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  3. Long-term pulmonary outcome of children with congenital diaphragmatic hernia: functional lung MRI using matrix-pencil decomposition enables side-specific assessment of lung function.
 

Long-term pulmonary outcome of children with congenital diaphragmatic hernia: functional lung MRI using matrix-pencil decomposition enables side-specific assessment of lung function.

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BORIS DOI
10.48350/189215
Date of Publication
June 2024
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Universitätsklinik fü...

Universitätsklinik fü...

Contributor
Streibel, Carmen
Universitätsklinik für Kinderheilkunde
Willers, Christoph Corinorcid-logo
Universitätsklinik für Kinderheilkunde
Bauman, Grzegorz
Pusterla, Andrea Orso
Universitätsklinik für Kinderheilkunde
Bieri, Oliver
Curdy, Marion
Horn, Matthias Thomas
Universitätsklinik für Kinderheilkunde
Casaulta, Carmenorcid-logo
Universitätsklinik für Kinderheilkunde
Berger, Steffen Michaelorcid-logo
Universitätsklinik für Kinderchirurgie
Dekany, Gabriela Marta
Universitätsklinik für Kinderchirurgie
Kieninger, Elisabethorcid-logo
Universitätsklinik für Kinderheilkunde
Bartenstein, Andreas
Universitätsklinik für Kinderchirurgie
Latzin, Philipporcid-logo
Universitätsklinik für Kinderheilkunde - Pneumologie / Allergologie
Universitätsklinik für Kinderheilkunde
Subject(s)

600 - Technology::610...

Series
European radiology
ISSN or ISBN (if monograph)
0938-7994
Publisher
Springer-Verlag
Language
English
Publisher DOI
10.1007/s00330-023-10395-8
PubMed ID
37982833
Uncontrolled Keywords

Children Congenital d...

Description
OBJECTIVES

In patients with congenital diaphragmatic hernia (CDH) the exact functional outcome of the affected lung side is still unknown, mainly due to the lack of spatially resolved diagnostic tools. Functional matrix-pencil decomposition (MP-) lung MRI fills this gap as it measures side-specific ventilation and perfusion. We aimed to assess the overall and side-specific pulmonary long-term outcomes of patients with CDH using lung function tests and MP-MRI.

METHODS

Thirteen school-aged children with CDH (seven with small and six with large defect-sized CDH, defined as > 50% of the chest wall circumference being devoid of diaphragm tissue) and thirteen healthy matched controls underwent spirometry, multiple-breath washout, and MP-MRI. The main outcomes were forced expiratory volume in 1 second (FEV1), lung clearance index (LCI2.5), ventilation defect percentage (VDP), and perfusion defect percentage (QDP).

RESULTS

Patients with a large CDH showed significantly reduced overall lung function compared to healthy controls (mean difference [95%-CIadjusted]: FEV1 (z-score) -4.26 [-5.61, -2.92], FVC (z-score) -3.97 [-5.68, -2.26], LCI2.5 (TO) 1.12 [0.47, 1.76], VDP (%) 8.59 [3.58, 13.60], QDP (%) 17.22 [13.16, 21.27]) and to patients with a small CDH. Side-specific examination by MP-MRI revealed particularly reduced ipsilateral ventilation and perfusion in patients with a large CDH (mean difference to contralateral side [95%-CIadjusted]: VDP (%) 14.80 [10.50, 19.00], QDP (%) 23.50 [1.75, 45.20]).

CONCLUSIONS

Data indicate impaired overall lung function with particular limitation of the ipsilateral side in patients with a large CDH. MP-MRI is a promising tool to provide valuable side-specific functional information in the follow-up of patients with CDH.

CLINICAL RELEVANCE STATEMENT

In patients with congenital diaphragmatic hernia, easily applicable MP-MRI allows specific examination of the lung side affected by the hernia and provides valuable information on ventilation and perfusion with implications for clinical practice, making it a promising tool for routine follow-up.

KEY POINTS

• Functional matrix pencil decomposition (MP) MRI data from a small sample indicate reduced ipsilateral pulmonary ventilation and perfusion in children with large congenital diaphragmatic hernia (CDH). • Easily applicable pencil decomposition MRI provides valuable side-specific diagnostic information on lung ventilation and perfusion. This is a clear advantage over conventional lung function tests, helping to comprehensively follow up patients with congenital diaphragmatic hernia and monitor therapy effects.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/171588
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s00330-023-10395-8.pdftextAdobe PDF1.48 MBpublishedOpen
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