2011
DOI: 10.1002/acr.20399
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An ask‐the‐expert service on a rheumatology web site: Who were the users and what did they look for?

Abstract: Objective. To analyze the inquiries sent to an online ask-the-rheumatologist service in order to identify the users' needs and requirements. Methods. The official web site of the German Competence Network Rheumatology (www.rheumanet.org) provided expert information for patients, relatives, and physicians. We analyzed the content of 1,133 inquiries posted over 5 years and the experts' answers were blinded for analyses. Results. Patients (60.0%), relatives (24.3%), and physicians (15.7%) addressed the experts. I… Show more

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Cited by 14 publications
(13 citation statements)
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References 30 publications
(66 reference statements)
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“… Four major topics of IN were identified: Qualitative study. Information on health care system: 30 (27.8 %) Information on individual access options to health care system: 31 (28.7 %) Information on regional service provider: 17 (15.8 %) Context-specific and disease-specific questions: 30 (27.8 %) Neumann et al (2011) [ 20 ] To identify and predict subgroups of IN among cancer patients. Cross-sectional design.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“… Four major topics of IN were identified: Qualitative study. Information on health care system: 30 (27.8 %) Information on individual access options to health care system: 31 (28.7 %) Information on regional service provider: 17 (15.8 %) Context-specific and disease-specific questions: 30 (27.8 %) Neumann et al (2011) [ 20 ] To identify and predict subgroups of IN among cancer patients. Cross-sectional design.…”
Section: Resultsmentioning
confidence: 99%
“…Information needs of patients were assessed in 12 studies [ 9 , 10 , 12 , 13 , 15 20 , 24 , 27 ], followed by information needs in the general population (4 studies) [ 11 , 21 , 25 , 26 ], of spouses/family members (4 studies) [ 14 , 15 , 18 , 20 ], and parents (2 studies) [ 22 , 23 ].…”
Section: Resultsmentioning
confidence: 99%
“…First, online utilities facilitating the search of registered users: almost 50 % of disease-focused online communities had a tool performing such search. The most frequent user-searching queries were gender, age, username, geographic area, and disease [23]. Second, entice of disclosure of PHI: all medical forums encourage participants to share their experience of illness and seek advice from other participants.…”
Section: Phl Leak Prevention In Online Communitiesmentioning
confidence: 99%
“…Several national organizations for persons with arthritis offer information about how intimate relationships and sexual life can be affected by RA. A recent investigation into a patient online helpline showed that 10% of the questions concerned sexual and reproductive issues (Richter et al 2011). And for most RA patients a wide concept of sexual health, including social functioning and an emotional perspective, is more important than a more mechanical description of disease consequences on sexual health (Couldrick, Gaynor, and Cross 2010 …”
Section: Informationmentioning
confidence: 99%
“…Ways of informing patients are by using material that often is available from organizations for persons with RA, both on-line and/or by leaflets. There are also on-line help-lines for persons with RA, where questions about sexual health have been presented (Richter et al 2011). It is possible that further use of such information including sexual health might assist the communication concerning sexual health between partners and perhaps also between persons with RA and health professionals.…”
Section: Introductionmentioning
confidence: 99%