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LIS-MEDICAL  May 2020

LIS-MEDICAL May 2020

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Subject:

[bims-librar] 2020-05-10, ten selections

From:

Thomas Krichel <[log in to unmask]>

Reply-To:

Thomas Krichel <[log in to unmask]>

Date:

Sun, 10 May 2020 02:12:00 +0000

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bims-librar       Biomed News on Biomedical librarianship
─────────────────────────────┐
Issue of 2020‒05‒10          │ 
ten papers selected by       │
Thomas Krichel (Open Library │
 Society)                    │
 http://e.biomed.news/librar │
                             │
                             │
                             └──────────────────────────────────────────────────
────────────────────────────────────────────────────────────────────────────────

 1. Effect of Online Health Information Seeking on Anxiety in Hospitalized 
     Pregnant Women: Cohort Study.
 2. TeamTat: a collaborative text annotation tool.
 3. Using Google Trends to assess the impact of global public health days 
     on online health information seeking behaviour in Central and South 
     America.
 4. The role of health classifications in health information management.
 5. [Use of health information on the internet: personal and motivational 
     influencing factors].
 6. [Toolbox for user-experience evaluation of online health information].
 7. The new International Classification of Diseases 11th edition: a 
     comparative analysis with ICD-10 and ICD-10-CM.
 8. SIB Literature Services: RESTful customizable search engines in 
     biomedical literature, enriched with automatically mapped biomedical 
     concepts.
 9. An assessment of the quality of current clinical meta-analyses.
10. Developing a strategy to improve data sharing in health research: A 
     mixed-methods study to identify barriers and facilitators.

────────────────────────────────────────────────────────────────────────────────

                                      JMIR Med Inform. 2020 May 06. 8(5): e16793
 1. Effect of Online Health Information Seeking on Anxiety in Hospitalized 
     Pregnant Women: Cohort Study.
   Coglianese F, Beltrame Vriz G, Soriani N, Piras GN, Comoretto RI, Clemente 
   L, Fasan J, Cristiano L, Schiavinato V, Adamo V, Marchesoni D, Gregori D
  BACKGROUND: There are approximately 1,000,000 pregnant women at high risk 
  for obstetric complications per year, more than half of whom require 
  hospitalization.
   OBJECTIVE: The aim of this study was to determine the relation between 
  online health information seeking and anxiety levels in a sample of 
  hospitalized woman with pregnancy-related complications.
   METHODS: A sample of 105 pregnant women hospitalized in northern Italy, all 
  with an obstetric complication diagnosis, completed different 
  questionnaires: Use of Internet Health-information (UIH) questionnaire about 
  use of the internet, EuroQOL 5 dimensions (EQ-5D) questionnaire on quality 
  of life, State-Trait Anxiety Inventory (STAI) questionnaire measuring 
  general anxiety levels, and a questionnaire about critical events occurring 
  during hospitalization.
   RESULTS: Overall, 98/105 (93.3%) of the women used the internet at home to 
  obtain nonspecific information about health in general and 95/105 (90.5%) of 
  the women used the internet to specifically search for information related 
  to their obstetric disease. Online health information-seeking behavior 
  substantially decreased the self-reported anxiety levels (P=.008).
   CONCLUSIONS: Web browsing for health information was associated with anxiety 
  reduction, suggesting that the internet can be a useful instrument in 
  supporting professional intervention to control and possibly reduce 
  discomfort and anxiety for women during complicated pregnancies.
   Keywords: anxiety; internet use; pregnant women; web health information
  DOI: https://doi.org/10.2196/16793
  URL: http://pubmed.ncbi.nlm.nih.gov/32374268

             Nucleic Acids Res. 2020 May 08. pii: gkaa333. [Epub ahead of print]
 2. TeamTat: a collaborative text annotation tool.
   Islamaj R, Kwon D, Kim S, Lu Z
  Manually annotated data is key to developing text-mining and 
  information-extraction algorithms. However, human annotation requires 
  considerable time, effort and expertise. Given the rapid growth of 
  biomedical literature, it is paramount to build tools that facilitate speed 
  and maintain expert quality. While existing text annotation tools may 
  provide user-friendly interfaces to domain experts, limited support is 
  available for figure display, project management, and multi-user team 
  annotation. In response, we developed TeamTat (https://www.teamtat.org), a 
  web-based annotation tool (local setup available), equipped to manage team 
  annotation projects engagingly and efficiently. TeamTat is a novel tool for 
  managing multi-user, multi-label document annotation, reflecting the entire 
  production life cycle. Project managers can specify annotation schema for 
  entities and relations and select annotator(s) and distribute documents 
  anonymously to prevent bias. Document input format can be plain text, PDF or 
  BioC (uploaded locally or automatically retrieved from PubMed/PMC), and 
  output format is BioC with inline annotations. TeamTat displays figures from 
  the full text for the annotator's convenience. Multiple users can work on 
  the same document independently in their workspaces, and the team manager 
  can track task completion. TeamTat provides corpus quality assessment via 
  inter-annotator agreement statistics, and a user-friendly interface 
  convenient for annotation review and inter-annotator disagreement resolution 
  to improve corpus quality.
  DOI: https://doi.org/10.1093/nar/gkaa333
  URL: http://pubmed.ncbi.nlm.nih.gov/32383756

                                           J Glob Health. 2020 Jun;10(1): 010403
 3. Using Google Trends to assess the impact of global public health days 
     on online health information seeking behaviour in Central and South 
     America.
   Havelka EM, Mallen CD, Shepherd TA
  Background: Public health awareness can help prevent illness and result in 
  earlier intervention when it does occur. For this reason, health promotion 
  and disease awareness campaigns have great potential to alleviate the global 
  burden of disease. Global Public Health Days (GPHD) are frequently 
  implemented with this intent, but research evaluating their effectiveness, 
  especially in the developing world setting, is scant.
   Objectives: We aimed to evaluate the impact of four GPHDs (World Cancer Day, 
  World Diabetes Day, World Mental Health Day, World AIDS Day) on online 
  health information seeking behaviour (OHISB) in five Central and South 
  American (CSA) countries which differ in their stage of economic development 
  and epidemiological transition (Uruguay, Chile, Brazil, Colombia, Nicaragua).
   Methods: Google Trends data was used as a 'surrogate' of OHISB. This was 
  measured on the 28 days leading up to the GPHD, on the date of the GPHD, and 
  on the seven days following it. The Joinpoint regression programme was used 
  to perform a time trend analysis on the Google Trends data. This allowed us 
  to identify statistically significant time points of a change in trend, 
  which reflect significant 'changes' to OHISB.
   Results: GPHDs were inconsistently effective at influencing internet search 
  query activity in the studied countries. In situations where an effect was 
  significant, this impact was consistently short-term, with Relative Search 
  Volume level returning to precampaign levels within 7 days of the GPHD.
   Conclusions: Our findings imply the need to revise GPHDs or create 
  alternative health awareness campaigns, perhaps with a more long-term 
  approach and tailored to the specific health needs of the CSA population. 
  Developing effective preventive strategies is vital in helping combat the 
  rising threat of NCDs in this region.
  DOI: https://doi.org/10.7189/jogh.10.010403
  URL: http://pubmed.ncbi.nlm.nih.gov/32373327

                                 Health Inf Manag. 2020 May 08. 1833358320905970
 4. The role of health classifications in health information management.
   Shepheard J, Groom A
  DOI: https://doi.org/10.1177/1833358320905970
  URL: http://pubmed.ncbi.nlm.nih.gov/32383407

     Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2020 May 04.
 5. [Use of health information on the internet: personal and motivational 
     influencing factors].
   Link E, Baumann E
  BACKGROUND AND OBJECTIVES: Taking an active role in healthcare requires 
  comprehensive health knowledge. One's own online search for health 
  information can contribute to an appropriate information base. Therefore, it 
  seems essential to determine the extent to which online services and health 
  apps are currently used in Germany as well as to analyze which personal and 
  motivational factors influence whether and how often the German public 
  search for health information online or use health apps.
   METHODS: We conducted an online survey among the German public in a sample 
  stratified by demographic characteristics (N = 3000). The questionnaire 
  measured the health-related use of the Internet and health apps as well as 
  possible personal and motivational factors. The relevance of these factors 
  for explaining the Internet use for health-related purposes was determined 
  by regression analyses.
   RESULTS: While health-related information searches using the Internet are 
  widespread in Germany, health apps are used less frequently. In particular 
  health information platforms are most frequently used to search for 
  information on disease symptoms. Turning to the Internet for health-related 
  purposes is mainly influenced by motivational factors. Having current health 
  problems and possessing information-seeking skills are particularly 
  influential factors for an individual's Internet use.
   CONCLUSIONS: In order to unfold the potential associated with health-related 
  online information-seeking behaviors, it is necessary that people are 
  motivated and feel competent to gather online information themselves. In 
  particular, the corresponding skills need to be promoted in order to reduce 
  the risk of increasing informational, health, and social disparities.
   Keywords: Empowered patients; Health promotion; Health-realted online 
    search; Uncertainty management
  DOI: https://doi.org/10.1007/s00103-020-03144-5
  URL: http://pubmed.ncbi.nlm.nih.gov/32367207

     Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2020 May 04.
 6. [Toolbox for user-experience evaluation of online health information].
   Thielsch MT, Salaschek M
  The Internet is now a central source of health information. An ideal design 
  of web services and e‑health programs requires valid evaluations of users' 
  perceptions, the so-called user experience. As part of a research project 
  with the German Federal Centre for Health Education (BZgA), a toolbox for 
  website evaluation (for screening and monitoring) was compiled for this 
  purpose from freely available quantitative empirical questionnaires. With 
  this toolbox, key aspects of the web user experience can be reliably and 
  validly assessed. In this article, we describe the toolbox's components, 
  underlying quality criteria, and practical experiences.The aim of the 
  toolbox is to facilitate methodically high-quality, comprehensive, and 
  time-efficient analyses. A total of nine standardized instruments and 
  supplementary single items from three areas are documented. In the standard 
  version of the toolbox, 35 items are used that can be answered in less than 
  10 min. For an extended examination of a website, the toolbox documents 
  additional measures on website content, usability, and aesthetics. We 
  discuss both the advantages and limitations of the toolbox and give an 
  outlook on possible future developments.
   Keywords: Digital health communication; Evaluation methods; E‑health; 
    Quality assurance; Usability
  DOI: https://doi.org/10.1007/s00103-020-03142-7
  URL: http://pubmed.ncbi.nlm.nih.gov/32367206

                              J Am Med Inform Assoc. 2020 May 01. 27(5): 738-746
 7. The new International Classification of Diseases 11th edition: a 
     comparative analysis with ICD-10 and ICD-10-CM.
   Fung KW, Xu J, Bodenreider O
  OBJECTIVE: To study the newly adopted International Classification of 
  Diseases 11th revision (ICD-11) and compare it to the International 
  Classification of Diseases 10th revision (ICD-10) and International 
  Classification of Diseases 10th revision-Clinical Modification (ICD-10-CM).
   MATERIALS AND METHODS: : Data files and maps were downloaded from the World 
  Health Organization (WHO) website and through the application programming 
  interfaces. A round trip method based on the WHO maps was used to identify 
  equivalent codes between ICD-10 and ICD-11, which were validated by limited 
  manual review. ICD-11 terms were mapped to ICD-10-CM through normalized 
  lexical mapping. ICD-10-CM codes in 6 disease areas were also manually 
  recoded in ICD-11.
   RESULTS: Excluding the chapters for traditional medicine, functioning 
  assessment, and extension codes for postcoordination, ICD-11 has 14 622 leaf 
  codes (codes that can be used in coding) compared to ICD-10 and ICD-10-CM, 
  which has 10 607 and 71 932 leaf codes, respectively. We identified 4037 
  pairs of ICD-10 and ICD-11 codes that were equivalent (estimated accuracy of 
  96%) by our round trip method. Lexical matching between ICD-11 and ICD-10-CM 
  identified 4059 pairs of possibly equivalent codes. Manual recoding showed 
  that 60% of a sample of 388 ICD-10-CM codes could be fully represented in 
  ICD-11 by precoordinated codes or postcoordination.
   CONCLUSION: In ICD-11, there is a moderate increase in the number of codes 
  over ICD-10. With postcoordination, it is possible to fully represent the 
  meaning of a high proportion of ICD-10-CM codes, especially with the 
  addition of a limited number of extension codes.
   Keywords: ICD-10; ICD-10-CM; ICD-11; controlled medical vocabularies; 
    medical terminologies
  DOI: https://doi.org/10.1093/jamia/ocaa030
  URL: http://pubmed.ncbi.nlm.nih.gov/32364236

             Nucleic Acids Res. 2020 May 07. pii: gkaa328. [Epub ahead of print]
 8. SIB Literature Services: RESTful customizable search engines in 
     biomedical literature, enriched with automatically mapped biomedical 
     concepts.
   Julien G, Déborah C, Pierre-André M, Luc M, Emilie P, Patrick R
  Thanks to recent efforts by the text mining community, biocurators have now 
  access to plenty of good tools and Web interfaces for identifying and 
  visualizing biomedical entities in literature. Yet, many of these systems 
  start with a PubMed query, which is limited by strong Boolean constraints. 
  Some semantic search engines exploit entities for Information Retrieval, 
  and/or deliver relevance-based ranked results. Yet, they are not designed 
  for supporting a specific curation workflow, and allow very limited control 
  on the search process. The Swiss Institute of Bioinformatics Literature 
  Services (SIBiLS) provide personalized Information Retrieval in the 
  biological literature. Indeed, SIBiLS allow fully customizable search in 
  semantically enriched contents, based on keywords and/or mapped biomedical 
  entities from a growing set of standardized and legacy vocabularies. The 
  services have been used and favourably evaluated to assist the curation of 
  genes and gene products, by delivering customized literature triage engines 
  to different curation teams. SIBiLS (https://candy.hesge.ch/SIBiLS) are 
  freely accessible via REST APIs and are ready to empower any curation 
  workflow, built on modern technologies scalable with big data: MongoDB and 
  Elasticsearch. They cover MEDLINE and PubMed Central Open Access enriched by 
  nearly 2 billion of mapped biomedical entities, and are daily updated.
  DOI: https://doi.org/10.1093/nar/gkaa328
  URL: http://pubmed.ncbi.nlm.nih.gov/32379317

                                   BMC Med Res Methodol. 2020 May 07. 20(1): 105
 9. An assessment of the quality of current clinical meta-analyses.
   Hameed I, Demetres M, Tam DY, Rahouma M, Khan FM, Wright DN, Mages K, 
   DeRosa AP, Nelson BB, Pain K, Delgado D, Girardi LN, Fremes SE, Gaudino M
  BACKGROUND: The objective of this study was to assess the overall quality of 
  study-level meta-analyses in high-ranking journals using commonly employed 
  guidelines and standards for systematic reviews and meta-analyses.
   METHODS: 100 randomly selected study-level meta-analyses published in ten 
  highest-ranking clinical journals in 2016-2017 were evaluated by medical 
  librarians against 4 assessments using a scale of 0-100: the Peer Review of 
  Electronic Search Strategies (PRESS), Preferred Reporting Items for 
  Systematic Reviews and Meta-Analyses (PRISMA), Institute of Medicine's (IOM) 
  Standards for Systematic Reviews, and quality items from the Cochrane 
  Handbook. Multiple regression was performed to assess meta-analyses 
  characteristics' associated with quality scores.
   RESULTS: The overall median (interquartile range) scores were: PRESS 
  62.5(45.8-75.0), PRISMA 92.6(88.9-96.3), IOM 81.3(76.6-85.9), and Cochrane 
  66.7(50.0-83.3). Involvement of librarians was associated with higher PRESS 
  and IOM scores on multiple regression. Compliance with journal guidelines 
  was associated with higher PRISMA and IOM scores.
   CONCLUSION: This study raises concerns regarding the reporting and 
  methodological quality of published MAs in high impact journals Early 
  involvement of information specialists, stipulation of detailed author 
  guidelines, and strict adherence to them may improve quality of published 
  meta-analyses.
   Keywords: Clinical; Cochrane; Epidemiology; IOM; Meta-analysis; 
    Methodology; PRESS; PRISMA; Quality
  DOI: https://doi.org/10.1186/s12874-020-00999-9
  URL: http://pubmed.ncbi.nlm.nih.gov/32380945

                                 Health Inf Manag. 2020 May 05. 1833358320917207
10. Developing a strategy to improve data sharing in health research: A 
     mixed-methods study to identify barriers and facilitators.
   Krahe MA, Wolski M, Mickan S, Toohey J, Scuffham P, Reilly S
  BACKGROUND: Data sharing presents new opportunities across the spectrum of 
  research and is vital for science that is open, where data are easily 
  discoverable, accessible, intelligible, reproducible, replicable and 
  verifiable. Despite this, it is yet to become common practice. Global 
  efforts to develop practical guidance for data sharing and open access 
  initiatives are underway, however evidence-based studies to inform the 
  development and implementation of effective strategies are lacking.
   OBJECTIVE: This study sought to determine the barriers and facilitators to 
  data sharing among health researchers and to identify the target behaviours 
  for designing a behaviour change intervention strategy.
   METHOD: Data were drawn from a cross-sectional survey of data management 
  practices among health researchers from one Australian research institute. 
  Determinants of behaviour were theoretically derived using well-established 
  behavioural models.
   RESULTS: Data sharing practices have been described for 77 researchers, and 
  6 barriers and 4 facilitators identified. The primary barriers to data 
  sharing included perceived negative consequences and lack of competency to 
  share data. The primary facilitators to data sharing included trust in 
  others using the data and social influence related to public benefit. 
  Intervention functions likely to be most effective at changing target 
  behaviours were also identified.
   CONCLUSION: Results of this study provide a theoretical and evidence-based 
  process to understand the behavioural barriers and facilitators of data 
  sharing among health researchers.
   IMPLICATIONS: Designing interventions that specifically address target 
  behaviours to promote data sharing are important for open researcher 
  practices.
   Keywords: data sharing; health information management; research
  DOI: https://doi.org/10.1177/1833358320917207
  URL: http://pubmed.ncbi.nlm.nih.gov/32367733

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