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Standards and Guidelines for Electronic Medical Record Systems in ...

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Purpose of this document<br />

This document provides guidance <strong>for</strong> EMR system developers <strong>and</strong> implementers, as well as health<br />

facilities <strong>in</strong> Kenya that are contemplat<strong>in</strong>g or currently us<strong>in</strong>g EMR systems to manage patient data.<br />

These guidel<strong>in</strong>es are based on various local <strong>and</strong> <strong>in</strong>ternational reference documents, <strong>in</strong>clud<strong>in</strong>g:<br />

· WHO <strong>and</strong> Kenyan HIV treatment guidel<strong>in</strong>es<br />

· The Kenya HIS strategic plan <strong>and</strong> policy<br />

· International <strong>and</strong> Kenyan health <strong>in</strong><strong>for</strong>matics st<strong>and</strong>ards, <strong>in</strong>clud<strong>in</strong>g those from the<br />

International Organization <strong>for</strong> St<strong>and</strong>ardization (ISO)<br />

· Experience from MOH <strong>and</strong> partners us<strong>in</strong>g EMRs <strong>in</strong> Kenya<br />

· Experience from groups us<strong>in</strong>g EMRs <strong>in</strong> other countries<br />

· Published medical <strong>and</strong> public health literature<br />

Audience<br />

This document is <strong>in</strong>tended <strong>for</strong> the follow<strong>in</strong>g audiences:<br />

· Developers of EMR systems <strong>for</strong> the Kenyan market<br />

· Health facilities or health systems currently us<strong>in</strong>g EMR systems<br />

· Health facilities or health systems consider<strong>in</strong>g procur<strong>in</strong>g, adapt<strong>in</strong>g, or <strong>in</strong>stall<strong>in</strong>g an EMR<br />

system, <strong>in</strong>clud<strong>in</strong>g public, private, mission, <strong>and</strong> NGO-supported facilities<br />

· Health policy makers at all levels<br />

· Donors provid<strong>in</strong>g resources to support the Kenyan health system<br />

Structure of the <strong>St<strong>and</strong>ards</strong> <strong>and</strong> <strong>Guidel<strong>in</strong>es</strong> Document<br />

This <strong>St<strong>and</strong>ards</strong> <strong>and</strong> <strong>Guidel<strong>in</strong>es</strong> <strong>for</strong> <strong>Electronic</strong> <strong>Medical</strong> <strong>Record</strong> <strong>Systems</strong> <strong>in</strong> Kenya document is<br />

divided <strong>in</strong>to 3 sections that provide requirements <strong>and</strong> offer guidance to discrete target audiences<br />

throughout the process of EMR systems development, deployment <strong>and</strong> implementation. The<br />

content <strong>in</strong> each volume is tailored to the underst<strong>and</strong><strong>in</strong>g <strong>and</strong> implementation roles of the identified<br />

target audiences.<br />

Section 1: Build<strong>in</strong>g an <strong>Electronic</strong> <strong>Medical</strong> <strong>Record</strong> System – This section outl<strong>in</strong>es the prerequisite<br />

processes of EMR system development <strong>and</strong> identifies basic functional requirements <strong>for</strong><br />

<strong>St<strong>and</strong>ards</strong> <strong>and</strong> <strong>Guidel<strong>in</strong>es</strong> <strong>for</strong> <strong>Electronic</strong> <strong>Medical</strong> <strong>Record</strong>s <strong>Systems</strong> <strong>in</strong> Kenya 9

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