Accreditation and regulatory implications of electronic health records for laboratory reporting

William Castellani, John H. Sinard, Myra L. Wilkerson, Mark S. Whitsitt, Walter H. Henricks

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The Clinical Laboratory Improvement Amendments of 1988 include strict regulations for reporting content, and it falls on the named director to ensure that this content is available to the caregiver. With the electronic health record serving as the conduit to the end user of the laboratory data, the laboratory generally, and the director specifically, must verify accurate transmission of these content components. An understanding of regulatory and accreditation requirements is essential both to allow the proper discharge of these mandated responsibilities and to enforce the role and authority that the pathologist must have to ensure that these requirements are satisfied by the reporting system. The regulatory requirements will be discussed in the context of the Clinical Laboratory Improvement Amendments of 1988 standards; however, interpretation and expansion on these regulations exist both in Clinical Laboratory Improvement Amendments of 1988 inspection guidelines from the Centers for Medicare and Medicaid Services and in accreditation program requirements. This regulatory expectation both places the laboratory director in a position of risk and provides leverage to ensure meaningful and accurate communication of laboratory information.

Original languageEnglish (US)
Pages (from-to)328-331
Number of pages4
JournalArchives of Pathology and Laboratory Medicine
Volume139
Issue number3
DOIs
StatePublished - Mar 1 2015

Fingerprint

Electronic Health Records
Accreditation
Centers for Medicare and Medicaid Services (U.S.)
Caregivers
Communication
Guidelines

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Medical Laboratory Technology

Cite this

Castellani, William ; Sinard, John H. ; Wilkerson, Myra L. ; Whitsitt, Mark S. ; Henricks, Walter H. / Accreditation and regulatory implications of electronic health records for laboratory reporting. In: Archives of Pathology and Laboratory Medicine. 2015 ; Vol. 139, No. 3. pp. 328-331.
@article{8ae0553c473541ec9774763edf319a34,
title = "Accreditation and regulatory implications of electronic health records for laboratory reporting",
abstract = "The Clinical Laboratory Improvement Amendments of 1988 include strict regulations for reporting content, and it falls on the named director to ensure that this content is available to the caregiver. With the electronic health record serving as the conduit to the end user of the laboratory data, the laboratory generally, and the director specifically, must verify accurate transmission of these content components. An understanding of regulatory and accreditation requirements is essential both to allow the proper discharge of these mandated responsibilities and to enforce the role and authority that the pathologist must have to ensure that these requirements are satisfied by the reporting system. The regulatory requirements will be discussed in the context of the Clinical Laboratory Improvement Amendments of 1988 standards; however, interpretation and expansion on these regulations exist both in Clinical Laboratory Improvement Amendments of 1988 inspection guidelines from the Centers for Medicare and Medicaid Services and in accreditation program requirements. This regulatory expectation both places the laboratory director in a position of risk and provides leverage to ensure meaningful and accurate communication of laboratory information.",
author = "William Castellani and Sinard, {John H.} and Wilkerson, {Myra L.} and Whitsitt, {Mark S.} and Henricks, {Walter H.}",
year = "2015",
month = "3",
day = "1",
doi = "10.5858/arpa.2013-0713-SO",
language = "English (US)",
volume = "139",
pages = "328--331",
journal = "Archives of Pathology and Laboratory Medicine",
issn = "0003-9985",
publisher = "College of American Pathologists",
number = "3",

}

Accreditation and regulatory implications of electronic health records for laboratory reporting. / Castellani, William; Sinard, John H.; Wilkerson, Myra L.; Whitsitt, Mark S.; Henricks, Walter H.

In: Archives of Pathology and Laboratory Medicine, Vol. 139, No. 3, 01.03.2015, p. 328-331.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Accreditation and regulatory implications of electronic health records for laboratory reporting

AU - Castellani, William

AU - Sinard, John H.

AU - Wilkerson, Myra L.

AU - Whitsitt, Mark S.

AU - Henricks, Walter H.

PY - 2015/3/1

Y1 - 2015/3/1

N2 - The Clinical Laboratory Improvement Amendments of 1988 include strict regulations for reporting content, and it falls on the named director to ensure that this content is available to the caregiver. With the electronic health record serving as the conduit to the end user of the laboratory data, the laboratory generally, and the director specifically, must verify accurate transmission of these content components. An understanding of regulatory and accreditation requirements is essential both to allow the proper discharge of these mandated responsibilities and to enforce the role and authority that the pathologist must have to ensure that these requirements are satisfied by the reporting system. The regulatory requirements will be discussed in the context of the Clinical Laboratory Improvement Amendments of 1988 standards; however, interpretation and expansion on these regulations exist both in Clinical Laboratory Improvement Amendments of 1988 inspection guidelines from the Centers for Medicare and Medicaid Services and in accreditation program requirements. This regulatory expectation both places the laboratory director in a position of risk and provides leverage to ensure meaningful and accurate communication of laboratory information.

AB - The Clinical Laboratory Improvement Amendments of 1988 include strict regulations for reporting content, and it falls on the named director to ensure that this content is available to the caregiver. With the electronic health record serving as the conduit to the end user of the laboratory data, the laboratory generally, and the director specifically, must verify accurate transmission of these content components. An understanding of regulatory and accreditation requirements is essential both to allow the proper discharge of these mandated responsibilities and to enforce the role and authority that the pathologist must have to ensure that these requirements are satisfied by the reporting system. The regulatory requirements will be discussed in the context of the Clinical Laboratory Improvement Amendments of 1988 standards; however, interpretation and expansion on these regulations exist both in Clinical Laboratory Improvement Amendments of 1988 inspection guidelines from the Centers for Medicare and Medicaid Services and in accreditation program requirements. This regulatory expectation both places the laboratory director in a position of risk and provides leverage to ensure meaningful and accurate communication of laboratory information.

UR - http://www.scopus.com/inward/record.url?scp=84923924567&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84923924567&partnerID=8YFLogxK

U2 - 10.5858/arpa.2013-0713-SO

DO - 10.5858/arpa.2013-0713-SO

M3 - Article

VL - 139

SP - 328

EP - 331

JO - Archives of Pathology and Laboratory Medicine

JF - Archives of Pathology and Laboratory Medicine

SN - 0003-9985

IS - 3

ER -