Evidence map›Paper›PMID 31412854›Full record

ArticleBMC health services research2019

Incomplete recording of Indigenous identification status under-estimates the prevalence of Indigenous population attending Australian general practices: a cross sectional study.

Belinda K Ford, Marlene Kong, James S Ward, Jane S Hocking, Christopher K Fairley, Basil Donovan, Rebecca Lorch, Simone Spark, Matthew Law, John Kaldor and 1 more

Abstract read
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Article in BMC health services research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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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

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Belinda K FordKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia. bford@georgeinstitute.org.au.ORCID http://orcid.org/0000-0003-4416-2389
Marlene KongKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.
James S WardSouth Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Jane S HockingCentre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.
Christopher K FairleyMonash University Central Clinical School and Melbourne Sexual Health Centre, Melbourne, Victoria, Australia.
Basil DonovanKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.
Rebecca LorchKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.
Simone SparkSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Matthew LawKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.
John KaldorKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.
Rebecca GuyKirby Institute, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAustralian Aboriginal and Torres Strait Islander (Indigenous) peoples face major health disadvantage across many conditions. Recording of patients' Indigenous status in general practice records supports equitable delivery of effective clinical services. National policy and accreditation standards mandate recording of Indigenous status in patient records, however for a large proportion of general practice patient records it remains incomplete. We assessed the completeness of Indigenous status in general practice patient records, and compared the patient self-reported Indigenous status to general practice medical records.

methodsA cross sectional analysis of Indigenous status recorded at 95 Australian general practices, participating in the Australian Chlamydia Control Effectiveness Pilot (ACCEPt) in 2011. Demographic data were collected from medical records and patient surveys from 16 to 29 year old patients at general practices, and population composition from the 2011 Australian census. General practitioners (GPs) at the same practices were also surveyed. Completeness of Indigenous status in general practice patient records was measured with a 75% benchmark used in accreditation standards. Indigenous population composition from a patient self-reported survey was compared to Indigenous population composition in general practice records, and Australian census data.

resultsIndigenous status was complete in 56% (median 60%, IQR 7-81%) of general practice records for 109,970 patients aged 16-29 years, and Indigenous status was complete for 92.5% of the 3355 patients aged 16-29 years who completed the survey at the same clinics. The median proportion per clinic of patients identified as Indigenous was 0.9%, lower than the 1.8% from the patient surveys and the 1.7% in clinic postcodes (ABS). Correlations between the proportion of Indigenous people self-reporting in the patient survey (5.2%) compared to status recorded in all patient records (2.1%) showed a fair association (r = 0.6468; p < 0.01). After excluding unknown /missing data, correlations weakened.

conclusionsIncomplete Indigenous status records may under-estimate the true proportion of Indigenous people attending clinics but have higher association with self-reported status than estimates which exclude missing/unknown data. The reasons for incomplete Indigenous status recording in general practice should be explored so efforts to improve recording can be targeted and strengthened.

trial registrationACTRN12610000297022 . Registered 13th April 2010.

Indexed as

AdolescentAdultAustraliaCross-Sectional StudiesFemaleGeneral PracticeHealthcare DisparitiesHumansMaleMedical Record LinkageMedical RecordsPatient Acceptance of Health CareYoung AdultAboriginal and/or Torres Strait islander peopleGeneral practiceHealth dataIndigenous statusMedical records

Identifiers

PMID31412854
PMCPMC6693211

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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.