Background Public access defibrillators (PADs) represent unique life-saving medical devices as they may be used by untrained lay rescuers. Collecting representative clinical data on these devices can be challenging. Here, we present results from a retrospective observational cohort study, describing real-world PAD utilisation over a 5-year period.
Methods Data were collected between October 2012 and October 2017. Responders voluntarily submitted electronic data downloaded from HeartSine PADs, and patient demographics and other details using a case report form in exchange for a replacement battery and electrode pack.
Results Data were collected for 977 patients (692 males, 70.8%; 255 females, 26.1%; 30 unknown, 3.1%). The mean age (SD) was 59 (18) years (range <1 year to 101 years). PAD usage occurred most commonly in homes (n=328, 33.6%), followed by public places (n=307, 31.4%) and medical facilities (n=128, 13.1%). Location was unknown in 40 (4.09%) events. Shocks were delivered to 354 patients. First shock success was 312 of 350 patients where it could be determined (89.1%, 95% CI 85.4% to 92.2%). Patients with reported response times ≤5 min were more likely to survive to hospital admission (89/296 (30.1%) vs 40/250 (16.0%), p<0.001). Response time was unknown for 431 events.
Conclusion This is the first study to report global PAD usage in voluntarily submitted, unselected real-world cases and demonstrates the real-world effectiveness of PADs, as confirmed by first shock success.
- ventricular fibrillation
- ventricular tachycardia
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What is already known about this subject?
Bystander automated external defibrillator (AED) use and rapid response times are associated with improved survival outcomes.
Public awareness and willingness to use public access defibrillators (PADs) varies from region to region and the number of patients who receive a shock before the arrival of emergency medical services is often suboptimal.
What does this study add?
This is the first analysis of data that were self-reported by the lay public and it gives a major insight into public access defibrillation.
The high first shock success demonstrates that public access AEDs can be successfully used in non-clinical environments by lay rescuers.
The paper presents an effective method of collecting post-market clinical follow-up data demonstrating safety and performance of PADs.
How might this impact on clinical practice?
This study may further disseminate the importance of AED use by lay rescuers and dispel the fear that is associated with using an AED in emergency situations.
Reassuring these rescuers of the safety and effectiveness of PADs could allow for earlier defibrillation and the potential for enhanced survival.
Out-of-hospital cardiac arrest (OHCA) is a leading cause of mortality in the USA and Europe, accounting for 347 000 to 700 000 deaths per year.1 2 Patients with ventricular fibrillation (VF) or pulseless ventricular tachycardia (VT) can be treated by transthoracic electrical shocks using an automated external defibrillator (AED). The likelihood of successful defibrillation and survival to hospital admission for patients presenting with VF or VT decreases with time.3 4 Rapid defibrillation and early initiation of chest compressions improve survival.5–7 The ‘Chain of Survival’ emphasises the time-sensitive responder actions which may improve survival from OHCA.8 To maximise survival, it is essential to increase awareness of OHCA, adoption of CPR training and availability of public access defibrillators (PADs).
PAD programmes targeting strategic placement of AEDs improve OHCA outcomes. The introduction of PAD programmes have shown that where PADs were readily available, patients were defibrillated sooner and had improved survival.9–11 However, public awareness and willingness to use PADs varies from region to region and the number of patients who receive a shock before the arrival of emergency medical services (EMS) is often suboptimal. A study of survival following PAD implementation in Stockholm reported underutilisation (n=74 of 474 patients, 16%), but when available and used, 70% of patients survived to 1 month post-arrest.12 Similarly, Wissenberg et al reported low PAD use in the Danish Cardiac Arrest Registry, highlighting that only 241 of 19 468 patients (1.4%) received treatment with a PAD. Importantly, patients treated by a bystander had improved survival outcomes.13
PADs are designed to enable a lay rescuer to terminate a shockable arrhythmia prior to the arrival of EMS. Survival to hospital admission, cardiac function or neurological outcome are influenced by numerous factors such as EMS response time and pre-existing medical conditions, meaning this metric would not provide a clear evaluation of PAD performance. As such, clinical assessment of PADs through analysis of first shock success represents the most appropriate evaluation of their efficacy.
The objective of this analysis was to report post-market clinical assessment data describing the effectiveness of real-world PAD utilisation over a 5-year period and to highlight an approach to PAD post-market clinical follow-up that can be adopted throughout the medical device industry.
Patient data collected from HeartSine PADs between October 2012 and October 2017 were analysed. Use of a PAD is defined as the responder turning on the device and placing electrodes on the patient to enable rhythm analysis. Following each use of the PADs, the end-user must replace the HeartSine Pad-Pak (single-use battery and electrode combination cartridge). To incentivise data collection, in return for a complete data package consisting of an Event Report Form and electronic event data downloaded from the PAD, the end-user was provided with a HeartSine Pad-Pak free of charge, allowing the PAD to be returned to service. HeartSine PADs have a sticker on the front and/or rear of the carry case instructing users to inform HeartSine via a web address if they use the PAD, and HeartSine distributors were instructed to inform users of this incentivised programme.
All HeartSine PADs use the same cardiac rhythm analysis algorithm and follow the same shock energy escalation protocol of 150 J–150 J–200 J. In addition, all HeartSine PADs provide at least basic CPR instruction, with some models providing CPR feedback.
Data were anonymised and audited prior to data entry and analysis.
Patients or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
The end-users, that is, rescuers who used the PAD, completed an Event Report Form after the OHCA. Data fields included patient age, gender and location of event, and details on survival (where known). The purpose of public access defibrillation is to provide OHCA patients with defibrillating shocks prior to their hospitalisation. For this reason, survival in this analysis is defined as a patient’s admission to hospital care.
In addition, end-user information such as CPR or CPR-Defibrillation training, and estimated response times were recorded. Response time was defined as the time from identification of cardiac arrest to arrival of the PAD.
Electronic event data downloaded from PAD
The end-user was asked to download the electronic event data from the PAD after each use. The electronic event data consists of an ECG (bipolar recording from the PAD electrodes) and impedance cardiogram trace, recorded through the electrode pads, with superimposed markers displaying audio prompts and key algorithm features. The ECG trace was analysed to determine cardiac rhythm and shock success. A shockable rhythm was defined as VF or VT with a rate >180 beats per minute. Similar to other published defibrillation studies, shock success was defined as the termination of a shockable rhythm for at least 5 s.14–16
Summary statistics were calculated for patient age and gender, location of event, user training, rescuer response time, survival outcomes, presenting arrhythmia and number of shocks delivered. Proportions were calculated for categorical data, and median and IQR were calculated where appropriate.
First shock success was determined, with 95% CIs based on the binomial distribution. Associations between age, gender and first shock success were investigated by fitting a logistic model with first shock success as the dependent variable and age and gender as covariates. The association between first shock success and survival to admission was investigated by fitting a logistic model with survival to admission as the dependent variable and first shock success as covariate, and the analysis was adjusted for age and gender.
Pearson’s χ2 test with Yates’ continuity correction was applied to test the independence between proportions.
R programming language and R Studio were used for all analyses. A p value of <0.05 was considered statistically significant.
Exact age of patients was not recorded in 49 cases, and in a further 8 cases age was recorded as, for example, ‘60+’, and these were treated as missing values. Similarly, 12 response times that were recorded qualitatively (eg, ‘quickly’ or ‘within minutes’) were not considered for analyses along with 419 unrecorded response times.
The ‘Full Dataset’ included all 977 cases. Electronic PAD downloads were available for all 977 cases. Analyses were performed on the subset of cases where response time was reported, defined as ‘Response Time Recorded’ and included 546 cases (55.9%).
Data were collated from events in 35 countries. Country was unknown in four events (table 1). Events from the USA, Australia, Germany, Spain and UK amounted to approximately 66% of the total cases.
PADs were used in all patients: 692 (70.8%) males and 255 (26.1%) females. Gender was missing in 30 (3.1%) cases. Female patients were typically older than the male patients (mean age (SD) 62 (20) years vs 58 (17) years, p=0.014) and more commonly presented in a non-shockable rhythm (n=206, 80.8%, vs n=391, 56.5%, p<0.001). Events with known gender and survival were considered (n=749), and of these events, male patients had a significantly higher survival to hospital admission compared with females (204 of 567 patients for whom survival was known (36.0%) compared with 45 of 182 patients for whom survival was known (24.7%), p<0.05) (a further two patients whose gender was not reported also survived to hospital admission). Of those patients whose gender was known and who received a shock (n=345), survival to admission was similar for males compared with females (174 of 293 male patients who received a shock, (59.4%) compared with 27 of 52 female patients who received a shock (51.9%)) (figure 1).
The mean age (SD) was 59 (18) years (range: less than 1 year to 101 years). The most frequent age of patient in this dataset was 60 years (n=42). Age was missing in 57 cases (49 cases where age was not reported, and 8 cases where age was reported as a range and was treated as a missing value). Eight (0.82%) patients were defined as paediatric patients, that is, less than 8 years old, as per American Heart Association (AHA) and European Resuscitation Council defibrillation guidelines.17 18 Grouped patient ages are presented in figure 2.
The most common location of PAD usage was at home (n=328, 33.6%). Location was not reported in 40 (4.1%) of events. The relationship between location, response time and survival to hospital admission is reported in table 2.
Most users (n=844, 86.4%) reported having either CPR or CPR-defibrillation training, and 35 (3.6%) users reported having no training. Information on user training was not reported in 98 (10.0%) of cases.
The median number of shocks a patient received was 1 (IQR 1–2), ranging from 1 to 13. The shock energy protocol for HeartSine PADs is 150 J–150 J–200 J, with all subsequent shocks 200 J.
There were 354 events where a shock was administered, and 350 events where first shock success could be determined. First shock success occurred in 312 events (89.1%, 95% CI 85.4% to 92.2%). For those patients who did not receive a shock (n=623), the most prevalent rhythm was asystole (n=333, 53.5%). A HeartSine PAD was applied to 49 (7.9%) patients who presented in sinus rhythm.
Age (p=0.60) and gender (p=0.11) were not associated with first shock success. The OR for gender as a predictor of shock success indicates that males are more likely to have a first shock success (OR 1.93, 95% CI 0.81 to 4.23).
Where survival outcomes were known, first shock success was significantly associated with survival to admission (OR 4.60, 95% CI 2.24 to 9.94, p<0.001). There was a significant negative association between increasing age and survival to hospital admission (p<0.001), demonstrated by the OR per 1-year increase in age as a predictor of survival to hospital admission (OR 0.98, 95% CI 0.98 to 0.99). However, it is important to note that other variables such as medical history and underlying aetiology may have influenced outcome—data for which are not available. Details on medical history were provided in only 39.6% of cases.
Survival to hospital admission information was unavailable for 223 events in ‘Full Dataset’, of which 49 (22.0%) presented in sinus rhythm. Cardiac arrest at initial presentation could not be verified in these patients during subsequent follow-up. Of the remaining 754 events, survival to admission was confirmed for 251 (33.3%) patients (table 2). Survival to admission for those patients who received a shock is reported in online supplementary table 1.
Response time recorded
As highlighted in the Chain of Survival,19 early recognition and treatment of OHCA is imperative to improving survival outcomes. There were a total of 546 (55.9%) events in this analysis where response time was reported (table 2, figure 3).
Only observations with reported response time were included in the following analysis. The median response time (minutes) was 4 (IQR 2–6). A total of 296 (54.2%) events had a rescuer response time of 5 min or less, and of these, 116 (39.2%) patients presented in a shockable rhythm and 114 (38.5%) of these events had at least one shock delivered. First shock success was achieved in 103 (90.4%) events. Survival to hospital admission in all patients in the ‘5 min or less’ group was 89 (30.1%). Similarly, of the 250 (45.8%) events with a rescuer response time of ‘greater than 5 min’, 77 (30.8%) patients presented in a shockable rhythm and all of these received at least one shock. First shock success was achieved in 68 (88.3%) events. Of the ‘greater than 5 min’ group, notably only 40 (16.0%) patients survived to hospital admission. This is statistically fewer than the ‘5 min or less’ group (p<0.001), yet the proportions of shockable rhythms and first shock successes are similar in both groups (p=0.83).
This analysis examined the use of PADs prior to EMS arrival and differs to other PAD studies in that the data were global real-world, unselected and not in pre-specified locations. The authors did not determine where the PADs should be located. The patient demographic data collected in this study are similar to that in previous OHCA studies.10 20–24 The dataset contains a low proportion of paediatric patients and more reports of males suffering OHCA. Males were also more likely to survive than their female counterparts.
It was noted that female patients were typically older, and more commonly presented an initial non-shockable rhythm than male patients, in line with a recent analysis of ROC Epistry data.25 More male than female patients received a shock (42.3% compared with 20.4%, p<0.001, figure 1), and their subsequent first shock success was comparable (89.1% compared with 80.8%, figure 1). Of those patients with known gender and survival (n=749), survival to hospital admission was significantly higher in male patients (36.0% compared with 24.7%, p<0.05), a result similar to the ROC Epistry-Cardiac Arrest data analysis26 who found that men were more likely to have sustained return of spontaneous circulation (ROSC) at hospital admission, although the difference in their analysis was not significant.
The home is often reported as the most common location of OHCA, with occurrences often reported to be as high as 87%.20 27 28 Our study identified only 33.6% of PAD uses in the home. When the relationship between location and survival to hospital admission was analysed, patients who were treated in the home were found to have the lowest rate of survival to hospital admission (13.2%). It is worth noting that patients at home are less likely to receive bystander CPR and early defibrillation than those in public places.29 As reported in similar studies, sports facilities have the highest proportion of patients who survived to hospital admission (n=75, 78.1%). Literature reports that OHCAs which occur in sports facilities are more commonly witnessed and bystander CPR is more likely to be performed.30 Our findings also identified sports facilities as the location with the fastest rescuer response time (median 2.5 (IQR 1–5)). OHCA occurring in sports facilities often involve younger people without a history of heart disease.30 Consequently, there is often particular focus on the placement of PADs in these locations and training of sports facility staff which may explain the fast response time and high survival to hospital admission reported in our analysis.
Effectiveness of PADs in this study was confirmed by first shock success. This was determined because, although PADs remind a user to call for emergency services and instruct on how to perform effective chest compressions, there are many other confounding factors such as underlying health status which may detrimentally affect survival outcomes. Shock success of PADs is not commonly reported on, as many PAD registry studies do not have access to the electronic ECG download from the AED. This study differs, as the electronic event data were available for every event. The PADs in this study use a low-energy shock escalation protocol, of 150 J–150 J–200 J. The results demonstrated that the PADs were effective, with termination of a shockable rhythm (first shock success) occurring in 89.1% (n=312) of events. Of those whose first shock was successful in terminating the shockable rhythm, and for whom survival was known (n=274), 69.7% (n=191) survived to hospital admission. There is often criticism of low-energy shock protocols, suggesting that low-energy defibrillation is less effective than higher-energy defibrillation. A systematic review by Morrison et al demonstrated that shock success for low-energy (150 J) defibrillators is comparable with higher-energy (200 J+) equivalents.31 The results from our study demonstrated a similarly high proportion of successful first shocks compared with that previously published.32 In addition, the proportion of patients who survived to hospital admission was high for those patients who received at least one shock (ranging from 41.9% to 90.7%; see online supplementary table 1).
There are few studies reporting the use of PADs by lay rescuers. Our study reported a high proportion of trained lay rescuers. Modern PADs are designed with simple user interfaces and audible instructions so that they could be used by anyone, regardless of training level. A survey by Brooks et al reported that 69.3% of their study population knew what an automated external defibrillator was, but only 2.1% of people would attempt to retrieve and use one in a cardiac arrest situation.33 As such, it is possible that our results contain data from trained individuals due to the higher awareness and willingness to use an AED compared with untrained individuals. The overall survival to hospital admission in our study analysis was higher than that reported in published studies assessing survival following bystander intervention, at 33.3% (table 2) compared with 21.8%13 as reported by Wissenberg et al. However, the improvement in survival outcomes is likely to be due to the improved availability of PADs and awareness of OHCA since the publication by Wissenberg et al.
Shorter response time is a well-known determinant of survival from OHCA.3–6 A PAD study in Denmark showed a reduction in response time from over 13 min to approximately 4 min34 35 due to the implementation of a PAD scheme and a corresponding smartphone application scheme which alerts a responder to a nearby OHCA and the location of the nearest PAD. In addition, a study from the Danish Registry found that after these initiatives to improve PAD usage, 30-day survival following defibrillation in public locations increased from 8.3% in 2001/2002 to 57.5% in 2011/2012.36
The results of our current data collection provide a median response time of 4 (IQR 2–6) min (table 2) which is comparable with response times of other PAD programmes.12 In our study, events with response times 5 min and less had higher survival to hospital admission in comparison with those events where response times were greater than 5 min (30.1% compared with 16.0%, p<0.001). Most notably, and to alleviate confounders, these two groups had similar proportions of patients initially presenting with a shockable rhythm (39.2% compared with 30.8%) (figure 3) and subsequent first shock successes (90.4% compared with 88.3%). In line with Weisfeldt and Becker’s three-phase time model,37 these results suggest other biological factors affect survival outcome, and that lowering response time is critical for patient survival.
In 1995, the AHA recommended development and deployment of simple, inexpensive AEDs which should be placed in public locations for use by emergency rescuers and lay users.38 Since then, AEDs have become smaller, lighter and include new technologies to assist lay rescuers to perform CPR effectively.39 In addition, new technologies, such as the GoodSAM smartphone application, have been introduced to assist improvements in rescuer response times and location of PADs.40 The placement of AEDs in public places has become more common, with AEDs becoming commonplace in airports, public streets and sports facilities. Our study shows that there are still improvements to be made to reduce response times and increase survival outcomes.
Our study reports easily obtainable data which can be used to evaluate safety and performance of PADs. Safety in this study was assessed by incidence of reported hands-on shocks or misuse of the PAD. Our study did not report any safety-related events or side-effects with using a PAD and ensured the acceptability of the risks already identified. The study did not identify any misuse.
This is the first example of proactive post-market clinical assessment of PADs and is an example of how PAD assessment can be performed. Overall, the results of this study report global PAD effectiveness and reiterate the importance of easily accessible PADs and rapid initiation of the Chain of Survival.
This study analyses data voluntarily submitted to HeartSine by end-users and does not encompass the entirety of the device use cases. We aimed to reduce any potential bias of returning only successful resuscitation attempts by incentivising the data collection, where the end-user was provided with a replacement Pad-Pak (battery and pads combination cartridge) regardless of the patient outcome. However, we do appreciate that lay responders have an unrealistic view of the success of resuscitation due to television and the media, and thus may feel that an unsuccessful resuscitation attempt was related to their actions rather than the true nature of OHCA. This could potentially lead to lack of reporting in these cases, but it should be noted that the incentive provided enables the PAD to be returned to commission without cost to the PAD owner.
There is limited information on the level of training of end-user. The Event Report Form required the end-user to self-report whether they had received CPR or CPR-D training and requirements for CPR and CPR-D training vary from region to region. As such, the level of competency displayed by ‘trained’ end-users is not quantified and may vary. A further limitation is in some of the reported demographic information. The Event Report Forms were completed retrospectively, which may affect the end-user’s perception of their response time. In addition, it is possible that the rescuer may have estimated patient age and without access to patient files, we cannot confirm accuracy.
There is limited information on the patients’ survival to hospital discharge and subsequent 30-day survival due to the end-user being responsible for the treatment only until EMS arrive. Related to this, we do not have information on sustained ROSC, as due to the nature of public access defibrillation, the PAD was removed from the patient before 20 min had elapsed. Due to patient confidentiality laws, it is difficult at present to collect further information.
This study is the first reporting global PAD use prior to the arrival of EMS and is the first representative, self-reported clinical assessment for PADs. The results of this study demonstrate the effectiveness of the PADs through a high proportion of first shock successes and highlight the relationship between rescuer response time and survival outcomes. The high proportion of events with a rescuer response time of greater than 5 min and the under-utilisation of PADs in the home identify areas for improvement.
The authors would like to thank the lay responders who submitted the anonymised PAD use data.
Contributors HT, OMA, RF, AH and BMC contributed to the research design. AK contributed to data entry. LD audited the dataset. OMA conducted the statistical analyses. HT was the primary author for the manuscript. AH, RB, DME and JA supervised the project. All authors contributed to the interpretation of the results and reviews and drafts of the manuscript. All authors approved the submitted manuscript.
Funding This research was funded by HeartSine Technologies Ltd.
Competing interests HT and OMA are employed by HeartSine Technologies Ltd and are PhD students at Ulster University. RB is employed by Ulster University. AH, AK, RF and BMC are employed by HeartSine Technologies Ltd. LD was employed by HeartSine Technologies Ltd at the time of data collection. JA is employed by the Belfast Health and Social Care Trust and is an unpaid member of the HeartSine Clinical Advisory Board. DME is employed by the Southern Health and Social Care Trust and is an unpaid member of the HeartSine Clinical Advisory Board.
Patient consent for publication Not required.
Ethics approval This study was reviewed by the Faculty of Computing, Engineering and Built Environment Filter Committee, Ulster University, and was assigned the identification number "19.12-Torney, Hannah".
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available on reasonable request.
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