the value of sonography in diagnosing pediatric necrotizing pneumonia
TRANSCRIPT
Posters / Paediatric Respiratory Reviews 14S2 (2013) S55–S85 S65
with MMP (n=21) and non-MP pneumonia (n = 20). We selected
patients during the same period with bronchial foreign body, airway
malformations and chronic cough as the control group (n =20). BALF
were collected from all cases at acute phase and recovery phase.
The levels of IL-5 and VEGF in BALF and serum were measured by
ELISA. All data is statistically analyzed by the application SPSS17.0.
Results:
1. The levels of IL-5 and VEGF in BALF and serum in patients
with wheeze were higher than those in non-wheeze, non-MP
pneumonia group and control group, there was a statistically
significant difference of them (P < 0.01).
2. The BALF in all patients was in accordance with serum in two
kinds of specimens examination result of the levels of IL-5 and
VEGF. The cytokine concentration in BALF was higher than that
of serum, both positive related.
3. There was no statistically significant difference between the
convalescence phase of MPP and the control group (P > 0.05).
Conclusion: IL-5 and VEGF may play important roles in airway
inflammation in children with mycoplasma pneumonia and
wheeze.
C07-186-1
Levels and clinical significance of MIP-1a, ECP in serum from
children with bronchiolitis
H.-M. Qiao1, J.-Z. Li2, L. Liu1, H.-L. You1, H.-J. Cheng1. 1First Hospital
of Jilin University, Changchun, China; 2Taizhou People’s Hospital,
Pediatrics, Taizhou, China
Objective: To investigate the levels and clinical significance of
MIP-1a, ECP in serum from children with bronchiolitis and analyze
the correlation between the levels of MIP-1a, ECP in the acute phase
of bronchiolitis and the more recurrent wheezing after recovery
period.
Methods: The object is the children enrolled with bronchiolitis.
Select the children without infection during the same period
as the control group. Double antibody sandwich enzyme-linked
immunosorbent assay is used to determine the levels of MIP-1aand ECP in acute phase, recovery phase and control group. We
followed up six to twelve months after the recovery of bronchiolitis
and observed whether the wheezing relapse. All data is statistically
analyzed by the application SPSS17.0.
Results:
1. The levels of serumMIP-1a and ECP in children with bronchiolitis
of the acute phasewere higher than those in the recovery phase
and the control group; the difference was statistically significant
(P < 0.01).
2. The levels of serumMIP-1a and ECP in children with bronchiolitis
of recovery phase were higher than the control group; the
difference was statistically significant (P < 0.05).
3. The levels of serum MIP-1a and ECP in children who had
wheezing relapse after the recovery of bronchiolitis were higher
than those who did not have wheezing again, P < 0.05.
4. The level of serum MIP-1a in children with bronchiolitis in acute
phase was positively correlated with ECP, r = 0.646, P < 0.01.
Conclusion: MIP-1a and ECP may play a role in the pathogenesis
of bronchiolitis. The level of serum MIP-1a in acute phase was
positively correlated with ECP.
C08-134-2
Results of QuantiFERON-TB Gold in-tube and skin testing
with recombinant proteins CFP-10-ESAT-6 in children and
adolescents with TB or latent TB infection
L.V. Slogotskaya1, V. Litvinov1, E. Ovsyankina1, D. Kudlay2,
P. Seltsovsky1, N. Seltsovsky, D. Ivanova1. 1Scientific and Clinical
Antituberculosis Center Clinical Research, Moscow, Russia; 2OJSC
“Pharmstandard” Research Department, Moscow, Russia
After decoding Mycobacterium tuberculosis genome and discovering
genes of specific proteins CFP-10 and ESAT-6 new in vitro
interferon-g release assays are commercially licensed. So,
QuantiFERON-TB Gold in tube (QFT-GIT) measure INF-g production
to three specific antigens – CFP-10, ESAT-6 and TB 7.7. But
application of laboratory tests in children is significantly restricted
by expensive costs, need for equipped laboratories and intravenous
manipulations. The solution was found in use of skin testing with
recombinant protein CFP-10-ESAT-6 (DIASKINTEST) (DST).
Aim: To compare results of skin test (DST) and QFT-GIT.
Subjects and Methods: 122 children and adolescents aged 6 to 17
(average age 12.9±3.34, median 12) were followed up. Pulmonary
TB was in 111 subjects (44% intrathoracic lymph nodes TB, 16%
focal TB, 23% primary TB complex, 12% infiltrative TB); LTBI in 11
(positive tuberculin and DST reactions). All the children received a
course of chemotherapy for at least 2 months (patients with LTBI)
and 6 months (with active TB). All the children were examined
within one day by two procedures: first QFT and then DST (0.2mkg
in 0.1ml).
Results: Positive skin test (DST) was observed in 108 out of 122
subjects (88.5%; 95%CI 81.5–93.6%). The mean positive reaction
was 16.6±4.56mm. Positive QFT-GIT was registered in 109 (89.3%;
95%CI 82.5–94.2%) subjects. The results of both tests agreed in
115 patients (94.3%; 95%CI 88.5–97.7%). The kappa coefficient of
concordance was 0.709 (95%CI 0.605–0.813; p < 0.0001). Discordant
reactions were observed in 7 (5.7%; 95%CI 2.3–11.5%) patients with
TB; moreover, in 4 patients with positive reactions to QFT and
negative reactions to DST the latter corresponded in clinical and
X-ray findings to the stage of the process (there was a phase
of resolution or calcination). This result was associated with the
reversion of a reaction to DST during cure. Three patients were
found to have a negative reaction to QFT (the level corresponded to
the threshold value) with a remaining positive reaction to DST.
Conclusion: DST and QFT-GIT have comparable high sensitivity
with a high agreement between the results; the discordance of
tests in 5.7% possibly results by near-threshold variability of QFT-
GIT values and dynamics of DST during chemotherapy.
C09-32
The value of sonography in diagnosing pediatric necrotizing
pneumonia
S.-H. Lai1, S.-L. Liao2, K.-S. Wong1. Department of Pediatrics, Chang
Gung Memorial Hospital and Chang Gung University, 1Taoyuan and2Keelung, Taiwan, Republic of China
Background: Necrotizing pneumonia (NP) is a severe complication
of pediatric community-acquired pneumonia, and the incidence
is increasing over recent years. NP is usually diagnosed by chest
computed tomography (CT). However, considering the medical costs
and radioactive exposure, CT exam should not be routinely used.
In this study, we aim to determine the role of sonography in early
diagnosis of NP.
Materials and Methods: We retrospectively reviewed the medical
records of children with pneumonia during the period of 2008–
2011. Children who underwent chest doppler sonography followed
by CT exam within 5 days were enrolled in the study. The diagnosis
of NP was based on findings of CT imaging. Doppler results
were classified as decreased or poor perfusion. Severity of lobar
necrosis was further graded to mild, moderate and severe necrosis.
The demographic data and clinical outcome were also reviewed.
Statistical analysis was performed by student t test, chi-square test,
and ROC curve.
Results: A total of 83 patients were enrolled with a mean age
of 5.16 years. Streptococcus pneumoniae was the most common
pathogen (68.3%). After analyzing the disease severity on CT and
sonographic findings by using ROC curve, moderate lobar necrosis
in CT imaging and decreased doppler perfusion had the highest area
under ROC curve with sensitivity of 77.8%, specificity of 91.5%, and
positive predictive value of 87.5%. Poor perfusion in sonography
and severe necrosis in CT imaging had a high relative risk (poor
S66 Posters / Paediatric Respiratory Reviews 14S2 (2013) S55–S85
perfusion, 10.56; severe necrosis, 16) for predicting the requirement
of lobectomy as a later rescue therapy for severe lobar necrosis.
Conclusion: Sonography is a valuable tool that is able to early detect
necrotizing pneumonia, especially in the presence of moderate lobar
necrosis. Poor lobar perfusion in sonography had a high sensitivity
and specificity in predicting subsequent rescue lobectomy for
severe NP. Routine and regular usage of sonography should be
advocated in clinical setting of pediatric community-acquired
pneumonia.
Category 4. Noninfectious Respiratory Disorders
D01-59
A single centre review of open lung biopsies in infants less
than 1 year of age
R. O’Reilly1, D. Kilner1, M. Ashworth2, P. Aurora1. 1Great Ormond
Street Hospital for Children Department of Paediatric Respiratory
Medicine, London, UK; 2Great Ormond Street Hospital for Children
Department of Pathology, London, UK
Introduction: Interstitial lung disease (ILD) in infants is rare, and
recommendations on classification and management are based
upon limited data. Clinical and radiological features are often non-
specific, and overlap with growth disorders and infection. Lung
biopsy is the gold standard for diagnosis, but the risk and diagnostic
yield of this procedure is incompletely understood.
Lung biopsies <1 year (n=27) Age 2.5 (0.1-11.6) months
Diffuse Developmental Disorders (n=6) Aveolar Capillary Dysplasia (n=6) Surfactant dysfunction disorders (n=4) Surfactant B deficiency (n=1) Surfactant like deficiency (n=1) Chronic pneumonitis of infancy (n=1) Non specific interstitial pneumonitis (n=1) Growth abnormalities reflecting deficient alveolarisation (n=3) Chronic neonatal lung disease (n=2) Chromosomal disorders (n=1) Pulmonary Interstitial Glycogenosis (n=1)* (also had surfactant C deficiency)
Chronic Cellular Interstitial Process (n=1) Meconium Aspiration Syndrome (n=2) Infection (n=2) Bordetella pertussis and Influenza B (n=1) CMV (n=1)
Pulmonary Lymphangiectasia (n=4) Aspiration (n=2) Normal lung architecture (n=1) Unclasssified (n=1)
Died shortly after lung biopsy (n=10) Followed up at local hospital (n=3)
Median age of last follow up (n=14) = 0.5 (0.39 -5.81) years 3 remain long term oxygen dependent 1 oxygen dependent and referred for transplant 1 death 18 months post lung biopsy from cardiac causes
Figure 1. Histopathological diagnosis in infants (<1 year) who had open lung biopsy
between 1/01/2005 and 31/3/2012.
Aim: To retrospectively review infants undergoing open lung
biopsy for suspected ILD at a large national referral centre; to
determine morbidity and mortality for the procedure; and to
describe subsequent diagnosis and outcome.
Methods: Lung biopsies performed in infants (aged <1 year)
between 1/01/2005 and 31/3/2012 were identified and clinical
data was collected from patient notes. Biopsies were reclassified
according to the ChILD classification system for diffuse lung
disorders in infants.
Results: 27 infants were identified, with the number of biopsies
performed each year increasing over the study period. Mortality
from the procedure was zero, and morbidity was negligible. The
range and proportions of diagnoses seen was very similar to that
reported by the ChILD network, Figure 1. Histopathological diagnosis
was not compatible with life in 10/27 (37%) of patients, and
management plans were altered appropriately. Of the 14 children
longitudinally followed up at our centre (median 0.5 (0.4–5.81)
years, only 4 continued to require supplemental oxygen.
Conclusion: Lung biopsy in infants with suspected ILD is a
safe procedure, and histopathological diagnosis frequently assists
treatment decisions, particularly with regard to withdrawal of care.
D02-171
Brain abscess caused by paradoxical embolism secondary to
pulmonary arteriovenous malformation. An unusual etiology.
Case report
G. Montesinos, I.E. Paredes, E. Lomas, P. Escobedo, E. Figueroa,
G. Vazquez, L. Hernandez. Hospital general Manuel Gea Gonzalez,
Distrito Federal, Mexico
Background: Cerebral abscess commonly occurs secondary to
trauma, hematogenous spread from distant infection or contiguity;
20% of these are called cryptogenic when it is not possible to identify
the cause. This might be as a result of the presence of rare entities
such as pulmonary arteriovenous fistula (PAVF), and because of this,
it is often overlooked. The following case reports a cerebral abscess
secondary to PAVF.
Case description: A 9-year-old girl entered the emergency room
with fatigue, headache, fever, projectile vomiting, right parasternal
noncardiac murmur, nail clubbing and positive meningeal
signs. Hemogram showed leukocytosis and polycythemia. Chest
radiograph revealed right basal opacity. Cranial computed
tomography (CT) demonstrated a left occipital intraparenchymal
brain abscess. The patient was treated with triple antibiotic
therapy and brain abscess drainage. Despite the treatment she
continued to rely on supplemental oxygen, with cyanosis and
oxygen saturation of 80–85%. High resolution chest CT evidenced
a right inferior pulmonary vein malformation (arteriovenous).
Pulmonary gammagram reported complex right basal PAVF. She
underwent percutaneous embolization of the fistula. After the
percutaneous procedure the patient had adequate clinical control.
Conclusions: Simple clinical features such as cyanosis, hypoxia and
polycythemia help early diagnosis suspect. The most prominent
associated complications of PAVF are neurologic events, including
brain abscesses. The high-resolution CT is the most sensitive
technique for diagnosis and percutaneous embolization has shown
good results. This report highlights the need to consider MAVP as
an etiology of cerebral abscess when no source is detected.
D03-149
Drowning: Clinical course of lung injury and outcomes in
children
W. Ratanakorn. Chonburi Hospital Pediatric Department, Chonburi,
Thailand
Background: Anoxic encephalopathy is the most dreaded
consequence of drowning accidents; respiratory involvement is also
very common in these patients.