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1.
Mymensingh Med J ; 31(3): 876-881, 2022 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-35780378

RESUMEN

Arrhythmogenic right ventricular dysplasia (ARVD) is a progressive degeneration and replacement of the right ventricular (RV) myocardial tissue by fat and fibrosis and produce clinical condition. Desmosome gene mutations are only the causative state for ARVD hereditary disorder. The arrhythmogenic right ventricular cardiomyopathy incidence is about 1/1000-5000. Mostly young people and athletes are bearing the clinical presentations include presyncope, syncope, ventricular tachycardias or ventricular fibrillation leading to cardiac arrest. We report about the first case of Cardiac magnetic resonance (CMR) imaging to diagnose a case Arrhythmogenic right ventricular dysplasia (ARVD) of a 34-year-old male from Savar, Dhaka, Bangladesh who was referred to cardiac emergency for the evaluation recurrent dizzy spells.


Asunto(s)
Displasia Ventricular Derecha Arritmogénica , Adolescente , Adulto , Displasia Ventricular Derecha Arritmogénica/diagnóstico por imagen , Displasia Ventricular Derecha Arritmogénica/genética , Bangladesh , Ventrículos Cardíacos , Humanos , Imagen por Resonancia Magnética/métodos , Espectroscopía de Resonancia Magnética , Masculino
2.
J Pharm Policy Pract ; 14(1): 73, 2021 Aug 31.
Artículo en Inglés | MEDLINE | ID: mdl-34465394

RESUMEN

BACKGROUND: One in four people experience a mental health problem every year and improving mental health care is an international priority. In the course of their work, pharmacists frequently encounter people with mental health problems. The experience of mental health teaching, including Mental Health First Aid (MHFA) training, in undergraduate pharmacy (MPharm) students in the UK and Ireland is not well documented. Students' viewpoints, contextualised with curricular overviews provided by staff, were analysed to understand their experience. METHODS: An anonymous, online questionnaire was distributed to MPharm students and staff in the UK and Ireland. Students were asked closed questions regarding their course and exposure to MHFA, which were analysed using descriptive statistics. Open questions were included to enable explanations and these data were used to contextualise the quantitative findings. One member of staff from each university was invited to answer a modified staff version of the questionnaire, to provide a curriculum overview and staff perspective. RESULTS: 232 students and 13 staff, from 22 universities, responded. Three-quarters of students did not agree with the statement that 'mental health was embedded throughout the MPharm'. Most students (80.6%) stated that they were taught neuropharmacology whilst 44.8% stated that their course included communicating with people about their mental health. One-third (33.2%) of students stated that their degree 'adequately prepared them to help people with their mental health'. Twenty-six students (11.6%) had completed MHFA training of which 89% would endorse inclusion of this within the MPharm. Of those who had not completed the training, 81% expressed a desire to do so. Those who completed MHFA training self-reported greater preparedness than those who did not, but student numbers were small. CONCLUSIONS: Mental health teaching for pharmacy undergraduates is more focussed on theoretical aspects rather than applied skills. MHFA was viewed by students as one way to enhance skill application. The association of the increased self-reported preparedness of those who completed MHFA could be confounded by a positive environmental cultural. MPharm programmes need sufficient focus on real-world skills such as communication and crisis response, to complement the fundamental science.

3.
Mymensingh Med J ; 28(3): 668-672, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31391442

RESUMEN

Hypertension is a global health problem and affects more than one billion people worldwide. Long term hypertension is associated with grave complications and therefore maintaining blood pressure within normal range is essential and ensuring patient's drug compliance is an important sector of patient care. Therefore, the purpose of our study was to find out the causes of poor compliance to antihypertensive medications. This cross sectional study was carried out in Medical Department of Ayub Teaching Hospital Abbottabad, Pakistan from 1st September 2017 to 30th October 2018. One hundred ninety three (193) patients were included through non probability consecutive sampling and were divided into two groups on the basis of compliance. The data was collected with the help of a structured questionnaire and analyzed using SPSS 20. Out of 193 hypertensive patients, 88(45.6%) were male while 105(54.4%) were females, with minimum age of 24 years and maximum age of 95 years and mean age of 61.98±12.81SD. Minimum duration of hypertension was 5 months and maximum was 30 years with mean duration of hypertension and standard deviation (SD) of 6.26±6.51 years. One hundred & Twenty (62.2%) patients were non-compliant, while 73(37.8%) were compliant to medication. Forgetfulness of medicine 85(70.8%) and non-affordability 62(52.5%) were the most common causes of noncompliance. This study documented a significantly higher proportion of medication non-adherence among hypertensive patients, with drug forgetfulness and affordability being found as the most common cause.


Asunto(s)
Antihipertensivos , Hipertensión , Cooperación del Paciente , Adulto , Anciano , Anciano de 80 o más Años , Antihipertensivos/uso terapéutico , Estudios Transversales , Femenino , Humanos , Hipertensión/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Pakistán , Atención Terciaria de Salud , Adulto Joven
4.
Microb Pathog ; 116: 200-208, 2018 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-29414608

RESUMEN

Silver nanoparticles showed enhanced biofilm inhibitory activity of clinical pathogens. Eleven isolates (45.8%) of E. coli bacteria were obtained from 24 wound specimens. Silver nanoparticles biosynthesized by E. coli culture supernatant with exhibition dark brown color after 24 hr of incubation. Scanning electron microscopy showed that Ag-NPs spherical particles and its size were (14.2-67.8) nm and its average was 33.6 nm. X-ray diffraction shows one high peak at 2ø (32.5°) compared with standard data. Fourier transform infrared spectroscopy analysis of Ag-NPs exposed the strong band at 1367.53 corresponds to OH-bend which influences the synthesis and stability of Ag-NPs, whereas the stretch for Ag-NPs found at 518.58 cm-1. The antibacterial effect of Ag-Nps against E. coli, P. aeruginosa, K. pneumoniae and S. aureus showed the inhibition zone of 10, 11, 13, and 10 mm, respectively. Strong biofilm formed by isolates of E. coli exhibited as black colonies on Congo red agar, while pink colonies on it with Ag-Nps, indicating a loss of biofilm formation ability in all tested bacterial isolates. Antibiofilm of 10 mM Ag-Nps by Microtiter plate exhibited lower biofilm inhibition against S. aureus reached to 22.2%, while 36.2% against E. coli, 30.4% for K. pneumonae, and P. aeruginosa 94.7%. Analysis of biofilm components after exposure to Ag-NPs by FT-IR reveals a low level of proteins, polysaccharides, lipids and nucleic acids compared with controls, then glucose formation measured and exhibited reduction of absorbance (0.146 nm) after treatment with Ag-Nps compared with control (0.347 nm), while the percentage of protein decreased completely (0%) compared with control (0.25%). The combined effect of Ag-NPs with antibiotics enhanced the antibiofilm activity which tested under inverted microscope (40X).


Asunto(s)
Antibacterianos/metabolismo , Biopelículas/efectos de los fármacos , Escherichia coli/metabolismo , Bacterias Gramnegativas/efectos de los fármacos , Bacterias Grampositivas/efectos de los fármacos , Nanopartículas , Plata/metabolismo , Antibacterianos/farmacología , Biopelículas/crecimiento & desarrollo , Escherichia coli/aislamiento & purificación , Infecciones por Escherichia coli/microbiología , Bacterias Gramnegativas/fisiología , Bacterias Grampositivas/fisiología , Humanos , Microscopía Electrónica de Rastreo , Plata/farmacología , Espectroscopía Infrarroja por Transformada de Fourier , Infección de Heridas/microbiología , Difracción de Rayos X
5.
Allergy ; 73(4): 744-764, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-28748641

RESUMEN

Hymenoptera venom allergy is a potentially life-threatening allergic reaction following a honeybee, vespid, or ant sting. Systemic-allergic sting reactions have been reported in up to 7.5% of adults and up to 3.4% of children. They can be mild and restricted to the skin or moderate to severe with a risk of life-threatening anaphylaxis. Patients should carry an emergency kit containing an adrenaline autoinjector, H1 -antihistamines, and corticosteroids depending on the severity of their previous sting reaction(s). The only treatment to prevent further systemic sting reactions is venom immunotherapy. This guideline has been prepared by the European Academy of Allergy and Clinical Immunology's (EAACI) Taskforce on Venom Immunotherapy as part of the EAACI Guidelines on Allergen Immunotherapy initiative. The guideline aims to provide evidence-based recommendations for the use of venom immunotherapy, has been informed by a formal systematic review and meta-analysis and produced using the Appraisal of Guidelines for Research and Evaluation (AGREE II) approach. The process included representation from a range of stakeholders. Venom immunotherapy is indicated in venom-allergic children and adults to prevent further moderate-to-severe systemic sting reactions. Venom immunotherapy is also recommended in adults with only generalized skin reactions as it results in significant improvements in quality of life compared to carrying an adrenaline autoinjector. This guideline aims to give practical advice on performing venom immunotherapy. Key sections cover general considerations before initiating venom immunotherapy, evidence-based clinical recommendations, risk factors for adverse events and for relapse of systemic sting reaction, and a summary of gaps in the evidence.


Asunto(s)
Venenos de Abeja/administración & dosificación , Desensibilización Inmunológica/métodos , Desensibilización Inmunológica/normas , Hipersensibilidad/etiología , Hipersensibilidad/prevención & control , Animales , Venenos de Abeja/inmunología , Humanos
6.
Allergy ; 73(4): 827-836, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-28850687

RESUMEN

PURPOSE: The European Academy of Allergy and Clinical Immunology (EAACI) has produced Guidelines on Allergen Immunotherapy (AIT). We sought to gauge the preparedness of primary care to participate in the delivery of AIT in Europe. METHODS: We undertook a mixed-methods, situational analysis. This involved a purposeful literature search and two surveys: one to primary care clinicians and the other to a wider group of stakeholders across Europe. RESULTS: The 10 papers identified all pointed out gaps or deficiencies in allergy care provision in primary care. The surveys also highlighted similar concerns, particularly in relation to concerns about lack of knowledge, skills, infrastructural weaknesses, reimbursement policies and communication with specialists as barriers to evidence-based care. Almost all countries (92%) reported the availability of AIT. In spite of that, only 28% and 44% of the countries reported the availability of guidelines for primary care physicians and specialists, respectively. Agreed pathways between specialists and primary care physicians were reported as existing in 32%-48% of countries. Reimbursement appeared to be an important barrier as AIT was only fully reimbursed in 32% of countries. Additionally, 44% of respondents considered accessibility to AIT and 36% stating patient costs were barriers. CONCLUSIONS: Successful working with primary care providers is essential to scaling-up AIT provision in Europe, but to achieve this, the identified barriers must be overcome. Development of primary care interpretation of guidelines to aid patient selection, establishment of disease management pathways and collaboration with specialist groups are required as a matter of urgency.


Asunto(s)
Desensibilización Inmunológica/normas , Hipersensibilidad/prevención & control , Guías de Práctica Clínica como Asunto , Desensibilización Inmunológica/métodos , Humanos
7.
Allergy ; 72(12): 1825-1848, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28543086

RESUMEN

BACKGROUND: To inform the development of the European Academy of Allergy and Clinical Immunology's (EAACI) Guidelines on Allergen Immunotherapy (AIT) for allergic asthma, we assessed the evidence on the effectiveness, cost-effectiveness and safety of AIT. METHODS: We performed a systematic review, which involved searching nine databases. Studies were screened against predefined eligibility criteria and critically appraised using established instruments. Data were synthesized using random-effects meta-analyses. RESULTS: 98 studies satisfied the inclusion criteria. Short-term symptom scores were reduced with a standardized mean difference (SMD) of -1.11 (95% CI -1.66, -0.56). This was robust to a prespecified sensitivity analyses, but there was evidence suggestive of publication bias. Short-term medication scores were reduced SMD -1.21 (95% CI -1.87, -0.54), again with evidence of potential publication bias. There was no reduction in short-term combined medication and symptom scores SMD 0.17 (95% CI -0.23, 0.58), but one study showed a beneficial long-term effect. For secondary outcomes, subcutaneous immunotherapy (SCIT) improved quality of life and decreased allergen-specific airway hyperreactivity (AHR), but this was not the case for sublingual immunotherapy (SLIT). There were no consistent effects on asthma control, exacerbations, lung function, and nonspecific AHR. AIT resulted in a modest increased risk of adverse events (AEs). Although relatively uncommon, systemic AEs were more frequent with SCIT; however no fatalities were reported. The limited evidence on cost-effectiveness was mainly available for sublingual immunotherapy (SLIT) and this suggested that SLIT is likely to be cost-effective. CONCLUSIONS: AIT can achieve substantial reductions in short-term symptom and medication scores in allergic asthma. It was however associated with a modest increased risk of systemic and local AEs. More data are needed in relation to secondary outcomes, longer-term effectiveness and cost-effectiveness.


Asunto(s)
Alérgenos/inmunología , Asma/inmunología , Asma/terapia , Desensibilización Inmunológica , Asma/diagnóstico , Análisis Costo-Beneficio , Desensibilización Inmunológica/efectos adversos , Desensibilización Inmunológica/métodos , Humanos , Inyecciones Subcutáneas , Calidad de Vida , Ensayos Clínicos Controlados Aleatorios como Asunto , Pruebas de Función Respiratoria , Inmunoterapia Sublingual , Evaluación de Síntomas , Factores de Tiempo , Resultado del Tratamiento
8.
Allergy ; 72(11): 1597-1631, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28493631

RESUMEN

BACKGROUND: The European Academy of Allergy and Clinical Immunology (EAACI) is in the process of developing Guidelines on Allergen Immunotherapy (AIT) for Allergic Rhinoconjunctivitis. To inform the development of clinical recommendations, we undertook a systematic review to assess the effectiveness, cost-effectiveness, and safety of AIT in the management of allergic rhinoconjunctivitis. METHODS: We searched nine international biomedical databases for published, in-progress, and unpublished evidence. Studies were independently screened by two reviewers against predefined eligibility criteria and critically appraised using established instruments. Our primary outcomes of interest were symptom, medication, and combined symptom and medication scores. Secondary outcomes of interest included cost-effectiveness and safety. Data were descriptively summarized and then quantitatively synthesized using random-effects meta-analyses. RESULTS: We identified 5960 studies of which 160 studies satisfied our eligibility criteria. There was a substantial body of evidence demonstrating significant reductions in standardized mean differences (SMD) of symptom (SMD -0.53, 95% CI -0.63, -0.42), medication (SMD -0.37, 95% CI -0.49, -0.26), and combined symptom and medication (SMD -0.49, 95% CI -0.69, -0.30) scores while on treatment that were robust to prespecified sensitivity analyses. There was in comparison a more modest body of evidence on effectiveness post-discontinuation of AIT, suggesting a benefit in relation to symptom scores. CONCLUSIONS: AIT is effective in improving symptom, medication, and combined symptom and medication scores in patients with allergic rhinoconjunctivitis while on treatment, and there is some evidence suggesting that these benefits are maintained in relation to symptom scores after discontinuation of therapy.


Asunto(s)
Conjuntivitis Alérgica/terapia , Desensibilización Inmunológica/métodos , Rinitis Alérgica Estacional/terapia , Alérgenos/inmunología , Bases de Datos Factuales , Humanos
9.
Allergy ; 72(3): 342-365, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-28120424

RESUMEN

BACKGROUND: The European Academy of Allergy and Clinical Immunology (EAACI) is in the process of developing the EAACI Guidelines on Allergen Immunotherapy (AIT) for the management of insect venom allergy. To inform this process, we sought to assess the effectiveness, cost-effectiveness and safety of AIT in the management of insect venom allergy. METHODS: We undertook a systematic review, which involved searching 15 international biomedical databases for published and unpublished evidence. Studies were independently screened and critically appraised using established instruments. Data were descriptively summarized and, where possible, meta-analysed. RESULTS: Our searches identified a total of 16 950 potentially eligible studies; of which, 17 satisfied our inclusion criteria. The available evidence was limited both in volume and in quality, but suggested that venom immunotherapy (VIT) could substantially reduce the risk of subsequent severe systemic sting reactions (OR = 0.08, 95% CI 0.03-0.26); meta-analysis showed that it also improved disease-specific quality of life (risk difference = 1.41, 95% CI 1.04-1.79). Adverse effects were experienced in both the build-up and maintenance phases, but most were mild with no fatalities being reported. The very limited evidence found on modelling cost-effectiveness suggested that VIT was likely to be cost-effective in those at high risk of repeated systemic sting reactions and/or impaired quality of life. CONCLUSIONS: The limited available evidence suggested that VIT is effective in reducing severe subsequent systemic sting reactions and in improving disease-specific quality of life. VIT proved to be safe and no fatalities were recorded in the studies included in this review. The cost-effectiveness of VIT needs to be established.


Asunto(s)
Venenos de Artrópodos/inmunología , Desensibilización Inmunológica , Hipersensibilidad/inmunología , Hipersensibilidad/terapia , Alérgenos/inmunología , Animales , Análisis Costo-Beneficio , Desensibilización Inmunológica/efectos adversos , Desensibilización Inmunológica/economía , Desensibilización Inmunológica/métodos , Manejo de la Enfermedad , Humanos , Mordeduras y Picaduras de Insectos/inmunología , Mordeduras y Picaduras de Insectos/terapia , Factores de Riesgo , Resultado del Tratamiento
10.
Part Fibre Toxicol ; 13: 10, 2016 Feb 24.
Artículo en Inglés | MEDLINE | ID: mdl-26911867

RESUMEN

BACKGROUND: Particulate matter (PM) is one of the six criteria pollutant classes for which National Ambient Air Quality Standards have been set by the United States Environmental Protection Agency. Exposures to PM have been correlated with increased cardio-pulmonary morbidity and mortality. Butadiene soot (BDS), generated from the incomplete combustion of 1,3-butadiene (BD), is both a model PM mixture and a real-life example of a petrochemical product of incomplete combustion. There are numerous events, including wildfires, accidents at refineries and tank car explosions that result in sub-acute exposure to high levels of airborne particles, with the people exposed facing serious health problems. These real-life events highlight the need to investigate the health effects induced by short-term exposure to elevated levels of PM, as well as to assess whether, and if so, how well these adverse effects are resolved over time. In the present study, we investigated the extent of recovery of mouse lungs 10 days after inhalation exposures to environmentally-relevant levels of BDS aerosols had ended. METHODS: Female BALB/c mice exposed to either HEPA-filtered air or to BDS (5 mg/m(3) in HEPA filtered air, 4 h/day, 21 consecutive days) were sacrificed immediately, or 10 days after the final BDS exposure. Bronchoalveolar lavage fluid (BALF) was collected for cytology and cytokine analysis. Lung proteins and RNA were extracted for protein and gene expression analysis. Lung histopathology evaluation also was performed. RESULTS: Sub-acute exposures of mice to hydrocarbon-rich ultrafine particles induced: (1) BALF neutrophil elevation; (2) lung mucosal inflammation, and (3) increased BALF IL-1ß concentration; with all three outcomes returning to baseline levels 10 days post-exposure. In contrast, (4) lung connective tissue inflammation persisted 10 days post-exposure; (5) we detected time-dependent up-regulation of biotransformation and oxidative stress genes, with incomplete return to baseline levels; and (6) we observed persistent particle alveolar load following 10 days of recovery. CONCLUSION: These data show that 10 days after a 21-day exposure to 5 mg/m(3) of BDS has ended, incomplete lung recovery promotes a pro-biotransformation, pro-oxidant, and pro-inflammatory milieu, which may be a starting point for potential long-term cardio-pulmonary effects.


Asunto(s)
Butadienos/toxicidad , Contaminantes Ambientales/toxicidad , Pulmón/efectos de los fármacos , Neumonía/inducido químicamente , Hollín/toxicidad , Administración por Inhalación , Aerosoles , Animales , Líquido del Lavado Bronquioalveolar/química , Butadienos/administración & dosificación , Contaminantes Ambientales/administración & dosificación , Femenino , Regulación de la Expresión Génica , Redes Reguladoras de Genes , Mediadores de Inflamación/metabolismo , Interleucina-1beta/metabolismo , Pulmón/metabolismo , Pulmón/patología , Ratones Endogámicos BALB C , Infiltración Neutrófila/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Tamaño de la Partícula , Neumonía/genética , Neumonía/metabolismo , Neumonía/patología , Recuperación de la Función , Medición de Riesgo , Hollín/administración & dosificación , Factores de Tiempo
12.
J Dev Areas ; 29(3): 371-88, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12346855

RESUMEN

PIP: Tarapur is a village in the district of Rajshahi, Bangladesh, covering an area of 821.05 acres. 342 households with a total population of 1981 were identified in the village by the 1985 census. The author investigated the use of time during 1984 and 1985 in busy, intermediate, and slack seasons among the village population to examine the variation in time use by gender and social class. Activity patterns were found to vary from one season to another, and also across social classes. The study highlights the need to refine some of the conceptual and methodological issues in the collection of data on women and work. The study also presents useful data on home-based production and market-oriented work. It could be useful to adopt an anthropological approach in order to understand the allocation of time by men and women from the perspective of household production and the local economy and culture. Study findings focus upon the following policy issues: the need for a better understanding and recognition of the significant role of women in field agriculture and postharvest processing, creation of further nontraditional employment and business opportunities for poor women in rural areas, and consciousness-raising and the challenge of cultural barriers affecting women. Rural women, especially those in need of employment and involved in market-oriented production, should be the target of mainstream development activities in future planning.^ieng


Asunto(s)
Relaciones Interpersonales , Población Rural , Estaciones del Año , Clase Social , Factores de Tiempo , Asia , Bangladesh , Demografía , Países en Desarrollo , Economía , Población , Características de la Población , Dinámica Poblacional , Factores Socioeconómicos
13.
Birthright ; 6(314): 12-3, 1971.
Artículo en Inglés | MEDLINE | ID: mdl-12276340

RESUMEN

PIP: This summarizes briefly teachings on family planning according to the consensus, or Ijma, of Muslim jurists. "Limitation of numbers" or family planning is permitted for preserving the good life, for ensuring economic security, for preserving the health of the wife, and, by implication, when the consent of the wife is given. Azl (coitus interruptus) is definitely permitted with the consent of the wife. New methods may be adopted subject to the principle of moral behavior. The wife can adopt any method with the consent of her husband in order to save her life. She can adopt it without his consent if she is in poor health. The use of qualified medical advice is emphasized. The view that contraception is killing children is extreme; the admonition in the Holy Koran not to recourse to infanticide is to discourage the killing of children, and is not directed at healthy methods of birth control. Islam stands for a positive life and does not give credence to the fatalism and pessimism of Malthusian calculus. It also does not uphold family planning as a negative factor in economics and society.^ieng


Asunto(s)
Servicios de Planificación Familiar , Coito Interrumpido
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