Evidence map›Paper›PMID 31748287›Full record

Observational studyBMJ open2019

Decomposition of the US black/white inequality in premature mortality, 2010-2015: an observational study.

Mathew V Kiang, Nancy Krieger, Caroline O Buckee, Jukka Pekka Onnela, Jarvis T Chen

Abstract readComparative StudyObservational Study
In one paragraph

Observational study in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Mathew V KiangCenter for Population Health Sciences, Stanford University, Palo Alto, California, USA mkiang@stanford.edu.ORCID 0000-0001-9198-150X
Nancy KriegerDepartment of Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Caroline O BuckeeDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Jukka Pekka OnnelaDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Jarvis T ChenDepartment of Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
Cohort filtering models to identify social program effects on health disparitiesDP2MD010478 · NIMHD · STANFORD UNIVERSITY · PI BASU, SANJAY · 2015 to 2015
$2.4M
Improving statistical methods for small area estimates of public health indicators and demographic characteristicsR01HD092580 · NICHD · EMORY UNIVERSITY · PI Lance A Waller · 2018 to 2026
$2.3M
NCI NIH HHS P30 CA006516NICHD NIH HHS R01 HD092580NIMHD NIH HHS DP2 MD010478
6 · The paper itself

Abstract

objectiveDecompose the US black/white inequality in premature mortality into shared and group-specific risks to better inform health policy.

settingAll 50 US states and the District of Columbia, 2010 to 2015.

participantsA total of 2.85 million non-Hispanic white and 762 639 non-Hispanic black US-resident decedents. PRIMARY AND SECONDARY OUTCOME MEASURES: The race-specific county-level relative risks for US blacks and whites, separately, and the risk ratio between groups.

resultsThere is substantial geographic variation in premature mortality for both groups and the risk ratio between groups. After adjusting for median household income, county-level relative risks ranged from 0.46 to 2.04 (median: 1.03) for whites and from 0.31 to 3.28 (median: 1.15) for blacks. County-level risk ratios (black/white) ranged from 0.33 to 4.56 (median: 1.09). Half of the geographic variation in white premature mortality was shared with blacks, while only 15% of the geographic variation in black premature mortality was shared with whites. Non-Hispanic blacks experience substantial geographic variation in premature mortality that is not shared with whites. Moreover, black-specific geographic variation was not accounted for by median household income.

conclusionUnderstanding geographic variation in mortality is crucial to informing health policy; however, estimating mortality is difficult at small spatial scales or for small subpopulations. Bayesian joint spatial models ameliorate many of these issues and can provide a nuanced decomposition of risk. Using premature mortality as an example application, we show that Bayesian joint spatial models are a powerful tool as researchers grapple with disentangling neighbourhood contextual effects and sociodemographic compositional effects of an area when evaluating health outcomes. Further research is necessary in fully understanding when and how these models can be applied in an epidemiological setting.

Indexed as

Health Status DisparitiesBlack or African AmericanFemaleHealth Services AccessibilityHumansMaleMortality, PrematurePovertySpatial AnalysisUnited StatesWhite PeopleBayesian joint modelracial/ethnic inequalityrisk decompositionspatial epidemiology

Identifiers

PMID31748287
PMCPMC6887068

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Registered trials

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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.