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1.
Innov Pharm ; 11(3)2020.
Artigo em Inglês | MEDLINE | ID: mdl-34007632

RESUMO

OBJECTIVE: The purpose of this study is to determine the effectiveness of individualized communication strategies and self-management action plans to improve A1c control at 3 months in patients with low health literacy. METHODS: A prospective, open-labeled, pilot study was conducted on 23 patients with diabetes mellitus in a pharmacist-led ambulatory care clinic. Patients who had a Rapid Estimate of Adult Literacy in Medicine- Revised (REALM-R) score of 6 or less and an A1c greater than 7% upon study entry were included. The first group received the teach-back method, personalized actions, and follow-up phone calls to assess comprehension (N = 12). The second group was assigned to usual care (N = 11). RESULTS: Patients receiving literacy-appropriate interventions had greater A1c percent reduction (A1c difference of -2.0 ± 1.3 vs -1.0 ± 2.2; P = 0.02) and less hyperglycemic events per week (0.1 vs. 2.1; P = 0.04). There were no differences in the number of hypoglycemic events, testing frequency, medication-adherence rates, or hospitalizations and emergency room visits related to diabetes. CONCLUSION: Literacy-appropriate methods such as the teach-back method, personalized action plans, and telephone follow-ups may improve glycemic control in low health literate patients with diabetes. PRACTICE IMPLICATIONS AND INNOVATIONS: The findings from this study suggest that pharmacists may improve diabetes outcomes when managing patients who possess low health literacy using simplified teaching methods.

2.
Pharmacotherapy ; 34(4): 389-95, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24390829

RESUMO

The rapid development and increased availability of novel pharmacologic therapies and pharmaceutical products has amplified the potential for drug exposure during pregnancy. Many drugs are beneficial for disease state management during pregnancy and provide significant fetal and maternal health benefits. However, a paucity of safety data combined with the imprecision of the current risk category system renders risk versus benefit assessment difficult. In response to decades of criticism, the U.S. Food and Drug Administration (FDA) is implementing a new pregnancy and lactation labeling rule designed to improve risk versus benefit assessment of drugs used in pregnant and nursing mothers. These recommendations will provide clear and detailed information for both patients and health care providers, and they will include three main categories: risk summary, clinical considerations, and data. The new labeling rules remove the previous letter risk categorization system (A, B, C, D, X). In this review, we summarize the upcoming FDA labeling changes and discuss their potential consequences on clinical practice.


Assuntos
Rotulagem de Medicamentos/legislação & jurisprudência , Feto/efeitos dos fármacos , Lactação/efeitos dos fármacos , Feminino , Humanos , Gravidez , Risco , Estados Unidos , United States Food and Drug Administration
3.
Pharmacotherapy ; 33(5): 549-57, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23450827

RESUMO

Family planning remains a high priority area for the United States, with goals to increase the proportion of pregnancies that are intended, reduce pregnancy rates among adolescents, and increase contraceptive use prioritized in the Healthy People 2020 objectives. Contraception intended for use after unprotected intercourse, known as emergency contraception, remains underutilized. Levonorgestrel is one method of oral emergency contraception, which prevents fertilization and does not disrupt an already established pregnancy; thus, timing of administration is critical. Despite data demonstrating safety and efficacy, evidence-based decision making has been overshadowed by politically charged actions involving levonorgestrel emergency contraception for over a decade. The Women's Health Practice and Research Network of the American College of Clinical Pharmacy supports expanded access to levonorgestrel emergency contraception and removal of barriers such as age restrictions on the nonprescription drug product. Pharmacists remain a key provider of emergency contraceptive services and can help ensure timely access. In states where direct pharmacy access to emergency contraception is available, pharmacists are encouraged to participate. Education, research, and advocacy are other important responsibilities for pharmacists in this arena.


Assuntos
Anticoncepção Pós-Coito/estatística & dados numéricos , Anticoncepcionais Pós-Coito , Acessibilidade aos Serviços de Saúde , Levanogestrel , Medicamentos sem Prescrição , Adolescente , Fatores Etários , Anticoncepcionais Pós-Coito/administração & dosagem , Anticoncepcionais Pós-Coito/efeitos adversos , Esquema de Medicação , Feminino , Regulamentação Governamental , Acessibilidade aos Serviços de Saúde/legislação & jurisprudência , Humanos , Levanogestrel/administração & dosagem , Levanogestrel/efeitos adversos , Medicamentos sem Prescrição/administração & dosagem , Educação de Pacientes como Assunto , Assistência Farmacêutica , Gravidez , Gravidez na Adolescência/prevenção & controle , Gravidez na Adolescência/estatística & dados numéricos , Sociedades Farmacêuticas , Estados Unidos , Serviços de Saúde da Mulher
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