Evidence map›Paper›PMID 25495664›Full record

ArticleBMC medical informatics and decision making2014

Is pathology necessary to predict mortality among men with prostate-cancer?

David Margel, David R Urbach, Lorraine L Lipscombe, Chaim M Bell, Girish Kulkarni, Jack Baniel, Neil Fleshner, Peter C Austin

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

David MargelDivision of Urology, Rabin Medical Center, Beilinson Campus, 39 Jabotinsky, Petah Tikva, 4941492, Israel. sdmargel@gmail.com.
David R UrbachDepartments of Surgery and Health Policy Management and Evaluation, University of Toronto, Toronto, Canada. david.urbach@uhn.ca.
Lorraine L LipscombeInstitute for Clinical Evaluative Sciences (ICES), Toronto, Canada. lorraine.lipscombe@wchospital.ca.
Chaim M BellInstitute for Clinical Evaluative Sciences (ICES), Toronto, Canada. cbell@mtsinai.on.ca.
Girish KulkarniInstitute for Clinical Evaluative Sciences (ICES), Toronto, Canada. Girish.Kulkarni@uhn.ca.
Jack BanielDivision of Urology, Rabin Medical Center, Beilinson Campus, 39 Jabotinsky, Petah Tikva, 4941492, Israel. jbaniel@clalit.org.il.
Neil FleshnerDivision of Urology, Department of Surgical Oncology, Princess Margaret Hospital, University Health Network, Toronto, Ontario, Canada. neil.fleshner@uhn.ca.
Peter C AustinInstitute for Clinical Evaluative Sciences (ICES), Toronto, Canada. peter.austin@ices.on.ca.

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundStatistical models developed using administrative databases are powerful and inexpensive tools for predicting survival. Conversely, data abstraction from chart review is time-consuming and costly. Our aim was to determine the incremental value of pathological data obtained from chart abstraction in addition to information acquired from administrative databases in predicting all-cause and prostate cancer (PC)-specific mortality.

methodsWe identified a cohort of men with diabetes and PC utilizing population-based data from Ontario. We used the c-statistic and net-reclassification improvement (NRI) to compare two Cox- proportional hazard models to predict all-cause and PC-specific mortality. The first model consisted of covariates from administrative databases: age, co-morbidity, year of cohort entry, socioeconomic status and rural residence. The second model included Gleason grade and cancer volume in addition to all aforementioned variables.

resultsThe cohort consisted of 4001 patients. The accuracy of the admin-data only model (c-statistic) to predict 5-year all-cause mortality was 0.7 (95% CI 0.69-0.71). For the extended model (including pathology information) it was 0.74 (95% CI 0.73-0.75). This corresponded to a change in category of predicted probability of survival among 14.8% in the NRI analysis. The accuracy of the admin-data model to predict 5-year PC specific mortality was 0.76 (95% CI 0.74-0.78). The accuracy of the extended model was 0.85 (95% CI 0.83-0.87). Corresponding to a 28% change in the NRI analysis.

conclusionsPathology chart abstraction, improved the accuracy in predicting all-cause and PC-specific mortality. The benefit is smaller for all-cause mortality, and larger for PC-specific mortality.

Indexed as

AgedCause of DeathComorbidityDiabetes MellitusHumansMaleOntarioPrognosisProportional Hazards ModelsProstatic NeoplasmsRegistriesRisk Assessment

Identifiers

PMID25495664
PMCPMC4275978

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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.