Abstract:IntroductionHealth laboratory services are a critical component of national health systems but face major operational challenges in resource-limited (RL) settings. New funding for health systems strengthening in RL countries has increased the demand for diagnostics and provided opportunities to address these constraints. An approach to sustainably strengthen national laboratory systems in sub-Saharan African countries is the Strengthening Laboratory Management Toward Accreditation (SLMTA) programme. External Q… Show more
“…Laboratory medicine can improve knowledge of the prevalence and demographics of diseases facilitating detection and improving patient outcomes further ensuring cost‐effective healthcare . In the developed world including countries such as the United States of America (USA), laboratory test results influence 60%‐70% of critical medical decisions, with approximately 50% of all testing being performed in peripheral, community‐based laboratories . In resource limited (RL) countries which include the majority of African countries, laboratory testing probably influence only 45% of medical decisions …”
Section: Discussionmentioning
confidence: 99%
“…In addition, it can identify training requirements. EQA providers and personnel should always be appropriately accredited …”
Introduction
Laboratory quality assurance (QA) includes internal quality control (IQC), external quality assurance (EQA) and quality improvement (QI). EQA identifies quality deviations and training needs. D‐dimers are breakdown products of thrombus and results guide various clinical decisions.
Methods
The National Health Laboratory Service (NHLS) in South Africa performs the pathology tests for more than 80% of the population. The NHLS Quality Assurance Department distributed 301 questionnaires to laboratories enquiring about D‐dimer testing. Two levels of STAGO® and Siemens® commercial D‐dimer assay control material were distributed for analysis and returned results analysed.
Results
A total of 64 (21.2%) completed questionnaires were returned and 26 (40.6%) laboratories were performing D‐dimers with 25 (97%) subscribing to an EQA scheme. All laboratories reported results in D‐dimer units with a negative result cut‐off of ≤0.25 mg/L but various testing platforms were in use. All returned interpretations of analyses on the blinded control material were correct. The results were also within the respective reference ranges of the controls apart from three outliers. One laboratory obtained a result on STAGO® pathological control that was above the cut‐off of the control reference range but the reason for this error could not be identified. Another obtained results on the STAGO® and on the Siemens® normal controls that were both below the cut‐off of the control reference range due to transcription errors.
Conclusion
The study demonstrated the feasibility of a local EQA scheme for D‐dimers based on commercial control material that could mitigate against the cost of international EQA scheme participation.
“…Laboratory medicine can improve knowledge of the prevalence and demographics of diseases facilitating detection and improving patient outcomes further ensuring cost‐effective healthcare . In the developed world including countries such as the United States of America (USA), laboratory test results influence 60%‐70% of critical medical decisions, with approximately 50% of all testing being performed in peripheral, community‐based laboratories . In resource limited (RL) countries which include the majority of African countries, laboratory testing probably influence only 45% of medical decisions …”
Section: Discussionmentioning
confidence: 99%
“…In addition, it can identify training requirements. EQA providers and personnel should always be appropriately accredited …”
Introduction
Laboratory quality assurance (QA) includes internal quality control (IQC), external quality assurance (EQA) and quality improvement (QI). EQA identifies quality deviations and training needs. D‐dimers are breakdown products of thrombus and results guide various clinical decisions.
Methods
The National Health Laboratory Service (NHLS) in South Africa performs the pathology tests for more than 80% of the population. The NHLS Quality Assurance Department distributed 301 questionnaires to laboratories enquiring about D‐dimer testing. Two levels of STAGO® and Siemens® commercial D‐dimer assay control material were distributed for analysis and returned results analysed.
Results
A total of 64 (21.2%) completed questionnaires were returned and 26 (40.6%) laboratories were performing D‐dimers with 25 (97%) subscribing to an EQA scheme. All laboratories reported results in D‐dimer units with a negative result cut‐off of ≤0.25 mg/L but various testing platforms were in use. All returned interpretations of analyses on the blinded control material were correct. The results were also within the respective reference ranges of the controls apart from three outliers. One laboratory obtained a result on STAGO® pathological control that was above the cut‐off of the control reference range but the reason for this error could not be identified. Another obtained results on the STAGO® and on the Siemens® normal controls that were both below the cut‐off of the control reference range due to transcription errors.
Conclusion
The study demonstrated the feasibility of a local EQA scheme for D‐dimers based on commercial control material that could mitigate against the cost of international EQA scheme participation.
“…Es necesario fortalecer la participación de los Laboratorios de Salud Pública y Secretarías de Salud en el programa de PEID de malaria (20), ya que aunque el objetivo de ajustar los criterios de envío de las láminas de malaria fue disminuir el número de láminas enviadas al LNR, todos los departamentos deben participar en esta actividad como parte del aseguramiento de la calidad del diagnóstico. Además, teniendo en cuenta el número de casos de infecciones mixtas y de complicaciones y mortalidades por malaria notificados al SIVIGI-LA durante estos años, no se está cumpliendo con los criterios de envío definidos por el LNR para este evento.…”
Introducción. Para el fortalecimiento de la calidad del diagnóstico de malaria en Colombia, sedesarrollan los Programas de Evaluación del Desempeño (PED) en los que participan laboratoriosprivados y públicos del país. Objetivo. Analizar los resultados obtenidos en los programas deevaluación del desempeño de malaria de los laboratorios de salud pública y privados de Colombiaen el lapso 2015-2016. Materiales y métodos. Se realizó un estudio de tipo retrospectivo mediantela revisión de los resultados obtenidos por los LSP y laboratorios privados participantes enlos programas de evaluación directa e indirecta del desempeño (PEDD, PEID) de malaria durantelos años 2015 y 2016 en términos de participación, concordancia de positividad y negatividad(Índice Kappa de Cohen), concordancia de especie, de formas parasitarias y de recuento (Z score).Resultados. La participación en el PEID se incrementó de 15% en 2015 a 51% en 2016, asícomo el total de láminas enviadas que en su mayoría cumplían con los criterios establecidos por elLaboratorio Nacional de referencia (LNR). La participación en el PEDD se incrementó de 88%en 2015 a 94% en 2016, con un Índice Kappa de Cohen de 0,97, una media de concordanciade especie parasitaria de 83,3% y de formas parasitarias de 62,5% y una concordancia del recuentoparasitario más frecuente entre -0,9 y 0,9, evidenciándose un mejor desempeño en 2016.Conclusión. Basados en los resultados obtenidos es necesario promover una mayor participaciónde los LSP en los PED de malaria, especialmente en el PEID y aumentar la participación de loslaboratorio privados.
“…Though, diagnostic laboratory services are a critical component of national health systems but face major operational challenges [18]. Lack of access to good-quality diagnostic tests in this region has been a major contributor to the enormous burden of infectious and non-infectious diseases [19].…”
Introduction: Laboratory services are crucial parts of the health system having a great contribution to disease prevention and management. The importance of accurate and reliable laboratory test results is less recognized in developing countries like Ethiopia where most medical decisions are based on clinical judgment. It is time for countries like Ethiopia to not only increase health care coverage but also improve access to essential diagnostic tests. Hence, this proposed study aims to assess essential in-vitro laboratory service provision in accordance with the WHO standards in Guragae Zone primary health care unit level, South Ethiopia. Methods: Health institution-based cross-sectional study was carried out. 30% randomly selected primary health care units were recruited. Each facility was visited with a WHO checklist by a trained data collector to assess the availability of essential diagnostics service provision. The proportion of available in-vitro diagnostics services was calculated. Results were presented as percentages in tables and figures. Result: Twenty-one primary health care facilities located in Guragae Zone were assessed between May and July 2019. All surveyed facilities had major gaps in essential test availability. Among essential diagnostic tests listed with WHO like C-reactive protein, lipid profile, Amylase and Lipase, TroponinT/I, hepatitis B e-antigen, IgM-specific antibodies to hepatitis B core antigen, Glucose-6-phosphate dehydrogenase activity, and anti-HIV/p24 rapid test were not provided in any facilities. However, essential diagnostic services like urine dipstick testing, random blood sugar, smear microscopy, and few serological tests were provided at all primary health care units. All surveyed facilities had limited major laboratory equipment and consumables. Conclusion and recommendation: The present study shows limited access to essential laboratory tests at the primary health care level. Hence, the responsible body should invest to make essential tests accessible at the primary care unit level within the framework of universal health coverage in the study area. The fact that access to essential diagnostic tests is the first key step in improving quality of care; such study has its own efforts to enable the implementation of essential diagnostic lists, and improve access to diagnostics in the country.
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