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Journal of Genetic Counseling, 14, 365-376.Īydinok Y, Kattamis A, Viprakasit V. Comparing Knowledge of ?-Thalassemia in Samples of Italians, Italian-Americans, and Non-ItalianAmericans. Diakses dari Online 14 November 2018.Īrmeli, C., Robbins, S.J., & Eunpu, D.L. Pemberdayaan Telenursing Menggunakan Aplikasi Skedit Untuk Edukasi Orang Tua Pasien Anak Dengan Talasemia. There was no difference in the level of adherence between the two groups (p: 0.987).Ĭonclusion: Providing education using WhatsApp through the SKEDit application and also booklets both effectively increase the level of parental knowledge and medication adherence of pediatric patients with thalassemia.Īndodo, C., (2019). There was no difference in the level of knowledge between the two groups (p: 0.994). There was no significant difference in the level of adherence of the pretest and posttest in the control group (p: 0.214). There was a significant difference in the level of adherence of the pretest and posttest in the intervention group (p: 0.028). Results: There was a significant difference in the level of knowledge in the pretest and posttest on the intervention group (p: 0.001) and the pretest and posttest in the control group (p: 0.001). The data were then analyzed using the Mann whitney and wilcoxon test. Parental knowledge was measured using a Parental knowledge about Thalassemia questionnaire and the level of adherence was measured using an indirect method known as 'Pill Count'.
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The total sample was 61 respondents with purposive sampling technique. Method: The study was quasi-experimental using pre and post-test with control group. Objective: To identify the effect of the implementation of education using WhatsApp through the SKEDit application compared to using booklets on parental knowledge and medication adherence in pediatric patients with thalassemia. The implementation of education using WhatsApp is expected to increase parental knowledge of the illness and children to adhere to iron chelation therapy. Background: Excess iron levels and low hemoglobin (Hb) levels are one of the complications of Beta-Thalassemia.