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1.
Hemodial Int ; 18(2): 495-506, 2014 Apr.
Article in English | MEDLINE | ID: mdl-26820998

ABSTRACT

There is a growing interest to use quality of life as one of the dialysis outcome measurement. Based on the Malaysian National Renal Registry data on 15 participating sites, 1569 adult subjects who were alive at December 31, 2012, aged 18 years old and above were screened. Demographic and medical data of 1332 eligible subjects were collected during the administration of the short form of World Health Organization Quality of Life questionnaire (WHOQOL-BREF) in Malay, English, and Chinese language, respectively. The primary objective is to evaluate the quality of life among dialysis patients using WHOQOL-BREF. The secondary objective is to examine significant factors that affect quality of life score. Mean (SD) transformed quality of life scores were 56.2 (15.8), 59.8 (16.8), 58.2 (18.5), 59.5 (14.6), 61.0 (18.5) for (1) physical, (2) psychological, (3) social relations, (4) environment domains, and (5) combined overall quality of life and general health, respectively. Peritoneal dialysis group scored significantly higher than hemodialysis group in the mean combined overall quality of life and general health score (63.0 vs. 60.0, P < 0.001). Independent factors that were associated significantly with quality of life score in different domains include gender, body mass index, religion, education, marital status, occupation, income, mode of dialysis, hemoglobin, diabetes mellitus, coronary heart disease, cerebral vascular accident and leg amputation. Subjects on peritoneal dialysis modality achieved higher combined overall quality of life and general health score than those on hemodialysis. Religion and cerebral vascular accident were significantly associated with all domains and combined overall quality of life and general health.


Subject(s)
Quality of Life , Renal Dialysis/psychology , Adult , Aged , Female , Humans , Male , Middle Aged , Peritoneal Dialysis/psychology , Surveys and Questionnaires
2.
Int J Clin Pharm ; 35(4): 621-8, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23661171

ABSTRACT

BACKGROUND: Cytochrome P450 2C19 (CYP2C19) loss-of-function polymorphisms are more common in Asian populations and have been associated with diminished antiplatelet response to clopidogrel. In this era of 'personalised medicine', combining genotyping and phenotyping as a strategy to personalise antiplatelet therapy warrants further exploration. OBJECTIVE: This study aimed to investigate the prevalence and impact of CYP2C19*2, *3 and *17 genotypes on clopidogrel responsiveness in a multiethnic Malaysian population planned for percutaneous coronary intervention. SETTING: Between October 2010 and March 2011, a total of 118 consecutive patients planned for percutaneous coronary intervention were enrolled in Sarawak General Hospital, Borneo. All patients received at least 75 mg aspirin daily for at least 2 days and 75 mg clopidogrel daily for at least 4 days prior to angiography. METHOD: Genotyping for CYP2C19*2 (rs4244285, 681G > A), *3 (rs4986893, 636G > A) and *17 (rs11188072, -3402C > T) alleles were performed by polymerase chain reaction-restriction fragment linked polymorphism method. Whole blood ADP-induced platelet aggregation was assessed with multiple electrode platelet aggregometry (MEA) using the Multiplate Analyzer. MAIN OUTCOME MEASURES: The distribution of CYP2C19*2, *3 and *17 among different ethnic groups and the association between genotype, clopidogrel responsiveness and clinical outcome were the main outcome measures. RESULTS: The highest prevalence of poor metabolisers (carriers of at least one copy of the *2 or *3 allele) was among the Chinese (53.7 %), followed by the Malays (26.9 %), Ibans (16.4 %) and other races (3.0 %). Poor metabolisers (PMs) had the highest mean MEA (303.6 AU*min), followed by normal metabolisers (NMs) with 270.5 AU*min and extensive metabolisers (EMs) with 264.1 AU*min (p = 0.518). Among poor responders to clopidogrel, 65.2 % were PMs and NMs, respectively, whereas none were EMs (p = 0.350). Two cardiac-related deaths were reported. CONCLUSION: There was a diverse inter-ethnic difference in the distribution of CYP2C19 polymorphism. The findings of this study echo that of other studies where genotype appears to have a limited impact on clopidogrel responsiveness and clinical outcome in low-risk patients.


Subject(s)
Aryl Hydrocarbon Hydroxylases/genetics , Percutaneous Coronary Intervention/methods , Platelet Aggregation Inhibitors/therapeutic use , Ticlopidine/analogs & derivatives , Adult , Aged , Alleles , Asian People/genetics , Aspirin/administration & dosage , Clopidogrel , Cytochrome P-450 CYP2C19 , Female , Follow-Up Studies , Genotype , Humans , Malaysia , Male , Middle Aged , Platelet Aggregation/drug effects , Platelet Aggregation Inhibitors/administration & dosage , Platelet Aggregation Inhibitors/pharmacology , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Prevalence , Ticlopidine/administration & dosage , Ticlopidine/pharmacology , Ticlopidine/therapeutic use , Treatment Outcome
3.
BMC Cardiovasc Disord ; 13: 10, 2013 Feb 25.
Article in English | MEDLINE | ID: mdl-23442728

ABSTRACT

BACKGROUND: Recent increases in cardiovascular risk-factor prevalences have led to new national policy recommendations of universal screening for primary prevention of cardiovascular disease in Malaysia. This study assessed whether the current national policy recommendation of universal screening was optimal, by comparing the effectiveness and impact of various cardiovascular screening strategies. METHODS: Data from a national population based survey of 24 270 participants aged 30 to 74 was used. Five screening strategies were modelled for the overall population and by gender; universal and targeted screening (four age cut-off points). Screening strategies were assessed based on the ability to detect high cardiovascular risk populations (effectiveness), incremental effectiveness, impact on cardiovascular event prevention and cost of screening. RESULTS: 26.7% (95% confidence limits 25.7, 27.7) were at high cardiovascular risk, men 34.7% (33.6, 35.8) and women 18.9% (17.8, 20). Universal screening identified all those at high-risk and resulted in one high-risk individual detected for every 3.7 people screened, with an estimated cost of USD60. However, universal screening resulted in screening an additional 7169 persons, with an incremental cost of USD115,033 for detection of one additional high-risk individual in comparison to targeted screening of those aged ≥35 years. The cost, incremental cost and impact of detection of high-risk individuals were more for women than men for all screening strategies. The impact of screening women aged ≥45 years was similar to universal screening in men. CONCLUSIONS: Targeted gender- and age-specific screening strategies would ensure more optimal utilisation of scarce resources compared to the current policy recommendations of universal screening.


Subject(s)
Cardiovascular Diseases/prevention & control , Developing Countries , Health Policy , Mass Screening , Policy Making , Preventive Health Services , Adult , Age Factors , Aged , Cardiovascular Diseases/economics , Cardiovascular Diseases/epidemiology , Cost-Benefit Analysis , Developing Countries/economics , Female , Health Care Costs , Health Policy/economics , Health Policy/legislation & jurisprudence , Humans , Malaysia/epidemiology , Male , Mass Screening/economics , Mass Screening/legislation & jurisprudence , Mass Screening/methods , Mass Screening/standards , Middle Aged , Practice Guidelines as Topic , Predictive Value of Tests , Prevalence , Preventive Health Services/economics , Preventive Health Services/legislation & jurisprudence , Preventive Health Services/methods , Preventive Health Services/standards , Risk Assessment , Risk Factors , Sex Factors
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