Lisa A. Davis
University of Colorado Denver
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Featured researches published by Lisa A. Davis.
Arthritis Care and Research | 2014
Gail S. Kerr; Mireille Aujero; John S. Richards; Harlan Sayles; Lisa A. Davis; Grant W. Cannon; Liron Caplan; Kaleb Michaud; Ted R. Mikuls
To evaluate the association of hydroxychloroquine (HCQ) use with lipid profiles in a Veterans Affairs Rheumatoid Arthritis (VARA) cohort.
Arthritis Care and Research | 2015
Bryant R. England; Harlan Sayles; Kaleb Michaud; Liron Caplan; Lisa A. Davis; Grant W. Cannon; Brian C. Sauer; Elizabeth Blair Solow; Andreas Reimold; Gail S. Kerr; Pascale Schwab; Josh F. Baker; Ted R. Mikuls
There has been limited investigation into cause‐specific mortality and the associated risk factors in men with rheumatoid arthritis (RA). We investigated all‐cause and cause‐specific mortality in men with RA, examining determinants of survival.
Antimicrobial Agents and Chemotherapy | 2015
Andrew J. Neville; Sydney J. Zach; Xiaofang Wang; Joshua J. Larson; Abigail K. Judge; Lisa A. Davis; Jonathan L. Vennerstrom; Paul H. Davis
ABSTRACT Toxoplasma gondii is an apicomplexan parasite of humans and other mammals, including livestock and companion animals. While chemotherapeutic regimens, including pyrimethamine and sulfadiazine regimens, ameliorate acute or recrudescent disease such as toxoplasmic encephalitis or ocular toxoplasmosis, these drugs are often toxic to the host. Moreover, no approved options are available to treat infected women who are pregnant. Lastly, no drug regimen has shown the ability to eradicate the chronic stage of infection, which is characterized by chemoresistant intracellular cysts that persist for the life of the host. In an effort to promote additional chemotherapeutic options, we now evaluate clinically available drugs that have shown efficacy in disease models but which lack clinical case reports. Ideally, less-toxic treatments for the acute disease can be identified and developed, with an additional goal of cyst clearance from human and animal hosts.
Arthritis Care and Research | 2013
Liron Caplan; Lisa A. Davis; Christina M. Bright; Gail S. Kerr; Deana Lazaro; Nasim A. Khan; J. Steuart Richards; Dannette S. Johnson; Grant W. Cannon; Andreas Reimold; Ted R. Mikuls
Obesity is a prevalent condition and a serious health concern. The relationship between obesity and rheumatoid arthritis (RA) disease activity and severity has not been adequately examined, and there are concerns that periarticular adipose tissue may reduce the utility of the joint examination.
The Journal of Rheumatology | 2013
Lisa A. Davis; Grant W. Cannon; Lauren F. Pointer; Leah M. Haverhals; Roger K. Wolff; Ted R. Mikuls; Andreas Reimold; Gail S. Kerr; J. Steuart Richards; Dannette S. Johnson; Robert J. Valuck; Allan V. Prochazka; Liron Caplan
Objective. C677T and A1298C polymorphisms in the enzyme methylenetetrahydrofolate reductase (MTHFR) have been associated with increased cardiovascular (CV) events in non-rheumatoid arthritis (RA) populations. We investigated potential associations of MTHFR polymorphisms and use of methotrexate (MTX) with time-to-CV event in data from the Veterans Affairs Rheumatoid Arthritis (VARA) registry. Methods. VARA participants were genotyped for MTHFR polymorphisms. Variables included demographic information, baseline comorbidities, RA duration, autoantibody status, and disease activity. Patients’ comorbidities and outcome variables were defined using International Classification of Diseases-9 and Current Procedural Terminology codes. The combined CV event outcome included myocardial infarction (MI), percutaneous coronary intervention, coronary artery bypass graft surgery, and stroke. Cox proportional hazards regression was used to model the time-to-CV event. Results. Data were available for 1047 subjects. Post-enrollment CV events occurred in 97 patients (9.26%). Although there was a trend toward reduced risk of CV events, MTHFR polymorphisms were not significantly associated with time-to-CV event. Time-to-CV event was associated with prior stroke (HR 2.01, 95% CI 1.03–3.90), prior MI (HR 1.70, 95% CI 1.06–2.71), hyperlipidemia (HR 1.57, 95% CI 1.01–2.43), and increased modified Charlson-Deyo index (HR 1.23, 95% CI 1.13–1.34). MTX use (HR 0.66, 95% CI 0.44–0.99) and increasing education (HR 0.87, 95% CI 0.80–0.95) were associated with a lower risk for CV events. Conclusion. Although MTHFR polymorphisms were previously associated with CV events in non-RA populations, we found only a trend toward decreased association with CV events in RA. Traditional risk factors conferred substantial CV risk, while MTX use and increasing years of education were protective.
Mayo Clinic Proceedings | 2014
Cory B. Pittman; Lisa A. Davis; Angelique Zeringue; Liron Caplan; Kent R. Wehmeier; Jeffrey F. Scherrer; Hong Xian; Francesca E. Cunningham; Jay R. McDonald; Alexis Arnold; Seth A. Eisen
OBJECTIVE To determine if bisphosphonates are associated with reduced risk of acute myocardial infarction (AMI). PATIENTS AND METHODS A cohort of 14,256 veterans 65 years or older with femoral or vertebral fractures was selected from national administrative databases operated by the US Department of Veterans Affairs and was derived from encounters at Veterans Affairs facilities between October 1, 1998, and September 30, 2006. The time to first AMI was assessed in relationship to bisphosphonate exposure as determined by records from the Pharmacy Benefits Management Database. Time to event analysis was performed using multivariate Cox proportional hazards regression. An adjusted survival analysis curve and a Kaplan-Meier survival curve were analyzed. RESULTS After controlling for atherosclerotic cardiovascular disease risk factors and medications, bisphosphonate use was associated with an increased risk of incident AMI (hazard ratio, 1.38; 95% CI, 1.08-1.77; P=.01). The timing of AMI correlated closely with the timing of bisphosphonate therapy initiation. CONCLUSION Our observations in this study conflict with our hypothesis that bisphosphonates have antiatherogenic effects. These findings may alter the risk-benefit ratio of bisphosphonate use for treatment of osteoporosis, especially in elderly men. However, further analysis and confirmation of these findings by prospective clinical trials is required.
Arthritis & Rheumatism | 2016
Joshua F. Baker; Brian C. Sauer; Grant W. Cannon; Chia Chen Teng; Kaleb Michaud; Said A. Ibrahim; Erik Jorgenson; Lisa A. Davis; Liron Caplan; Amy C. Cannella; Ted R. Mikuls
Unintentional weight loss is important and can be predictive of long‐term outcomes in patients with rheumatoid arthritis (RA). This study was undertaken to assess how primary therapies for RA may influence changes in body mass index (BMI) in RA patients from a large administrative database.
eGEMs (Generating Evidence & Methods to improve patient outcomes) | 2013
Lisa A. Davis; Alyse Mann; Grant W. Cannon; Ted R. Mikuls; Andreas Reimold; Liron Caplan
Objective: To assess the accuracy of International Classification of Diseases, Ninth Revision, and Current Procedural Terminology codes for identifying cardiovascular (CV) events (myocardial infarction [MI], stroke, coronary artery bypass graft [CABG], and percutaneous coronary intervention [PCI]) in enrollees of the Veterans Affairs Rheumatoid Arthritis (VARA) registry. Design: We performed a validation study from VARA enrollment until 6/1/2010 to compare the accuracy of CV events in those with and without CV-event coding in inpatient and outpatient records to evaluate for CV events +/− 3 months of the coding. The positive predictive value (PPV) was calculated, and codes with a PPV ≥50% were included in a composite coding algorithm. Results: We evaluated 107 individuals for 21 CV-event codes and 60 individuals without CV-event coding. The PPV varied between 0–100%. Composite coding algorithms’ PPV ranged from 70–100%. Conclusions: Validation of these algorithms allows for identification of acute CV events with known accuracy. The sensitivity and PPV of coding algorithms for CABG and PCI exceed that of stroke and MI.
Lupus | 2015
Itziar Quinzanos; Lisa A. Davis; Angela Keniston; Alyssa Nash; Jinoos Yazdany; Rebecca Fransen; Joel M. Hirsh; JoAnn Zell
Objectives Quality indicators (QIs) are evidence-based processes of care designed to represent the current standard of care. Reproductive health QIs for the care of patients with systemic lupus erythematosus (SLE) have recently been developed, and examine areas such as pregnancy screening for autoantibodies, treatment of pregnancy-associated antiphospholipid syndrome, and contraceptive counseling. This study was designed to investigate our performance on these QIs and to explore potential gaps in care and demographic predictors of adherence to the QIs in a safety-net hospital. Methods We performed a record review of patients with a diagnosis of SLE at Denver Health Medical Center (DH) through an electronic query of existing medical records and via chart review. Data were limited to female patients between the ages of 18 and 50 who were seen between July 2006 and August 2011. Results A total of 137 female patients between the ages of 18 and 50 were identified by ICD-9 code and confirmed by chart review to have SLE. Of these, 122 patients met the updated 1997 American College of Rheumatology SLE criteria and had intact reproductive systems. Only 15 pregnancies were documented during this five-year period, and adherence to autoantibody screening was 100 percent. We did not have any patients who were pregnant and met criteria for pregnancy-associated antiphospholipid syndrome. Sixty-five patients (53%) received potentially teratogenic medications, and 30 (46%) had documented discussions about these medications’ potential risk upon their initiation. Predictors of whether patients received appropriate counseling included younger age (OR 0.92, CI 0.87–0.98) and those who did not describe English as their primary language (OR 0.24, CI 0.07–0.87) in the multivariate analysis. Conclusions We were able to detect an important gap in care regarding teratogenic medication education to SLE patients of childbearing potential in our public health academic clinic, as only one in two eligible patients had documented appropriate counseling at the initiation of a teratogenic medication.
Arthritis Care and Research | 2018
Bryant R. England; Joshua F. Baker; Harlan Sayles; Kaleb Michaud; Liron Caplan; Lisa A. Davis; Grant W. Cannon; Brian C. Sauer; E. Blair Solow; Andreas Reimold; Gail S. Kerr; Ted R. Mikuls
To examine associations of body mass index (BMI) and weight loss with cause‐specific mortality in rheumatoid arthritis (RA).