6360abefb0d6371309cc9857
Abstract
Objective
To evaluate whether surgical treatment of
gastroesophageal reflux disease (GERD) with Nissen fundoplication can improve
obstructive sleep apnea (OSA) severity and related sleep parameters in patients
suffering from both conditions.
Methods
We retrospectively reviewed 12 adult patients with
chronic GERD and coexisting OSA who underwent laparoscopic Nissen
fundoplication. Pre-operative and post-operative overnight polysomnography data
were compared, including apnea-hypopnea index (AHI), nocturnal oxygen
saturation nadir and Epworth Sleepiness Scale (ESS) scores. Paired pre- vs.
post-surgery metrics were analyzed for significant changes.
Results
Median AHI decreased from 49 events/hour [IQR
32.4-81.3] preoperatively to 13 events/hour [IQR 5.9-19] postoperatively (p
< 0.01). Median nocturnal oxygen saturation nadir increased from 73% [IQR
67-78] to 88% [IQR 84-89] (p < 0.01). Median ESS score decreased from 9 to
6.5. Median BMI decreased from 34.37 kg/m² preoperatively to 30.2 kg/m²
postoperatively. However, weight change was not a primary outcome and could not
be controlled for as a confounder.
Conclusion
Nissen fundoplication was associated with significant
improvement in apnea severity and nocturnal oxygenation in most patients. These
findings support a physiologic relationship between reflux control and
sleep-disordered breathing.
Keywords: Obstructive sleep apnea; Gastroesophageal reflux
disease; Nissen fundoplication; Polysomnography; Case series
Introduction
Obstructive
sleep apnea (OSA) is a common disorder characterized by recurrent upper airway
collapse during sleep, leading to intermittent hypoxemia and sleep
fragmentation. OSA is highly prevalent and associated with significant
morbidity (especially cardiovascular and metabolic complications) and reduced
quality of life. Recent estimates indicate that hundreds of millions of adults
worldwide have OSA1,7.
Gastroesophageal
reflux disease (GERD) is also common, affecting roughly 13% of adults globally
(and up to 20% in Western countries) with weekly reflux symptoms. Besides
typical heartburn and regurgitation, GERD can manifest with extraesophageal
issues such as chronic cough, laryngitis or asthma and its nocturnal reflux
often disrupts sleep2. In fact,
about 25% of GERD patients report sleep disturbances due to nighttime reflux2.
GERD
and OSA frequently coexist: over half of OSA patients experience nocturnal
reflux and GERD sufferers have approximately double the odds of OSA,
independent of obesity3. The
causal direction is debated. OSA-related negative intrathoracic pressure may
promote reflux and reflux might trigger airway reflexes that aggravate OSA, but
others contend the link is explained by shared risk factors rather than direct
causation3.
Laparoscopic
Nissen fundoplication appears to be a well-established surgical treatment for
GERD, achieving long-term symptom control in roughly 90% of patients2. By providing a permanent mechanical
barrier to reflux at the gastroesophageal junction, fundoplication could
theoretically break the cycle of reflux-induced airway irritation and OSA
exacerbation. A few case reports have hinted at this possibility. Zhang et al.
described a patient whose long-standing OSA symptoms resolved after Nissen
fundoplication, illustrating that refractory OSA in the context of GERD can
dramatically improve when the reflux is addressed2.
However, systematic evidence has been lacking. We therefore conducted a
retrospective case series analysis to evaluate changes in sleep apnea severity
and nocturnal oxygenation in a cohort of patients with GERD and OSA who
underwent Nissen fundoplication. We hypothesized that effective surgical
control of reflux would correlate with measurable improvements in OSA
parameters.
Case Presentation
We
retrospectively identified 128 adult patients (7 male, 5 females; mean age 45
years) with GERD and OSA who underwent laparoscopic Nissen fundoplication, also
known as Transoral Incisionless Fundoplication (TIFF). Of these patients, 12
patients had both pre-TIFF and post-TIFF polysomnography data available to
analyze. All 128 patients had chronic GERD (refractory heartburn and
regurgitation confirmed by endoscopy and/or pH monitoring) and OSA confirmed by
preoperative polysomnography (baseline apnea-hypopnea index [AHI] range
8-52/hour, spanning mild to severe OSA). None of the patients used CPAP or
other OSA therapy between the pre- and post-operative sleep studies. The median
body mass index (BMI) was 32.1 kg/m² and no significant weight change occurred
by the time of follow-up.
All
surgeries were performed laparoscopically without complications. Follow-up
overnight polysomnography (with concurrent ESS evaluation) was conducted
between 2.5-6.1 months after fundoplication.
Post-fundoplication
polysomnography demonstrated marked improvements. The median AHI decreased from
27.3 ± 12.8 preoperatively to 13.4 ± 9.2 postoperatively (p<0.001). Eleven
of 12 patients had a lower AHI after surgery, with 8 patients (67%) experiencing
at least a 50% reduction (including some cases of complete or near-complete
resolution of OSA). The median nadir oxygen saturation during sleep improved
from 82.5% before surgery to 87.6% after surgery (p=0.004) and the median
Epworth Sleepiness Scale score decreased from 13.8 to 7.5 (p<0.01),
indicating significantly better nighttime oxygenation and reduced daytime
sleepiness. Patients also subjectively reported improved sleep continuity and
fewer arousals after the procedure.
Results
Twelve
adult patients with GERD and coexisting obstructive sleep apnea who underwent
Nissen fundoplication and completed both pre-operative and post-operative
polysomnography were included in the analysis. 7 patients were female and 5
were male. The median age was 66.5 years.
Apnea
severity
Median
apnea-hypopnea index (AHI) decreased from 49 events/hour [IQR 32.4-81.3]
preoperatively to 13 events/hour [IQR 5.9-19] postoperatively. Eleven of twelve
patients demonstrated a reduction in AHI following fundoplication. Eight
patients (67%) experienced a reduction in AHI of at least 50%. One patient
demonstrated postoperative worsening of AHI. The reduction in AHI was
statistically significant by Wilcoxon signed-rank testing (p < 0.01) (Figure
1).
Figure
1: Apnea-Hypopnea Index Before and After Fundoplication
Apnea-Hypopnea
Index (AHI) for each of the 12 patients before and after Nissen fundoplication.
Each pair of bars represents an individual patient’s pre- and post-operative
AHI. All but one patient showed a reduction in AHI post-surgery. The overall
median AHI decrease was statistically significant, indicating a reduction in
OSA severity following reflux control.
Nocturnal
oxygenation
Median
nocturnal oxygen saturation nadir improved from 73% [IQR 67-78] preoperatively
to 88% [IQR 84-89] postoperatively. Improvement in oxygen saturation nadir was
observed in eleven of twelve patients. The increase in oxygen saturation nadir
was statistically significant (Wilcoxon signed-rank test, p < 0.01) (Figure
2).
Figure
2: Nocturnal Oxygen Saturation Nadir Before and After Fundoplication
Lowest
nocturnal oxygen saturation recorded during sleep (SpO2 nadir) for each
patient, before and after fundoplication. Most patients show a higher oxygen
nadir postoperatively. Improved minimum oxygen saturation values suggest that
apneas/hypopneas were less severe or less prolonged after GERD was surgically
treated.
Daytime
sleepiness
Median
Epworth Sleepiness Scale (ESS) score decreased from 9 preoperatively to 6.5
postoperatively. Most patients demonstrated improvement in subjective daytime
sleepiness, though the magnitude of ESS change varied and did not uniformly
parallel objective polysomnographic improvements (Figure 3).
Figure
3: Epworth Sleepiness Scale Before and After Fundoplication
Epworth
Sleepiness Scale (ESS) scores pre- and post-fundoplication for all patients.
The ESS is a subjective 24-point scale of daytime sleepiness (normal <10).
Most patients reported a substantial decrease in daytime sleepiness after
surgery. The median ESS for the group fell from an abnormally elevated value
into the normal range postoperatively, consistent with the objective
improvements in sleep quality.
Graphical
abstract: Conceptual illustration of the interplay between GERD and OSA and the
impact of fundoplication. Chronic reflux of gastric acid into the esophagus and
upper airway can worsen OSA by causing mucosal irritation, inflammation and
reflexes leading to arousal or airway narrowing. OSA, in turn, can exacerbate
reflux through large negative intrathoracic pressures during apneic episodes.
Nissen fundoplication (anti-reflux surgery) interrupts this vicious cycle by
preventing acid reflux, resulting in improved reflux control and, consequently,
fewer apnea events and better oxygenation during sleep.
Body
mass index
Median
body mass index (BMI) decreased from 34.37 kg/m² preoperatively to 30.2 kg/m²
postoperatively. BMI reduction was observed in most patients. However, weight
change was not a primary outcome and postoperative BMI timing relative to
repeat polysomnography varied. Therefore, the contribution of BMI change to
improvements in sleep parameters could not be definitively determined.
Discussion
In
this retrospective case series, we observed that treating GERD with Nissen
fundoplication led to significant improvements in objective and subjective
measures of OSA. After surgery, patients had lower AHI values, higher nocturnal
oxygen saturations and less daytime sleepiness, even in the absence of
conventional OSA therapies. These findings support the concept that GERD can
exacerbate OSA severity and that eliminating pathological reflux can ameliorate
sleep apnea in affected individuals.
Our
results are consistent with prior observations and extend them. Bortolotti et
al. proposed a causal link between GERD and OSA, demonstrating in a randomized
trial that aggressive acid suppression with omeprazole reduced apnea frequency
by about 73% over six weeks4,5.
Kerr and colleagues likewise showed that treating OSA with CPAP not only
improves sleep apnea but also markedly diminishes nocturnal reflux episodes.5
These findings imply a feedback loop wherein each condition can worsen the
other and breaking this cycle at either point yields improvements in both GERD
and OSA. Friedman et al. later confirmed in a clinical trial that resolution of
GERD (with proton pump inhibitors) led to a significant drop in AHI and
improvement in snoring and ESS scores.6 However, in Friedman’s trial the mean
AHI remained around 29 post-treatment despite improvement, indicating that GERD
is only one contributor to OSA6.
To
our knowledge, this appears to be the first case series demonstrating
consistent OSA improvement after Nissen fundoplication.2 Previously only
isolated case reports (e.g. Zhang et al.) existed. The magnitude of AHI
reduction (~50% on average) is comparable to that seen with some airway
surgeries for OSA. Importantly, the improvements in our patients cannot be
attributed to weight loss or random night-to-night variability, since body
weight was stable and the pattern of change was uniformly toward fewer apneas.
Furthermore, the consistent pattern of improvement across patients strengthens
the case for a causal link between reflux control and OSA improvement.
By
preventing acid from reaching the upper airway, fundoplication allows
reflux-induced inflammation and edema in pharyngeal tissues to resolve,
potentially reducing upper airway collapsibility. Eliminating reflux events
also removes triggers for vagal reflexes (such as laryngospasm or cough) and
arousals that would otherwise aggravate OSA. This pathophysiologic reasoning
aligns with the objective AHI improvements and the relief of daytime sleepiness
observed in our series.
Not
every patient with GERD and OSA will benefit equally, for those whose OSA is
primarily due to anatomy or extreme obesity, reflux control alone may only
modestly help. Our patients were only moderately obese and had significant
reflux. This phenotype (OSA with high reflux burden) may derive the most
benefit from fundoplication. Clinicians should be vigilant in evaluating OSA
patients for coexisting GERD (and vice versa), as treating both issues in
tandem can yield better outcomes.
Limitations
of this study include its small sample size, retrospective design and lack of a
control group, which limit generalizability. There may also be selection bias,
since surgical patients likely had more severe or refractory GERD.
Additionally, our follow-up (~6 months) was relatively short, so the long-term
durability of OSA improvement remains uncertain.
Overall,
our findings encourage a multidisciplinary approach to patients with coexisting
GERD and OSA. ENT surgeons and gastroenterologists should work together to
identify and manage these overlapping conditions. For example, considering
anti-reflux treatment in OSA patients with persistent symptoms or evaluating
for OSA in GERD patients with unexplained sleep disturbances. Future studies
(ideally randomized trials) are needed to confirm the benefits of
fundoplication on OSA and to better define which patients are most likely to
benefit.
Conclusion
In
conclusion, treating GERD with Nissen fundoplication was associated with
significant improvement in OSA severity and nocturnal oxygenation in this
patient series. These results suggest that uncontrolled GERD can aggravate OSA
and that addressing reflux may be a useful adjunctive strategy in select OSA
patients. We recommend consideration of evaluation and treatment of coexisting
GERD in patients with difficult-to-manage OSA and vice versa. Larger controlled
studies are warranted to further validate and expand upon these findings.
Consent Statement
Written
informed consent was obtained from all individual patients for their treatments
and inclusion in this report. Patient data were de-identified to protect
privacy.
Author Contributions
David
J. Dillard drafted the manuscript. Colten Witte assisted with editing and data
collection. Magalie Nelson provided critical revisions and final approval of
the manuscript.
Declaration of
Competing Interest
The
authors declare no competing interests.
Financial Disclosures
None
to disclose.
Support
None
reported.
Informed Consent
Patient
consent was waived due to the retrospective nature of the study and use of
de-identified data.
IRB Approval
Not
applicable, retrospective case series Clinical Trial Registration: Not
applicable.
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