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1.
Arterioscler Thromb Vasc Biol ; 41(4): 1459-1473, 2021 04.
Article in English | MEDLINE | ID: mdl-33567869
2.
Ann Otol Rhinol Laryngol ; 129(7): 649-652, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32005077

ABSTRACT

INTRODUCTION: Double aortic arch is a rare congenital malformation of the aortic arch that most frequently presents in childhood. Early surgical intervention typically yields excellent outcomes. OBJECTIVES: To describe aortotracheal fistula as a rare, yet serious complication of vascular ring and subsequent aortic aneurysm in an adult patient. METHODS: Clinical history, as well as radiographic and endoscopic imaging were obtained to describe the development, diagnosis, and clinical course of this patient's aortotracheal fistula. Additionally, follow up data was obtained to document the healing of this fistula after surgical repair. RESULTS: We describe a case of a 46-year-old male with DiGeorge Syndrome and a double aortic arch, repaired in childhood, which developed into an aortotracheal fistula after tracheostomy placement as an adult. CONCLUSIONS: This case demonstrates that dangerous complications of a double aortic arch can persist into adulthood, even after surgical repair in infancy. Each patient's unique anatomy must be considered when thinking about airway management and prevention of complications of this rare congenital anomaly.


Subject(s)
Aortic Aneurysm, Thoracic/surgery , Aortic Diseases/surgery , Fistula/surgery , Postoperative Complications/surgery , Tracheal Diseases/surgery , Tracheomalacia/surgery , Vascular Ring/surgery , Aortic Aneurysm, Thoracic/complications , Aortic Aneurysm, Thoracic/diagnostic imaging , Aortic Diseases/complications , Aortic Diseases/diagnostic imaging , DiGeorge Syndrome/complications , Fistula/complications , Fistula/diagnostic imaging , Humans , Male , Middle Aged , Thoracic Surgical Procedures , Tomography, X-Ray Computed , Tracheal Diseases/complications , Tracheal Diseases/diagnostic imaging , Tracheomalacia/complications , Tracheostomy , Vascular Grafting , Vascular Ring/complications
3.
JAMA Otolaryngol Head Neck Surg ; 145(1): 21-26, 2019 01 01.
Article in English | MEDLINE | ID: mdl-30383170

ABSTRACT

Importance: Because of the recurrent nature of idiopathic subglottic stenosis, routine follow-up is necessary for monitoring progression of stenosis. However, no easily accessible, standardized objective measure exists to monitor disease progression. Objective: To determine whether peak expiratory flow (PEF) can be used as a reliable and easily accessible biometric indicator of disease progression relative to other validated spirometry measures in patients with idiopathic subglottic stenosis. Design, Setting, and Participants: Prospectively collected data on PEF, expiratory disproportion index (EDI), and total peak flow (TPF) from 42 women with idiopathic subglottic stenosis without comorbid lower airway or parenchymal lung disease who were treated at a single tertiary referral center between 2014 and 2018 were analyzed. The mean follow-up period was 18.2 months (range, 2-40 months). Ten patients initially screened were not included in the analysis owing to comorbid glottic or supraglottic stenosis or nonidiopathic etiology. Main Outcomes and Measures: Measurements of PEF, EDI, and TPF were taken at preoperative visits and at all other visits. Results: Forty-two women (mean age, 51.5 years; 98% white [n = 41]) met the inclusion criteria. The area under the curve for PEF was 0.855 (95% CI, 0.784-0.926). The optimal cutoff value was 4.4 liters per second (264 L/min), with a sensitivity and specificity of 84.4% and 82.0%, respectively. The area under the curve for EDI was 0.853 (95% CI, 0.782-0.925). For TPF, this was 0.836 (95% CI, 0.757-0.916). Conclusions and Relevance: This study provides evidence supporting the use of PEF as a simple, efficient, and accessible way of monitoring progression of idiopathic subglottic stenosis and predicting receipt of surgical intervention. Sensitivity and specificity of PEF were comparable to those of the more complex measures of TPF and EDI.


Subject(s)
Laryngostenosis/diagnosis , Spirometry , Adult , Aged , Disease Progression , Female , Follow-Up Studies , Humans , Laryngostenosis/physiopathology , Laryngostenosis/surgery , Middle Aged , Peak Expiratory Flow Rate , Prognosis , Retrospective Studies , Sensitivity and Specificity
4.
Laryngoscope ; 123(9): 2170-5, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23729204

ABSTRACT

OBJECTIVES/HYPOTHESIS: Black patients generally present with advanced head and neck cancer resulting in decreased survival. The objective of this study was to determine whether equal access to laryngeal cancer care in a tertiary care Veterans Affairs (VA) Medical Center would result in similar survival for white and black patients. STUDY DESIGN: Retrospective chart review. METHODS: Patient and tumor characteristics, compliance with National Comprehensive Cancer Network (NCCN) guidelines, and survival outcomes were collected for 205 male patients with squamous cell carcinoma of the larynx treated between 2000 and 2012 at the Michael E. DeBakey Veterans Affairs Medical Center. RESULTS: Black patients constituted 33% of the entire cohort, were older (mean age, 65.1 vs. 62.1 years), and consumed less tobacco (46.6 vs. 65.8 mean pack-years) than white patients. Disease stage and compliance with NCCN guidelines were not affected by race. Mean follow up time was 3.6 years. A higher recurrence rate was noted among white patients (24% vs. 15%, P < .05). Neither disease-free survival (DFS) nor overall survival (OS) was significantly different between black and white patients (DFS 69% vs. 68%, P = .7; OS 68% vs. 77%, P = .1). CONCLUSIONS: Utilization of a multidisciplinary approach to laryngeal cancer care at the VA medical center allows for high compliance with NCCN guidelines and excellent oncologic outcomes. Ethnicity did not impact stage at presentation, treatment selection, or treatment intensity in this patient cohort. Our data suggest that cancer care at a VA medical center results in clinical outcomes that do not significantly vary based on patient race.


Subject(s)
Black or African American/statistics & numerical data , Carcinoma, Squamous Cell/ethnology , Carcinoma, Squamous Cell/pathology , Laryngeal Neoplasms/ethnology , Laryngeal Neoplasms/pathology , Neoplasm Recurrence, Local/mortality , Aged , Carcinoma, Squamous Cell/mortality , Carcinoma, Squamous Cell/therapy , Chemotherapy, Adjuvant , Cohort Studies , Combined Modality Therapy , Ethnicity , Hospitals, Veterans , Humans , Kaplan-Meier Estimate , Laryngeal Neoplasms/mortality , Laryngeal Neoplasms/therapy , Laryngectomy/methods , Male , Middle Aged , Neoplasm Recurrence, Local/ethnology , Neoplasm Recurrence, Local/pathology , Prognosis , Racial Groups , Radiotherapy, Adjuvant , Retrospective Studies , Risk Assessment , Survival Analysis , Treatment Outcome
5.
J Immunother ; 35(3): 276-82, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22421945

ABSTRACT

CD40, a member of the tumor necrosis factor receptor superfamily, is broadly expressed on antigen-presenting cells and other cells, including fibroblasts and endothelial cells. Binding of CD40 and its natural ligand CD40L (CD154) triggers cytokine secretion, and increased expression of costimulatory molecules is required for T-cell activation and proliferation. However, to our knowledge, the use of agonistic antibodies to CD40 to boost adoptively transferred T cells in vivo has not been investigated. The purpose of this study was to determine whether anti-CD40 monoclonal antibody (mAb) in combination with interleukin (IL)-2 could improve the efficacy of in vitro-activated T cells to enhance antitumor activity. Mice bearing B16 melanoma tumors expressing the gp100 tumor antigen were treated with cultured, activated T cells transgenic for a T-cell receptor specifically recognizing gp100, with or without anti-CD40 mAb. In this model, the combination of anti-CD40 mAb with IL-2 led to expansion of adoptively transferred T cells and induced a more robust antitumor response. Furthermore, the expression of CD40 on bone marrow-derived cells and the presence of CD80/CD86 in the host were required for the expansion of adoptively transferred T cells. The use of neutralizing mAb to IL-12 provided direct evidence that enhanced IL-12 secretion induced by anti-CD40 mAb was crucial for the expansion of adoptively transferred T cells. Collectively, these findings provide a rationale to evaluate the potential application of anti-CD40 mAb in adoptive T-cell therapy for cancer.


Subject(s)
Adoptive Transfer , Antibodies, Monoclonal/immunology , CD40 Antigens/immunology , Melanoma, Experimental/immunology , Melanoma, Experimental/therapy , T-Lymphocytes/immunology , Animals , Antibodies, Monoclonal/pharmacology , Antigen Presentation/immunology , B7-1 Antigen/metabolism , B7-2 Antigen/metabolism , Bone Marrow Cells/immunology , Bone Marrow Cells/metabolism , CD40 Antigens/agonists , Cell Line , Female , Interleukin-2/immunology , Interleukin-2/metabolism , Mice , Mice, Inbred C57BL , Mice, Knockout , T-Lymphocytes/drug effects , T-Lymphocytes/metabolism , gp100 Melanoma Antigen/metabolism
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