Literature DB >> 16684166

The qualitative experience of Chinese parents with children diagnosed of cancer.

Maggie Y-F Wong1, Sally W-C Chan.   

Abstract

AIM: The present study aimed to describe the coping experiences of Chinese parents with children diagnosed as having cancer during the treatment stage.
BACKGROUND: Cancer is the second major cause of death among children in Hong Kong, it claims the lives of 60-70 children per year. Childhood cancer has tremendous impact on the family, especially the parents. It is, therefore, important to understand parents' psychological functioning and coping experience.
METHODS: A phenomenological approach was used. Data were collected by qualitative interviews and analysed following Colaizzi's phenomenological methodology. A purposive sample of nine parents whose children were diagnosed of having childhood cancer was recruited from a regional hospital in Hong Kong.
RESULTS: Four themes emerged describing parents' coping experiences: shock and denial, establishing the meaning or the situation, confronting the reality and establishing a new perspective. The initial reactions of the parents to the diagnosis were shock, denial and worry. However, they quickly accepted the reality and regarded their child's illness as their 'fate' that they had to accept. They were committed to the care of the sick child and seek informational and emotional support to cope with the situation. All of them were able to identify positive aspects from the illness experience and establish hope for the future. Chinese cultural beliefs might help the parents cope positively and avoid negative emotions.
CONCLUSION: This study found some commonalities of coping experience in both Western and Chinese culture. It adds knowledge to the coping experience of Chinese parents at the treatment phase of their children's illness and highlighted the need for emotional and information support for parents. RELEVANCE TO CLINICAL PRACTICE: Education programme and mutual support group would be helpful to parents. Nurses have to learn how different cultural groups and subcultural groups in the society cope to provide competent cultural care.

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Year:  2006        PMID: 16684166     DOI: 10.1111/j.1365-2702.2006.01297.x

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  12 in total

1.  Comparability of the Patient-Reported Outcomes Measurement Information System Pediatric short form symptom measures across culture: examination between Chinese and American children with cancer.

Authors:  Yanyan Liu; Changrong Yuan; Jichuan Wang; Jeanne Geiger Brown; Fen Zhou; Xiufang Zhao; Min Shen; Pamela S Hinds
Journal:  Qual Life Res       Date:  2016-05-10       Impact factor: 4.147

Review 2.  Family adjustment to childhood cancer: a systematic review.

Authors:  Kristin A Long; Anna L Marsland
Journal:  Clin Child Fam Psychol Rev       Date:  2011-03

3.  The emotional distress of children with cancer in China: an item response analysis of C-Ped-PROMIS Anxiety and Depression short forms.

Authors:  Yanyan Liu; Jingting Wang; Pamela S Hinds; Jichuan Wang; Nanping Shen; Xiufang Zhao; Jian Ding; Changrong Yuan
Journal:  Qual Life Res       Date:  2014-12-16       Impact factor: 4.147

4.  The effectiveness of solution-focused brief therapy for psychological distress among Chinese parents of children with a cancer diagnosis: a pilot randomized controlled trial.

Authors:  Anao Zhang; QingYing Ji; Jennifer Currin-McCulloch; Phyllis Solomon; YuTing Chen; Yaxi Li; Barbara Jones; Cynthia Franklin; Jack Nowicki
Journal:  Support Care Cancer       Date:  2018-03-15       Impact factor: 3.603

5.  Predictors of stress of parents of a child with cancer: a Jordanian perspective.

Authors:  Rami Masa'Deh; Jacqueline Collier; Carol Hall; Fadwa Alhalaiqa
Journal:  Glob J Health Sci       Date:  2013-09-04

6.  Parents' Voice in Managing the Pain of Children with Cancer during Palliative Care.

Authors:  Rina Mariyana; Allenidekania Allenidekania; Nani Nurhaeni
Journal:  Indian J Palliat Care       Date:  2018 Apr-Jun

7.  Information Needs Assessment among Parents of Children with Cancer.

Authors:  Mohammad Esmail Motlagh; Mehdi Mirzaei-Alavijeh; Seyyed Nasrollah Hosseini
Journal:  Asian Pac J Cancer Prev       Date:  2019-06-01

8.  The Effect of the Family-Centered Empowerment Model (FCEM) on the Care Burden of the Parents of Children Diagnosed with Cancer.

Authors:  Mahnaz Shoghi; Bahareh Shahbazi; Naimeh Seyedfatemi
Journal:  Asian Pac J Cancer Prev       Date:  2019-06-01

9.  Comparison of child and family reports of health-related quality of life in pediatric acute lymphoblastic leukemia patients after induction therapy.

Authors:  Shohei Nakajima; Iori Sato; Takafumi Soejima; Katsuyoshi Koh; Motohiro Kato; Yasuhiro Okamoto; Toshihiko Imamura; Miho Maeda; Yasushi Ishida; Atsushi Manabe; Kiyoko Kamibeppu
Journal:  BMC Pediatr       Date:  2020-08-19       Impact factor: 2.125

10.  Fear of abortion and emotional divorce in women with minor thalassemia: a population-based study in Yazd, Iran.

Authors:  Zohreh Rahaei; Mohammad Ali Sahami; Reza Bidaki
Journal:  BMC Womens Health       Date:  2021-12-07       Impact factor: 2.809

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