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印度农村地区父母对孩子癫痫适应情况的预测因素

Predictors of parental adjustment to children's epilepsy in rural India.

作者信息

Pal D K, Chaudhury G, Das T, Sengupta S

机构信息

Neurosciences Unit, Institute of Child Health, University College London, UK.

出版信息

Child Care Health Dev. 2002 Jul;28(4):295-300. doi: 10.1046/j.1365-2214.2002.00278.x.

Abstract

BACKGROUND

Negative societal attitudes towards disability affect the adjustment of parents when their child is diagnosed with epilepsy. Recent studies have suggested that parental and child outcomes, including adjustment, can be influenced by non-directed social support to mothers of children with disability. The objective of our study was to test the hypothesis that maternal satisfaction with social support, measured at the beginning of treatment, would predict parental adjustment to the child's epilepsy after 1 year of treatment.

METHODS

We enrolled 46 mothers of children aged 6-18 years with epilepsy in the study. We measured social support using the modified Dunst family support scale, and parental adjustment using a locally validated instrument (S-PAM). Correlation was tested using a multiple linear regression model, allowing for confounding variables.

RESULTS

Parental adjustment at outcome was positively independently correlated with satisfaction with social support at baseline,and negatively with severity of the child's epilepsy. The regression model explained 34% of the total variance.

CONCLUSIONS

Taken together with evidence from previous studies, this finding supports the idea that helping parents to find more satisfaction within their (new or existing) social networks will promote adjustment to their child's disability.

摘要

背景

社会对残疾的负面态度会影响孩子被诊断出患有癫痫症时父母的适应情况。最近的研究表明,包括适应情况在内的父母和孩子的结果可能会受到对残疾儿童母亲的非定向社会支持的影响。我们研究的目的是检验这样一个假设,即在治疗开始时测量的母亲对社会支持的满意度能够预测治疗1年后父母对孩子癫痫症的适应情况。

方法

我们招募了46名6至18岁癫痫患儿的母亲参与研究。我们使用改良的邓斯特家庭支持量表测量社会支持,并使用经过本地验证的工具(S-PAM)测量父母的适应情况。使用多元线性回归模型检验相关性,同时考虑混杂变量。

结果

结果显示,父母的适应情况与基线时对社会支持的满意度呈正相关,与孩子癫痫症的严重程度呈负相关。回归模型解释了总方差的34%。

结论

结合先前研究的证据,这一发现支持了这样一种观点,即帮助父母在其(新的或现有的)社交网络中找到更多满足感将促进他们对孩子残疾状况的适应。

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