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The Experience of Dementia¡¯s Families¡¯s Defecation Care Experience

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KMID : 0607320080170020204
ÀÌÁ¤¼· ( Lee Jung-Seop ) - ÇѾç´ëÇб³ °£È£Çаú

ÇÏÁø ( Ha Jin ) - º¸°Çº¹Áö°¡Á·ºÎ ³ëÀÎÁ¤Ã¥°ú

Abstract

Purpose: This study was to understand the experience of dementia patient¡¯s families¡¯ experience of defecation care.

Methods: Colaizzi¡¯s phenomenology guided the data collection and analysis. Data was collected through in depth interviews of 20 families in a day care center and attendants at family education for dementia.

Results: 142 meaningful statements, 25 concepts, and 5 concept clusters of experience of dementia patient¡¯s families¡¯ defecation management were identified. The essential result of dementia¡¯s families¡¯s defecation care were ¡®Burden of patient¡¯s action¡¯, ¡®Environmental difficulty related to patient¡¯, ¡®Self dilemma¡¯, ¡®Burden of weakness of general condition¡¯, and ¡®Effort of resolution in one¡¯s own way¡¯.

Conclusion: The result of this study could help care givers to understand care experiences of the dementias¡¯ family with defecation care. Future research is needed to develop a public support system and nursing interventions for defecation care.
KeyWords
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Dementia, Family, Defecation, Careexperience
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ÇмúÁøÈïÀç´Ü(KCI) KoreaMed