Evidence map›Paper›PMID 39773635›Full record

Observational studyBMC health services research2025

Consumer perspectives on the national electronic health record and barriers to its adoption in Germany: does health policy require a change in communication?

Saskia Kröner, Björn Schreiweis, Veronika Strotbaum, Lea Christine Brandl, Monika Pobiruchin, Martin Wiesner

Abstract readObservational Study
In one paragraph

Observational study in BMC health services research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. [Digital transformation in healthcare to strengthen patient autonomy].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2026
    Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Saskia KrönerHealth Informatics Research Group, University AS Osnabrück, Osnabrück, Germany. s.kroener@hs-osnabrueck.de.ORCID http://orcid.org/0009-0001-1387-4853
Björn SchreiweisInstitute for Medical Informatics and Statistics, University Hospital Schleswig-Holstein and Kiel University, Kiel, Germany.ORCID http://orcid.org/0000-0002-1748-1563
Veronika StrotbaumConsumer Health Informatics special interest group of the German Association for Medical Informatics, Biometry and Epidemiology (GMDS e. V.), Cologne, Germany.ORCID http://orcid.org/0000-0003-1098-9417
Lea Christine BrandlInstitute of Telematics, University of Lübeck, Lübeck, Germany.ORCID http://orcid.org/0000-0001-6655-6763
Monika PobiruchinHeilbronn University, Heilbronn, Germany.ORCID http://orcid.org/0000-0002-9925-2173
Martin WiesnerHeilbronn University, Heilbronn, Germany.ORCID http://orcid.org/0000-0003-3346-9633

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe national health record (ePA) was introduced January 1

methodsAn exploratory, observational, cross-sectional online survey was conducted one year after ePA introduction, followed by descriptive statistical analysis.

resultsThe top three ePA use cases were medical document collection, simplified data exchange between medical institutions, and emergency medical information. Adoption barriers included lack of information and access, privacy concerns, and perceived lack of necessity. Participants that felt informed about the ePA, reported they received information primarily from health insurances, the media, and educational or professional sources, mainly through printed brochures, social media, or via emails. Most participants (86.5%) preferred being informed through conversations, particularly with health insurance providers (81.5%) and doctors (61.0%). Written information was highly desired (94.5%), preferably via email or information letters/flyers. However, more than half of the participants (55.6%) reported being uninformed about the ePA introduction.

conclusionThe study revealed a communication gap between providers and consumers, leading to a low acceptance rate of digital health technologies. Comparisons with other countries showed low adoption rates for opt-in systems. The authors suggest changing communication strategies, given users prefer direct information from doctors or health insurance companies. Adopting an opt-out system with professional social media and marketing campaigns could increase nationwide ePA adoption.

Indexed as

Electronic Health RecordsHealth PolicyAdultAgedCommunicationConsumer BehaviorCross-Sectional StudiesFemaleGermanyHumansMaleMiddle AgedSurveys and QuestionnairesYoung AdultAdoptionBarriersCommunicationConsumersNational electronic health record

Identifiers

PMID39773635
PMCPMC11706193

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.