ArticleBMC pharmacology & toxicology2017
Multifaceted interventions for improving spontaneous reporting of adverse drug reactions in a general hospital in China.
Article in BMC pharmacology & toxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.
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Who cites it
13 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Improving adverse drug event reporting by healthcare professionals.The Cochrane database of systematic reviews · 2024Pooled it
- Problems lowering the study quality in traditional medicine, introspection from an example of meta-analysis of acupuncture.BMC complementary medicine and therapies · 2020Pooled it
- Temporal trends in the incidence of adverse effects of medical treatment in BRICS countries from 1990 to 2021: an age-period cohort analysis.Frontiers in public health · 2025Article
- Impact of multifaceted interventions on the knowledge, attitude, and practice of adverse drug reactions reporting among healthcare workers in Vietnam: a comparative intervention study.Frontiers in pharmacology · 2024Article
- Strategies and interventions to strengthen pharmacovigilance systems in low-income and middle-income countries: a scoping review.BMJ open · 2023Article
- A Mobile App Leveraging Citizenship Engagement to Perform Anonymized Longitudinal Studies in the Context of COVID-19 Adverse Drug Reaction Monitoring: Development and Usability Study.JMIR human factors · 2022Article
- Evaluation of the reliability of the criteria for assessing prescription quality in Chinese hospitals among pharmacists in China.BMC health services research · 2022Article
- Traditional Lectures Actually Improve the Body of Knowledge, Skills, and Attitudes of Health Care Professional for Health Incident Reporting System.Hospital pharmacy · 2021Article
- Translation, transcultural adaptation and validation to Brazilian Portuguese of tools for adverse drug reaction assessment in children.BMC medical research methodology · 2021Article
- Rapid review of suspected adverse drug events due to remdesivir in the WHO database; findings and implications.Expert review of clinical pharmacology · 2021Article
- Investigation of the characteristics of medication errors and adverse drug reactions using pharmacovigilance data in China.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020Article
- Mechanisms Underlying the Prevention and Treatment of Cholelithiasis Using Traditional Chinese Medicine.Evidence-based complementary and alternative medicine : eCAM · 2019Review
- Analysis of a pharmacist-led adverse drug event management model for pharmacovigilance in an academic medical center hospital in China.Therapeutics and clinical risk management · 2018Article
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10 authors.
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Abstract
backgroundThe present study investigates changes in spontaneous reporting (SR) compliance and ADR patterns following adoption of a new hospital SR system, and multiple interventions designed for its improvement use under modified drug administration guidelines.
methodsIn total, 1389 ADR cases were reviewed. Cases were divided into two groups, cases from period 1 (n = 557, from January 2006 to June 2011) under the old SR system and cases in period 2 (n = 832, from July 2011 to December 2016) under the new SR system with multiple interventions to improve physician SR compliance. General information, drug information, and clinical manifestations were investigated and compared between periods.
resultsInterventions for improved clinician training, education on knowledge, attitudes, and practices (KAP), and economic incentives substantially improved SR adherence. We also found that changing drug usage patterns (based on the new drug administration guidelines) greatly influenced ADR occurrence and type.
conclusionsWe found the SR compliance can be improved by multifaceted interventions. Drug usage patterns also influence ADR occurrence, so programs tailored for rational use are essential. These results could lead to further improvements in the SR system for ADRs in China, and provide guidance for establishing better methods of pharmacovigilance.
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