Abstract

BackgroundIn the early days of neurosurgery, extradural haemorrhages (EDHs) contributed to a high mortality rate after craniotomies. Almost a century ago, Walter Dandy reported dural tenting sutures as an effective way to prevent postoperative EDH. Over time, his technique gained in popularity and significance to finally become a neurosurgical standard. Yet, several retrospective reports and one prospective report have questioned the ongoing need for dural tenting sutures. Dandy’s explanation that the haemostasis observed under hypotensive conditions is deceiving and eventually causes EDH may be obsolete. Today, proper intra- and postoperative care, including maintenance of normovolemia and normotension and the use of modern haemostatic agents, may be sufficient for effective haemostasis. Thus, there is a fundamental need to evaluate the necessity of dural tenting sutures in a solid, unbiased, evidence-based manner.MethodsThis study is designed as a randomised, multicentre, double-blinded, controlled interventional trial with 1:1 allocation. About one half of the participants will undergo craniotomy without dural tenting sutures and will be considered an intervention group. The other half will undergo craniotomy with these sutures. Both groups will be followed clinically and radiologically. The primary outcome is reoperation due to extradural haematoma. Secondary outcomes aim to evaluate the impact of dural tenting sutures on mortality, readmission risk, postoperative headaches, size of extradural collection, cerebrospinal fluid leak risk and the presence of any new neurological deficit. The study protocol follows the SPIRIT 2013 statement.DiscussionIt is possible that many neurosurgeons around the globe are tenting the dura in elective craniotomies which brings no benefit and only extends the operation. Unfortunately, there is not enough data to support or reject this technique in modern neurosurgery. This is the first study that may produce strong, evidence-based recommendations on using dural tenting sutures.Trial registration, ethics and disseminationThe Bioethics Committee of the Medical University of Warsaw approved the study protocol (KB/106/2018). The trial is registered at http://www.clinicaltrials.gov (NCT03658941) on September 6, 2018. The findings of this trial will be submitted to a peer-reviewed neurosurgical journal. s will be submitted to relevant national and international conferences.Trial statusProtocol version and date: version 1.5, 14.01.2020First recruitment: September 7, 2018Estimated recruitment completion: September 1, 2021

Highlights

  • In the early days of neurosurgery, extradural haemorrhages (EDHs) contributed to a high mortality rate after craniotomies

  • It is possible that many neurosurgeons around the globe are tenting the dura in elective craniotomies which brings no benefit and only extends the operation

  • There have been several retrospective and prospective reports that questioned the ongoing need for dural tenting sutures [2,3,4]

Read more

Summary

Methods

The trial is registered at http://www.clinicaltrials.gov (NCT03658941), and any important changes in the protocol will be implemented there (World Health Organisation Trial Registration Data Set). Each consecutive participant is assigned a randomisation number, specific to each centre, which has had already been allocated to the intervention or control group. The following study procedures will be in place to ensure double-blind administration of the study: Access to the randomisation code will be strictly controlled; The surgeon will receive information on each subject’s allocation after the surgery has commenced in a sealed envelope containing the allocation information of the participant and detailed allocation instructions. Primary outcome The primary outcome is the risk of reoperation due to extradural haematoma (EDH occurrence) This endpoint, as opposed to overall mortality, was chosen because of the main objective of trial, which is to assess the necessity of prophylactic use of dural tenting sutures. This outcome will be evaluated during the postoperative hospitalisation of each patient

Discussion
Introduction
Postoperative 30-day mortality
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call