Integrating instruments and the laboratory information system

American Journal of Clinical Pathology

Volumn 105, Issue 4 SUPPL. 1, 1996, Pages

  Chou, David ^a,b  

^a LERNER RESEARCH INSTITUTE   (United States)

^b Cleveland Clinic Foundation ^*

Author keywords

Automation; Instrumentation; Laboratory Information Systems; Robotics

Indexed keywords

AUTOANALYZER; CLINICAL LABORATORY; COMPUTER INTERFACE; INFORMATION SYSTEM; PRIORITY JOURNAL; PRODUCTIVITY; REVIEW; STANDARD;

CLINICAL LABORATORY INFORMATION SYSTEMS; EQUIPMENT DESIGN; HUMANS; SYSTEMS INTEGRATION;

EID: 0029872092     PISSN: 00029173     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Electronic Industries Association. EIA Standard RS-232-C. Washington, DC: Electronic Industries Association, 1969.
2. ASTM E1381-91, specification for low-level protocol to transfer messages between clinical laboratory instruments and computer systems. 1995 Annual Book of ASTM Standards, Volume 14.01. Philadelphia: American Society for Testing and Materials, 1995, pp 287-291.
3. ASTM E1394-91, standard specification for transferring information between clinical instruments and computer systems. 1995 Annual Book of ASTM Standards, Volume 14.01. Philadelphia: American Society for Testing and Materials, 1995, pp 311-325.
4. ASTM E1466-92, standard specification for use of bar codes on specimen tubes in the clinical laboratory. 1995 Annual Book of ASTM Standards, Volume 14.01. Philadelphia: American Society for Testing and Materials, 1995, pp 383-385.
5. ASTM E1238-94, standard specification for transferring clinical laboratory data messages between independent computer systems. 1995 Annual Book of ASTM Standards, Volume 14.01. Philadelphia: American Society for Testing and Materials, 1995, pp 104-182.
6. McDonald CJ, Hammond WE. Standards formats for electronic transfer of data. Ann Intern Med 1989;110:333-335.
7. Health Level Seven: An Application Protocol for Electronic Data Interchange in Health Care Environments, Version 2.1. Ann Arbor MI: HL7, 1991.
8. Application of the medical device GMPS to computerized devices and manufacturing processes: Medical device GMP guidance for FDA investigators, first draft. Rockville, MD: Office of Compliance and Surveillance, Division of Compliance Programs, Food and Drug Administration, Public Health Service, Department of Health and Human Services, 1990.
9. Weilert M, Tilzer LL. Putting bar codes to work for improved patient care. Clin Lab Med 1991;11:227-238.
10. Bar Code Label Specifications Guide, Version 1.0. Indianapolis, IN: Boehringer-Mannheim Diagnostics, 1988.