IndiCleft – A web-based standardized research tool and resource for cleft anomalies

O. Kharbanda, A. Grover, Savita Dawar, Karoon Aggarwal, S. Sharma, M. Singhal, S. Chauhan, H. Singh, M. Kabra, Neeraja Gupta, V. Scaria, M. Rajkhowa, ArtiGarg, Nitika Monga, Ravinder Singh, R. Dhaliwal
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引用次数: 1

Abstract

Introduction: In India, approximately 35,000 new cleft patients are born every year. Many patients receive suboptimum, improper, little, or no treatment. The cumulative burden of cleft care is up to 1 million cases. The spectrum of problems is varied, the caseload is enormous, and the logistics of treatment delivery are complicated. The Indian Council of Medical Research (ICMR) task force project was launched in 2012 to evaluate the status of cleft care in India and develop strategies to provide comprehensive cleft care through a dynamic multidisciplinary and multidimensional tool. ICMR task force project (2012–14) was conducted in Delhi, and the National Capital Region reported that at least 50% of studied cases had complex and multiple treatment needs. The needs identified were related to surgical, orthodontic, dental, ENT and Speech, rehabilitation of mutilated dentition, and various psychological disturbances among patients with Cleft anomalies. Aim: The aim of this study was to develop and test web-based application to create a system for national data of patients with cleft anomalies and digitize the patient records in a standardized preagreed format. Methods and Results: Corresponding to contemporary digital technologies and evolutionary improvements in data collection, web-based data collection instrument, including text, photographs, X-rays, and audio files, was considered the most appropriate. The experts from varied domains in consultation with ICMR and National Informatics Centre evolved a web-based data collection instrument which is named the “IndiCleft tool.” The tool has been tested and used over the years and is presently being upgraded to dynamic version for a national data and patient care registry. Conclusion: The present article describes the process of the development of a “dynamic” web-based data collection instrument. The IndiCleft tool is the national resource on cleft data in India.
IndiCleft -一个基于网络的腭裂异常标准化研究工具和资源
简介:在印度,每年约有35000名新的腭裂患者出生。许多患者接受了次优、不当、很少或根本没有治疗。唇裂护理的累计负担高达100万例。问题种类繁多,案件数量巨大,提供治疗的后勤工作也很复杂。印度医学研究委员会(ICMR)工作组项目于2012年启动,旨在评估印度的腭裂护理状况,并制定战略,通过一个动态的多学科和多层面工具提供全面的腭裂护理。ICMR特别工作组项目(2012-2014)在德里进行,国家首都地区报告称,至少50%的研究病例有复杂和多种治疗需求。确定的需求与手术、正畸、牙科、耳鼻喉科和言语、残齿列的康复以及腭裂患者的各种心理障碍有关。目的:本研究的目的是开发和测试基于网络的应用程序,以创建一个全国性腭裂畸形患者数据系统,并以标准化的预先准备的格式将患者记录数字化。方法和结果:与当代数字技术和数据收集的进化改进相对应,基于网络的数据收集工具,包括文本、照片、X光片和音频文件,被认为是最合适的。来自不同领域的专家与ICMR和国家信息学中心协商,开发了一种基于网络的数据收集工具,称为“IndiCleft工具”。该工具经过多年的测试和使用,目前正在升级为国家数据和患者护理登记处的动态版本。结论:本文描述了“动态”网络数据采集工具的开发过程。IndiCleft工具是印度关于裂隙数据的国家资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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