A recurring rollercoaster ride: a qualitative study of the emotional experiences of parents of children with juvenile idiopathic arthritis

被引:41
作者
Gomez-Ramirez, Oralia [1 ]
Gibbon, Michele [2 ]
Berard, Roberta [3 ,4 ]
Jurencak, Roman [5 ,6 ]
Green, Jayne [7 ]
Tucker, Lori [8 ,9 ]
Shiff, Natalie [10 ,11 ]
Guzman, Jaime [8 ,9 ]
机构
[1] Univ British Columbia, Dept Anthropol, 6303 NW Marine Dr, Vancouver, BC V6T 1Z1, Canada
[2] Childrens Hosp Eastern Ontario, Div Rheumatol, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada
[3] Univ Western Ontario, Dept Pediat, 800 Commissioners Rd East, London, ON N6A 5W9, Canada
[4] Childrens Hosp, London Hlth Sci Ctr, 800 Commissioners Rd East, London, ON N6A 5W9, Canada
[5] Univ Ottawa, Dept Pediat, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada
[6] Childrens Hosp Eastern Ontario, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada
[7] British Columbia Childrens Hosp, Room K4-116,4480 Oak St, Vancouver, BC V6H 3V4, Canada
[8] Univ British Columbia, Dept Pediat, 4480 Oak St, Vancouver, BC V6H 3V4, Canada
[9] British Columbia Childrens Hosp, 4480 Oak St, Vancouver, BC V6H 3V4, Canada
[10] Univ Florida, Dept Pediat, 1600 Archer Rd, Gainesville, FL USA
[11] Univ Saskatchewan, Dept Epidemiol & Community Hlth, 1600 Archer Rd, Gainesville, FL USA
关键词
Juvenile arthritis; Emotions; Parents; Canada; Qualitative research; Secondary analysis; HEALTH-CARE; OF-LIFE; ATTITUDES; MOTHERS; FATHERS; DIAGNOSIS; OUTCOMES; GENDER; HEART;
D O I
10.1186/s12969-016-0073-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Despite the wealth of clinical research carried out in children with juvenile idiopathic arthritis (JIA), little is known about the emotional experiences of their parents. This article describes the predominant emotional experiences reported by parents of children with JIA in two Canadian cities. Methods: Research participants included 15 experienced parents and 8 novice parents (<6 months since children's JIA diagnosis). Their children were 2 to 16 years old with various JIA categories. A qualitative dataset including audio recordings and verbatim transcripts of three focus groups, and written reports of 59 reciprocal interviews (parents interviewing each other) were examined by a multidisciplinary research team following a four-step qualitative analytical process. Results: Parents of children with JIA experienced recurrent mixed negative and positive emotions that varied over time. Between disease onset and diagnosis, mounting anxiety, fear and confusion were the predominant emotions. Shortly after diagnosis there were shock, disbelief, and fear, with a sense of having being blindsided by the disease. At times of disease quiescence there was hope and gratitude, but also fatigue and frustration with ongoing treatment and fear of flares. During periods of increasing or ongoing symptoms there was admiration and sympathy for the courageous way children coped with JIA, as well as sorrow and frustration for ongoing pain and limitations. There were at times, frustration and indignation with peers and teachers unable to understand the child's fluctuations in physical activity and schoolwork. Throughout the disease, parents felt an underlying anxiety and powerlessness. Conclusions: Parents of children with JIA described complex emotional journeys akin to the recurring ups and downs of rollercoaster rides, instead of ordered emotional phases ending in resolution. This has implications for healthcare providers who need to be aware of the complexity of these emotional journeys to support parents more effectively, thereby helping improve patient outcomes.
引用
收藏
页数:11
相关论文
共 47 条
  • [31] Parents' Emotional and Social Experiences of Caring for a Child Through Cleft Treatment
    Nelson, Pauline A.
    Kirk, Susan A.
    Caress, Ann-Louise
    Glenny, Anne-Marie
    [J]. QUALITATIVE HEALTH RESEARCH, 2012, 22 (03) : 346 - 359
  • [32] Long-term outcomes and predictors of outcomes for patients with juvenile idiopathic arthritis
    Oen, K
    [J]. BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2002, 16 (03): : 347 - 360
  • [33] Illness trajectories in Mexican children with juvenile idiopathic arthritis and their parents
    Pelaez-Ballestas, I.
    Romero-Mendoza, M.
    Ramos-Lira, L.
    Caballero, R.
    Hernandez-Garduno, A.
    Burgos-Vargas, R.
    [J]. RHEUMATOLOGY, 2006, 45 (11) : 1399 - 1403
  • [34] Attitudes Toward HPV Vaccination Among Low-Income and Minority Parents of Sons: A Qualitative Analysis
    Perkins, Rebecca B.
    Tipton, Hailey
    Shu, Elaine
    Marquez, Cecilia
    Belizaire, Myrdell
    Porter, Courtney
    Clark, Jack A.
    Pierre-Joseph, Natalie
    [J]. CLINICAL PEDIATRICS, 2013, 52 (03) : 231 - 240
  • [35] Plutchik R, 2001, AM SCI, V89, P344, DOI 10.1511/2001.4.344
  • [36] Qualitative research in health care - Analysing qualitative data (Reprinted from Qualitative Research in Health Care)
    Pope, C
    Ziebland, S
    Mays, N
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2000, 320 (7227): : 114 - 116
  • [37] Assessing the minimal important difference in symptoms: A comparison of two techniques
    Redelmeier, DA
    Guyatt, GH
    Goldstein, RS
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 1996, 49 (11) : 1215 - 1219
  • [38] Safeguarding precarious survival: Parenting children who have life-threatening heart disease
    Rempel, Gwen R.
    Harrison, Margaret J.
    [J]. QUALITATIVE HEALTH RESEARCH, 2007, 17 (06) : 824 - 837
  • [39] How do parents of children with juvenile idiopathic arthritis (JIA) perceive their therapies?
    Rouster-Stevens, Kelly
    Nageswaran, Savithri
    Arcury, Thomas A.
    Kemper, Kathi J.
    [J]. BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2008, 8 (1):
  • [40] Determinants of Health-Related Quality of Life in Children Newly Diagnosed With Juvenile Idiopathic Arthritis
    Seid, Michael
    Huang, Bin
    Niehaus, Stacey
    Brunner, Hermine I.
    Lovell, Daniel J.
    [J]. ARTHRITIS CARE & RESEARCH, 2014, 66 (02) : 263 - 269