Parents' experiences of family and daily life after their child's stay in the pediatric intensive care unit: a qualitative descriptive study

被引:0
作者
Stalder, Sandra [1 ]
Handler-Schuster, Daniela [1 ,2 ,3 ]
Benedetti, Franzisca Domeisen [1 ]
机构
[1] ZHAW Zurich Univ Appl Sci, Inst Nursing, Sch Hlth Sci, Katharina Sulzer Pl 9, CH-8401 Winterthur, Switzerland
[2] Private Univ Hlth Sci, Inst Nursing, Dept Nursing Sci & Gerontol, Med Informat & Technol UMIT, Hall In Tirol, Austria
[3] Te Herenga Waka Victoria Univ Wellington Te Hereng, Fac Hlth, Sch Nursing Midwifery & Hlth Practice, Wellington, New Zealand
关键词
Experience; Pediatric intensive care unit; Critically ill child; Follow-up; Parents; Family and daily life; POSTTRAUMATIC STRESS; INTERVENTIONS; DEATH;
D O I
10.1186/s12887-024-04883-z
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
IntroductionThe stay of a critically ill child in a pediatric intensive care unit (PICU) is a significant experience for the family. Thus far, little is known regarding the impact of this stay on parents and their healthy children for whom no continuous aftercare services are offered. This study aimed to capture the post-stay experience and needs of parents after this traumatic event so that they could return to family and everyday life.MethodsThis qualitative descriptive study was conducted in collaboration with four pediatric intensive care units in Switzerland. It included parents whose children had fully recovered after a stay and who did not require continuous medical follow-up. All children were hospitalized in the PICU for at least 48 h. Data were collected through narrative pairs (n = 6) and individual interviews (n = 8). Interviews were audio recorded, transcribed, coded inductively according to Salda & ntilde;a, and analyzed.ResultsThe results showed three related phases that influence each other to restore normality in daily life: Trust and inclusion in the treatment process during the stay (1), processing after the stay (2), and returning to everyday life (3).ConclusionFollow-up meetings should be available to all parents whose children have been hospitalized in the PICU. In particular, it should also be available to parents whose children have fully recovered and no longer have any medical disabilities.
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页数:9
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