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Figure.  Flowchart Illustrating the Study Selection Process
Flowchart Illustrating the Study Selection Process

EU indicates European Union.

Table 1.  Results of Included Studies With a Lower Risk of Bias
Results of Included Studies With a Lower Risk of Bias
Table 2.  Results of Included Studies With a Higher Risk of Bias
Results of Included Studies With a Higher Risk of Bias
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    1 Comment for this article
    TASER(R) Update.
    Gary Ordog, MD, DABEM, DABMT | County of Los Angeles, Department of Health Services, (retired)
    I read your study on "conducted electrical weapons" with interest. I am not surprised that your study of controlled experimentation on CEW in humans was fraught with difficulty. Why did you only go back to 2000? The TASER(R) was first used in a major law enforcement department in 1980, in Los Angeles, California, USA. We examined all of the recipients of "CEW" seen at a major medical center from then on, and reported the results in a peer-reviewed medical journal. Like ours, most of the major clinical trials were conducted before the year 2000. After examining hundreds of cases, the conclusion was that the TASER(R) was 'relatively' "safe" when used to "control" healthy people and by using the other safety use guidelines. But, the mortalities occurred when it was used on people who were already not medically stable, and especially those intoxicated with illicit drugs. The other factor that was associated with mortality was the excessive use of shocks by time and number, probably causing respiratory, then cardiac arrest. You are correct that a prospective controlled study cannot emulate what is happening in real life, and no one would be able to get ethical committee authorization to do so. 
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    Original Investigation
    Public Health
    February 12, 2021

    Human Health Risks of Conducted Electrical Weapon Exposure: A Systematic Review

    Author Affiliations
    • 1Netherlands Institute for Health Services Research (Nivel), Utrecht, the Netherlands
    • 2ARQ National Psychotrauma Centre, Diemen, the Netherlands
    • 3University of Groningen, Groningen, the Netherlands
    JAMA Netw Open. 2021;4(2):e2037209. doi:10.1001/jamanetworkopen.2020.37209
    Key Points

    Question  What are the health risks associated with exposure to an electrical weapon?

    Findings  This systematic review of 33 studies on use of conducted electrical weapons found no evidence that electrical weapon exposure is associated with adverse health outcomes. However, most of the existing studies recruited healthy and physically fit individuals and had important methodologic limitations.

    Meaning  It is unlikely that the existing evidence constitutes a good representation of real-life field situations.


    Importance  Conducted electrical weapons (CEWs) are used broadly as a less-lethal force option for police officers. However, there is no clear picture of the possible health risks in humans on the basis of rigorously assessed scientific evidence from the international peer-reviewed literature.

    Objective  To synthesize and systematically evaluate the strength of published evidence for an association between exposure to different models of CEWs and adverse acute as well as chronic conditions.

    Evidence Review  Following a preregistered review protocol, the literature search strategy was based on a search of reviews published between January 1, 2000, and April 24, 2020, of PubMed, MEDLINE, EMBASE, Web of Science, PsycINFO, and Cochrane Library, as well as relevant online databases and bibliographic sources, such as reference sections of recent publications. The identified studies were independently assessed in terms of scope, relevance, methodologic bias, and quality. Peer-reviewed publications of human studies were included, using original data and with a focus on the use of taser CEWs in the context of law enforcement. Eligible studies examined clearly defined health outcomes as dependent variables following exposure to a CEW. The review followed the relevant sections of the Preferred Reporting Items for Systematic Reviews and Meta-analyses reporting guideline. A meta-analysis could not be conducted.

    Findings  Of the 1081 unique records screened, 33 relevant studies were identified, all of them of experimental design and conducted in the US. Eleven studies had a low risk of bias and 22 had a higher bias risk. Studies focused on outcomes such as physiologic stress responses, heart rate, blood pressure, arrhythmias, or cognitive performance. Independently of bias risk, the studies reported few or no acute health problems, apart from the wounds caused by the darts. Furthermore, no long-term outcomes were studied. Most of the studies were performed on healthy, physically fit individuals (eg, police officers) in a controlled setting, with short exposure duration (5 seconds). Half of the studies, mainly those with a higher risk of bias, were at least partly funded by the manufacturer.

    Conclusions and Relevance  Based on the findings of the reviewed studies, the risk for adverse health outcomes due to CEW exposure can be currently estimated as low. However, most of the reviewed studies had methodologic limitations. Considering that recruited participants were not representative of the population that usually encounters a CEW deployment, it is not possible to draw conclusions regarding exposure outcomes in potentially vulnerable populations or high-risk groups, such as those under the influence of substances.


    Given that police personnel must regularly deal with dangerous and often life-threatening situations, availability of appropriate equipment is important. The use of firearms comes with risks for the offenders as well as the police officers and in some cases for bystanders. In recent years, there has been a shift to alternative, less-lethal law enforcement options, such as conducted electrical weapons (CEWs), pepper spray, and batons. In this article, the focus is on the taser, a type of CEW.1 Over the past 2 decades, the taser CEW has been considered a means of law enforcement and especially self-defense during encounters with aggressive or violent individuals, particularly those who may not respond to alternatives to the use of force.2,3 The term taser (Thomas A. Swift electronic rifle) refers to a specific type of CEW, produced by Axon Enterprise Inc (formerly TASER International Inc).1,4 The taser CEW was developed in the US and is currently, as in many other countries, part of basic police equipment.4,5 Several types of taser CEWs exist (eTable 1 in the Supplement) as do different deployment methods. Such CEWs can be used in 2 ways: either by firing a barbed dart or by using the stun mode. The first option produces an electric current that causes muscle contraction, leading to a temporary incapacitation of the victim, and the second option provokes physical discomfort/pain.1,4,5

    Currently, CEWs are used broadly as a less-lethal force option for police, but their use has been controversial from the early stages of production and their safety has been a subject of debate in both the media6,7 and scientific community.8 Despite the increasing availability of CEWs within the police force internationally, there is no clear picture of possible adverse health outcomes on the basis of rigorously assessed scientific evidence. Axon Enterprise Inc has published guidelines regarding taser CEW use,9 suggesting that exposure is safe for healthy people who are not under the influence of substances, are not pregnant, are not children or older individuals, and have no psychiatric disorders, and if the exposure lasts no longer than a few seconds and only in certain parts of the body. However, to date, most of the existing literature has focused on the technical aspects of CEWs, anecdotal or non–peer-reviewed reports, or animal studies.

    To our knowledge, scientific evidence from the international peer-reviewed literature on the potential health effects of exposure to CEWs in humans has not been systematically reviewed following rigorous and replicable methods. Our systematic review aimed to fill this gap in the literature by identifying relevant studies conducted in the past 20 years to synthesize and systematically assess the strength of evidence for an association between exposure to different models of taser CEWs and acute as well as chronic adverse conditions. In addition, this review examined whether any possible risk groups can be distinguished based on the current evidence.

    Primary Search Strategy

    This study followed the relevant sections of the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline for systematic reviews.10 The study methodology protocol has been preregistered in the PROSPERO platform.11 A meta-analysis was not conducted because of high heterogeneity among the studies.

    A wide range of relevant search terms regarding exposure to CEWs was used to form the search strategy (eg, taser, Axon, electrical weapon, and electric shock weapon). Before the definitive strategy and search term selection were developed, a pilot search was conducted on PubMed and MEDLINE where the number and applicability of various search terms were tested. The detailed search per main database is included in eAppendix 6 in the Supplement. As a first step, we made an inventory of key publications, such as reviews, based on a pilot search on PubMed and MEDLINE. Second, we developed our literature research strategy protocol on the basis of relevant search terms from the identified articles and exchange of feedback within the project team. The search strategy was based on an extensive literature search in the following major databases: PubMed, including all records of MEDLINE; Web of Science; PsycINFO; EMBASE; and Cochrane Central Register of Controlled Trials.

    In addition, a basic search was conducted using the following relevant online databases: register, European Union (EU) Clinical Trials register, US National Institute of Justice database, and the CEPOL (EU Agency for Law Enforcement Training) database. Furthermore, the reference sections of several articles were screened to check whether any relevant studies were missed in the primary and additional searches.

    Selection Criteria

    Several major inclusion and exclusion criteria were established a priori. Studies were included by 3 of us (C.B., J.G., and C.J.Y.) if the following criteria were met: published or accepted for publication between January 1, 2000, and April 24, 2020; primary scientific studies including original data; published in English, Dutch, French, German, or Spanish; published in peer-reviewed journals; had explicit focus on the use of taser CEWs in the context of law enforcement; assessed clearly defined (self-reported or physician-diagnosed/objectively assessed) health symptoms and conditions, health status or symptom scores, and/or physiologic measures as dependent variables; included only humans; and focused on CEWs as the exposure source (only models from taser and Axon Enterprise Inc, in particular, M26, X26[P], X3, X2, XREP, and/or more recent models). Studies focusing on equipment/devices that did not fall within this classification, such as stun guns, batons/prods, and belts, were excluded.

    There was no restriction in terms of demographic characteristics or investigated health outcomes. Purely descriptive studies in which no clear exposure-outcome associations were tested, reviews, and case studies were excluded. Additional details are presented in eTable 2 in the Supplement.


    Given that the risk of methodologic bias and study and reporting quality are not synonymous,12 both the risk of bias and general study quality were independently assessed by 2 of us (C.B. and J.G.). After consensus and pilot testing within the research team, a modified version of the AXIS (Appraisal tool for Cross-Sectional Studies) quality assessment tool13,14 was used so as to be applicable to different study designs15 (eAppendix 1 in the Supplement).

    Bias risk was based on 3 items of the AXIS tool related to 3 fundamental methodologic aspects: statistical power, sampling, and statistical methods and replicability (numbers 3 [Was the sample size justified?], 4 [Was the target population clearly defined with appropriate population base/unbiased sampling?], and 6 [Were methods, including statistical methods, sufficiently described to enable them to be repeated?]). A study was classified as having a high risk of bias if it scored 0 on at least 2 of those 3 items. For the studies with a lower risk of bias, hierarchy of evidence based on study design was also documented following the Quality Rating Scheme for Studies and Other Evidence16: a modified classification was applied as follows: higher evidence quality (properly conducted randomized clinical trials, controlled trials without randomization, or prospective, comparative cohort trials) and lower evidence quality (nonrandomized, uncontrolled experimental studies or observational studies).

    Regarding general study quality, a score was generated based on all items of the modified AXIS tool (maximum score, 10, 11, or 12, depending on the study design) and divided into 3 categories: low, moderate, and high. The involvement of sponsors was evaluated separately by documenting the funding source for each of the included studies. Assessment of risk of bias and study quality was performed a posteriori and was not a prerequisite for considering a study as eligible for the review.


    During the first phase of the screening, duplicate records from the pool of identified studies were excluded. The members of the project team independently screened the titles and abstracts of the identified studies using the selection protocol formed on the basis of the aforementioned broader inclusion and exclusion criteria. Studies that clearly did not meet the inclusion criteria at this stage of the screening process were excluded. Possible eligible studies underwent a full-text assessment.

    During the second phase of the screening, the potentially relevant studies were assessed by 2 of us (C.B. and J.G.). Discrepancies in terms of scope or relevance of a particular article during the screening were resolved by the involvement of a third reader (C.J.Y.) and discussion among the project team members until consensus was reached. For a third of the studies screened for relevance by both researchers, interrater reliability was calculated based on Cohen κ assessment for binary assessments.17,18 The value of the Cohen κ indicated good agreement (87%, κ = 0.75).

    In the third phase, bias evaluation and general quality assessment were carried out independently by 2 of us (C.B. and J.G.) for all relevant studies, with raters being blind to each other's assessment. Interrater reliability was good (good agreement at 88%, κ = 0.75) and discrepancies between assessments were resolved by the involvement of a third researcher (C.J.Y.). Regarding general quality assessment, interrater reliability was evaluated for a third of all included studies, reaching agreement in all classifications after discussion about minor differences in assessments.

    The selection process was documented in a PRISMA flowchart.10 For the extraction of data, we used a form that was tested on a selection of 10 relevant studies. After agreement was reached on the form, the data were extracted, coded, and imported into tables and the accuracy of the extraction was checked. Differences in assessment or interpretation were resolved through consultation among us. The following characteristics were extracted for each study: authors of the article, year of publication, country in which the study was conducted, CEW model and exposure duration, sample size and type, study design, general study quality, main findings, and funding source.

    Literature Search and Study Characteristics

    The PRISMA flowchart (Figure) shows the literature search process. Of the 1081 unique records screened, 362 potentially relevant studies underwent full-text assessment, and 329 studies were excluded. During this stage of the search, we identified and documented 16 solely descriptive studies on the topic (eAppendix 2 in the Supplement), 60 case studies (eAppendix 3 in the Supplement), and 30 review or overview papers (eAppendix 4 in the Supplement). As a result of this process, 33 research articles from the peer-reviewed literature were included in this review.

    Most of the studies (n = 29) were nonrandomized trials (namely provocation studies with or without a control group), while 4 were randomized clinical trials. Most of the studies (26 [79%]) were conducted in the US and focused on the taser X26 as the exposure source. Twenty-seven studies reported that they involved law enforcement officers as participants, sometimes together with medical personnel or civilians (taser CEW trainees), and 19 studies (58%) recruited less than 30 participants. In 30 studies (91%), the maximum exposure duration to the CEW current was 15 seconds (up to 5 seconds in 19 studies), and the darts were often replaced by sprung metal clips (alligator clips). In one study the duration reached 30 seconds. Most of the investigated outcomes concerned physiologic measures of different aspects of the person’s psychophysiologic state, such as heart rate, blood pressure, cognitive skills, and conditions such as cardiac arrhythmias and acidosis.

    In terms of general quality assessment, 6 studies (18%) scored high, 25 (76%) had a moderate score, and 2 (6%) had a low score. Eleven studies were assessed as having a low risk of bias regarding statistical power, sampling, and statistical methods and replicability. The design of 4 of those studies (12%) referred to a higher quality of evidence (randomized clinical trial and controlled studies). Seventeen studies were at least partly funded by the manufacturer (Axon Enterprises Inc). In 4 studies the funding source was not reported. In addition, the sample sizes of studies receiving funding from the CEW manufacturer appeared to be consistently lower.

    Association Between CEW Exposure and Outcomes

    Independently of the general quality of the included studies, findings were categorized based on the possible risk of methodologic bias (Table 119-29 and Table 230-51). Table 1 presents information on the 11 included studies that were found to have a lower possible risk of bias. These studies generally showed few or no acute health outcomes other than superficial wounds caused by the darts in some cases. Except for sporadically observed increases in blood pressure, no significant changes occurred in heart rhythm and physiologic stressors, such as markers of acidosis, following prolonged exposure. Two studies assessing cognitive skills showed contradictory findings.29,36 The study with the smallest sample (n = 4) looked at possible adverse outcomes associated with CEW exposure on people with a pacemaker and reported no significant alterations in heart rate or blood pressure, or any interference with the implanted device.24

    Assessment of the 22 studies with a higher risk of bias also did not yield consistent associations (Table 2). Thirteen of these studies were financed by Axon Enterprise Inc. Exposure duration was, on average, somewhat higher compared with that in the studies with a lower bias risk. In one study,44 exposure reached 30 seconds, and the investigators reported that prolonged exposure to CEWs was associated with mild lactic acidosis. Some other findings suggested small increases in blood pressure and heart rate with CEW exposure, as well as in creatine kinase levels, but no significant changes in troponin levels, body temperature, respiratory rate, and metabolic effects were observed, even after alcohol consumption. When exposure to CEWs was compared with exposure to other types of police intervention (eg, pepper spray and a police dog search and attack exercise), neurocognitive ability was reduced for a maximum duration of 1 hour for all exposed groups, but group measures did not differ statistically significantly from each other.

    Most industry-funded studies, as well as those funded by other sources, showed no statistically significant findings. Among the 17 studies that reported receiving funding from the manufacturer, 5 reported changes in the examined physiologic measurements that were generally described as mild, and 1 study reported more serious effects in 1 participant after exposure to an experimental device that was later not approved for use. Regarding the studies reporting another funding source, 6 mentioned statistically significant changes in some of the physiologic response levels, with 4 studies stating that the measures shortly returned to baseline. Three additional studies reported some statistically significant changes as well, but those were considered as not being clinically relevant or significant.


    This systematic review identified and assessed evidence in the peer-reviewed literature during the past 20 years of the possible human health risks to individuals exposed to a taser CEW in the law enforcement context. With the search strategies used, our established a priori–defined inclusion criteria, and consideration of the methodologic soundness of the included studies, we identified 33 eligible studies. All studies were of experimental design and focused on outcomes such as physiologic stress responses, heart rate, blood pressure, arrhythmias, blood acidity, or cognitive performance.

    Most of the studies suggested either no significant association between CEW exposure and adverse health outcomes or reported contradictory findings. Exposure to the electrical current of a CEW does not seem to be associated with serious health problems, especially when maximum duration ranges between 5 and 15 seconds. The risk for adverse health outcomes associated with CEW exposure can therefore be estimated as low. However, most studies on the topic had methodologic limitations; 22 of 33 studies had a higher risk of methodologic bias, particularly regarding sample size and selection. Nevertheless, both studies with a lower and a higher risk of bias showed in general no significant associations between exposure and the examined measures. In this review, an additional distinction was made based on the funding source of each study. From our assessment it was not apparent that the results of the Axon Enterprise Inc–financed studies were substantially more likely to suggest that CEW exposure is less harmful, compared with studies that were financed by other sources, as suggested by Azadani et al.52 However, the latter study had a different scope and approach and focused on the broader literature on the effects of electrical weapons, including animal studies. Nevertheless, a consistent difference we observed was that the Axon Enterprise Inc–sponsored studies seemed to analyze small sample sizes more frequently.

    Representativeness of the study population and generalizability of the existing evidence constitute major limitations of the current body of literature on the topic. Most studies exclusively relied on law enforcement officers as the study population, meaning that recruited participants were generally healthy and physically fit and therefore not representative of the population that would usually encounter a CEW deployment. In several cases, a reward was promised (eg, a CEW for personal use) as an incentive to participate. It is therefore questionable whether the existing evidence constitutes a good representation of real-life field situations, since it is not possible to draw solid conclusions regarding exposure effects in potentially vulnerable populations or high-risk groups, such as pregnant women, people with psychiatric problems, or those under the influence of substances. The only studies introducing potential vulnerability factors, such as physical exhaustion and alcohol consumption, suggested no clinically significant associations.42,46,48 Taking the current findings into account, the health warning issued by Axon Enterprise Inc9 regarding vulnerable groups cannot be substantiated on the basis of existing human studies. However, that lack of evidence does not mean that the possibility of adverse health outcomes should be ignored, given that research evidence on the dose-response effects among potential high risk groups is, to our knowledge, nonexistent and not feasible owing to ethical restrictions.

    Lack of generalizability seems to be a major shortcoming in even more aspects. For instance, in European countries, such as the Netherlands, the taser X2 is being used, however, in most of the reviewed studies, only the possible effects of the taser X26 were examined.53 This limited variation in the models reviewed also makes it difficult to differentiate health responses by taser CEW model or maximum exposure duration thresholds on the basis of the included studies. Furthermore, almost all of the reviewed studies were conducted in the US, a country with legal, cultural, and systemic differences compared with Western Europe, and it is unclear whether these findings are applicable to the situation in other countries.

    Heterogeneity in examined health outcomes, definitions, and methodologic aspects makes it difficult to directly compare some of the results of the relevant literature. For example, some studies consider the wounds caused by the barbs of the CEW as injury, while other studies do not. In addition, all reviewed studies focused on physiologic measures/stressors (eg, levels of lactate, pH, blood pressure, and creatine kinase levels), despite the unclear clinical relevance and lack of a broadly accepted hypothesis behind the choice to investigate these outcomes, but research on symptoms (eg, headache, dizziness, and sleep problems) and pain reaction is scarce. Investigation of such stressors could probably provide some information regarding the occurrence of an extreme state, often referred to as excited delirium,54 which does not have a formal diagnosis.55

    Amnesty International as well as Reuters news agency6,7 have pointed out the possible dangers associated with CEWs for vulnerable groups. Reuters has created a database with possible deaths due to CEW use mostly in the US based on media reports, self-report by the operator of the CEW, and, in a minority of cases, an autopsy report.7 In 163 of these cases, the autopsy report confirmed that CEW was the cause of death or one of the contributing factors.56 In many cases death occurred in people who were under the influence of drugs.56 In the literature, exposure to CEWs has rarely been documented as the sole cause of death; in several articles, a CEW was reported as a possible contributing factor in a number of mortality cases, when long-term and/or repetitive exposure was combined with drug use or cardiovascular disease (eAppendix 5 in the Supplement). Based on the current literature, it is not possible to state that there is a direct negative effect of CEW exposure on the health of vulnerable groups; at the same time, it has not been scientifically substantiated that use of a CEW on these groups is safe. The responsibility for the safe use of a CEW lies with the police officer who uses it and is well trained in all aspects of its use. To consider the extensive use of CEWs in law enforcement, it is crucial to look at both the advantages and disadvantages compared with the use of other weapons or police equipment. The use of firearms can often become lethal, while a CEW may possibly serve as a less-lethal substitute, minimizing physical violence while allowing a relatively secure distance from the possible perpetrator or threat. The use of batons and pepper spray is another alternative; however, there is possible risk associated with their use.57,58

    There is in general little evidence on the risk of injuries associated with the stun mode. Studies tend to use alligator clips on the clothes during provocation tests instead of barbed darts shot into the skin or deeper into the body, given that purposefully putting the participants at risk of physical injury is not applicable and is not ethically acceptable. It is also difficult to estimate the actual risk of this type of injury in real-life conditions. Based on descriptive studies (eAppendix 2 in the Supplement), an estimate can be made of the risk of injury. According to El-Sayed et al,59 in approximately 1 of 200 000 cases, the CEW darts had to be removed in the hospital. Bozeman et al60 reported that, in 99.75% of CEW deployment cases, there were no injuries or only superficial injuries due to penetration from the darts. In other studies, however, the prevalence seems to be higher: according to Haileyesus et al,61 11 of 100 cases involved nonfatal injuries treated in a hospital without any significant injuries among minors. In another study, 20% of a sample of minors had mild injuries, such as bruises and scrapes.62 A large multicenter study showed that the position of the exposed individual (prone vs nonprone) during exposure did not seem to be associated with sudden in-custody death rates.63 It is often challenging to compare these findings, given the differences in methods and the definition and documentation of the injuries. There is, in any case, some risk of injury with exposure to a CEW, but that chance appears to be small. eTable 3 in the Supplement provides a summary of case studies identified during the literature searches, categorizing the injuries per organ system.

    Further investigation into the possible causal mechanisms between CEW use and human health effects is needed. Although a large part of the literature concerns animal studies, animal models do not necessarily approximate the possible effects of CEWs on the human body and the hypothesis that the impact of CEW exposure on animals (eg, swine) and humans is similar, seems to be problematic.64-66

    For research transparency and replicability, the methods of experimental studies and clinical trials on the human health effects of CEWs should be preregistered in the form of an open-access protocol. Investigation of health outcomes could be expanded, assessing a broader range of possible health outcomes, such as somatic and psychological symptoms in association with CEW exposure. Although in terms of design, randomized clinical trials are used for the clarification of causal relationships, the methodologic flaws of the existing literature and ethical considerations in this field of research make the performance of observational studies the next timely step that would allow the investigation of longer-term outcomes at the population level. A reliable monitoring system should be established in which diagnosed health conditions, injuries, symptoms, and the extent to which a CEW was deployed will be routinely registered in primary, secondary, or forensic health care services.

    Strengths and Limitations

    To our knowledge, this is the first systematic review that focused on the association between CEW exposure and human health effects based on a preregistered protocol and a comprehensive search strategy. No meta-analysis was possible owing to the high heterogeneity in the type and operationalization of the outcomes investigated in the reviewed studies.


    Based on currently published evidence in the peer-reviewed literature, the risk for adverse health outcomes associated with CEW exposure may be estimated as low, when the same deployment guidelines are applied as in the studies. However, it is not possible to draw conclusions about the extent to which the existing evidence constitutes a good representation of real-life field situations. For this reason, and until further data are available from more methodologically sound studies, it is recommended to follow the precautionary principle, when applicable. By systematically evaluating the health effects of CEW use in daily policing practice (physical as well as mental), it will become clear to what extent the results reported in this review apply to real-life conditions. The involvement of a physician or nurse in the health evaluation of cases in which a CEW was used and the development of a health care database in which the associated health outcomes would be routinely registered would provide further insight into the possible health impact of CEWs, especially for potential at-risk groups.

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    Article Information

    Accepted for Publication: December 22, 2020.

    Published: February 12, 2021. doi:10.1001/jamanetworkopen.2020.37209

    Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2021 Baliatsas C et al. JAMA Network Open.

    Corresponding Author: Christos Baliatsas, PhD, Netherlands Institute for Health Services Research (Nivel), Otterstraat 118, 3513 CR, Utrecht, the Netherlands (

    Author Contributions: Dr Baliatsas and Ms Gerbecks had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.

    Concept and design: All authors.

    Acquisition, analysis, or interpretation of data: All authors.

    Drafting of the manuscript: Baliatsas, Yzermans.

    Critical revision of the manuscript for important intellectual content: All authors.

    Obtained funding: Dückers.

    Administrative, technical, or material support: Dückers.

    Supervision: Baliatsas, Dückers, Yzermans.

    Conflict of Interest Disclosures: No disclosures were reported.

    Funding/Support: This work was supported by the Dutch Ministry of Justice and Security, Research and Documentation Centre (project 3030).

    Role of the Funder/Sponsor: The funding organization had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

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