Literature DB >> 29737504

Inadequate harms reporting in randomized control trials of antibiotics for pediatric acute otitis media: a systematic review.

Stephanie W Hum1, Su Golder2, Nader Shaikh3,4.   

Abstract

INTRODUCTION: Reporting of harms in randomized control trials is often inconsistent and inadequate.
OBJECTIVE: To assess the quality of harms reporting in randomized control trials evaluating the efficacy of antibiotics used to treat pediatric acute otitis media and to investigate whether connections to pharmaceutical companies or the publication of the CONSORT-Harms extension influenced the quality of harms reporting. STUDY DESIGN AND
SETTING: We considered randomized control trials that evaluated the efficacy and safety of antibiotic treatment for uncomplicated acute otitis media in children aged 0-19. We evaluated the quality of harms reporting using a 19-item checklist addressing the recommendations endorsed in the CONSORT-Harms extension.
RESULTS: 160 studies met our inclusion criteria. Overall quality of reporting relating to harms was low; on average studies adhered to 55.2% of the checklist items on the quality of harms reporting. The reporting of methods relating the measurement of harms was particularly lacking; studies adhered to an average of only 33.2% of the checklist items. The overall quality of reporting did not change after the publication of the CONSORT-Harms extension. The overall quality of reporting did not differ significantly in reports with or without declared connections to pharmaceutical companies (mean quality score of 56.8% vs 52.0%, respectively).
CONCLUSIONS: Harms reporting in pediatric randomized trials, especially the reporting of methods used to collect harms data, remains inadequate.

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Year:  2018        PMID: 29737504     DOI: 10.1007/s40264-018-0680-0

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  15 in total

Review 1.  Low quality of reporting adverse drug reactions in paediatric randomised controlled trials.

Authors:  Tjalling W de Vries; Eric N van Roon
Journal:  Arch Dis Child       Date:  2010-06-15       Impact factor: 3.791

Review 2.  The quality of safety reporting in trials is still suboptimal: survey of major general medical journals.

Authors:  Anna-Bettina Haidich; Charis Birtsou; Theodore Dardavessis; Ilias Tirodimos; Malamatenia Arvanitidou
Journal:  J Clin Epidemiol       Date:  2010-06-17       Impact factor: 6.437

3.  Antibiotic prescribing in ambulatory pediatrics in the United States.

Authors:  Adam L Hersh; Daniel J Shapiro; Andrew T Pavia; Samir S Shah
Journal:  Pediatrics       Date:  2011-11-07       Impact factor: 7.124

Review 4.  The reporting of harms in randomized controlled trials of hypertension using the CONSORT criteria for harm reporting.

Authors:  Nitin Babulal Bagul; Jamie J Kirkham
Journal:  Clin Exp Hypertens       Date:  2012-05-09       Impact factor: 1.749

5.  Reporting of safety results in published reports of randomized controlled trials.

Authors:  Isabelle Pitrou; Isabelle Boutron; Nizar Ahmad; Philippe Ravaud
Journal:  Arch Intern Med       Date:  2009-10-26

Review 6.  Reporting of harms by randomised controlled trials in ophthalmology.

Authors:  Roderick O'Day; Richard Walton; Richard Blennerhassett; Mark C Gillies; Daniel Barthelmes
Journal:  Br J Ophthalmol       Date:  2014-02-10       Impact factor: 4.638

Review 7.  Adverse event reporting in cancer clinical trial publications.

Authors:  Shanthi Sivendran; Asma Latif; Russell B McBride; Kristian D Stensland; Juan Wisnivesky; Lindsay Haines; William K Oh; Matthew D Galsky
Journal:  J Clin Oncol       Date:  2013-12-09       Impact factor: 44.544

Review 8.  Adverse Event Reporting in Clinical Trials of Intravenous and Invasive Pain Treatments: An ACTTION Systematic Review.

Authors:  Mark R Williams; Andrew McKeown; Zachary Pressman; Matthew Hunsinger; Kendrick Lee; Paul Coplan; Ian Gilron; Nathaniel P Katz; Michael P McDermott; Srinivasa N Raja; Bob A Rappaport; Michael C Rowbotham; Dennis C Turk; Robert H Dworkin; Shannon M Smith
Journal:  J Pain       Date:  2016-08-12       Impact factor: 5.820

Review 9.  Adherence to CONSORT harms-reporting recommendations in publications of recent analgesic clinical trials: an ACTTION systematic review.

Authors:  Shannon M Smith; Daniel R Chang; Anthony Pereira; Nirupa Shah; Ian Gilron; Nathaniel P Katz; Allison H Lin; Michael P McDermott; Bob A Rappaport; Michael C Rowbotham; Cristina Sampaio; Dennis C Turk; Robert H Dworkin
Journal:  Pain       Date:  2012-09-15       Impact factor: 6.961

10.  Reporting of adverse events in randomised controlled trials of antiepileptic drugs using the CONSORT criteria for reporting harms.

Authors:  Arif A Shukralla; Catrin Tudur-Smith; Graham A Powell; Paula R Williamson; Anthony G Marson
Journal:  Epilepsy Res       Date:  2011-10-14       Impact factor: 3.045

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  4 in total

Review 1.  Analysis and reporting of adverse events in randomised controlled trials: a review.

Authors:  Rachel Phillips; Lorna Hazell; Odile Sauzet; Victoria Cornelius
Journal:  BMJ Open       Date:  2019-03-01       Impact factor: 2.692

2.  Reporting of data monitoring committees and adverse events in paediatric trials: a descriptive analysis.

Authors:  Allison Gates; Patrina Caldwell; Sarah Curtis; Leonila Dans; Ricardo M Fernandes; Lisa Hartling; Lauren E Kelly; Ben Vandermeer; Katrina Williams; Kerry Woolfall; Michele P Dyson
Journal:  BMJ Paediatr Open       Date:  2019-03-20

Review 3.  Statistical methods for the analysis of adverse event data in randomised controlled trials: a scoping review and taxonomy.

Authors:  Rachel Phillips; Odile Sauzet; Victoria Cornelius
Journal:  BMC Med Res Methodol       Date:  2020-11-30       Impact factor: 4.615

4.  Understanding current practice, identifying barriers and exploring priorities for adverse event analysis in randomised controlled trials: an online, cross-sectional survey of statisticians from academia and industry.

Authors:  Rachel Phillips; Victoria Cornelius
Journal:  BMJ Open       Date:  2020-06-11       Impact factor: 2.692

  4 in total

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