Evidence map›Paper›PMID 27166576›Full record

ArticleJournal of visualized experiments : JoVE2016

Measuring Pressure Volume Loops in the Mouse.

DeWayne Townsend

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 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

1 author.

DeWayne TownsendDepartment of Integrative Biology and Physiology, University of Minnesota; town0045@umn.edu.

Funding

Improving dystrophin gene therapy through understanding dystrobrevin functionR01HL114832 · NHLBI · UNIVERSITY OF MINNESOTA · PI TOWNSEND, DEWAYNE · 2013 to 2017
$1.8M
Coronary Regulation in Dystrophic CardiomyopathyK08HL102066 · NHLBI · UNIVERSITY OF MINNESOTA · PI TOWNSEND, DEWAYNE · 2010 to 2014
$641k
NHLBI NIH HHS K08 HL102066NHLBI NIH HHS R01 HL114832
6 · The paper itself

Abstract

Understanding the causes and progression of heart disease presents a significant challenge to the biomedical community. The genetic flexibility of the mouse provides great potential to explore cardiac function at the molecular level. The mouse's small size does present some challenges in regards to performing detailed cardiac phenotyping. Miniaturization and other advancements in technology have made many methods of cardiac assessment possible in the mouse. Of these, the simultaneous collection of pressure and volume data provides a detailed picture of cardiac function that is not available through any other modality. Here a detailed procedure for the collection of pressure-volume loop data is described. Included is a discussion of the principles underlying the measurements and the potential sources of error. Anesthetic management and surgical approaches are discussed in great detail as they are both critical to obtaining high quality hemodynamic measurements. The principles of hemodynamic protocol development and relevant aspects of data analysis are also addressed.

Indexed as

AnimalsBlood PressureBlood Pressure MonitorsHeartHeart DiseasesHemodynamicsMice

Identifiers

PMID27166576
PMCPMC4942027

What OpenQuestion holds

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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.