1.Radiation Safety in Emergency Medicine: Balancing the Benefits and Risks
Raja Rizal AZMAN ; Mohammad Nazri Md SHAH ; Kwan Hoong NG
Korean Journal of Radiology 2019;20(3):399-404
The use of computed tomography (CT) in emergency departments has increased over several decades, as physicians increasingly depend on imaging for diagnoses. Patients and medical personnel are put at risk due to frequent exposure to and higher levels of radiation, with very little evidence of improvements in outcomes. Here, we explore why CT imaging has a tendency to be overused in emergency departments and the obstacles that medical personnel face in ensuring patient safety. The solution requires cooperation from all emergency care stakeholders as well as the continuous education of doctors on how CT scans help in particular cases.
Diagnosis
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Education
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Emergencies
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Emergency Medical Services
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Emergency Medicine
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Emergency Service, Hospital
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Humans
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Patient Safety
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Private Practice
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Radiation, Ionizing
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Risk Assessment
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Tomography, X-Ray Computed
2.‘Sub-superscan’ in Bone Scan – An Important Feature of Extensive Bone Metastases
Khadijah Abdul Hamid ; Mohammad Nazri Md Shah
Malaysian Journal of Medicine and Health Sciences 2020;16(Supp 2, May):75-77
A Superscan is described as a ‘beautiful bone scan’. In a superscan, the uptake of 99mTc-Methelene Diphosphonate (MDP) is prominent in the skeleton relative to soft tissue with absent or faint visualisation of the kidneys. This finding could be misinterpreted as a normal bone scan. A ‘Sub-superscan’ is a term used for scan findings in which the uptake is atypical of a superscan, but the patient has extensive bone metastases, as presented in our case report.
3.SPECT-CT in Differentiating Metastatic and Degenerative Lesions of the Spine
Khadijah Abdul Hamid ; Sazilah Ahmad Sarji ; Mohammad Nazri Md Shah ; Ibrahim Lutfi Shuaib
Malaysian Journal of Medicine and Health Sciences 2020;16(Supp 2, May):31-37
Introduction: The purpose of this study was to determine the usefulness of SPECT-CT in differentiating metastatic and degenerative disease of the spine. Methods: Twenty-eight patients aged 50 years and above diagnosed with various cancers were referred for whole body (WB) planar bone scintigraphy. Those with a maximum three foci of tracer uptake in the spine were selected for the study. SPECT-CT of these areas of uptake was performed and the lesions were classified as degenerative, indeterminate or metastasis. A repeat study (WB planar bone scintigraphy and SPECT-CT) was performed between 3 to 12 months later. These areas of uptake were reassessed and compared with the first WB planar bone scintigraphy and SPECT-CT. The second SPECT-CT was used as the standard for the diagnosis. Results: Thirty-seven lesions in 28 patients were assessed. The sensitivity of the first WB planar bone scintigraphy, second WB planar bone scintigraphy and first SPECT-CT is 75%, 62.5% and 75% respectively. The specificity of the first WB planar bone scintigraphy, second WB planar bone scintigraphy and first SPECT-CT is 86%, 93%, 90% respectively. There was 2.7% of ‘indeterminate lesion’ in the first WB planar bone scintigraphy, 5.4% in the second WB planar bone scintigraphy, and 5.4% in the first SPECT-CT. The indeterminate lesions were resolved in the second SPECT-CT. Conclusion: SPECT- CT is useful in differentiating degenerative disease from metastatic lesions in the spine.
4.Allelic Diversity of the Hemochromatosis Gene (HFE) in Malays, Chinese and Indians
Che Ghazali Norul Hajar ; Suhaida Md. Akhir ; Zulkafli Zefarina ; Nor Suhaila Md. Riffin ; Tuan Hulwani Tuan Mohammad ; Mohd Nazri Hassan ; Sabreena Safuan ; Mohd Yusmaidie Aziz ; Siddhartha Pati ; Geoffrey Keith Chambers ; Hisham Atan Edinur
Malaysian Journal of Medicine and Health Sciences 2021;17(No.3):49-54
Introduction: Hereditary hemochromatosis (HH) is an autosomal recessive disorder that causes accumulation of iron in circulating blood and organs. The disease is associated with H63D, S65C and C282Y variants of the haemochromatosis (HFE) gene and, if not treated can cause organ damage and may prove fatal. The main objectives of the present survey were to screen these genetic variants and establish risk profiles for developing HH in Malays, Chinese and Indians. Methods: A total of two hundred and twenty-two unrelated and healthy individuals together representing Malay, Chinese and Indian ethnicities in Malaysia were scored for the H63D, S65C and C282Y variants using a polymerase chain reaction-restriction fragment length polymorphism technique. Results: There are clear differences in H63D, S65C and C282Y allele and genotype frequency distributions between Malays, Chinese and Indians. In particular, H63D is more common in Chinese (5.19%) and Indians (7.29%), while S65C is more common in Malays (1.03%) and Chinese (1.04%). In addition, a susceptibility genotype for HH (the compound heterozygote for C282Y and H63D) was only detected in Indians (0.02%). Conclusion: Overall, our study is the first to provide data on the prevalence of H63D, S65C, and C282Y genetic variants and HH risk profiles for Malays, Chinese and Indians.