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Reporting of Adverse Events in Surgical Trials: Critical Appraisal of Current Practice
9 references·5 citing·48 second hop
Reporting of Adverse Events in Surgical Trials: Critical Appraisal of Current Practice (2014)Reporting of Adverse Events in Surgical T…Comparison of Randomized Controlled Trial Registry Entries and Content of Reports in Surgery Journals (2013)Comparison of Randomized Cont…Developing core outcome sets for clinical trials: issues to consider (2012)Developing core outcome sets …CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updat…CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updat…Extending the CONSORT Statement to Randomized Trials of Nonpharmacologic Treatment: Explanation and Elaboration (2008)Extending the CONSORT Stateme…Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement (2004)Better Reporting of Harms in …Quality of Complication Reporting in the Surgical Literature (2002)Quality of Complication Repor…Completeness of safety reporting in randomized trials: an evaluation of 7 medical areas. (2001)Completeness of safety report…Reporting of safety data from randomised trials (1998)Reporting of safety data from…Strengthening the reporting of harms of all interventions in clinical trials (2022)Strengthening the reporting o…Reporting Adverse Events in Plastic Surgery: A Systematic Review of Randomized Controlled Trials (2018)Reporting Adverse Events in P…Reporting adverse events in cancer surgery randomized trials: A systematic review of published trials in oesophago-gastric and gynecological cancer patients (2016)Reporting adverse events in c…Definition and Classification of Intraoperative Complications (CLASSIC): Delphi Study and Pilot Evaluation (2015)Definition and Classification…Adverse event methods were heterogeneous and insufficiently reported in randomized trials on persistent depressive disorder (2015)Adverse event methods were he…Reporting results of cancer treatment (1981)The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials (2001)The Revised CONSORT Statement for Reporting Randomized Trials: Explanation and Elaboration (2001)The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement (2007)CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)Cumulative Meta-Analysis of Therapeutic Trials for Myocardial Infarction (1992)Improving the quality of reporting of randomized controlled trials. The CONSORT statement (1996)Meta-Analysis, Decision Analysis, and Cost-Effectiveness Analysis (1999)Reporting bias in medical research - a narrative review (2010)PRISMA harms checklist: improving harms reporting in systematic reviews (2016)Assessing the Risk of Bias of Individual Studies in Systematic Reviews of Health Care Interventions (2017)The magical number seven, plus or minus two: Some limits on our capacity for processing information. (1956)Intraclass correlations: Uses in assessing rater reliability. (1979)The magical number seven, plus or minus two: Some limits on our capacity for processing information. (1994)The problem with the existing reporting standards for adverse event and medical error research (2025)Improving the Quality of Reporting of Randomized Controlled Trials (1996)The CONSORT Statement: Revised Recommendations for Improving the Quality of Reports of Parallel-Group Randomized Trials (2001)Inadequate use and regulation of interventions against publication bias decreases their effectiveness: a systematic review (2015)A systematic review of the processes used to link clinical trial registrations to their published results (2017)Outcome reporting discrepancies between trial entries and published final reports of orthodontic randomized controlled trials (2018)Core outcome domains for chronic pain clinical trials: IMMPACT recommendations (2003)Systematic Review of the Empirical Evidence of Study Publication Bias and Outcome Reporting Bias (2008)The COSMIN checklist for assessing the methodological quality of studies on measurement properties of health status measurement instruments: an international Delphi study (2010)How to select outcome measurement instruments for outcomes included in a “Core Outcome Set” – a practical guideline (2016)The COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN) and how to select an outcome measurement instrument (2016)Guidelines for Inclusion of Patient-Reported Outcomes in Clinical Trial Protocols (2018)Assessing the quality of randomized controlled trials: An annotated bibliography of scales and checklists (1995)Opportunities and challenges for improving the quality of reporting clinical research: CONSORT and beyond (2004)Safety Reporting in Randomized Trials of Mental Health Interventions (2004)The quality of safety reporting in trials is still suboptimal: Survey of major general medical journals (2010)The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement (2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. (2009)Better reporting of interventions: template for intervention description and replication (TIDieR) checklist and guide (2014)Standards for Reporting Qualitative Research (2014)Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation (2015)Empirical Evidence of Bias (1995)Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration (2007)The Behavior Change Technique Taxonomy (v1) of 93 Hierarchically Clustered Techniques: Building an International Consensus for the Reporting of Behavior Change Interventions (2013)CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)Standards for Surgical Complication Reporting in Urologic Oncology: Time for a Change (2007)AHRQ Series Paper 4: Assessing harms when comparing medical interventions: AHRQ and the Effective Health-Care Program (2008)Reporting and Grading of Complications After Urologic Surgical Procedures: An ad hoc EAU Guidelines Panel Assessment and Recommendations (2011)CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials (2013)Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis (TRIPOD): Explanation and Elaboration (2015)
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References

  • 2010CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials13,365 cited
  • 2010CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials9,314 cited
  • 2008Extending the CONSORT Statement to Randomized Trials of Nonpharmacologic Treatment: Explanation and Elaboration2,290 cited
  • 2012Developing core outcome sets for clinical trials: issues to consider1,659 cited
  • 2004Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement1,588 cited
  • 2002Quality of Complication Reporting in the Surgical Literature620 cited
  • 2001Completeness of safety reporting in randomized trials: an evaluation of 7 medical areas.564 cited
  • 1998Reporting of safety data from randomised trials97 cited
  • 2013Comparison of Randomized Controlled Trial Registry Entries and Content of Reports in Surgery Journals50 cited

Cited by

  • 2015Definition and Classification of Intraoperative Complications (CLASSIC): Delphi Study and Pilot Evaluation167 cited
  • 2015Adverse event methods were heterogeneous and insufficiently reported in randomized trials on persistent depressive disorder45 cited
  • 2022Strengthening the reporting of harms of all interventions in clinical trials24 cited
  • 2018Reporting Adverse Events in Plastic Surgery: A Systematic Review of Randomized Controlled Trials15 cited

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  • 2016Reporting adverse events in cancer surgery randomized trials: A systematic review of published trials in oesophago-gastric and gynecological cancer patients13 cited