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A questionnaire-based analysis of parental perspectives on pediatric cochlear implant (CI) re/habilitation services: a pilot study from a developing CI service in India

机译:对儿科耳蜗植入物(CI)RE / HAPILITITE服务的父母视角的基于调查分析:印度CI服务的试点研究

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摘要

Objective: To study parental perspectives on re/habilitation services offered for pediatric cochlear implant (CI) users at a non-profit organization in India. Methodology: A non-standardized questionnaire comprising 46 items was created to understand perspectives of parents of pediatric CI users. Questions were designed to examine re/habilitation services from the angles of service delivery, parental stress levels, reasons for delay in obtaining services, sources of emotional support, concerns, and fears during each stage starting from diagnosis of hearing loss to CI surgery, re/habilitation services and parents' views of their children post-CI. The questionnaire was posed to 30 parents and responses were recorded and coded. Results and discussion: Qualitative and quantitative analyses based on parents' responses identified several factors that significantly influenced parental perspectives during each stage. The major factors delaying the decision to go for CI included a fear of surgery, lack of funds for CI and the subsequent re/habilitation process, and limited knowledge. Key concerns were the child's academic performance and social acceptance.
机译:目的:研究在印度非营利组织的儿科耳蜗植入物(CI)用户提供的重新/居住服务的父母视角。方法论:包括46项的非标准化问卷,以了解儿科CI用户父母的透视。问题旨在从服务交付的角度,父母压力水平,延迟原因,从诊断到CI手术的诊断开始,从服务交付的角度,父母压力水平,延迟原因,情绪支持,担忧和恐惧的担忧。 /居住服务和父母对其子女的看法。调查问卷被提交给30名父母,并记录并编码答复。结果与讨论:基于父母的响应的定性和定量分析确定了几种影响每个阶段的父母观点的因素。延迟决定的主要因素包括对手术的恐惧,缺乏CI和随后的重新/居住过程以及知识有限的资金。关键问题是孩子的学术表现和社会验收。

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