Citations

Showing 10 of 108036 citations.

Elevated International Normalized Ratio After Initiation of Niacin and Niacinamide Chemoprophylaxis for Patients on Warfarin
Markham, Dane J. , Barbosa, Naiara S. , Degesys, Catherine A.

Mayo Clinic

Dermatologic Surgery | February 29, 2024 | Volume: 50 | Issue: 7 | Pages: 690-692

10.1097/dss.0000000000004144 | PMID 38422208 Get It

Multimodality Imaging of a Mass Arising from a Cor Triatriatum Sinister Membrane
Gonzalez, Tomas V. , Bookwalter, Candice A., François, Christopher J. , François, Christopher

Mayo Clinic

Radiology: Cardiothoracic Imaging | February 29, 2024 | Volume: 6 | Issue: 1 | Pages: No page available

10.1148/ryct.230225 | PMID 38421274 Get It

Salvage Therapy for Prostate Cancer: AUA/ASTRO/SUO Guideline Part II: Treatment Delivery for Non-metastatic Biochemical Recurrence After Primary Radical Prostatectomy
Morgan, Todd M. , Boorjian, Stephen A. , Buyyounouski, Mark K. , Chapin, Brian F. , Chen, David Y.T. , Jacene, Heather A. , Kim, Sennett K., Kirkby, Erin, Nathanson, B.J., Posadas, Edwin M. , Morgan, Todd M , Cheng, Heather H. , Chou, Roger , Kamran, Sophia C. , Luckenbaugh, Amy N. , Nathanson, Ben J., Nyame, Yaw A. , Tran, Phuoc T , Chen, Ronald C.

Mayo Clinic

Journal of Urology | February 29, 2024 | Volume: 211 | Issue: 4 | Pages: 518-525

10.1097/ju.0000000000003891 | PMID 38421243 Get It

Salvage Therapy for Prostate Cancer: AUA/ASTRO/SUO Guideline Part I: Introduction and Treatment Decision-Making at the Time of Suspected Biochemical Recurrence after Radical Prostatectomy
Morgan, Todd M. , Boorjian, Stephen A. , Buyyounouski, Mark K. , Chapin, Brian F. , Chen, David Y.T. , Jacene, Heather A. , Kim, Sennett K., Kirkby, Erin, Nathanson, B.J., Posadas, Edwin M. , Morgan, Todd M , Cheng, Heather H. , Chou, Roger , Kamran, Sophia C. , Luckenbaugh, Amy N. , Nathanson, Ben J., Nyame, Yaw A. , Tran, Phuoc T , Chen, Ronald C.

Mayo Clinic

Journal of Urology | February 29, 2024 | Volume: 211 | Issue: 4 | Pages: 509-517

10.1097/ju.0000000000003892 | PMID 38421253 Get It

Antimicrobial susceptibilities of Campylobacter fetus: report from a reference laboratory
Zhang, M. , Melton, Tanner A., Akhtar, Haris, Shah, Aditya , Schuetz, Audrey N. , Clement, Josh , Stevens, Ryan W. , Zhang, Ming May , Schuetz, Audrey N , Stevens, Ryan W , Akhtar, Haris

Mayo Clinic

Journal of Clinical Microbiology | February 29, 2024 | Volume: 62 | Issue: 4 | Pages: No page available

10.1128/jcm.01447-23 | PMID 38421164 Get It

ABSTRACT Campylobacter fetus is known to cause human disease, particularly in elderly and immunocompromised hosts. There are limited published data for antimicrobial susceptibility patterns with this organism, and no interpretive criteria are available. We reviewed antimicrobial susceptibilities of C. fetus isolates tested at a tertiary care center and reference laboratory over an 11-year period. C. fetus isolates from patients treated at Mayo Clinic and those sent as referrals for identification and susceptibility were included. Antimicrobial susceptibility testing was performed using agar dilution for ciprofloxacin, doxycycline, erythromycin, gentamicin, meropenem, and tetracycline. Geographic distribution, culture source, organism minimal inhibitory concentration (MIC) distributions, and MIC 50 and MIC 90 were examined. Excluding duplicates, 105 unique isolates were identified from 110 positive cultures. Blood cultures represented the most common source, followed by body fluids, skin and soft tissue, and central nervous system. Gentamicin and meropenem had favorable MIC 50 and MIC 90 of 1 µg/mL. Ciprofloxacin demonstrated an MIC 50 of 1 µg/mL; however, the MIC 90 was >2 µg/mL. Erythromycin demonstrated MIC 50 and MIC 90 of 2 µg/mL. Tetracycline and doxycycline were tested on a limited number of isolates and showed a wide range of MICs. Gentamicin and meropenem demonstrated favorable MICs in C. fetus isolates. These may represent therapeutic options for consideration in serious C. fetus infections, pending susceptibility results. Ciprofloxacin, which showed variable results, may be more appropriate for use only after susceptibility testing. C. fetus interpretive criteria are needed to aid clinicians in selection of both empiric and definitive therapies. IMPORTANCE Our findings contribute to the scant literature on Campylobacter fetus antimicrobial susceptibility test results. We used a reference test method of agar dilution and provide MICs for a large number of organisms and antimicrobial agents.
New onset refractory status epilepticus: Summary of the NORSE Institute roundtable during the 2023 American Epilepsy Society meeting, Orlando, Florida
Hanin, Aurélie , Eschbach, Krista , Gofton, Teneille , Howe, Charles L. , Lai, Yi‐Chen , Koh, Sookyong , Shen, Haying, Hirsch, Lawrence J. , Gofton, Teneille E , Howe, Charles L , Lai, Yi-Chen , Hirsch, Lawrence J , Eschbach, Krista , Hanin, Aurelie , Gopaul, Margaret

Mayo Clinic

Epilepsia | February 29, 2024 | Volume: 65 | Issue: 4 | Pages: 1145-1146

10.1111/epi.17934 | PMID 38421053 Get It

Improved Risk-Stratification Scheme for Mismatch-Repair Proficient Stage II Colorectal Cancers Using the Digital Pathology Biomarker QuantCRC
Wu, Christina , Pai, Reetesh K. , Kosiorek, Heidi , Banerjee, Imon , Pfeiffer, Ashlyn , Hartley, Christopher , Graham, Rondell P. , Sonbol, Mohamad Bassam , Bekaii‐Saab, Tanios , Patel, Bhavik N. , Shivji, Sameer , Conner, James , Swallow, Carol J. , Cyr, David P. , Kirsch, Richard , Pai, Rish K. , Hagen, Catherine E , Hartley, Christopher P , Graham, Rondell P , Sonbol, Mohamad B , Bekaii-Saab, Tanios S , Xie, Hao , Sinicrope, Frank A , Patel, Bhavik , Westerling-Bui, Thomas , Shivji, Sameer , Conner, James , Swallow, Carol , Savage, Paul , Cyr, David P , Kirsch, Richard , Pai, R K , Banerjee, Imon , Kosiorek, Heidi E , Wu, Christina , Hagen, Catherine E. , Xie, Hao , Sinicrope, Frank A. , Savage, Paul

Mayo Clinic

Clinical Cancer Research | February 29, 2024 | Volume: 30 | Issue: 9 | Pages: 1811-1821

10.1158/1078-0432.ccr-23-3211 | PMID 38421684 Get It

Abstract Purpose: There is a need to improve current risk stratification of stage II colorectal cancer to better inform risk of recurrence and guide adjuvant chemotherapy. We sought to examine whether integration of QuantCRC, a digital pathology biomarker utilizing hematoxylin and eosin–stained slides, provides improved risk stratification over current American Society of Clinical Oncology (ASCO) guidelines. Experimental Design: ASCO and QuantCRC-integrated schemes were applied to a cohort of 398 mismatch-repair proficient (MMRP) stage II colorectal cancers from three large academic medical centers. The ASCO stage II scheme was taken from recent guidelines. The QuantCRC-integrated scheme utilized pT3 versus pT4 and a QuantCRC-derived risk classification. Evaluation of recurrence-free survival (RFS) according to these risk schemes was compared using the log-rank test and HR. Results: Integration of QuantCRC provides improved risk stratification compared with the ASCO scheme for stage II MMRP colorectal cancers. The QuantCRC-integrated scheme placed more stage II tumors in the low-risk group compared with the ASCO scheme (62.5% vs. 42.2%) without compromising excellent 3-year RFS. The QuantCRC-integrated scheme provided larger HR for both intermediate-risk (2.27; 95% CI, 1.32–3.91; P = 0.003) and high-risk (3.27; 95% CI, 1.42–7.55; P = 0.006) groups compared with ASCO intermediate-risk (1.58; 95% CI, 0.87–2.87; P = 0.1) and high-risk (2.24; 95% CI, 1.09–4.62; P = 0.03) groups. The QuantCRC-integrated risk groups remained prognostic in the subgroup of patients that did not receive any adjuvant chemotherapy. Conclusions: Incorporation of QuantCRC into risk stratification provides a powerful predictor of RFS that has potential to guide subsequent treatment and surveillance for stage II MMRP colorectal cancers.
MRI Surveillance and Breast Cancer Mortality in Women With BRCA1 and BRCA2 Sequence Variations
Møller, Pål , Eisen, Andrea , Peck, Larissa , Bordeleau, Louise , Zakalik, Dana , Stempa, Klaudia , Dungan, J.S., Cullinane, Carey A., Olopade, Olufunmilayo I. , Metcalfe, Kelly , Sun, Ping , Narod, Steven A. , Sweet, Kevin , Velsher, Lea, McCuaig, Jeanna , Panchal, Seema, Poll, Aletta, Lemire, Edmond G., Serfas, Kim, Costalas, Josephine Wagner, Blum, Joanne L. , Olopade, Olufunmilayo I , Metcalfe, Kelly A , Eisen, Andrea , Bordeleau, Louise , Lubiński, Jan , Kotsopoulos, Joanne , Pal, Tuya , Karlan, Beth Y. , Aeilts, Amber M. , Eng, Charis , Foulkes, William D. , Tung, Nadine , Couch, Fergus J. , Fruscio, Robert , Cajal, Teresa Ramón y , Singer, Christian F. , Neuhausen, Susan L. , Cybulski, Cezary , Gronwald, Jacek , Huzarski, Tomasz , Senter, Leigha , Saal, Howard M. , Armel, Susan Randall , Reilly, Richard B. , Cohen, Stephanie A.

Mayo Clinic

JAMA Oncology | February 29, 2024 | Volume: 10 | Issue: 4 | Pages: 493

10.1001/jamaoncol.2023.6944 | PMID 38421676 Get It

Importance Magnetic resonance imaging (MRI) surveillance is offered to women with a pathogenic variant in the BRCA1 or BRCA2 gene who face a high lifetime risk of breast cancer. Surveillance with MRI is effective in downstaging breast cancers, but the association of MRI surveillance with mortality risk has not been well defined. Objective To compare breast cancer mortality rates in women with a BRCA1 or BRCA2 sequence variation who entered an MRI surveillance program with those who did not. Design, Setting, and Participants Women with a BRCA1 or BRCA2 sequence variation were identified from 59 participating centers in 11 countries. Participants completed a baseline questionnaire between 1995 and 2015 and a follow-up questionnaire every 2 years to document screening histories, incident cancers, and vital status. Women who had breast cancer, a screening MRI examination, or bilateral mastectomy prior to enrollment were excluded. Participants were followed up from age 30 years (or the date of the baseline questionnaire, whichever was later) until age 75 years, the last follow-up, or death from breast cancer. Data were analyzed from January 1 to July 31, 2023. Exposures Entrance into an MRI surveillance program. Main Outcomes and Measures Cox proportional hazards modeling was used to estimate the hazard ratios (HRs) and 95% CIs for breast cancer mortality associated with MRI surveillance compared with no MRI surveillance using a time-dependent analysis. Results A total of 2488 women (mean [range] age at study entry 41.2 [30-69] years), with a sequence variation in the BRCA1 (n = 2004) or BRCA2 (n = 484) genes were included in the analysis. Of these participants, 1756 (70.6%) had at least 1 screening MRI examination and 732 women (29.4%) did not. After a mean follow-up of 9.2 years, 344 women (13.8%) developed breast cancer and 35 women (1.4%) died of breast cancer. The age-adjusted HRs for breast cancer mortality associated with entering an MRI surveillance program were 0.20 (95% CI, 0.10-0.43; P < .001) for women with BRCA1 sequence variations and 0.87 (95% CI, 0.10-17.25; P = .93) for women with BRCA2 sequence variations. Conclusion and Relevance Results of this cohort study suggest that among women with a BRCA1 sequence variation, MRI surveillance was associated with a significant reduction in breast cancer mortality compared with no MRI surveillance. Further studies of women with BRCA2 sequence variations are needed to ascertain these women obtain the same benefits associated with MRI surveillance.
Salvage Therapy for Prostate Cancer: AUA/ASTRO/SUO Guideline Part III: Salvage Therapy After Radiotherapy or Focal Therapy, Pelvic Nodal Recurrence and Oligometastasis, and Future Directions
Morgan, Todd M. , Boorjian, Stephen A. , Buyyounouski, Mark K. , Chapin, Brian F. , Chen, David Y.T. , Jacene, Heather A. , Kim, Sennett K., Kirkby, Erin, Nathanson, B.J., Posadas, Edwin M. , Morgan, Todd M , Cheng, Heather H. , Chou, Roger , Kamran, Sophia C. , Luckenbaugh, Amy N. , Nathanson, Ben J., Nyame, Yaw A. , Tran, Phuoc T , Chen, Ronald C.

Mayo Clinic

Journal of Urology | February 29, 2024 | Volume: 211 | Issue: 4 | Pages: 526-532

10.1097/ju.0000000000003890 | PMID 38421252 Get It

Should we operate on patients with acute type A aortic dissection who present with cardiopulmonary resuscitation?
Beckmann, Erik , Martens, Andreas , Krueger, Heike, Korte, Wilhelm, Shrestha, Pamila, Kaufeld, Tim , Shrestha, Malakh

Mayo Clinic

European Journal of Cardio-Thoracic Surgery | February 29, 2024 | Volume: 65 | Issue: 3 | Pages: No page available

10.1093/ejcts/ezae046 | PMID 38420648 Get It

Abstract OBJECTIVES Acute aortic dissection type A (AADA) is a life-threatening medical emergency. Emergent surgical repair is the gold standard but mortality remains high. Mortality is even higher in patients who arrive at the hospital in poor condition, especially after cardiopulmonary resuscitation (CPR). This study was designed to analyse the outcome of patients who underwent surgery for AADA and who require preoperative CPR. METHODS Between 2000 and 2023, 810 patients underwent emergent surgery for AADA at our centre. Of these, 63 had preoperative CPR. We performed a retrospective analysis with follow-up. RESULTS Mean age was 64 ± 13 years and 37 (59%) patients were male. Further, 50 (79%) patients had preoperative intubation, and 54 (86%) had pericardial effusion. Twenty-four (38%) patients had out-of-hospital CPR, 19 (30%) required CPR in hospital and 20 (32%) needed CPR in the operating room. Successful CPR with return of spontaneous circulation was achieved in 41 (65%) patients, and 22 (35%) underwent emergent surgery under ongoing CPR. The median time of CPR was 10 (interquartile range 12) min, and the median time from onset of symptoms to start of the operation was 5.5 (interquartile range 4.8) h. The majority of patients underwent ascending aortic replacement with hemiarch repair (n = 37, 59%). Further, 26 (41%) patients underwent full root replacement. Another 15 (24%) patients underwent total arch repair with or without (frozen) elephant trunk repair. Postoperative stroke was present in 8 (13%) patients. The 30-day mortality was 29 (46%). The 30-day mortality of patients with preoperative intubation was not significantly higher (n = 15/28, 54%, P = 0.446). The 1-, 5- and 10-year survival rates of the entire group were 42, 39 and 36%. CONCLUSIONS Early mortality for patients undergoing surgery for AADA with preoperative CPR is extremely high (almost 50%). However, this means that also ∼50% of patients benefit from surgery despite poor preoperative prognosis. Patients with preoperative intubation after CPR and unknown neurological condition should also undergo surgery. Patients who survive the initial operation for AADA have acceptable long-term survival. Emergent surgery should be offered for all patients with AADA regardless of the preoperative condition, even after CPR.