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1.
S Afr J Surg ; 60(1): 40-43, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35451268

ABSTRACT

BACKGROUND: Few studies have assessed the impact of COVID-19 on surgical training in low- and middle-income countries. The aim of this study was to survey the effect of the COVID-19 pandemic on postgraduate surgical training, research and registrar wellbeing in South Africa. METHODS: A cross-sectional study was conducted as an online survey from 5 October 2020 to 1 December 2020. The study population was registrars from all surgical disciplines at the Faculty of Medicine and Health Sciences of Stellenbosch University. The survey consisted of 26 multiple-choice and five open-ended qualitative questions on the impact of COVID-19 on physical and mental wellbeing, skills acquisition and postgraduate research. RESULTS: Of 98 surgical registrars, 35 (36%) responded. Twenty-three (65.7%) reported missed planned surgical rotations, 30 (85.7%) decreased surgical training time, and 22 (62.9%) reported a perceived decrease in training quality. Simulated skills training was only available to eight (22.9%) participants. Twenty-four (68.6%) experienced burnout and/or depression symptoms during the pandemic. Twenty-seven (77.1%) reported that postgraduate research was unaffected by the pandemic. CONCLUSION: During the COVID-19 pandemic, surgical trainees at this institution reported a decrease in the quality of surgical training and skills acquisition and a negative impact on their mental wellbeing.


Subject(s)
COVID-19 , COVID-19/epidemiology , Cross-Sectional Studies , Humans , Pandemics , SARS-CoV-2 , Surveys and Questionnaires
2.
Diabet Med ; 24(5): 498-504, 2007 May.
Article in English | MEDLINE | ID: mdl-17381501

ABSTRACT

AIMS: Thioredoxin interacting protein (TXNIP) is an attractive candidate gene for diabetes or diabetic dyslipidaemia, since TXNIP is the strongest glucose-responsive gene in pancreatic B-cells, TXNIP deficiency in a mouse model is associated with hyperlipidaemia and TXNIP is located in the 1q21-1q23 chromosomal Type 2 diabetes mellitus (DM) locus. We set out to investigate whether metabolic effects of TXNIP that were previously reported in a murine model are also relevant in human Type 2 DM. METHODS: The frequency distribution of a 3' UTR single nucleotide polymorphism (SNP) in TXNIP was investigated in subjects with normal glucose tolerance (NGT; n = 379), impaired glucose tolerance (IGT; n = 228) and Type 2 DM (n = 230). Metabolic data were used to determine the effect of this SNP on parameters associated with lipid and glucose metabolism. RESULTS: The frequency of the TXNIP variation did not differ between groups, but within the group of diabetic subjects, carriers of the TXNIP-T variant had 1.6-fold higher triglyceride concentrations (P = 0.015; n = 136) and a 5.5-mmHg higher diastolic blood pressure (P = 0.02; n = 212) than homozygous carriers of the common C-allele, whereas in non-diabetic subjects fasting glucose was 0.26 mmol/l lower (P = 0.002; n = 478) in carriers of the T-allele. Moreover, a significant interaction between plasma glucose concentrations and TXNIP polymorphism on plasma triglycerides was observed (P = 0.012; n = 544). CONCLUSION: This is the first report to implicate TXNIP in a human disorder of energy metabolism, Type 2 diabetes. The effect of TXNIP on triglycerides is influenced by plasma glucose concentrations, suggesting that the biological relevance of TXNIP variations may be particularly relevant in recurrent episodes of hyperglycaemia.


Subject(s)
Blood Pressure/genetics , Carrier Proteins/genetics , Diabetes Mellitus, Type 2/genetics , Hypertriglyceridemia/genetics , Polymorphism, Genetic/genetics , Triglycerides/blood , Aged , Animals , Blood Glucose/metabolism , Diabetes Mellitus, Type 2/blood , Diabetic Angiopathies/blood , Diabetic Angiopathies/genetics , Female , Genetic Predisposition to Disease , Humans , Male , Mice , Middle Aged , Triglycerides/analysis
3.
Arterioscler Thromb Vasc Biol ; 24(4): 744-9, 2004 Apr.
Article in English | MEDLINE | ID: mdl-14751815

ABSTRACT

OBJECTIVE: The present study addresses the presence of distinct metabolic phenotypes in familial combined hyperlipidemia (FCHL) in relation to small dense low-density lipoprotein (sd LDL) and very low-density lipoprotein (VLDL) subclasses. METHODS AND RESULTS: Hyperlipidemic FCHL relatives (n=72) were analyzed for LDL size by gradient gel electrophoresis. Pattern B LDL (sd LDL, particle size <258 A) and pattern A LDL (buoyant LDL, particle size > or =258 A) were defined. Analyses showed bimodal distribution of LDL size associated with distinct phenotypes. Subjects with predominantly large, buoyant LDL showed a hypercholesterolemic phenotype and the highest apo B levels. Subjects with predominantly sd LDL showed a hypertriglyceridemic, low high-density lipoprotein (HDL) cholesterol phenotype, with moderately elevated apoB, total cholesterol level, and LDL cholesterol level. Subjects with both buoyant LDL and sd LDL (pattern AB, n=7) showed an intermediate phenotype, with high normal plasma triglycerides. VLDL subfraction analysis showed that the sd LDL phenotype was associated with a 10-times higher number of VLDL1 particles of relatively lower apo AI and apo E content, as well as smaller VLDL2 particles, in combination with increased plasma insulin concentration in comparison to pattern A. CONCLUSIONS: The present observations underscore the importance of the VLDL triglyceride metabolic pathway in FCHL as an important determinant of the phenotypic heterogeneity of the disorder.


Subject(s)
Hyperlipidemia, Familial Combined/blood , Lipoproteins, LDL/classification , Lipoproteins, VLDL/classification , Adult , Apolipoprotein A-I/blood , Apolipoproteins E/blood , Blood Protein Electrophoresis , Female , Humans , Hypercholesterolemia/blood , Hypercholesterolemia/genetics , Hyperlipidemia, Familial Combined/genetics , Hyperlipoproteinemia Type IV/blood , Hyperlipoproteinemia Type IV/genetics , Insulin/blood , Lipoproteins, LDL/blood , Lipoproteins, VLDL/blood , Male , Particle Size , Phenotype
4.
Int J Technol Assess Health Care ; 17(3): 316-28, 2001.
Article in English | MEDLINE | ID: mdl-11495376

ABSTRACT

OBJECTIVE: To describe how scientific evidence has influenced healthcare policy making in Belgium in the field of sickness prevention for mammography, PSA testing in prostate cancer screening, and use of ultrasound in pregnancy. METHODS: Review of published and gray literature and interviews with stakeholders and experts. RESULTS: At the end of 1999, a systematic national/regional screening program had not yet been implemented for any of the three screening strategies. A systematic breast cancer screening program is being prepared for implementation only in Flanders. This limited impact can be attributed to the fragmentation in healthcare policy, the different options among the different regions, fragmentation in healthcare practice, the strong impact of healthcare stakeholders (provider groups and sickness funds) on decision making, and limited attention to scientific evidence in health policy and technology assessment. CONCLUSIONS: Health technology assessment has had very little impact on policy and practice in use of mammography, PSA testing, and ultrasound in pregnancy in Belgium.


Subject(s)
Health Policy , Mammography/statistics & numerical data , Mass Screening/statistics & numerical data , Prostate-Specific Antigen/blood , Technology Assessment, Biomedical , Ultrasonography, Prenatal/statistics & numerical data , Adolescent , Adult , Aged , Belgium , Breast Neoplasms/diagnosis , Breast Neoplasms/prevention & control , Child , Child, Preschool , Diagnostic Tests, Routine/statistics & numerical data , Female , Humans , Infant , Male , Middle Aged , Pregnancy , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/prevention & control
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