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1.
Med Ref Serv Q ; 35(2): 135-44, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27054531

RESUMEN

The ORCID (Open Researcher and Contributor ID) registry helps disambiguate authors and streamline research workflows by assigning unique 16-digit author identifiers that enable automatic linkages between researchers and their scholarly activities. This article describes how ORCID works, the benefits of using ORCID, and how librarians can promote ORCID at their institutions by raising awareness of ORCID, helping researchers create and populate ORCID profiles, and integrating ORCID identifiers into institutional repositories and other university research information systems.


Asunto(s)
Autoria/normas , Bibliotecólogos , Bibliotecas Médicas/normas , Bibliotecología/educación , Bibliotecología/normas , Humanos
2.
Med Ref Serv Q ; 34(2): 190-201, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25927511

RESUMEN

Scopus and Web of Science are the two major citation databases that collect and disseminate bibliometric statistics about research articles, journals, institutions, and individual authors. Liaison librarians are now regularly called upon to utilize these databases to assist faculty in finding citation activity on their published works for tenure and promotion, grant applications, and more. But questions about the accuracy, scope, and coverage of these tools deserve closer scrutiny. Discrepancies in citation capture led to a systematic study on how Scopus and Web of Science compared in a real-life situation encountered by liaisons: comparing three different disciplines at a medical school and nursing program. How many articles would each database retrieve for each faculty member using the author-searching tools provided? How many cited references for each faculty member would each tool generate? Results demonstrated troubling differences in publication and citation activity capture between Scopus and Web of Science. Implications for librarians are discussed.


Asunto(s)
Bibliometría , Bases de Datos Bibliográficas , Almacenamiento y Recuperación de la Información/métodos , Bibliotecas Médicas , Ginecología , Enfermería , Obstetricia , Publicaciones Periódicas como Asunto , Farmacia
3.
J Hosp Palliat Nurs ; 23(5): 406-420, 2021 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-33883525

RESUMEN

Dyspnea is a subjective experience of breathing discomfort that consists of qualitatively distinct sensations, varies in intensity, and can only be known through the patient's report. Dyspnea is akin to suffocation and is one of the most distressing symptoms experienced by patients with advanced illness and at the end of life. Common approaches to dyspnea management, such as pulmonary rehabilitation, breathing strategies, or supplemental oxygen, have become accepted through pragmatic use or because studies do not include dyspnea as a measured outcome. Patients and clinicians urgently need evidence-based treatments to alleviate this frightening symptom. To fill this gap, a group of dyspnea researchers with expertise to conduct a literature review of evidence-based interventions for dyspnea in patients with serious illness produced these guidelines. We present the evidence from the strongest recommendations for practice to the weakest recommendations and include practical considerations for clinical nurses.


Asunto(s)
Muerte , Disnea , Disnea/etiología , Disnea/terapia , Humanos
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