Evidence map›Paper›PMID 40610969›Full record

Observational studyBMC nephrology2025

Dilemma of missing specific disease codes: an approach to assess the incidence and prevalence of a rare nephrology disease.

Matthias Roll, Amadeus Gladbach, Isabella Selinger, Thomas Hardt, Helena Himmelhaus, Christian Jacob, Timotheus Stremel, Julia Theil, Jürgen Floege

Abstract readObservational Study
In one paragraph

Observational study in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Matthias RollCSL Vifor, München, Germany. matthias.roll@viforpharma.com.
Amadeus GladbachCSL Vifor, München, Germany.
Isabella SelingerCSL Vifor, München, Germany.
Thomas HardtCSL Vifor, München, Germany.
Helena HimmelhausPharmaLex GmbH, part of Cencora Inc., Hannover, Germany.
Christian JacobPharmaLex GmbH, part of Cencora Inc., Hannover, Germany.
Timotheus StremelPharmaLex GmbH, part of Cencora Inc., Hannover, Germany.
Julia TheilPharmaLex GmbH, part of Cencora Inc., Hannover, Germany.
Jürgen FloegeDivisions of Nephrology and Cardiology, RWTH Aachen University Hospital, Aachen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEstimating disease epidemiology using health insurance claims data is challenging due to the lack of specific diagnostic codes. This study demonstrates an approach to estimate the epidemiology of primary immunoglobulin A nephropathy (IgAN) using German Statutory Health Insurance (SHI) claims data.

methodsA retrospective observational study was conducted using data from January 1

resultsThe mean prevalence rate from 2017-2022 ranged from 4.5 (restrictive codes) to 38.3 (inclusive codes) cases per 100,000 individuals, demonstrating the orphan nature of primary IgAN. Mean incidence rates ranged from 0.2 to 0.6 cases per 100,000 individuals. In 2022, this corresponded to an estimated 4,043 to 32,229 prevalent cases and 164 to 538 incident cases in Germany.

conclusionThis study presents an approach for estimating disease epidemiology in the absence of specific diagnostic codes, using primary IgAN as an example. While our dual-algorithm method provides valuable insights into the incidence and prevalence of primary IgAN in Germany, it also highlights the need for consistent coding practices and specific diagnostic codes for accurate epidemiological assessments.

Indexed as

Clinical CodingGlomerulonephritis, IGARare DiseasesAdultAgedAlgorithmsFemaleGermanyHumansIncidenceInternational Classification of DiseasesMaleMiddle AgedPrevalenceRetrospective StudiesYoung AdultClaims dataEpidemiologyGermanyIgANPrimary immunoglobulin a nephropathyStatutory health insurance

Identifiers

PMID40610969
PMCPMC12231908

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.