Alemayehu Bekele
American Public Health Association
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BMC Research Notes | 2016
Yusuf Mohammed; Alemayehu Bekele
BackgroundA transfusion transmissible infection (TTI) is any infection that is transmissible from person to- person through parenteral administration of blood or blood products. The magnitude of transfusion-transmitted infections (TTI) varies from country to country depending on TTI’s load in that particular population. Measuring their severity, WHO (World Health Organization) has recommended pre-transfusion blood test for Human immunodeficiency virus (HIV), Hepatitis B virus (HBV), Hepatitis C Virus (HCV) and Syphilis as mandatory. The aim of the current study was to assess the trend and prevalence of TTI among blood donors in Jijiga Blood Bank between 2010 and 2013.MethodsA Retrospective cross-sectional study was conducted by reviewing the records from 2010 to 2013 at Jijiga Blood Bank. All blood donors who presented to the blood bank and screened for TTI during the study period were included. The data was collected, entered and analyzed using Epi Info 3.5.1 & Microsoft Excel 2007. The descriptive statistics were determined in means of percentages. Chi-square was used for trend analysis and p-value was used to declare the statistical significance between the variable.ResultThere were a total of 4224 people donated blood during study period. Males formed the majority of the donor population accounting for 4171 (98.7xa0%). Majority 4139 (98xa0%) of donors were Replacement donors. The overall prevalence of transfusion-transmitted infection was 487/4224 (11.5xa0%). The prevalence for HBsAg, HCV, HIV, & Syphilis antibodies was 460 (10. 9xa0%), 17 (0.4xa0%), 6 (0.1xa0%) and 4 (0.1xa0%) respectively. Majority 460/487 (94.5xa0%) of infection was HBsAg. Statistically significant difference was observed in number of donation as well as sero-positivity from year 2010 to 2013 (Chi-square 9.24, p valuexa0=xa00.02), in Trends of HBsAg from year to year (Chi-square 11.14, p valuexa0=xa00.01), HIV virus was seen as the age of donors increases (Chi-square 8.37, p valuexa0=xa00.01) and There was also statistically significance difference (p valuexa0=xa00.01) in prevalence of HBsAg distribution by sex.ConclusionThe present study clearly documents high Seroprevalence (487 out of 4,224, 11.5xa0%) of TTI, low percentage of voluntary donors and low participation of female donors. Promoting the culture of voluntary donors, recruitment of female blood donors and proper testing of donor’s blood by using standard methods are recommended.
BMC Public Health | 2018
Teklu Weldegebreal; Ismael Ahmed; Abiyou Muhiye; Shoandagne Belete; Alemayehu Bekele; Mirgissa Kaba
BackgroundOpportunistic diseases cause morbidity and mortality among human immunodeficiency virus (HIV) infected persons. There is dearth of evidence on the magnitude and predictors of opportunistic diseases among PLHIV in Ethiopia. This study was conducted to determine the magnitude and predictors of opportunistic diseases among adults enrolled in the national HIV/AIDS care and treatment services and generate information for program planning and medicine quantification in the country.MethodsA health facility-based cross-sectional study was conducted. Probability proportional to size and random sampling methods were employed to select health facilities and medical records of adult HIV-infected patients respectively. A total of 7826 medical records were reviewed from 60 health facilities nationwide. Socio-demographic and clinical data including diagnosis of opportunistic diseases were collected from the medical records. Period prevalence of opportunistic diseases over one year period was determined. Bivariate and multivariate logistic regression was used to measure associations between independent variables and the dependent variable, occurrence of opportunistic diseases.ResultsOf the total of 7826 study participants, 3748 (47.9%) were from hospitals and 4078 were from health centers. The majority (61.8%) were female. The median age was 32xa0years with interquartile range (IQR) of 27–40. The median duration of stay in HIV care was 56 (IQRu2009=u200928–80) months; 7429 (94.9%) were on antiretroviral treatment. A total of 1665 cases of opportunistic diseases were recorded with an overall prevalence estimated at 21.3% (95% confidence interval (CI): 20.36, 22.18%). Skin diseases (4.1%), diarrhea (4.1%), bacterial pneumonia (3.6%), recurrent upper respiratory tract infections (3.1%) and tuberculosis (2.7%) were the leading opportunistic diseases. Isoniazid preventive therapy coverage among eligible patients was 24.8%. Persons with a CD4 count <u2009200 cells/mm3 [adjusted odds ratio (AOR) 1.80, 95% CI: 1.45, 2.23]; and who were bed ridden or ambulatory functional status [AOR (95% CI)u2009=u20093.19 (2.32, 4.39)] were independent predictors of diagnosis of opportunistic diseases.ConclusionOpportunistic diseases were found to be pervasive among HIV infected adults in Ethiopia. Proactive identification and management, and prevention of opportunistic diseases should be strengthened especially among females, ambulatory or bed-ridden, and patients with low CD4 cell count.
BMC Infectious Diseases | 2018
Munira Nasser Hassen; Abyot Bekele Woyessa; Mekonen Getahun; Berhane Beyene; Lucy Buluanger; Ayesheshem Ademe; Alemayehu Bekele; Adamu Addissie; Amha Kebede; Daddi Jima
BackgroundMeasles is a highly infectious and serious respiratory viral disease which caused by a virus. It is a significant cause of illness and death worldwide. This data analysis was conducted to describe the trend and determine the reporting rate of measles cases in Addis Ababa to make recommendation for the government of the city to strengthening measles control interventions.MethodsWe obtained and extracted ten years (2005–2014) Addis Ababa city’s measles surveillance data from national database. We carried out retrospective descriptive data analysis by time, place and person variables. We calculated cumulative and specific reporting rates by dividing measles cases (lab confirmed, epidemiologically linked and compatible cases) to respective population and multiplying by 100,000. We divided average of ten years measles cases to midyear population and multiplied by 100,000 to calculate annualized reporting rate. We analyzed non-measles febrile rash rate by dividing laboratory negative cases to total population and multiplying by 100,000.ResultsA total of 4203 suspected measles cases were identified. Among them 1154 (27.5%) were laboratory confirmed, 512 (12.2%) were clinically compatible, 52 (1.2%) were epidemiologically linked cases and the rest 2485 (59.1%) were IgM negative for measles which makes total measles cases 1718 (40.9%). Median age was 5xa0years with 2–18xa0years interquartile-range. The annualized measles reporting rate was 5.9, which was 40.2 among >u20091xa0year, 11.5 among 1–4xa0years, 6.0 among 5–14xa0years, 4.1 among 15–44xa0years and 0.01 among ≥u200945xa0years per 100,000 population. Among the total measles cases; 380 (22%) were received at least one dose of measles containing vaccine (MCV) while 415 (24%) cases were not vaccinated and the vaccination status of 923 (54%) cases were not known.ConclusionOur analysis revealed that the reporting rate was higher among young children than older age group. Among all the patients 22% were received at least one dose of measles vaccine whereas 13% were not vaccinated against measles antigen. Routine immunization should be strengthened to reach all children through well monitored vaccine cold chain management.
The Ethiopian Journal of Health Development | 2018
Kassahun Amenu; Terefe Gelibo; Misrak Getnet; Tefera Tadele; Theodros Getachew; Atkure Defar; Habtamu Teklie; Geremew Gonfa; Girum Taye; Fasil Shiferaw; Mulugeta Guta; Yeweyenhareg Feleke; Alemayehu Bekele; Dujuma Yadeta; Tedla Kebede; Mussie G; Michael; Feyissa Challa; Yabestse Girma; Kissi Mudie; Yewondwossen Tadesse; Abebe Bekel
The Ethiopian Journal of Health Development | 2018
Terefe Gelibo; Kassahun Amenu; Tefera Tadele; Misrak Getnet; Theodros Getachew; Atkure Defar; Habtamu Teklie; Alemayehu Bekele; Fasil Shiferaw; Mussie G; Michael; Feyissa Challa; Yabestse Girma; Mulugeta Guta; Geremew Gonfa; Kissi Mudie; Yeweyenhareg Feleke; Dejuma Yadeta; Tedla Kebede; Amaha Kebede; Abebe Bekele
The Ethiopian Journal of Health Development | 2018
Habtamu Teklie; Geremew Gonfa; Theodros Getachew; Atkure Defar; Alemayehu Bekele; Abebe Bekele; Terefe Gelibo; Kassahun Amenu; Tefera Tadele; Girum Taye; Misrak Getinet; Feyissa Chala; Kissi Mudie; Mulugeta Guta; Yeweyenharg Feleke; Fassil Shiferaw; Yewondwossen Tadesse; Dujuma Yadeta; Mussie G; Michael; Yabetse Girma; Tedla Kebede; Solomon Teferra
The Ethiopian Journal of Health Development | 2018
Feyissa Challa; Yewondwossen Tadesse; Kissi Mudie; Girum Taye; Terefe Gelibo; Alemayehu Bekele; Meron Sileshi; Tigist Getahun; Zeleke Geto; Abenezer Ayalkebet; Bikila Nagasa; Habtamu Teklie; Tefera Taddele; Theodros Getachew; Yeweyenhareg Feleke; Mulugeta Guta; Fassil Shiferaw; Mussie Gebremichael; Yabetse Girma; Dejuma Yadeta; Tedla Kebede; Atkure Defar; Kassahun Amenu; Misrak Getnet; Geremew Gonfa; Abebe Bekele
The Ethiopian Journal of Health Development | 2018
Abebe Bekele; Terefe Gelibo; Kassahun Amenu; Theodros Getachew; Atkure Defar; Habtamu Teklie; Tefera Taddele; Girum Taye; Misrak Getnet; Geremew Gonfa; Alemayehu Bekele; Tedla Kebede; Yeweyenhareg Feleke; Dejuma Yadeta; Mussie G; Michael; Mulugeta Guta; Fassil Shiferaw; Feyissa Challa; Yabetse Girma; Kissi Mudie; Yewondwossen Tadesse; Yibeltal Assefa; Amha Kebede; Kebede Worku
The Ethiopian Journal of Health Development | 2018
Atkure Defar; Theodros Getachew; Habtamu Teklie; Alemayehu Bekele; Geremew Gonfa; Terefe Gelibo; Kassahun Amenu; Tefera Taddele; Girum Taye; Misrak Getinet; Yabetse Girma; Feyissa Challa; Kissi Mudie; Mulugeta Guta; Yeweyenhareg Feleke; Fassil Shiferaw; Yewondwossen Tadesse; Dejuma Yadeta; Mussie G; Michael; Tedla Kebede; Abebe Bekele; Solomon Teferra
The Ethiopian Journal of Health Development | 2018
Habtamu Teklie; Geremew Gonfa; Theodros Getachew; Atkure Defar; Alemayehu Bekele; Abebe Bekele; Guta Mulugeta; Yeweyenhareg Feleke; Fassil Shiferaw; Yewondwossen Tadess; Dejuma Yadeta; Mussie G; Michael; Yabetse Girma; Tedla Kebede; Solomon Teferra