Experiences and psychological issues affecting parents of children born with atypical genitalia in India.

IF 1.3 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Pediatric Endocrinology & Metabolism Pub Date : 2024-11-11 DOI:10.1515/jpem-2024-0372
Tanvi Bindal, Rajni Sharma, Vandana Jain, Rajesh Sagar
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Abstract

Background: Parents of children with differences of sex development (DSD) are known to suffer from psychological distress at the time of diagnosis and thereafter. We analyzed the prevalence of anxiety and depression in Indian parents of children with DSD and its associated risk factors, as well as their experiences, perceptions and expectations from the healthcare system.

Methods: This cross-sectional study included parents of children aged ≤6 years with atypical genitalia. Data was collected through face-to-face semi-structured interview using specially designed questionnaire. Depression and anxiety have been assessed using PHQ9 (Patient health questionnaire) and GAD-7 (Generalized anxiety disorder scale), respectively.

Results: The current mean age of the 43 children (46,XY=26, 46,XX=16 and chromosomal DSD=1) was 36.5 ± 21.4 months with a median age of diagnosis of 5 months (range- 0-60 months). 68 parents (35 mothers and 33 fathers) were interviewed. The score was above the cut-off for clinically significant depression in 27.2 and 25.7 % of the fathers and mothers, respectively; and for clinically significant anxiety in 15.1 and 28.6 % of the fathers and mothers, respectively. The most significant factor associated with psychological distress was rearing a boy with lower EMS in fathers and lower literacy levels (with higher perception of stigma) in mothers. Absence of family support was associated with high levels of distress in both parents.

Conclusions: There is a high level of depression and anxiety amongst Indian parents of children born with atypical genitalia and requirement for psychological support and counseling.

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影响印度先天性非典型生殖器儿童父母的经历和心理问题。
背景:众所周知,性发育差异(DSD)患儿的父母在确诊时及其后都会遭受心理困扰。我们分析了印度 DSD 患儿家长焦虑和抑郁的患病率及其相关风险因素,以及他们的经历、对医疗系统的看法和期望:这项横断面研究包括年龄≤6 岁的非典型生殖器畸形儿童的父母。采用专门设计的问卷,通过面对面的半结构式访谈收集数据。抑郁和焦虑分别使用 PHQ9(患者健康问卷)和 GAD-7(广泛性焦虑症量表)进行评估:43 名儿童(46,XY=26 人,46,XX=16 人,染色体 DSD=1 人)目前的平均年龄为 36.5 ± 21.4 个月,诊断年龄中位数为 5 个月(范围为 0-60 个月)。68 名家长(35 名母亲和 33 名父亲)接受了访谈。分别有 27.2% 和 25.7% 的父亲和母亲的得分超过了具有临床意义的抑郁临界值;分别有 15.1% 和 28.6% 的父亲和母亲的得分超过了具有临床意义的焦虑临界值。与心理压力相关的最重要因素是抚养男孩,父亲的 EMS 水平较低,母亲的文化水平较低(对耻辱感的认识较高)。缺乏家庭支持与父母双方的高抑郁水平有关:印度先天性非典型生殖器儿童的父母抑郁和焦虑程度较高,需要心理支持和咨询。
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来源期刊
CiteScore
2.70
自引率
7.10%
发文量
176
审稿时长
3-6 weeks
期刊介绍: The aim of the Journal of Pediatric Endocrinology and Metabolism (JPEM) is to diffuse speedily new medical information by publishing clinical investigations in pediatric endocrinology and basic research from all over the world. JPEM is the only international journal dedicated exclusively to endocrinology in the neonatal, pediatric and adolescent age groups. JPEM is a high-quality journal dedicated to pediatric endocrinology in its broadest sense, which is needed at this time of rapid expansion of the field of endocrinology. JPEM publishes Reviews, Original Research, Case Reports, Short Communications and Letters to the Editor (including comments on published papers),. JPEM publishes supplements of proceedings and abstracts of pediatric endocrinology and diabetes society meetings.
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