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العنوان
Quality of Life Among Children Suffering from Congenital Heart Disease /
المؤلف
Sayeh, Manal Mahmoud,
هيئة الاعداد
باحث / Manal Mahmoud Sayeh
مشرف / Seham Guirguis Ragheb
مشرف / Waleed Mohamed ELguindy
مناقش / Rasmia Abd Elsttar Ali
تاريخ النشر
2016.
عدد الصفحات
P.182. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
المجتمع والرعاية المنزلية
تاريخ الإجازة
1/1/2016
مكان الإجازة
جامعة عين شمس - كلية التمريض - تمريض صحة المجتمع
الفهرس
Only 14 pages are availabe for public view

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from 182

Abstract

The diagnosis of a child’s congenital heart disease is a stressful event for parents especially the mother who is considered to be a main caregiver for the child. Parental responses to the diagnosis of their child’s congenital heart commonly include disbelief, denial anger, frustration and confusion. Mothers of the congenitally heart experience stressors which are usually multiple and ongoing as they confront stressors at the time of diagnosis and during the developmental transition. Community health nurses must be aware of the ongoing responses, needs and quality of life of the congenitally heart child and his/her mother. (www.en.wikepidia_org/wiki/congenital heart, 2015).
Aim of the study:
The aim of the current study was to assess quality of life among children suffering from congenital heart disease.
Setting:
The study was conducted at cardiopulmonary outpatient clinic of pediatrics hospital affiliated to Ain Shams University Hospital.
Sampling: Sampling of the study involved 200 children suffering from congenital heart disease and their mothers, form both sexes, with age at birth – 4 years.
Tools for data collection:
Data obtained through an interview with the congenitally heart children and their accompanying mothers through using the following tools:
* The first tool:
• Child interviewing questionnaire was developed by investigator and it was written in simple Arabic language, it included the following:
• Socio-demographic data of children include age, gender, and child rank.
• Socio-demographic data of mothers and fathers include age, educational level occupation.
• Environmental assessment for children living in.
• Data regarding the child’s medical history.
• Data regarding assessing mother’s knowledge about congenital heart disease, definition, causes, signs, symptoms and treatment.
• Data regarding children health needs and problem related to congenital heart disease by mother’s role towards the needs and problem for the children.
* The second tools:
• Quality of life inventory scale by (Varni, 2003) it was used to assess level of quality of life for children with congenital heart disease. It is consists of four items physical, psychological, social, spiritual and general will being every items contain some of point.
* The third tools:
• Child’s medical record to assess health status of children which included diagnosis, when the disease started, the time of the treatment initiation and evaluated physical circulatory, respiratory urinary tract, nervous, motor system and skin condition for the child also included the results of laboratory investigations.
Pilot study
• A pilot study was conducted on 10% of children and their mothers to test the feasibility of the tools and the time consumed for filling in the questionnaire and also to test the language clarify of the tools. Data obtained from the pilot study was analyzed and accordingly the necessary modifications were done. The number of the pilot study was excluded from the study sample.