1.Development and validation of the Salt Intake-Related Knowledge, Attitude, and Practice Questionnaire for Malaysian adults
Zainorain Natasha Zainal Arifen ; Ngoh Wan Hwah ; Hng Jie Wei ; Siti Aishah Ismail ; Maryam Hanis Fairuzam ; Hasnah Haron
Malaysian Journal of Nutrition 2024;30(No.1):73-86
		                        		
		                        			
		                        			Introduction: Malaysian adults consume excessive amounts of salt daily, which 
could lead to hypertension. Understanding knowledge, attitudes, and practices 
(KAP) surrounding salt intake is crucial for designing effective interventions to 
reduce excessive consumption and its associated health risks. Therefore, this study 
aimed to adapt an existing salt intake-related KAP questionnaire that was previously 
employed in a local population-based survey and to validate and test its reliability. 
Methods: This cross-sectional study comprised two phases: (1) adaptation, content 
validation (CV), and face validation (FV); (2) pilot testing and reliability testing. CV 
and FV involved a total of seven experts and ten Malaysian adults from the Klang 
Valley, respectively. Pilot testing involved 139 Malaysian adults to determine the 
questionnaire’s reliability. Content validity index (CVI) and Face validity index 
(FVI) values were calculated to analyse CV and FV. Reliability of each domain was 
analysed by obtaining Cronbach’s alpha (α) values. Results: A self-administered 
questionnaire comprising six items each for knowledge, attitude, and practice was 
developed. The questionnaire demonstrated acceptable item-level CVI (I-CVI) and 
item-level FVI (I-FVI) values of at least 0.83, indicating that the items were relevant, 
clear, non-ambiguous, and simple. Reliability test showed acceptable α values 
of at least 0.70 for each domain, suggesting that the questionnaire was reliable. 
Conclusion: This tool could be considered valid and reliable for assessing the level 
of KAP towards salt intake among adults in Malaysia.
		                        		
		                        		
		                        		
		                        	
2.Kaedah Diagnostik Semasa dan Penggunaan Ujian Titik Penjagaan Pantas (POC) Bagi Mendiagnos Hiperkolesterolemia Famili (FH) (Current Diagnostic Techniques and the Use of Rapid Point-of-Care (POC) Testing to Diagnose Familial Hypercholesterolemia (FH))
LINA KHIALIDA SAIDI ; ZAM ZUREENA MD RANI ; SITI AISHAH SILAIMAN ; ISMAIL AZIAH ; ANIS AMIRAH ALIM ; SHARIPAH NADZIRAH SYED AHMAD AYOB ; DEE CHANG FU ; AZRUL AZLAN HAMZAH ; NOR AZIAN ABDUL MURAD
Malaysian Journal of Health Sciences 2023;21(No.2):35-45
		                        		
		                        			
		                        			Familial hypercholesterolemia (FH) is an autosomal dominant inherited genetic disease characterized by increased 
concentrations of low-density lipoprotein (LDL-C) cholesterol in the blood. The risk of premature coronary heart 
disease in FH patients may increase without early treatment. Advancement in molecular biology techniques has enable 
early detection and diagnosis of FH. These techniques are cost-effective and have a shorter turnaround time. The 
current diagnostic tools available for FH diagnosis involving algorithm-based scoring criteria and various molecular 
diagnosis methods including next-generation sequencing (NGS), Sanger sequencing, Multiplex ligation-dependent 
probe amplification (MLPA) and DNA hybridisation assay are discussed in this review. However, molecular genetic 
testing is not widely available due to time-consuming procedures, high cost and requires trained personnel. Thus, this 
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review highlights the use of point of care (POC) testing as an approach to diagnose FH, particularly in countries 
lacking infrastructure and expertise in this field. Lateral flow testing (LFA) has gained attention as a POC diagnostic 
tool due to its simplicity, low cost and involved simple procedure and settings. The advantages of LFA made this technique 
a potential tool in addressing challenges in diagnosing FH, particularly for early diagnosis of family members.
		                        		
		                        		
		                        		
		                        	
            

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