Parents Need More Support: A Qualitative Study of the Experiences of Australian Parents Who Are Waiting for Surgical Intervention for Their Children With Otitis Media

被引:4
|
作者
Stephens, Jacqueline H. [1 ,2 ]
O'Keefe, Maree [3 ]
Schembri, Mark [4 ]
Baghurst, Peter A. [3 ]
机构
[1] Univ Adelaide, Adelaide Med Sch, Discipline Paediat, Adelaide, SA, Australia
[2] South Australian Hlth & Med Res Inst, Aboriginal Hlth Equ, Adelaide, SA, Australia
[3] Univ Adelaide, Fac Hlth & Med Sci, Adelaide, SA, Australia
[4] Womens & Childrens Hosp, Ear Nose & Throat Dept, Adelaide, SA, Australia
来源
JOURNAL OF PATIENT EXPERIENCE | 2020年 / 7卷 / 05期
关键词
qualitative research; child; otitis media; ear health;
D O I
10.1177/2374373519883495
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objective: To explore the experiences, expectations, and motivations of parents/caregivers of children with otitis media who were booked to undergo tympanostomy tube insertion. Method: A cross-sectional cohort study was conducted using semistructured interviews with 39 parents. Interviews were conducted via telephone and analyzed for key themes. Results: Three themes emerged that incorporated a range of subthemes: (1) the impact of the child's underlying condition on the family, (2) the cues and prompts that influenced parents to seek intervention, and (3) the parents' expectations of the health-care system. The child's otitis media disrupted the day-to-day functioning of the family and the child's well-being, but despite this, the families found ways to adapt and cope. Parents were influenced by their friends, family, and medical practitioners when making treatment decisions and had differing expectations of the health-care system. Conclusion: Parents need support during their child's illness to help with pressures placed on the family and also in making health-care decisions for their child. Clinicians should consider these issues when discussing treatment options with parents.
引用
收藏
页码:717 / 725
页数:9
相关论文
共 50 条
  • [41] Experiences and changes in parents of children with infant cerebral palsy: a qualitative study
    Fernandez-Alcantara, M.
    Garcia-Caro, M. P.
    Berrocal-Castellano, M.
    Benitez, A.
    Robles-Vizcaino, C.
    Laynez-Rubio, C.
    ANALES DEL SISTEMA SANITARIO DE NAVARRA, 2013, 36 (01) : 9 - 20
  • [42] The views of parents and carers on managing acute otitis media in urban Aboriginal and Torres Strait Islander children: a qualitative study
    Reath, Jennifer S.
    O'Brien, Sarah
    Campbell, Letitia
    Gunasekera, Hasantha
    Tyson, Claudette A.
    Askew, Deborah A.
    Hu, Wendy
    Usherwood, Tim
    Kong, Kelvin
    Morris, Peter
    Leach, Amanda J.
    Walsh, Robyn
    Abbott, Penelope A.
    MEDICAL JOURNAL OF AUSTRALIA, 2024, 220 (04) : 202 - 207
  • [43] Experiences of peer support amongst parents of children with neurodevelopmental disorders: A qualitative systematic review
    Wong, Tiffany Shi Min
    Shorey, Shefaly
    JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES, 2022, 67 : E92 - E99
  • [44] Why parents of children with neurodevelopmental disabilities requiring gastrostomy feeding need more support
    Craig, GM
    Scambler, G
    Spitz, L
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2003, 45 (03): : 183 - 188
  • [45] A qualitative study of parent to parent support for parents of children with special needs
    Ainbinder, JG
    Blanchard, LW
    Singer, GHS
    Sullivan, ME
    Powers, LK
    Marquis, JG
    Santelli, B
    JOURNAL OF PEDIATRIC PSYCHOLOGY, 1998, 23 (02) : 99 - 109
  • [46] Parents of preterm-born children; sources of stress and worry and experiences with an early intervention programme - a qualitative study
    Kynø N.M.
    Ravn I.H.
    Lindemann R.
    Smeby N.A.
    Torgersen A.M.
    Gundersen T.
    BMC Nursing, 12 (1)
  • [47] Being parents of extremely preterm children, from a long-term perspective: A qualitative study of parents' experiences
    Starke, Veronica
    Diderholm, Barbro
    Heyman, Maria
    Blomqvist, Ylva Thernstrom
    EARLY HUMAN DEVELOPMENT, 2023, 183
  • [48] Parents Are the Experts: A Qualitative Study of the Experiences of Parents of Children With Severe Neurological Impairment During Decision-Making
    Bogetz, Jori F.
    Trowbridge, Amy
    Lewis, Hannah
    Shipman, Kelly J.
    Jonas, Danielle
    Hauer, Julie
    Rosenberg, Abby R.
    JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2021, 62 (06) : 1117 - 1125
  • [49] Dressing material in children with epidermolysis bullosa A qualitative study on experiences of parents and affected children
    Hartenstein-Pinter, Almut
    Huebner-Moehler, Bettina
    Zernikow, Boris
    Wager, Julia
    SCHMERZ, 2020, 34 (02): : 156 - 165
  • [50] Experiences of parents who have children with chronic kidney disease: A systematic review of qualitative studies
    Tong, Allison
    Lowe, Alison
    Sainsbury, Peter
    Craig, Jonathan C.
    PEDIATRICS, 2008, 121 (02) : 349 - 360