Literature DB >> 22367767

Pain experience in children with advanced cancer.

Lois Van Cleve1, Cynthia E Muñoz, Matt L Riggs, Laura Bava, Marilyn Savedra.   

Abstract

BACKGROUND: It is important for health care professionals to understand the pain experience in children with advanced cancer. There has been increased attention to this topic, but systematic studies are limited.
OBJECTIVE: To examine pain symptoms and management in children with advanced cancer using child self-report and nurse documentation.
METHODS: A prospective, longitudinal method was used to collect data from 62 children over a 5-month period. Children were English and Spanish speaking, ages 6 to 17 years, with advanced cancer. Nurses also provided data.
RESULTS: Across all interviews, pain was reported 56% of the time by all children. Nurses documented pain only 23% of the time. Children most frequently reported head pain (31%), followed by abdomen, lower back, leg, and feet pain (20% to 30%). Children consistently reported more intense pain compared with nurses. Nonopioids were used more frequently (45%) than opioids (32%), and nurses' perception of pain intensity was more highly correlated with administration of opioids (r = .72, P < .001). Children who died during their participation in this study received more opioids over time. Pain intensity was relatively stable over time. Nurses noted ethnicity related differences with higher pain levels for Caucasian children, who received analgesics more frequently. DISCUSSION: The children consistently reported pain. Child self-report and nurse documentation of pain differed, as did pain management among children who died compared with those who did not. Ethnicity differences in the identification and management of pain by nurses begs further study. Overall, nurses were aware of and responsive to pain and pain management.

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Year:  2012        PMID: 22367767     DOI: 10.1177/1043454211432295

Source DB:  PubMed          Journal:  J Pediatr Oncol Nurs        ISSN: 1043-4542            Impact factor:   1.636


  4 in total

1.  Perspectives of children, family caregivers, and health professionals about pediatric oncology symptoms: a systematic review.

Authors:  Lei Cheng; Liying Wang; Mengxue He; Sheng Feng; Yehui Zhu; Cheryl Rodgers
Journal:  Support Care Cancer       Date:  2018-05-17       Impact factor: 3.603

2.  Palliative and end-of-life care for children with diffuse intrinsic pontine glioma: results from a London cohort study and international survey.

Authors:  Sophie E M Veldhuijzen van Zanten; Charlotte L L I van Meerwijk; Marc H A Jansen; Jos W R Twisk; Anna-Karenia Anderson; Lucy Coombes; Maggie Breen; Olivia J Hargrave; June Hemsley; Finella Craig; Ofelia Cruz; Gertjan J L Kaspers; Dannis G van Vuurden; Darren R Hargrave
Journal:  Neuro Oncol       Date:  2015-10-11       Impact factor: 12.300

3.  Quality of Life and Pain Experienced by Children and Adolescents With Cancer at Home Following Discharge From the Hospital.

Authors:  Joana Duran; Lilian Bravo; Vanessa Torres; Alexandra Craig; Jasmine Heidari; Kathleen Adlard; Rita Secola; Renee Granados; Eufemia Jacob
Journal:  J Pediatr Hematol Oncol       Date:  2020-01       Impact factor: 1.170

4.  Consistency of pediatric pain ratings between dyads: an updated meta-analysis and metaregression.

Authors:  Huaqiong Zhou; Matthew A Albrecht; Pam A Roberts; Paul Porter; Phillip R Della
Journal:  Pain Rep       Date:  2022-09-22
  4 in total

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