Neonatal Screening
"Neonatal Screening" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The identification of selected parameters in newborn infants by various tests, examinations, or other procedures. Screening may be performed by clinical or laboratory measures. A screening test is designed to sort out healthy neonates (INFANT, NEWBORN) from those not well, but the screening test is not intended as a diagnostic device, rather instead as epidemiologic.
Descriptor ID |
D015997
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MeSH Number(s) |
E01.370.225.910 E01.370.500.580 E05.200.910 E05.318.308.250.580.580 N02.421.143.827.233.443.816 N05.715.360.300.375.500.575 N06.850.520.308.250.580.580 N06.850.780.500.580
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Concept/Terms |
Neonatal Screening- Neonatal Screening
- Neonatal Screenings
- Screening, Neonatal
- Screenings, Neonatal
- Infant, Newborn, Screening
- Newborn Infant Screening
- Newborn Infant Screenings
- Screening, Newborn Infant
- Screenings, Newborn Infant
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Below are MeSH descriptors whose meaning is more general than "Neonatal Screening".
Below are MeSH descriptors whose meaning is more specific than "Neonatal Screening".
This graph shows the total number of publications written about "Neonatal Screening" by people in UAMS Profiles by year, and whether "Neonatal Screening" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2024 | 2 | 0 | 2 | 2023 | 2 | 0 | 2 | 2022 | 1 | 3 | 4 | 2020 | 1 | 0 | 1 | 2019 | 1 | 1 | 2 | 2017 | 0 | 1 | 1 | 2016 | 2 | 1 | 3 | 2015 | 5 | 1 | 6 | 2014 | 1 | 0 | 1 | 2013 | 2 | 0 | 2 | 2010 | 1 | 0 | 1 | 2009 | 1 | 1 | 2 | 2008 | 2 | 0 | 2 | 2007 | 0 | 1 | 1 | 2004 | 2 | 0 | 2 | 1996 | 1 | 0 | 1 | 1995 | 1 | 0 | 1 | 1993 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Neonatal Screening" by people in Profiles over the past ten years.
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Rose NR, Dabbs SG, O'Hagan EC, Guimbellot JS. Literary evidence of the impact of nonbiological risk factors on CRMS/CFSPID: A scoping review. Pediatr Pulmonol. 2024 Dec; 59(12):3095-3105.
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El-Khawam R, Dumpa V, Islam S, Kohn B, Hanna N. Early blood glucose screening in asymptomatic high-risk neonates. J Pediatr Endocrinol Metab. 2024 Aug 27; 37(8):686-692.
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Bower C, Reilly BK, Richerson J, Hecht JL. Hearing Assessment in Infants, Children, and Adolescents: Recommendations Beyond Neonatal Screening. Pediatrics. 2023 09 01; 152(3).
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Ellis EW, Smetak MR, Alving-Trinh A, Golinko M, Phillips JD, Belcher RH. An Enhanced Audiologic Protocol for Early Identification of Conductive Hearing Loss in Patients with Cleft Palate. Cleft Palate Craniofac J. 2024 Oct; 61(10):1657-1662.
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Ivanic S, Tong LS, Laird A, Malhotra A, Nataraja RM, Lang C, Pacilli M. The Newborn Infant Parasympathetic Evaluation (NIPE?) monitor predicts post-operative pain in children undergoing day-procedures: A prospective observational study. J Pediatr Surg. 2023 Apr; 58(4):684-688.
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Prakash S, Penn JD, Jackson KE, Dean LW. Newborn screening for Pompe disease: Parental experiences and follow-up care for a late-onset diagnosis. J Genet Couns. 2022 12; 31(6):1404-1420.
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Nicholson N, Rhoades EA, Glade RE. Analysis of Health Disparities in the Screening and Diagnosis of Hearing Loss: Early Hearing Detection and Intervention Hearing Screening Follow-Up Survey. Am J Audiol. 2022 Sep; 31(3):764-788.
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Mak D, Akinseye L, Lahoti A, Diaz-Thomas A. Abnormal Newborn Screen During a Pandemic. Neoreviews. 2022 03 01; 23(3):e212-e215.
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Chorath K, Garza L, Tarriela A, Luu N, Rajasekaran K, Moreira A. Clinical practice guidelines on newborn hearing screening: A systematic quality appraisal using the AGREE II instrument. Int J Pediatr Otorhinolaryngol. 2021 Feb; 141:110504.
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Alanazi AA, Nicholson N. Audiology and Speech-Language Pathology Simulation Training on the 1-3-6 Early Hearing Detection and Intervention Timeline. Am J Audiol. 2019 Jun 10; 28(2):348-361.
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Hays LH. Societal value of newborn screening for severe combined immune deficiency in Arkansas: An economic analysis. Public Health Nurs. 2019 07; 36(4):541-544.
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Chung EK, Gable EK, Golden WC, Hudson JA, Hackman NM, Andrews JP, Jackson DS, Beavers JB, Mirchandani DR, Kellams A, Krevitsky ME, Monroe K, Madlon-Kay DJ, Stratbucker W, Campbell D, Collins J, Rauch D. Current Scope of Practice for Newborn Care in Non-Intensive Hospital Settings. Hosp Pediatr. 2017 08; 7(8):471-482.
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Zhou Y, Bai S, Bornhorst JA, Elhassan NO, Kaiser JR. The Effect of Early Feeding on Initial Glucose Concentrations in Term Newborns. J Pediatr. 2017 02; 181:112-115.
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Mitchell AJ, Hall RW, Golianu B, Yates C, Williams DK, Chang J, Anand KJ. Does noninvasive electrical stimulation of acupuncture points reduce heelstick pain in neonates? Acta Paediatr. 2016 Dec; 105(12):1434-1439.
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Alanazi AA, Nicholson N, Atcherson SR, Franklin C, Anders M, Nagaraj N, Franklin J, Highley P. Use of Baby Isao Simulator and Standardized Parents in Hearing Screening and Parent Counseling Education. Am J Audiol. 2016 Sep 01; 25(3):211-23.
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Lavin LR, Higby N, Abramo T. Newborn Screening: What Does the Emergency Physician Need to Know? Pediatr Emerg Care. 2015 Sep; 31(9):661-7; quiz 667-9.
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Schaefer GB, Larson IA, Bolick J, Williamson-Dean L. What is the role of clinical genetics in the patient-centered medical home?: A commentary from the Medical Home Workgroup of the Heartland Regional Genetics and Newborn Screening Collaborative. Genet Med. 2016 05; 18(5):440-2.
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Reefhuis J, Gilboa SM, Anderka M, Browne ML, Feldkamp ML, Hobbs CA, Jenkins MM, Langlois PH, Newsome KB, Olshan AF, Romitti PA, Shapira SK, Shaw GM, Tinker SC, Honein MA. The National Birth Defects Prevention Study: A review of the methods. Birth Defects Res A Clin Mol Teratol. 2015 Aug; 103(8):656-69.
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Chasteen S, Golden WE, Smith N. Newborn screening improvements in Arkansas. J Ark Med Soc. 2015 May; 111(12):252-3.
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Wong D, Tortorelli S, Bishop L, Sellars EA, Schimmenti LA, Gallant N, Prada CE, Hopkin RJ, Leslie ND, Berry SA, Rosenblatt DS, Fair AL, Matern D, Raymond K, Oglesbee D, Rinaldo P, Gavrilov D. Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening. Genet Med. 2016 Feb; 18(2):162-7.
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Tinker SC, Carmichael SL, Anderka M, Browne ML, Caspers Conway KM, Meyer RE, Nembhard WN, Olney RS, Reefhuis J. Next steps for birth defects research and prevention: The birth defects study to evaluate pregnancy exposures (BD-STEPS). Birth Defects Res A Clin Mol Teratol. 2015 Aug; 103(8):733-40.
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