Weiyi Chen1, Ziyue Wu2, Sally L. Davidson Ward3, Michael C.K. Khoo4, and Krishna S. Nayak1
1Electrical Engineering, University of Southern California, Los Angeles, CA, United States, 2Alltech Medical Systems USA, Solon, OH, United States, 3Children's Hospital Los Angeles, Los Angeles, CA, United States, 4Biomedical Engineering, University of Southern California, Los Angeles, CA, United States
Synopsis
We demonstrate a novel experiment that captures the upper airway’s
instantaneous response to changes in air pressure. We apply rapid changes in continuous positive airway pressure (CPAP) during real-time
simultaneous multi-slice MRI. This reveals the airway area does NOT only depend on
pressure level but also different airway sections and previous muscle tone status.
This technique also enables characterization of airway collapsibility, and is
relevant to the assessment of obstructive sleep apnea (OSA) and treatment
planning. Purpose
Obstructive sleep apnea
(OSA) is characterized by repetitive upper airway (UA) collapse during sleep. Invasive
endoscopy has shown that airway cross sectional area change during Mueller
maneuver (MM) is correlated to the severity of OSA
1. MM is a
voluntary effort with poor reproducibility. Continuous positive airway pressure (CPAP) can
produce similar and well-controlled positive pressure, and is the most widely
used therapy for OSA
2. The direct effects of CPAP on soft tissues
surrounding the upper airway have been extensively studied using static MRI
3. However, the underlying mechanisms of airway response to pressure change
remains unknown. In this study, we perform real-time multi-slice MRI during
rapid changes to the CPAP pressure level, and for the first time, fully resolve
the soft tissue response to pressure change.
Methods
Acquisition: Experiments were performed on a clinical 3T MRI
(GE EXCITE HDxt) with a 6-channel carotid coil. Physiological signals including
facemask pressure, respiratory effort bellow displacement, oxygen saturation
and heart rate were simultaneously collected. The facemask was connected to a
CPAP machine (Philips Respironics System One) in the MRI control room. The
maximum pressure level in the facemask was set to a pre-titrated value that
maintained patent airway, determined during an overnight sleep study using standard
polysomnography. During each study, the CPAP level in the facemask was
alternated between the maximum value and 4cm H2O. Note some positive pressure is required, due to
resistance in the long tube between CPAP and facemask. The imaging sequence,
described in Ref4 utilized a simultaneous multi-slice golden angle
radial CAIPIRINHA fast gradient echo acquisition, providing 1mm in-plane
spatial resolution, 4 simultaneous slices (2-retroglossal 2-retropalatal), with
96ms temporal resolution.
Image analysis: A semi-automated region growing algorithm4 was used to segment the airway in each 2D slice. The lateral and
anterior-posterior dimensions of the patent airway were calculated using the
segmented images, by subtracting the
left-right and anterior-posterior extents of the airway, respectively.
Results
Fig.1
contains representative images from a patient with OSA (15 yrs., male, AHI 11.6),
with the top row at 4cm H
2O, and bottom row at 11cm H
2O, covering from soft palate to epiglottis (left to right).
Fig.2 contains the temporal changes in
airway area for all four slices during sudden pressure rise at t=1 sec (4 to 11
cm H
2O) and drop at t=16sec (11 to 4 cm H
2O). The
pressure remained at 11cm H
2O in between these two time points, however,
the airway area gradually changed during that timespan, and with tidal
breathing, indicating a highly dynamic process.
Fig.3 shows the temporal change in airway dimension along the
lateral and anterior-posterior directions, corresponding to the right two
columns in Fig.1. Airway change in our (n=4) cohort was
mediated primarily by lateral expansion. The collapse pattern has been observed
for all 4 subjects to date, conforms to similar observation in Ref
3.
Discussion
Pathological mechanisms
underlying OSA have been studied by measuring physiological changes during
immediate drops in CPAP
5. The proposed technique allows one to fully
resolve the dynamics secondary to sudden pressure change, therefore has the potential to provide visual and quantitative information for pathological
assessment. Furthermore, simultaneous multi-slice acquisition allows identification
of the more responsive site to CPAP change. For example, the tissues in the
right two columns (retroglossal) deform
more than the other two columns (retropalatal), and can be positively
identified as the more compliant sites for this particular subject.
A previous study using static MRI
3 showed airway area enlarged with
progressively increased pressure. However, the fully resolved dynamics (highlighted
area in
Fig.2) reveals that airway
area depends on many factors in addition to the pressure level.
Conclusion
We demonstrate a novel experiment
that captured the upper airways’ instantaneous response to pressure changes. By
performing real-time multi-slice MRI during the application of CPAP, we
demonstrate that airway area change is dynamic and depends on factors including pressure
level, airway section and previous muscle tone status.
Acknowledgements
GRANT SPONSOR: NIH R01-HL105210. References
[1] Schwatz et al. J.
Otolartngol Head Neck Surg 2015 44(1): 32-39
[2] American Thoracic Society. Am. J. Respir. Crit. Care Med. 1994. 150:1738-1745.
[3] Schwab et al. Am. J. Respir. Crit. Care Med. 1996. 154:1106-1116.
[4] Wu et al. Proc ISMRM 2015, p242.
[5] Edwards et al. Sleep 2014
37(7):1227-36