Evidence map›Paper›PMID 26376722›Full record

ArticleCritical care (London, England)2015

THAM reduces CO2-associated increase in pulmonary vascular resistance - an experimental study in lung-injured piglets.

Staffan Höstman, João Batista Borges, Fernando Suarez-Sipmann, Kerstin M Ahlgren, Joakim Engström, Göran Hedenstierna, Anders Larsson

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 38% 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.

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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 1 institution in 2 countries.

Staffan HöstmanHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. staffan.hostman@surgsci.uu.se.
João Batista BorgesHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. joao.batista_borges@medsci.uu.se.
Fernando Suarez-SipmannHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. fsuarezsipmann@gmail.com.
Kerstin M AhlgrenHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. kerstin.ahlgren@surgsci.uu.se.
Joakim EngströmHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. joakim@me.com.
Göran HedenstiernaHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. goran.hedenstierna@medsci.uu.se.
Anders LarssonHedenstierna Laboratory, Uppsala University, Uppsala, Sweden. anders.larsson@surgsci.uu.se.
Uppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLow tidal volume (VT) ventilation is recommended in patients with acute respiratory distress syndrome (ARDS). This may increase arterial carbon dioxide tension (PaCO2), decrease pH, and augment pulmonary vascular resistance (PVR). We hypothesized that Tris(hydroxymethyl)aminomethane (THAM), a pure proton acceptor, would dampen these effects, preventing the increase in PVR.

methodsA one-hit injury ARDS model was established by repeated lung lavages in 18 piglets. After ventilation with VT of 6 ml/kg to maintain normocapnia, VT was reduced to 3 ml/kg to induce hypercapnia. Six animals received THAM for 1 h, six for 3 h, and six serving as controls received no THAM. In all, the experiment continued for 6 h. The THAM dosage was calculated to normalize pH and exhibit a lasting effect. Gas exchange, pulmonary, and systemic hemodynamics were tracked. Inflammatory markers were obtained at the end of the experiment.

resultsIn the controls, the decrease in VT from 6 to 3 ml/kg increased PaCO2 from 6.0±0.5 to 13.8±1.5 kPa and lowered pH from 7.40±0.01 to 7.12±0.06, whereas base excess (BE) remained stable at 2.7±2.3 mEq/L to 3.4±3.2 mEq/L. In the THAM groups, PaCO2 decreased and pH increased above 7.4 during the infusions. After discontinuing the infusions, PaCO2 increased above the corresponding level of the controls (15.2±1.7 kPa and 22.6±3.3 kPa for 1-h and 3-h THAM infusions, respectively). Despite a marked increase in BE (13.8±3.5 and 31.2±2.2 for 1-h and 3-h THAM infusions, respectively), pH became similar to the corresponding levels of the controls. PVR was lower in the THAM groups (at 6 h, 329±77 dyn∙s/m(5) and 255±43 dyn∙s/m(5) in the 1-h and 3-h groups, respectively, compared with 450±141 dyn∙s/m(5) in the controls), as were pulmonary arterial pressures.

conclusionsThe pH in the THAM groups was similar to pH in the controls at 6 h, despite a marked increase in BE. This was due to an increase in PaCO2 after stopping the THAM infusion, possibly by intracellular release of CO2. Pulmonary arterial pressure and PVR were lower in the THAM-treated animals, indicating that THAM may be an option to reduce PVR in acute hypercapnia.

Indexed as

AnimalsCarbon DioxideDisease Models, AnimalHemodynamicsHypercapniaLungRespiratory Distress SyndromeSwineTidal VolumeTromethamineVascular ResistanceVentilator-Induced Lung InjuryCarbon DioxideTromethamine

Identifiers

PMID26376722
PMCPMC4573471
OpenAlexW2149926614

What OpenQuestion holds

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LicenceCC BY
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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.