Sunflower Health Plan Orthognathic Surgery (PDF) Form
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This policy describes the medical necessity requirements for orthognathic surgery to improve
form and function through correction of an underlying skeletal deformity.1
Policy/Criteria
I. It is the policy of health plans affiliated with Centene Corporation® that orthognathic surgery
is medically necessary when all of the following are met:
A. When any of the following skeletal deformities (associated with masticatory
malocclusion) are present:
1. Anteroposterior discrepancy, one of the following:
a. Maxillary/mandibular incisor relationship: overjet of greater than 5 mm, or a zero
to negative value (norm = 2 mm);
b. Maxillary/mandibular anteroposterior molar relationship discrepancy of greater
than 4 mm (norm = 0 to 1 mm);
2. Vertical discrepancy, one of the following:
a. Presence of a vertical facial skeletal deformity which is two or more standard
deviations from published norms for accepted skeletal landmarks;
b. Open bite with no vertical overlap of anterior teeth or unilateral or bilateral
posterior open bite greater than 2 mm;
c. Deep overbite with impingement of palatal soft tissue;
d. Supraeruption of a dentoalveolar segment resulting from lack of occlusion when
dentition in segment is intact;
3. Transverse discrepancy, one of the following:
a. Presence of a transverse skeletal discrepancy which is two or more standard
deviations from published norms;
b. Total bilateral palatal cusp to mandibular fossa discrepancy of 4 mm or greater, or
a unilateral discrepancy of 3 mm or greater, given normal axial inclination of the
posterior teeth;
4. Anteroposterior, transverse or lateral asymmetries greater than 3 mm, with
concomitant occlusal asymmetry.
B. Presence of any of the following functional impairments:
1. Persistent difficulties with mastication and swallowing after causes such as
neurological or metabolic diseases have been excluded;
2. Malnutrition, significant weight loss, or failure-to-thrive secondary to facial skeletal
deformity;
3. Speech dysfunction directly related to a jaw deformity as determined by a speech and
language pathologist;
4. Myofascial pain secondary to facial skeletal deformity that has persisted for at least
six months, despite conservative treatment such as physical therapy and splints;
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5. Airway obstruction, such as obstructive sleep apnea, documented by polysomnogram,
when both of the following criteria are met:
a. Criteria for positive airway pressure (PAP) met and individual has proved
intolerant to or failed a trial of PAP;
b. Individual has failed prior less invasive surgical procedures OR has craniofacial
skeletal abnormalities that are associated with a narrowed posterior airway space
and tongue-base obstruction.
II. It is the policy of Centene Corporation that orthognathic surgery is not medically necessary
when any of the following are present:
A. When the sole purpose is to improve appearance, regardless of whether it is associated
with psychological disorders, because it is considered cosmetic in nature;
B. When the member/enrollee is still developing and the deformity could be corrected with
less intrusive treatment (e.g., expander or head gear).
Background
Orthognathic surgery is the surgical correction of abnormalities of the mandible, maxilla, or
both. The underlying abnormality may be present at birth or may become evident as the patient
grows and develops or may be the result of traumatic injuries or systemic diseases. Often, the
severity of these deformities precludes adequate treatment through dental treatment alone. Such
skeletal abnormalities may cause difficulties with eating or chewing, abnormal speech patterns,
or dysfunction of the temporomandibular joint (TMJ). The overall goal of treatment is to
improve function through correction of the underlying skeletal deformity.1
Abnormalities generally occur as a result of a differential in growth between the upper facial
skeleton and the lower facial skeleton, resulting in a discrepancy of the normal relationship that
exists between the upper jaw (maxilla) and lower jaw (mandible). Genetic predisposition and
environmental factors can influence the normal growth of the facial skeleton. Genetic causes can
include cleft palate and other syndromes, such as Apert and Crouzon.1,9 Traumatic events can
displace the normal structural elements or may disturb future normal growth. Other etiologies
that can result in significant dentofacial anomalies include neoplasms, surgical resection and
iatrogenic radiation. Developmental anomalies, however, are the most common condition. All of
these deformities may result in diminished bite forces, restricted mandibular excursions,
abnormal chewing patterns, speech deficits, malocclusions and/or abnormal facial appearance.
There is a relationship between facial skeletal abnormalities and malocclusions, including Class
II (disto-occlusion), Class III (mesio-occlusion) and open-bite (teeth do not meet) deformities.1
The American Association of Oral and Maxillofacial Surgeons (AAOMS) classification of
occlusion/malocclusion1
Class I: Exists with the teeth in a normal relationship when the mesial-buccal cusp of the
maxillary first permanent molar coincides with the buccal groove of the mandibular first molar.
Class II: Malocclusion occurring when the mandibular teeth are behind the normal relationship
with the maxillary teeth. This can be due to a deficiency of the lower jaw (Type 1) or an excess
of the upper jaw (Type 2).
Class III: Commonly referred to as an under bite, Class III malocclusion occurs when the lower
dental arch is in front of (mesial to) the upper dental arch. People with this type of occlusion
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usually have a strong or protrusive chin, which can be due to either horizontal mandibular excess
or horizontal maxillary deficiency.
Surgical Procedures
In orthognathic surgery, an osteotomy is made in the affected jaw, and the bones are repositioned
in a more normal alignment. The bones are held in position with plates, screws and/or wires.
Intermaxillary fixation, a procedure in which arch bars are placed on both jaws, may also be
needed to provide added stability. Simultaneous osteotomies may be performed when
deformities must be corrected in both jaws. Grafts from the ribs, hip or skull may be performed
for patients with deficient bone tissue; alloplastic bone replacement may also be required.
Orthognathic surgery, which was initially introduced in the 19th century, is generally performed
under general anesthesia on an inpatient basis.7 The gold standard for treatment of malocclusion
is orthodontic management followed by surgery; however, over the last few decades, support has
been increasing for a surgery first approach.8 Although sometimes performed for cosmetic
purposes, orthognathic surgery is generally considered to be medically necessary when
performed to treat a significant abnormality (e.g., mandible forward to cranial base, increase
mandibular length, short ramal length or obtuse gonial angle) that is causing considerable
functional impairment.7,9
Coding Implications
This clinical policy references Current Procedural Terminology (CPT®). CPT® is a registered
trademark of the American Medical Association. All CPT codes and descriptions are copyrighted
2022, American Medical Association. All rights reserved. CPT codes and CPT descriptions are
from the current manuals and those included herein are not intended to be all-inclusive and are
included for informational purposes only. The following codes are for informational purposes
only. They are current at time of review of this policy. Inclusion or exclusion of any codes does
not guarantee coverage. Providers should reference the most up-to-date sources of professional
coding guidance prior to the submission of claims for reimbursement of covered services.
CPT®*
Codes
21110 Application of interdental fixation device for conditions other than fracture or
dislocation, includes removal
21120 Genioplasty; augmentation (autograft, allograft, prosthetic material)
21121 Genioplasty; sliding osteotomy, single piece
21122 Genioplasty; sliding osteotomies, 2 or more osteotomies (eg, wedge excision or bone
wedge reversal for asymmetrical chin)
21123 Genioplasty; sliding, augmentation with interpositional bone grafts (includes
obtaining autografts)
21125 Augmentation, mandibular body or angle; prosthetic material
21127 Augmentation, mandibular body or angle; prosthetic; with bone graft, onlay or
interpositional includes obtaining autograft)
21141 Reconstruction midface, LeFort I; single piece, segment movement in any direction
(eg, for Long Face Syndrome), without bone graft
21142 Reconstruction midface, LeFort I; two pieces, segment movement in any direction,
without bone graft
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CPT®*
Codes
21143 Reconstruction midface, LeFort I; three or more pieces, segment movement in any
direction, without bone graft
21145 Reconstruction midface, LeFort I; single piece, segment in any direction, requiring
bone grafts (includes obtaining autografts)
21146 Reconstruction midface, LeFort I; two pieces, segment movement in any direction,
requiring bone grafts (includes obtaining autografts) (e,g., ungrafted unilateral
alveolar cleft)
21147 Reconstruction midface, LeFort I; three or more pieces, segment movement in any
direction, requiring bone grafts (includes obtaining autografts) (e.g., ungrafted
bilateral alveolar cleft or multiple osteotomies)
21150 Reconstruction midface, LeFort II; anterior intrusion (eg, Treacher-Collins
Syndrome)
21151 Reconstruction midface, LeFort II; any direction, requiring bone grafts (includes
obtaining autografts)
21154 Reconstruction midface, LeFort III; (extracranial), any type, requiring bone grafts
(includes obtaining autografts); without LeFort I
21155 Reconstruction midface, LeFort III; (extracranial), any type, requiring bone grafts
(includes obtaining autografts); with LeFort I
21159 Reconstruction midface, LeFort III (extra and intracranial) with forehead
advancement (eg, mono bloc), requiring bone grafts (includes obtaining autografts);
without LeFort I
21160 Reconstruction midface, LeFort III (extra and intracranial) with forehead
advancement (eg, mono bloc), requiring bone grafts (includes obtaining autografts);
with LeFort I
21188 Reconstruction midface, osteotomies (other than LeFort type) and bone grafts
(includes obtaining autografts)
21193 Reconstruction of mandibular rami, horizontal vertical, C”, or “L” osteotomy;
without bone graft
21194 Reconstruction of mandibular rami, horizontal vertical, “C”, or “L” osteotomy; with
bone graft (includes obtaining graft)
21195 Reconstruction of mandibular rami and/or body, sagittal split; without internal rigid
fixation
21196 Reconstruction of mandibular rami and/or body, sagittal split; with internal rigid
fixation
21198 Osteotomy, mandible, segmental
21199 Osteotomy, mandible, segmental; with genioglossus advancement
21206 Osteotomy, maxilla, segmental (e.g., Wassmund or Schuchard)
21208 Osteoplasty, facial bones; augmentation (autograft, allograft, or prosthetic implant)
21209 Osteoplasty, facial bones; reduction
21210 Graft, bone; nasal, maxillary or malar areas (include obtaining graft)
21215 Graft, bone; mandible (includes obtaining graft)
21244 Reconstruction of mandible, extraoral, with transosteal bone plate (e.g., mandibular
staple bone plate)
21245 Reconstruction of mandible or maxilla, superiosteal implant; partial
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CPT®*
Codes
21246 Reconstruction of mandible or maxilla, superiosteal implant; complete
21247 Reconstruction of mandibular condyle with bone and cartilage autografts (includes
obtaining grafts) (e.g., for hemifacial microsomia)
21248 Reconstruction of mandible or maxilla, endosteal implant (eg, blade, cylinder);
partial
21249 Reconstruction of mandible or maxilla, endosteal implant (eg, blade, cylinder);
complete
Reviews, Revisions, and Approvals
Policy developed.
All instances of “member” replaced with “member/enrollee.” Transferred
to CNC template from WellCare CCG HS-87. References reviewed and
updated.
Annual review complete. Updated 1.A.1.a. from >5mm to ≥5mm and
updated 1.A.1.b.>4mm to ≥4mm. Added, "or irritation of buccal or
lingual soft tissues of the opposing arch" to 1.A.2.c. Specified "maxillary"
palatal cusp in 1.A.3.b. Minor verbiage updates with no clinical
significance. Added CPT codes 21120, 21121, 21122, 21123, 21159, and
21160. Removed CPT codes 21248 and 21249. Removed ICD-10 code
table. References reviewed, updated, and reformatted. Changed “review
date” in the header to “date of last revision” and “date” in the revision log
header to “revision date.” Reviewed by specialist.
Annual review completed. Reformatted criteria II. and added II.B. as
additional non-medically necessary indication. Additional minor
rewording with no clinical significance. Background updated. CDT codes
removed from policy. References revised and updated. Reviewed by
external and internal specialists.
Annual review. Added CPT codes 21248 and 21249. References reviewed
and updated.
Review
Date
3/11
10/20
Approval
Date
3/11
10/20
10/21
10/21
10/22
10/22
10/23
10/23