Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 + 6712 word(s) 6712 2022-03-16 04:36:10 |
2 formating Meta information modification 6712 2022-03-22 07:30:09 |

Video Upload Options

Do you have a full video?

Confirm

Are you sure to Delete?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Corey, J. Persons Experiencing Homelessness during COVID-19. Encyclopedia. Available online: https://encyclopedia.pub/entry/20803 (accessed on 07 July 2024).
Corey J. Persons Experiencing Homelessness during COVID-19. Encyclopedia. Available at: https://encyclopedia.pub/entry/20803. Accessed July 07, 2024.
Corey, Julia. "Persons Experiencing Homelessness during COVID-19" Encyclopedia, https://encyclopedia.pub/entry/20803 (accessed July 07, 2024).
Corey, J. (2022, March 21). Persons Experiencing Homelessness during COVID-19. In Encyclopedia. https://encyclopedia.pub/entry/20803
Corey, Julia. "Persons Experiencing Homelessness during COVID-19." Encyclopedia. Web. 21 March, 2022.
Persons Experiencing Homelessness during COVID-19
Edit

Persons experiencing homelessness are at heightened risk for infection, morbidity, and mortality from COVID-19. However, health consequences of the pandemic extend far beyond those directly caused by the virus, including fear of infection, access to housing, hygiene, PPE, food, as well as mental health, substance use, other health-related outcomes and treatment services.

homelessness health COVID-19

1. Introduction

Since the emergence of SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), more than 350 million people worldwide have experienced a confirmed infection, and more than 5.6 million have died [1]. Despite widespread reductions in risk of COVID-19 transmission and severe disease as a consequence of vaccine rollouts [2], the virus continues to pose a serious threat to human health, particularly for vulnerable populations [3][4]. Persons experiencing homelessness (PEH) appear to be at higher risk for infection, morbidity, and mortality due to COVID-19 than the general population [5][6][7][8][9]. Several factors may contribute to this increased risk, including lack of safe housing, inadequate access to healthcare, difficulties following public health guidelines, closure of regularly attended support services, and heightened risk for comorbidities including chronic diseases, mental health issues, and addiction [6][10].
While PEH have been disproportionately affected by the pandemic [5][8], the health consequences reach far beyond those of just infection and illness from COVID-19. For example, the large-scale closure of public buildings and facilities reduced access to toilets and basic hygiene and sanitation for those who were unsheltered [11][12]. Less financial support from the general public due to stay-at-home advisories and closure or reorganisation of food and social support services also contributed to difficulties accessing food assistance and hygiene products [12][13]. Restrictions on international travel and freedom of movement interrupted alcohol and drug supply chains, increasing costs [14] and reducing access, leading some persons who use drugs to shift from using their preferred substance to potentially more dangerous substances [15]. In some cases, harm reduction, treatment, and support services for PEH were closed, limited, or inaccessible due to commute barriers [16][17][18][19]. These new challenges have exacerbated existing mental health issues; studies have reported increased rates of self-harm, depression, and anxiety among PEH [20][21], as well as increased difficulties in accessing mental health services [13].
Despite the negative impact the pandemic has had on PEH, unprecedented changes in policies and services brought about to reduce the spread of COVID-19 have also improved the health and well-being of PEH in some communities. Positive changes have included the rapid rehousing and shielding of PEH [22][23], expansion of harm reduction and treatment services [22][24][25], and cross-sector collaboration of services that increased access to mental health services [26].

2. SARS-CoV-2 Infection and Morbidity

A number of included studies reported infection attack rates of SARS-CoV-2 among study participants: 29 studies measured positivity rates (i.e., current infection) [13][27][28][29][30][31][32][33], seven measured seroprevalence (i.e., prevalence of antibodies for SARS-CoV-2, indicating historic infection) [34][35][36][37][38][39][40], and four measured both positivity and seroprevalence rates [41][42][43][44]. Additionally, data regarding SARS-CoV-2 symptoms reported by study participants were provided by 32 articles [7][8][27][28][29][30][32]. Positivity rates among PEH ranged from 0 to 66%, while seropositivity among PEH ranged from 0 to 94%. Among studies that measured positivity rates, 13 included testing of participants in response to an outbreak [28][30][32][33][45][46]. In addition, surveillance testing (i.e., testing not prompted by a confirmed or suspected outbreak) was conducted for all participants regardless of symptoms in 16 studies [27][29][30][32][45][47]]. Of these, six reported that routine surveillance testing occurred regularly [29][47][48][49][50]. Eight studies described close-contact- or symptom-based testing strategies [30][48][51], and one study did not specify reasons participants were tested [52]. Two studies reported positivity rates using retrospective [53] or prospective (person-level data from COVID-19 surveillance and reporting systems) [31] data from cohorts of the populations that were tested for SARS-CoV-2. One study by Jatt et al. [30] described how testing progressed from only symptomatic individuals and close contacts to outbreak testing and finally to routine surveillance testing from 11 March to 29 April 2020 in a large healthcare facility in Los Angeles. Of the 33 studies that measured infection rates, polymerase chain reaction (PCR) tests were the most commonly reported tests used for diagnosis (n = 24) [28][30][45][43][44][54]. Other measures included self-reported positive test results (n = 3) [13][55][43], antigen testing (n = 1) [29], and assays (n = 1) [27]. Five studies did not specify tests used for SARS-CoV-2 diagnosis [31][32][33][56][53].
Multiple unique risk factors for SARS-CoV-2 positivity were identified among PEH. Three studies reported that PEH were at increased risk for infection compared to the general population [31][35][57], though one study found that among people living with HIV, experiencing homelessness was not associated with seropositivity [37]. Among haemodialysis patients, Rincón et al. [58] found that living in a nursing home or experiencing homelessness was an independent risk factor for testing positive for SARS-CoV-2. Three studies reported risk of COVID-19 based on specific shelters of residence [46][59][41]. While no statistical significance was reported, Rogers et al. [48] noted that most positive cases (79%) were detected among shelters housing older male residents and with shared day services, showering facilities, and rotating staff. Similarly, Ghinai et al. [60] reported that increased numbers of private bathrooms were associated with lower prevalence rates. Living in a congregate or crowded setting [34] and shared sleeping arrangements [60] were also identified as risk factors. In addition, a study by Roland et al. [42] reported that persons who shared a room with someone who tested positive, or did not know, were significantly more likely to test positive. Rogers et al. [48] reported that 86% of positive cases in their study of homeless shelters in King County, Washington slept in a communal space in the past week, compared with 78% of residents with negative tests; however, no statistical significance was provided. Three articles noted that the shelters in their studies with the largest outbreaks had more transient resident populations [27][29][61]. Similarly, Ghinai et al. [60] reported an association between the proportion of residents leaving and returning each day and increased prevalence rates. A study of congregate shelters in Rhode Island found that 70% of participants with negative tests had spent more than two weeks at their shelter, compared with 43% of participants with positive tests [61]. The same study reported that three shelters that had stopped accepting new residents at least two weeks prior had zero cases at the time of testing [61].
Additional risk factors were identified by several studies. Two studies found the presence of symptoms to be associated with testing positive for SARS-CoV-2 [59][34], while four studies found no statistical significance between symptoms of persons testing positive and negative [27][32][61][42]. Two studies reported a relationship between older age and increased likelihood of testing positive among PEH [32][60], though this relationship was not statistically significant in the study by Kiran et al. [32], and after adjusting for individual level factors and clustering at shelters, positivity rates no longer differed significantly by age in the study by Ghinai et al. [60]. Another study by Ly et al. [59] reported that younger PEH (18–34 years old) had more than three times higher odds of testing positive. Karb et al. [61] reported no statistical differences in age between people testing positive and negative. One study reported that 84% of PEH testing positive for SARS-CoV-2 were male, though men accounted for 72% of participants [62], and three found no significant difference in gender between people testing positive or negative [61][60][42]. Prevalence of the virus was higher among non-Hispanic white PEH than among non-Hispanic Black PEH in a study by Ghinai et al. [60], though after adjusting for individual-level factors, the positivity rates no longer differed. Karb et al. [61] also reported no differences in race between persons testing positive or negative. PEH in Belgium with an Urgent Medical card had significantly higher proportions of SARS-CoV-2 infections than those without access to the health system (7% vs. 3%, respectively) [42], and shelter residents in Toronto who tested positive were significantly less likely to have a provincial health insurance card than those who tested negative (54% vs. 72%, respectively) [32]. In France, Rahi et al. [63] found that PEH were more likely to be infected during lockdown (17 March–11 May 2020) than before (5% vs. 1%, respectively). One study reported significantly lower seroprevalence among shelter residents consuming tobacco (3%) compared to those who did not (8%) [34], and another study similarly found that current smoking among shelter residents was associated with lower prevalence of infection, compared with never smoking [60]. PEH who tested positive in a study by Karb et al. [61] had significantly lower prevalence of comorbidities than those testing negative (20% vs. 40%, respectively). Seroprevalence was also reported to be lower among PEH with psychiatric and/or addiction comorbidities than among those without (3% vs. 6%, respectively) in a study by Loubiere et al. [34]. Prior chronic respiratory disease [42] and self-reported medical history [60] were not significantly associated with positivity status in two other studies [60][42].

3. COVID-19-Related Hospitalisation

Nine studies provided information regarding COVID-19 related hospitalisations among PEH [8][28][60][51][56][41][64][65][66], among which six provided hospitalisation rates [28][60][51][56][41][64]. A study by Imbert et al. [64] reported that 8% of shelter residents who tested positive between 5 April and 15 April 2020 required hospitalisation, and a study by Tobolowsky et al. [56] reported that 20% of residents that tested positive between 30 March and 1 April 2020 were hospitalised. Among symptomatic persons with COVID-19, significantly more PEH were hospitalised than those in the general population (29% vs. 11%, respectively) in a study by Fields et al. [51]. Another article reported that among the 13% of shelter residents that were hospitalised due to COVID-19 (testing positive between 1 April and 1 May 2020), 33% required intensive care unit (ICU) admission [60]. In Paris, 24% of residents across three homeless shelters that tested positive were hospitalised, of which 12% were transferred to an ICU [41]. Data from one shelter in the same study indicated that patients over 65 years old, those with heart conditions, those with chronic kidney disease, and those with more than two risk factors were hospitalised more often [41]. In a Toronto refugee shelter, 4% of residents that tested positive for SARS-CoV-2 were admitted to the hospital for isolation requirements rather than clinical severity; there were no reported cases of ICU admission at the time of the study (20–21 April 2020) [28]. A U.S. study by Cha et al. [66] reported that among patients experiencing homelessness hospitalised with COVID-19, 54% were hospitalised for >4 days, 17% were admitted to the ICU, and 11% had mechanical ventilation, most commonly patients > 65 years (20%) and those with no underlying health conditions (21%). Schrooyen et al. [8] reported that incidences of hospitalisation for COVID-19 were three times higher among PEH (650 per 100,000) compared to the general population (194 per 100,000). Among all adult patients with COVID-19 treated from 1 March to 18 May 2020 at the Boston Medical Centre (BMC), PEH accounted for 16% of all patients, 24% of non-ICU inpatients, 16% of ICU admissions without mechanical ventilation, and 15% of ICU admissions with mechanical ventilation [67]. Hospitalisations among COVID-19 positive PEH in the BMC system were reduced by 28% following the opening of the COVID-19 Recuperation Unit, located adjacent to the BMC, which provided space for PEH to isolate, quarantine, and receive treatment for substance use [65].

4. COVID-19-Related Mortality

Mortality from COVID-19 among PEH was evaluated in 12 studies [5][8][31][67][68]. Data regarding case fatality rates (CFRs) were available from eight studies [5][31][60][69][41][70][64][66], with six studies reporting at least one death [5][31][60][51][69][41][64][66]. A study from France by Husain et al. [41] reported the highest CFR (6%) among the included studies, using data from PEH in shelters who received positive PCR tests for SARS-CoV-2 between 1 March 2020 and 31 May 2020. Leifheit et al. [5] found that, when compared to the wider population, CFRs in Los Angeles were significantly increased for PEH under the age of 65, and that the opposite was true for those ages 65 and over. A study by Hsu et al. [67] reported that among adult patients with confirmed COVID-19 that were treated at BMC, 15% of those who died were PEH. Additionally, 15% of deaths among PEH in Wales between February and July 2020 were registered as COVID-19 involved, compared with 14% among the general population [68], though no statistical significance was provided. One study reported no significant association between housing problems and mortality from COVID-19 [8].

5. Fear of COVID-19

Fear or perceived threat of COVID-19 among PEH was discussed by ten studies [12][13][71][72]. Fear varied across studies; in Los Angeles, 65% of tenants of permanent supportive housing surveyed by Henwood et al. [73] in March 2020 regarded COVID-19 as a serious risk to their health, while 33% of those surveyed in Los Angeles by Kuhn et al. [74] from December 2020 to February 2021 perceived it as a high threat. A third study in Los Angeles carried out from April to June 2020 reported that 53% of young PEH (18–25 years old) were not at all worried about COVID-19, and 15% were very or extremely worried [71]. One study by Rodriguez et al. [12] reported that PEH in Tippecanoe County, Indiana had an overall low risk perception of COVID-19, while researchers of a study in France found that PEH felt that the virus was indeed a threat but was not a major concern compared to the other risks they regularly faced [13]. Using data from Hamburg, Hajek et al. [72] found that increased fear of COVID-19 among PEH was associated with younger age, absence of chronic alcohol consumption, increased perceived own risk of contracting the virus one day, and a higher agreement that a diagnosis of COVID-19 would ruin their life. Similarly, Henwood et al. [73] reported that having a pre-existing health condition was associated with increased odds of perceiving COVID-19 as a serious health risk among PEH. They also noted that men in their study had significantly lower odds of perceiving the virus as a serious health risk than women [73].
PEH’s perceived threat of COVID-19 impacted some aspects of their health and behaviour. In one study, increased loneliness was associated with a high self-perceived risk of contracting COVID-19 [75]. Kuhn et al. [74] reported PEH in their study who perceived the virus as a high threat were significantly less likely to be vaccine hesitant. Perceiving COVID-19 as a serious threat was also associated with increased odds of handwashing and social distancing among PEH in a study by Henwood et al. [73]. Finnigan [76] found that 27% of PEH surveyed in Sacramento, California, reported avoiding shelters due to fear of the virus. One study in Hamburg reported increased physician visits or likelihood of hospitalisation was not associated with fear of COVID-19 among PEH [77].

6. COVID-19 Vaccine Acceptance

Five studies measured attitudes toward COVID-19 vaccination. Three studies took place during December 2020 or later, when vaccines first became available in the U.S. and Italy [55][74][78], while two were conducted earlier in 2020, before vaccines received any emergency use authorisation [79][80]. Four studies examined attitudes exclusively among PEH [55][79][74][80]; vaccine hesitancy was reported as 41% [79] and 48% [74] in two studies, while vaccine acceptance was found to be 56% [80] and 64% [55] in another two studies. Fear of side effects (37%), wanting more information (30%), or rejecting all vaccines (37%) were cited as reasons for vaccine hesitancy among PEH in a study by Kuhn et al. [74]. Moore et al. [78] reported that housing insecurity was associated with more than sevenfold increased odds of vaccine resistance among American Americans living in the southern U.S.
Several factors that may contribute to vaccine hesitancy among PEH were identified. In France, Longchamps et al. [79] found increased odds of vaccine hesitancy among females (vs. males) and those living with a partner (vs. living alone) and decreased odds of vaccine hesitancy among those with no legal residence (vs. French/legal residence) and those with higher health literacy (vs. low). Similarly, Iacoella et al. [55] found that vaccine acceptance was higher among male PEH in Rome than females (74% vs. 59%, respectively). Kuhn et al. [74] reported that those trusting official sources were significantly less likely to be hesitant, and those engaging in highly protective behaviour were significantly more likely. A study in Los Angeles reported no significant differences regarding vaccine attitudes or uptake based on race/ethnicity, gender identity, sexual orientation, or testing history among young PEH (18–26 years old) [80]. Nearly 80% of participants in the same study felt that having access to primary prevention services and personal protective equipment (PPE) were important to promoting uptake, and 70% expressed that access to COVID-19 treatments, text-based prevention information and support, and the ability to get vaccinated in non-traditional medical settings were crucial for them to be vaccinated [80].

7. Housing

Many included studies reported substantial impacts of the pandemic on housing for PEH. Three studies indicated that the pandemic may have led to an increase in persons experiencing homelessness [21][76][81]. Between February and May 2020, Irwin et al. [21] reported a 91% increase in persons experiencing unsheltered homelessness in Arlington County, Virginia and noted an 88% increase in Black individuals and 48% increase in white individuals. Several studies also noted that the pandemic led some people to experience homelessness or be recognised by homeless support services for the first time [13][23][82]. Barbu et al. [83] reported that some persons newly experiencing homelessness during the pandemic had difficulties accessing emergency accommodation.
Several studies described how the pandemic exacerbated insecure living conditions for PEH. Four studies reported shelters restricting new admissions [12][61][84][85], and three reported shelters closing during the pandemic [48][64][83]. One study reported that authorities in France dismantled a squat [33], and in Salamanca, Spain, PEH were not allowed to live on the street during the initial lockdown period [26]. Additionally, Allaria et al. [13] reported 42% of PEH in their study changed accommodation since the onset of the pandemic. Court proceedings delayed due to the pandemic slowed intake of some PEH, particularly those leaving incarceration, into shelters, according to a study by Pixley et al. [86]. A study in Los Angeles by Tucker et al. [71] reported that 29% of young PEH (18–25 years old) indicated that the pandemic made finding a safe place to spend the night more difficult, and 42% indicated that it was now harder to find or keep stable housing. Some shelter residents in a study by Parkes et al. [23] also felt that support within accommodations was reduced during the pandemic.
Despite the negative impact of the pandemic on housing insecurity, many studies described instances in which housing supports were provided or improved for PEH. Ten articles noted that shelter services were expanded, or new temporary shelters were established, as part of the pandemic response [26][30][60][87], and 21 reported that PEH were temporarily housed in repurposed hotels [7][12][23][32][88][89]. Two studies mentioned participants staying in hotels but did not indicate whether their stay was related to temporary pandemic housing programmes [74][90]. Two studies reported that those leaving non-congregate hotel accommodation were given support in finding permanent housing [50][91]; 83% of participants in the study by Aitken [91] found suitable alternative accommodation. An additional four studies reported those leaving medical care sites were supported with a discharge plan for housing [70][91][92][93]. However, a report by Barbu et al. [83] noted that when some temporary accommodation supports eventually closed, some PEH to returned to rough sleeping. In Ireland, some PEH in temporary emergency accommodations expressed concern over uncertainties of future accommodations [87]. Three studies indicated changes made to reduce crowding provided increased privacy in shelters [48][85] or non-congregate settings [86]. Leonardi and Stefani [85] also noted that shelters in Turin, Italy began operating 24 hours a day, which fostered a sense of community among residents. Two studies reported shelters using incentives such as free meals, cigarettes, TV, and religious or spiritual events to keep clients indoors during the pandemic and reduce exposure to SARS-CoV-2 [40][44]. Both reported no positive cases among residents [40][44].
Isolation or quarantine accommodation for PEH who were symptomatic, confirmed cases was noted in 44 articles. Of these, the majority reported that access to temporary facilities to safely isolate or quarantine was provided, with 15 specifically describing hotels converted for the purpose. Fuchs et al. [69] found that premature discontinuation of hotel isolation or quarantine was associated with experiencing unsheltered homelessness and requiring quarantine as a close contact. Wang et al. [93] described the implementation of a trauma-informed care site in Chicago, with high satisfaction reported among patients. Three studies mentioned isolation of individuals who were symptomatic or positive but did not provide further details as to where isolation occurred [60][41][94]. Six studies mentioned that PEH were unable to safely isolate or quarantine [25][33],[85], three of which described a lack of safe isolation services in March and April 2020 [25][42][85]. Two studies noted that PEH were unable to quarantine or isolate in place if needed because of a lack of necessities such as food [73][82], hygiene, or medication [73].

8. Access to Personal Hygiene and PPE

Multiple studies discussed personal hygiene. Unmet need for showers [12][33], bathrooms [86], and other hygiene products or services [48][86] for PEH during the pandemic were reported by several studies. In a study by Riley et al., [95] 66% of women experiencing homelessness or unstable housing reported one or more subsistence needs, defined as insufficient access to food, clothing, housing, or hygiene resources. In some cases, barriers to hygiene were exacerbated by the pandemic; reduced access to showers [71][83][96], toilets [83], laundry [71][83], and other personal hygiene products and services [13] were discussed by several studies, with some noting that barriers were due, at least in part, to public closures [12][83][86][96]. However, some studies indicated that PEH had access to showers [33][45],[97], toilets [33][97], or laundry [83][97]. Access to general hygiene products or services was also noted in five studies [60][87], all of which were provided by organisations or shelters. In a few studies, access to showers [33][56] and hygiene products [11] was reported as improving for some PEH during the pandemic.
Other personal hygiene concerns brought up by studies included cleaning supplies and sharing of substances. One study reported that PEH had access to cleaning supplies [52], three reported unmet need [13][45][83], and one indicated decreased access as a result of the pandemic [11]. Sharing of substances among PEH as an infection risk was brought up by three studies [12][71][94]. One study noted that cigarettes were commonly shared among PEH [12], and one found that many PEH avoided sharing cigarettes or drugs because of the pandemic [71]. In addition, Steer et al. [94] reported positive outcomes of a disposable cup intervention to reduce drink sharing among PEH, particularly among those using alcohol.
Hand hygiene among PEH was discussed by numerous studies. Many noted that PEH were able to wash their hands [11][13][47][97], access soap [11][98][59][71], or access hand sanitiser [11][33][45]. Use [97] or provision [39] of gloves to PEH was also mentioned by two studies. However, unmet needs for handwashing facilities [11][12][71], soap [11][71], and hand sanitiser [11][45][56][71][83] were also reported. Montgomery et al. [11] reported that public closures and price surges of hand hygiene supplies triggered by the pandemic reduced access to soap, hand sanitiser, and handwashing facilities for PEH in Atlanta, Georgia, though supplies and handwashing stations were later provided. The same study found that unsheltered PEH were more likely to rely on hand sanitiser, bottled water, and disinfecting wipes for hand hygiene, and some PEH in shelters expressed concerns about crowding and long lines to wash hands [11]. Henwood et al. [73] reported that among PEH living in Skid Row, those living in single room occupancies with shared bathrooms and those with mental health conditions were nearly half as likely to report hand washing compared to those in studios.
Personal protective equipment (PPE) was discussed in several studies. PEH were reported as having access to facemasks or face coverings in 21 studies, among which nine reported that these were required to be worn in shelters [12][27][47][97] or quarantine and isolation sites [99]. Three studies noted that PPE generally was available to PEH [25][50][97]. PPE [26] and masks [76] were also reported as being worn during interviews for two studies. Additional studies noted that facemasks were enforced during health check-ups [20] or in public [98], and encouraged while awaiting test results and in general patient areas of a health facility [100]. Rodriguez et al. [12] described difficulties enforcing masks among PEH in shelters, with some giving up and only requiring them to be worn by staff. Unmet need for facemasks/face coverings [45][56][71][83] or PPE [23][42][86] for PEH was discussed in seven studies.
Physical distancing was also noted in several included articles. PEH were reportedly able to follow social distancing guidelines in 14 studies [13][27][33][45][47][98][48][61][59][49][99][71][82][101][97], among which seven reported that distancing was enforced in shelters [45][47][48][49][101][97] or quarantine and isolation sites [99]. Eight studies reported that some PEH were unable to follow social distancing guidelines [12][25][27][33][61][71][83][88], sometimes even despite markers indicating recommended spacing [25][88]. Reluctance to follow and ambivalence regarding the importance of social distancing among PEH was noted in four studies [12][23][25][82]. Physical distancing was enforced among some PEH accessing homeless support services in the U.S. [86], during health check-ups in Salamanca [20], and during interviews for a study in Spain [26] and encouraged among patients accessing a psychiatric emergency room in Los Angeles [100] and shelter residents in Washington State [56]. One study in Ireland reported accommodation services were expanded to support social distancing [87]. Henwood et al. [73] reported that among PEH living in Skid Row, those living in single room occupancies and those with mental health conditions were nearly half as likely to report consistent social distancing than those in studios. In a study by Kuhn et al. [74], 42% of PEH reported high COVID-19 protective behaviour, measured by frequency of wearing a mask, washing hands, distancing from others, and avoiding touching their face.

9. Access to Food

There were mixed impacts of the COVID-19 pandemic on access to food for PEH. Three studies reported unmet need for food during the pandemic [73][86][95]. Riley et al. [95] measured subsistence needs, defined as insufficient access to food, clothing, housing, or hygiene resources, and found that 66% of women experiencing homelessness in the study had at least one unmet subsistence need. Additionally, when asked if they would be able to shelter in place for 14 days if needed, 45% of PEH in a study in Los Angeles responded no, with 91% citing lack of food as a reason [73]. Three studies reported finances as a barrier to PEH accessing food [71][82][83]. In addition, five studies reported that food services for PEH were reduced or halted because of COVID-19 [12][25][86][102][96]; three reported that these were closed or limited because of risk of virus transmission among PEH accessing services [12][25][102], and two did not provide specific reasons for closure [86][96]. Several studies noted that COVID-19 reduced access to food for PEH [12][13][71][83][103]. In a study by Tucker et al. [71], 54% of PEH indicated that the pandemic made it harder to get enough food to eat. In a large city in France, when compared with PEH in shelters, persons sleeping rough were significantly more likely to have difficulty accessing food (24% vs. 60%, respectively) and water (5% vs. 39%, respectively) as a result of the pandemic [13]. The same study noted that access to food assistance was especially reduced for those more recently homeless compared with those living rough or in slums longer, who had established networks [13]. In Scotland, restrictions on movements limited options for some PEH, who were no longer able to travel to places with cheaper food [103]. Transportation barriers were also noted in a study by Gaeta et al. [99].
Some articles did report examples of food needs being met, or even improving, as a consequence of the pandemic. Two studies reported outreach services were able to meet food needs for PEH [52][96], and one study noted that several participants felt they had easier and more regular access to food due to the support received during the pandemic [91]. It was also frequently noted that meals were provided to individuals as patients [47][50][70][99][87] or residents of temporary accommodation [25][26][27][61][69][50][40][44][83][85][101][91][97][87][102][103]. However, a report from Scotland explained that while asylum seekers were rehoused into hotels and provided meals, the food was often poor in nutrition or culturally inappropriate, leading to malnourishment and mental health issues [103]. In Ireland, PEH in temporary emergency accommodation felt that lack of cooking facilities was a barrier to eating proper meals, and several suggested improved quality and frequency of meals [87].

10. Substance Use

Active substance use among PEH during the pandemic was noted in 36 studies [8][11][12][13][20][23][25][26][32][59][100][34][35][41][70][66][68][77][75][71][72][81][83][85][91][87][102][88][89][93][104][94][105][106][107]. Substances used included alcohol [8][13][23][25][26][59][34][35][41][70][77][75][71][72][83][91][87][102][104][94][107], tobacco [8][12][13][32][34][35][41][71][104], cannabis [23][26][100][35][71][104], cocaine [26][100][35][70][105], methamphetamines [70][89][106], heroin [35][91][105], stimulants [104][94][105], unprescribed benzodiazepines [23][70][105], fentanyl [89][105], amphetamines [100], and gamma-hydroxybutyrate [104]. An additional four studies noted general opioid use [26][70][104][105], and 17 reported current substance use without further specification [11][12][13][20][25][32][59][34][41][66][81][85][87][102][88][93][94][106]. Increased use of substances was reported in four studies [20][23][71][89]. Increased use of marijuana (28%), tobacco (20%), and alcohol (20%) during the pandemic was reported by some young PEH (18–25 years old) in Los Angeles [71]. In Scotland, the emotional impact of lockdown, isolation, and reduced support services contributed to increased drug use among some PEH [23]. Similarly, individuals in a study by Scallan et al. [89] reported increasing substance use following loss of housing supports. Aguilar et al. [20] reported an increase in relapses among PEH during the first ten weeks of confinement in Spain, though the finding was reported in the discussion only, and supporting data was not available. One study reported reduced drug use among some PEH was facilitated by increased privacy and sense of safety they experienced since shielding or self-isolating in emergency accommodations [87].
Many included studies discussed access to substance use treatment for PEH during the pandemic. Treatment was reported as available in 22 studies, and access or uptake was noted as improving in 12 studies [23][25][26][105]. Tucker et al. [71] reported that 13% of young PEH (18–25 years old) in their study found substance use services easier to access since the onset of the pandemic. Nine studies noted that access to treatment improved within the context of accommodation services [23][26][50][70][104], five of which specifically noted that PEH initiated treatment for the first time within the service [23][70][91][87][104]. Participants in a study by Pixley et al. [86] reported that PEH were more open and accepting to substance use treatment following the rollout of alternative services and improved housing standards in noncongregate sheltering. Both Fitzpatrick et al. [102] and Parkes et al. [23] reported that reduced financial support from the public led PEH to seek prescription medication rather than illicit substances. The use of telehealth to support treatment was noted in seven studies [20][25][38][105]. Preventative measures implemented for fatal overdoses among PEH were reported in two studies, with both reporting no fatal overdoses at the time of the studies [70][104].
Five studies discussed reduced access to substance use treatment services during the pandemic [12][23][25][87], three of which specifically noted that services for alcohol use disorders were limited [23][25][87]. Tucker et al. [71] reported that 32% of participants in their study reported that accessing substance treatment services was harder since the onset of the pandemic. Service providers interviewed by Rodriguez et al. [12] also expressed concerns regarding PEHs’ access to substance treatment, with some noting that reduced addiction treatment services led some individuals to relapse. Another study in California by Appa et al. [81] reported that fatal overdoses increased among PEH in the eight months following the onset of the pandemic (defined as 17 March 2020) compared with the eight months prior.

11. Mental Health

Numerous studies discussed the impact the pandemic has had on PEH’s mental health. Poor mental health was reported in five studies [100][75][87][95][107]. A survey of PEH in Hamburg revealed that 32% of PEH had problems with anxiety or depression and that those with health insurance had lower odds of experiencing these conditions [107]. Another study using the same dataset from Hamburg reported that 49% of those surveyed felt lonely, with increased loneliness associated with male gender, being single, originating from Germany, high frequency of sharing a sleeping space with more than three people, and a higher self-perceived risk of contracting COVID-19 [75]. In San Francisco, 55% of women experiencing homelessness and unstable housing had depression, and 42% had anxiety; factors significantly associated with depression and anxiety included recent homelessness, unmet subsistence needs, and social isolation [95]. Increased difficulties accessing care for chronic medical conditions also increased risk of screening positive for anxiety more than threefold, and for depression, sixfold [95]. Cardenas et al. [100] reported that the majority of individuals presenting to a psychiatric emergency room in Los Angeles were PEH.
Nine studies indicated that the pandemic led to poorer mental health outcomes among PEH [12][20][23][25][71][83][85][86][87]. Disruptions to routines [12], feelings of loneliness [71][83][85][87], exclusion, confinement, [83] nervousness, [83][87] hopelessness [71], exacerbation of pre-existing mental health problems [23], and reduced access to services and counselling [12][87] were all seen as contributing to negative mental health during the pandemic. In temporary emergency accommodations in Ireland, 39% of PEH surveyed in May and June 2020 reported worse mental health than one year prior, and 21% self-harmed, attempted suicide, or had suicidal thoughts in the past month [87]. Aguilar et al. [20] reported increased psychological destabilisation among PEH during the first ten weeks of confinement in Spain, though supporting data for the finding were not available. Three studies noted mental health improving for some PEH during the pandemic [85][87][108]. In Turin, Leonardi and Stefani [85] described how night shelters that shifted to 24/7 services became residential communities, providing stability and improving mental health for some residents. A study by the Irish Health Service Executive (HSE) [87] reported that 39% of PEH surveyed in emergency accommodations self-reported improved mental health compared with one year prior; increased privacy, sense of safety, and rebuilding relationships with family since shielding or self-isolating was noted by some as contributing to improved mental health. Additionally, a positive association was found in changes in moderate or total physical activity and mental well-being and self-esteem among young PEH (16–24 years old) between the four weeks before and after the initial lockdown in the UK in a study by Thomas et al. [108].
Access to mental health services was addressed in 11 studies [23][25][26][50][40][70][71][86][91][87][92]. Of these, five indicated that mental health support was provided within temporary accommodations [50][40][70][87][92], and four indicated that PEH’s access to support improved during the pandemic [25][26][91][87]. Parkes et al. [25] reported that telephone and online support groups helped PEH in Scotland to maintain and improve their mental health. In a temporary shelter in Spain, significantly more patients were prescribed psychotropic drugs by the end of the programme than at the beginning (82% vs. 59%, respectively) [26]. Aitken [91] reported that hotel accommodation provided a safe space for PEH experiencing mental health conditions and increased willingness to engage with support. Two studies reported that some PEH were discharged to mental health programmes after leaving temporary accommodations [26][70]. Unmet need for mental health services was noted in five studies [13][23][71][86][87]. In France, 24% of PEH in a study by Allaria et al. [13] reported unmet mental health needs, with the highest unmet need reported among those sleeping rough (33%), and the lowest, among those living in squats (17%). Parkes et al. [23] reported that telephone and online support groups were not enough to offset increased social isolation due to the pandemic. Similarly, Pixley et al. [86] noted barriers to accessing online support among PEH. In Ireland, some PEH in temporary accommodations noted that they were unable to access their psychiatrists and that provided mental health services could be improved [87]. A study in Los Angeles by Tucker et al. [71] reported that 44% of young PEH (18–25 years old) felt that accessing mental health counselling was more difficult since the onset of the pandemic.

12. Access to Health Services

Beyond healthcare directly related to COVID-19, substance use, or mental health, several studies discussed PEH access to healthcare during the pandemic. Seven articles reported unmet health needs [12][13][38][87][107][109][110]. In Marseille, France, 17% of PEH reported unmet physical health needs, with the highest unmet need reported among those in shelters (21%), followed by those living rough (18%) and in squats (12%) [13]. van Rüth et al. found that only 69% of PEH living in Hamburg during the pandemic reported having health insurance [107]. In Ireland, 32% of surveyed PEH in temporary emergency accommodations did not have an up-to-date care plan, and 15% did not know [87]. Substantially fewer PEH in county Dublin (35%) reported having an up-to-date care plan than in Galway, Limerick, Clare, and Tipperary (70%) [87]. For some, the large shift toward telemedicine was a barrier to health services. In Indiana, PEH were unable to avail of telehealth services because of lack of access to phones, computers, or places to charge or store devices [12]. Another study found that U.S. veterans experiencing homelessness were 11% less likely to use video care during the pandemic than those not experiencing homelessness [109]. Similarly, Hickey et al. [38] reported that PEH accounted for 9% of those reached prior to a scheduled telehealth visit and 17% of those not reached. At a large HIV clinic in San Francisco, Spinelli et al. [110] reported that PEH were offered telehealth visits significantly less often than the average population (32% vs. 54%, respectively) and had fewer no-shows during shelter-in-place (1–30 April 2020) than the average population pre-shelter-in-place (1 December 2019–29 February 2020), and that viral non-suppression was higher among PEH during the pandemic than before. Barriers to primary healthcare were also exacerbated by the pandemic, with PEH in Edinburgh being turned away from the A&E for problems unrelated to COVID-19 and unable to meet with general practitioners (GPs) or access wound care, sexual health, or dentistry services [23]. Reduced access to STD services such as condoms, testing, or PrEP due to the COVID-19 pandemic was also reported in a Los Angeles-based study [71].
While some articles described unmet healthcare needs among some PEH, eight studies reported instances in which health needs of PEH were supported during the pandemic [25][52][44][91][97][93][96][106]. Three studies described medication delivery for PEH; two described it in relation to enabling PEH to shield [25][44], while the third delivered prescriptions to PEH who were isolating with COVID-19 [93]. In addition to prescription delivery, PEH isolating in care sites in Chicago were supported through telehealth visits and transportation to and from outpatient haemodialysis [93], and those residing in three shelters on the Slovakia borders received regular GP visits [44]. Some patients admitted to an Intermediary Care Unit in Edinburgh for recovery from acute illnesses were able to reengage with primary care, access hepatitis-C treatment, or receive care for chronic health conditions [91]. One HIV clinic in San Francisco reported that the proportion of PEH visiting the clinic each month was similar before and during the pandemic and that viral suppression did not worsen among patients [106]. In addition, 15% of the patients were temporarily housed in hotels, enabling navigators to conduct both phone and in-person outreach [106]. An intervention for persons living with HIV with experience of homelessness in Boston provided phones to patients without devices, facilitating biweekly contact to ensure that medical and prescription needs were met [52]. The intervention found that 57% of patients that were unhoused kept their appointments with their HIV primary care providers, though it was a significantly lower proportion than among those who were currently housed (75%) [52]. Redondo-Sama et al. [96] described collaboration between social workers and health services, enabling advocacy for vulnerable patients, and Brown and Edwards [97] reported that health support was delivered to unsheltered homeless encampments in California by the Emergency Operation Centre, though details of the health support were not provided.
In some cases, the pandemic improved access to health services for PEH. Some residents of temporary emergency accommodation in Ireland reported accessing new supports, such as primary care services, on-site nursing, housing support, and project worker support [87]. The same study noted that the number of respondents engaging with keyworkers or case managers increased during the outbreak period (April–June 2020) compared with before (September 2019–March 2020) [87]. In England, homeless services’ closer connections with the health services helped PEH to receive better health assessments [102]. In addition, some providers of HCV test and treat interventions for those temporarily housed in England reported that increased freedom and flexibility allowed them to provide clients all of their medication upon treatment initiation, reducing the consequences of losing contact while people moved between accommodations [88]. Providers also felt that the lockdown and accommodations provided time and space for some PEH to reflect on and reengage with their health [88]. A study by Cironi et al. [84] in New Orleans reported that 60% of those testing positive for HCV as part of a pilot program among persons in COVID-19 temporary housing were previously unaware of their infection. The program was therefore able to communicate diagnoses with residents and link them with follow-up care [84].

13. Other Health Impacts

A few studies explored other health impacts of the pandemic, such as violence [86][90], sense of safety [87], physical activity [87][108], emergency department use [87][90], local health centre use, quality of life, and general health status [87]. Pixley et al. [86] explained that while domestic and interpersonal violence had been associated with homelessness and housing insecurity prior to the pandemic, new financial fears or fear of SARS-CoV-2 may prevent some individuals from leaving violent or abusive situations. A study by Riley et al. [90] noted that 33% of women experiencing homelessness or housing insecurity in San Francisco decided where to sleep based on avoiding violence during the pandemic. In Ireland, 70% of surveyed PEH in temporary emergency accommodation reported feeling safe or very safe in May and June 2020, and 46% reported feeling safer than they did one year prior [87]. Regarding physical activity, some participants in the same study in Ireland noted more appreciation for exercise in the emergency accommodations while others felt that not having a gym or facing difficulties walking negatively impacted their well-being [87]. Thomas et al. [108] found that physical activity among young PEH (16–24 years old) generally increased in the UK during the four weeks following lockdown restrictions introduced in March 2020 compared with four weeks before. Increased physical activity following lockdown was significantly higher in participants considered ‘inactive’ prior to lockdown than in those considered ‘active’ [108]. Riley et al. [90] reported that, unlike the general population, women experiencing homelessness and housing insecurity in San Francisco did not reduce emergency department use during the pandemic. Experiencing homelessness was significantly associated with emergency department use [90]. In Ireland, visits to local health centres and the emergency department declined among PEH who were accessing emergency accommodations in most areas during the outbreak period (April–June 2020), except county Galway, where a 17% increase in emergency department use was reported [87]. In the same study, 54% of respondents described their quality of life as good, very good, or excellent; 28% described it as fair; and 18% self-reported poor or very poor quality of life [87]. Respondents also self-reported their general health status; 46% described it as better than one year prior, 34% reported it as worse, and 30% indicated no change [87].

References

  1. Worldometer. Coronavirus Statistics. Available online: https://www.worldometers.info/coronavirus/ (accessed on 26 January 2022).
  2. Moghadas, S.M.; Vilches, T.N.; Zhang, K.; Wells, C.R.; Shoukat, A.; Singer, B.H.; Meyers, L.A.; Neuzil, K.M.; Langley, J.M.; Fitzpatrick, M.C.; et al. The Impact of Vaccination on Coronavirus Disease 2019 (COVID-19) Outbreaks in the United States. Clin. Infect. Dis. 2021, 73, 2257–2264.
  3. Calderón-Larrañaga, A.; Dekhtyar, S.; Vetrano, D.L.; Bellander, T.; Fratiglioni, L. COVID-19: Risk accumulation among biologically and socially vulnerable older populations. Ageing Res. Rev. 2020, 63, 101149.
  4. Tregoning, J.S.; Flight, K.E.; Higham, S.L.; Wang, Z.; Pierce, B.F. Progress of the COVID-19 vaccine effort: Viruses, vaccines and variants versus efficacy, effectiveness and escape. Nat. Rev. Immunol. 2021, 21, 626–636.
  5. Leifheit, K.M.; Chaisson, L.H.; Medina, J.A.; Wahbi, R.N.; Shover, C.L. Elevated Mortality Among People Experiencing Homelessness With COVID-19. Open Forum Infect. Dis. 2021, 8, ofab301.
  6. Perri, M.; Dosani, N.; Hwang, S.W. COVID-19 and people experiencing homelessness: Challenges and mitigation strategies. CMAJ 2020, 192, E716–E719.
  7. Roederer, T.; Mollo, B.; Vincent, C.; Nikolay, B.; Llosa, A.E.; Nesbitt, R.; Vanhomwegen, J.; Rose, T.; Goyard, S.; Anna, F.; et al. Seroprevalence and risk factors of exposure to COVID-19 in homeless people in Paris, France: A cross-sectional study. Lancet Public Health 2021, 6, e202–e209.
  8. Schrooyen, L.; Delforge, M.; Lebout, F.; Vanbaelen, T.; Lecompte, A.; Dauby, N. Homeless people hospitalized with COVID-19 in Brussels. Clin. Microbiol. Infect. 2021, 27, 151–152.
  9. Tsai, J.; Wilson, M. COVID-19: A potential public health problem for homeless populations. Lancet Public Health 2020, 5, e186–e187.
  10. Silva, D.S.; Smith, M.J. Social distancing, social justice, and risk during the COVID-19 pandemic. Can. J. Public Health 2020, 111, 459–461.
  11. Montgomery, M.P.; Carry, M.G.; Garcia-Williams, A.G.; Marshall, B.; Besrat, B.; Bejarano, F.; Carlson, J.; Rutledge, T.; Mosites, E. Hand hygiene during the COVID-19 pandemic among people experiencing homelessness—Atlanta, Georgia, 2020. J. Community Psychol. 2021, 49, 2441–2453.
  12. Rodriguez, N.M.; Lahey, A.M.; MacNeill, J.J.; Martinez, R.G.; Teo, N.E.; Ruiz, Y. Homelessness during COVID-19: Challenges, Responses, and Lessons Learned from Homeless Service Providers in Tippecanoe County, Indiana. BMC Public Health 2021, 21, 1657.
  13. Allaria, C.; Loubière, S.; Mosnier, E.; Monfardini, E.; Auquier, P.; Tinland, A. “Locked down outside”: Perception of hazard and health resources in COVID-19 epidemic context among homeless people. SSM Popul. Health 2021, 15, 100829.
  14. Farhoudian, A.; Radfar, S.R.; Mohaddes Ardabili, H.; Rafei, P.; Ebrahimi, M.; Khojasteh Zonoozi, A.; De Jong, C.A.J.; Vahidi, M.; Yunesian, M.; Kouimtsidis, C.; et al. A Global Survey on Changes in the Supply, Price, and Use of Illicit Drugs and Alcohol, and Related Complications During the 2020 COVID-19 Pandemic. Front. Psychiatry 2021, 12, 1134.
  15. Ali, F.; Russell, C.; Nafeh, F.; Rehm, J.; LeBlanc, S.; Elton-Marshall, T. Changes in substance supply and use characteristics among people who use drugs (PWUD) during the COVID-19 global pandemic: A national qualitative assessment in Canada. Int. J. Drug Policy 2021, 93, 103237.
  16. Glick, S.N.; Prohaska, S.M.; LaKosky, P.A.; Juarez, A.M.; Corcorran, M.A.; Des Jarlais, D.C. The Impact of COVID-19 on Syringe Services Programs in the United States. AIDS Behav. 2020, 24, 2466–2468.
  17. Picchio, C.A.; Valencia, J.; Doran, J.; Swan, T.; Pastor, M.; Martró, E.; Colom, J.; Lazarus, J.V. The impact of the COVID-19 pandemic on harm reduction services in Spain. Harm Reduct. J. 2020, 17, 87.
  18. Radfar, S.R.; De Jong, C.A.J.; Farhoudian, A.; Ebrahimi, M.; Rafei, P.; Vahidi, M.; Yunesian, M.; Kouimtsidis, C.; Arunogiri, S.; Massah, O.; et al. Reorganization of Substance Use Treatment and Harm Reduction Services During the COVID-19 Pandemic: A Global Survey. Front. Psychiatry 2021, 12, 349.
  19. Vasylyeva, T.I.; Smyrnov, P.; Strathdee, S.; Friedman, S.R. Challenges posed by COVID-19 to people who inject drugs and lessons from other outbreaks. J. Int. AIDS Soc. 2020, 23, e25583.
  20. Aguilar, L.; Vicente-Hernández, B.; Remón-Gallo, D.; García-Ullán, L.; Valriberas-Herrero, I.; Maciá-Casas, A.; Pérez-Madruga, A.; Garzón, M.Á.; Álvarez-Navares, A.; Roncero, C. A real-world ten-week follow-up of the COVID outbreak in an outpatient drug clinic in Salamanca (Spain). J. Subst. Abus. Treat 2021, 125, 108303.
  21. Irwin, M.D.; Amanuel, Y.; Bickers, B.; Nguyen, M.A.; Russell, O.W. Impacts of the COVID-19 Pandemic on Preexisting Racial and Ethnic Disparities, and Results of an Integrated Safety Net Response in Arlington County, Virginia. Health Secur. 2021, 19, S62–S71.
  22. O’Carroll, A.; Duffin, T.; Collins, J. Harm reduction in the time of COVID-19: Case study of homelessness and drug use in Dublin, Ireland. Int. J. Drug Policy 2021, 87, 102966.
  23. Parkes, T.; Carver, H.; Masterton, W.; Falzon, D.; Dumbrell, J.; Grant, S.; Wilson, I. “You know, we can change the services to suit the circumstances of what is happening in the world”: A rapid case study of the COVID-19 response across city centre homelessness and health services in Edinburgh, Scotland. Harm Reduct. J. 2021, 18, 64.
  24. Krawczyk, N.; Fawole, A.; Yang, J.; Tofighi, B. Early innovations in opioid use disorder treatment and harm reduction during the COVID-19 pandemic: A scoping review. Addict. Sci. Clin. Pract. 2021, 16, 68.
  25. Parkes, T.; Carver, H.; Masterton, W.; Falzon, D.; Dumbrell, J.; Grant, S.; Wilson, I. ‘They already operated like it was a crisis, because it always has been a crisis’: A qualitative exploration of the response of one homeless service in Scotland to the COVID-19 pandemic. Harm Reduct. J. 2021, 18, 26.
  26. Martin, C.; Andrés, P.; Bullón, A.; Villegas, J.L.; de la Iglesia-Larrad, J.I.; Bote, B.; Prieto, N.; Roncero, C. COVID pandemic as an opportunity for improving mental health treatments of the homeless people. Int. J. Soc. Psychiatry 2021, 67, 335–343.
  27. Samuels, E.A.; Karb, R.; Vanjani, R.; Trimbur, M.C.; Napoli, A. Congregate Shelter Characteristics and Prevalence of Asymptomatic SARS-CoV-2. medRxiv 2020.
  28. Redditt, V.; Wright, V.; Rashid, M.; Male, R.; Bogoch, I. Outbreak of SARS-CoV-2 infection at a large refugee shelter in Toronto, April 2020: A clinical and epidemiologic descriptive analysis. CMAJ Open 2020, 8, E819–E824.
  29. Aranda-Díaz, A.; Imbert, E.; Strieff, S.; Graham-Squire, D.; Evans, J.L.; Moore, J.; McFarland, W.; Fuchs, J.; Handley, M.A.; Kushel, M. Implementation of Rapid and Frequent SARS-CoV2 Antigen Testing and Response in Congregate Homeless Shelters. medRxiv 2021.
  30. Jatt, L.P.; Winnett, A.; Graber, C.J.; Vallone, J.; Beenhouwer, D.O.; Goetz, M.B. Widespread severe acute respiratory coronavirus virus 2 (SARS-CoV-2) laboratory surveillance program to minimize asymptomatic transmission in high-risk inpatient and congregate living settings. Infect. Control Hosp. Epidemiol. 2020, 41, 1331–1334.
  31. Wang, L.; Ma, H.; Yiu, K.C.Y.; Calzavara, A.; Landsman, D.; Luong, L.; Chan, A.K.; Kustra, R.; Kwong, J.C.; Boily, M.-C.; et al. Heterogeneity in testing, diagnosis and outcome in SARS-CoV-2 infection across outbreak settings in the Greater Toronto Area, Canada: An observational study. CMAJ Open 2020, 8, E627–E636.
  32. Kiran, T.; Craig-Neil, A.; Das, P.; Lockwood, J.; Wang, R.; Nathanielsz, N.; Rosenthal, E.; Snider, C.; Hwang, S.W. Factors associated with SARS-CoV-2 positivity in 20 homeless shelters in Toronto, Canada, from April to July 2020: A repeated cross-sectional study. CMAJ Open 2021, 9, E302–E308.
  33. Le Bihan, C.; Faucherre, V.; Le Moing, V.; Mehenni, A.; Nantes, D.; Da Silva, A.; Jaume, C.; Lassalle, F.; Makinson, A. COVID-19: The forgotten cases of hidden exiles. Infect. Dis. Now 2021, 51, 387–390.
  34. Loubiere, S.; Monfardini, E.; Allaria, C.; Mosnier, M.; Allibert, A.; Ninove, L.; Bosetti, T.; Farnarier, C.; Hamouda, I.; Auquier, P. Seroprevalence of SARS-CoV-2 antibodies among homeless people living rough, in shelters and squats: A large population-based study in France. PLoS ONE 2021, 16, e0255498.
  35. Röthlin Eriksen, A.R.; Fogh, K.; Hasselbalch, R.B.; Bundgaard, H.; Nielsen, S.D.; Jørgensen, C.S.; Scharff, B.F.S.S.; Erikstrup, C.; Sækmose, S.G.; Holm, D.K.; et al. SARS-CoV-2 antibody prevalence among homeless people, sex workers and shelter workers in Denmark: A nationwide cross-sectional study. medRxiv 2021.
  36. Routledge, I.; Epstein, A.; Takahashi, S.; Janson, O.; Hakim, J.; Duarte, E.; Turcios, K.; Vinden, J.; Sujishi, K.; Rangel, J.; et al. Citywide serosurveillance of the initial SARS-CoV-2 outbreak in San Francisco using electronic health records. Nat. Commun. 2021, 12, 3566.
  37. Spinelli, M.A.; Lynch, K.L.; Yun, C.; Glidden, D.V.; Peluso, M.J.; Henrich, T.J.; Gandhi, M.; Brown, L.B. SARS-CoV-2 seroprevalence, and IgG concentration and pseudovirus neutralising antibody titres after infection, compared by HIV status: A matched case-control observational study. Lancet HIV 2021, 8, e334–e341.
  38. Hickey, M.D.; Sergi, F.; Zhang, K.; Spinelli, M.A.; Black, D.; Sola, C.; Blaz, V.; Nguyen, J.Q.; Oskarsson, J.; Gandhi, M. Pragmatic randomized trial of a pre-visit intervention to improve the quality of telemedicine visits for vulnerable patients living with HIV. J. Telemed. Telecare 2020, 1357633X20976036.
  39. Ralli, M.; Cedola, C.; Urbano, S.; Latini, O.; Shkodina, N.; Morrone, A.; Arcangeli, A.; Ercoli, L. Assessment of SARS-CoV-2 infection through rapid serology testing in the homeless population in the City of Rome, Italy. Preliminary results. J. Public Health Res. 2020, 9, 1986.
  40. Krcmery, V.; Bucko, L.; Kimuli, A.; Jackulikova, M.; Kozon, V.; Olah, M.; Kovac, R.; Jancovic, M.; Holkova, J.; Mikolasova, G.; et al. Cohortation and testing of elderly homeless within COVID pademics in an urban environment—Example of a life island mission model. Acta Missiol. 2020, 1, 76–78.
  41. Husain, M.; Rachline, A.; Cousien, A.; Rolland, S.; Rouzaud, C.; Ferre, V.M.; Gomez, M.V.; Le Teurnier, M.; Wicky-Thisse, M.; Descamps, D.; et al. Impact of the COVID-19 pandemic on the homeless: Results from a retrospective closed cohort in France (March–May 2020). Clin. Microbiol. Infect. 2021, 27, 1520.e1–1520.e5.
  42. Roland, M.; Ben Abdelhafidh, L.; Déom, V.; Vanbiervliet, F.; Coppieters, Y.; Racapé, J. SARS-CoV-2 screening among people living in homeless shelters in Brussels, Belgium. PLoS ONE 2021, 16, e0252886.
  43. Storgaard, S.F.; Eiset, A.H.; Abdullahi, F.; Wejse, C. First wave of COVID-19 did not reach the homeless population in Aarhus. Dan. Med. J. 2020, 67, A08200594.
  44. Gombita, P.; Olah, M.; Kovac, R.; Jurasek, M.; Kosticova, M.; Taziarova, M.; Zabavova, S.; Haluskova, E.; Jackulikova, M.; Zemko, R. Senior Homeless Population was COVID-19 Free in 3 shelter communities after adapting the Life Island model (Note). Clin. Soc. Work Health Interv. 2020, 11, 78–79.
  45. Yoon, J.C.; Montgomery, M.P.; Buff, A.M.; Boyd, A.T.; Jamison, C.; Hernandez, A.; Schmit, K.; Shah, S.; Ajoku, S.; Holland, D.P.; et al. Coronavirus Disease 2019 (COVID-19) Prevalences Among People Experiencing Homelessness and Homelessness Service Staff During Early Community Transmission in Atlanta, Georgia, April–May 2020. Clin. Infect. Dis. 2021, 73, e2978–e2984.
  46. Mosites, E.; Parker, E.M.; Clarke, K.E.N.; Gaeta, J.M.; Baggett, T.P.; Imbert, E.; Sankaran, M.; Scarborough, A.; Huster, K.; Hanson, M. Assessment of SARS-CoV-2 infection prevalence in homeless shelters—four US cities, March 27–April 15, 2020. Morb. Mortal. Wkly. Rep. 2020, 69, 521.
  47. Marquez, H.; Ramers, C.; Northrup, A.; Tam, A.; Liu, J.; Rojas, S.; Klaman, S.; Khasira, M.; Madbak, J.; Matthews, E.; et al. Response to the Coronavirus Disease 2019 Pandemic Among People Experiencing Homelessness in Congregant Living Settings in San Diego, California. Clin. Infect. Dis. 2021, 73, e805–e807.
  48. Rogers, J.H.; Link, A.C.; McCulloch, D.; Brandstetter, E.; Newman, K.L.; Jackson, M.L.; Hughes, J.P.; Englund, J.A.; Boeckh, M.; Sugg, N. Characteristics of COVID-19 in homeless shelters: A community-based surveillance study. Ann. Intern. Med. 2021, 174, 42–49.
  49. Ralli, M.; Morrone, A.; Arcangeli, A.; Ercoli, L. Asymptomatic patients as a source of transmission of COVID-19 in homeless shelters. Int. J. Infect. Dis. 2021, 103, 243–245.
  50. Montgomery, M.P.; Paulin, H.N.; Morris, A.; Speers, A.; Boyd, A.T.; Buff, A.M.; Mathews, D.; Wells, A.; Marchman, C.; Gaffga, N. Establishment of Isolation and Noncongregate Hotels During COVID-19 and Symptom Evolution Among People Experiencing Homelessness—Atlanta, Georgia, 2020. J. Public Health Manag. Pract. 2021, 27, 285–294.
  51. Fields, V.L.; Kiphibane, T.; Eason, J.T.; Hafoka, S.F.; Lopez, A.S.; Schwartz, A.; Henry, A.; Tran, C.H.; Tate, J.E.; Kirking, H.L. Assessment of contact tracing for COVID-19 among people experiencing homelessness, Salt Lake County Health Department, March–May 2020. Ann. Epidemiol. 2021, 59, 50–55.
  52. Brody, J.K.; Rajabiun, S.; Strupp Allen, H.J.; Baggett, T. Enhanced Telehealth Case Management Plus Emergency Financial Assistance for Homeless-Experienced People Living With HIV During the COVID-19 Pandemic. Am. J. Public Health 2021, 111, 835–838.
  53. Sachdev, D.; Mara, E.; Hsu, L.; Scheer, S.; Rutherford, G.; Enanoria, W.; Gandhi, M. COVID-19 Susceptibility and Outcomes Among People Living With HIV in San Francisco. J. Acquir. Immune. Defic. Syndr. 2021, 86, 19–21.
  54. Ly, T.D.A.; Edouard, S.; Badiaga, S.; Tissot-Dupont, H.; Hoang, V.T.; Pommier de Santi, V.; Brouqui, P.; Raoult, D.; Gautret, P. Epidemiology of respiratory pathogen carriage in the homeless population within two shelters in Marseille, France, 2015–2017: Cross sectional 1-day surveys. Clin. Microbiol. Infect. 2019, 25, e241–e249.
  55. Iacoella, C.; Ralli, M.; Maggiolini, A.; Arcangeli, A.; Ercoli, L. Acceptance of COVID-19 vaccine among persons experiencing homelessness in the City of Rome, Italy. Eur. Rev. Med. Pharmacol. Sci. 2021, 25, 3132–3135.
  56. Tobolowsky, F.A.; Gonzales, E.; Self, J.L.; Rao, C.Y.; Keating, R.; Marx, G.E.; McMichael, T.M.; Lukoff, M.D.; Duchin, J.S.; Huster, K. COVID-19 outbreak among three affiliated homeless service sites—King County, Washington, 2020. Morb. Mortal. Wkly. Rep. 2020, 69, 523.
  57. Rozenfeld, Y.; Beam, J.; Maier, H.; Haggerson, W.; Boudreau, K.; Carlson, J.; Medows, R. A model of disparities: Risk factors associated with COVID-19 infection. Int. J. Equity Health 2020, 19, 126.
  58. Rincón, A.; Moreso, F.; López-Herradón, A.; Fernández-Robres, M.A.; Cidraque, I.; Nin, J.; Méndez, O.; López, M.; Pájaro, C.; Satorra, À. The keys to control a COVID-19 outbreak in a haemodialysis unit. Clin. Kidney J. 2020, 13, 542–549.
  59. Ly, T.D.A.; Nguyen, N.N.; Goumballa, N.; Louni, M.; Canard, N.; Dao, T.L.; Medkour, H.; Borg, A.; Bardy, K.; Esteves-Vieira, V. Screening of SARS-CoV-2 among homeless people, asylum-seekers and other people living in precarious conditions in Marseille, France, March–April 2020. Int. J. Infect. Dis. 2021, 105, 1–6.
  60. Ghinai, I.; Davis, E.S.; Mayer, S.; Toews, K.-A.; Huggett, T.D.; Snow-Hill, N.; Perez, O.; Hayden, M.K.; Tehrani, S.; Landi, A.J. Risk factors for severe acute respiratory syndrome coronavirus 2 infection in homeless shelters in Chicago, Illinois—March–May, 2020. Open Forum Infect. Dis. 2020, 7, ofaa477.
  61. Karb, R.; Samuels, E.; Vanjani, R.; Trimbur, C.; Napoli, A. Homeless shelter characteristics and prevalence of SARS-CoV-2. West. J. Emerg. Med. 2020, 21, 1048.
  62. Baggett, T.P.; Keyes, H.; Sporn, N.; Gaeta, J.M. Prevalence of SARS-CoV-2 infection in residents of a large homeless shelter in Boston. JAMA 2020, 323, 2191–2192.
  63. Rahi, M.; Le Pluart, D.; Beaudet, A.; Ismaël, S.; Parisey, M.; Poey, N.; Tarhini, H.; Lescure, F.-X.; Yazdanpanah, Y.; Deconinck, L. Sociodemographic characteristics and transmission risk factors in patients hospitalized for COVID-19 before and during the lockdown in France. BMC Infect. Dis. 2021, 21, 812.
  64. Imbert, E.; Kinley, P.M.; Scarborough, A.; Cawley, C.; Sankaran, M.; Cox, S.N.; Kushel, M.; Stoltey, J.; Cohen, S.; Fuchs, J.D. Coronavirus Disease 2019 Outbreak in a San Francisco Homeless Shelter. Clin. Infect. Dis. 2021, 73, 324–327.
  65. Barocas, J.A.; Gai, M.J.; White, L.F.; Faretra, D.; Sachs, K.; Komaromy, M. Implementation of a Recuperation Unit and Hospitalization Rates Among People Experiencing Homelessness With COVID-19. JAMA Netw. Open 2021, 4, e212826.
  66. Cha, S.; Henry, A.; Montgomery, M.P.; Laws, R.L.; Pham, H.; Wortham, J.; Garg, S.; Kim, L.; Mosites, E.; Team, C.-N.S. Morbidity and Mortality among Adults Experiencing Homelessness Hospitalized with COVID-19. J. Infect. Dis. 2021, 224, 425–430.
  67. Hsu, H.E.; Ashe, E.M.; Silverstein, M.; Hofman, M.; Lange, S.J.; Razzaghi, H.; Mishuris, R.G.; Davidoff, R.; Parker, E.M.; Penman-Aguilar, A. Race/ethnicity, underlying medical conditions, homelessness, and hospitalization status of adult patients with COVID-19 at an urban safety-net medical center—Boston, Massachusetts, 2020. Morb. Mortal. Wkly. Rep. 2020, 69, 864.
  68. Song, J.; Grey, C.N.B.; Davies, A.R. Creating an e-cohort of individuals with lived experience of homelessness and subsequent mortality in Wales, UK. J. Public Health 2021, fdab180.
  69. Fuchs, J.D.; Carter, H.C.; Evans, J.; Graham-Squire, D.; Imbert, E.; Bloome, J.; Fann, C.; Skotnes, T.; Sears, J.; Pfeifer-Rosenblum, R. Assessment of a Hotel-Based COVID-19 Isolation and Quarantine Strategy for Persons Experiencing Homelessness. JAMA Netw. Open 2021, 4, e210490.
  70. Komaromy, M.; Harris, M.; Koenig, R.M.; Tomanovich, M.; Ruiz-Mercado, G.; Barocas, J.A. Caring for COVID’s most vulnerable victims: A safety-net hospital responds. J. Gen. Intern. Med. 2020, 36, 1006–1010.
  71. Tucker, J.S.; D’Amico, E.J.; Pedersen, E.R.; Garvey, R.; Rodriguez, A.; Klein, D.J. Behavioral health and service usage during the COVID-19 pandemic among emerging adults currently or recently experiencing homelessness. J. Adolesc. Health 2020, 67, 603–605.
  72. Hajek, A.; Bertram, F.; van Rüth, V.; Kretzler, B.; Püschel, K.; Heinrich, F.; König, H.-H. Prevalence and factors associated with fear of COVID-19 among homeless individuals during the COVID-19 pandemic: Evidence from the hamburg survey of homeless individuals. Risk Manag. Healthc. Policy 2021, 14, 2689.
  73. Henwood, B.F.; Redline, B.; Lahey, J. Surveying Tenants of Permanent Supportive Housing in Skid Row about COVID-19. J. Health Care Poor Underserved 2020, 31, 1587–1594.
  74. Kuhn, R.; Henwood, B.; Lawton, A.; Kleva, M.; Murali, K.; King, C.; Gelberg, L. COVID-19 vaccine access and attitudes among people experiencing homelessness from pilot mobile phone survey in Los Angeles, CA. PLoS ONE 2021, 16, e0255246.
  75. Bertram, F.; Heinrich, F.; Fröb, D.; Wulff, B.; Ondruschka, B.; Püschel, K.; König, H.-H.; Hajek, A. Loneliness among Homeless Individuals during the First Wave of the COVID-19 Pandemic. Int. J. Environ. Res. Public Health 2021, 18, 3035.
  76. Finnigan, R. Self-reported impacts of the COVID-19 pandemic for people experiencing homelessness in Sacramento, California. J. Soc. Distress Homelessness 2021.
  77. Hajek, A.; Bertram, F.; Heinrich, F.; van Rüth, V.; Ondruschka, B.; Kretzler, B.; Schüler, C.; Püschel, K.; König, H.-H. Determinants of health care use among homeless individuals: Evidence from the Hamburg survey of homeless individuals. BMC Health Serv. Res. 2021, 21, 317.
  78. Moore, J.X.; Gilbert, K.L.; Lively, K.L.; Laurent, C.; Chawla, R.; Li, C.; Johnson, R.; Petcu, R.; Mehra, M.; Spooner, A. Correlates of COVID-19 vaccine hesitancy among a community sample of African Americans living in the Southern United States. Vaccines 2021, 9, 879.
  79. Longchamps, C.; Ducarroz, S.; Crouzet, L.; Vignier, N.; Pourtau, L.; Allaire, C.; Colleville, A.-C.; El Aarbaoui, T.; Melchior, M.; ECHO Study Group. COVID-19 vaccine hesitancy among persons living in homeless shelters in France. Vaccine 2021, 39, 3315–3318.
  80. Hsu, H.-T.; Petering, R.; Onasch-Vera, L. Implications of COVID-19 vaccine uptake among young adults experiencing homelessness: A brief report. J. Soc. Distress Homelessness 2021, 1–6.
  81. Appa, A.; Rodda, L.N.; Cawley, C.; Zevin, B.; Coffin, P.O.; Gandhi, M.; Imbert, E. Drug Overdose Deaths Before and After Shelter-in-Place Orders During the COVID-19 Pandemic in San Francisco. JAMA Netw. Open 2021, 4, e2110452.
  82. Ramaswamy, M.; Hemberg, J.; Faust, A.; Wickliffe, J.; Comfort, M.; Lorvick, J.; Cropsey, K. Criminal justice–involved women navigate COVID-19: Notes from the field. Health Educ. Behav. 2020, 47, 544–548.
  83. Barbu, S.; Perez, S.; Silk, R.; Coyne, A. The Impact of COVID-19 on Homeless Service Providers & Homeless People: The Migrant Perspective; FEANTSA: Brussels, Belgium, 2021.
  84. Cironi, K.A.; Jones, A.T.; Hauser, E.M.; Olsen, J.W.; Kissinger, P.J. Human Immunodeficiency Virus and Hepatitis C Linkage-to-Care Initiative for New Orleans Residents Experiencing Homelessness During the COVID-19 Pandemic. Sex. Transm. Dis. 2021, 48, 595–600.
  85. Leonardi, D.; Stefani, S. The pandemic and homeless people in the Turin area: The level of housing adequacy shapes experiences and well-being. Hous. Care Support 2021, 24, 93–104.
  86. Pixley, C.L.; Henry, F.A.; DeYoung, S.E.; Settembrino, M.R. The role of homelessness community based organizations during COVID-19. J. Community Psychol. 2021, 1–15.
  87. National Social Inclusion Office. National COVID-19 Homeless Service User Experience Survey—Report of Findings; HSE: Dublin, Ireland, 2020.
  88. Wilkinson, R.; Mandal, S.; Phipps, E. Evaluation of Hepatitis C Test and Treat Interventions Targeted at Homeless Populations (Outside London) in England During the COVID-19 Pandemic. Clin. Liver Dis. 2021, 17, 90–94.
  89. Scallan, E.; Bodkin, C.; Wiwcharuk, J.; O’Shea, T.; Lennox, R. Finding stability amidst the COVID-19 pandemic: The impact of emergency temporary housing for people who use drugs. Drug Alcohol Rev. 2021, 41, 7–8.
  90. Riley, E.D.; Raven, M.C.; Dilworth, S.E.; Braun, C.; Imbert, E.; Doran, K.M. Using a “Big Events” framework to understand emergency department use among women experiencing homelessness or housing instability in San Francisco during the COVID-19 pandemic. Int. J. Drug Policy 2021, 97, 103405.
  91. Aitken, E. COVID-19: Opportunity to improve crisis responses to homelessness? J. R. Coll. Physicians Edinb. 2021, 51, S53–S62.
  92. Ramírez-Cervantes, K.L.; Romero-Pardo, V.; Pérez-Tovar, C.; Martínez-Alés, G.; Quintana-Diaz, M. A medicalized hotel as a public health resource for the containment of COVID-19: More than a place for quarantining. J. Public Health 2021, 43, 89–97.
  93. Wang, C.Y.; Palma, M.L.; Haley, C.; Watts, J.; Hinami, K. Rapid Creation of a Multiagency Alternate Care Site for COVID-19—Positive Individuals Experiencing Homelessness. Am. J. Public Health 2021, 111, 1227–1230.
  94. Steer, K.J.D.; Klassen, D.C.; O’Gorman, C.M.; Webster, M.; Mitchell, M.; Krichevsky, L.; Christiansen, K.; Benham, J.L.; Schindler, R.S. Cups for COVID: Rapid implementation of a harm reduction initiative to support populations experiencing homelessness during the COVID-19 pandemic. Can. J. Public Health 2021, 112, 29–35.
  95. Riley, E.D.; Dilworth, S.E.; Satre, D.D.; Silverberg, M.J.; Neilands, T.B.; Mangurian, C.; Weiser, S.D. Factors associated with symptoms of depression and anxiety among women experiencing homelessness and unstable housing during the COVID-19 pandemic. JAMA Netw. Open 2021, 4, e2117035.
  96. Redondo-Sama, G.; Matulic, V.; Munté-Pascual, A.; de Vicente, I. Social work during the COVID-19 crisis: Responding to urgent social needs. Sustainability 2020, 12, 8595.
  97. Brown, D.; Edwards, F.L. Sheltering the Homeless during COVID-19 in San Jose, California. Int. J. Public Adm. 2021, 44, 952–962.
  98. Ly, T.D.A.; Hoang, V.T.; Goumballa, N.; Louni, M.; Canard, N.; Dao, T.L.; Medkour, H.; Borg, A.; Bardy, K.; Esteves-Vieira, V.; et al. Variations in respiratory pathogen carriage among a homeless population in a shelter for men in Marseille, France, March-July 2020: Cross-sectional 1-day surveys. Eur. J. Clin. Microbiol. Infect. Dis. 2021, 40, 1579–1582.
  99. Gaeta, J.M.; De Las Nueces, D.; Munson, D.G.; Barocas, J.A.; Walsh, K.E. Case 21–2020: A 66-year-old homeless man with COVID-19. N. Engl. J. Med. 2020, 383, 170–178.
  100. Cardenas, J.; Roach, J.; Kopelowicz, A. Prevalence of COVID 19 Positive Cases Presenting to a Psychiatric Emergency Room. Community Ment. Health J. 2021, 57, 1240–1243.
  101. Kelly, D.; Murphy, H.; Vadlamudi, R.; Kraut, R.; Dalessio, K.; Malani, A.N.; Glabach, M.; Marquez, J.L. Successful public health measures preventing coronavirus disease 2019 (COVID-19) at a Michigan homeless shelter. Infect. Control Hosp. Epidemiol. 2021, 42, 1155–1156.
  102. Fitzpatrick, S.; Watts, B.; Sims, R. Homelessness Monitor England 2020: COVID-19 Crisis Response Briefing; Crisis: London, UK, 2020.
  103. Dempsey, D.; Pautz, H. Food Insecurity in Times of COVID-19—An Insight into a Deepening Crisis; UWS-Oxfam Partnership: Scotland, UK, 2021.
  104. Mehtani, N.J.; Ristau, J.T.; Snyder, H.; Surlyn, C.; Eveland, J.; Smith-Bernardin, S.; Knight, K.R. COVID-19: A catalyst for change in telehealth service delivery for opioid use disorder management. Subst. Abus. 2021, 42, 205–212.
  105. Harris, M.; Johnson, S.; Mackin, S.; Saitz, R.; Walley, A.Y.; Taylor, J.L. Low barrier tele-buprenorphine in the time of COVID-19: A case report. J. Addict. Med. 2020, 14, e136–e138.
  106. Hickey, M.D.; Imbert, E.; Glidden, D.V.; Del Rosario, J.B.; Chong, M.; Clemenzi-Allen, A.; Oskarsson, J.; Riley, E.D.; Gandhi, M.; Havlir, D.V. Viral suppression during COVID-19 among people with HIV experiencing homelessness in a low-barrier clinic-based program. AIDS 2021, 35, 517–519.
  107. van Rüth, V.; König, H.H.; Bertram, F.; Schmiedel, P.; Ondruschka, B.; Püschel, K.; Heinrich, F.; Hajek, A. Determinants of health-related quality of life among homeless individuals during the COVID-19 pandemic. Public Health 2021, 194, 60–66.
  108. Thomas, J.; Bowes, N.; Meyers, R.; Thirlaway, K. Mental well-being and physical activity of young people experiencing homelessness before and during COVID-19 lockdown: A longitudinal study. Ment. Health Phys. Act. 2021, 21, 100407.
  109. Ferguson, J.M.; Jacobs, J.; Yefimova, M.; Greene, L.; Heyworth, L.; Zulman, D.M. Virtual care expansion in the Veterans Health Administration during the COVID-19 pandemic: Clinical services and patient characteristics associated with utilization. J. Am. Med. Inform. Assoc. 2021, 28, 453–462.
  110. Spinelli, M.A.; Hickey, M.D.; Glidden, D.V.; Nguyen, J.Q.; Oskarsson, J.J.; Havlir, D.; Gandhi, M. Viral suppression rates in a safety-net HIV clinic in San Francisco destabilized during COVID-19. AIDS 2020, 34, 2328–2331.
More
Information
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
View Times: 350
Revisions: 2 times (View History)
Update Date: 22 Mar 2022
1000/1000
Video Production Service