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. 2015 Mar 24;19(1):112. doi: 10.1186/s13054-015-0837-5

Increase in cerebral oxygenation during advanced life support in out-of-hospital patients is associated with return of spontaneous circulation

Cornelia Genbrugge 1,2,✉, Ingrid Meex 1,2, Willem Boer 2, Frank Jans 1,2, René Heylen 2, Bert Ferdinande 3, Jo Dens 1,3, Cathy De Deyne 1,2
PMCID: PMC4377035  PMID: 25887259

Abstract

Introduction

By maintaining sufficient cerebral blood flow and oxygenation, the goal of cardiopulmonary resuscitation (CPR) is to preserve the pre-arrest neurological state. To date, cerebral monitoring abilities during CPR have been limited. Therefore, we investigated the time-course of cerebral oxygen saturation values (rSO2) during advanced life support in out-of-hospital cardiac arrest. Our primary aim was to compare rSO2 values during advanced life support from patients with return of spontaneous circulation (ROSC) to patients who did not achieve ROSC.

Methods

We performed an observational study to measure rSO2 using Equanox™ (Nonin, Plymouth, MI) from the start of advanced life support in the pre-hospital setting.

Results

rSO2 of 49 consecutive out-of-hospital cardiac arrest patients were analyzed. The total increase from initial rSO2 value until two minutes before ROSC or end of advanced life support efforts was significantly larger in the group with ROSC 16% (9 to 36) compared to the patients without ROSC 10% (4 to 15) (P = 0.02). Mean rSO2 from the start of measurement until two minutes before ROSC or until termination of advanced life support was higher in patients with ROSC than in those without, namely 39% ± 7 and 31% ± 4 (P = 0.05) respectively.

Conclusions

During pre-hospital advanced life support, higher increases in rSO2 are observed in patients attaining ROSC, even before ROSC was clinically determined. Our findings suggest that rSO2 could be used in the future to guide patient tailored treatment during cardiac arrest and could therefore be a surrogate marker of the systemic oxygenation state of the patient.

Introduction

The goal of cardiopulmonary resuscitation (CPR) is to preserve the pre-arrest neurological state by maintaining sufficient cerebral blood flow and oxygenation. By generating sufficient oxygenated blood flow, ischemic brain damage is minimized [1]. However, only a minority of patients following out-of hospital cardiac arrest (OHCA) experience survival without neurological injury [2-4]. Good quality bystander basic life support, shorter time between collapse and start of CPR and early defibrillation increase the chance of survival with good neurological outcome [5]. Unfortunately, it is still impossible to obtain any information about organ perfusion, in particular cerebral perfusion, and ensuing ischemic organ damage during CPR. Current monitoring of the OHCA patient during CPR is limited to rhythm assessments, pulse checks between two episodes of chest compressions and end-tidal carbon dioxide [6]. Currently, the latter is the only parameter proven to correlate with the likelihood of return of spontaneous circulation (ROSC), although its value for the prediction of long-term outcome has not been established and gives no particular information about the brain [7].

An ideal monitor during out-of hospital CPR should be readily available for use, non-invasively, independent of a pulsatile signal and should provide information about the condition of the brain. Cerebral near-infrared spectroscopy (NIRS), a non-invasive technique, measures the regional difference between oxygenated and deoxygenated hemoglobin, an expression of the difference in oxygen supply and demand. NIRS is independent of a pulsatile signal and continuously measures cerebral oxygen saturation (rSO2) [8]. This technique has recently been introduced in the cardiac arrest setting [9-17]. These studies suggest that rSO2 measured during CPR may correlate with ROSC and survival. Unfortunately, all currently available data were obtained during in-hospital CPR efforts of OHCA patients or during CPR of in-hospital cardiac arrest patients. Until now, no data are available on rSO2 monitoring from start of advanced life support (ALS) in patients suffering from OHCA. The purpose of this study was to measure rSO2 in OHCA patients from the start of ALS until ROSC or until the resuscitation efforts were terminated. We aimed to investigate whether any difference existed in the time course of rSO2 between patients who did or did not experience ROSC.

Methods

In this prospective, observational, single-center study (Ziekenhuis Oost-Limburg, Genk, Belgium) we measured pre-hospital rSO2 in consecutive OHCA patients. The primary aim of this study was to investigate whether there was any difference in rSO2 during OHCA ALS between patients who achieved ROSC and patients who do not. Furthermore, the difference in highest, lowest and initial rSO2 was also investigated as the proportion of time during ALS spent below 30%. The study protocol was approved by the local institutional review board (Commissie Medische Ethiek Ziekenhuis Oost-Limburg, 13–044 U). Informed consent was obtained from patient’s next of kin. In circumstances in which it was not possible to obtain informed consent, the requirement for informed consent was waived, in agreement with the protocol.

An emergency vehicle, staffed by a physician trained in emergency medicine or anesthesiology and a nurse, equipped with a portable cerebral oximeter (Equanox™ 7600; Nonin Medical Inc., Plymouth, MN, USA) drove to the scene of an OHCA after an emergency call. The physician placed a single sensor on the right side of the forehead of the patient as soon as possible, in some cases immediately and in some cases after endotracheal intubation. If the sensor was applied before endotracheal intubation, 100% oxygen was delivered through a bag valve mask. All patients were intubated and ventilated with 100% oxygen. Only one rSO2 sensor was applied to minimize the time delay to the gold standard of care. rSO2 was continuously measured and registered every 4 seconds during pre-hospital ALS until CPR efforts were terminated or until the patient with ROSC arrived at the emergency department. ALS was performed following current European Resuscitation guidelines [6]. In all patients, manual chest compressions were performed. None of the patients received mechanical chest compressions. If ROSC was achieved, the emergency physician pressed the event button of the cerebral oximeter and/or noted the time of ROSC on the Utstein forms [18,19]. Patients were pronounced dead pre hospital or they achieved sustained ROSC (>20 minutes) and were transported to the hospital. No patient was transported with ongoing CPR.

Exclusion criteria were age younger than 18, obvious traumatic cause of cardiac arrest and ROSC before or within 1 minute after start of rSO2 measurement. Emergency physicians were not blinded to rSO2 values because visual confirmation of the measurement and quality of the NIRS signal is necessary. However, they had not received any pre-study information regarding the interpretation of rSO2 values. The rSO2 values were therefore not used in the clinical decision-making and all patients received the best available care regardless of rSO2 values. The decision to stop resuscitation efforts was at the discretion of the medical emergency team. The accuracy and reliability of the used cerebral oximeter (Equanox™ 7600; Nonin Medical Inc.) has been validated against a mix of 70% jugular bulb saturation and 30% arterial saturation [20].

Baseline characteristics were prospectively collected from Utstein templates and emergency medical charts [18,19]. rSO2 data were downloaded from the portable device according to the manufacturer’s instructions and exported to SPSS 20.00 (SPSS, Armonk, NY, USA) for statistical analysis. Patients were defined as achieving ROSC if ROSC was sustained for more than 20 minutes.

Because the goal of this prospective study was to investigate the rSO2 values in OHCA patients during ALS as a prediction for ROSC and to avoid interference from rSO2 measurements when ROSC was already achieved, only data obtained until 1 or 2 minutes before ROSC were used in the following data analysis. We compared initial, mean and maximum rSO2 values as well as the increase in rSO2 and the percentage of ALS time spent below a rSO2 value of 30%.

Statistical analysis

Patients’ characteristics were compared using Student’s t test if normally distributed or the Mann–Whitney test if not normally distributed and expressed as respectively mean ± standard deviation or median with first and third quartiles. The chi-square test and Fisher’s exact test were used when comparing categorical values. Descriptive statistics were used for continuously measured rSO2 values and are expressed as mean ± standard deviation or median with first and third quartiles. P <0.05 was considered statistically significant. All tests were performed using SPSS 20.00. Figures were made using GraphPad Prism 5.01 (GraphPad Software, La Jolla, CA, USA).

Results

Between December 2011 and November 2013, there were 100 eligible OHCA patients. Out of these 100 patients, rSO2 was measured in 56 OHCA patients (Figure 1). Data for seven patients were excluded from the analysis for the following reasons: obvious noncardiac cause of arrest (hanging) in two patients, four patients already had ROSC when rSO2 measurement was started, and data from one patient could not be used due to a technical defect during transfer of data. Eventually 49 patients were prospectively included, 19 (39%) patients achieved sustained ROSC whereas 30 patients (61%) did not and died pre hospital. Of the 19 patients with ROSC, 10 patients (20%) died in the emergency department and eventually three (6%) patients survived with good neurological outcome (Cerebral Performance Category 1 and 2) at hospital discharge and one patient survived with Cerebral Performance Category 4.

Figure 1.

Figure 1

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Enrollment of study patients. ROSC, return of spontaneous circulation.

Comparing ROSC with no ROSC, there were significantly more male patients in the group without ROSC (77% vs. 42%, P = 0.03). Age, initial rhythm, witnessed arrest, amount of epinephrine given and the number of patients in which basic life support by bystanders was started were similar in both groups (Table 1). Patients with ROSC had a shorter median duration of basic life support, initiated by bystander, general practitioners or paramedics (10 (4 to 12) minutes vs. 13 (10 to 17) minutes, P <0.01) and shorter median duration of ALS (16 (10 to 30) minutes vs. 25 (20 to 33) minutes, P = 0.02). The median time between the emergency call and the start of ALS was 14 (12 to 17) minutes in the group without ROSC and 12 (8 to 15) minutes in the group with ROSC (P = 0.01).

Table 1.

Patient demographics and characteristics

Total No ROSC ROSC P value
( n  = 49) ( n  = 30) 19)
Male 31 (63) 23 (77) 8 (42) 0.03
Age 73 (±17) 69 (±17) 70 (16) 0.85
First recorded rhythm
 Ventricular fibrillation 12 (24) 6 (20) 6 (32) 0.50
 Asystole 31 (63) 20 (67) 11 (58) 0.56
 Pulseless electric activity 6 (15) 4 (13) 2 (11) 1.00
Bystander witnessed cardiac arrest 26 (53) 14 (47) 12 (63) 0.38
EMS witnessed cardiac arrest 3 (6) 1 (3) 2 (11) 0.55
Bystander CPR 29 (59) 20 (67) 9 (47) 0.24
BLS duration (minutes)
 Total 12 (9 to 16) 13 (10 to 16.75) 10 (4 to 12) 0.01
 Bystander 10 (5.5 to 15) 10 (7.5 to 15) 5 (4 to 11.5) 0.02
 Paramedic 6.5 (4 to 10) 8 (5 to 12) 4 (4 to 8.5) 0.03
ALS duration (minutes) 21 (15.5 to 31) 25 (20 to 32.75) 16 (10 to 30) 0.02
Response time (minutes)
 Time (call to ALS) 13 (11 to 15) 14 (12 to 17.25) 12 (8 to 15) 0.01
 Time (call to BLS) 0 (0 to 4) 0 (0 to 4.75) 2 (0 to 4) 0.48
 Time (ALS to sensor placement) 3 (1 to 9) 5 (1.75 to 12) 2 (0 to 6) 0.15
Epinephrine dosage (mg) 5 (3 to 8) 5 (4 to 8) 4 (2 to 8) 0.11
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Data are presented as number (percentage), mean (± standard deviation) or median (interquartile range). Demographic data of studied patients. ALS, advanced life support; BLS, basic life support; CPR, cardiopulmonary resuscitation; EMS, emergency medical system; ROSC, return of spontaneous circulation.

The total median increase from initial rSO2 values until 2 minutes before ROSC or the end of ALS efforts was significantly larger in the group with ROSC (16% (9 to 32)) compared with the patients without ROSC 10% (4 to 15) (P = 0.02). All results are summarized in Table 2.

Table 2.

Cerebral saturation values

No ROSC ROSC P value
( n  = 30) ( n  = 19)
Initial rSO2 20 % (±13) 28% (±20) 0.07
Initial rSO2, lowest value of the first minute 19% (7 to 30) 24% (8 to 39) 0.10
Initial rSO2, mean of the first minute 27% (14 to 33) 35% (8 to 43) 0.11
Lowest rSO2 value 19% (7 to 3) 24 %(8 to 39) 0.14
Highest rSO2 value, ROSC included 40% (±16) 56% (±14) <0.01
Highest rSO2 until 2 minutes before ROSC 40% (±16) 52% (±14) <0.01
Mean rSO2, ROSC included 31% (±4) 42% (±8) 0.02
Mean rSO2 until 2 minutes before ROSC 31% (±4) 39% (±7) 0.05
Increase in rSO2, ROSC included 10% (4 to 15) 18% (15 to 33) <0.01
Increase in rSO2 until 2 minutes before ROSC 10% (4 to 15) 16% (9 to 32) 0.02
Increase in rSO2 until 16 minutes 11% (6 to 19) (14 pts) 16% (11 to 36) (19 pts) 0.05
% time spent rSO2 ≤ 30%, ROSC included 25 (0 to 100) 1 (0 to 37) 0.03
% time spent rSO2 ≤ 30% until 2 minutes before ROSC 25 (0 to 100) 2 (0 to 36) 0.05
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Parametric data expressed as mean (± standard deviation), nonparametric data as median (interquartile range). rSO2, cerebral tissue saturation; ROSC, return of spontaneous circulation.

The median duration of ALS until ROSC was 16 (10 to 30) minutes. If we compare rSO2 from the start of measurement until ROSC or until 16 minutes in the no ROSC group (only available in 14 patients), a significant difference in median increase is observed – namely 11% (5.75 to 19) for the no ROSC group versus 16% (11 to 36) for the ROSC group (P = 0.05).

Patients who did not achieve ROSC spent a significantly higher portion of time during ALS with rSO2 ≤ 30% (P < 0.03). The median proportion of time spent ≤30% until 2 minutes before ROSC was 25% (0 to 100) of the time for the no ROSC group compared with 2% (0 to 36) of the time for the ROSC group (P = 0.05). Figure 2 represents the course of rSO2 values in both groups during ALS.

Figure 2.

Figure 2

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Course of cerebral oxygen saturation during advanced life support. Mean cerebral oxygen saturation (rSO2) values ± standard error of mean during advanced life support (ALS) in patients with return of spontaneous circulation (ROSC) and no ROSC.

The mean maximum rSO2 value until 2 minutes before ROSC recorded during ALS was significantly higher in the group that achieved ROSC (52% ± 14 vs. 40% ± 16, P <0.01). The median minimal rSO2 value recorded during ALS, 24% (8 to 39) in the ROSC group compared with 18% (7 to 29) in the no ROSC group, did not differ (P = 0.14) between both groups.

There was no statistically significant difference in the mean initial recorded rSO2 value between the ROSC group compared with the no ROSC group (28% ± 20 vs. 20% ± 13, P = 0.07). The mean rSO2 over the first minute after the start of measurement was not different between both groups, 35% (8 to 43) in the ROSC group and 27% (14 to 33) in the no ROSC group (P = 0.11).

The mean rSO2 from the start of measurement until 2 minutes before ROSC or until ALS was terminated was higher in the ROSC group compared with the no ROSC group, respectively 39% ± 7 and 31% ± 4 (P = 0.05).

The mean initial rSO2 value of the three patients with good neurological outcome was 44% (±26). The mean rSO2 until 2 minutes before ROSC was 54% (±4) and the increase until 2 minutes before ROSC was 13% (±6).

Discussion

During pre-hospital ALS, a higher increase in rSO2 is observed in patients attaining ROSC, even before ROSC was clinically determined. rSO2 monitoring was started immediately on the arrival of the medical emergency team at the scene of cardiac arrest. During the entire course of ALS, rSO2 values were recorded, until ROSC or until the decision to stop ALS. Apart from three small feasibility studies, all previously published studies on this topic reported only data obtained in the emergency department, and therefore a considerable time after the cardiac arrest [14,17,21]. As a result of our early pre-hospital start of rSO2 monitoring, it was possible to monitor patients with short ALS duration and a possibly positive neurological outcome. The time delay between start of CPR and rSO2 monitoring in all published studies was much longer, without information on the duration of low rSO2 values pre hospital and with exclusion of OHCA patients with short time to ROSC [10].

As stated by others and in accordance with our results, rSO2 seems more useful when it is used as a dynamic information tool rather than a static one, so that a single threshold rSO2 value might be insufficient to predict outcome [10,11,22]. However, use of the mean rSO2 as the threshold is not clinically useful. We used data until 2 minutes before ROSC to enable a comparison of rSO2 during ALS between two equivalent groups of patients: a first group who achieved ROSC and a second group in which ALS efforts were halted, but both still in cardiac arrest. We analyzed the difference in rSO2 increase during ALS between patients who achieved ROSC and those who did not. We found a significant difference in the increase in rSO2 between these groups, with an increase in rSO2 even before ROSC was clinically determined by means of pulse check [23]. These observations support the idea for the use of cerebral saturation as a monitor during ALS. Asim and colleagues also analyzed the increase in rSO2 during CPR, and found a gradual increase of 5% (0 to 18) in the patients without ROSC compared with 52% (17 to 52) (P <0.001) in the patients with ROSC [16]. The higher increase, compared with our findings, could be due to the device used to measure rSO2, the Invos™ 5100C (Covidien, Boulder, CO, USA), which does not measure values below 15%. Secondly, the inclusion of rSO2 values at the moment of ROSC together with the rather small number of patients included (23 patients) will exacerbate differences between survivors and nonsurvivors. Thirdly, these findings are of limited added clinical value because ROSC was already determined.

In addition to the increase from start of rSO2 measurement until ROSC, a significant difference was also observed between the ROSC group and the no ROSC group if we compared the increase from start of ALS until 16 minutes of ALS (median duration of ALS in the ROSC group). Both findings could be a surrogate marker for better systemic oxygenation with ROSC as a result. These differences in the increase of rSO2 between the ROSC group and the no ROSC group suggest a high sensitivity of rSO2 to hemodynamic changes, which can be important during ALS for early determination of ROSC and rearrest, especially in the pre-hospital setting where monitoring modalities are limited in contrast to in-hospital cardiac arrest.

Analysis of the current results did not enable determination of a critical threshold of increase predicting ROSC with acceptable specificity/sensitivity. Probably, larger patient numbers will be needed and our ongoing multicenter trial (ClinicalTrials.gov NCT01806844) could enable us to analyze whether this critical threshold for rSO2 increase can be determined.

We observed no significant difference in initial rSO2 between patients who achieved ROSC and patients who did not achieve ROSC. The absence of a significant difference in initial rSO2 between the ROSC group and the no ROSC group was unexpected. We hypothesized that patients with shorter time between the emergency call and start of ALS would have a higher initial rSO2 value, which in turn is supported by a significantly shorter time between the emergency call and start of ALS in patients achieving ROSC. The findings therefore seem contradictory, but this could be linked to the relatively small patient population studied and the observed trend for higher initial rSO2 in the ROSC group. Initial rSO2 could be clinically interesting because it is a fast and easy observation. Although only rSO2 data during CPR were included, we were able to confirm the results of Parnia and colleagues that patients with ROSC had a majority of rSO2 values >30% during CPR [11]. Despite this confirmation, it is important to take into consideration that, amongst our group of survivors, initial rSO2 values of 0% were measured.

In a recent multicenter study, Ito and colleagues measured rSO2 in 672 OHCA patients during a 1-minute period at hospital arrival [15]. A significant difference between patients with transient or sustained ROSC and no ROSC was observed. Surprisingly, only the lowest measured rSO2 values were used in their analysis, introducing a bias caused by suboptimal measurement. It remains unclear how the authors processed rSO2 values <15% in their results because the NIRS device used does not measure below rSO2 of 15% (Invos™ 5100). As the study design is fundamentally different and the measuring device (NIRS) is different, comparison with our study is not possible.

This study has several limitations. Firstly, it is a small, observational, single-center study. Larger, multicenter studies are necessary to confirm current results. Secondly, the physician of the emergency medical team was not blinded to the rSO2 values, although there are no indications that the rSO2 values were used in the decision to cease or continue resuscitation efforts. Moreover, the emergency physician did not receive any information about interpretation of rSO2 data. Thirdly, despite the fact that we used ROSC >20 minutes as the endpoint, only nine patients survived until arrival at the ICU and eventually only four patients survived until hospital discharge. Larger studies are necessary to compare rSO2 values during ALS between survivors to hospital discharge and nonsurvivors (neurological outcome). Fourthly, we could not compare our findings with end-tidal capnography, which is currently the only monitoring tool generally used during CPR, due to lack of end-tidal carbon dioxide data. Finally, none of the patients in the no ROSC group underwent an autopsy, and therefore we can only presume an arrest of cardiac origin.

Conclusion

We found a significant difference in increase of rSO2 during ALS between patients who achieved ROSC and those who did not, even before ROSC was achieved. Our findings suggest that rSO2 could become a surrogate marker of systemic oxygenation because a significant increase in rSO2 was observed before ROSC. Cerebral oximetry could have the potential to guide treatment and decision-making during cardiopulmonary resuscitation, possibly together with capnography. Currently, no initial rSO2 or gradient cutoff value can be defined to predict ROSC. This will remain particularly difficult as high specificity is warranted for such a cutoff value, and observed rSO2 values vary within a wide range. Although there is no doubt that in the clinical (pre) hospital setting a tool to quickly determine whether a patient will achieve ROSC would prove invaluable, these results are promising – but there is still a way to go.

Key messages

  • Limited information and monitoring possibilities are available during ALS in the OCHA setting.

  • Patients who achieve ROSC have a statistically significant higher increase in cerebral saturation from start of measurement until 2 minutes before ROSC or until end of CPR efforts.

  • Further research is necessary in larger patient groups to explore the monitoring possibilities to guide CPR efforts and to correlate cerebral saturation values with neurological outcome.

Acknowledgements

The authors wish to thank the residents, nursing and medical staff of the emergency unit of Ziekenhuis Oost-Limburg for their cooperation and support in this study. They also want to thank Francesca Solmi for statistical support and Eric Caers for English grammar advice. This study is part of the Limburg Clinical Research Program UHasselt-ZOL-Jessa, supported by the foundation Limburg Sterk Merk, Hasselt University, Ziekenhuis Oost-Limburg and Jessa Hospital.

Abbreviations

ALS

advanced life support

CPR

cardiopulmonary resuscitation

NIRS

near-infrared spectroscopy

OHCA

out-of hospital cardiac arrest

ROSC

return of spontaneous circulation

rSO2

cerebral oxygen saturation

Footnotes

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

CG contributed to conception, design, data collection and analysis, and interpretation of the results of the present study and drafted the manuscript. IM contributed to conception, design, data collection and interpretation of the results and was involved in drafting the manuscript. WB contributed to conception, design and interpretation of the results and helped to draft the manuscript. FJ contributed to the design of the study and the interpretation of the results and revised it critically for important intellectual content. RH contributed to the manuscript with his critical remarks on the results and the manuscript. BF critically interpreted the results and helped to draft the manuscript. JD contributed to conception and design of the study and also to the critical interpretation of the results and drafting the manuscript. CDD contributed to conception and design of the study and the critical interpretation of the results and has been involved in revising the manuscript critically for important intellectual content. All authors read and approved the final manuscript.

Contributor Information

Cornelia Genbrugge, Email: cornelia.genbrugge@uhasselt.be.

Ingrid Meex, Email: ingrid.meex@uhasselt.be.

Willem Boer, Email: willem.boer@zol.be.

Frank Jans, Email: frank.jans@zol.be.

René Heylen, Email: rene.heylen@zol.be.

Bert Ferdinande, Email: bert.ferdinande@zol.be.

Jo Dens, Email: jo.dens@zol.be.

Cathy De Deyne, Email: Cathy.dedeyne@zol.be.

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