CC BY 4.0 · J Neurol Surg B Skull Base 2023; 84(05): 423-432
DOI: 10.1055/a-1886-5500
Original Article

Generating Operative Workflows for Vestibular Schwannoma Resection: A Two-Stage Delphi's Consensus in Collaboration with the British Skull Base Society. Part 1: The Retrosigmoid Approach

1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
2   Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London, London, United Kingdom
,
Danyal Z. Khan
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
2   Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London, London, United Kingdom
,
Justin Collins
3   Department of Urooncology, University College London Hospitals National Health Service Foundation Trust, London, United Kingdom
,
Stephen Cooke
4   Department of Neurosurgery, Belfast Health and Social Care Trust, Belfast, United Kingdom
,
Simon R. Freeman
5   Department of Otolaryngology, Manchester Centre for Clinical Neurosciences, Salford Royal Hospital, Salford, United Kingdom
,
Nihal Gurusinghe
6   Department of Neurosurgery, Lancashire Teaching Hospital, Preston, United Kingdom
,
Susie Hampton
7   Department of Ear, Nose and Throat, Belfast Health and Social Care Trust, Belfast, United Kingdom
,
Carl Hardwidge
8   Department of Neurosurgery, University Hospital Sussex, Brighton, United Kingdom
,
Richard Irving
9   Department of Ear, Nose and Throat, Queen Elizabeth Hospital, Birmingham, United Kingdom
,
Neil Kitchen
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
,
Andrew King
10   Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Manchester, United Kingdom
11   Northern Care Alliance National Health Service Group, University of Manchester, Manchester, United Kingdom
,
Sherif Khalil
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
12   The Royal National Throat, Nose and Ear Hospital, London, United Kingdom
,
Chan H. Koh
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
2   Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London, London, United Kingdom
,
Colin Leonard
7   Department of Ear, Nose and Throat, Belfast Health and Social Care Trust, Belfast, United Kingdom
,
Hani J. Marcus
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
2   Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London, London, United Kingdom
,
William Muirhead
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
2   Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London, London, United Kingdom
,
Rupert Obholzer
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
12   The Royal National Throat, Nose and Ear Hospital, London, United Kingdom
,
Omar Pathmanaban
13   Department of Neurosurgery, Manchester Centre for Clinical Neurosciences, Salford Royal Hospital, Salford, United Kingdom
,
Iain J. A. Robertson
14   Department of Neurosurgery, Nottingham University Hospitals, Nottingham, United Kingdom
,
Jonathan Shapey
15   Department of Neurosurgery, Kings College Hospital, London, United Kingdom
,
Danail Stoyanov
2   Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London, London, United Kingdom
,
Mario Teo
16   Bristol Institute of Clinical Neuroscience, Southmead Hospital, Bristol, United Kingdom
,
James R. Tysome
17   Department of Ear, Nose and Throat, Cambridge University Hospitals, Cambridge, United Kingdom
,
Shakeel R. Saeed*
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
12   The Royal National Throat, Nose and Ear Hospital, London, United Kingdom
,
Patrick Grover*
1   Victor Horsley Department of Neurosurgery, National Hospital for Neurology and Neurosurgery, London, United Kingdom
› Institutsangaben
 

Abstract

Objective An operative workflow systematically compartmentalizes operations into hierarchal components of phases, steps, instrument, technique errors, and event errors. Operative workflow provides a foundation for education, training, and understanding of surgical variation. In this Part 1, we present a codified operative workflow for the retrosigmoid approach to vestibular schwannoma resection.

Methods A mixed-method consensus process of literature review, small-group Delphi's consensus, followed by a national Delphi's consensus, was performed in collaboration with British Skull Base Society (BSBS). Each Delphi's round was repeated until data saturation and over 90% consensus was reached.

Results Eighteen consultant skull base surgeons (10 neurosurgeons and 8 ENT [ear, nose, and throat]) with median 17.9 years of experience (interquartile range: 17.5 years) of independent practice participated. There was a 100% response rate across both Delphi's rounds. The operative workflow for the retrosigmoid approach contained three phases and 40 unique steps as follows: phase 1, approach and exposure; phase 2, tumor debulking and excision; phase 3, closure. For the retrosigmoid approach, technique, and event error for each operative step was also described.

Conclusion We present Part 1 of a national, multicenter, consensus-derived, codified operative workflow for the retrosigmoid approach to vestibular schwannomas that encompasses phases, steps, instruments, technique errors, and event errors. The codified retrosigmoid approach presented in this manuscript can serve as foundational research for future work, such as operative workflow analysis or neurosurgical simulation and education.


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Introduction

Vestibular schwannomas are typically resected through one of the following three approaches: (1) retrosigmoid, (2) translabyrinthine, and (3) middle fossa.[1] The retrosigmoid and translabyrinthine are the most commonly utilized approaches and provide good outcomes relating to safety and efficacy profiles.[1] [2] [3] The middle fossa approach is rarely performed in the United Kingdom due to the high risks of damage to the facial nerve and seizures caused by temporal lobe manipulation.[4] [5] [6] There is variability between surgeons and centers on how to perform the operation, based on surgeon preference and training, tumor location, and characteristics, all of which may result in differing surgical outcomes.[1] [6] [7] Additionally, lateral skull base procedures are technically challenging, have steep learning curves, and centers have varying degrees of collaboration with ear, nose, and throat (ENT) surgeons for different parts of the operation.

An initial step to understanding how an operation is performed is to deconstruct an operation and create a common language. A technique to systematically deconstruct complex procedures into defined tasks and errors is known as “operative workflow analysis.”[8] [9] The surgical procedure is broken down into phases which contain a series of steps, generating a workflow framework.[9] During each step (e.g., suturing), surgical instruments (e.g., forceps) are used to perform maneuvers (e.g., knot tying) via a series of gestures (e.g., grasping and pulling suture).[10] Similarly, at each step, there is the potential for technical errors, lapses in surgical technique, and adverse events, an event which may lead to adverse outcomes or postoperative complications.[9] Deconstructing a complex procedure into a systematic operative workflow requires expert consensus. Existing literature has demonstrated subject experts generating comprehensive and standardized workflow framework for nonneurosurgical proceedures[11] [12] [13] and more recently a neurosurgical procedure.[14] The Delphi technique allows the generation of group consensus through iterative questionnaires/surveys, interspersed with feedback.[13]

The management of vestibular schwannomas has benefitted from international, multidisciplinary consensus statements relating to stereotactic radiosurgery,[15] reporting outcomes,[16] and, more recently, large vestibular schwannomas.[17] Currently, there is no consensus on the operative workflow for the retrosigmoid or translabyrinthine approaches for vestibular schwannomas. Expert, consensus-driven operative workflows can provide multiple benefits: (1) workflow analysis; (2) training; (3) creation of high-fidelity simulation models; (4) objective assessment of procedure-specific surgical skills; (5) evaluation of novel technologies or techniques; (6) operating room efficiency improvements.[9] [11] [18] [19]

We created an operative workflow for the retrosigmoid approach for vestibular schwannoma, through an expert consensus process in collaboration with the British Skull Base Society (BSBS). This operative workflow aimed to digitize the approaches and provide foundational research in which to build, for example, the application of artificial intelligence to vestibular schwannoma resection.


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Methods

Overview

The methodology was drawn from previous work from our group.[14] [20] This process aimed to generate a comprehensive workflow framework which captured how each approach could reasonably be performed. We did not aim to dictate how an operation should be done. The beginning of the operation was taken as the first incision, adhering to the American College of Surgeon's definition of surgery, “structurally altering the human body by the incision or destruction of tissues.”[21] [22] Therefore, variation relating to position of the patient and incision analysis was not within the scope of this work, although the authors recognize that positioning plays a critical role for any given procedure. The components for workflow analysis and associated definitions are listed in [Table 1]. Expert input will be derived through an iterative, mixed-methods consensus process ([Fig. 1]).

Zoom Image
Fig. 1 Schematic diagram of Delphi's process, highlighting the generation of a surgical workflow through iterative consensus from British Skull Base Society expert members.[20] Adapted from Marcus et al.[14]
Table 1

Definition of operative workflow terminology per domain

Domain

Definition

Example

Phase

A major event occurring during a surgical procedure, composed of several steps[6]

Approach and exposure - encompassing the beginning of surgery until tumor debulking

Step

A sequence of activities used to achieve a surgical objective[24]

Seal mastoid air cells

Instrument

A tool or device for performing specific actions (such as cutting, dissecting, grasping, holding, retracting, or suturing) during a surgical step

Bone wax

Technical error

Lapses in operative technique while performing a surgical step[25]

Failure to seal mastoid air cells

Adverse event

An intraoperative event which is a result of a technical error and has the potential to lead to a post-operative adverse outcome/complication[25]

Cerebrospinal fluid rhinorrhea


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Modified Delphi's Process and Sampling

Literature Review

We performed a literature review of Greenberg's Handbook of Neurosurgery, Youmans and Winn Neurological Surgery, and Operative Cranial Neurosurgical Anatomy, and undertook a PubMed and EMBASE search using the keywords “retrosigmoid,” “translabyrinthine,” and “vestibular schwannoma resection”[1] [2] [3] ([Fig. 1]).


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Delphi's Round 1

The initial literature-based operative workflow was reviewed by a group of five consultant skull base surgeons, including neurosurgery and ENT, based at the National Hospital for Neurology and Neurosurgery, London, United Kingdom. Each consultant surgeon reviewed the operative workflow individually via computerized document with the definitions of phases, steps, instruments, technical errors, and adverse events as above ([Table 1]). Each expert was asked a series of questions via e-mail, seeking to assess the completeness and accuracy of the workflow ([Supplementary Material A], available in the online version).[14] Any additional suggestions were reviewed and added to the workflow matrix if in scope and not duplicate. According to the Delphi technique, circulation and iterative revision of the workflow was repeated until data saturation was achieved, that is, all experts were satisfied that the operative workflow was complete and accurate.[14]


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Delphi's Round 2

The refined workflow was circulated nationally with skull base surgeons (neurosurgeons and ENT) who were members of the BSBS,[25] the United Kingdom and Ireland's society primarily focused on skull base pathology. The entirety of the BSBS was invited to participate via e-mail. All contributing authors are specialist of lateral skull base surgeons with an independent surgical practice in vestibular schwannoma surgery who are members of the BSBS (either neurosurgery or ENT). Consultant surgeon members from the BSBS were asked to assess the workflow and suggest any amendments to encompass possible variation in practice and technique. Additional suggestions were reviewed and added to the workflow if (1) in scope and (2) not duplicate.[14] Round 2 was completed until all surgeons agreed that the workflow captured the operative practice and that there were no additional suggestions for the workflow from the participant group. Both the retrosigmoid and translabyrinthine approaches were completed in parallel: surgeons within the BSBS were given the opportunity to contribute to either approach depending on their personal clinical practice and expertise. Experience for all authors was calculated from the date they were added to the General Medical Council's Specialist Register, a list of doctors who have completed their postgraduate training and eligible to work as a consultant.[26]


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Administration

Invitations to participate in the Delphi's process were sent via direct e-mail only. Workflow documents were presented using Microsoft Word (Version 16.4, Microsoft, United States) in both rounds and supported by Google Forms in Round 2 (Google LLC, United States).


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Data Collection and Analysis

Participant demographics collected included surgical specialty and unit. The collected data regarding the surgical workflow were quantitative (whether participants agree that it is complete and accurate) and qualitative (additional suggestions or comments).[14] Content analysis was used to analyze free-text responses: to remove out-of-scope suggestions, group similar suggestions together, and compare them to existing data points in the workflow. Data analysis and workflow updates were performed in duplicate by two independent analyzers (H.L.H. and P.G.).


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Ethics

This study is independent of national health services and does not require ethical approval – interrogated via online Health Research Authority decision tool ([Supplementary Material B], available in the online version).[27] [26]


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Results

Participants

The Delphi Round 1 was completed by a group of five consultant skull base surgeons. Two neurosurgeons at the National Hospital for Neurology and Neurosurgery, London, United Kingdom, and three ENT surgeons at the Royal National Throat, Nose, and Ear Hospital, London, United Kingdom. Cumulatively, they had a median of 12.3 years and interquartile range (IQR) 16.0 years of experience (IQR: 1 9.6 years; IQR: 3 25.5 years). The Delphi Round 1 was repeated four times during a 4-month period (October 2020–February 2021) until saturation.

The Delphi Round 2 was completed by 10 neurosurgeons and 8 ENT surgeons based at 11 centers across the United Kingdom. All contributing authors are specialist lateral skull base surgeons with an independent surgical practice in vestibular schwannoma surgery who are members of the BSBS (either neurosurgery or ENT). Cumulatively, they had a median of 17.9 years and IQR of 17.5 years of experience (IQR: 1 8.0 years; IQR: 3 25.5 years). Round 2 was repeated twice during a 3-month period (May–July 2021) until saturation. There was a 100% response rate and no attrition across both the Delphi Rounds.


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Retrosigmoid Approach

Three distinct operative phases were delineated: (1) approach and exposure, (2) tumor debulking and excision, and (3) closure. The operative workflow had 40 unique steps. Preoperative set-up and postoperative protocols were recognized as important but not included as per the defined study scope.

Phase 1: Approach and Exposure

This phase consisted of 10 steps from retroauricular incision, approaching the cerebellopontine angle, and dissection of the arachnoid plane from the tumor capsule ([Table 2]).

Table 2

Retrosigmoid operative workflow phase 1: approach and exposure

No.

Steps

Instruments

Technique error

Event error

1

Retroauricular incision to bone ± pericranial graft

Scalpel, monopolar, retractors

•Vertebral artery injury

•Soft tissue dissection too far lateral

•Vertebral artery bleeding or infarct

•Laceration

2

Hemostasis

Monopolar, bipolar, suction, bone wax

3

 ± Retrosigmoid craniectomy ± collection of bone dust

Cutting burr, Kerrison's punch, periosteal elevator, bone wax

•Dural sinus injury

•Opening of mastoid air cells without repair

•Hemorrhage

•Air embolism

•Sinus thrombosis

•CSF rhinorrhea

4

 ± Retrosigmoid craniotomy

Perforator, Penfield's dissector, McDonald's dissector, matchstick burr, cutting burr, craniotome, bone wax

•Dural sinus injury

•Opening of mastoid air cells without repair

•Hemorrhage

•Air embolism

•Sinus thrombosis

•CSF rhinorrhea

5

Seal mastoid air cells

Bone wax

•Failure to seal mastoid air cells

•CSF rhinorrhea

6

Durotomy

Scalpel, blunt hook, Cottonoid patties, dural scissors

•Dural sinus injury

•Hemorrhage

•Air embolism

•Sinus thrombosis

7

Suture to dural edges

Suture

•Dural sinus injury

•Hemorrhage

•Air embolism

•Sinus thrombosis

8

Cisterna magna opening

Microscope, brain retractor, scalpel, sharp hook, Cottonoid patties

•Failure to open cisterna magna

•Insufficient CSF egress

•Excessive retraction

•Cerebellar swelling and retraction injury

•Hemorrhage

9

Approach to cerebellopontine angle and retraction of cerebellum

Microscope, microdissector, microscissors, suction, retractors, linteens, Cottonoid patties, rubber dam

•Stretching of cranial nerves

•Excessive retraction

•CN VII, XI, X palsy

•Superior petrosal vein injury

•Tearing of bridging veins and hemorrhage

•Cerebellar swelling and retraction injury

10

Dissection of arachnoid plane from tumor capsule

Microscope, bipolar, suction, microdissector, microscissors, Cottonoid patties, nontoothed bayonet fine tip forceps

•Loss of arachnoid plane or entry into incorrect plane

•Excessive traction on capsule

•Hemorrhage

•CN injury

Abbreviations: CFS, cerebrospinal fluid; CN, cranial nerve.



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Phase 2: Tumor Debulking and Excision

This phase consisted of 21 steps, starting with identification of the facial nerve using a stimulator, tumor debulking at the superior, and inferior poles, with lateral–medial and medial–lateral dissection, and culminating with stepwise rolling and debulking of the tumor ([Table 3]). It is acknowledged that the exact order of the tumor debulking is surgeon and tumor characteristic dependent. As such, each operation will contain the steps listed within this phase, but perhaps in a different order as written depending on intraoperative findings. Further, facial nerve reanimation may or may not take place intraoperatively, and the type of nerve graft used is surgeon dependent.

Table 3

Retrosigmoid operative workflow phase 2: tumor debulking and excision

No.

Steps

Instruments

Technique error

Event error

1

Posterior aspect of tumor stimulated for facial nerve

Microscope, facial nerve stimulator

 •Failure to identify CN VII

 •CN VII palsy

2

Tumor capsule opened and primary debulking

Microscope, facial nerve stimulator, bipolar, suction, microdissector, Cottonoid patties, ultrasonic aspirator, tumor holding forceps, rongeur

 •Incomplete hemostasis

 •CN injury

 •Hemorrhage

 •CN palsy

3

Tumor biopsy

Tumor holding forceps, rongeur

 Hemorrhage

4

Inferior pole resection and separation from lower cranial nerves and vessels

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, ultrasonic aspirator, tumor holding forceps

 •Injury to CN IX, X, XI

 •Injury to vessels: AICA, PICA

 •Incomplete tumor excision

 •CN IX, X, XI palsy

 •Hemorrhage

 •Infarct

5

Identification of CN VIII at brainstem and dissection of arachnoid medially

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, knife

 •Incorrect arachnoid plane

 •Perforating vessel injury

 •Injury to CN VII or VIII

 •Brainstem, peduncle infarct

 •CN VII palsy

 •Hearing loss if preservation intended

6

 ± Identification of dorsal cochlear nucleus for DNAP electrode if considering cochlear preservation

DNAP electrode

7

Identification of the root entry of CN VII which lies ventral and inferior to root entry of CN VIII

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties

 •Vessel injury

 •Injury to CN VII

 •Hemorrhage or infarct

 •CN VII palsy

8

 ± FREMAP electrode

FREMAP electrode

9

Superior pole resection

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, ultrasonic aspirator, tumor holding forceps

 •Injury to CN V or VII

 •Injury to petrosal vein or SCA

 •Incomplete tumor excision

 •CN V, VII palsy

 •Hemorrhage

 •SCA infarct

10

Identification and protection of petrosal vein ± coagulation and division of petrosal vein only if absolutely necessary

Microscope, bipolar, suction, microdissector, microscissors, Cottonoid patties, scalpel

 •Traction on petrosal vein

 •Injury to SCA

 •Sinus injury

 •Venous infarct or hematoma

 •Air embolism

 •Sinus thrombosis

11

Dissection of tumor capsule from CN V

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties

 •Injury to CN IV or V

 •Injury to SCA

 •CN IV or V palsy

 •SCA infarct

12

Medial to lateral dissection and rolling of the tumor from cerebellar peduncle and brain stem

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, tumor holding forceps, ultrasonic aspirator

 •CN VII injury at root entry zone

 •Injury to perforating vessels

 •Incomplete tumor excision

 •CN VII palsy

 •Peduncle or brainstem infarct

13

Drilling of internal auditory canal

Drill, irrigation, (± cutting, ± diamond burr), curette, bone wax, facial nerve stimulator

 •Air cell opening without repair

 •Opening of the labyrinth or endolymphatic duct

 •Jugular bulb injury

 •Injury to CN VII or cochlear nerve

 •Hearing loss

 •CSF leak

 •Hemorrhage

 •Air embolism

 •CN VII or cochlear nerve palsy

14

Incise dura of IAM and reflect away from tumor

Drill, irrigation, (± cutting, ± diamond burr), curette, bone wax, facial nerve stimulator

 •CN injury

 •Vessel injury

 •Hemorrhage

 •CN palsy

15

Locate fundus of IAM and dissect superior vestibular nerve as laterally as possible

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, knife

 •Injury to CN VII or cochlear nerve

 •Incomplete tumor excision

 •CN VII or cochlear nerve palsy

16

 ± Sacrifice of cochlear nerve in large tumors

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, knife, blunt hook, facial nerve stimulator

 •Failure to identify CN VII in distal canal as distinct from tumor and other CN

 •Injury to cochlear nerve in attempted hearing preservation surgery

 •CN VII palsy

 •Hearing loss

17

Continue dissection with lateral to medial dissection to the porous

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, knife

 •Failure to keep CN VII visualized at all times

 •Failure to maintain plane between tumor and CN VII

 •Incomplete tumor excision

 •CN VII palsy

18

Resection of tumor in the CPA until lateral–medial and medial–lateral dissections to join together

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, ultrasonic aspirator, tumor holding forceps

 •CN injury

 •Vessel injury

 •Incomplete tumor excision

 •Hemorrhage

 •CN palsy

19

Removal of tumor after stepwise rolling and debulking of tumor as above

Microscope, facial nerve stimulator, bipolar, suction, microdissector, microscissors, Cottonoid patties, ultrasonic aspirator, tumor holding forceps

 •CN injury

 •Vessel injury

 •Brainstem or peduncle injury

 •Incomplete tumor excision

 •Hemorrhage

 •CN palsy

 •Brainstem or peduncle edema or infarct

20

 ± In circumstance when facial nerve is not preserved, perform facial nerve graft (proximal and distal stump anastomosis using nerve ± sural or greater auricular nerve)

Scalpel, monopolar, retractor, microscope, suture

 •Incomplete anastomosis

 •CN injury

 •CN VII palsy

Abbreviations: AICA, anterior inferior cerebellar artery; CN, cranial nerve; CPA, cerebellopontine angle; CSF, cerebrospinal fluid; DNAP, dorsal cochlear nucleus action potential; FREMAP, facial nerve root exit zone–elicited compound muscle action potential; IAM, internal auditory meatus; IQR, interquartile range; PICA, posterior inferior cerebellar artery; SCA, superior cerebellar artery.


Note: We appreciate the exact order of the following steps will be surgeon and tumor characteristic dependent.



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Phase 3: Closure Phase

This phase consisted of nine steps, beginning with facial nerve stimulation, hemostasis, dural repair, and multilayer closure ([Table 4]).

Table 4

Retrosigmoid operative workflow phase 3: closure

No.

Steps

Instruments

Technique error

Event error

1

CN VII stimulation to confirm response at low level (0.05 mA)

Facial nerve stimulator

 •No stimulation

 •CN VII palsy

2

Hemostasis

Bipolar, fibrin sealant, oxidized cellulose matrix, Cottonoid patties

 •Incomplete hemostasis

 •Hematoma

3

Seal mastoid air cells

Bone wax, fibrin glue

 •Failure to seal mastoid air cells

 •CSF leak

4

Resection cavity inspection

 •Failure to identify residual tumor

 •Recurrence or incomplete tumor resection

5

Dural repair

Suture, ± synthetic dural substitute, ± dural sealant glue, ± pericranium graft

 •Incomplete closure

 •CSF leak

 •Pseudomeningocoele

6

 ± Replacement of bone flap

Bone flap, miniplates, screws, ± bone substitute, ± bone flap clamp system

 •Incomplete closure

 •CSF leak

 •Pseudomeningocoele

7

 ± Replacement of bone dust or bone cement

Bone dust or bone cement

 •Incomplete closure

 •CSF leak

8

Closure of muscle layer and fascia

Suture

 •Incomplete closure

 •CSF leak

 •Infection

9

Skin closure

Suture, clips

 •Poor opposition of skin edges

 •CSF leak

 •Wound infection

Abbreviations: CFS, cerebrospinal fluid; CN, cranial nerve.



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Discussion

Principal Findings

We present a consensus-derived codified operative workflow for retrosigmoid approach to vestibular schwannoma that considers the phases, steps, technique errors, and event errors of the operation. The operative workflow was achieved through national collaboration with the BSBS following an open invitation to all members to participate. This comprised 18 independently practicing neurosurgeons and ENT surgeons from 11 centers across the United Kingdom.

The retrosigmoid approach operative workflow comprised three distinct phases as follows: (1) approach and exposure, (2) tumor debulking and excision, and (3) closure, with a total of 40 individual steps. Participants felt strongly about protecting the petrosal vein and avoiding sacrifice if it all possible to prevent the risk of venous infarct or hemorrhage. Regarding tumor debulking and excision, the Phase 2, the aim is to achieve maximal tumor resection while preserving the facial nerve. As such, the tumor debulking and excision phase presented is an illustrative example. The exact sequence of resection is tumor and surgeon specific. We acknowledge that it is a systematic, stepwise debulking of the superior and inferior poles, and joining of medial–lateral and lateral–medial dissections but that depending on local experience and expertise, intraoperative findings, and the sequence of resection might differ from our operative workflow.

Vestibular schwannoma resection is a challenging surgery, with nuance relating to many aspects of the procedure. The retrosigmoid approach can be performed with the patient in a sitting, lateral, or supine position. Further, the incision and how to deal with the muscles during opening is important to avoid muscle atrophy or numbness. We acknowledge the heterogeneity in practice relating to local expertise and surgeon preference. The codified retrosigmoid approach presented in this manuscript can serve as foundational research for further work, such as operative workflow analysis or neurosurgical education.

Utilizing the Operative Workflow for Simulation and Education

Vestibular schwannomas cause unilateral hearing loss, tinnitus, imbalance, and headaches.[28] Zhang et al[29] reported a large retrospective series of 1,006 patients undergoing vestibular schwannoma resection. The mortality was 0.3%, risk of meningitis was 1.2%, and risk of cerebrospinal fluid (CSF) leak was in 9% of cases. Their reported CSF leak rate and the need for revision surgery decreased over time, while House–Brackmann facial nerve grade and hearing preservation after surgery improved over time. The authors cite improvement in functional outcomes that is due to increasing experience on smaller vestibular schwannomas.[29] In modern practice, smaller vestibular schwannomas are often managed nonsurgically with stereotactic radiosurgery.[4] This heralds an issue for current neurosurgical and ENT trainees, as there is a reduction in the number of smaller tumors to resect, train on, and enhance operative skills. Additionally, the learning curve for vestibular schwannoma resection is steep,[30] such that limited surgical experience in low-volume centers can result in poor functional outcomes and increased morbidity.[31] Adequate training and experience are essential in reducing mortality and morbidity. Operative workflows can provide a medium to explore and improve simulation, through the creation of high-fidelity models.[32] This can improve training experience and reduce mortality and morbidity.

Postoperative complications resulting from intraoperative errors during microsurgery for vestibular schwannoma resection are well known and have been well reported traditionally.[33] [34] Seventy-five percent of errors within neurosurgery are deemed as preventable and technical in nature.[35] For example, injury to the venous sinuses or the cerebellar arteries can have devastating consequences for patients during vestibular schwannoma resection.[33] [34] [36] [37] Our operative workflows contain information on technique errors and event errors,[38] paired with an exact sequence of phases and steps. This provides a framework for the development of high-fidelity models which encompass the importance of error awareness, avoidance, and management. This can be integrated with a model using augmented reality overlay to simulate a vessel injury and subsequent bleeding.[39] This gives the surgical trainee the opportunity to face and deal with intraoperative complications in a safe environment with no harm to patients. High-fidelity simulation models incorporating the operative workflows, as presented here, may become an integral component of surgical training in the future. For example, Realists spinal models ( https://www.realists.de/realspine ) already simulate bleeding and complications.

Models must be valid, and appropriate for the task. “Validity” comprises face validity (realism), content validity (usefulness as a training skill), and construct validity (experts perform better than novices).[40] To validate the content of a model simulating the retrosigmoid approach, there must be an agreed operative workflow with which to compare. The operative workflows presented in this study therefore offer a mean to validate the content of retrosigmoid surgical simulators. The codified operative workflow also provides the opportunity to generate a specific technical skills assessment for trainees, adapting traditional examples, such as the Objective Structured Assessment of Technical Skills (OSATS), which can be further used to examine construct validity of the model. The retrosigmoid approach in this codified operative workflow is related to vestibular schwannoma resection, but Phase-1 approach and exposure and Phase-3 closure, could be applicable to all retrosigmoid approaches to the cerebellopontine angle. Therefore, future research could explore the different pathologies to generate codified workflows for different skull base pathologies utilizing the retrosigmoid approach.


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Strengths and Limitations

This study presents the first consensus-derived operative workflow that considers and digitizes the phases, steps, technique errors, and event errors for the retrosigmoid to vestibular schwannoma resection. Our methodology follows the precedence of existing literature and includes national experts with many years of experience of performing such surgeries. The operative workflows provide a platform to further explore the complexity of vestibular schwannoma resection within an existing framework and common language. It also provides a framework in which to assess and validate “cadaver freed training models,” such as UpSurgeon's Retrosigmoid model ( www.upsurgeon.com ).

The operative workflows do not include some controversial aspects of vestibular schwannoma surgery, such as the indications for the approach, patient positioning, or intraoperative decision-making if aiming for subtotal resection. However, we took a constraint-based, pragmatic approach to create a foundational digitized operative workflow as the first stage in developing this operative workflow research. Although we reached consensus with colleagues from the BSBS, the operative workflows only reflect practice across the United Kingdom. Further collaboration with our European and international colleagues to generate worldwide consensus would broaden the scope of application.


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Conclusion

We present a national, multicenter, consensus-derived codified operative workflow for the retrosigmoid approach to vestibular schwannoma resection. The workflows provide a framework detailing the phases, steps, technical errors, and event errors. The codified retrosigmoid approach presented in this manuscript can serve as foundational research for future work, such as operative workflow analysis or neurosurgical simulation and education.


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Conflict of Interest

J.C. receives research grants and consultancy fees from Medtronic (Dublin, Ireland). J.C. is the associate medical director of CMR surgical (Cambridge, United Kingdom). D.S. is a shareholder in Odin Vision Ltd. (London, United Kingdom) and is an employee of Digital Surgery (London, United Kingdom). H.L.H., H.J.M., C.H.K., and W.M. are supported by the Wellcome/EPSRC Centre for Interventional and Surgical Sciences, University College London. D.Z.K. is supported by an National Institute for Health and Care Research (NIHR) Academic Clinical Fellowship. H.J.M. is also funded by the NIHR Biomedical Research Centre at University College London.

All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers' bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or nonfinancial interest (such as personal or professional relationships, affiliations, knowledge, or beliefs) in the subject matter or materials discussed in this manuscript.

Previous Presentations

This work has not been presented, either partly or wholly.


Authors' Contributions

Study conception and methodology was led by H.J.M., J.C., M.F., M.G., D.Z.K., C.H.K., H.L.H. and W.M. Material preparation, data collection and analysis were performed by H.L.H., D.Z.K., J.C., S.C., S.R.F., N.G., S.H., C.H., R.I., N.K., A.K., S.K., C.H.K., C.L., H.J.M., W.M., R.O., O.P., I.J.A.R., J.S., D.S., M.T., J.R.T., S.R.S., and P.G. contributed to data collection. The first draft of the manuscript was written by H.L.H., H.J.M. and P.G. All authors reviewed and edited subsequent versions of the manuscript. All authors read and approved the final manuscript.


Ethical and Informed Consent

Ethical approval and informed consent were unnecessary due to the nature of the study (consensus process amongst health care professionals).


Data Availability

The data for this article is available upon reasonable request.


* Denotes joint senior authorship.


Supplementary Material

  • References

  • 1 Chamoun R, MacDonald J, Shelton C, Couldwell WT. Surgical approaches for resection of vestibular schwannomas: translabyrinthine, retrosigmoid, and middle fossa approaches. Neurosurg Focus 2012; 33 (03) E9
  • 2 Lin EP, Crane BT. The management and imaging of vestibular schwannomas. AJNR Am J Neuroradiol 2017; 38 (11) 2034-2043
  • 3 Silk PS, Lane JI, Driscoll CL. Surgical approaches to vestibular schwannomas: what the radiologist needs to know. Radiographics 2009; 29 (07) 1955-1970
  • 4 Gupta VK, Thakker A, Gupta KK. Vestibular schwannoma: what we know and where we are heading. Head Neck Pathol 2020; 14 (04) 1058-1066
  • 5 Irving RM, Jackler RK, Pitts LH. Hearing preservation in patients undergoing vestibular schwannoma surgery: comparison of middle fossa and retrosigmoid approaches. J Neurosurg 1998; 88 (05) 840-845
  • 6 Ansari SF, Terry C, Cohen-Gadol AA. Surgery for vestibular schwannomas: a systematic review of complications by approach. Neurosurg Focus 2012; 33 (03) E14
  • 7 Gharabaghi A, Samii A, Koerbel A, Rosahl SK, Tatagiba M, Samii M. Preservation of function in vestibular schwannoma surgery. Neurosurgery 2007; 60(02, Suppl 01) ONS124–ONS127, discussion ONS127–ONS128
  • 8 Lalys F, Jannin P. Surgical process modelling: a review. Int J CARS 2014; 9 (03) 495-511
  • 9 Sarker SK, Chang A, Albrani T, Vincent C. Constructing hierarchical task analysis in surgery. Surg Endosc 2008; 22 (01) 107-111
  • 10 Vedula SS, Malpani AO, Tao L. et al. Analysis of the structure of surgical activity for a suturing and knot-tying task. PLoS One 2016; 11 (03) e0149174
  • 11 Dijkstra FA, Bosker RJI, Veeger NJGM, van Det MJ, Pierie JPEN. Procedural key steps in laparoscopic colorectal surgery, consensus through Delphi methodology. Surg Endosc 2015; 29 (09) 2620-2627
  • 12 Dharamsi A, Gray S, Hicks C, Sherbino J, McGowan M, Petrosoniak A. Bougie-assisted cricothyroidotomy: Delphi-derived essential steps for the novice learner. CJEM 2019; 21 (02) 283-290
  • 13 Okoli C, Pawlowski SD. The Delphi method as a research tool: an example, design considerations and applications. Inf Manage 2004; 42: 15-29
  • 14 Marcus HJ, Khan DZ, Borg A. et al. Pituitary society expert Delphi consensus: operative workflow in endoscopic transsphenoidal pituitary adenoma resection. Pituitary 2021; 24 (06) 839-853
  • 15 Tsao MN, Sahgal A, Xu W. et al. Stereotactic radiosurgery for vestibular schwannoma: International Stereotactic Radiosurgery Society (ISRS) Practice Guideline. J Radiosurg SBRT 2017; 5 (01) 5-24
  • 16 Kanzaki J, Tos M, Sanna M, Moffat DA, Monsell EM, Berliner KI. New and modified reporting systems from the consensus meeting on systems for reporting results in vestibular schwannoma. Otol Neurotol 2003; 24 (04) 642-648 , discussion 648–649
  • 17 Starnoni D, Giammattei L, Cossu G. et al. Surgical management for large vestibular schwannomas: a systematic review, meta-analysis, and consensus statement on behalf of the EANS skull base section. Acta Neurochir (Wien) 2020; 162 (11) 2595-2617
  • 18 Strauss G, Fischer M, Meixensberger J. et al. Workflow analysis to assess the efficiency of intraoperative technology using the example of functional endoscopic sinus surgery [in German]. HNO 2006; 54 (07) 528-535
  • 19 Krauss A, Muensterer OJ, Neumuth T. et al. Workflow analysis of laparoscopic Nissen fundoplication in infant pigs- a model for surgical feedback and training. J Laparoendosc Adv Surg Tech A 2009; 19 (suppl 1): S117-S122
  • 20 Layard HorsfallH, Khan DZ, Collins J. et al. Generating Operative Workflows for Vestibular (Schwannoma Resection: A Two-Stage Delphi's Consensus in Collaboration with the British Skull Base Society. Part 2: The Translabyrinthine Approach. J Neurol Surg B Skull Base 2023; 84 (05) 433-443
  • 21 State of the states: defining surgery. Accessed July 13, 2022 at: https://bulletin.facs.org/2012/05/state-of-the-states-defining-surgery/
  • 22 Greenberg MS. Handbook of Neurosurgery. New York, NY: Thieme Medical Publishers; 2019
  • 23 Winn H. Youmans and Winn Neurological Surgery. Philadelphia, PA: Elsevier; 2016
  • 24 Gagliardi F, Gragnaniello G, Mortini P, Caputy A. Operative Cranial Neurosurgical Anatomy. New York, NY: Thieme Medical Publishers; 2019
  • 25 The British Skull Base Society. The UK's society for clinicians involved in the care of patients with skull base pathology. Accessed July 13, 2022 at: https://skullbase.co.uk/
  • 26 General Medical Council. The specialist register. Accessed July 13, 2022 at: https://www.gmc-uk.org/registration-and-licensing/the-medical-register/a-guide-to-the-medical-register/specialist-registration
  • 27 Is my study research?. Accessed July 13, 2022 at: http://www.hra-decisiontools.org.uk/research/
  • 28 Blakeley JO, Evans DG, Adler J. et al. Consensus recommendations for current treatments and accelerating clinical trials for patients with neurofibromatosis type 2. Am J Med Genet A 2012; 158A (01) 24-41
  • 29 Zhang Z, Nguyen Y, De Seta D. et al. Surgical treatment of sporadic vestibular schwannoma in a series of 1006 patients. Acta Otorhinolaryngol Ital 2016; 36 (05) 408-414
  • 30 Wang AY, Wang JT, Dexter M, Da Cruz M. The vestibular schwannoma surgery learning curve mapped by the cumulative summation test for learning curve. Otol Neurotol 2013; 34 (08) 1469-1475
  • 31 Ward BK, Gourin CG, Francis HW. Vestibular schwannoma surgical volume and short-term outcomes in Maryland. Arch Otolaryngol Head Neck Surg 2012; 138 (06) 577-583
  • 32 Davids J, Manivannan S, Darzi A, Giannarou S, Ashrafian H, Marcus HJ. Simulation for skills training in neurosurgery: a systematic review, meta-analysis, and analysis of progressive scholarly acceptance. Neurosurg Rev 2021; 44 (04) 1853-1867
  • 33 Betka J, Zvěřina E, Balogová Z. et al. Complications of microsurgery of vestibular schwannoma. BioMed Res Int 2014; 2014: 315952
  • 34 Sade B, Mohr G, Dufour J-J. Vascular complications of vestibular schwannoma surgery: a comparison of the suboccipital retrosigmoid and translabyrinthine approaches. J Neurosurg 2006; 105 (02) 200-204
  • 35 Cobb MI-PH, Taekman JM, Zomorodi AR, Gonzalez LF, Turner DA. Simulation in neurosurgery-A brief review and commentary. World Neurosurg 2016; 89: 583-586
  • 36 Guazzo E, Panizza B, Lomas A. et al. Cerebral venous sinus thrombosis after translabyrinthine vestibular schwannoma-a prospective study and suggested management paradigm. Otol Neurotol 2020; 41 (02) e273-e279
  • 37 Abou-Al-Shaar H, Gozal YM, Alzhrani G, Karsy M, Shelton C, Couldwell WT. Cerebral venous sinus thrombosis after vestibular schwannoma surgery: a call for evidence-based management guidelines. Neurosurg Focus 2018; 45 (01) E4
  • 38 Bruce J, Russell EM, Mollison J, Krukowski ZH. The measurement and monitoring of surgical adverse events. Health Technol Assess 2001; 5 (22) 1-194
  • 39 Vávra P, Roman J, Zonča P. et al. Recent development of augmented reality in surgery: a review. J Healthc Eng 2017; 2017: 4574172
  • 40 McDougall EM. Validation of surgical simulators. J Endourol 2007; 21 (03) 244-247

Address for correspondence

Hugo Layard Horsfall, MRCS
National Hospital for Neurology and Neurosurgery, Queen Square
London, WC1N 3BG
United Kingdom   

Publikationsverlauf

Eingereicht: 03. März 2022

Angenommen: 20. Juni 2022

Accepted Manuscript online:
28. Juni 2022

Artikel online veröffentlicht:
10. Oktober 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

  • References

  • 1 Chamoun R, MacDonald J, Shelton C, Couldwell WT. Surgical approaches for resection of vestibular schwannomas: translabyrinthine, retrosigmoid, and middle fossa approaches. Neurosurg Focus 2012; 33 (03) E9
  • 2 Lin EP, Crane BT. The management and imaging of vestibular schwannomas. AJNR Am J Neuroradiol 2017; 38 (11) 2034-2043
  • 3 Silk PS, Lane JI, Driscoll CL. Surgical approaches to vestibular schwannomas: what the radiologist needs to know. Radiographics 2009; 29 (07) 1955-1970
  • 4 Gupta VK, Thakker A, Gupta KK. Vestibular schwannoma: what we know and where we are heading. Head Neck Pathol 2020; 14 (04) 1058-1066
  • 5 Irving RM, Jackler RK, Pitts LH. Hearing preservation in patients undergoing vestibular schwannoma surgery: comparison of middle fossa and retrosigmoid approaches. J Neurosurg 1998; 88 (05) 840-845
  • 6 Ansari SF, Terry C, Cohen-Gadol AA. Surgery for vestibular schwannomas: a systematic review of complications by approach. Neurosurg Focus 2012; 33 (03) E14
  • 7 Gharabaghi A, Samii A, Koerbel A, Rosahl SK, Tatagiba M, Samii M. Preservation of function in vestibular schwannoma surgery. Neurosurgery 2007; 60(02, Suppl 01) ONS124–ONS127, discussion ONS127–ONS128
  • 8 Lalys F, Jannin P. Surgical process modelling: a review. Int J CARS 2014; 9 (03) 495-511
  • 9 Sarker SK, Chang A, Albrani T, Vincent C. Constructing hierarchical task analysis in surgery. Surg Endosc 2008; 22 (01) 107-111
  • 10 Vedula SS, Malpani AO, Tao L. et al. Analysis of the structure of surgical activity for a suturing and knot-tying task. PLoS One 2016; 11 (03) e0149174
  • 11 Dijkstra FA, Bosker RJI, Veeger NJGM, van Det MJ, Pierie JPEN. Procedural key steps in laparoscopic colorectal surgery, consensus through Delphi methodology. Surg Endosc 2015; 29 (09) 2620-2627
  • 12 Dharamsi A, Gray S, Hicks C, Sherbino J, McGowan M, Petrosoniak A. Bougie-assisted cricothyroidotomy: Delphi-derived essential steps for the novice learner. CJEM 2019; 21 (02) 283-290
  • 13 Okoli C, Pawlowski SD. The Delphi method as a research tool: an example, design considerations and applications. Inf Manage 2004; 42: 15-29
  • 14 Marcus HJ, Khan DZ, Borg A. et al. Pituitary society expert Delphi consensus: operative workflow in endoscopic transsphenoidal pituitary adenoma resection. Pituitary 2021; 24 (06) 839-853
  • 15 Tsao MN, Sahgal A, Xu W. et al. Stereotactic radiosurgery for vestibular schwannoma: International Stereotactic Radiosurgery Society (ISRS) Practice Guideline. J Radiosurg SBRT 2017; 5 (01) 5-24
  • 16 Kanzaki J, Tos M, Sanna M, Moffat DA, Monsell EM, Berliner KI. New and modified reporting systems from the consensus meeting on systems for reporting results in vestibular schwannoma. Otol Neurotol 2003; 24 (04) 642-648 , discussion 648–649
  • 17 Starnoni D, Giammattei L, Cossu G. et al. Surgical management for large vestibular schwannomas: a systematic review, meta-analysis, and consensus statement on behalf of the EANS skull base section. Acta Neurochir (Wien) 2020; 162 (11) 2595-2617
  • 18 Strauss G, Fischer M, Meixensberger J. et al. Workflow analysis to assess the efficiency of intraoperative technology using the example of functional endoscopic sinus surgery [in German]. HNO 2006; 54 (07) 528-535
  • 19 Krauss A, Muensterer OJ, Neumuth T. et al. Workflow analysis of laparoscopic Nissen fundoplication in infant pigs- a model for surgical feedback and training. J Laparoendosc Adv Surg Tech A 2009; 19 (suppl 1): S117-S122
  • 20 Layard HorsfallH, Khan DZ, Collins J. et al. Generating Operative Workflows for Vestibular (Schwannoma Resection: A Two-Stage Delphi's Consensus in Collaboration with the British Skull Base Society. Part 2: The Translabyrinthine Approach. J Neurol Surg B Skull Base 2023; 84 (05) 433-443
  • 21 State of the states: defining surgery. Accessed July 13, 2022 at: https://bulletin.facs.org/2012/05/state-of-the-states-defining-surgery/
  • 22 Greenberg MS. Handbook of Neurosurgery. New York, NY: Thieme Medical Publishers; 2019
  • 23 Winn H. Youmans and Winn Neurological Surgery. Philadelphia, PA: Elsevier; 2016
  • 24 Gagliardi F, Gragnaniello G, Mortini P, Caputy A. Operative Cranial Neurosurgical Anatomy. New York, NY: Thieme Medical Publishers; 2019
  • 25 The British Skull Base Society. The UK's society for clinicians involved in the care of patients with skull base pathology. Accessed July 13, 2022 at: https://skullbase.co.uk/
  • 26 General Medical Council. The specialist register. Accessed July 13, 2022 at: https://www.gmc-uk.org/registration-and-licensing/the-medical-register/a-guide-to-the-medical-register/specialist-registration
  • 27 Is my study research?. Accessed July 13, 2022 at: http://www.hra-decisiontools.org.uk/research/
  • 28 Blakeley JO, Evans DG, Adler J. et al. Consensus recommendations for current treatments and accelerating clinical trials for patients with neurofibromatosis type 2. Am J Med Genet A 2012; 158A (01) 24-41
  • 29 Zhang Z, Nguyen Y, De Seta D. et al. Surgical treatment of sporadic vestibular schwannoma in a series of 1006 patients. Acta Otorhinolaryngol Ital 2016; 36 (05) 408-414
  • 30 Wang AY, Wang JT, Dexter M, Da Cruz M. The vestibular schwannoma surgery learning curve mapped by the cumulative summation test for learning curve. Otol Neurotol 2013; 34 (08) 1469-1475
  • 31 Ward BK, Gourin CG, Francis HW. Vestibular schwannoma surgical volume and short-term outcomes in Maryland. Arch Otolaryngol Head Neck Surg 2012; 138 (06) 577-583
  • 32 Davids J, Manivannan S, Darzi A, Giannarou S, Ashrafian H, Marcus HJ. Simulation for skills training in neurosurgery: a systematic review, meta-analysis, and analysis of progressive scholarly acceptance. Neurosurg Rev 2021; 44 (04) 1853-1867
  • 33 Betka J, Zvěřina E, Balogová Z. et al. Complications of microsurgery of vestibular schwannoma. BioMed Res Int 2014; 2014: 315952
  • 34 Sade B, Mohr G, Dufour J-J. Vascular complications of vestibular schwannoma surgery: a comparison of the suboccipital retrosigmoid and translabyrinthine approaches. J Neurosurg 2006; 105 (02) 200-204
  • 35 Cobb MI-PH, Taekman JM, Zomorodi AR, Gonzalez LF, Turner DA. Simulation in neurosurgery-A brief review and commentary. World Neurosurg 2016; 89: 583-586
  • 36 Guazzo E, Panizza B, Lomas A. et al. Cerebral venous sinus thrombosis after translabyrinthine vestibular schwannoma-a prospective study and suggested management paradigm. Otol Neurotol 2020; 41 (02) e273-e279
  • 37 Abou-Al-Shaar H, Gozal YM, Alzhrani G, Karsy M, Shelton C, Couldwell WT. Cerebral venous sinus thrombosis after vestibular schwannoma surgery: a call for evidence-based management guidelines. Neurosurg Focus 2018; 45 (01) E4
  • 38 Bruce J, Russell EM, Mollison J, Krukowski ZH. The measurement and monitoring of surgical adverse events. Health Technol Assess 2001; 5 (22) 1-194
  • 39 Vávra P, Roman J, Zonča P. et al. Recent development of augmented reality in surgery: a review. J Healthc Eng 2017; 2017: 4574172
  • 40 McDougall EM. Validation of surgical simulators. J Endourol 2007; 21 (03) 244-247

Zoom Image
Fig. 1 Schematic diagram of Delphi's process, highlighting the generation of a surgical workflow through iterative consensus from British Skull Base Society expert members.[20] Adapted from Marcus et al.[14]