Obstructive sleep apnea (OSA) is a growing health concern. Approximately 2%–4% of middle-aged people suffer from OSA.1 OSA is characterized by repetitive collapse and reopening of the upper airway during sleep resulting in intermittent hypoxia and sleep fragmentation.2 Intermittent hypoxia is a condition when apnea/hypopnea occurs, and oxygen supply to the blood is reduced. Intermittent hypoxia results in systemic inflammation and oxidative stress and may induce airway inflammation.3 To alleviate this symptoms, continuous positive airway pressure (CPAP) or surgery are common treatments applied to OSA.
CPAP reduces reflux events and improves clinical symptoms of gastroesophageal reflux disease (GERD) and laryngopharyngeal reflux (LPR) in patients with OSA, like heartburn complaints.4–6 As an effective and noninvasive treatment for OSA, CPAP maintains a certain positive pressure in the upper airway to improve upper airway collapse. Research has shown that CPAP decreases both GERD and LPR attacks by increasing esophageal internal pressure,4,7 and reflex contraction of the lower esophageal sphincter (LES),8 limiting reflux duration and reducing esophageal acidification. OSA and LPR are two conditions that cause chronic upper airway inflammation. In OSA patients, coexistence with LPR is very frequent, being found in 20%–67% of patients.9,10 Although the association between OSA and LPR has been recently investigated, it still remains controversial. While some studies have demonstrated that CPAP treatment significantly improves reflux symptoms in OSA patients,11 only few have investigated the effect of surgery treatment for OSA on reflux disease.
Uvulopalatopharyngoplasty (UPPP) is a widely accepted surgery for OSA12 and first suggested by Fujita et al.13 It has been recently improved14 with the goal of reducing the oropharyngeal obstruction by eliminating redundant mucosal folds, hypertrophic tonsils, and an excessively thickened and elongated soft palate.15 UPPP may relieve the severity of OSA in patients whose obstruction site is located at the palatopharyngeal level.
LPR is defined as gastric content reflux to the laryngopharynx; it is characterized by laryngeal mucosal inflammation and damage,16 and a common disease in otolaryngology outpatient clinics.9 Although 24 h pH monitoring is the gold standard for diagnosing LPR, the reflux symptom index (RSI) and reflux finding score (RFS) are more commonly used for routine clinical practice and to quantify the severity of LPR symptoms.9,17
The aim of this study was to evaluate the changes in LPR symptoms and signs after UPPP for OSA based on patients' responses to the RSI and RFS questionnaires.
METHODS Procedure and participantsAdult participants were recruited from patients at the Sleep Laboratory of the Second Xiangya Hospital, Central South University, between January 2016 and January 2017. Of the 128 participants, 21 (16%) declined to participate and 16 (13%) were ineligible, leaving 91 (71%) participants in the present study. The study included patients newly diagnosed with OSA as confirmed by Polysomnography (PSG). Controls were selected among patients without OSA as confirmed by PSG. According to the Apnea and hypopnea index (AHI), participants were classified into non-OSA (AHI <5) and OSA group (AHI ≥5). The OSA group was assigned as follows: mild to moderate, AHI >5 and ≤30; or severe, AHI >30. Participants with OSA were diagnosed with LPR if both RSI scores >13 and RFS >7. The study design is shown in Figure 1.
The inclusion criteria were as follows: (1) clinical symptoms and signs compatible with clinical OSA suspicion,18 (2) aged between 18 and 60 years, (3) no central sleep apnoea, (4) no disease of the nasal cavity and nasopharynx, (5) no history of taking anti-reflux drugs, and (6) provided informed consent. Clinical suspicion was defined as snoring and ≥1 of the following symptoms: witnessed apnoea, nonrestful sleep, or daytime sleepiness. Participants were excluded if they had NYHA grade IV heart failure, chronic renal failure (stage 4–5), degenerative cerebrovascular disease, or severe lung disease. The Epworth Sleepiness Scale (ESS) questionnaire, which is widely used to assess daytime sleepiness, was also completed by the patients at the same visit. Demographic data including sex, age, body mass index (BMI), AHI, minimum oxygen saturation, and oxygen saturation <90% were also obtained.
Approval by the Human Research Ethics CommitteeThe study was approved by the ethics committee of the Second Xiangya Hospital, Central South University in China (LYF2020014), and all participants provided written informed consent.
LPR was defined as both the RSI score >13 and RFS >7.19 The RSI was developed by Belafsky et al.17 As a validated quality-of-life instrument, the RSI is a 9-item questionnaire administered to document the presence and severity of LPR characteristic signs and symptoms. It is a useful instrument in diagnosing LPR, along with other measures, such as that of the composite pH score, and for devising the appropriate potential therapies. The questionnaire included hoarseness, throat clearing, postnasal drip, swallowing difficulty, coughing, breathing difficulty, annoying cough, lump sensation, and heartburn. During the initial visit, all patients were asked to complete the RSI questionnaire to assess the severity of LPR-related symptoms. They were asked if they had a specific set of symptoms indicating LPR. Each item is scored from 0 (no problem) to 5 (severe problem), with a maximum score of 45. A score ≥13 was not normal and supported a diagnosis of LPR.
The RFS contains an 8-item clinical severity scale for judging laryngoscopy findings and is a useful tool to assess and follow-up LPR patients. To identify the most specific laryngoscopic signs of LPR, Belafsky et al.16 developed the RFS based on the findings of video laryngoscopy. The laryngoscopic findings used for the diagnosis of LPR are nonspecific signs of laryngeal irritation and inflammation, including subglottic edema, ventricular obliteration, erythema, vocal fold edema, diffuse laryngeal edema, vocal fold edema, posterior commissure hypertrophy, granulation tissue, and thick endolaryngeal mucus. Laryngoscopy was reviewed by an otolaryngologist blinded to patient RSI and PSG information. They rated eight LPR-associated findings on a variably weighted scale from 0 to 4, and the results ranged from 0 (normal) to 26 (worst possible score). According to their analysis, a patient with a score ≥7 has LPR with 95% certainty.
UPPP relieves airway obstruction at the palate level by eliminating redundant mucosal folds, hypertrophic tonsils, and excessively thickened and elongated soft palates. We performed a revised UPPP with uvular preservation. Bilateral tonsillectomy was performed. Then, the redundant bilateral mucosa and submucosal tissue were resected to enlarge the oropharyngeal lumen. Two inverted U-shaped incisions were performed on the surface of the soft palate along both sides of the uvula. Mucosal membrane and surplus submembranous adipose tissue in the U-shaped incisions were removed. The soft palate length to remove was determined preoperatively according to the anatomy of the patient's pharynx and sleep apnoea severity. The incision was higher in severe patients and lower in mild patients. The dorsal surface of the soft palate was incised, and the levator palatini muscle and tensor palatini muscle were preserved. The dorsal and ventral margins of the preserved mucosal membrane of the uvula were closed with interrupted sutures forming a long new uvula. The new uvula was shortened when considered too long. The palatoglossal arch, the soft tissue of the tonsillar fossa, and the palatopharyngeal arch were also closed with interrupted sutures, thus enlarging the oropharyngeal cavity.
Patients who underwent UPPP surgery met the following inclusion criteria: (1) observed loud snoring, sleep apnoea, daytime sleepiness, and arousal from sleep; (2) AHI ≥5 events/hour of sleep (from PSG); (3) thickened and elongated soft palate; (4) Friedman stage I or II; (5) nonadherence with CPAP treatment or rejecting CPAP treatment. The exclusion criteria included (1) serious psychiatric, cardiopulmonary, or neurological disease or an American Society of Anesthesiologists (ASA) classification >3; (2) severe nasal congestion; (3) BMI≥40 kg/m2; (3) history of surgical therapy for OSA (for example, tonsillectomy); (4) Friedman stage III; and (5) anti-reflux treatment before or after surgery. A surgeon (L. S. S.) performed all UPPP surgeries. Surgical success was defined as ≥50% reduction in preoperative AHI and a postoperative AHI <20 per hour.20
Follow-upAll patients were re-evaluated at our sleep disorder centre at follow-up visits 6 months after UPPP surgery. PSG, RSI, RFS, and ESS questionnaire were obtained from each patient. The investigator (L. S. S.) was not involved in the care of any patient.
Statistical analysisData were analyzed using a SPSS (version 24.0; SPSS Inc., Chicago, IL). A Chi-square test was used for categorical variables and a t-test or Mann–Whitney U test for continuous variables. Regression analysis was performed to show the effect of different variables on the outcome data. Statistical significance was set at P <.05.
RESULTS Population characteristicsThe characteristics of the 64 patients with OSA (AHI ≥5 events/h) and 27 controls are presented in Table 1. There were no significant differences in age or BMI between groups. Patients with OSA had lower blood oxygen saturation, higher AHI and epworth sleepiness scores. As anticipated, the RSI score and RFS of patients with OSA were higher than those of the controls.
TABLE 1 Initial characteristics of study participants
Note: Data are presented as median ± SD.
Abbreviations: AHI: apnea/hypopnea index; BMI: body mass index; CT90%: percentage of recording time when oxygen saturation of arterial blood<90%; ESS: Epworth Sleepiness Scale (range 0–24); L-SpO2: lowest blood oxygen saturation during recording time; RFS: reflux finding score; RSI: reflux symptom index.
Relationship betweenIn 64 OSA patients, both AHI and CT90 were positively correlated with the RSI score and RFS, indicating that the degree of OSA is associated with LPR severity (Figure 2A,B). Lowest blood oxygen saturation during the recording time (L-SpO2) was negatively correlated with the RSI score and RFS (Figure 2C). In addition, the RSI score and RFS of patients with severe OSA were higher than those of patients with mild to moderate OSA (Table 2).
TABLE 2 Reflux symptom index and reflux finding score between mild-moderate obstructive sleep apnea (OSA) and severe OSA patients before uvulopalatopharyngoplasty
Note: Data are presented as median ± SD.
Abbreviations: RFS: reflux finding score; RSI: reflux symptom index.
Surgical outcomesTable 3 shows that postoperative AHI, night-time SpO2 (CT90 and L-SpO2), and ESS scores decreased after UPPP surgery in 34 OSA patients. Moreover, both the RSI score and RFS decreased after treatment with UPPP.
TABLE 3 Various factors before and after uvulopalatopharyngoplasty surgery
Note: Data are presented as median ± SD.
Abbreviations: AHI, apnea/hypopnea index; BMI, body mass index; CT90%, percentage of recording time when oxygen saturation of arterial blood<90%; ESS, Epworth Sleepiness Scale (range 0–24); L-SpO2, lowest blood oxygen saturation during recording time; RFS, reflux finding score; RSI: reflux symptom index.
Patients whose AHI decreased by 50% from baseline and AHI <20 per hour after surgery were considered as surgical success.20 The surgical success rate was 73.53% (25/34). In 25 successful surgery patients, the RSI score and RFS were lower than before surgery, and the LPR prevalence changed immediately after successful UPPP surgery (Table 4).
TABLE 4 Changes between reflux symptom index and reflux finding score in patients with uvulopalatopharyngoplasty surgery
Note: Data are presented as median ± SD.
Abbreviations: RFS: reflux finding score; RSI: reflux symptom index.
Figure 3A shows that all individual RSI variables improved significantly after surgery (P <.05), except for hoarseness (P = .054). When we compared the pre- and postsurgery individual RSI variables in patients in the successful or unsuccessful surgery group, all RSI variables improved significantly after successful surgery (P <.05, Figure 3B), except for hoarseness and postnasal drip (P = .117 and P = .052, respectively), but no RSI variables significantly changed after unsuccessful surgery (Figure 3C).
This study investigated the effect of UPPP surgery for OSA on LPR symptoms based on patient responses to the RSI and RFS questionnaires. We found: (1) a close correlation between OSA and LPR: LPR is more prevalent in OSA patients than in the general population, and AHI and CT90 were positively and L-SpO2 negatively correlated with LPR symptoms, and (2) UPPP surgery, especially when successful, significantly lowered the mean RSI score and RFS but also individual RSI variables.
The coexistence of OSA with LPR has been reported to have a prevalence of 20%–67%.21,22 Although previous studies could not demonstrate a direct relationship between them, they suggested a possible causative relationship.23 Our results indicate that the degree of OSA is associated with LPR severity, and that there is a close correlation between OSA and LPR. An interaction between them could explain our results, namely, OSA causes inflammatory injury, low intrathoracic pressure, and leakage of the lower esophageal sphincter; in turn, LPR (Acid reflux) results in injury to the esophagus, larynx, and pharynx mucosa as well as laryngopharyngeal symptoms.
Anti-reflux therapy may improve the symptoms and PSG parameters of OSA.24 Simultaneously, other studies report that CPAP can reduce GER events and improve nocturnal GER symptoms in OSA patients.20,21 However, few studies report on the effect of surgical treatment for OSA on LPR.25 UPPP is usually not the first choice of treatment in most patients with OSA compared to CPAP. If CPAP is refused or the obstructive plane is defined, surgery can be considered as a treatment for OSA, especially multilevel surgery. UPPP is indicated in patients who only have airway collapse at the level behind the palate, and our study included participants whose level of collapse was presumed to be in the oropharynx was in the oropharynx. The present study demonstrated that postoperative AHI, night-time SpO2 (CT90 and L-SpO2), the RSI score, and the RFS were greatly improved after surgery. Interestingly, when we compared the pre- and postsurgery changes in the mean RSI score and mean RFS among patients in the successful and unsuccessful surgery groups, the successful surgery group experienced a significant decrease in the RSI score and RFS, but there was only one significant difference (mean RFS) in the unsuccessful group. We proposed that successful UPPP surgery lowered RSI scores and RFSs, and unsuccessful surgery improved the RFS only.
In our study, we presumed that effective UPPP surgery could improve LPR symptoms and signs in three ways. First, published studies have proposed that mouth breathing and snoring aggravate pharyngeal inflammation and LPR, and chronic intermittent hypoxia can lead to systemic inflammation of the whole body and respiration in OSA.24,26,27 UPPP solves the problem of OSA-induced inflammatory injury by reducing airflow obstruction and increasing nocturnal blood oxygen saturation. Second, successful UPPP lowers OSA-induced esophageal changes. It has been postulated that OSA causes lower intrathoracic pressure and leakage of the lower esophageal sphincter28: (1) when either apnoea or hypopnea occur, OSA patients overcome hypoxia by sleep breathing effort, which produces increased transdiaphragmatic pressure and decreased intrathoracic pressure, exacerbating the LES pressure gradient and favoring acid reflux into the esophagus, resulting in laryngeal mucosal injury.29–31 (2) the inflammation accompanying OSA may predispose the patient to dysphagia by hypoxia-reoxygenation, promoting upper airway narrowing.32,33 Additionally, the hypoxia inducible factor (HIF)-2α may play an important role in reflux esophagitis, indicating that low nocturnal oxygen saturation may aggravate LPR symptoms.34,35 (3) OSA-induced airway resistance causes reflux events coexisting with transient LES pressure relaxation.35,36 Third, LPR-induced inflammation cannot be ignored in the cycle between OSA and LPR. Previous studies have proposed that LPR results in esophagus, larynx, and pharynx mucosal injury and promote: (1) tissue thickening and hypertrophy caused by chronic inflammation which can directly narrow upper airways and (2) increased sensitivity of the laryngopharyngeal mucosa, inflammation-mediated tissue damage, and sensory impairment contributing to upper respiratory collapse.23 UPPP improves LPR in two aspects mentioned above, breaking the OSA and LPR cycle.
Patients often have postoperative complaints after UPPP surgery, including pharyngeal pain, swallowing difficulty, and lump sensation, which might result from surgical wound scarification. Most of these symptoms were similar to those reported in the RSI questionnaire. However, our study found that most symptoms improved significantly after UPPP surgery, probably resulting from removal of the upper airway obstruction.
Our study had several limitations. First, a more objective and easy measure to evaluate the effects of UPPP on LPR is needed to clarify our results and evaluate the obstruction level. There are several reasons we chose the RSI score and RFS instead of 24 h pH monitoring to diagnose LPR and evaluate UPPP effects: (1) RSI and RFS questionnaires are not only easy to conduct for both patients and doctors, but also convenient for follow-up; (2) twenty-four hour pH monitoring is difficult for patients to accept, leading to poor adherence. Second, OSA patients often complain of similar symptoms (lump sensation, throat clearing, and difficulty swallowing) in the RSI questionnaire after surgery treatment, which are difficult to distinguish. Further studies are needed to compare the preoperative and postoperative states of each item in the RSI and RFS questionnaires. Third, UPPP can solve intermittent hypoxia or upper airway resistance in patients with OSA, but future studies including more cases are necessary to explore whether removing intermittent hypoxia or upper airway resistance can improve LPR.
CONCLUSIONIn summary, LPR symptoms are prevalent in OSA patients, and the coexistence of OSA and LPR cannot be ignored. Successful UPPP surgery against OSA potentially reduces laryngeal reflux symptoms and improves laryngoscopic signs by alleviating sleep respiratory disorders.
CONFLICT OF INTERESTThe authors declared that there is no other funding, financial relationships, or conflicts of interest to disclose.
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Abstract
Purpose
To estimate laryngopharyngeal reflux (LPR) changes after uvulopalatopharyngoplasty (UPPP) for obstructive sleep apnea (OSA) using the reflux symptom index (RSI) and reflux finding score (RFS) questionnaires.
Methods
A total of 91 participants were recruited and divided into three groups: control (n = 27), OSA mild to moderate (n = 29), and OSA severe (n = 35) groups according to polysomnography. All participants completed the preoperative RSI, and underwent blinded evaluation on videolaryngoscopy using the RFS questionnaire. Thirty‐four OSA patients who underwent UPPP surgery completed postoperative polysomnography and questionnaires again after a 6‐month follow‐up.
Results
The RSI score and RFS were higher in patients with OSA than in those without OSA. Patients with severe OSA also had a higher RSI score and RFS than those with mild to moderate OSA. Apnea and hypopnea index degree and percentage of recording time for <90% oxygen saturation showed positive correlation with LPR symptoms. But the lowest blood oxygen saturation during the recording time was negatively correlated with LPR symptoms. The mean RSI score and RFS before UPPP surgery were 15.88 ± 4.85 and 13.18 ± 4.80, after surgery decreasing to 9.53 ± 4.16 and 8.65 ± 4.87, respectively (
Conclusions
LPR symptoms are common among OSA patients, and the coexistence of OSA and LPR cannot be ignored. Successful UPPP surgery potentially reduces LPR symptoms and improves laryngoscopic signs by alleviating sleep respiratory disorders.
Level of Evidence: 3.
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