Publications by authors named "D J Bezuidenhout"

This article offers a comprehensive and user-friendly guide to visualizing causal theories using Single World Intervention Graphs (SWIGs). We begin with a discussion of the potential outcomes approach to causality and limitations of using Directed Acyclic Graphs (DAGs) under this framework. We then introduce SWIGs as a simple but powerful tool for integrating potential outcomes explicitly into causal diagrams.

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Background: Household contact investigations are effective for finding tuberculosis (TB) cases but are hindered by low referral uptake for clinic-based evaluation and testing. We assessed the acceptability and feasibility of in-home testing of household contacts (HHC) using the GeneXpert Edge platform.

Methods: We conducted a 2-arm, randomized study in Eastern Cape, South Africa.

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The concentration of the polymer in the electrospinning solution greatly influences the mechanical behaviour of electrospun vascular grafts due to the influence on scaffold morphology. The scaffold morphology (fiber diameter, fiber orientation and inter-fiber voids) of the grafts plays an important role in their behaviour during use. Even though manual methods and complex algorithms have been used so far for characterisation of the morphology of electrospun architecture, they still have several drawbacks that limit their reliability.

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Article Synopsis
  • Cabamiquine is a new antimalarial drug that targets Plasmodium falciparum translation elongation factor 2 and was tested for its ability to prevent malaria in healthy, malaria-naive volunteers through a phase 1b clinical trial in the Netherlands.
  • The study involved 39 participants divided into cohorts, receiving different doses of cabamiquine or a placebo after being inoculated with malaria sporozoites, with various outcomes measured including the development of parasitaemia and safety profiles.
  • Results from the trial are still being evaluated to determine the effectiveness and safety of cabamiquine as a potential chemoprophylactic treatment for malaria.
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Background: Evaluation of parasite clearance patterns in experimental human infection trials helps increase understanding of drug action. In a previously reported phase Ib trial of a new investigational anti-malarial drug M5717, parasite clearance showed a biphasic linear pattern: slow removal phase with a near flat clearance rate followed by a fast clearance phase with a steep slope. In this study three statistical approaches were implemented and compared to estimate the parasite clearance rate for each phase and the time point corresponding to the change of clearance rates (changepoint between the two phases).

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