The TYPHOON Study

  • Research type

    Research Study

  • Full title

    The TYPHOON Study: Tonsillectomy Postoperative Haemorrhage Outcomes and Observations National Cohort Study

  • IRAS ID

    345168

  • Contact name

    Catriona Douglas

  • Contact email

    catriona.douglas@ggc.scot.nhs.uk

  • Sponsor organisation

    NHS Greater Glasgow and Clyde

  • Duration of Study in the UK

    0 years, 2 months, 21 days

  • Research summary

    Tonsillectomy is one of the most commonly performed surgical procedures in Ear, Nose, Throat (ENT) surgery, with an estimated 28 000 procedures performed in the UK 2019/20. Historical data from the UK National Prospective Tonsillectomy Audit in 2005 suggested a post-tonsillectomy bleed (PTB) rate of 4.9% in adults, which has since been widely quoted to patients in the consent taking process. Specifically, the study found a three-times increased risk of PTB with “hot” surgical techniques for both dissection and haemostasis compared to cold steel tonsillectomy without the use of any “hot” techniques. National guidance released halfway through the audit changed practice and reduced rates of haemorrhage. However, data collection for this audit concluded over 20 years ago, and recent unpublished data from Hospital Episode Statistics indicates a significant increase in the PTB rate to 15.6% over the period 2022-2023, the reasons for which are currently unclear and need to be urgently addressed.

    We plan to conduct a national, prospective, multicentre collaborative cohort study of all consecutive adult patients undergoing tonsillectomy over 28 days. The study will be run by INTEGRATE, the UK ENT Trainee Collaborative Network, on a voluntary basis. Patients will be expected to fill in a questionnaire on how their sore throat is impacting their quality of life (TOI 14 – Tonsillectomy Outcome Inventory). We will collect granular data on patient characteristics, previous episodes of sore throat, surgical and anaesthetic characteristics and post-operative management including analgesia. We will also telephone the patient at 28 days following surgery to determine if they have had any episodes of bleeding and how this was managed.

    The aim of this study is to better understand the risk factors associated with an increased risk of PTB and how we can change our practice to reduce this risk for patients.

  • REC name

    HSC REC B

  • REC reference

    24/NI/0152

  • Date of REC Opinion

    24 Dec 2024

  • REC opinion

    Further Information Favourable Opinion