Literature DB >> 17906889

The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome.

A Kyburz1, U Bauersfeld, A Schinzel, M Riegel, M Hug, M Tomaske, E R Valsangiacomo Büchel.   

Abstract

BACKGROUND: This study aimed to evaluate the cardiac outcome for children with microdeletion 22q11.2 and congenital heart defect (CHD).
METHODS: A total of 49 consecutive children with 22q11.2 and CHD were retrospectively identified. The CHD consisted of tetralogy of Fallot and variances (n = 22), interrupted aortic arch (n = 10), ventricular septal defect (n = 8), truncus arteriosus (n = 6), and double aortic arch (n = 1). Extracardiac anomalies were present in 46 of 47 children.
RESULTS: The median follow-up time was 8.5 years (range, 3 months to 23.5 years). Cardiac surgical repair was performed for 35 children, whereas 5 had palliative surgery, and 9 never underwent cardiac surgery. The median age at repair was 7.5 months (range, 2 days to 5 years). The mean hospital stay was 35 days (range, 7-204 days), and the intensive care unit stay was 15 days (range, 3-194 days). Significant postoperative complications occurred for 26 children (74%), and surgery for extracardiac malformations was required for 21 patients (43%). The overall mortality rate was 22% (11/49), with 1-year survival for 86% and 5-year survival for 80% of the patients. A total of 27 cardiac reinterventions were performed for 16 patients (46%) including 15 reoperations and 12 interventional catheterizations. Residual cardiac findings were present in 25 patients (71%) at the end of the follow-up period.
CONCLUSIONS: Children with microdeletion 22q11.2 and CHD are at high risk for mortality and morbidity, as determined by both the severity of the cardiac lesions and the extracardiac anomalies associated with the microdeletion.

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Year:  2007        PMID: 17906889     DOI: 10.1007/s00246-007-9074-2

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  29 in total

1.  Guidelines for 22q11 deletion screening of patients with conotruncal defects.

Authors:  M C Digilio; B Marino; A Giannotti; R Mingarelli; B Dallapiccola
Journal:  J Am Coll Cardiol       Date:  1999-05       Impact factor: 24.094

2.  Influence of chromosome 22q11.2 microdeletion on surgical outcome after treatment of tetralogy of fallot with pulmonary atresia.

Authors:  Adriano Carotti; Bruno Marino; Roberto M Di Donato
Journal:  J Thorac Cardiovasc Surg       Date:  2003-11       Impact factor: 5.209

3.  Truncus arteriosus repair: outcomes, risk factors, reoperation and management.

Authors:  J W Brown; M Ruzmetov; Y Okada; P Vijay; M W Turrentine
Journal:  Eur J Cardiothorac Surg       Date:  2001-08       Impact factor: 4.191

Review 4.  Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).

Authors:  K Momma; R Matsuoka; A Takao
Journal:  Pediatr Cardiol       Date:  1999 Mar-Apr       Impact factor: 1.655

5.  Long-term results after repair of truncus arteriosus communis in neonates and infants.

Authors:  M V Ullmann; M Gorenflo; C Sebening; H E Ulmer; S Hagl
Journal:  Thorac Cardiovasc Surg       Date:  2003-08       Impact factor: 1.827

6.  A cohort study of neurodevelopmental outcome in children with DiGeorge syndrome following cardiac surgery.

Authors:  M Maharasingam; I Ostman-Smith; M G Pike
Journal:  Arch Dis Child       Date:  2003-01       Impact factor: 3.791

7.  Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

Authors:  R Matsuoka; A Takao; M Kimura; S Imamura; C Kondo; K Joh-o; K Ikeda; M Nishibatake; M Ando; K Momma
Journal:  Am J Med Genet       Date:  1994-11-15

8.  Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Authors:  D A Driscoll; N B Spinner; M L Budarf; D M McDonald-McGinn; E H Zackai; R B Goldberg; R J Shprintzen; H M Saal; J Zonana; M C Jones
Journal:  Am J Med Genet       Date:  1992-09-15

9.  Anatomic patterns of conotruncal defects associated with deletion 22q11.

Authors:  B Marino; M C Digilio; A Toscano; S Anaclerio; A Giannotti; C Feltri; M A de Ioris; A Angioni; B Dallapiccola
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

10.  Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Authors:  A K Ryan; J A Goodship; D I Wilson; N Philip; A Levy; H Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; M Prieur; A Aurias; F L Raymond; J Clayton-Smith; E Hatchwell; C McKeown; F A Beemer; B Dallapiccola; G Novelli; J A Hurst; J Ignatius; A J Green; R M Winter; L Brueton; K Brøndum-Nielsen; P J Scambler
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

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  8 in total

1.  Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.

Authors:  Daniel Seung Kim; Jerry H Kim; Amber A Burt; David R Crosslin; Nancy Burnham; Cecilia E Kim; Donna M McDonald-McGinn; Elaine H Zackai; Susan C Nicolson; Thomas L Spray; Ian B Stanaway; Deborah A Nickerson; Patrick J Heagerty; Hakon Hakonarson; J William Gaynor; Gail P Jarvik
Journal:  J Thorac Cardiovasc Surg       Date:  2015-11-10       Impact factor: 5.209

2.  Independent risk factors for cardiac operations in adults with congenital heart disease: a retrospective study of 543 operations for 500 patients.

Authors:  Manfred Otto Vogt; Jürgen Hörer; Sophie Grünewald; Daniela Otto; Harald Kaemmerer; Christian Schreiber; John Hess
Journal:  Pediatr Cardiol       Date:  2011-09-08       Impact factor: 1.655

3.  The Impact of 22q11.2 Microdeletion on Cardiac Surgery Postoperative Outcome.

Authors:  Goran Cuturilo; Danijela Drakulic; Ida Jovanovic; Slobodan Ilic; Jasna Kalanj; Irena Vulicevic; Misela Raus; Dejan Skoric; Marija Mijovic; Biljana Medjo; Snezana Rsovac; Milena Stevanovic
Journal:  Pediatr Cardiol       Date:  2017-09-22       Impact factor: 1.655

Review 4.  22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects.

Authors:  Carolina Putotto; Flaminia Pugnaloni; Marta Unolt; Stella Maiolo; Matteo Trezzi; Maria Cristina Digilio; Annapaola Cirillo; Giuseppe Limongelli; Bruno Marino; Giulio Calcagni; Paolo Versacci
Journal:  Children (Basel)       Date:  2022-05-25

5.  22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot.

Authors:  Laura Mercer-Rosa; Nelangi Pinto; Wei Yang; Ronn Tanel; Elizabeth Goldmuntz
Journal:  J Thorac Cardiovasc Surg       Date:  2013-01-11       Impact factor: 5.209

6.  22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive cases.

Authors:  Shabnam Peyvandi; Philip J Lupo; Jennifer Garbarini; Stacy Woyciechowski; Sharon Edman; Beverly S Emanuel; Laura E Mitchell; Elizabeth Goldmuntz
Journal:  Pediatr Cardiol       Date:  2013-04-21       Impact factor: 1.655

7.  Cardiac abnormalities and facial anthropometric measurements in children from the Free State and Northern Cape provinces of South Africa with chromosome 22q11.2 microdeletion.

Authors:  S C Brown; B D Henderson; D A Buys; M Theron; M A Long; F Smit
Journal:  Cardiovasc J Afr       Date:  2010 Jan-Feb       Impact factor: 1.167

8.  Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples.

Authors:  Harini Ravi; Gabriel McNeill; Shruti Goel; Steven D Meltzer; Nathan Hunkapiller; Allison Ryan; Brynn Levy; Zachary P Demko
Journal:  PLoS One       Date:  2018-02-23       Impact factor: 3.240

  8 in total

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