Is there a standardised consent process within the surgical specialties?

Surgeon

Department of General and Colorectal Surgery, Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester, UK.

Published: December 2020

AI Article Synopsis

  • The consent process in surgery is increasingly recognized as a staged procedure, especially after important legal cases, and the survey aimed to explore how surgeons follow national guidelines in this area.
  • Among the 325 surveyed surgeons, most obtained consent on the day of surgery, with few having scheduled pre-consent meetings, and many used local pre-printed consent forms.
  • There is significant variability in how surgeons implement consent practices, highlighting the need for better time allocation and infrastructure to improve the consent process.

Article Abstract

Introduction: The consent process is central to surgical practice. Subsequent to landmark cases such as Montgomery and Thefaut there is increasing consensus that consent should be a staged process. The aim of our survey was to identify if there was any homogeneity in the practice of surgeons with regards to the consent process in comparison to national guidelines.

Methods: Our survey was distributed to a broad range of surgical specialties via an anonymous Google Forms questionnaire available online. Consultant Surgeons and Specialist registrars across the United Kingdom were then contacted via their relevant surgical societies and professional. Data collection was based on the Montgomery principles: consent location; face to face meetings; information leaflets (including their source); distribution of copies of letters and consent forms; use of percentage risks; use of pre-printed consent forms.

Results: The total number of replies was 325. The majority of consent was taken on the day of surgery (166/319; 50.8%). Scheduled meeting for the consent process occurred routinely in only 87 cases (87/319; 27.3%). 103 (103/319; 32.9%) responders indicated the use of pre-printed consent forms. Of which 93 (93/103; 90.3%) were produced locally. Risk percentages were routinely used by 103 responders (103/319; 32.9%) Nearly two-thirds never write specific risk percentages routinely (205/319; 64.3%). Copies of consent forms were routinely given out by 210 responders (210/319; 65.8%). Supporting information was routinely given to patients in 248 cases (248/319; 77.7%).

Conclusion: Our survey documents significant variation in the practice of consent despite clear guidance on best practice. We believe that most surgeons welcome a more thorough and robust consent process, but hey need the time and infrastructure to be able to do it Introduction.

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Source
http://dx.doi.org/10.1016/j.surge.2020.06.004DOI Listing

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