Background: Worldwide thalassemia poses a serious public health problem due to the high prevalence. Globally, 15 million people are suffering from clinically thalassemic disorders. Objective: To describe the lived experience of thalassaemic children in Bangladesh. Methods: This study was conducted following a descriptive qualitative research approach. Twenty thalassemic children were recruited purposively in the present study. Semi-structured individual's interview guidelines were used to collect in depth information. In addition, digital recorder was used to capture the children's voice. Data were analyzed using the process of content analysis. This study was approved by the Institutional Review Board (IRB), NIANER. Results: The mean age of the thalassemic children was (16.05) SD = 1.877. Most of the children were Muslim (95.0%) and they study at school (70.0%). Most of their mothers were (90.0%) housewife. This study revealed four major themes and eleven subthemes based on the experience of thalassemic children: 1) understanding of children meaning of thalassaemia: perception of children, unable to perform daily activities, and educational impact, 2) feeling frustrating experience and disease management: feelings about long term treatment, coping and altered body image, 3) family relationship: differences from siblings, parental attention and feeling burden, and 4) social interactions: sharing with peer, inability to social interaction. Conclusion: This study indicated that thalassaemia has affected negatively on several areas of health of these children including physical, emotional, social financial and educational areas. Reducing these problems requires comprehensive constant support and surveying health and medical status of these children to promote care and decrease the suffering of thalassaemic children. The findings of the present study are grounds for further research in a wider range to describe the different areas of the experience of thalassaemic children.
Background: Diabetes Mellitus (DM) has been a global epidemic in the new millennium and the majority of all diabetic patients constitute Type 2 diabetes mellitus. Medication adherence to prescribed treatments is a key determinant to achieve therapeutic success reduces diabetic complications. Objectives: The aim of the study was to examine the level of medication adherence to Type 2 diabetic patients hospitalized at tertiary care hospital in Bangladesh. Methods: The study was descriptive cross-sectional design. A total of 112 Type 2 diabetic patients were conveniently recruited from tertiary care hospital in Bangladesh. Results: The mean age of the participants was 57.46 (SD=11.65) years. More than half of the patients (60.7%) were male and majority of them (94.6%) were married. The mean score of diabetic medication adherence was calculated as 26.46 (SD=1.58). Adherence to diabetic medications was significantly associated with age (p=.01), occupation (p=.003), duration of DM (p=.003), oral hypoglycemic agents (p=.02), HbA1c (p=< .01) and Fasting Blood Ssugar (p=< .01). Medication non-adherence significantly found in patients with presence of diabetic retinopathy (p=<.01), microabuminuria (p=.01), dyslipidemia (p=.006), hypertension (p=.01) and other chronic diseases (p=.01). Conclusion: The level of medication adherence among Type 2 diabetic patients was found to be suboptimal. Good adherence has beneficial effects on HbA1c and FBS. For improving adherence particular focus should pay to diabetic patients with different age groups and the presence of comorbidities. Keywords: Medication Adherence; Type 2 Diabetes Mellitus; Oral Hypoglycemic Agents; Comorbidities.
Background: The childhood cancer is increasing throughout the world. The incidence of children and adolescent (1-19 years old) mortality by cancer was 4.49 by 2006 (Korea Statistics, 2014). Mothers of children experienced a difficult situation in coping when their children were diagnosed with cancer. Based on Mishel's Uncertainty in Illness Theory, maternal uncertainty and perceived social support are important factors that may have an impact on maternal coping in mothers of children with cancer. Therefore, it was worth to investigate this phenomenon in the context of Korea where no such study was conducted. Objective: To identify the factors affecting maternal coping in mothers of children with cancer. Methods: The study was conducted by using a descriptive design. This study was approved by the Institutional Review Board, Yonsei Health System, Severance Hospital, Seoul, Korea and informed consent forms were obtained from the participants. Fifty-nine mothers completed three questionnaires: 1) Parent's Perception of Uncertainty Scale, 2) Multidimensional Scale of Perceived Social Support, and 3) Coping Health Inventory for Parents. The internal consistency of these instruments was satisfactory, all with alpha coefficients over 0.86. Results: Hierarchical multiple regression analysis revealed that perceived social support and maternal uncertainty together explained 35% of the variance in the maternal coping in mothers of children with cancer (R 2 = 0.353, F = 15.255, p = 0.000). Perceived social support and maternal uncertainty had an impact on maternal coping. Conclusions: The findings provided information that could be used in a further intervention study to increase maternal coping in mothers of children with cancer.
Background: Globally, maternal and infant morbidity and mortality is a serious public health problem. Maternal mortality rate in Bangladesh is 176 per lack live births which remain high as Government set target to be achieved by 2016. Antenatal care is extremely important health care service for the mothers' and unborn fetus during pregnancy. It is well recognized that good antenatal care improves maternal, perinatal and neonatal outcomes. Objective: To identify the maternal awareness of antenatal care on impact of mothers' and newborn health in Bangladesh. Methods: The study was conducted by using descriptive and cross-sectional design. This study was approved by the appropriate authority and informed consent forms were obtained from the participants. Two hundred forty-one of rural and two hundred one urban mothers completed three sets of questionnaires: 1) Socio-demographic, 2) Maternal Awareness and 3) Impact of Awareness. Content validity was done by the experts and internal consistency of these instruments was satisfactory with Cronbach's alpha over 0.74. Result: The average awareness scores of rural and urban mothers were 18.54 ± 2.77 and 19.69 ± 2.16 respectively. The mean scores of impact on rural and urban mothers were 9.41 ± 2.13 and 9.39 ± 2.25 respectively. Maternal' awareness of antenatal care; impact of mothers' and newborn health were found statistically significant (t = 68.54, p < 0.001) and (t = 59.11, p < 0.001) different among rural and urban mother's. It was observed that maternal' awareness of antenatal care and impact of mothers' and newborn health were significantly difference between rural and urban mothers' (x 2 = 211.869, p 0.004 and (x 2 = 157.772, p 0.002 respectively). Conclusions: The findings indicated that maternal' awareness of antenatal care on impact of mothers' and newborn health was statistically significant different between How to cite this paper: Khatun, M
Background: Complementary feeding is a significant milestone that has nutritional, developmental, and health implications. Worldwide, 33% of the deaths are linked to malnutrition. Objective: To describe the mothers' experience about complementary feeding practice with child aged less than two years in Bangladesh. Method: A descriptive qualitative study was conducted from July 2018 to June 2019. This study was approved by the Institutional Review Board (IRB) NIANER. 20 mothers of children of 6 -24 months of age were recruited purposively who live in Sattalla slum. Descriptive statistics were used to analyze the mothers' demographic characteristics and thematic analysis was used to describe mothers' experience about complementary feeding practice. Results: The study showed that the average age of the mothers was 25 (SD = 4.75) years. Only 5% of the mothers have higher education. Through the findings, two main themes have been identified. Moreover, first main theme includes three subthemes. Fifty percent of the mothers stated that appropriate time to start complementary food for their babies is from 6 months of age. Mothers feed various types of complementary foods. Most of the mothers have knowledge about complementary feeding but they do not practice appropriately. Almost all of the mothers (95%) stated that their babies do not like to eat anything, and 45% of mothers feed only breast milk. Conclusion: Findings of the study will provide information for the nurses resulted in increasing the rate of complementary feeding practice among mothers of children in Bangladesh. Future study is needed to identify the factors influencing complementary feeding practice among mothers of 6 -24 months old children in Bangladesh.
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