Citations

Clear

1323 citation(s) found for "Mayo, Angela".

Sepsis and Shock Response Team: Impact of a Multidisciplinary Approach to Implementing Surviving Sepsis Campaign Guidelines and Surviving the Process
Grek, Ami , Booth, Sandra, Festić, Emir , Shirazi, Ehsan, Thompson, Kristine M., Starbuck, Angela, McRee, Chad, Naessens, James M. , Maniaci, Michael, Thompson, Kristine, Moreno Franco, Pablo, Maniaci, Michael J. , Franco, Pablo Moreno

Mayo Clinic

American Journal of Medical Quality | November 12, 2016 | Volume: 32 | Issue: 5 | Pages: 500-507

10.1177/1062860616676887 | PMID 27837163 Get It

The Surviving Sepsis Campaign guidelines are designed to decrease mortality through consistent application of a 7-element bundle. This study evaluated the impact of improvement in bundle adherence using a time-series analysis of compliance with the bundle elements before and after interventions intended to improve the process, while also looking at hospital mortality. This article describes interventions used to improve bundle compliance and hospital mortality in patients admitted through the emergency department with sepsis, severe sepsis, or septic shock. Quality improvement methodology was used to develop high-impact interventions that led to dramatically improved adherence to the Surviving Sepsis Campaign guidelines bundle. Improved performance was associated with a significant decrease in the in-hospital mortality of severe sepsis patients presenting to the emergency department.
Clinical spectrum of Castleman disease–associated neuropathy
Naddaf, Elie , Dispenzieri, Angela , Mandrekar, Jay , Mauermann, Michelle L. , Dispenzieri, Angela , Naddaf, Elie , Mauermann, Michelle L

Mayo Clinic

Neurology | November 3, 2016 | Volume: 87 | Issue: 23 | Pages: 2457-2462

10.1212/wnl.0000000000003405 | PMID 27807187 Get It

Beta‐blockers improve survival outcomes in patients with multiple myeloma: a retrospective evaluation
Hwa, Yi L. , Shi, Qian , Kumar, Shaji , Lacy, Martha Q. , Kapoor, Prashant , Dingli, David , Go, Ronald S. , Hayman, Suzanne R. , Russell, Stephen J. , Lust, John A., Lin, Yi , Dispenzieri, Angela , Buadi, Francis K. , Go, Ronald S , Russell, Stephen, Gertz, Morie A. , Leung, Nelson , Gonsalves, Wilson I. , Rajkumar, S. Vincent , Dispenzieri, Angela , Russell, Stephen J , Shi, Qian , Dingli, David , Lin, Yi

Mayo Clinic

American Journal of Hematology | October 13, 2016 | Volume: 92 | Issue: 1 | Pages: 50-55

10.1002/ajh.24582 | PMID 27733010 Get It

A preclinical study demonstrated anti‐proliferative and apoptotic effect of propranolol on multiple myeloma (MM) cell. Clinical studies suggested that beta‐blocker (BB) might impact the prognosis of breast, prostate, colorectal, ovarian, lung, and skin cancer. This retrospective study evaluated the effect of BB in MM disease‐specific survival (DSS) and overall survival (OS). Among 1,971 newly diagnosed MM patients seen at Mayo Clinic between 1995 and 2010, usage of BB and other cardiac (or antihypertensive) medications were abstracted. Cumulative incidence function and Kaplan–Meier method were used to estimate 5‐year cumulative incidence rate (CIR) of MM death and OS rate, respectively. Nine hundred and thirty (47.2%) patients had no intake of cardiac medications; 260 (13.2%) used BB alone; 343 (17.4%) used both BB/non‐BB cardiac medications; and 438 (22.2%) had non‐BB cardiac drugs. Superior MM DSS was observed in BB only users, compared to patients without any cardiac drugs ( , 0.53, 95% confidence interval [CI], 0.42–0.67, Padj.<0.0001) and non‐BB cardiac drugs users ( , 0.49, 95% CI, 0.38–0.63, Padj.<0.0001). Patients on both BB and other cardiac drugs showed superior DSS than non‐cardiac drugs users ( , 0.54, 95% CI, 0.44–0.67, Padj.<0.0001) and non‐BB cardiac drug users. ( , 0.50, 95% CI, 0.40–0.62, Padj.<0.0001). MM DSS did not differ between BB users with and without other cardiac drugs (Padj.=0.90). Multivariable analysis showed the same pattern for OS. In patients with MM, BB intake is associated with a reduced risk of disease‐specific death and overall mortality in comparison to non‐BB or no use of cardiac drugs. Am. J. Hematol. 92:50–55, 2017. © 2016 Wiley Periodicals, Inc.
The prognostic value of multiparametric flow cytometry in AL amyloidosis at diagnosis and at the end of first-line treatment
Muchtar, Eli , Jevremović, Dragan , Dispenzieri, Angela , Dingli, David , Lacy, Martha Q. , Hayman, Suzanne R. , Kapoor, Prashant , Russell, Stephen J. , Lust, John A., Lin, Yi , Chakraborty, Rajshekhar , Zeldenrust, Steven R., Kumar, Shaji , Kyle, Robert A. , Gertz, Morie A , Buadi, Francis K. , Gonsalves, Wilson I. , Leung, Nelson , Go, Ronald S. , Rajkumar, S. Vincent , Gertz, Morie A. , Muchtar, E , Dispenzieri, Angela , Russell, Stephen J , Jevremovic, Dragan , Chakraborty, Rajshekhar , Dingli, David , Lin, Yi

Mayo Clinic

Blood | October 12, 2016 | Volume: 129 | Issue: 1 | Pages: 82-87

10.1182/blood-2016-06-721878 | PMID 27729322 Get It

Key PointsThe monotypic and polytypic PC compartments assessed by MFC are prognostic in AL amyloidosis. MFC may play a role in the definition of hematologic response to treatment.
Patient- and Provider-Centered Design of an Outpatient Diabetes Technology Clinic
Cramer, A , Scalzo, Patty , Bach, Sarah M., Kudva, Yogish C. , Cramer, Angela M, Bach, Sarah M.

Mayo Clinic

Journal of Diabetes Science and Technology | October 11, 2016 | Volume: 11 | Issue: 3 | Pages: 499-505

10.1177/1932296816672690 | PMID 28745100 Get It

Dying With a Left Ventricular Assist Device as Destination Therapy
Strand, Jacob J. , Wordingham, Sara E., Stulak, John M., Luckhardt, Angela J., Dunlay, Shannon M. , Swetz, Keith M.

Mayo Clinic

Circulation: Heart Failure | October 6, 2016 | Volume: 9 | Issue: 10 | Pages: No page available

10.1161/circheartfailure.116.003096 | PMID 27758809 Get It

Background— Despite the ability of left ventricular assist device as destination therapy (DT-LVAD) to prolong survival for many patients with advanced heart failure, little is known about the eventual end-of-life care that patients with DT-LVAD receive. Methods and Results— All patients undergoing DT-LVAD at the Mayo Clinic in Rochester, Minnesota, from January 1, 2007, to September 30, 2014, who subsequently died before July 1, 2015, were included. Information about end-of-life care was obtained from documentation in the electronic medical record. Of 89 patients who died with a DT-LVAD, the median (25th–75th percentile) time from left ventricular assist device implantation to death was 14 (4–31) months. The most common causes of death were multiorgan failure (26%), hemorrhagic stroke (24%), and progressive heart failure (21%). Nearly half (46%) of the patients saw palliative care within 1 month before death; however, only 13 (15%) patients enrolled in hospice a median 11 (range 1–315) days before death. Most patients (78%) died in the hospital, of which 88% died in the intensive care unit. In total, 49 patients had their left ventricular assist device deactivated before death, with all but 3 undergoing deactivation in the hospital. Most patients died within an hour of left ventricular assist device deactivation and all within 26 hours. Conclusions— In contrast to the general heart failure population, most patients with DT-LVAD die in the hospital and few use hospice. Further work is needed to understand these differences and to determine whether patients with DT-LVAD are receiving optimal end-of-life care.
Randomized phase 2 trial of ixazomib and dexamethasone in relapsed multiple myeloma not refractory to bortezomib
Kumar, Shaji , LaPlant, Betsy, Reeder, Craig B. , Halvorson, Alese E. , Bergsagel, P. Leif , Thompson, Melanie , Crawley, Jamie , Kapoor, Prashant , Stewart, Keith, Hayman, Suzanne R. , Hwa, Yi L. , Dingli, David , Lin, Yi , Rivera, Candido E., Lacy, Martha Q. , Nahi, Hareth , Bergsagel, P. Leif , Kumar, Shaji K , LaPlant, Betsy R, Mıkhael, Joseph , Roy, Vivek , Buadi, Francis K. , Gertz, Morie A. , Dispenzieri, Angela , Gonsalves, Wilson I. , Witzig, Thomas E. , Ailawadhi, Sikander , Go, Ronald S. , Rajkumar, S. Vincent , Dingli, David , Lin, Yi , Nahi, Hareth

Mayo Clinic

Blood | October 4, 2016 | Volume: 128 | Issue: 20 | Pages: 2415-2422

10.1182/blood-2016-05-717769 | PMID 27702799 Get It

Key Points The combination of ixazomib and dexamethasone has clinical activity in patients with relapsed and or refractory multiple myeloma. Higher dose of ixazomib leads to improved response rates but with higher rates of treatment related adverse events.
Phase II trial of nab‐paclitaxel in patients with relapsed or refractory multiple myeloma
Jain, Tania , Dueck, Amylou C. , Ginos, Brenda, Mayo, Angela, Reeder, Craig B. , Chesi, Marta , Stewart, A. Keith, Bergsagel, P. Leif , Bergsagel, P. Leif , Ginos, Brenda F, Mıkhael, Joseph , Dueck, A. C. , Kosiorek, Heidi , Fonseca, Rafaël , Jain, Tania

Mayo Clinic

American Journal of Hematology | September 1, 2016 | Volume: 91 | Issue: 12 | Pages: No page available

10.1002/ajh.24548 | PMID 27581088 Get It

Chronic Daily Headache: Ten Steps for Primary Care Providers to Regain Control
Sheeler, Robert D. , Garza, Ivan , Vargas, Bert B., O’Neil, Angela E.

Mayo Clinic

Headache: The Journal of Head and Face Pain | August 23, 2016 | Volume: 56 | Issue: 10 | Pages: 1675-1684

10.1111/head.12881 | PMID 27552176 Get It

Background Chronic daily headache (CDH) affects 2% to 4% of the North American and European population. Various pathways lead to this condition, although chronification of migraine and the occurrence of central sensitization in tension headache are the 2 most common. Medication overuse headaches complicate a substantial portion of other primary headaches that have become chronic and often make their treatment more complex and less successful. Methods/Results A 10‐step process to help primary care providers evaluate and treat CDH patients begins with excluding secondary headache disorders, then moves on to classification of the primary underlying headache disorder. Next, the exacerbating factors, as well as relevant comorbid conditions, are identified. The patient's current acute therapy is examined, and attempts are made to identify and resolve medication overuse if present. Past preventive therapies are reviewed, allowing for thoughtful design of a headache action plan with preventive, acute, and lifestyle components. Patients are asked to keep a headache diary, used to initiate a cycle of continuous improvement in a patient's response to acute and preventive therapeutic approaches. Conclusions A systematic approach and partnership with patients often make it possible to convert CDH to episodic headache that is responsive to both acute and preventive therapies.