8 research outputs found

    Mapping of children with malnutrition in kelantan utilizing open geographic information system (gis) and remote sensing platform

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    The Mapping of Children with Malnutrition in Kelantan Utilizing Open Source Geographic Information System (GIS) and Remote Sensing Platform" study was started at 31 October until 30 September 2010 and extends till 31 December 2010. This study was one of the university research {RU) grant headed by Prof. Zabidi Azhar Husin @ Mohd Hussin. The main objective of this study was to identify malnourish children (severe) from 1 day to 6 years old from 12 clinics in Kota Bharu via mapping the location of children with USM Growth Monitor and Geoinformation System {GIS).In this study, data collection was done through the "USM Growth Monitor" online system produced in this study. Through this system, raw data from all the clinic were entered by the nurses involve at the clinic and is able to retrieve direct to research centre at USM. Data regarding Geoinformation System such as soil structure, water source and so on were getting from Malaysian Remote Sensing Agency (ARSM). Kota Bharu district was chosen as a study area for this research from 10 districts in Kelantan after successful research at Tum pat {2007). At the beginning of the study, Anthropometric data such as date of birth, birth weight, birth length and also weaning information of the children aged between 1 day to 6 years old were assemble from every health clinic (Kiinik Kesihatan in Kota Bharu District. Birth weight and length data according to children age were converting to nutritional status using Epilnfo programme (Epi Info'" Version 3.4). The total of 4616 data were collected consist of 2285 {49.5%) boys and 2331{50.5%) girls. Outcome from nutritional status analysis shown that 3.4% of the children were Overweight, 15.3% were undernourished [10.3% were moderate undernourished {-2SD) and 4.5% were severe undernourished {-3SD)]. From this preliminary result, Remote sensing techniques were using to identify the home location of the children and correlation with GIS information and nutritional status were assessed

    Makanlah sayang... resepi sihat & mudah untuk anak-anak

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    Buku ini diterbitkan dengan tujuan membantu ibu bapa atau penjaga anak-anak, khususnya anak-anak istimewa dalam menyediakan makanan alternatif bagi mempelbagaikan jenis makanan di dalam diet seharian anak-anak mereka. Setiap menu ini mempunyai kandungan tenaga yang tinggi serta memenuhi kriteria makanan lengkap, mengandungi semua kelas makanan dan vitamin serta mineral khusus. Maklumat nutrien untuk setiap makanan telah dilakukan melalui pengiraan mengunakan perisian NutritionistPro. Menu sebegini diperlukan terutama untuk kanak-kanak yang mempunyai kebolehan mengunyah dan menelan yang terhad. Kandungan tenaga, protein, vitamin dan setiap mineral telah dibandingkan mengikut Saranan Pengambilan Nutrient (RNI, 2017). Manakala kandungan kanji (karbohidrat), lemak dan serat telah dibandingkan mengikut saranan Institute of Medicine (2005). Saranan ini sesuai untuk kanak-kanak yang berusia 2 hingga 18 tahun

    The study of glucose-6-phosphate dehydrogenase (G6PD) gene by restriction enzyme by restriction enzyme digestion in the Kelantan population

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    The most common diseases producing enzymopathy affecting the human population is glucose-6-phosphate dehydrogenase (G6PD) deficiency. It is estimated that about 400 million people worldwide are affected and this disease is commonest seen in the tropical and subtropical zones of the Eastern hemisphere. Molecular analysis has confirmed that the basis for G6PD deficiency is widely heterogeneous. Different mutants are responsible for the G6PD deficiency in the various parts of the world where this abnormality is prevalent. This study involved a sequential analysis whereby the blood from Malay neonates with neonatal jaundice admitted to Hospital Universiti Sains Malaysia and Kota Bharu Hospital were analyzed and polymerase chain reaction based analysis using serial multiplex primer method was done on those DNA samples. Samples that are found to be abnormal were then sequenced. Out of the 45 samples studied, 8 were found to have the Mediterranean mutation, two have the Mahidol mutation, two have Canton mutation and three have Kaiping mutation. Thus the molecular basis for the Malay neonatal jaundice in Kelantan is described with further prospect of population screening

    Psychological distress and associated factors in parents of children with cancer

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    Introduction: Diagnosis of cancer in children poses a challenging situation for parents to cope with. Method: Seventy-nine (N = 79) parents whose children are receiving treatment for cancer in Hospital Universiti Sains Malaysia participated in this cross-sectional descriptive study. They completed a set questionnaire measuring their level of anxiety and stress, knowledge about cancer, and amount of activities they perform with or for the child to enhance the child’s coping abilities, in addition to children’s psychological problems. Socio-demographic information was obtained. Results: Parents with higher cancer knowledge reported reduced stress (p<0.01) and anxiety (p<0.05). The higher the income (p<0.05) and education (p<0.01), the higher cancer knowledge. Parental stress was negatively correlated with income (p<0.05) and education (p<0.01), indicating that the better educated and higher the salary, less stress symptoms. Highly educated parents engaged in more activities with their children (p<0.05). Parental anxiety was correlated significantly with children’s current treatment including chemotherapy procedure (p<0.01), ‘In-patient’ Vs ‘Outpatient’ (p<0.01), and children’s condition (p<0.01). Parents of hospitalized children who underwent chemotherapy were significantly more anxious than their counterparts. Parents who perceived their children’s current condition as ‘very good’, reported reduced anxiety, compared to those who reported their child’s condition as ‘ok’. The more psychological problems the children had, the higher parental anxiety (p<0.05) and stress symptoms (p<0.01). Discussion: Some groups of parents reported more psychological difficulties compared to others. Ongoing psychological assessment and intervention may reduce parental stress by increasing coping and reducing children psychological problems

    Together we stand, divided we fall: Interprofessional collaborative practice competencies from Malaysian medical professionals' perspectives

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    أهداف البحث: إن المطالب على نظام الرعاية الصحية في تزايد٬ وهناك المزيد من الأصوات تتضمن المناهج الصحية التعليم المتداخل بين التخصصات. ولكن٬ لم يتم الوصول إلى نتائج بعد، وهناك معلومات محددة لتوجيه المعلمين. تهدف هذه الدراسة لاستكشاف المهنية الطبية من وجهة نظر أصحاب التخصصات الطبية الماليزية وعلى وجه التحديد٬ ممارسة الكفاءات التعاونية التخصصية المتداخلة المتوقعة من الطبيب في الحالة الماليزية. طرق البحث: أجرينا مناقشة جماعية مركزة على الأطباء في ماليزيا للحصول على خبرات المشاركين ووجهات نظرهم على الأهداف المنشودة. ثم أجرينا تحليلا موضوعيا للنصوص. تم التعامل مع البيانات بواسطة برنامج الأطلس. تاي. النتائج: تم مشاركة عدد ٢٢ طبيبا أكاديميا و غير أكاديمي في هذه الدراسة. وظهرت ثمانية مواضيع من المناقشة لوصف المهنية الطبية في ماليزيا. صُنفت هذه المواضيع إلى شائعة٬ مكملة وكفاءات تعاونية. ووجدنا أن الكفاءات التعاونية في ماليزيا تتضمن” مهارات القيادة والتداخل بين التخصصات “ و”الأولوية للمرضى“. الاستنتاجات: قدمت هذه الدراسة وصفا أوليا عن المهنية الطبية والكفاءات التعاونية المتوقعة في ماليزيا. وتقدم نتائج هذه الدراسة هيكلة لدراسات مستقبلية لاستراتيجيات التعليم الفعال وأدوات التقييم لمعرفة التعليم المتداخل بين التخصصات

    Nerve Conduction Study Among Healthy Malays. The Influence of Age, Height and Body Mass Index on Median, Ulnar, Common Peroneal and Sural Nerves

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    Nerve conduction study is essential in the diagnosis of focal neuropathies and diffuse polyneuropathies. Age, height and body mass index (BMI) can affect nerve velocities as reported by previous studies. We studied the effect of these factors on median, ulnar, common peroneal and sural nerves among healthy Malay subjects. We observed slowing of nerve conduction velocities (NCVs) with increasing age and BMI (except ulnar sensory velocities). No demonstrable trend can be seen across different height groups except in common peroneal nerve

    Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy

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    Abortion has been largely avoided in Muslim communities. However, Islamic jurists have established rigorous parameters enabling abortion of fetuses with severe congenital abnormalities. This decision-making process has been hindered by an inability to predict the severity of such prenatally-diagnosed conditions, especially in genetic disorders with clinical heterogeneity, such as spinal muscular atrophy (SMA). Heterogeneous phenotypes of SMA range from extremely severe type 1 to very mild type 4. Advances in molecular genetics have made it possible to perform prenatal diagnosis and to predict the types of SMA with its potential subsequent severity. Such techniques will make it possible for clinicians working in predominantly Muslim countries to counsel their patients accurately and in harmony with their religious beliefs. In this paper, we discuss and postulate that with our current knowledge of determining SMA types and severity with great accuracy, abortion is legally applicable for type 1 SMA
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