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Friday, January 4, 2019

Management of Carotid Artery Injury in Endonasal Surgery





Management of Carotid Artery Injury in Endonasal Surgery

Address for correspondence Peter-John Wormald, MD, FRACS, FRCS Department of Otolaryngology, Head and Neck Surgery, The Queen Elizabeth Hospital, 28 Woodville Road, Woodville South, South Australia 5011, Australia, ua.ude.edialeda@dlamrow.jretep

Introduction

Across the world, the transnasal endoscopic approach is fast becoming the method of choice for managing pathology of the ventral skull base including the clivus and craniocervical junction.1 Endoscopic techniques employed for the surgical management of inflammatory and neoplastic diseases in the paranasal sinuses have been expanded and combined with a better understanding of endonasal skull base anatomy to facilitate surgery in this region.2 Otolaryngologists and neurosurgeons appreciate the advantages of this method including the avoidance of skin incisions, minimal sacrifice of intervening structures, improved visualization, reduced postoperative pain, and shorter hospital admissions.3

Despite these significant advantages, the limitations of this approach must also be appreciated. These include longer operating times and a reported higher postoperative cerebrospinal fluid leak rate.4 5 The most feared and disastrous complication, however, is that of carotid artery injury. In the immediate operative setting, this can result in overwhelming blood loss and place the patient's life at imminent risk.6These patients may also be susceptible to pseudoaneurysm formation, vessel spasm, thrombosis, embolism with consequent cerebral insult, and even the formation of a caroticocavernous fistula.7

The incidence of carotid artery injury in endoscopic sinus surgery is rare, with only 29 case reports described in the literature.2 The incidence is higher in transsphenoidal pituitary surgery at 1.1% and higher still in extended endonasal approaches, such as for craniopharyngiomas, clival chordomas, and chondrosarcomas, at 5 to 9%.8

Currently, there is no standard protocol for the management of carotid artery injury. Literature in this area is largely limited to case reports and anecdotal evidence. With the increasing frequency of endonasal procedures performed and the willingness to tackle more complex pathologies, the appropriate management of this catastrophic complication has become increasingly important. As such, attention has been turned toward prospective research, which has been aided by the development of a sheep model of carotid bleeding.9 This, in combination with the emergence of vascular training workshops, has allowed surgeons to gain the expertise necessary to manage this scenario safely.10 11 12

This article aims to review the preoperative, operative, and postoperative evidence-based management of carotid artery injury.

Review of the Literature

Preoperative Considerations

The successful evolution of endoscopic skull base surgery from paranasal sinus surgery has relied on the surgeon's thorough understanding of anatomy. This anatomical knowledge can be an integral part of the prevention of carotid artery injury. Adoption of a classification system based on different endoscopic approaches, such as the one described by Kassam et al, can help minimize neurovascular complications by augmenting the surgeon's anatomical knowledge.13 14 15

Identifying at-risk patients, however, is the mainstay of carotid artery injury prevention. A recent review article by Valentine and Wormald identified anatomical, tumor, and patient factors that may contribute to carotid artery injury.8

Anatomical Factors

Appreciation of the relationship between the internal carotid artery (ICA) and the sphenoid sinus is paramount. The bony wall overlying the ICA is less than 0.5 mm thick and is not sufficient to protect the artery.16 Also, in up to 22% of cases the lateral sphenoid wall may in fact be dehiscent with only dura and sphenoid sinus mucosa overlying the ICA.16 17 An ICA that approaches the midline may also predispose to injury. It has been found that in 71% of cases the artery may be up to 4 mm from the midline, with some authors also describing the distance between both ICAs within the sphenoid to be as close as 4 mm.18 19 In the majority of patients, the bony sphenoid septum or sphenoid septation inserts onto the ICA canal wall, and surgery on this septation may place the artery at risk.20

Potential cavernous ICA anomalies also need to be taken into account. Cavernous ICA aneurysm makes up ∼12% of all intracranial aneurysms, with some authors showing an association with pituitary adenomas. Of concern are several reports of unrecognized preoperative cavernous ICA aneurysms, which have resulted in ICA rupture.8

Tumor Factors

Tumors closely adherent to the ICA require careful attention. Vessel encasement by the tumor not only predisposes to injury but may also be associated with vasospasm, which can result in altered mental status and/or hemiparesis.21 Vasospasm can occur as a result of tumor dissection away from the ICA or due to displacement of the ICA within the cavernous sinus during attempted hemostasis.22 The authors advocate whenever possible to use blunt instruments, such as suction Freer dissectors and pituitary ring curettes, when working in close proximity to the artery. If bone is required to be removed, then a grasping and twisting motion should be avoided. Performing bony osteotomies before removal can help prevent inadvertent laceration. In addition, diamond burrs should be utilized in preference to cutting burrs.

Taking into account both anatomical and tumor factors requires imaging to be a mandatory part of the preoperative process. High-definition, thin-sliced computed tomography (CT) scans can be useful to thoroughly visualize the bony anatomy of the sella region and delineate vessel anatomy and its relationship to the sphenoid sinus. Magnetic resonance imaging (MRI) scans can demonstrate preoperative ICA aneurysms, with follow-up magnetic resonance angiogram (MRA) useful to confirm such suspicions.2 8Intraoperative CT can provide up-to-date information for image guidance and can detect vascular complications.2 In addition, neurophysiologic monitoring of cortical and brainstem function during surgery can be helpful in the event of major bleeding to assess cerebral blood flow.2

Patient Factors

A careful patient history is integral to the preoperative workup. Several authors have described the association between cavernous ICA injuries and patients who have had previous radiotherapy, revision surgery, and/or bromocriptine therapy. Also, acromegalic patients tend to have more tortuous and ectatic carotid arteries, often with tumor in contact or surrounding the carotid.6 8 22 23

Intraoperative Management

A major vascular injury such as a carotid artery injury represents one of the most challenging scenarios for a surgeon. The high-pressure, high-flow environment can prove difficult for even the most experienced surgeon to gain visualization and control. Before attempting hemostasis, it is important for the surgical team to appropriately control the surgical field to prevent a panicked and disordered approach, to promote safe maneuvers, and to ensure controlled management.

Controlling the Surgical Field

The literature relating to the endoscopic control of major vascular injury is limited. Through the development of an animal model of the endoscopic, endonasal vascular injury,9 Valentine and Wormald were able to reproduce the high-pressure, high-volume field encountered during carotid artery injury and as such described key steps in its control.10

Key points include10:

  • Two surgeons are engaged, allowing one surgeon to control the bloodstream, directing it away from the endoscope, while the other obtains visualization to attempt hemostasis (Fig. 1).
    An external file that holds a picture, illustration, etc.  Object name is 10-1055-s-0034-1395266-i18s2a1ra-1.jpg

    Controlling the surgical field: suction device directs blood flow away from endoscope to allow attempt at hemostasis with Wormald vascular clamp (Medtronic, Jacksonville, Florida, United States).

  • Two large-bore (10F) suction devices and, if available, a lens cleaning system for the endoscope should be used.
  • The second surgeon uses suction downside the nose with predominant bleeding to direct flow away from the other side.
  • The primary surgeon places the endoscope down the contralateral side, using the posterior septal edge as a shield from the blood flow.
  • The primary surgeon clears blood ahead of the endoscope using the second suction device. A pedicled septal flap should also be cleared and pushed into the nasopharynx.
  • The second surgeon is then free to "hover" the suction device directly over the site of injury to help gain visualization for the primary surgeon.

Hemostasis

A variety of methods to gain control of a vascular catastrophe have been reported. Emergency surgical ligation in the neck has been a traditional approach; however, this can result in stroke or death and will be ineffective in the patient with good collateral flow. Ligation will also terminate access for any potential endovascular procedure.6 24 25 Nasal packing is currently therefore the mainstay of management.8 25 26

A number of adjunct maneuvers and procedures have been described to aid in hemostasis and pack placement. Head elevation and controlled hypotension are not necessary given the significant hypotensive effect of the bleeding. If suction devices and hypotension cannot allow for adequate nasal packing, then ipsilateral common carotid artery compression can be performed.8 Weidenbecher et al advocated bilateral carotid artery compression in the neck, with concurrent surgical widening of the sphenoid sinus ostium, to facilitate nasal pack placement.17 It is also widely recommended that normotension be maintained through resuscitative measures to preserve adequate cerebral perfusion.8

Several packing agents have been described in the literature. These include Teflon (Medox Medical, Oakland, NJ) and methyl methacrylate patch, fibrin glue, Gelfoam (Pfizer, New York City, NY), oxidized cellulose packing thrombin-gelatin matrix, oxygel, and glue and muslin gauze.8 26 Valentine and Wormald's review article found that despite numerous options, gauze was most frequently used due to its availability and ease of use.8 Packing is not without its own complications, however. Raymond et al reported on 12 cases in which carotid artery injury was treated with nasal packing. Eight of these cases had ICA occlusion, and four had carotid stenosis secondary to the packing. It was concluded that overpacking contributed to patient morbidity and mortality.6 Skull base surgery requires wide exposure of the surgical field and exposure of many critical neurovascular structures. Overpacking is indeed an important consideration in preventing compression injury to these structures. Furthermore, compressive nasal packing is not considered an option if the dura is opened as blood is likely to track back into the subdural space.2As such, attention has therefore turned to alternate methods.

Muscle Patch

Considerable effort has been made in our department to add to the relative paucity of prospective research in the management of carotid artery injury. Valentine et al compared the hemostatic efficacy of various absorbable and biocompatible hemostats in an animal model of carotid bleeding. These included oxidized cellulose, thrombin-gelatin matrix, and a crushed muscle patch. The crushed muscle patch was the only method that succeeded in gaining hemostasis in all instances.11 Its effectiveness has been described in case reports in the past, with the use of quadriceps muscle as an effective permanent tamponade for ICA bleeding.17

Valentine's work was followed by Padhye et al's study in which the muscle patch was trialed not only on a linear injury type but also punch and stellate injuries. The muscle patch again achieved hemostasis in all cases. Long-term complications were also assessed, and although muscle patch use incurred low rates of destabilization and pseudoaneurysm in certain injury types, it was shown to maintain normal vessel characteristics and patency in all cases.12

In the clinical setting, muscle is harvested from the thigh (usually prepared for fascia lata graft in skull base cases) or sternocleidomastoid in the neck. A 2 × 1.5 × 1-cm graft is harvested then crushed between two metal kidney basins and, after gaining control of the surgical field, it is placed directly over the injury site with Blakesley forceps (Fig. 2).27 It should be placed with enough force to stay in contact with the vessel injury site but should not compress or occlude the vessel, and it may take up to 12 minutes to gain hemostasis.11 12 If the carotid is likely to be exposed to the nasal cavity, the muscle patch should be reinforced with an overlying septal flap. If the vessel is intracranial, the patch should be secured with oxidized cellulose and fibrin glue.

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Muscle patch placed over carotid injury site with Blakesley forceps.

Direct Vessel Closure

In the situation where there is adequate exposure of the vasculature during surgery and the vessel injury site is not enclosed by bone or difficult to access, direct closure of the injury is possible.2 8 26

Laws and Solares et al have previously described the use of direct suture repair and a Sundt-type clip graft in cases of carotid artery injury; however, outcomes of these methods are not known.2 22 Valentine et al used of U-clip anastomotic device (Medtronic, Jacksonville, Florida, United States) to repair the injury site after clamping with a Wormald endoscopic vascular clamp (Medtronic) and found it to be very effective in gaining hemostasis in an animal model of carotid catastrophe.11 Long-term outcomes of this method are also unknown, and unfortunately Medtronic has ceased production of the U-clip.

Padhye et al studied different carotid injury types and their long-term complications and found that a T2 Aneurysm Clip (Mizuho, Tokyo, Japan) was able to gain hemostasis in all injury types as well as prevent pseudoaneurysm occurrence in an animal model of carotid bleeding (Fig. 3). Careful attention to placement was needed to avoid contributing to carotid stenosis.12

An external file that holds a picture, illustration, etc.  Object name is 10-1055-s-0034-1395266-i18s2a1ra-3.jpg

T2 aneurysm clip (Mizuho, Tokyo, Japan) placement on carotid injury site.

Bipolar electrocauterization has also been described2; however, long-term outcomes in a clinical setting are unknown. Padhye et al trialed bipolar electrocauterization on different injury types in an animal model of bleeding, and although effective at times in gaining hemostasis, there was an association with delayed secondary hemorrhage as well as total carotid occlusion. In addition, this technique can in certain cases worsen the injury, enlarging the defect. Therefore, this technique cannot be recommended.12

Endovascular Techniques

In some patients, hemostasis may not be achievable, and in these cases urgent transfer for endovascular intervention must be sought.25 28 29 These interventions are designed to either occlude the vessel or maintain vascular flow.8 In these cases, as much hemostasis as possible should be achieved endoscopically before transfer to the angiography suite.

Endovascular occlusion of the artery is generally performed using a balloon or coil and should be performed at the wall defect to prevent extravasation of blood from both anterograde and retrograde vessel filling.25 Deployment of an endovascular balloon or coil can be associated with distal migration due to the high-pressure, high-flow environment of the artery.30 This can place the ophthalmic artery at imminent risk due to its location distal to the cavernous ICA.6 If occlusive intervention is sought and time permits, prior assessment of collateral circulation should be undertaken and can be done in a variety of ways. In addition to angiography, balloon occlusion test (BOT) of the ICA in combination with electroencephalogram, transcranial Doppler, xenon-CT, and single-photon emission computed tomography are useful to assess the collateral circulation.17 It should be noted, however, that Mathis et al found that of 192 patients who passed the BOT, 4.7% developed permanent stroke.31 The BOT may not always be possible in the emergency situation, where hemostasis has not been achieved and occlusion intervention may be the only way to save a patient's life.

An alternative to occlusion intervention is placement of a stent graft to seal the injury site and maintain vascular flow. This is, however, technically challenging to place in the tortuous cavernous carotid siphon; stent grafts are also associated with distant migration as well as ICA spasm.8 29 In addition, there is a 4.4% risk of stroke within the first 30 days of stent placement32 as well as requirement of concurrent anticoagulation therapy, which confers its own potential risks.8

Postoperative Considerations

Postoperative care largely involves the prevention of potential complications of carotid artery injury, which include pseudoaneurysm formation and caroticocavernous fistula.2 8 17 25 26 A pseudoaneurysm is a tear through all layers of an artery with persistent flow outside the vessel into a space contained by surrounding tissue.33 Its incidence after carotid artery injury can be as high as 60% and carries with it a risk of rupture for up to 3 months.8 Therefore prompt identification and treatment is required for successful long-term management.

Once hemostasis has been achieved intraoperatively, the patient should be transferred for urgent angiographic investigation to assess the repair and ascertain if further endovascular intervention in required.2 8 26 Angiography should include the external carotid artery if no abnormality is found within the ICA. In addition, the cosurgeons should be available to loosen the packing if localization of the injury site is not possible due to overly tight packing.2 If the immediate postoperative angiogram is normal, then the authors advocate monitoring the patient in the intensive care unit until the packing is removed and another angiogram is performed, usually at 1 week postsurgery. If this is again normal, then the angiogram is repeated at 6 weeks, 3 months, and 1 year.

If pseudoaneurysm is detected, then three main treatment options exist: stent-graft placement, isolated endovascular occlusion of aneurysm lumen, or surgery (bypass or aneurysmal clipping).8 Coil or balloon occlusion has been associated with an increased complication profile as the pseudoaneurysm lacks a wall on which the coil/balloon can sit, and rupture or dissection of the ICA wall can still occur. It is accepted that extracranial/intracranial surgery has a relatively high complication rate, and therefore stent-graft placement in this situation is the safest option. Caroticocavernous fistula, which occurs between the carotid sinus and the cavernous sinus, is treated in much the same way; however, detachable balloons may be used in this setting to occlude the fistula while maintaining parent vessel patency.8 34

Discussion

Endoscopic carotid artery injury is a devastating complication that can induce panic and management paralysis in the surgical team if the surgeons have no experience with this complication and no clear plan of how to manage this event. Review of the English literature reveals several important steps that a surgeon can take to successfully manage this complication. First, optimal preoperative assessment with preoperative planning for such a potential complication is important. Second, skilled operative maneuvers can successfully achieve hemostasis. And third, postoperative assessments and comprehensive management of potential complications will result in the best possible outcome for the patient.

Preoperatively, surgeons must be familiar and competent with the endoscopic approach and anatomy to minimize neurovascular complications.13 14 15 Studious assessment of preoperative CT scans is required, including appreciation of the relationship of the cavernous ICA and the lateral sphenoidal wall,16 17 as well as the potential midline lie of the artery.18 19 Obtainment of MRI or MRA to confirm suspicion of ICA anomalies is also supported as is close assessment of tumor relationship to ICA.8 Factors such as previous radiotherapy, revision surgery, bromocriptine therapy, and acromegaly are helpful to identify the at-risk patient.6 8 22 23 These patients may warrant preoperative assessment of collateral cerebral circulation if their risk is deemed high enough.

Intraoperatively, during a carotid artery injury, emphasis is on controlling the surgical field through the two-surgeon, four-handed technique, to gain vision and better decision making regarding hemostasis.10There are several courses available that allow surgeons to train on animal models so that surgeons may practice the necessary surgical maneuvers that allow successful hemostasis. Having experience in this situation and having a clear surgical plan can be lifesaving for the patient.8 9 10 Nasal packing has been widely described as the method of choice; however, overpacking has been seen to incur its own complications secondary to compression of critical neurovascular structures.8 Use of a crushed muscle patch has been shown to be effective in gaining primary hemostasis and maintains normal vessel characteristics in more than one injury type. However, it has been associated with destabilization and pseudoaneurysm if used as the lone treatment.11 12 In the clinical setting, the authors would advocate for prompt follow-up angiography with endovascular intervention if required.

If the surgical field permits, direct vessel closure techniques such as the U-clip and the T2 aneurysm clip have been shown to be effective in a sheep model of carotid bleeding. The aneurysm clip was not associated with pseudoaneurysm formation; however, placement may influence long-term carotid flow.1112 Reports have also been made on the use of direct suture repair and bipolar.2

If hemostasis cannot be achieved promptly, packing and transfer for angiography and endovascular intervention with balloon, coil, or stent graft is indicated.8 25 28 29 Where possible, assessment of collateral cerebral circulation should be undertaken.17

Postoperative management is focused on the prevention of complications of carotid artery injury, namely pseudoaneurysm and caroticocavernous fistula. After intraoperative intervention, immediate postoperative angiography should be undertaken, followed by repeat investigations at 1 week, 6 weeks, 3 months, and 1 year.8 Preference is given to stent-graft placement over coil or balloon occlusion and surgery due to its comparatively lower complication rate. Detachable balloons, however, may be more appropriate in caroticocavernous fistula.8 34

Disclosures P.J. Wormald receives royalties from Medtronic ENT for instruments designed and is a consultant for Neilmed Pharmaceuticals.

Final Comments

Prevention and management of carotid artery injury is a combination of appropriate patient selection, surgical competency, and teamwork, culminating in the formulation and execution of a surgical plan. In this anxiety-provoking situation, the need for appropriate training cannot be underestimated. In addition to clinical training, targeted vascular workshops utilizing cadaveric and live animal specimens will help surgeons acquire technical expertise as well as skills in teamwork and plan formulation necessary to gain the most favorable outcome for the patient.

References

1. Carrau R L Kassam A B Snyderman C H Pituitary surgery Otolaryngol Clin North Am 20013461143–1155., ix [PubMed]
2. Solares C A, Ong Y K, Carrau R L. et al. Prevention and management of vascular injuries in endoscopic surgery of the sinonasal tract and skull base. Otolaryngol Clin North Am. 2010;43(4):817–825. [PubMed]
3. Casler J D, Doolittle A M, Mair E A. Endoscopic surgery of the anterior skull base. Laryngoscope. 2005;115(1):16–24. [PubMed]
4. Dehdashti A R Ganna A Witterick I Gentili F Expanded endoscopic endonasal approach for anterior cranial base and suprasellar lesions: indications and limitations Neurosurgery 2009644677–687., discussion 687–689 [PubMed]
5. Snyderman C H, Pant H, Carrau R L, Prevedello D, Gardner P, Kassam A B. What are the limits of endoscopic sinus surgery?: The expanded endonasal approach to the skull base. Keio J Med. 2009;58(3):152–160. [PubMed]
6. Raymond J, Hardy J, Czepko R, Roy D. Arterial injuries in transsphenoidal surgery for pituitary adenoma; the role of angiography and endovascular treatment. AJNR Am J Neuroradiol. 1997;18(4):655–665. [PubMed]
7. Berker M, Aghayev K, Saatci I, Palaoğlu S, Onerci M. Overview of vascular complications of pituitary surgery with special emphasis on unexpected abnormality. Pituitary. 2010;13(2):160–167. [PubMed]
8. Valentine R, Wormald P J. Carotid artery injury after endonasal surgery. Otolaryngol Clin North Am. 2011;44(5):1059–1079. [PubMed]
9. Valentine R, Wormald P J. A vascular catastrophe during endonasal surgery: an endoscopic sheep model. Skull Base. 2011;21(2):109–114. [PMC free article] [PubMed]
10. Valentine R, Wormald P J. Controlling the surgical field during a large endoscopic vascular injury. Laryngoscope. 2011;121(3):562–566. [PubMed]
11. Valentine R, Boase S, Jervis-Bardy J, Dones Cabral J D, Robinson S, Wormald P J. The efficacy of hemostatic techniques in the sheep model of carotid artery injury. Int Forum Allergy Rhinol. 2011;1(2):118–122. [PubMed]
12. Padhye V Valentine R Paramasivam S et al. Early and late complications of endoscopic hemostatic techniques following different carotid artery injury characteristic Int Forum Allergy Rhinol 2014. (e-pub ahead of print) [PubMed]
13. Kassam A, Snyderman C H, Mintz A, Gardner P, Carrau R L. Expanded endonasal approach: the rostrocaudal axis. Part I. Crista galli to the sella turcica. Neurosurg Focus. 2005;19(1):E3. [PubMed]
14. Kassam A, Snyderman C H, Mintz A, Gardner P, Carrau R L. Expanded endonasal approach: the rostrocaudal axis. Part II. Posterior clinoids to the foramen magnum. Neurosurg Focus. 2005;19(1):E4.[PubMed]
15. Kassam A B, Gardner P, Snyderman C, Mintz A, Carrau R. Expanded endonasal approach: fully endoscopic, completely transnasal approach to the middle third of the clivus, petrous bone, middle cranial fossa, and infratemporal fossa. Neurosurg Focus. 2005;19(1):E6. [PubMed]
16. Fujii K, Chambers S M, Rhoton A L Jr. Neurovascular relationships of the sphenoid sinus. A microsurgical study. J Neurosurg. 1979;50(1):31–39. [PubMed]
17. Weidenbecher M, Huk W J, Iro H. Internal carotid artery injury during functional endoscopic sinus surgery and its management. Eur Arch Otorhinolaryngol. 2005;262(8):640–645. [PubMed]
18. Renn W H, Rhoton A L Jr. Microsurgical anatomy of the sellar region. J Neurosurg. 1975;43(3):288–298. [PubMed]
19. Lee K J The sublabial transseptal transsphenoidal approach to the hypophysis Laryngoscope 197888(7 Pt 2, Suppl 10):10, 1–65 [PubMed]
20. Koitschev A, Baumann I, Remy C T, Dammann F. [Rational CT diagnosis before operations on the paranasal sinuses] HNO. 2002;50(3):217–222. [PubMed]
21. Bejjani G K Sekhar L N Yost A M Bank W O Wright D C Vasospasm after cranial base tumor resection: pathogenesis, diagnosis, and therapy Surg Neurol 1999526577–583., discussion 583–584 [PubMed]
22. Laws E R Jr. Vascular complications of transsphenoidal surgery. Pituitary. 1999;2(2):163–170.[PubMed]
23. Hatam A, Greitz T. Ectasia of cerebral arteries in acromegaly. Acta Radiol Diagn (Stockh) 1972;12(4):410–418. [PubMed]
24. Chaloupka J C, Putman C M, Citardi M J, Ross D A, Sasaki C T. Endovascular therapy for the carotid blowout syndrome in head and neck surgical patients: diagnostic and managerial considerations. AJNR Am J Neuroradiol. 1996;17(5):843–852. [PubMed]
25. Koitschev A, Simon C, Löwenheim H, Naegele T, Ernemann U. Management and outcome after internal carotid artery laceration during surgery of the paranasal sinuses. Acta Otolaryngol. 2006;126(7):730–738. [PubMed]
26. Inamasu J Guiot B H Iatrogenic carotid artery injury in neurosurgery Neurosurg Rev 2005284239–247., discussion 248 [PubMed]
27. Wormald P J. New York, NY: Thieme; 2013. Endoscopic Sinus Surgery: Anatomy, Three-Dimensional Reconstruction, and Surgical Technique. 3rd ed.
28. Biswas D, Daudia A, Jones N S, McConachie N S. Profuse epistaxis following sphenoid surgery: a ruptured carotid artery pseudoaneurysm and its management. J Laryngol Otol. 2009;123(6):692–694.[PubMed]
29. Kocer N, Kizilkilic O, Albayram S, Adaletli I, Kantarci F, Islak C. Treatment of iatrogenic internal carotid artery laceration and carotid cavernous fistula with endovascular stent-graft placement. AJNR Am J Neuroradiol. 2002;23(3):442–446. [PubMed]
30. Park Y S, Jung J Y, Ahn J Y, Kim D J, Kim S H. Emergency endovascular stent graft and coil placement for internal carotid artery injury during transsphenoidal surgery. Surg Neurol. 2009;72(6):741–746. [PubMed]
31. Mathis J M, Barr J D, Jungreis C A. et al. Temporary balloon test occlusion of the internal carotid artery: experience in 500 cases. AJNR Am J Neuroradiol. 1995;16(4):749–754. [PubMed]
32. Wholey M H, Wholey M H, Jarmolowski C R, Eles G, Levy D, Buecthel J. Endovascular stents for carotid artery occlusive disease. J Endovasc Surg. 1997;4(4):326–338. [PubMed]
33. Kalapatapu V R, Shelton K R, Ali A T, Moursi M M, Eidt J F. Pseudoaneurysm: a review. Curr Treat Options Cardiovasc Med. 2008;10(2):173–183. [PubMed]
34. Higashida R T, Halbach V V, Dowd C F, Barnwell S L, Hieshima G B. Intracranial aneurysms: interventional neurovascular treatment with detachable balloons—results in 215 cases. Radiology. 1991;178(3):663–670. [PubMed]

Articles from International Archives of Otorhinolaryngology are provided here courtesy of Thieme Medical Publishers

Endoscopic Endonasal Repair of Internal Carotid Artery Injury during Endoscopic Endonasal Surgery. Repair the injury with a temporalis muscle patch. The ability to repair the ICA using endoscopic techniques is limited by the narrow surgical field and inability of suturing. Pressure application or bipolar cautery has been suggested in cases of small defects in the vessel wall. However, in cases of significant bleeding during EES, endovascular treatment is suggested as definitive treatment.

Endoscopic Endonasal Repair of Internal Carotid Artery Injury during Endoscopic Endonasal Surgery

Address for correspondence Ziv Gil, MD, PhD Department of Otolaryngology Head and Neck Surgery, Rambam Medical Center, Technion – Israel Institute of Technology, 8 Ha'Aliya Street, POB 9602, Haifa 31096, Israel, gro.lluksfoesab@viz

Introduction

Intraoperative injury to the internal carotid artery (ICA) during endoscopic endonasal surgery (EES) of the skull base is a rare (0.2–1%) complication that can potentially be associated with high rates of morbidity and mortality. 1 The most common site of injury within the ICA is the cavernous segment, with left-sided injuries occurring more frequently than right-sided injuries. Traumatic injury to the ICA during EES may cause massive hemorrhaging, leading to hypotension and shock. Massive hemorrhage can be difficult to control due to limited access to the sphenoid sinus and rapid obscuring of the visual field. Bleeding from this vital artery can become lethal within minutes. Even when the bleeding is controlled, permanent neurological deficits (such as altered mental status, cranial nerve deficits, and palsies) frequently persist. 1Long-term complications include the formation of a pseudoaneurysm or carotid cavernous fistula. Management of ICA injuries involves emergent hemostasis. Many techniques have been developed to manage ICA injury including controlled hypotension, ipsilateral and contralateral neck pressure, proximal control through neck dissection, surgical ligation, aneurysm clippings, direct suture repair, or muscle/fascia grafts, with varying degrees of success. Once hemorrhage has been controlled and resuscitation efforts are underway, patients often need emergent angiography and neuroradiological intervention, such as balloon occlusions or coil embolization. The size of the arterial damage, its nature (small perforator avulsion vs. large, direct injury), and its site determine its treatment and the ability to control the injury while preserving the vessel. The ability to repair the ICA using endoscopic techniques is limited by the narrow surgical field and inability of suturing. Pressure application or bipolar cautery has been suggested in cases of small defects in the vessel wall. However, in cases of significant bleeding during EES, endovascular treatment is suggested as definitive treatment. The incidence of reported cases of ICA injury during EES is low, and thus development of an evidence-based management strategy is difficult. 1 In this case report, we provide a detailed description of an endoscopic repair of ICA injury during EES.

Case Report

A 57-year-old otherwise healthy woman was referred to our clinic due to complaints of intense headaches, speech difficulties, and dysphagia for 2 weeks. Upon physical examination, the patient demonstrated slurred speech with tongue deviation toward the left. Neck examination and endoscopic flexible fiber optic evaluation were normal. No other neurological deficits were observed. Magnetic resonance imaging demonstrated an enhanced clival mass, 48 × 36 × 55 mm, invading the right sphenoid sinus, occipital condyles, dens, and anterior arch of C1 ( Fig. 1 ). The mass was pushing the pituitary gland upward, invading the parapharyngeal space as well as the upper, middle, and lower parts of the clivus with intradural extension through the midclival region pushing the pons and basilar trunk. Inferiorly, the mass invaded the occipital condyle on both sides, the anterior ring of C1 and the upper dens. Radiological features were consistent with chordoma. The patient was scheduled for an endonasal endoscopic resection.

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Preoperative gadolinium-enhanced T2-weighted ( A ) axial and ( B ) coronal magnetic resonance imaging sections. An enhanced clival mass, 48 × 36 × 55 mm, is shown, invading the right sphenoid sinus, the occipital condyles, the dens, and the anterior arch of C1. Radiological features were consistent with chordoma.

Surgical Technique

The operation was performed under general anesthesia using an intraoperative frameless navigation. The surgery was conducted under electrophysiological monitoring. After inferior turbinate lateralization, middle turbinectomy, middle antrostomy, anterior and posterior ethmoidectomy, posterior septectomy, and elevation of a nasoseptal flap, the tumor was exposed in the sphenoid sinus. Using a high-speed coarse drill, the rostrum and clival tumor extensions were drilled out. The anterior wall of the sphenoid sinus was removed to provide better access to the tumor mass. Due to its rubbery consistency, the tumor could not be suctioned out. Instead, tumor removal was performed using Kerrison rongeur forceps and a drill. When the tumor was extirpated from the left sphenoid wall, bleeding from the left ICA in the cavernous segment was noticed. An immediate pressure with a neurosurgical gauze was applied over the defect. The operating team and the anesthesiologist were immediately notified. Packed cells and fresh-frozen plasma were delivered to the operating room and a second anesthesiologist joined the team. Vital signs were monitored carefully. Arterial blood was drawn to monitor blood gases and hematocrit levels. Neither hemodynamic compromise nor deviation from normal ranges of any of the monitored parameters was noted. Two attempts to correct the injury with Surgicel (Ethicon, West Somerville, New Jersey, United States) were unsuccessful. It was then decided to repair the injury with a temporalis muscle patch. At this point, the head and neck surgeon started prepping the temporalis area, while the neurosurgeon placed a neurosurgical gauze directly on the injured part of the left ICA applying local pressure for packing. Full control of the bleeding was maintained. Next, a 2 × 2 cm muscle patch flap was quickly harvested from the left temporalis muscle through a scalp incision at the superior temporal line in a coronal plane by the head and neck surgeon. After harvesting, the gauze was removed, and the muscle flap was inserted and positioned directly over the injured ICA. Gentle pressure was applied with overlying cotton patties for exactly 10 minutes. During that time, blood pressure was maintained above 100/60 mm Hg. After 10 minutes, the cotton patties were removed without evidence of residual bleeding. The total blood loss was <250 mL, and there was no hemodynamic compromise. Vital signs, including blood pressure, as well as laboratory results, including arterial blood gases, hemoglobin and hematocrit levels, were all within normal ranges. The patient received 1 unit of packed red blood cells (300 mL/unit) and 2 units of fresh-frozen plasma. After hemostasis was achieved, there was a question whether to discontinue the surgery. Based on the patient's stability during the time from the injury recognition until the bleeding was fully controlled, and given that a large portion of the tumor mass had already been removed prior to the injury, the operating team and anesthesiologist decided it was safe to proceed with the surgery. The operation continued for less than an hour. The degree of resection was also limited by the consistency of the tumor, which was firm and fibrotic. As most of the tumor was located below the vidian canal, the injury to the ICA did not limit the access to the rest of the tumor. Before injury, 50% of the tumor was resected, and by the end of the operation, 80% of the tumor had been removed. Throughout surgery, the right cranial nerve XII (CN XII) was monitored and preserved, while the left nerve was nonfunctional prior to surgery. Immediately after surgery, a computed tomography (CT) scan with contrast was performed, without evidence for pneumocephalus, pseudoaneurysm, or intracranial bleeding. After the operation, the patient was extubated uneventfully and transferred to the intensive care unit for observation. No postoperative complications were encountered. On 1-month follow-up, the patient was asymptomatic, maintained good outpatient oral intake, with great relief of preoperative complaints. There were no neurological deficits except for the known preoperative left CN XII palsy, which improved following surgery. The surgical wounds were intact, without evidence of infection or inflammation, and no local pain. High-quality CT angiogram was performed 6 weeks after surgery to rule out delayed pseudoaneurysm, an event with 50 to 60% prevalence. The CT angiogram showed no evidence for pseudoaneurysm nor narrowing of the artery. We believe that CT angiogram should be considered early after such an event. Pathological analysis of the specimen demonstrated clival chordoma. The patient was referred for adjuvant radiotherapy.

Discussion

Dissection around the cavernous, paraclival, and petrous segments of the ICA may be associated with vascular injury. 1 The cavernous portion of the ICA has the highest rate of injury due to its intimate relationship with the sphenoid sinus. Thus, the identification of the ICA is essential when operating in the cavernous region. Gardner et al 2 described their experience of seven ICA injuries in 2,015 endoscopic endonasal skull base cases over a 13-year period, reporting an incidence of 0.3%. Most injuries involved the left ICA, and the most common diagnosis was chondroid neoplasm. Injury of the ICA might be associated with long-term neurological deficits. 1 Therefore, when such a life-threatening complication occurs, prompt identification and intervention are crucial. Furthermore, proper preparation for such a complication is essential when planning operation on a tumor adjacent to the ICA. In light of the reported case, we propose and adopted the following changes to the operative protocol: first, in operations with high risk of ICA injury, the temporalis site should be prepped into the surgical field while setting up the surgery. Second, due to the high risk for vascular injury, we advise against the use of small cutting burrs for drilling near the ICA.

Several additional hemostatic techniques have been proposed and shown to be effective at achieving vascular control. These include muscle patch treatment (harvested sternocleidomastoid), as well as the use of Floseal (Baxter International; Deerfield, Illinois, United States), oxidized regenerated cellulose (Surgicel Nu-Knit; Ethicon), MicroFrance Wormald vascular clamps (Medtronic; Jacksonville, Florida, United States), and U-Clip anastomotic sutures (Medtronic) to suture the vascular defect. 3 Packing and placing adequate pressure have the potential to stop the bleeding; however, this may lead to complete occlusion of the artery. 1 Thus, despite controlling the bleeding, the same complications of exsanguination may occur as a result of reduced blood flow to the brain. Applying pressure can lead to pseudoaneurysm formation, especially following endovascular recanalization. 1 As Linskey et al reported in their literature review, abrupt ICA occlusion is associated with a stroke rate of up to 26% and a mortality rate of 12%. 4 Roski et al reported a 16.6% incidence of stroke in their long-term follow-up (average 12.5 years) after ligation of the ICA for an ICA aneurysm. 5 Endovascular techniques (balloon occlusion and coil embolization by stent graft) are valid options if endonasal repair is not achieved. 1 In such cases, following packing, the patient is delivered intubated to the endovascular suite.

Conclusion

There is no clear protocol to manage injury to the ICA during EES, although many have been proposed. The mortality and morbidity of an ICA injury during EES can be decreased if the team is properly trained for this event. The following steps are the basis of successful control of ICA bleeding: (1) early recognition of the ICA injury, (2) briefing of the team and preparations, (3) packing, (4) harvesting of temporalis muscle patch, (5) endoscopic placement of the muscle patch over the defect, and (6) gentle compression for 10 minutes. Using this technique, the continuity of the vessel is maintained and neurological complications can be avoided.

Financial Disclosure

None.

Conflict of Interest None.

Note

This is an original article reviewed by all the authors and not under consideration for publication elsewhere.

References

1. Chin O Y, Ghosh R, Fang C H, Baredes S, Liu J K, Eloy J A. Internal carotid artery injury in endoscopic endonasal surgery: a systematic review. Laryngoscope. 2016;126(03):582–590. [PubMed]
2. Gardner P A, Tormenti M J, Pant H, Fernandez-Miranda J C, Snyderman C H, Horowitz M B. Carotid artery injury during endoscopic endonasal skull base surgery: incidence and outcomes Neurosurgery201373(2, suppl operative):ons261–ons269., discussion ons269–ons270 [PubMed]
3. Valentine R, Wormald P J. Controlling the surgical field during a large endoscopic vascular injury. Laryngoscope. 2011;121(03):562–566. [PubMed]
4. Linskey M E, Jungreis C A, Yonas H et al. Stroke risk after abrupt internal carotid artery sacrifice: accuracy of preoperative assessment with balloon test occlusion and stable xenon-enhanced CT. AJNR Am J Neuroradiol. 1994;15(05):829–843. [PubMed]
5. Roski R A, Spetzler R F, Nulsen F E. Late complications of carotid ligation in the treatment of intracranial aneurysms. J Neurosurg. 1981;54(05):583–587. [PubMed]

Articles from Journal of Neurological Surgery Reports are provided here courtesy of Thieme Medical Publishers

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681346/

Internal carotid artery injury in endoscopic endonasal surgery

Laryngoscope. 
doi: 10.1002/lary.25748. Epub 2015 Nov 3.
Internal carotid artery injury in endoscopic endonasal surgery: A systematic review.
Chin OY1, Ghosh R1, Fang CH1, Baredes S1,2, Liu JK2,3, Eloy JA1,2,3,4.
Author information
1
Department of Otolaryngology-Head and Neck Surgery, Rutgers New Jersey Medical School, Newark, New Jersey, U.S.A.
2
Center for Skull Base and Pituitary Surgery, Neurological Institute of New Jersey, Rutgers New Jersey Medical School, Newark, New Jersey, U.S.A.
3
Department of Neurological Surgery, Rutgers New Jersey Medical School, Newark, New Jersey, U.S.A.
4
Department of Ophthalmology and Visual Science, Rutgers New Jersey Medical School, Newark, New Jersey, U.S.A.
Abstract
OBJECTIVES/HYPOTHESIS:
Internal carotid artery (ICA) injury during endoscopic endonasal surgery (EES) is a known and feared complication of paranasal sinus and skull base procedures. These ICA injuries can result in stroke, cranial nerve palsies, and death. This review examines the setting of injury along with the treatment approaches, and patient outcomes.

STUDY DESIGN:
Systematic review using PubMed/MEDLINE and EMBASE.

METHODS:
The databases were searched for articles reporting cases of ICA injury during EES. Variables analyzed included patient demographics, operative approach, preoperative diagnosis, setting of injury, repair method, imaging studies, patient outcomes, and follow-up.

RESULTS:
Twenty-five articles with 50 cases were included in this review. The EES approach was used for skull base procedures in 34 cases and for inflammatory disease in 16 cases. The most commonly injured ICA segment was the cavernous (34 cases), followed by the ophthalmic (three cases). Injuries occurred more commonly on the left (1.3:1). Injury occurred in the setting of various steps during EES with instruments. Stereotactic image guidance was reported in two cases. Initial hemostasis was achieved with packing in 35 cases, endoscopic clip sacrifice in four cases, bipolar coagulation with the intent to seal defect in three cases, and bipolar coagulation with the intent to sacrifice the ICA in one case. Intraoperative or immediate postoperative angiography was reported in 27 cases.

CONCLUSIONS:
The incidence of reported cases of ICA injury during EES remains low. Left-sided injuries to the cavernous segment of the ICA occurred more frequently than injuries on the right.

LEVEL OF EVIDENCE:
NA Laryngoscope, 126:582-590, 2016.

© 2015 The American Laryngological, Rhinological and Otological Society, Inc.

KEYWORDS:
Endoscopic sinus surgery; ICA injury; endoscopic endonasal approach; internal carotid artery injury; intraoperative complication; skull base surgery

PMID: 26525334 DOI: 10.1002/lary.25748
[Indexed for MEDLINE]
https://www.ncbi.nlm.nih.gov/pubmed/26525334