ArticleJournal of robotic surgery2025
Consensus regarding transoral robotic surgery (TORS) complications for use in a proposed standardised consent form.
Article in Journal of robotic surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Ethical and Linguistic Quality of Participant Information Sheets and Their Association with Recruitment Outcomes : An Empirical Bioethics Study of Clinical Trials.Journal of bioethical inquiry · 2026Article
- Haemorrhage following transoral robotic surgery in head and neck cancer.Journal of robotic surgery · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Consenting patients for surgery is a vital process with ethical and legal implications. The use of a standardised consent form may provide a solution to issues related to poor communication surrounding the consenting process. To date, there is no standardised consent form available for use specifically for transoral robotic surgery (TORS) across robotic centres. In an attempt to improve the consenting process relating specifically to TORS, this study aims to develop a standardised consent form using a modified Delphi process. A modified Delphi process was employed to define consensus for complications to be used in a standardised consent form for TORS. An initial iteration was devised using a literature search with experts rating each item using a Likert scale. The process was repeated until consensus was reached for all items. Two rounds were completed with seven experts detailing key risks to be included on a standardised TORS consent form. This study is the first to propose a standardised consent form for use specifically in TORS. The authors agree with other literature that suggests that the use of standardised consent forms provide numerous advantages over handwritten forms. Future studies are needed to evaluate its implementation across multiple centres in order to assess the proposed benefits to both clinicians and patients.
Indexed as
Identifiers
40372502What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.