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1.
MMWR Morb Mortal Wkly Rep ; 69(49): 1853-1856, 2020 12 11.
Article in English | MEDLINE | ID: mdl-33301432

ABSTRACT

American Indian/Alaska Native (AI/AN) persons experienced disproportionate mortality during the 2009 influenza A(H1N1) pandemic (1,2). Concerns of a similar trend during the coronavirus disease 2019 (COVID-19) pandemic led to the formation of a workgroup* to assess the prevalence of COVID-19 deaths in the AI/AN population. As of December 2, 2020, CDC has reported 2,689 COVID-19-associated deaths among non-Hispanic AI/AN persons in the United States.† A recent analysis found that the cumulative incidence of laboratory-confirmed COVID-19 cases among AI/AN persons was 3.5 times that among White persons (3). Among 14 participating states, the age-adjusted AI/AN COVID-19 mortality rate (55.8 deaths per 100,000; 95% confidence interval [CI] = 52.5-59.3) was 1.8 (95% CI = 1.7-2.0) times that among White persons (30.3 deaths per 100,000; 95% CI = 29.9-30.7). Although COVID-19 mortality rates increased with age among both AI/AN and White persons, the disparity was largest among those aged 20-49 years. Among persons aged 20-29 years, 30-39 years, and 40-49 years, the COVID-19 mortality rates among AI/AN were 10.5, 11.6, and 8.2 times, respectively, those among White persons. Evidence that AI/AN communities might be at increased risk for COVID-19 illness and death demonstrates the importance of documenting and understanding the reasons for these disparities while developing collaborative approaches with federal, state, municipal, and tribal agencies to minimize the impact of COVID-19 on AI/AN communities. Together, public health partners can plan for medical countermeasures and prevention activities for AI/AN communities.


Subject(s)
/statistics & numerical data , American Indian or Alaska Native/statistics & numerical data , COVID-19/ethnology , COVID-19/mortality , Health Status Disparities , Adult , Female , Humans , Male , Middle Aged , United States/epidemiology , Young Adult
2.
Genet Med ; 20(6): 608-613, 2018 06.
Article in English | MEDLINE | ID: mdl-29758563

ABSTRACT

PurposeTo determine feasibility and utility of newborn screening for spinal muscular atrophy (SMA) in New York State.MethodsWe validated a multiplex TaqMan real-time quantitative polymerase chain reaction assay using dried blood spots for SMA. From January 2016 to January 2017, we offered, consented, and screened 3,826 newborns at three hospitals in New York City and tested newborns for the deletion in exon 7 of SMN1.ResultsNinety-three percent of parents opted in for SMA screening. Overall the SMA carrier frequency was 1.5%. We identified one newborn with a homozygous SMN1 deletion and two copies of SMN2, which strongly suggests the severe type 1 SMA phenotype. The infant was enrolled in the NURTURE clinical trial and was first treated with Spinraza at age 15 days. She is now age 12 months, meeting all developmental milestones, and free of any respiratory issues.ConclusionOur pilot study demonstrates the feasibility of population-based screening, the acceptance by families, and the benefit of newborn screening for SMA. We suggest that SMA be considered for addition to the national recommended uniform screening panel.


Subject(s)
Muscular Atrophy, Spinal/diagnosis , Neonatal Screening/methods , Survival of Motor Neuron 1 Protein/genetics , Exons , Female , Gene Deletion , Gene Dosage , Humans , Infant , Infant, Newborn , Male , Muscular Atrophy, Spinal/genetics , New York , Pilot Projects , Survival of Motor Neuron 1 Protein/physiology
3.
Genet Med ; 15(12): 978-82, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23598714

ABSTRACT

PURPOSE: Treatment of inherited metabolic disorders is accomplished by use of specialized diets employing medical foods and medically necessary supplements. Families seeking insurance coverage for these products express concern that coverage is often limited; the extent of this challenge is not well defined. METHODS: To learn about limitations in insurance coverage, parents of 305 children with inherited metabolic disorders completed a paper survey providing information about their use of medical foods, modified low-protein foods, prescribed dietary supplements, and medical feeding equipment and supplies for treatment of their child's disorder as well as details about payment sources for these products. RESULTS: Although nearly all children with inherited metabolic disorders had medical coverage of some type, families paid "out of pocket" for all types of products. Uncovered spending was reported for 11% of families purchasing medical foods, 26% purchasing supplements, 33% of those needing medical feeding supplies, and 59% of families requiring modified low-protein foods. Forty-two percent of families using modified low-protein foods and 21% of families using medical foods reported additional treatment-related expenses of $100 or more per month for these products. CONCLUSION: Costs of medical foods used to treat inherited metabolic disorders are not completely covered by insurance or other resources.


Subject(s)
Insurance, Health, Reimbursement/statistics & numerical data , Metabolism, Inborn Errors/diet therapy , Adolescent , Child , Child, Preschool , Costs and Cost Analysis , Data Collection , Diet Therapy/economics , Dietary Supplements/economics , Food, Formulated/economics , Humans , Infant , Infant, Newborn , Insurance, Health, Reimbursement/economics , Metabolism, Inborn Errors/economics
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