Citations

Mayo Clinic

Showing 10 of 108506 citations.

Precision Oncology: An Overview
Garraway, Levi A. , Verweij, Jaap, Ballman, Karla V.

Journal of Clinical Oncology | April 15, 2013 | Volume: 31 | Issue: 15 | Pages: 1803-1805

10.1200/jco.2013.49.4799 | PMID 23589545 Get It

Efatutazone, an Oral PPAR-γ Agonist, in Combination With Paclitaxel in Anaplastic Thyroid Cancer: Results of a Multicenter Phase 1 Trial
Smallridge, Robert C., Copland, John A. , Brose, Marcia S. , Wadsworth, J. Trad , Houvras, Yariv , Menefee, Michael E., Bible, Keith C. , Shah, Manisha H. , Gramza, Ann W., Klopper, Joshua , Marlow, Laura A. , Roemeling, Reinhard von, Heckman, Michael G. , Marlow, Laura

The Journal of Clinical Endocrinology & Metabolism | April 15, 2013 | Volume: 98 | Issue: 6 | Pages: 2392-2400

10.1210/jc.2013-1106 | PMID 23589525 Get It

Improved Resident Physician Confidence With Advance Care Planning After an Ambulatory Clinic Intervention
Tung, Ericka E. , Verdoorn, Brandon P. , Mauck, Karen F. , Post, Jason , Thomas, Matthew R. , Bundrick, John B., Jaeger, Thomas M. , Cha, Stephen S., Thomas, Kris G., Wieland, Mark L. , Cha, Stephen S.

American Journal of Hospice and Palliative Medicine® | April 15, 2013 | Volume: 31 | Issue: 3 | Pages: 275-280

10.1177/1049909113485636 | PMID 23588577 Get It

Many primary care providers feel uncomfortable discussing end-of-life care. The aim of this intervention was to assess internal medicine residents’ advance care planning (ACP) practices and improve residents’ ACP confidence. Residents participated in a facilitated ACP quality improvement workshop, which included an interactive presentation and chart audit of their own patients. Pre- and postintervention surveys assessed resident ACP-related confidence. Only 24% of the audited patients had an advance directive (AD), and 28% of the ACP-documentation was of no clinical utility. Terminally ill patients (odds ratio 2.8, P < .001) were more likely to have an AD. Patients requiring an interpreter were less likely to have participated in ACP. Residents reported significantly improved confidence with ACP and identified important training gaps. Future studies examining the impact on ACP quality are needed.
Oxytocin and vasopressin
Benarroch, Eduardo E.

Neurology | April 15, 2013 | Volume: 80 | Issue: 16 | Pages: 1521-1528

10.1212/wnl.0b013e31828cfb15 | PMID 23589638 Get It

Favorable Stage Distribution in the NELSON Trial
Midthun, David E. , Gould, Michael K.

American Journal of Respiratory and Critical Care Medicine | April 15, 2013 | Volume: 187 | Issue: 8 | Pages: 792-793

10.1164/rccm.201302-0314ed | PMID 23586379 Get It

Management of unruptured intracranial aneurysms
Williams, Lindsy N., Brown, Robert D.

Neurology Clinical Practice | April 15, 2013 | Volume: 3 | Issue: 2 | Pages: 99-108

10.1212/cpj.0b013e31828d9f6b | PMID 23914319 Get It

Targeting deregulated epigenetic control in cancer
Zaidi, Sayyed K. , Wijnen, André J. van , Lian, Jane B. , Stein, Janet L. , Stein, Gary S. , van Wijnen, Andre J

Journal of Cellular Physiology | April 15, 2013 | Volume: 228 | Issue: 11 | Pages: 2103-2108

10.1002/jcp.24387 | PMID 23589100 Get It

AbstractCancer is a multifaceted disease that involves acquisition of genetic mutations, deletions, and amplifications as well as deregulation of epigenetic mechanisms that fine‐tune gene regulation. Key epigenetic mechanisms that include histone modifications, DNA methylation, and non‐coding RNA‐mediated gene silencing are often deregulated in a variety of cancers. Subnuclear localization of key proteins in the interphase nucleus and bookmarking of genes by lineage commitment factors in mitosis—a new dimension to epigenetic control of fundamental biological processes—is also modified in cancer. In this review, we discuss the various aspects of epigenetic control that are operative in a variety of cancers and their potential for risk assessment, early detection, targeted therapy, and personalized medicine. J. Cell. Physiol. 228: 2103–2108, 2013. © 2013 Wiley Periodicals, Inc.
Defining acceptable limits for the metrological traceability of specific measurands
Bais, Renze, Armbruster, Dave, Jansen, Rob, Klee, George G., Panteghini, Mauro , Passarelli, J, Sikaris, Ken

Clinical Chemistry and Laboratory Medicine | April 15, 2013 | Volume: 51 | Issue: 5 | Pages: 973-979

10.1515/cclm-2013-0122 | PMID 23525873 Get It

Abstract Although manufacturers are compelled by the European IVD Directive, 98/79/EC, to have traceability of the values assigned to their calibrators if suitable higher order reference materials and/or procedures are available, there is still no equivalence of results for many measurands determined in clinical laboratories. The adoption of assays with metrological traceable results will have a significant impact on laboratory medicine in that results will be equivalent across different laboratories and different analytical platforms. The IFCC WG on Allowable Errors for Traceable Results has been formed to define acceptable limits for metrological traceability chains for specific measurands in order to promote the equivalence of patient results. These limits are being developed based on biological variation for the specific measurands. Preliminary investigations have shown that for some measurands, it is possible for manufacturers to assign values to assay calibrators with a measurement uncertainty that allows the laboratory enough combined uncertainty for their routine measurements. However, for other measurands, e.g., plasma sodium, current assays are too imprecise to fulfil limits based on biological variation. Although an alternative approach based on probability theory is being investigated, the most desirable approach would be for industry to improve measurement methods so that they meet clinical requirements.
Hydrogen Sulfide Signaling in the Gastrointestinal Tract
Linden, David R.

Antioxidants & Redox Signaling | April 15, 2013 | Volume: 20 | Issue: 5 | Pages: 818-830

10.1089/ars.2013.5312 | PMID 23582008 Get It

Significance: The current literature regarding the effects of the gaseous signal molecule hydrogen sulfide (H 2 S) in the gastrointestinal system is reviewed. Bacterial, host and pharmaceutical-derived H 2 S are all considered and presented according to the physiological or pathophysiological effects of the gaseous signal molecule. These subjects include the toxicology of intestinal H 2 S with emphasis on bacterial-derived H 2 S, especially from sulfate-reducing bacteria, the role of endogenous and exogenous H 2 S in intestinal inflammation, and the roles of H 2 S in gastrointestinal motility, secretion and nociception. Recent Advances: While its pro- and anti-inflammatory, smooth muscle relaxant, prosecretory, and pro- and antinociceptive actions continue to remain the major effects of H 2 S in this system; recent findings have expanded the potential molecular targets for H 2 S in the gastrointestinal tract. Critical Issues: Numerous discrepancies remain in the literature, and definitive molecular targets in this system have not been supported by the use of competitive antagonism. Future Directions: Future work will hopefully resolve discrepancies in the literature and identify molecular targets and mechanisms of action for H 2 S. It is clear from the current literature that the long-appreciated relationship between H 2 S and the gastrointestinal tract continues to be strong as we endeavor to unravel its mysteries. Antioxid. Redox Signal . 20, 818–830.
A multicenter evaluation of a new therapeutic plasma exchange procedure
Winters, Jeffrey L. , Burgstaler, Edwin A. , Gottschall, Jerome L. , Balogun, Rasheed A. , Houghton, Jaime, Lee, Wanda J., Snyder, Edward L. , Winters, Jeffrey L

Transfusion | April 15, 2013 | Volume: 53 | Issue: 12 | Pages: 3269-3278

10.1111/trf.12189 | PMID 23581280 Get It

BackgroundThe AMICUS (Fenwal, Inc.) was cleared in the United States for platelet (PLT) and plasma collection in 1996 with subsequent clearances for the collection of other blood products. Although not previously used for therapeutic plasma exchange (TPE), new disposables, software, and hardware were developed to enable TPE on the AMICUS.Study Design and MethodsA multicenter, randomized, nonblinded, crossover paired treatment protocol was performed. Thirty patients with orders for at least two TPE procedures were randomly assigned to the AMICUS or the COBE Spectra (TerumoBCT) for the first treatment. Each patient was crossed over to the other device using the same procedure settings from the first procedure. The primary objective compared efficiency of plasma removal (EPR) with secondary objectives of comparing PLT and hemoglobin (Hb) waste plasma content, coagulation factor and complement activation, fluid balance tracking accuracy, procedure length, and adverse events.ResultsThe EPR for the AMICUS (81.9 ± 7.62%) was superior to that of the COBE Spectra (75.2 ± 6.29%; p = 0.00001). The AMICUS also demonstrated statistically higher fluid balance accuracy (99.84%) compared to that of the COBE Spectra (98.83%; p < 0.0001) and a statistically shorter procedure time (103.9 ± 30.8 vs. 110.5 ± 27.1 min, p < 0.001). No significant differences with regard to PLT and Hb content in the waste plasma, change in patient PLT count, or changes in markers of coagulation and complement cascade activation were seen. Frequency and severity of adverse reactions were similar.ConclusionThe AMICUS separator can effectively perform TPE. The AMICUS demonstrated superior plasma removal efficiency compared to the COBE Spectra with no evidence of significant differences in PLT removal, hemolysis, and coagulation or complement activation.