Literature DB >> 34760556

A 9-year audit of fetal chest masses in an Australian maternal-fetal medicine cohort.

Saranya Gopikrishna1, Amanda Henry1,2,3, Simren Kaur4, Antonia W Shand1,2,5, Ashish Jiwane6, Kate Dyer2, Alec W Welsh1,2.   

Abstract

INTRODUCTION: To assess fetal vs. neonatal diagnoses, pregnancy outcomes and need for surgery in babies prenatally diagnosed with congenital pulmonary airway malformation (CPAM) or bronchopulmonary sequestration (BPS).
METHODS: Retrospective single-centre cohort study of fetuses with a prenatal diagnosis of CPAM or BPS between 2006 and 2014. Data collected included serial antenatal ultrasound information and neonatal/infant diagnoses and outcomes.
RESULTS: Initial ultrasound diagnosis (n = 63) was CPAM in 51 and BPS in 12: nineteen (30%) fetuses had mediastinal shift and 2 (3%) had hydrops. All neonates with known birth outcome (n = 56) were liveborn. Final diagnosis in 52 infants (83%) with neonatal imaging and/or histopathology confirmed CPAM in 17/44 (39%) and BPS in 6/9 (67%). Of 34 prenatally suspected but unconfirmed CPAM lesions: 10 had no lesion on neonatal imaging, one no neonatal imaging performed, five confirmed BPS, 11 other lung/thoracic lesions, seven were lost to follow-up. There was one infant death. 27/63 infants (43%) had post-natal surgery. More neonates requiring neonatal respiratory support/resuscitation had surgery compared to those who did not (67% vs. 29%, P = 0.008). Patients with suspected CPAM or BPS on both initial and final ultrasound were more likely to have post-natal surgical management than when a lesion was no longer visible on final antenatal ultrasound (68% vs. 23%, P = 0.001).
CONCLUSIONS: Over 50% of antenatally suspected CPAM/BPS either regressed or had an alternate post-natal diagnosis. Perinatal outcome was good, with the majority of neonates/infants conservatively managed. Persistently visible antenatal lesion and need for neonatal respiratory support predicted ultimate surgical management.
© 2019 Australasian Society for Ultrasound in Medicine.

Entities:  

Keywords:  bronchopulmonary sequestration; congenital cystic adenomatoid malformation; congenital pulmonary airway malformation; ultrasound

Year:  2019        PMID: 34760556      PMCID: PMC8411682          DOI: 10.1002/ajum.12161

Source DB:  PubMed          Journal:  Australas J Ultrasound Med        ISSN: 1836-6864


  28 in total

1.  Prediction of pediatric outcome after prenatal diagnosis and expectant antenatal management of congenital cystic adenomatoid malformation.

Authors:  Paul J Yong; Peter Von Dadelszen; Daniela Carpara; Ken Lim; Nancy Kent; Francine Tessier; Marie-France Delisle; Titus Wong; Geoffrey Blair; Erik D Skarsgard
Journal:  Fetal Diagn Ther       Date:  2012-02-03       Impact factor: 2.587

Review 2.  Systematic review and meta-analysis of the postnatal management of congenital cystic lung lesions.

Authors:  Michael Stanton; Ike Njere; Niyi Ade-Ajayi; Shailesh Patel; Mark Davenport
Journal:  J Pediatr Surg       Date:  2009-05       Impact factor: 2.545

3.  Management of the upper airway and congenital cystic lung diseases in neonates.

Authors:  T Nicolai
Journal:  Semin Fetal Neonatal Med       Date:  2008-10-02       Impact factor: 3.926

4.  The increasing incidence of foetal echogenic congenital lung malformations: an observational study.

Authors:  Linden J Stocker; Diana G Wellesley; Michael P Stanton; Rajeswari Parasuraman; David T Howe
Journal:  Prenat Diagn       Date:  2014-11-04       Impact factor: 3.050

5.  Outcome of antenatally suspected congenital cystic adenomatoid malformation of the lung: 10 years' experience 1991-2001.

Authors:  J K Calvert; P A Boyd; P C Chamberlain; S Syed; S Said; K Lakhoo
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2005-08-30       Impact factor: 5.747

6.  Prenatal diagnosis and management of congenital cystic adenomatoid malformation of the lung.

Authors:  Gregory J Duncombe; Jan E Dickinson; Colin S Kikiros
Journal:  Am J Obstet Gynecol       Date:  2002-10       Impact factor: 8.661

7.  Fetal lung lesions: management and outcome.

Authors:  N S Adzick; M R Harrison; T M Crombleholme; A W Flake; L J Howell
Journal:  Am J Obstet Gynecol       Date:  1998-10       Impact factor: 8.661

8.  Long-term outcome of asymptomatic patients with congenital cystic adenomatoid malformation.

Authors:  A Wong; D Vieten; S Singh; J G Harvey; Andrew J A Holland
Journal:  Pediatr Surg Int       Date:  2009-04-30       Impact factor: 1.827

Review 9.  Current outcome of antenally diagnosed cystic lung disease.

Authors:  Mark Davenport; S A Warne; S Cacciaguerra; S Patel; A Greenough; K Nicolaides
Journal:  J Pediatr Surg       Date:  2004-04       Impact factor: 2.545

10.  The natural history of prenatally diagnosed congenital cystic lung lesions: long-term follow-up of 119 cases.

Authors:  James Cook; Lyn S Chitty; Paolo De Coppi; Michael Ashworth; Colin Wallis
Journal:  Arch Dis Child       Date:  2017-06-05       Impact factor: 3.791

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