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52
C. Bachert etal.
Table 5.1
Eosinophils found in sinus specimen Comorbid asthma (may be before or after CRSwNP diagnosis) Aspirin or other non-steroidal anti-inammatory sensitivity Recurrence of nasal polyposis after surgery Serum eosinophilia (>150 cells/mL of intermediate association, >300 cells/mL strongly
associated) Clinically relevant allergic rhinitis or other allergic comorbidities (weak association)
Clinical signs for presence of type 2 inammatory disease
smell and/or taste, nasal obstruction, rhinorrhea and/or post-nasal drip, and facial pain/pressure despite medical therapy. Uncontrolled CRSwNP is dened as per­sistent or recurring rhinosinusitis symptoms despite long-term(intranasal cortico­steroids) INCS, at least one course of systemic corticosteroids in the preceding 2years (or having a medical contraindication to receiving systemic corticoste­roids) and/or previous sinonasal surgery (or having a contraindication/unwilling­ness to undergo surgery).
Indications andSurgical Considerations forReboot Procedure
In patients who have failed previous surgical intervention for type 2 CRSwNP and report uncontrolled or severe recalcitrant CRSwNP, the reboot procedure can be considered as an additional surgical option. Additional considerations for the reboot procedure are included in Table5.2.
When former surgery is reported, an estimation of the kind and extent of this operation should be deduced from available reports, nasal endoscopy, and eventu­ally CT scanning. Which sinuses have been approached (were the frontal and sphe­noid sinuses included?), and has a “ventilation and drainage” approach or a “mucosal” approach been performed? Have the sinuses been opened and clearly thickened mucosa been removed (partially) or did the surgeon aim to (almost) com­pletely remove the sinus mucosa, as described under the terms “nasalization” [13] or “reboot” [14]? Are those openings still functional, and can the sinuses be inspected with the endoscope? What is the condition of the sinus mucosa in the vari­ous sinuses? Healthy, thickened, are there secretions and crusts? The ultimate aim of surgical intervention is to provide an open ostium and a non-inamed relatively thin sinus mucosa without colored secretions in all sinuses (Fig.5.2).
If these sinus conditions are not achieved and the patient still has symptoms derived from remaining pan-sinus disease, a reboot surgery approach in severe CRSwNP should be considered. The authors also advocate consideration of the reboot procedure as a primary procedure in patients who suffer from severe uncon­trolled bilateral type 2 CRSwNP disease.
5 The Reboot Procedure forSevere Chronic Rhinosinusitis withNasal Polyps
53
Table 5.2
indications for reboot procedure in patients with CRSwNP
Fig. 5.2 View into the ethmoid after Reboot surgery; maxillary and sphenoid sinuses accessible, no polyps visible
Potential
Involvement of equal to or more than two sinuses on both sides
Comorbid asthma Comorbid aspirin sensitivity (NSAID) Increased blood eosinophils Failure of previous surgical intervention with return of
nasal polyposis
Surgical Principles andConsiderations
For the reboot procedure, standard techniques for endoscopic sinus surgery should be applied, with an emphasis on broad openings of each of the sinuses. Once this is obtained, the inamed mucosa of the sinuses should be removed. Typically, the inamed mucosa of the sinuses is easily removable with the typical instruments for sinus surgery including grasping instruments like the antrum grasping forceps “Heuwieser” or Blakesley’s forceps. The principles of reboot surgery are listed in Table5.3.
Removal of mucosa may lead to some bleeding from the underlying bone upon immediate removal. This tends to improve quickly but may also be aided by the application of topical vasoconstrictors and/or foam-based hemostatic agents. Nasal packing may be necessary for additional hemostasis.
After completion of the surgery, the nasal re-mucosalization will extend from the edges of the stripped mucosa in the nose into the sinuses within just a few days, and often can be observed to cover most of the maxillary and ethmoidal sinuses after
54
C. Bachert etal.
Table 5.3
(a) Broadly opening of the ethmoid, maxillary, frontal and sphenoid sinuses (b) Completely removing the sinus mucosa of the maxillary and ethmoid sinuses (c) Completely removing the sinus mucosa of the sphenoid and frontal sinuses. In cases where
these sinuses demonstrate normal mucosa, the mucosa can be spared (d) Preservation of the nasal mucosa of the inferior turbinate, middle turbinate (if without
polyp growth), superior turbinate, the lateral nasal mucosa of the pre-maxillary and pre­ethmoidal regions, the olfactory cleft mucosa
Principles of reboot surgery
just 1 week. After 2 weeks, the total surgical eld is often fully re-mucosalized with a thin, but functional mucosa. It is important in this period of wound healing to avoid infections. The authors will often provide doxycycline 200mg initially, then 100mg/day, given prophylactically for up to 4weeks to minimize the risk of infec­tion. These patients should be closely observed to ensure sinus stenosis does not occur. The authors advocate for early and frequent use of topical sinus irrigations twice daily and debridement of the sinuses at 1 and 2weeks post-operatively. Any early stenosis should be promptly dilated and scar bands cut. We see the patients post-operatively for cleaning and control of pain up to once a week for the rst 4 week. The post-operative wound healing period is mostly completed within 8–12weeks.
Only occasionally, the frontal sinus ostia have to be enlarged with the help of bougies or balloons, or small single polyps from any sinus have to be removed within that time. At the end of this period, all sinuses should be accessible, free of infection and edema formation. Temporary hyposmia is anticipated but does improve. Within 6–12months, >80% of the formerly anosmic subjects regain smell. To avoid CRSwNP recurrence and to support the smell potential, topical steroid rinses are continued after surgery twice daily for up to 3 years and once daily there­after, provided the mucosa remains free of polyp burden.
Another approach is the combination of surgery with biologic drugs such as Omalizumab, Mepolizumab, Dupilumab, or Benralizumab [811]. The indication for biologics is discussed in Chap. 25 of this book; however, when Reboot surgery is planned and the sinus mucosa is completely removed, a combination with biolog­ics may not be needed.

Reported Outcomes

The authors’ own data show that markers of Type-2 inammation in secretions decrease post-operatively, and smell improves within one to 3 months and is main­tained at a functional level over a follow-up of 6months or longer (up to 5years documented). Recurrence of nasal polyps rarely occurs, and if so, mostly localized areas of minor disease may occur. In these cases, small polyps can be removed inlocal anesthesia. The need for revision surgery for CRSwNP is low (below 10% over 5years).
5 The Reboot Procedure forSevere Chronic Rhinosinusitis withNasal Polyps
55
Tips and Pearls
• Create a relatively large enough ostium such that you can visualize the complete
sinus cavities and visibly verify complete removal of the sinus mucosa.
• For removal of the maxillary oor sinus mucosa, the “Heuwieser” bended grasp-
ing forceps or frontal instruments may be helpful.
• The frontal sinus ostium enlargement anteriorly and medially can be achieved
with the Bachert frontal sinus punch, which can be used to remove the bony
frontal sinus oor.
• Blakesley’s with different angles (up to 90°) are helpful for the maxillary ostium
and the anterior ethmoid approach to the frontal sinus.
• The inferior turbinate as well as the middle turbinate should be maintained as
much as possible, as they only seldomly develop nasal polyps and serve the
humidication of the ambient air post-operatively.
• Strictly avoid stripping of mucosa in the olfactory cleft or removal of the superior
turbinate to minimize the risk of postoperative hyposmia.

References

1. Bachert C, Wagenmann M, Hauser U, Rudack C.IL-5 is upregulated in human nasal polyp tissue. J Allergy Clin Immunol. 1997;99:837–42.
2. Tomassen P, Vandeplas G, van Zele T, Cardell LO, Arebro J, Olze H, Förster-Ruhrmann U, Kowalski ML, Olszewska-Ziąber A, Holtappels G, De Ruyck N, Wang XD, Van Drunen C, Mullol J, Hellings P, Hox V, Toskala E, Scadding G, Lund V, Zhang L, Fokkens W, Bachert C.Inammatory endotypes of chronic rhinosinusitis based on cluster analysis of biomarkers. J Allergy Clin Immunol. 2016;137(5):1449–56.
3. De Loof M, De Leenheer EMR, Holtappels G, Bachert C.Cytokine prole of nasal and middle ear polyps in a patient with Woakes’ syndrome and eosinophilic otitis media. BMJ Case Rep. 2016;2016:bcr2016215054.
4. Alsharif S, Jonstam K, van Zele T, Gevaert P, Holtappels G, Bachert C. Endoscopic sinus surgery for Type-2 CRSwNP: an Endotype-based retrospective study. Laryngoscope. 2019;129(6):1286–92.
5. Bachert C, Han JK, Wagenmann M, Hosemann W, Lee SE, Backer V, Mullol J, Gevaert P, Klimek L, Prokopakis E, Knill A, Cavaliere C, Hopkins C, Hellings P. EUFOREA expert board meeting on uncontrolled severe chronic rhinosinusitis with nasal polyps (CRSwNP) and biologics: denitions and management. J Allergy Clin Immunol. 2021;147(1):29–36.
6. Bachert C, Zhang N, Holtappels G, De Lobel L, van Cauwenberge P, Shixi L, Lin P, Bousquet J, van Steen K.Presence of IL-5 protein and IgE-antibodies to staphylococcal enterotoxins in nasal polyps is associated with co-morbid asthma. JACI. 2010;126:962–8.
7. Bachert C, Zhang N, Holtappels G, Tomassen P, Liu S, Lin P, Bousquet J.Nasal polyp endo­types: IL-5 and asthma co-morbidity. J Allergy Clin Immunol. 2011.
8. Gevaert P, Omachi T, Corren J, Mullol J, Han J, Lee SE, Kaufman D, Ligueros-Saylan M, Howard M, Zhu R, Owen R, Wong K, Islam L, Bachert C.Efcacy and safety of omalizumab in nasal polyposis: two randomized 1 phase III trials. JACI. 2020;146:595–605.
9. Han JK, Bachert C, Fokkens W, Desrosiers M, Wagenmann M, Lee SE, Smith SG, Martin N, Mayer B, Yancey SW, Sousa AR, Chan R, Hopkins C, SYNAPSE study investigators. Mepolizumab for chronic rhinosinusitis with nasal polyps (SYNAPSE): a randomised, double­blind, placebo-controlled, phase 3 trial. Lancet. Respir Med. 2021;9(10):1141–53.
10. Bachert C, Han JK, Desrosiers M, Hellings PW, Amin N, Lee SF, Mullol J, Greos LS, Bosso JV, Laidlaw TM, Cervin A, Maspero JF, Hopkins C, Olze H, Canonica GW, Paggiaro P, Cho
https://doi.org/10.1136/bcr- 2016- 215054.
56
SH, Fokkens W, Fujieda S, Zhang M, Lu Y, Fan C, Draikiwicz S, Kamat SA, Khan A, Pirozzi GL, Patel N, Graham N, Ruddy M, Staudinger H, Weinreich CD, Stahl N, Yancopoulos GD, Mannent LP.Dupilumab efcacy and safety in severe chronic rhinosinusitis with nasal polyps in the multicentre, randomised, double-blind, placebo-controlled, parallel group phase 3 trials LIBERTY NP SINUS-24 and LIBERTY NP SINUS-52. Lancet. 2019;394(10209):1638–50.
11. Bachert C, Han JK, Desrosiers MY, Gevaert P, Hefer E, Hopkins C, Tversky JR, Barker P, Cohen D, Emson C, Martin UJ, Shih VH, Necander S, Kreindler JL, Jison M, Werkström V.Efcacy and safety of Benralizumab in chronic rhinosinusitis with nasal polyps: a random­ized, placebo-controlled trial. J Allergy Clin Immunol. 2021;S0091–6749(21):01459–7.
12. Calus L, Van Bruaene N, Bosteels C, Dejonckheere S, Van Zele T, Holtappels G, Bachert C, Gevaert P.Twelve-year follow-up study after endoscopic sinus surgery in patients with chronic rhinosinusitis with nasal polyposis. Clin Transl Allergy. 2019;9:30.
13. Jankowski R, Rumeau C, Nguyen DT, Gallet P.Updating nasalisation: from concept to tech­nique and results. Eur Ann Otorhinolaryngol Head Neck Dis. 2018;135(5):327–34.
14. Costa Gomes S, Cavaliere C, Masieri S, Van Zele T, Gevaert P, Holtappels G, Zhang N, Ramasamy P, Voegels RL, Bachert C.Reboot surgery for CRSwNP: recurrence and smell kinetics. Eur Arch Otorrinolaringol. 2022;279:5691.
C. Bachert etal.
Sphenoid Drill-out forRecalcitrant Chronic Sphenoid Rhinosinusitis
WilliamDerekLeight andDonaldArthurLeopold
Key Points
• The management of chronic sphenoid rhinosinusitis (CSR) recalcitrant to medi-
cal therapy is time consuming and difcult.
• Sphenoid drill-out is a safe and effective technique that allows large volume
irrigation to the sphenoid analogous to a Draf III with a procedure time and degree of invasiveness similar to a Draf IIb.
• It is a versatile technique that can be combined with other extended approaches
to the frontal and maxillary sinuses, as well as previously described extended sphenoid surgery techniques, such as mini-nasoseptal ap or nasoseptal res­cue ap.
• The technique is a natural transition for most sinus surgeons who perform endo-
scopic approaches to the pituitary.
• The sphenoid drill-out should be reserved for recalcitrant disease and revision
surgery, or in cases of difcult primary disease with high likelihood of recur­rence due to anatomic factors.
6
Donald Arthur Leopold passed away during the composition of this chapter.
Supplementary Information The online version contains supplementary material available at
https://doi.org/10.1007/978- 3- 031- 89191- 5_6.
W. D. Leight (*) · D. A. Leopold Ear, Nose and Throat Institute, Boys Town National Research Hospital, Boys Town, NE, USA e-mail: William.Leight@boystown.org
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2025 J. T. Lee et al. (eds.), Advances in Surgical and Medical Interventions for Recalcitrant Chronic Rhinosinusitis,
https://doi.org/10.1007/978-3-031-89191-5_6
57
58
W. D. Leight and D. A. Leopold

Background

Chronic sphenoid rhinosinusitis (CSR) recalcitrant to medical and surgical therapy may result from advanced chronic infectious or inammatory disease, anatomic fac­tors, or inadequate initial surgical/postoperative management of primary chronic sphenoid rhinosinusitis. It is often multifactorial [1]. Persistent inammatory dis­ease in the sphenoid more commonly results from systemic factors leading to sphe­noid sinusitis in the setting of chronic pansinusitis (Fig.6.1) and occasionally from local factors resulting in isolated chronic sphenoid rhinosinusitis (Fig.6.2).
In cases of revision sinus surgery, the sphenoid will be involved approximately 30–50% of the time [2, 3]. The goal of surgical management in recalcitrant chronic sphenoid rhinosinusitis is to improve sphenoid function and mucociliary clearance by removing irreversibly inamed mucosa, neo-osteogenic bone, and scar. In most cases of refractory chronic sphenoid inammation, long-term topical therapy will be required, and optimizing the sphenoid for maximal high volume, low pressure saline irrigation is therefore also key in long term management [4]. While a tradi­tional type I, II, or III sphenoidotomy [5] is highly effective in the management of most cases of primary surgery for chronic sphenoid rhinosinusitis, extended proce­dures are sometimes needed for advanced disease [6].
The sphenoid drill-out is a modication of the traditional bilateral sphenoidot­omy that allows for the creation of a single common sphenoid cavity by removal of the rostrum, posterior nasal septum and sphenoid intersinus septum in order to max­imize irrigation volume and topical drug delivery (Fig.6.3). In the surgical hierar­chy of chronic sphenoid rhinosinusitis, it lies between traditional sphenoidotomy and sphenoid marsupialization, which requires extensive drilling of the clivus to fully eliminate the need for mucociliary transport [7]. Although it is conceptually similar to a Draf III in the frontal sinus in that a single common cavity is created, in the degree of invasiveness and time required, it is more similar to a Draf IIb. This allows it to be readily performed in the same setting as extended approaches to the maxillary and frontal sinuses [8, 9].
Fig. 6.1 Coronal and axial computed tomography (CT) images of a patient with aspirin exacer­bated respiratory disease after 3 previous surgeries
6 Sphenoid Drill-out forRecalcitrant Chronic Sphenoid Rhinosinusitis
Fig. 6.2 Coronal and axial CT images of a patient with an isolated sphenoid sinus mycetoma without prior surgical intervention. Notice intense inammatory changes and neo-osteogenesis and absence of a portion of sphenoid intersinus septum despite no prior surgery
Fig. 6.3 Long-term postoperative result from a patient who has undergone sphenoid drill-out. Notice absence of rostrum and intersinus septum as right (R) and left (L) sphenoid cavity can be appreciated together in the same eld as the planum sphenoidale (P) using a 0-degree endoscope
59

Surgical Indications

Sphenoid drill-out should be considered primarily for surgical salvage. Patients requiring sphenoid drill-out have typically had one or more prior sphenoidotomies. Only rarely should it be performed in the primary surgical setting [8, 9]. Patients typically have impaired mucociliary clearance and advanced mucosal disease (Table 6.1). Advanced chronic rhinosinusitis with and without nasal polyps
60
W. D. Leight and D. A. Leopold
Table 6.1
1. Recalcitrant sphenoid sinusitis in the presence of: (a) Isolated sphenoid sinusitis with neo-osteogenesis and/or aggressive synechiae formation (b) Recurrent sphenoid mycetoma (c) Sphenoid mycetoma with severe neo-osteogenesis (d) Chronic rhinosinusitis with and without nasal polyposis (e) Eosinophilic mucin chronic rhinosinusitis with nasal polyposis (f) Aspirin exacerbated respiratory disease (AERD) (g) Eosinophilic granulomatosis with polyangiitis (EGPA) (h) Granulomatosis with polyangiitis (GPA) (i) Recurrent allergic fungal rhinosinusitis (j) Cystic brosis (k) Primary ciliary dyskinesia
2. Neoplasia
3. Recurrent sphenoid mucocele with neo-osteogenesis or bone erosion
Indications for sphenoid drill-out
Fig. 6.4 On the left, axial CT image from a patient with AFRS after two previous surgeries. Note extensive inammatory disease, bony remodeling, high density inltrates, and multiple areas of skull base dehiscence. On the right, 0-degree endoscopic view of same patient 5years after a sphe­noid drill-out procedure
(CRSwNP, CRSsNP), eosinophilic mucin chronic rhinosinusitis with nasal polyps (eCRSwNP), allergic fungal rhinosinusitis (AFRS) (Fig.6.4), aspirin exacerbated respiratory disease (AERD) (Fig.6.1), cystic brosis, sphenoid mycetoma (Fig.6.2), sphenoid mucocele (Fig.6.5), and eosinophilic granulomatous polyangiitis (EGPA) with CRS are some of the conditions that are more likely to require a sphenoid drill-out.
6 Sphenoid Drill-out forRecalcitrant Chronic Sphenoid Rhinosinusitis
Fig. 6.5 Coronal CT image revealing a mucocele surrounded by severe osteoneogenesic bone in the right sphenoid
61

Surgical Technique

The technique has similar elements to an endoscopic approach to lesions of the sella. Stereotactic computed tomography (CT) guidance is recommended due to the enhanced difculty usually encountered in terms of anatomic landmarks, inamma­tory change, scar, neo-osteogenesis, increased blood loss, and presence of vital neu­rovascular structures in the region. 1% lidocaine with 1:100,000 epinephrine is injected into the lateral nasal wall just anterior to the sphenopalatine foramen, as well as into the posterior nasal septum. In the absence of other mitigating factors, the less diseased sphenoid is addressed rst. This allows for better access and visu­alization when addressing the more severely diseased sinus later.
Any revision surgery that needs to be accomplished in the maxillary and ethmoid sinuses is performed rst. If a Draf III is planned, the entire sphenoid drill-out is performed prior to addressing the frontal sinuses. Most commonly, a trans-ethmoid approach to the sphenoid is used, as most of these cases are done in the setting of refractory pansinusitis; however a trans-nasal approach is possible.
If present, the superior turbinate or its remnant is partially resected. The natural or surgical ostium of the sphenoid is identied if present. If small, a stapes curette or J-curette are typically used to gently enlarge the ostium initially. A wide sphe­noidotomy is then performed with a variety of Kerrison rongeurs using a standard push-pull technique. These are ideal instruments for revision sphenoid surgery, as they allow for forceful removal of thickened bone and mucosa in a controlled fash­ion that minimizes risk to nearby structures. Having a wide array of rongeurs of different angles and sizes can greatly aid this portion of the dissection. As the initial sphenoidotomy is being performed, care is taken to identify the important land­marks of the sphenoid including the sella, carotid artery, optico-carotid recess, optic nerve, and lateral recess (if present) with V2 and vidian nerves.