ASSESSMENT OF HEALTH QUALITY OF LIFE UPON SCHOOL AGE CHILDREN (6 – 12 ) WITH THALASSEMIA AT THALASSEMIA CENTRE IN IBN- BALADI HOSPITAL.

Authors

  • Khetam Mutsher AL-Mosooi

Abstract

Objectives: assess the QOL of thalassemia school age children and relation ship with some variables.  Methodology:  Non- probability (purposive) sample of (40) patient school age children with thalassemia hospitalized for management were selected .The questionnaire format designed for the purpose of the study, two instrument were used include : sample demographic characteristics QOL domain of thalassemia school children .  Data were analyzed by using frequencies, percentage. and multi-regression analysis Results: The result of the study indicated that the majority of the sample was the age group (9-11) and (6-8) and 75% of the subject of the study have (1-2) affected brothers . Regarding the age of onset shows that the majority of thalassemia have the disease between the (6-10) month of there life ,57.5% of the patient suffer from thalassemia major and 67.5% had family history. Over half (72.5%) of patient feel tired when he or she gait due to sign and symptom of there disease , majority of the sample  87.5% depended on blood transfusion and 85% of thalassemia patient need to desferal. While the majority of the patient 85% feel bad because can't do what their friend doing and 70% of patient felt comfort from other supported (nurse, doctor)  emotional and psychologically in the center and provide  what they need. Recommendation: The study recommend further studies should consider more generic measure of psychological and social functioning related QOL. In addition need for Educational program for those patients should be designed to help them live a better life  with hemophilia disease , the patients emphasize the importance of how to cope with their problems for a good QOL.

References

- Al-mosooi ,K.M: Burden of hemophilia type A and its treatment upon adolesent quality of life " University of Baghdad, Nursing College, June, 2004.

- Kuo Ht,Penq CT, Tsai MY (Pilot study on parental stress and behavioral adjustment to the thalassemia major disease process in children undergoing iron-chelation in western Taiwan) Hemoglobin 2006;30(2):301-9.

- Wonke- B( clinical management of bete- Thalassaemia Major) Semin- Hematol-2001 Oct., 38C4):350-q

- Datt, parul, Pediatric nursing ( second edition) Jaypee brothers medical publishers,2009, page:342-344

- Tiosano, -D and Hochberg, Z (Endocrine Complication of Thalassemia) Toural- Enabcrinal –Invest.2001 oct;24(9):716-23.

- WWW-Iron disorder.org,(2001).

- Aziz, P.M: Burdens of care upon family of Thalassemic children Sulaymania Governorate. University, 2000.

- Anie, K-A, Massaglia , -P(Psychological + Therapies for Thalassaemia), Cochrane- Dababass- Syst- Rew.2001,(S).

- Wong, D: Whaley and Wong’s essentials of pediatric nursing, (5th ed.), St.Louis: Mosby Company, 1997

- Donald, L.P.and Pennifer, E.:Health status and Health Policy Quality of life in health Care.Evaluation and Research Allocation.Newyourk, Oxford university, 1995,pp. 20-26.

Downloads

Published

2021-06-14

Issue

Section

Articles