The overall objective of this cross-sectional study is to measure the effect of the HCI-supported collaborative to improve the quality of services for PLWHA on client satisfaction, provider satisfaction, and HIV services. The study will include an exposed group and an unexposed group. Pilot sites that participated in the collaborative improvement effort will be included in the exposed group and sites that received no quality program will be counted among the non-exposed group.
Ce rapport décrit les résultats de la phase de démonstration d’une collaborative d'amélioration en Cote d'Ivoire mis en œuvre par le Projet de l’Amélioration des Soins de Santé de l’USAID (HCI), le Programme National de Prise en Charge Médicale des Personnes Vivant avec le VIH (PNPEC), et le Ministère de la Santé et de l’Hygiène Publique pour améliorer la qualité des services VIH.
This technical report describes results achieved during the demonstration phase of an improvement collaborative implemented in Cote d’Ivoire by the USAID Health Care Improvement Project (HCI), the National Program for the Medical Management of People Living with HIV/AIDS (PNPEC), and the Ministry of Health and Public Hygiene in order to improve the quality of HIV services.
An initial evaluation of the quality of care and treatment for persons living with HIV (PLHIV) was conducted from July – August 2008 in 33 health care centers throughout Cote d’Ivoire in order to draw attention to the need for improvements among different components of care and treatment services. After the restitution of the results of the initial evaluation and the establishment of the elements of an improvement collaborative, 41 sites were selected to participate in the demonstration phase of the collaborative. Of these 41 sites, 34 provide prevention of mother to child transmission of HIV (PMTCT) services, and 38 provide anti-retroviral (ARV) treatment services.
La Côte d’Ivoire a une prévalence élevée du VIH, avec 4,7 % de la population infectée par le virus. Cependant en 2008, une évaluation nationale de la prévention de la transmission mère-enfant du VIH (PTME) et les services de thérapie antirétrovirale (ARV) ont montré un écart important dans la qualité des soins tant dans le secteur privé que public. Pour mesurer les effets du collaboratif quant à la réduction des écarts, le Projet d’Amélioration des soins de santé de l’USAID (HCI) en Côte d’Ivoire, a comparé les résultats obtenus dans les sites de démonstration et ceux obtenus sur de nouveaux sites qui allaient rejoindre le projet. Ce rapport décrit le collaboratif d’amélioration qui a été mis en place par HCI en 2009 pour améliorer les soins et services ARV/PTME offerts aux PVVIH (Personne Vivant avec le VIH).
Pour répondre à la problématique des Orphelins et Enfants Vulnérables (OEV) en Côte d’Ivoire, le Projet d’Amélioration des soins de santé (HCI) de l’USAID, le Ministère de la Femme, de la Famille et des Affaires Sociales (MFFAS), et le Programme National de prise en charge des OEV (PN-OEV) ont engagés le processus d’Amélioration de la Qualité des services pour découvrir les insuffisances des soins et soutiens offerts aux OEV et à leurs familles. Ce rapport décrit les interventions mis en œuvre par HCI et leurs partenaires pour améliorer la qualité des services offerts aux OEV qui a démarré en 2009.
En 2008, à la demande du Ministère de la santé, avec l’appui financier du PEPFAR, le Projet d’Amélioration des Soins de Santé de l’USAID (HCI) a été invité à assister le Programme National de Prise en Charge des personnes vivant avec le VIH (PNPEC) pour conduire une évaluation nationale de la qualité des soins dans le domaine du VIH en Côte d’Ivoire. HCI et les partenaires de mise en œuvre ont conduit une évaluation nationale de la qualité des soins et services offerts aux PVVIH. Sur la base de l’évaluation, un comité technique dirigé par le PNPEC avec l’appui technique d’URC a développé un paquet de changement pour améliorer la documentation, le suivi et la rétention des patients. Ce rapport décrit les résultats du collaboratif d’amélioration d’ARV/PTME.
High-perfoming quality improvement teams are the cornerstone for identifying and testing local strategies to improve care. This study was conducted in the context of a collaborative improvement initiative launched by The Ministry of Health of Cote d’Ivoire and its National Program for HIV Care and Treatment (PNPEC) and the USAID Health Care Improvement Project (HCI) in December 2008 to study the performance of quality improvement teams.
In 2008, the USAID Health Care Improvement Project (HCI) took on the challenge of improving the learning system for health care improvement. This learning system includes the processes of harvesting, analyzing, and synthesizing knowledge about what teams do to improve health care and the process of sharing what they learn with other QI teams. Using experience to date and some innovations, HCI developed a set of four tools—collectively known as the “Standard Evaluation System” (SES) tools—for teams and their coaches to use to facilitate these knowledge management processes. The SES tools include a QI team-level Journal, a QI team-level Synthesis Form, and two databases for results indicator data—one for QI teams and the other for the collaborative level. These tools were created to help support the collaborative learning system by which teams examine which of their changes were most effective and sharing this learning with other teams in the collaborative. This report summarizes the results of testing these SES tools to strengthen documentation, analysis, and sharing of QI team efforts to improve care through testing of changes.
Lessons Lessons learned from OVC programs have revealed the need to improve service quality and to strengthen harmonization across partners around the questions: How can our programs make a measurable difference in children’s well-being? What are the essential actions that we all agree need to be part of a service to best to mitigate the impact of HIV/AIDS on children and families, in the pursuit of efficiency, effectiveness, equity, reach, and scale and sustainability? In response to the observed need to improve the quality of services provided to orphans and vulnerable children, in 2007, PEPFAR, through the United States Agency for International Development (USAID), sought to create a regional initiative to support countries and implementing partners in improving the quality of OVC programming. With support from the USAID Health Care Improvement Project (HCI), a regional OVC quality improvement initiative was organized. The initiative, which has come to be known as Care that Counts, has engaged national stakeholders, program implementers, and donor agencies throughout sub-Saharan Africa in improving the quality of OVC programming.
This short report describes the efforts of the Care that Counts Initiative to support to implementers at the country level to:
1) Build constituencies and commitment for quality in OVC programming,
2) Develop OVC service standards through consensus processes involving key stakeholders, including children and their families,
3) Undertake quality improvement activities at the point of service delivery with community-based volunteers and organizations, and
4) Gather evidence that standards and other quality improvement approaches have a measurable impact.
This short report describes assistance that the USAID Health Care Improvement Project is providing to the National Program for HIV Care and Treatment (PNPEC) of the Ministry of Health, implementing partners, the National Program for Orphans and Vulnerable Children (PN-OEV) and the Ministry of the Family, Women and Social Affairs (MFFAS) in Cote d'Ivoire to apply improvement methods to improve the quality of antiretroviral therapy services, PMTCT, OVC programs, and peer prevention of HIV. The report also highlights results from 41 sites that have been engaged in an improvement collaborative on ART and PMTCT since 2008.
The assessment, conducted in July and August 2008, collected data from interviews with providers or heads of HIV services, as well as cohort data from medical records and registers used for prevention of mother-to-child transmission (PMTCT), voluntary counseling and testing (VCT), antiretroviral therapy (ART) and HIV care services. The first cohort, made of patients already on ART, was defined as patients who had a documented ART initiation date in their medical records as of June 2007. The second cohort, the "pre-ART" cohort, consisted of patients who had tested HIV-positive, were in HIV care, but who had not initiated ART in the first three months of HIV care. A third cohort was drawn from PMTCT registers and consisted of prenatal care clients who had tested HIV-positive and for whom data might be available for a potential period of 18 months.
The assessment found that for both the pre-ART and the ART cohorts, adherence to standards of care during the initial visit at the assessed sites was good. It was better among ART patients compared to pre-ART patients, and generally better among children compared to adults. Basic HIV care standards of HIV typing, weighing, clinical staging, and CD4+ T cell count assessment were all performed in at least 65% of patients. Adherence to standards of care was lower in the second semester of care for both cohorts. A number of clinical activities that were not conducted during clinical visits represent low-effort opportunities for providing care, including clinical staging, weight-taking, and patient counseling. Retention of patients in HIV care was found to be poor. Six months after initiating care, two out of three pre-ART patients and 45% of ART patients were lost to follow-up, comparing unfavorably with retention figures from other studies in the African context. While some sites worked with local groups providing community HIV care, coordination of this care was a challenge.
Reliance on information documented in medical records and registers limited this assessment, which was illustrated when medical record data for the ART cohort patients were compared with pharmacy data.