Trial reportChest2026
The Effects of Targeted Mild Hypercapnia on Right Ventricular Function After Out-of-Hospital Cardiac Arrest: A Substudy of the Targeted Therapeutic Mild Hypercapnia After Resuscitated Cardiac Arrest Trial.
Trial report in Chest, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03114033 (TAME Cardiac Arrest Trial), which is not on this map. Not yet cited in PubMed.
What it found
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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.
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.
TAME Cardiac Arrest Trial: Targeted Therapeutic Mild Hypercapnia After Resuscitated Cardiac Arrest: A Phase III Multi-Centre Randomised Controlled Trial
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundTargeting hypercapnia during invasive mechanical ventilation with subsequent respiratory acidosis may impair right ventricular (RV) function and cause RV failure. RV dysfunction is common after cardiac arrest and may be associated with poor outcomes. RESEARCH QUESTION: Does targeting mild hypercapnia after out-of-hospital cardiac arrest (OHCA) adversely affect RV function, and is RV failure after OHCA associated with increased mortality? STUDY DESIGN AND
methodsIn this single-center, preplanned substudy of the Targeted Therapeutic Mild Hypercapnia After Resuscitated Cardiac Arrest (TAME) trial, patients were randomized to mild hypercapnia (Paco
resultsA total of 111 patients were randomized and evaluated with echocardiography. RHC was performed in 84 patients. TAPSE similarly was reduced in both treatment groups at ICU admission. During the intervention, TAPSE, S', and FAC were higher in the hypercapnia group (P < .05). Accordingly, 13 patients (25%) in the hypercapnia group demonstrated RV systolic dysfunction compared with 37 patients (64%) in the normocapnia group (P < .001). RV failure was present in 30 patients: 8 patients in the hypercapnia group and 22 patients in the normocapnia group (P = .011). RV failure was associated with increased 6-month mortality (hazard ratio, 2.89; 95% CI, 1.37-6.10; P = .005).
interpretationAmong patients resuscitated from OHCA, targeting mild hypercapnia compared with normocapnia was not associated with worsened RV function, but rather with less RV dysfunction and failure. RV failure was associated with increased 6-month mortality. CLINICAL
trial registrationClinicalTrials.gov; No.: NCT03114033; URL: www. CLINICALTRIALS: gov.
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