9 results on '"Richard S. Olney"'
Search Results
2. Adrenoleukodystrophy Newborn Screening in California Since 2016: Programmatic Outcomes and Follow-Up
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Jamie Matteson, Stanley Sciortino, Lisa Feuchtbaum, Tracey Bishop, Richard S. Olney, and Hao Tang
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adrenoleukodystrophy ,newborn screening ,follow-up ,evaluation ,Pediatrics ,RJ1-570 - Abstract
X-linked adrenoleukodystrophy (ALD) is a recent addition to the Recommended Uniform Screening Panel, prompting many states to begin screening newborns for the disorder. We provide California’s experience with ALD newborn screening, highlighting the clinical and epidemiological outcomes observed as well as program implementation challenges. In this retrospective cohort study, we examine ALD newborn screening results and clinical outcomes for 1,854,631 newborns whose specimens were received by the California Genetic Disease Screening Program from 16 February 2016 through 15 February 2020. In the first four years of ALD newborn screening in California, 355 newborns screened positive for ALD, including 147 (41%) with an ABCD1 variant of uncertain significance (VUS) and 95 males diagnosed with ALD. After modifying cutoffs, we observed an ALD birth prevalence of 1 in 14,397 males. Long-term follow-up identified 14 males with signs of adrenal involvement. This study adds to a growing body of literature reporting on outcomes of newborn screening for ALD and offering a glimpse of what other large newborn screening programs can expect when adding ALD to their screening panel.
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- 2021
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3. The First Year Experience of Newborn Screening for Pompe Disease in California
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Hao Tang, Lisa Feuchtbaum, Stanley Sciortino, Jamie Matteson, Deepika Mathur, Tracey Bishop, and Richard S. Olney
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pompe disease ,newborn screening ,california ,Pediatrics ,RJ1-570 - Abstract
The California Department of Public Health started universal newborn screening for Pompe disease in August 2018 with a two-tier process including: 1) acid alpha-glucosidase (GAA) enzyme activity assay followed by, 2) GAA gene sequencing analysis. This study examines results from the first year of screening in a large and diverse screening population. With 453,152 screened newborns, the birth prevalence and GAA enzyme activity associated with various types of Pompe disease classifications are described. The frequency of GAA gene mutations and allele variants are reported. Of 88 screen positives, 18 newborns were resolved as Pompe disease, including 2 classic infantile-onset and 16 suspected late-onset form. The c.-32-13T>G variant was the most common pathogenic mutation reported. African American and Asian/Pacific Islander newborns had higher allele frequencies for both pathogenic and pseudodeficiency variants. After the first year of Pompe disease screening in California, the disease distribution in the population is now better understood. With the ongoing long-term follow-up system currently in place, our understanding of the complex genotype-phenotype relationships will become more evident in the future, and this should help us better understand the clinical significance of identified cases.
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- 2020
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4. Late Detection of Critical Congenital Heart Disease Among US Infants: Estimation of the Potential Impact of Proposed Universal Screening Using Pulse Oximetry
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Suzanne M. Gilboa, Elizabeth C. Ailes, Suzan L. Carmichael, Matthew E. Oster, Tiffany Riehle-Colarusso, Cora Peterson, David E Fixler, Gary M. Shaw, Richard S. Olney, and Cynthia H. Cassell
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Heart Defects, Congenital ,Pediatrics ,medicine.medical_specialty ,Population ,Coarctation of the aorta ,Autopsy ,Article ,Prevalence ,Medicine ,Humans ,Mass Screening ,Oximetry ,Critical congenital heart disease ,education ,Mass screening ,Estimation ,education.field_of_study ,medicine.diagnostic_test ,business.industry ,Infant ,medicine.disease ,United States ,Pulse oximetry ,Pediatrics, Perinatology and Child Health ,business ,Pulmonary atresia - Abstract
Importance Critical congenital heart disease (CCHD) was added to the Recommended Uniform Screening Panel for Newborns in the United States in 2011. Many states have recently adopted or are considering requirements for universal CCHD screening through pulse oximetry in birth hospitals. Limited previous research is directly applicable to the question of how many US infants with CCHD might be identified through screening. Objectives To estimate the proportion of US infants with late detection of CCHD (>3 days after birth) based on existing clinical practice and to investigate factors associated with late detection. Design, setting, and participants Descriptive and multivariable analysis. Data were obtained from a multisite population-based study of birth defects in the United States, the National Birth Defects Prevention Study (NBDPS). We included all live-born infants with estimated dates of delivery from January 1, 1998, through December 31, 2007, and nonsyndromic, clinically verified CCHD conditions potentially detectable through screening via pulse oximetry. Main outcomes and measures The main outcome measure was the proportion of infants with late detection of CCHD through echocardiography or at autopsy under the assumption that universal screening at birth hospitals might reduce the number of such late diagnoses. Secondary outcome measures included prevalence ratios for associations between selected demographic and clinical factors and late detection of CCHD. Results Of 3746 live-born infants with nonsyndromic CCHD, late detection occurred in 1106 (29.5% [95% CI, 28.1%-31.0%]), including 6 (0.2%) (0.1%-0.4%) first receiving a diagnosis at autopsy more than 3 days after birth. Late detection varied by CCHD type from 9 of 120 infants (7.5% [95% CI, 3.5%-13.8%]) with pulmonary atresia to 497 of 801 (62.0% [58.7%-65.4%]) with coarctation of the aorta. In multivariable analysis, late detection varied significantly by CCHD type and study site, and infants with extracardiac defects were significantly less likely to have late detection of CCHD (adjusted prevalence ratio, 0.58 [95% CI, 0.49-0.69]). Conclusions and relevance We estimate that 29.5% of live-born infants with nonsyndromic CCHD in the NBDPS received a diagnosis more than 3 days after birth and therefore might have benefited from routine CCHD screening at birth hospitals. The number of infants in whom CCHD was detected through screening likely varies by several factors, including CCHD type. Additional population-based studies of screening in practice are needed.
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- 2014
5. Cost-Effectiveness of Routine Screening for Critical Congenital Heart Disease in US Newborns
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Matthew E. Oster, Scott D. Grosse, Richard S. Olney, Cora Peterson, and Cynthia H. Cassell
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Heart Defects, Congenital ,Male ,Pediatrics ,medicine.medical_specialty ,Delayed Diagnosis ,Cost effectiveness ,Cost-Benefit Analysis ,Article ,Cohort Studies ,Neonatal Screening ,Cause of Death ,Medicine ,Humans ,Oximetry ,Critical congenital heart disease ,health care economics and organizations ,Cause of death ,Inpatient care ,Cost–benefit analysis ,business.industry ,Delivery Rooms ,Infant, Newborn ,Infant ,Infant mortality ,United States ,Quality-adjusted life year ,Hospitalization ,Survival Rate ,Pediatrics, Perinatology and Child Health ,Female ,Quality-Adjusted Life Years ,business ,Cohort study - Abstract
OBJECTIVES: Clinical evidence indicates newborn critical congenital heart disease (CCHD) screening through pulse oximetry is lifesaving. In 2011, CCHD was added to the US Recommended Uniform Screening Panel for newborns. Several states have implemented or are considering screening mandates. This study aimed to estimate the cost-effectiveness of routine screening among US newborns unsuspected of having CCHD. METHODS: We developed a cohort model with a time horizon of infancy to estimate the inpatient medical costs and health benefits of CCHD screening. Model inputs were derived from new estimates of hospital screening costs and inpatient care for infants with late-detected CCHD, defined as no diagnosis at the birth hospital. We estimated the number of newborns with CCHD detected at birth hospitals and life-years saved with routine screening compared with no screening. RESULTS: Screening was estimated to incur an additional cost of $6.28 per newborn, with incremental costs of $20 862 per newborn with CCHD detected at birth hospitals and $40 385 per life-year gained (2011 US dollars). We estimated 1189 more newborns with CCHD would be identified at birth hospitals and 20 infant deaths averted annually with screening. Another 1975 false-positive results not associated with CCHD were estimated to occur, although these results had a minimal impact on total estimated costs. CONCLUSIONS: This study provides the first US cost-effectiveness analysis of CCHD screening in the United States could be reasonably cost-effective. We anticipate data from states that have recently approved or initiated CCHD screening will become available over the next few years to refine these projections.
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- 2013
6. Maternal periconceptional occupational exposure to pesticides and selected musculoskeletal birth defects
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Carissa M. Rocheleau, Richard S. Olney, Yanyan Cao, Bonnie Chapman, Martha A. Waters, Patricia A. Stewart, Paul A. Romitti, Shao Lin, Christine Kielb, Christina C. Lawson, Charlotte M. Druschel, Michele L. Herdt-Losavio, and Erin M. Bell
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Adult ,Male ,medicine.medical_specialty ,Insecticides ,Population ,Limb Deformities, Congenital ,Article ,Craniosynostoses ,Young Adult ,Occupational hygiene ,Pregnancy ,Risk Factors ,Occupational Exposure ,Odds Ratio ,Medicine ,Humans ,Young adult ,Occupations ,education ,Gastroschisis ,Hernia, Diaphragmatic ,education.field_of_study ,business.industry ,Obstetrics ,Herbicides ,Public Health, Environmental and Occupational Health ,Case-control study ,Infant, Newborn ,Pregnancy Outcome ,Odds ratio ,medicine.disease ,Confidence interval ,United States ,Surgery ,Fungicides, Industrial ,Logistic Models ,Maternal Exposure ,Case-Control Studies ,Environmental Pollutants ,Female ,business ,Hernias, Diaphragmatic, Congenital - Abstract
This population-based U.S. study investigated the association between major musculoskeletal malformations and periconceptional maternal occupational pesticide exposure for a wide range of occupations. We conducted a multi-site case–control analysis using data from the National Birth Defects Prevention Study among employed women with due dates from October 1, 1997 through December 31, 2002. Cases included 871 live-born, stillborn, or electively terminated fetuses with isolated craniosynostosis, gastroschisis, diaphragmatic hernia, or transverse limb deficiencies. Controls included 2857 live-born infants without major malformations. Using self-reported maternal occupational information, an industrial hygienist used a job-exposure matrix and expert opinion to evaluate the potential for exposure to insecticides, herbicides or fungicides for each job held during one month pre-conception through three months post-conception. Exposures analyzed included any exposure (yes/no) to pesticides, to insecticides only, to both insecticides and herbicides (I + H) and to insecticides, herbicides and fungicides (I + H + F). We used logistic regression to evaluate the association between exposures and defects, controlling for infant and maternal risk factors. Occupational exposure to I + H + F was associated with gastroschisis among infants of women aged 20 years or older (adjusted odds ratio [aOR] = 1.88; 95% confidence interval [CI]: 1.16–3.05), but not for women under age 20 (aOR = 0.48; 95% CI: 0.20–1.16). We found no significant associations for the other defects. Additional research is needed to validate these findings in a separate population.
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- 2013
7. Maternal Corticosteroid Use and Hypospadias
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Suzan L. Carmichael, Chen Ma, Gary M. Shaw, Martha M. Werler, and Richard S. Olney
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Male ,medicine.medical_specialty ,medicine.drug_class ,medicine.medical_treatment ,Article ,Folic Acid ,Adrenal Cortex Hormones ,Pregnancy ,Administration, Inhalation ,medicine ,Humans ,Adverse effect ,Maternal-Fetal Exchange ,Gynecology ,Hypospadias ,business.industry ,Obstetrics ,Case-control study ,Infant, Newborn ,Odds ratio ,medicine.disease ,Health Surveys ,Confidence interval ,United States ,Nasal spray ,Case-Control Studies ,Pediatrics, Perinatology and Child Health ,Dietary Supplements ,Vitamin B Complex ,Corticosteroid ,Female ,business - Abstract
Objective To explore whether women who reported corticosteroid use during pregnancy were more likely to deliver an infant with hypospadias than women who did not. Study design The analysis encompassed data on deliveries with an estimated due date between 1997 and 2004 from the National Birth Defects Prevention Study, a large population-based, case-control study conducted in the United States. Included were 1165 cases of moderate to severe hypospadias and 3000 nonmalformed male controls. Results The mothers of 39 cases (3.3%) and 62 controls (2.1%) reported using a corticosteroid medication during the period extending from 4 weeks before conception to 14 weeks after conception. The odds ratio (OR) for any corticosteroid exposure versus no corticosteroid exposure was 1.6 (95% confidence interval [CI] = 1.1 to 2.5); after adjustment for maternal race/ethnicity, education, age, and study site, it was 1.3 (95% CI = 0.8 to 2.0). Analyses by route of administration and specific component suggest that elevated ORs occurred only for nasal spray/inhaled corticosteroids (OR = 1.5; 95% CI = 0.9 to 2.6). Conclusions Maternal use of corticosteroid medications was weakly associated with risk of hypospadias, but the association was negligible after adjustment for potential confounders.
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- 2009
8. Vitamin supplements and the risk for congenital anomalies other than neural tube defects (This article was prepared by a group consisting of both United States Government employees and non-United States Government employees and as such is subject to...
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Lorenzo D. Botto, Richard S. Olney, and J. David Erickson
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CLINICAL trials ,FOLIC acid ,NEURAL tube defect prevention ,VITAMIN B complex ,CLINICAL medicine ,MEDICAL experimentation on humans - Abstract
Randomized trials, supported by many observational studies, have shown that periconceptional use of folic acid, alone or in multivitamin supplements, is effective for the primary prevention of neural tube defects (NTDs). Whether this is true also for other congenital anomalies is a complex issue and the focus of this review. It is useful to consider the evidence not only for specific birth defects separately but, importantly, also for all birth defects combined. For the latter, the Hungarian randomized clinical trial indicated, for periconceptional multivitamin use, a reduction in the risk for all birth defects (odds ratio (OR) = 0.53, 95% confidence interval (CI) = 0.350.70), even after excluding NTDs (OR = 0.53, 95% CI = 0.380.75). The Atlanta population-based case-control study, the only large observational study to date on all major birth defects, also found a significant risk reduction for all birth defects (OR = 0.80, 95% CI = 0.690.93) even after excluding NTDs (OR = 0.84, 95% CI = 0.720.97). These and other studies also evaluated specific anomalies, including those of the heart, limb, and urinary tract, as well as orofacial clefts, omphalocele, and imperforate anus. For cardiovascular anomalies, two studies were negative, whereas three, including the randomized clinical trial, suggest a possible 2550% overall risk reduction, more marked for some conotruncal and septal defects. For orofacial clefts, six of seven case-control studies suggest an apparent reduced risk, which could vary by cleft type and perhaps, according to some investigators, by pill dosage. For limb deficiencies, three case-control studies and the randomized trial estimated approximately a 50% reduced risk. For urinary tract defects, three case-control studies and the randomized trial reported reduced risks, as did one study of nonsyndromic omphalocele. All these studies examined multivitamin supplement use. With respect to folic acid alone, a reduced rate of imperforate anus was observed among folic acid users in China. We discuss key gaps in knowledge, possible avenues for future research, and counseling issues for families concerned about occurrence or recurrence of these birth defects. © 2004 Wiley-Liss, Inc. [ABSTRACT FROM AUTHOR]
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- 2004
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9. The association between race/ethnicity and major birth defects in the United States, 1999-2007.
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Canfield MA, Mai CT, Wang Y, O'Halloran A, Marengo LK, Olney RS, Borger CL, Rutkowski R, Fornoff J, Irwin N, Copeland G, Flood TJ, Meyer RE, Rickard R, Alverson CJ, Sweatlock J, and Kirby RS
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- Birth Certificates, Humans, Population Surveillance, Prevalence, Risk Factors, United States epidemiology, Congenital Abnormalities ethnology, Ethnicity statistics & numerical data, Racial Groups statistics & numerical data
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Objectives: We investigated the relationship between race/ethnicity and 27 major birth defects., Methods: We pooled data from 12 population-based birth defects surveillance systems in the United States that included 13.5 million live births (1 of 3 of US births) from 1999 to 2007. Using Poisson regression, we calculated prevalence estimates for each birth defect and 13 racial/ethnic groupings, along with crude and adjusted prevalence ratios (aPRs). Non-Hispanic Whites served as the referent group., Results: American Indians/Alaska Natives had a significantly higher and 50% or greater prevalence for 7 conditions (aPR = 3.97; 95% confidence interval [CI] = 2.89, 5.44 for anotia or microtia); aPRs of 1.5 to 2.1 for cleft lip, trisomy 18, and encephalocele, and lower, upper, and any limb deficiency). Cubans and Asians, especially Chinese and Asian Indians, had either significantly lower or similar prevalences of these defects compared with non-Hispanic Whites, with the exception of anotia or microtia among Chinese (aPR = 2.08; 95% CI = 1.30, 3.33) and Filipinos (aPR = 1.90; 95% CI = 1.10, 3.30) and tetralogy of Fallot among Vietnamese (aPR = 1.60; 95% CI = 1.11, 2.32)., Conclusions: This is the largest population-based study to our knowledge to systematically examine the prevalence of a range of major birth defects across many racial/ethnic groups, including Asian and Hispanic subgroups. The relatively high prevalence of birth defects in American Indians/Alaska Natives warrants further attention.
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- 2014
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