- Open Access
Effect of the Cardio First Angel™ device on CPR indices: a randomized controlled clinical trial
Critical Care volume 20, Article number: 147 (2016)
The Commentary to this article has been published in Critical Care 2016 20:182
A number of cardiopulmonary resuscitation (CPR) adjunct devices have been developed to improve the consistency and quality of manual chest compressions. We investigated whether a CPR feedback device would improve CPR quality and consistency, as well as patient survival.
We conducted a randomized controlled study of patients undergoing CPR for cardiac arrest in the mixed medical-surgical intensive care units of four academic teaching hospitals. Patients were randomized to receive either standard manual CPR or CPR using the Cardio First Angel™ CPR feedback device. Recorded variables included guideline adherence, CPR quality, return of spontaneous circulation (ROSC) rates, and CPR-associated morbidity.
A total of 229 subjects were randomized; 149 were excluded; and 80 were included. Patient demographics were similar. Adherence to published CPR guidelines and CPR quality was significantly improved in the intervention group (p < 0.0001), as were ROSC rates (72 % vs. 35 %; p = 0.001). A significant decrease was observed in rib fractures (57 % vs. 85 %; p = 0.02), but not sternum fractures (5 % vs. 17 %; p = 0.15).
Use of the Cardio First Angel™ CPR feedback device improved adherence to published CPR guidelines and CPR quality, and it was associated with increased rates of ROSC. A decrease in rib but not sternum fractures was observed with device use. Further independent prospective validation is warranted to determine if these results are reproducible in other acute care settings.
ClinicalTrials.gov identifier: NCT02394977. Registered on 5 Mar 2015.
Effective chest compression remains the cornerstone of successful cardiopulmonary resuscitation (CPR) and is vital for patient survival and good neurological recovery [1–12]. International guidelines note the critical importance of the quality of manual chest compression components, including hand position, position of rescuer and victim, and compression rate and depth [9, 13–20]. Several devices have been developed to improve the consistency and quality of chest compressions [8, 14, 18, 21]. These include active compression-passive decompression (ACPD) devices and active compression-active decompression devices. Some of these devices are coupled to feedback technology to help guide or inform the rescuer about CPR. CPR feedback technology ranges in complexity from a simple metronome to more complex devices that monitor and provide real-time audiovisual feedback [22–24]. Some devices are designed for use by both medical personnel and laypersons [25–29]. While guidelines currently do not recommend any of these circulatory adjuncts, owing to insufficient data, some are being used routinely in resuscitation as alternatives to standard manual chest compressions [8, 30, 31].
The feedback devices may be divided into those associated or not with automated external defibrillators (AEDs). The non-AED ACPD devices are small, lightweight, portable devices that are positioned between the patient and rescuer. These devices are positioned on the patient’s chest where the rescuer’s hands would normally be positioned during manual CPR, and compressions are performed on the device. To date, four non-AED-associated and five AED-associated CPR feedback devices have been tested in clinical and training environments .
Feedback devices rely on either pressure or acceleration measurements as surrogates for compression depth to determine compression adequacy. The Cardio First Angel™ (CFA; INOTECH, Nubberg, Germany) is an ACPD CPR feedback system designed for use by both laypersons and healthcare professionals. We sought to determine if the addition of CFA to routine manual CPR would impact the quality and consistency of CPR and patient survival.
Study design and settings
We conducted a randomized, controlled, single-blind study of patients undergoing CPR for cardiac arrest in the mixed medical-surgical intensive care units (ICUs) of four academic teaching hospitals in Tehran, Iran, between 1 June and 31 October 2014. Patients were randomized in the emergency department at the time of ICU admission. The intervention and control groups were labeled groups 1 and 2, respectively. The assessment tool was scored by the principal investigator and an ICU nurse. The data analyzer was blinded to group randomization and was not present during CPR.
Patients were eligible for study participation if they met the following criteria: (1) age ≥18 years, (2) admitted to the ICU, (3) full code status, and (4) informed consent was obtained from the patient, legal guardian, or healthcare surrogate upon ICU admission (before cardiac arrest event). Patients with any limitation of code status including but not limited to “no code” or “do not resuscitate” and “do not intubate” were excluded from study participation. Decisions to cease resuscitation efforts were made in accordance with American Heart Association guidelines and included (1) >30 minutes of resuscitation process without any events of ventricular fibrillation or ventricular tachycardia, (2) asystole due to irreversible cause, (3) initial rhythm of asystole, (4) injury not compatible with life, or (5) severity of comorbidities, in the presence of normothermia.
Patients were enrolled consecutively from among available admitted ICU patients. Randomization was accomplished using Random Allocation Software© (Informer Technologies, Inc., Madrid, Spain) (Fig. 1). Block randomization was performed with a computer-generated random number list by an expert statistician who had no clinical involvement in the trial. Allocation assignment was accomplished through confidential communication between the patient’s nurse and a third party who was not involved in the recruitment process.
All parts of the study were reviewed according to the Consolidated Standards of Reporting Trials (CONSORT) statement (Fig. 1) [32, 33]. The trial is registered with ClinicalTrials.gov with the identifier NCT02394977. The protocol was approved by the institutional review boards at the four participating medical centers in Tehran: Baqiyatallah Hospital, Masih Daneshvari Hospital, Loghman Hakim Hospital, and Shahid Modares Hospital. Consent covered both study participation and consent to publish the findings. Informed consent was required. Surrogate consent from the patient’s legal guardian or healthcare proxy was permitted in cases where the patient did not have decision-making capacity.
Chest compressions were performed by ICU nurses. Before the start of the study, all ICU nurses at approved study sites received standardized CPR training in accordance with published guidelines, in addition to formal training with the CFA device [9, 20]. Upon CPR initiation, patients in the control group received CPR in accordance with published guidelines, and patients in the intervention group received CPR in accordance with published guidelines using the CFA device per the manufacturer’s instructions. Compressor rotation was not standardized and was dependent on clinical staffing as well as the physical health, condition, and stamina of those providing compressions. Invasive hemodynamics were not measured during the resuscitation, as this was outside the scope of this study.
Cardio First Angel ™ device
The Cardio First Angel™ is a lightweight device (130 g, 4.5 oz) that consists of three components (Fig. 2). The rescuer-side portion consists of a red, round push-button that fits in the palm of the rescuer’s hand as it would lie on the sternum during manual CPR. This rescuer-side component displays a pictogram illustrating proper device use. The center unit is composed of a stable plastic base that contains a complex arrangement of springs to transfer force to the patient’s thorax. The patient side of the device consists of liquid-absorbent polyurethane foam that disperses the compression force evenly across the device footprint. Application of 400 ± 30 N of force (41 kg or 90 lb of pressure), which correlates to a sternum compression depth of 50–60 mm, is followed by an audible “click” sound to alert the rescuer to cease compression. The “click” sound is also audible upon spring decompression, alerting the rescuer to resume compression.
The data collection tool included both demographic and CPR-specific variables. The assessment tools were developed during two 90-minute meetings by a consensus multidisciplinary panel consisting of 11 physicians representing critical care (n = 3), anesthesia (n = 3), cardiology (n = 2), pulmonology (n = 1), internal medicine (n = 1), and forensic medicine (n = 1), in addition to 10 critical care nurses. The assessment tool was scored by the principal investigator and an ICU nurse. Tool validation was performed using the Delphi technique. Assessment of interrater reliability yielded a κ score of 0.9.
Collected demographic data included age, sex, invasive mechanical ventilation status upon code onset (yes or no), ICU length of stay, diagnoses, presence of known osteoporosis (yes or no), and incidence of sternum or rib fractures (on x-ray or autopsy). Also recorded were initial rhythm and therapeutic agents administered during the resuscitation. Time of resuscitation occurrence (morning, midday, evening, or night) and nurse’s level (years) of critical care nursing experience were recorded. CPR effectiveness was evaluated on a scale of 0 (lowest) to 10 (highest) based upon patient position, CPR event frequency, presence of a working intravenous line, use of a CPR board or deflation of air mattress, environmental management, CPR duration, and return of spontaneous circulation (ROSC). Observation of the adherence to CPR guidelines on a scale of 0 (lowest) to 10 (highest) was recorded using a checklist. Assessment of guideline adherence was based upon timeliness of compression initiation, effective team coordination and observation of preassigned roles, compression rate, compression depth, rescuer position, airway management, medication administration, and appropriate use of defibrillation and pacing. Both checklists were validated on the basis of content validity ratio (0.54) and content validity index (0.89).
All analyses were performed using IBM SPSS 22.0 software (IBM, Armonk, NY, USA). Frequency (percent) and mean (SD) were presented for qualitative and quantitative variables. The normality of study variables was assessed with the one-sample Kolmogorov-Smirnov test. The median value (quartile 1 to quartile 3) was presented as a summary statistic for nonnormative variables, including CPR duration, nurse satisfaction with CPR quality, CPR evaluation, and observation of CPR guidelines. Frequency was presented as a summary statistic for ROSC and incidence of rib and sternum fractures. Non-Gaussian variables were compared with the Mann-Whitney U test, χ 2 test, or Fisher’s exact test as appropriate. Demographic variables were compared using a t test, χ 2 test, or Fisher’s exact test as appropriate. Statistical significance was defined as a p value <0.05.
Of 229 consecutive patients eligible for study enrollment, 149 were excluded and 80 were included (Fig. 1). Patient demographics were similar between groups (Table 1). The percentage of female patients was similar between groups (55 % vs. 65.5 %; p = 0.56) as was patient age (59 ± 13 years vs. 62 ± 13 years; p = 0.32). Admission diagnoses were similar (Table 2). All cases of cardiac arrest occurred in the ICU. Identified initial rhythms compared between intervention and control groups included asystole (30 % vs. 33 %), ventricular tachycardia (45 % vs. 45 %), ventricular fibrillation (12.5 % vs. 12.5 %), and bradyarrhythmia (12.5 % vs. 10 %).
Use of resuscitation therapies was similar between groups (Table 3). No significant difference was observed between groups in total dose of electricity administered for defibrillation. No significant difference in either the rate of administration or the dose of administered epinephrine, vasopressin, atropine, amiodarone, calcium gluconate, or sodium bicarbonate was observed (Table 3). Although the frequency of lidocaine administration was similar between groups, there was a significant increase in dose administered in the intervention group (p < 0.0001).
When we considered risk factors for CPR-associated morbidity, we found that the percentage of patients with osteoporosis was similar between groups (90 % vs. 82 %; p = 0.52). Moreover, the shift of CPR occurrence (morning, midday, evening, night) was similar between groups (p = 0.78).
Adherence to published CPR guidelines as well as CPR quality were improved in the intervention group (p < 0.0001) (Table 4). No significant difference in CPR duration was observed between groups (34 minutes vs. 36 minutes; p = 0.076) (Table 5). ROSC was observed more frequently in the intervention group (72 % vs. 35 %; p = 0.001). A significant decrease in rib fractures was identified between groups (57 % vs. 85 %; p = 0.02). No significant difference in sternum fractures was observed (5 % vs. 17 %; p = 0.15).
Effective chest compression remains the cornerstone of successful CPR and is vital for survival and good neurological recovery [1–12]. As such, the quality of chest compression remains a focal point of international guidelines [9, 13–20]. Both compression rate and depth are of critical importance, with compression frequencies of <75 and >125 per minute being associated with decreased incidence of ROSC . Moreover, use of proper compression force and depth is important to minimize CPR-associated injuries . A number of CPR adjunct devices have been developed to improve the consistency and quality of chest compressions [8, 14, 18, 21]. Many of these devices incorporate an auditory tool to guide the compression rate. This is based on a number of clinical studies in which researchers noted that audible rate guidance during chest compressions may improve CPR performance [34, 35]. With few exceptions , researchers in early simulation studies of CPR feedback devices have generally reported improved CPR quality as defined by compression rate and depth [25, 37–40]. To date, only the AED-associated CPR feedback devices have been tested clinically, and reports on their efficacy for improving CPR quality have been conflicting [36, 40, 41]. Even when chest compression frequency does not differ significantly from the ideal set out in the guidelines, analysis of “no-flow times” may be significantly longer for the first CPR cycle . Moreover, devices based on accelerometer technology are not accurate on surfaces that are not firm and flat. They also do not correct for the compression of an underlying mattress, leading to significant undercompression of the chest during CPR [24, 43]. Both the increase in “no-flow times” and undercompression may be clinically relevant impediments to high-quality CPR [44, 45].
Before the present study, four non-AED CPR feedback devices had been tested in clinical or medical simulation environments. Although none have been tested clinically, each has been tested in simulated resuscitation environments. The CPRmeter™ (Laerdal, Wappingers Falls, NY, USA) uses an accelerometer to calculate compression depth, as well as a pressure sensor to determine the adequacy of chest wall release or recoil during decompression. Although early reports suggested that the CPRmeter™ significantly improved chest compression quality performed by students inexperienced in CPR , a later report suggested that compression quality was inferior to standard basic life support. Moreover, device use caused a substantial delay in CPR initiation . Similar findings were reported with use of the Zoll Pocket CPR™ device (Zoll Medical Corp., Chelmsford, MA, USA) . Although statistically significant, it is unclear if this delay in CPR initiation is clinically significant.
Both the CPREzy™ (Health Affairs Ltd., Berkhamsted, UK) and CPR PLUS™ devices (Kelly Medical Products, Princeton, NJ, USA) rely on direct measurements of pressure. The CPREzy™ device is battery-powered and relies on light-emitting diodes to notify the rescuer when appropriate compression force has been applied. In one study, the CPREzy™ was associated with a higher number of incorrectly placed compressions (26 % vs. 3.9 % standard CPR; p < 0.001) . This was largely due to a higher number of low compressions (26 % of total compressions for CPREzy vs. 1 % for standard CPR; p < 0.001) . Use of the CPREzy™ device may be associated with rescuer fatigue, as it is associated with a 21–26.5 % increase in rescuer work . Moreover, use was associated with a significant risk of soft tissue injury of the rescuer’s hand .
The CPR PLUS™ device measures compressive pressure and reports this measure to the rescuer via a meter with a movable needle. In a medical simulation study, use of the CPR PLUS™ device resulted in an improved number of correctly applied compressions and reduction in excessive pressure application compared with standard CPR . Limitations of this device include a meter that is difficult to read in real time and a shape that does not fit the rescuer’s hand in an ergonomic fashion.
The Cardio First Angel™ is a non-AED CPR feedback device that uses direct pressure measurement to provide an auditory stimulus to guide both compression and decompression. When it is used properly, rescuers may deliver approximately 100–120 compressions per minute. By measuring pressure directly rather than relying on a calculated pressure based upon movement of an accelerometer, it avoids the limitations of the Laerdal CPRmeter™ and Zoll Pocket CPR™ devices. The Cardio First Angel™ device improves on the CPREzy™ and CPR PLUS™ devices by employing an auditory stimulus to direct compression-decompression, which frees the rescuer to look in other directions and potentially participate in other aspects of the resuscitation. This may be advantageous for environments with few (one to three) rescuers as compared with acute care environments where considerably more assistance may be available.
To our knowledge, this is the first study to show improved ROSC with the use of a non-AED CPR feedback device. Multiple reasons likely exist for the larger-than-expected increase in mortality, and it remains unclear how much of the increase is directly attributable to use of the device. Interestingly, adherence to CPR guidelines was significantly higher in the intervention group and likely also contributed in part to the improved mortality. It remains unclear whether device use directly promoted improved adherence to CPR guidelines or whether an unmeasured variable such as hypervigilance on the part of providers using a new CPR device contributed. Regardless of these considerations, the findings of the present study warrant prospective independent validation, ideally with direct comparison to other devices and standard CPR.
CPR guideline adherence was significantly higher in the intervention group. It remains unclear to what degree this is a direct reflection of device use vs. other unmeasured variables. Additionally, although rates of lidocaine administration were similar between groups, the dose was significantly higher in the intervention group. Although this relates to a relatively small percentage of the study patients, both the reason for and the impact of this discrepancy remains unclear.
One criticism of devices that encourage right-not right, one-size-fits-all CPR is that they do not account for complex changes that occur during CPR. Like other CPR feedback devices, the CFA accounts for neither complex changes in chest wall compliance and elasticity nor the compressibility of the surface on which the patient is lying (e.g., a mattress). Additionally, there are unique aspects to the ICUs at the enrolling sites in the present study that limit the generalizability of the findings. For example, only experienced ICU nurses were observed. It remains unclear to what degree the level of nursing experience impacted findings or whether these findings are generalizable to less experienced nurses or nurses in other acute care environments.
Last, the incidence of cardiac arrest was higher than one might anticipate at academic medical centers in Europe or the United States. The reason for this is likely multifactorial. It may in part relate to the availability and allocation of ICU resources. For example, Iran has far fewer ICU beds per 100,000 population than the United States does [48–50]. Additionally, demand may dictate that patients with “do not resuscitate” status or those with more minor critical illnesses may be managed outside the ICU. This may potentially result in a more acutely ill ICU population at higher risk for cardiac arrest.
Use of the Cardio First Angel™ CPR feedback device improved adherence to published CPR guidelines, CPR quality, and nurse satisfaction and was associated with increased rates of ROSC in patients with cardiac arrest in four academic ICUs. Although no difference in sternum fractures was observed, a decrease in rib fractures was observed with device use. Further independent prospective validation is warranted to determine if our results are reproducible in other acute care settings.
active compression-passive decompression
automated external defibrillator
Cardio First Angel™
Consolidated Standards of Reporting Trials
intensive care unit
return of spontaneous circulation
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We thank all physicians, nurses, and support staff who contributed to the expert panel sessions, study implementation, and direct patient care. We thank Dr. Dorothea McAreavey of the National Institutes of Health for her thoughtful manuscript review and feedback. We also thank doctoral candidate Stephen Davis of West Virginia University for his assistance with the statistical analysis.
The authors declare that they have no competing interests.
Substantial contributions to conception and design, or acquisition or analysis of data: AVA, MH, AA, HJ, MI, SJM, and SMRH. Manuscript drafting and revision: AVA, MH, HJ, AA, MI, SJM, SMRH, and ACM. All authors read and approved the final manuscript.