Literature DB >> 17003536

Understanding the information needs of general practitioners managing a rare genetic disorder (osteogenesis imperfecta).

Philip Zack1, Catherine Devile, Christine Clark, Robert Surtees.   

Abstract

BACKGROUND: Lack of adequate knowledge is a common problem in medicine, but is a particular problem in a rapidly advancing field like genetics. This study uses the example of a rare genetic disorder (osteogenesis imperfecta) to understand the information needs of primary care physicians (GPs).
OBJECTIVES: To determine whether a knowledge gap is recognised, how GPs currently attempt to overcome it, and what features of an information resource are preferred by GPs.
METHODS: GPs of children affected by osteogenesis imperfecta in and around Greater London were interviewed, using both questionnaire-based semi-structured interview and a qualitatively analysed open-ended discussion. Consultations in both primary and tertiary care settings over a 5-year period were compared.
RESULTS: Problems due to osteogenesis imperfecta were presented to GPs in about one third of consultations with these patients. GPs reported finding such patients difficult to manage due to lack of knowledge. Knowledge from tertiary sources, which was authoritative, accessible and relevant, was preferred, particularly when reasoning was explained. Primary literature and clinical guidelines were not favoured.
CONCLUSIONS: Empirical evidence supports and elaborates theoretical models for provision of clinically useful information. A model for improved information services using authoritative web-based information linked to electronic patient records is suggested.

Entities:  

Mesh:

Year:  2006        PMID: 17003536     DOI: 10.1159/000094475

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  5 in total

1.  Barriers and facilitators to clinical information seeking: a systematic review.

Authors:  Christopher A Aakre; Lauren A Maggio; Guilherme Del Fiol; David A Cook
Journal:  J Am Med Inform Assoc       Date:  2019-10-01       Impact factor: 4.497

2.  Enhancing the diagnosis of fabry disease in cardiology with a targeted information: a before-after control-impact study.

Authors:  Anne-Louise Savary; Remy Morello; Carole Brasse-Lagnel; Paul Milliez; Soumeya Bekri; Fabien Labombarda
Journal:  Open Heart       Date:  2017-03-13

3.  How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners.

Authors:  W R H Evans; J Tranter; I Rafi; J Hayward; N Qureshi
Journal:  J Community Genet       Date:  2020-03-03

4.  Severe Combined Immunodeficiency: Knowledge and Information Needs Among Healthcare Providers.

Authors:  Oksana Kutsa; Angela Gwaltney; Alissa Creamer; Melissa Raspa
Journal:  Front Pediatr       Date:  2022-02-21       Impact factor: 3.418

5.  Initial report of the osteogenesis imperfecta adult natural history initiative.

Authors:  Laura L Tosi; Matthew E Oetgen; Marianne K Floor; Mary Beth Huber; Ann M Kennelly; Robert J McCarter; Melanie F Rak; Barbara J Simmonds; Melissa D Simpson; Carole A Tucker; Fergus E McKiernan
Journal:  Orphanet J Rare Dis       Date:  2015-11-14       Impact factor: 4.123

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.