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1.
Mil Med ; 189(1-2): 13-16, 2024 Jan 23.
Artigo em Inglês | MEDLINE | ID: mdl-37201200

RESUMO

The number of women in the military has more than tripled over the past 50 years, increasing from 5% in the 1970s to 17% in 2023, making them essential for global health engagement and military operations. Provider competence and confidence are barriers to the consistent availability of preventive, gynecologic, and reproductive services for women across service locations and duty platforms. The Defense Health Board recommends standardizing services and improving the availability and scope of services for women at every point of care. In direct conflict with these recommendations, however, is a congressional call for a drawdown of medical forces, which creates a need for operationally trained clinicians with a broad skill set including comprehensive care for women. Advanced practice registered nurses, such as family and women's health nurse practitioners, are key assets to fill this gap on military medical health-care teams. At the request of the U.S. Air Force, the Graduate School of Nursing at the Uniformed Services University began offering a Women's Health Nurse Practitioner (WHNP) program in 2014. The WHNP curriculum was layered onto the existing Family Nurse Practitioner program so that Family Nurse Practitioner students receive enhanced education in women's health and WHNP students are prepared to meet the holistic, primary care needs of patients across the lifespan in addition to caring for women with obstetric and urogenital health concerns. This article highlights the value of dual-certified Family Nurse Practitioners and WHNPs in the military health-care system. These Uniformed Services University alumni are uniquely prepared to provide comprehensive primary and specialty care for female warfighters across the lifecycle from stable, well-resourced duty stations to austere, operational settings or deployment platforms.


Assuntos
Prática Avançada de Enfermagem , Educação de Pós-Graduação em Enfermagem , Medicina , Profissionais de Enfermagem , Feminino , Humanos , Saúde da Mulher
2.
Nurse Educ ; 48(1): 43-48, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-35977345

RESUMO

BACKGROUND: Nurse practitioner (NP) faculty assess student acquisition of knowledge through examinations, simulation, and clinical performance. PROBLEM: Developing appropriately leveled curriculum, assessments, and clinical expectations that accurately capture student maturation presents a challenge. APPROACH: The Reporter, Interpreter, Manager, Educator (RIME) provided the framework for doctor of nursing practice NP curriculum redesign to enhance student performance and content mastery. Faculty used a gap analysis approach, iteratively leveling specialty content, course competencies, examination questions, simulation cases, and clinical expectations using the building blocks of RIME. OUTCOMES: Objective scores on student evaluations for clinical courses exceeded the threshold established, including 83% of simulation encounters. Faculty implemented targeted methods to remediate areas of underperformance. CONCLUSIONS: Structuring the course competencies and preceptor feedback around RIME made it easier to pinpoint specific deficiencies and target remediation. It also helped guide discussions about the minimum acceptable standard for student performance.


Assuntos
Currículo , Profissionais de Enfermagem , Humanos , Pesquisa em Educação em Enfermagem
3.
J Am Assoc Nurse Pract ; 34(8): 954-956, 2022 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-36330549

RESUMO

ABSTRACT: Mitochondrial disorders arise from DNA mutations in either the mitochondrial DNA (mtDNA) or nuclear DNA genomes. This article focuses on a mtDNA base-pair mutation associated with neuropathy, ataxia, and retinitis pigmentosa and Leigh syndrome and the large-scale mtDNA deletion associated with Kearns-Sayre syndrome. Disease sequelae and management strategies are reviewed, along with implications for the nurse practitioner in primary or specialty care.


Assuntos
Síndrome de Kearns-Sayre , Doenças Mitocondriais , Humanos , DNA Mitocondrial/genética , Mutação Puntual/genética , Doenças Mitocondriais/genética , Doenças Mitocondriais/complicações , Síndrome de Kearns-Sayre/complicações , Síndrome de Kearns-Sayre/genética , Mutação
4.
J Am Assoc Nurse Pract ; 34(5): 698-700, 2022 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-35486866

RESUMO

ABSTRACT: Anemia, the overall reduction of red blood cell (RBC) mass in an individual, occurs as a result of an underlying condition. It is probably the most common pathological state worldwide and can be acute, chronic, congenital, or acquired. It can be placed in one of three broad categories: blood loss, hypoproliferative, and hemolytic. The most common and easiest to correct is hypoproliferative anemia caused by nutritional deficiencies. The most common genetic anemias are caused by mutations on the alpha- or beta-globin genes, but there are other mutations that alter red cell membrane function or decrease the bone marrow's ability to manufacture RBCs. Understanding the mechanisms of anemia can help providers interpret the symptom(s)/presentation and guide the clinical workup. Nurse practitioners, especially those in primary care, should be able to recognize when a microcytic anemia is not caused by iron deficiency because these anemias are not corrected by iron supplementation and will need additional workup and referral to hematology.


Assuntos
Anemia Hemolítica Congênita , Anemia Hipocrômica , Anemia , Anemia/complicações , Anemia/etiologia , Anemia Hemolítica Congênita/complicações , Anemia Hemolítica Congênita/genética , Anemia Hipocrômica/etiologia , Humanos , Ferro , Atenção Primária à Saúde
5.
J Am Assoc Nurse Pract ; 34(2): 217-219, 2022 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-35120083

RESUMO

ABSTRACT: Mitochondrial diseases are genetic disorders that can arise either from maternally inherited mitochondrial DNA (mtDNA) or from mutations in nuclear DNA. This article is the second in a series of papers reviewing mitochondrial genetics and several of the disorders associated with mitochondrial gene variants. With a prevalence of 1:∼4,300 persons, mitochondrial disorders are diagnostic entities with which nurse practitioners should be familiar. In describing genetic mutations, numbering nucleotides (nuclear or mtDNA) is critical for communicating exactly where a variation has occurred in a stretch of nucleotides. This article discusses the nomenclature associated with mtDNA mutations, using the examples of mutations causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes and Leber hereditary optic neuropathy. Pathophysiology, symptoms, and treatment options for these disease entities are discussed.


Assuntos
Acidose Láctica , Atrofia Óptica Hereditária de Leber , Acidente Vascular Cerebral , DNA Mitocondrial/genética , Humanos , Encefalomiopatias Mitocondriais , Mutação/genética , Atrofia Óptica Hereditária de Leber/genética
6.
Nurs Outlook ; 70(2): 337-346, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-34911643

RESUMO

BACKGROUND: Clinical competency validation is essential for nurse practitioner (NP) education and public accountability. While there has been robust discussion around what constitutes clinical competency and assessment, clear and consistent definitions and measurements remain elusive. PURPOSE: This article describes the PRIME-NP clinical competency model that is scalable, reproducible and accurately documents NP student competency across clinical courses. METHODS: To develop the model, work in 5 discrete domains was necessary: (a) model development, (b) assessment tool to be used in Objective Structured Clinical Exams (OSCE), (c) rubrics to accompany the OSCE exam, (d) faculty education, and (e) evaluating the model use. FINDINGS: Faculty and student outcomes reveal that the model and assessment tool acceptability and effectiveness of the model, especially for early identification for at risk students. CONCLUSION: The PRIME-NP offered faculty the opportunity to identify at-risk students, identify a more nuanced remediation plan, and assess student competency in simulated environments.


Assuntos
Prática Avançada de Enfermagem , Profissionais de Enfermagem , Competência Clínica , Avaliação Educacional , Humanos , Profissionais de Enfermagem/educação , Estudantes
7.
J Am Assoc Nurse Pract ; 32(11): 764-770, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-33177337

RESUMO

Transgender individuals have a long-standing history of honorable service in the United States Military. However, politics have had an impact on their ability to openly serve in uniform as policies continually change rapidly with each new administration. This article describes the shifting political landscape of policies related to whether (or not) transgender individuals can serve in the military, and how this has affected the health care experiences of transgender individuals and the ability for nurse practitioners to provide quality health care to the transgender population serving on active duty.


Assuntos
Medicina Militar/legislação & jurisprudência , Militares/legislação & jurisprudência , Pessoas Transgênero/legislação & jurisprudência , Humanos , Medicina Militar/métodos , Estados Unidos
8.
J Am Assoc Nurse Pract ; 32(9): 630-637, 2020 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-31702603

RESUMO

ABSTRACT: Exploring new roles and responsibilities available to clinicians offers a path to renovate a nurse practitioner's career. The role of academician and nurse faculty broadens career horizons, presents a sense of autonomy, and offers unique opportunities to teach, participate in research, build leadership skills, and contribute to the health care delivery system at a higher level. Advance practice nurses often consider a shift to academia but are concerned about the unfamiliarity of the entire process. This article offers elements a clinician will likely encounter throughout the transition to a faculty role. These include expectations for the application and interview, negotiating for a position, and orientation to the role of an academic.


Assuntos
Mobilidade Ocupacional , Docentes de Enfermagem/tendências , Liderança , Docentes de Enfermagem/psicologia , Humanos
9.
Semin Oncol Nurs ; 35(1): 22-33, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30660356

RESUMO

OBJECTIVE: To provide an overview of key considerations for somatic testing for the purpose of targeting cancer treatment. DATA SOURCES: Literature; research reports. CONCLUSION: Genomic testing of cancer cells to identify variants that drive the carcinogenic process is becoming common in clinical settings. Providers and patients need to weigh the potential benefits of testing with technologic and logistic issues. IMPLICATIONS FOR NURSING PRACTICE: Testing is available for thousands of genomic variants to identify one or more to guide targeted treatment. Oncology nurses need to understand the benefits and limitations of participating in patient-centered implementation of this testing.


Assuntos
Mutação , Neoplasias/genética , Antineoplásicos Imunológicos/uso terapêutico , Carcinogênese/genética , Aconselhamento Genético , Testes Genéticos , Humanos , Neoplasias/diagnóstico , Neoplasias/tratamento farmacológico , Neoplasias/enfermagem , Prognóstico
11.
J Am Assoc Nurse Pract ; 30(11): 600-602, 2018 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-30422875

RESUMO

Hypophosphatasia is a rare, progressive metabolic disorder inherited in either an autosomal dominant or an autosomal recessive fashion. Affected individuals may have unusual bone development. Infants may be diagnosed with infantile rickets. Symptoms then abate during adolescence, with bony abnormalities manifesting again as mid-life osteopenia or osteoporosis. Long-term management is focused on minimizing complications, so consultations and periodic visits with a variety of specialists is often warranted. New therapies are on the horizon, but some agents used to treat bone diseases are contraindicated in this population. At-risk relatives should be referred to genetic professionals to determine mode of inheritance and discuss options.


Assuntos
Hipofosfatasia/complicações , Hipofosfatasia/diagnóstico , Doenças Genéticas Inatas/genética , Humanos , Hipofosfatasia/fisiopatologia , Síndrome
12.
Mil Med ; 181(11): 1404-1406, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27849472

RESUMO

Despite efforts to increase patient safety, hundreds of thousands of lives are lost each year to preventable health care errors. The Institute of Medicine and other organizations have recommended that facilitating effective interprofessional health care team work can help address this problem. While the concept of interprofessional health care teams is known, understanding and organizing effective team performance have proven to be elusive goals. Although considerable research has been conducted in the civilian sector, scholars have yet to extend research to the military context. Indeed, delivering the highest caliber of health care to our service men and women is vitally important. This commentary describes a new initiative as the Uniformed Services University of the Health Sciences aimed at researching the characteristics of successful military interprofessional teams and why those characteristics are important. It also describes the interprofessional education initiative that Uniformed Services University is launching to help optimize U.S. military health care.


Assuntos
Comportamento Cooperativo , Relações Interprofissionais , Medicina Militar/educação , Militares , Equipe de Assistência ao Paciente/normas , Humanos , Medicina Militar/métodos , Equipe de Assistência ao Paciente/tendências , Desenvolvimento de Programas
13.
Nurse Pract ; 39(10): 18-28; quiz 28-9, 2014 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-25208040

RESUMO

The public expects nurse practitioners (NPs) to be informed about scientific advances and adjust practice as disease screening and management evolves with new research findings. No discipline has evolved more quickly than genomics. This article describes six areas in genomics in which NPs should be competent, concluding with three case studies.


Assuntos
Competência Clínica , Genômica/tendências , Profissionais de Enfermagem , Padrões de Prática em Enfermagem/normas , Pesquisa Biomédica , Predisposição Genética para Doença , Testes Genéticos/ética , Testes Genéticos/legislação & jurisprudência , Humanos , Papel do Profissional de Enfermagem , Avaliação em Enfermagem , Educação de Pacientes como Assunto , Medição de Risco
14.
J Nurs Scholarsh ; 45(1): 89-95, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23368403

RESUMO

PURPOSE: Some forms of genetic skin disease are highly prevalent and others are exceedingly rare, but collectively, genetic skin disorders (or genodermatoses) are often poorly understood. The purpose of this article, therefore, is to increase nurses' awareness and understanding of some of the physical, psychological, social, and ethical issues facing patients with inherited skin disorders. ORGANIZING CONSTRUCT: This article offers an overview of genetic skin diseases; highlights the complexity and prevalence of the genodermatoses; describes inheritance patterns, genetics, and treatment for six genodermatoses; and reviews some of the ethical, privacy, technological, and resource issues nurses should consider when caring for patients with genetic skin disorders. CONCLUSIONS: Because genodermatoses are found in all age groups, across all populations, and within all healthcare settings, nurses are uniquely positioned to address the educational and healthcare needs of patients and families with inherited skin disorders. CLINICAL RELEVANCE: Over the past two decades, genetics has evolved from a niche specialty into general practice. To ensure that patients and their families receive appropriate services and resources, nurses must have a working knowledge of genetic concepts. This article reinforces key genetic concepts while discussing many of the issues and concerns important to caring for patients with genetic skin disease.


Assuntos
Dermatopatias/genética , Dermatopatias/enfermagem , Ética em Enfermagem , Predisposição Genética para Doença , Testes Genéticos , Genoma Humano , Humanos , Papel do Profissional de Enfermagem , Fatores de Risco , Dermatopatias/psicologia
15.
Prehosp Disaster Med ; 28(1): 61-8, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23149111

RESUMO

INTRODUCTION: Military health care providers (HCPs) have an integral role during disaster, humanitarian, and civic assistance (DHCA) missions. Since 50% of patients seen in these settings are children, military providers must be prepared to deliver this care. PURPOSE: The purpose of this systematic, integrative review of the literature was to describe the knowledge and clinical skills military health care providers need in order to provide care for pediatric outpatients during DHCA operations. DATA SOURCES: A systematic search protocol was developed in conjunction with a research librarian. Searches of PubMed and CINAHL were conducted using terms such as Disaster*, Geological Processes, and Military Personnel. Thirty-one articles were included from database and manual searches. CONCLUSIONS: Infectious diseases, vaccines, malnutrition, sanitation and wound care were among the most frequently mentioned of the 49 themes emerging from the literature. Concepts included endemic, environmental, vector-borne and vaccine-preventable diseases; enhanced pediatric primary care; and skills and knowledge specific to disaster, humanitarian and civic assistance operations. IMPLICATIONS FOR PRACTICE: The information provided is a critical step in developing curriculum specific to caring for children in DHCA. While the focus was military HCPs, the knowledge is easily translated to civilian HCPs who provide care to children in these situations.


Assuntos
Proteção da Criança , Desastres , Pessoal de Saúde/normas , Militares , Socorro em Desastres/normas , Adolescente , Altruísmo , Criança , Distúrbios Civis , Controle de Doenças Transmissíveis/métodos , Bases de Dados Bibliográficas , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Desnutrição/terapia , Saneamento/métodos , Ferimentos e Lesões/terapia
16.
Genet Med ; 10(9): 659-67, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18978677

RESUMO

PURPOSE: The aim of this article was to determine the accuracy and efficiency of World Wide Web ("Web") resources to help nongeneticists answer four clinical questions about each of five common genetic conditions. METHODS: Correct answers were established by literature review. Two open-access genetics resources and seven general subscription resources were reviewed. Scoring criteria were established to define complete, partial, vague, inconsistent, not found, and wrong answers. The main outcome measures were number of answers found, accuracy, and completeness of answers. Efficiency (time per answer found) was a secondary measure. RESULTS: Overall, the databases contained complete answers 33.3% of the time but contained no information as frequently (33.9%). The best database had complete answers 70% of the time, whereas the worst contained no complete answers. Five of the seven subscription databases had a total of eight wrong answers. The other two subscription databases and the two open-access genetics databases had no wrong answers. Search time ranged from 3.2 to 18.3 minutes per complete answer. CONCLUSIONS: Nongeneticist providers do not have a Web resource that is accessible, accurate, and efficient to answer genetic questions that might arise in practice.


Assuntos
Bases de Dados Factuais , Armazenamento e Recuperação da Informação , Internet , Serviços de Informação
17.
J Genet Couns ; 17(2): 152-60, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18259847

RESUMO

Genetic Counselors (GCs) spend years learning about genetics and practicing counseling techniques in classroom environments. From the learner perspective, teaching may seem straightforward: provide appropriate information, develop tests or assignments and submit grades. When asked to teach for the first time, however, clinicians suddenly realize that there is a lot more to education than standing in front of a class and talking. This article introduces clinical educators to strategies and learning principles that help make the teaching/learning process more interesting and successful for faculty and students alike. The instructional concepts presented here are useful across the entire spectrum of learning situations; a 1 hour discussion with a lay audience, a 3 hour workshop at a professional meeting, a 15 week graduate course, or a series of courses culminating in an advanced degree. The article offers suggestions for writing course competencies, selecting instructional approaches, embedding learning engagement options, leveling course content and choosing evaluation strategies.


Assuntos
Docentes de Medicina , Aconselhamento Genético , Genética Médica/educação , Currículo , Avaliação Educacional , Testes Genéticos , Humanos , Modelos Educacionais
18.
Nurs Educ Perspect ; 25(5): 232-7, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15508562

RESUMO

Innovative use of standardized patients (SPs) in a telemedicine environment can improve learning outcomes and clinical competencies. This randomized, cross-over study examined the relationship of technology-based strategies and the improvement of knowledge outcomes and competencies. Results showed that the innovative use of SPs and telemedicine, compared to a traditional distance learning teaching methodology, significantly improved learning outcomes. In addition, there was a significant increase in performance motivation and an interesting decrease in student satisfaction that may be linked to the pressure of performance-based learning. This article addresses knowledge improvement only.


Assuntos
Educação a Distância/métodos , Educação de Pós-Graduação em Enfermagem , Simulação de Paciente , Consulta Remota , Comunicação por Videoconferência , Adulto , Análise de Variância , Avaliação Educacional , Humanos , Pesquisa em Educação em Enfermagem , Estudos Prospectivos , Estados Unidos
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