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1.
Epidemiol Infect ; 152: e34, 2023 Dec 15.
Article in English | MEDLINE | ID: mdl-38097277

ABSTRACT

The devastating effects of the coronavirus disease (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may not end when the acute illness has terminated. A subset of COVID-19 patients may have symptoms that persist for months. This condition has been described as 'long COVID'. From a historical perspective, it has been recognized that serious long-term neurological sequelae have been associated with RNA viruses such as influenza viruses and coronaviruses. A potential intervention for early post-COVID-19 neuropsychiatric impairment may be the commonly employed, readily available, reasonably priced macrolide antibiotic, azithromycin. We have observed a favourable clinical response with azithromycin in three patients with neurological symptoms associated with long COVID-19. We recommend considering formal clinical trials using azithromycin for patients with post-COVID-19 infection neurological changes including 'COVID fog' or the more severe neurological symptoms that may later develop.


Subject(s)
Azithromycin , COVID-19 , Humans , Azithromycin/therapeutic use , SARS-CoV-2 , Post-Acute COVID-19 Syndrome , COVID-19 Drug Treatment
2.
Dermatol Ther ; 33(4): e13785, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32510734

ABSTRACT

The devastating effects of the coronavirus designated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have led to urgent attempts to find effective therapeutic agents for inpatient and outpatient treatment of COVID-19. Initial enthusiasm for the combination of hydroxychloroquine and azithromycin has abated. However, as a result of positive clinical experience with azithromycin used alone during the first few days of the flu-like illness caused by this coronavirus, we recommend formal clinical trials using azithromycin early in the course of a COVID-19 infection. There is one clinical trial initiated, the individually randomized, telemedicine-based, "Azithromycin for COVID-19 Treatment in Outpatients Nationwide" based at the University of California San Francisco. This placebo-controlled trial is designed to determine the efficacy of a single 1.2-g dose of oral azithromycin to prevent COVID-19 patient progression to hospitalization. We recommend formal clinical trials of azithromycin in its prepackaged form at the first sign of COVID-19 infection in adults and children, using an initial adult dose of 500 mg followed by 250 mg per day for 4 days, a total cumulative dose of 1.5 g, and for children 5 to 18 years of age, 10 mg/kg on the first day followed by 5 mg/kg for 4 days.


Subject(s)
Azithromycin/therapeutic use , Betacoronavirus , Coronavirus Infections/drug therapy , Pneumonia, Viral/drug therapy , Adult , Anti-Bacterial Agents/therapeutic use , COVID-19 , Child , Coronavirus Infections/epidemiology , Dose-Response Relationship, Drug , Humans , Pandemics , Pneumonia, Viral/epidemiology , SARS-CoV-2
3.
BMC Med Educ ; 18(1): 185, 2018 Aug 06.
Article in English | MEDLINE | ID: mdl-30081897

ABSTRACT

BACKGROUND: Every curriculum needs to be reviewed, implemented and evaluated; it must also comply with the regulatory standards. This report demonstrates the value of curriculum mapping (CM), which shows the spatial relationships of a curriculum, in developing and managing an integrated medical curriculum. METHODS: A new medical school developed a clinical presentation driven integrated curriculum that incorporates the active-learning pedagogical practices of many educational institutions worldwide while adhering to the mandated requirements of the accreditation bodies. A centralized CM process was run in parallel as the curriculum was being developed. A searchable database, created after the CM data was uploaded into an electronic curriculum management system, was used to ensure placing, integrating, evaluating and revising the curricular content appropriately. RESULTS: CM facilitated in a) appraising the content integration, b) identifying gaps and redundancies, c) linking learning outcomes across all educational levels (i.e. session to course to program), c) organizing the teaching schedules, instruction methods, and assessment tools and d) documenting compliance with accreditation standards. CONCLUSIONS: CM is an essential tool to develop, review, improve and refine any integrated curriculum however complex. Our experience, with appropriate modifications, should help other medical schools efficiently manage their curricula and fulfill the accreditation requirements at the same time.


Subject(s)
Curriculum/standards , Learning , Schools, Medical , Accreditation , Advisory Committees
4.
J Trop Pediatr ; 50(5): 271-5, 2004 10.
Article in English | MEDLINE | ID: mdl-15510757

ABSTRACT

In the developing world, diarrhoeal disease is a significant cause of childhood morbidity especially amongst severely malnourished children. As a direct result of improved acute-phase management of this group of patients, there has been a 47 per cent reduction in the death rate among severely malnourished children hospitalized at the ICDDR,B in Bangladesh. The change in the risk factors for death among children aged under 5 years presenting with diarrhoea was reassessed. The charts of 366 children under 5 years of age who were hospitalized for diarrhoeal disease in the year 1998 were retrospectively analysed. One hundred and eighty-three of these patients died and 183 of those who survived acted as controls. Univariate analysis found 12 significant risk factors on admission that impacted outcome. Only two factors, female sex and positive blood culture, remained significant in the multivariate analysis with odds ratios (95 per cent CI) of 2.05 (1.1-4.0) and 4.6 (1.7-12.4), respectively. Prior to the change in the protocol involving the management of severely malnourished children, only severe malnutrition and non-breastfeeding were found to be significant predictors of mortality.


Subject(s)
Clinical Protocols , Critical Pathways , Diarrhea/mortality , Diarrhea/therapy , Anti-Bacterial Agents/therapeutic use , Bangladesh/epidemiology , Case-Control Studies , Child, Preschool , Confidence Intervals , Dehydration/therapy , Diarrhea/diet therapy , Diarrhea, Infantile/mortality , Diarrhea, Infantile/therapy , Diet Therapy/statistics & numerical data , Female , Fluid Therapy/statistics & numerical data , Humans , Infant , Infant, Newborn , Male , Odds Ratio , Retrospective Studies , Risk Factors , Severity of Illness Index
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