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Optimal Approach and Strategies to Strengthen Pharmacovigilance in Sub-Saharan Africa: A Cohort Study of Patients Treated with First-Line Artemisinin-Based Combination Therapies in the Nanoro Health and Demographic Surveillance System, Burkina Faso.
- Source :
-
Drug design, development and therapy [Drug Des Devel Ther] 2020 Apr 16; Vol. 14, pp. 1507-1521. Date of Electronic Publication: 2020 Apr 16 (Print Publication: 2020). - Publication Year :
- 2020
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Abstract
- Background and Purpose: Resource-limited countries face challenges in setting up effective pharmacovigilance systems. This study aimed to monitor the occurrence of adverse events (AEs) after the use of artemisinin-based combination therapies (ACTs), identify potential drivers of reporting suspected adverse drug reactions (ADRs) and monitor AEs among women who were inadvertently exposed to ACTs in the first trimester of pregnancy.<br />Patients and Methods: We conducted a prospective observational study from May 2010 to July 2012 in Nanoro Health and Demographic Surveillance System (HDSS), Burkina Faso. The HDSS area was divided into active and passive surveillance areas to monitor AEs among patients (regardless of age or sex) who received a first-line ACT (artemether-lumefantrine or artesunate-amodiaquine). In the active surveillance area, patients were followed up for 28 days, while in the passive surveillance area, patients were encouraged to return voluntarily to the health facility to report any occurrence of AEs until day 28 after drug intake. We assessed the crude incidence rates of AEs in both cohorts and performed Cox regression with mixed random effects to identify potential drivers of ADR occurrence.<br />Results: In total, 3170 participants were included in the study. Of these, 40.3% had reported at least one AE, with 39.6% and 44.4% from active and passive surveillance groups, respectively. The types of ADRs were similar in both groups. The most frequent reported ADRs were anorexia, weakness, cough, dizziness and pruritus. One case of abortion and eight cases of death were reported, but none of them was related to the ACT. The variance in random factors showed a high variability of ADR occurrence between patients in both groups, whereas variability between health facilities was low in the active surveillance group and high in passive surveillance group. Taking more than two concomitant medications was associated with high hazard in ADR occurrence, whereas the rainy season was associated with low hazard.<br />Conclusion: This study showed that both passive and active surveillance approaches were useful tools. The HDSS allowed us to capture a few cases of exposure during the first trimester of pregnancy. The passive surveillance approach, which is more likely to be implemented by malaria control programs, seems to be more relevant in the Sub-Saharan African context.<br />Competing Interests: The authors report no conflicts of interest in this work.<br /> (© 2020 Rouamba et al.)
- Subjects :
- Adolescent
Amodiaquine administration & dosage
Amodiaquine adverse effects
Antimalarials administration & dosage
Antimalarials adverse effects
Artemisinins administration & dosage
Artemisinins adverse effects
Burkina Faso
Child
Child, Preschool
Cohort Studies
Dose-Response Relationship, Drug
Drug Therapy, Combination
Female
Humans
Infant
Infant, Newborn
Lumefantrine administration & dosage
Lumefantrine adverse effects
Male
Pregnancy
Prospective Studies
Structure-Activity Relationship
Amodiaquine therapeutic use
Antimalarials therapeutic use
Artemisinins therapeutic use
Lumefantrine therapeutic use
Malaria drug therapy
Pharmacovigilance
Subjects
Details
- Language :
- English
- ISSN :
- 1177-8881
- Volume :
- 14
- Database :
- MEDLINE
- Journal :
- Drug design, development and therapy
- Publication Type :
- Academic Journal
- Accession number :
- 32368010
- Full Text :
- https://doi.org/10.2147/DDDT.S224857