Evidence map›Paper›PMID 30185185›Full record

ArticleBMC musculoskeletal disorders2018

Cohort identification of axial spondyloarthritis in a large healthcare dataset: current and future methods.

Jessica A Walsh, Shaobo Pei, Gopi K Penmetsa, Jianwei Leng, Grant W Cannon, Daniel O Clegg, Brian C Sauer

Abstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  3. Utility of the Current Procedural Terminology Codes for Prophylactic Stabilization for Defining Metastatic Femur Disease.Journal of the American Academy of Orthopaedic Surgeons. Global research & reviews · 2020
    Article
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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

7 authors.

Jessica A WalshDivision of Rheumatology School of Medicine, 30 North 1900 East, Salt Lake City, UT, 84132, USA. jessica.walsh@hsc.utah.edu.ORCID http://orcid.org/0000-0002-4563-0845
Shaobo PeiGeorge E. Wahlen Veteran Affairs Medical Center, 500 Foothill Boulevard, Salt Lake City, UT, 84148, USA.
Gopi K PenmetsaDivision of Rheumatology School of Medicine, 30 North 1900 East, Salt Lake City, UT, 84132, USA.
Jianwei LengGeorge E. Wahlen Veteran Affairs Medical Center, 500 Foothill Boulevard, Salt Lake City, UT, 84148, USA.
Grant W CannonGeorge E. Wahlen Veteran Affairs Medical Center, 500 Foothill Boulevard, Salt Lake City, UT, 84148, USA.
Daniel O CleggDivision of Rheumatology School of Medicine, 30 North 1900 East, Salt Lake City, UT, 84132, USA.
Brian C SauerGeorge E. Wahlen Veteran Affairs Medical Center, 500 Foothill Boulevard, Salt Lake City, UT, 84148, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBig data research is important for studying uncommon diseases in real-world settings. Most big data studies in axial spondyloarthritis (axSpA) have been limited to populations identified with billing codes for ankylosing spondylitis (AS). axSpA is a more inclusive concept, and reliance on AS codes does not produce a comprehensive axSpA study population. The first objective was to describe our process for establishing an appropriate sample of patients with and without axSpA for developing accurate axSpA identification methods. The second objective was to determine the classification performance of AS billing codes against the chart-reviewed axSpA reference standard.

methodsVeteran Health Affairs clinical and administrative data, between January 2005 and June 2015, were used to randomly select patients with clinical phenotypes that represented high, moderate, and low likelihoods of an axSpA diagnosis. With chart review, the sampled patients were classified as Yes axSpA, No axSpA or Uncertain axSpA, and these classification assignments were used as the reference standard for determining the positive predictive value (PPV) and sensitivity of AS ICD-9 codes for axSpA.

resultsSix hundred patients were classified as Yes axSpA (26.8%), No axSpA (68.3%), or Uncertain axSpA (4.8%). The PPV and sensitivity of an AS ICD-9 code for axSpA were 83.3% and 57.3%, respectively.

conclusionsStandard methods of identifying axSpA patients in a large dataset lacked sensitivity. An appropriate sample of patients with and without axSpA was established and characterized for developing novel axSpA identification methods that are anticipated to enable previously impractical big data research.

Indexed as

Big DataAdultAgedCohort StudiesDatabases, FactualDelivery of Health CareFemaleForecastingHumansMaleMiddle AgedRandom AllocationSpondylarthritisSpondylitis, AnkylosingUnited StatesUnited States Department of Veterans AffairsAnkylosing spondylitisDatabasesHealth services researchSpondyloarthropathy

Identifiers

PMID30185185
PMCPMC6123987

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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.