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1283 citation(s) found for "Fu, Wayne".

Outcomes of Intralesional Interferon-α2B for the Treatment of Peyronie Disease
Trost, Landon , Ateş, Erhan , Powers, Mary K., Sikka, Suresh C. , Hellstrom, Wayne J.G. , Trost, Landon W

Journal of Urology | May 18, 2013 | Volume: 190 | Issue: 6 | Pages: 2194-2199

10.1016/j.juro.2013.05.022 | PMID 23688848 Get It

A critical analysis of the surgical outcomes for the treatment of Peyronie’s disease
Mandava, Sree Harsha , Trost, Landon , Hellstrom, Wayne J.G.

Arab Journal of Urology | May 6, 2013 | Volume: 11 | Issue: 3 | Pages: 284-293

10.1016/j.aju.2013.03.007 | PMID 26558094 Get It

Pseudoinsulinoma Syndrome from Inadvertent Tolazamide Ingestion
Ahlquist, David A. , NELSON, ROGER L., CALLAWAY, C. WAYNE, NELSON, ROGER L., CALLAWAY, C. WAYNE

Annals of Internal Medicine | April 12, 2013 | Volume: 93 | Issue: 2 | Pages: 281-282

10.7326/0003-4819-93-2-281 | PMID 6250435 Get It

Calcium Tablets for Hypertension?
Heath, Hunter, CALLAWAY, C. WAYNE, CALLAWAY, C. WAYNE

Annals of Internal Medicine | April 12, 2013 | Volume: 103 | Issue: 6_Part_1 | Pages: 946-947

10.7326/0003-4819-103-6-946 | PMID 4062095 Get It

Weight Standards: Their Clinical Significance
Callaway, C. Wayne

Annals of Internal Medicine | April 12, 2013 | Volume: 100 | Issue: 2 | Pages: 296-298

10.7326/0003-4819-100-2-296 | PMID 6691671 Get It

Acute Myocardial Infarction and Renal Dysfunction: A High-Risk Combination
Wright, R. Scott , Reeder, Guy S., Herzog, Charles A. , Albright, Robert C. , Williams, Brent A. , Dvorak, David L., Murphy, Joseph G. , Kopecky, Stephen L. , Jaffe, Allan S. , Miller, Wayne L. , Jaffe, Allan S.

Annals of Internal Medicine | April 12, 2013 | Volume: 137 | Issue: 7 | Pages: 563-570

10.7326/0003-4819-137-7-200210010-00007 | PMID 12353943 Get It

The Effect of T-Cell Depletion on Enhanced Basophil Histamine Release after In Vitro Incubation with Live Influenza A Virus
Huftel, M. A., Swensen, Cheri A., Borcherding, Wayne, Dick, E. C., Kita, Hisaaki, Gleich, G.J., Kita, Hirohito , Hong, Robert , Busse, William W. , Kita, H

American Journal of Respiratory Cell and Molecular Biology | April 3, 2013 | Volume: 7 | Issue: 4 | Pages: 434-440

10.1165/ajrcmb/7.4.434 | PMID 1382480 Get It

Abstract A number of mechanisms participate in virus-induced asthma. Previously, we described enhanced basophil histamine release (HR) during an experimentally induced rhinovirus infection and after in vitro incubation of peripheral blood mononuclear cells (PBMC) with influenza virus. This study extends our previous observations and examines the effect of influenza A virus on basophil leukotriene C4 (LTC4) release as well as the effect of T-cell depletion on virus-enhanced basophil HR. PBMC were isolated from ragweed-allergic subjects and incubated with live influenza A virus or control medium (allantoic fluid). After incubation with influenza A, ragweed antigen (AgE) stimulated LTC4 and HR were enhanced (P < 0.05). To further define the role of T cells in virus-enhanced basophil secretion, PBMC were isolated and divided into two aliquots. In one aliquot, T cells were removed by magnetic bead separation of mouse monoclonal anti-CD3-coated lymphocytes. T-cell-depleted and nontreated PBMC suspensions were incubated with influenza A or control medium, collected, and challenged with AgE to release histamine. Basophil HR was enhanced in the virus-treated group of PBMC that had not undergone T-cell depletion. In contrast, virus incubation did not enhance HR in the T-cell-depleted fraction. Finally, preliminary analysis of the supernate from virus-treated leukocytes indicates the presence of interferon-γ. These findings suggest that T cells, and their cytokine products, play an integral role in the process by which viruses enhance basophil HR.
Managing the Difficult Penile Prosthesis Patient
Trost, Landon , Baum, Neil , Hellstrom, Wayne J.G.

The Journal of Sexual Medicine | April 1, 2013 | Volume: 10 | Issue: 4 | Pages: 893-907

10.1111/jsm.12115 | PMID 23551538 Get It

ABSTRACT Introduction Inflatable penile prostheses (IPPs) are associated with excellent long-term outcomes and patient/partner satisfaction. A small percentage of patients remain dissatisfied, despite acceptable surgical results. Aims This study aims to evaluate factors associated with patient satisfaction and dissatisfaction, define patient characteristics, which may identify elevated risk of postoperative dissatisfaction, and describe management strategies to optimize functional and psychological patient outcomes. Methods A review of urologic and non-urologic cosmetic surgery literature was performed to identify factors associated with patient satisfaction/dissatisfaction. Emphasis was placed on articles defining “high risk” or psychologically challenging patients. Main Outcome Measures Preoperative factors associated with patient satisfaction/dissatisfaction and character traits, which may identify elevated risk of postoperative dissatisfaction or otherwise indicate a psychologically challenging patient. Results Contemporary patient and partner satisfaction rates following IPP are 92–100% and 91–95%, respectively. Factors associated with satisfaction include decreased preoperative expectations, favorable female partner sexual function, body mass index ≤30, and absence of Peyronie's disease or prior prostatectomy. Determinants of dissatisfaction include perceived/actual loss of penile length, decreased glanular engorgement, altered erectile/ejaculatory sensation, pain, diminished cosmetic outcome, difficulty with device function, partner dissatisfaction and perception of unnatural sensation, complications, and extent of alternative treatments offered. Personality characteristics which may indicate psychologically challenging IPP patients include obsessive/compulsive tendencies, unrealistic expectations, patients undergoing revision surgery, those seeking multiple surgical opinions, feeling of entitlement, patients in denial of their prior erectile/sexual function and current disease status, or those with other psychiatric disorders. The mnemonic CURSED Patient is presented: “Compulsive/obsessive, Unrealistic, Revision, Surgeon Shopping, Entitled, Denial, and Psychiatric.” Conclusions Although the majority of IPP patients experience excellent, durable satisfaction and outcomes, a challenging subset of patients may be at increased risk of postoperative dissatisfaction. Appropriate recognition/prevention and management of this cohort may help to establish and strengthen relationships, reduce physical, emotional, and legal risk, and ultimately enhance patient satisfaction.
Genetic Susceptibility to Triple-Negative Breast Cancer
Stevens, Kristen N., Vachon, Celine M. , Couch, Fergus J., Purrington, Kristen S. , Vachon, Celine M. , Purrington, Kristen S

Cancer Research | March 28, 2013 | Volume: 73 | Issue: 7 | Pages: 2025-2030

10.1158/0008-5472.can-12-1699 | PMID 23536562 Get It

Abstract Triple-negative breast cancers (TNBC), defined by the absence of estrogen receptor, progesterone receptor, and HER-2 expression, account for 12% to 24% of all breast cancers. TNBC is associated with early recurrence of disease and poor outcome. Germline mutations in the BRCA1 and BRCA2 breast cancer susceptibility genes have been associated with up to 15% of TNBC, and TNBC accounts for 70% of breast tumors arising in BRCA1 mutation carriers and 16% to 23% of breast tumors in BRCA2 carriers. Whether germline mutations in other breast cancer susceptibility genes also predispose to TNBC remains to be determined. Common variation in a subset of the 72 known breast cancer susceptibility loci identified through genome-wide association studies and other large-scale genotyping efforts have also been associated with risk of TNBC (TOX3, ESR1, RAD51L1, TERT, 19p13.1, 20q11, MDM4, 2p24.1, and FTO). Furthermore, variation in the 19p13.1 locus and the MDM4 locus has been associated with TNBC, but not other forms of breast cancer, suggesting that these are TNBC-specific loci. Thus, TNBC can be distinguished from other breast cancer subtypes by a unique pattern of common and rare germline predisposition alleles. Additional efforts to combine genetic and epidemiologic data are needed to better understand the etiology of this aggressive form of breast cancer, to identify prevention and therapeutic targets, and to impact clinical practice through the development of risk prediction models. Cancer Res; 73(7); 2025–30. ©2012 AACR.
Androgen Deprivation Therapy Impact on Quality of Life and Cardiovascular Health, Monitoring Therapeutic Replacement
Trost, Landon , Şerefoğlu, Ege Can , Gökçe, Ahmet , Linder, Brian J. , Sartor, Alton Oliver, Hellstrom, Wayne J.G. , Linder, Brian J

The Journal of Sexual Medicine | February 6, 2013 | Volume: 10 | Issue: Supplement_1 | Pages: 84-101

10.1111/jsm.12036 | PMID 23387914 Get It

ABSTRACTIntroductionAndrogen deprivation therapy (ADT) is commonly utilized in the management of both localized and advanced adenocarcinoma of the prostate. The use of ADT is associated with several adverse events, physical changes, and development of medical comorbidities/mortality.AimThe current article reviews known adverse events associated with ADT as well as treatment options, where available. Current recommendations and guidelines are cited for ongoing monitoring of patients receiving ADT.MethodsA PubMed search of topics relating to ADT and adverse outcomes was performed, with select articles highlighted and reviewed based on level of evidence and overall contribution.Main Outcome MeasuresReported outcomes of studies detailing adverse effects of ADT were reviewed and discussed. Where available, randomized trials and meta-analyses were reported.ResultsADT may result in several adverse events including decreased libido, erectile dysfunction, vasomotor symptoms, cognitive, psychological and quality of life impairments, weight gain, sarcopenia, increased adiposity, gynecomastia, reduced penile/testicular size, hair changes, periodontal disease, osteoporosis, increased fracture risk, diabetes and insulin resistance, hyperlipidemia, and anemia. The definitive impact of ADT on lipid profiles, cardiovascular morbidity/mortality, and all-cause mortality is currently unknown with available data. Treatment options to reduce ADT-related adverse events include changing to an intermittent treatment schedule, biophysical therapy, counseling, and pharmacotherapy.ConclusionsPatients treated with ADT are at increased risk of several adverse events and should be routinely monitored for the development of potentially significant morbidity/mortality. Where appropriate, physicians should reduce known risk factors and counsel patients as to known risks and benefits of therapy.