Evidence map›Paper›PMID 31341958›Full record

ArticleNPJ digital medicine2019

City-wide electronic health records reveal gender and age biases in administration of known drug-drug interactions.

Rion Brattig Correia, Luciana P de Araújo Kohler, Mauro M Mattos, Luis M Rocha

Open access · goldAbstract read
In one paragraph

Article in NPJ digital medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 18% of its field
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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Inherent Bias in Electronic Health Records: A Scoping Review of Sources of Bias.medRxiv : the preprint server for health sciences · 2024
    Article
  9. Design and Evaluation of EMPATHICA: A Chatbot for Enhancing Medication Literacy.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Drug-Drug-Gene Interactions in Cardiovascular Medicine.Pharmacogenomics and personalized medicine · 2022
    Review
  15. The distance backbone of complex networks.Journal of complex networks · 2021
    Article
  16. Article
  17. 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

4 authors at 2 institutions in 3 countries.

Rion Brattig Correia1School of Informatics, Computing & Engineering, Indiana University, Bloomington, IN 47408 USA.ORCID 0000-0001-5460-9397
Luciana P de Araújo Kohler4Universidade Regional de Blumenau (FURB), Blumenau, SC 89030-903 Brazil.ORCID 0000-0002-8219-1343
Mauro M Mattos4Universidade Regional de Blumenau (FURB), Blumenau, SC 89030-903 Brazil.ORCID 0000-0002-0631-687X
Luis M Rocha1School of Informatics, Computing & Engineering, Indiana University, Bloomington, IN 47408 USA.ORCID 0000-0001-9402-887X
Indiana University Bloomington · USUniversidade Regional de Blumenau · BR

Funding

Evidence-based Drug-Interaction Discovery: In-Vivo, In-Vitro and ClinicalR01LM011945 · NLM · INDIANA UNIVERSITY INDIANAPOLIS · PI LI, LANG, ROCHA, LUIS M · 2014 to 2017
$1.8M
myAURA: Personalized Web Service for Epilepsy ManagementR01LM012832 · NLM · TRUSTEES OF INDIANA UNIVERSITY · PI BORNER, KATY, MILLER, WENDY RENEE · 2018 to 2021
$1.3M
NLM NIH HHS R01 LM011945NLM NIH HHS R01 LM012832
6 · The paper itself

Abstract

The occurrence of drug-drug-interactions (DDI) from multiple drug dispensations is a serious problem, both for individuals and health-care systems, since patients with complications due to DDI are likely to reenter the system at a costlier level. We present a large-scale longitudinal study (18 months) of the DDI phenomenon at the primary- and secondary-care level using electronic health records (EHR) from the city of Blumenau in Southern Brazil (pop. ≈340,000). We found that 181 distinct drug pairs known to interact were dispensed concomitantly to 12% of the patients in the city's public health-care system. Further, 4% of the patients were dispensed drug pairs that are likely to result in major adverse drug reactions (ADR)-with costs estimated to be much larger than previously reported in smaller studies. The large-scale analysis reveals that women have a 60% increased risk of DDI as compared to men; the increase becomes 90% when considering only DDI known to lead to major ADR. Furthermore, DDI risk increases substantially with age; patients aged 70-79 years have a 34% risk of DDI when they are dispensed two or more drugs concomitantly. Interestingly, a statistical null model demonstrates that age- and female-specific risks from increased polypharmacy fail by far to explain the observed DDI risks in those populations, suggesting unknown social or biological causes. We also provide a network visualization of drugs and demographic factors that characterize the DDI phenomenon and demonstrate that accurate DDI prediction can be included in health care and public-health management, to reduce DDI-related ADR and costs.

Indexed as

Computational scienceDrug regulationEpidemiologyPublic healthRisk factors

Identifiers

PMID31341958
PMCPMC6650500
OpenAlexW2794244028

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.