Table 2.
Author, Year | Funding/COI Disclosures of Review Authors | Objectives | Date Range of Literature Search | Evidence Type | Health Outcome Measures | Study Designs | Population | Number of Included Studies | Exposure | Vaping Devices | |
---|---|---|---|---|---|---|---|---|---|---|---|
Acute | Chronic | ||||||||||
Glasser et al., 2017 [28] | N/A | Synthesize empirical studies on electronic nicotine delivery systems across a broad range of topics, including the health effects. | Through 31 May 2016 | Human | Lung function, changes in COPD/asthma disease symptoms (time of assessment unspecified). | Experimental, quasi-experimental, observational (including case control, cohort and cross-sectional), case reports, case series, qualitative studies, mixed methods. | N/A | 116 articles on the impact of vaping on human health. | Exposure to vapor (duration not specified). | N/A | |
Gualano et al., 2014 [17] | N/A | A systematic review of published studies in order to investigate the efficacy and the adverse effects of the EC. | Through April 2014 | Human | Respiratory resistance | N/A | Experimental | N/A | One study | Short-term use of EC (duration not specified). | N/A |
Pisinger & Dossing, 2014 [21] | Authors report no conflict of interest. | (1) Systematic and critical review of the existing literature on the health consequences of ECs and discuss the implications of our findings for public health; and (2) to investigate how many of the published articles have a conflict of interest. | Through 24 August 2014 | Human, Animal | Acute changes in airway resistance, obstruction, and spirometry-assessed lung function. | N/A | Experimental | Human studies: Generally healthy participants. The results show that three studies included participants with asthma/COPD. Animal: mice. | Six human and one animal studies on pulmonary health effects. | Short-term EC use (minutes) * Intra-tracheal application of a diluted e-liquid solution 2× week for 2 weeks. |
N/A |
Bozier et al., 2020 [18] | None declared | (1) To provide a comprehensive update of data on the potential health effects of ECs since the NASEM report. (2) To provide a focused discussion of the scientific literature that will help inform the general public, health-care practitioners, and policy makers of the effects of EC use on health. | February 2017 through May 2019 | Human, Animal | Changes in lung function in animals and humans. Changes in respiratory symptoms in COPD/asthma patients. | Experimental, observational, and case reports. | Not specified. | 14 studies on respiratory/pulmonary health effects. | Short-term and long-term EC use or exposure to EC vapor (no data on the duration). | N/A | |
Harrell et al., 2014 [19] | The authors report no conflicts of interests. One co-author reports to be receiving research support from a pharmaceutical company, which is also a manufacturer of a stop smoking medication. | To have a summary of the current, relevant literature on EC safety and efficacy. | Through November 2013 | Human | Acute changes in respiratory resistance, lung function (no definition of “acute”). | N/A | Case series and case reports. | Not specified. The results show that some studies included smokers and never smokers. No information on their health. | Eight studies on acute physiological effects. | EC use (no data on the duration). | EC devices reported partially in a Table with study characteristic. No summary or discussion provided. |
NASEM, 2018 [16] | N/A | To evaluate the available evidence of the health effects related to the use of electronic nicotine delivery systems (ENDS) and identify future federally funded research needs. | 1 February 2017–31 August 2017 | Human | Intermediate outcomes (measurements of lung function and lung structure, quantification of inflammatory cell numbers from bronchoalveolar lavage (BAL), pro-inflammatory cytokines from bronchial biopsies, and improvement and progression of existing respiratory diseases. | Development of respiratory conditions, such as asthma, pneumonia, and COPD. | Experimental, observational. | Subjects with or without preexisting respiratory disease. | 17 human studies. | Acute (minutes to hours) and long-term (not further defined) vaping. | |
Ioakeimidis et al., 2016 [20] | N/A | To highlight the efficacy for smoking cessation and the potential hazards of EC use. | Through June 2015 | Human | Acute effects on pulmonary function (No definition of “acute”). | N/A | Not specified. Original studies as well as review articles and statements. | N/A | 20 original studies and 8 review articles and statements | EC use (no data on the duration) | N/A |
Bravo-Gutierrez et al., 2021 [27] | Authors declared no conflicts of interest. | To describe the adverse effects on the respiratory system in consumers of ECs. | January 2013–August 2020 | Human, animal, in vitro | Acute and sub-acute effects on DNA damage, inflammation mechanisms, and reactive oxygen species (ROS) presence. | Chronic effects on DNA damage, inflammation mechanisms, ROS presence. | Experimental, laboratory. | N/A | N/A | Acute (2 h daily for 3 days), sub-acute (2 h daily, 5 days a week for 30 days), and chronic (no definition) inhalation | N/A |
Chand & Hosseinzadeh, 2021 § [31] | Authors declared no conflicts of interest. | To evaluate the most recent studies exploring the association between EC use and asthma worldwide. | 2007–March 2021 | Human | Self-reported asthma diagnosis. | Observational | Youth and adult current EC users, ever EC users and dual EC and TC users. | 13 cross-sectional studies. | Current EC use (past 30 days), ever EC use (ever use but not in past 30 days), dual use (use of EC and TC in past 30 days). | N/A | |
Larue et al., 2021 § [29] | No competing interests for this work were declared. The review protocol declares that a family member of the lead author works in tobacco industry. | To assess the immediate respiratory effects of acute EC use. | Through 20 May 2021 | Human | Augmentation index, fraction of exhaled nitric oxide (FeNO), and spirometry measures. | N/A | Experimental | Mostly healthy participants. Current smokers and non-smokers. | 17 cross over and randomized trial studies. | Duration of EC use (with and without nicotine) ranged from 3 to 30 min. Assessment time occurred between 1 and 30 min post use. | Different brands of ECs with varying nicotine content. |
Xian & Chen, 2021 § [25] | Authors declared no conflicts of interest. | To explore the relationship between ECs and the risk of asthma. | Through August 2020 | Human | Asthma diagnosis | Observational | Adolescents and adults with diagnosed asthma, who are current or former EC users or smokers (comparators). | 11 cross-sectional studies. | Current and former EC use (no further definition). | N/A | |
Goniewicz et al., 2020 [24] | First author received research grant from Pfizer and personal fees from Johnson & Johnson outside of this work. Other authors have nothing to declare. | To conduct a systematic review of epidemiological studies that estimated the odds of key respiratory outcomes among EC users who formerly smoked, compared with current smokers who do not use ECs. | Through September 2020 | Human | Respiratory outcomes (COPD, chronic bronchitis, emphysema, asthma, and wheezing). | Observational | Adult former smokers who transitioned to EC use and current exclusive TC smokers (as a comparator). | Two cross-sectional and one prospective. | EC use (no data on the duration). | N/A | |
Wills et al., 2021 § [23] | Authors declared no conflicts of interest. | To provide a comprehensive review and meta-analysis of evidence from epidemiological studies about the association of EC use with asthma and COPD in human populations. | Through March 2020 | Human | Asthma and COPD. | Observational | General population of adolescents and adults. | 15 studies on asthma and nine for COPD (seven cross-sectional and two prospective). | EC use (current use, 30-day use, and long-term use). | N/A |
§ Meta-analysis. COI = conflict of interest; EC = electronic cigarettes; TC = traditional cigarettes; COPD = chronic obstructive pulmonary disease; ROS = reactive oxygen species; FeNo = fraction of exhaled nitric oxide; and N/A = not available. * Duration of exposure varied according to the followed intervention protocols.