Meconium Aspiration Imaging

Updated: Jul 02, 2019

Author: Lynne M Smith, MD, FAAP; Chief Editor: Eugene C Lin, MD

Practice Essentials

Meconium is the first substance discharged from the gastrointestinal tract in the perinatal period and consists of a mixture of water (75-95%), mucopolysaccharides (80% dry weight), gastrointestinal secretions (bile salts and pancreatic and liver enzymes), solids (vernix caseosa, lanugo, and squamous cells), blood, minerals, and lipids (free fatty acids). Meconium aspiration syndrome involves aspiration of meconium through the trachea into the bronchial tree, sometimes down to the alveoli. Meconium is rarely found in the amniotic fluid before 34 weeks' gestation, probably because its passage likely requires neural stimulation of a mature gastrointestinal tract; thus, meconium aspiration syndrome, in which the newborn aspirates the meconium-containing amniotic fluid, chiefly affects infants at term and post-term.[1]

Three classes of alveoli are described: (1) those not ventilated due to complete proximal obstruction (atelectatic), (2) those with partial meconium obstruction, and (3) those with no proximal obstruction. Alveoli with partial meconium obstruction are thought to trap air because of a ball-valve mechanism by which gas reaches the alveoli on inflation but is trapped secondary to reduced airway diameter during expiration. It is challenging to oxygenate babies with meconium aspiration syndrome, because the alveoli where gas trapping occurs may rupture, leading to air leak. Also, meconium in the alveoli may deactivate surfactant.[2, 3, 4, 5]

Meconium aspiration is a frequent problem in the newborn; meconium-stained amniotic fluid is noted in 10-15% of deliveries, and males and females are affected equally. Of such deliveries, 5-15% of the infants develop symptoms of respiratory distress.[6] In fact, infants born through meconium-stained amniotic fluid are at 100-fold greater risk of developing respiratory distress than those born with clear amniotic fluid.[2]

In addition to obstruction of the airway, the aspiration leads to an inflammatory response in the lung parenchyma (chemical pneumonitis). It is this inflammation, not the meconium itself, that results in the patchy infiltrates seen on chest radiography (see the images below). It is not clear which component(s) of meconium triggers the inflammatory response. However, bile and liver enzymes have been suggested as the causative agents. The viscosity of the meconium and the response to aspiration are highly variable, and pulmonary hypertension is a significant comorbidity that is not obvious on chest radiography. Therefore, the clinical picture may be poorly correlated with the radiographic findings.

Preferred imaging study

Chest radiography is the preferred examination.[3, 7, 4, 8] However, the inflammatory process of meconium aspiration may have various presentations on chest radiography, and it is initially indistinguishable from transient tachypnea of the newborn or neonatal pneumonia. Without visualization of meconium below the vocal cords during resuscitation, the diagnosis is made on the basis of the clinical course and the results of follow-up imaging studies. If neurologic damage is suspected, neuroimaging modalities such as computed tomography (CT) scanning, magnetic resonance imaging (MRI), and ultrasonography[9] may be considered.[10] An echocardiogram is needed in severe cases of meconium aspiration syndrome with prolonged respiratory distress to evaluate cardiac function in the setting of potential persistent pulmonary hypertension of the newborn (PPHN) and congenital cardiovascular problems.

Meconium aspiration. Serial radiographs in a newborn with uncomplicated meconium aspiration. Radiograph obtained shortly after birth shows ill-defined, predominantly perihilar opacities in the lungs; these are more severe on the right than on the left. The lungs are hyperexpanded. The neonate's heart size is within normal limits. The abnormalities on the initial chest radiograph, aside from the presence of an endotracheal tube and an umbilical artery catheter, are identical to those seen in severe cases of transient tachypnea of the newborn.

Meconium aspiration. Radiograph obtained 2 days after that of the previous image shows almost complete resolution of the pulmonary opacities.

Meconium aspiration. Radiographic abnormalities in a patient with meconium aspiration who was treated with extracorporeal membrane oxygenation (ECMO). The lungs are airless because of pulmonary bypass. A cannula (arrows) enters from the right neck and extends to the right atrium, providing venous-venous ECMO. An endotracheal tube, a nasogastric tube, and an umbilical artery catheter are also in place.

Differential diagnosis and other problems to consider

Transient tachypnea of the newborn usually demonstrates patchy opacities on radiographs caused by pulmonary fluid in the process of resorption. Follow-up radiographs show rapid clearing of infiltrates, in contrast with meconium aspiration syndrome or pneumonia.

Neonatal pneumonia usually has patchy opacities representing consolidation, with pleural effusion present in up to two thirds of cases. Lung volumes are usually normal, but the lung fields may be hyperinflated.

Respiratory distress syndrome usually has a uniform distribution of opacities, classically with a ground-glass appearance and decreased lung volumes due to alveolar collapse. Air bronchograms may be seen. Pleural effusions are rare. This is most often seen in preterm infants (in contrast to those with meconium aspiration syndrome).

In addition to persistent pulmonary hypertension of the newborn (PPHN), other issues of neonates should be considered, including sepsis, pulmonary hypoplasia, congenital anatomic pulmonary anomalies, congenital diaphragmatic hernia, and congenital heart disease. PPHN can be confirmed with echocardiography.

Also, keep in mind that some cases of meconium aspiration syndrome result in litigation when parents discover that their infant requires long-term care due to sequelae of prolonged perinatal hypoxia.

Radiography

Chest radiography typically shows hyperinflation with patchy opacities. These findings represent areas of atelectasis mixed with areas of air trapping. Air leaks are common, leading to pneumothorax, pneumomediastinum, pneumopericardium, and/or pulmonary interstitial emphysema. Pleural effusions may be present. Note that it is important to assess the positioning of tubes (endotracheal, nasogastric), lines (umbilical arterial/venous catheters, peripherally inserted central catheters), and other devices. This disease is primarily a clinical diagnosis, and patients should be treated on the basis of their clinical presentation.[9] In isolation, chest radiographs are neither sensitive nor specific for the diagnosis of meconium aspiration syndrome. (See the following images.)

Meconium aspiration. Radiographic findings in a more severe case of meconium aspiration. This initial radiograph obtained shortly after birth shows patchy, coarse parenchymal opacities and severe hyperexpansion. In addition, pneumomediastinum is present on the right (arrows), outlining the right lobe of the thymus (T).

Meconium aspiration. Follow-up radiograph of the patient in the previous image. This image was obtained after placement of bilateral thoracostomy tubes for pneumothoraces and shows pneumopericardium (arrows) and extensive imaging lucencies in the lungs. These findings indicate pulmonary interstitial emphysema.

Ultrasonography

Lung ultrasonography has been found to correspond well with radiographic findings of meconium aspiration, while providing real-time bedside imaging with limited radiation exposure in neonates.[11, 12, 13]

In study of 117 newborns with meconium aspiration syndrome and 100 controls, the main lung ultrasonographic findings in patients with meconium aspirations were as follows[11] :

Pulmonary consolidation with air bronchogram was found in all patients.
Pleural line anomalies and the disappearance of the A-line were found in all patients.
Atelectasis was found in 19 (16.2%) severe cases, who demonstrated severe massive atelectasis and visible lung pulse.
Pleural effusion was found in 16 patients (13.7%).
Alveolar-interstitial syndrome or B-line in the nonconsolidation area was found in all patients with meconium aspiration.

Author

Lynne M Smith, MD, FAAP Associate Professor, Department of Pediatrics, University of California, Los Angeles, David Geffen School of Medicine; Director of Education, Neonatal-Perinatal Medicine Fellowship, Director, Level ll Nursery, Harbor-University of California at Los Angeles Medical Center

Lynne M Smith, MD, FAAP is a member of the following medical societies: American Academy of Pediatrics, Phi Beta Kappa, Society for Pediatric Research, Western Society for Pediatric Research, Perinatal Research Society

Disclosure: Nothing to disclose.

Coauthor(s)

Michael J Diament, MD Associate Professor, Department of Radiology, University of California at Los Angeles School of Medicine

Michael J Diament, MD is a member of the following medical societies: American Roentgen Ray Society, Radiological Society of North America, Society for Pediatric Radiology

Disclosure: Nothing to disclose.

Virender Rehan, MD, FAAP Professor, Department of Pediatrics, Director, Neonatal Intensive Care Unit, Division of Neonatology, Harbor-University of California at Los Angeles Medical Center; Director, Harbor-UCLA/CHOC Neonatal Fellowship Program

Virender Rehan, MD, FAAP is a member of the following medical societies: American Academy of Pediatrics, Rhode Island Medical Society, Royal College of Physicians, Society for Pediatric Research, Canadian Paediatric Society, Western Society for Pediatric Research, Indian Academy of Pediatrics, Royal College of Physicians of Ireland

Disclosure: Nothing to disclose.

Specialty Editor Board

Bernard D Coombs, MB, ChB, PhD Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand

Disclosure: Nothing to disclose.

David A Stringer, MBBS, FRCR, FRCPC Professor, National University of Singapore; Head, Diagnostic Imaging, KK Women's and Children's Hospital, Singapore

David A Stringer, MBBS, FRCR, FRCPC is a member of the following medical societies: Royal College of Physicians and Surgeons of Canada, Royal College of Radiologists, Society for Pediatric Radiology, British Columbia Medical Association, European Society of Paediatric Radiology

Disclosure: Nothing to disclose.

Chief Editor

Eugene C Lin, MD Attending Radiologist, Teaching Coordinator for Cardiac Imaging, Radiology Residency Program, Virginia Mason Medical Center; Clinical Assistant Professor of Radiology, University of Washington School of Medicine

Eugene C Lin, MD is a member of the following medical societies: American College of Nuclear Medicine, American College of Radiology, Radiological Society of North America, Society of Nuclear Medicine and Molecular Imaging

Disclosure: Nothing to disclose.

Additional Contributors

Henrique M Lederman, MD, PhD Professor of Radiology and Pediatric Radiology, Chief, Division of Diagnostic Imaging in Pediatrics, Federal University of Sao Paulo, Brazil

Henrique M Lederman, MD, PhD is a member of the following medical societies: Society for Pediatric Radiology

Disclosure: Nothing to disclose.

Acknowledgements

Daryoush Bassiri, MD Neonatology Fellow, Department of Pediatrics, Harbor-University of California at Los Angeles Medical Center, Children's Hospital of Orange County

Disclosure: Nothing to disclose.

Michael Leu, MD Staff Physician, Department of Pediatrics, Harbor-University of California at Los Angeles Medical Center