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World Health Organization WHO, Food and Agriculture Organization FAO, World Organization for Animal Health OIE
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World Health Organization WHO, Regional Office of Europe
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World Health Organization, TB HIV working group, Stop TB Partnership
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World Health Organization, UNAIDS, United Nations Office on Drugs and Crime
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World Health Organization, Western Pacific
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World Health Organization. Regional Office for Europe
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X. Chen
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Y. Keynan, D. Marin et al.
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Y. M. F. Moreno
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Y. Zhang
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Yaria, J.
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Yebyo, Henock G., Mussie A. Gebreselassie, and Alemayehu B. Kahsay
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Yimer, G. et al.
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Yotsu,R.R.
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Yuyun, M.F.
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Z. Brihnu
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Z. Diaz-Bello, C. Colmenares, et al.
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Zhang, H-X.
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Васильева Ирина Анатольевна, Самойлова Анастасия Геннадьевна, Эргешов Атаджан Эргешович et al.
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ВОЗ и Международная организация по проблемам болезни Альцгеймера
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Всемирная организация здравоохранения (ВОЗ)
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Всемирная организация здравоохранения (Европа)
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Всемирная организация здравоохранения (Европейское)
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Г-жа M. Mansfeld
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Г-н Z. T. Gavry
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Д-р M. Dara
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Департамент "Остановить туберкулез", ВОЗ
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Департамент по ВИЧ/СПИД, Департамент «Остановить ТБ», Всемирная организация здравоохранения
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Жилберт Жерро, Николас Кларк
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Назим Агазаде, Ирина Михайловна Никольская, Игорь Валерьевич Добряков et al.
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Раздорская В. В., Воскресенская О. Н., Юдина Г. К.
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Саратовский научно-медицинский журнал
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Сорос-Кыргызстан
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федеральное государственное бюджетное учреждение центральный научно-исследовательский институт туберкулеза российской академии медицинских наук, Американский международный союз здравоохранения
Cystic fibrosis (CF) was earlier thought to be a disease prevalent in the West among Caucasians. However, quite a number of recent studies have uncovered CF cases outside of this region, and reported hundreds of unique and novel variant forms of CFTR. Here, we discuss the evidence of CF in parts of
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the world earlier considered to be rare; Africa, and Asia. This review also highlighted the CFTR mutation variations and new mutations discovered in these regions. This discovery implies that the CF data from these regions were earlier underestimated. The inadequate awareness of the disease in these regions might have contributed towards the poor diagnostic facilities, under-diagnosis or/and under-reporting, and the lack of CF associated health policies. Overall, these regions have a high rate of infant, childhood and early adulthood mortality due to CF. Therefore, there is a need for a thorough investigation of CF prevalence and to identify unique and novel variant mutations within these regions in order to formulate intervention plans, create awareness, develop mutation specific screening kits and therapies to keep CF mortality at bay.
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These policy guidelines provide a strategic approach and new recommendations for integrated TB and HIV services for patients suffering from substance-abuse addiction. The key recommendations fall under three main categories: joint planning, key interventions, and overcoming barriers.
This interim guidance to national health authorities and blood transfusion services outlines the steps required to collect convalescent whole blood (CWB) or plasma (CP) from Ebola virus disease (EVD) recovered patients for transfusion to patients with early EVD, as an empirical treatment modality.
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Document contents:
Guidance on donor selection, screening, donation and handling of blood and plasma units;
guidance on transfusion of convalescent whole blood or plasma;
other considerations.
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Cochrane Database of Systematic Reviews 2015, Issue 2. Art. No.: CD011386. DOI: 10.1002/14651858.CD011386.pub2
Free access from the website http://onlinelibrary.wiley.com/enhanced/doi/10.1002/14651858.CD011386.pub2
Watch a short film which accompanies this Cochrane Review and talks about applying
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the findings in relevant clinical settings at http://www.cochrane.org/news/new-evidence-helps-health-workers-fight-against-ebola
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The primary audience for the guideline is health programme managers, including governmental and non-governmental organizations, and policy makers who are responsible for designing maternal, newborn and child health programmes, primarily in low-income settings. The guideline is also aimed at health p
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roviders and teaching institutions, to increase knowledge of interventions. Development programmes and organizations supporting women’s empowerment and rights will also find this guideline of use.
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Technical Update
Areas of Africa endemic for Buruli ulcer (BU), caused by Mycobacterium ulcerans, also have a high prevalence of human immunodeficiency virus (HIV), with adult prevalence rates between 1% and 5% (Maps). However, there is limited information on the prevalence of BU–HIV coinfection.
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Preliminary
evidence suggests that HIV infection may increase the risk of BU disease (1–3). In the Médecins Sans Frontières project in Akonolinga, Cameroon, HIV prevalence was approximately 3–6 times higher among BU patients than the regional estimated HIV prevalence (2). Similarly in Benin and Ghana, BU
patients were 8 times and 3 times respectively more likely to have HIV infection than those without BU (1, 3). Further study is needed to clarify this association and enhance knowledge about the prevalence ofBU–HIV coinfection in endemic areas.
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The approach is in line with two of the five objectives outlined in the Every Newborn Action Plan (ENAP): Strategic Objective 2 – Improve the quality of maternal and newborn care; and Strategic Objective 5 – Count every newborn through measurement, programme-tracking and accountability to genera
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te data for decision-making and action.
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