安博维MedInfo电子病历(EMR)模板编辑器使用手册-V3.0

EMR999电子病历操作手册三九集团深圳九明珠信息科技有限公司目录第一章系统的进入与基本维护 (3)1.1系统的进入 (3)1.2系统的退出 (4)1.3修改密码 (4)1.4系统注销 (5)第二章系统维护 (6)2.1.系统参数设置 (6)2.2医疗服务机构维护 (7)2.3.科室资料维护 (8)2.4.医生资料维护 (8)2.5.用户权限配置 (10)2.6.报表管理 (12)第三章病历设计管理 (15)3.1.科室病历配置 (15)3.2.病种模板管理 (21)3.3.病历样式库管理 (22)第四章病人控制台 (24)4.1 病人控制台的进入 (24)4.2 病人控制台的界面分布 (25)4.3 病人资料卡 (25)第五章书写病历 (29)5.1 首页 (29)5.2 病人病历记录的书写 (30)5.3 其他记录 (34)5.4 医疗文书 (35)5.5 病历模板的使用 (36)5.6 打印 (39)第六章病历文件夹 (42)第七章阅改事件 (44)第一章系统的进入与基本维护1.1系统的进入双击桌面快捷图标，即可进入电子病历的登录界面，如（图1-1）所示：（图1-1）（注：本操作说明以外三科工号为1001的王将医生为例）登陆步骤如下：1、录入操作员的工号。

2、按【Enter】键，则系统会自动获取操作员的姓名。

3、输入密码（注：初始密码为医生的工号）。

4、选择自己所对应的科室5、点击【确定】即可进入该主界面（由于进入系统的过程中需要读取数据，所以需要等待几秒钟的时间）。

如（图1-2）所示：注：登陆界面之后，系统默认进入的主界面是电子病历的病人控制台界面。

（图1-2）1.2系统的退出若需退出系统，则点击左下角【开始】—【关闭系统】(如图1-3)，即可退出系统。

（图1-3）1.3修改密码若操作员需要修改密码，则需点击【开始】—【用户密码维护】（如图1-3），即可进入修改密码界面，如（图1-4）所示：（图1-4）修改密码步骤如下：1、录入操作员的旧密码（初始密码为操作员工号）2、录入新密码3、录入确认密码：与新密码相同4、点击【确定】按钮即可修改密码成功。

电子病历系统用户使用手册（V3.0）北京安博维科技发展有限公司版权所有不得复制目录约定 (3)名词术语 (3)一、系统简介 (3)二、登陆系统 (3)三、登陆住院医生工作站 (4)3.1菜单介绍 (5)3.2查找患者 (8)四、书写病历 (9)4.1 工具栏 (9)4.2 模板选择 (13)4.3 写病历 (15)约定【】：用‘【】‘引起来的内容是相关按钮或者是比较重要的文字。

名词术语一、系统简介本系统是基于国产操作平台下开发的医疗信息系统，适用于目前中国国情。

本系统的一个最大的亮点就是引入了安博维公司自主开发的【电子病历编辑器】，应用面向医疗的语义识别技术及面向医疗的知识库归集和应用技术，使病历的编辑走上了电子化的道路，使以往全凭医生经验决定病历质量，以及病历书写中用词不统一，不规范，病历的查询、统计不方便甚至无法进行查询、统计等情况得到了极大的改善，使得病历的编辑真正的做到了电子化、规范化。

系统包括【患者管理】和【病历编辑】两个部分，由【患者管理】模块确定一个病人后进入【病历编辑】模块书写该患者的病历。

二、登陆系统双击桌面电子病历快捷方式，弹出如图2.1所示登陆界面，输入医生工号、密码点击【登陆】按钮进入电子病历系统，界面如图2.2所示。

登陆问题提示：1、正确录入工号和密码后系统提示：连接服务器端失败，请检查本机网络是否已连接，或者服务器端未正常提供登陆服务，请联系管理员。

2、正确录入工号和密码后系统提示：该工号已登陆，此时表明其他人已使用您的工号密码登陆系统，有权限修改您的病历不留下痕迹，请妥善保管密码。

您将无法登陆系统，请联系管理员。

（图2.1）电子病历登陆界面图2.2电子病历主界面三、登陆住院医生工作站 双击图标进入住院医生工作站选择患者界面，如（图3.1）所示。

包括查询、添加、删除三项功能，界面如（图3.1）所示。

（图3.1） 选择患者界面3.1菜单介绍(图 3.2)业务菜单 (图3.3)工具菜单左上角的菜单栏上有【业务】、【工具】、【帮助】三个菜单，其中，【业务】中有“病历编写”功能；使用方法：在选择患者界面（图3.1）选择某个病人后，再点击“业务”中的“病历编写”直接进入该病人的病历书写界面，如（图4.1）所示。

文档编号：电子病历编辑器—0001—TEMPL电子病历编辑器模板制作用户手册（版本3.0.0）河南省新星科技有限公司二OO 九年目录1.模板制作说明 (5)1.1 操作环境 (5)1.2 总体描述 (5)1.3 重要提示 (5)2.编辑器的书写功能及符号说明 (6)2.1 编辑器“工具栏”有哪些功能？ (6)2.2 模板中的名称定义 (6)2.3 模板中引入元素的意义 (7)2.4 保留标题 (7)2.5 非保留标题 (7)2.6 行选、单项选择、多项选择、有无选择 (7)2.7 关键词 (10)2.8 录入提示 (10)2.9 宏 (10)2.10 使用图形 (10)2.11 使用表格 (13)2.11.1 创建表格 (13)2.11.2 表格操作 (13)3.模板元素制作详细说明 (14)3.1 模板制作菜单介绍 (14)3.2 从外部获取数据来设计模板 (14)3.3 常用排版功能 (14)3.4 系统注册的宏和可替换的项目 (15)3.5 单选设置 (16)3.5.1 属性设置 (17)3.5.2 条目设置 (18)3.6 多选设置 (20)3.7 有无选择设置 (21)3.8 录入提示 (21)3.9 格式化录入 (24)3.9.1 日期型的设置 (24)3.9.2 数值型的设置 (24)3.10 关键词 (25)3.11 保留标题 (26)3.11.1 层次序号 (27)3.11.2 内容 (27)3.12 非保留标题 (27)3.13 图像 (28)3.14 横线 (30)3.15 分页符 (30)3.16 分号、页数、日期时间 (31)3.17 月经史公式 (31)3.18 删除元素 (31)3.19 元素静态属性 (31)4.表格制作详细说明 (32)4.1 新建表格 (32)4.1.1 创建表格 (32)4.1.2 表格操作 (32)4.2 表格应用 (33)4.2.1 无边框表格 (33)4.2.2 表格属性 (33)4.2.3 单元格属性 (35)4.2.4 有框表格 (35)5.段落排版 (36)5.1 段落排版包含的功能 (36)5.2 段落连接符设置 (37)5.3 段落属性设置 (37)6.关键词制作要求 (38)1.模板制作说明1.1 操作环境电子病历 V3.0 版本的模板制作直接采用编辑器就可处理，不需要安装特殊的软件。

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用户手册Visante™ OCT■Model 1000Visante™ OCT 用户手册修订版控制部件号修订版软件版本说明发布日期60899-6 A 1.0Visante™ OCT 用户手册（中文）2006.01版权所有© Carl Zeiss Meditec Inc. 保留所有权利。

商标Visante™ 是 Carl Zeiss Meditec Inc. 的商标。

本文档中所有其它商标均为其各自所有者的财产。

目录目录(1)简介...................................................................................................1-1•使用说明..................................................................................................1-1•本用户手册的目的.................................................................................1-1• Visante OCT 技术......................................................................................1-2• Visante OCT 系统硬件.............................................................................1-3•警告：用户对软件或硬件的更改.......................................................1-4•仪器安装.................................................................................................1-4•避免损坏的窍门.....................................................................................1-4•嵌入的 Windows 许可证........................................................................1-5•产品遵从性.............................................................................................1-5•产品安全性.............................................................................................1-5•电磁兼容性 (EMC)...................................................................................1-6•附属设备.................................................................................................1-9•符号和标签............................................................................................1-10•仪器处置................................................................................................1-12•安装和使用可选的电源台...................................................................1-13 (2)操作概述...........................................................................................2-1•章节概述.................................................................................................2-1•启动和登录系统.....................................................................................2-1•初始系统设置.........................................................................................2-4•状态栏信息.............................................................................................2-8•操作模式和窗口.....................................................................................2-9•标题栏、菜单和工具栏......................................................................2-10•性能验证检查........................................................................................2-13•关闭系统电源........................................................................................2-16 (3)获取扫描...........................................................................................3-1•章节概述.................................................................................................3-1•准备患者.................................................................................................3-1•确定患者.................................................................................................3-2•选择检查程序.........................................................................................3-6•校准眼睛并获取扫描............................................................................3-7•查看扫描：保存或重试......................................................................3-11•获取之前的调整（可选）...................................................................3-15 (4)检查程序和扫描类型.......................................................................4-1•章节概述.................................................................................................4-1•检查程序.................................................................................................4-1• Exam Protocols 对话框............................................................................4-3•扫描类型.................................................................................................4-7目录(5)扫描分析...........................................................................................5-1•章节概述.................................................................................................5-1•访问分析.................................................................................................5-1• Analysis 窗口............................................................................................5-2•工具选项板.............................................................................................5-6•眼角膜厚度分析...................................................................................5-10•演示文稿导出........................................................................................5-13•打印.........................................................................................................5-15•示例报告................................................................................................5-15 (6)数据管理...........................................................................................6-1•章节概述.................................................................................................6-1• admin 用户...............................................................................................6-1•创建机构名称和徽标............................................................................6-1• Equipment（设备）：创建 Station Name（站名）............................6-3•人员登记.................................................................................................6-3•记录搜索.................................................................................................6-6•创建、编辑和删除患者记录.............................................................6-10•合并患者记录........................................................................................6-14•将患者记录分类....................................................................................6-16 (7)存档和检索.......................................................................................7-1•章节概述..................................................................................................7-1•患者数据库..............................................................................................7-1•数据维护要求.........................................................................................7-2•清除检查数据.........................................................................................7-2•存档建议.................................................................................................7-4•存档管理.................................................................................................7-5•手动存档.................................................................................................7-9•检索检查数据........................................................................................7-10 (8)例行维护...........................................................................................8-1•章节概述.................................................................................................8-1•更换保险丝.............................................................................................8-1•处理错误消息.........................................................................................8-4•硬盘碎片整理.........................................................................................8-5•例行清洁.................................................................................................8-5•用户更换部件列表................................................................................8-6(9)规格..................................................................................................9-1(10)法律声明..........................................................................................10-1•有限担保...............................................................................................10-1•服务合同...............................................................................................10-2•软件版权...............................................................................................10-2•软件许可证协议...................................................................................10-2目录附录 (A) 联网指导....................................................................................A-1•注意..........................................................................................................A-1•网络功能.................................................................................................A-1•警告：Internet 连接的风险...................................................................A-1•禁止的活动.............................................................................................A-2•不支持的网络活动................................................................................A-2•网络文件服务器最低要求....................................................................A-2•网络文件服务器建议............................................................................A-2•使用网络文件服务器............................................................................A-3•直接导出至个人计算机的配置...........................................................A-5附录 (B) 网络存储设备的配置.................................................................B-1•简介..........................................................................................................B-1• NAS 设备安全警告.................................................................................B-1• NAS 设备要求..........................................................................................B-1• NAS 设备建议..........................................................................................B-2•安装和配置 NAS 设备............................................................................B-2• NAS 设备清洁..........................................................................................B-5附录 (C) 打印机配置................................................................................C-1•简介..........................................................................................................C-1•打印机安全警告.....................................................................................C-1•认可的打印机.........................................................................................C-1•安装概述.................................................................................................C-2•点对点的无线配置................................................................................C-2•网络配置.................................................................................................C-6• USB 配置..................................................................................................C-7附录 (D) 测量数据....................................................................................D-1• Visante OCT 的精确性、重复性和再现性............................................D-1•眼角膜厚度数据....................................................................................D-2• LASIK 角膜瓣和基质数据.....................................................................D-4索引...................................................................................................I-1目录简介(1) 简介ZEISS Visante™ OCT Model 1000 (Visante™ OCT) 能够对眼前段进行详细的 in vivo 检查，而无需接触眼睛。

12HCV BLOT 3.0使用说明书MAD 0013-CHN-4 产品型号：18人份/盒―11139-018 36人份/盒―11139-0361. 通用名称：丙型肝炎病毒 (HCV) 抗体检测试剂 盒 (免疫印迹法)2. 英文名称：HCV BLOT3.018人份/盒，36人份/盒。

本产品用于定性检测人血清或血浆中的丙型肝炎病毒抗体。

安倍生物医学亚太私人有限公司 (MP Biomedicals Asia Pacific) 生产的丙型肝炎病毒(HCV) 抗体检测试剂盒 (HCV BLOT 3.0) 是对人血清或血浆中的丙型肝炎病毒抗体进行体外检测的定性酶免疫测定方法。

该试剂盒做为特异性更高的补充确认试验，用于对筛查方法 (如:酶联免疫吸附试验) 检测重复呈阳性的样本进行确认。

硝酸纤维素膜条上含有来自HCV 基因组中核抗原、NS3、NS4和NS5区的重组蛋白条带。

重组蛋白以谷胱甘肽转移酶融合表达，因此膜上也包含一条谷胱甘肽转移酶质控带，用以提示个别样本对谷胱甘肽转移酶的反应性。

膜上还包含一条IgG 和一条抗-IgG 质控带。

膜条与稀释的血清或血浆样本一起孵育。

如果样本中存在HCV 的特异性抗体，则2～8°C 储存，有效期24个月。

1.在不使用时，应将HCV BLOT 3.0试剂盒及其组分储存在2-8˚C 环境中。

2. 在失效期前，储存在2-8˚C 环境中的试剂组份和试剂膜条是稳定的，试剂不能冰冻。

A. 试剂膜条• 避免试剂膜条不必要地暴露于光线下。

B. 试剂• 用原装的瓶子盛装试剂，盖紧盖子储存。

• 在冷藏的情况下取用试剂，用完后尽快将试剂放回到2-8˚C 储存。

• 底物液在2-8˚C 储存时，可能会有沉淀形成，但不影响试剂盒的正常使用。

注意：避免底物液不必要地暴露于光线下。

生产日期及失效日期见标签。

1. 去离子水或蒸馏水。

2. 一次性手套。

3. 摇床(每分钟12-16次，摆动角度5-10度，以均匀地清洗膜条)或全自动蛋白免疫印迹仪(推荐使用型号AutoBlot System 20)。

目录MedWin 概述 (1)MedWin 集成开发环境的特点 (1)MedWin 对系统的要求 (2)快速入门适用范围 (2)内容安排 (2)一、安装MedWin (3)二、设置MedWin (6)三、MedWin 开发入门 (11)四、MedWin 调试实例 (18)五、MedWin 断点功能 (24)六、MedWin 菜单命令 (26)七、MedWin 右键弹出式菜单 (2)八、MedWin 的表达式 (4)MedWin 概述MedWin 是万利电子有限公司Insight® 系列仿真开发系统的高性能集成开发环境。

集编辑、编译/ 汇编、在线及模拟调试为一体，VC 风格的用户界面，内嵌自主版权的宏汇编器和连接器，并完全支持Franklin/Keil C 扩展OMF 格式文件，支持所有变量类型及表达式，配合Insight® 系列仿真器，是您开发80C51 系列单片机的理想开发工具。

图1:MedWin 集成开发环境窗口界面MedWin 集成开发环境的特点1. 完美的Windows 版集成开发环境MedWin2. 内嵌自主版权的宏汇编器A51 和连接器L51,并支持Keil/Franklin 编译、连接工具3. 具有分别独立控制项目文件的工程项目管理器4. 在工程项目管理下，实现多模块和混合语言编程调试5. VC 风格的窗口停驻、窗口切分和工作簿模式界面6. 在线编辑、编译/ 汇编、连接下载运行和错误关联定位7. 符合编程语言语法的彩色文本显示8. 完全的表达式分析，支持所有数据类型变量的观察9. 无须点击的感应式鼠标提示功能10. 外部功能部件编程向导11. 不限制打开数据区观察窗口的数目12. 调试状态下用户程序自动重装功能13. 提供真实的软件模拟仿真开发环境MedWin 对系统的要求为使MedWin 集成开发环境能够正常地运行，您必须提供以下软硬件环境：1. 586 以上的PC 及兼容机2. 100M 以上的剩余硬盘空间3. 分辨率为800x600 以上的显示器4. 具有SPP 功能的打印机接口5. 中文或英文Windows/95/98，Windows/Me，Windows 2000/NT,Windows XP6. 尽量减少DOS 自动批处理中关于系统路径及环境变量的设置，或删除DOS 下的批处理文件Autoexec.bat 文件快速入门适用范围1. MedWin 集成开发环境V2.3x2. 标准80C51 系列仿真器SE-52P,ME-52A,ME52P,AE-52E3. 标准扩展80C51 系列仿真器ME-52H/SE-52H,ME-32004. 专用80C51 系列仿真器ME-12055. PHILIPS 51LPC 系列仿真器SE-764内容安排本书从以下八部分，介绍MedWin 集成开发环境的快速入门方法：一、安装MedWin二、设置MedWin三、Med Win 开发入门四、MedWin 调试实例五、MedWin 断点功能六、MedWin 菜单命令七、MedWin 右键弹出式菜单八、MedWin 的表达式一、安装MedWin本章分三节介绍怎样获得MedWin 集成开发环境安装程序、MedWin 集成开发环境对系统的要求和安装MedWin 集成开发环境步骤。

USER GUIDE LISTINGMSI Contact ListNOTE: See Other Resources on Page 2APPOINTMENT SCHEDULINGAppointment SchedulingSetup/Maintain Master Appointment Scheduler Verification of Benefits/Precerts BASIC CONCEPTSHelp TextKeyboard StandardsOperational Assistant/Commands Standard Function Keys & Options BATCH ENTRYAnesthesia Charge Entry Batch Charge EntryBatch Charge Entry Reverse Rekey Charge Function Bulk Payment Entry Discrepancy Report HPSA PaymentsNSF/Stop Payment/Stale Checks Payment Posting Tips Regular Payment EntrySNF/Home Health/Hospice Billing – Medicare & LA Medicaid System Charge Balance AdjustmentTo Work Credit Open Items and Unapplied Pymt-Adj CLOSING & SPECIAL FUNCTIONSArchive Account InstructionsF10 Restricted Commands Work With Objects Locks(Contact Software Support ) F10 Special CommandsiSeries Initialize Tape-Entire System Backup MSI iSeries EOD/EOM/EOY Closing To Create a Condition/Rule COLLECTION TASK MODULECollection/Task Module ELECTRONIC CLAIMSEMC ERA Carrier Parameters EMC Errors/Electronic Claims ListEmdeon Vision for Claim ManagementERA Receive/Prepare/Create Unprocessed Batch Download ERA 835 File via PaySpan MREP Split ERATo Complete EDI (EMC, ERA & EFT) Setup for BCBS LA, LA Medicare, LA Medicaid & Clearinghouse To Reset LA Medicare EMC/ERA Access FRONT DESKCo-Pay Feature Front DeskFront Desk Charge Ticket List F15 Authorization RecordInsurance Card – Drivers License Scanning Instructions List Incomplete Masters (Orphaned Insurance Card Scans) ReportOB Billing GridUnproc/Proc List Transactions Reports Vaccines & Administration HISTORY & DEMOGRAPHICSAdd/Change/Delete Insurance Information Patient HistoryINDUSTRIAL MEDICINE MODULEIndustrial Medicine INSURANCE/LABELSGenerate LabelsMedicare Policy # / MBIMedicare – Replacement/Advantage (MCRR) Products IdentificationSelected Insurance Re-files: Adjustments and Void Claims System Deletion of Claims Outstanding 0-Cr Bal Chgs System Refiles/Generate Insurance EMC Preparation AndSubmittalTo Work “Secondary Claims Held Over ## Days” ReportInstructionsMEDEHR/MEDSUITESee MEDEHR Resources section of the MEDTRON website(https:///).MEDICAID GUIDESLA Medicaid Community Care Monthly Capitation Fee (CAP) LA Medicaid Community Care Referral Exempt LA Medicaid Community Care VA MedallionMISC TRAININGAccounts Receivable Analysis ToolsAdvance Beneficiary Notice (ABN) and Medical Necessity (MN) Audit LogAvoid Low CollectionsClaim Information Reference Number CMS Web Based Training CoursesEnable User Sign-on (Contact Software Support ) External EHR Interface with MPMS Global GuidelinesHow To Setup A Join Me SessionInstalling Insurance Card Scanning Software Ver 3-1 Inscards 3.1 Interface/Download Programs PQRS PrefaceTo Add-Delete Users to-from iSeries – iSeries Clients Only(Contact Software Support )To Add Transfer Data Function for Office 2007 iSeries Access forWindowsTo Change MEDPM (iSeries) Default Color Scheme To Clear Cache in Firefox BrowserTo Convert iSeries Reports using the iSeries Navigator To Create an Excel Spreadsheet From iSeries Data (SQLCommand)To Obtain Tax or Employer ID Numbers and CP575 Letters PATIENT INFORMATIONAccount Status Codes Combine Patient Accounts Online Eligibility RequestsPatient Demographics Add & Change Search and Scan OptionsSystem Transfer To Patient Responsibility Workers’ Comp Accounts and Claims RECOMMENDATIONSComments (Common Abbreviations) REPORTSBell Curve ReportsCharge Application Report EDC ReportList/Delete Unused Insurance Codes List Patients W/ Specific InsuranceRelative Value Units (RVU) Productivity Report Reports OverviewReports For Work Prior To EOM Close Transaction History Report SETUP & SUPPORTCMS 1500/ANSI Field Completion Situational Field Comments Collector CodesDMERC Claims SetupInsurance (Claim) Directives: Electronic & Split/Break to New Claim Medical NecessityNational Correct Coding Initiative (NCCI) NPI Registry Search Search FeatureSetup/Maintain ERA Comments/Messages Setup/Maintain Insurance Company Master Setup/Maintain Letters/Labels Setup/Maintain Location MasterSetup/Maintain Referral Source Master Setup/Maintain Setup & Support Files Setup/Maintain Specific Action Master Setup/Maintain Transaction Master Setup Online EligibilityTo Obtain/Edit a National Provider Identifier (NPI) TPL UpdatesSTATEMENT/LETTERSGenerate Letters StatementsFinance-Statement ChargesTo Print Patient Demographics for Labcorp Order FormVFC Medicaid ImmunizationsThe above User Guides are linked to the most current published version. All User Guides are updated as new information is made available and therefore may be in the process of being revised. Check back often to ensure most recent version is being used. If a User Guide presents in black with no link, this User Guide is in the process of being created.If a User Guide presents in black, the guide is in the process of being updated/revised, please contact Support Dept via email: or phone (985) 234-0599 to request us to expedite its completion.A User ID and Password are required to access all of the User Guides. If the further assistance or a User ID and password is needed, please contact our Support Dept via email: or phone (985) 234-0599.MEDTRON Software Intelligence – All rights reserved.OTHER RESOURCES MSI Contact List USER FORMS:MDS-MSI Client User Access Agreement - Security PolicyMDS/MSI Menu OptionsE&M RESOURCES:E&M Information PacketMEDICARE RESOURCES:CMS RVU and Payment Policy IndicatorsCMS RVU List (per CMS Website)PRACTICE FORMS:Demographics Intake Form – Web versionDemographics Intake Form – iSeries versionOTHER RESOURCES:Acronym List/Glossary of Healthcare TermsCarrier Precertification/Prior Authorization (PA) ListingCMS Medicare Fraud & Abuse – Prevention, Detection, and Reporting Fact Sheet (False Claims Act)MSI 2018 CPT-HCPCS Code Resource GridMSI ICD-10-CM Code Resource GridLCD/Medical Policy ListingsTherapy Billing GridModifier Staff Training Presentation。

P/N 12195-000 3/04Medi-Temp III FW601 Blood/Fluid WarmerOperator’s Manual/Service ManualTable of ContentsSec Topic Page1.0Indications for Use (1)2.0Product Description (2)3.0Instructions for Use (4)4.0Safety Systems (7)5.0Cleaning (7)6.0Functional Check/Safety Inspection (8)7.0Troubleshooting (10)8.0Technical Specifications (11)Before you begin . . .ImportantBefore using the Medi-Temp III FW601 Blood/FluidWarmer, please read and understand this Operator’sManual and the SAFETY PRECAUTIONS prior to use.If you have any questions, please contact your localdealer for assistance.WarrantyThe Medi-Temp III FW601 Blood/Fluid Warmer iswarranted free of defects in material and workmanshipfor a period of one (1) year.The Disposable Warming Sets are warranted free ofdefects in material and workmanship for a singleapplication.A copy of the warranty is available upon request.Gaymar disclaims all implied warranties including, butnot limited to, the implied warranties ofmerchantability and of fitness for a particular purpose.MET I N/P n o i t p i r c s eD1000-83111r e v o cp o T2230-59609e s u F3000-63111r e v o ct h g i R4000-93419we r c s l e v i wS5000-41680pma l ce l o pV I6520-97419we r c sp a ct e k c o S7000-49121l e b a l s g n i t a R8000-24111r e v i e c e rp a r te l b b u B9711-47009t emmo r gn o i t a l u s n I01720-67009g n i h s u b f e i l e rn i a r t so c y eHMET I N/P n o i t p i r c s eD11000-66211d r o cr ewo P21000-98211l e b a l p a r te l b b u B31000-02311l e b a l t o de u l B41000-19730p a r t se s oH51000-73111r e v o ct f e L61000-88221l e b a l t n o r F71000-39211l e b a l e s u F81710-91519)nwo h s t o n4y t qr e v o cp o t r o F(we r c Sc i t s a l P91400-82209)nwo h s t o n(p i l ce l b aC02000-59121)nwo h s t o n(l a u n ams,r o t a r e pO13Figure 11—Replacement Parts1.0Indications for UseThis device is intended to aid in the prevention of inadvertent hypothermia during administration of blood, blood products, and other fluids.1.1Safety Precautions112.p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R .p m e T .s i s e R )C °()s m h o ()C °()s m h o ()C °()s m h o ()C °()s m h o ()C °()s m h o ()C °()s m h o ()C °()s m h o ()C °()s m h o ()C °()s m h o (53174183003114251144320174019051183552765846951851.5356411.8359211.1484111.4491011.747091.058081.352271.656461.959752.5395412.8309212.1434112.4451012.743092.055082.358172.654462.957753.5335413.8358213.1493113.4411013.740093.052083.356173.651463.955754.5374414.8397214.1443114.4470014.746984.059974.354174.659364.953755.5314415.8347215.1492115.4430015.743985.056975.351175.657365.951756.5353416.8396216.1452116.449996.749886.053976.359076.654366.959657.5392417.8346217.1402117.445997.746887.050977.356077.652367.957658.5332418.8395218.1461118.441998.742888.057878.353078.650368.955659.5371419.8345219.1421119.448899.749789.054879.351079.657269.953656311419394212470115448984678151874589675526061651.6350411.9344211.2430111.540891.842781.158771.455961.753262.6300412.9393212.2489012.546792.849682.155772.453962.750263.6349313.9343213.2449013.542793.846683.152773.450963.758164.6388314.9392214.2409014.548694.842684.159674.458864.756165.6338315.9342215.2458015.545695.849585.157675.455865.754166.6377316.9391216.2418016.541696.846586.154676.453866.751167.6317317.9341217.2477017.547597.843587.151677.450867.759068.6366318.9390218.2437018.544598.849488.158578.458768.757069.6306319.9340219.2486019.540599.846489.155579.455769.7550673553104991134460164649943482525755376853061.7394311.0459111.3406011.642491.940481.258471.550761.850062.7344312.0409112.3465012.649392.946382.257472.558662.858953.7383313.0458113.3425013.645393.943383.254473.555663.856954.7333314.0408114.3474014.642394.940384.251474.553664.854955.7372315.0467115.3434015.648295.947285.258375.550665.852956.7322316.0417116.3493016.644296.944286.255376.558566.850957.7361317.0466117.3453017.641297.941287.253377.555567.857858.7311318.0416118.3413018.647198.947188.250378.553568.855859.7360319.0475119.3472019.644199.944189.257279.551569.85385Figure 10—Resistance temperature chart (Gaymar FWT1 Temperature Sensor)Figure 1—FW601 Blood/Fluid WarmerWhen this occurs, an LED temperature display located on the front panel will display the actual fluid temperature or the setpoint temperature in °C.The setpoint is user selectable from 38.0°C–41.0°C in 1.0°C increments, by use of the SETPOINT switch on the front panel. Also located on the front of the unit is a slot for insertion of the disposable warming set. On the right side of the unit, just below the IV pole clamp,is a receiver for the disposable warming set’s bubble trap.2.2Disposable setsThe Medi-Temp III FW601 Blood/Fluid warming unit is designed to be used only with Gaymar seriesdisposable warming sets. The following warming sets (figure 2) are designed for use up to 300 mm Hg pressure. Contact your local dealer for more information.2.0Product DescriptionThe Medi-Temp III FW601 Blood/Fluid Warmer is a dry-heat device designed for safe and rapid warming of blood, blood products and other fluids through the utilization of disposable blood/fluid warming sets. The warmer does not provide fluid flow rate control.Blood, blood products and other fluids normallyrefrigerated, can be rapidly warmed to user selectable temperatures of between 38.0°C–41.0°Cat flow rates up to 300 ml/min. Room temperature fluids can be warmed at flow rates up to 500 ml/min.The disposable Blood/Fluid warming sets are available in Standard, Standard with Extensions, Pediatric, and High Flow models.2.1WarmerThe warming unit is designed to be IV pole mounted. The device has no on/off switch.Connection to the AC supply is indicated by a green STANDBY mode indicator, located on the front panel. In STANDBY mode, no power can be applied to the heater. To begin normal operation,the RUN/STANDBY button must be pressed.2switch IV pole clampbutton Cassette slotBubble trap receiver STANDBY indicatorREMOVE FROM USE indicator118.0 Technical SpecificationsFigure 9—SpecificationsFigure 3—Warming set and bubble trapAet t e s s a C Br o t a n i m i l E r i A l a u n a M )e v l a V f e i l e R (C p a r T e l b b u B D pm a l C E )t n e i t a P o t (r e u L e l a M Fre u L e l a m e F )e c r u o S d i u l F /d o o l B o t (Gli a R e d i u G e u l B 3Figure 2—Gaymar series warming setsno i t p i r c s e D go l a t a C d r a d n a t S r e b m u N go l a t a C s s e l d e e N re b m u N n o i t a c i l p p A g n i m i r P e m u l o V dr a d n a t S E C 04352D —n i m /l m 051—O V K l m 93n o i s n e t x e "84h t i w d r a d n a t S E C 01352D LN 01352D n i m /l m 051—O V K l m 84n o i s n e t x e "06h t i w d r a d n a t S EC 51352D —n i m /l m 051—O V K l m 05n o i s n e t x e "03h t i w c i r t a i d e P —L N 02352D n i m /l m 001—O V K l m 03n o i s n e t x e "84h t i w w o l F h g i HE C 03352D LN 03352D n i m /l m 005—001l m 97no i t a g i r r I 0753R R I —xa m n i m /l m 005AN ne p o s n i e v p e e k o t d e r i u q e r w o lf m u m i n i m =O V K 10mo t p m y S se s u a c e l b a b o r P no i t c a d e r i u q e R s e h s a l f y l e t a n r e t l a y a l p s i D d i u l f e h t d n a O L er u t a r e p m e t s a h e r u t a r e p m e t d i u l f t u p t u O .C °43d e h c a e r t e y t o n .s e t u n i m 2r o f n u r o t t i n u w o l l A ,e s a e r c n i t o n s e o d e r u t a r e p m e t f I .e c i v r e s t s e u q e r d n a e s u m o r f e v o m e r s e h s a l f y l e t a n r e t l a y a l p s iD d i u l f e h t d n a I H er u t a r e p m e t s a h c u s ,e c n a b r u t s i d t n e i s n a r t A ,e t a r w o l f n i e g n a h c n e d d u s a e r u t a r e p m e t d i u l f e h t d e s u a c s a h .C °34e v o b a e s i r o t l a m r o n e m u s e r l l i w t i n u —E N O N s p o r d e r u t a r e p m e t n e h w n o i t a r e p o .C °34w o l e b d n a s d n u o s m r a l a e l b i d u A e h t d n a O L s e h s a l f y a l p s i d e r u t a r e p m e t d i u l f s a h e r u t a r e p m e t d i u l f t u p t u O .C °43w o l e b d e p p o r d .s e t u n i m 2r o f n u r o t t i n u w o l l A ,e s a e r c n i t o n s e o d e r u t a r e p m e t f I .e c i v r e s t s e u q e r d n a e s u m o r f e v o m e r d n a s d n u o s m r a l a e l b i d u A _A F s e t a c i d n i y a l p s i d e v a h s c i t s o n g a i d c i n o r t c e l e e h T .m e l b o r p l a n r e t n i n a d e t c e t e d .e c i v r e s t s e u q e r d n a e s u m o r f e v o m e R s d n u o s m r a l a e l b i d u A w o l l e y d n a y l s u o u n i t n o c ti l s i t h g i l U F R e v a h s e r u t a r e p m e t d i u l f l a n r e t n I p u k c a b d n a C °54d e d e e c x e .d e t a v i t c a n e e b s a h m e t s y s d n a ,e t t e s s a c d r a c s i d ,w o l f d i u l f p o t S .e c i v r e s t s e u q e r o t t l u c if f i d s i e t t e s s a C ti n u g n i m r a w o t n i t r e s n i o t r o i r p d e m i r p e t t e s s a C .n o i t r e s n i .t r e s n i e r d n a e t t e s s a c n i a r D y a m t i n u g n i m r a w f o t o l s e d i s n I e h t n o n o i t a n i m a t n o c e v a h .s e t a l p r e t a e h g n i w o l l o f y b t i n u f o e d i s n i n a e l C )0.5n o i t c e s (e r u d e c o r p g n i n a e l c ot t l u c i f f i d s i e t t e s s a C ti n u g n i m r a w m o r f e v o m e r .d e z i r u s s e r p l l i t s s i e t t e s s a C t u p t u o n e p o d n a p m a l c t u p n i e s o l C .n i a r d o t d i u l f w o l l A .p m a l c 7.0 TroubleshootingFigure 8—Troubleshooting chartFigure 4—Inserting the cassette3.0Instructions for Use(see figures 3—5)•Attach warming unit to IV pole and secure with clamp on side of unit.•Plug the power cord into a properly grounded outlet.•Remove the warming set from it’s sterile packagingNOTE: The warming set is designed so it can be inserted into the warmer in only oneorientation. Orient the cassette so that the blue guide rail is inserted into the bottom of the warming unit.n Grasp each rail (see figure 4). Insert the front endof the cassette into the front of the warming unit,with the blue guide rail facing down. Align the rails to each of the slotted openings.Move hands to the rail protrusions and continue to insert the cassette until the clear guide rail is almost flush with the front of the unit. (The blueguide rail will protrude slightly for easy removal.)4Figure 5—Setup instructions91.Insert any D25000 series Warming cassette into the warming unit. Using hot tap water (46°C–50°C), flow hot water through the cassette for approximately 1-3 minutes.2.Connect AC power to the warming unit. Thedevice should immediately sound the audible alarm and light the RFU light.6.4Ground Resistance CheckUse a current leakage/ground resistance tester tomeasure the resistance between the ground pin on the power plug and the mounting screw on the IV pole clamp.The resistance value should not exceed 0.50 ohms.Figure 7—Test setup6.5Current Leakage TestMeasure the maximum earth leakage current (ground open). Measure all combinations of line polarity with neutral open and closed. Values should not exceed the following;Neutral closed....................150µA Neutral open ......................200µAo Close warming set input clamp. Remove theprotector from the female luer of the warming set and connect it to the male luer on the IVadministration set. Remove the protector from the male luer of the warming set. To minimize temperature drop and priming volume, remove unnecessary lead extensions at this time.p Invert the bubble trap.q Open warming set input clamp. Allow fluid toprime the set. When the bubble trap fills to approximately (2/3) full, close the output clamp.r Re-invert the bubble trap and place it into thebubble trap receiver on the side of the warming unit.s Press the RUN/STANDBY switch on thefront of the unit.Upon successful completion of self-diagnostics,the display will flash the setpoint for approximately 3 seconds, then begin warming the fluid to the selected temperature.The setpoint most recently used is retained in memory, even after power is removed.SETPOINT This will cause the setpoint to be displayed and flash for approximately 3 seconds. While thedisplay is flashing the setpoint, the user may select any setpoint between 38.0°C and 41.0°C in 1.0°C increments by repeatedly pressing the SETPOINT switch.NOTE: holding down the SETPOINT switch indefinitely will not increment the setpoint.After the selection has been made, the display will continue to flash this setpoint for approximately 3 seconds, then revert to displaying the actual fluid temperature. The setpoint can be checked at any time during the procedure by momentarily pressing the SETPOINT switch.t If required, connect an extension for patientconnection.u Purge air from remaining length of tubing byopening output clamp and allowing fluid to flow.586.0 Functional Check and Safety InspectionTo assure optimum performance, dependability, and safety, the following should be performed every twelve months or as specified in the facility’s preventive maintenance program.Equipment or tools requiredAny Gaymar D25340 series Blood/Fluid Warming SetTemperature measurement device: •Gaymar D25340 Blood/Fluid WarmingSet; and •Temperature sensor (Gaymar catalogFWT1) and an ohmmeter (accuracy,1.5% of reading; maximum excitation current of 100uA) and the resistance temperature chart. See figure 10 (p. 12). or•Any Gaymar D25000 seriesBlood/Fluid Warming Set; and •Waterproof temperature sensor/meter with an accuracy of ± 0.3%across the range of 30°C to 60°C and a thermal time constant of 2seconds or faster.Flow measurement device (Gaymar catalog FWT2 flowmeter):•Fluid source with calibrated flowmeter and a minimum accuracy of ± 12 ml/minute or•Fluid source with adjustable flowcontrol, Use a stop watch and graduated cylinder to adjust flow rate.Current Leakage/Ground resistance testerAC multimeter6.1 Physical InspectionCheck that the following items are in good condition and secure.Labels, if peeling or missingScrews in cover Bubble trap receiver Power cordIV pole clamp6.2 Output Fluid Temperature VerificationThe FW601 Blood/Fluid Warmer is factory calibrated at a flow rate of 100 ml/min.To verify the output fluid temperature is correct:1.The ambient room temperature must be between 20°C to 24°C.2.Connect the test setup (see figure 7). Attach the Gaymar FWT1 temperature sensor to the output of the bubble trap.Alternate method: Put a hole in the top of the bubble trap and insert a temperaturemeasurement device through this hole. Make certain sensor is completely submerged in fluid then seal the hole in the bubble trap.3.Connect the FWT2 flowmeter or flowmeasurement/control device to the output of the FWT1 temperature sensor.Alternate method: If using the sensor in the bubble trap method, connect the FWT2 flowmeter or flow measurement/control device directly to the output of the bubble trap.4.Flow room temperature water through the warmer at 100 ml/min (cc/min). Verify that the bubble trap is maintained 1/2 to 2/3 full.5.Turn the warmer on. Adjust the SETPOINT to 41.0°C. Allow it to run for 10 minutes.6.Verify that the output water temperature is 41.0°C ± 1.1°C. If using the FWT1 temperature sensor and an ohmmeter, verify that the resistance is within 1103—1204 ohms.If temperature or resistance values are not met, check setup and repeat test. If still not within range, contact your dealer for service.This device is factory calibrated and cannot be field adjusted.6.3Overtemp Protection VerificationProper operation of the overtemp protection system is verified each time the unit is switched from STANDBY to RUN mode. Therefore, periodic testing of this system is not necessary. However, the following procedure may be used to force an OVERTEMP condition in order to observe that the overtemp protection system works:3.1Effect of Flow Rate on Fluid TemperatureFluid temperatures exiting the patient line are affected by flow rate. The following flow vs. output fluidtemperature curve is typical for the FW601 warming unit. See figure 6 above.NOTE: Output fluid temperature for this curve is measured at the end of the patient line.Figure 6—Typical fluid temperature vs. flow rate63.2Warming Set RemovalThe cassette cannot be removed from the warming unit while under pressure. To remove the cassette:1.Close the warming set input clamp first, while leaving the output clamp open.2.Close the warming set output clamp.3.Following steps 1 and 2 will allow fluid to drain from the cassette. Gently pull on blue guide rail to remove cassette from warming unit.4.Dispose of warming set per facility protocol.Temperature at the End of Patient Line20253035404550100150200250300350400450500550600Flow in ml/minT e m p e r a t u r e°CSetpoint 41.0°CAmbient 22°C74.0Safety Systems4.1Over Temperature ProtectionA backup system within the warmer is independent of the main controller and monitors fluid temperature continuously. If the output fluid temperature exceeds 45.0°C, the backup system will immediately interrupt power to the heaters. If the over-temperaturecondition is a temporary occurrence as a result of a sudden change in flow rate, the display will alternately flash HI and the fluid temperature. When the fluid temperature returns to acceptable temperature levels,normal operation will resume. If, however, the backup system detects that the over-temperature condition is a result of a failure of the main controller, an audible alarm will sound, the RFU (REMOVE FROM USE)indicator will light, and the device will shut down.If this occurs, immediately stop the fluid flow, discard the warming set, and contact your dealer for service.4.2Self-diagnosticsEach time the warming unit is switched from STANDBY mode to RUN mode, a self-test is initiated. If the backup system is not functioning properly, an error message will be displayed and the unit will shut down.In addition, self-tests are routinely performed during RUN mode to ensure continued safe operation of the warming unit.4.3Control Alarm LOIf the warming unit senses a fluid temperature less than 34.0°C, the audible alarm will chime and the display will alternately indicate the symbol LO , and the actual fluid temperature.Exception:The unit will not alarm until the fluidtemperature has initially surpassed the 34.0°C threshold.5.0CleaningPerform the following care and cleaning between patient use or per facility protocol. •Unplug unit prior to cleaning•To clean the external surfaces of the warmer, usea non-abrasive cleaning solution (such as warm soap water) and a clean cloth.•Clean inside of cassette slot with disposable brush.Carefully flush using squeeze bottle with water.Replacement cleaning kit P/N 78350-000.•Apply a disinfectant such as 10% chlorinatedbleach solution (chlorinated bleach with 5.25%sodium hypochlorite) to both the outside of the unit and the cassette slot and allow to dry.。

VE 2023.0.0.0 Release NotesContentsVE 2023 (3)ApacheHVAC (3)ApacheSim (3)Approved Document O (3)Building Template Manager (3)Component Library (3)Constructions Database (4)Content Store (4)Design Options (4)Energy Sources and Meters (4)General (4)Kiva (4)MagiCAD Navigator (5)MicroFlo (5)ModelIT (5)Navigator for ASHRAE 90.1 PRM (5)Navigator for NECB (5)Navigator for Title 24 2022 (5)Navigator for Title 24 2019 (5)RadianceIES (6)Reports (6)SunCast (6)Tabular Space Data (6)UK Compliance (6)VE Scripts (7)VistaPro (7)VE 2023ApacheHVACCentral Plant Heat Pump modelling option added. [Id-52062]: Air to Water and Water to Water Heat Pump modelling options added that can be used as heat/cool source on hot water and/or chilled water loops.Auxiliary Heat Source option added. [Id-51783]: A Hot Water boiler or Part Load Curve heat source can be specified downstream of the hot water loop primary heat source.HVAC Wizard improvements. [Id-126626]: Fixed issue where Primary Cooling and Heating sources for the AHU coils were not editable on the Waterside and Plant Equipment Selection page and issue with importing multiple systems via the wizard where IDs became duplicated.Fixed issue with 'Design - Waterside and Plant Equipment Selection' page in HVAC Wizard [ID-122590]: When editing an existing file in the HVAC Wizard no additional plants or water loops were available for selection. This has been corrected and all plants and water loops are available for selection.Unchecked state for Set Design cooling capacity of chillers on CHWL relative to CHWL capacity works only for manual editing of CHWL Capacity, not for Autosizing. [ID-44729]: When the set design capacity option is unchecked only the % capacity value is updated after auto-sizing. The checkbox is hidden when the 'Force loop capacity...' check box on the Chilled water loop tab is selected.08b HVAC System has Incorrect Default Link for Dry-bulb Sensor/Controller. [ID-44986]: System 08b now has the default link for the specified controller set to Cooling coil - AHU cool LATApacheSimEnergy Meters interface enhanced [ID-52057]: The Energy Meters interface is updated to allow easier creation and management of meters (and sub-meters) for large projects.Total Electricity variable discrepancy resolved [ID-47199]: The Building Energy Total Electricity variable matches the value reported under Electricity in the Meters and End Uses variables.Approved Document OApproved Doc O: 2021 Overheating Script improved. [ID-123781]: Generating the overheating report in some cases caused the application to stall, this has been resolved so the report can generate.Building Template ManagerMissing profile data in BTM Comfort tab has been fixed [ID-73938]: The BTM Comfort tab now displays assigned profiles and profile options are available for selection in the dropdowns.Component LibraryComponent items wrongly identified as selected in ModelIT. [ID-84569]: Components are no longer incorrectly shown as selected when going down to component level.Constructions DatabaseCorrected link in Project Construction - Glazed: Electrochromic Control Function. [ID-81632]: Link updated top open the online Help site.Content StoreExtract proposed and baseline content store script error with PCI calculation. [ID-48879]: The PCI in the graphic and the table are matching and when set to 4 d.p the value is as expected. The EUI calc has corrected the MMBtu to kBtu conversion.Design OptionsDesign options crashes VE if project name/path contains extended-ascii character. [ID-44989]: Creating new design option does not crash the VE if the project name/path contains extended-ascii characters i.e.ø, etc. Energy Sources and MetersEnergy Meters can crash the VE. [ID-124921]: VE meters no longer crashes the VE when attempting to create its internal structure due to naming meters the same.GeneralStandard Data and Weather files being re-installed when not required. [ID-123961]: Duplicated Shared Content no longer being installed.Standard data and weather files out of date download link updated. [ID-45976]: The link has been updated when an older version of Shared Content is detected to direct the user to download the latest 64-bit version.False Alert removed - Unsupported Energy Sources in Electricity Generators. [ID-84368]: Alert no longer incorrectly displayed to the user.Updated 'DHW Zones' grouping scheme [ID-43309]: The 'DHW Zones' grouping scheme can no longer be renamed. A new 'Non-ApHVAC spaces' room group has been added alongside the existing 'Plenums and Voids' group. This new group will contain all space types other than rooms using the 'ApHVAC' HVAC methodology option to prevent these from being placed in a DHW Zone. When upgrading a model any applicable spaces will be placed in this group automatically.KivaFixed issue with kiva deep-ground boundary condition selection [ID-124945]: The selected deep-ground boundary condition option now persists after closing the kiva settings dialog and upon loading a saved project. Failed to create foundation geometry because of multiple ground floor foundation polygons detected. [ID-89350]: Error when calculating and writing to Kiva foundations file fixed in certain geometry cases.Kiva - Controls at Insulation details tab will be converted to a 'PLACEHOLDER' or 'Static' pressing the'Enter' key. [ID-124573]: Kiva Insulations detail dialog no longer displays placeholder labels over correct displays.Investigation for crash in third party KIVA (ASHRAE loads calc impacted) [ID-81828]: Third party Kiva library updated preventing crash.Kiva foundation zero-volume blocks should not be allowed [ID-74417]: Insulation blocks now require a min value of 0.001cm to be entered for width and when attempting to enter a lesser value this is prevented with a warning message.Kiva foundation custom blocks should allow some negative values [ID-74418]: Kiva foundation custom blocks now allow negative values for X pos, Depth and Width.MagiCAD NavigatorMagiCAD Navigator added. [ID-82806]: A Navigator is available to allow Heating and Cooling Loads calculation results to be exported out to MagiCAD via CSV.MicroFlo45 deg rotated CFD component not showing results. [ID-124900]: CFD simulation now displays results for the rotated component, error caused by the way component broken down during simulation.ModelITInconsistent behaviour with locks/snaps when using the Add window/door to wall (in Plan) tool. [ID-81076]: Width setting no longer superseding the grid setting causing strange behaviour when placing openings/windows.Units error on Object Bar for annotation location. [ID-122535]: The x, y, z, radius and height values are displayed and converted correctly for labels/trees when switching between units.Navigator for ASHRAE 90.1 PRM90.1 2013 ECB prototype data ApacheHVAC PTHP efficiencies are not correct (DX Cooling Types) [ID-45021]: The two DX Cooling PTHP units have been updated in the PRM systems library so that they now match the lower ECB units.Florida compliance report shows room floor area value in m2 instead of ft2. [ID-56181]: Report now shows value in ft2 and has the units in the column header.Navigator for NECBError Occurred: KeyError('ROOMID') due to use of voids. [ID-81633]: Error when generating the NECB report prevented when models contain Voids.Navigator for Title 24 2022Navigator for Title 24 2022 added. [ID-52066]: The Navigator for Title 24 2022 is approved to give a fully accredited alternative compliance solution for the Title 24 2022 code cycle.Navigator for Title 24 2019T24 CBECC Multifamily export – ResidentialOtherZone support added. [ID-51684]: Models containing spaces marked as ResidentialOtherZone can be included in xml that is accepted when imported to CBECC.RadianceIESBRE 209 Simulation option for seasonal variation of foliage added. [ID-52189]: Analysis option to assess BRE 209 allows simulation of Daylight Factor and Annual Illuminance taking into account seasonal variation of foliage (trees and hedges).Radiance multi view doesn't load UDI-C results. [ID-125373]: Multiview can successfully display all working plane grid results file types.Discard NULLdata when counting hours in CBDM results. [ID-82541]: When running a CBDM simulation Null values are no longer reported as daylit hours.Multi-view can show values on grid points. [ID-126078]: Multi-view extended to give option to display the values for each grid point as well as colour bands when viewing results of dynamic simulation on WP Grid tab. ReportsPrevented crash when generating heating and cooling report [ID-44581]: Prevented a crash when using compliance simulation results to generate heating and cooling reports in VistaPro after generating a report using the notional or actual .aps file the VE would crash when attempting to generate another report using the other.aps file.Loads report script error KeyError: 0 corrected. [ID-43255]: Loads report script improved to handle case that previously caused KeyError: 0 in some modelsSunCastSunCast solar energy or exposure analyses - objects on layers that are OFF are included. [ID-129651]: Layers that are configured to be off are no longer used within the SunCast simulation.Solar energy analysis - result Display unit corrected. [ID-84394]: Energy units displayed when viewing solar energy results on model viewer 2 instead of displaying energy values with Hours shown as units. General legend improvements to improve display.Tabular Space DataPaste from clipboard data in cfm units doesn't get pasted in primary and exhaust air change requirements. [ID-50670]: When the Primary and Exhaust Air Change values are pasted in from Excel (or imported from a tab-delimited/csv file), the value correctly respects the appropriate unit that is indicated in the import data (as specified Primary Air Change Req. Unit and Air Change Req Unit columns on the row).UK ComplianceText missing from Calculated useful generation capacity is exceeded message in Section 6 2022. [ID-123993]: Full text correctly displayed when relevant.Model combo indicates Notional building active even if creation of the notional failed. [ID-73081]: Without a valid model messages will show when trying to switch buildings, the existing one telling you to set the building type or a new error will be shown saying the NB can't be created due to a zero floor area. If the model is valid, then tab edit will display the correct text when switching between buildings.Unknown keyword in rooms file: GL. [ID-125251]: Issue resulting in incorrect thermal template being assigned in some cases resolved.VE ScriptsPython API - VEMacroflo.set() not updating dependent vars. [ID-47815]: Dependant variables/span updated as expected in tabular MacroFlo data dialog, after running python script. The values are also updated in types dialog.Adaptive comfort variables cannot be read from Python API. [ID-89368]: Basic Adaptive comfort variables now return valid results from the Python API.VistaProN/A (no value) variables are plotted on charts. [ID-47668]: N/A values are no longer being plotted on VistaPro charts.Fixed error with hours in range test tool run over year end [ID-47863]: When a simulation was run over year end the range test tool was not accounting for any hours beyond December.Units for annual water corrected. [ID-74795]: The IP unit of annual water correctly displays 1000 gallons instead of 1000 cu. Ft。