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青春期脑瘫相关残疾少女的月经问题的影响。

The impact of menstruation in adolescents with disabilities related to cerebral palsy.

机构信息

Department of Endocrinology and Diabetes, The Royal Children's Hospital, Parkville, Melbourne, Victoria 3052, Australia.

出版信息

Arch Dis Child. 2010 Jul;95(7):526-30. doi: 10.1136/adc.2009.174680. Epub 2010 May 10.

Abstract

BACKGROUND

Information regarding menstrual difficulties for adolescents with developmental disabilities and their families is limited.

AIM

To assess the impact of menstruation on adolescents with developmental disabilities and their families, and to compare this to previously reported experiences of age-matched normal girls.

METHODS

Families of girls aged 12-18 years with known disabilities, attending the Royal Children's Hospital, Melbourne, were recruited into a questionnaire based study evaluating issues of menstruation and associated problems, together with the consequent psychological, social and emotional impact on their families and carers. Information was sought regarding menstrual management strategies, outcome satisfaction and specific areas of family concern.

RESULTS

103 questionnaires were completed. The average age of participating girls was 15.11 years, mean menarchal age 12.3 years. 79 girls were postmenarchal. The severity of menstrual problems was similar to a normal population. 59 (76%) were happy with the impact of menses on their social activities. More than 50% sought menstrual advice before menarche. Advice seeking strongly correlated with disability severity (p=0.01) and impact of menses on social activities (p=0.01), which in turn were highly predictive of seeking assistance (p=0.005). Carer satisfaction with current management inversely correlated with treatment seeking behaviour (p=0.034).

CONCLUSIONS

Menstrual characteristics in this population are similar to those without disabilities. There is a high level of parental anxiety regarding the impact of menses, particularly when disability is severe. Medical therapies may be required but information for families is lacking. Clinicians should play a proactive and educational role with families and adolescents with disabilities.

摘要

背景

青少年发育障碍患者及其家庭的月经困难相关信息有限。

目的

评估月经对发育障碍青少年及其家庭的影响,并与年龄匹配的正常女孩的既往报告进行比较。

方法

招募了墨尔本皇家儿童医院就诊的 12-18 岁已知发育障碍女孩的家庭,参与基于问卷的研究,评估月经及相关问题,以及对其家庭和照顾者的心理、社会和情感影响。我们寻求了月经管理策略、结果满意度以及家庭关注的具体领域的信息。

结果

完成了 103 份问卷。参与女孩的平均年龄为 15.11 岁,初潮年龄为 12.3 岁。79 名女孩已经经历初潮。月经问题的严重程度与普通人群相似。59 名(76%)女孩对月经对其社交活动的影响感到满意。超过 50%的人在初潮前寻求月经建议。寻求建议与残疾严重程度(p=0.01)和月经对社交活动的影响(p=0.01)强烈相关,而这两个因素又高度预测了寻求帮助(p=0.005)。照顾者对当前管理的满意度与寻求治疗的行为呈负相关(p=0.034)。

结论

该人群的月经特征与无残疾人群相似。父母对月经的影响感到非常焦虑,尤其是当残疾严重时。可能需要医疗治疗,但家庭缺乏相关信息。临床医生应与发育障碍的家庭和青少年积极主动地进行教育。

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