52 research outputs found

    Exploring the perceptions of Patients with Chronic Respiratory Diseases and their insights into Pulmonary Rehabilitation in Bangladesh

    Get PDF
    Background: Chronic respiratory diseases (CRDs) require holistic management reflecting patient preferences, appropriate pharmacotherapy, pulmonary rehabilitation, and integrated care. We aimed to understand the perceptions of people with CRDs about their condition and pulmonary rehabilitation in Bangladesh.Methods: We conducted semi-structured interviews with a maximum variation sample of people with CRD who had participated in a feasibility study of pulmonary rehabilitation in 2021/ 2022. Interviews were transcribed verbatim, analysed in Bengali using a grounded theory approach and interpreted by a multidisciplinary team.Results: We interviewed 15 participants with COPD, asthma, or post-tuberculosis. Analysis revealed three themes. 1) Understanding CRD: patients characterised their condition by the symptoms (e.g., ‘Hapani’ meaning ‘breathlessness’) rather than describing a disease entity. Some identified occupation, previous infection or family history that they believed was the cause. 2) Perceptions of pulmonary rehabilitation: Exercise was counterintuitive as it exacerbated the breathlessness symptom that defined their disease. Views varied, though many acknowledged the benefits after a few sessions. Even with home-based programmes, participants described practical barriers to finding time for the sessions and adopted strategies to overcome the challenges. 3) Implementation: Participants highlighted the need for raising awareness of CRD and the potential of pulmonary rehabilitation in the community, adapting to the local context, and establishing an accessible resourced service. Conclusion: Understanding how patients and their communities perceive their condition and the barriers (both conceptual and logistical) to acceptance is the first step to embedding this highly effective intervention into routine healthcare services in Bangladesh with potential benefits for the increasing number of people living with CRDs in LMICs.<br/

    Structural characteristics of camel-bone gelatin by demineralization and extraction

    Get PDF
    Camel bone was demineralized through HCl acidulation process at different concentrations (0.0%, 1.5%, 3.0%, and 6.0%) over 1–5 days. The level of demineralization was acid concentration and soaking time dependent. Highest demineralization (62.0%) was recorded in bone sample treated with 6.0% dilute acid for 5 days. Energy dispersive X-ray spectroscopy (EDX) elemental analysis revealed reduction in Ca and increase in N and H, while O remains unaffected. Particulate characteristics by scanning electron microscope showed an increased surface roughness of bone after demineralization. Fourier transform infrared (FT-IR) analysis of ossein depicted the presence of functional group similar to that of bone protein (collagen). Statistical optimization by central composite design (CCD) revealed a significant quadratic model for optimum values of extraction temperature, pH, and extraction time. The highest gelatin yield from camel bone was 23.66% at optimum extraction condition (71.87°C, pH 5.26, and 2.58 h) and the bloom was 205.74 g. Camel bone is suitable for production of gelatin with good potentials in food and nonfood applications. © 2017 Taylor & Francis Group, LLC

    A Sensitive DNA Enzyme-Based Fluorescent Assay for Bacterial Detection

    No full text
    Bacterial detection plays an important role in protecting public health and safety, and thus, substantial research efforts have been directed at developing bacterial sensing methods that are sensitive, specific, inexpensive, and easy to use. We have recently reported a novel “mix-and-read” assay where a fluorogenic DNAzyme probe was used to detect model bacterium E. coli. In this work, we carried out a series of optimization experiments in order to improve the performance of this assay. The optimized assay can achieve a detection limit of 1000 colony-forming units (CFU) without a culturing step and is able to detect 1 CFU following as short as 4 h of bacterial culturing in a growth medium. Overall, our effort has led to the development of a highly sensitive and easy-to-use fluorescent bacterial detection assay that employs a catalytic DNA
    corecore