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1.
J Clin Hypertens (Greenwich) ; 25(9): 801-807, 2023 09.
Article En | MEDLINE | ID: mdl-37551050

Hypertension is the leading cause of death worldwide, affecting 1.4 billion people. Treatment options include the widely used calcium channel blockers, among which amlodipine, a dihydropyridine, has unique characteristics that distinguish it from other drugs within this class. This review aims to provide an updated overview of the evidence supporting the use of amlodipine over the past 30 years and highlights its cardiovascular benefits in current hypertension management. Amlodipine has low renal clearance (7 mL/min/mg) and long half-life (35-50 h) and duration of action, which allows it to sustain its anti-hypertensive effect for more than 24 h following a single dose. Additionally, blood pressure (BP) control is maintained even when a dose has been missed, providing continuous protection in case of incidental noncompliance. It has proven to reduce BP variability and successfully lower BP. Amlodipine also controls BP in patients with a systolic/diastolic BP of 130/80 mm Hg or higher, diabetes, or chronic kidney disease without worsening glycemic or kidney function. Additionally, amlodipine is a wise choice for older adults due to its ability to control BP and protect against stroke and myocardial infarction. Side effects of amlodipine include edema, palpitations, dizziness, and flushing, which are more common with the higher dose of 10 mg. Amlodipine is cost effective and predicted to be cost saving when compared with usual care.


Amlodipine , Hypertension , Humans , Aged , Amlodipine/adverse effects , Antihypertensive Agents/adverse effects , Calcium Channel Blockers/adverse effects , Blood Pressure
2.
Am J Med ; 133(6): e260-e268, 2020 06.
Article En | MEDLINE | ID: mdl-31877267

BACKGROUND: Hospital readmission is a major burden for patients, caregivers, and health systems. Some readmissions may be avoided through timely follow-up in a transition clinic with an interprofessional approach to care. METHODS: We prospectively evaluated a cohort of adults >18 years, n = 203, who are patients of an affiliated academic internal medicine clinic with University of Florida Health and discharged from the hospital between November 1, 2016, and May 1, 2017. We sought to determine if follow-up in an interprofessional transition-of-care (TCM) clinic after discharge was associated with a reduction in hospital readmission when compared to standard follow-up at 30, 60, and 90 days. RESULTS: Follow-up in the TCM clinic was associated with reduced odds of hospital readmission at 90 days by 60%, (odds ratio [OR]: 0.40, P = 0.044, 95% confidence interval [CI] 0.16-0.97). Although the clinic failed to demonstrate a statistically significant association between clinic follow-up and in readmission at 30 (OR: 0.66, P = 0.36, 95% CI 0.27-1.59) and 60 days (OR: 0.67, P = 0.31, 95% CI 0.31-1.47), fewer readmissions were seen in patients seen by the TCM clinic. CONCLUSIONS: A primary care nested interprofessional transition-of-care clinic was associated with a reduction in hospital readmission.


Patient Readmission/statistics & numerical data , Primary Health Care/methods , Transitional Care/organization & administration , Aftercare , Aged , Cohort Studies , Female , Home Care Agencies , Humans , Internal Medicine , Male , Middle Aged , Nurses , Patient Care Team , Pharmacists , Primary Health Care/organization & administration , Prospective Studies , Social Workers
3.
J Sex Marital Ther ; 44(1): 1-15, 2018 Jan 02.
Article En | MEDLINE | ID: mdl-28287913

This study compared the effectiveness of a skill-based bibliotherapy intervention and a placebo pill intervention purported to be efficacious in increasing women's sexual desire. Forty-five participants were randomized into the two groups after completing pretest measures of sexual desire and functioning. After completing their interventions, participants completed 6-week posttest and 12-week follow-up measures. Results demonstrated that when compared to the placebo pill group, the bibliotherapy group made statistically greater gains from pretest to follow-up in sexual desire and satisfaction. Nevertheless, the placebo pill group evidenced short-term improvements in sexual desire over time. Findings have implications for future research and current treatments for low sexual desire in women.


Bibliotherapy/methods , Personal Satisfaction , Sexual Dysfunction, Physiological/therapy , Sexual Dysfunctions, Psychological/therapy , Adult , Androgens/administration & dosage , Female , Humans , Libido , Middle Aged , Treatment Outcome
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