Steroid Treatment After Resuscitated Out-of-Hospital Cardiac Arrest

Cardiac Arrest Clinical Trial

— STEROHCA  

Official title:

Steroid Treatment as Anti-inflammatory and Neuroprotective Agent Following Out-of-Hospital Cardiac Arrest. A Randomized Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04624776
• Other study ID #: EudraCT: 2020-000855-11
• Status: Completed
• Phase: Phase 2
• Start date: October 10, 2020
• Est. completion date: February 28, 2023

Study information

• Verified date: March 2023
• Source: Rigshospitalet, Denmark
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Comatose patients resuscitated from Out-of-Hospital Cardiac Arrest (OHCA) often develop a complicated systemic inflammatory response and have a poor prognosis with neurological damage being the most common cause of death. This study will investigate the anti-inflammatory and neuroprotective effect of early treatment with the glucocorticoid methylprednisolone measured by interleukin-6 and neuron-specific enolase levels in resuscitated comatose OHCA-patients.

Description:

BACKGROUND: Each year approximately 5400 individuals suffer from Out-of-Hospital Cardiac Arrest (OHCA) in Denmark and despite an improved prognosis 30-day mortality is around 90%. For OHCA patients resuscitated successfully and admitted to an Intensive Care Unit (ICU) the 30-day mortality remains higher than 50% due to a complicated systemic response, referred to as the Post Cardiac Arrest Syndrome (PCAS). PCAS consists of four interacting components: 1) ischemic/reperfusion brain injury, 2) myocardial dysfunction, 3) a systemic inflammatory response and 4) persistent stress from the triggering cause of the cardiac arrest, e.g. acute myocardial infarction. PCAS progresses during the first 1-2 days following resuscitated cardiac arrest, and the treatment aims to reduce neurologic injury by cooling the patient to 33-36° C, circulatory support with vasopressors, inotropics or mechanical devices as well as identification and treatment of reversible causes to the cardiac arrest, e.g. acute revascularization of an AMI. Several studies have shown that the systemic inflammatory response is associated with a high risk of poor outcome following OHCA. Inflammatory markers associated with poor outcome include interleukin (IL) 6, high sensitivity C-reactive protein (hsCRP), leucocytes, IL-1b, IL-10, IL-13, tumor necrosis factor alpha (TNF-alpha) and procalcitonin. Despite of this, there is no specific treatment that addresses this complicated and life-threatening systemic response, and guidelines remain inconclusive in this field. Anoxic irreversible brain injury remains the leading cause of death following resuscitated OHCA. The complex mechanism is one of the components in the PCAS and is thought to develop due to neuron apoptosis and reperfusion/ischemic injury. Further, the biomarker neuron-specific enolase (NSE) is correlated to neuron damage in the blood stream and has a strong predictive value for poor outcome following OHCA. Inhibiting the causes of the systemic inflammatory response and thereby potentially the brain injury in the very early stages following resuscitation from OHCA may therefore be key to optimizing post-cardiac arrest care. Following resuscitated OHCA, the function of the adrenal gland is compromised due to global ischemia and reduced levels of the hormone steroid, glucocorticoid, are produced. Glucocorticoid has an important role in several physiologic processes including an anti-inflammatory systemic response. As a result, resuscitated cardiac arrest patients are affected by a severe inflammatory response, while the natural defense mechanism of the body to modulate inflammation is suppressed. Systemic treatment with steroids serves as an anti-inflammatory mediator and counteracts acute microcirculation injury and free radical formation, resulting in diminished vasodilation and reduction of edema, e.g. brain edema. Two small studies have shown signs of improved survival and neurologic outcome among patients who was given injections with glucocorticoids after in-hospital cardiac arrest. The incidence of adverse events was not higher in patients receiving glucocorticoids. Long-term treatment with glucocorticoids is associated with a series of side effects, whereas short-term treatment only has a few side effects. Systemic treatment with glucocorticoids could therefore be an important and safe factor in the treatment of resuscitated cardiac arrest patients that could potentially improve survival and neurological outcome. Methylprednisolone and other glucocorticoids are used in pulse doses (>250 mg prednisolone equivalent a day) in various acute immunologically mediated conditions/diseases such as organ transplantation to prevent organ rejection and certain rheumatic diseases with acute deterioration. All these conditions are associated with a severe inflammatory response, as seen in PCAS, and therefore methylprednisolone doses as high as 30 mg/kg (equivalent of 2.1 g for a person weighing 70 kg) are used in pulse therapy to obtain an adequate response and effect. Further, the advantage of pulse dose glucocorticoid treatment is better efficacy, but also a decrease in side effects due to a reduced need for longer lasting therapy exceeding days or weeks. The literature reports of possible cardiovascular side effects as bradycardia and arrhythmias associated to infusion of pulse doses of methylprednisolone/glucocorticoids if given within a short period of time, but the evidence is limited and not well supported. The Danish summary of product characteristics recommends an initial infusion of Solu-Medrol to be administered over a period of at least five minutes. Based on the above knowledge the intervention in this study is 250 mg of methylprednisolone administered intravenously as a bolus infusion over five minutes. In summary, following resuscitated OHCA, PCAS, a severe and life-threatening condition, is often developed. PCAS is associated with increased mortality and poor neurological outcome. Inhibition of this inflammatory response may have an important, yet relatively unknown, role in post-cardiac arrest care. HYPOTHESIS: Bolus infusion of 250 mg methylprednisolone in the pre-hospital setting will inhibit the systemic inflammatory response and minimize the degree of neurological injury in comatose, resuscitated Out-of-Hospital Cardiac Arrest (OHCA) patients. SAMPLE SIZE: The trial is powered at the co-primary endpoint. The investigators chose a priori to power the trial at the 'weakest' of the two endpoints, ensuring a sufficient power for both endpoints. As the investigators were not able to find data regarding the effect of methylprednisolone on IL-6 levels or NSE levels from OHCA admission, the trial was powered towards a single measurement drawn 48 hours after admission. In 171 patients from the investigators institution the mean (logarithmically transformed to approximate normal distribution) IL-6 level after 48 hours from admission was 4.19±1.27 (unpublished data). The investigators assumed that methylprednisolone would reduce the IL-6 level by 20%. With an α-level of 0.025, the trial would achieve a power of 0.90 if 112 patients were included. The mean (logarithmically transformed to approximate normal distribution) NSE level after 48 hours was 3.21±0.96 after 48 hours from admission (unpublished data). The investigators assumed that methylprednisolone would reduce the NSE level by 20%. With an α-level of 0.025, the trial would achieve a power of 0.90 if 114 patients were included. The investigators aimed to include 120 patients, to adjust for missingness due to withdrawn consent. Further, since a proportion of the patients were expected to die before complete assessment of the co-primary endpoint (i.e. blood sampling at 72 hours), randomization of patients will continue until a total of 120 patients have survived to blood sampling at 72 hours.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 158
• Est. completion date: February 28, 2023
• Est. primary completion date: July 15, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age =18 years

2. OHCA of presumed cardiac cause

3. Unconsciousness (GCS =8) upon pre-hospital randomization

4. Sustained ROSC for at least 5 minutes

5. Randomization and start of study medicine infusion within 30 minutes of sustained ROSC.

Exclusion Criteria:

1. Advanced life support termination-of-resuscitation exclusion criteria

2. Asystole as primary ECG rhythm

3. Women of childbearing capacity

4. Known therapy limitation

5. Known allergy to methylprednisolone

6. Known pre-arrest modified Rankin Scale (mRS) score of 4-5

7. Temperature upon randomization <30° C

8. >30 minutes to sustained ROSC.

Related Conditions & MeSH terms

• Cardiac Arrest
• Cardiac Arrest With Successful Resuscitation
• Heart Arrest
• Neurological Injury
• Out-Of-Hospital Cardiac Arrest
• Post Cardiac Arrest Syndrome
• Post-Cardiac Arrest Syndrome
• Syndrome
• Systemic Inflammatory Response Syndrome
• Trauma, Nervous System

Intervention

Drug:
• Methylprednisolone
A dosis of 250 mg methylprednisolone is suspended in isotonic saline to a total volume of 4 mL prior to infusion.
• Isotonic saline
A bolus infusion of 4 mL isotonic saline (NaCl 0.9%).

Locations

Country	Name	City	State
Denmark	Rigshospitalet	Copenhagen
Denmark	Gentofte Hospital	Gentofte

Sponsors (1)

Lead Sponsor	Collaborator
Christian Hassager

Country where clinical trial is conducted

Denmark, 

References & Publications (32)

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* Note: There are 32 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Concentration of IL-6	Interleukin 6 (ng/L)	Daily measurements from admission to 72 hours after admission
Primary	Concentration of NSE	Neuron-specific-enolase (ng/L)	Daily measurements from admission to 72 hours after admission
Secondary	Markers of inflammation, biomarkers	High sensitivity C-reactive protein (hsCRP, mg/L) and plasma cytokine levels exemplified by IL-6 (ng/L)	Daily measurements the first three days following admission
Secondary	Markers of inflammation, cell count	Leucocyte- and differential count (thousand cells/µL)	Daily measurements the first three days following admission
Secondary	Markers of kidney and hepatic injury	Creatinine, ALAT, ASAT, BF and bilirubin (all in mg/L)	Daily measurements the first three days following admission
Secondary	Marker of the coagulation system, biomarker	Plasma fibrinogen (mg/L)	Plasma fibrinogen the first three days from admission
Secondary	Marker of the coagulation system, functional analysis	Thromboelastography (TEG, measured in minutes)	Thromboelastography at admission and at 48 hours
Secondary	Hemodynamics, Swan-Ganz catheter	Measurements on Swan-Ganz catheter (CVP, PAP, PCWP - all in mmHg)	Daily Swan-Ganz catheter measurements the first five days from admission
Secondary	Hemodynamics, arterial blood gasses (Lactate)	Arterial blood gasses (Lactate in mmol/L)	Arterial blood gasses bihourly the first 36 hours
Secondary	Hemodynamics, arterial blood gasses	Arterial blood gasses (PaO2 and PaCO2 in kPa)	Arterial blood gasses bihourly the first 36 hours
Secondary	Neuroprotection, biomarkers	Biomarkers TAU, NFL, NFM, NFH and GFAP (all in mmol/L)	Biomarkers the first three days from admission
Secondary	Cardiac protection, biomarkers	TnT, TnI and CKMB (all in mmol/L).	Biomarkers the first three days from admission
Secondary	Clinical endpoint, survival	Survival (yes/no, register based data from "The Medical Register of Births and Deaths" in Denmark)	180 days following discharge
Secondary	Clinical endpoint, neurological outcome by mRS score	Neurological outcome (modified Rankin Scale score, 0-6 symptom scale with higher scores indicating more severe symptoms)	After five days of admission and at 30- and 180- days following discharge
Secondary	Safety, adverse events	Cumulated incidence of adverse events	From admission till 7 days following admission