The TAME Cardiac Arrest trial will study the ability of higher arterial carbon dioxide (PaCO2) levels to reduce brain damage, comparing giving patients 'normal' to 'slightly higher than normal' blood PaCO2 levels and assessing their ability to return to normal life-tasks. It will be the largest trial ever conducted in heart attack patients in the intensive care unit. This therapy is cost free and, if shown to be effective, will improve thousands of lives, transform clinical practice, and yield major savings.
Cardiac arrest is a common and catastrophic event with substantial human and financial costs. It is well understood that cardiac arrest leads to brain injury. However, what is not widely appreciated is that, after circulation has been restored, cerebral hypoperfusion continues. Ongoing cerebral vasoconstriction and cerebral hypoxia has been demonstrated using technologies that include positron emission tomography, ultrasound, jugular bulb oxygen saturation and cerebral oximetry. A likely mechanism responsible for sustained early cerebral hypoperfusion relates to impaired cerebrovascular auto-regulation. Such impaired cerebral auto-regulation may make even a normal arterial carbon dioxide tension (PaCO2) (the major physiological regulator of cerebral blood flow) insufficient to achieve and maintain adequate cerebral perfusion and, consequently, cerebral oxygenation. However, PaCO2 is the major determinant of cerebral blood flow and an increased PaCO2 (hypercapnia) markedly increases cerebral blood flow. Moreover, arterial carbon dioxide is modifiable and, as such, is a potential therapeutic target. The TAME Cardiac Arrest Trial is a definitive phase III multi-centre randomised controlled trial in resuscitated cardiac arrest patients. This trial will determine whether targeted therapeutic mild hypercapnia (TTMH) applied during the first 24 hours of mechanical ventilation in the intensive care unit (ICU) improves neurological outcome at 6 months compared to standard care (targeted normocapnia (TN). Supported by compelling preliminary data, significant improvements in patient outcomes are achievable with this proposed simple and cost free therapy. Recruiting 1,700 patients, for multiple sites in many countries, this will be the largest trial ever conducted involving resuscitated cardiac arrest patients admitted to the ICU. If the TAME Cardiac Arrest Trial confirms that TTMH is effective, its findings will improve the lives of many, transform clinical practice and yield major economic gains worldwide.
Study Type
INTERVENTIONAL
Allocation
Patients allocated to the TTMH protocol will be sedated to achieve moderate to deep sedation (a target Richmond Agitation Scale Score of -4). Arterial blood gases and end- tidal carbon dioxide levels will be measured at baseline and then used to guide respiratory rate adjustments of minute ventilation to remain within the target PaCO2 range of 50-55 mmHg. Arterial blood gases will be repeated every 4 hours for 24 hours following randomisation or if end-tidal carbon dioxide values change \>5 mmHg
Patients allocated to the standard care (TN) protocol will be managed according to current practice and in accordance with ILCOR guidelines which recommend maintaining normocapnia in these patients. They will be sedated to achieve moderate to deep sedation (a target Richmond Agitation Scale Score of - 4). Arterial blood gases and end-tidal carbon dioxide levels will be measured at baseline and then used to guide respiratory rate adjustments of minute ventilation to remain within the target PaCO2 range of 35-45 mmHg. Arterial blood gases will be repeated every 4 hours for 24 hours following randomisation or if end-tidal carbon dioxide values change \>5 mmHg.
Neurological outcome
Proportion of patients with a favourable (score ≥5) neurological outcome as assessed using the Glasgow Outcomes Score Extended (GOSE) method.
Time frame: 6 months following enrolment
Mortality at intensive care unit discharge
Mortality at intensive care unit discharge
Time frame: 6 months after randomisation
Mortality at hospital discharge
Mortality at hospital discharge
Time frame: 6 months after randomisation
Health-related Quality of Life (EQ-5D-5L)
Health-related Quality of Life (EQ-5D-5L) at 6 months
Time frame: 6 months after randomisation
modified Rankin scale (mRS)
modified Rankin scale (mRS) with favourable score of equal to or less than 3
Time frame: 6 months after randomisation
Montreal Cognitive Assessment (MoCA-blind)
Montreal Cognitive Assessment (MoCA-blind) at 6 months
Time frame: 6 months after randomisation
Mortality at 6 months
Mortality at 6 months
Time frame: 6 months after randomisation
Informant Questionnaire on Cognitive Decline in the Elderly-Cardiac Arrest (IQCODE)
IQCODE
Time frame: 6 months after randomisation
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RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
1,700
St Vincent's Hospital Sydney
Darlinghurst, New South Wales, Australia
Nepean Hospital
Penrith, New South Wales, Australia
Royal North Shore Hospital
St Leonards, New South Wales, Australia
Wollongong Hospital
Wollongong, New South Wales, Australia
Royal Darwin Hospital
Tiwi, Northern Territory, Australia
Royal Brisbane and Women's Hospital
Brisbane, Queensland, Australia
Princess Alexandra Hospital
Brisbane, Queensland, Australia
Prince Charles Hospital
Chermside, Queensland, Australia
Gold Coast University Hospital
Southport, Queensland, Australia
Nambour Hospital
Sunshine Coast, Queensland, Australia
...and 42 more locations
Symbol Digit Modality Test
SDMT at 6 months
Time frame: 6 months after randomisation