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1.
Surg Obes Relat Dis ; 15(12): 2060-2065, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31668944

ABSTRACT

BACKGROUND: Intragastric balloon (IGB) placement can provide a mean percent total weight loss (%TWL) of 10.2% at 6-month follow-up. OBJECTIVES: We aimed to evaluate 30-day outcomes and safety of patients undergoing IGB placement. SETTING: Metabolic and Bariatric Surgery Accreditation and Quality Improvement Program. METHODS: The 2016 to 2017 Metabolic and Bariatric Surgery Accreditation and Quality Improvement Program was queried for adult patients who underwent primary IGB placement. Demographic characteristics and preoperative risk factors were collected. Postoperative outcomes included %TWL, percent excess weight loss, and complications rates and causes. Subset analysis was done for outcomes comparison between surgeons or gastroenterologists performing the procedure. Statistical analysis was performed using SPSS 25.0. RESULTS: A total of 1221 patients were included. The majority was female (81.9%), Caucasian (81.2%), with a mean age of 48 ± 11.3 years and a mean preoperative body mass index of 34.9 ± 11.2 kg/m2. Of patients, 98.8% were discharged within 24 hours of the procedure. Two patients were admitted to the intensive care unit, and 7.2% received postoperative treatment for dehydration. Reoperation and readmission rates were 1.1% and 7.2%, respectively, mainly due to nausea, vomiting, and poor nutritional status (n = 22). The intervention rate was 6.2%. Patients in this cohort achieved a mean %TWL of 6.2% (standard deviation, 5.52%) and mean TWL of 6.8 kg within 30 days postoperatively (n = 147; 24-30 d). CONCLUSIONS: Our data show patients met approximately 50% of their target weight loss 30 days after IGB placement. Nausea, vomiting, and poor nutrition status were the most common complications within 30 days of the procedure. Long-term follow-up is necessary to determine if these patients are able to sustain their weight loss and for how long.


Subject(s)
Gastric Balloon , Obesity, Morbid/surgery , Postoperative Complications/therapy , Weight Loss , Dehydration/therapy , Female , Humans , Male , Middle Aged , Nutrition Disorders/therapy , Patient Readmission/statistics & numerical data , Postoperative Nausea and Vomiting/therapy , Reoperation/statistics & numerical data , Risk Factors , Time Factors
2.
J Health Care Poor Underserved ; 30(2): 618-636, 2019.
Article in English | MEDLINE | ID: mdl-31130541

ABSTRACT

PURPOSE: Using the RE-AIM framework, the primary purpose of this qualitative study was to conduct focus groups to identify areas for future adaptation of an evidence-based cardiovascular disease (CVD) risk intervention (COACH) developed for an urban primary care setting to urban American Indian (AI)-serving settings. METHODS: This qualitative study involved conducting three focus groups with 31 urban AI patients with two or more CVD risk factors to maximize reach and efficacy of COACH. The patients had not yet participated in an adapted COACH program. RESULTS: Findings from the focus groups indicate that a culturally adapted CVD risk reduction program modeled after COACH would be acceptable among urban AI populations. Recommendations for cultural adaptation include a need for images of AI people, traditional AI exercise activities and AI foods, information on the portion sizes of traditional foods, and expanded information on tobacco use and resources. CONCLUSION: With cultural adaptations, the COACH program can be pilot-tested in urban AI-serving primary care settings to address health concerns and behaviors that affect cardiovascular health outcomes.


Subject(s)
Cardiovascular Diseases/prevention & control , Indians, North American , Risk Reduction Behavior , Adult , Aged , Cardiovascular Diseases/ethnology , Evidence-Based Practice/methods , Female , Focus Groups , Humans , Male , Middle Aged , Program Development/methods , Risk Factors , Urban Population
3.
Am J Pharm Educ ; 75(5): 89, 2011 Jun 10.
Article in English | MEDLINE | ID: mdl-21829263

ABSTRACT

The Feik School of Pharmacy collaborated with a commercial software development company to create a Web-based e-portfolio system to document student achievement of curricular outcomes and performance in pharmacy practice experiences. The multi-functional system also could be used for experiential site selection and assignment and continuing pharmacy education. The pharmacy school trained students, faculty members, and pharmacist preceptors to use the e-portfolio system. All pharmacy students uploaded the required number of documents and assessments to the program as evidence of achievement of each of the school's curricular outcomes and completion of pharmacy practice experiences.


Subject(s)
Education, Pharmacy/methods , Educational Technology/methods , Internet , Curriculum , Documentation , Educational Status , Faculty/organization & administration , Humans , Pharmacists/organization & administration , Preceptorship , Software , Students, Pharmacy
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