Brian J. Wells
Wake Forest University
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Featured researches published by Brian J. Wells.
Journal of Diabetes | 2016
Subramanian Kannan; Kevin M. Pantalone; Simone Matsuda; Brian J. Wells; Matthew Karafa; Robert S. Zimmerman
The aim of the present study was to assess the risk of overall mortality, coronary artery disease (CAD), and congestive heart failure (CHF) in patients with type 2 diabetes mellitus (T2DM) treated with metformin (MF) and an additional antidiabetic agent.
Diabetes Care | 2016
Kevin M. Pantalone; Brian J. Wells; Kevin Chagin; Flavia Ejzykowicz; Changhong Yu; Alex Milinovich; Janine M. Bauman; Michael W. Kattan; Swapnil Rajpathak; Robert S. Zimmerman
OBJECTIVE “Clinical inertia” has been used to describe the delay in the intensification of type 2 diabetes treatment among patients with poor glycemic control. Previous studies may have exaggerated the prevalence of clinical inertia by failing to adequately monitor drug dose changes and nonmedication interventions. This project evaluated the intensification of diabetes therapy and hemoglobin A1c (A1C) goal attainment among patients with newly diagnosed type 2 diabetes when metformin monotherapy failed. RESEARCH DESIGN AND METHODS The electronic health record at Cleveland Clinic was used to identify patients with newly diagnosed type 2 diabetes between 2005 and 2013 who failed to reach the A1C goal after 3 months of metformin monotherapy. A time-dependent survival analysis was used to compare the time until A1C goal attainment in patients who received early intensification of therapy (within 6 months of metformin failure) or late intensification. The analysis was performed for A1C goals of 7% (n = 1,168), 7.5% (n = 679), and 8% (n = 429). RESULTS Treatment was intensified early in 62%, 69%, and 72% of patients when poor glycemic control was defined as an A1C >7%, >7.5%, and >8%, respectively. The probability of undergoing an early intensification was greater the higher the A1C category. Time until A1C goal attainment was shorter among patients who received early intensification regardless of the A1C goal (all P < 0.05). CONCLUSIONS A substantial number of patients with newly diagnosed type 2 diabetes fail to undergo intensification of therapy within 6 months of metformin monotherapy failure. Early intervention in patients when metformin monotherapy failed resulted in more rapid attainment of A1C goals.
BMJ Open | 2017
Kevin M. Pantalone; Todd M. Hobbs; Kevin Chagin; Sheldon X. Kong; Brian J. Wells; Michael W. Kattan; Jonathan Bouchard; Brian Sakurada; Alex Milinovich; Wayne Weng; Janine M. Bauman; Anita D. Misra-Hebert; Robert S. Zimmerman; Bartolome Burguera
Objective To determine the prevalence of obesity and its related comorbidities among patients being actively managed at a US academic medical centre, and to examine the frequency of a formal diagnosis of obesity, via International Classification of Diseases, Ninth Revision (ICD-9) documentation among patients with body mass index (BMI) ≥30 kg/m2. Design The electronic health record system at Cleveland Clinic was used to create a cross-sectional summary of actively managed patients meeting minimum primary care physician visit frequency requirements. Eligible patients were stratified by BMI categories, based on most recent weight and median of all recorded heights obtained on or before the index date of 1July 2015. Relationships between patient characteristics and BMI categories were tested. Setting A large US integrated health system. Results A total of 324 199 active patients with a recorded BMI were identified. There were 121 287 (37.4%) patients found to be overweight (BMI ≥25 and <29.9), 75 199 (23.2%) had BMI 30–34.9, 34 152 (10.5%) had BMI 35–39.9 and 25 137 (7.8%) had BMI ≥40. There was a higher prevalence of type 2 diabetes, pre-diabetes, hypertension and cardiovascular disease (P value<0.0001) within higher BMI compared with lower BMI categories. In patients with a BMI >30 (n=134 488), only 48% (64 056) had documentation of an obesity ICD-9 code. In those patients with a BMI >40, only 75% had an obesity ICD-9 code. Conclusions This cross-sectional summary from a large US integrated health system found that three out of every four patients had overweight or obesity based on BMI. Patients within higher BMI categories had a higher prevalence of comorbidities. Less than half of patients who were identified as having obesity according to BMI received a formal diagnosis via ICD-9 documentation. The disease of obesity is very prevalent yet underdiagnosed in our clinics. The under diagnosing of obesity may serve as an important barrier to treatment initiation.
Respiratory Care | 2018
Umur Hatipoğlu; Brian J. Wells; Kevin Chagin; Dhruv Joshi; Alex Milinovich; Michael B. Rothberg
BACKGROUND: The pneumonia 30-d readmission rate has been endorsed by the National Quality Forum as a quality metric. Hospital readmissions can potentially be lowered by improving in-hospital care, transitions of care, and post-discharge disease management programs. The purpose of this study was to create an accurate prediction model for determining the risk of 30-d readmission at the point of discharge. METHODS: The model was created using a data set of 1,295 hospitalizations at the Cleveland Clinic Main Campus with pneumonia over 3 y. Candidate variables were limited to structured variables available in the electronic health record. The final model was compared with the Centers for Medicare and Medicaid Services (CMS) model among subjects 65 y of age and older (n = 628) and was externally validated. RESULTS: Three hundred thirty subjects (25%) were readmitted within 30 d. The final model contained 13 variables and had a bias-corrected C statistic of 0.74 (95% CI 0.71–0.77). Number of admissions in the prior 6 months, opioid prescription, serum albumin during the first 24 h, international normalized ratio and blood urea nitrogen during the last 24 h were the predictor variables with the greatest weight in the model. In terms of discriminative performance, the Cleveland Clinic model outperformed the CMS model on the validation cohort (C statistic 0.69 vs 0.60, P = .042). CONCLUSIONS: The proposed risk prediction model performed better than the CMS model. Accurate readmission risk prediction at the point of discharge is feasible and can potentially be used to focus post-acute care interventions in a high-risk group of patients.
Journals of Gerontology Series A-biological Sciences and Medical Sciences | 2018
Leon Lenchik; Kristin M Lenoir; Josh Tan; Robert D. Boutin; Kathryn E. Callahan; Stephen B. Kritchevsky; Brian J. Wells
BACKGROUND Opportunistic assessment of sarcopenia on CT examinations is becoming increasingly common. This study aimed to determine relationships between CT-measured skeletal muscle size and attenuation with 1-year risk of mortality in older adults enrolled in a Medicare Shared Savings Program (MSSP). METHODS Relationships between skeletal muscle metrics and all-cause mortality were determined in 436 participants (52% women, mean age 75 years) who had abdominopelvic CT examinations. On CT images, skeletal muscles were segmented at the level of L3 using two methods: (a) all muscles with a threshold of -29 to +150 Hounsfield units (HU), using a dedicated segmentation software, (b) left psoas muscle using a free-hand region of interest tool on a clinical workstation. Muscle cross-sectional area (CSA) and muscle attenuation were measured. Cox regression models were fit to determine the associations between muscle metrics and mortality, adjusting for age, sex, race, smoking status, cancer diagnosis, and Charlson comorbidity index. RESULTS Within 1 year of follow-up, 20.6% (90/436) participants died. In the fully-adjusted model, higher muscle index and muscle attenuation were associated with lower risk of mortality. A one-unit standard deviation (SD) increase was associated with a HR = 0.69 (95% CI = 0.49, 0.96; p = .03) for total muscle index, HR = 0.67 (95% CI = 0.49, 0.90; p < .01) for psoas muscle index, HR = 0.54 (95% CI = 0.40, 0.74; p < .01) for total muscle attenuation, and HR = 0.79 (95% CI = 0.66, 0.95; p = .01) for psoas muscle attenuation. CONCLUSION In older adults, higher skeletal muscle index and muscle attenuation on abdominopelvic CT examinations were associated with better survival, after adjusting for multiple risk factors.
Journal of Diabetes | 2018
Kevin M. Pantalone; Anita D. Misra-Hebert; Todd M. Hobbs; Brian J. Wells; Sheldon X. Kong; Kevin Chagin; Tanujit Dey; Alex Milinovich; Wayne Weng; Janine M. Bauman; Bartolome Burguera; Robert S. Zimmerman; Michael W. Kattan
The aim of the present study was to assess the longitudinal accumulation of diabetes‐related complications and the effect of glycemic control on the Diabetes Complications Severity Index (DCSI) score in people with newly diagnosed type 2 diabetes (T2D).
Diabetes, Obesity and Metabolism | 2017
Robert S. Zimmerman; Todd M. Hobbs; Brian J. Wells; Sheldon X. Kong; Michael W. Kattan; Jon Bouchard; Kevin Chagin; Changhong Yu; Brian Sakurada; Alex Milinovich; Wayne Weng; Janine M. Bauman; Kevin M. Pantalone
To assess the potential impact of glucagon‐like peptide‐1 receptor agonist (GLP‐1RA) exposure on cardiovascular disease (CVD) and mortality outcomes in patients with type 2 diabetes (T2D), using a large retrospective cohort.
International Orthopaedics | 2018
Austin V. Stone; Alexander H. Jinnah; Brian J. Wells; Hal H. Atkinson; Anna N. Miller; Wendell Futrell; Kristin M Lenoir; Cynthia L. Emory
Clinical Medicine Insights: Endocrinology and Diabetes | 2016
Kevin M. Pantalone; Todd M. Hobbs; Brian J. Wells; Sheldon X. Kong; Michael W. Kattan; Jonathan Bouchard; Kevin Chagin; Changhong Yu; Brian Sakurada; Alex Milinovich; Wayne Weng; Janine M. Bauman; Robert S. Zimmerman
Journal of Clinical Oncology | 2018
Kathryn E. Weaver; Heidi D. Klepin; Tiffany P. Avery; Zanetta S. Lamar; Nicholas M. Pajewski; William Gregory Hundley; Brian J. Wells; Aimee Johnson; Randi E. Foraker