Citations

Mayo Clinic

Clear

277 citation(s) found for "O'Shea, C".

300 Final analysis of a prospective, randomized, double-blind, placebo-controlled phase IIb trial of tumor lysate, particle-loaded, dendritic cell vaccine in stage III/IV melanoma: 36-month analysis
Adams, Lexy, Chick, Robert C. , Vreeland, Timothy J. , McCarthy, Patrick M. , Bohan, P. Kemp, Hickeron, Annelies, Myers, John , Cindass, Jessica L., Hale, Diane F. , Faries, Mark B. , Hyngstrom, John , Berger, Adam C. , Shaheen, Montaser , Wagner, Thomas E., Peoples, George E. , McCarthy, Patrick , Clifton, Guy T. , O’Shea, Anne E. , Jakub, James W. , Sussman, Jonathan

Regular and young investigator award abstracts | November 9, 2020 | Volume: No volume available | Issue: No issue available | Pages: A183.2-A184

10.1136/jitc-2020-sitc2020.0300 Get It

Rate of infection following revision anterior cruciate ligament reconstruction and associated patient‐ and surgeon‐dependent risk factors: Retrospective results from MOON and MARS data collected from 2002 to 2011
Group, MARS, Brophy, Robert H. , Wright, Rick W. , Huston, Laura J. , Haas, Amanda K. , Anderson, Allen F., Cooper, Daniel E. , Dunn, Warren R. , Lantz, Brett A., Mann, Barton J., Albright, John P., Amendola, Annunziato, Andrish, Jack T. , Annunziata, Christopher C., Arciero, Robert A. , Bach, Bernard R. , Baker, Champ L., Bartolozzi, Arthur R. , Baumgarten, Keith M. , Bechler, Jeffery R., Berg, Jeffrey H., Bernas, Geoffrey A., Brockmeier, Stephen F. , Bush‐Joseph, Charles A., Butler, J. Brad, Carey, James L. , Carpenter, James E. , Cole, Brian J. , Cox, Charles L. , Creighton, R. Alexander , Dahm, Diane L., Flanigan, David C. , Frederick, Robert W., Ganley, Theodore J. , Garofoli, Elizabeth A. , Gatt, Charles J. , Gecha, Steven R., Giffin, J. Robert , Hame, Sharon L. , Hannafin, Jo A., Harner, Christopher D. , Harris, Norman Lindsay, Hechtman, Keith S., Hershman, Elliott B., Hoellrich, Rudolf G., Hosea, Timothy M., Johnson, David C. , Johnson, Timothy S. , Kaeding, Christopher C. , Kamath, Ganesh V. , Klootwyk, Thomas E., Levy, Bruce A. , Benjamin, Chunbong, Maiers, G. Peter, Marx, Robert G. , Matava, Matthew J. , Mathien, Gregory M., McAllister, David R. , McCarty, Eric C. , McCormack, Robert G. , Miller, Bruce S. , Nissen, Carl W. , O’Neill, Daniel F., Parker, Richard D., Purnell, Mark L., Ramappa, Arun J. , Rauh, Michael A. , Rettig, Arthur C., Sekiya, Jon K., Sherman, Orrin H. , Li, Xulei, Slauterbeck, James R., Smith, Matthew V. , Spang, Jeffrey T. , Svoboda, LTC Steven J., Taft, Timothy N., Tenuta, Joachim J., Tingstad, Edwin M., Vidal, Armando F. , Viskontas, Darius G., White, Richard A., Williams, James S., Wolcott, Michelle L., Wolf, Brian R. , York, James J. , Svoboda, Steven J. , Brophy, Robert H. , McCarty, Eric C , Group, MARS, Allen, Christina R. , DeBerardino, Thomas M. , Mann, Barton, Spindler, Kurt P , Stuart, Michael J., Campbell, John , Cooper, Jonathan M., David, Tal S. , Johnson, David C., Jones, Morgan H. , Owens, Brett D. , Shea, Kevin G. , Li, Xulei

Journal of Orthopaedic Research | October 1, 2020 | Volume: 39 | Issue: 2 | Pages: 274-280

10.1002/jor.24871 | PMID 33002248 Get It

AbstractInfection is a rare occurrence after revision anterior cruciate ligament reconstruction (rACLR). Because of the low rates of infection, it has been difficult to identify risk factors for infection in this patient population. The purpose of this study was to report the rate of infection following rACLR and assess whether infection is associated with patient‐ and surgeon‐dependent risk factors. We reviewed two large prospective cohorts to identify patients with postoperative infections following rACLR. Age, sex, body mass index (BMI), smoking status, history of diabetes, and graft choice were recorded for each patient. The association of these factors with postoperative infection following rACLR was assessed. There were 1423 rACLR cases in the combined cohort, with 9 (0.6%) reporting postoperative infections. Allografts had a higher risk of infection than autografts (odds ratio, 6.8; 95% CI, 0.9–54.5; p = .045). Diabetes (odds ratio, 28.6; 95% CI, 5.5–149.9; p = .004) was a risk factor for infection. Patient age, sex, BMI, and smoking status were not associated with risk of infection after rACLR.
Relationship between Physicochemical Characteristics and Pathogenic Leptospira in Urban Slum Waters
Oliveira, Daiana de , Querino, Vladimir Airam, Lee, Yeonsoo Sara , Cunha, Marcelo, Perelo, Louisa Wessels , Alva, Juan Carlos Rossi , Ko, Albert I. , Reis, Mitermayer Galvão dos , Casanovas‐Massana, Arnau , de Oliveira, Daiana , Sara Lee, Yeonsoo , Casanovas-Massana, Arnau , Nery, Nívison , Costa, Federico

Tropical Medicine and Infectious Disease | September 16, 2020 | Volume: 5 | Issue: 3 | Pages: 146

10.3390/tropicalmed5030146 | PMID 32947807 Get It

Leptospirosis, a zoonosis caused by pathogenic Leptospira, primarily affects tropical, developing regions, especially communities without adequate sanitation. Outbreaks of leptospirosis have been linked with the presence of pathogenic Leptospira in water. In this study, we measured the physicochemical characteristics (temperature, pH, salinity, turbidity, electrical conductivity, and total dissolved solids (TDS)) of surface waters from an urban slum in Salvador, Brazil, and analyzed their associations with the presence and concentration of pathogenic Leptospira reported previously. We built logistic and linear regression models to determine the strength of association between physicochemical parameters and the presence and concentration of Leptospira. We found that salinity, TDS, pH, and type of water were strongly associated with the presence of Leptospira. In contrast, only pH was associated with the concentration of the pathogen in water. The study of physico-chemical markers can contribute to a better understanding of the occurrence of Leptospira in water and to the identification of sources of risk in urban slum environments.
Women's Health in Times of Emergency: We Must Take Action
Lee, Yeonsoo Sara , Behn, Maya , Lee, Yeonsoo S, Sara Lee, Yeonsoo , Rexrode, Kathryn M.

Journal of Women's Health | September 2, 2020 | Volume: 30 | Issue: 3 | Pages: 289-292

10.1089/jwh.2020.8600 | PMID 32877307 Get It

Women have historically faced gendered patterns of disadvantage during times of emergency. Evidence demonstrates differences in gendered exposures and inequities during acute crises such as natural disasters and pandemics, including Covid-19, and longer-term emergencies such as climate change. These patterns, without intervention, may be perpetuated in future crises. Threats to women's health in times of emergency can arise from restricted access to health care, economic disadvantages, and harmful social norms. During crises, women face additional barriers to accessing maternal, contraceptive, and abortion care, likely exacerbating existing inequities in reproductive health outcomes. Gendered inequalities in financial and economic stability can become even more stark. Globally, women perform the majority of health care and unpaid caregiving work, but face barriers to affording costs of living and obtaining health insurance due to over-representation in low-wage jobs. Finally, gendered expectations of social roles contribute to increased vulnerabilities, such as displacement and poverty. Violence against women rises in times of emergency and pathways to escaping trauma can be limited. In addition to directly addressing women's unique barriers and providing support in times of emergency through bolstering health care access, economic, and social support systems, thoughtful solutions such as trauma-informed care, increasing the number of women in leadership roles, educational initiatives, and advocacy from health professionals are needed to protect and advance women's health.
Screening Cancer Immunotherapy: When Engineering Approaches Meet Artificial Intelligence
Qu, Moyuan , Tebon, Peyton , Jiang, Xing , Wang, Canran , Zhu, Jixiang , Zhang, Shiming , Öklü, Rahmi , Sengupta, Shiladitya , Sun, Wujin , Khademhosseini, Ali, Khademhosseini, Ali , Oklu, Rahmi , Zhou, Xingwu , Xue, Yumeng

Advanced Science | August 14, 2020 | Volume: 7 | Issue: 19 | Pages: No page available

10.1002/advs.202001447 | PMID 33042756 Get It

AbstractImmunotherapy is a class of promising anticancer treatments that has recently gained attention due to surging numbers of FDA approvals and extensive preclinical studies demonstrating efficacy. Nevertheless, further clinical implementation has been limited by high variability in patient response to different immunotherapeutic agents. These treatments currently do not have reliable predictors of efficacy and may lead to side effects. The future development of additional immunotherapy options and the prediction of patient‐specific response to treatment require advanced screening platforms associated with accurate and rapid data interpretation. Advanced engineering approaches ranging from sequencing and gene editing, to tumor organoids engineering, bioprinted tissues, and organs‐on‐a‐chip systems facilitate the screening of cancer immunotherapies by recreating the intrinsic and extrinsic features of a tumor and its microenvironment. High‐throughput platform development and progress in artificial intelligence can also improve the efficiency and accuracy of screening methods. Here, these engineering approaches in screening cancer immunotherapies are highlighted, and a discussion of the future perspectives and challenges associated with these emerging fields to further advance the clinical use of state‐of‐the‐art cancer immunotherapies are provided.
Bioactive‐Tissue‐Derived Nanocomposite Hydrogel for Permanent Arterial Embolization and Enhanced Vascular Healing
Hu, Jingjie , Altun, İzzet , Zhang, Zefu , Albadawi, Hassan , Salomao, Marcela , Mayer, Joseph L. , Hemachandra, L. P. Madhubhani P. , Rehman, Suliman, Öklü, Rahmi , Salomao, Marcela A, Oklu, Rahmi , Salomao, Marcela

Advanced Materials | June 24, 2020 | Volume: 32 | Issue: 33 | Pages: No page available

10.1002/adma.202002611 | PMID 32578337 Get It

AbstractTranscatheter embolization is a minimally invasive procedure that uses embolic agents to intentionally block diseased or injured blood vessels for therapeutic purposes. Embolic agents in clinical practice are limited by recanalization, risk of non‐target embolization, failure in coagulopathic patients, high cost, and toxicity. Here, a decellularized cardiac extracellular matrix (ECM)‐based nanocomposite hydrogel is developed to provide superior mechanical stability, catheter injectability, retrievability, antibacterial properties, and biological activity to prevent recanalization. The embolic efficacy of the shear‐thinning ECM‐based hydrogel is shown in a porcine survival model of embolization in the iliac artery and the renal artery. The ECM‐based hydrogel promotes arterial vessel wall remodeling and a fibroinflammatory response while undergoing significant biodegradation such that only 25% of the embolic material remains at 14 days. With its unprecedented proregenerative, antibacterial properties coupled with favorable mechanical properties, and its superior performance in anticoagulated blood, the ECM‐based hydrogel has the potential to be a next‐generation biofunctional embolic agent that can successfully treat a wide range of vascular diseases.
Fetal Dosimetry at CT: A Primer
Sensakovic, William F. , Royall, Ivey, Hough, Matthew , Potrebko, P, Grekoski, Vincent, Vicenti, Rebecca, Potrebko, Peter

RadioGraphics | June 19, 2020 | Volume: 40 | Issue: 4 | Pages: 1061-1070

10.1148/rg.2020190166 | PMID 32559149 Get It

Breast Cancer Metastasis Presenting as Colonic Polyps
Bering, Jamie , Ryan, Margaret , Gurudu, Suryakanth, Gurudu, Suryakanth R

ACG Case Reports Journal | June 16, 2020 | Volume: 7 | Issue: 6 | Pages: e00411

10.14309/crj.0000000000000411 | PMID 33062785 Get It

ABSTRACT Breast cancer is the most common malignancy among women and is the second leading cause of cancer-related death among women in the United States. Rarely, breast cancer can metastasize to the gastrointestinal tract. We present a case of metastatic breast cancer diagnosed after finding metastatic lesions appearing as polyps during a colonoscopy.
ABVD followed by BV consolidation in risk-stratified patients with limited-stage Hodgkin lymphoma
Park, Steven , Shea, Thomas C., Olajide, Oludamilola, Reddy, Nishitha , Budde, Lihua E. , Deal, Allison M. , Noe, Jeanne F., Ansell, Stephen M. , Park, Steven I , Ghosh, Nilanjan , Deal, Allison

Blood Advances | June 9, 2020 | Volume: 4 | Issue: 11 | Pages: 2548-2555

10.1182/bloodadvances.2020001871 | PMID 32516414 Get It

Abstract Approximately 90% of limited-stage Hodgkin lymphoma (HL) patients are projected to be cured with standard therapy, but many do not live their expected life span because of late treatment–related complications. New treatment paradigms are needed to reduce the use of radiation therapy (RT) as well as conventional chemotherapy drugs while improving upon current standard-of-care survival outcomes. In this phase 2 multicenter study, patients with non-bulky limited-stage HL received doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) followed by brentuximab vedotin (BV) consolidation. Forty-one patients were enrolled, and patient characteristics included median age of 29 years (range, 19 to 67 years), 58% were female, 45% had unfavorable disease, and 98% had stage II disease. Based on positron emission tomography (PET)–based risk stratification, patients received 2 to 6 cycles of ABVD followed by 6 cycles of BV. After ABVD followed by BV, 95% of evaluable patients (37 out of 39; 95% confidence interval [CI], 83%-99%) achieved PET-negative status. In the intent-to-treat patient population, the estimated 3-year progression-free survival (PFS) rate was 92%, and the overall survival (OS) rate was 97%, with a median follow-up of 47 months. All 37 patients who achieved negative PET status after BV consolidation effectively avoided RT and remain in remission with estimated 3-year PFS and OS rates of 100%. In conclusion, BV demonstrates encouraging clinical activity when it follows ABVD therapy in limited-stage HL. Early incorporation of BV may reduce the use of RT as well as conventional chemotherapy drugs while achieving favorable survival outcomes in risk-stratified patients with non-bulky limited-stage HL. This trial was registered at www.clinicaltrials.gov as #NCT01578967.
PROTOCOL: When and how to replicate systematic reviews
Karunananthan, Sathya , Maxwell, Lara , Pardo, Jordi Pardo , Avey, Marc T. , Baptiste-Ngobi, John, Batista, Ricardo , Curran, Janet , Ghogomu, Elizabeth Tanjong , Graham, Ian D. , Ioannidis, John P. A. , Jordan, Zoe , Jull, Janet , Lyddiatt, Anne , Pottie, Kevin , Shamseer, Larissa , Shea, Beverley , Siontis, Konstantinos C. , Tschirhart, Naomi , Wells, George A. , Ioannidis, John P A , Pottie, Kevin , Welch, Vivian Andrea , Petkovic, Jennifer , Rader, Tamara , Batista, Ricardo, Grimshaw, Jeremy , Moher, David , Petticrew, Mark P. , G, Gabriel Rada , Vachon, Brigitte , White, Howard , Tugwell, Peter

Campbell Systematic Reviews | May 28, 2020 | Volume: 16 | Issue: 2 | Pages: No page available

10.1002/cl2.1087 | PMID 37131421 Get It

Abstract This is a protocol for a co‐registered Cochrane and Campbell Review (Methodology). The objectives are as follows: To identify, describe and assess methods for: when to replicate a systematic review; how to replicate a systematic review.