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Development of a Document Management System for the Standardization of Clinical Laboratory Documents

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Background: Documentation is very important; a considerable number of documents exist for use in accreditation inspection. However, most laboratories do not effectively manage the processes of documentation, organization, and storage. The purpose of this study was to facilitate the establishment of a strategically effective and sustainably standardized document management system. Methods: A document code formatting system was modified by comparing the document list data received from 3 major university hospitals. In addition, a questionnaire regarding document code standardization was created and sent to 268 institutes to establish document classifications and generate a standard coding scheme. A computerized document management system was developed. Results: Only 32% (8 out of 25 institutes) answered that they were able to identify all of the document types and their numbers. In total, 76% of institutes (19 out of 25) answered that a systematic document management system was necessary. Disorganized document files were systemized by classifying them into 8 major groups according to their characteristics: patient test records (T), test quality control (Q), manuals (M), equipment and environment management (E), statistics (S), division administration (A), department administration (R), and others (X). Conclusions: Our documentation system may serve as a basis for the standardization of documents and the creation of a document management system for all hospital laboratories.

Abstract

Background: Documentation is very important; a considerable number of documents exist for use in accreditation inspection. However, most laboratories do not effectively manage the processes of documentation, organization, and storage. The purpose of this study was to facilitate the establishment of a strategically effective and sustainably standardized document management system. Methods: A document code formatting system was modified by comparing the document list data received from 3 major university hospitals. In addition, a questionnaire regarding document code standardization was created and sent to 268 institutes to establish document classifications and generate a standard coding scheme. A computerized document management system was developed. Results: Only 32% (8 out of 25 institutes) answered that they were able to identify all of the document types and their numbers. In total, 76% of institutes (19 out of 25) answered that a systematic document management system was necessary. Disorganized document files were systemized by classifying them into 8 major groups according to their characteristics: patient test records (T), test quality control (Q), manuals (M), equipment and environment management (E), statistics (S), division administration (A), department administration (R), and others (X). Conclusions: Our documentation system may serve as a basis for the standardization of documents and the creation of a document management system for all hospital laboratories.

참고문헌 (4)

  1. Wagner LR, "The College of American Pathologists, 1946-1996: laboratory standards", Arch Pathol Lab Med, 121, pp.536~541 (1997)
  2. Lee WG, "Clinical pathology laboratory inspection and accreditation in Korea I: development of the system and its trial", Korean J Clin Pathol, 21, pp.86~92 (2001)
  3. 이위교, "임상검사실 표준화 심사 및 신임 인증제도에 관한 연구 Ⅱ: 1차년도 인증심사 분석", Annals of Laboratory Medicine, 23(5), pp.363~369 (2003), 대한진단검사의학회
  4. Clinical and Laboratory Standards Institute, "Laboratory documents: developement and control; Approved guideline. 5th ed, GP2-A5" (2006), Clinical and Laboratory Standards Institute

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