Lung structure and function on MRI in preterm born school children with and without BPD: A feasibility study

Background and Objective The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory outcomes. However, also preterm children without BPD may show similar adverse respiratory outcomes. There is a need for a...

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Published inPediatric pulmonology Vol. 57; no. 12; pp. 2981 - 2991
Main Authors Elders, Bernadette B. L. J., Tiddens, Harm A. W. M., Pijnenburg, Mariëlle W. H., Reiss, Irwin K. M., Wielopolski, Piotr A., Ciet, Pierluigi
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.12.2022
John Wiley and Sons Inc
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Abstract Background and Objective The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory outcomes. However, also preterm children without BPD may show similar adverse respiratory outcomes. There is a need for a safe imaging modality for preterm children with and without BPD for disease severity assessment and risk stratification. Our objective was to develop a magnetic resonance imaging (MRI) protocol in preterm children with and without BPD at school age. Methods Nine healthy volunteers (median age 11.6 [range: 8.8–12.8] years), 11 preterm children with BPD (11.0 [7.2–15.6] years), and 9 without BPD (11.1 [10.7–12.6] years) underwent MRI. Images were scored on hypo‐ and hyperintense abnormalities, bronchopathy, and architectural distortion. MRI data were correlated to spirometry. Ventilation and perfusion defects were analyzed using Fourier Decomposition (FD) MRI. Results On MRI, children with BPD had higher %diseased lung (9.1 (interquartile range [IQR] 5.9–11.6)%) compared to preterm children without BPD (3.4 (IQR 2.5–5.4)%, p < 0.001) and healthy volunteers (0.4 (IQR 0.1–0.8)%, p < 0.001). %Diseased lung correlated negatively with %predicted FEV1 (r = −0.40, p = 0.04), FEV1/FVC (r = −0.49, p = 0.009) and FEF75 (r = −0.63, p < 0.001). Ventilation and perfusion defects on FD sequence corresponded to hypointense regions on expiratory MRI. Conclusion Chest MRI can identify structural and functional lung damage at school age in preterm children with and without BPD, showing a good correlation with spirometry. We propose MRI as a sensitive and safe imaging method (without ionizing radiation, contrast agents, or the use of anesthesia) for the long‐term follow‐up of preterm children.
AbstractList Abstract Background and Objective The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory outcomes. However, also preterm children without BPD may show similar adverse respiratory outcomes. There is a need for a safe imaging modality for preterm children with and without BPD for disease severity assessment and risk stratification. Our objective was to develop a magnetic resonance imaging (MRI) protocol in preterm children with and without BPD at school age. Methods Nine healthy volunteers (median age 11.6 [range: 8.8–12.8] years), 11 preterm children with BPD (11.0 [7.2–15.6] years), and 9 without BPD (11.1 [10.7–12.6] years) underwent MRI. Images were scored on hypo‐ and hyperintense abnormalities, bronchopathy, and architectural distortion. MRI data were correlated to spirometry. Ventilation and perfusion defects were analyzed using Fourier Decomposition (FD) MRI. Results On MRI, children with BPD had higher %diseased lung (9.1 (interquartile range [IQR] 5.9–11.6)%) compared to preterm children without BPD (3.4 (IQR 2.5–5.4)%, p  < 0.001) and healthy volunteers (0.4 (IQR 0.1–0.8)%, p  < 0.001). %Diseased lung correlated negatively with %predicted FEV 1 ( r  = −0.40, p  = 0.04), FEV 1 /FVC ( r  = −0.49, p  = 0.009) and FEF 75 ( r  = −0.63, p  < 0.001). Ventilation and perfusion defects on FD sequence corresponded to hypointense regions on expiratory MRI. Conclusion Chest MRI can identify structural and functional lung damage at school age in preterm children with and without BPD, showing a good correlation with spirometry. We propose MRI as a sensitive and safe imaging method (without ionizing radiation, contrast agents, or the use of anesthesia) for the long‐term follow‐up of preterm children.
Background and ObjectiveThe most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory outcomes. However, also preterm children without BPD may show similar adverse respiratory outcomes. There is a need for a safe imaging modality for preterm children with and without BPD for disease severity assessment and risk stratification. Our objective was to develop a magnetic resonance imaging (MRI) protocol in preterm children with and without BPD at school age.MethodsNine healthy volunteers (median age 11.6 [range: 8.8–12.8] years), 11 preterm children with BPD (11.0 [7.2–15.6] years), and 9 without BPD (11.1 [10.7–12.6] years) underwent MRI. Images were scored on hypo‐ and hyperintense abnormalities, bronchopathy, and architectural distortion. MRI data were correlated to spirometry. Ventilation and perfusion defects were analyzed using Fourier Decomposition (FD) MRI.ResultsOn MRI, children with BPD had higher %diseased lung (9.1 (interquartile range [IQR] 5.9–11.6)%) compared to preterm children without BPD (3.4 (IQR 2.5–5.4)%, p < 0.001) and healthy volunteers (0.4 (IQR 0.1–0.8)%, p < 0.001). %Diseased lung correlated negatively with %predicted FEV1 (r = −0.40, p = 0.04), FEV1/FVC (r = −0.49, p = 0.009) and FEF75 (r = −0.63, p < 0.001). Ventilation and perfusion defects on FD sequence corresponded to hypointense regions on expiratory MRI.ConclusionChest MRI can identify structural and functional lung damage at school age in preterm children with and without BPD, showing a good correlation with spirometry. We propose MRI as a sensitive and safe imaging method (without ionizing radiation, contrast agents, or the use of anesthesia) for the long‐term follow‐up of preterm children.
The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory outcomes. However, also preterm children without BPD may show similar adverse respiratory outcomes. There is a need for a safe imaging modality for preterm children with and without BPD for disease severity assessment and risk stratification. Our objective was to develop a magnetic resonance imaging (MRI) protocol in preterm children with and without BPD at school age. Nine healthy volunteers (median age 11.6 [range: 8.8-12.8] years), 11 preterm children with BPD (11.0 [7.2-15.6] years), and 9 without BPD (11.1 [10.7-12.6] years) underwent MRI. Images were scored on hypo- and hyperintense abnormalities, bronchopathy, and architectural distortion. MRI data were correlated to spirometry. Ventilation and perfusion defects were analyzed using Fourier Decomposition (FD) MRI. On MRI, children with BPD had higher %diseased lung (9.1 (interquartile range [IQR] 5.9-11.6)%) compared to preterm children without BPD (3.4 (IQR 2.5-5.4)%, p < 0.001) and healthy volunteers (0.4 (IQR 0.1-0.8)%, p < 0.001). %Diseased lung correlated negatively with %predicted FEV (r = -0.40, p = 0.04), FEV /FVC (r = -0.49, p = 0.009) and FEF (r = -0.63, p < 0.001). Ventilation and perfusion defects on FD sequence corresponded to hypointense regions on expiratory MRI. Chest MRI can identify structural and functional lung damage at school age in preterm children with and without BPD, showing a good correlation with spirometry. We propose MRI as a sensitive and safe imaging method (without ionizing radiation, contrast agents, or the use of anesthesia) for the long-term follow-up of preterm children.
Background and Objective The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory outcomes. However, also preterm children without BPD may show similar adverse respiratory outcomes. There is a need for a safe imaging modality for preterm children with and without BPD for disease severity assessment and risk stratification. Our objective was to develop a magnetic resonance imaging (MRI) protocol in preterm children with and without BPD at school age. Methods Nine healthy volunteers (median age 11.6 [range: 8.8–12.8] years), 11 preterm children with BPD (11.0 [7.2–15.6] years), and 9 without BPD (11.1 [10.7–12.6] years) underwent MRI. Images were scored on hypo‐ and hyperintense abnormalities, bronchopathy, and architectural distortion. MRI data were correlated to spirometry. Ventilation and perfusion defects were analyzed using Fourier Decomposition (FD) MRI. Results On MRI, children with BPD had higher %diseased lung (9.1 (interquartile range [IQR] 5.9–11.6)%) compared to preterm children without BPD (3.4 (IQR 2.5–5.4)%, p < 0.001) and healthy volunteers (0.4 (IQR 0.1–0.8)%, p < 0.001). %Diseased lung correlated negatively with %predicted FEV1 (r = −0.40, p = 0.04), FEV1/FVC (r = −0.49, p = 0.009) and FEF75 (r = −0.63, p < 0.001). Ventilation and perfusion defects on FD sequence corresponded to hypointense regions on expiratory MRI. Conclusion Chest MRI can identify structural and functional lung damage at school age in preterm children with and without BPD, showing a good correlation with spirometry. We propose MRI as a sensitive and safe imaging method (without ionizing radiation, contrast agents, or the use of anesthesia) for the long‐term follow‐up of preterm children.
Author Reiss, Irwin K. M.
Elders, Bernadette B. L. J.
Tiddens, Harm A. W. M.
Ciet, Pierluigi
Pijnenburg, Mariëlle W. H.
Wielopolski, Piotr A.
AuthorAffiliation 2 Department of Radiology and Nuclear Medicine, Erasmus MC—Sophia Children's Hospital University Medical Centre Rotterdam Rotterdam The Netherlands
3 Department of Neonatology, Erasmus MC—Sophia Children's Hospital University Medical Centre Rotterdam Rotterdam The Netherlands
1 Department of Paediatric Pulmonology and Allergology, Erasmus MC—Sophia Children's Hospital University Medical Centre Rotterdam Rotterdam The Netherlands
AuthorAffiliation_xml – name: 2 Department of Radiology and Nuclear Medicine, Erasmus MC—Sophia Children's Hospital University Medical Centre Rotterdam Rotterdam The Netherlands
– name: 1 Department of Paediatric Pulmonology and Allergology, Erasmus MC—Sophia Children's Hospital University Medical Centre Rotterdam Rotterdam The Netherlands
– name: 3 Department of Neonatology, Erasmus MC—Sophia Children's Hospital University Medical Centre Rotterdam Rotterdam The Netherlands
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CitedBy_id crossref_primary_10_1002_ppul_26468
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Issue 12
Keywords spirometry
bronchopulmonary dysplasia
MRI
imaging
paediatric
Language English
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Snippet Background and Objective The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and...
The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and impaired respiratory...
Abstract Background and Objective The most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung...
Background and ObjectiveThe most common respiratory complication of prematurity is bronchopulmonary dysplasia (BPD), leading to structural lung changes and...
SourceID pubmedcentral
proquest
crossref
pubmed
wiley
SourceType Open Access Repository
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Index Database
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StartPage 2981
SubjectTerms bronchopulmonary dysplasia
Bronchopulmonary Dysplasia - diagnostic imaging
Child
Feasibility Studies
Follow-Up Studies
Forced Expiratory Volume
Humans
imaging
Infant, Newborn
Lung - diagnostic imaging
Magnetic Resonance Imaging
MRI
Original
paediatric
Spirometry
Ventilation
Title Lung structure and function on MRI in preterm born school children with and without BPD: A feasibility study
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fppul.26119
https://www.ncbi.nlm.nih.gov/pubmed/35982507
https://www.proquest.com/docview/2737359349
https://pubmed.ncbi.nlm.nih.gov/PMC9826116
Volume 57
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