Showing posts with label Burkina Faso. Show all posts
Showing posts with label Burkina Faso. Show all posts

Monday, March 28, 2016

Missed Opportunities of Inclusion of HIV-Infected Children to Initiate Antiretroviral Treatment Before the Age of Two in West Africa, 2011 to 2013

INTRODUCTION:
The World Health Organization (WHO) 2010 guidelines recommended to treat all HIV-infected children less than two years of age. We described the inclusion process and its correlates of HIV-infected children initiated on early antiretroviral therapy (EART) at less than two years of age in Abidjan, Côte d'Ivoire, and Ouagadougou, Burkina Faso.

METHODS:
All children with HIV-1 infection confirmed with a DNA PCR test of a blood sample, aged less than two years, living at a distance less than two hours from the centres and whose parents (or mother if she was the only legal guardian or the legal caregiver if parents were not alive) agreed to participate in the MONOD ANRS 12206 project were included in a cohort to receive EART based on lopinavir/r. We used logistic regression to identify correlates of inclusion.

RESULTS:
Among the 217 children screened and referred to the MONOD centres, 161 (74%) were included and initiated on EART. The main reasons of non-inclusion were fear of father's refusal (48%), mortality (24%), false-positive HIV infection test (16%) and other ineligibility reasons (12%). Having previously disclosed the child's and mother's HIV status to the father (adjusted odds ratio (aOR): 3.20; 95% confidence interval (95% CI): 1.55 to 6.69) and being older than 12 months (aOR: 2.05; 95% CI: 1.02 to 4.12) were correlates of EART initiation. At EART initiation, the median age was 13.5 months, 70% had reached WHO Stage 3/4 and 57% had a severe immune deficiency.

CONCLUSIONS:
Fear of stigmatization by the father and early competing mortality were the major reasons for missed opportunities of EART initiation. There is an urgent need to involve fathers in the care of their HIV-exposed children and to promote early infant diagnosis to improve their future access to EART and survival.

Below:  Cohort profile ofthe ANRS 12206 MONOD study, Abidjan, Ouagadougou, May 2011 to February 2013



Full article at:   http://goo.gl/ILmMTv

  • 1MONOD Project, ANRS 12206, Centre de Recherche Internationale pour la Santé, Ouagadougou, Burkina Faso.
  • 2Inserm, U1219, Institut de Santé Publique, Epidémiologie et Développement, University of Bordeaux, Bordeaux, France.
  • 3Centre Muraz, Bobo-Dioulasso, Burkina Faso; ddahourou@gmail.com; ddahourou@gmail.com.
  • 4PACCI Programme, Site ANRS, Projet Monod, Abidjan, Côte d'Ivoire.
  • 5Pediatric Department, CHU of Cocody, Abidjan, Côte d'Ivoire.
  • 6Centre Muraz, Bobo-Dioulasso, Burkina Faso.
  • 7University of Ouagadougou, Ouagadougou, Burkina Faso.
  • 8Pediatric Department, Centre Hospitalier Universitaire (CHU) de Yopougon, Abidjan, Côte d'Ivoire.
  • 9Department of Infection and Immunity, Luxembourg Institute of Health, Luxembourg.
  • 10Pediatric Department, CHU Charles de Gaulle, Ouagadougou, Burkina Faso.
  • 11Pediatric Department, Hôpital Universitaire des Enfants de la Reine Fabiola, Université Libre de Bruxelles, Brussels, Belgium.
  • 12Inserm, U1027, Université Toulouse, Toulouse, France. 
  •  2016 Mar 23;19(1):20601. doi: 10.7448/IAS.19.1.20601.



Sunday, March 20, 2016

Prevention & Care of Pediatric HIV Infection in Ouagadougou, Burkina Faso: Knowledge, Attitudes & Practices of the Caregivers

Background
The paediatric Human Immunodeficiency Virus (HIV) epidemic still progresses because of operational challenges in implementing prevention of mother-to-child HIV transmission (PMCT) programs. We assessed the knowledge, attitudes and practices (KAP) of children’s caregivers regarding mother-to-child transmission (MTCT) of HIV, paediatric HIV infection, early infant diagnosis (EID), and paediatric antiretroviral treatment in Ouagadougou, Burkina Faso.

Methods
We undertook a qualitative survey in the four public hospitals managing HIV exposed or infected children, in Ouagadougou in 2011. A sociologist used a semi-structured questionnaire to interview caregivers of children less than 5 years old attending the paediatrics wards on their KAP. Study participants were divided into four groups as follows:
those who did not yet know their children’s HIV infection status, those who were waiting for their children’s HIV test results, those who were waiting for antiretroviral treatment, and those who were already on antiretroviral treatment.

Results
A total of 37 caregivers were interviewed. The mean age was 32.5 years, and 29 (78 %) were mothers. Twenty seven (73 %) caregivers had primary or higher level of education, and 15 (40 %) described their occupation as “housewife”. Overall, 36 (97 %) of caregivers knew that the main route of HIV transmission for infants was through MTCT and 14 (38 %) specified that it occurred during pregnancy or delivery. Five percent thought that MTCT of HIV occurred during conception. PMTCT interventions could help prevent infant HIV infection according to 32 (87 %) caregivers. Thirty five percent of caregivers stated EID as a prevention strategy. Fifty-four percent of the participants believed that replacement feeding option would prevent MTCT of HIV; 24 (65 %) stated that they would prefer medical practitioners seek caregivers’ consent before carrying out any HIV-test for their child, and that caregivers’ consent was not compulsory before antiretroviral treatment. All caregivers thought that it was necessary to treat HIV-infected children, although they did not know what interventions could be done.

Conclusions
This study highlighted the low level of caregivers’ knowledge on paediatric HIV prevention and care in Ouagadougou. Awareness programs targeting caregivers need to be strengthened in order to improve the uptake of HIV early infant diagnosis and care.

Caregivers’ knowledge, attitudes and perceptions in Ouagadougou, Burkina Faso, 2011
Total N = 37 100 %Group 1 N = 11 100 %Group 2 N = 4 100 %Group 3 N = 5 100 %Group 4 N = 17 100 %Groups 1 + 2 + 3 N = 20 100 %P-value (Group 1 + 2 + 3 vs Group 4)
Caregiver’s knowledge of existing interventions to prevent MTCT of HIV
 Yes30 (81)7 (64)4 (100)3 (60)16 (94)14 (70)0.16
 No1 (3)0 (0)0 (0)1 (20)0 (0)1 (5)
 No response6 (16)4 (36)0 (0)1 (20)1 (6)5 (25)
Caregiver’s knowledge regarding existing methods of infant HIV diagnosis
 Yes32 (86)8 (73)4 (100)5 (100)15 (88)17 (85)0.77
 No5 (14)3 (27)0 (0)0 (0)2 (12)3 (15)
Caregiver’s knowledge regarding existing treatment of HIV-infected infants
 Yes37 (100)11 (100)4 (100)5 (100)17 (100)Not applicable
 No0 (0)0 (0)0 (0)0 (0)0 (0)
Caregiver’s attitude regarding the practice of their child systematic HIV testing
 For31 (84)11 (100)3 (75)4 (80)13 (76)18 (90)0.26
 Against6 (16)0 (0)1 (25)1 (20)4 (24)2 (10)
Caregiver’s attitude regarding the antiretroviral treatment of HIV-infected children
 For37 (100)11 (100)4 (100)5 (100)17 (100)20 (100)Not applicable
 Against0 (0)0 (0)0 (0)0 (0.0)0 (0.0)0 (0)
Parent’s consent needed for child HIV-test
 Yes24 (65)8 (73)3 (75)4 (80)9 (53)15 (75)0.16
 No13 (35)3 (27)1 (25)1 (20)8 (47)5 (25)
Parent’s consent needed for child treatment
 Yes11 (30)6 (55)0 (0)1 (20)4 (24)7 (35)0.25
 No24 (65)4 (36)3 (75)4 (80)13 (76)11 (55)
 No response2 (5)1 (9)1 (25)0 (0)0 (0)2 (10)
Group 1: caregivers of HIV-infected child currently treated with antiretroviral therapy
Group 2: caregivers of HIV-infected child not yet initiated on antiretroviral therapy
Group 3: caregivers waiting for their child’s HIV post-test result
Group 4: caregivers attending paediatric ward, with an unknown HIV child status
Vs versus

Full article at:   http://goo.gl/1Dwg43

Projet MONOD, ANRS 12206, Centre de Recherche Internationale pour la Santé, 09 BP 168 Ouagadougou, Burkina Faso
Centre Muraz, Bobo Dioulasso, Burkina Faso
CHU Charles De Gaules, Service de Pédiatrie médicale, Ouagadougou, Burkina Faso
CHU Yalgado Ouédraogo, Service de Pédiatrie, Ouagadougou, Burkina Faso
Inserm U1219, Institut de Santé Publique, Epidémiologie et Développement, Université de Bordeaux, Bordeaux, France
Inserm U1027 Université Paul Sabatier, Toulouse 3, Toulouse, France




Sunday, February 7, 2016

HIV Risk & Behaviour among Part-Time vs Professional Female Sex Workers: Baseline Report of an Interventional Cohort in Burkina Faso

OBJECTIVE:
To readjust HIV control programmes in Africa, we assessed the factors associated with high-risk behaviours and HIV infection among young female sex workers (FSW) in Burkina Faso.

METHODS:
We carried out a cross-sectional study from September 2009 to September 2010 in Ouagadougou, the capital city. FSW were categorised as professionals and part-time sex workers (PTSW). After a face-to-face questionnaire, blood and urine samples were collected for HIV, HSV-2, genital infections and pregnancy. High-risk behaviour was defined as a recent unprotected sex with either casual clients, regular clients or regular partners.

RESULTS:
We recruited 609 FSW including 188 (30.9%) professionals. Their median age was 21 years (IQR 19-23), and the prevalence of HIV was 10.3% among professionals and 6.5% among PTSW. Only 3 of 46 HIV-infected women were aware of their status. Overall, 277 (45.6%) women reported high-risk behaviours (41.2% among professionals and 47.5% among PTSW), which were driven mainly by non-systematic condom use with regular partners. In multivariable analysis, PTSW and having a primary or higher education level remained associated with high-risk behaviours. HIV infection was associated with older age with being married/cohabiting and with Trichomonas vaginalis infection, while history of HIV testing was associated with a decreased risk.

CONCLUSIONS:
This study highlights the need for targeted interventions among young FSW focusing particularly on PTSW, sexual behaviours with regular partners and regular HIV testing.

Purchase full article at:   http://goo.gl/NJ4Vb1

  • 1Department of Clinical Research, Centre Muraz, Bobo-Dioulasso, Burkina Faso.
  • 2Centre of International Research for Health, University of Ouagadougou, Ouagadougou, Burkina Faso.
  • 3Department of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK.
  • 4CHU Montpellier & INSERM U1058, Montpellier, France.
  • 5Department of Public Health, Centre Muraz, Bobo-Dioulasso, Burkina Faso Department of Public Health, University of Ouagadougou, Ouagadougou, Burkina Faso. 
  •  2016 Feb 1. pii: sextrans-2015-052038. doi: 10.1136/sextrans-2015-052038.



Friday, January 15, 2016

The Impact of Support Groups for People Living with HIV on Clinical Outcomes: A Systematic Review of the Literature

Background
Support groups for people living with HIV (PLHIV) are integrated into Human Immunodeficiency Virus (HIV) care and treatment programs as a modality for increasing patient literacy and as an intervention to address the psychosocial needs of patients. However, the impact of support groups on key health outcomes has not been fully determined.

Methods
We searched electronic databases from January 1995 through May 2014 and reviewed relevant literature on the impact of support groups on mortality, morbidity, retention in HIV care, quality of life, and ongoing HIV transmission, as well as their cost effectiveness.

Results
Of 1809 citations identified, 20 met inclusion criteria. One reported on mortality, seven on morbidity, five on retention in care, seven on quality of life, and seven on ongoing HIV transmission. Eighteen (90%) of the articles reported largely positive results on the impact of support group interventions on key outcomes. Support groups were associated with reduced mortality and morbidity, increased retention in care and improved quality of life. Due to study limitations, the overall quality of evidence was rated as fair for mortality, morbidity, retention in care, and quality of life, and poor for HIV transmission.

Conclusions
Implementing support groups as an intervention is expected to have a high impact on morbidity and retention in care and a moderate impact on mortality and quality of life of PLHIV. Support groups improve disclosure with potential prevention benefits but the impact on ongoing transmission is uncertain. It is unclear if this intervention is cost-effective given the paucity of studies in this area.

...The review found largely positive results. Although limited by the quality of the included studies, the data suggest potential benefit of support groups on key health outcomes. We rated the expected impact of support groups as an intervention in PLHIV as high in terms of reducing morbidity and improving retention in care. Support groups also have the potential to influence mortality, quality of life and prevention of ongoing HIV transmission. Specific positive benefits associated with support group membership include enhancing treatment success and improving the quality of life through equipping PLHIV with coping skills.

With development of community-based care models in some settings, support groups could provide an opportunity for PLHIV to share experiences and become more engaged in their care. Given the severe human resource challenges in sub-Saharan Africa, specifically the shortage of trained health care providers, support groups can play an increasingly larger role in care models, particularly with regard to retaining HIV-infected persons in care. Based on success of the pilot program developed by Médecins Sans Frontières (MSF) and provincial health officials in Mozambique reported in this review , , the Mozambique Ministry of Health is scaling up CAGs nationally.

We did not specifically search for adherence as an outcome in this review. However five studies reported increased adherence to ART , , ,  associated with support group participation. In Wouters et al., 89.9% of support group members reported that support group meetings helped create a forum for sharing knowledge and experiences, some of which related to taking medications. In Mozambique PLHIV enrolled in support groups reported increased adherence. 

Two studies described negative outcomes. In a South Africa study, male participants in support groups felt under pressure to conform to a lifestyle that was not consistent with established gender roles , while a large mixed methods study with participants from Burkina Faso, Kenya, Malawi and Uganda showed that membership in a support group was associated with non-disclosure to partners.  These issues will need to be addressed to maximize the potential of support groups as an intervention...
  
Full article at:   http://goo.gl/HNJv2T

By:  Moses Bateganya, MBChB, MMed, MPH,1,§ Ugo Amanyeiwe, BDS, FWACS, MS,2 Uchechi Roxo, MSc,2 and Maxia Dong, MD, PhD1
1Division of Global AIDS, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia
2Office of HIV and AIDS, United States Agency for International Development
§Corresponding author: Moses H Bateganya, MBChB, MMed, MPH, Centers for Disease Control and Prevention (CDC), 1600 Clifton Rd NE, MS E-04, Atlanta, GA 30333, USA ;  vog.cdc@aynagetaBM ; phone: 404-639-3220, fax: 404-639-8114




Wednesday, January 13, 2016

Female Genital Mutilation/Cutting: Risk Management and Strategies for Social Workers and Health Care Professionals

Female genital mutilation/cutting (FGM/C) is a traditional practice originating in Africa. Its worst forms cause irreparable harm to girls and women and have no medical justification. Based on a literature review of global responses to FGM/C and conversations with Australian women who migrated from FGM/C practicing countries, this paper provides some background on FGM/C and its epidemiology, outlining its prevalence, types, and health risks and complications for women and girls. It discusses risk-prevention strategies, first, for health practitioners in identifying, screening, and supporting women affected by FGM/C and, second, for welfare and social workers and health care professionals to identify, work with, and prevent girls from being cut. Consistent with international trends in addressing the risks of FGM/C, the paper suggests practice responses for coordinated responses between professionals, communities from practicing countries, and governments of different countries.

Countries grouped according to prevalence, types I, II, and III and laws against FGM/C
CategoriesPrevalence of girls and women of reproductive age who report having been cut, and Type of FGC/MCountriesCountries with laws against FGM/C
1. Very high prevalence countries, almost universalOver 80% of girls and women of reproductive age reported having been cut, 30% Type IIISomalia (98%), Guinea (96%), Djibouti (93%), Egypt (91%). Eritrea (89%), Mali (89%), Sierra Leone (88%), Sudan (88%).Djibouti, Egypt. Eritrea, Guinea, Somalia, Sudan.
2. Moderately high prevalence countriesBetween 51% and 80% of girls and women cut, predominantly Types I and IIGambia (76%), Burkina Faso (76%), Ethiopia (74%), Mauritania (69%), Liberia (66%).Burkina Faso, Ethiopia, Mauritania.
3. Moderately low prevalence countriesBetween 26% and 50% of girls and women cut, predominantly Types I and IIGuinea Bissau (50%), Chad (44%), Cote D’Ivoire (38%), Kenya (27%), Nigeria (27%), Senegal (26%).Chad, Cote D’Ivoire, Kenya, Senegal, Guinea Bissau, Nigeria.
4. Low prevalenceBetween 10 and 25%, predominantly Types I and IICentral African Republic (24%), Yemen (23%), United Republic of Tanzania (15%), Benin (13%).Central African Republic, Benin, United Republic of Tanzania.
5. Very low prevalenceBelow 10%Iraq (8%), Ghana (4%), Togo (4%), Niger (2%), Cameroon (1%), Uganda (1%).Ghana, Niger, Togo.
Notes: Data from UNICEF 2013,4 and Macfarlane and Dorkenoo.15
Abbreviation: FGM/C, female genital mutilation/cutting.

Full article at:   http://goo.gl/h2My9U

School of Global, Urban and Social Studies, RMIT University, Melbourne, VIC, Australia
Correspondence: Susan Costello, School of Global, Urban and Social Studies, RMIT University, 360 Swanston Street, Melbourne 3001, VIC, Australia, Email ua.ude.timr@olletsoc.nasus