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Functional endoscopic sinus surgery

Functional endoscopic sinus surgery (FESS) is a minimally invasive surgical that utilizes rigid endoscopes inserted through the nostrils to enlarge the natural drainage pathways of the , restoring and treating inflammatory conditions such as chronic rhinosinusitis (CRS) that are refractory to medical management. This mucosal-sparing approach avoids external incisions and focuses on preserving sinus physiology while removing obstructing tissue like polyps, bone fragments, or inflamed mucosa to improve ventilation, drainage, and access for topical therapies. The development of FESS traces back to early 20th-century attempts at nasal endoscopy, with Adolf Hirschmann credited for the first use of a modified cystoscope in 1901, though practical advancements came later with Harold Hopkins' rod-lens system in the 1960s, which improved visualization. In the 1970s, Austrian otolaryngologist Wolfgang Messerklinger pioneered functional endoscopic diagnostic techniques, emphasizing the ostiomeatal complex's role in sinus pathology and laying the groundwork for therapeutic applications. David Kennedy and others popularized FESS in the United States during the 1980s, with the first formal training course held at Johns Hopkins in 1985, shifting sinus surgery from open, ablative methods to targeted, physiology-preserving procedures. Over the subsequent decades, innovations like high-resolution computed tomography (CT) imaging in 1987, microdebriders, and balloon sinuplasty have refined the technique, expanding its use beyond CRS to include tumor resection, orbital decompression, and skull base access. The procedure is typically performed under general anesthesia as an outpatient operation lasting 1-3 hours, guided by preoperative scans to map and identify . Surgeons employ angled endoscopes (0°, 30°, or 45°) and specialized instruments to perform targeted interventions, such as anterior/posterior ethmoidectomy, maxillary antrostomy, sphenoidotomy, or frontal otomy, while avoiding damage to surrounding structures like the or skull base. Postoperative care involves nasal irrigations, , and short-term antibiotics or steroids to promote healing, with most patients experiencing mild bleeding and fatigue for 1-2 weeks. Indications for FESS include medically refractory CRS (with or without nasal polyps), recurrent acute (≥4 episodes per year), , mucoceles, sinonasal tumors, and complications like orbital abscesses, confirmed by nasal and CT evidence of ostial obstruction or mucosal thickening despite maximal medical therapy (e.g., 4-12 weeks of antibiotics, oral/intranasal steroids, and saline irrigations). Ophthalmic applications encompass orbital decompression for Graves' orbitopathy and for lacrimal obstruction. Outcomes demonstrate significant improvements in , symptom scores, and endoscopic findings, with success rates of 76-97.5% and durable benefits up to 10 years post-surgery, though complications like leaks (0.5-2%) or orbital injury (0.5-3%) require vigilant intraoperative monitoring.

Overview

Definition and principles

Functional endoscopic sinus surgery (FESS) is a minimally invasive surgical procedure that utilizes nasal endoscopes to directly visualize and access the , enabling the targeted removal of diseased tissue such as polyps or obstructive mucosa while preserving normal anatomical structures and healthy mucosa. This approach aims to restore normal sinus function by addressing pathology at its source, particularly in conditions like , without the need for external incisions. Rigid endoscopes with viewing angles of 0°, 30°, and 45° are typically employed to provide optimal visualization of the and sinus ostia during the procedure. The core principles of FESS emphasize "functional" surgery, focusing on the restoration of sinus ventilation and rather than radical excision of sinus contents, thereby promoting natural drainage and reducing the risk of postoperative complications. This philosophy, which prioritizes preservation of the sinus mucosa and avoidance of excessive tissue removal, was pioneered through the foundational techniques developed by Walter Messerklinger and Wolfgang Wigand in the 1970s. The Messerklinger technique employs a conservative, uninarial approach to relieve obstructions in the ostiomeatal unit, targeting inflammation in the maxillary, frontal, and anterior ethmoid sinuses with minimal intervention. In contrast, the Wigand technique adopts a more extensive binostril method, involving complete ethmoidectomy and wider sinus ostia enlargement for severe , while still adhering to the functional goal of enhancing . Anatomically, FESS relies on access to the —air-filled cavities including the , , ethmoid, and sphenoid sinuses—through key drainage pathways centered on the ostiomeatal complex (OMC). The OMC, located in the middle meatus of the , comprises the uncinate process, ethmoid infundibulum, ostium, and frontal recess, serving as the primary conduit for mucus drainage from the anterior ethmoid air cells, , and . Obstruction at this complex is a common pathophysiological basis for sinus disease, and FESS targets these sites to reopen natural ostia and facilitate airflow. In comparison to traditional open sinus surgeries, such as the Caldwell-Luc procedure, FESS represents a significant advancement due to its endonasal, endoscopic nature, which minimizes tissue trauma, reduces postoperative morbidity, and avoids external scarring. The Caldwell-Luc approach, involving an external incision through the to access the , often requires mucosal stripping and carries higher risks of recurrence and complications like facial swelling or dental injury. By contrast, FESS preserves mucosal integrity and focuses on functional restoration, leading to improved long-term patency and patient outcomes with lower revision rates.

Indications and patient selection

Functional endoscopic sinus surgery (FESS) is primarily indicated for chronic rhinosinusitis (CRS) that remains to appropriate medical , typically after at least 12 weeks of including antibiotics, nasal corticosteroids, and saline , accompanied by persistent symptoms such as nasal obstruction, , or facial pain. Other primary indications include nasal polyposis causing significant obstruction or impacting control, allergic fungal rhinosinusitis, such as fungus balls, and conditions like tumors or mucoceles that lead to obstruction or complications. Secondary indications for FESS encompass revision surgery for previously failed sinus procedures where residual disease persists despite initial intervention, as well as adjunctive roles in managing orbital or skull base pathologies, such as decompression in Graves' ophthalmopathy or repair of cerebrospinal fluid leaks. Patient selection for FESS requires objective evidence of disease, including coronal computed tomography (CT) findings demonstrating mucosal disease or obstruction, alongside endoscopic confirmation of pathology such as polyps or purulent discharge. Contraindications include uncontrolled coagulopathy or active untreated infection, which must be addressed prior to considering surgery. In pediatric patients, FESS is approached more cautiously due to the developing facial and potential impact on growth, with surgery limited to targeted procedures like anterior ethmoidectomy or maxillary antrostomy after failure of 4-6 weeks of medical therapy. It shows particular utility in children with cystic fibrosis-related CRS, where higher success rates are observed compared to other etiologies, though overall indications mirror adults but emphasize prior and avoidance of extensive dissection.

Procedure

Preoperative evaluation and preparation

The preoperative evaluation for functional endoscopic sinus surgery (FESS) begins with a comprehensive patient history, focusing on symptom duration exceeding 12 weeks for chronic rhinosinusitis (CRS), prior medical treatments, and associated factors such as allergies. Allergy testing, including skin prick or serum IgE assessments, is considered in patients with comorbid to identify potential contributors to CRS and guide management. is performed to visualize mucosal inflammation, polyps, or anatomical obstructions, providing objective confirmation of disease severity. Imaging plays a central role in anatomical mapping, with computed tomography (CT) scans being essential for preoperative planning. Coronal CT views are preferred for evaluating the ostiomeatal complex, nasal septum variants, and critical structures like the cribriform plate and lamina papyracea, using a systematic multiplanar approach (coronal for drainage pathways, axial for basal lamella, sagittal for frontal recess) to identify variants that could predispose to complications. Key landmarks, such as the Keros classification for olfactory fossa depth and dehiscences in the or , are assessed to mitigate risks during surgery. (MRI) is optionally employed when soft tissue details, such as fungal elements or tumors, require further delineation beyond CT capabilities. Patient optimization involves a trial of maximal therapy prior to to reduce and confirm . This typically includes a 12-week course of intranasal corticosteroids and saline irrigations for all CRS patients, with short courses of oral antibiotics added if bacterial is suspected based on purulent discharge or cultures (for CRS without nasal s) or systemic corticosteroids for reduction (for CRS with nasal s). As part of enhanced recovery after () protocols, comprehensive patient education and counseling on expectations and care are provided, along with minimization of preoperative to reduce and improve outcomes. is advised at least 3-4 weeks preoperatively to enhance mucosal healing and reduce complication risks. Comorbidities, such as or aspirin sensitivity, are controlled through multidisciplinary coordination, as uncontrolled conditions like eosinophilic can worsen outcomes. Discontinuation of anticoagulants, nonsteroidal drugs, and supplements (e.g., , ginkgo) is recommended 2 weeks prior to minimize bleeding risks. The process entails a detailed discussion of procedure-specific risks, including bleeding, , orbital injury, and , tailored to the patient's from imaging findings. planning is individualized, with general preferred for most cases due to the need for airway control and controlled , though with may suffice for limited procedures; positioning in reverse Trendelenburg is standard to reduce venous bleeding. Surgical planning incorporates advanced tools for complex cases, such as revision surgeries or distorted , where image-guided systems are registered using preoperative to provide real-time anatomical localization and avoid critical structures like the or . prophylaxis, if administered, follows guidelines for clean-contaminated head and procedures, typically involving a single dose of (2 g IV within 60 minutes of incision) or clindamycin (600-900 mg IV) for β-lactam-allergic patients, though evidence for routine use in uncomplicated FESS remains moderate.

Surgical techniques

Functional endoscopic sinus surgery (FESS) is performed under general , often incorporating hypotensive techniques to minimize intraoperative and enhance . The patient is positioned on the with the head elevated in reverse Trendelenburg at approximately 30 degrees to further reduce venous congestion in the surgical field. Access to the sinuses is achieved transnasally using rigid endoscopes, typically 4 mm in diameter with 0°, 30°, or 70° angled lenses, allowing magnified without external incisions. Preoperative decongestion of the is accomplished with topical agents such as or cocaine-soaked pledgets, and the eyes are protected with corneal shields. The procedure begins with medialization of the middle turbinate using a Freer elevator to expose the uncinate process, followed by uncinectomy, where the uncinate is incised with a sickle knife or backbiter and removed using to reveal the natural maxillary . Next, maxillary antrostomy enlarges the posteriorly and inferiorly to approximately 1 cm in diameter, employing through-cutting instruments like Kerrison rongeurs or a powered microdebrider to remove bone while preserving surrounding mucosa and avoiding injury to the or . Anterior ethmoidectomy then involves penetrating the ethmoid with a J-shaped curette, followed by systematic removal of ethmoid air cell septations using forceps or microdebriders, clearing the region up to the skull base while safeguarding the lamina papyracea. Posterior ethmoidectomy extends this dissection by perforating the basal lamella and exenterating posterior cells to the sphenoid face. If disease involves the , sphenoidotomy is performed by identifying the natural ostium medial to the superior turbinate and enlarging the opening with curettes or mushroom punches, ensuring wide patency for drainage. For frontal sinus involvement, dissection of the frontal recess targets the cell and any obstructing structures using angled endoscopes and curved instruments, with advanced cases requiring a "drill-out" to remove from the frontal beak using a high-speed . Throughout, the emphasis is on mucosal preservation to maintain ciliary function and prevent iatrogenic , with all steps guided by the goal of restoring sinus ventilation and . Key instruments include handheld tools such as backbiters, Blakesley and mushroom punches, and curettes for precise bone removal, alongside powered microdebriders that combine suction, irrigation, and cutting for efficient tissue resection with reduced blood loss. High-speed drills are employed for bony work in challenging areas like the frontal recess. Image-guided systems, such as the StealthStation, integrate preoperative imaging with real-time endoscopic views to correlate and enhance safety in distorted or revision cases. Variations in FESS extent depend on disease distribution, ranging from limited procedures addressing only the anterior ethmoid and to extended approaches incorporating sphenoid and frontal sinuses. Hybrid techniques may augment traditional FESS with , where inflatable catheters dilate ostia in the maxillary, sphenoid, or frontal sinuses to facilitate access and improve patency with minimal tissue trauma.

Postoperative management

Following functional endoscopic sinus surgery (FESS), immediate postoperative care focuses on monitoring for or epistaxis, managing , and minimizing nasal to promote mucosal healing. Patients are typically observed in a recovery area for several hours to assess for significant hemorrhage, which occurs in approximately 2-5% of cases and is managed with nasal compression, topical vasoconstrictors like , or, if severe, return to the operating room for control. Nasal packing is avoided when possible to prevent crusting and adhesions, but if used for in cases of extensive surgical , bioresorbable materials such as carboxymethylcellulose or foams are preferred over traditional or nonabsorbable packs, as they reduce postoperative discomfort, upon removal, and synechia formation while dissolving within days. is generally mild and controlled with analgesia, including scheduled acetaminophen (up to 3-4 g/day) and nonsteroidal anti-inflammatory drugs (NSAIDs) like ibuprofen starting the day after surgery, with opioids reserved for breakthrough to limit side effects like ; early mobilization is encouraged as part of ERAS protocols to enhance . Follow-up protocols emphasize wound care to facilitate sinus drainage and prevent . Saline nasal irrigations, using high-volume low-pressure devices (e.g., 240 mL per side twice daily), are initiated on postoperative day 1 to clear and reduce inflammation, continuing for at least 2-3 months. In-office via removes crusts and promotes ostial patency, typically scheduled at 1 week, 3 weeks, and 6 weeks postoperatively, with frequency adjusted based on healing; weekly sessions in the first 2-3 weeks optimize outcomes by reducing adhesions and improving symptom scores. Systemic antibiotics are prescribed for 7-10 days only if indicated by intraoperative , results, or factors like , as routine use does not reduce rates and may promote resistance. Patients receive detailed instructions to support recovery and identify complications early. Head elevation during sleep (using 2-3 pillows) and environmental humidification (via cool-mist humidifier) are advised for the first 1-2 weeks to minimize and crusting. Avoidance of , straining (e.g., heavy lifting >10 lbs or Valsalva maneuvers), and irritants like smoke is recommended for 7-10 days to prevent bleeding or pressure changes; sneezing should occur with the mouth open. Patients are educated on warning signs, including persistent clear nasal discharge suggestive of (CSF) leak, severe unilateral headache, or fever >101°F, prompting immediate contact with the surgeon. Long-term maintenance involves ongoing medical therapy to sustain surgical benefits and assess for revision needs. Intranasal sprays (e.g., mometasone or fluticasone, one spray per daily) are restarted 1-2 weeks postoperatively and continued indefinitely for control, particularly in patients with polyps. Revision FESS is considered if persistent nasal obstruction or recurrent symptoms occur after 3 months despite maximal medical management, with preoperative confirming ostial closure or scarring.

Historical Development

Early history

The pre-endoscopic era of sinus surgery relied on open, external approaches that prioritized radical removal of diseased tissue but often resulted in substantial morbidity. The Caldwell-Luc procedure, first described by George W. Caldwell in 1893 and refined by Henri Luc in 1897, accessed the maxillary sinus via an incision through the canine fossa above the upper teeth, allowing removal of infected mucosa and creation of a drainage antrostomy into the nasal cavity. This method, while effective for severe chronic sinusitis, was notably invasive, frequently leading to complications such as facial swelling in up to 90% of cases, transient or permanent numbness of the cheek or teeth due to infraorbital nerve injury, oroantral fistulas, and chronic pain. For more extensive maxillary sinus pathology, the Denker operation, introduced by Alfred Denker in 1906, offered a radical alternative involving partial anterior maxillectomy to expose and excise diseased tissue from the sinus walls. This approach provided wide access but amplified risks, including significant facial scarring, bone defects, and higher rates of nerve damage and compared to less aggressive techniques. Such procedures underscored the era's emphasis on eradication over mucosal preservation, often sacrificing normal sinus physiology and contributing to long-term functional deficits. The introduction of endoscopy began to shift paradigms toward intranasal visualization in the early . In 1901, Alfred Hirschmann of performed the first recorded endoscopic nasal examination using a modified cystoscope originally designed for , successfully visualizing the through the natural without external incisions. This pioneering effort demonstrated the potential for direct internal access, though limited by poor illumination and rigid instrumentation that restricted maneuverability in curved nasal passages. Early extensions to the occurred in the , with experimental endoscopies attempting to navigate the complex frontal recess, but these remained rudimentary due to technological constraints. By the mid-20th century, otolaryngologists in the 1950s and 1960s increasingly incorporated headlights for enhanced illumination and suction devices to clear blood and debris during intranasal ethmoidectomies and polyp removals, reducing reliance on external approaches. However, widespread endoscopic adoption was hindered by the limitations of available tools, including the straight-line view of rigid endoscopes and the distorted, low-resolution images from emerging flexible fiberoptic scopes, which proved inadequate for precise sinus navigation. A breakthrough in the 1960s was the rod-lens telescope system invented by physicist Harold Hopkins, which provided superior brightness and clarity, facilitating more effective intranasal endoscopy. These advancements nonetheless facilitated a gradual transition from mutilating external incisions to mucosa-sparing intranasal techniques, setting the foundation for functional preservation in later developments.

Evolution and key milestones

The development of functional endoscopic sinus surgery (FESS) began in the with pioneering work in , where Messerklinger introduced the concept of middle meatal antrostomy in 1978, emphasizing preservation of normal sinus mucosa to restore physiological drainage and ventilation. Concurrently, Manfred Wigand developed a posterior-to-anterior surgical approach using rigid endoscopes, which allowed for more extensive sinus access while minimizing external incisions. These innovations laid the groundwork for minimally invasive techniques, shifting away from traditional open procedures. In 1985, Heinz Stammberger in and David Kennedy independently popularized the term "functional endoscopic sinus surgery," highlighting its focus on functional restoration rather than radical tissue removal. During the 1990s and , FESS gained widespread adoption through technological integrations that enhanced precision and safety. Image-guided navigation systems, introduced in the early , utilized preoperative computed tomography scans to provide real-time intraoperative localization, particularly beneficial in complex anatomies like revision surgeries. In the late , microdebriders were incorporated into FESS, enabling efficient removal of diseased tissue while sparing healthy mucosa, which improved operative efficiency and reduced bleeding. Procedure volumes surged during this period; for instance, in , the annual number of endoscopic sinus surgeries increased from approximately 6,800 in 2010 to over 8,200 by 2019, reflecting broader clinical acceptance and refined indications for chronic rhinosinusitis. Advancements from the to 2025 further refined FESS with innovative tools and approaches. Robotic-assisted systems emerged around 2020, offering enhanced dexterity and for delicate dissections, though primarily in investigational and early clinical use to improve in challenging cases. Navigation technologies integrated by 2023–2024, enabling predictive modeling of surgical paths and overlays to reduce errors in real-time. Bioresorbable packing materials, such as steroid-eluting implants, became standard in the , promoting faster and lower rates without requiring removal. Combined procedures, like FESS with vidian , showed long-term efficacy in managing chronic with nasal polyps and in 2025 studies, with sustained symptom relief observed up to five years post-surgery. Post-2020 trends included techniques incorporating for ostial dilation alongside traditional FESS, expanding options for refractory cases. The global dissemination of FESS accelerated through standardized training and guidelines, such as the European Position Paper on Rhinosinusitis and Nasal Polyps (EPOS) 2020, which updated evidence-based recommendations for surgical indications and integrated care pathways to promote uniform adoption worldwide.

Clinical Outcomes

Efficacy and success rates

Functional endoscopic sinus surgery (FESS) demonstrates high efficacy in treating chronic rhinosinusitis (CRS), with studies reporting 80-90% of adult patients experiencing significant symptom improvement, including reductions in nasal obstruction, discharge, and facial pain. A meta-analysis of 335 patients showed a mean SNOT-22 score reduction of 23.58 points (95% CI: 10.70-36.46, p < 0.001), exceeding the minimal clinically important difference of 8.9-9 points and indicating substantial quality-of-life gains. Success rates range from 76% to 97.5%, with notable improvements in SNOT-22 scores (e.g., from 34.87 to 22 post-primary surgery) and endoscopic findings like Lund-Kennedy scores. For CRS with nasal polyps (CRSwNP), FESS alone yields polyp recurrence rates of 15-22% over 2-5 years, but adjunctive biologics such as dupilumab significantly lower this to under 20% at 2 years by delaying regrowth and enhancing long-term control (p < 0.01). Outcomes are influenced by disease severity, with non-polypoid CRS showing better symptom resolution (up to 87% improvement) compared to polypoid forms, where recurrence risks increase with factors like asthma or high-grade polyps. Surgeon experience plays a key role, as high-volume practitioners (>63 cases/year) achieve 40% lower revision rates (HR: 0.63, 95% CI: 0.46-0.86) than low-volume ones (1-17 cases/year), correlating with 15-20% higher overall success through more complete procedures. Adherence to postoperative follow-up, including topical therapies, further boosts efficacy by reducing recurrence. Meta-analyses confirm FESS superiority over medical therapy alone for CRS, with a 2024 review reporting 85-87% patient satisfaction and sustained SNOT-22 improvements (p < 0.001) versus ongoing medications. The EPOS 2020 guidelines endorse FESS for cases failing 6-12 weeks of adequate medical , noting 70-100% subjective in symptom and quality-of-life metrics like VAS and scores, particularly when preoperative SNOT-22 exceeds 20. Long-term data indicate 70-80% sustained benefit at 5 years, with 65-75% achieving clinically meaningful SNOT-22 reductions (≥8.9 points) and acceptable disease control (19.5% fully controlled, 36.8% partly controlled), though 40% may require revisions in severe CRSwNP without adjuncts. The SNOT-22 tool validates these gains, highlighting FESS's role in enhancing olfaction and overall well-being in validated cohorts.

Complications and risks

Functional endoscopic sinus surgery (FESS) carries a low overall risk of complications, with major adverse events occurring in approximately 0.36% of primary cases. Common minor complications include postoperative , crusting, and , which typically resolve with conservative measures. Minor , often manifesting as epistaxis, affects about 2-3% of patients and is usually managed with nasal packing or . Crusting and minor are common, primarily due to disrupted mucosal healing, and are prevented through regular postoperative and prophylaxis. Synechiae or adhesions form in 2-4% of patients, potentially obstructing sinus , and are mitigated by meticulous surgical and postoperative stenting if needed. Major risks, though rare, can be severe and include (CSF) leak, orbital injury, and vascular damage. CSF leaks occur in 0.13-0.28% of procedures, with higher rates during sphenoid sinus interventions, and are often repaired intraoperatively using mucosal grafts or flaps. Orbital injuries, including or extraocular muscle damage leading to potential blindness, affect 0.23-0.44% of cases and are avoided by adhering to anatomical landmarks such as the lamina papyracea. Vascular injuries, particularly to the , are exceedingly rare at less than 0.1% and require immediate or . Risk factors for complications include anatomical variants identifiable on preoperative computed tomography (CT), such as Haller cells, which protrude into the maxillary sinus roof and increase the risk of orbital or maxillary injury. Image-guided navigation systems may reduce the risk of major complications, enhancing precision in complex cases. Postoperative monitoring is essential for early detection of issues like meningitis, which occurs in about 0.24% of patients. Management of complications employs a multidisciplinary approach; for instance, persistent CSF leaks may necessitate neurosurgical consultation for layered closure with or grafts. Incidence trends show a modest decline in certain complications, such as (annual percent change of -3.42% since the ), attributable to technological advances like and improved , with overall major event rates decreasing by around 20% over the past decade.

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