Didier K. Ekouevi
University of Bordeaux
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Featured researches published by Didier K. Ekouevi.
Tropical Medicine & International Health | 2010
Didier K. Ekouevi; Eric Balestre; Franck-Olivier Ba-Gomis; Serge Eholié; Moussa Y. Maiga; Clarisse Amani-Bosse; Albert Minga; Eugène Messou; Papa Salif Sow; Charlotte Lewden; Hamar Allassane Traoré; Emmanuel Bissagnene; François Dabis
Objective To study factors associated with the probability of retention in antiretroviral therapy (ART) programmes in West Africa.
The Journal of Infectious Diseases | 2000
Isabelle Pellegrin; Isabelle Garrigue; Didier K. Ekouevi; Lionel Couzi; Pierre Merville; Patrick Merel; Geneviève Chêne; Marie-Hélène Schrive; Pascale Trimoulet; Marie-Edith Lafon; Hervé Fleury
Thirty renal transplant recipients, after transplantation, were tested weekly with the following assays: cytomegalovirus (CMV) antigenemia (pp65 Ag), plasma qualitative Amplicor CMV (P-AMP), plasma and peripheral blood leukocyte quantitative Amplicor CMV monitor (P- and PBL-CMM), peripheral blood leukocyte (PBL) quantitative Quantiplex bDNA CMV, version 2.0 (bDNA), and whole-blood Nuclisens pp67 CMV (pp67). Eleven patients developed symptomatic CMV disease, and 7 developed asymptomatic CMV infection. For prediction of CMV disease, the sensitivity, specificity, and positive and negative predictive values, respectively, were as follows: 100%, 63%, 61%, and 100% for pp65 Ag; 100%, 42%, 50%, and 100% for bDNA; 91%, 47%, 50%, and 90% for PBL-CMM; 55%, 74%, 55%, and 74% for P-AMP; 55%, 74%, 55%, and 74% for P-CMM; and 64%, 79%, 64%, and 79% for pp67. First positive results in PBL were obtained 9-10 days before symptoms of CMV disease, compared with 5-6 days in plasma and 0 days in whole blood. PBL assays appear to be more appropriate than plasma assays when pre-emptive therapy is required to prevent the rapid progression from the first detection of the virus to CMV disease.
PLOS ONE | 2012
Aristophane Tanon; Antoine Jaquet; Didier K. Ekouevi; Jocelyn Akakpo; Innocent Adoubi; Isidore Diomande; Fabien Houngbe; Marcel Zannou; Annie J. Sasco; Serge Eholié; François Dabis; Emmanuel Bissagnene
Background Cancer is a growing co-morbidity among HIV-infected patients worldwide. With the scale-up of antiretroviral therapy (ART) in developing countries, cancer will contribute more and more to the HIV/AIDS disease burden. Our objective was to estimate the association between HIV infection and selected types of cancers among patients hospitalized for diagnosis or treatment of cancer in West Africa. Methods A case-referent study was conducted in referral hospitals in Côte d’Ivoire and Benin. Each participating clinical ward enrolled all adult patients seeking care for a confirmed diagnosis of cancer and clinicians systematically proposed an HIV test. HIV prevalence was compared between AIDS-defining cancers and a subset of selected non-AIDS defining cancers to a referent group of non-AIDS defining cancers not reported in the literature to be positively or inversely associated with HIV. An unconditional logistic model was used to estimate odds ratios (OR) and their 95% confidence intervals (CI) of the risk of being HIV-infected for selected cancers sites compared to a referent group of other cancers. Results The HIV overall prevalence was 12.3% (CI 10.3–14.4) among the 1,017 cancer cases included. A total of 442 patients constituted the referent group with an HIV prevalence of 4.7% (CI 2.8–6.7). In multivariate analysis, Kaposi sarcoma (OR 62.2 [CI 22.1–175.5]), non-Hodgkin lymphoma (4.0 [CI 2.0–8.0]), cervical cancer (OR 7.9 [CI 3.8–16.7]), anogenital cancer (OR 11.6 [CI 2.9–46.3]) and liver cancer (OR 2.7 [CI 1.1–7.7]) were all associated with HIV infection. Conclusions In a time of expanding access to ART, AIDS-defining cancers remain highly associated with HIV infection. This is to our knowledge, the first study reporting a significant association between HIV infection and liver cancer in sub-Saharan Africa.
Journal of the International AIDS Society | 2014
Stephany N. Duda; Amanda M. Farr; Mary Lou Lindegren; Meridith Blevins; C. William Wester; Kara Wools-Kaloustian; Didier K. Ekouevi; Matthias Egger; Jennifer Hemingway-Foday; David A. Cooper; Richard D. Moore; Catherine C. McGowan; Denis Nash
HIV care and treatment programmes worldwide are transforming as they push to deliver universal access to essential prevention, care and treatment services to persons living with HIV and their communities. The characteristics and capacity of these HIV programmes affect patient outcomes and quality of care. Despite the importance of ensuring optimal outcomes, few studies have addressed the capacity of HIV programmes to deliver comprehensive care. We sought to describe such capacity in HIV programmes in seven regions worldwide.
BMC Health Services Research | 2014
Boris Tchounga; Antoine Jaquet; Patrick A. Coffie; Apollinaire Horo; Catherine Sauvaget; Innocent Adoubi; Privat Guie; François Dabis; Annie J. Sasco; Didier K. Ekouevi
BackgroundCervical cancer is the most common cancer among women and the leading cause of cancer deaths in women in Côte d’Ivoire. Low resource countries can now prevent this cancer by using HPV vaccine and effective and affordable screening tests. However the implementation of these prevention strategies needs well-trained human resources. Part of the solution could come from midwives by integrating cervical cancer prevention into reproductive health services. The aim of this survey was to assess knowledge, attitudes and practices of midwives towards cervical cancer prevention in Abidjan, Côte d’Ivoire, and to find out factors associated with appropriate knowledge.MethodsA cross-sectional survey was conducted among midwives in the urban district of Abidjan, using a self-administered questionnaire. Knowledge was assessed by two scores. Factors associated with appropriate knowledge were determined using a logistic regression analysis. Attitudes and practices were described and compare using the Chi2 test.ResultsA total of 592 midwives were enrolled, including 24.5% of final-year students. 55.7% of midwives had appropriate knowledge on cervical cancer, and 42.4% of them had appropriate knowledge on cervical cancer prevention strategies. Conferences, courses taken at school of midwifery and special training sessions on cervical cancer (OR = 4.9, 95% CI [1.9 to 12.6], p <0.01) were associated with good knowledge on the management of this disease. Among these midwives, 18.4% had already benefited from a screening test for themselves, 37.7% had already advised screening to patients and 8.4% were able to perform a visual inspection. 50.3% of midwives knew HPV vaccine as a preventive method; among them 70.8% usually recommended it to young girls.ConclusionDespite sufficient knowledge about cervical cancer prevention, attitudes and practices of midwives should be improved by organizing capacity building activities. This would ensure the success of integration of cervical cancer prevention into reproductive health services in countries like Côte d’Ivoire.
The American Journal of Gastroenterology | 2000
Pascale Trimoulet; Victor de Ledinghen; Didier K. Ekouevi; Pierre-Henri Bernard; Patrick Merel; Geneviève Chêne; Patrice Couzigou; Hervé Fleury
OBJECTIVE:The pathogenic role of TT virus (TTV) is not well known, especially during chronic hepatitis C virus (HCV) infection. We retrospectively investigated the presence of TTV DNA in the plasma of patients with chronic HCV infection and compared the characteristics of TTV-DNA–positive and -negative groups.METHODS:Between November 1996 and November 1998, 234 patients were included. Inclusion criteria were persistently elevated serum alanine aminotransferase (ALT) levels, anti-HCV and HCV-RNA positivity, and seronegativity for hepatitis B virus and human immunodeficiency virus markers. TTV DNA was amplified in nested polymerase chain reaction with TTV-specific primers, and products were analyzed by agarose-gel electrophoresis. Data were analyzed using the χ2, Fishers exact test, or Mann-Whitney test, as appropriate.RESULTS:TTV DNA was detected in 19 (8.1%; 95% confidence interval: 4.6–11.6%) patients. TTV-DNA–positive and TTV-DNA–negative patients did not differ statistically for age, gender ratio, source of HCV infection, HCV disease duration, biological parameters, histological grade, HCV-RNA load, or HCV genotype. Although nonsignificant (p = 0.21), there was a trend for a higher prevalence of TTV DNA in patients with an unknown cause of HCV infection (4/22, 18.2%) than in intravenous drug users (4/84; 4.8%), in those exposed to potential risk factors (4/49; 8.2%), or in those having received blood transfusion (7/79; 8.9%).CONCLUSIONS:Because the rates of HCV replication and the severity of liver lesions in TTV-DNA–negative and -positive patients were similar, the hepatic pathogenicity of TTV in chronic hepatitis C patients is questionable.
Journal of the International AIDS Society | 2016
Eric Balestre; Didier K. Ekouevi; Boris Tchounga; Serge P. Eholie; Eugène Messou; Adrien Sawadogo; Rodolphe Thiébaut; Margaret T May; Jonathan A C Sterne; François Dabis
Response to antiretroviral therapy (ART) among individuals infected with HIV‐2 is poorly described. We compared the immunological response among patients treated with three nucleoside reverse‐transcriptase inhibitors (NRTIs) to boosted protease inhibitor (PI) and unboosted PI‐based regimens in West Africa.
Journal of the International AIDS Society | 2017
Antoine Jaquet; Gilles Wandeler; Marcellin Nouaman; Didier K. Ekouevi; Judicaël Tine; Akouda Patassi; Patrick A Coffie; Aristophane Tanon; M. Seydi; Alain Attia; François Dabis
Introduction: Liver fibrosis is often the first stage of liver disease in people living with HIV (PLWHIV) in industrialized countries. However, little is known about liver fibrosis and its correlates among PLWHIV in sub‐Saharan Africa.
Journal of the International AIDS Society | 2014
Camille Ndondoki; Fatoumata Dicko; Patrick A. Coffie; Tanoh Eboua; Didier K. Ekouevi; Kouakou Kouadio; Addi Edmond Aka; Karen Malateste; François Dabis; Clarisse Amani-Bosse; Pety Touré; Valériane Leroy
We assessed the rate of treatment failure of HIV‐infected children after 12 months on antiretroviral treatment (ART) in the Paediatric IeDEA West African Collaboration according to their perinatal exposure to antiretroviral drugs for preventing mother‐to‐child transmission (PMTCT).
The American Journal of Gastroenterology | 2000
Pascale Trimoulet; Victor de Ledinghen; Didier K. Ekouevi; Pierre-Henri Bernard; Patrick Merel; Geneviève Chêne; Patrice Couzigou; Hervé Fleury
OBJECTIVE: The pathogenic role of TT virus (TTV) is not well known, especially during chronic hepatitis C virus (HCV) infection. We retrospectively investigated the presence of TTV DNA in the plasma of patients with chronic HCV infection and compared the characteristics of TTV-DNA–positive and -negative groups. METHODS: Between November 1996 and November 1998, 234 patients were included. Inclusion criteria were persistently elevated serum alanine aminotransferase (ALT) levels, anti-HCV and HCV-RNA positivity, and seronegativity for hepatitis B virus and human immunodeficiency virus markers. TTV DNA was amplified in nested polymerase chain reaction with TTV-specific primers, and products were analyzed by agarose-gel electrophoresis. Data were analyzed using the χ2, Fisher’s exact test, or Mann-Whitney test, as appropriate. RESULTS: TTV DNA was detected in 19 (8.1%; 95% confidence interval: 4.6–11.6%) patients. TTV-DNA–positive and TTV-DNA–negative patients did not differ statistically for age, gender ratio, source of HCV infection, HCV disease duration, biological parameters, histological grade, HCV-RNA load, or HCV genotype. Although nonsignificant (p = 0.21), there was a trend for a higher prevalence of TTV DNA in patients with an unknown cause of HCV infection (4/22, 18.2%) than in intravenous drug users (4/84; 4.8%), in those exposed to potential risk factors (4/49; 8.2%), or in those having received blood transfusion (7/79; 8.9%). CONCLUSIONS: Because the rates of HCV replication and the severity of liver lesions in TTV-DNA–negative and -positive patients were similar, the hepatic pathogenicity of TTV in chronic hepatitis C patients is questionable.