Psychosocial Impairment and Lower Quality of Life among Childhood Cancer Survivors in Egypt, Single Institution Experince.

Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 5528-5528
Author(s):  
Mona Elsamahy ◽  
Ashraf Abdelmonem ◽  
Shahinda Abdelrahman

Abstract Survival itself has, until recently, been the marker of successful cancer therapy, but now more attention is being focused on the long-term effects of cancer therapy and the quality of life (QOL)of the survivors. OBJECTIVE: To assess health related quality of life and behavior and emotional problems among childhood cancer survivors at Ain Shams Pediatric Oncology Clinic, Cairo, Egypt. DESIGN: This study was conducted on 30 childhood cancer survivors attending the cancer survivors’ clinic at Ain Sham Children’s University Hospital in the period of October 2004–April 2005. The PedsQL™ 4.0 Generic Core Scales (physical, emotional, social and, school functioning) translated into Arabic language has been utilized. Parallel child self-report and parent proxy-report questionnaire formats have been used. Items were reverse-scored and linearly transformed to a 0–100 scale, so that higher scores indicate better QOL. Assessment of behavioral and emotional disturbance was performed using The Child Behavior Checklist (CBCL) Results: Age range 6–16 years with a mean age of 10.7±2.9 years, 18 (60%) were males and 12(40%) were females. Seventeen patients (56.6%) were acute leukemia survivors and 10(43.4%) lymphomas and solid tumors. There was statistically significant (p<0.001) decrease in the overall generic PedsQL in cancer survivors (mean 67±11.6) compared to normal children (mean 83.9±12.5) with school functioning area being the most affected (score 47.5±13). ALL survivors had significantly lower mean QOL (62.5±11.8) compared to other cancer survivors (72.8±8.8) (p<0.05). Gender (females) and CNS-directed therapy were risk factors for poorer QOL. Strong agreement between parents and their children QOL rating was seen in most of the QOL domains {overall QOL (p=0.001) physical well being (p=0.04), emotional feelings (p=0.0004), and social interaction (p=0.003) with the strongest correlation in the school domain (p=0.000004)}. Fifty three percent of the survivors showed clinical range of social incompetence with survivors who were diagnosed before the age of 3 were less socially competent than those who were diagnosed after this age (p<0.05), 63% expressed Internalizing behavioral problems and while 23% had Externalizing problems. CONCLUSION: This results demonstrate Chidhood cancer survivors are at significant risk of poor psychosocial functioning and QOL.

2004 ◽  
Vol 13 (1) ◽  
pp. 49-56 ◽  
Author(s):  
Sigrid Pemberger ◽  
Reinhold Jagsch ◽  
Eva Frey ◽  
Rosemarie Felder-Puig ◽  
Helmut Gadner ◽  
...  

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 1319-1319 ◽  
Author(s):  
Hyeon Jin Park ◽  
Yoon Yi Kim ◽  
Young Ae Kim ◽  
Young Ho Yun ◽  
Byung Ho Nam ◽  
...  

Abstract Purpose : Remarkable improvements in survival of children with cancer have resulted in a growing population of Korean childhood cancer survivors. However, long-term survivors are at risk for developing a broad spectrum of adverse outcomes. Therefore increasing emphasis is now being placed on health-related quality of life (HRQL) of Korean childhood cancer survivors. The Minneapolis-Manchester Quality of Life Instrument (MMQL) is a standardized patient self-report instrument designed to assess HRQL in childhood cancer survivors. In order to create an appropriate scale for the HRQL assessment of Korean childhood cancer survivors, the Korean version of MMQL-Youth Form (YF) (8 to 12 years) and MMQL-Adolescent Form (AF) (13 to 20 years) were cross-culturally adapted into Korean and its reliability and validity were evaluated. Patients and Methods : The translation procedure followed the standard Functional Assessment of Chronic Illness Therapy (FACIT) translation methodology. The patients who were given the diagnosis of cancer participated in this study. The subjects consist of 4 groups, which are 8–12 and 13–20 aged patients undergoing treatment after the diagnosis of cancer, and 8–12 and 13–20 aged patients who were more than 1 year after terminating treatment. Factor analysis uses the pattern of inter-item correlations to produce clusters of items that have substantial correlations with one another. The stability was tested by readministering the MMQL to a subset of participants of each group after a 2-week interval. Cronbach’s coefficient alpha was used to assess the internal consistency. Discriminate validity was determined by comparing children undergoing treatment with children off therapy. Construct validity was conducted by comparing the patient responses of MMQL with their mothers responses of Child Health Questionnaire Parent version (CHQ-PF50). Results : The MMQL-YF were administered to 63 children undergoing treatment and their mothers and 66 off-therapy cancer survivors and their mothers. The MMQL-AF were administered to 60 children undergoing treatment and their mothers and 85 off-therapy cancer survivors and their mothers. Test-retest reliability of MMQL-YF (Cronbach’s a=0.76) and MMQL-AF (Cronbach’s a=0.82) demonstrated that both instruments were stable in all questionnaires. For internal consistency reliability, overall Cronbach’s alpha coefficient was 0.86 for the Korean version of MMQL–YF and 0.90 for the Korean version of AF. These results indicate that the items constituting the MMQL-YF and MMQL-AF were consistent internally. The MMQL-YF and MMQL-AF were able to discriminate between children undergoing treatment and off-therapy cancer survivors. The scales of MMQL-YF and MMQL-AF were highly correlated with similar CHQ-PF50 domains. Conclusion : This study provides evidence for the reliability and validity of the Korean version of MMQL-YF and MMQL-AF as a comprehensive, multidimensional self-report instrument for measuring HRQL among Korean childhood cancer survivors.


2012 ◽  
Vol 35 (6) ◽  
pp. 447-455 ◽  
Author(s):  
Ho Cheung William Li ◽  
Oi Kwan Joyce Chung ◽  
Ka Yan Eva Ho ◽  
Sau Ying Chiu ◽  
Violeta Lopez

Author(s):  
Keagan G. Lipak ◽  
Joseph R. Rausch ◽  
Rachel S. Fisher ◽  
Kemar V. Prussien ◽  
Olivia E. Clark ◽  
...  

2007 ◽  
Vol 16 (7) ◽  
pp. 1211-1220 ◽  
Author(s):  
Tara E. O’Leary ◽  
Lisa Diller ◽  
Christopher J. Recklitis

Author(s):  
Mary S. McCabe ◽  
Stacie Corcoran

Being told you are cancer-free does not mean you are free of the consequences of the disease. Seventy-six percent of cancer survivors are over age 60 years and have coexisting medical conditions that complicate posttreatment recovery to maximum health. Childhood cancer survivors also carry a heavy burden of medical and psychological problems resulting from their experience with cancer. Cancer diagnosis and treatment affects the family as well as the patient. Improvements are needed in the coordination of care for cancer survivors to assure optimal quality of life.


2010 ◽  
Vol 91 (5) ◽  
pp. 865-876 ◽  
Author(s):  
Yasushi Ishida ◽  
Misato Honda ◽  
Shuichi Ozono ◽  
Jun Okamura ◽  
Keiko Asami ◽  
...  

2011 ◽  
Vol 19 (9) ◽  
pp. 1275-1287 ◽  
Author(s):  
Anne F. Klassen ◽  
Samantha J. Anthony ◽  
Aalia Khan ◽  
Lillian Sung ◽  
Robert Klaassen

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