Evidence map›Paper›PMID 26871665›Full record

ReviewShock (Augusta, Ga.)2016

MITOCHONDRIAL FUNCTION IN SEPSIS.

Nishkantha Arulkumaran, Clifford S Deutschman, Michael R Pinsky, Brian Zuckerbraun, Paul T Schumacker, Hernando Gomez, Alonso Gomez, Patrick Murray, John A Kellum, ADQI XIV Workgroup

Abstract readReview
In one paragraph

Review in Shock (Augusta, Ga.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed, 2 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

111 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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51 more citing papers are in PubMed but not listed here.

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

10 authors.

Nishkantha Arulkumaran*Bloomsbury Institute of Intensive Care Medicine, University Hospital London, UK †Department of Pediatrics and Molecular Medicine, Hofstra-North Shore-Long Island Jewish School of Medicine, New Hyde Park, New York ‡Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania §Departments of Pediatrics-Neonatology, Cell and Molecular Biology and Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois ||Department of Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania ¶Center for Critical Care Nephrology, University of Pittsburgh, Pittsburgh, Pennsylvania #Academia Colombiana de Medicina Critica (ACOMEC) **Division of Critical Care Medicine, Clínica Palermo, Bogotá, Colombia ††University College Dublin, Dublin, Ireland.
Clifford S Deutschman
Michael R Pinsky
Brian Zuckerbraun
Paul T Schumacker
Hernando Gomez
Alonso Gomez
Patrick Murray
John A Kellum
ADQI XIV Workgroup

Funding

Analysis and Characterization of Trauma-Induced CoagulopathyUM1HL120877 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MORRISSEY, JAMES H., WISNIEWSKI, STEPHEN R · 2013 to 2019
$26.6M
Predicting Patient Instability Noninvasively for Nursing Care-Two (PPINNC-2)R01NR013912 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AL-ZAITI, SALAH S, CLERMONT, GILLES · 2012 to 2025
$7.0M
Multidisciplinary Training in Critical Care Outcomes ResearchT32HL007820 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Timothy D Girard, Jeremy M Kahn · 1996 to 2026
$6.4M
Respiratory and Metabolic Adaptation to HypoxiaR01HL035440 · NHLBI · UNIVERSITY OF CHICAGO · PI SCHUMACKER, PAUL T · 1986 to 2018
$5.0M
Myocardial Ischemia and Vasospasm in Aneurysmal SAHR01HL074316 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOROWITZ, MICHAEL B · 2004 to 2008
$2.8M
Metabolic Regulation of Pulmonary Vascular RemodelingR01HL122062 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHUMACKER, PAUL T · 2014 to 2017
$2.0M
Heart-Lung Interactions &Cardiovascular InsufficiencyK24HL067181 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PINSKY, MICHAEL R · 2002 to 2011
$1.4M
NHLBI NIH HHS HL074316NHLBI NIH HHS HL07820NHLBI NIH HHS HL120877NHLBI NIH HHS HL122062NHLBI NIH HHS HL35440NHLBI NIH HHS K24 HL067181NHLBI NIH HHS R01 HL035440NHLBI NIH HHS R01 HL074316NHLBI NIH HHS R01 HL122062NHLBI NIH HHS T32 HL007820NHLBI NIH HHS UM1 HL120877NINR NIH HHS NR013912NINR NIH HHS R01 NR013912Wellcome Trust
6 · The paper itself

Abstract

Mitochondria are an essential part of the cellular infrastructure, being the primary site for high-energy adenosine triphosphate production through oxidative phosphorylation. Clearly, in severe systemic inflammatory states, like sepsis, cellular metabolism is usually altered, and end organ dysfunction is not only common, but also predictive of long-term morbidity and mortality. Clearly, interest is mitochondrial function both as a target for intracellular injury and response to extrinsic stress have been a major focus of basic science and clinical research into the pathophysiology of acute illness. However, mitochondria have multiple metabolic and signaling functions that may be central in both the expression of sepsis and its ultimate outcome. In this review, the authors address five primary questions centered on the role of mitochondria in sepsis. This review should be used both as a summary source in placing mitochondrial physiology within the context of acute illness and as a focal point for addressing new research into diagnostic and treatment opportunities these insights provide.

Indexed as

Oxidative PhosphorylationSignal TransductionAnimalsHumansMitochondriaSepsis

Identifiers

PMID26871665
PMCPMC4755359

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.