Background
Clefts of the lip, alveolus and palate are the most common congenital malformations of the head and neck and the second most common of all congenital malformations in general [
1]. Both cleft lip and cleft palate (CP) occur when tissues in the face and mouth do not fuse properly by the 2nd or 3rd month of pregnancy. Although considerably progress has been made in the last 30 years in the treatment of CP, multiple surgical procedures are still required followed by endless clinical visits and emotional and physical stress both for patients and their families [
2,
3]. The current state of CP treatment relies on a multidisciplinary approach starting from the examination by a paediatrician who oversees the development of the child, a plastic or oral surgeon and an otolaryngologist [
4].
Malformations affecting the soft and hard palate influence the functionality of the Eustachian tube, interfering with the ear ventilation and drainage from the ear [
5]. Therefore, Eustachian tube dysfunction may lead to middle ear effusion and otitis media recurrence, thus affecting auditory function [
6,
7]. The recovery rate of Eustachian tube function after palatal surgery ranges from 40 to 86% [
8,
9]. Although the surgical closure of the palate with the pterygoid and tensor of the soft palate muscle integrity may improve middle ear status, the simple closure of the palate is insufficient unless a good velar sphincter is formed [
10,
11].
The list of specialists required for the proper treatment of CP is not complete without the identification of ear, nose and throat (ENT) manifestations associated with CP. Follow-up examination involves a maxillofacial surgeon who monitors the development of dentition and palate, an otolaryngologist who evaluates the middle ear status, an audiologist who monitors hearing loss, and a speech and language pathologist. Recommendations for surgical correction and treatment of middle ear pathology are based on otologic and audiometric evaluations. To date, there is still a lack of evidence indicating that a greater degree of alteration of the palate is associated with increased velopalatal and Eustachian tube dysfunction and consequently an increased rate of chronic otitis media (COM) and increased hearing loss [
6,
12]. In this regard, understanding Eustachian tube dysfunction is an important component of CP management [
13]. Furthermore, the majority of children with CP display acute otitis media at some point in their development. The incidence of acute otitis media in these children is not comparable to that of the general population until adolescence [
14].
In the short term, patients treated early with ear tubes exhibit better audiometric results as well as better articulation and speech development compared with patients treated conservatively, whereas no significant differences have been observed regarding mid- or long-term outcomes. Since early placement of tympanic ventilation tubes has been the standard in the care of CP children and often accompanied by an increased rate of tympanic membrane abnormalities indicative of COM, it is important to assess whether this is a result of the insertion of multiple tympanostomy tubes or it is intrinsic to the natural history of middle ear inflammatory disease of such patients [
15].
Here, we studied a cohort of CP patients who underwent operation at the Vall d’Hebron Hospital in Barcelona to determine how CP type or degree may affect the presence of tympanic membrane abnormalities indicative of COM among patients who underwent operation for this type of malformation. The impact of CP type and number of ventilation tubes received on otologic, audiologic, and speech outcomes was investigated. Therefore, the state of the ear was reviewed by otoendoscopy/otomicroscopy, and audiometry was performed in external consultations. This information was related to the type of CP not with the type of surgery because we agreed that this variable was uniform in all cases.
Methods
Study design
This research is an observational cross-sectional study on a group of patients. Otologic, audiometric, tympanometric and speech evaluation were conducted for a cohort of children (> 6 years) with cleft repair between 2000 and 2014. All individuals were followed by the ENT service of our centre. The type and degree of velopalatal malformation, presence/absence of hearing loss, and number of surgeries for insertion of ear tubes were recorded. The indication used in our service for the placement of the tympanostomy tubes is the presence of persistent seromucosa otitis media (with at least 3 months of evolution) associated with conductive hearing loss greater than 30–35 dB (predominantly in the low frequencies) and/or a delay/alteration in the acquisition of language to a greater or lesser degree.
In addition, patients were classified according to the presence/absence of tympanic membrane abnormalities indicative of COM. The procedures described within the present study are part of routine clinical care.
Selection criteria
The inclusion criteria were age greater than or equal to 6 years, repair of cleft palate +/− cleft lip between 2000 and 2014, repair performed in our centre, follow-up by ENT in our centre, and complete otoscopic, audiometric, impedance and speech evaluation at the time of the study.
The exclusion criteria were malformative syndrome affecting the facial mass and/or accompanied by alteration of the Central Nervous System, isolated cleft lip, cleft repair at outside hospital, no ENT follow-up, or no otoscopic, audiometric impedance and/or speech testing at the time of this study.
Otologic measurements
Tympanic membranes were evaluated using microscopic otoscopy. The term chronic otitis media refers to intractable middle ear or mastoid tissue pathology behind an intact or perforated tympanic membrane. The presence of cholesteatoma, deep attic retraction pockets, persistent membrane perforations (> 3 months), atelectasis or severe adhesive membranes were considered as COM. Ears that had a lower degree of shrinkage or persistent otitis media with effusion (> 3 months) without further tympanic alterations were considered abnormal but not as COM. In the same way, the presence of tympanostomy tubes without the presence of other changes in the tympanic membrane, apart from these at the time of examination, was not considered COM. Finally, the presence of isolated myringosclerosis was not considered abnormal, as this finding has not been suggested as a risk factor in the development of COM.
Audiometric measurements and hearing loss
Pure-tone audiometry was performed on all patients using an audiometer MAICO MA-51 (CE certificate 0124) (Berlin, Germany) and headphones (Telephonics TDH 39-P, New York, USA) properly calibrated in accordance with the manufacturer’s manuals. Five pure tone averages (PTA) at 500, 1000, 2000, 4000, and 8000 Hz were calculated. The degree of hearing loss was evaluated as classified by Northern and Downs [
16]. Briefly, 0–15 dB was considered normal hearing, 16–25 dB was considered very mild hearing loss (but included as normal hearing loss during analyses), 26–40 dB was considered mild hearing loss, 41–70 dB was considered moderate hearing loss, 71–90 dB was considered severe hearing loss, and greater than 91 dB was considered profound hearing loss.
Impedance measurements/tubal evaluation
Middle ear impedance was measured using Titan (Interacoustics, Interacoustics A/S, Middelfart, Denmark).
Type A tympanograms with peak pressures within {plus minus} 50 daPa and compliance of 0.2–1.4 cc were considered normal because it is a normal curve where the pressure in the middle ear corresponds to the atmospheric and therefore to that of the external auditory canal. However, the tympanograms Ad, As, B and C are pathological curves.
Speech
Speech parameters assessed included nasal resonance and articulation errors. Hypernasality was ranked on a scale of 0–3, which corresponds to the absence of nasal resonance (0), mild (1), moderate (2) and severe (3) hypernasality. Speech articulation was evaluated by demonstrating the presence or absence of errors.
Statistics
The continuous variables of the study were summarized by descriptive statistics: mean and standard deviation (sd). Similarly, categorical variables were summarized by frequency statistics: number of cases and percentage.
The following relationships were evaluated using Chi-squared or Fisher’s exact test: Veau classification-COM, Veau classification-hypoacusis, Veau classification-abnormal impedance, Veau classification-hypernasality, Veau classification-number of ventilation tube surgeries, number of ventilation tube surgeries-COM, and number of ventilation tube surgeries-hypoacusis.
Multivariate analysis by using the multiple linear regressions was performed to assess the association with Veau classification, age, number of ventilation tubes inserted, degree of hearing loss (independent variables) and COM (dependent variable).
The SPSS program (version 16.0) (Chicago, IL, USA) for data management and the Stata program (version 13.1) (College Station, TX, USA) were used for the remainder of the calculations.
A level of significance α = 0.05 was established in all tests performed.
Discussion
The association of CP with ear pathology and hearing loss has been studied for greater than a century. CP is believed to be associated with COM of infants and children due to poor Eustachian tube function and other anatomic problems. The current study aimed to determine whether Veau classification or number of ventilation tubes is associated with the presence of COM, hearing loss or speech alteration.
Despite the results obtained, we cannot be sure whether the positive relationship between COM and the number of surgeries is related to surgery or with the natural course of a more aggressive ear pathology that makes it necessary to place a greater number of ventilation tubes in this type of patient. However, we can confirm that those patients with tympanic and/or middle ear alterations present worse hearing compared with patients with a relatively normal otoscopy. In a previous study, the rate of type A and B tympanograms, the proportion of discharge during myringotomy, and the indwelling period of the first ventilating tube insertion also influenced the probability of additional ventilation tube insertion in CP patients [
19].
Little information is known about the natural history of CP patients who have not been subjected to palatoplasty or any intervention at the otologic level. Based on the vocal quality characteristics of children with CP, a comprehensive speech and language pathology intervention is recommended [
20]. However, one of the earlier works on Dutch CP patients demonstrated only small differences between speech pathologists with and without expertise in CP speech [
21]. Studies performed in India and China on patients with unrepaired CP revealed that a significant percentage of these patients demonstrated hearing loss and abnormal tympanometry that persisted in adolescence and adulthood [
22]. Another audiological study in Turkey revealed that the prevalence of middle ear disease of children whose palates were repaired during the first two years of life and who did not have access to otolaryngology care was considerably reduced compared with patients who did not receive an operation for palatoplasty or treated by the otorhinolaryngologist. This comparative data analysis demonstrated that palate repair is an independent variable in reducing the prevalence of middle ear pathology [
23]. Although there is no definite evidence that a specific CP repair technique results in superior middle ear function, one previous study demonstrated that patients who underwent Furlow Z-plasty required fewer tympanostomy tubes compared with those who underwent traditional techniques [
24].
The type of palatine defect plays an important role in the development of mucosal otitis media (OM) and has been observed in patients with major defects requiring additional surgeries for the insertion of tympanostomy tubes [
25]. It is not universally accepted that an early and successful closure of the palate reduces the possibility of permanent otological pathology. The initial hypothesis for the early (up to 4 months) closure of the palate that prevents middle ear complications in CP patients is no longer supported. It seems to be clear is that an improvement in hearing is associated with child growth with minimal loss observed after 10 years of age. The variability in the time and course of this recovery suggests that the improvement is not exclusively the result of palatal surgery but a combination of factors, including surgical correction, developmental factors and treatment of middle ear pathology [
22].
The number of tympanostomy tubes inserted appears to be related to the abnormal mid-term and long-term tympanic findings. However, atrophy, retraction, and COM may also appear as sequelae in children with persistent mucosal OM who never had tympanostomy tubes [
26]. The long-term consequences of drainage insertion are particularly important in CP children. An increased rate of abnormal tympanic membranes between ears previously treated with ventilation tubes in children with CP who underwent operation was previously observed by Ovesen and Belgvad-Andersen [
27], and an increased incidence of complications and worse audiological status appears in the studies performed by Robson et al. [
28]. However, it is unclear whether children with early placed ventilation tubes later developed mucosal OM.
Focal atrophy and tympanosclerosis are two well-documented types of complications of ventilation tube insertion. The tympanic membrane with tympanosclerosis is considered in numerous abnormal studies despite its small tendency to progress to COM with a minimal effect on hearing. Persistent perforations (9.13%) may also occur, particularly after insertions of repeated tubes, interventions at very early age, or the insertion of permanent drainage tubes, such as Goode’s T-tubes [
29].
Cholesteatoma appears in studies as a complication of ventilation tube insertion, especially after insertion of T-tubes. The relationship between COM and cholesteatoma is clear in CP patients, with rates ranging from 0.90 to 9.20% for cholesteatoma. In our case, the frequency of cholesteatomatous COM was 2.06% as it was only observed in 5 patients with this type of pathology. The incidence of COM in this type of patients is variable (11–37%). Persistent tympanic perforation (1.30–19%), tympanic retraction (11.50–36.80%), tympanic sclerosis (11–37%), secondary cholesteatoma (0–3.80%) and otorrhea (up to 11.50%) present with great variability based on the revised study. In our study, we exclusively focused on membrane changes, such as retraction and ‘pexia’, that could be considered to be risk factors for the possible progression to COM when tympanosclerosis is not considered to be an abnormal appearance of the tympanic membrane.
The involvement of COM in CP remains debated. A recent study on 105 CP Turkish patients demonstrates a statistically significant relationship between the middle ear disease, function of Eustachian tube, treatment outcomes, middle ear pressure, CP type and bilateralism of the disease [
30]. A study from the Nova Scotia Hearing Center proposed COM with effusion following CP repair as a clinical predictor for secondary velopharyngeal insufficiency [
31]. A recommendation for the outcomes that should be measured has been recently proposed by a group of UK clinics performing management of COM in children with CP [
14].
In our study, we observed no statistical association between CP type and COM. Accordingly, no statistically significant relationship was noted between palate type and COM (p = 0.546), the need for an increased number of ventilation tubes inserted (p = 0.820) and grade of hearing loss (p = 0.616). Although these results did not imply a difference between the groups, patients with a grade III or IV Veau fissure exhibit an increased frequency of COM (59 and 42.86%, respectively) and a greater degree of hearing loss (up to 38% of patients with grade IV fissures had hearing loss). Similarly, patients with more complex palatine fissures (grades III and IV) require a greater number of surgeries for insertion of ventilation tubes (approximately 50% of patients compared with 30% for patients with Veau grade I or II). Given the lack of significance of the results obtained, we conclude that further studies would be necessary to determine whether this finding was influenced by sample size or whether the relationship described was not significant.
According to our data, ears with an abnormal otoscopic appearance were almost identical to those with a greater number of tubes. A significant correlation was noted between abnormal otoscopy and reduced hearing. The association between the number of inserted ventilation tubes and the increased prevalence of abnormal otoscopy and hearing has been reported. However, it was impossible to determine to what degree the finding is due to the number of surgeries and to what extent the nature of a more severe inflammatory process makes it necessary to place more drainage tubes. It is important to note that our study does not contemplate those patients who have been treated at other centres, some of whom may have developed otological problems. This fact may lead to over- or underestimation of the presence of COM in CP patients who underwent operation. Moreover, it is possible that the children included in our study have developed COM since the end of the study period.
Hearing loss is a known complication of CP patients, but its magnitude is not always appreciated. The majority of the studies focus on the development of a competent velopharyngeal sphincter and normal facial development in this type of patient, while the complication of hearing loss is neglected [
32]. Some evidence revealed that children growing with CP exhibited an improved audiological status. Accordingly the drainage can correct the auditory deficit associated with short-term mucosal OM [
6,
7].
Recent studies on hearing loss among CP infants revealed no significant difference in patients with or without CP [
33]. Another study examining the association among CP grade, palate repair technique, and hearing outcomes in children from northern Finland aged 3–9 years revealed that only 3.30% of CP patients exhibited abnormal hearing [
34]. Our analyses of the audiometric and otologic measurements made for the group of CP patients who underwent operation at the Vall d’Hebron Hospital (Barcelona, Spain) revealed no significant association between hearing loss and Veau classification or Eustachian tube function (Table
3b).
In our study, most ears examined (n = 242) exhibited mild hearing loss (49.17%). In addition, 34.30% of the ears evaluated exhibited normal hearing (0–25 dB), 14.04% had moderate hearing loss and only 2.47% of the ears had severe hearing loss. Profound hearing loss was not noted in any patient. It seems likely that patients who received a greater number of ventilation tubes displayed an increased rate of COM and worse audiometric results in the long term. Up to 86% of the patients in our study who had COM underwent operation for at least two occasions of transtympanic drainage. Only 17.24% of these patients had strictly normal hearing.
Conclusions
Our results demonstrate that the CP type did not affect articulation, speech development or hearing loss and was also not associated with COM. By contrast, these parameters seemed to vary depending on the number of tympanostomy tubes inserted. These results do not support improvements in speech, hearing, or tympanic membrane abnormalities indicative of COM with tympanostomy tubes. Although the placement of tympanic ventilation tubes has been often accompanied by an increased rate of COM, it is important to assess whether this is a result of the number of ventilation tubes inserted or it is intrinsic to the natural history of middle ear inflammatory disease of such patients, so more studies are needed.
In the case of children, CP is believed to be associated with COM due to poor Eustachian tube function and other anatomic problems, so understanding Eustachian tube dysfunction is an important component of CP management.
There are many reasons to suggest that mucous OM in these children should be treated conservatively in early childhood. Given that conservative management of mucosal OM is relatively safe and has no long-term sequelae and that other forms of auditory rehabilitation, such as a hearing aid, are available, clinicians could consider more conservative management in light of these data; however, more studies are needed. Nevertheless, the improvement is not exclusively the result of palatal surgery but a combination of factors, including surgical correction, developmental factors, treatment of middle ear pathology and a multidisciplinary approach.