Chronic pain prevalence and quality of life in survivors of paediatric cancer: A systematic review

Anna Hurley-Wallace; Daniel Schoth; Christina Liossi

doi:10.1002/pon.4639

Chronic pain prevalence and quality of life in survivors of paediatric cancer: A systematic review

Anna Hurley-Wallace^*, Daniel Schoth (Editor), Christina Liossi (Editor)

^*Corresponding author for this work

Bristol Medical School (THS)

Research output: Contribution to conference › Conference Poster › peer-review

Abstract

Background: As survival rates of paediatric cancers continue to improve, there is a growing need for research into survivorship, particularly in children and adolescents.

Aims: This study will a) systematically review current literature on the prevalence of chronic pain (CP) in survivors of childhood cancer, b) review the relationship between pain prevalence in paediatric cancer survivors and health-related quality of life (HRQOL), and c) compare CP and HRQOL between adult survivors of paediatric cancer (18+) and survivors within the paediatric age range (0-18).

Methods: A systematic review will be conducted in accordance with PRISMA guidelines. Studies will be identified via a search of Medline, PsychINFO, Web of Science, CINAHL, PubMed, Scopus, Cochrane Library, Google Scholar and OpenGrey databases from inception of the databases to November 2017.

We will include all study formats reporting any point or period prevalence estimates, from a survivor sample (i.e., not currently receiving cancer treatment), diagnosed with cancer between 0 and 18 years and experiencing chronic pain, i.e., defined as pain in one or more body locations, lasting for a period of 3 months or longer.

The articles will be appraised using a risk of bias tool developed specifically for prevalence studies (Hoy et al., 2012).

Results: The studies will be synthesised and pooled prevalence estimates will be calculated for chronic pain in adult and paediatric survivors of childhood cancer. The results will be discussed in light of relevant findings.

Conclusions: Recommendations for further research will be made regarding the clinical care of survivors.

Original language	English
DOIs	https://doi.org/10.1002/pon.4639
Publication status	Published - 1 Mar 2018
Event	2018 Annual Conference of the British Psychosocial Oncology Society - Southampton, United Kingdom Duration: 8 Mar 2018 → 9 Mar 2018

Conference

Conference	2018 Annual Conference of the British Psychosocial Oncology Society
Country/Territory	United Kingdom
City	Southampton
Period	8/03/18 → 9/03/18

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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@conference{880aa4684f7d44e5bf1e4c72b0e5b90b,

title = "Chronic pain prevalence and quality of life in survivors of paediatric cancer: A systematic review ",

abstract = "Background: As survival rates of paediatric cancers continue to improve, there is a growing need for research into survivorship, particularly in children and adolescents. Aims: This study will a) systematically review current literature on the prevalence of chronic pain (CP) in survivors of childhood cancer, b) review the relationship between pain prevalence in paediatric cancer survivors and health-related quality of life (HRQOL), and c) compare CP and HRQOL between adult survivors of paediatric cancer (18+) and survivors within the paediatric age range (0-18). Methods: A systematic review will be conducted in accordance with PRISMA guidelines. Studies will be identified via a search of Medline, PsychINFO, Web of Science, CINAHL, PubMed, Scopus, Cochrane Library, Google Scholar and OpenGrey databases from inception of the databases to November 2017. We will include all study formats reporting any point or period prevalence estimates, from a survivor sample (i.e., not currently receiving cancer treatment), diagnosed with cancer between 0 and 18 years and experiencing chronic pain, i.e., defined as pain in one or more body locations, lasting for a period of 3 months or longer. The articles will be appraised using a risk of bias tool developed specifically for prevalence studies (Hoy et al., 2012). Results: The studies will be synthesised and pooled prevalence estimates will be calculated for chronic pain in adult and paediatric survivors of childhood cancer. The results will be discussed in light of relevant findings. Conclusions: Recommendations for further research will be made regarding the clinical care of survivors. ",

author = "Anna Hurley-Wallace and Daniel Schoth and Christina Liossi",

year = "2018",

month = mar,

day = "1",

doi = "10.1002/pon.4639",

language = "English",

note = "2018 Annual Conference of the British Psychosocial Oncology Society ; Conference date: 08-03-2018 Through 09-03-2018",

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Chronic pain prevalence and quality of life in survivors of paediatric cancer: A systematic review . / Hurley-Wallace, Anna; Schoth, Daniel (Editor); Liossi, Christina (Editor).
2018. Poster session presented at 2018 Annual Conference of the British Psychosocial Oncology Society , Southampton, United Kingdom.

Research output: Contribution to conference › Conference Poster › peer-review

TY - CONF

T1 - Chronic pain prevalence and quality of life in survivors of paediatric cancer

T2 - 2018 Annual Conference of the British Psychosocial Oncology Society

AU - Hurley-Wallace, Anna

A2 - Schoth, Daniel

A2 - Liossi, Christina

PY - 2018/3/1

Y1 - 2018/3/1

N2 - Background: As survival rates of paediatric cancers continue to improve, there is a growing need for research into survivorship, particularly in children and adolescents. Aims: This study will a) systematically review current literature on the prevalence of chronic pain (CP) in survivors of childhood cancer, b) review the relationship between pain prevalence in paediatric cancer survivors and health-related quality of life (HRQOL), and c) compare CP and HRQOL between adult survivors of paediatric cancer (18+) and survivors within the paediatric age range (0-18). Methods: A systematic review will be conducted in accordance with PRISMA guidelines. Studies will be identified via a search of Medline, PsychINFO, Web of Science, CINAHL, PubMed, Scopus, Cochrane Library, Google Scholar and OpenGrey databases from inception of the databases to November 2017. We will include all study formats reporting any point or period prevalence estimates, from a survivor sample (i.e., not currently receiving cancer treatment), diagnosed with cancer between 0 and 18 years and experiencing chronic pain, i.e., defined as pain in one or more body locations, lasting for a period of 3 months or longer. The articles will be appraised using a risk of bias tool developed specifically for prevalence studies (Hoy et al., 2012). Results: The studies will be synthesised and pooled prevalence estimates will be calculated for chronic pain in adult and paediatric survivors of childhood cancer. The results will be discussed in light of relevant findings. Conclusions: Recommendations for further research will be made regarding the clinical care of survivors.

AB - Background: As survival rates of paediatric cancers continue to improve, there is a growing need for research into survivorship, particularly in children and adolescents. Aims: This study will a) systematically review current literature on the prevalence of chronic pain (CP) in survivors of childhood cancer, b) review the relationship between pain prevalence in paediatric cancer survivors and health-related quality of life (HRQOL), and c) compare CP and HRQOL between adult survivors of paediatric cancer (18+) and survivors within the paediatric age range (0-18). Methods: A systematic review will be conducted in accordance with PRISMA guidelines. Studies will be identified via a search of Medline, PsychINFO, Web of Science, CINAHL, PubMed, Scopus, Cochrane Library, Google Scholar and OpenGrey databases from inception of the databases to November 2017. We will include all study formats reporting any point or period prevalence estimates, from a survivor sample (i.e., not currently receiving cancer treatment), diagnosed with cancer between 0 and 18 years and experiencing chronic pain, i.e., defined as pain in one or more body locations, lasting for a period of 3 months or longer. The articles will be appraised using a risk of bias tool developed specifically for prevalence studies (Hoy et al., 2012). Results: The studies will be synthesised and pooled prevalence estimates will be calculated for chronic pain in adult and paediatric survivors of childhood cancer. The results will be discussed in light of relevant findings. Conclusions: Recommendations for further research will be made regarding the clinical care of survivors.

U2 - 10.1002/pon.4639

DO - 10.1002/pon.4639

M3 - Conference Poster

Y2 - 8 March 2018 through 9 March 2018

ER -

Chronic pain prevalence and quality of life in survivors of paediatric cancer: A systematic review

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