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Neonatal Pneumonia

A male infant was born at 36 weeks gestation to a mother who tested positive for GBS one week prior. After birth, the infant had periods of stopped breathing, fast and labored breathing, and was admitted to the NICU. His oxygen levels dropped below 85% and he was intubated. His chest X-ray and symptoms were consistent with neonatal pneumonia likely caused by GBS acquired before or during birth. He required supportive treatment including ventilation and antibiotics to treat the infection while balancing the risks of ventilator-associated complications.

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100% found this document useful (1 vote)
2K views16 pages

Neonatal Pneumonia

A male infant was born at 36 weeks gestation to a mother who tested positive for GBS one week prior. After birth, the infant had periods of stopped breathing, fast and labored breathing, and was admitted to the NICU. His oxygen levels dropped below 85% and he was intubated. His chest X-ray and symptoms were consistent with neonatal pneumonia likely caused by GBS acquired before or during birth. He required supportive treatment including ventilation and antibiotics to treat the infection while balancing the risks of ventilator-associated complications.

Uploaded by

elyuchan
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd
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Case

A male infant is born at 36 weeks gestation to a


mother who tested (+) for GBS (Group B
Streptococcus) one week prior to delivery.

She came to the ER with contractions and leaking of


fluid for ~15 hours. By the time she delivered vaginally,
she had been ruptured for >24 hours.

She also had a low grade fever just before delivery, but
was otherwise well.
Case
After birth the baby is not as active as expected. He
has moments when he stops breathing briefly. At
times his breathing is fast & labored with both nasal
flaring and intercostal retractions. He is also noted to
be “moaning” on examination.
He is administered oxygen and admitted in the NICU
for more evaluation.
There is no improvement and oxygen saturations are
<85%. Infant is intubated, placed on a ventilator and a
CXR is taken.
Case
Neonatal Pneumonia
Neonatal Pneumonia
Presentation of bacterial sepsis & concurrent pneumonia
Common cause of significant neonatal morbidity &
mortality
Transmission
Predominantly ascending infection from GU tract
Trans-placental infection or blood borne
Risk factors
PROM > 12 Hr
Maternal chorioamnionitis
Prematurity
Neonatal Pneumonia
Pathogens
Group-B Streptococci or GBS, common (1-4/1000 births)
E.coli, Klebsiella, Listeria monocytogenes,
Pneumococci,
H. influenza, Staph. Aureus, Pseudomonas, Staph-Epi.,
Chlamydia, Viral and Fungal pneumonias
Neonatal Pneumonia
Clinical Features
Tachypnea, Grunting, Flaring & Retractions
Cyanosis, Apnea, Lethargy, CVS instability
Diagnosis
Clinical, blood count, CXR, blood cultures
Laboratory findings
↑ WBC, ↑ band count, thrombocytopenia
Abnormal CXR & +ve blood / tracheal culture
Neonatal Pneumonia
Chest X-ray
Lobar streaky densities (focal or multi-focal)
Basal confluent opacities (unilateral or bilateral)
Differential Dx
RDS, edema or aspiration syndromes
Neonatal Pneumonia
Can present with either diffuse reticulonodular
densities similar to respiratory distress syndrome
or with patchy, asymmetric infiltrates with
hyperaeration similar to meconium aspiration.
 The presence of a small pleural effusion is a useful
distinguishing feature as it is a common finding in
neonatal pneumonia (up to 2/3 thirds) and is
uncommon in respiratory distress syndrome.
Neonatal Pneumonia
Treatment
Supportive, NPO, IVF, O2 & Antibiotics
Ventilation & Surfactant needed sometimes
Neonatal Pneumonia
Complications
The neonatologist must maintain a balance between the
ventilatory needs of the infant and the complications
that can result from positive pressure ventilation.
The lung volumes on the daily neonatal CXR are used as
a guide to determine the ventilator settings.
If the compliance of the lungs is too low, or the mean
airway pressure is too high, barotrauma will result.
 Pulmonary interstitial emphysema (PIE)

 Pneumothorax
Neonatal Pneumonia
Pulmonary interstitial emphysema (PIE) results from
rupture of the alveoli with air accumulating in the
peribronchial and perivascular spaces.
Linear lucencies radiating from the hilum
Can also be cystic in appearance, which can be
difficult to distinguish from chronic lung disease.
Occurs early and is associated with high ventilatory
settings
Chronic lung disease occurs later in the hospital
course with lower ventilatory settings
Neonatal Pneumonia
 PIE is an ominous sign because it indicates the
poor compliance of the lungs and is frequently
followed by a pneumothorax.
In addition to adjusting the ventilatory settings as
much as tolerated, it is helpful to put the most
affected side down.
Example of unilateral PIE with a pneumothorax
Close up of left lung
demonstrating the
streaky lucencies of the
air in the interstitium
(red arrows)
 Complicated by a
pneumothorax (yellow
arrow).
 This patient was treated
with a chest tube and by
placing the left side
down. The PIE resolved
after 2 days.

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