Evidence map›Paper›PMID 38326635›Full record

ArticleRadiologie (Heidelberg, Germany)2024

Morphological chest CT changes in cystic fibrosis and massive hemoptysis.

Martha Dohna, Hilmar Kühl, Sivagurunathan Sutharsan, Nora Bruns, Van Dai Vo Chieu, Susanne Hellms, Norman Kornemann, Michael J Montag

Abstract read
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Article in Radiologie (Heidelberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Martha DohnaDepartment of Diagnostic and Interventional Radiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany. dohna.martha@mh-hannover.de.
Hilmar KühlSt. Bernhard-Hospital Kamp-Lintfort, Bürgermeister-Schmelzing-Str. 90, 47475, Kamp-Lintfort, Germany.
Sivagurunathan SutharsanDivision of Cystic Fibrosis, Department of Pulmonary Medicine, University Medicine Essen -Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
Nora BrunsDepartment of Pediatrics I, University Medicine Essen, Hufelandstr. 55, 45147, Essen, Germany.
Van Dai Vo ChieuSt. Vicenz-Hospital Paderborn, Am Busdorf 2, 33098, Paderborn, Germany.
Susanne HellmsDepartment of Diagnostic and Interventional Radiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Norman KornemannDepartment of Diagnostic and Interventional Radiology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Michael J MontagClinic for Radiology, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMassive hemoptysis (MH) is a rare but potentially life-threatening condition of patients with mainly advanced cystic fibrosis (CF). Morphological lung changes are aggravated with disease progression. The aim of this study was to determine whether morphological lung changes differ between patients with CF (pwCF) who have MH and pwCF without MH.

methodsChest computed tomography (CT) scans of pwCF and MH acquired at a maximum of 4 months prior to MH (1/2008 to 2/2015) were evaluated for morphological changes and bronchial artery (BA) diameters. Lung lobes with MH were compared with lobes without MH and with matched control patients with end-stage CF and no hemoptysis using the Helbich scoring system.

resultsThe study included 26 patients with MH (P

conclusionMorphological changes are more severe in lobes with MH in the same patient, but there is no difference when compared with matched control patients. Besides abscess/sacculation, no specific changes for MH were identified. Other factors such as BA hypertrophy might play a pivotal role in the pathogenesis of MH in pwCF. Commonly used scores to evaluate chest CT in pwCF cannot be used to assess MH, and other factors, e.g., hypertrophied BA, not represented and not measured in these scores, might be more suitable for assessing the risk for MH.

Indexed as

Cystic FibrosisHemoptysisTomography, X-Ray ComputedAdultCase-Control StudiesFemaleHumansLungMaleRadiography, ThoracicRetrospective StudiesYoung AdultBronchial arteryChest CTHelbich scoring systemMorphological lung changesRisk factor

Identifiers

PMID38326635
PMCPMC11602869

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.