Clinical UM Guideline
|Subject:||Functional Endoscopic Sinus Surgery (FESS)|
|Guideline #:||CG-SURG-24||Current Effective Date:||10/14/2014|
|Status:||Reviewed||Last Review Date:||08/14/2014|
This document addresses the use of functional endoscopic sinus surgery (FESS), an endoscopic surgical procedure used to treat various conditions of the nasal sinuses, including but not limited to chronic sinusitis.
Note: Please see the following document for related information:
Functional endoscopic sinus surgery (FESS) is considered medically necessary for the treatment of sinusitis, polyposis, or sinus tumor when any one of the following circumstances is present:
Nasal or sinus cavity debridement following FESS is considered medically necessary for any of the following circumstances:
Not Medically Necessary:
Functional endoscopic sinus surgery is considered not medically necessary for the treatment of sinusitis, polyposis, sinus tumor, or any other condition when the criteria above are not met.
Nasal or sinus cavity debridement following FESS is considered not medically necessary when criteria above are not met.
The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.
|31237||Nasal/sinus endoscopy, surgical; with biopsy, polypectomy or debridement [when specified as debridement following sinus surgery]|
|31254||Nasal/sinus endoscopy, surgical; with ethmoidectomy, partial (anterior)|
|31255||Nasal/sinus endoscopy, surgical; with ethmoidectomy, total (anterior and posterior)|
|31256||Nasal/sinus endoscopy, surgical, with maxillary antrostomy|
|31267||Nasal/sinus endoscopy, surgical, with maxillary antrostomy; with removal of tissue from maxillary sinus|
|31276||Nasal/sinus endoscopy, surgical with frontal sinus exploration, with or without removal of tissue from frontal sinus|
|31287||Nasal/sinus endoscopy, surgical, with sphenoidotomy|
|31288||Nasal/sinus endoscopy, surgical, with sphenoidotomy; with removal of tissue from the sphenoid sinus|
|S2342||Nasal endoscopy for post-operative debridement following functional endoscopic sinus surgery, nasal and/or sinus cavity(s), unilateral or bilateral|
|ICD-9 Procedure||[For dates of service prior to 10/01/2015]|
|ICD-9 Diagnosis||[For dates of service prior to 10/01/2015]|
|039.0-039.9||Actinomycotic infections (actinomycotic mycetoma)|
|212.0||Benign neoplasm of nasal cavities, middle ear, and accessory sinuses|
|235.9||Neoplasm of uncertain behavior of other and unspecified respiratory organs (accessory sinuses)|
|239.1||Neoplasms of unspecified nature, respiratory system|
|325||Phlebitis and thrombophlebitis of intracranial venous sinuses|
|V58.49||Other specified aftercare following surgery|
|ICD-10 Procedure||[For dates of service on or after 10/01/2015]|
|095P4ZZ-095X4ZZ||Destruction of sinus, percutaneous endoscopic approach [accessory, maxillary, frontal ethmoid or sphenoid; includes codes 095P4ZZ, 095Q4ZZ, 095R4ZZ, 095S4ZZ, 095T4ZZ, 095U4ZZ, 095V4ZZ, 095W4ZZ, 095X4ZZ]|
|099P40Z-099X4ZZ||Drainage of sinus, percutaneous endoscopic approach [with or without device, accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 099P40Z, 099P4ZZ, 099Q40Z, 099Q4ZZ, 099R40Z, 099R4ZZ, 099S40Z, 099S4ZZ, 099T40Z, 099T4ZZ, 099U40Z, 099U4ZZ, 099V40Z, 099V4ZZ, 099W40Z, 099W4ZZ, 099X40Z, 099X4ZZ]|
|09BP4ZZ-09BX4ZZ||Excision of sinus, percutaneous endoscopic approach [accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 09BP4ZZ, 09BQ4ZZ, 09BR4ZZ, 09BS4ZZ, 09BT4ZZ, 09BU4ZZ, 09BV4ZZ, 09BW4ZZ, 09BX4ZZ]|
|09CP4ZZ-09CX4ZZ||Extirpation of matter from sinus, percutaneous endoscopic approach [accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 09CP4ZZ, 09CQ4ZZ, 09CR4ZZ, 09CS4ZZ, 09CT4ZZ, 09CU4ZZ, 09CV4ZZ, 09CW4ZZ, 09CX4ZZ]|
|09DP4ZZ-09DX4ZZ||Extraction of sinus, percutaneous endoscopic approach [accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 09DP4ZZ, 09DQ4ZZ, 09DR4ZZ, 09DS4ZZ, 09DT4ZZ, 09DU4ZZ, 09DV4ZZ, 09DW4ZZ, 09DX4ZZ]|
|09JY4ZZ||Inspection of sinus, percutaneous endoscopic approach|
|09NP4ZZ-09NX4ZZ||Release sinus, percutaneous endoscopic approach [accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 09NP4ZZ, 09NQ4ZZ, 09NR4ZZ, 09NS4ZZ, 09NT4ZZ, 09NU4ZZ, 09NV4ZZ, 09NW4ZZ, 09NX4ZZ]|
|09QP4ZZ-09QX4ZZ||Repair sinus, percutaneous endoscopic approach [accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 09QP4ZZ, 09QQ4ZZ, 09QR4ZZ, 09QS4ZZ, 09QT4ZZ, 09QU4ZZ, 09QV4ZZ, 09QW4ZZ, 09QX4ZZ]|
|09TP4ZZ-09TX4ZZ||Resection of sinus, percutaneous endoscopic approach [accessory, maxillary, frontal, ethmoid or sphenoid; includes codes 09TP4ZZ, 09TQ4ZZ, 09TR4ZZ, 09TS4ZZ, 09TT4ZZ, 09TU4ZZ, 09TV4ZZ, 09TW4ZZ, 09TX4ZZ]|
|ICD-10 Diagnosis||[For dates of service on or after 10/01/2015]|
|D14.0||Benign neoplasm of nasal cavities, middle ear, and accessory sinuses|
|D38.5||Neoplasm of uncertain behavior of other respiratory organs (accessory sinuses)|
|D38.6||Neoplasm of uncertain behavior of respiratory organ, unspecified|
|G08||Intracranial and intraspinal phlebitis and thrombophlebitis|
|J01.00- J01.91||Acute sinusitis|
|Z48.89||Encounter for other specified surgical aftercare|
Functional Endoscopic Sinus Surgery (FESS)
FESS is the most commonly used surgical technique to treat medically unresponsive chronic sinusitis and other serious conditions of the nasal sinuses that result in impaired sinus drainage. FESS utilizes small fiberoptic tools to access the nasal sinuses through the nasal opening to remove diseased tissue and bone, resulting in opened sinus passageways, improved mucus drainage, and promotion of healthy tissue growth.
Prior to the creation and adoption of FESS, the standard treatment method involved the creation of a surgical opening in the upper jaw above the front teeth. The use of FESS allows for a much less invasive and traumatic procedure, resulting in shorter surgery and healing times, less postoperative discomfort, and fewer surgical complications.
Despite having been widely adopted as the standard of care, only a few controlled trials evaluating the use of FESS for various conditions are currently available in the medical literature. One randomized controlled trial by Blomqvist (2001) compared medical treatment for nasal polyps with surgery followed by medical treatment in 32 subjects with a follow-up of 1 year. The authors reported that surgery reduced the polyp score and improved nasal obstruction symptoms, but did not help with hyposmia (reduced sense of smell). Another study by Penttila (1997) reported the results of a randomized study comparing FESS vs. the Caldwell-Luc (C-L) open procedure for the treatment of chronic maxillary sinusitis. Follow-up ranged from 5 to 9 years with 128 individuals responding. The authors report that the outcomes for the FESS group were approximately equivalent to that in the C-L group.
A prospective, randomized, controlled trial of medical vs. surgical treatment of polypoid and nonpolypoid chronic rhinosinusitis (CRS) is described by Ragab and colleagues (2004). In this study, 90 people with CRS were randomized to either medical or surgical therapy with FESS. The study found that both the medical and surgical treatments for CRS significantly improved almost all subjective and objective parameters of CRS with no significant difference being found between the two groups. The authors conclude that CRS should initially be treated with maximal medical therapy (e.g., antibiotics and topical steroids), with surgical treatment being reserved for cases refractory to medical therapy.
Finally, a Cochrane review of FESS for the indication of chronic rhinosinusitis from May 2006 concluded:
The evidence available does not demonstrate that FESS, as practiced in the included trials, is superior to medical treatment with or without sinus irrigation in patients with chronic rhinosinusitis. There were no major complications in any of the included trials and FESS appears to be a safe procedure. More randomised controlled trials comparing FESS with medical and other treatments, with long-term follow up, are required.
Although the literature-based evidence addressing FESS is limited, the clinical experience over the past decade has demonstrated the safety and efficacy of this procedure compared to more invasive techniques.
There have been several studies addressing the use of nasal or sinus postoperative debridement after FESS surgery, although the results have been mixed with regard to whether or not there is benefit of this procedure. A small study found no significant benefit from debridement (Nilssen, 2002), and another found only minor symptomatic benefit when debridement was performed during the first postoperative week (Kemppainen, 2008). Another study found that debridement significantly reduces crusting and postoperative adhesions as compared with saline irrigation, but was associated with significantly more postoperative pain (Bugten, 2006). The authors reported that at 12 weeks after surgery, there were no significant differences between individuals receiving or not receiving debridement in terms of polyps, edema, crusting, and discharge. A very small randomized trial suggested that 1 week intervals were optimal for performing debridement, which the authors indicate is currently most often performed in a large number of clinical settings (Lee, 2008). Fishman and colleagues conducted a prospective, randomized controlled, single-blinded, within-subject trial involving 24 subjects who underwent FESS and were followed for 3months posoperatively (2011). Each subject had frequent endoscopic cleaning on one side versus minimal intervention on the other in the early post-operative period. The authors reported that there was no overall statistically significant difference between the two groups (p = 0.37). A post-hoc subgroup analysis revealed a significant effect of regular suction clearance on adhesions at 3 months (p=0.048), but not on edema, polyps, granulation, discharge or crusting. An RCT reported by Alsaffar (2013) involving 58 subjects randomized to receive either 2 postoperative debridements at 2 and 4 weeks (n=28) or no debridement (n=30). The authors reported that at 4 weeks there was no difference between the groups in regard to Lund-Kennedy Endoscopic Score (p=0.59) or SNOT-21 scores (p=0.47). Similar results were reported at 6 months (Lund-Kennedy Endoscopic Score, p=0.46; SNOT-21, p=0.71). Although both groups reported low overall levels of pain in the early postoperative time period based on visual analog scale measurements, the debridement group had significantly higher overall pain score vs. controls (p=0.019). Finally, the authors investigated the difference in inconvenience between the two groups using the Post-Operative Inconvenience Scale (POIS). A significant difference between groups was reported, with the debridement group significantly more inconvenienced than the control group (p=0.002).
Postoperative debridement may need to occur for longer periods in some individuals with conditions that may lead to the development of complications. Such individuals include those with severe resistant nasal polyposis, neoplasm, or allergic fungal sinusitis. However, even in these individuals, debridement should be prompted by symptoms which arise as a consequence of the more extensive surgery or underlying disease. There is no evidence that debridement absent symptoms, even with these risk factors for complications after FESS, is associated with improved outcomes.
Peer Reviewed Publications:
Government Agency, Medical Society, and Other Authoritative Publications:
Functional Endoscopic Sinus Surgery
|Reviewed||08/14/2014||Medical Policy & Technology Assessment Committee (MPTAC) review. No change to clinical indications. Updated Rationale and Reference sections.|
|Revised||08/08/2013||MPTAC review. Clarified medically necessary criteria regarding CT findings for uncomplicated sinusitis and allergy assessment. Updated Coding and Reference sections.|
|07/01/2013||Updated Coding section to remove CPT 31240 (not applicable).|
|Revised||08/09/2012||MPTAC review. Revised mucocele indication in MN statement to add "causing chronic sinusitis". Added "Cavernous sinus thrombosis caused by chronic sinusitis" to MN statement. Updated Coding and Reference sections.|
|Revised||05/10/2012||MPTAC review. Revised statement regarding uncomplicated sinusitis. Revision of debridement statement regarding symptoms of nasal obstruction.|
|Revised||08/18/2011||MPTAC review. Added language to not medically necessary section regarding the use of FESS for all other indications.|
|Revised||11/18/2010||MPTAC review. Added medically necessary and not medically necessary statements regarding postoperative debridement following FESS. Updated rationale and references.|
|Reviewed||08/19/2010||Medical Policy & Technology Assessment Committee (MPTAC) review. Updated Reference section.|
|Reviewed||08/27/2009||MPTAC review. No change to guideline position. Updated Reference section.|
|Reviewed||08/28/2008||MPTAC review. No change to guideline position.|
|Reviewed||08/23/2007||MPTAC review. No change to guideline position.|
|New||09/14/2006||MPTAC initial guideline development.|