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1.
Educ Health (Abingdon) ; 20(1): 18, 2007 May.
Article in English | MEDLINE | ID: mdl-17647184

ABSTRACT

INNOVATIVE EDUCATION: The FHS, Moi University has been an active member of Community Based Education and Service (COBES) network. To achieve this, FHS uses innovative educational strategies that encourage active learning and self-directed learning. However, since these educational strategies are very resource intensive, the faculty has been forced to establish links with health programs. SUSTAINABILITY OF INNOVATIONS: Although higher learning institutions have been urged to become more innovative and responsive to a globally competitive knowledge market, support from governments has been declining. This has forced institutions to develop new links with service systems to enable them to sustain innovations. It is undisputable that investments in higher learning generate major community benefits through returns from research, technology application and service provision. Collaboration, which is a mechanism of working together in a harmonious and supportive way with other agencies, is vital for sustaining innovations. POTENTIAL HEALTH PROGRAMS FOR COLLABORATION: In Kenya, where programs such as Health Education and Maternal Child Health that undertake outreach health services exist, Higher Learning Institutions need to collaborate with these programs to enable them make best use of resources and increase efficiency. In this paper, a framework for collaboration in developing countries where resources are meager is suggested.


Subject(s)
Community Health Services , Community-Institutional Relations , Education, Professional , Teaching/methods , Education, Professional/organization & administration , Humans , Kenya , Models, Educational , Organizational Innovation , Program Development
2.
Microbiol Immunol ; 37(9): 679-88, 1993.
Article in English | MEDLINE | ID: mdl-7505875

ABSTRACT

Parenteral immunization with either formalin-fixed whole cells of the fimbriate Bgd17 strain or purified fimbriae protected against Vibrio cholerae O1 infection in rabbits, independent of biotype and serotype. Parenteral immunization of adult rabbits with purified fimbriae prior to V. cholerae O1 challenge resulted in a reduction of 2 to 3 orders of magnitude in the number of bacteria recovered from the small intestines of immunized rabbits in comparison to non-immunized controls. IgG and IgA antibodies against fimbrillin of V. cholerae O1 were detected in the convalescent sera of patients with cholera; however, little fimbrial antigen was detected in the commercially available cholera vaccines when examined by polyclonal and monoclonal antibodies against fimbriae. These data suggest that fimbrial hemagglutinin is a major adhesin of V. cholerae O1 and that parenteral immunization with fimbriae generates a specific immune response in the gut that may serve as one means of mitigating subsequent V. cholerae O1 gut infection.


Subject(s)
Cholera Vaccines/immunology , Cholera/prevention & control , Fimbriae, Bacterial/immunology , Polysaccharides, Bacterial/immunology , Vibrio cholerae/immunology , Animals , Antibodies, Bacterial/blood , Antibody Formation , Convalescence , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin G/blood , O Antigens , Rabbits
3.
East Afr Med J ; 69(7): 398-401, 1992 Jul.
Article in English | MEDLINE | ID: mdl-1396198

ABSTRACT

Successful treatment of infections with Trichomonas vaginalis (TV) is difficult because of many confounding factors such as poor abstinence from sex during chemotherapy, lack of standardised chemotherapy, difficulties in understanding transmission patterns and low detection rates among infected individuals. The purpose of this study was to establish the present efficacy of the available drugs at their recommended single or double dosages for Kenya. Adult symptomatic females (age 17-39 years) with positive High Vaginal Swabs but without pregnancy were recruited into the study; and asked to swallow one of the following medicine: nimorazole 2G (Naxogin Farmitalia Carlo Erba, Italy), nimorazole 4G in two equally divided doses 24 hours apart (2GBD), nimorazole 3G, tinidazole 2G (Fasigyn, Pfizer Ltd) and ornidazole 1.5G (Tiberal, Roche, Switzerland). All patients were reviewed 48 hours after the drugs administration and 24 hours after the last dose for the group which received nimorazole 2GBD. 153 patients were recruited into the study. 121 came for follow up out of which 49 were dropped from the study for involvement in sexual intercourse leaving only 72 for the final analysis. Clinical cure was 100% for the group receiving nimorazole 2GBD and nimorazole 3G. Parasitological cure was highest for the group on nimorazole 2GBD (100%) and lowest for the group on tinidazole (50%). Instruction to avoid sex during treatment were withheld from patients. This made it easier during the follow up to pick out and drop from the study those who had had sexual contact.


Subject(s)
Nitroimidazoles/therapeutic use , Trichomonas Vaginitis/drug therapy , Adolescent , Adult , Female , Hospitals, District , Hospitals, Public , Humans , Kenya , Nitroimidazoles/administration & dosage , Nitroimidazoles/adverse effects , Outpatient Clinics, Hospital , Trichomonas Vaginitis/diagnosis , Trichomonas Vaginitis/parasitology
4.
East Afr Med J ; 69(3): 135-9, 1992 Mar.
Article in English | MEDLINE | ID: mdl-1505401

ABSTRACT

Three hundred and three children under 5 years old with acute measles and diarrhoea (cases) and 300 other age-matched children with diarrhoea (controls) were examined for enteroadherent E. coli (EAEC) and other agents including rotavirus and Cryptosporidium. EAEC was determined by tissue culture of HEP-2 cells. Other agents were determined by conventional methods. EAEC was identified from both cases and control accounting for 10.3% (31/303) and 15.2% (46/300) respectively. Other bacterial agents were: 10.3% (31/303) from cases and 12.8% (39/300) from controls. A higher detection rate of enteroparasites was found among cases 15% (45/300) than controls 8.9% (27/300) whereas rotavirus was the reverse, 3% (9/303) in cases and 30.3% (92/300) in controls. To our knowledge characterization of EAEC has not been done before and therefore might be attributing factor to some of our unexplained diarrhoeal cases.


Subject(s)
Diarrhea/etiology , Escherichia coli Infections/complications , Escherichia coli/classification , Measles/complications , Child, Preschool , Escherichia coli Infections/epidemiology , Escherichia coli Infections/microbiology , Hospitals, Public , Humans , Infant , Infant, Newborn , Kenya/epidemiology , Microbial Sensitivity Tests , Prevalence , Serotyping
8.
East Afr Med J ; 62(12): 835-41, 1985 Dec.
Article in English | MEDLINE | ID: mdl-3835063

ABSTRACT

PIP: 3 groups of children aged 0-5 years were studied at Kenyatta National Hospital between September 1983 and September 1984 to determine the incidence of enteric agents causing diarrhea in infants and children. The 1st group consisted of children with diarrhea alone, the 2nd group had diarrhea and kwashiorkor, and the 3rd had diarrhea and marasmus. Diarrhea occurring alone peaked in the 0-5 month age group; diarrhea and marasmus peaked in the 6-11 month group, and diarrhea and kwashiorkor, the 6-17 month group. Isolation rates of enteric agents (Campylobacter, Shigella, Salmonella, Rotavirus) for the 3 groups were not significantly different; however E. coli was isolated with a higher frequency from children who had diarrhea with marasmus. The most common mixed infection was that of E. coli and Rotavirus, occurring more often in children with marasmus. Most children had a history of diarrhea for 3-5 days duration. Among agents isolated from cases of more than 8 days duration, Campylobacter was most common, and was only isolated from malnourished children. Results indicate that duration of diarrhea before admission was longer in kwashiorkor or marasmic children than children with diarrhea alone. Treatment for diarrhea in all cases should be similar.^ieng


Subject(s)
Diarrhea/complications , Enterobacteriaceae Infections/complications , Nutrition Disorders/complications , Diarrhea/etiology , Humans , Infant
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