Parental reaction to diagnosis of infant hearing loss

IF 1.4 Q3 PSYCHIATRY Advances in Mental Health Pub Date : 2020-01-02 DOI:10.1080/18387357.2019.1651661
V. Green
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引用次数: 8

Abstract

ABSTRACT Objective This study aimed to investigate parental reactions to a diagnosis of Permanent Childhood Hearing Loss (PCHL) and the implications for engagement in medical investigations and early intervention services. The study sought to determine the impact of type of hearing loss, presence of parental depression or anxiety, and parental reflective function on timely engagement with services for children with bilateral PCHL. Method Questionnaires were completed by 27 parents of babies aged 3-5 months, diagnosed with bilateral hearing loss. Measures included the DASS 21, DMRF (Diamond Maternal Reflective Function Scale), and demographic items. Clinical charts were accessed six months later to ascertain timing of engagement with medical and early intervention services. Results 86% of families attended all required medical appointments following diagnosis. Early intervention services were attended by 65.5% of families. Parental anxiety was the only significant factor in engagement with early intervention services. There was no impact of reflective functioning, parent education and additional medical needs of the child on engagement. The participants also had lower levels overall of anxiety and depression (compared to normative data) but higher levels of stress on the DASS. Discussion While many factors may impact on the likelihood of timely attendance at medical appointments and engagement with early intervention services (EI), support needs to be tailored to each family to ameliorate any potential barriers and ensure that access is easily available, particularly when there may be parental anxiety. This study shows that higher levels of anxiety were significantly associated with decreased engagement with EI.
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父母对婴儿听力损失诊断的反应
摘要目的本研究旨在探讨父母对永久性儿童听力损失(PCHL)诊断的反应,以及参与医学调查和早期干预服务的意义。该研究旨在确定听力损失类型、父母抑郁或焦虑的存在以及父母反思功能对双侧PCHL儿童及时参与服务的影响。方法对27例3-5月龄双侧听力损失患儿父母进行问卷调查。测量包括DASS 21, DMRF(钻石产妇反射功能量表)和人口统计项目。六个月后查阅了临床图表,以确定接受医疗和早期干预服务的时间。结果86%的家庭在诊断后参加了所有要求的医疗预约。65.5%的家庭参加了早期干预服务。父母焦虑是参与早期干预服务的唯一重要因素。反思功能、父母教育和儿童的额外医疗需求对参与没有影响。参与者的焦虑和抑郁总体水平也较低(与规范数据相比),但DASS上的压力水平较高。虽然许多因素可能影响到及时就诊和参与早期干预服务(EI)的可能性,但需要为每个家庭量身定制支持,以改善任何潜在障碍,并确保容易获得,特别是在父母可能感到焦虑的情况下。这项研究表明,较高的焦虑水平与EI参与度的下降显著相关。
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来源期刊
CiteScore
3.20
自引率
7.10%
发文量
19
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