Evidence map›Paper›PMID 32459638›Full record

ArticleJMIR research protocols2020

Prediction Model for Timing of Death in Potential Donors After Circulatory Death (DCD III): Protocol for a Multicenter Prospective Observational Cohort Study.

Angela M M Kotsopoulos, Piet Vos, Nichon E Jansen, Ewald M Bronkhorst, Johannes G van der Hoeven, Wilson F Abdo

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in JMIR research protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04123275 (DCD III Study), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 30% of its field
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.

NCT04123275 completednot on this map

DCD III Study: a Multicentre Prospective Study to Identify Parameters Predicting Time to Death in Controlled Circulatory Death (cDCD) Donors and Prospective Validation of Previous Derived Prediction Models on Time to Death.

TypeobservationalSponsorRadboud University Medical CenterRan2015 to 2018Enrolled400ConditionsTissue and Organ ProcurementArmsNo intervention wil be done. Patient characteristics and the standard care before and after withdrawal of life-sustaining treatment in all potential cDCD donors, will be studied. .
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Angela M M KotsopoulosDepartment of Intensive Care, Radboudumc, Nijmegen, Netherlands.ORCID https://orcid.org/0000-0003-4380-6744
Piet VosDepartment of Intensive Care, Elisabeth-TweeSteden Hospital, Tilburg, Netherlands.ORCID https://orcid.org/0000-0003-2701-5459
Nichon E JansenDutch Transplant Foundation, Leiden, Netherlands.ORCID https://orcid.org/0000-0003-2952-3799
Ewald M BronkhorstDepartment of Health Evidence, Radboud Institute for Health Sciences, Radboudumc, Nijmegen, Netherlands.ORCID https://orcid.org/0000-0003-0953-8053
Johannes G van der HoevenDepartment of Intensive Care, Radboudumc, Nijmegen, Netherlands.ORCID https://orcid.org/0000-0001-5362-0244
Wilson F AbdoDepartment of Intensive Care, Radboudumc, Nijmegen, Netherlands.ORCID https://orcid.org/0000-0002-5783-8643
Radboud University Nijmegen · NLElisabeth-TweeSteden Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundControlled donation after circulatory death (cDCD) is a major source of organs for transplantation. A potential cDCD donor poses considerable challenges in terms of identification of those dying within the predefined time frame of warm ischemia after withdrawal of life-sustaining treatment (WLST) to circulatory arrest. Several attempts have been made to develop models predicting the time between treatment withdrawal and circulatory arrest. This time window determines whether organ donation can occur and influences the quality of the donated organs. However, the selected patients used for these models were not always restricted to potential cDCD donors (eg, patients with cancer or severe infections were also included). This severely limits the generalizability of those data.

objectiveThe objectives of this study are the following: (1) to develop a model predicting time to death within 60 minutes in potential cDCD patients; (2) to validate and update previous prediction models on time to death after WLST; (3) to determine timing and patient characteristics that are associated with prognostication and the decision-making process that leads to initiating end-of-life care; (4) to evaluate the impact of timing of family approach on organ donation approval; and (5) to assess the influence of variation in WLST processes on postmortem organ donor potential and actual postmortem organ donors.

methodsIn this multicenter observational prospective cohort study, all patients admitted to the intensive care unit of 3 university hospitals and 3 teaching hospitals who met the criteria of the cDCD protocol as defined by the Dutch Transplant Foundation were included. The target of enrolment was set to 400 patients. Previously developed models will be refitted in our data set. To further update previous prediction models, we will apply least absolute shrinkage and selection operator (LASSO) as a tool for efficient variable selection to develop the multivariable logistic regression model.

resultsThis protocol was funded in August 2014 by the Dutch Transplant Foundation. We expect to have the results of this study in July 2020. Patient enrolment was completed in July 2018 and data collection was completed in April 2020.

conclusionsThis study will provide a robust multimodal prediction model, based on clinical and physiological parameters, that can predict time to circulatory arrest in cDCD donors. In addition, it will add valuable insight in the process of WLST in cDCD donors and will fill an important knowledge gap in this essential field of health care.

trial registrationClinicalTrials.gov NCT04123275; https://clinicaltrials.gov/ct2/show/NCT04123275. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/16733.

Indexed as

circulatory deathclinical prediction ruleclinical protocolscohort studydonation after circulatory deathend-of-life careintensive care unitorgan donationorgan donororgan transplanttissue and organ procurementwithdrawal of life-sustaining treatment

Identifiers

PMID32459638
PMCPMC7380979
OpenAlexW3022226207

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Registered trials

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.