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Institution

Makerere University

EducationKampala, Uganda
About: Makerere University is a education organization based out in Kampala, Uganda. It is known for research contribution in the topics: Population & Public health. The organization has 7220 authors who have published 12405 publications receiving 366520 citations. The organization is also known as: Makerere University Kampala & MUK.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the authors developed briquettes from coffee and rice husks agricultural wastes as sustainable fuel sources for domestic cooking applications, using both clay and cassava starch as binders.

86 citations

Journal ArticleDOI
TL;DR: The prevalence and factors associated with Helicobacter pylori colonization in apparently healthy children aged 0-12 years in urban Kampala, Uganda are determined and the impact of Helicobacterial infection on children's health in Uganda needs to be further clarified.
Abstract: Background: Helicobacter pylori is one of the most common causes of bacterial infection in human beings. Studies have showed a high prevalence of Helicobacter pylori among people in low-income countries and colonization early in life. A monoclonal antigen test, performed on faeces, HpSA®ImmunoCardSTAT, has a high sensitivity, specificity and accuracy and the faecal test can be performed in all ages, also in resource-limited settings. The main objective of this study was to determine the prevalence and factors associated with Helicobacter pylori colonization in apparently healthy children aged 0-12 years in urban Kampala, Uganda. Method: We tested 427 apparently healthy children, age 0-12 years (211 males, 216 females), in a cross sectional survey for Helicobacter pylori colonization using HpSA ® ImmunoCardSTAT. A short standardized interview with sociodemographic information and medical history was used to assess risk factors. Results: The overall prevalence of Helicobacter pylori in the 427 children was 44.3% (189 out of 427). Early colonization was common, 28.7%, in children younger than 1 year of age. The age specific rates were 46.0% in children age 1- < 3 years, 51.7% in children age 3- < 6 years, 54.8% in children age 6- < 9 years and 40.0% in children age 9- < 12 years. There was a significant difference in prevalence by gender; female 38.5% versus male 49.8% and by type of housing; permanent house 38.5% versus semi-permanent house 48.6%. Congestive living and education level of the female caretaker showed a clear trend for a difference in prevalence. Factors independently associated with Helicobacter pylori colonization included: drugs taken last three months, using a pit latrine, sources of drinking water and wealth index. Conclusion: The prevalence of Helicobacter pylori colonization among urban Ugandan children is high at an early age and increases with age. The impact of Helicobacter pylori colonization on children's health in Uganda needs to be further clarified.

86 citations

01 Jan 2015
TL;DR: The Global Burden of Disease Study 2013 (GBD 2013) aims to bring together all available epidemiological data using a coherent measurement framework, standardised estimation methods, and transparent data sources to enable comparisons of health loss over time and across causes, age-sex groups, and countries as discussed by the authors.
Abstract: Background The Global Burden of Disease Study 2013 (GBD 2013) aims to bring together all available epidemiological data using a coherent measurement framework, standardised estimation methods, and transparent data sources to enable comparisons of health loss over time and across causes, age–sex groups, and countries. The GBD can be used to generate summary measures such as disability-adjusted life-years (DALYs) and healthy life expectancy (HALE) that make possible comparative assessments of broad epidemiological patterns across countries and time. These summary measures can also be used to quantify the component of variation in epidemiology that is related to sociodemographic development. Methods We used the published GBD 2013 data for age-specific mortality, years of life lost due to premature mortality (YLLs), and years lived with disability (YLDs) to calculate DALYs and HALE for 1990, 1995, 2000, 2005, 2010, and 2013 for 188 countries. We calculated HALE using the Sullivan method; 95% uncertainty intervals (UIs) represent uncertainty in age-specific death rates and YLDs per person for each country, age, sex, and year. We estimated DALYs for 306 causes for each country as the sum of YLLs and YLDs; 95% UIs represent uncertainty in YLL and YLD rates. We quantified patterns of the epidemiological transition with a composite indicator of sociodemographic status, which we constructed from income per person, average years of schooling after age 15 years, and the total fertility rate and mean age of the population. We applied hierarchical regression to DALY rates by cause across countries to decompose variance related to the sociodemographic status variable, country, and time. Findings Worldwide, from 1990 to 2013, life expectancy at birth rose by 6·2 years (95% UI 5·6–6·6), from 65·3 years (65·0–65·6) in 1990 to 71·5 years (71·0–71·9) in 2013, HALE at birth rose by 5·4 years (4·9–5·8), from 56·9 years (54·5–59·1) to 62·3 years (59·7–64·8), total DALYs fell by 3·6% (0·3–7·4), and age-standardised DALY rates per 100 000 people fell by 26·7% (24·6–29·1). For communicable, maternal, neonatal, and nutritional disorders, global DALY numbers, crude rates, and age-standardised rates have all declined between 1990 and 2013, whereas for non–communicable diseases, global DALYs have been increasing, DALY rates have remained nearly constant, and age-standardised DALY rates declined during the same period. From 2005 to 2013, the number of DALYs increased for most specific non-communicable diseases, including cardiovascular diseases and neoplasms, in addition to dengue, food-borne trematodes, and leishmaniasis; DALYs decreased for nearly all other causes. By 2013, the five leading causes of DALYs were ischaemic heart disease, lower respiratory infections, cerebrovascular disease, low back and neck pain, and road injuries. Sociodemographic status explained more than 50% of the variance between countries and over time for diarrhoea, lower respiratory infections, and other common infectious diseases; maternal disorders; neonatal disorders; nutritional deficiencies; other communicable, maternal, neonatal, and nutritional diseases; musculoskeletal disorders; and other non-communicable diseases. However, sociodemographic status explained less than 10% of the variance in DALY rates for cardiovascular diseases; chronic respiratory diseases; cirrhosis; diabetes, urogenital, blood, and endocrine diseases; unintentional injuries; and self-harm and interpersonal violence. Predictably, increased sociodemographic status was associated with a shift in burden from YLLs to YLDs, driven by declines in YLLs and increases in YLDs from musculoskeletal disorders, neurological disorders, and mental and substance use disorders. In most country-specific estimates, the increase in life expectancy was greater than that in HALE. Leading causes of DALYs are highly variable across countries. Interpretation Global health is improving. Population growth and ageing have driven up numbers of DALYs, but crude rates have remained relatively constant, showing that progress in health does not mean fewer demands on health systems. The notion of an epidemiological transition—in which increasing sociodemographic status brings structured change in disease burden—is useful, but there is tremendous variation in burden of disease that is not associated with sociodemographic status. This further underscores the need for country-specific assessments of DALYs and HALE to appropriately inform health policy decisions and attendant actions.

86 citations

Journal ArticleDOI
TL;DR: Differences in food types as well as non-uniform protocols for sampling and identification might have contributed to high heterogeneity although some high prevalence data could be factual with extensive varieties of raw and RTE foods.

85 citations

Journal ArticleDOI
TL;DR: In this paper, a review explores the drivers of soil organic carbon (SOC) concentration relevant for the establishment of thresholds and further evaluates existing SOC thresholds for provoking no yield response or significant response to added N fertilizer.
Abstract: Soil organic carbon (SOC) is a potential soil fertility indicator for regulating nitrogen application in tropical farming systems. However, there are limited studies that have discussed SOC thresholds above or below which crop production could be diminished, or at which no or high response to nitrogen (N) application can be realized. This review explores the drivers of SOC concentration relevant for the establishment of thresholds. We further evaluate existing SOC thresholds for provoking no yield response or significant response to added N fertilizer. Key drivers for SOC concentration relevant in establishing thresholds are mainly climate, topography, texture, and land use management. Soil organic carbon threshold for sustaining soil quality is widely suggested to be about 2% below which deterioration may occur. For added N fertilizer management, specific SOC thresholds seem quite complex and are only valid after assuming other factors are non-limiting. In some soils, SOC levels as low as 0.5% result in fertilizer responses and soils as high as 2% SOC also respond to small N doses. Minimum SOC thresholds can be identified for a given soil type, but maximum thresholds depend on crop N requirements, crop N use efficiency and amount of N applied. However, there seem to exist critical total SOC ranges that could be targeted for optimal indigenous N supply and integrative soil functional benefits. These can be targeted as minimum levels in soil fertility restoration. In all, it is still difficult to establish a single minimum or maximum SOC threshold value that can be universally or regionally accepted.

85 citations


Authors

Showing all 7286 results

NameH-indexPapersCitations
Pete Smith1562464138819
Joy E Lawn10833055168
Philip J. Rosenthal10482439175
William M. Lee10146446052
David R. Bangsberg9746339251
Daniel O. Stram9544535983
Richard W. Wrangham9328829564
Colin A. Chapman9249128217
Ronald H. Gray9252934982
Donald Maxwell Parkin8725971469
Larry B. Goldstein8543436840
Paul Gepts7826319745
Maria J. Wawer7735727375
Robert M. Grant7643726835
Jerrold J. Ellner7634717893
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202343
202289
20211,200
20201,120
2019900
2018790