Neonatal Pneumonia Imaging 

Neonatal Pneumonia Imaging 

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Other than hematologic testing, blood biochemistry, and searches for the offending microorganism, chest radiographic imaging is considered to be an essential component in making the diagnosis of neonatal pneumonia, despite the potentially limited predictive value of radiographic and laboratory findings. [1] Attempts to identify and culture the causative microorganisms are often unsuccessful.

Diagnostic imaging is involved not only to initially assess the neonate’s condition and to establish a diagnosis but also to monitor the progress of the disease and the effects of interventional therapeutic measures. [2, 3, 4, 5, 6, 7] Bedside studies obtained using portable equipment are often limited but can provide much useful information when a careful, detailed approach is used to produce the radiograph and interpret the results. Conventional chest radiography remains the mainstay of diagnosis in neonates with respiratory symptoms (see the images below). [8, 9, 10, 11, 12]

Ultrasound is a useful technique in the detection of pleural fluid and guided aspiration of pleural effusions. CT scanning or MRI may be helpful in excluding tumors, aberrant vessels, sequestered lobes, or other primary pulmonary anomalies (see the images below). These studies may also help establish the presence of an infiltrate. Routine follow-up chest radiographs are not needed in childhood community-acquired pneumonia if the child has a clinically uneventful recovery. [2]

The findings on chest radiography are nonspecific and have a wide differential diagnosis. Several lung dysplasias may mimic viral pneumopathy, especially in newborns. [13] Ultrasound detects pleural effusions with a wide differential diagnosis. CT scanning and MRI are expensive tests, and neonates may require heavy sedation or general anesthetic to undergo them. The radiation dose from CT scanning is high. In addition, although intravenous contrast may not be required to detect pulmonary abnormalities, when used, it can have nephrotoxic effects.

Wahlgren et al looked at 346 children to evaluate whether radiologic findings and healing time in children with pneumonia correlated to etiologic agent and suggested that conclusions about etiology could not be drawn from the chest radiograph findings and that laboratory examinations must be used to confirm the radiologic diagnosis of viral pneumonias. [3]

Radiologic findings did not differ between etiologic groups but correlated significantly with patient age. The radiologic healing frequency on follow-up radiographs was significantly lower in children with mixed bacterial and viral etiology than in children from each of the other groups and to the material as a whole.

Thoracentesis is indicated when significant pleural fluid is detected with chest radiography or ultrasound (US). The procedure may be therapeutic or diagnostic. Diagnostic aspiration is usually performed for Gram stain, culture, and biochemical tests, while a therapeutic aspiration is indicated in neonates with respiratory distress. [14] US guidance can aid in the procedure. Stretching the skin down over the entry site may minimize the risk of pneumothorax or injury to the intercostal vessels: release after the procedure permits the return of tissues to their usual location to occlude the path of the needle. Needle puncture over the superior rib margin reduces the chance of laceration of the intercostal vessels. Care is taken to avoid further needle penetration once a fluid sample has been obtained. Aspiration should be continuous once the skin is penetrated.

Bronchoscopy may be used to obtain biopsy material or brush specimens or to perform guided aspiration. A direct rigid bronchoscope may be used in larger infants; however, the fiberoptic bronchoscope technique is preferred in smaller infants or in infants in whom distal sites cannot be reached with rigid bronchoscopes. Noncontaminated specimens may be difficult to obtain because of oral or airway commensals. It may be difficult to obtain samples from distal bronchial sites.

Direct lung aspiration is a useful method to sample lung infiltrate for culture or biopsy analysis. This procedure is associated with a higher risk of air leaks, as it usually requires a larger-bore needle than is used to obtain pleural fluid. Because of this risk, the procedure is reserved for (1) infants in whom empiric therapy has failed and for (2) infants who continue to deteriorate and in whom less invasive methods have failed to obtain microbial cultures. With advances in surgical techniques, clinicians may perform open surgical biopsy, as the success of obtaining adequate samples is much greater and complications may be dealt with directly.

MRI may be helpful to exclude tumors, aberrant vessels, sequestered lobes, or congenital hernias. Magnetic resonance angiography (MRA) and computed tomographic angiography (CTA) are relatively noninvasive techniques that may be substituted for angiography if required. More experience is required in using MRI to characterize neonatal intrathoracic abnormalities. MRI is not indicated in lung parenchymal abnormalities. Sequestrated lung segment is considered one of the differential diagnoses of neonatal pneumonia. Angiography represents the criterion standard in the detection and characterization of sequestrated lung segment but is being replaced with the relatively less invasive computed tomographic angiography (CTA) and the noninvasive technique of color Doppler ultrasonography. Angiography is an invasive technique, and a false-negative examination is possible with atypical arterial supply and venous drainage.

In neonates, most chest radiographs are obtained supine and in the anteroposterior projection (see the images below). Radiographs should be well centered and at the right penetration.

Other views may be required to explain anatomic relationships and detect air-fluid levels. Although neonatal pneumonia has no characteristic appearance, many chest radiographic findings are consistent with neonatal pneumonia. Some of the patterns described include the following:

Diffuse opacification of the lung parenchyma resembling the ground-glass appearances of respiratory distress syndrome. [14] This pattern is encountered with a hematogenous process; however, the appearances are nonspecific, and aspiration of infected fluid with secondary bloodstream infection can give rise to a similar appearance.

Patchy opacification or consolidation is generally regarded as a complication of antepartum or intrapartum aspiration, particularly when the peripheral parts of the lungs are involved. Patchy densities at the lung bases, more pronounced on the right, suggest postnatal aspiration.

The presence of pneumatoceles associated with pleural effusions indicates an infective pneumonic process.

Hyperinflation associated with patchy consolidation suggests partial airway obstruction from a mucous plug or inflammatory debris.

An air bronchogram usually suggests extensive consolidation, but the appearances are nonspecific and may be encountered in pulmonary hemorrhage or edema.

A tumefactive-type lobar consolidation in neonatal pneumonia is rare.

Images reflect conditions only at the instant in which the study is performed. Since neonatal lung diseases, including pneumonia, are dynamic, initially suggestive images may require reassessment based on the subsequent clinical course and findings in later studies.

Neonates in intensive care units frequently undergo radiographic examinations. It is of great importance that because of greater radiosensitivity and longer life expectancy of the neonates and premature babies, the radiation dose is optimized and kept to a minimum.

Faghihi et al studied 50 neonates, mostly premature, with different weights and gestational ages in 5 hospitals, mostly suffering from respiratory distress syndrome and pneumonia, and calculated the radiation dose involved using the values of entrance skin dose (ESD), dose area products (DAPs), energy imparted (EI), whole-body dose, and effective dose. [15] The risk of childhood cancer was estimated using 3 methods, including direct method (using thermoluminescence dosimetry [TLD] chips), indirect method (using tube output), and Monte Carlo (MC) method (using MCNP4C code).

In the first step, the ESD of the neonates was directly measured using TLD-100 chips. The values of ESD to neonates were indirectly obtained from the tube output in different imaging techniques. The results indicate that the mean ESD per radiograph estimated by the direct, indirect, and MC methods are 56.6±4.1, 50.1±3.1, and 54.5±3.3 μGy, respectively. The mean risk of childhood cancer estimated in this study varied between 4.21×10-7 and 2.72×10-6. [15]

Tracheoesophageal fistula is a rare malformation but should be suspected in neonates who present with coughing bouts and cyanosis after feeding and when radiography shows aspiration pneumonia, atelectasis, and gas within the colon. [16]

In a study of the chest radiographs of 30 infants with autopsy-proven pulmonary infections, the most common abnormality identified was bilateral alveolar densities (77%). Of these patients, one third had characteristically extensive, dense alveolar changes with numerous air bronchograms. A pattern of radiographic abnormalities consistent with transient tachypnea of the newborn was found in 17% of patients, and a second pattern resembling hyaline membrane disease was found in 13%. The authors suggested that the presence of a pleural effusion (in cases of the hyaline membrane disease pattern) and persistence beyond 1-2 days (in the transient tachypnea pattern) are helpful features in the diagnosis of neonatal pneumonia. Recognition of the spectrum of expected radiographic changes can aid in the diagnosis of neonatal pneumonia, particularly if this information is correlated with the clinical features. [17]

Cordero et al studied the changes that occur in chest radiographs at the time of gram-negative bacilli (GNB) nosocomial bloodstream infection (BSI) and determined the contribution of bronchopulmonary dysplasia (BPD). Radiographic signs of air space disease accompanied by the recovery of GNB respiratory pathogens from the blood and from a previously uncolonized airway strongly supported the clinical diagnosis of GNB nosocomial pneumonia. Radiologic signs of BPD were found to be stable in relation to nosocomial bloodstream infection (BSI) caused by GNB, but BPD radiologic scores were higher in infants who also had a newly acquired respiratory GNB. In newborns on ventilation, BSI, new respiratory tract GNB, and BPD were found to be critical associations for the clinical interpretation of radiographic changes. [18]

Flores described 10 newborn babies who developed respiratory distress and whose chest radiographs demonstrated a miliary nodular pattern. All patients received a diagnosis of bacterial pneumonia and appeared to respond favorably to antibiotic therapy. The pulmonary abnormalities resolved. The children were clinically well in less than 3 weeks. Flores suggests that hematogenous bacterial dissemination may produce the miliary pattern, one of the radiologic patterns of neonatal pneumonia. [19]

Dominguez et al described radiologic findings in the lungs of 16 hospitalized neonates with disseminated herpes simplex infection. [20] The authors devised a sequential picture of 4 stages in the evolution of the pneumonitis of this hematogenous infection. The radiologic stages were as follows:

Stage I, normal chest

Stage II, prominent perihilar interstitial markings

Stage III, coalescent areas of pulmonary infiltrates

Stage IV, diffuse alveolar and interstitial disease (“white-out” lungs)

In general, the pulmonary abnormalities were widespread and without air trapping. Pleural effusions were noted in one case. All affected neonates died, and antemortem clinical and radiologic findings were correlated with multiple-organ postmortem histopathologic evidence of viral infection, especially with the associated pneumonia.

Korppi et al examined 61 children with microbiologically verified viral pneumonia or radiologically verified bacterial pneumonia. [21] Their results suggested that the presence of an alveolar infiltrate on a chest radiograph is a specific but insensitive indicator of bacterial pneumonia. Korppi et al concluded that patients with alveolar pneumonia should be treated with antibiotics. However, in patients with interstitial pneumonia, a viral or bacterial etiology is possible.

CT scanning (see the images below) may be helpful to exclude tumors, aberrant vessels, sequestered lobes, or other primary pulmonary anomalies and to establish the presence of an infiltrate.

Chronic pneumonitis of infancy (CPI) is a rare entity. Olsen et al described chest radiography and high-resolution CT (HRCT) findings in a child with histologically confirmed chronic pneumonitis of infancy. The child was admitted for intensive care 18 hours after birth and died at age 39 days. Diffuse ground-glass change, interlobular septal thickening, and discrete centrilobular nodules were observed on HRCT. [4] An accurate diagnosis is crucial for correct management; however, several entities with the same HRCT findings are recognized.

CT scanning is also useful in the diagnosis of pulmonary sequestration. Wassia et al described a 2-day-old newborn with extrapulmonary sequestration that manifested as persistent Staphylococcus epidermidis pneumonia and high-output cardiac failure. [5] CT scanning of the chest without angiography established the diagnosis. Radiographic evaluation of pulmonary sequestration includes delineation of the aberrant systemic feeding artery and venous drainage. Color Doppler ultrasound, spiral CT scanning, and MR angiography are often sufficient to make the diagnosis.

HRCT in children remains a technically challenging procedure, both to perform optimally and to interpret correctly. Much remains to be learned about the optimal application of HRCT. However, HRCT can clarify often confusing or nonspecific chest radiographs, as well as clarify the diagnosis and evolution of both common and unusual pediatric lung diseases. As new therapies become available for these disorders and CT becomes faster and easier to perform, HRCT will be used more often for more accurate diagnosis and for better evaluation of therapeutic effects. [6]

Ultrasonography (US) is a useful adjunct to radiography in selected circumstances. [22] Sonograms are particularly useful for identifying and localizing fluid in the pleural and pericardial spaces. US is a noninvasive technique ideally suited to neonates, as sedation is seldom required. [23] US has high sensitivity in the detection of pleural effusions and detects consolidation at the lung bases. No radiation is involved, and the procedure may be repeated many times without untoward effects.

US is not ideal to detect air space disease. It is an operator-dependent procedure, and the modality produces many artifacts, which may result in false-positive and false-negative results. For example, soft tissue surgical emphysema following pleural intubation may degrade US examination quality.

Bober and Swietlinski assessed the diagnostic use of ultrasonography in respiratory distress syndrome (RDS) in 131 consecutive newborns and concluded that in RDS, 100% sensitivity and 92% specificity characterize US examination. Nevertheless, US cannot replace chest radiography in the evaluation for respiratory failure because it overestimates the diagnosis; however, US may be useful in excluding RDS as a cause of respiratory insufficiency in newborns. [7, 24]

Zar HJ, Andronikou S, Nicol MP. Advances in the diagnosis of pneumonia in children. BMJ. 2017 Jul 26. 358:j2739. [Medline].

Virkki R, Juven T, Mertsola J, Ruuskanen O. Radiographic follow-up of pneumonia in children. Pediatr Pulmonol. 2005 Sep. 40(3):223-7. [Medline].

Wahlgren H, Mortensson W, Eriksson M, Finkel Y, Forsgren M, Leinonen M. Radiological findings in children with acute pneumonia: age more important than infectious agent. Acta Radiol. 2005 Jul. 46(4):431-6. [Medline].

Olsen E OE, Sebire NJ, Jaffe A, Owens CM. Chronic pneumonitis of infancy: high-resolution CT findings. Pediatr Radiol. 2004 Jan. 34(1):86-8. [Medline].

Wassia HL, Hussein H, Binyaheb S. CT scan diagnosis of extralobar pulmonary sequestration: angiography not required. Saudi Med J. 2003 May. 24(5 Suppl):S35.

Kuhn JP, Brody AS. High-resolution CT of pediatric lung disease. Radiol Clin North Am. 2002 Jan. 40(1):89-110. [Medline].

Bober K, Swietlinski J. Diagnostic utility of ultrasonography for respiratory distress syndrome in neonates. Med Sci Monit. 2006 Oct. 12(10):CR440-6. [Medline].

Alzahrani SA, Al-Salamah MA, Al-Madani WH, Elbarbary MA. Systematic review and meta-analysis for the use of ultrasound versus radiology in diagnosing of pneumonia. Crit Ultrasound J. 2017 Dec. 9 (1):6. [Medline]. [Full Text].

Beer M, Ammann B. [Radiological diagnostics of pediatric lungs]. Radiologe. 2015 Jul. 55 (7):554-60. [Medline].

Ibrahim M, Omran A, Ibrahim M, Bioumy N, El-Sharkawy S. Lung Ultrasound in Early Diagnosis of Neonatal Ventilator Associated Pneumonia before Any Radiographic or Laboratory Changes. Case Rep Pediatr. 2016. 2016:4168592. [Medline].

Rath C, Suryawanshi P. Point of Care Neonatal Ultrasound – Head, Lung, Gut and Line Localization. Indian Pediatr. 2016 Oct 8. 53 (10):889-899. [Medline].

Rodríguez-Fanjul J, Balcells C, Aldecoa-Bilbao V, Moreno J, Iriondo M. Lung Ultrasound as a Predictor of Mechanical Ventilation in Neonates Older than 32 Weeks. Neonatology. 2016. 110 (3):198-203. [Medline].

Randaccio M. [Radiological aspects of viral respiratory diseases in childhood]. Minerva Med. 1980 Dec 8. 71(49):3617-26. [Medline].

Tudor J, Young L, Wigglesworth JS, Steiner RE. The value of radiology in the idiopathic respiratory distress syndrome: a radiological and pathological correlation study. Clin Radiol. 1976 Jan. 27(1):65-75. [Medline].

Faghihi R, Mehdizadeh S, Sina S, Alizadeh FN, Zeinali B, Kamyab GR, et al. Radiation dose to neonates undergoing X-ray imaging in special care baby units in Iran. Radiat Prot Dosimetry. 2012 Jun. 150(1):55-9. [Medline].

Sahnoun L, Aloui S, Nouri S, Ksia A, Krichene I, Mekki M. [Isolated congenital tracheoesophageal fistula]. Arch Pediatr. 2013 Feb. 20(2):186-91. [Medline].

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Cordero L, Coley BD, Hogan MJ, Ayers LW. Radiological pulmonary changes during gram-negative bacillary nosocomial bloodstream infection in premature infants. J Perinatol. 1998 Jul-Aug. 18(4):291-6. [Medline].

Flores JA. Miliary pattern in neonatal pneumonia. Pediatr Radiol. 1988. 18(4):355-6. [Medline].

Dominguez R, Rivero H, Gaisie G, Talmachoff P, Amortegui A, Young LW. Neonatal herpes simplex pneumonia: radiographic findings. Radiology. 1984 Nov. 153(2):395-9. [Medline].

Korppi M, Kiekara O, Heiskanen-Kosma T, Soimakallio S. Comparison of radiological findings and microbial aetiology of childhood pneumonia. Acta Paediatr. 1993 Apr. 82(4):360-3. [Medline].

Xin H, Li J, Hu HY. Is Lung Ultrasound Useful for Diagnosing Pneumonia in Children?: A Meta-Analysis and Systematic Review. Ultrasound Q. 2018 Mar. 34 (1):3-10. [Medline].

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Marini C, Bulleri A, Cambi L, Marinari A, Bernardini M, Bartalena L, et al. [The neonatal respiratory insufficiency syndrome: the role of the chest radiogram]. Radiol Med (Torino). 1997 Nov. 94(5):463-7. [Medline].

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Ali Nawaz Khan, MBBS, FRCS, FRCP, FRCR Consultant Radiologist and Honorary Professor, North Manchester General Hospital Pennine Acute NHS Trust, UK

Ali Nawaz Khan, MBBS, FRCS, FRCP, FRCR is a member of the following medical societies: American Association for the Advancement of Science, American Institute of Ultrasound in Medicine, British Medical Association, Royal College of Physicians and Surgeons of the United States, British Society of Interventional Radiology, Royal College of Physicians, Royal College of Radiologists, Royal College of Surgeons of England

Disclosure: Nothing to disclose.

Saeed Saleh Emam Mohammed, MD, MB, ChB Consulting Staff, Department of Medical Imaging, King Fahad National Guard Hospital, Saudi Arabia

Saeed Saleh Emam Mohammed, MD, MB, ChB is a member of the following medical societies: Royal College of Surgeons in Ireland

Disclosure: Nothing to disclose.

Klaus L Irion, MD, PhD Consulting Staff, The Cardiothoracic Centre Liverpool NHS Trust, The Royal Liverpool University Hospital, UK

Klaus L Irion, MD, PhD is a member of the following medical societies: American Roentgen Ray Society, Radiological Society of North America

Disclosure: Nothing to disclose.

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.

Henrique M Lederman, MD, PhD Consulting Staff, Department of Radiology, LeBonheur Children’s Medical Center and St Jude Children’s Research Hospital; 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.

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: British Columbia Medical Association, European Society of Paediatric Radiology, Royal College of Physicians and Surgeons of Canada, Royal College of Radiologists, and Society for Pediatric Radiology

Disclosure: Nothing to disclose.

Neonatal Pneumonia Imaging 

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