The impact of thalassemia on Southeast Asian and Asian Indian families in the United States: A qualitative study

Robert I Liem*, Brynnan Gilgour, Stephanie A. Pelligra, Maryann Mason, Alexis A Thompson

*Corresponding author for this work

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Objective: To describe the challenges, including sociocultural and socioeconomic barriers, faced by an urban immigrant population in the United States affected by thalassemia major. Design: Ethnographic, semi-structured, 1-on-1 interviews using an interview guide developed for this study. Digital recordings were transcribed and data analyzed using constant comparative method. Setting: University-based, Comprehensive Thalassemia Program at Children's Memorial Hospital, Chicago, IL, USA. Participants: Fourteen Southeast Asian and Asian Indian parents of children with transfusion dependent thalassemia. Main Outcome Measure: Qualitative descriptions of parental experiences, frequency of codes applied to interviews and emergent themes. Results: Thalassemia has its greatest impact on the emotional and social well-being of affected children and their parents. Current and future concerns were related to disease-specific complications and challenges with management such as transfusions and chelation therapy. These perceptions were tied to parental hope for a cure, a frequently coded coping mechanism. Despite their availability, few parents relied on support systems beyond immediate family members due to perceived public knowledge gaps about thalassemia. Culturally based past experiences and barriers did not emerge as dominant themes in our analysis. Conclusion: The impact of thalassemia is tremendous for affected children and their parents and is due more to factors that were either disease-specific or common to other chronic disease models rather than those influenced by culture. The unmet needs of these families require additional investigation to facilitate the development of initiatives aimed at improving quality of life and lessening overall impact of thalassemia.

Original languageEnglish (US)
Pages (from-to)361-369
Number of pages9
JournalEthnicity and Disease
Volume21
Issue number3
StatePublished - Jun 1 2011

Fingerprint

Thalassemia
Parents
Interviews
Hope
Chelation Therapy
Urban Population
beta-Thalassemia
Chronic Disease
Quality of Life
Outcome Assessment (Health Care)

Keywords

  • Asian Indian
  • Qualitative research
  • Southeast Asian
  • Thalassemia

ASJC Scopus subject areas

  • Epidemiology

Cite this

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title = "The impact of thalassemia on Southeast Asian and Asian Indian families in the United States: A qualitative study",
abstract = "Objective: To describe the challenges, including sociocultural and socioeconomic barriers, faced by an urban immigrant population in the United States affected by thalassemia major. Design: Ethnographic, semi-structured, 1-on-1 interviews using an interview guide developed for this study. Digital recordings were transcribed and data analyzed using constant comparative method. Setting: University-based, Comprehensive Thalassemia Program at Children's Memorial Hospital, Chicago, IL, USA. Participants: Fourteen Southeast Asian and Asian Indian parents of children with transfusion dependent thalassemia. Main Outcome Measure: Qualitative descriptions of parental experiences, frequency of codes applied to interviews and emergent themes. Results: Thalassemia has its greatest impact on the emotional and social well-being of affected children and their parents. Current and future concerns were related to disease-specific complications and challenges with management such as transfusions and chelation therapy. These perceptions were tied to parental hope for a cure, a frequently coded coping mechanism. Despite their availability, few parents relied on support systems beyond immediate family members due to perceived public knowledge gaps about thalassemia. Culturally based past experiences and barriers did not emerge as dominant themes in our analysis. Conclusion: The impact of thalassemia is tremendous for affected children and their parents and is due more to factors that were either disease-specific or common to other chronic disease models rather than those influenced by culture. The unmet needs of these families require additional investigation to facilitate the development of initiatives aimed at improving quality of life and lessening overall impact of thalassemia.",
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The impact of thalassemia on Southeast Asian and Asian Indian families in the United States : A qualitative study. / Liem, Robert I; Gilgour, Brynnan; Pelligra, Stephanie A.; Mason, Maryann; Thompson, Alexis A.

In: Ethnicity and Disease, Vol. 21, No. 3, 01.06.2011, p. 361-369.

Research output: Contribution to journalArticle

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T1 - The impact of thalassemia on Southeast Asian and Asian Indian families in the United States

T2 - A qualitative study

AU - Liem, Robert I

AU - Gilgour, Brynnan

AU - Pelligra, Stephanie A.

AU - Mason, Maryann

AU - Thompson, Alexis A

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N2 - Objective: To describe the challenges, including sociocultural and socioeconomic barriers, faced by an urban immigrant population in the United States affected by thalassemia major. Design: Ethnographic, semi-structured, 1-on-1 interviews using an interview guide developed for this study. Digital recordings were transcribed and data analyzed using constant comparative method. Setting: University-based, Comprehensive Thalassemia Program at Children's Memorial Hospital, Chicago, IL, USA. Participants: Fourteen Southeast Asian and Asian Indian parents of children with transfusion dependent thalassemia. Main Outcome Measure: Qualitative descriptions of parental experiences, frequency of codes applied to interviews and emergent themes. Results: Thalassemia has its greatest impact on the emotional and social well-being of affected children and their parents. Current and future concerns were related to disease-specific complications and challenges with management such as transfusions and chelation therapy. These perceptions were tied to parental hope for a cure, a frequently coded coping mechanism. Despite their availability, few parents relied on support systems beyond immediate family members due to perceived public knowledge gaps about thalassemia. Culturally based past experiences and barriers did not emerge as dominant themes in our analysis. Conclusion: The impact of thalassemia is tremendous for affected children and their parents and is due more to factors that were either disease-specific or common to other chronic disease models rather than those influenced by culture. The unmet needs of these families require additional investigation to facilitate the development of initiatives aimed at improving quality of life and lessening overall impact of thalassemia.

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