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110 citation(s) found for "Mangold, A R".

Improving Access to Care Through the Establishment of a Local, Teledermatology Network
Costello, Collin M. , Cumsky, Helen J.L., Maly, Connor , Harvey, Jamison A. , Buras, Matthew , Pallagi, Peter J. , Gustaveson, Anna L., Nelson, Steven A. , Pittelkow, Mark R. , Mangold, Aaron R. , Maly, Connor J, Mangold, A R , Buras, Matthew R , Costello, Collin M , Singh, Davinder

Mayo Clinic

Telemedicine and e-Health | October 15, 2019 | Volume: 26 | Issue: 7 | Pages: 935-940

10.1089/tmj.2019.0051 | PMID 31613713 Get It

Supporting the Transition to Practice for Nurse Residents on a Multispecialty Unit
Mangold, Kara , Crockett, Cynthia, Crockett, Cynthia Cindy

Mayo Clinic

Critical Care Nurse | October 1, 2019 | Volume: 39 | Issue: 5 | Pages: 76-79

10.4037/ccn2019165 | PMID 31575598 Get It

Regression of mycosis fungoides with large‐cell transformation following skin biopsy
Besch‐Stokes, Jake , Costello, Collin M. , Bhullar, Puneet , Maly, Connor , DiCaudo, David J. , Pittelkow, Mark R. , Mangold, Aaron R. , Besch-Stokes, J G , Mangold, A R , Costello, Collin M , Rosenthal, Allison

Mayo Clinic

Journal of the European Academy of Dermatology and Venereology | October 1, 2019 | Volume: 34 | Issue: 2 | Pages: No page available

10.1111/jdv.15976 | PMID 31566801 Get It

Uniformly low serum cobalt levels after modular dual-mobility total hip arthroplasties with ceramic heads
Mangold, D. G., Hanssen, Arlen D. , Pagnano, Mark W. , Trousdale, Robert T. , Chalmers, Brian P. , Abdel, Matthew P.

Mayo Clinic

The Bone & Joint Journal | May 31, 2019 | Volume: 101-B | Issue: 6_Supple_B | Pages: 57-61

10.1302/0301-620x.101b6.bjj-2018-1403.r1 | PMID 31146553 Get It

Aims Modular dual-mobility constructs reduce the risk of dislocation after revision total hip arthroplasty (THA). However, questions about metal ions from the cobalt-chromium (CoCr) liner persist, and are particularly germane to patients being revised for adverse local tissue reactions (ALTR) to metal. We determined the early- to mid-term serum Co and Cr levels after modular dual-mobility components were used in revision and complex primary THAs, and specifically included patients revised for ALTR. Patients and Methods Serum Co and Cr levels were measured prospectively in 24 patients with a modular dual-mobility construct and a ceramic femoral head. Patients with CoCr heads or contralateral THAs with CoCr heads were excluded. The mean age was 63 years (35 to 83), with 13 patients (54%) being female. The mean follow-up was four years (2 to 7). Indications for modular dual-mobility were prosthetic joint infection treated with two-stage exchange and subsequent reimplantation (n = 8), ALTR revision (n = 7), complex primary THA (n = 7), recurrent instability (n = 1), and periprosthetic femoral fracture (n = 1). The mean preoperative Co and Cr in patients revised for an ALTR were 29.7 μg/l (2 to 146) and 21.5 μg/l (1 to 113), respectively. Results Mean Co and Cr levels were 0.30 μg/l and 0.76 μg/l, respectively, at the most recent follow-up. No patient had a Co level ≥ 1 μg/l. Only one patient had a Cr level ≥ 1 μg/l. That patient’s Cr level was 12 μg/l at 57 months after revision THA for ALTR (and decreased ten-fold from a preoperative Cr of 113 μg/l). Conclusion At a mean of four years, no patient with a modular dual-mobility construct and ceramic femoral head had elevated Co levels, including seven patients revised specifically for ALTR. While further studies are required, we support the selective use of a modular dual-mobility construct in revision and complex primary THAs for patients at high risk for instability. Cite this article: Bone Joint J 2019;101-B(6 Supple B):57–61.
Impact of standardized templates and skin cancer learning modules for teledermatology consultations
Cumsky, Helen J.L., Maly, Connor , Costello, Collin M. , Buras, Matthew , Ranieri, LeeAnn M., Grover, Michael , Comfere, Nneka I. , Nelson, Steven A. , Pittelkow, Mark R. , Mangold, Aaron R. , Maly, Connor J, Grover, Michael L, Mangold, A R , Buras, Matthew R , Costello, Collin M

Mayo Clinic

International Journal of Dermatology | March 28, 2019 | Volume: 58 | Issue: 12 | Pages: 1423-1429

10.1111/ijd.14437 | PMID 30916785 Get It

AbstractBackgroundLittle research has been done in teledermatology to examine the effects of standardized templates and subject‐specific learning modules.MethodsWe performed a prospective study examining the effects of standardized templates and standardized cutaneous oncology learning modules on teledermatology referrals at Mayo Clinic. This data was then compared to previous teledermatology referrals before standardized templates were adopted.ResultsA total of 42 teledermatology consultations were performed during the 4‐month study period. The use of standardized templates resulted in an absolute reduction in face‐to‐face referrals. Teledermatology consultation increased the absolute diagnostic and management concordance by 26.2% (P = 0.02) and 33.3% (P < 0.01), respectively, and decreased the absolute diagnostic and management discordance by 19.1% (P = 0.03) and 31.0% (P < 0.01), respectively. The largest knowledge gaps were identified in cutaneous oncology. Educational intervention improved theoretical referral rates and confidence in diagnosis and management overall.ConclusionThe implementation of standardized intake templates reduces the rate of face‐to‐face referrals. Teledermatology improves primary care‐based dermatological care and reduces theoretical referral rates.
Survival and Glycemic Control in Patients With Coexisting Melanoma and Diabetes Mellitus
Karlin, Nina J. , Mangold, Aaron R. , Amin, Shailja B , Buras, Matthew , Verona, Patricia M , Cook, Curtiss B. , Mangold, A R , Buras, Matthew R , Kosiorek, Heidi

Mayo Clinic

Future Science OA | March 7, 2019 | Volume: 5 | Issue: 3 | Pages: No page available

10.4155/fsoa-2018-0084 | PMID 30906566 Get It

Chemoprevention agents for melanoma: A path forward into phase 3 clinical trials
Jeter, Joanne, Bowles, Tawnya L. , Curiel‐Lewandrowski, Clara , Filipp, Fabian V. , Geskin, Larisa J. , Brewer, Jerry D., Gershenwald, Jeffrey E. , Chu, Emily Y. , Kirkwood, John M. , Funchain, Pauline , Fisher, David E. , Kendra, Kari , Marghoob, Ashfaq A. , Chen, Suephy C. , Ming, Michael E. , Albertini, Mark R. , Vetto, John T. , Margolin, Kim , Hay, Jennifer L. , Ellis, Darrel L., Kashani–Sabet, Mohammed , Mangold, Aaron R. , Nelson, Kelly C. , Powers, Jennifer G. , Sahni, Debjani, Sekulić, Aleksandar , Sondak, Vernon K. , Wei, Maria L. , Thompson, John A. , Weinstock, Martin A. , Cassidy, Pamela B. , Filipp, Fabian V , Mangold, A R , Funchain, Pauline , Jeter, Joanne , Swetter, Susan M. , ABDEL‐MALEK, ZALFA A. , Arbiser, Jack L. , Box, Neil F. , Pagoto, Sherry , Grossman, Douglas , Markovic, Svetomir N. , Robinson, June K. , Zager, Jonathan S. , Dellavalle, Robert Paul , Leachman, Sancy A.

Mayo Clinic

Cancer | October 5, 2018 | Volume: 125 | Issue: 1 | Pages: 18-44

10.1002/cncr.31719 | PMID 30281145 Get It

Recent progress in the treatment of advanced melanoma has led to unprecedented improvements in overall survival and, as these new melanoma treatments have been developed and deployed in the clinic, much has been learned about the natural history of the disease. Now is the time to apply that knowledge toward the design and clinical evaluation of new chemoprevention agents. Melanoma chemoprevention has the potential to reduce dramatically both the morbidity and the high costs associated with treating patients who have metastatic disease. In this work, scientific and clinical melanoma experts from the national Melanoma Prevention Working Group, composed of National Cancer Trials Network investigators, discuss research aimed at discovering and developing (or repurposing) drugs and natural products for the prevention of melanoma and propose an updated pipeline for translating the most promising agents into the clinic. The mechanism of action, preclinical data, epidemiological evidence, and results from available clinical trials are discussed for each class of compounds. Selected keratinocyte carcinoma chemoprevention studies also are considered, and a rationale for their inclusion is presented. These data are summarized in a table that lists the type and level of evidence available for each class of agents. Also included in the discussion is an assessment of additional research necessary and the likelihood that a given compound may be a suitable candidate for a phase 3 clinical trial within the next 5 years.
INPP5a expression as a prognostic marker in cutaneous squamous cell carcinoma (cSCC).
Liang, Helen J, DiCaudo, David J. , Schmidt, Jessica, Pittelkow, Mark R. , Sekulić, Aleksandar , Mangold, Aaron R. , Mangold, A R , Liang, Helen J

Mayo Clinic

Journal of Clinical Oncology | September 5, 2018 | Volume: 36 | Issue: 15_suppl | Pages: e21567-e21567

10.1200/jco.2018.36.15_suppl.e21567 Get It

Reverse Shoulder Arthroplasty With Proximal Humeral Replacement for the Management of Massive Proximal Humeral Bone Loss
Lee, Julia , Mangold, Devin R., Cofield, Robert H. , Sperling, John W. , Shukla, Dave R. , Sánchez‐Sotelo, Joaquín

Mayo Clinic

Journal of Shoulder and Elbow Arthroplasty | June 1, 2018 | Volume: 2 | Issue: No issue available | Pages: No page available

10.1177/2471549218779845 Get It

Background Substantial proximal humeral bone loss may compromise reverse shoulder arthroplasty secondary to limited implant support, insufficient soft tissue tension due to shortening, lack of attachment sites for the posterosuperior cuff when present, and lack of lateral offset of the deltoid. In these circumstances, use of a proximal humeral replacement may be considered. Patients/Methods Between 2012 and 2014, 34 consecutive reverse shoulder arthroplasties were performed using a proximal humeral replacement system. The indications were failed shoulder arthroplasty (15), oncology reconstruction (9), humeral malunion/nonunion (7), prior resection arthroplasty (2), and intraoperative fracture (1). All patients were included in the survival analysis. Twenty-two patients with minimum 2-year follow-up were included in analysis of clinical results. Results Among the cohort of 34 patients, there were 8 additional reoperations: humeral loosening (3), periprosthetic fracture (2), irrigation and debridement (2), and glenoid loosening (1). Humeral component loosening occurred exclusively in patients undergoing revision shoulder arthroplasty. The 4 patients had an average 3.75 prior procedures before the proximal humeral replacement. Two of the revisions were from cemented to uncemented stems. Among the 23 patients with minimum 2-year follow-up, there was significant improvement in pain scores (4.1 vs 0.6), forward elevation (31 vs 109) degrees, and 81% were satisfied. Conclusion Use of a proximal humeral replacement when performing a reverse shoulder arthroplasty in the complex setting of substantial proximal humerus bone loss provides good clinical results and a particularly low dislocation rate. However, the rate of loosening of the humeral component in the revision setting suggests that proximal humeral replacement components should be cemented when revising a previously cemented stem. IRB 16-006966.
The Use of Central Pathology Review With Digital Slide Scanning in Advanced-stage Mycosis Fungoides and Sézary Syndrome
Gru, Alejandro A. , Pulitzer, Melissa , Guitart, Joan , Wood, Gary S. , Cerroni, Lorenzo , Pawade, Joya, Schaffer, András , Pincus, Laura B. , Tetzlaff, Michael T. , Scarisbrick, Julia , Mangold, Aaron R. , DiCaudo, David J. , Shinohara, Michi M. , Hong, Eric, Horton, Bethany J. , Mangold, A R , Gru, Alejandro , Shinohara, M M , Kim, Jinah , Battistella, Maxime , Kempf, Werner , Willemze, Rein , Querfeld, Christiane , Duvic, Madeleine , Porcu, Pierluigi , Kim, Youn H

Mayo Clinic

American Journal of Surgical Pathology | March 15, 2018 | Volume: 42 | Issue: 6 | Pages: 726-734

10.1097/pas.0000000000001041 | PMID 29543675 Get It

This pathology PILOT study aims to define the role and feasibility of centralized pathology review in a cohort of 75 patients from different centers in the United States and Europe using digital slide scanning. The pathologic material from 75 patients who had been diagnosed with mycosis fungoides/Sézary syndrome and were clinically staged as IIb or above was retrieved from 11 participating centers. Each pathology reviewer was provided with the pathologic diagnosis (by the referring pathologist), and the following list of histopathologic criteria (presence or absence) from the initial report: epidermotropism, folliculotropism (FT), large cell transformation, syringotropism, and granulomas. Patients with advance stage were selected for this study as this is a population where there is significant variability in the diagnosis of pathologic prognostic and predictive biomarkers. The slides were digitally scanned with an Aperio scanner and consensus review of cases occurred when major or minor discrepancies between the referral diagnosis and central pathology review occurred. Among the 75 cases, 70 (93.3%) had a final consensus diagnosis between the 3 central review pathologists. The overall agreement between the consensus review and the referring pathologist was 60%. The overall agreement was also higher between the reviewers and consensus review, compared with the referring pathologist and consensus. 65.3% of cases had some type of discrepancy (major or minor) between the outside and consensus review. Major discrepancies were seen in 34 of 73 cases (46.6%; 73 cases indicated a yes or no response). Minor discrepancies were seen in 32 of 75 (42.7%) of cases. Most of the major discrepancies were accounted by a difference in interpretation in the presence or absence of large cell transformation or FT. Most minor discrepancies were explained by a different interpretation in the expression of CD30. We found digital slide scanning to be a beneficial, reliable, and practical for a methodical approach to perform central pathology review in the context of a large clinical prospective study.