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ABSTRACT: A substantial portion of patients with obstructive sleep apnea (OSA) seek alternatives to positive airway pressure (PAP), the usual first-line treatment for the disorder. One option is upper airway surgery. As an adjunct to the American Academy of Sleep Medicine (AASM) Standards of Practice paper, we conducted a systematic review and meta-analysis of literature reporting outcomes following various upper airway surgeries for the treatment of OSA in adults, including maxillomandibular advancement (MMA), pharyngeal surgeries such as uvulopharyngopalatoplasty (UPPP), laser assisted uvulopalatoplasty (LAUP), and radiofrequency ablation (RFA), as well as multi-level and multi-phased procedures. We found that the published literature is comprised primarily of case series, with few controlled trials and varying approaches to pre-operative evaluation and post-operative follow-up. We include surgical morbidity and adverse events where reported but these were not systematically analyzed. Utilizing the ratio of means method, we used the change in the apnea-hypopnea index (AHI) as the primary measure of efficacy. Substantial and consistent reductions in the AHI were observed following MMA; adverse events were uncommonly reported. Outcomes following pharyngeal surgeries were less consistent; adverse events were reported more commonly. Papers describing positive outcomes associated with newer pharyngeal techniques and multi-level procedures performed in small samples of patients appear promising. Further research is needed to better clarify patient selection, as well as efficacy and safety of upper airway surgery in those with OSA.
Sleep 10/2010; 33(10):1396-407. · 5.05 Impact Factor
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ABSTRACT: The purpose of our study was to evaluate the dose and image quality performance of a dedicated cone-beam CT (CBCT) scanner in comparison with an MDCT scanner.
The conventional dose metric, CT dose index (CTDI), is no longer applicable to CBCT scanners. We propose to use two dose metrics, the volume average dose and the mid plane average dose, to quantify the dose performance in a circular cone-beam scan. Under the condition of equal mid plane average dose, we evaluated the image quality of a CBCT scanner and an MDCT scanner, including high-contrast spatial resolution, low-contrast spatial resolution, noise level, CT number uniformity, and CT number accuracy.
For the sinus scanning protocol, the CBCT system had comparable high-contrast resolution and inferior low-contrast resolution to those obtained with the MDCT scanner when the doses were matched (mid plane average dose 9.2 mGy). The CT number uniformity and accuracy were worse on the CBCT scanner. The image artifacts caused by beam hardening and scattering were also much more severe on the CBCT system.
With a matched radiation dose, the CBCT system for sinus study has comparable high-contrast resolution and inferior low-contrast resolution relative to the MDCT scanner. Because of the more severe image artifacts on the CBCT system due to the small field of view and the lack of accurate scatter and beam-hardening correction, the utility of the CBCT system for diagnostic tasks related to soft tissue should be carefully assessed.
American Journal of Roentgenology 02/2010; 194(2):W193-201. · 2.78 Impact Factor
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ABSTRACT: Asthmatic chronic rhinosinusitis with nasal polyps (aCRSwNP) is a common disruptive eosinophilic disease without effective medical treatment. Therefore, we sought to identify gene expression changes, particularly those occurring early, in aCRSwNP. To highlight expression changes associated with eosinophilic epithelial inflammation, we further compared the changes in aCRSwNP with those in a second eosinophilic epithelial disease, atopic dermatitis (AD), which is also closely related to asthma.
Genome-wide mRNA levels measured by exon array in both nasosinus inflamed mucosa and adjacent polyp from 11 aCRSwNP patients were compared to those in nasosinus tissue from 17 normal or rhinitis subjects without polyps. Differential expression of selected genes was confirmed by qRT-PCR or immunoassay, and transcription changes common to AD were identified. Comparison of aCRSwNP inflamed mucosa and polyp to normal/rhinitis tissue identified 447 differentially transcribed genes at > or = 2 fold-change and adjusted p-value < 0.05. These included increased transcription of chemokines localized to chromosome 17q11.2 (CCL13, CCL2, CCL8, and CCL11) that favor eosinophil and monocyte chemotaxis and chemokines (CCL18, CCL22, and CXCL13) that alternatively-activated monocyte-derived cells have been shown to produce. Additional transcription changes likely associated with Th2-like eosinophilic inflammation were prominent and included increased IL1RL1 (IL33 receptor) and EMR1&3 and decreased CRISP2&3. A down-regulated PDGFB-centric network involving several smooth muscle-associated genes was also implicated. Genes at 17q11.2, genes associated with alternative activation or smooth muscle, and the IL1RL1 gene were also differentially transcribed in AD.
Our data implicate several genes or gene sets in aCRSwNP and eosinophilic epithelial inflammation, some that likely act in the earlier stages of inflammation. The identified gene expression changes provide additional diagnostic and therapeutic targets for aCRSwNP and other eosinophilic epithelial diseases.
PLoS ONE 01/2010; 5(7):e11450. · 4.09 Impact Factor
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ABSTRACT: To assess the role of uvulopalatopharyngoplasty (UPPP) in the treatment of obstructive sleep apnea (OSA) using polysomnography (PSG) data within 6 months before and after surgery.
We analyzed PSG and body mass index (BMI) data from patients with OSA who were 18 years or older and who underwent UPPP between January 1, 1988, and August 31, 2006.
Sixty-three patients (51 men [81.0%]; mean +/- SD age, 42.1+/-13.9 years; mean +/- SD BMI, 34.9+/-7.2) underwent PSG a mean +/- SD of 50+/-47 days before and 88.5+/-34.0 days after UPPP. Surgical cure was defined as a postoperative apnea-hypopnea index (AHI) of 5 or less. Fifteen patients (24%) achieved a surgical cure. Twenty-one patients (33%) had a postoperative AHI of 10 or less, whereas 32 (51%) achieved a 50% or greater reduction in AHI and/or an AHI of 20 or less. No significant changes were noted in BMI before and 6 months after UPPP. Patients who attained an AHI of 5 or less were younger (mean +/- SD age, 35.9+/-13.1 vs 44+/-13.7 years; P=.05), had lower BMIs (mean +/- SD, 30.8+/-6.5 vs 34.6+/-6.6; P=.05), and had less severe OSA (mean +/- SD AHI, 38.1+/-33.6 vs 69.6+/-32.8; P=.004). Of the 48 patients (76%) with a post-UPPP AHI greater than 5, 35 (56%) received continuous positive airway pressure, with a mean reduction in pressure of 1.4 cm H(2)O (95% confidence interval, -0.4 to -2.4 cm H(2)O).
Independent of changes in BMI, in our retrospective analysis, UPPP achieved an AHI of 5 or less in 24% and an AHI of 10 or less in 33% of patients with OSA who underwent PSG 6 months before and after surgery. In those with residual OSA who received continuous positive airway pressure, the required pressure setting decreased by 1.4 cm H(2)O.
Mayo Clinic Proceedings 10/2009; 84(9):795-800. · 5.70 Impact Factor
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ABSTRACT: The presence of stridor in patients with multiple system atrophy (MSA) is associated with poor prognosis, mainly due to a high risk of complete airway obstruction at night. Continuous positive airway pressure (CPAP) therapy has been proposed as a treatment of MSA-associated stridor, but, until now, there has been no visual documentation of the effect of CPAP on laryngeal patency during nonpharmacologically induced spontaneous sleep of a patient with MSA. We present a video-laryngoscopic documentation of a 57-year-old woman with MSA who was evaluated for nocturnal stridor. Direct laryngoscopy during sleep without pharmacologic sedation documented inspiratory adduction of the vocal cords with downward displacement of the larynx. Application of CPAP resulted in improvement of stridor, distension of the hypopharynx, abduction of vocal cords, and reduction of the downward displacement of the larynx. We discuss the possible mechanisms of action of CPAP in MSA-associated stridor.
Journal of clinical sleep medicine: JCSM: official publication of the American Academy of Sleep Medicine 03/2009; 5(1):65-7. · 3.23 Impact Factor
