Saki Nader, Bayat Arash, Nikakhlagh Soheila, Karimi Majid, Nikafrooz Mohammad, Daneshi Ahmad, Zarandi Masoud Motesadi, Ajalloueyan Mohammad, Hashemi Seyed Basir, Ghasemi Mohammad Mehdi, Eftekharian Ali, Abtahi Seyyed Hamidreza, Amizadeh Maryam, Farahani Farhad, Naderpour Masoud
Hearing Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran Hearing Research Center Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran.
Department of Education, University of Farhangian Teacher Education, Chamran Branch, Iran Department of Education University of Farhangian Teacher Education Chamran Branch Iran.
Int Tinnitus J. 2019 Sep 4;23(2):74-78. doi: 10.5935/0946-5448.20190013.
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.
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.
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.
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.
在伊朗,接受人工耳蜗植入(CI)的患者构成了一个庞大群体。这一群体需要对长期疗效、教育安置和生活质量进行定期监测。目前,伊朗尚无关于人工耳蜗使用者长期疗效的国家或地区登记系统。本研究旨在介绍伊朗人工耳蜗接受者国家患者疗效登记系统的设计与实施情况。这个伊朗人工耳蜗登记系统(ICIR)为人工耳蜗研究中的数据收集与共享、科学交流与合作提供了一个综合框架。
国家ICIR是一个针对在伊朗各中心接受植入手术患者的前瞻性患者疗效登记系统。该登记系统基于一个综合数据库,利用安全的网络平台,通过电子病例报告表(e-CRFs)在预定时间间隔从临床医生和患者代理人处收集应答数据。在初次设备激活前(作为基线变量)以及之后每三个月随访一次,直至24个月,此后每年对人工耳蜗候选者进行一组标准化和非标准化问卷评估。
ICIR登记系统的软件应用程序设计了用户友好的图形界面和不同的输入字段。收集到的数据分为四个子集,包括个人信息、临床数据、手术数据和调试结果。主要参数包括患者的听力测量表现、设备使用情况、患者合并症、设备使用情况、生活质量以及与健康相关的效用,涉及不同制造商生产的不同类型人工耳蜗设备。
伊朗日益增长的人工耳蜗中心网络可以使用ICIR数据库。临床医生、学术和产业研究人员以及医疗保健政策制定者可以利用这个数据库开发更有效的人工耳蜗设备,更好地管理接受者,并制定国家指南。