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. 2021 Mar 12;70:124–133. doi: 10.1016/j.genhosppsych.2021.03.006

Mental disorder prevalence among populations impacted by coronavirus pandemics: A multilevel meta-analytic study of COVID-19, MERS & SARS

Matt Boden a,, Nichole Cohen b, Jessilyn M Froelich c, Katherine J Hoggatt d, Hoda S Abdel Magid e, Swapandeep S Mushiana f
PMCID: PMC8058549  PMID: 33894561

Abstract

Objective

Through a systematic review and meta-analysis of research on COVID-19, severe acute respiratory syndrome (SARS) and middle east respiratory syndrome (MERS) pandemics, we investigated whether mental disorder prevalence: (a) was elevated among populations impacted by coronavirus pandemics (relative to unselected populations reported in the literature), and (b) varied by disorder (undifferentiated psychiatric morbidity, anxiety, depressive, posttraumatic stress disorders [PTSD]) and impacted population (community, infected/recovered, healthcare provider, quarantined).

Method

From 68 publications (N = 87,586 participants), 808 estimates were included in a series of multilevel meta-analyses/regressions including random effects to account for estimates nested within studies.

Results

Median summary point prevalence estimates varied by disorder and population. Psychiatric morbidity (20–56%), PTSD (10–26%) and depression (9–27%) were most prevalent in most populations. The highest prevalence of each disorder was found among infected/recovered adults (18–56%), followed by healthcare providers (11–28%) and community adults (11–20%). Prevalence estimates were often notably higher than reported for unselected samples. Sensitivity analyses demonstrated that overall prevalence estimates moderately varied by pandemic, study location, and mental disorder measure type.

Conclusion

Coronavirus pandemics are associated with multiple mental disorders in several impacted populations. Needed are investigations of causal links between specific pandemic-related stressors, threats, and traumas and mental disorders.

Keywords: Coronavirus, Pandemic, Mental health, Depression, PTSD, Anxiety, Healthcare provider, COVID-19

1. Introduction

Numerous studies document the often-substantial adverse mental health impact of coronavirus pandemics [1,2]. With the onset of COVID-19, useful information will be gained from a systematic review of this literature and quantitative summary of prevalence of mental disorders that may be common to populations impacted by coronaviruses. Through a systematic review and meta-analysis of COVID-19, severe acute respiratory syndrome (SARS) and middle east respiratory syndrome (MERS) pandemic research literatures, we addressed two questions. First, is mental disorder prevalence elevated among populations impacted by coronavirus pandemics relative to unselected populations reported in the literature? Second, does mental disorder prevalence vary by disorder (undifferentiated psychiatric morbidity, anxiety, depressive, posttraumatic stress disorders [PTSD]) and impacted population (community, infected/recovered, healthcare provider, quarantined)? We focused our investigation on disorders that are common in the general population and/or theoretically or empirically linked to stressors, threats and traumas that we hypothesized would be prevalent during coronavirus pandemics (see below). As the mental health impact of a coronavirus might not manifest in distinguishable disorders in the acute phases of pandemics, we also investigated undifferentiated psychiatric morbidity (i.e., distress commensurate with a mental disorder diagnosis).

Physical exposure to a virus (e.g., through job duties), media exposure, exposure to illness and death, movement restrictions, interpersonal loss, and (for COVID-19) unemployment and economic deprivation are key pandemic-related threats, stressors and traumas that are likely to increase the risk of a mental disorder [1,[3], [4], [5], [6]]. Populations experiencing a greater frequency or intensity of pandemic-related stressors are likely to be at greater risk of experiencing a mental disorder [7]. Among adults infected with a coronavirus, threats to health and mortality, and disruption to routines (e.g., absence from work) will be pronounced and more impactful the greater the severity of infection [[8], [9], [10]]. Functional impairment and disability may further increase risk for mental disorders among recovered adults [2,[11], [12], [13], [14]]. Healthcare providers, especially front-line treatment providers who contend with threats, stressors and traumas such as repeated exposure to infected and dying people and morally ambiguous decisions regarding who receives treatment [5,6,12] may be at increased risk of mental disorders. Quarantined adults may be at increased risk of mental disorders due to threats to health, lack of social contact, and disruptions to routine [1]. Anxiety and depressive disorders are likely to be common as any given person may experience multiple threats and stressors that contribute to such disorders [15,16]. Infected/recovered adults and healthcare providers, in particular, may experience traumatic events (e.g., invasive treatments, witnessing death) that increase risk of post-traumatic stress disorder (PTSD; [2,5]).

Based on a systematic review of COVID-19, SARS, and MERS research, we conducted multilevel meta-analyses/regressions to derive summary prevalence estimates for multiple disorders (undifferentiated psychiatric morbidity, anxiety, depressive, PTSD) in adult populations (community [including students], infected/recovered, healthcare provider, quarantined). We investigated whether mental disorder prevalence was elevated among populations impacted by coronavirus pandemics relative to unselected populations reported in the literature. For example, a meta-analysis of 157 studies from 59 countries (N ~ 660,000; [17]) found a 12-month prevalence of 15.4% for combined mood (including bipolar) and anxiety (including PTSD) disorders. Twelve-month (or less) prevalence has also been reported in epidemiological studies including unselected samples representative of the adult populations of: (a) China (any disorder = 9.3%; anxiety disorder = 5.%0; depressive disorder = 3.6%; PTSD = 0.2%; [18]), (b) Europe (anxiety disorder = 6.4%, major depression = 3.9%; [19]), and (c) the United States (any disorder = 26.2%, anxiety disorder = 18.1%, depressive disorder = 6.7%, PTSD = 3.5%; [20]). We hypothesized that, relative to these estimates, all disorders would be more prevalent in all populations that we investigated given the frequent and often impactful threats, stressors and traumas associated with coronavirus pandemics. As the frequency and impact of particular threats, stressors and traumas is likely to vary in type and by population, we further hypothesized that mental disorder prevalence would vary by disorder and impacted population.

As individual studies often provided estimates of multiple disorders from the same population, we utilized three-level meta-analytic models including random effects to account for estimates nested within studies. The use of multilevel models allowed us to include all relevant prevalence estimates (e.g., by sex, age, income-level), thus further maximizing the information provided by any given study. By investigating mental disorder prevalence in multiple populations potentially impacted by coronavirus pandemics, our study provides information not found in published meta-analyses related to the aims of the current paper [21,22], which focused on single populations (healthcare providers, severely infected/recovered). Comparison of mental disorder prevalence across populations can inform targeted research on populations most impacted by coronavirus, and downstream resource allocation to populations most in need.

2. Method

This study is part of a broad registered protocol [23], and was conducted according to PRISMA [24] and MOOSE guidelines [25].

2.1. Literature search strategy & criteria

From April 15, 2020 until June 1, 2020, two study staff (MB, NC) conducted a key-word search of electronic databases PubMED, PsychINFO and Google Scholar (with focused searches by author additionally conducted in Scopus and Web of Science) for peer-reviewed, English language publications. We searched for a broad set of studies by forming all combinations of key words (a) avian flu, coronavirus, COVID, Ebola, equine flu, flu, H1N1, Influenza, MERS, quarantine, swine flu, SARS, respiratory, crossed with (b) emotional distress, mental health, anxiety, depression, psychological distress, posttraumatic (and separately, post traumatic and PTSD/PTS/PTST, the latter on the advice of a peer-reviewer). Because the literature search was intended to inform several projects in addition to this meta-analysis, search terms unrelated to coronavirus pandemics were included (e.g., Ebola; [23]). We examined reference lists of identified publications and lists of cited studies to identify additional studies.

2.2. Study sample

Studies meeting the following criteria were included in this meta-analysis: (1) available in English language, (2) peer-reviewed (no grey literature or preprints), (3) reported source data (no reviews), (4) focused on mental disorders (undifferentiated psychiatric morbidity, anxiety, depression or PTSD) related to COVID-19, MERS, SARS, (5) included quantitative estimates of mental disorder prevalence assessed by clinician diagnosis or measures with published psychometric validation data, (6) included adult participants (age ≥18). Electronic database searches yielded a total of 4142 publications that potentially met inclusion criteria. Screening of titles and abstracts yielded 279 studies that were coded (including studies of non-coronavirus outbreaks/epidemics coded as part of the broader project), with 68 studies meeting inclusion criteria (see Fig. 1 ).

Fig. 1.

Fig. 1

Study screening, selection, coding and analysis.

2.3. Coding of study and effect characteristics

Publications were first coded by one of four study authors (MB, NC, SM, JF), with the majority coded by the first author. The first author developed the coding scheme and trained all other study coders through didactics, iterative feedback on coding of a subset of studies, and confirmation of codes by the first author. Study coders identified studies that met inclusion criteria, and extracted data based on the coding scheme developed the first author. A subset of studies (144/279) was coded a second time to ensure consistency of coding. Disagreements between primary and secondary codes were resolved by the first author.

Coded study attributes include mental disorder prevalence in terms of: (a) sample size and (b) size of sample positive for a disorder, (c) type of disorder (undifferentiated psychiatric morbidity, anxiety, depression, PTSD), (d) sample population (community [including university students], infected/recovered, healthcare providers, quarantined), (e) pandemic (COVID-19, SARS, MERS), (f) location (Canada, China, Hong Kong, Korea, Saudi Arabia, Singapore, Taiwan, Italy, United States, Multi: Singapore and India), (g) timing (acute, within 1-year of main outbreak, more than 1-year after main outbreak), and (h) measures (see Supplement A). Measures of psychiatric morbidity included questionnaires assessing psychological/emotional distress and specific types of psychopathology (e.g., Hospital Anxiety and Depression Scale) and clinician assessment of an unspecified mental disorder.

We coded all relevant estimates provided in each study, including estimates for different disorders and the same disorder assessed by different measures, at different time-points, or among different populations and subpopulations (e.g., quarantined versus community, males versus females, doctors versus nurses). Thus, we coded sociodemographic and socioeconomic characteristics but did not include them in moderator analyses due to inconsistent reporting across studies. We also coded study attributes not included in the reported analyses (i.e., means and standard deviation for continuous measures of mental disorders/symptoms).

We manually calculated size of sample positive for a disorder when not reported by the study. For questionnaire measures, we coded size of sample positive for a disorder consistent with the study authors, who typically utilized established cutoffs reported in prior research. Estimates obtained from non-standard cutoffs were identified for sensitivity analysis. When severity thresholds (only) were provided (e.g., mild, moderate, severe), participants in moderate or higher categories were coded as positive for a disorder unless otherwise specified in prior research. Estimates obtained from total but not subscale scores (e.g., PTSD hyperarousal) were included in analyses.

Study quality was assessed by the Systematic Assessment of Quality in Observation Research (SAQOR) tool [26] with several changes to increase the applicability of the system to our coding of prevalence (see Supplement B).

2.4. Computation of effect sizes and data analysis

Using the metafor [27] package in R, we conducted a series of mixed-effect multilevel meta-analyses/regressions. Our main analyses consisted of four meta-analyses/regressions, each of which included a random effect for studies and estimates within studies. First, we conducted a meta-analysis to obtain an overall summary prevalence estimate across disorders and populations. Second, we conducted a meta-regression including (dummy-coded) disorder as a fixed effect moderator to obtain summary prevalence of each disorder across populations. We conducted a third meta-regression including (dummy-coded) population to obtain overall mental disorder prevalence in each population. The fourth meta-regression, including dummy-coded disorder, population, and their product, provided summary estimates of individual disorders in individual populations. Studies that utilized the same samples were analyzed as a single study.

Models were implemented using restricted maximum-likelihood estimation. Study prevalence estimates (i.e., sample size with disorder divided by total sample size) and 95% confidence intervals (CI) were Freeman-Tukey double arcsine transformed [28] for improved statistical properties. Fixed effects and CI were back-transformed [29] to provide summary prevalence estimates. The I 2 statistic measured percentage of heterogeneity due to true between-study and between-estimate differences, and the interclass correlation coefficient (ICC), the association between underlying estimates. Profile plots indicated whether all variance components were statistically identifiable.

As part of sensitivity/quality analyses, we re-conducted our four main analyses using a cluster-robust estimator of standard errors (similar to the Eicker-Huber-White method) useful when multiple, dependent outcomes come from individual studies [30]. Additionally, in a series of meta-regressions, we examined whether the overall summary effect varied by: (1) pandemic, (2) location, (3) timing, (4) measure (self-report questionnaire versus clinician assessment; for a related example see [31]), (5) scoring (non-standard/unknown versus standard scoring of measure), and (6) study quality (very low, low, moderate). Analysis of publication bias was not conducted as most studies did not use inferential statistics to test hypotheses regarding prevalence, and thus, were not more likely to be published because of statistically significant results.

3. Results

From 68 publications (of which six studies/three-pairs utilized the same or partially overlapping samples) including 87,586 participants, 808 individual estimates were obtained. Summing I 2 values representing between- and within-study heterogeneity, approximately 99% of variance between- and within-studies was due to true variation rather than sampling error in main analyses. As expected, between-study heterogeneity was larger (Range I 2 = 72.7–73.6%) than within-study heterogeneity (Range I 2 = 25.0–26.2%). ICC ranged from 0.74 to 0.75, indicating a strong association between estimates within studies. Models with random effects fit significantly better than respective models without (all p < .001). Profile plots indicated that all variance components were statistically identifiable. Summary estimates for individual disorders/populations were based on varying numbers of studies, individual effects and participants (see Table 1 ). CI were large for summary estimates derived from few studies/estimates (e.g., quarantined), thus indicating greater imprecision.

Table 1.

Sample size and meta-analysis/regression results, including summary estimates/prevalence and 95% confidence intervals by disorder and population.

Population Disorder Study N IE N Sample N SE 95% CI LB 95% CI UB SPP SPP 95% CI LB SPP 95% CI UB
All All 65a 808 87,586 0.46 0.41 0.51 0.19 0.15 0.23
Psych. morbidity 20 232 10,818 0.60 0.55 0.65 0.31 0.26 0.36
Anxiety 29 168 33,263 0.37 0.32 0.41 0.12 0.09 0.15
Depression 31 162 24,794 0.44 0.39 0.49 0.17 0.14 0.21
PTSD 39 246 18,711 0.45 0.40 0.49 0.18 0.14 0.22
Community All 21 210 49,229 0.42 0.35 0.49 0.16 0.11 0.21
Psych. morbidity 4 35 4446 0.47 0.38 0.57 0.20 0.13 0.28
Anxiety 11 85 21,538 0.39 0.32 0.46 0.13 0.09 0.19
Depression 10 46 13,685 0.44 0.36 0.51 0.17 0.12 0.23
PTSD 11 44 9560 0.36 0.28 0.43 0.11 0.07 0.17
Infected/recovered All 25 352 30,191 0.57 0.48 0.66 0.29 0.21 0.38
Psych. morbidity 11 108 5664 0.84 0.74 0.95 0.56 0.46 0.66
Anxiety 8 40 8537 0.45 0.36 0.54 0.18 0.11 0.26
Depression 9 79 9399 0.56 0.47 0.65 0.27 0.19 0.36
PTSD 16 125 6591 0.55 0.46 0.64 0.26 0.19 0.35
Healthcare providers All 14 173 3375 0.46 0.39 0.52 0.19 0.14 0.24
Psych. morbidity 4 31 521 0.56 0.49 0.63 0.28 0.22 0.34
Anxiety 8 38 944 0.35 0.28 0.42 0.11 0.06 0.16
Depression 9 33 1000 0.42 0.36 0.49 0.16 0.11 0.21
PTSD 9 71 910 0.47 0.40 0.53 0.20 0.15 0.25
Quarantined All 6 73 4791 0.34 0.22 0.46 0.10 0.04 0.19
Psych. morbidity 1 58 187 0.56 0.24 0.88 0.28 0.05 0.60
Anxiety 3 5 2244 0.22 0.08 0.37 0.04 0.00 0.12
Depression 3 4 710 0.33 0.16 0.49 0.09 0.02 0.21
PTSD 3 6 1650 0.34 0.19 0.48 0.10 0.03 0.21
a

Independent studies reporting data from the same sample (N = 3 pairs) were coded as single studies that provided multiple effect sizes. IE = Individual estimate. SE = Summary estimate. CI = Confidence interval. LB = Lower bound. UB = Upper bound. SPP = Summary point prevalence (i.e., back-transformed Freeman-Tukey double arcsine transformed estimates; [29]).

The median summary point prevalence for mental disorders across disorders and populations was 19% (95%CI = 15–23%). Prevalence estimates of 20% or higher were found for 9 (36%) disorders/populations with a high of 56% for psychiatric morbidity among infected/recovered adults (see Table 1). Occurring in 31% (95%CI = 26–36%) of the overall sample, psychiatric morbidity had the highest prevalence across all populations (see Fig. 2 ). Across populations, PTSD had the second highest prevalence (18%, 95%CI = 14–22%), closely followed by depression (17%, 95%CI = 14–21%) and anxiety (12%, 95%CI = 9–15%).

Fig. 2.

Fig. 2

Summary point prevalence estimates and 95% confidence intervals grouped by disorder (Panel A) and population (Panel B).

Across disorders, the highest prevalence was found for infected/recovered adults (29%, 95%CI = 21–38%), followed by healthcare providers (19%, 95%CI = 14–24%), community adults (16%, 95%CI = 11–21%), and quarantined adults (10%, 95%CI = 4–19%). The highest prevalence of each disorder was found for infected/recovered adults (18–56%). Healthcare providers had high psychiatric morbidity prevalence (28%, 95%CI = 22–34%) and PTSD (20%, 95%CI = 15–25%) relative to other disorders. Adults in the community had high prevalence of psychiatric morbidity (20%, 95%CI = 13–28%) and depression (17%, 95%CI = 12–23%) relative to other disorders. Quarantined adults had much higher prevalence of psychiatric morbidity (28%, 95%CI = 5–60%) than other disorders, but summary estimates based on few studies/individual estimates were imprecisely estimated.

In sensitivity analyses, use of the robust estimator resulted in wider confidence intervals on average for summary estimates (Mean Difference = 0.02, Range = −0.64 to 0.19) and back-transformed point prevalence estimates (Mean Difference = 0.02, Range = −0.55 to 0.16). Most studies (a) focused on SARS, (b) were conducted in China and (separately) Hong Kong, included estimates (c) measured during the acute phase, and obtained (d) via questionnaire and (e) with standard scoring, and (f) were of low or very low quality (see Table 2 ). Overall prevalence estimates across disorders and populations were higher for studies/estimates: (1) focused on SARS or MERS versus COVID-19 (22/23% vs. 12%), (2) conducted in the United States, Hong Kong, Korea or Taiwan (23–40%) versus other locations (4–18%), (3) measured post-acute versus acute phase (20/21% versus 18%), obtained (4) via questionnaire versus clinician assessment (20% vs. 10%) and (5) with standard versus non-standard scoring (20% vs. 17%), and (6) of moderate or very low versus low quality (22/20% vs. 17%).

Table 2.

Sample size and sensitivity meta-analysis/regression results, including summary estimates/prevalence and 95% confidence intervals by pandemic, location, timing, measure, scoring and study quality.

Factor Categories Study N IE N Sample N SE 95% CI LB 95% CI UB SPP 95% CI LB 95% CI UB
Pandemic COVID-19 20 287 62,180 0.37 0.29 0.45 0.12 0.07 0.18
MERS 8 24 2695 0.49 0.36 0.62 0.22 0.11 0.33
SARS 37 497 22,711 0.50 0.45 0.56 0.23 0.18 0.28
Location Canada 5 31 3858 0.44 0.28 0.61 0.18 0.06 0.32
China 21 421 52,473 0.38 0.31 0.46 0.13 0.08 0.19
Hong Kong 14 138 6069 0.55 0.45 0.64 0.26 0.18 0.36
Korea 7 23 2521 0.52 0.38 0.66 0.24 0.13 0.38
Saudi Arabia 1 1 174 0.22 −0.19 0.63 0.04 0.00 0.34
Singapore 7 102 4229 0.45 0.32 0.59 0.18 0.09 0.30
Taiwan 7 74 5977 0.50 0.37 0.64 0.23 0.12 0.35
Italy 1 12 6873 0.53 0.18 0.88 0.25 0.02 0.59
United States 1 3 2694 0.69 0.32 1.05 0.40 0.09 0.76
Multi: Singapore & India 1 3 2718 0.24 −0.12 0.61 0.05 0.00 0.32
Timing Acute 41 436 73,237 0.45 0.39 0.50 0.18 0.14 0.22
Within 1-year post 16 171 6286 0.49 0.41 0.57 0.21 0.15 0.28
After 1-year post 12 201 8063 0.47 0.39 0.56 0.20 0.13 0.27
Measure Questionnaire 62 696 86,064 0.47 0.43 0.52 0.20 0.16 0.24
Clinician assessment 9 112 1522 0.35 0.28 0.41 0.10 0.07 0.15
Scoring Standard 55 668 63,186 0.47 0.42 0.51 0.20 0.16 0.24
Non-standard 22 140 24,400 0.43 0.38 0.48 0.17 0.13 0.21
Qualitya Very low 28 297 33,920 0.47 0.10 0.54 0.20 0.14 0.26
Low 34 427 49,113 0.44 0.38 0.50 0.17 0.13 0.23
Moderate 5 84 4553 0.50 0.34 0.66 0.22 0.10 0.38
a

Two studies with same or overlapping samples but different quality ratings were treated as separate studies. IE = Individual estimate. SE = Summary estimate. CI = Confidence interval. LB = Lower bound. UB = Upper bound. SPP = Summary point prevalence (i.e., back-transformed Freeman-Tukey double arcsine transformed estimates; [29]).

4. Discussion

Across 68 individual studies, about one-in-five adults in populations impacted by a coronavirus pandemic demonstrated or reported signs or symptoms indicative of a mental disorder diagnosis. Undifferentiated psychiatric morbidity was the most prevalent disorder in most of our study populations followed by PTSD and depression, then anxiety. Infected recovered adults were most at risk of a mental disorder, followed by healthcare providers and adults in the community, then quarantined adults. As we discuss below in relation to these populations, our summary estimates tended to be higher, often substantially than 12-month or shorter prevalence estimates from a meta-analysis and systematic review [17,32] and from epidemiological studies of the adult populations of China [18], Europe [19], and the United States [20,33]. Our results suggest that coronavirus pandemics are associated with an adverse mental health impact as manifested by elevated rates of multiple mental disorders in multiple populations. Our search strategy and analytical methods allowed us to utilize all relevant data from individual studies, while accounting for dependencies in those data. Furthermore, our focus on peer-reviewed studies utilizing standardized measures strengthens our confidence in the validity of our results. Despite these strengths, our results do not provide an indication of causal relations between coronavirus pandemics and mental disorders, as the majority of the observational studies included in our meta-analysis did not include adequate control/comparison groups, and we did not examine related differences.

Infected or recovered adults had the highest prevalence of all disorders and each individual disorder, with notably higher prevalence relative to unselected adults in prior studies [[18], [19], [20],33]. For example, 56% of infected/recovered adults were positive for undifferentiated psychiatric morbidity compared to the 9% [18] to 26% of adults [20] who were positive for ‘any disorder’ studies of unselected adults. Prevalence of PTSD (26%) was much higher than found among unselected adults in China (0.2% [18]), Europe (0.9% [19]), and the United States (3.5%; [20]), and comparable to lifetime prevalence of PTSD among combat veterans [34] and prevalence of PTSD among survivors of intensive care unit treatment [35]. The latter comparison is informative, as the high prevalence of PTSD among infected/recovered adults may be attributable in-part to their experiences of intensive care and associated treatment, such as mechanic ventilation [8]. Prevalence of depression (27%) was also much higher than the 3–10% prevalence of mood/depressive disorders or major depressive disorder found in studies of unselected adult populations [[17], [18], [19], [20],33]. Prevalence of anxiety was higher than prevalence found among unselected adults in several studies (e.g., [17]; also see [32]), but identical to unselected adults in the United States (18%; [20]). Our results suggest that severe infection is a potent risk factor for mental disorders, and as demonstrated by prior studies (e.g., [2]), may contribute to functional impairment and disability that continues to adversely impact the mental health of recovered patients. We hypothesize that even minor infections may be quite threatening and stressful in people with pre-existing physical or mental health conditions. Nuanced investigations of causal links between infection severity, symptom presentation and medical treatments, and mental disorders and facets of (dys)function post recovery will be useful for mental health intervention planning in relation to COVID-19 and future pandemics.

Healthcare providers had high prevalence of most disorders relative to unselected adult population samples [[17], [18], [19], [20],32,33]. Prevalence of undifferentiated psychiatric morbidity (28%) was somewhat higher than found in a study of emergency room physicians and trainees (26.8%; [36]). Prevalence of PTSD (20%) was higher than found in multiple studies of trauma-exposed physicians (see [37]) and lower than found in a study of critical care nurses (24–29%; [38]). Prevalence of depression (16%) was higher than found in some [39,40], but not other studies of healthcare providers [41], though Ford et al. [39] and Frank and Dingle [41] provided lifetime estimates, which tend to be higher than point- or 12-month prevalence. Notably high PTSD prevalence may reflect exposure to numerous potentially traumatic events (e.g., suffering and death of patients, morally ambiguous decisions and moral injury), whereas job stresses (e.g., long and inflexible hours, fluid work environments and job duties) may contribute to high prevalence of psychiatric morbidity and depression, along with burnout [36]. Considered together, the results above suggest that healthcare providers are at risk for mental disorders, and especially, traumatic-stress disorders during a coronavirus pandemic. Future observational research testing this hypothesis will benefit from case-control and cohort designs that more clearly establish causal links between particular stressors, threats and traumas experienced by healthcare providers, and development of various mental disorders.

Prevalence of depression (17%) and PTSD (11%) was notably elevated among adults in the community relative to those found among samples of unselected adult [[17], [18], [19], [20],32,33]. Prevalence of anxiety (13%) and undifferentiated psychiatric morbidity (20%) was higher than comparable rates found in some [[17], [18], [19]], but not other studies of unselected adult samples [20]. These results suggest coronavirus pandemics have a nuanced impact on adults in the community. The high prevalence of depression, in particular, might reflect the stress of living and coping with the threat of infection, societal dysfunction, and/or limited availability of routines and resources. Thus, countries that continue to be impacted by COVID-19 may experience increased incidence of depression in the general population over time. Longitudinal studies including adequate control/comparison groups will be useful in testing this and related hypotheses.

Quarantined adults had rates of undifferentiated psychiatric morbidity (28%), anxiety (4%) and depression (9%) that were higher than some studies of unselected adults [18,33], and lower than others [20]. Prevalence of PTSD (10%), on the other hand, was higher than found in multiple studies of unselected adults [[18], [19], [20]]. Yet, these findings must be interpreted more cautiously than findings for other populations given the small number of studies/estimates from which summary estimates were derived. As a front-line defense against coronavirus pandemics with substantial benefits as well as costs, quarantine draws advocates and critics in equal measure. Additional research is needed, especially to investigate for whom and under what conditions quarantine is associated with mental disorders. There a likely multiple mediators and moderators of links between quarantine and mental disorders, including degree of restriction/isolation (e.g., shelter-in-place, isolation on an intensive care unit), demographic factors (age, sex, relationship status, parental status), and supports that mitigate the impact of quarantine (e.g., food delivery to people with limited mobility). Future research that provides rigorous and actionable data can facilitate effective responding by communities and countries.

Several issues should be considered when interpreting the results of this meta-analysis. First, as indicated by large CI, some studies produced imprecise summary prevalence estimates, likely due to small sample sizes. Second, most studies were of low or very low quality. Summary estimates varied somewhat by study quality, though summary estimates were identical for moderate and very low quality studies. Third, the true prevalence of diagnosable mental disorders in populations impacted by coronavirus epidemics is likely to be lower than the magnitude of summary estimates, derived mostly from studies using self-report questionnaires that do not precisely assess mental disorder diagnostic criteria. Only a subset of included studies utilized gold-standard clinical interviews (e.g., Structured Clinical Interview for DSM) and assessment instruments specifically designed to screen for mental disorders (e.g., [42]). Indeed, sensitivity analyses revealed higher overall summary prevalence obtained from questionnaires versus clinician assessment. Somewhat mitigating this concern: (a) almost all studies utilizing questionnaires implemented empirically validated cutoffs to identify participants with mental disorders (e.g., [43]); and (b) studies that did not implement standard questionnaire cutoffs (and those that utilized unknown scoring algorithms to identify mental disorders) yielded similar overall summary prevalence estimates as those that did.

As applied to understanding and planning for COVID-19 [23], summary estimates must be interpreted cautiously. Overall prevalence of all disorders across all populations was lower for COVID-19 versus MERS and SARS. SARS and MERS have higher mortality rates and higher average severity than does COVID-19. The greater threat to health and mortality of SARS and MERS, and the challenges of long-term recovery from severe infection may have potentially increased risk for mental disorders among those infected with and recovered from these viruses, healthcare workers treating infected patients, and the general public who worried about severe infection, disability and death. Also potentially accounting for differences, all COVID-19 studies focused on mental disorder prevalence during the acute phase of the pandemic, whereas MERS and SARS studies included acute and longer time-frames, thus capturing mental dysfunction across a longer period of time. Yet, the overall mental disorder prevalence varied little between acute and longer time-frames. In relation to COVID-19, it will be important to investigate whether mental disorder prevalence is elevated in countries with prolonged periods of infection and economic hardship (e.g., United States, Brazil). Further suggesting the need for such investigations, our sensitivity analyses demonstrated differences in prevalence by country, with the United States, Hong Kong, Korea and Taiwan having notably higher prevalence than Canada, Singapore, Taiwan, China and Saudi Arabia. Caution is advised when comparing prevalence rates by country, as estimates were derived from a varying number of studies for each country, and a single study provided estimates for some countries (e.g., United States). Regardless, we hypothesize that countries and areas within countries that experience prolonged infection, quarantine and economic hardship will experience increased rates of the disorders examined in this study, in addition to disorders of despair (e.g., alcohol dependence; [44]) and related to disease threat (e.g., illness anxiety disorder, somatic symptom disorder). Furthermore, the raw number of mental disorders attributable to COVID-19 will be substantial and magnitudes higher than attributable to MERS and SARS due to the vast scope and ongoing nature of the pandemic.

Preliminary evidence suggests that COVID-19 exacerbates existing inequalities that harm racial/ethnic minorities, economically disadvantaged people, people with ‘essential’ job types, etc. [45,46]. Additional research is needed to quantify the mental health impact of COVID-19 in these subpopulations, and to document disparities in assessment and treatment of COVID-19-related mental disorders. Future research that examines the potentially manifold pathways to individual outcomes among subpopulations most at-risk will be instrumental in intervening in a cost-effective, effective and equitable manner. Future research that utilizes rigorous and validated subject recruitment and mental disorder assessment methods can improve upon the low quality of the majority of studies included in our study. Additional limitations can be addressed through assessment of pre-existing mental disorders among study samples, rigorous assessment of time-periods at risk, and/or inclusion of control conditions (e.g., people exposed to but not infected by COVID-19 as a comparator for infected/recovered people). Studies that do so will more directly measure the impact of COVID-19-related threats, stressors and traumas on mental disorder prevalence, incidence, and rate ratios, which will be essential to intervention planning and implementation.

Comparison of our synthesized prevalence rates across populations and disorder demonstrate the nuanced mental health impact of coronavirus pandemics. These data may prove a useful guide for future research and data collection that results in actionable information that can inform mental health treatment and resource allocation and policy. In addition to examining specific disorders in targeted and vulnerable populations, this research should examine between-country, and even, between-community and neighborhood variation that results from the confluence of specific threats, stressors and traumas prevalent in a given area.

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Acknowledgements

Dr. Boden consulted for Beneath the Surface Foundation. We thank Susanna Martins, Suzanne Tamang and Esther Meerwijk for providing guidance and feedback. The views expressed here do not necessarily represent those of the Department of Veterans Affairs or any other U.S. government agency or entity.

Footnotes

Study included in meta-analysis.

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.genhosppsych.2021.03.006.

Supplementary data

Supplementary material

mmc1.docx (28.2KB, docx)

Data availability

Data will be made available on request.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary material

mmc1.docx (28.2KB, docx)

Data Availability Statement

Data will be made available on request.


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