Lifestyle and Risk Factors for Knee Arthroplasty: A South African Perspective

Author(s):  
Zia Maharaj ◽  
Jurek Rafal Tomasz Pietrzak
Author(s):  
Leanne Pillay ◽  
Isaac Dennis Amoah ◽  
Nashia Deepnarain ◽  
Kriveshin Pillay ◽  
Oluyemi Olatunji Awolusi ◽  
...  

2021 ◽  
Vol 6 (1) ◽  
pp. e003499
Author(s):  
Ryan G Wagner ◽  
Nigel J Crowther ◽  
Lisa K Micklesfield ◽  
Palwende Romauld Boua ◽  
Engelbert A Nonterah ◽  
...  

IntroductionCardiovascular disease (CVD) risk factors are increasing in sub-Saharan Africa. The impact of these risk factors on future CVD outcomes and burden is poorly understood. We examined the magnitude of modifiable risk factors, estimated future CVD risk and compared results between three commonly used 10-year CVD risk factor algorithms and their variants in four African countries.MethodsIn the Africa-Wits-INDEPTH partnership for Genomic studies (the AWI-Gen Study), 10 349 randomly sampled individuals aged 40–60 years from six sites participated in a survey, with blood pressure, blood glucose and lipid levels measured. Using these data, 10-year CVD risk estimates using Framingham, Globorisk and WHO-CVD and their office-based variants were generated. Differences in future CVD risk and results by algorithm are described using kappa and coefficients to examine agreement and correlations, respectively.ResultsThe 10-year CVD risk across all participants in all sites varied from 2.6% (95% CI: 1.6% to 4.1%) using the WHO-CVD lab algorithm to 6.5% (95% CI: 3.7% to 11.4%) using the Framingham office algorithm, with substantial differences in risk between sites. The highest risk was in South African settings (in urban Soweto: 8.9% (IQR: 5.3–15.3)). Agreement between algorithms was low to moderate (kappa from 0.03 to 0.55) and correlations ranged between 0.28 and 0.70. Depending on the algorithm used, those at high risk (defined as risk of 10-year CVD event >20%) who were under treatment for a modifiable risk factor ranged from 19.2% to 33.9%, with substantial variation by both sex and site.ConclusionThe African sites in this study are at different stages of an ongoing epidemiological transition as evidenced by both risk factor levels and estimated 10-year CVD risk. There is low correlation and disparate levels of population risk, predicted by different risk algorithms, within sites. Validating existing risk algorithms or designing context-specific 10-year CVD risk algorithms is essential for accurately defining population risk and targeting national policies and individual CVD treatment on the African continent.


2019 ◽  
Vol 5 (1) ◽  
pp. 1704601
Author(s):  
Bongolethu Diko ◽  
Sogo Angel Olofinbiyi ◽  
Jean Steyn

1988 ◽  
Vol 30 (1) ◽  
pp. 95
Author(s):  
J. K. Elliott ◽  
J. H. Petzer ◽  
P. J. Hartin

PLoS ONE ◽  
2014 ◽  
Vol 9 (3) ◽  
pp. e90768 ◽  
Author(s):  
Ian Louis Ross ◽  
Ragnhildur Bergthorsdottir ◽  
Naomi Levitt ◽  
Joel Alex Dave ◽  
Desmond Schatz ◽  
...  

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