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368 citation(s) found for "Wolf, DM".

Effect of High-Grade Preoperative Knee Laxity on Anterior Cruciate Ligament Reconstruction Outcomes
Magnussen, Robert A., Reinke, Emily K. , Huston, Laura J. , Group, MOON, Hewett, Timothy E. , Andrish, Jack T. , Jones, Morgan H. , Parker, Richard D., McCarty, Eric C. , Marx, Robert G. , Amendola, Annunziato , Wolf, Brian R. , Flanigan, David C. , Kaeding, Christopher C. , Brophy, Robert H. , Matava, Matthew J. , Wright, Rick W. , Dunn, Warren R. , Magnussen, Robert A. , Group, MOON, Spindler, Kurt P , Brophy, Robert H. , Jones, Morgan H , McCarty, Eric C

Mayo Clinic

The American Journal of Sports Medicine | August 1, 2016 | Volume: 44 | Issue: 12 | Pages: 3077-3082

10.1177/0363546516656835 | PMID 27480978 Get It

Background: Knee laxity in the setting of suspected anterior cruciate ligament (ACL) injury is frequently assessed through physical examination using the Lachman, pivot-shift, and anterior drawer tests. The degree of laxity noted on these examinations may influence treatment decisions and prognosis. Hypothesis: Increased preoperative knee laxity would be associated with increased risk of subsequent revision ACL reconstruction and worse patient-reported outcomes 2 years postoperatively. Study Design: Cohort study; Level of evidence, 2. Methods: From an ongoing prospective cohort study, 2333 patients who underwent primary isolated ACL reconstruction without collateral or posterior cruciate ligament injury were identified. Patients reported by the operating surgeons as having an International Knee Documentation Committee (IKDC) grade D for Lachman, anterior drawer, or pivot-shift examination were classified as having high-grade laxity. Multiple logistic regression modeling was used to evaluate whether having high-grade preoperative laxity was associated with increased odds of undergoing revision ACL reconstruction within 2 years of the index procedure, controlling for patient age, sex, Marx activity level, level of competition, and graft type. Multiple linear regression modeling was used to evaluate whether having high-grade preoperative laxity was associated with worse IKDC score or Knee injury and Osteoarthritis Outcome Score Knee-Related Quality of Life subscale (KOOS-QOL) scores at a minimum 2 years postoperatively, controlling for baseline score, patient age, ethnicity, sex, body mass index, marital status, smoking status, sport participation, competition level, Marx activity rating score, graft type, and articular cartilage and meniscus status. Results: Pre-reconstruction laxity data were available for 2325 patients (99.7%). Two-year revision data were available for 2259 patients (96.8%), and patient-reported outcomes were available for 1979 patients (84.8%). High-grade preoperative laxity was noted in 743 patients (31.9%). The mean postoperative IKDC score was 81.8 ± 15.9, and the mean KOOS-QOL score was 72.0 ± 22.0. The presence of high-grade pre-reconstruction laxity was associated with significantly increased odds of ACL graft revision (odds ratio [OR] = 1.87 [95% CI, 1.19-2.95]; P = .007). The presence of high-grade pre-reconstruction laxity was not associated with any difference in postoperative IKDC (β = −0.56, P = .44) or KOOS-QOL (β = 0.04, P = .97). Conclusion: The presence of high-grade pre-reconstruction knee laxity as assessed by manual physical examination under anesthesia is associated with significantly increased odds of revision ACL surgery but has no association with patient-reported outcome scores at 2 years after ACL reconstruction.
To the Point: Integrating Patient Safety Education Into the Obstetrics and Gynecology Undergraduate Curriculum
Abbott, Jodi , Pradhan, Archana , Buery-Joyner, Samantha D. , Casey, Petra M., Chuang, Alice, Dugoff, Lorraine , Dalrymple, John L. , Hampton, Brittany Star, Hueppchen, Nancy A. , Kaczmarczyk, J, Katz, Nadine T. , Nuthalapaty, Francis S., Page-Ramsey, Sarah M. , Wolf, Abigail , Cullimore, Amie J., Forstein, David A.

Mayo Clinic

Journal of Patient Safety | July 28, 2016 | Volume: 16 | Issue: 1 | Pages: e39-e45

10.1097/pts.0000000000000250 | PMID 27465297 Get It

Abstract This article is part of the To the Point Series prepared by the Association of Professors of Gynecology and Obstetrics Undergraduate Medical Education Committee. Principles and education in patient safety have been well integrated into academic obstetrics and gynecology practices, although progress in safety profiles has been frustratingly slow. Medical students have not been included in the majority of these ambulatory practice or hospital-based initiatives. Both the Association of American Medical Colleges and Accreditation Council for Graduate Medical Education have recommended incorporating students into safe practices. The Accreditation Council for Graduate Medical Education milestone 1 for entering interns includes competencies in patient safety. We present data and initiatives in patient safety, which have been successfully used in undergraduate and graduate medical education. In addition, this article demonstrates how using student feedback to assess sentinel events can enhance safe practice and quality improvement programs. Resources and implementation tools will be discussed to provide a template for incorporation into educational programs and institutions. Medical student involvement in the culture of safety is necessary for the delivery of both high-quality education and high-quality patient care. It is essential to incorporate students into the ongoing development of patient safety curricula in obstetrics and gynecology.
Splenic Hematopoiesis in Polycythemia Vera: A Morphologic and Immunohistologic Study
Wolf, Barbara C., Banks, Peter M. , Mann, Risa B., Neiman, Richard S.

Mayo Clinic

American Journal of Clinical Pathology | March 17, 2016 | Volume: 89 | Issue: 1 | Pages: 69-75

10.1093/ajcp/89.1.69 | PMID 3276145 Get It

Non-Hodgkin's Lymphomas of the Gastrointestinal Tract: An Evaluation of Paraffin Section Immunostaining
Wolf, Barbara C., Martin, Alvin W., Ree, H. J., Banks, Peter M. , Smith, Susie I., Neiman, Richard S.

Mayo Clinic

American Journal of Clinical Pathology | March 17, 2016 | Volume: 93 | Issue: 2 | Pages: 233-239

10.1093/ajcp/93.2.233 | PMID 1689097 Get It

Unmet Needs of African Americans and Whites at the Time of Palliative Care Consultation
Bull, Janet , Wolf, Steven , Portman, Diane , Strand, Jacob J. , Johnson, Kimberly S. , Strand, Jacob, Kamal, Arif H.

Mayo Clinic

American Journal of Hospice and Palliative Medicine® | February 17, 2016 | Volume: 34 | Issue: 5 | Pages: 461-465

10.1177/1049909116632508 | PMID 26888883 Get It

Context: Differences among patient populations that present to consultative palliative care are not known. Such an appreciation would inform health-care delivery tailored to unique populations. Objectives: We aimed to compare characteristics and palliative care needs of African Americans (AAs) and whites during initial palliative care consultation. Methods: We analyzed patient-reported, clinician-entered clinical encounter data from a large, multisite community-based, nonhospice palliative care collaborative. We included first specialty palliative care consultations from January 1, 2014, to July 2, 2015, across 15 sites within the Global Palliative Care Quality Alliance registry. Demographics, disease, performance status, advance care planning, and symptom prevalence/severity were compared. Results: Of 775 patients, 12.9% (N = 100) were AA. African Americans were younger (63 vs 75.4 years, P < .0001). A larger proportion of AAs had a diagnosis of cancer (45.0% vs 36.3%, P = .09) and in the hospital (71% vs 61.8%, P = .07). African Americans were more likely to have a Palliative Performance Score of 0 to 30 (35.6% vs 23.7%, P = .049). Around 50% in both racial groups were full code; slightly more than 40% had an advance directive. Nearly two-thirds in both racial groups reported 3 or more symptoms of any severity; one-third reported 3 or more moderate or severe symptoms. A larger proportion of Africans than whites reported pain of any severity (66.0% vs 56.1%, P = .06). Conclusion: All patients present to palliative care consultations with significant symptom and advance care planning needs. Further research is needed to identify how to deliver palliative care: earlier, in noncancer conditions, and improve pain management in AA populations.
Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network
Crosslin, DR, Owusu‐Obeng, Aniwaa, Wallace, John R. , Almoguera, Berta , Basford, MA, Bielinski, Suzette J. , Carrell, DS, Connolly, John J. , Doheny, KF, Gallego, CJ, Gordon, Allan , Kirby, Jacqueline, Kitchner, Terrie, Manzi, Shannon , Mejia, A R, Pan, Vivian , Perry, Cassandra, Peterson, JF, Prows, CA, Ralston, James D. , Scott, Stuart A. , Scrol, Aaron, Smith, Maureen E. , Stallings, SC, Veldhuizen, Tamra L., Wolf, W.A., Volpi, Simona , Wiley, Kenneth L , Manolio, Teri A. , Böttinger, Erwin P. , Brilliant, MH, Carey, David J. , Chisholm, Rex L. , Chute, CG, Jl, Haines, Håkonarson, Håkon , Harley, JB, Holm, Ingrid A. , Kullo, IJ, Jarvik, GP, Larson, EB, McCarty, Catherine A. , Williams, MS, Denny, Joshua C. , Rasmussen‐Torvik, LJ, Roden, DM, Ritchie, MD, Rasmussen‐Torvik, Laura J. , Jarvik, Gail P. , Peterson, Josh F. , Bush, William S. , Wallace, J, Crawford, Dana C. , Keating, Brendan J. , Perry, CL, Peterson, JF, Stallings, SC, Li, R, Roden, DM, Ritchie, M.D., Holm, Ingrid A , Hakonarson, Hakon , Denny, Joshua C , Jarvik, Gail P , Bielinski, Suzette , Gordon, Adam S , Connolly, John J , Peterson, Josh F , Scott, Stuart A , Rasmussen-Torvik, Laura J

Mayo Clinic

Clinical Pharmacology & Therapeutics | February 9, 2016 | Volume: 100 | Issue: 2 | Pages: 160-169

10.1002/cpt.350 | PMID 26857349 Get It

Genetic variation can affect drug response in multiple ways, although it remains unclear how rare genetic variants affect drug response. The electronic Medical Records and Genomics (eMERGE) Network, collaborating with the Pharmacogenomics Research Network, began eMERGE‐PGx, a targeted sequencing study to assess genetic variation in 82 pharmacogenes critical for implementation of “precision medicine.” The February 2015 eMERGE‐PGx data release includes sequence‐derived data from ∼5,000 clinical subjects. We present the variant frequency spectrum categorized by variant type, ancestry, and predicted function. We found 95.12% of genes have variants with a scaled Combined Annotation‐Dependent Depletion score above 20, and 96.19% of all samples had one or more Clinical Pharmacogenetics Implementation Consortium Level A actionable variants. These data highlight the distribution and scope of genetic variation in relevant pharmacogenes, identifying challenges associated with implementing clinical sequencing for drug treatment at a broader level, underscoring the importance for multifaceted research in the execution of precision medicine.
Transition of Care for Inpatient Hematology Patients Receiving Chemotherapy: Development of Hospital Discharge Huddle Process and Effects of Implementation
Warsame, Rahma , Kasi, Pashtoon Murtaza , Gallenberg, DeWayne, Matt-Hensrud, Natasha , Grethen, Kimberly, Colborn, Lisa K., Zeldenrust, Steven R., Lacy, Martha Q. , Thompson, Carrie A. , Kasi, Pashtoon M, Villasboas-Bisneto, Jose C, Wolf, Robert, Ward, James, Colborn, Lisa, Zeldenrust, Steven, Kasi, Pashtoon Murtaza , Villasboas, José C. , Wolf, Robert Christian , Ward, James

Mayo Clinic

Journal of Oncology Practice | January 13, 2016 | Volume: 12 | Issue: 1 | Pages: e88-e94

10.1200/jop.2015.005785 | PMID 26374861 Get It

Developing a systematic approach to hospital discharges can lead to improvements and serve a model for other inpatient wards.
Pre‐clinical heterotopic intrathoracic heart xenotransplantation: a possibly useful clinical technique
Abicht, Jan‐Michael , Mayr, Tanja, Reichart, Bruno , Buchholz, Stefan, Werner, Fabian, Lutzmann, Isabelle, Schmoeckel, Michael , Thormann, Michael , Langenmayer, Martin C. , Herbach, Nadja , Pohla, Heike , Herzog, Rudolf, McGregor, Christopher G.A. , Ayares, David , Wolf, Eckhard , Klymiuk, Nikolai , Baehr, Andrea , Kind, Alexander, Hagl, Christian, Ganswindt, Ute , Belka, Claus , Guethoff, Sonja , Brenner, Paolo , Bauer, Andreas , Herzog, Rudolf

Mayo Clinic

Xenotransplantation | November 25, 2015 | Volume: 22 | Issue: 6 | Pages: 427-442

10.1111/xen.12213 | PMID 26602740 Get It

AbstractBackgroundAs a step towards clinical cardiac xenotransplantation, our experimental heterotopic intrathoracic xenotransplantation model offers a beating and ejecting donor heart while retaining the recipient′s native organ as a backup in case of graft failure. Clinically applicable immunosuppressive regimens (IS) were investigated first, then treatments known to be effective in hypersensitized patients or those with recalcitrant rejection reactions.MethodsConsecutive experiments were carried out between 2009 and 2013. Twenty‐one genetically modified pigs (GGTA1‐knockout/hCD46/± thrombomodulin, in one caseHLA‐E instead) were used as donors. In all experiments, two cycles of immunoabsorption reduced preformed antibodies. Recipient baboons were divided into two groups according toISregimen:In group one (n = 10), pre‐treatment started either one (anti‐CD20) or four weeks (anti‐CD20 plus the proteasome inhibitor bortezomib) prior to transplantation. The extended conventional (as for allotransplantation) immunosuppressive maintenance regimen included anti‐thymocyte globuline, tacrolimus, mycophenolate mofetil, methylprednisolone and weekly anti‐CD20.In group two (n = 11), myeloablative pre‐treatment as in multiple myeloma patients (long and short regimens) was added to extended conventionalIS; postoperative total thoracic and abdominal lymphoid irradiation (TLI; single dose of 600cGY) was used to further reduce antibody‐producing cells.ResultsIn the perioperative course, the surgical technique was safely applied: 19 baboons were weaned off extracorporeal circulation and 17 extubated. Nine animals were lost in the early postoperative course due to causes unrelated to surgical technique orISregimen.Excluding these early failures, median graft survival times of group 1 and 2 were 18.5 (12–50) days and 16 (7–35) days. Necropsy examination of group 1 donor organs revealed hypertrophy of the left ventricular wall in the six longer‐lasting grafts; myocardial histology confirmed pre‐clinical suspicion of humoral rejection, which was not inhibited by the extended conventional IS including intensified treatments, and signs of thrombotic microangiopathy.Grafts of group 2 presented with only mild‐to‐moderate features of humoral rejection and thrombotic microangiopathy, except in one case of delayed rejection on day 17. The other experiments in this group were terminated because of untreatable pulmonary oedema, recurring ventricular fibrillation, Aspergillus sepsis, as well as a combination of a large donor organ and late toxic side effects due toTLI.ConclusionsLonger‐term results were difficult to achieve in this model due to theISregimens used. However, we conclude that heterotopic intrathoracic heart transplantation may be an option for clinical xenotransplantation.