Risk Assessment as a Management Tool Used to Assess the Effect of Pesticide Use in an Irrigation System,Situated in a Semi-Desert Region

A preliminary study undertaken by the CSIR in July 1993 on the health effects of aerial crop spraying of pesticides in the Vaalharts irrigation area in South Africa indicated that potential health risks could exist for the inhabitants of this area. An extensive scientific health risk assessment and epidemiological study to determine the actual health risks, is very expensive and requires medical and financial justification. The aim of this study was to develop a theoretical health risk model, which could be used as a predictive tool to determine as accurately as possible from the data available if a complete scientific health risk assessment study is justified. The actual amounts of pesticides sold in the Vaalharts area by two major pesticide manufacturers were used to perform a theoretical health risk assessment. The risks were assessed by making use of RISK*ASSISTANT, a computer modeling system and chemical database. The United States Environmental Protection Agency's (EPA) health risk model was applied to the data to identify the hazards, assess the exposures and dose response, and characterize the risks. Three exposure scenarios, namely, the ingestion of food and water and the inhalation of air were evaluated. The method used to calculate the risks varied according to the type of health hazard and the results were characterized accordingly. The acute health effects due to exposure to pesticides are well known and the risks are easy to determine. However, the risks associated with chronic health hazards were more difficult to calculate. For this reason a ranking model was developed which made use of a point scoring system. This model highlights those pesticides which have the greatest possibility of causing chronic health effects. From the results it can be concluded that very large amounts of pesticides are used in the Vaalharts area and that the community might be at risk to chronic health effects. Although the theoretical health risk assessment model was successfully used in this study, its effectiveness as a predictive tool still has to be proven by a complete scientific study. Received: April 1996/Revised: 21 July 1996     

Whole blood intra-operative salvage and reinfusion in patients undergoing venous thrombectomy

Concern regarding the risk of disease transmission via blood transfusion together with periodic shortages of homologous blood has stimulated an interest in and the usage of autologous blood. Forty-nine patients had shed blood salvaged during venous thrombectomy. Between 200-3800 ml of blood were salvaged and reinfused using Solcotrans. No patient in this study required an homologous blood transfusion. The haematological parameters studied showed figures within the normal, acceptable range post-reinfusion. No patient experienced a clinical coagulopathy or showed evidence of renal dysfunction. The device is simple to use, safe and effective.     

Pseudarthrosen

The treatment of fracture healing disorders is complex and often associated with a long-term course of treatment. After clinical radiological confirmation of delayed fracture healing, the treating physician has to decide on the optimal timing of an intervention. Waiting for 6 months is not always the best approach under these circumstances. Revision surgery can be necessary even in the early phase of fracture healing disorders, particularly in the event of a biomechanical insufficiency (early material fatigue with implant breakage) or a local infection in the fracture region. An early intervention potentially prevents long-term problems, including pain and functional limitations for the patient as well as high socioeconomic costs.     

An ovine model of maternal iron poisoning in pregnancy

An ovine model of maternal iron poisoning in pregnancy was used to examine the placental transport of deferoxamine and ferrioxamine and to follow maternal and fetal serum iron concentrations when maternal serum iron levels exceeded total iron-binding capacity. Ewes in the third stage of gestation underwent hysterotomy and delivery of the fetal head through an abdominal incision while under ketamine and halothane anesthesia. The fetal external jugular vein was catheterized for sampling of venous blood while the fetus remained in utero. Administration of deferoxamine mesylate or ferrioxamine mesylate IV to ewes was not accompanied by measurable deferoxamine or ferrioxamine in fetal blood. In a final experiment, four gravid ewes in a control group received 2 mg/kg maternal body wt iron IV over 60 minutes. An experimental group comprising another four ewes received similar doses of iron but then received 50 mg/kg deferoxamine mesylate IV over 15 minutes. Control and deferoxamine ewes reached similar peak maternal serum iron concentrations (2,479 +/- 266 and 2,121 +/- 343 micrograms/dL, respectively). The markedly elevated maternal serum iron concentrations were not accompanied by meaningful elevations in fetal serum iron levels over baseline values. Maternal deferoxamine infusion resulted in a more rapid fall in maternal serum iron concentrations but had no effect on fetal serum iron levels. The ovine fetus appears to be protected from elevated maternal serum iron concentrations in the last trimester of pregnancy. It could not be demonstrated that meaningful quantities of deferoxamine or ferrioxamine cross the placenta in the last trimester.(ABSTRACT TRUNCATED AT 250 WORDS)     

Multi‐centre reproducibility of diffusion MRI parameters for clinical sequences in the brain

The purpose of this work was to assess the reproducibility of diffusion imaging, and in particular the apparent diffusion coefficient (ADC), intra‐voxel incoherent motion (IVIM) parameters and diffusion tensor imaging (DTI) parameters, across multiple centres using clinically available protocols with limited harmonization between sequences. An ice–water phantom and nine healthy volunteers were scanned across fives centres on eight scanners (four Siemens 1.5T, four Philips 3T). The mean ADC, IVIM parameters (diffusion coefficient D and perfusion fraction f) and DTI parameters (mean diffusivity MD and fractional anisotropy FA), were measured in grey matter, white matter and specific brain sub‐regions. A mixed effect model was used to measure the intra‐ and inter‐scanner coefficient of variation (CV) for each of the five parameters. ADC, D, MD and FA had a good intra‐ and inter‐scanner reproducibility in both grey and white matter, with a CV ranging between 1% and 7.4%; mean 2.6%. Other brain regions also showed high levels of reproducibility except for small structures such as the choroid plexus. The IVIM parameter f had a higher intra‐scanner CV of 8.4% and inter‐scanner CV of 24.8%. No major difference in the inter‐scanner CV for ADC, D, MD and FA was observed when analysing the 1.5T and 3T scanners separately. ADC, D, MD and FA all showed good intra‐scanner reproducibility, with the inter‐scanner reproducibility being comparable or faring slightly worse, suggesting that using data from multiple scanners does not have an adverse effect compared with using data from the same scanner. The IVIM parameter f had a poorer inter‐scanner CV when scanners of different field strengths were combined, and the parameter was also affected by the scan acquisition resolution. This study shows that the majority of diffusion MRI derived parameters are robust across 1.5T and 3T scanners and suitable for use in multi‐centre clinical studies and trials. © 2015 The Authors NMR in Biomedicine Published by John Wiley & Sons Ltd.