2012, Number 4
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Rev Cubana Hematol Inmunol Hemoter 2012; 28 (4)
Questionnaire to assess health-related quality of life in sickle cell adults
Martínez-Triana R, Martínez-Rodríguez M, Guerra-Romero C, Guerra-González EM, Machado- Almeida T, Machín-García S, Espinosa-Martínez E
Language: Spanish
References: 16
Page: 385-397
PDF size: 519.79 Kb.
ABSTRACT
Studies related to quality of life (HRQOL) in sickle cell disease are scarce and there
are no specific tools for assessment in Spanish. This article described the
development and validation of a brief specific questionnaire on quality of life in
sickle cell disease (CEB-S), which has been created to assess the quality of life in
patients with sickle cell disease on the basis of their own assessment on how this
disease affects their quality of life. The development of this instrument included
stages: creation of questions, pilot study and field study. The draft consisted of 33
Likert-type closed questions applied to 20 men and 20 women with sickle cell
disease. After an analysis, a second 4-scale thirty question version was
accomplished and then applied to 104 patients. Psychometric analysis included:
evaluation of reliability, validity, sensitivity, specificity, and efficiency. The reliability
of this questionnaire in terms of internal consistency by Cronbach index (physical
area 0.82; social area 0.82; emotional area 0.76; pain 0.85 and total 0.92) was
determined. Sixty nine patients yielded strong validity criterion consistent with the
SF-36 health questionnaire. CEB-S discriminant validity was demonstrated, by
comparing the results obtained in patients with any symptoms related to this
disease, with those obtained in asymptomatic patients and with the stratification of
patients according to the severity of anemia at the time of application. This version
was considered final.
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