Evidence map›Paper›PMID 23193230›Full record

ArticleIEEE transactions on bio-medical engineering2013

Assessing the effects of pharmacological agents on respiratory dynamics using time-series modeling.

Kin Foon Kevin Wong, Jen J Gong, Joseph F Cotten, Ken Solt, Emery N Brown

Abstract read
In one paragraph

Article in IEEE transactions on bio-medical engineering, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

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

5 authors.

Kin Foon Kevin WongDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA 02129, USA. kfwong@partners.org
Jen J Gong
Joseph F Cotten
Ken Solt
Emery N Brown

Funding

A Systems Neuroscience Approach for the Study of General AnesthesiaDP1OD003646 · OD · MASSACHUSETTS GENERAL HOSPITAL · PI BROWN, EMERY N · 2007 to 2011
$4.4M
Volatile Anesthetic Regulation of TASK Tandem Pore Potassium ChannelsK08GM083216 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI COTTEN, JOSEPH F · 2008 to 2012
$757k
Active Induction of Emergence from General AnesthesiaK08GM094394 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI SOLT, KEN · 2010 to 2013
$469k
NIGMS NIH HHS K08 GM083216NIGMS NIH HHS K08-GM083216NIGMS NIH HHS K08 GM094394NIGMS NIH HHS K08-GM094394NIH HHS DP1 OD003646NIH HHS DP1-OD003646
6 · The paper itself

Abstract

Developing quantitative descriptions of how stimulant and depressant drugs affect the respiratory system is an important focus in medical research. Respiratory variables-respiratory rate, tidal volume, and end tidal carbon dioxide-have prominent temporal dynamics that make it inappropriate to use standard hypothesis-testing methods that assume independent observations to assess the effects of these pharmacological agents. We present a polynomial signal plus autoregressive noise model for analysis of continuously recorded respiratory variables. We use a cyclic descent algorithm to maximize the conditional log likelihood of the parameters and the corrected Akaike's information criterion to choose simultaneously the orders of the polynomial and the autoregressive models. In an analysis of respiratory rates recorded from anesthetized rats before and after administration of the respiratory stimulant methylphenidate, we use the model to construct within-animal z-tests of the drug effect that take account of the time-varying nature of the mean respiratory rate and the serial dependence in rate measurements. We correct for the effect of model lack-of-fit on our inferences by also computing bootstrap confidence intervals for the average difference in respiratory rate pre- and postmethylphenidate treatment. Our time-series modeling quantifies within each animal the substantial increase in mean respiratory rate and respiratory dynamics following methylphenidate administration. This paradigm can be readily adapted to analyze the dynamics of other respiratory variables before and after pharmacologic treatments.

Indexed as

Models, BiologicalSignal Processing, Computer-AssistedAlgorithmsAnesthetics, InhalationAnimalsCentral Nervous System StimulantsCluster AnalysisDrug Evaluation, PreclinicalIsofluraneMaleMethylphenidatePlethysmographyRatsRats, Sprague-DawleyRespiratory RateTidal VolumeAnesthetics, InhalationCentral Nervous System StimulantsIsofluraneMethylphenidate

Identifiers

PMID23193230
PMCPMC6376979

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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.