Document Detail


Contribution of genetic disorders to neonatal mortality in a regional intensive care setting.
MedLine Citation:
PMID:  8198647     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We examined the contribution of chromosomal abnormalities, mendelian disorders, and birth defects to mortality in a regional neonatal intensive care unit by medical record review of neonatal deaths in that unit. Of a total of 296 infant deaths during the 5-year period June 1986 to May 1991, 69 (23.3%) had a genetic disorder. By diagnostic category, 18.8% had a chromosomal abnormality, 10.1% had a mendelian condition, 42% had a single primary defect in development, and 29% had an unrecognized pattern of malformation. The rate of autopsy and genetic evaluation differed markedly between these diagnostic categories. A comparison was made of underlying cause of death determined from medical records with underlying cause as classified by vital statistics nosologic procedures. No death certificate was on file for two of the deaths; for the remaining 67, 27 (40.3%) had an erroneous or misleading underlying cause of death as determined from vital statistics. The important contribution of genetic disorders to neonatal mortality in this high-risk population and the relative underrecognition of these disorders by vital statistics sources indicate that efforts aimed at reducing neonatal mortality will require a full range of preventive health activities, including preconception, prenatal and perinatal assessment, and counseling. Improved data collection techniques need to be developed to understand the contribution of this group of conditions to total neonatal mortality.
Authors:
S M Hudome; R S Kirby; J W Senner; C Cunniff
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  American journal of perinatology     Volume:  11     ISSN:  0735-1631     ISO Abbreviation:  Am J Perinatol     Publication Date:  1994 Mar 
Date Detail:
Created Date:  1994-07-07     Completed Date:  1994-07-07     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  8405212     Medline TA:  Am J Perinatol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  100-3     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Arkansas Children's Hospital, Little Rock 72202-3591.
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MeSH Terms
Descriptor/Qualifier:
Cause of Death*
Chromosome Aberrations / mortality*
Chromosome Disorders
Congenital Abnormalities / mortality*
Hospital Mortality
Humans
Infant
Infant Mortality
Infant, Newborn
Intensive Care Units, Neonatal

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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