Open Access

Targeted therapeutic mild hypercapnia after cardiac arrest

Critical Care201721:196

https://doi.org/10.1186/s13054-017-1770-6

Published: 31 July 2017

The original article was published in Critical Care 2017 21:90

We read the paper entitled “Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model” by Sekhon et al. published in Critical Care [1]. We agree that the clinical pathophysiologic impact of hypoxic ischemic brain injury after cardiac arrest (CA) is multi-factorial and complex. We are concerned, however, that the description of carbon dioxide management fails to address the potential therapeutic role of mild hypercapnia and identify current research directions underway to explicitly investigate targeted mild hypercapnia in the early post-resuscitation period.

Previously, from a large retrospective audit involving >16,000 patients from 125 Australian and New Zealand (ANZ) intensive care units (ICUs) following CA between 2000 and 2011, we found that, compared with normocapnia, hypercapnia was associated with a greater likelihood of discharge home among survivors [2]. More recently, the findings of our prospective phase II multi-centre randomised trial, the CCC trial, showed that targeting therapeutic mild hypercapnia (TTMH) (PaCO2 50-55 mmHg), compared to targeted normocapnia (TN) (PaCO2 35-45 mmHg) was feasible, appeared safe and resulted in attenuation of neuron specific enolase (NSE) release (a biomarker of brain injury) in resuscitated CA patients [3]. While at this stage only hypothesis generating, such findings suggest that mild hypercapnia could have neuro-protective properties during the immediate post-resuscitation phase. If proven to be beneficial, induction of hypercapnia would be an easy to apply intervention at minimal cost to most CA patients.

We agree that the current best evidence indicates that hypocapnia should be avoided, there is uncertainly whether normocapnia or TTMH is the optimal approach in the immediate post-resuscitation phase. There is sufficient uncertainty to justify a definitive trial to evaluate the potential benefit of mild hypercapnia. Indeed, we have now initiated the TAME Cardiac Arrest trial (Clinicaltrials.gov NCT03114033). This phase III multi-centre randomised controlled trial will determine whether TTMH, applied during the early post-resuscitation period, improves neurological outcome of resuscitated adult cardiac arrest patients admitted to the intensive care unit.

Authors’ response

  • Mypinder S. Sekhon,
  • Philip N. Ainslie and
  • Donald E. Griesdale
  • To the editor:

    We acknowledge Eastwood et al. for their insightful comments to our narrative review entitled “Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two hit” model”. They identify the importance of preventing secondary cerebral injury after cardiac arrest and the crucial role of arterial carbon dioxide induced modulation of cerebral blood flow and oxygen delivery. This effect occurs through the modulation of extracellular pH and is rendered less effective over time. Clearly, episodes of hypocapnia are associated with adverse outcome, stemming from cerebral vasoconstriction, reduced cerebral blood flow and oxygen delivery [1]. Conversely, in a large multicenter observational study, Schneider et. al demonstrated that patients with hypercapnia (PaCO2 > 45 mmHg on one blood gas in the first 24 hours) had higher rates of discharge home among survivors (OR 1.16, 95%CI: 1.03 – 1.32) [2].

    Biologically, the phenomenon of “no reflow”, characterized by cerebral vasoconstriction, microvascular thrombi and subsequent cerebral oligemia early after resuscitation is well established [1]. It follows that mild hypercapnia to induce cerebral vasodilation may augment blood flow during this critical period and mitigate secondary injury. We commend Eastwood et al. for undertaking a foundational randomized control trial to investigate the role of mild hypercapnia (PaCO2 50-55 mmHg) after cardiac arrest compared with normocapnia (PaCO2 35-45 mmHg) (TAME trial; Clinicaltrials.gov NCT03114033) and eagerly await the results.

    This trial will no doubt provide important insights into the management of post-resuscitative care of cardiac arrest patients. However, it should be noted that there is likely significant within-patient heterogeneity with respect to individual pathophysiology of hypoxic ischemic brain injury [1]. Randomized control trials of single physiological interventions in critical care may fail to account for these nuances. For example, two recent randomized trials of single physiological interventions aimed at mitigating secondary injury after cardiac arrest and traumatic brain injury, specifically targeted temperature management and transfusion thresholds, respectively, were negative [4, 5]. Hence our belief is that we should shift the paradigm to delineating the underlying individualized pathophysiology and establish personalized physiologic resuscitation targets following cardiac arrest. Our research group has recently demonstrated the ability to monitor cerebral autoregulation in real time after cardiac arrest to identify optimal and individualized mean arterial pressure [6]. We acknowledge that it remains unknown if individualized perfusion targets are associated with improved outcome after cardiac arrest. However, this strategy represents an intriguing shift towards personalized physiological resuscitation in the management of this catastrophic and complex disease.

    Notes

    Abbreviations

    CA: 

    Cardiac arrest

    TN: 

    Targeted normocapnia

    TTMH: 

    Targeted therapeutic mild hypercapnia

    Declarations

    Acknowledgements

    Not applicable.

    Funding

    No funding source.

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    Not applicable.

    Authors’ contributions

    GE, AN and MW wrote and edited the letter and all authors read and approved the final manuscript.

    Ethics approval and consent to participate

    Not applicable.

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    Not applicable.

    Competing interests

    The authors declare that they have no competing interests.

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    Authors’ Affiliations

    (1)
    Department of Intensive Care, Austin Hospital
    (2)
    Australia and New Zealand Intensive Care Research Centre, Monash University
    (3)
    Department of Intensive Care, Alfred Hospital
    (4)
    Irish Critical Care- Clinical Research Network, University College Dublin / St Vincent’s University Hospital
    (5)
    Adult Critical Care, University Hospital of Wales

    References

    1. Sekhon MS, Ainslie PN, Griesdale DE. Clinical pathophysiology of hypoxic ischemic brain injury after cardiac arrest: a “two-hit” model. Crit Care. 2017;21:90.View ArticlePubMedPubMed CentralGoogle Scholar
    2. Schneider AG, Eastwood GM, Bellomo R, et al. Arterial carbon dioxide tension and outcome in patients admitted to the intensive care unit after cardiac arrest. Resuscitation. 2013;84:927–34.View ArticlePubMedGoogle Scholar
    3. Eastwood GM, Schneider AG, Suzuki S, et al. Targeted therapeutic mild hypercapnia after cardiac arrest: A phase II multi-centre randomised controlled trial (the CCC trial). Resuscitation. 2016;104:83–90.View ArticlePubMedGoogle Scholar
    4. Nielsen N, Wetterslev J, Cronberg T, Erlinge D, Gasche Y, Hassager C, et al. Targeted temperature management at 33 °C versus 36 °C after cardiac arrest. N Engl J Med. 2013;369:2197–206.View ArticlePubMedGoogle Scholar
    5. Robertson CS, Hannay HJ, Yamal J-M, Gopinath S, Goodman JC, Tilley BC, et al. Effect of erythropoietin and transfusion threshold on neurological recovery after traumatic brain injury: a randomized clinical trial. JAMA. 2014;312:36–47.View ArticlePubMedPubMed CentralGoogle Scholar
    6. Sekhon MS, Smielewski P, Bhate TD, Brasher PM, Foster D, Menon DK, et al. Using the relationship between brain tissue regional saturation of oxygen and mean arterial pressure to determine the optimal mean arterial pressure in patients following cardiac arrest: A pilot proof-of-concept study. Resuscitation. 2016;106:120–5.View ArticlePubMedGoogle Scholar

    Copyright

    © The Author(s). 2017

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