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The effect of rapid exome sequencing on downstream health care utilization for infants with suspected genetic disorders in an intensive care unit.
Rodriguez Llorian, Elisabet; Dragojlovic, Nick; Campbell, Teresa M; Friedman, Jan M; Osiovich, Horacio; Elliott, Alison M; Lynd, Larry D.
Afiliação
  • Rodriguez Llorian E; Collaboration for Outcomes Research and Evaluation, Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Dragojlovic N; Collaboration for Outcomes Research and Evaluation, Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.
  • Campbell TM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Friedman JM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Osiovich H; Division of Neonatology, Department of Paediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Elliott AM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Lynd LD; Collaboration for Outcomes Research and Evaluation, Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada; Centre for Health Evaluation and Outcome Sciences, St. Paul's Hospital, Vancouver, British Columbia, Canada. Electronic address: larry.lynd@ubc
Genet Med ; 24(8): 1675-1683, 2022 08.
Article em En | MEDLINE | ID: mdl-35622065
PURPOSE: This study aimed to compare downstream utilization of medical services among critically ill infants admitted to intensive care units who received rapid exome sequencing (ES) and those who followed alternative diagnostic testing pathways. METHODS: Using propensity score-weighted regression models including sex, age at admission, and severity indicators, we compared a group of 47 infants who underwent rapid ES with a group of 211 infants who did not receive rapid ES. Utilization and cost indicators were compared between cohorts using negative binomial models for utilization and two-part models for costs. RESULTS: After controlling for patients' sociodemographic and clinical characteristics, we found no statistically significant difference in outpatient visits, hospitalizations, intensive care unit or total length of stay, or length of stay-associated costs between the cohorts at 12- or 26-month follow-up. Similarly, there was no evidence of higher utilization or costs by the ES group when infants who died were removed from the analysis. CONCLUSION: When examining utilization during and beyond the diagnostic trajectory, there is no evidence that ES changes frequency of outpatient visits or use of in-hospital resources in critically ill infants with suspected genetic disorders.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estado Terminal / Exoma Tipo de estudo: Prognostic_studies Limite: Humans / Infant Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estado Terminal / Exoma Tipo de estudo: Prognostic_studies Limite: Humans / Infant Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá