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571 citation(s) found for "Wagner, M".

AOFAS Position Statement Regarding Patient-Reported Outcome Measures
Kitaoka, Harold B. , Meeker, James E. , Phisitkul, Phinit, Adams, Samuel B. , Kaplan, Jonathan , Wagner, Emilio

Mayo Clinic

Foot & Ankle International | October 31, 2018 | Volume: 39 | Issue: 12 | Pages: 1389-1393

10.1177/1071100718809066 | PMID 30379085 Get It

Outcome measures evaluate various aspects of patient health, and when appropriately utilized can provide valuable information in both clinical practice and research settings. The orthopedic community has placed increasing emphasis on patient-reported outcome measures, recognizing their value for understanding patients’ perspectives of treatment outcomes. Patient-reported outcomes are information directly reported by patients regarding their perceptions of health, quality of life, or functional status without interpretation by healthcare providers. The American Orthopaedic Foot & Ankle Society (AOFAS) supports the use of validated patient-reported outcome (PRO) instruments to assess patient general health, functional status, and outcomes of treatment. It is not possible to recommend a single instrument to collect quality orthopedic data as the selection is dependent on the population being examined and the question being asked. We support the use of the PROMIS Physical Function Computerized Adaptive Test (PF CAT) or Lower Extremity Computerized Adaptive Test (LE CAT), which can be assessed with other domains such as Pain Interference. In addition, a disease-specific measure can be used when available.
Proposed surgical technique to facilitate targeted reinnervation of the infraspinatus: A cadaveric feasibility study
Wyles, Cody C. , Maldonado, Andrés A. , Wagner, Eric R. , Lachman, Nirusha , Spinner, Robert J. , Lachman, Nirusha , Spinner, Robert J , Wagner, Eric R , Wyles, Cody C , Houdek, Matthew T. , Maldonado, Andres A.

Mayo Clinic

Clinical Anatomy | October 26, 2018 | Volume: 32 | Issue: 1 | Pages: 131-136

10.1002/ca.23310 | PMID 30362668 Get It

Restoration of shoulder lateral rotation remains a significant challenge following brachial plexus injury. Transfer of the accessory nerve to suprascapular nerve (SSN) has been widely performed, although with generally poor outcomes for lateral rotation. A recent report suggested a selective infraspinatus reinnervation technique using a radial nerve branch for SSN transfer. This cadaveric study was performed in 7 specimens (14 shoulders). We present technical modifications to achieve additional length to the recipient nerve (suprascapular) that would facilitate direct repair. Key elements of the technique are (1) isolation of the SSN immediately distal to its motor branch to supraspinatus near the superior transverse scapular ligament; and (2) delivery of the transected SSN through the spinoglenoid notch and deep to the infraspinatus for emergence in the infraspinatus‐teres minor interval. Nerve overlap of at least 21 mm was observed in all 14 dissected shoulders between the harvested SSN and radial nerve branches. The mean nerve overlap between harvested branches was 26 mm (range 21–32 mm). The mean harvested SSN length was 59 mm (range 46–80 mm). The mean length of the harvested radial nerve branch was 72 mm (range 65–85 mm). No measurements were significantly different between left and right shoulders or between males and females (smallest P value = 0.1249). Nerve diameter of the two harvested branches was judged to be appropriately compatible for surgical coaptation in all 14 dissected shoulders. We present a variation on a described technique to increase recipient suprascapular nerve length. Additional length of the recipient nerve is achieved through utilization of a more proximal dissection of the suprascapular nerve near the level of the superior transverse scapular ligament and delivering the nerve through the teres minor‐infraspinatus interval. These surgical modifications are of clinical interest when selective reinnervation of the infraspinatus muscle is considered. We believe such a targeted approach can potentially increase shoulder lateral rotation function. Clin. Anat. 32:131–136, 2019. © 2018 Wiley Periodicals, Inc.
Arthroscopic Treatment of Massive Posterosuperior Rotator Cuff Tears
Wagner, Eric R. , Welp, Kathryn M., Elhassan, Bassem T. , Higgins, Laurence D. , Warner, Jon J.P. , Warner, Jon J P , Wagner, Eric R , Woodmass, Jarret Murray , Chang, Michelle J.

Mayo Clinic

JBJS Reviews | September 28, 2018 | Volume: 6 | Issue: 9 | Pages: e3-e3

10.2106/jbjs.rvw.17.00199 | PMID 30204644 Get It

* Massive rotator cuff tears that are treated nonoperatively demonstrate increases in tear size, fatty infiltration, muscular atrophy, and arthritis. * The pooled retear rate following complete repair of massive rotator cuff tears is 79%. * Absorbable and nonabsorbable graft augmentation following rotator cuff repair can reduce the retear rate and improve functional outcomes. * Irreparable tears can be predicted preoperatively by evaluating the degree of fatty infiltration, muscular atrophy, and tendon length. * Latissimus dorsi transfer, lower trapezius transfer, and superior capsular reconstruction provide improvements in terms of pain, range of motion, and function in patients with irreparable tears.
The Selinexor in Advanced Liposarcoma (SEAL) study: A phase 2/3, multicenter, randomized, double blind study of selinexor versus placebo in patients with advanced, unresectable, dedifferentiated liposarcoma (DDLS).
Gounder, Mrinal M. , Wagner, Andrew J. , Somaiah, Neeta , Riedel, Richard F. , Attia, Steven , Razak, Albiruni R. Abdul, Cranmer, Lee D. , Okuno, Scott H. , Choe-Juliak, Cassandra, Shacham, Sharon, Kauffman, Michael , Chawla, Sant P. , Riedel, Richard F , Schwartz, Gary K. , Milhem, Mohammed

Mayo Clinic

Journal of Clinical Oncology | September 6, 2018 | Volume: 34 | Issue: 15_suppl | Pages: TPS11072-TPS11072

10.1200/jco.2016.34.15_suppl.tps11072 Get It

E3311 trial of transoral surgery for oropharynx cancer: Implementation of a novel surgeon credentialing and quality assurance process.
Weinstein, Gregory S., Mehra, Ranee , García, Joaquín J. , Chung, Christine H. , Gillison, Maura L. , Ringash, Jolie , Méndez, Eduardo, Richmon, Jeremy D. , Magnuson, Scott, Smith, Russel B., Thomas, Giovana R. , Richmon, Jeremy D , Li, Shuli , Ferris, Robert L. , Holsinger, F. Christopher , Quon, Harry , Wagner, Lynne I. , Lewin, Jan S. , Ridge, John Andrew , Bell, R. Bryan , Burtness, Barbara

Mayo Clinic

Journal of Clinical Oncology | September 6, 2018 | Volume: 34 | Issue: 15_suppl | Pages: 6054-6054

10.1200/jco.2016.34.15_suppl.6054 Get It

Hand-foot skin reaction (HFSR) and outcomes in the phase 3 CORRECT trial of regorafenib for metastatic colorectal cancer (mCRC).
Huang, Liping , Wagner, Andrea, Grothey, Axel , Wagner, Andrea, Cutsem, Eric Van

Mayo Clinic

Journal of Clinical Oncology | September 6, 2018 | Volume: 35 | Issue: 15_suppl | Pages: 3551-3551

10.1200/jco.2017.35.15_suppl.3551 Get It

3551 Background: Cutaneous toxicity is a known adverse effect of multikinase inhibitors and has been associated with clinical outcomes (Granito 2016). In the phase 3 CORRECT trial (NCT01103323), the multikinase inhibitor regorafenib significantly improved overall survival (OS) vs placebo in patients with mCRC (hazard ratio [HR] 0.77, 95% CI 0.64, 0.94; 1-sided P = 0.0052). This retrospective analysis explored whether HFSR was associated with outcomes in CORRECT. Methods: Patients randomized to receive regorafenib 160 mg/day during the first 3 weeks of each 4-week cycle were divided into subgroups based on whether or not they had HFSR. Estimates of OS and progression-free survival (PFS) (95% CI) were calculated using the Kaplan–Meier method. Patients who were randomized, but not treated, were included in the no HFSR group for the analysis of survival. Results: Of the 505 randomized patients, 500 received at least one dose of regorafenib. Among the treated patients, 47% (n = 235) had HFSR of any grade and 17% (n = 83) had HFSR grade 3. Of the patients who had HFSR, 69% (n = 162) had their first HFSR event (any grade) during the first treatment cycle. There was some imbalance in baseline characteristics between groups (Table). Survival was improved in patients who had HFSR at any time vs those who did not (Table). The OS benefit was also observed in patients who had the first HFSR event during Cycle 1 vs those who did not (median OS 7.2 vs 5.7 months; HR 0.66, 95% CI 0.51, 0.87). Conclusions: This post-hoc exploratory analysis suggests that patients who had HFSR had a greater treatment benefit from regorafenib. Since HFSR and survival are post-baseline assessments, results may be confounded by baseline factors or other unknown factors. Clinical trial information: NCT01103323. [Table: see text]
Phase II study of alisertib, irinotecan, and temozolomide in children with relapsed and refractory neuroblastoma: A report from the New Approaches to Neuroblastoma Therapy (NANT) consortium.
DuBois, Steven G. , Marachelian, Araz , Fox, Elizabeth , Kudgus, Rachel A. , Groshen, Susan , Malvar, Jemily , Wagner, Lars M. , Hawkins, Randall A., Lai, Hollie , Boucher, Najee, Czarnecki, Scarlett, Mossé, Yaël P. , Reid, Joel M. , Bagatell, Rochelle , Maris, John M. , Courtier, Jesse , Goodarzian, Fariba , Shimada, Hiroyuki , Tsao-Wei, Denice D , Matthay, Katherine K.

Mayo Clinic

Journal of Clinical Oncology | September 6, 2018 | Volume: 34 | Issue: 15_suppl | Pages: 10556-10556

10.1200/jco.2016.34.15_suppl.10556 Get It

Effect of bortezomib on complete remission (CR) rate when added to bendamustine-rituximab (BR) in previously untreated high-risk (HR) follicular lymphoma (FL): A randomized phase II trial of the ECOG-ACRIN Cancer Research Group (E2408).
Evens, Andrew M. , Gascoyne, Randy D. , Quon, Andrew , Ansell, Stephen M. , Petrich, Adam M., Chang, Julie , O’Brien, Timothy E., Cheema, P. , Cescon, Terrence P., Sturtz, Keren , Evens, Andrew M , Hong, Fangxin , Habermann, Thomas M. , Advani, Ranjana H. , Witzig, Thomas E. , Wagner, Lynne I. , Kahl, Brad S.

Mayo Clinic

Journal of Clinical Oncology | September 6, 2018 | Volume: 34 | Issue: 15_suppl | Pages: 7507-7507

10.1200/jco.2016.34.15_suppl.7507 Get It

SU2C-SARC032: A phase II randomized controlled trial of neoadjuvant pembrolizumab with radiotherapy and adjuvant pembrolizumab for high-risk soft tissue sarcoma.
Riedel, Richard F. , Brigman, Brian E. , Attia, Steven , Meyer, Christian F. , Schuetze, Scott M. , Dickson, Mark A. , Hartner, Lee , Tinoco, Gabriel , Tine, Brian Andrew Van, Wagner, Andrew J. , Kirsch, David G. , Riedel, Richard F , Tinoco, Gabriel , Mowery, Yvonne Marie , Ballman, Karla V. , Burgess, Melissa , Chmielowski, Bartosz , Milhem, Mohammed , Reinke, Denise K.

Mayo Clinic

Journal of Clinical Oncology | September 5, 2018 | Volume: 36 | Issue: 15_suppl | Pages: TPS11588-TPS11588

10.1200/jco.2018.36.15_suppl.tps11588 Get It

Phase 2 results of selinexor in advanced de-differentiated (DDLS) liposarcoma (SEAL) study: A phase 2/3, randomized, double blind, placebo controlled cross-over study.
Gounder, Mrinal M. , Somaiah, Neeta , Attia, Steven , Chawla, Sant P. , Villalobos, Víctor M. , Riedel, Richard F. , Wagner, Andrew J. , Mudenda, Boyd, Sadanowicz, Mara , Shah, Jatin J., Shacham, Sharon, Kauffman, Michael , Razak, Albiruni Ryan Abdul, Riedel, Richard F , Chmielowski, Bartosz , Burgess, Melissa , Schwartz, Gary K. , Mehren, Margaret von , Choy, Edwin , Verma, Shailendra , Li, Lingling

Mayo Clinic

Journal of Clinical Oncology | September 5, 2018 | Volume: 36 | Issue: 15_suppl | Pages: 11512-11512

10.1200/jco.2018.36.15_suppl.11512 Get It