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Education and employment status of children and adults with thalassemia in North America
Author(s) -
Pakbaz Zahra,
Treadwell Marsha,
Kim HaeYoung,
Trachtenberg Felicia,
Parmar Nagina,
Kwiatkowski Janet L.,
Cunningham Melody J.,
Martin Marie,
Sweeters Nancy,
Neufeld Ellis J.,
Giardina Patricia J.,
Olivieri Nancy,
Yamashita Robert C.,
Vichinsky Elliott
Publication year - 2010
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.22565
Subject(s) - medicine , thalassemia , life expectancy , ethnic group , pediatrics , demography , multivariate analysis , deferiprone , chelation therapy , gerontology , population , environmental health , sociology , anthropology
Abstract Background Advances in the management of thalassemia have resulted in increased life expectancy and new challenges. We conducted the first survey of education and employment status of people with thalassemia in North America. Procedures A total of 633 patients (349 adults and 284 school age children) enrolled in the Thalassemia Clinical Research Network (TCRN) registry in Canada and the U.S. were included in the data analysis. Predictors considered for analysis were age, gender, race/ethnicity, site of treatment (Canada vs. United States), transfusion and chelation status, serum ferritin, and clinical complications. Results Seventy percent of adults were employed of which 67% reported working full‐time. Sixty percent had a college degree and 14% had achieved some post‐college education. Eighty‐two percent of school age children were at expected grade level. In a multivariate analysis for adults, Whites (OR = 2.76, 95% CI: 1.50–5.06) were more likely to be employed compared to Asians. Higher education in adults was associated with older age (OR = 1.67, 95% CI: 1.29–2.15), female gender (OR = 2.08, 95% CI: 1.32–3.23) and absence of lung disease (OR = 14.3, 95% CI: 2.04–100). Younger children (OR = 5.7 for 10‐year increments, 95% CI: 2.0–16.7) and Canadian patients (OR = 5.6, 95% CI: 1.5–20) were more likely to be at the expected education level. Neither transfusion nor chelation was associated with lower employment or educational achievement. Conclusions Individuals with thalassemia in North America can achieve higher education; however, full‐time employment remains a problem. Transfusion and chelation do not affect employment or education status of this patient population. Pediatr Blood Cancer. 2010;55:678–683. © 2010 Wiley‐Liss, Inc.