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1.
JMIR Med Educ ; 4(1): e15, 2018 Jun 15.
Article in English | MEDLINE | ID: mdl-29907558

ABSTRACT

BACKGROUND: As electronic health records have become a more integral part of a physician's daily life, new electronic health record tools will continue to be rolled out to trainees. Patient access to provider notes is becoming a more widespread practice because this has been shown to increase patient empowerment. OBJECTIVE: In this analysis, we compared differences between resident and attending physicians' perceptions prior to implementation of patient access to provider notes to facilitate optimal use of electronic health record features and as a potential for patient empowerment. METHODS: This was a single-site study within an academic internal medicine program. Prior to implementation of patient access to provider notes, we surveyed resident and attending physicians to assess differences in perceptions of this new electronic health record tool using an open access survey provided by OpenNotes. RESULTS: We surveyed 37% (20/54 total) of resident physicians and obtained a 100% response rate and 72% (31/44 total) of attending physicians. Similarities between the groups included concerns about documenting sensitive topics and anticipation of improved patient engagement. Compared with attending physicians, resident physicians were more concerned about litigation, discussing weight, offending patients, and communicated less overall with patients through electronic health record. CONCLUSIONS: Patient access to provider notes has the potential to empower patients but concerns of the resident physicians need to be validated and addressed prior to its utilization.

2.
Circulation ; 137(2): 134-143, 2018 01 09.
Article in English | MEDLINE | ID: mdl-29021322

ABSTRACT

BACKGROUND: In individuals with a low diastolic blood pressure (DBP), the potential benefits or risks of intensive systolic blood pressure (SBP) lowering are unclear. METHODS: SPRINT (Systolic Blood Pressure Intervention Trial) was a randomized controlled trial that compared the effects of intensive (target <120 mm Hg) and standard (target <140 mm Hg) SBP control in 9361 older adults with high blood pressure at increased risk of cardiovascular disease. The primary outcome was a composite of cardiovascular disease events. All-cause death and incident chronic kidney disease were secondary outcomes. This post hoc analysis examined whether the effects of the SBP intervention differed by baseline DBP. RESULTS: Mean baseline SBP and DBP were 139.7±15.6 and 78.1±11.9 mm Hg, respectively. Regardless of the randomized treatment, baseline DBP had a U-shaped association with the hazard of the primary cardiovascular disease outcome. However, the effects of the intensive SBP intervention on the primary outcome were not influenced by baseline DBP level (P for interaction=0.83). The primary outcome hazard ratio for intensive versus standard treatment was 0.78 (95% confidence interval, 0.57-1.07) in the lowest DBP quintile (mean baseline DBP, 61±5 mm Hg) and 0.74 (95% confidence interval, 0.61-0.90) in the upper 4 DBP quintiles (mean baseline DBP, 82±9 mm Hg), with an interaction P value of 0.78. Results were similar for all-cause death and kidney events. CONCLUSIONS: Low baseline DBP was associated with increased risk of cardiovascular disease events, but there was no evidence that the benefit of the intensive SBP lowering differed by baseline DBP. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifier: NCT01206062.


Subject(s)
Antihypertensive Agents/therapeutic use , Blood Pressure/drug effects , Hypertension/drug therapy , Acute Coronary Syndrome/epidemiology , Aged , Aged, 80 and over , Antihypertensive Agents/adverse effects , Diastole/drug effects , Female , Humans , Hypertension/diagnosis , Hypertension/mortality , Hypertension/physiopathology , Incidence , Male , Middle Aged , Myocardial Infarction/epidemiology , Puerto Rico , Renal Insufficiency, Chronic/epidemiology , Risk Factors , Time Factors , Treatment Outcome , United States
3.
Prog Community Health Partnersh ; 10(1): 123-32, 2016.
Article in English | MEDLINE | ID: mdl-27018361

ABSTRACT

BACKGROUND: Evidence-based interventions exist for prevention of chronic disease in older adults. Partnering with community organizations may provide a mechanism for disseminating these interventions. OBJECTIVE: To describe the partnership and program implementation by the Arthritis Foundation (AF) and the University of Pittsburgh. METHODS: The AF Exercise Program (AFEP; an existing evidence-based program) was enhanced with the "10 Keys"™ to Healthy Aging (a prevention-focused program bundling the most common risk factors for chronic disease and disability in older adults and applies behavior change strategies to enhance prevention). The program was delivered in 20 sessions over 10 weeks by community health workers in a cluster-randomized trial. LESSONS LEARNED: Partnering with an organization having an existing infrastructure supports program delivery at the community level. This partnership provided programming in 54 sites across Pittsburgh and surrounding communities. CONCLUSIONS: This collaborative partnership created a productive synergy maximizing strengths in both research and program delivery.


Subject(s)
Aging , Community-Based Participatory Research/methods , Delivery of Health Care, Integrated/methods , Health Promotion/methods , Health Services for the Aged , Program Evaluation , Aged , Aged, 80 and over , Cluster Analysis , Community Health Workers , Cooperative Behavior , Exercise , Female , Humans , Male , Middle Aged , Pennsylvania
4.
Obesity (Silver Spring) ; 20(3): 636-43, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21494228

ABSTRACT

The Women on the Move through Activity and Nutrition (WOMAN) study was designed to test whether a nonpharmacological intervention including qualitative and quantitative dietary changes to induce weight loss and increased physical activity levels would reduce blood triglyceride levels and number of low-density lipoprotein particles (LDL-P). Such decreases in lipoproteins and other risk factors could reduce or slow progression of subclinical cardiovascular disease (CVD). Study participants were randomized to either the intervention (Lifestyle Change) or assessment (Health Education) group. Most of the intervention ended at the 30-month visit. The last 48-month examination was completed in 9/2008. There was very substantial weight loss and increased exercise during the first 30 months of the trial resulting in significant decreases in CV risk factors. Most of the intervention effect was lost through 48 months. Weight loss was 3.4 kg in Lifestyle Intervention and 0.2 kg in the Health Education at 48 months (P = 0.000). There were no significant changes at 48 months in lipid levels, blood pressure (BP), glucose, insulin, or in the subclinical measures of coronary calcium, carotid intima media thickness, or plaque. There was a significant decrease in long-distance corridor walk time in the Lifestyle vs. Health Education groups. Significant lifestyle changes can be achieved that result in decreases in CV risk factors. Whether such changes reduce CV outcomes is still untested in clinical trials of weight loss or exercise. Long-term maintenance of successful lifestyle changes, weight loss and reduced risk factors is the hurdle for lifestyle interventions attempting to prevent CV and other chronic diseases.


Subject(s)
Cardiovascular Diseases/prevention & control , Feeding Behavior , Health Behavior , Health Education , Motor Activity , Obesity/prevention & control , Risk Reduction Behavior , Biomarkers/blood , Cardiovascular Diseases/epidemiology , Cardiovascular Diseases/physiopathology , Cholesterol, LDL/blood , Energy Intake , Exercise , Female , Humans , Middle Aged , Obesity/epidemiology , Obesity/physiopathology , Risk Factors , Triglycerides/blood , United States/epidemiology , Weight Loss , Women's Health
5.
Contemp Clin Trials ; 30(6): 540-51, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19665588

ABSTRACT

BACKGROUND: The primary form of treatment for obesity today is behavioral therapy. Self-monitoring diet and physical activity plays an important role in interventions targeting behavior and weight change. The SMART weight loss trial examined the impact of replacing the standard paper record used for self-monitoring with a personal digital assistant (PDA). This paper describes the design, methods, intervention, and baseline sample characteristics of the SMART trial. METHODS: The SMART trial used a 3-group design to determine the effects of different modes of self-monitoring on short- and long-term weight loss and on adherence to self-monitoring in a 24-month intervention. Participants were randomized to one of three conditions (1) use of a standard paper record (PR); (2) use of a PDA with dietary and physical activity software (PDA); or (3), use of a PDA with the same software plus a customized feedback program (PDA + FB). RESULTS: We screened 704 individuals and randomized 210. There were statistically but not clinically significant differences among the three cohorts in age, education, HDL cholesterol, blood glucose and systolic blood pressure. At 24 months, retention rate for the first of three cohorts was 90%. CONCLUSIONS: To the best of our knowledge, the SMART trial is the first large study to compare different methods of self-monitoring in a behavioral weight loss intervention and to compare the use of PDAs to conventional paper records. This study has the potential to reveal significant details about self-monitoring patterns and whether technology can improve adherence to this vital intervention component.


Subject(s)
Diet , Exercise , Monitoring, Ambulatory/methods , Obesity/therapy , Adult , Body Weights and Measures , Clinical Protocols , Computers, Handheld , Female , Humans , Male , Middle Aged , Monitoring, Ambulatory/instrumentation , Patient Compliance , Patient Dropouts/statistics & numerical data , Research Design , Socioeconomic Factors , Weight Loss , Young Adult
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