A preterm infant with mild respiratory insufficiency resulting from respiratory distress syndrome developed a pneumatocele after the start of nasal continuous positive airway pressure. Pneumonia was excluded by sputum and blood cultures. Treatment with high frequency oscillation ventilation resulted in complete recovery.
- nasal continuous positive airway pressure
- CPAP, continuous positive airway pressure
- HFOV, high frequency oscillation ventilation
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A preterm infant was admitted to the neonatal intensive care unit because of progressive respiratory insufficiency. He was born in another hospital after 34 weeks gestation by caesarean section because of a transverse lie. Steroids had not been administered antenatally. Membranes were ruptured for less than 24 hours. Apgar scores were 7, 7, and 10 after 1, 5, and 10 minutes respectively, and humidified oxygen was provided for several minutes. No bag and mask ventilation was required. Birth weight was 2460 g (50th percentile (weight according to gestational age)).
The patient developed signs of respiratory distress several hours after birth consisting of nasal flaring, grunting, intercostal and subcostal retractions, and tachypnoeic respiration with increased oxygen requirement until 60%. Breath sounds were normal. A chest radiograph suggested respiratory distress syndrome I–II (fig 1). Differential diagnosis included group B streptococcal pneumonia or wet lung. The patient was treated with continuous positive airway pressure (CPAP) with extra oxygen through nasal prongs (Babylog; Dräger Medizintechnik, Lübeck, Germany). CPAP was initiated five hours after birth. The patient was suctioned with a controlled length of suction catheter, excluding the possibility that the pneumatocele had been caused by improper suction. After blood cultures and nasopharyngeal aspirate had been taken, antibiotics were administered because pneumonia could not be excluded. During the next 48 hours, the patient developed progressive respiratory insufficiency with increasing oxygen requirement to 70% despite the positive end expiratory pressure being raised from 4 cm H2O to 6 cm H2O. Although the clinical situation deteriorated, capillary blood gases remained stable, with pH between 7.32 and 7.36, carbon dioxide levels between 5.6 and 6.2 kPa, and bicarbonate levels between 23.1 and 23.5 mmol/l.
Twenty four hours after birth the chest radiograph showed a progressive cyst located retrocardially (fig 2). Thoracic computed tomography showed a cystic malformation located retrocardially, which had its origin in a proximal bronchus. There was no connection to the lung parenchyma. Other parts of the lung did not show any abnormalities (fig 3). A diagnosis of pneumatocele due to increased airway pressure from CPAP was made.
In neonates, pneumatocele formation is described as a complication of pneumonia. It is reported to occur after infection with Staphylococcus aureus, Streptococcus pneumoniae, Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, or Pseudomonas aeruginosa.1–3 It has also been described as a complication of artificial ventilation in older children and adults.4,5 Therapeutic options include appropriate intravenous antimicrobial treatment. If this fails, surgery may be necessary.6–9 Several invasive methods have been described. Decompression by percutaneous computed tomographic guided catheter placement or direct tube thoracostomy have been suggested as well as surgical resection of the pneumatocele. Complications of surgical intervention include pulmonary abscess and persistent fistula.4 Little information is available about the natural history of pneumatoceles. Rupture and development of tension pneumothorax have been described in an older patient.4 However, to our knowledge, no large series of neonates with pneumatoceles have been described.
In our patient, the pneumatocele was located centrally, which complicates surgical resection and percutaneous catheter related decompression. We chose to treat him with high frequency oscillation ventilation (HFOV; Sensormedics 3100A, Bilthoven, The Netherlands), which produces compression of the pneumatocele and distention in other parts of the lung. The initial continuous distending pressure was 13 cm H2O and the amplitude 33 cm H2O with a normal volume HFOV strategy. Gradually decreasing the continuous distending pressure caused the pneumatocele to reduce in size and finally disappear after 10 days. Surfactant was not given. Cultures of blood and nasopharyngeal aspirate remained negative, confirming CPAP as the cause of the pneumatocele.
In conclusion, this report describes a neonate who developed a pneumatocele as a complication of CPAP. HFOV was found to be an efficient, non-invasive treatment. Another non-invasive option that can be used if HFOV fails to resolve the pneumatocele may be selective intubation and ventilation of a main bronchus.
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