United States Health Information Knowledgebase

 

You are viewing the Abridged Children's EHR Format.
To view the Full Children's EHR Format, you must first agree to the HL7 License Agreement.

Children's EHR Format Requirement Comparison

(No Match) Requirement ID: Req-281: Documentation of Care, Measurements and Results Req-823: Newborn Screening Decision Support
(Matches) Release Package: 2013 Format 2013 Format
(No Match) Title: Documentation of Care, Measurements and Results Newborn Screening Decision Support
(No Match) Description: System will document Care, Measurements and Results
ONC and HRSA are actively developing use cases and other health IT resources around newborn screening. A use case is available at: http://www.hhs.gov/healthit/usecases/documents/NBSDetailedUseCase.pdf [1]. The U.S. National Library of Medicine (NLM) has published the Newborn Screening Coding and Terminology to promote and facilitate the use of electronic health data standards for the conditions recommended for screening by the HHS Secretary's Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC). This is available at: http://newbornscreeningcodes.nlm.nih.gov/ [2].

The National Newborn Screening and Genetics Resource Center (http://genes-r-us.uthscsa.edu/ [3]) provides continuously updated information on the conditions screened for in each state. In addition, links are available to each state program. The Resource Center also provides educational materials for clinicians and family members.
Well-described clinical algorithms have been developed to guide general pediatricians and subspecialists in the process of newborn screening. These are available at: http://pediatrics.aappublications.org/content/121/1/192.abstract[4]. The requirements were designed to support these algorithms. In addition, these requirements support the transition from diagnosis through screening to chronic condition management and long-term follow-up as described in Kemper AR, Boyle CA, Aceves J, et al. Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children. Genet Med. 2008:10:259-261

Links:
------
[1] http://www.hhs.gov/healthit/usecases/documents/NBSDetailedUseCase.pdf
[2] http://newbornscreeningcodes.nlm.nih.gov/
[3] http://genes-r-us.uthscsa.edu/
[4] http://pediatrics.aappublications.org/content/121/1/192.abstract
(No Match) Topic Area(s): Activity Clearance, Children with Special Healthcare Needs, EPSDT, Growth Data, Immunizations, Medication Management, Newborn Screening, Primary Care Management, Records Management, Registry Linkages, Specialized Scales/Scoring, Well Child/Preventive Care Newborn Screening
(No Match) Provenance: HL7 EHR FM R1 SME
(Matches) Achievability:
(Matches) Requirement Type: Header Header
(Matches) Shall/Should/May:
(Matches) Critical/Core: no no
(Matches) Status: Released Released
(No Match) Links: Clinical Algorithms: Well-described clinical algorithms have been developed to guide general pediatricians and subspecialists in the process of newborn screening. These are available at this linkhttp://pediatrics.aappublications.org/cgi/content/abstract/121/1/192National Newborn Screening and Genetics Resource Center: The National Newborn Screening and Genetics Resource Center provides continuously updated information on the conditions screened for in each state. In addition, links are available to each state program. The Resource Center also provides educational material for clinicians and family members.http://genes-r-us.uthscsa.edu/Newborn Screening Coding and Terminology: The U.S. National Library of Medicine (NLM) has published the Newborn Screening Coding and Terminology to promote and facilitate the use of electronic health data standards for the conditions recommended for screening by the HHS Secretary's Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC). This is available at this linkhttp://newbornscreeningcodes.nlm.nih.gov/Recommended Uniform Screening Panel: Recommended Uniform Screening Panel of the Secretary's Advisory Committee on Heritable Disorders in Newborns and Childrenhttp://www.hrsa.gov/advisorycommittees/mchbadvisory/heritabledisorders/recommendedpanel/uniformscreeningpanel.pdfNewborn Screening AHIC Use Case: Newborn Screening American Health Information Community (AHIC) Detailed Use Casehttp://www.hhs.gov/healthit/usecases/documents/NBSDetailedUseCase.pdf
(Matches) See Also:
(Matches) Comments:
(No Match) Additional Information: ONC and HRSA newborn screening use cases: ONC and HRSA developed a detailed use case related to newborn screening, at http://www.hhs.gov/healthit/usecases/documents/NBSDetailedUseCase.pdf This is a Newborn Screening Use Case document developed by the Office of the National Coordinator for Health Information Technology (ONC) to represent the AHIC priorities and provide context for the national agenda activities, beginning with the selection of harmonized standards by the Healthcare Information Technology Standards Panel (HITSP). AHIC specifically requested that the Newborn Screening Use Case focus on the ability to order and communicate the results from screenings in various clinical domains. [Last accessed 27 September 2012]
(Matches) Implementation Notes:
Scroll To Top