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1572 citation(s) found for "Wu, Samuel".

A New Era in Critical Care Ultrasound: Professionalization
Brown, Samuel M. , Sekiguchi, Hiroshi , Pinsky, Michael R.

Annals of the American Thoracic Society | November 7, 2017 | Volume: 14 | Issue: 12 | Pages: 1747-1749

10.1513/annalsats.201708-624ps | PMID 29112479 Get It

Dose-Response Association of CD8 + Tumor-Infiltrating Lymphocytes and Survival Time in High-Grade Serous Ovarian Cancer
Goode, Ellen L. , Block, Matthew S. , Kalli, Kimberly R., Vierkant, Robert A. , Fogarty, Zachary C. , Tołoczko, Aleksandra, Hein, Alexander , Bouligny, Aliecia L., Jensen, Allan , Osório, Ana , Ryan, Andy , Magliocco, Anthony M., Hartmann, Arndt , Gao, Bo , McCauley, Bryan M. , Kennedy, Catherine J. , Karpinskyj, Chloe , Sousa, Christiani Bisinoto de, Tiezzi, Daniel Guimarães , Wachter, David L., Herpel, Esther , Taran, Florin‐Andrei , Nelson, Gregg , Menkiszak, Janusz , Alsop, Jennifer , Lester, Jenny , García-Donás, Jesús , Nation, Jill, Hung, Jillian A., Palacios, José , Rothstein, Joseph H. , Kelley, Joseph L., Andrade, Jurandyr Moreira de , Robles-Díaz, Luis, Intermaggio, Maria P., Widschwendter, Martin , Beckmann, Matthias W. , Ruebner, Matthias , Jimenez‐Liñan, Mercedes , Singh, Naveena , Oszurek, Oleg, Harnett, Paul R. , Rambau, Peter , Sinn, Hans‐Peter , Wagner, Philipp , Sharma, Raghwa , Ness, Roberta B., Oršulić, Sandra , Johnatty, Sharon E., Longacre, Teri A. , Eilber, Ursula, McGuire, Valerie , Sieh, Weiva , Natanzon, Yanina , Li, Zheng , Whittemore, Alice S. , DeFazio, Anna , Staebler, Annette , Bowtell, David D.L. , Høgdall, Estrid , Reis, Francisco José Cândido dos , Steed, Helen , Campbell, Ian , Benı́tez, Javier , Koziak, Jennifer M. , Chang‐Claude, Jenny, Moysich, Kirsten B. , Kelemen, Linda E. , Goodman, Marc T. , García, María J. , Fasching, Peter A. , Kommoss, Stefan , Deen, Suha , Menon, Usha , Chenevix‐Trench, Georgia , Huntsman, David G. , Köbel, Martin , Ramus, Susan J. , Winham, Stacey J. , Fazio, Anna de , Ramus, Susan J , Köbel, Martin , Hein, Alexander , Jensen, Allan , Vierkant, Robert A , Menon, Usha , Moysich, Kirsten , Campbell, Ian G , García-Donas, Jesús , Kennedy, Catherine J , Menkiszak, Janusz , Sinn, Peter , Widschwendter, Martin , Fogarty, Zachary C , Sieh, Weiva , Benitez, Javier , Chenevix-Trench, Georgia , Høgdall, Estrid , Bowtell, David D , Chen, Wenqian , Gentry‐Maharaj, Aleksandra , Bouligny, Aliecia, Hartkopf, Andreas D , Chudecka-Glaz, Anita Monika , Jung, Audrey , Hernandez, Brenda Y. , Fridley, Brooke L. , Wang, Chen , Modugno, Francesmary , Lubiński, Jan , Robles-Díaz, Luis, Ghatage, Prafull , Edwards, Todd , Brucker, Sara Yvonne , Karlan, Beth Y. , Gilks, C. Blake , Gronwald, Jacek , Cook, Linda S. , Kjær, Susanne K. , Brenton, James D. , Pharoah, Paul D.P. , Nelson, Gregg S , Harnett, Paul R , Steed, Helen , Goodman, Marc T

JAMA Oncology | October 19, 2017 | Volume: 3 | Issue: 12 | Pages: e173290

10.1001/jamaoncol.2017.3290 | PMID 29049607 Get It

Mortality and Cerebrovascular Events After Heart Rhythm Disorder Management Procedures
Lee, Justin Z. , Ling, Jayna, Diehl, Nancy N. , Hodge, David O. , Padmanabhan, Deepak , Killu, Ammar M. , Madhavan, Malini , Cha, Yong‐Mei , Deshmukh, Abhishek , Shen, Win-Kuang, Friedman, Paul A. , Munger, Thomas M. , Asirvatham, Samuel J. , Packer, Douglas L. , Mulpuru, Siva K. , Kapa, Suraj , Asirvatham, Samuel J , Noseworthy, Peter A. , McLeod, Christopher J. , Srivathsan, Komandoor , Kusumoto, Fred

Circulation | October 18, 2017 | Volume: 137 | Issue: 1 | Pages: 24-33

10.1161/circulationaha.117.030523 | PMID 29046320 Get It

Background: Recognition of rates and causes of hard, patient-centered outcomes of death and cerebrovascular events (CVEs) after heart rhythm disorder management (HRDM) procedures is an essential step for the development of quality improvement programs in electrophysiology laboratories. Our primary aim was to assess and characterize death and CVEs (stroke or transient ischemic attack) after HRDM procedures over a 17-year period. Methods: We performed a retrospective cohort study of all patients undergoing HRDM procedures between January 2000 and November 2016 at the Mayo Clinic. Patients from all 3 tertiary academic centers (Rochester, Phoenix, and Jacksonville) were included in the study. All in-hospital deaths and CVEs after HRDM procedures were identified and were further characterized as directly or indirectly related to the HRDM procedure. Subgroup analysis of death and CVE rates was performed for ablation, device implantation, electrophysiology study, lead extraction, and defibrillation threshold testing procedures. Results: A total of 48 913 patients (age, 65.7±6.6 years; 64% male) who underwent a total of 62 065 HRDM procedures were included in the study. The overall mortality and CVE rates in the cohort were 0.36% (95% confidence interval [CI], 0.31–0.42) and 0.12% (95% CI, 0.09–0.16), respectively. Patients undergoing lead extraction had the highest overall mortality rate at 1.9% (95% CI, 1.34–2.61) and CVE rate at 0.62% (95% CI, 0.32–1.07). Among patients undergoing HRDM procedures, 48% of deaths directly related to the HDRM procedure were among patients undergoing device implantation procedures. Overall, cardiac tamponade was the most frequent direct cause of death (40%), and infection was the most common indirect cause of death (29%). The overall 30-day mortality rate was 0.76%, with the highest being in lead extraction procedures (3.08%), followed by device implantation procedures (0.94%). Conclusions: Half of the deaths directly related to an HRDM procedure were among the patients undergoing device implantation procedures, with cardiac tamponade being the most common cause of death. This highlights the importance of the development of protocols for the quick identification and management of cardiac tamponade even in procedures typically believed to be lower risk such as device implantation.
Alcohol consumption, variability in alcohol dehydrogenase genes and risk of renal cell carcinoma
Antwi, Samuel O. , Eckel‐Passow, Jeanette E. , Diehl, Nancy D., Serie, Daniel, Custer, Kaitlynn, Wu, Kevin J. , Cheville, John C. , Thiel, David D. , Leibovich, Bradley C. , Parker, Alexander S. , Antwi, Samuel O

International Journal of Cancer | October 12, 2017 | Volume: 142 | Issue: 4 | Pages: 747-756

10.1002/ijc.31103 | PMID 29023769 Get It

Alcohol consumption has been associated inversely with renal cell carcinoma (RCC) risk; however, no study has examined effect modification by germline variation in alcohol‐metabolizing genes. We investigated whether the association between alcohol intake and RCC risk is modulated by germline variants in alcohol dehydrogenase genes in a large case–control study. Data from 652 RCC cases and 1,366 non‐cancer controls were analyzed. Alcohol intake was assessed using a standardized risk factor questionnaire. Three previously genotyped polymorphisms in ADH6 and ADH7 with the TaqMan assay were examined. Odds ratios (ORs) and 95% confidence interval (CI) were calculated using logistic regression, adjusting for covariates. Compared to non‐drinkers, ever consumption of alcohol was associated with lower RCC risk (OR = 0.52, 95% CI = 0.42–0.65). Analysis with cubic spline regression curve showed a “J‐shaped” relationship between alcohol drinks/day and RCC risk, such that there was no added benefit against RCC for consumption of more than two drinks/day. We observed effect modification by variation in rs1154454 (ADH7) (pinteraction = 0.007); a per unit increase in alcohol drink/day was associated with 35% lower RCC risk among non‐minor allele carriers, a 27% lower risk among those who carry one copy of the minor allele, but no association was observed among those with two copies of the minor allele. These findings indicate that alcohol consumption is associated with lower RCC risk. Consuming more than two drinks a day does not confer additional protection against RCC. The association between alcohol intake and RCC risk appears to be modulated by inter‐individual germline variation in alcohol‐metabolizing genes.
Effect of atrial fibrillation duration on plasma von Willebrand factor level
Wysokiński, Waldemar E. , Cohoon, Kevin P. , Konik, Ewa, Melduni, Rowlens M. , Ammash, Naser M., Asirvatham, Samuel J. , McBane, Robert D. , Konik, Ewa A, Wysokinski, Waldemar , McBane, Robert , Asirvatham, Samuel J

European Journal of Haematology | September 27, 2017 | Volume: 99 | Issue: 6 | Pages: 569-576

10.1111/ejh.12975 | PMID 28952167 Get It

AbstractAimsvon Willebrand factor (VWF) is an independent risk factor for adverse events in patients with non‐valvular atrial fibrillation (NVAF). However, it is unclear if VWF level remains elevated and predictive of stroke during entire course of NVAF.Methods and ResultsIn order to determine if VWF is a time‐dependent blood variable, VWF antigen measured by latex immunoassay in 425 NVAF patients and 100 controls with normal sinus rhythm (NSR) was analyzed according to NVAF duration (<1 month: n = 76, 1‐12 months: n = 98, and >12 months: n = 251). The mean VWF antigen level in NVAF patients with <1‐month duration (167 ± 59%) was not different compared to those with 1‐12 months (157 ± 50%, P = .24) and >12 months duration (156 ± 54%, P = .11) but higher compared to NSR controls (143 ± 48%, P = .003). Higher VWF level correlated with higher CHADS2 scores and with progressing intensity of blood stasis in the left atrium and thrombus formation in all three time periods of atrial fibrillation duration. Patients not treated with warfarin had VWF 30% higher in the first month compared to following months.Conclusionsvon Willebrand Factor is steadily elevated throughout the course of dysrhythmia in NVAF patients treated with warfarin and in those with higher intensity of left atrium blood stasis.
Patient Outcomes from Lung Cancer and Diabetes Mellitus: A Matched Case–Control Study
Karlin, Nina J. , Amin, Shailja B , Buras, Matthew , Verona, Patricia M , Cook, Curtiss B. , Buras, Matthew R , Kosiorek, Heidi

Future Science OA | September 26, 2017 | Volume: 4 | Issue: 1 | Pages: No page available

10.4155/fsoa-2017-0081 | PMID 29255620 Get It

Genetic deletion of sphingosine kinase 1 suppresses mouse breast tumor development in an HER2 transgenic model
Shimizu, Yoshiko, Furuya, Hideki , Tamashiro, Paulette M, Iino, Kayoko, Chan, Owen , Goodison, Steve , Hokutan, Kanani , Peres, Rafael , Loo, Lenora W. M. , Naing, Aung , Chong, Clayton, Rosser, Charles J. , Kawamori, Toshihiko, Furuya, Hideki , Pagano, Ian , Hernandez, Brenda Y.

Carcinogenesis | September 7, 2017 | Volume: 39 | Issue: 1 | Pages: 47-55

10.1093/carcin/bgx097 | PMID 28968647 Get It

History of Comorbidities and Survival of Ovarian Cancer Patients, Results from the Ovarian Cancer Association Consortium
Minlikeeva, Albina N. , Freudenheim, Jo L. , Eng, Kevin H., Cannioto, Rikki , Friel, Grace , Szender, J. Brian, Odunsi, Kunle , Mayor, Paul , Diergaarde, Brenda , Zsíros, Emese , Kelemen, Linda E. , Köbel, Martin , Steed, Helen , DeFazio, Anna , Jordan, Susan J. , Fasching, Peter A. , Beckmann, Matthias W. , Rossing, Mary Anne, Chang‐Claude, Jenny , Goodman, Marc T. , Dörk, Thilo , Edwards, Robert P., Ness, Roberta B., Matsuo, Keitaro , Goode, Ellen L. , Høgdall, Estrid , Schildkraut, Joellen M. , Terry, Kathryn L. , Paddock, Lisa E. , Kiemeney, Lambertus A. , Massuger, Leon F.A.G. , Sutphen, Rebecca , Menon, Usha , Gayther, Simon A. , Ramus, Susan J. , Pearce, Celeste Leigh , Wu, Anna H. , Kupryjańczyk, Jolanta , Jensen, Allan , Webb, Penelope M. , Moysich, Kirsten B. , Bowtell, David D.L. , Fazio, Anna de , Dörk, Thilo , Kiemeney, Lambertus A , Ramus, Susan J , Webb, Penelope M , Köbel, Martin , Jensen, Allan , Menon, Usha , Moysich, Kirsten , Matsuo, Keitaro , Kupryjanczyk, Jolanta , Høgdall, Estrid , Bowtell, David D , Segal, Brahm H. , Risch, Harvey A. , Doherty, Jennifer A. , Modugno, Francesmary , Mizuno, Mika , Karlan, Beth Y. , Kjær, Susanne K. , Cramer, Daniel W. , Bandera, Elisa V. , Anton‐Culver, Hoda , Ziogas, Argyrios , Gentry‐Maharaj, Aleksandra , Diergaarde, Brenda , Steed, Helen , Goodman, Marc T

Cancer Epidemiology, Biomarkers & Prevention | September 1, 2017 | Volume: 26 | Issue: 9 | Pages: 1470-1473

10.1158/1055-9965.epi-17-0367 | PMID 28864456 Get It

Abstract Background: Comorbidities can affect survival of ovarian cancer patients by influencing treatment efficacy. However, little evidence exists on the association between individual concurrent comorbidities and prognosis in ovarian cancer patients. Methods: Among patients diagnosed with invasive ovarian carcinoma who participated in 23 studies included in the Ovarian Cancer Association Consortium, we explored associations between histories of endometriosis; asthma; depression; osteoporosis; and autoimmune, gallbladder, kidney, liver, and neurological diseases and overall and progression-free survival. Using Cox proportional hazards regression models adjusted for age at diagnosis, stage of disease, histology, and study site, we estimated pooled HRs and 95% confidence intervals to assess associations between each comorbidity and ovarian cancer outcomes. Results: None of the comorbidities were associated with ovarian cancer outcome in the overall sample nor in strata defined by histologic subtype, weight status, age at diagnosis, or stage of disease (local/regional vs. advanced). Conclusions: Histories of endometriosis; asthma; depression; osteoporosis; and autoimmune, gallbladder, kidney, liver, or neurologic diseases were not associated with ovarian cancer overall or progression-free survival. Impact: These previously diagnosed chronic diseases do not appear to affect ovarian cancer prognosis. Cancer Epidemiol Biomarkers Prev; 26(9); 1470–3. ©2017 AACR.
International survey of knowledge, attitudes, and practices of cardiologists regarding prevention and management of cardiac implantable electronic device infections
DeSimone, Daniel C. , Chahal, C. Anwar A. , Asirvatham, Samuel J. , Friedman, Paul A. , Sohail, M. Rizwan , Chahal, Anwar A, Friedman, Paul A , Asirvatham, Samuel J , Sohail, M Rizwan , Chahal, Choudhary Anwar A , DeSimone, Daniel C , DeSimone, Christopher V. , Baddour, Larry M.

Pacing and Clinical Electrophysiology | August 28, 2017 | Volume: 40 | Issue: 11 | Pages: 1260-1268

10.1111/pace.13183 | PMID 28846153 Get It

AbstractBackgroundCardiovascular implantable electronic devices (CIEDs) can be life‐saving. However, complications from CIED infection can be life‐threatening, often requiring device removal. Despite publication of CIED infection management guidelines, there remains marked variation in clinical practice.ObjectiveTo better understand and quantify these differences, we conducted a multinational survey of practitioners of CIED management.MethodsAn electronic survey was sent to Heart Rhythm Society members, spanning 70 countries across six continents. All responses were collected anonymously.Results227 out of 3,600 (6.3%) responded to the survey. The majority of surveys were completed by practitioners from the United States (168; 68.3%) and 53.8% of these practiced in academic medical centers. The large majority (92.7%) of sites had protocols to ensure appropriate timing of prophylactic antibiotics. Superficial (incisional) site infections were treated with antibiotics alone 52.5% of the time (consistent with guidelines); in contrast, deep pocket infections were treated with antibiotics (with device removal) in accordance to guidelines only 37.4% of the time. Almost all providers (98.7%) were inclined to perform complete hardware removal in cases of CIED‐related endocarditis. In contrast, 82.2% of survey participants suggested complete CIED system removal in patients with an occult Gram‐positive bacteremia, 65.5% with occult Gram‐negative bacteremia, and 59.3% with prolonged bacteremia due to a source other than CIED.ConclusionsThese data suggest wide variability in clinical practice in managing CIED infection with significant deviations from published guidelines. There is critical need to increase awareness and develop institutional protocols to ensure adherence with evidence‐based guidelines to optimize outcomes.
Long‐term weight loss after colorectal cancer diagnosis is associated with lower survival: The Colon Cancer Family Registry
Kocarnik, Jonathan , Hua, Xinwei , Hardikar, Sheetal , Lindor, Noralane M. , Win, Aung Ko , Figueiredo, Jane C. , Gallinger, Steven , Cotterchio, Michelle , Adams, Scott V. , Phipps, Amanda I. , Kocarnik, Jonathan M , Figueiredo, Jane C , Newcomb, Polly A. , Win, Aung K , Robinson, Jamaica R.M. , Hopper, John L. , Potter, John D. , Campbell, Peter T. , Cohen, Stacey A.

Cancer | August 25, 2017 | Volume: 123 | Issue: 23 | Pages: 4701-4708

10.1002/cncr.30932 | PMID 28841225 Get It

BACKGROUNDBody weight is associated with colorectal cancer (CRC) risk and survival, but to the authors' knowledge, the impact of long‐term postdiagnostic weight change is unclear. Herein, the authors investigated whether weight change over the 5 years after a diagnosis of CRC is associated with survival.METHODSCRC cases diagnosed from 1997 to 2008 were identified through 4 population‐based cancer registry sites. Participants enrolled within 2 years of diagnosis and reported their height and weight 2 years prior. Follow‐up questionnaires were administered approximately 5 years after diagnosis. Associations between change in weight (in kg) or body mass index (BMI) with overall and CRC‐specific survival were estimated using Cox regression analysis adjusted for age, sex, American Joint Committee on Cancer stage of disease, baseline BMI, nonsteroidal anti‐inflammatory drug use, smoking, time between diagnosis and enrollment, and study site.RESULTSAt the 5‐year postdiagnostic survey, 2049 participants reported higher (53%; median plus 5 kg), unchanged (12%), or lower (35%; median ‐4 kg) weight. Over a median of 5.1 years of subsequent follow‐up (range, 0.3‐9.9 years), 344 participants died (91 of CRC). Long‐term weight loss (per 5 kg) was found to be associated with poorer overall survival (hazard ratio, 1.13; 95% confidence interval, 1.07‐1.21) and CRC‐specific survival (hazard ratio, 1.25; 95% confidence interval, 1.13‐1.39). Significantly lower survival was similarly observed for relative weight loss (>5% vs ≤5% change), BMI reduction (per 1 unit), or BMI category change (overweight to normal vs remaining overweight).CONCLUSIONSWeight loss 5 years after a diagnosis of CRC was found to be significantly associated with decreased long‐term survival, suggesting the importance of avoiding weight loss in survivors of CRC. Future research should attempt to further evaluate this association, accounting for whether this weight change was intentional or represents a marker of declining health. Cancer 2017;123:4701‐4708. © 2017 American Cancer Society.