Mandibular distraction in neonates: indications, technique, results
© Sesenna et al; licensee BioMed Central Ltd. 2012
Received: 26 July 2011
Accepted: 2 February 2012
Published: 2 February 2012
The Pierre Robin Sequence features were first described by Robin in 1923 and include micrognathia, glossoptosis and respiratory distress with an incidence estimated as 1:8,500 to 1:20,000 newborns. Upper airway obstruction and feeding difficulties are the main concerns related to the pathology. Mandibular distraction should be considered a treatment option (when other treatments result inadequate).
Patients and methods
Ten patients between the ages of 1 month and 2 years with severe micrognathia and airway obstruction were treated with Mandibular Distraction Osteogenesis (MDO).
All patients underwent fibroscopic examination of the upper airway and a radiographic imaging and/or computed tomography scans to detect malformations and to confirm that the obstruction was caused by posterior tongue displacement. All patients were evaluated by a multidisciplinary team. Indications for surgery included frequent apneic episodes with severe desaturation (70%). Gavage therapy was employed in all patients since oral feeding was not possible. The two tracheotomy patients were 5 months and 2 years old respectively, and the distraction procedure was performed to remove the tracheotomy tube. All patients were treated with bilateral mandibular distraction: two cases with an external multivector distraction device, six cases with an internal non-resorbable device and two cases with an internal resorbable device. In one case, the patient with Goldenhar's Syndrome, the procedure was repeated.
The resolution of symptoms was obtained in all patients, and, when present, tracheotomy was removed without complications. Of the two patients with pre-existing tracheotomies, in the younger patient (5 months old) the tracheotomy was removed 7 days postoperatively. In the Goldenhar's syndrome case (2 years old) a Montgomery device was necessary for 6 months due to the presence of tracheotomy-inducted tracheomalacia. Patients were discharged when the endpoint was obtained: symptoms and signs of airway obstruction were resolved, PAS and maxillomandibular relationship improved, and tracheotomy, when present, removed. During the follow-up, no injury to the inferior alveolar nerve was noted and scarring was significant in only the two cases treated with external devices.
Mandibular Distraction Osteogenesis is a good solution in solving respiratory distress when other procedures are failed in paediatric patients with severe micrognatia.
Infants with congenital craniofacial anomalies (CFAs) often display associated severe mandibular hypoplasia causing obstruction of the airway through retro-positioning of the tongue-base into the posterior pharyngeal airway .
Retro/micrognathia may be a feature of isolated Pierre Robin sequence (PRS), when PRS is not associated with other malformations (referred as non-syndromic PRS), or is part of several congenital craniofacial syndromes, such as Treacher Collins syndrome, Goldenhar syndrome, Nager syndrome, temporomandibular joint ankylosis and velocardiofacial syndrome [2–4].
The features of PRS were first described by Robin  and include micrognathia, glossoptosis and respiratory distress. Its incidence has been estimated as 1:8,500 to 1:20,000 newborns in the general population, with no gender predilection .
Robin  later revised the characteristics of the syndrome and included cleft palate as an additional factor that could be present. A wide range of clinical manifestations exists, but the main clinical problems faced by clinicians include upper airway obstruction and feeding difficulties .
It is clear that not every child with mandibular hypoplasia displays airway obstruction [8, 9]. However, some patients may present an adequate airway when awake, but the obstruction may arise during feeding or sleeping when the pharyngeal muscle tone decreases. Thus, management regimes differ depending on the degree of upper airway obstruction (such as feeding difficulties, pulmonary infections).
Current treatments include non-surgical (prone positioning, nasopharyngeal tube/stenting, prolonged intubation), or surgical options (tongue-lip adhesion, tracheotomy, mandibular distraction osteogenesis). Recently, in neonates, mandibular distraction osteogenesis has been popularized in the literature and it is now widely accepted as the procedure of choice in the early management of airway obstruction due to craniofacial disproportion [4, 10–13].
In this study, we report 10 selected paediatric patients with severe micrognathia and airway obstruction. The patients were treated by mandibular distraction osteogenesis when other non-surgical treatments failed to avoid tracheotomy or to remove the tracheotomy itself if present.
Patients and methods
Discussion and conclusions
Children with isolated PRS or associated with a range of other congenital malformations typically display a degree of airway obstruction . The understanding of the pathogenesis of airway obstruction in PRS has rapidly evolved . The dynamics of airway obstruction seems to be multi-factorial, with both anatomic and neuromuscular components. Anatomic abnormalities include retroposition of the mandible and reduced effectiveness of the genioglossus muscle in exerting anterior traction on the tongue. Delorme et al.  suggested that in such patients the genioglossus fibres are too short or too tight. They also noted that the tongue is not pushed back but is rotated posteriorly on its base. They proposed that the retruded mandible is the result, not the cause, of the tongue position.
Caouette-Laberge et. al. 1994 proposed the following clinical classification based on the severity of respiratory symptoms .
Group I: adequate respiration in the prone position and bottle feeding.
Group II: adequate respiration in the prone position but feeding difficulties requiring gavage.
Group III: children with respiratory distress requiring respiratory support and gavage.
The clinical expression was heterogeneous: the severity of the airway complication varied from mild respiratory distress to extreme episodes of asphyxia.
Children with a mild degree of obstruction may present only subtle clinical signs, such as restless sleep, intermittent waking, and crying . A lack of weight gain despite adequate nutritional intake is an additional indication of persistent airway obstruction. This is caused by the increased effort of breathing and increased calorie consumption in these children . Severe airway distress is clinically manifested by persistent inspiratory stridor, several sternal and rib retractions, feeding difficulties (the necessity of tube feeding is frequent among these patients), and cyanosis that can result in cerebral hypoxia . The priority in patients with severe micrognathia should be to maintain the free airway to avoid chronic obstruction that can lead to carbon dioxide retention, the development of pulmonary vasoconstriction, hypertension with right ventricular failure, and associated delayed development.
Micrognathia in the isolated PRS often improves or spontaneously resolves within the first 2 years of life, without surgical intervention for the mandible. This is possible because mandibular growth improves pharyngeal neuromuscular control and increases the airway space. This is clearly not valid in cases of syndromic infants with micrognathia who display an intrinsic anomaly in mandibular growth. From previous reports, it is evident that the management of syndromic children differs from isolated PRS . Several authors have proposed an algorithm for the management of neonatal upper airway obstruction to avoid many of the unsuccessful outcomes [19, 20]. According to these guidelines, we treated non-syndromic PRS patients with mandibular distraction when other treatments were inadequate.
In cases of mild upper airway obstruction, children can be managed by non-surgical treatment, including careful instruction regarding appropriate feeding techniques, an alertness to symptoms of increased obstruction, and lateral or prone positioning, where the infant is placed in ventral decubitus to displace the tongue anteriorly.
Nasopharyngeal intubation is recommended initially to alleviate the immediate hypoxia and present an adequate solution for a short time period but clinical evaluation is necessary to observe the adequacy of the procedure. The aim of this procedure is to maintain a good respiratory pattern by reducing the duration of tube feeding, promoting weight gain . It is usually maintained for 7-10 days, when definitive treatment can be performed. When used as a definitive therapy it may be left in place for up to 8 weeks.
Patients with severe or refractory upper airway obstruction require more aggressive management. Surgical options most commonly include tongue-lip adhesion (TLA), tracheotomy, and mandibular distraction osteogenesis (MDO).
The tongue-lip adhesion procedure was introduced by Shukowsky in 1911  and popularized by Douglas in 1946 . It was designed to alleviate upper airway obstruction by correcting abnormal tongue positioning. The procedure is clearly not physiological, because it prevents the normal tongue movements and reported complications include dehiscence, tongue lacerations, injuries to the Wharton's ducts, wound infection, scar deformation and pneumonia "ab ingestis" [2, 14, 24].
Mandibular traction devices have also been used: Stellmach  reported the use of two circummandibular wires in the symphyseal area, attached to a 70-g weight, with an upwards traction. The use of circummandibular wires attached to a skull cap with an "outrigger" bar as an adjunct to glossopexy has also been reported. These treatment modalities can be effective, but must be performed for a long time period (2-3 months) and require hospitalization .
Others procedures that have been described include transfixion of the tongue by a transmandibular Kirschner wire placed anterior to the mandibular angle, as proposed by Hadley 1963 , but problems with this procedure include instability and impracticability. Hyomandibulopexy (by Bergoin 1971  and by Lapidot 1976 ) is designed to anchor the hyoid bone to the mandible anteriorly and to bring the base of the tongue forward. Interference with mandibular growth is considered a drawback of this procedure. Subperiosteal release of the floor of the mouth musculature was described by Delorme  with the concept that the musculature of the floor of the mouth when under increased tension pushes the tongue upwards and backwards. Early release of this musculature should allow the tongue to return to a more normal position. However, there are no published studies with objective measurements that demonstrate the benefits of this technique . In 1998, Myer  reported the use of tracheotomy regarding the issue of long-term airway management. Tracheotomy in neonatal airway obstruction may be life-saving but is associated with complications and developmental problems. This procedure can also be associated with severe complications, such as accidental decannulation and obstruction of the tube, which can occur at any time during the entire period of the tracheotomy. Early complications include haemorrhage from stomal varices, pneumothorax, pneumomediastinum, and minor complications include tracheitis, pneumonia, tracheal granulations, respiratory infections, subglottic stenosis, and cricoid cartilage injury [4, 29]. Once in place, the tracheotomy is usually necessary for 1-4 years. During the time of cannulation, home care remains a significant burden for the family and medical care systems. Additionally, typically, skilled home care for a child with a tracheostomy is difficult to obtain.
The average age at decanulation is 3.1 years and long-term problems, such as growth retardation, delayed speech, articulation difficulties, and behavioural problems  are present in up to 50-75% of cases . The most frequent complication is tracheomalacia.
Recently, MDO has emerged as an alternative method for relieving airway obstruction in paediatric patients with severe mandibular hypoplasia to avoid tracheotomy and improve oral feeding. Distraction osteogenesis is a surgical orthopaedic technique that was first introduced to lengthen the long bones of the body . This technique is based on the principle that tension stimulates histogenesis with bone formation (Codivilla of Bologna, Italy, described the technique as early as 1905) .
McCarthy et al. applied these concepts to treat underdeveloped mandibles in the early 1990s . From that time, numerous reports have been published, and the technique has evolved and been applied throughout the craniofacial skeleton, including the maxilla, midface, orbits, and cranium.
Mandibular lengthening obtained with MDO provides an alternative to traditional methods of airway management in infants with micrognathia. As the mandible is lengthened, the tongue base moves forward by its anterior muscular attachments to the mandible, increasing the airway space and relieving airway obstruction.
This procedure has been found to be safe and the surgical scars cosmetically acceptable. Some complications include damage to the inferior alveolar nerves, infections, failure of distraction, dislodgement of pins or distractors and damage to the tooth buds.
Distraction osteogenesis consists of four primary and consistent phases: (1) device placement and osteotomy, (2) a latency period of primary healing (not in these patients), (3) active distraction (at a rate of 2 mm/d until the desired level of distraction is achieved). Patients are given 5 days of antibiotics, and are restricted to a soft diet. At the end of the procedure (4), after completing the distraction, the devices are left in place for an additional 4-6 weeks to allow the regenerated bone to consolidate .
Three types of device exist: external, internal and resorbable, and uni/multivectorial. External devices are easier to apply but cause scarring due to the pins. Other problems such as pin site infections and the dislodgement of devices has been observed. External devices can be removed with local aesthesia but frequently require revision of the scar caused by the pin moving through the skin (Figure 3).
Internal devices are placed directly on the mandibular bone with improved compliance by the patients and parents. When the end point of active distraction is reached, some internal devices offer the possibility to remove the activation bar that emerges from the skin during the activation phase.
Written informed consent was obtained from the patient for publication of this article and accompanying images.
List of abbreviations
congenital craniofacial anomalies
Mandibular Distraction Osteogenesis
Pierre Robin sequence
posterior airway space
- Morovic CG, Monasterio L: Distraction osteogenesis for obstructive apneas in patients with congenital malformation. Plast Reconstr Surg. 2000, 105: 2324-2330. 10.1097/00006534-200006000-00003.View ArticlePubMedGoogle Scholar
- St-Hilaire H, Buchbinder D: maxillofacial pathology and management of Pierre Robin sequence. Otolaryngol Clin North Am. 2000, 33: 1241-1256. 10.1016/S0030-6665(05)70279-6.View ArticlePubMedGoogle Scholar
- Shprintzen RJ: The implications of the diagnosis of Robin sequence. Cleft palate Craniofacial J. 1992, 29: 205-209. 10.1597/1545-1569(1992)029<0205:TIOTDO>2.3.CO;2.View ArticleGoogle Scholar
- Chigurupati R, Myall R: Airway Management in Babies With Micrognathia: The Case Against Early Distraction. J Oral Maxillofac Surg. 2005, 63: 1209-1215. 10.1016/j.joms.2005.04.011.View ArticlePubMedGoogle Scholar
- Robin P: La chute de la base de la langue consideree comme une nouvelle cause de gene dans la respiration nasopharyngienne. Bull Acad Med Paris. 1923, 89: 37-41.Google Scholar
- Robin P: Glossoptosis due to atresia and hypotrophy of the mandible. Am J Dis Child. 1934, 48: 541-547.Google Scholar
- Cole A, Lynch P, Slator R: A new grading if Pierre Robin sequence. Cleft Palate Craniofac J. 2008, 45: 603-6. 10.1597/07-129.1.View ArticlePubMedGoogle Scholar
- Meyer AC, LidskY ME, Sampson DE, Lander TA, Liu M, Sidman JD: Airway intervention in children with Pierre Robin Sequence. Otolaryngology-Head and Neck Surgery. 2008, 138: 782-787. 10.1016/j.otohns.2008.03.002.View ArticlePubMedGoogle Scholar
- Dauria D, Marsh JL: Mandibular distraction osteogenesis for Pierre Robin's sequence: Wath percentage of neonates need it?. J Craniofac Surg. 2008, 19: 1237-1243. 10.1097/SCS.0b013e3181843293.View ArticlePubMedGoogle Scholar
- Darrow D, Weiss DD: Management of sleep-related breathing disordes in children. Operative technique in otolaryngology-head and neck surgery. 2002, 13: 111-118. 10.1053/otot.2002.126224.View ArticleGoogle Scholar
- Burstein FD, Williams JK: Mandibular Distraction Osteogenesis in Pierre Robin Sequence:Application of a New Internal Single-Stage Resorbable Device. Plas Reconstr Surg. 2005, 115 (No 1): 61-67.Google Scholar
- Burstein FD: Resorbable Distraction of the Mandible: Technical Evolution and Clinical Experience. J Craniofac Surg. 2008, 19 (3): 637-643. 10.1097/SCS.0b013e31816b6c8f.View ArticlePubMedGoogle Scholar
- Iatrou I, Theologie-Lygidakis N, Schoinohoriti O: Mandibular distraction osteogenesis for severe airway obstruction in Robon Sequence. Case report. J Craniomaxillofac Surg. 2010, 38 (6): 431-5. 10.1016/j.jcms.2009.10.019.View ArticlePubMedGoogle Scholar
- Myer CM, Reed JM, Cotton RT, Willging JP, Shott SR: Airway management in Pierre Robin sequence. Otolaryngol Head Neck Surg. 1998, 118: 630-635.View ArticlePubMedGoogle Scholar
- Cohen MM: The Robin anomalad-its nonspecificity and associated syndromes. J Oral Surg. 1976, 34: 587-593.PubMedGoogle Scholar
- Delorme RP, Laroque Y, Caouette-Laberge L: Innovative surgical approach for the P. Robin anomalad: subperiosteal release of the floor of the mouth musculature. Plast Reconst Surg. 1989, 83: 960-964. 10.1097/00006534-198906000-00004.View ArticlePubMedGoogle Scholar
- Caouette-Laberge L, Bayet B, Larocque Y: The Pierre Robin sequence: Review of 125 cases and evolution of treatment modalities. Plas Reconst Sur. 1994, 93: 934-942.View ArticleGoogle Scholar
- Randall P: The Robin sequence:Micrognatia and glossoptosis with airway obstruction. Plast Surgery. Edited by: Mc Carthy JG. 1990, Philadelphia, PA, Saunders, 4: 3123-3134. 2Google Scholar
- Schaefer RB, Stadler JA, Gosain AK: To distract or not to distract: an algorithm for airway management in isolated Pierre Robin sequence. Plast Reconstr Surg. 2004, 113: 1113-1125. 10.1097/01.PRS.0000110323.50084.21.View ArticlePubMedGoogle Scholar
- Cruz MJ, Kershner JE, Beste DJ, Conley SF: Pierre Robin sequences: secondary respiratory difficulties and intrinsic feeding abnormalities. Laryngoscope. 1999, 109 (10): 1632-1636. 10.1097/00005537-199910000-00016.View ArticlePubMedGoogle Scholar
- Marques IL, de Sousa TV, Carneiro AF, Peres SP, Barbieri MA, Bettiol H: Robin sequenze: a single treatment protocol. J Pediatr (Rio J). 2005, 81 (1): 14-22.View ArticleGoogle Scholar
- Shukowsky WP: Zur atiologie des stridor inspiratorius congenitus. Jahrb Kinderheilk. 1911, 73: 459-Google Scholar
- Douglas B: The treatment of micrognathia with obstruction by a plasic procedure. Plast Reconstructive Surgery. 1946, 1: 300-10.1097/00006534-194611000-00007.View ArticleGoogle Scholar
- Darrow DH: Surgery for pediatric sleep apnea. Otolaringol Clin North Am. 2007, 40 (4): 855-875. 10.1016/j.otc.2007.04.008.View ArticleGoogle Scholar
- Stellmach R: Die funktionelle Behandlung der Mikrogenie beim Syndrom Pierre Robin. Dtsch Zahn-Mund_Kieferheilk. 1957, 27: 224-234.Google Scholar
- Hadley RC, Johnson JB: Utilization of the Kirschner wire in Pierre Robin syndrome. Plast Recontr Surg. 1963, 31: 587-596. 10.1097/00006534-196306000-00010.View ArticleGoogle Scholar
- Bergoin M, Giraud JP, Chaix C: Hyomandibulopexy in the treatment of severe forms of Pierre Robin syndrome. Ann Chir Infant. 1971, 12 (1): 85-90.PubMedGoogle Scholar
- Lapidot A, Rezvani F, Terrefe D, Ben-Hur N: A new functional approach to the surgical management of Pierre Robin syndrome: experimental and clinical report. Laryngoscope. 1976, 86 (7): 979-983. 10.1288/00005537-197607000-00011.View ArticlePubMedGoogle Scholar
- Izadi K, Yellon R, Mandell DL, Smith M, Song SY, Bidic S, Bradley : Correction of upper airway obstruction in the newborn with internal mandibular distraction osteogenesis. J Craniofac Surg. 2003, 14: 493-499. 10.1097/00001665-200307000-00019.View ArticlePubMedGoogle Scholar
- Judge B, Hamlar D, Rimell FL: Mandibular distraction osteogenesis in a neonate. Arch Otolaryngol Head Neck Surg. 1999, 125 (9): 1029-1032.View ArticlePubMedGoogle Scholar
- Denny A, Amm C: New technique for airway correction in neonates with severe Pierre Robin sequence. J Pediatr. 2005, 147: 97-101. 10.1016/j.jpeds.2005.02.018.View ArticlePubMedGoogle Scholar
- Ilizarov GA, Devyatov AA, Karnerim VK: Plastic reconstruction of longitudinal bone defects by means of compression and subsequent distraction. Acta Chir Plast. 1980, 22: 32-41.PubMedGoogle Scholar
- Codivilla A: On the means of lengthening, in the lower limbs, the muscles and tissues which are shortened through deformity. J Bone Joint Surg Am. 1905, s2-2: 353-369.Google Scholar
- McCarty JG, Schreiber J, Karp N, Thorne CH, Grayson BH: Lengthening of the human mandible by gradual distraction. Plas Reconstr Surg. 1992, 89: 1-8.View ArticleGoogle Scholar
- Allen GC: Mandibular distraction osteogenesis for neonatal airway obstruction. Operative Techniques in Otolaryngology. 2005, 16: 187-193. 10.1016/j.otot.2005.09.003.View ArticleGoogle Scholar
- Villani S, Brevi B, Sesenna E: Distraction osteogenesis in a newborn infant with Pierre Robin sequence. Mund Kiefer Gesichtschir. 2002, 6: 197-201. 10.1007/s10006-002-0378-3.View ArticlePubMedGoogle Scholar
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