| Literature DB >> 31683953 |
Antonio Di Mauro1, Angela Ammirabile2, Michele Quercia3, Raffaella Panza4, Manuela Capozza5, Mariano M Manzionna6, Nicola Laforgia7.
Abstract
INTRODUCTION: Viral bronchiolitis is a common cause of lower respiratory tract infection in the first year of life, considered a health burden because of its morbidity and costs. Its diagnosis is based on history and physical examination and the role of radiographic examination is limited to atypical cases. Thus far, Lung Ultrasound (LUS) is not considered in the diagnostic algorithm for bronchiolitis.Entities:
Keywords: Bronchiolitis; Bronchiolitis [Mesh]; Lung Ultrasound; Ultrasonography [Mesh]; Viral [Mesh], Lung Ultrasound
Year: 2019 PMID: 31683953 PMCID: PMC6963954 DOI: 10.3390/diagnostics9040172
Source DB: PubMed Journal: Diagnostics (Basel) ISSN: 2075-4418
Summary of the analyzed studies about the role of Lung Ultrasound (LUS) in the management of bronchiolitis.
| Authors | Type of study | Number of cases | LUS pattern | Results | Conclusions |
|---|---|---|---|---|---|
| Caiulo et al [ | Prospective observational study | 52 patients with bronchiolitis who had undergone a CXR for clinical reasons, median age 2.1 months |
Mildest form: a prevalence of few isolate B-lines Moderate disease: a higher frequency of single subpleural consolidation and areas of white lung Severe disease: the presence of multiple lung consolidations, pleural line anomalies and pleural effusions |
Positive tests for diagnosis of bronchiolitis: 47/52 for LUS vs. 38/52 for CXR. 9 patients with a clinical course of bronchiolitis had with normal CXR and abnormal LUS. Mean time of tests interpretation: 0 m (during the scan) for LUS vs. 4.45 h for CXR. Statistically significant LUS findings ( Not statistically significant LUS findings ( LUS findings not revealed by CXR: minimal pleural effusion (3/52 infants), small pneumothorax (1/52 infants) |
Higher reliability of LUS for diagnosis and follow-up of bronchiolitis, due to identification of lung abnormalities not revealed by CXR |
| Jaszczolt et al [ | Retrospective study | 23 children aged 2 weeks to 24 months and 3 children older than 24 months with confirmed respiratory syncytial virus infection plus a separate specific group composed by 3 children over the age of 2 years also diagnosed with bronchiolitis |
Liver-like hypoechoic consolidations (small subpleural < 10 mm in diameter and > 10 mm in diameter with air bronchogram), Interstitial syndrome with B7 lines (7mm between two different lines), Alveolar-interstitial syndrome with B3 lines (distance around 3mm between two different lines), Pleural effusion Higher involvement of inferior and posterior areas |
Positive tests for diagnosis of bronchiolitis: 21/26 for LUS vs. 4/26 for CXR. 5 children showed absence of abnormalities at LUS and CXR. Statistically significant LUS findings ( |
LUS as a useful tool in the diagnosis of bronchiolitis, considering its superiority in the detection of small amounts of pleural effusions or intraparenchymal lesions, and also in the monitoring of treatment efficacy. Greater ability of CXR in showing bronchi and hilar regions or lung hyperinflation. Direct comparison of specificity and sensitivity of both methods is not possible |
| Basile et al [ | Observational cohort study | 106 infants, median age of 71 days: 74 infants with mild bronchiolitis, 30 infants with moderate bronchiolitis, 2 infants with severe bronchiolitis |
Presence of B-lines, subpleural lung consolidations, bilateral involvement of intercostal spaces Higher involvement of posterior and paravertebral areas |
High agreement between the attending physician and the paediatric sonographer on the severity of bronchiolitis (agreement: 90.6%; expected agreement: 52.3%; K = 0.8; Standard error = 0.0765; z = 10.19; Excellent inter-observer concordance on the basis of the US findings between the two different sonographers (Cohen’s kappa coefficient: agreement = 89.6%; expected agreement 46.4%; K = 0.8; Std error = 0.07; z = 11.33; LUS identification of those infants in need of supplementary oxygen with a specificity of 98.7% (95% CI: 93% to 99.8%), a sensitivity of 96.6% (95% CI: 82.2% to 99.4%), a positive predictive value of 96.6% (95% CI: 82.2% to 99.4%) and a negative predictive value of 98.7% (95% CI: 92.95% to 99.8%): True Positive (TP) as LUS score > 3 indicating the need of supplementary oxygen. |
High agreement (90.6%) between the clinical and sonographic scores and an excellent inter-observer ultrasound diagnosis concordance Identification of children in need of supplementary oxygen with a very high specificity (98.7%) and sensitivity (96.6%) |
| Zoido Garrote et al [ | Prospective observational study | 59 patients with mild-to-moderate AB, median age of 90 days |
Pleural line anomalies with thickening and loss of lung sliding, extent of interstitial syndrome as shown by B-lines up to the white lung appearance, the presence of subpleural consolidations with a classification according to their number and their dimension. |
Moderate linear association between the sonographic score, especially the degree of AIS and SCs, and the clinical scores—modified WDFM (rho = 0.504, High interrater intraclass correlation coefficient (absolute agreement between individual measurements) for the total score in the LUS-Sc (agreement = 0.917, 95% CI, 0.854–0.956). Association between the sonographic score and the admission to PICU (OR 2.5; 95% CI: 1.1–5.9; Association between each 5-point increase in the LUS-Sc and increase in the probability of admission to PICU (OR, 2.5; 95% CI, 1.1–5.9; |
Moderate correlation between findings at early LUS (at the time of admission) and the severity of acute bronchiolitis, taking also its clinical progression into consideration |
| Bueno-Campaña et al [ | Prospective multicentre study | 145 infants with acute bronchiolitis, median age of 1.7 months |
Lung sliding, ≥3 B-lines per intercostal space (uni or bilaterally located), confluent B-lines (uni or bilaterally located), and subpleural consolidations (larger or smaller than 1 cm). |
Multivariate final predictive model: age less than 1 month (1.5 point), WDFS ≥ 6 points (2.5 points), more than 3 B lines per intercostal space (1.5 point) and confluent B lines bilaterally in anterior area (1 point) and posterior consolidations of any size (1 point if < 1 cm and 3 points if > 1 cm). Predictive capacity for the need of respiratory support of a cut-off point of 3.5: sensitivity of 89.1% (CI95%:78.2–94.9%), specificity of 56% (CI95%: 45.3–66.1%), PPV of 57% (CI95%:46.4–66.9%), and NPV of 88.7% (CI95%:77.4–94.7) with an area under ROC: 0.845 (CI95%:0.781–0.909). Statistically significant correlation ( |
Presence of at least one posterior consolidation > 1 cm as main factor associated to the need of respiratory support (non-invasive or invasive ventilation, except conventional low-flow oxygen through nasal sprongs) in the acute phase of bronchiolitis |
| Taveira et al [ | Prospective observational single-center study | 47 infants under 6 months of age with severe acute viral bronchiolitis |
Mild disease: mild interstitial-syndrome with few B-lines Moderate disease: severe interstitial syndrome with compact B-lines and with lung appearance Severe disease: presence of consolidations seen as a hypoechoic area with blurred margins and air bronchograms |
Absence of statistically significant correlation between the LUS score on admission (3.5 ± 2.6) and length of NIV (69 ± 68.6 hours, rho = 0.1, Statistically significant correlation between the number of affected intercostal spaces on the right and length of NIV (3 ± 3.4, Spearman’s Rho 0.318; |
Statistically significant correlation between the number of affected intercostal spaces on the right side and the length on the oxygen therapy (days), considered a secondary endpoint Absence of confirmation of the primary aim, i.e. the prediction of NIV length (CPAP or high-flow nasal cannula) nor an association with length of hospitalization or the clinical score m-WCAS. |
| Varshney et al [ | Prospective cross-sectional study | 94 patients with signs of a respiratory tract infection (rhinorrhea and/or cough) and wheeze, median age of 11.1 months and |
Pathological LUS (≥1 finding): ≥3 B-lines per intercostal space, consolidation, pleural line abnormalities or fluid |
Good reliability between novice and expert sonologist: Kappa statistic 0.68 (95% CI 0.54 to 0.82) for a positive LUS (≥1 positive findings). Good to almost perfect agreement between raters for each finding: kappa statistic 0.88 (95% CI 0.78 to 0.98) for ≥ 3 B-lines per intercostal space, 0.62 (95% CI 0.42 to 0.82) for small consolidations, 0.88 (95% CI 0.66 to 1.00) for large consolidations and 0.55 (95% CI 0.26 to 0.84) for pleural abnormalities. Proportion of positive LUS, along with their diagnostic accuracy (sensitivity, specificity), for children with bronchiolitis, asthma, pneumonia and asthma/pneumonia: 46% (45.8%, 72.7%), 0% (0%, 51.3%), 100% (100%, 61.1%), 50% (50%, 58.9%), respectively. Positive LUS in 46% (33/72) of patients with bronchiolitis, 0% (0/14) of patients with asthma, 100% (4/4) of patients with pneumonia and in 50% (2/4) of those with concomitant asthma and pneumonia when categorised by final diagnosis. |
Possibility to rule out the diagnosis of asthma in case of positive LUS that could direct the clinician toward a diagnosis of pneumonia (100% of patients) or bronchiolitis (46% of patients) |
| Biagi et al [ | Prospective study | 87 children with a diagnosis bronchiolitis that undergone CXR because of a suspicion of concomitant pneumonia |
Subpleural consolidations, absence of air bronchograms, pleural line abnormalities, single or confluent B lines Higher number of consolidations in the posterior lung areas |
Sensitivity and specificity of LUS for the diagnosis of pneumonia 100% and 83.9% respectively, vs. sensitivity and specificity of CXR of 96% and 87.1%. When only consolidation > 1cm was considered consistent with pneumonia, the specificity of LUS increased to 98.4% and the sensitivity decreased to 80.0%, Strong correlation between CXR and LUS in diagnosing bacterial pneumonia (rs = 0.638, No strong correlation between positive LUS (consolidations with bronchograms) and clinical/laboratory data (fever > 38 °C, SatO2 < 92%, WBC > 15,000/mmc, CRP > 4mg/dL), probably for the impossibility to clearly differentiate bacterial from viral disease and to predict severity of paediatric pneumonia. Weak positive correlation between positive LUS and SatO2 < 92%, CRP > 4mg/dL and TC > 38 °C when all consolidations with bronchograms were included in the LUS positive findings. Identification of all the cases of bronchiolitis with concomitant bacterial pneumonia with LUS. |
Higher sensitivity of LUS for the diagnosis of pneumonia than CXR (100% vs. 96%) and its specificity can reach 98.4% when only consolidations > 1 cm are considered |