Literature DB >> 23612637

Impact of inborn errors of metabolism on admission in a neonatal intensive care unit: a 4-year report.

Meng Meng, Yu-Ping Zhang.   

Abstract

Inborn errors of metabolism (IEM) have greater repercussions in neonatology units. The aim of our study was to evaluate the impact of IEM in a neonatal intensive care unit (NICU) and the resources required to care for these neonates. All patients with IEM admitted in our unit during a 4-year period were evaluated for specific diagnosis, demographic data, clinical features, biochemical characteristics at admission, need for mechanical ventilation, use of extracorporeal removal therapy, and outcome at NICU discharge. The study group comprised 2742 infants, 39 of which required admission to the NICU (1.42% of admissions) because of severe symptoms and/or newborn screening. Five of the 39 had an earlier diagnosis and treatment because of expanded newborn screening. The average age at admission was 5 days [interquartile range (IQR, 3-9 days)] and the median length of stay in the NICU for the study population was 5 days (IQR, 3-12 days). Aggressive support was often necessary (extracorporeal removal therapy, mechanical ventilation). Ten patients died; thus the death rate was 25.6%. Overall mortality in the NICU was 10.4% during the study period. These observations shown that IEM may be very common in our population. Most patients with IEM admitted to a NICU require aggressive support (including mechanical ventilation and extracorporeal removal therapies), and consume significant resources for relatively shorter stays.

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Year:  2013        PMID: 23612637     DOI: 10.1515/jpem-2013-0021

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  4 in total

1.  Newborn Sequencing in Genomic Medicine and Public Health.

Authors:  Jonathan S Berg; Pankaj B Agrawal; Donald B Bailey; Alan H Beggs; Steven E Brenner; Amy M Brower; Julie A Cakici; Ozge Ceyhan-Birsoy; Kee Chan; Flavia Chen; Robert J Currier; Dmitry Dukhovny; Robert C Green; Julie Harris-Wai; Ingrid A Holm; Brenda Iglesias; Galen Joseph; Stephen F Kingsmore; Barbara A Koenig; Pui-Yan Kwok; John Lantos; Steven J Leeder; Megan A Lewis; Amy L McGuire; Laura V Milko; Sean D Mooney; Richard B Parad; Stacey Pereira; Joshua Petrikin; Bradford C Powell; Cynthia M Powell; Jennifer M Puck; Heidi L Rehm; Neil Risch; Myra Roche; Joseph T Shieh; Narayanan Veeraraghavan; Michael S Watson; Laurel Willig; Timothy W Yu; Tiina Urv; Anastasia L Wise
Journal:  Pediatrics       Date:  2017-01-17       Impact factor: 7.124

2.  Genetic disorders and mortality in infancy and early childhood: delayed diagnoses and missed opportunities.

Authors:  Monica H Wojcik; Talia S Schwartz; Inbar Yamin; Heather L Edward; Casie A Genetti; Meghan C Towne; Pankaj B Agrawal
Journal:  Genet Med       Date:  2018-04-12       Impact factor: 8.822

3.  Medium-chain acyl-CoA dehydrogenase deficiency: Two novel ACADM mutations identified in a retrospective screening.

Authors:  Andraz Smon; Urh Groselj; Marusa Debeljak; Mojca Zerjav Tansek; Sara Bertok; Magdalena Avbelj Stefanija; Katarina Trebusak Podkrajsek; Tadej Battelino; Barbka Repic Lampret
Journal:  J Int Med Res       Date:  2018-01-19       Impact factor: 1.671

4.  Molecular autopsy by proxy in preconception counseling.

Authors:  Malak Ali Alghamdi; Ameinah Alrasheedi; Esra Alghamdi; Nouran Adly; Wajeih Y AlAali; Amal Alhashem; Abdulaziz Alshahrani; Hanan Shamseldin; Fowzan S Alkuraya; Majid Alfadhel
Journal:  Clin Genet       Date:  2021-08-30       Impact factor: 4.296

  4 in total

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