標(biāo)準(zhǔn)號:ANSI/ASTM E2117-2006
中文標(biāo)準(zhǔn)名稱:醫(yī)療記錄質(zhì)量保證計劃的鑒定和確立用分類指南
英文標(biāo)準(zhǔn)名稱:Classifications Guide for Identification and Establishment of a Quality Assurance Program for Medical Transcription
標(biāo)準(zhǔn)類型:C00
發(fā)布日期:2006/10/24 12:00:00
實施日期:1999/12/31 12:00:00
中國標(biāo)準(zhǔn)分類號:C00
國際標(biāo)準(zhǔn)分類號:03.120.10;11.020
適用范圍: This guide covers the establishment of a quality assurance program for dictation, medical transcription, and related processes. Quality assurance (QA) is necessary to ensure the accuracy of healthcare documentation. Quality documentation protects healthcare providers, facilitates reimbursement, and improves communication among healthcare providers, thus improving the overall quality of patient care. This guide establishes essential and desirable elements for quality healthcare documentation, but it is not purported to be an exhaustive list. The QA personnel for medical transcription should have an understanding of the processes and variables or alternatives involved in the creation of medicolegal documents and an understanding of quality assurance issues as they pertain to medical transcription. Qualified personnel include certified medical transcriptionists (CMTs), quality assurance professionals, or individuals who hold other appropriately related credentials or degrees. The medical transcriptionist (MT) and QA reviewer should establish a cooperative partnership so that the review outcomes are objective and educational to include corrective actions and remedies. Policies should be developed to minimize subjective review, which can lead to forceful implementation of one style at the expense of other reasonable choices. Objective review, including an appeals process, should follow organizational standards that have been agreed upon by the full team of QA personnel, MTs, and management staff.
相關(guān)標(biāo)準(zhǔn)
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
《GB/T 16886.1-2011》醫(yī)療器械生物學(xué)評價 第1部分 風(fēng)險管理過程中的評價與試驗 GB/T 16886.1-2011
《GB/T14233.2-2005》醫(yī)用輸液、輸血、注射器具檢驗方法第二部分:生物實驗方法 GB/T14233.2-2005
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