Akindeh Mbuh Nji
University of Yaoundé I
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Publication
Featured researches published by Akindeh Mbuh Nji.
Tropical Medicine & International Health | 2011
Lindsay Mangham; Bonnie Cundill; Olivia Achonduh; Joel N Ambebila; Albertine K. Lele; Theresia N. Metoh; Sarah N. Ndive; Ignatius C. Ndong; Rachel L. Nguela; Akindeh Mbuh Nji; Barnabas Orang-Ojong; Virginia Wiseman; Joelle Pamen-Ngako; Wilfred F. Mbacham
Objective To investigate the quality of malaria case management in Cameroon 5 years after the adoption of artemisinin‐based combination therapy (ACT). Treatment patterns were examined in different types of facility, and the factors associated with being prescribed or receiving an ACT were investigated.
Malaria Journal | 2010
Wilfred F. Mbacham; Marie-Solange Evehe; Palmer Masumbe Netongo; Patrice Nsangou Mimche; Anthony Ajua; Akindeh Mbuh Nji; Domkam Irenee; Justin B Echouffo-Tcheugui; Bantar Tawe; Rachel Hallett; Cally Roper; Geoffrey Targett; Brian Greenwood
BackgroundThe efficacy of amodiaquine (AQ), sulphadoxine-pyrimethamine (SP) and the combination of SP+AQ in the treatment of Cameroonian children with clinical malaria was investigated. The prevalence of molecular markers for resistance to these drugs was studied to set the baseline for surveillance of their evolution with time.MethodsSeven hundred and sixty children aged 6-59 months with uncomplicated falciparum malaria were studied in three ecologically different regions of Cameroon - Mutengene (littoral equatorial forest), Yaoundé (forest-savannah mosaic) and Garoua (guinea-savannah). Study children were randomized to receive either AQ, SP or the combination AQ+SP. Clinical outcome was classified according to WHO criteria, as either early treatment failure (ETF), late clinical failure (LCF), late parasitological failure (LPF) or adequate clinical and parasitological response (ACPR). The occurrence of mutations in pfcrt, pfmdr1, dhfr and dhps genes was studied by either RFLP or dot blot techniques and the prevalence of these mutations related to parasitological and therapeutic failures.ResultsAfter correction for the occurrence of re-infection by PCR, ACPRs on day 28 for AQ, SP and AQ+SP were 71.2%, 70.1% and 80.9%, in Garoua, 79.2%, 62.5%, and 81.9% in Mutengene, and 80.3%, 67.5% and 76.2% in Yaoundé respectively. High levels of Pfcrt 76T (87.11%) and Pfmdr1 86Y mutations (73.83%) were associated with quinoline resistance in the south compared to the north, 31.67% (76T) and 22.08% (86Y). There was a significant variation (p < 0.001) of the prevalence of the SGK haplotype between Garoua in the north (8.33%), Yaoundé (36.29%) in the savannah-forest mosaic and Mutengene (66.41%) in the South of Cameroon and a weak relation between SGK haplotype and SP failure. The 540E mutation on the dhps gene was extremely rare (0.3%) and occurred only in Mutengene while the pfmdr1 1034K and 1040D mutations were not detected in any of the three sites.ConclusionIn this study the prevalence of molecular markers for quinoline and anti-folate resistances showed high levels and differed between the south and north of Cameroon. AQ, SP and AQ+SP treatments were well tolerated but with low levels of efficacy that suggested alternative treatments were needed in Cameroon since 2005.
Trials | 2012
Virginia Wiseman; Lindsay Mangham; Bonnie Cundill; Olivia Achonduh; Akindeh Mbuh Nji; Abanda Ngu Njei; Clare Chandler; Wilfred F. Mbacham
BackgroundGovernments and donors all over Africa are searching for sustainable, affordable and cost-effective ways to improve the quality of malaria case management. Widespread deficiencies have been reported in the prescribing and counselling practices of health care providers treating febrile patients in both public and private health facilities. Cameroon is no exception with low levels of adherence to national guidelines, the frequent selection of non-recommended antimalarials and the use of incorrect dosages. This study evaluates the effectiveness and cost-effectiveness of introducing two different provider training packages, alongside rapid diagnostic tests (RDTs), designed to equip providers with the knowledge and practical skills needed to effectively diagnose and treat febrile patients. The overall aim is to target antimalarial treatment better and to facilitate optimal use of malaria treatment guidelines.Methods/DesignA 3-arm stratified, cluster randomized trial will be conducted to assess whether introducing RDTs with provider training (basic or enhanced) is more cost-effective than current practice without RDTs, and whether there is a difference in the cost effectiveness of the provider training interventions. The primary outcome is the proportion of patients attending facilities that report a fever or suspected malaria and receive treatment according to malaria guidelines. This will be measured by surveying patients (or caregivers) as they exit public and mission health facilities. Cost-effectiveness will be presented in terms of the primary outcome and a range of secondary outcomes, including changes in provider knowledge. Costs will be estimated from a societal and provider perspective using standard economic evaluation methodologies.Trial RegistrationClinicalTrials.gov: NCT00981877
Malaria Research and Treatment | 2018
Marcel N. Moyeh; Dieudonne L. Njimoh; Marie Solange Evehe; Innocent M. Ali; Akindeh Mbuh Nji; Dominique N. Nkafu; Palmer N. Masumbe; Atogho-Tiedeu Barbara; Valentine Ndikum; Wilfred F. Mbacham
Background As a result of the spread of parasites resistant to antimalarial drugs, Malaria treatment guidelines in Cameroon evolved from nonartemisinin monotherapy to artemisinin-based combination therapy. The aim of this study was to assess the effect of these therapy changes on the prevalence of molecular markers of resistance from 2003 to 2013 in Mutengene, Cameroon. Methodology Dry blood samples (collected in 2003–2005 and 2009–2013) were used for parasite DNA extraction. Drug resistance genes were amplified by PCR and hybridized with oligonucleotide probes or subjected to restriction digestion. The prevalence of individual marker polymorphisms and haplotypes was compared in these two study periods using the Chi square test. Results Alleles conferring resistance to 4-aminoquinolines in the Pfcrt 76T and Pfmdr1 86Y, 184F, and 1246Y genotypes showed a significant reduction of 97.0% to 66.9%, 83.6% to 45.2%, 97.3% to 56.0%, and 3.1% to 0.0%, respectively (P < 0.05). No difference was observed in SNPs associated with antifolate drugs resistance 51I, 59R, 108N, or 540E (P > 0.05). Haplotype analysis in the Pfmdr1 gene showed a reduction in the YFD from 75.90% to 42.2%, P < 0.0001, and an increase in the NYD (2.9% to 30.1%; P < 0.0001). Conclusions The results indicated a gradual return of the 4-aminoquinoline sensitive genotype while the antifolate resistant genotypes increased to saturation.
The Pan African medical journal | 2015
Armand Seraphin Nkwescheu; Joseph Fokam; Patrice Tchendjou; Akindeh Mbuh Nji; Hermann Ngouakam; Bita Fouda Andre; Sobngwi Joelle; Benjamin Uzochukwu; Kingsley K. Akinroye; Wilfred F. Mbacham; Vittorio Colizzi; Rose Leke; Cesar G. Victora
As the study of disease occurrence and health indicators in human populations, Epidemiology is a dynamic field that evolves with time and geographical context. In order to update African health workers on current epidemiological practices and to draw awareness of early career epidemiologists on concepts and opportunities in the field, the 3rd African Epidemiology Association and the 1st Cameroon Society of Epidemiology Conference was organized in June 2-6, 2014 at the Yaoundé Mont Febe Hotel, in Cameroon. Under the theme«Practice of Epidemiology in Africa: Stakes, Challenges and Perspectives», the conference attracted close to five hundred guest and participants from all continents. The two main programs were the pre-conference course for capacity building of African Early Career epidemiologists, and the conference itself, providing a forum for scientific exchanges on recent epidemiological concepts, encouraging the use of epidemiological methods in studying large disease burden and neglected tropical diseases; and highlighting existing opportunities.
Malaria Journal | 2015
Akindeh Mbuh Nji; Innocent M. Ali; Marcel N Moyeh; Eric-Oliver Ngongang; Aristide M Ekollo; Jean-Paul Chedjou; Valentine N Ndikum; Marie Solange Evehe; Guenter Froeschl; Christian Heumann; Ulrich Mansmann; Olumide Ogundahunsi; Wilfred F. Mbacham
African Journal of Biotechnology | 2009
Wilfred F. Mbacham; M Evehe; Palmer Masumbe Netongo; Innocent M. Ali; N Nfor; A Akaragwe; Patrice Nsangou Mimche; Akindeh Mbuh Nji; C Djoko; B Tawe
African Journal of Biotechnology | 2008
Wilfred F. Mbacham; Patrice Nsangou Mimche; Palmer Masumbe Netongo; Evehe Bebandoue Marie-Solange; Akindeh Mbuh Nji; Immaculate Amunom; Johanna P. Daily; Valerie Makoge; Kayla F. Laserson; Songmbe Michael Yong; Nicoline Lomah; Peter Enyong; Vincent P.K. Titanji; Dyann F. Wirth
BMC Pediatrics | 2018
Habakkuk Azinyui Yumo; C. Kuaban; Rogers Awoh Ajeh; Akindeh Mbuh Nji; Denis Nash; Anastos Kathryn; Marcus Beissner; Thomas Loescher
Journal of Tuberculosis Research | 2016
Irene Ane-Anyangwe; Wilfred F. Mbacham; Henry Dilonga Meriki; Teyim Pride; Theresa Nkuo-Akenji; Veronique Mbeng Penlap; Leopold Djomkam Tietcheu; Damian Nota Anong; Akindeh Mbuh Nji; Vincent P.K. Titanji