A National Iranian Cochlear Implant Registry (ICIR): cochlear implanted recipient observational study.

Q3 Medicine
Nader Saki, Arash Bayat, Soheila Nikakhlagh, Majid Karimi, Mohammad Nikafrooz, Ahmad Daneshi, Masoud Motesadi Zarandi, Mohammad Ajalloueyan, Seyed Basir Hashemi, Mohammad Mehdi Ghasemi, Ali Eftekharian, Seyyed Hamidreza Abtahi, Maryam Amizadeh, Farhad Farahani, Masoud Naderpour
{"title":"A National Iranian Cochlear Implant Registry (ICIR): cochlear implanted recipient observational study.","authors":"Nader Saki,&nbsp;Arash Bayat,&nbsp;Soheila Nikakhlagh,&nbsp;Majid Karimi,&nbsp;Mohammad Nikafrooz,&nbsp;Ahmad Daneshi,&nbsp;Masoud Motesadi Zarandi,&nbsp;Mohammad Ajalloueyan,&nbsp;Seyed Basir Hashemi,&nbsp;Mohammad Mehdi Ghasemi,&nbsp;Ali Eftekharian,&nbsp;Seyyed Hamidreza Abtahi,&nbsp;Maryam Amizadeh,&nbsp;Farhad Farahani,&nbsp;Masoud Naderpour","doi":"10.5935/0946-5448.20190013","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objective: </strong>Patients who receive cochlear implants (CIs) constitutes a significant population in Iran. This population needs regular monitor on long-term outcomes, educational placement and quality of life. Currently, there is no national or regional registry on the long term outcomes of CI users in Iran. The present study aims to introduce the design and implementation of a national patient-outcomes registry on CI recipients for Iran. This Iranian CI registry (ICIR) provides an integrated framework for data collection and sharing, scientific communication and collaboration inCI research.</p><p><strong>Methods: </strong>The national ICIR is a prospective patient-outcomes registry for patients who are implanted in one of Iranian centers. The registry is based on an integrated database that utilizes a secure web-based platform to collect response data from clinicians and patient's proxy via electronic case report forms (e-CRFs) at predefined intervals. The CI candidates are evaluated with a set of standardized and non-standardized questionnaires prior to initial device activation(as baseline variables) and at three-monthly interval follow-up intervals up to 24 months and annually thereafter.</p><p><strong>Results: </strong>The software application of the ICIR registry is designed in a user-friendly graphical interface with different entry fields. The collected data are categorized into four subsets including personal information, clinical data, surgery data and commission results. The main parameters include audiometric performance of patient, device use, patient comorbidities, device use, quality of life and health-related utilities, across different types of CI devices from different manufacturers.</p><p><strong>Conclusion: </strong>The ICIR database could be used by the increasingly growing network of CI centers in Iran. Clinicians, academic and industrial researchers as well as healthcare policy makers could use this database to develop more effective CI devices and better management of the recipients as well as to develop national guidelines.</p>","PeriodicalId":39842,"journal":{"name":"International Tinnitus Journal","volume":"23 2","pages":"74-78"},"PeriodicalIF":0.0000,"publicationDate":"2019-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Tinnitus Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5935/0946-5448.20190013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 10

Abstract

Background and objective: Patients who receive cochlear implants (CIs) constitutes a significant population in Iran. This population needs regular monitor on long-term outcomes, educational placement and quality of life. Currently, there is no national or regional registry on the long term outcomes of CI users in Iran. The present study aims to introduce the design and implementation of a national patient-outcomes registry on CI recipients for Iran. This Iranian CI registry (ICIR) provides an integrated framework for data collection and sharing, scientific communication and collaboration inCI research.

Methods: The national ICIR is a prospective patient-outcomes registry for patients who are implanted in one of Iranian centers. The registry is based on an integrated database that utilizes a secure web-based platform to collect response data from clinicians and patient's proxy via electronic case report forms (e-CRFs) at predefined intervals. The CI candidates are evaluated with a set of standardized and non-standardized questionnaires prior to initial device activation(as baseline variables) and at three-monthly interval follow-up intervals up to 24 months and annually thereafter.

Results: The software application of the ICIR registry is designed in a user-friendly graphical interface with different entry fields. The collected data are categorized into four subsets including personal information, clinical data, surgery data and commission results. The main parameters include audiometric performance of patient, device use, patient comorbidities, device use, quality of life and health-related utilities, across different types of CI devices from different manufacturers.

Conclusion: The ICIR database could be used by the increasingly growing network of CI centers in Iran. Clinicians, academic and industrial researchers as well as healthcare policy makers could use this database to develop more effective CI devices and better management of the recipients as well as to develop national guidelines.

伊朗国家人工耳蜗注册(ICIR):人工耳蜗植入受体观察性研究。
背景和目的:接受人工耳蜗(CIs)的患者在伊朗占很大比例。这一人群需要对长期结果、教育安置和生活质量进行定期监测。目前,伊朗没有关于CI使用者长期结果的国家或地区登记。本研究旨在介绍伊朗CI受者的国家患者结局登记处的设计和实施。这个伊朗CI注册表(ICIR)为CI研究的数据收集和共享、科学交流和合作提供了一个综合框架。方法:国家ICIR是对在伊朗某一中心植入的患者进行前瞻性患者结局登记。该登记处以一个综合数据库为基础,该数据库利用一个安全的基于网络的平台,以预先确定的时间间隔通过电子病例报告表格(e-CRFs)收集临床医生和患者代理的应答数据。CI候选人在初始设备激活之前(作为基线变量)通过一组标准化和非标准化问卷进行评估,并在三个月的随访时间间隔至24个月,之后每年进行一次随访。结果:ICIR注册表的软件应用程序设计为具有不同输入字段的友好图形界面。收集的数据分为四个子集,包括个人信息、临床数据、手术数据和委托结果。主要参数包括来自不同制造商的不同类型CI设备的患者听力测量性能、设备使用、患者合并症、设备使用、生活质量和与健康相关的实用程序。结论:ICIR数据库可用于伊朗日益增长的CI中心网络。临床医生、学术和工业研究人员以及医疗保健政策制定者可以使用该数据库开发更有效的CI设备,更好地管理接受者,并制定国家指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
International Tinnitus Journal
International Tinnitus Journal Medicine-Otorhinolaryngology
CiteScore
0.70
自引率
0.00%
发文量
11
期刊介绍: The International Tinnitus Journal is the first peer review journal to provide a forum for exchange of information of on-going basic and clinical science efforts for understanding tinnitus and its application to patient diagnosis and treatment. Subject areas to be covered range from fundamental theory to clinical applications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信