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LACK OF ASSOCIATION OF INITIAL VASOPRESSOR DOSING WITH SURVIVAL AND

CARDIAC RE-ARREST LIKELIHOOD AFTER RETURN OF SPONTANEOUS

CIRCULATION

Emergency Medicine

7/28/23

Abigail R. Sharpe, PHARMD, Kelly Richardson, PHARMD,∗ Matthew Stanton, PHARMD, BCPS, DABAT, Cathyyen Dang, PHARMD, BCPS,∗ Jessica Feih, PHARMD, BCPS,∗ Ruta Brazauskas, PHD, Bi Qing Teng, MS, and Ryan Feldman, PHARMD, BCPS, DABAT∗

Background

Background

Objectives

Cardiac Arrest

Cardiac Arrest

Adult Advanced Life Support: 2020 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations

2 types of cardiac arrest:

  • Shockable Rhythm

  • Non-shockable Rhythm

Cardiac Arrest with a Shockable Rhythm

ACLS algorithm for shockable rhythms (pulseless ventricular tachycardia and ventricular fibrilation)

When using amiodarone:

300 mg for 1st dose, 150 mg for 2nd dose

When using Lidocaine:

1 to 1.5 mg/kg for 1st dose, 0.5 to 0.75 mg/kg for 2nd dose

Cardiac Arrest Without a Shockable Rhythm

ACLS algorithm for non-shockable rhythms (pulseless electrical activity and asystole)

Post-cardiac Arrest Care

Temperature Managment:

  • Goal temp 89.6 to 96.8F
  • Improved neurologic outcomes
  • AKA therapeutic hypothermia

Ventilator optimization:

  • Maintain arterial O2 of 92 to 98%

Hemodynamic optimization:

  • Goal MAP of 65 mmHg or more

Other:

  • Glycemic control within normal range
  • coronary reperfusion via PCI

Post-cardiac Arrest Care

IV infusions for hypotension:

  • IV Fluid Bolus: Give 1-2 L of normal saline or LR
  • Epinephrine 2-10 mcg/min
  • Dopamine 5-20 mcg/kg/min
  • Norepinephrine 0.1-0.5 mcg/kg/min

Objective of the study

Objectives

this study aimed to assess the association between the initial dose of vasopressors in patients who experienced cardiac arrest in ranges from low doses to very high doses of vasopressors

Methods

Study Design and Study Setting

Inclusion Crtieria and Exclusion Criteria

Interventions

Endpoints

Statistical analysis

Design and Setting

Study Design

Single-center, retrospective record analysis of patients in the Froedtert Hospital Emergency Department

Study Location

Froedtert Hospital Milwaukee, Wisconsin

Study period 11/1/2015 to 10/31/2020

Study Criteria

Inclusion Criteria

Exclusion Criteria

Study Criteria

Inclusion

  • all patients 18+ who experienced cardiac arrest prior to arrival
  • patient achieved ROSC
  • Started on a norepinephrine, epinephrine, or vasopressin infusion

Exclusion Criteria

Exclusion

  • Known pregnancy
  • DNR status
  • transfer from OSH
  • vasopressor infusion initiated prior to hospital arrival
  • vasopressor started >1 hour after ROSC
  • patients who recieved dopamine infusion

4 Study arms

Interventions

Low dose (<0.25 mcg/kg/min)

Middle dose (0.25 to 0.49 mcg/kg/min)

High dose (0.5 to 0.99 mcg/kg/min)

Very high dose (1 or more mcg/kg/min)

Endpoints

Primary and Secondary Endpoints

Primary Endpoint

Primary

Incidence of cardiac re-arrest within 1 hour of vasopressor initiation

Secondary Endpoints

Secondary

  • Need for second vasopressor in the ED
  • % of MAP at goal (65 mmHg +)
  • Incidence of malignant hypertension (SBP > 180 mmHg) during ED stay
  • Incidence of atrial or ventricular dysrythmia
  • Survival to ICU admission
  • Survival to hospital discharge

Data Analysis

Statiscial Analysis

  • Fischer's Exact Test and Kruskal-Wallis Test for continuous and categorical measurements between groups
  • chi-squared or 2-tailed T-test were used for inter-group comparisons

Results

Baseline Study Characteristics

Number lost to follow-up

Study Outcomes

Participant Characteristics

Average age of participants was 63 (+/- 16) years old

predominantly male (58.4% of all participants)

Most commonly observed rhythm was asystole/PEA (68.6%)

Pateints excluded from regression analysis

Number Lost to Follow-up

2

1 - d/t Hypokalemia as cause of arrest rather than hyperkalemia

2 - Time and date of ROSC not recorded

Outcomes

Re-arrests within 1 hour

Secondary Outcomes

Primary Outcome - Re-arrests

There was no significant difference in re-arrests within 1 hour of vassopressor initiation regardless of dose

There was no diference between number of re-arrests regardless of vasopressor dose

Secondary Endpoints

no difference in MAP at goal , incidence of malignant hypertension, or dysrhythmia development in the ED,

Patients initiated at very high doses were more likely to require additional vasopressors to meet hemodynamic support needs

Patients in the high dose group were less likely to survive to hospital discharge than the low dose or medium dose groups

Additional Findings

This study supported existing data regarding metabolic acidosis being associated with poor outcomes in ICU patients

  • Higher post-ROSC pH and longer time to initiation of vasopressors were associated with decreased likelihood of re-arrest

Additional Findings

Longer duration of arrest and hyperkalemia as etiology of arrest was associated with increased incidnce of re-arrest

Hyperkalemia is associated with reduced survival at time of discharge

Discussion

Strengths and Weaknesses

Conclusions

Clinical Significance

Strengths of the study

Strengths

  • The study was exended over a long time frame allowing for a larger study population
  • Matching the study period to the AHA ALS guideline timeline allows for greater internal validity. Providers would be held to the same standard per guideline recommendations for the duration of the study period.

Weaknesses of the study

Weaknesses

  • Assessment of pre-existing comorbidities and bystander CPR prior to EMS arrival were not assessed reducing internal validty.
  • retrospective study design limits data to what was collected during admission or via outside medical record systems
  • Setting of a single hospital limits patient enrollment and overall external validity of this study.

Conclusions

Author's Conclusions

Author's conclusions

  • Dose of vasopressors initiated within 1 hour of ROSC do not have a significant impact on incidence of re-arrest.
  • Patients started on higher initial doses of vasopressors may have been more acutely unwell than those started on lower doses
  • More studies are needed to assess initial vasopressor dose post ROSC in patients presenting to emergency departments to better understand the relationship between dose and re-arrest

My conclusion

My conclusions

I think more research is required before we can conclude that a particular regimen is efficacious at reducing re-arrest in patients who have acheived ROSC following cardiac arrest

What does this study tell us?

Clinical Significance

To date, there is not substantial data on the dose of vasopressor following cardiac arrest to reduce morbidity and mortality.

This study was meant to fill a gap in care; however, the study findings did not provide a clear direction for dosing of vasopressors following cardiac arrest. Provider preferrance should continue guiding vasopressor dose following ROSC after cardiac arrest untill more data comes out supporting a particular dosing regimen.

I look forward to hearing more information about advances in post-cardiac arrest care in the future in order to increase patient survival to hospital discharge in the future.

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