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1.
J Womens Health (Larchmt) ; 28(12): 1614-1622, 2019 12.
Article in English | MEDLINE | ID: mdl-31390282

ABSTRACT

Background: Menopause is a time often fraught with changes and symptoms, which may require difficult choices and decision-making. During this period, women would benefit from a better understanding and in-depth discussions with providers regarding menopause, associated conditions, and appropriate therapy. Patient portals offer a potential means to improve knowledge and shared decision-making (SDM) about menopause. Materials and Methods: This protocol article explores the feasibility of using the secure messaging (SM) function of the Veterans Affairs (VA) Patient Portal, "My HealtheVet" to implement an educational intervention and measure its impact on knowledge and SDM in the management of menopause. Results: This is a quality improvement pilot study in which women veterans of menopausal age in the Miami VA are offered an educational intervention via a patient portal, while women veterans in two neighboring VA facilities are not. Intervention participants receive weekly SMs with information on menopause symptoms, and treatment. After 6-months, all participants are surveyed on menopause knowledge, SDM, and satisfaction with the program. Conclusion: This study is among the first to assess the impact of an innovative patient portal intervention to improve knowledge and SDM between patients and providers regarding menopause. If successful, our program will add to the "meaningful use" of patient portals and offer a scalable and timely resource for SDM about menopause.


Subject(s)
Internet-Based Intervention , Menopause , Patient Portals , Veterans/education , Decision Making , Female , Humans , Middle Aged , Patient Participation , Pilot Projects , Proof of Concept Study , Research Design , Surveys and Questionnaires , United States , United States Department of Veterans Affairs
2.
Telemed J E Health ; 24(12): 1006-1013, 2018 12.
Article in English | MEDLINE | ID: mdl-29672218

ABSTRACT

Background:We studied the feasibility of using the Veteran Health Administration's electronic health record (EHR), My HealtheVet, as an educational and monitoring tool for veterans with heart failure (HF).Methods:We enrolled 120 HF patients with a mean age (±standard deviation): 64.8 ± 9.6, range: 41-91 years. There were 105 (87.5%) non-Hispanics, 15 (12.5%) Hispanics, 91 (75.8%) whites, and 20 (16.5%) blacks, and 62 (51.7%) were married. Study participants received educational material on managing their HF and were monitored on their weight and HF symptoms weekly. Surveys on My HealtheVet use and secondary outcomes including knowledge of their illness, quality of life (QoL), and self-efficacy were conducted at baseline and 26 weeks after enrollment.Results:Among the participants, 55 (45.8%) had used My HealtheVet. The number of weeks each user responded to the weekly messages by the care coordinator ranged from 1 (4%) to 26 (100%) with a median of 8. Secondary outcome data were available for 54 patients (24 users and 30 nonusers) who participated in both baseline and 26-week surveys. There was a significant improvement in QoL (p < 0.01) among users of My HealtheVet compared with nonusers. There were no significant differences with respect to self-efficacy or HF knowledge. Use of My HealtheVet and ease in using the HealtheVet portal increased from baseline to follow-up.Conclusions:EHR-based interventions have potential for HF monitoring and case management, and may be feasible in improving QoL for patients.


Subject(s)
Electronic Health Records/organization & administration , Health Knowledge, Attitudes, Practice , Heart Failure/therapy , Patient Education as Topic/organization & administration , Veterans , Adult , Aged , Aged, 80 and over , Female , Heart Failure/physiopathology , Heart Failure/psychology , Humans , Male , Middle Aged , Quality of Life , Self Efficacy , United States , United States Department of Veterans Affairs
3.
Telemed J E Health ; 24(3): 203-209, 2018 03.
Article in English | MEDLINE | ID: mdl-28686082

ABSTRACT

PURPOSE: Veterans with dementia and their caregivers in remote areas may not have access to specialists to provide diagnosis, treatment, and education. The purpose of this clinical demonstration project was to examine the feasibility, acceptability, and impact of a video consultations clinic for veterans with dementia or memory complaints and their caregivers. METHODS: The dementia clinical video telehealth (CVT) consultation clinic was established to identify, diagnose, and treat dementia in veterans at sites distant from the main medical center. A geriatrician at the main facility provided video consultation to patients and caregivers at seven satellite facilities. Diagnoses made and services provided were recorded after the initial consultation. Patient and caregiver satisfaction with the CVT clinic were assessed. FINDINGS: Ninety-four patients were evaluated in the CVT dementia clinic (average age = 74.7; average Mini-Mental State Exam = 24.4). Forty patients had a prior dementia diagnosis, 15 received a new dementia diagnosis, and 20 a new mild cognitive impairment diagnosis. Of the remaining patients evaluated for memory complaints, seven were found to have depression, three had hearing loss, and three had traumatic brain injury. After CVT consultation, common referrals included social work (n = 43), neuropsychology (n = 36), and brain imaging (n = 26). Patients and caregivers expressed high satisfaction with the video consultation and 90% of caregivers indicated they would rather use CVT than travel to see the specialist in person. CONCLUSIONS: Video consultation was well accepted by both dementia patients and caregivers. CVT may facilitate timely diagnosis and management and provide support for rural dementia patients and caregivers.


Subject(s)
Dementia/diagnosis , Dementia/therapy , Patient Satisfaction , Remote Consultation/organization & administration , Rural Population , Adult , Aged , Aged, 80 and over , Brain Injuries, Traumatic/diagnosis , Brain Injuries, Traumatic/therapy , Caregivers/psychology , Cognitive Dysfunction/diagnosis , Cognitive Dysfunction/therapy , Depression/diagnosis , Depression/therapy , Female , Hearing Loss/diagnosis , Humans , Male , Mental Status and Dementia Tests , Middle Aged , Referral and Consultation , Veterans , Videoconferencing
4.
Telemed J E Health ; 23(7): 544-554, 2017 07.
Article in English | MEDLINE | ID: mdl-28051761

ABSTRACT

BACKGROUND: Chronic heart failure (HF) is a complex and costly disease. Daily weight and symptom monitoring is the cornerstone of HF management. Little information exists about feasibility of a mobile monitoring intervention among minority patients with HF. METHODS: We developed and tested usability of a mobile-monitoring system in minority patients with HF in a 2:1 randomized controlled trial. We tracked usage and obtained feedback on usability and the system overall at 1, 2, and 3 months. RESULTS: Forty-two participants aged 53.0 ± 9.4 years (mean ± standard deviation) were randomized to the mobile-monitoring intervention group. They included the following: 67% males, 76% White Hispanics, 21% African Americans, and 52% with high school education or less. Over the 3-month intervention period, 26 (62%) participants used the system over 50% of the time. Overall, on a 1.0-7.0 scale for both, program satisfaction scores were excellent (mean 6.84 ± 0.46), and the usability ratings were all above 6.0. Comparing 1- to 3-month responses, there was a substantial increase in the percentage of participants who felt the system was easy to use after they had gotten used to it (84% vs. 94%) and that navigating the system was not complicated (78% vs. 84%). Almost all participants said that the program made them feel more secure about their health and that they would stay enrolled in a program like this. None of them had used a similar system before. CONCLUSIONS: A mobile phone-based disease management program is feasible in a minority county hospital population and offers a modality to help reduce ethnic disparity.


Subject(s)
Cell Phone , Chronic Disease/therapy , Heart Failure/diagnosis , Heart Failure/therapy , Minority Groups/statistics & numerical data , Patient Satisfaction/statistics & numerical data , Telemedicine , Adult , Black or African American/statistics & numerical data , Aged , Aged, 80 and over , Female , Hispanic or Latino/statistics & numerical data , Hospitals, County/statistics & numerical data , Hospitals, Urban/statistics & numerical data , Humans , Male , Middle Aged , Monitoring, Physiologic/methods , Surveys and Questionnaires , United States , Urban Population/statistics & numerical data , White People/statistics & numerical data
5.
J Rehabil Res Dev ; 50(7): 931-40, 2013.
Article in English | MEDLINE | ID: mdl-24301430

ABSTRACT

The rehabilitation of U.S. military servicemembers (SMs) who have sustained a traumatic loss of one or both lower limbs requires outcome measures that can assess their physical capabilities in comparison with their uninjured colleagues. Describing reference ranges for the 6-minute walk test (6MWT) in both populations will help clinicians develop appropriate goals for rehabilitation and document progress toward those goals. A convenience sample of 118 male U.S. SMs with and 97 without traumatic lower-limb loss participated in this study. All participants completed a 6MWT, and comparisons were made between SMs with and without limb loss and among the levels of limb loss. The SMs without lower-limb loss performed significantly better than all SMs with lower-limb loss. The SMs with transtibial limb loss performed significantly better than those with all other levels of limb loss. Statistically significant and clinically relevant differences were also noted between the other levels of limb loss. No differences were found between different prosthetic components. Reference ranges were established for U.S. SMs with and without various levels of limb loss, and the 6MWT was able to identify functional differences between groups.


Subject(s)
Amputation, Traumatic/physiopathology , Body Size , Military Personnel , Walking/physiology , Adult , Amputation, Traumatic/rehabilitation , Artificial Limbs , Case-Control Studies , Disability Evaluation , Exercise Test , Femur/injuries , Humans , Leg , Male , Prosthesis Design , Reference Values , Tibia/injuries , United States , Young Adult
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