Evidence map›Paper›PMID 30758518›Full record

ArticleEuropean journal of clinical pharmacology2019

Fall-risk-increasing adverse reactions-is there value in easily accessible drug information? A case-control study.

Susanne Schiek, Katja Hildebrandt, Olaf Zube, Thilo Bertsche

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Article in European journal of clinical pharmacology, 2019. 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
0.5field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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 1 institution in 1 country.

Susanne SchiekInstitute of Pharmacy, Department of Clinical Pharmacy and Drug Safety Center, Leipzig University and University Hospital of Leipzig, Bruederstraße 32, 04103, Leipzig, Germany.
Katja HildebrandtPharmacy Department, Military Hospital, Lesserstraße 180, 22049, Hamburg, Germany.
Olaf ZubePharmacy Department, Military Hospital, Lesserstraße 180, 22049, Hamburg, Germany.
Thilo BertscheInstitute of Pharmacy, Department of Clinical Pharmacy and Drug Safety Center, Leipzig University and University Hospital of Leipzig, Bruederstraße 32, 04103, Leipzig, Germany. thilo.bertsche@medizin.uni-leipzig.de.
Leipzig University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe individual fall risk of a patient is often multifactorial. Polymedication contributes to an additional risk of fall-risk-increasing adverse reactions (FRIARs). Previous studies have not sufficiently investigated the complexity facing prescribers when balancing the therapeutic benefits of individual drugs against their potential fall risk.

methodsAn expert panel identified drugs with FRIARs based on the Summary of Product Characteristics (SmPC). These FRIARs and other parameters (such as the total number of drugs, dosage, dose adjustments, and drug changes) were then analyzed for their impact on falls in a case-control study using logistic regression.

resultsDuring a 1-year period, 112 (1%) of 11,481 hospital patients experienced at least one fall event. Complete data was available for evaluation from 87 of them (case group). We matched these patients to another 87 patients who had no fall events (control group). FRIAR drugs were more frequently prescribed in the case group (4.26 (Q25-Q75, 3.75-4.78) per patient; p = 0.033) than in the control group (3.48 (2.97-3.99)). Drugs with FRIARs (β = 0.137; p = 0.035) and the total number of FRIARs (β = 0.033; p = 0.031) increased the fall risk. The total number of drugs, dosage, dose adjustments, and drug changes showed no influence.

conclusionsFRIARs were associated with a higher number of falls. To consider FRIARs offers a chance to address the complexity of the individual medication. This data can support future computerized physician order entries with clinical decision support.

Indexed as

Accidental FallsAgedAged, 80 and overCase-Control StudiesDrug-Related Side Effects and Adverse ReactionsFemaleHospitals, MilitaryHumansInpatientsMalePotentially Inappropriate Medication ListRisk FactorsAdverse reactionsDrug labelDrug therapyFall-risk-increasing drugsInpatientsPatient safety

Identifiers

PMID30758518
OpenAlexW2913208066

What OpenQuestion holds

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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.