목차
서 론
1. 연구의 필요성
2. 연구목적
연 구 방 법
1. 연구설계
2. 연구참여자 선정
3. 자료수집 및 분석
4. 윤리적 고려
5. 연구자의 준비
6. 연구의 엄격성 확보
연 구 결 과
1. 부담스러웠으나 어쩔 수 없이 받아들임
2. 두려움이 엄습함
3. 혼자 감당해야 하는 무게
4. 어렵고 생소하기만 한 모든 것들
5. 그래도 우리집
6. 다른 가족들에게 미안함
논 의
결 론 및 제 언
REFERENCES
초록
Purpose: This study was conducted to identify the experiences of families caring for patients with home mechanical ventilation. The question was, “What is the caregiving experience of a family who has a member with home mechanical ventilation?”. Methods: This study was a qualitative study to explore and describe the implications of experiences of families caring through a phenomenological approach. One-on-one in-depth interviews were conducted with family caregivers who worked as full-time for caring for patients with home mechanical ventilation, and the results were analyzed using Colaizzi’s (1978) phenomenological method. Participants’ relationships to patients were 1 spouse, 1 father, and 6 mother. The ages of the participants were between 33 and 59, with an average of 45.1. Results: In this study, family members’ caregiving experience was emerged. Analysis revealed the following themes: Felt burdened but had to accept it; Seized by fear; The weight I must bear alone; Everything is difficult and unfamiliar; Still, my home; and Sorry for the other family members. It was found that caregivers had decided to discharge their loved ones from the hospital out of a sense of duty. Conclusion: The families took care of the patients with responsibility and love. The study results should help with the understanding of a family with a member with home mechanical ventilation and should be used to develop nursing, mediating, and consulting programs for these caregivers