Evidence map›Paper›PMID 26646582›Full record

ArticleStatistics in medicine2016

Time-varying effect modeling with longitudinal data truncated by death: conditional models, interpretations, and inference.

Jason P Estes, Danh V Nguyen, Lorien S Dalrymple, Yi Mu, Damla Şentürk

Abstract read
In one paragraph

Article in Statistics in medicine, 2016. 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.

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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

5 authors.

Jason P EstesDepartment of Biostatistics, University of California, Los Angeles, 90095, California, U.S.A.
Danh V NguyenDepartment of Medicine, UC Irvine School of Medicine, Orange, 92868-3298, California, U.S.A.
Lorien S DalrympleDivision of Nephrology, Department of Medicine, University of California, Sacramento, 95817, California, U.S.A.
Yi MuGraduate Group in Epidemiology, University of California, Davis, 95616, California, U.S.A.
Damla ŞentürkDepartment of Biostatistics, University of California, Los Angeles, 90095, California, U.S.A.

Funding

University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
UC Davis Clinical and Translational Science CenterUL1TR000002 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BERGLUND, LARS F · 2012 to 2015
$12.2M
Institute for Clinical and Translational ScienceUL1TR000153 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$12.1M
Multilevel Time-Dynamic Modeling of Hospitalization and Survival in Patients on DialysisR01DK092232 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KURUM, ESRA, NGUYEN, DANH V · 2011 to 2025
$4.9M
Infection in Dialysis Patients: Risk Factors and OutcomesK23DK093584 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DALRYMPLE, LORIEN SKY · 2012 to 2014
$447k
NCATS NIH HHS UL1 TR000002NCATS NIH HHS UL1 TR000153NCATS NIH HHS UL1 TR001414NIDDK NIH HHS K23 DK093584NIDDK NIH HHS R01 DK092232
6 · The paper itself

Abstract

Recent studies found that infection-related hospitalization was associated with increased risk of cardiovascular (CV) events, such as myocardial infarction and stroke in the dialysis population. In this work, we develop time-varying effects modeling tools in order to examine the CV outcome risk trajectories during the time periods before and after an initial infection-related hospitalization. For this, we propose partly conditional and fully conditional partially linear generalized varying coefficient models (PL-GVCMs) for modeling time-varying effects in longitudinal data with substantial follow-up truncation by death. Unconditional models that implicitly target an immortal population is not a relevant target of inference in applications involving a population with high mortality, like the dialysis population. A partly conditional model characterizes the outcome trajectory for the dynamic cohort of survivors, where each point in the longitudinal trajectory represents a snapshot of the population relationships among subjects who are alive at that time point. In contrast, a fully conditional approach models the time-varying effects of the population stratified by the actual time of death, where the mean response characterizes individual trends in each cohort stratum. We compare and contrast partly and fully conditional PL-GVCMs in our aforementioned application using hospitalization data from the United States Renal Data System. For inference, we develop generalized likelihood ratio tests. Simulation studies examine the efficacy of estimation and inference procedures.

Indexed as

Models, StatisticalAgedCardiovascular DiseasesComputer SimulationFemaleHospitalizationHumansInfectionsLikelihood FunctionsLinear ModelsLongitudinal StudiesMaleRenal DialysisRisk FactorsUnited Statescardiovascular outcomesend-stage renal diseasefully conditional modelpartially linear generalized varying coefficient modelstime-varying effectsUnited States Renal Data System

Identifiers

PMID26646582
PMCPMC4828268

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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.