Literature DB >> 35122416

Going beyond the chest X-ray: Investigating laterality defects in primary ciliary dyskinesia.

Wallace B Wee1,2, Kimberley R Kaspy3, Michael G Sawras4, Michael R Knowles5, Maimoona A Zariwala6, Margaret W Leigh7, Sharon D Dell2,8, Adam J Shapiro3.   

Abstract

BACKGROUND: Organ laterality defects in primary ciliary dyskinesia (PCD) are common, ranging from complete mirror image organ arrangement, situs inversus totalis (SIT), to situs ambiguus (SA), which falls along the spectrum of situs solitus (SS) and SIT. Targeted investigations for organ laterality defects are not universally recommended in PCD consensus statements. Without investigations beyond chest radiography (CXR), clinically significant defects may go undetected leading to increased morbidity. We hypothesize that clinically significant SA defects remain undetected on CXR and targeted investigations are needed to detect various laterality defects associated with morbidity.
METHODS: This retrospective study collected data from PCD clinics at two Canadian children's hospitals from 2012 to 2020. Participants <30 years old with a confirmed or clinical diagnosis of PCD were enrolled. CXR images were reviewed, and reports of other targeted investigations, including chest computed tomography, abdominal ultrasound, echocardiogram, upper gastrointestinal series, and splenic function studies, were extracted from medical records. Situs classifications from CXR alone versus CXR with add-on targeted investigations were compared using Cochran's q and McNemar tests.
RESULTS: One hundred and fifty-nine PCD patients were included, median age at PCD diagnosis of 6.1 years (range: 0-28). The situs classification differed significantly from CXR images alone versus CXR with add-on targeted investigations (p < 0.001); SS 88 (55%) versus 75 (47%), SIT 59 (37%) versus 46 (29%), and SA 12 (8%) versus 38 (24%). Identified SA defects were cardiovascular (21, 13%), intestinal (9, 6%), and/or splenic (16,10%).
CONCLUSIONS: In PCD patients, clinically significant SA defects may not be detected by CXR alone. Our results suggest that the routine use of CXR with add-on targeted investigations may be justified.
© 2022 Wiley Periodicals LLC.

Entities:  

Keywords:  bronchiectasis; epidemiology; imaging; primary ciliary dyskinesia; pulmonology

Mesh:

Year:  2022        PMID: 35122416      PMCID: PMC9186022          DOI: 10.1002/ppul.25853

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  19 in total

1.  A human syndrome caused by immotile cilia.

Authors:  B A Afzelius
Journal:  Science       Date:  1976-07-23       Impact factor: 47.728

2.  Congenital heart disease and the specification of left-right asymmetry.

Authors:  Richard J B Francis; Adam Christopher; William A Devine; Lawrence Ostrowski; Cecilia Lo
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-03-09       Impact factor: 4.733

3.  Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.

Authors:  Heike Olbrich; Miriam Schmidts; Claudius Werner; Alexandros Onoufriadis; Niki T Loges; Johanna Raidt; Nora Fanni Banki; Amelia Shoemark; Tom Burgoyne; Saeed Al Turki; Matthew E Hurles; Gabriele Köhler; Josef Schroeder; Gudrun Nürnberg; Peter Nürnberg; Eddie M K Chung; Richard Reinhardt; June K Marthin; Kim G Nielsen; Hannah M Mitchison; Heymut Omran
Journal:  Am J Hum Genet       Date:  2012-09-27       Impact factor: 11.025

4.  Evaluating a management strategy for malrotation in heterotaxy patients.

Authors:  Paulette I Abbas; Heather A Dickerson; David E Wesson
Journal:  J Pediatr Surg       Date:  2016-02-13       Impact factor: 2.545

5.  Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

Authors:  Adam J Shapiro; Stephanie D Davis; Thomas Ferkol; Sharon D Dell; Margaret Rosenfeld; Kenneth N Olivier; Scott D Sagel; Carlos Milla; Maimoona A Zariwala; Whitney Wolf; Johnny L Carson; Milan J Hazucha; Kimberlie Burns; Blair Robinson; Michael R Knowles; Margaret W Leigh
Journal:  Chest       Date:  2014-11       Impact factor: 9.410

Review 6.  Is Screening of Intestinal Foregut Anatomy in Heterotaxy Patients Really Necessary?: A Systematic Review in Search of the Evidence.

Authors:  Paul S Cullis; Sotirios Siminas; Paul D Losty
Journal:  Ann Surg       Date:  2016-12       Impact factor: 12.969

7.  Nomenclature and classification of congenital heart disease.

Authors:  M J Tynan; A E Becker; F J Macartney; M Q Jiménez; E A Shinebourne; R H Anderson
Journal:  Br Heart J       Date:  1979-05

8.  Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents.

Authors:  Margaret W Leigh; Thomas W Ferkol; Stephanie D Davis; Hye-Seung Lee; Margaret Rosenfeld; Sharon D Dell; Scott D Sagel; Carlos Milla; Kenneth N Olivier; Kelli M Sullivan; Maimoona A Zariwala; Jessica E Pittman; Adam J Shapiro; Johnny L Carson; Jeffrey Krischer; Milan J Hazucha; Michael R Knowles
Journal:  Ann Am Thorac Soc       Date:  2016-08

9.  Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype.

Authors:  Stephanie D Davis; Margaret Rosenfeld; Hye-Seung Lee; Thomas W Ferkol; Scott D Sagel; Sharon D Dell; Carlos Milla; Jessica E Pittman; Adam J Shapiro; Kelli M Sullivan; Keith R Nykamp; Jeffrey P Krischer; Maimoona A Zariwala; Michael R Knowles; Margaret W Leigh
Journal:  Am J Respir Crit Care Med       Date:  2019-01-15       Impact factor: 30.528

10.  The ciliary protein Ftm is required for ventricular wall and septal development.

Authors:  Christoph Gerhardt; Johanna M Lier; Stefanie Kuschel; Ulrich Rüther
Journal:  PLoS One       Date:  2013-02-28       Impact factor: 3.240

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