Literature DB >> 14681831

The burden of genetic disease on inpatient care in a children's hospital.

Shawn E McCandless1, Jeanne W Brunger, Suzanne B Cassidy.   

Abstract

The important role of genetics in pediatric illness has been increasingly recognized, but the true impact has not been well delineated. An important study of pediatric inpatient admissions to a children's hospital in 1978 found a genetic basis for disease in just less than half of admitted patients. We sought to update this study in light of current hospitalization practices and new knowledge about genetics. We systematically reviewed the records of 5,747 consecutive admissions (4,224 individuals), representing 98% of patients admitted in 1996 to Rainbow Babies and Children's Hospital (Cleveland, OH). Each patient was assigned to one of five groups on the basis of the presence or absence of an underlying chronic medical condition and whether that condition had a genetic basis or susceptibility. An underlying disorder with a significant genetic component was found in 71% of admitted children. The vast majority (96%) of underlying chronic disorders in children in this study were either clearly genetic or had a genetic susceptibility. Total charges for 1996 were >$62 million, of which $50 million (81%) was accounted for by disorders with a genetic determinant. The 34% of admissions with clearly genetic underlying disorders accounted for 50% (>$31 million) of the total hospital charges. The mean length of stay was 40% longer for individuals with an underlying disease with a genetic basis than for those with no underlying disease. Charges and length of stay were similar for children with underlying chronic disorders, regardless of the cause. This study begins to quantify the enormous impact of genetic disease on inpatient pediatrics and the health care system. Additional study and frank public discourse are needed to understand the implications on the future health care workforce and on the utilization of health care resources.

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Year:  2003        PMID: 14681831      PMCID: PMC1181899          DOI: 10.1086/381053

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  14 in total

1.  Genetic aspects of admissions to a paediatric intensive care unit.

Authors:  D R FitzPatrick; C H Skeoch; J L Tolmie
Journal:  Arch Dis Child       Date:  1991-05       Impact factor: 3.791

2.  Frequency and load of congenital anomalies in a neonatal intensive care unit, prenatal diagnosis, and perinatal management.

Authors:  E W Ling
Journal:  Semin Perinatol       Date:  1992-12       Impact factor: 3.300

3.  The incidence of genetic disease in a University hospital population.

Authors:  N Day; L B Holmes
Journal:  Am J Hum Genet       Date:  1973-05       Impact factor: 11.025

4.  The impact of birth defects and genetic diseases.

Authors:  J G Hall
Journal:  Arch Pediatr Adolesc Med       Date:  1997-11

5.  Annual summary of vital statistics: 2000.

Authors:  D L Hoyert; M A Freedman; D M Strobino; B Guyer
Journal:  Pediatrics       Date:  2001-12       Impact factor: 7.124

6.  Human complement factor H deficiency associated with hemolytic uremic syndrome.

Authors:  N Rougier; M D Kazatchkine; J P Rougier; V Fremeaux-Bacchi; J Blouin; G Deschenes; B Soto; V Baudouin; B Pautard; W Proesmans; E Weiss; L Weiss
Journal:  J Am Soc Nephrol       Date:  1998-12       Impact factor: 10.121

7.  Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study.

Authors:  P W Yoon; R S Olney; M J Khoury; W M Sappenfield; G F Chavez; D Taylor
Journal:  Arch Pediatr Adolesc Med       Date:  1997-11

8.  The frequency of genetic disease and congenital malformation among patients in a pediatric hospital.

Authors:  C R Scriver; J L Neal; R Saginur; A Clow
Journal:  Can Med Assoc J       Date:  1973-05-05       Impact factor: 8.262

9.  Contribution of heritable disorders to mortality in the pediatric intensive care unit.

Authors:  C Cunniff; J L Carmack; R S Kirby; D H Fiser
Journal:  Pediatrics       Date:  1995-05       Impact factor: 7.124

10.  Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.

Authors:  M Noris; P Ruggenenti; A Perna; S Orisio; J Caprioli; C Skerka; B Vasile; P F Zipfel; G Remuzzi
Journal:  J Am Soc Nephrol       Date:  1999-02       Impact factor: 10.121

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  57 in total

Review 1.  Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.

Authors:  Laurie D Smith; Laurel K Willig; Stephen F Kingsmore
Journal:  Cold Spring Harb Perspect Med       Date:  2015-12-18       Impact factor: 6.915

Review 2.  Therapeutic in vivo gene transfer for genetic disease using AAV: progress and challenges.

Authors:  Federico Mingozzi; Katherine A High
Journal:  Nat Rev Genet       Date:  2011-05       Impact factor: 53.242

Review 3.  Rare-disease genetics in the era of next-generation sequencing: discovery to translation.

Authors:  Kym M Boycott; Megan R Vanstone; Dennis E Bulman; Alex E MacKenzie
Journal:  Nat Rev Genet       Date:  2013-09-03       Impact factor: 53.242

4.  How is the progress in genetics relevant to children's health care.

Authors:  Judith G Hall
Journal:  Paediatr Child Health       Date:  2004-04       Impact factor: 2.253

5.  Using Public-Private Partnerships to Mitigate Disparities in Access to Genetic Services: Lessons from Wisconsin.

Authors:  Laura Senier; Matthew Kearney; Jason Orne
Journal:  Adv Med Sociol       Date:  2015

6.  The unforeseen toll of birth defects and their economic burden at a tertiary care public institute in Mumbai.

Authors:  Mamta Muranjan; P Vijayalakshmi
Journal:  Indian J Pediatr       Date:  2014-04-26       Impact factor: 1.967

7.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

8.  Frequency of genetic diseases and health coverage of children requiring admission in a general pediatric clinic of northern Greece.

Authors:  Theodoros Lialiaris; Elpis Mantadakis; Dimitra Kareli; Panagiotis Mpountoukas; Aggelos Tsalkidis; Athanassios Chatzimichail
Journal:  Ital J Pediatr       Date:  2010-01-26       Impact factor: 2.638

Review 9.  When to suspect a genetic syndrome.

Authors:  Benjamin D Solomon; Maximilian Muenke
Journal:  Am Fam Physician       Date:  2012-11-01       Impact factor: 3.292

10.  The cycle of genome-directed medicine.

Authors:  Janet A Buchanan; Andrew R Carson; David Chitayat; David Malkin; M Stephen Meyn; Peter N Ray; Cheryl Shuman; Rosanna Weksberg; Stephen W Scherer
Journal:  Genome Med       Date:  2009-02-02       Impact factor: 11.117

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