Benitz WE, Zaoutis TE, et al. Management of neonates born at ≥35 0/7 weeks' gestation with suspected or proven early-onset bacterial sepsis. Pediatrics. 2018 Dec;142(6):e20182894. https://publications.aap.org/pediatrics/article/142/6/e20182894/37522/Management-of-Neonates-Born-at-35-0-7-Weeks http://www.ncbi.nlm.nih.gov/pubmed/30455342?tool=bestpractice.com Treatment with antibiotics should be discontinued if 48-hour blood cultures are negative, unless there is clear evidence of site-specific infection.[54]Puopolo KM, Benitz WE, Zaoutis TE, et al. Management of neonates born at ≥35 0/7 weeks' gestation with suspected or proven early-onset bacterial sepsis. Pediatrics. 2018 Dec;142(6):e20182894. https://publications.aap.org/pediatrics/article/142/6/e20182894/37522/Management-of-Neonates-Born-at-35-0-7-Weeks http://www.ncbi.nlm.nih.gov/pubmed/30455342?tool=bestpractice.com If blood cultures are positive, antibiotics should be continued for up to 7 days.
Preventive measures for babies born through meconium-stained amniotic fluid have been investigated. Such interventions include amnioinfusion, oropharyngeal suctioning of the baby at the perineum, tracheal suction, and gastric aspiration. None of these interventions has been shown to reduce the risk of MAS, and their routine use is not recommended.[29]Wiswell TE, Gannon CM, Jacob J, et al. Delivery room management of the apparently vigorous meconium-stained neonate: results of the multicenter, international collaborative trial. Pediatrics. 2000 Jan;105(1 Pt 1):1-7.
http://www.ncbi.nlm.nih.gov/pubmed/10617696?tool=bestpractice.com
[33]Fraser WD, Hofmeyr J, Lede R, et al; Amnioinfusion Trial Group. Amnioinfusion for the prevention of the meconium aspiration syndrome. N Engl J Med. 2005 Sep 1;353(9):909-17.
http://www.nejm.org/doi/full/10.1056/NEJMoa050223#t=article
http://www.ncbi.nlm.nih.gov/pubmed/16135835?tool=bestpractice.com
[34]Velaphi S, Vidyasagar D. The pros and cons of suctioning at the perineum (intrapartum) and post-delivery with and without meconium. Semin Fetal Neonatal Med. 2008 Dec;13(6):375-82.
http://www.ncbi.nlm.nih.gov/pubmed/18474453?tool=bestpractice.com
[35]Vain NE, Szyld EG, Prudent LM, et al. Oropharyngeal and nasopharyngeal suctioning of meconium-stained neonates before delivery of their shoulders: multicentre, randomised controlled trial. Lancet. 2004 Aug 14-20;364(9434):597-602.
http://www.ncbi.nlm.nih.gov/pubmed/15313360?tool=bestpractice.com
[36]Falciglia HS, Henderschott C, Potter P, et al. Does DeLee suction at the perineum prevent meconium aspiration syndrome? Am J Obstet Gynecol. 1992 Nov;167(5):1243-9.
http://www.ncbi.nlm.nih.gov/pubmed/1442972?tool=bestpractice.com
[37]Chettri S, Adhisivam B, Bhat BV. Endotracheal suction for nonvigorous neonates born through meconium stained amniotic fluid: a randomized controlled trial. J Pediatr. 2015;166:1208-1213.
http://www.ncbi.nlm.nih.gov/pubmed/25661412?tool=bestpractice.com
[38]Nangia S, Sunder S,Biswas R, et al. Endotracheal suction in term nonvigorous meconium stained neonates - a pilot study. Resuscitation. 2016;105:79-84.
http://www.ncbi.nlm.nih.gov/pubmed/27255954?tool=bestpractice.com
[39]Kiremitci S, Tuzun F, Yesilirmak DC, et al. Is gastric aspiration needed for newborn management in delivery room? Resuscitation. 2011 Jan;82(1):40-4.
http://www.ncbi.nlm.nih.gov/pubmed/20951491?tool=bestpractice.com
[40]Yadav SK, Venkatnarayan K, Adhikari KM, et al. Gastric lavage in babies born through meconium stained amniotic fluid in prevention of early feed intolerance: a randomized controlled trial. J Neonatal Perinatal Med. 2018;11(4):393-7.
http://www.ncbi.nlm.nih.gov/pubmed/30149474?tool=bestpractice.com
[41]Gidaganti S, Faridi MM, Narang M, et al. Effect of gastric lavage on meconium aspiration syndrome and feed intolerance in vigorous infants born with meconium stained amniotic fluid: a randomized control trial. Indian Pediatr. 2018 Mar 15;55(3):206-10.
http://www.ncbi.nlm.nih.gov/pubmed/29629694?tool=bestpractice.com
[ ]
What are the benefits and harms of amnioinfusion for meconium‐stained liquor during labor in settings with standard peripartum surveillance?/cca.html?targetUrl=https://www.cochranelibrary.com/cca/doi/10.1002/cca.2208/fullShow me the answer
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
mild MAS
oxygen therapy plus supportive care
Infants with mild respiratory distress, tachypnoea, mild cyanosis, and retractions should be admitted to the neonatal intensive care unit (NICU) for treatment and observation.
Infants should be placed in Isolette, or under an infant warmer, and oxygen saturation should be monitored continuously.
Oxygen should be given by hood or nasal cannula to maintain oxygen saturations at 92% to 97%. Usually, may require FiO₂ <0.40 for a short duration of 48 to 72 hours. As respiratory distress begins to improve, FiO₂ should be decreased by 5% at a time, as tolerated, depending on pulse oximeter reading.
Intravenous fluids (10% dextrose in water) should be started on day 1. On subsequent days, switching to nasogastric or oral feeds, as tolerated, should be considered if the infant's respiratory status improves. If feedings are not adequate, intravenous fluid should be increased (80-90 mL/kg/day, adding NaCl at 2-4 mmol/kg/day [2-4 mEq/kg/day] plus amino acids) to meet the daily requirement. Giving intravenous fluids containing glucose 6 to 8 mg/minute/kg is indicated in those with hypoglycaemia until resolution.
Other measures may include providing partial exchange to lower the haematocrit and improve blood flow in infants with high haemoglobin, or blood transfusion if haemoglobin is low (<130 g/L [<13 g/dL]).
antibiotics
Additional treatment recommended for SOME patients in selected patient group
Indicated in the presence of risk factors or laboratory findings suggestive of infection, such as chorioamnionitis, prolonged rupture of membranes, oligohydramnios, fetal heart rate abnormalities, post-maturity. Broad-spectrum antibiotics used include ampicillin and gentamicin.[54]Puopolo KM, Benitz WE, Zaoutis TE, et al. Management of neonates born at ≥35 0/7 weeks' gestation with suspected or proven early-onset bacterial sepsis. Pediatrics. 2018 Dec;142(6):e20182894. https://publications.aap.org/pediatrics/article/142/6/e20182894/37522/Management-of-Neonates-Born-at-35-0-7-Weeks http://www.ncbi.nlm.nih.gov/pubmed/30455342?tool=bestpractice.com
Treatment with antibiotics should be discontinued if 48-hour blood cultures are negative, unless there is clear evidence of site-specific infection.[54]Puopolo KM, Benitz WE, Zaoutis TE, et al. Management of neonates born at ≥35 0/7 weeks' gestation with suspected or proven early-onset bacterial sepsis. Pediatrics. 2018 Dec;142(6):e20182894. https://publications.aap.org/pediatrics/article/142/6/e20182894/37522/Management-of-Neonates-Born-at-35-0-7-Weeks http://www.ncbi.nlm.nih.gov/pubmed/30455342?tool=bestpractice.com If blood cultures are positive, antibiotics should be continued for up to 7 days.
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
moderate MAS
CPAP ventilation
Patients in this group include infants with moderate respiratory distress who do not respond to oxygen therapy, or infants with moderate respiratory distress at presentation.
In infants with spontaneous breathing and good respiratory effort, continuous positive airway pressure (CPAP) should be started with nasal prongs if FiO₂ needs exceed 0.40 to maintain saturations within normal limits. Starting CPAP is 4 to 6 cm of H₂O. Further increase of CPAP level is determined by presence of atelectasis and work of breathing. CPAP should be avoided in the presence of air leaks and air trapping on CXR. Complications include abdominal distension, air trapping because of underlying ball-valve mechanisms or excessive flow, and distending pressure. These potential complications warrant close monitoring. CPAP reduces the need for mechanical ventilation in infants with MAS who have peripheral oxygen saturations <90% and respiratory distress score >4.[55]Pandita A, Murki S, Oleti TP, et al. Effect of nasal continuous positive airway pressure on infants with meconium aspiration syndrome: a randomized clinical trial. JAMA Pediatr. 2018 Feb 1;172(2):161-5. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839267 http://www.ncbi.nlm.nih.gov/pubmed/29204652?tool=bestpractice.com
Arterial blood gases should be obtained every 4 to 6 hours, and FiO₂ should be adjusted to maintain oxygen saturations between 92% and 97% or higher, and PaO₂ of 80 to 100 mmHg (10.3 to 13.0 kPa).
antibiotics plus supportive care
Treatment recommended for ALL patients in selected patient group
Treatment with intravenous broad-spectrum antibiotics (e.g., ampicillin and gentamicin) is initiated in all patients.
Supportive care includes parenteral nutrition with amino acid solution and intralipid solution to meet caloric requirements.
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
vasopressor/inotrope
Additional treatment recommended for SOME patients in selected patient group
Infants with MAS are prone to developing hypertension, especially after receiving sedatives. Inotropes such as dopamine, dobutamine, and adrenaline (epinephrine) may be administered to maintain a higher systemic pressure and avoid hypotension from simultaneous administration of sedatives. Due to dopamine’s non-selective systemic and pulmonary vasoconstriction it can often lead to increased pulmonary vascular resistance. Expert consensus therefore now supports the use of dobutamine and/or adrenaline (which is also a vasopressor) to support cardiac function in MAS, particularly when pulmonary hypertension is suspected.[61]Jain A, Giesinger RE, Dakshinamurti S, et al. Care of the critically ill neonate with hypoxemic respiratory failure and acute pulmonary hypertension: framework for practice based on consensus opinion of neonatal hemodynamics working group. J Perinatol. 2022 Jan;42(1):3-13. http://www.ncbi.nlm.nih.gov/pubmed/35013586?tool=bestpractice.com [62]Osman A, Halling C, Crume M, et al. Meconium aspiration syndrome: a comprehensive review. J Perinatol. 2023 Oct;43(10):1211-21. http://www.ncbi.nlm.nih.gov/pubmed/37543651?tool=bestpractice.com
Consult a specialist for guidance on suitable inotrope/vasopressor regimens and doses.
surfactant
Additional treatment recommended for SOME patients in selected patient group
Pulmonary surfactant may be altered or inactivated in babies with MAS. A bolus dose of surfactant may be given through the endotracheal tube. If pneumothorax is present, it should be treated before giving surfactant therapy. Evidence suggests that surfactant administration in infants with moderate to severe MAS decreases the risk of progressive respiratory failure that requires support with extracorporeal membrane oxygenation (ECMO).[56]El Shahed AI, Dargaville P, Ohlsson A, et al. Surfactant for meconium aspiration syndrome in term and late preterm infants. Cochrane Database Syst Rev. 2014 Dec 14;(12):CD002054. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD002054.pub3/full http://www.ncbi.nlm.nih.gov/pubmed/25504256?tool=bestpractice.com [57]Abdelaal MA, Abushanab D, Al-Badriyeh D. Surfactant therapy for meconium aspiration syndrome in neonates: a systematic overview of systematic reviews and recent clinical trials. J Comp Eff Res. 2020 Jun;9(8):527-36. http://www.ncbi.nlm.nih.gov/pubmed/32394731?tool=bestpractice.com [58]Arayici S, Sari FN, Kadioglu Simsek G, et al. Lung lavage with dilute surfactant vs. bolus surfactant for meconium aspiration syndrome. J Trop Pediatr. 2019 Oct 1;65(5):491-7. https://academic.oup.com/tropej/article/65/5/491/5299597 http://www.ncbi.nlm.nih.gov/pubmed/30690595?tool=bestpractice.com
Lung lavage with diluted surfactant in intubated infants in small aliquots may be considered, especially in units where further ECMO support is not available. Lung lavage with diluted surfactant may be beneficial, but further clinical trials are needed to determine long-term outcomes.[59]Dargaville PA, Copnell B, Mills JF, et al; lessMAS Trial Study Group. Randomized controlled trial of lung lavage with dilute surfactant for meconium aspiration syndrome. J Pediatr. 2011 Mar;158(3):383-9;e2.
https://www.jpeds.com/article/S0022-3476(10)00742-0/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/20947097?tool=bestpractice.com
[60]Hahn S, Choi HJ, Soll R, et al. Lung lavage for meconium aspiration syndrome in newborn infants. Cochrane Database Syst Rev. 2013 Apr 30;(4):CD003486.
http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD003486.pub2/full
http://www.ncbi.nlm.nih.gov/pubmed/23633311?tool=bestpractice.com
[ ]
Is there randomized controlled trial evidence to support the use of lung lavage in newborn infants with meconium aspiration syndrome?/cca.html?targetUrl=https://cochranelibrary.com/cca/doi/10.1002/cca.1001/fullShow me the answer Only an experienced specialist should perform lung lavage, as it is associated with severe desaturations.
Primary options
beractant intratracheal: 100-150 mg/kg endotracheal bolus
conventional mechanical ventilation
Infants who continue to exhibit respiratory distress should be intubated and mechanically ventilated. Intubation criteria include FiO₂ >0.60, increased work of breathing or apnoea, and deteriorating ABG values showing low PaO₂ (<50 mmHg, PaCO₂ 70 mmHg, dropping pH to <7.25). Once the infant is intubated and stabilised, blood gases and CXR should be obtained to reassess the condition.
In mechanically ventilated patients, sedation is preferable to muscle paralysis, although evidence-based recommendations to support this are lacking. Sedation decreases the agitation and frequent desaturation seen in these infants.
antibiotics plus supportive care
Treatment recommended for ALL patients in selected patient group
Treatment with intravenous broad-spectrum antibiotics (e.g., ampicillin and gentamicin) is initiated in all patients.
Supportive care includes parenteral nutrition with amino acid solution and intralipid solution to meet caloric requirements.
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
vasopressor/inotrope
Additional treatment recommended for SOME patients in selected patient group
Infants with MAS are prone to developing hypertension, especially after receiving sedatives. Inotropes such as dopamine, dobutamine, and adrenaline (epinephrine) may be administered to maintain a higher systemic pressure and avoid hypotension from simultaneous administration of sedatives. Due to dopamine’s non-selective systemic and pulmonary vasoconstriction it can often lead to increased pulmonary vascular resistance. Expert consensus therefore now supports the use of dobutamine and/or adrenaline (which is also a vasopressor) to support cardiac function in MAS, particularly when pulmonary hypertension is suspected.[61]Jain A, Giesinger RE, Dakshinamurti S, et al. Care of the critically ill neonate with hypoxemic respiratory failure and acute pulmonary hypertension: framework for practice based on consensus opinion of neonatal hemodynamics working group. J Perinatol. 2022 Jan;42(1):3-13. http://www.ncbi.nlm.nih.gov/pubmed/35013586?tool=bestpractice.com [62]Osman A, Halling C, Crume M, et al. Meconium aspiration syndrome: a comprehensive review. J Perinatol. 2023 Oct;43(10):1211-21. http://www.ncbi.nlm.nih.gov/pubmed/37543651?tool=bestpractice.com
Consult a specialist for guidance on suitable inotrope/vasopressor regimens and doses.
conventional or high-frequency ventilation plus inhaled nitric oxide (iNO)
Infants who are refractory to mechanical ventilation with high oxygen inspiration and surfactant treatment invariably have concomitant persistent pulmonary hypertension (PPHN). iNO should be given with a starting concentration of 20 ppm, along with conventional or high-frequency ventilation, if dual pulse oximetry or echocardiography demonstrates right-to-left shunt and oxygen index is >25.[63]Kinsella JP, Truog WE, Walsh WF, et al. Randomized, multicenter trial of inhaled nitric oxide and high-frequency oscillatory ventilation in severe, persistent pulmonary hypertension of the newborn. J Pediatr. 1997 Jul;131(1 Pt 1):55-62. http://www.ncbi.nlm.nih.gov/pubmed/9255192?tool=bestpractice.com [64]Barrington KJ, Finer N, Pennaforte T, et al. Nitric oxide for respiratory failure in infants born at term or near term. Cochrane Database Syst Rev. 2017 Jan 5;(1):CD000399. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD000399.pub3/full http://www.ncbi.nlm.nih.gov/pubmed/28056166?tool=bestpractice.com Echocardiographic evaluation is recommended before initiating iNO therapy to rule out cardiac disease and to assess pulmonary artery pressure and ventricular function. About 60% of infants with PPHN respond to iNO therapy.[63]Kinsella JP, Truog WE, Walsh WF, et al. Randomized, multicenter trial of inhaled nitric oxide and high-frequency oscillatory ventilation in severe, persistent pulmonary hypertension of the newborn. J Pediatr. 1997 Jul;131(1 Pt 1):55-62. http://www.ncbi.nlm.nih.gov/pubmed/9255192?tool=bestpractice.com
Once FiO₂ can be weaned to 0.60, then iNO should be weaned gradually. Methaemoglobin should be monitored.
In patients who are difficult to wean from iNO, sildenafil (a phosphodiesterase-5 inhibitor) can be added;[68]Steinhorn RH. Nitric oxide and beyond: new insights and therapies for pulmonary hypertension. J Perinatol. 2008 Dec;28(suppl 3):S67-71. https://www.nature.com/jp/journal/v28/n3s/full/jp2008158a.html http://www.ncbi.nlm.nih.gov/pubmed/19057613?tool=bestpractice.com [69]Kelly LE, Ohlsson A, Shah PS. Sildenafil for pulmonary hypertension in neonates. Cochrane Database Syst Rev. 2017 Aug 4;(8):CD005494. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD005494.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/28777888?tool=bestpractice.com however, it should be used cautiously (i.e., when the benefit-risk profile is acceptable) with appropriate cardiac evaluation, and high doses and long-term use should be avoided due to an increased risk of mortality in paediatric patients. Revatio (sildenafil): drug safety communication - FDA clarifies warning about pediatric use for pulmonary arterial hypertension Opens in new window
In mechanically ventilated patients, sedation is preferable to muscle paralysis, although evidence-based recommendations to support this are lacking. Sedation decreases the agitation and frequent desaturation seen in these infants.
antibiotics plus supportive care
Treatment recommended for ALL patients in selected patient group
Treatment with intravenous broad-spectrum antibiotics (e.g., ampicillin and gentamicin) is indicated in all patients.
Supportive care includes giving intravenous fluids. Infants with severe MAS may need initial fluid bolus (10 mL/kg). However, it subsequently should be restricted to 70 to 80 mL/kg/day, unless infant is asphyxiated, in which case it should be restricted even further (60 mL/kg/day). Sodium can be initiated at 1 to 2 mmol/kg/day (1-2 mEq/kg/day) on the first day.
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
vasopressor/inotrope
Additional treatment recommended for SOME patients in selected patient group
Infants with MAS are prone to developing hypertension, especially after receiving sedatives. Inotropes such as dopamine, dobutamine, and adrenaline (epinephrine) may be administered to maintain a higher systemic pressure and avoid hypotension from simultaneous administration of sedatives. Due to dopamine’s non-selective systemic and pulmonary vasoconstriction it can often lead to increased pulmonary vascular resistance. Expert consensus therefore now supports the use of dobutamine and/or adrenaline (which is also a vasopressor) to support cardiac function in MAS, particularly when pulmonary hypertension is suspected.[61]Jain A, Giesinger RE, Dakshinamurti S, et al. Care of the critically ill neonate with hypoxemic respiratory failure and acute pulmonary hypertension: framework for practice based on consensus opinion of neonatal hemodynamics working group. J Perinatol. 2022 Jan;42(1):3-13. http://www.ncbi.nlm.nih.gov/pubmed/35013586?tool=bestpractice.com [62]Osman A, Halling C, Crume M, et al. Meconium aspiration syndrome: a comprehensive review. J Perinatol. 2023 Oct;43(10):1211-21. http://www.ncbi.nlm.nih.gov/pubmed/37543651?tool=bestpractice.com
Consult a specialist for guidance on suitable inotrope/vasopressor regimens and doses.
severe MAS
high-frequency mechanical ventilation plus inhaled nitric oxide (iNO)
Patients in this group include infants who are refractory to mechanical ventilation with high oxygen inspiration and surfactant treatment or with severe respiratory distress at presentation. These infants are best managed at a level III neonatal intensive care unit (NICU; or IV, if no extracorporeal membrane oxygenation available at level III) under the care of a neonatologist.
Treatment consists of high-frequency ventilation plus iNO. Echocardiographic evaluation is recommended before initiating iNO therapy to rule out cardiac disease and to assess pulmonary artery pressure and ventricular function.
iNO should be given with starting concentration of 20 ppm, along with conventional or high-frequency ventilation, if dual pulse oximetry or echocardiography demonstrates right-to-left shunt and oxygen index is >25.[63]Kinsella JP, Truog WE, Walsh WF, et al. Randomized, multicenter trial of inhaled nitric oxide and high-frequency oscillatory ventilation in severe, persistent pulmonary hypertension of the newborn. J Pediatr. 1997 Jul;131(1 Pt 1):55-62. http://www.ncbi.nlm.nih.gov/pubmed/9255192?tool=bestpractice.com [64]Barrington KJ, Finer N, Pennaforte T, et al. Nitric oxide for respiratory failure in infants born at term or near term. Cochrane Database Syst Rev. 2017 Jan 5;(1):CD000399. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD000399.pub3/full http://www.ncbi.nlm.nih.gov/pubmed/28056166?tool=bestpractice.com
Once FiO₂ can be weaned to 0.60, then iNO should be weaned gradually. Methaemoglobin should be monitored.
In patients who are difficult to wean from iNO, sildenafil (a phosphodiesterase-5 inhibitor) can be added;[68]Steinhorn RH. Nitric oxide and beyond: new insights and therapies for pulmonary hypertension. J Perinatol. 2008 Dec;28(suppl 3):S67-71. https://www.nature.com/jp/journal/v28/n3s/full/jp2008158a.html http://www.ncbi.nlm.nih.gov/pubmed/19057613?tool=bestpractice.com [69]Kelly LE, Ohlsson A, Shah PS. Sildenafil for pulmonary hypertension in neonates. Cochrane Database Syst Rev. 2017 Aug 4;(8):CD005494. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD005494.pub4/full http://www.ncbi.nlm.nih.gov/pubmed/28777888?tool=bestpractice.com however, it should be used cautiously (i.e., when the benefit-risk profile is acceptable) with appropriate cardiac evaluation, and high doses and long-term use should be avoided due to an increased risk of mortality in paediatric patients. Revatio (sildenafil): drug safety communication - FDA clarifies warning about pediatric use for pulmonary arterial hypertension Opens in new window
In mechanically ventilated patients, sedation is preferable to muscle paralysis, although evidence-based recommendations to support this are lacking. Sedation decreases the agitation and frequent desaturation seen in these infants.
antibiotics plus supportive care
Treatment recommended for ALL patients in selected patient group
Treatment with intravenous broad-spectrum antibiotics (e.g., ampicillin and gentamicin) is initiated in all patients.
Supportive care includes parenteral nutrition with amino acid solution and intralipid solution to meet caloric requirements.
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
vasopressor/inotrope
Treatment recommended for ALL patients in selected patient group
Inotropes such as dobutamine can be used in infants with MAS and PPHN to maintain higher systemic pressure and avoid hypotension from simultaneous administration of sedatives. Adrenaline (epinephrine) may also be used for its combined inotrope and vasopressor properties. Arterial blood pressure must be maintained in suprasystemic pressure to overcome a right-to-left shunt at the ductal level secondary to PPHN.
Consult a consultant for guidance on suitable inotrope/vasopressor regimens and doses.
surfactant
Additional treatment recommended for SOME patients in selected patient group
Pulmonary surfactant may be altered or inactivated in babies with MAS. A bolus dose of surfactant may be given through the endotracheal tube. If pneumothorax is present, it should be treated before giving surfactant therapy. Evidence suggests that surfactant administration in infants with moderate to severe MAS decreases the risk of progressive respiratory failure that requires support with extracorporeal membrane oxygenation (ECMO).[56]El Shahed AI, Dargaville P, Ohlsson A, et al. Surfactant for meconium aspiration syndrome in term and late preterm infants. Cochrane Database Syst Rev. 2014 Dec 14;(12):CD002054. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD002054.pub3/full http://www.ncbi.nlm.nih.gov/pubmed/25504256?tool=bestpractice.com [57]Abdelaal MA, Abushanab D, Al-Badriyeh D. Surfactant therapy for meconium aspiration syndrome in neonates: a systematic overview of systematic reviews and recent clinical trials. J Comp Eff Res. 2020 Jun;9(8):527-36. http://www.ncbi.nlm.nih.gov/pubmed/32394731?tool=bestpractice.com [58]Arayici S, Sari FN, Kadioglu Simsek G, et al. Lung lavage with dilute surfactant vs. bolus surfactant for meconium aspiration syndrome. J Trop Pediatr. 2019 Oct 1;65(5):491-7. https://academic.oup.com/tropej/article/65/5/491/5299597 http://www.ncbi.nlm.nih.gov/pubmed/30690595?tool=bestpractice.com
Lung lavage with diluted surfactant in intubated infants in small aliquots may be considered, especially in units where further ECMO support is not available. Lung lavage with diluted surfactant may be beneficial, but further clinical trials are needed to determine long-term outcomes.[59]Dargaville PA, Copnell B, Mills JF, et al; lessMAS Trial Study Group. Randomized controlled trial of lung lavage with dilute surfactant for meconium aspiration syndrome. J Pediatr. 2011 Mar;158(3):383-9;e2.
https://www.jpeds.com/article/S0022-3476(10)00742-0/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/20947097?tool=bestpractice.com
[60]Hahn S, Choi HJ, Soll R, et al. Lung lavage for meconium aspiration syndrome in newborn infants. Cochrane Database Syst Rev. 2013 Apr 30;(4):CD003486.
http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD003486.pub2/full
http://www.ncbi.nlm.nih.gov/pubmed/23633311?tool=bestpractice.com
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Is there randomized controlled trial evidence to support the use of lung lavage in newborn infants with meconium aspiration syndrome?/cca.html?targetUrl=https://cochranelibrary.com/cca/doi/10.1002/cca.1001/fullShow me the answer Only an experienced specialist should perform lung lavage, as it is associated with severe desaturations.
Primary options
beractant intratracheal: 100-150 mg/kg endotracheal bolus
extracorporeal membrane oxygenation (ECMO)
If there is no response to iNO therapy along with high-frequency ventilation, infants should be placed on ECMO. Indications include alveolar-arterial oxygen gradient >610 mmHg and oxygen index ≥40.[65]Radhakrishnan RS, Lally PA, Lally KP, et al. ECMO for meconium aspiration syndrome: support for relaxed entry criteria. ASAIO J. 2007 Jul-Aug;53(4):489-91. http://www.ncbi.nlm.nih.gov/pubmed/17667237?tool=bestpractice.com [66]Bartlett RH, Gazzaniga AB, Huxtable RF, et al. Extracorporeal circulation (ECMO) in neonatal respiratory failure. J Thorac Cardiovasc Surg. 1977 Dec;74(6):826-33. http://www.ncbi.nlm.nih.gov/pubmed/926812?tool=bestpractice.com
In mechanically ventilated patients, sedation is preferable to muscle paralysis, although evidence-based recommendations to support this are lacking. Sedation decreases the agitation and frequent desaturation seen in these infants.
antibiotics plus supportive care
Treatment recommended for ALL patients in selected patient group
Treatment with intravenous broad-spectrum antibiotics (e.g., ampicillin and gentamicin) is indicated in all patients.
Supportive care includes parenteral nutrition with amino acid solution and intralipid solution to meet caloric requirements.
Primary options
ampicillin: 50-100 mg/kg/day intravenously given in divided doses every 6-12 hours depending on age and weight
and
gentamicin: 4-5 mg/kg/day intravenously given in divided doses depending on age and weight
vasopressor/inotrope
Treatment recommended for ALL patients in selected patient group
Inotropes such as dobutamine can be used in infants with MAS and PPHN to maintain higher systemic pressure and avoid hypotension from simultaneously giving sedatives. Adrenaline (epinephrine) may also be used for its combined inotrope and vasopressor properties. Arterial blood pressure must be maintained in suprasystemic pressure to overcome a right-to-left shunt at the ductal level secondary to PPHN.
Consult a consultant for guidance on suitable inotrope/vasopressor regimens and doses.
Choose a patient group to see our recommendations
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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