Dmitry Dukhovny
Oregon Health & Science University
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Featured researches published by Dmitry Dukhovny.
Pediatrics | 2015
Timmy Ho; Dmitry Dukhovny; John A.F. Zupancic; Donald A. Goldmann; Jeffrey D. Horbar; DeWayne M. Pursley
BACKGROUND: The use of unnecessary tests and treatments contributes to health care waste. The “Choosing Wisely” campaign charges medical societies with identifying such items. This report describes the identification of 5 tests and treatments in newborn medicine. METHODS: A national survey identified candidate tests and treatments. An expert panel of 51 individuals representing 28 perinatal care organizations narrowed the list over 3 rounds of a modified Delphi process. In the final round, the panel was provided with Grading of Recommendation, Assessment, Development and Evaluation (GRADE) literature summaries of the top 12 tests and treatments. RESULTS: A total of 1648 candidate tests and 1222 treatments were suggested by 1047 survey respondents. After 3 Delphi rounds, the expert panel achieved consensus on the following top 5 items: (1) avoid routine use of antireflux medications for treatment of symptomatic gastroesophageal reflux disease or for treatment of apnea and desaturation in preterm infants, (2) avoid routine continuation of antibiotic therapy beyond 48 hours for initially asymptomatic infants without evidence of bacterial infection, (3) avoid routine use of pneumograms for predischarge assessment of ongoing and/or prolonged apnea of prematurity, (4) avoid routine daily chest radiographs without an indication for intubated infants, and (5) avoid routine screening term-equivalent or discharge brain MRIs in preterm infants. CONCLUSIONS: The Choosing Wisely Top Five for newborn medicine highlights tests and treatments that cannot be adequately justified on the basis of efficacy, safety, or cost. This list serves as a starting point for quality improvement efforts to optimize both clinical outcomes and resource utilization in newborn care.
Journal of Personalized Medicine | 2015
Kurt D. Christensen; Dmitry Dukhovny; Uwe Siebert; Robert C. Green
Despite dramatic drops in DNA sequencing costs, concerns are great that the integration of genomic sequencing into clinical settings will drastically increase health care expenditures. This commentary presents an overview of what is known about the costs and cost-effectiveness of genomic sequencing. We discuss the cost of germline genomic sequencing, addressing factors that have facilitated the decrease in sequencing costs to date and anticipating the factors that will drive sequencing costs in the future. We then address the cost-effectiveness of diagnostic and pharmacogenomic applications of genomic sequencing, with an emphasis on the implications for secondary findings disclosure and the integration of genomic sequencing into general patient care. Throughout, we ground the discussion by describing efforts in the MedSeq Project, an ongoing randomized controlled clinical trial, to understand the costs and cost-effectiveness of integrating whole genome sequencing into cardiology and primary care settings.
Pediatrics | 2017
Jonathan S. Berg; Pankaj B. Agrawal; Donald B. Bailey; Alan H. Beggs; Steven E. Brenner; Amy Brower; Julie A. Cakici; Ozge Ceyhan-Birsoy; Kee Chan; Flavia Chen; Robert 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 D. Lantos; Steven Leeder; Megan A. Lewis; Amy L. McGuire; Laura V. Milko; Sean D. Mooney; Richard B. Parad; Stacey Pereira; Joshua E. Petrikin; Bradford C. Powell
The rapid development of genomic sequencing technologies has decreased the cost of genetic analysis to the extent that it seems plausible that genome-scale sequencing could have widespread availability in pediatric care. Genomic sequencing provides a powerful diagnostic modality for patients who manifest symptoms of monogenic disease and an opportunity to detect health conditions before their development. However, many technical, clinical, ethical, and societal challenges should be addressed before such technology is widely deployed in pediatric practice. This article provides an overview of the Newborn Sequencing in Genomic Medicine and Public Health Consortium, which is investigating the application of genome-scale sequencing in newborns for both diagnosis and screening.
Pediatrics | 2016
Dmitry Dukhovny; DeWayne M. Pursley; Haresh Kirpalani; Jeffrey H. Horbar; John A.F. Zupancic
Rising health care costs challenge governments, payers, and providers in delivering health care services. Tremendous pressures result to deliver better quality care while simultaneously reducing costs. This has led to a wholesale re-examination of current practice methods, including explicit consideration of efficiency and waste. Traditionally, reductions in the costs of care have been considered as independent, and sometimes even antithetical, to the practice of high-quality, intensive medicine. However, it is evident that provision of evidence-based, locally relevant care can result in improved outcomes, lower resource utilization, and opportunities to reallocate resources. This is particularly relevant to the practice of neonatology. In the United States, 12% of the annual birth cohort is affected by preterm birth, and 3% is affected by congenital anomalies. Both of these conditions are associated with costly health care during, and often long after, the NICU admission. We will discuss how 3 drivers of clinical practice in neonatal care (evidence-based medicine, evidence-based economics, and quality improvement) can together optimize clinical and fiscal outcomes.
Genetics in Medicine | 2018
Kurt D. Christensen; Jason L. Vassy; Kathryn A. Phillips; Carrie Blout; Danielle R. Azzariti; Christine Y. Lu; Jill O. Robinson; Kaitlyn Lee; Michael P. Douglas; Jennifer M. Yeh; Kalotina Machini; Natasha K. Stout; Heidi L. Rehm; Amy L. McGuire; Robert C. Green; Dmitry Dukhovny
PurposeGreat uncertainty exists about the costs associated with whole-genome sequencing (WGS).MethodsOne hundred cardiology patients with cardiomyopathy diagnoses and 100 ostensibly healthy primary care patients were randomized to receive a family-history report alone or with a WGS report. Cardiology patients also reviewed prior genetic test results. WGS costs were estimated by tracking resource use and staff time. Downstream costs were estimated by identifying services in administrative data, medical records, and patient surveys for 6 months.ResultsThe incremental cost per patient of WGS testing was
Pediatrics | 2018
Sunah S. Hwang; Dmitry Dukhovny; Daksha Gopal; Howard Cabral; Stacey A. Missmer; Hafsatou Diop; Eugene Declercq; Judy E. Stern
5,098 in cardiology settings and
Journal of Perinatology | 2017
S. C. Hay; Haresh Kirpalani; C. Viner; Roger F. Soll; Dmitry Dukhovny; Wenyang Mao; Jochen Profit; Sara B. DeMauro; John A.F. Zupancic
5,073 in primary care settings compared with family history alone. Mean 6-month downstream costs did not differ statistically between the control and WGS arms in either setting (cardiology: difference = −
Journal of Perinatology | 2016
D Wei; C Osman; Dmitry Dukhovny; J Romley; M Hall; S Chin; Timmy Ho; P S Friedlich; A Lakshmanan
1,560, 95% confidence interval −
Journal of Perinatology | 2018
Leah Yieh; Cindy McEvoy; Scott W. Hoffman; Aaron B. Caughey; Kelvin D. MacDonald; Dmitry Dukhovny
7,558 to
Respiratory Care | 2017
Brian Montenegro; Michael Amberson; Lauren Veit; Christina Freiberger; Dmitry Dukhovny; Lawrence Rhein
3,866, p = 0.36; primary care: difference =