Introduction
Oesophageal atresia (OA) is a congenital malformation, characterized by an interruption in the continuity of the oesophagus [
11,
22]. OA affects one in 2500 to 4500 live births and is fatal without surgical treatment. The prognosis is influenced by the occurrence of associated morbidities [
11,
17,
21]. Other congenital malformations are present in more than 50 % of children with OA [
17]. The co-occurrence of the most frequent congenital anomalies is named the VACTERL association (vertebral, anorectal, cardiac, tracheo-oesophageal, renal and limb defects) [
11,
17,
22]. During the previous two decades, survival rates of children with OA have improved to a current rate of more than 90 % [
12,
17,
21,
22]. Despite this improved survival, significant numbers of children with repaired OA still have to deal with short- and long-term morbidity. This has led to increased interest in the identification of morbidity in these patients [
10‐
12,
21,
23].
Dysphagia is a common problem [
12,
20,
23]. Due to the dysphagia, many children develop adaptive feeding behaviours [
11,
20]. Dysphagia can occur in association with gastro-oesophageal reflux [
5,
6]. Moreover, serious consequences of dysphagia like failure to thrive and aspiration may occur [
11]. Two issues limit the up-to-date knowledge of dysphagia in this population. First, different definitions are used to describe dysphagia [
10,
14,
20], which probably explains the wide variability in prevalence of 45 to 70 % [
12,
13,
18,
23]. Second, dysphagia can occur in one or more phases of the swallowing process, respectively, the oral, pharyngeal and oesophageal phase. Abnormalities in different phases require different treatment approaches [
1,
8]. The extent to which dysphagia occurs in the oropharyngeal swallowing phase remains unclear [
9,
26].
A clear definition and an objective tool are essential to accurately report the prevalence and severity of dysphagia during follow-up. According to the American Speech-Language-Hearing Association (ASHA) (www.
asha.org), paediatric dysphagia is defined as ‘difficulty with any step of the feeding process, from accepting foods and liquids into the mouth to the entry of food into the stomach and intestines’. Appropriate non-invasive evaluation of change in dysphagia and its severity over time can be obtained using the Functional Oral Intake Scale [
4]. To our best knowledge, no studies have described change in prevalence and severity of dysphagia over time using this functional oral intake scale in children with repaired OA.
Concerning the different swallowing phases, it is important to identify the specific phase in which dysphagia occurs. The videofluoroscopic swallow study (VFSS) is generally accepted as the best investigation to objectively assess the oropharyngeal phase of the swallow function [
1,
8]. So far, occurrence of dysphagia in the oropharyngeal phase of the swallow has hardly been studied in children with repaired OA [
9,
26].
Material and methods
Patient population and materials
A retrospective cohort study in patients with OA, born between January 1996 and July 2013, was performed at the Radboudumc Amalia Children’s Hospital, Nijmegen, the Netherlands. Patients with OA treated in this tertiary paediatric centre were identified using the OA registration list of the Paediatric Surgery Department and were included in the clinical cohort. Patients with any of the following criteria were excluded: death within the first 6 months of life, patients with a follow-up less than 6 months, patients lost to follow-up or no available paediatric and paediatric surgery medical records. The medical records were reviewed from birth through December 2014.
Additionally, all first VFSSs of the included patients with repaired OA performed at the research location were identified. All included VFSSs were performed between June 2002 and November 2014. Patients included in the VFSS review will be referred to as ‘VFSS cohort’.
Patient characteristics
Medical records of included patients in the clinical and VFSS cohort were reviewed for the following patient characteristics: data on gender, birth weight, gestational age, type of OA based on the Gross classification [
7], associated malformations/syndromes, type of surgery to correct OA, oesophageal dilatation for anastomotic stricture, the reported presence of GORD and fundoplication. Our patients received standard anti-acid medication until the age of 6 months. Therefore, GORD was defined as use of anti-acid medication because of reflux symptoms after 6 months of age.
Data collection
Medical records of patients included in the clinical cohort were systematically reviewed. The occurrence of dysphagia, sensations of food impaction, oesophageal dilatation and GORD was determined in four age groups: respectively <1, 1–4, 5–11 and 12–18 years. Patients were assigned to the age groups from birth until the age at last follow-up as stated in their medical record. The ordination of these age groups was based on anatomic differences of the swallowing mechanism in infants and adults [
2], clinical experience of the paediatrician (JD) and two speech language pathologists (LE, SG) involved in this study.
Dysphagia
To determine the prevalence and severity of dysphagia, the FOIS was used. This objective dysphagia scale was originally validated to determine change in the occurrence and severity of dysphagia in an adult population over time [
4]. The FOIS was chosen since no appropriate functional oral intake tool exists to estimate change in dysphagia occurrence and severity over time in children [
3]. The FOIS includes seven levels concerning functional oral intake, ranging from nothing by mouth (level 1) to total oral diet with no restrictions (level 7) as shown in Table
1 [
4]. Based on information on oral intake as stated in the medical records, each patient was assigned to one of the FOIS levels in the four age groups. If no information concerning diet was stated, the oral diet was considered normal and rated as oral diet with no restrictions (level 7). If multiple levels were applicable within one age group, the lowest level was assigned.
Table 1
Functional Oral Intake Scale (FOIS) according to Crary et al. [
4]: children 1–18 years
Level 1 | Nothing by mouth |
Level 2 | Tube dependent with minimal attempts of food or liquids |
Level 3 | Tube dependent with consistent oral intake of food or liquids |
Level 4 | Total oral diet of a single consistency |
Level 5 | Total oral diet with multiple consistencies, but requiring special preparations or compensations |
Level 6 | Total oral diet with multiple consistencies without special preparation, but with specific food limitations |
Level 7 | Total oral diet with no restrictions |
Modifications in the FOIS were made in order to assign this scale to patients in age group <1 year, since infants at this age are still expanding their oral diet from liquid (milk) to pureed and solid foods. These modifications were made based on Christiaanse et al. [
3] and based on the distinct stages in the process of expanding the diet in infants [
16]. Normal expansion of oral diet was considered reached when introduction of solid foods in pureed form started before 9 months of age and the introduction of mashed foods and soft lumps started before 12 months of age. According to age group <1 year, the following FOIS modifications were made: level 4–level 6 were merged and assigned if expansion of oral diet was not reached. Level 7 was assigned if expansion of oral diet was reached (Table
2).
Table 2
Modified Functional Oral Intake Scale (FOIS): children <1 year
Level 1 | Nothing by mouth |
Level 2 | Tube dependent with minimal attempts of food or liquids |
Level 3 | Tube dependent with consistent oral intake of food or liquids |
Levels 4–6 | Expansion of oral diet not reacheda
|
Level 7 | Expansion of oral diet reacheda
|
Dysphagia was defined as a FOIS level below 7; meaning total oral diet had specific food limitations or was more restricted. The severity of dysphagia was expressed in FOIS level (level 1–level 6). The occurrence of dysphagia was subdivided in oropharyngeal and oesophageal dysphagia. Therefore, sensations of food impaction and oesophageal dilatation in history were determined in the same age group. Dysphagia was considered to occur in the oesophageal phase if sensations of food impaction or oesophageal dilatation were reported.
Videofluoroscopic swallow studies
Since the FOIS does not determine the aetiology of dysphagia, the prevalence of oral and pharyngeal dysphagia based on VFSS will give advanced insight in different possible causes of dysphagia in our population. The VFSS images were stored on video home system (VHS) or on the Digital Swallowing Workstation (Kay Pentax Swallowing Workstation, Lincoln Park, New Jersey). VFSS procedures in children are individualized according to the child’s age and developmental level. VFSS were completed with different volumes and three different nutritional consistencies if applicable for the patient, namely thin liquid (i.e. milk), liquid (i.e. pureed food) and solid food (i.e. bread). Contrast (Xenetic 300 mg or Barium; Guerbet, Brussels, Belgium) was used to visualize the swallow act [
8,
24].
Assessment procedure
The VFSS images were assessed according to structural and functional findings in the oral, pharyngeal and upper oesophageal phase of the swallowing process according to van den Engel-Hoek et al. [
24]. The presence or absence of these findings was scored dichotomously.
As literature shows experience and training influences reliability, the following procedure was conducted in order to achieve accurate assessment of VFSS images [
15]. First, two experienced speech language pathologists (LE, SG) assessed the VFSS images in real time and slow motion separately. The ratings were compared, and inconsistencies between the two raters were determined. These inconsistent VFSS ratings were reviewed and discussed until consensus was reached. In order to present the most reliable results, consensus was used to rate the identified abnormalities in the oral, pharyngeal and upper oesophageal phase.
Statistical analyses
Data were analysed using SPSS statistics 20.0. Descriptive statistics were used for patients’ characteristics, prevalence and severity of dysphagia and VFSS findings. Categorical variables were described as number and percentage; continuous variables were described as median and interquartile range (IQR). The prevalence of dysphagia in patients with repaired OA was calculated in the four age groups. Additionally, the prevalence rate was subdivided in percentages oropharyngeal and oesophageal dysphagia. To provide a clear overview of changes in severity of dysphagia over time, severity was expressed by compromising the 7 FOIS levels into three categories, namely tube-dependent feeding (levels 1–3), oral diet with restrictions (levels 4–6) and oral diet without restrictions (level 7 = no dysphagia). Additional analyses were performed in order to compare patient’s characteristics and to determine if dysphagia was associated with GORD in the four age groups. For that, the two-tailed Fisher’s exact test was used with a significance level of 0.05. In order to compare change in dysphagia prevalence over time, a mixed logistic regression model with random intercept for subjects was used. This statistical model was chosen since each patient is present in multiple (>1) age groups and the variable of interest is on a dichotomous scale. A significance level of 0.05 was chosen.
Discussion
This retrospective study primarily assessed the prevalence of dysphagia, based on abnormal functional oral intake using the FOIS, in children (aged 0–18 years) with repaired OA. Prevalence of dysphagia was above 50 % in age groups <1 and 1–4 years. In age groups 5–11 and 12–18 years, prevalence rates decreased to approximately 20 %. The present study is the first reporting prevalence on dysphagia using the FOIS in children with repaired OA.
The prevalence of dysphagia in our study is consistent to other studies with regards to age groups <1 and 1–4 years [
12,
13]. However, the prevalence of dysphagia in the age groups 5–11 and 12–18 years was lower than other literature reports, although our population was similar to those in previously published studies [
12,
13,
18,
23]. In general, dysphagia in children is underreported as stated in literature [
19]. Differences between our study and previously reported results might be explained by the use of various dysphagia definitions. In our study, we used the objective-modified FOIS. Obvious smaller differences were seen in prevalence rates compared to previous studies, if children with FOIS level 7 (no dysphagia) and sensations of bolus impaction or oesophageal dilatation in history were included in our prevalence analyses, respectively, 79 % in age group <1 year, 71 % in age group 1–4 years, 56 % in age group 5–11 years and 38 % in age group 12–18 years. This highlights the influence of dysphagia definitions on prevalence rates.
This study is, to our best knowledge, the only study in children with repaired OA grading severity of dysphagia using the objective-modified FOIS. Accurate determination of change in dysphagia severity is important to improve follow-up and evaluate treatment interventions [
4]. Our results showed an overall decrease in prevalence and severity over the age groups. Application of an objective dysphagia scale to report change in dysphagia severity in OA patients might be a contributing factor to follow-up.
Our study confirmed the association of dysphagia with GORD, with or without fundoplication, in children with repaired OA. This is in accordance with previous research, which indicates abnormal oesophageal motility as common etiologic factor [
5,
6]. Dysphagia and GORD can both cause aspiration, respectively, anterograde or retrograde aspiration [
25]. The co-occurrence of dysphagia and GORD highlights the need to determine the aetiology of aspiration in children with repaired OA.
In our clinical cohort, dysphagia was subdivided into different swallowing phases. So far, this subdivision has not been applied before in dysphagia prevalence studies in children with OA [
12,
13,
18,
23]. In our results, oropharyngeal dysphagia was present in children with repaired OA based on review of medical records. To objectively determine dysphagia in different swallowing phases, VFSS could be helpful [
1,
8].
This study identified the aetiology of dysphagia based on VFSS findings in a limited number of patients. In our study, oral dysphagia was present in one third of our patients and pharyngeal dysphagia in more than three quarter of the patients in the VFSS cohort. Only Hörmann et al. [
16] and Yalcin et al. [
26] performed a VFSS study in children with repaired OA. First, differences in dysphagia prevalence should be considered in the light of a limited number of children in the studied cohorts. Hörmann et al. [
9] published an article focusing on dysphagia in different swallowing phases using VFSS. In this study [
9], all children had abnormalities in the pharyngeal phase, and none had abnormalities in the oral phase
. Compared to this study, our percentage of oral dysphagia was higher, while pharyngeal dysphagia in our study was lower. A possible explanation for these results is the use of different consistencies in our study, whereby Hörmann et al. [
9] only used thin liquid. Other consistencies can reveal additional abnormalities causing dysphagia [
25].
Yalcin et al. [
26] recently published a study to evaluate the functional disorders of deglutition in children with repaired EA with VFSS. They showed oral dysphagia in 10 % of the children with repaired esophageal atresia, suggesting that oral dysphagia may be associated with late onset of oral feeding. Our results support their hypothesis, since three of our four patients with oral dysphagia were tube dependent (FOIS levels 1–2 in age group <1 year). The percentage of pharyngeal dysphagia was more frequent in our population. This result may be explained by the fact that dysphagia was present in all our VFSS patients, while in Yalcin et al., dysphagia was absent in the majority of patients [
26]. One of the issues that emerges from these findings is the correct indication of VFSS.
As a consequence of the retrospective study design, follow-up data were limited and therefore, not always straightforward. One researcher (CC) reviewed medical records and obtained data. However, in case of ambiguities, data were discussed with the involved paediatrician (JD) until consensus was reached. Concerning the VFSS findings, these do not reflect the overall OA population since selection of patients was based on the presence or absence of VFSS performed. Nevertheless, this study is the first to combine prevalence of dysphagia using the FOIS and identification of dysphagia in different swallowing phases using VFSS in children with repaired OA.
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