Introduction

Epinephrine (adrenaline) has been employed for cardiac resuscitation for more than a century, despite the knowledge that it can cause beta-mimetic complications [1–3]. Vasopressin is a potent vasopressor that could become a useful therapeutic alternative in the treatment of cardiac arrest because it has very little effect on pulmonary circulation and ventilation/perfusion mismatch [4–6]. Our previous study shows that vasopressin could become a better alternative to epinephrine [6]. Recent studies have shown that vasopressin is especially beneficial when combined with epinephrine during cardiopulmonary resuscitation (CPR) [1, 7].

Several studies show a strong correlation between end-tidal carbon dioxide tension (petCO2) and cardiac output, coronary perfusion pressure (CPP) and cerebral perfusion pressure, restoration of spontaneous circulation (ROSC), and hospital discharge [8–13]. In addition, clinical studies were performed to demonstrate the correlation between mean arterial blood pressure (MAP) and survival as well as the neurological outcome after CPR [14, 15].

The aim of this prehospital study was to compare the values of petCO2 and MAP in patients who suffered a cardiac arrest. They were divided in two groups; one was treated with epinephrine and the other with vasopressin. Our goal was to demonstrate that the use of vasopressin during CPR contributes to higher petCO2 and MAP values and thus may have a beneficial impact on survival rate as well as on neurological outcome.

Materials and methods

In this observational prospective study in the town of Maribor, Slovenia (approximately 200,000 inhabitants), we collected data from January 2000 to April 2006 with the approval of the ethical review board of the Ministry of Health. All emergency calls in this period which were classified as out-of-hospital cardiac arrest (OHCA) in adults older than 18 years and which were dispatched to the prehospital emergency unit were included. In the Centre for Emergency Medicine Maribor, we have two prehospital emergency teams, which are advanced life support (ALS) units of three members with adequately equipped road vehicles (an emergency physician and two registered nurses or medical technicians). ALS was provided using a regional protocol that incorporates the standards and guidelines of the European Resuscitation Council (Antwerp, Belgium).

Exclusion criteria of the study were documented terminal illness, successful defibrillation without administration of a vasopressor, and severe hypothermia (< 30°C). We compared petCO2 and MAP in two treatment groups of resuscitated OHCA patients. In the epinephrine group, patients received 1 mg of epinephrine intravenously every three minutes. In the vasopressin/epinephrine group, patients received 40 units of arginine vasopressin (Pitressin; Goldshield Pharmaceuticals Ltd, Surrey, UK) intravenously only or followed by 1 mg of epinephrine every three minutes during CPR. Patient allocation into these two groups depended on the year of incident (vasopressin has been the first therapy in ventricular fibrillation since November 2003 and in asystole since January 2005) and on accessibility of vasopressin in our prehospital unit (intermittently available since November 2000 and regularly available since November 2003). After successful resuscitation, patients were transferred to the intensive care unit of the Teaching Hospital Maribor.

Data were collected and analyzed according to the Utstein criteria. Demographic information, medical data, and petCO2 values were recorded for each patient by the emergency physician.

During resuscitation, the petCO2 values were measured and recorded every minute beginning with the initial postintubation petCO2 (first petCO2 value obtained) and ending with the final petCO2 value at admission to the hospital. The initial MAP was the first measurement of MAP after ROSC, and the final MAP was recorded at admission to the hospital. Measurements of petCO2, arterial blood pressure, and other parameters were performed with a LIFEPACK 12 defibrillator monitor (Physio-Control, Inc., part of Medtronic, Inc., Minneapolis, MN, USA). Hospital records were used for outcome analysis, including assessment of cerebral performance category (CPC), for patients discharged alive.

Data were expressed as mean ± standard deviation or as number (percentage). For analysis of variables, we used the Fisher exact test and the Wilcoxon rank sum test. The Bonferroni correction was applied for multiple comparisons. The null hypothesis was considered to be rejected at p values of less than 0.05. Analyses of independent predictors for ROSC and survival from univariate analysis were performed using a multivariate logistic regression. For statistical analysis, we used SPSS software (version 12.01; SPSS Inc., Chicago, IL, USA).

Results

Out of 636 patients, 38 were excluded from the study because they were successfully defibrillated without administration of a vasopressor. Patients from the recent vasopressin study [6] (patients with initial ventricular fibrillation) were included in this study. There were no significant differences between demographic and initial clinical characteristics in the compared groups: first monitored rhythm, location of arrest, witnessed arrest, etiology of arrest, gender, age, time to initiation of CPR, and initial petCO2 (Tables 1 to 3).

Table 1 Utstein reporting for cardiopulmonary resuscitation in epinephrine and vasopressin groups
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Table 2 Demographic and clinical characteristics of out-of-hospital cardiac arrest patients
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Table 3 End-tidal pressure of carbon dioxide and mean arterial blood pressure in two groups of cardiac arrest patients
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The initial, average, and final values of petCO2 were significantly higher in patients with ROSC on admission to the hospital compared with patients without ROSC in both groups (p < 0.01). All patients with ROSC had an initial petCO2 value greater than 1.33 kPa. The average petCO2 values in patients with and without ROSC and the final petCO2 values in patients with ROSC were significantly higher in the vasopressin/epinephrine group (p < 0.01). The average values of initial and final MAP were significantly higher in the vasopressin/epinephrine group (p < 0.01) (Table 3).

In multivariate analysis, initial, average, and final petCO2 values, initial MAP, and use of vasopressin were associated with ROSC and admission to the hospital (Table 4); initial, average, and final petCO2 values, final MAP, and use of vasopressin were associated with survival at 24 hours (Table 5); initial, average, and final petCO2 values and final MAP were associated with final survival and hospital discharge (Table 6). Vasopressin/epinephrine therapy was not associated with improved hospital discharge.

Table 4 Variables associated with restoration of spontaneous circulation and hospital admission
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Table 5 Variables associated with survival at 24 hours
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Table 6 Variables associated with hospital discharge
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In outcome analysis, we found significantly higher rates of ROSC and survival at 24 hours in the vasopressin/epinephrine group (p < 0.05) (Table 1). There was no difference in survival to hospital discharge between groups (p = 0.19), but when analyzing the subgroup of patients in asystole, we found a significantly higher hospital discharge rate in patients treated with vasopressin (epinephrine subgroup 17/183 [9.3%] versus vasopressin/epinephrine subgroup 10/44 [22.7%]; p = 0.04; Fisher exact test). In the epinephrine group, significantly higher doses of additional epinephrine were needed, CPR lasted longer, and significantly more patients needed additional atropine, bicarbonate, and inotropic agents than in the vasopressin/epinephrine group (p < 0.05).

Out of all cases of cardiac arrest, 90 patients in the epinephrine group and 36 in the vasopressin/epinephrine group were discharged alive from the hospital. Forty-seven discharged patients in the epinephrine group were with CPC-1 or CPC-2 (52% of survivors), 37 patients with CPC-3 or CPC-4 (41%), and 6 patients with CPC-5 (7%). In the vasopressin/epinephrine group, 26 discharged patients were with CPC-1 or CPC-2 (72%), 8 patients with CPC-3 or CPC-4 (22%), and 2 patients with CPC-5 (6%). Neurological outcome of discharged patients was better (CPC-1 or CPC-2) in the vasopressin/epinephrine group (p = 0.04).

Discussion

In previous studies, the relationship between petCO2 and prognosis was established in prehospital CPR [11–13]. In this study, however, the main focus was on the relationship between petCO2 and MAP and subsequent outcomes. The relevant hemodynamic parameters of resuscitated patients treated with epinephrine only and patients treated with vasopressin (only or in combination with epinephrine) were compared along with their prognostic value in CPR outcome.

The results of this study are similar to those of the studies of Wenzel and colleagues [4] and Guyette and colleagues [5] and show higher rates of ROSC and survival at 24 hours in the group of patients treated with vasopressin. In addition, this study shows that the patients who had asystole as the initial arrest rhythm and who were treated with vasopressin have a higher hospital discharge rate. The average and final petCO2 values in vasopressin-treated patients with ROSC were significantly higher. The initial and the final MAP values were significantly higher in the vasopressin group as well. These results suggest that vasopressin could be more potent than epinephrine in increasing the cardiac output.

Using an animal model, Isserles and Breen [16] established a linear relationship between changes in petCO2 and cardiac output. The authors claim that, during a decreased cardiac output, reduced carbon dioxide delivery to the lung decreases alveolar carbon dioxide pressure and thus causes part of the decrease in petCO2. The remaining reduction in petCO2 results from the increase in alveolar dead space due to the lower pulmonary perfusion pressure (dilution of carbon dioxide from perfused alveolar spaces). Gazmuri and colleagues [17, 18] confirmed that both petCO2 and PaCO2 (arterial partial pressure of carbon dioxide) correspond with the pulmonary blood flow and therefore with cardiac output generated by precordial compressions during CPR.

In an animal study, Yannopoulos and colleagues [19] demonstrated a linear correlation between MAP, cerebral perfusion pressure and CPP, and petCO2. A strong correlation between MAP and neurological outcome was observed in a few other studies [20–22]. In a study using a pig model of ventricular fibrillation cardiac arrest, Lindner and colleagues [23] concluded that administration of vasopressin led to a significantly higher CPP, myocardial blood flow, and total cerebral flow during CPR. In a study conducted by Morris and colleagues [24] using a human model of prolonged cardiac arrest, 40% of the patients receiving vasopressin had a significant increase in CPP. Our study shows that higher values of petCO2 and MAP in patients treated with vasopressin are consistent with the better outcomes in the vasopressin group. In a multivariate analysis, we determined that the chances for survival are improved in patients with a higher MAP on admission to the hospital (for every 1.33-kPa increase in MAP, the chances for survival were 1.4 times better). We also determined that the chances for ROSC, survival at 24 hours, and hospital discharge are associated with the year in which CPR was administered (Tables 4 to 6). Various factors may cause differences between the two observed time periods. These include implementation of new CPR guidelines, renewal of dispatch protocols, application of vasopressin as first therapy, and improved phone communication.

In our study, we had significantly more patients with CPC-1 and CPC-2 in the vasopressin group than in the epinephrine group. In the postresuscitation period, MAP is usually kept at a normal level (80 to 100 mm Hg) or at least at a level that secures coronary perfusion (that is, 65 mm Hg). Results from the study by Bell and colleagues [25] indicate that, to secure cerebral perfusion and prevent secondary cerebral injury, MAP should be kept at a level higher than commonly accepted. In our study, vasopressin contributed to a higher average final MAP (approximately 105 mm Hg), thus preserving cerebral perfusion in the critical postresuscitation period of absent cerebral autoregulation.

Several investigations have demonstrated that vasopressin could improve hemodynamic variables in advanced vasodilatatory or hemorrhagic shock [26–32]. The study by Friesenecker and colleagues [27] showed that, under normal physiological conditions, vasopressin exerted significantly stronger vasoconstriction on large arterioles than norepinephrine. This observation could explain, in part, why vasopressin can be effective in advanced shock that is unresponsive to increases of catecholamines in the standard shock therapy.

In the epinephrine group, resuscitation efforts lasted longer and a significantly higher quantity of additional epinephrine was needed. Adrenergic stimulation by additional doses of epinephrine is associated with adverse cardiac effects, including postresuscitation myocardial dysfunction and increased myocardial oxygen consumption. That is one of the reasons why significantly larger doses of additional therapy (inotropes, vasopressors, atropine, and bicarbonate) were needed in the epinephrine group in comparison with the vasopressin group.

Increased doses of epinephrine have a direct impact on lowering the petCO2 value [33]. Tang and colleagues [34] in an experimental model and Cantineau and colleagues [35] in a prospective human study established that epinephrine induces pulmonary ventilation/perfusion defects as a result of redistribution of pulmonary blood flow. Other studies show that high doses of epinephrine significantly decrease cardiac output and petCO2 but enhance myocardial perfusion pressure and myocardial blood flow [36, 37]. Lindberg and colleagues [38] confirmed that an injection of epinephrine during chest compressions decreased petCO2 and pulmonary blood flow and increased CPP (which then slowly decreased), but the effects on petCO2 and pulmonary blood flow were prolonged. Therefore, epinephrine initially increases CPP and the chances of ROSC, but decreases petCO2 value induced by critical deterioration in cardiac output and thereby diminishes oxygen delivery.

Tang and colleagues [39] confirmed that the beta-adrenergic action of epinephrine has a detrimental effect on postresuscitation myocardial function because it increases myocardial oxygen consumption and decreases postresuscitation survival. In the study by Pan and colleagues [40], CPP was increased after vasopressin application and a significant positive correlation between petCO2 and CPP was observed, suggesting that vasopressin has very little effect on pulmonary circulation and ventilation/perfusion mismatch.

Unlike vasopressin, epinephrine during CPR can, to some extent, reduce petCO2 values because of its impact on the pulmonary circulation. Nevertheless, the values of petCO2, together with MAP, reliably reflect changes in cardiac output.

Conclusion

PetCO2 and MAP values are prognostic factors for the outcome of OHCA. During a cardiac arrest, petCO2 can be considered an indirect parameter for the evaluation of cardiac output in prehospital monitoring together with MAP, when spontaneous circulation is restored. Patients treated with vasopressin alone or followed by epinephrine during CPR have higher average and final petCO2 values as well as higher initial and final MAP values on admission to the hospital than patients treated with epinephrine only. The combination of vasopressor therapy (vasopressin followed by epinephrine) in CPR improves ROSC as well as short-term survival and neurological outcome. In the subgroup of patients with asystole as the initial rhythm, it improves the hospital discharge rate. Our findings suggest that the current guidelines for resuscitation established by the European Resuscitation Council, in which vasopressin is not considered even as a secondary alternative to epinephrine, should be revised.

Key messages

  • During CPR, higher petCO2 and MAP values were observed when vasopressin was used.

  • PetCO2 and MAP are strong prognostic factors for the outcome of cardiac arrest.

  • Compared to epinephrine, vasopressin in CPR improves ROSC as well as short-term survival and neurological outcome.