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Trigger tools to identify adverse drug events in hospitalised children: A systematic review.
Arab, Rama; Cornu, Catherine; Kilo, Roubi; Portefaix, Aurélie; Fretes-Bonett, Beatriz; Hergibo, Fanny; Kassai, Behrouz; Nguyen, Kim An.
Affiliation
  • Arab R; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France. Electronic address: ramaarab15@gmail.com.
  • Cornu C; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France; Centre d'investigation clinique, Inserm CIC1407, EPICIME department of clinical epdiemiology, Hospices civils de Lyon, 69500 Bron, France.
  • Kilo R; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France; Pôle de santé publique, Hospices civils de Lyon, 69008 Lyon, France.
  • Portefaix A; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France; Centre d'investigation clinique, Inserm CIC1407, EPICIME department of clinical epdiemiology, Hospices civils de Lyon, 69500 Bron, France.
  • Fretes-Bonett B; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France.
  • Hergibo F; Département médical, Teva Pharma Belgique NV, 1000 Bruxelles, Belgique.
  • Kassai B; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France; Département d'épidémiologie clinique, Hospices civils de Lyon, 69008 Lyon, France.
  • Nguyen KA; Laboratoire de biométrie et biologie évolutive, CNRS, UMR 5558, université de Claude-Bernard Lyon 1, 8, rue Guillaume-Paradin, Bât B 69008, 69008 Lyon, France.
Therapie ; 77(5): 527-539, 2022.
Article in En | MEDLINE | ID: mdl-35190187
ABSTRACT

AIMS:

To identify all available trigger tools applicable to the pediatric population in hospital settings to detect adverse drug events (ADEs) and to describe their performances by positive predictive value (PPV).

METHODS:

PubMed® was searched until December 2021. The reference sections were also consulted for new articles. Studies were selected when they used one or more triggers to identify AEs and used data on pediatric inpatient settings. Studies mentioning triggers related to AEs that were only caused by care procedures were excluded. Only triggers related to ADEs were included. PPVs of triggers were reported. Mean PPVs were calculated for multi-study triggers. The interest of each trigger in a real-time detection system was assessed.

RESULTS:

Thirty studies were included. A total of 271 unique triggers were identified, 179 of which were related to drug-induced harms. Among them, 68 could be used for prevention of ADEs, 80 for verification and 31 for reporting. Nineteen triggers (11%) had a mean PPV between 50% and 100%, including 5 that had a 100% PPV.

CONCLUSION:

The performances of individual triggers need to be more adequately studied. The detection of ADEs through computerized triggers and/or real-time detection systems remains an emerging field, very much needed in children especially, due to frequent off-label use.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adverse Drug Reaction Reporting Systems / Drug-Related Side Effects and Adverse Reactions Type of study: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limits: Child / Humans Language: En Journal: Therapie Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adverse Drug Reaction Reporting Systems / Drug-Related Side Effects and Adverse Reactions Type of study: Diagnostic_studies / Prognostic_studies / Systematic_reviews Limits: Child / Humans Language: En Journal: Therapie Year: 2022 Document type: Article