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Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015
INTRODUCTION: Medicines have the potential to cause adverse drug reactions and because of this Zimbabwe monitor reactions to medicines through the Adverse Drug Reaction Surveillance System. The Medicines Control Authority of Zimbabwe monitors reactions to medicines through the Adverse Drugs Reaction...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554661/ https://www.ncbi.nlm.nih.gov/pubmed/28819477 http://dx.doi.org/10.11604/pamj.2017.27.55.11090 |
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author | Muringazuva, Caroline Chirundu, Daniel Mungati, More Shambira, Gerald Gombe, Notion Bangure, Donewell Juru, Tsitsi Tshimanga, Mufuta |
author_facet | Muringazuva, Caroline Chirundu, Daniel Mungati, More Shambira, Gerald Gombe, Notion Bangure, Donewell Juru, Tsitsi Tshimanga, Mufuta |
author_sort | Muringazuva, Caroline |
collection | PubMed |
description | INTRODUCTION: Medicines have the potential to cause adverse drug reactions and because of this Zimbabwe monitor reactions to medicines through the Adverse Drug Reaction Surveillance System. The Medicines Control Authority of Zimbabwe monitors reactions to medicines through the Adverse Drugs Reactions Surveillance System. The system relies on health professionals to report adverse drug reactions to maximize patient safety. We report results of an evaluation of the Adverse Drugs Reactions Surveillance System in Kadoma District. METHODS: A descriptive cross-sectional study was conducted using the updated CDC guidelines in six health facilities in Kadoma City. Data were collected using a pretested interviewer administered questionnaire, checklists and records review. Data was analyzed using Epi Info(TM) to calculate frequencies and means. Qualitative data were analyzed manually. Written informed consent was obtained from all study participants. RESULTS: The surveillance system did not meet up to its objectives as it failed to detect the adverse drug reactions and there was no monitoring of increases in known events. Fewer than half (43%) of the participants were aware of at least 2 objectives of the surveillance system but 83% of health workers willing to participate. However the system was not acceptable, 79% did not perceive the system to be necessary with the majority saying ''why should we fill in the forms when the reactions were already known or minor''. Though the system was supposed to identify potential patient risk factors for particular types of events health workers were reluctant to participate as evidenced by only one form filled out of 20 reactions experienced in the district. The system was simple as the notification form has 16 fields which require easily obtainable information from the patient records. CONCLUSION: The surveillance system was not useful and was not acceptable to health workers but was simple and stable. Health workers lacked knowledge. Sharing of results with the Medicines Control Authority of Zimbabwe through the Matrons facilitated training of health workers in Kadoma City. Health workers were encouraged to notify any drug reaction and to completely fill in the notification forms. Patients were also encouraged to report any drug reaction to health care workers. |
format | Online Article Text |
id | pubmed-5554661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-55546612017-08-17 Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 Muringazuva, Caroline Chirundu, Daniel Mungati, More Shambira, Gerald Gombe, Notion Bangure, Donewell Juru, Tsitsi Tshimanga, Mufuta Pan Afr Med J Research INTRODUCTION: Medicines have the potential to cause adverse drug reactions and because of this Zimbabwe monitor reactions to medicines through the Adverse Drug Reaction Surveillance System. The Medicines Control Authority of Zimbabwe monitors reactions to medicines through the Adverse Drugs Reactions Surveillance System. The system relies on health professionals to report adverse drug reactions to maximize patient safety. We report results of an evaluation of the Adverse Drugs Reactions Surveillance System in Kadoma District. METHODS: A descriptive cross-sectional study was conducted using the updated CDC guidelines in six health facilities in Kadoma City. Data were collected using a pretested interviewer administered questionnaire, checklists and records review. Data was analyzed using Epi Info(TM) to calculate frequencies and means. Qualitative data were analyzed manually. Written informed consent was obtained from all study participants. RESULTS: The surveillance system did not meet up to its objectives as it failed to detect the adverse drug reactions and there was no monitoring of increases in known events. Fewer than half (43%) of the participants were aware of at least 2 objectives of the surveillance system but 83% of health workers willing to participate. However the system was not acceptable, 79% did not perceive the system to be necessary with the majority saying ''why should we fill in the forms when the reactions were already known or minor''. Though the system was supposed to identify potential patient risk factors for particular types of events health workers were reluctant to participate as evidenced by only one form filled out of 20 reactions experienced in the district. The system was simple as the notification form has 16 fields which require easily obtainable information from the patient records. CONCLUSION: The surveillance system was not useful and was not acceptable to health workers but was simple and stable. Health workers lacked knowledge. Sharing of results with the Medicines Control Authority of Zimbabwe through the Matrons facilitated training of health workers in Kadoma City. Health workers were encouraged to notify any drug reaction and to completely fill in the notification forms. Patients were also encouraged to report any drug reaction to health care workers. The African Field Epidemiology Network 2017-05-24 /pmc/articles/PMC5554661/ /pubmed/28819477 http://dx.doi.org/10.11604/pamj.2017.27.55.11090 Text en © Caroline Muringazuva et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Muringazuva, Caroline Chirundu, Daniel Mungati, More Shambira, Gerald Gombe, Notion Bangure, Donewell Juru, Tsitsi Tshimanga, Mufuta Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 |
title | Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 |
title_full | Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 |
title_fullStr | Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 |
title_full_unstemmed | Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 |
title_short | Evaluation of the adverse drug reaction surveillance system Kadoma City, Zimbabwe 2015 |
title_sort | evaluation of the adverse drug reaction surveillance system kadoma city, zimbabwe 2015 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554661/ https://www.ncbi.nlm.nih.gov/pubmed/28819477 http://dx.doi.org/10.11604/pamj.2017.27.55.11090 |
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