Despite all the advancements in dental prevention over the past decades, the problem of early childhood caries (ECC) still exists. Evidence suggests that whereas the prevalence of caries among older children, youth, and adults has declined, the prevalence of ECC in the preschool population has increased. [1][2][3] For many children with ECC, dental surgery under general anaesthesia is the only treatment option. 4 In-hospital day surgery to treat ECC is the most common day surgical procedure in Canada. 5 A 2013 report from the Canadian Institute of Health Information revealed that the
The COVID-19 pandemic pushed dental health officials around the world to reassess and adjust their existing healthcare practices. As studies on controlled COVID-19 transmission remain challenging, this review focuses on particles that can carry the virus and relevant approaches to mitigate the risk of pathogen transmission in dental offices. This review gives an overview of particles generated in clinical settings and how size influences their distribution, concentration, and generation route. A wide array of pertinent particle characterization and counting methods are reviewed, along with their working range, reliability, and limitations. This is followed by a focus on the effectiveness of personal protective equipment (PPE) and face shields in protecting patients and dentists from aerosols. Direct studies on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are still limited, but the literature supports the use of masks as an important and effective non-pharmaceutical preventive measure that could reduce the risk of contracting a respiratory infection by up to 20%. In addition to discussing about PPE used by most dental care professionals, this review describes other ways by which dental offices can protect patients and dental office personnel, which includes modification of the existing room design, dental equipment, and heating, ventilation, and air conditioning (HVAC) system. More affordable modifications include positioning a high-efficiency particulate air (HEPA) unit within proximity of the patient's chair or using ultraviolet germicidal irradiation in conjunction with ventilation. Additionally, portable fans could be used to direct airflow in one direction, first through the staff working areas and then through the patient treatment areas, which could decrease the number of airborne particles in dental offices. This review concludes that there is a need for greater awareness amongst dental practitioners about the relationship between particle dynamics and clinical dentistry, and additional research is needed to fill the broad gaps of knowledge in this field.
Objective Histopathological studies suggest that parasite load is different between acute and chronic forms of cutaneous leishmaniasis (CL). However, highly sensitive detection methods are still needed to distinguish different forms of leishmaniasis. In the present study, we developed a quantitative real-time polymerase chain reaction (PCR) to detect and quantify Leishmania tropica parasites in paraffin-embedded tissue samples. Results The ability of real-time PCR for leishmania detection was higher than histopathological evaluation. The quantitative real-time PCR (qPCR) quantified parasite loads were highly correlated with microscopic results (r = 0.598; P < 0.001). Among patients, the parasite load was inversely correlated with disease duration (acute CL lesions had very higher parasite load than chronic CL lesions), but there was no difference in the parasite load according to the patients’ age and sex as well as location of the lesions. In contrast to Ridley scoring system (P < 0.001), there were no statistically significant differences in the relative number of parasites among the lupoid and non-lupoid forms of chronic lesions in real-time PCR (P = 0.549), which indicates the superiority of histopathological evaluation for chronic forms differentiation.
Molecular diffusive membranes play crucial roles in the field of microfluidics for biological applications e.g., 3D cell culture and biosensors. Hydrogels provide a range of benefits such as free diffusion of small molecules, cost-effectiveness, and the ability to be produced in bulk. Among various hydrogels, Pluronic F127 can be used for cell culture purposes due to its biocompatibility and flexible characteristics regarding its environment. Aqueous solutions of Pluronic F127 shows a reversible thermo-thickening property, which can be manipulated by introduction of ions. As a result, controlled diffusion of ions into the solution of Pluronic F127 can result in a controlled gel formation. In this study, the flow of immiscible solutions of Pluronic and sodium phosphate inside a Y-shaped microchannel is simulated using the level set method, and the effects of volume flow rates and temperature on the gel formation are investigated. It is indicated that the gel wall thickness can decrease by either increasing the Pluronic volume flow rate or increasing both volume flow rates while increasing the saline volume flow rate enhances the gel wall thickness. Below a critical temperature value, no gel wall is formed, and above that, a gel wall is constructed, with a thickness that increases with temperature. This setup can be used for drug screening, where gel wall provides an environment for drug-cell interactions.Article Highlights Parallel flow of Pluronic F127 and saline solutions inside a Y-shaped microchannel results in formation of a gel wall at their interface. The numerical analysis reveals the impact of each inlet flow rate and temperature on gel wall thickness and movement. The findings indicate that the gel wall has a low but steady velocity toward the saline solution. Graphical abstract
objective: Histopathological studies suggest that parasite load is different between acute and chronic forms of cutaneous leishmaniasis (CL). However, highly sensitive detection methods are still needed to distinguish different forms of leishmaniasis. In the present study, we developed a quantitative realtime polymerase chain reaction (PCR) to detect and quantify leishmania tropica parasites in paraffinembedded tissue samples. Results: The ability of real-time PCR for leishmania detection was higher than histopathological evaluation. The parasite loads were quantified by qPCR assay and microscopic evaluation were highly correlated ( r =0.598; P <0.001). Among patients, the parasite load was inversely correlated with disease duration (acute CL lesions had very higher parasite loads than chronic CL lesions), but there was no difference in parasite load according to the patients' age and sex as well as location of the lesions. In contrast to Ridley scoring system (P<0.001), there were no statistically significant differences in the relative number of parasites among the lupoid and nonlupoid forms of chronic lesions in real-time PCR (P=0.549), which indicates the superiority of histopathological evaluation in CL forms differentiation.
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