Dennis M. Lyu
Anschutz Medical Campus
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Featured researches published by Dennis M. Lyu.
Proceedings of the American Thoracic Society | 2009
Dennis M. Lyu; Martin R. Zamora
As short- and long-term survival rates for lung transplantation continue to improve, and as more lung transplantations are occurring with each year, a multitude of medical complications are encountered by the clinician. This article reviews the long-term non-pulmonary noninfectious medical complications that arise beyond the postoperative period in patients who have undergone lung transplantation. This article reviews the development of renal failure, diabetes, cardiovascular complications of hypertension and atherosclerosis, osteoporosis and avascular necrosis, hematologic complications, thromboembolic disease, gastrointestinial complications, neurologic complications, and malignancy, including post-transplant lymphoproliferative disorder.
Transplant Infectious Disease | 2010
Adriana Weinberg; Dennis M. Lyu; Shaobing Li; J. Marquesen; Martin R. Zamora
A. Weinberg, D.M. Lyu, S. Li, J. Marquesen, M.R. Zamora. Incidence and morbidity of human metapneumovirus and other community‐acquired respiratory viruses in lung transplant recipients Transpl Infect Dis 2010: 12: 330–335. All rights reserved.
American Journal of Transplantation | 2013
K. Schoeppler; Dennis M. Lyu; Todd J. Grazia; J.T. Crossno; K.M. Vandervest; Martin R. Zamora
Evidence supports the use of 12 months of cytomegalovirus prophylaxis in all at‐risk lung transplants; whether cytomegalovirus serostatus can be used to further optimize this duration remains to be determined. The purpose of this retrospective study was to determine if cytomegalovirus serostatus of both donor and recipient were associated with late‐onset cytomegalovirus. The primary outcome was the proportion of lung transplants that developed cytomegalovirus infection or disease during the 180‐day period following 6 months of prophylaxis in each at‐risk serotype. Two hundred forty‐four consecutive lung transplants were evaluated, 131 were included. The proportion of recipients with cytomegalovirus differed significantly between serotypes (20 of 41 [48.8%] D+/R‐ vs. 19 of 56 [33.9%] D+/R+ vs. 2 of 34 [5.9%] D‐/R+; p < 0.001). In a multivariate model, older age (odds ratio [OR], 1.05, 95% confidence interval [CI] 1.004–1.099; p = 0.03) and D+/R‐ serostatus (OR, 3.83; 95% CI 1.674–8.770; p = 0.002) were associated with cytomegalovirus. Among R+ lung transplants, D‐ serostatus was associated with the absence of cytomegalovirus (OR, 0.12; 95% CI 0.0263–0.563; p = 0.007). These findings suggest that in the valganciclovir era, cytomegalovirus serostatus of both donor and recipient may identify lung transplants at heightened risk for late‐onset cytomegalovirus.
The Journal of Thoracic and Cardiovascular Surgery | 2008
T. Brett Reece; John D. Mitchell; Martin R. Zamora; David A. Fullerton; Joseph C. Cleveland; Marvin Pomerantz; Dennis M. Lyu; Frederick L. Grover; Michael J. Weyant
OBJECTIVE Single-lung transplantation is an accepted treatment for end-stage lung disease caused by chronic obstructive pulmonary disease. A complication unique to single-lung transplantation for chronic obstructive pulmonary disease is graft dysfunction due to compression caused by native lung hyperinflation. We hypothesized that patients with functional compromise from native lung hyperinflation would benefit from native lung volume reduction surgery. METHODS The charts of all patients undergoing single-lung transplantation for chronic obstructive pulmonary disease were reviewed for lung volume reduction surgery of their native lung. Data regarding length of stay, surgical morbidity and mortality, overall survival, type of lung volume reduction surgery, and pulmonary function were recorded to evaluate the effect of lung volume reduction surgery. RESULTS Between February 1992 and May 2007, 206 single-lung transplantations were performed for chronic obstructive pulmonary disease. Ten (5%) patients had clinically significant graft compression from native lung hyperinflation. After excluding other causes for functional decline, these patients underwent a modified lung volume reduction surgery between 12 and 142 months after single-lung transplantation (mean, 50 months). Lung volume reduction surgery consisted of anatomic resection. Two (20%) of 10 patients died during their hospitalization. Of the remaining 8 patients, 7 (87.5%) have demonstrated functional improvement on the basis of forced expiratory volume in 1 second improving from 12% to 200% (mean improvement, 57%). Within 6 months of lung volume reduction surgery, mean 6-minute walk values improved significantly (866 to 1055 feet), whereas desaturation with exertion decreased significantly. CONCLUSIONS Lung volume reduction surgery by means of formal lobectomy in patients with native lung hyperinflation undergoing single-lung transplantation and significant graft compression appears feasible. Additionally, improvements in forced expiratory volume in 1 second can be accomplished in nearly all properly selected patients. Lung volume reduction surgery should be considered in patients with decreasing graft function caused by graft compression from native lung hyperinflation.
Annals of the American Thoracic Society | 2015
Carolyn H. Welsh; Tisha S. Wang; Dennis M. Lyu; Jeremy E. Orr; Keith C. Meyer; Allan R. Glanville; Geert Verleden; Kevin C. Wilson; Carey C. Thomson
Pulmonary Medicine, Denver Veterans Affairs Medical Center, Denver, Colorado; Division of Pulmonary and Critical Care Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California; Division of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado Denver, Denver, Colorado; Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of California San Diego School of Medicine, San Diego, California; Section of Allergy, Pulmonary, and Critical Care Medicine, Department of Internal Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin; Thoracic Medicine, St. Vincent’s Hospital, Darlinghurst, New South Wales, Australia; Department of Clinical and Experimental Medicine, University of Leuven, Leuven, Belgium; Division of Pulmonary, Allergy, Sleep, and Critical Care Medicine, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts; and Division of Pulmonary and Critical Care Medicine, Department of Medicine, Mt. Auburn Hospital, Harvard Medical School, Boston, Massachusetts
Case reports in transplantation | 2015
Kelly E. Schoeppler; Martin R. Zamora; Noelle M. Northcutt; Gerard R. Barber; Gayle O'Malley-Schroeder; Dennis M. Lyu
Because of the high incidence of morbidity and mortality associated with invasive fungal infections, antifungal prophylaxis is often used in solid organ transplant recipients. However, this prophylaxis is not universally effective and may contribute to the selection of emerging, resistant pathogens. Here we present a rare case of invasive infection caused by Microascus trigonosporus species complex in a human, which developed during voriconazole prophylaxis in a lung transplant recipient. Nebulized liposomal amphotericin B was used in addition to systemic therapy in order to optimize antifungal drug exposure; this regimen appeared to reduce the patients fungal burden. Despite this apparent improvement, the patients pulmonary status progressively declined in the setting of multiple comorbidities, ultimately leading to respiratory failure and death.
Clinical Transplantation | 2012
Dennis M. Lyu; Todd J. Grazia; Alex B. Benson; Linda R. Cagle; Brian M. Freed; Martin R. Zamora
Journal of Heart and Lung Transplantation | 2012
K. Schoeppler; Dennis M. Lyu; I. Kim; Todd J. Grazia; J.T. Crossno; Uwe Christians; Martin R. Zamora
Archive | 2015
Carolyn H. Welsh; Tisha S. Wang; Dennis M. Lyu; Jeremy E. Orr; Keith C. Meyer; Allan R. Glanville; Geert Verleden; Kevin C. Wilson; Carey C. Thomson
Journal of Heart and Lung Transplantation | 2015
Kelly E. Schoeppler; Dennis M. Lyu; K.M. Vandervest; Todd J. Grazia; J.T. Crossno; Martin R. Zamora