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1.
Clin Infect Dis ; 2023 Apr 20.
Article in English | MEDLINE | ID: covidwho-2295602

ABSTRACT

In response to longstanding healthcare inequities unmasked by the COVID-19 pandemic, the Infectious Diseases Section at the Yale School of Medicine designed and implemented a pilot curriculum integrating Diversity, Equity, and Anti-racism (ID2EA) into Infectious Disease educational training and measured program outcomes. We herein describe a mixed-methods assessment of Section members on whether the ID2EA curriculum impacted their beliefs and behaviors regarding racism and healthcare inequities. Participants rated the curriculum as useful (92% averaging across sessions) and effective in achieving stated learning objectives (89% averaging across sessions), including fostering understanding of how inequities and racism are linked to health disparities and identifying strategies to effectively deal with racism and inequities. Despite limitations in response rates and assessment of longer-term behavioral change, this work demonstrates that training in diversity, equity, and anti-racism can be successfully integrated into Infectious Disease physicians' educational activities and impact physicians' perspectives on these topics.

2.
Geriatrics (Basel) ; 7(6)2022 Dec 06.
Article in English | MEDLINE | ID: covidwho-2154949

ABSTRACT

Ukraine imposed a COVID-19 lockdown in March 2020. From April to June 2020, we surveyed 123 older people with HIV (OPWH) by phone to assess their mental health, engagement in HIV and other healthcare, and substance use using standardised scales. Variables of key interest were symptoms of depression and symptoms of anxiety. Univariate and multivariable Firth logistic regression models were built to assess factors associated with: (1) symptoms of depression, and (2) symptoms of anxiety. Findings indicated high suicidal ideation (10.6%); 45.5% met the screening criteria for moderate to severe depression; and 35.0% met the criteria for generalised anxiety disorder (GAD). Independent correlates of having moderate to severe depression included being female (AOR: 2.83, 95%CI = 1.19-7.05), having concerns about potential barriers to HIV treatment (AOR: 8.90, 95%CI = 1.31-104.94), and active drug use (AOR: 34.53, 95%CI = 3.02-4885.85). Being female (AOR: 5.30, 95%CI = 2.16-14.30) and having concerns about potential barriers to HIV treatment (AOR: 5.33, 95%CI = 1.22-28.45) were independently correlated with GAD, and over half (58.5%) were willing to provide peer support to other OPWH. These results highlight the impact of the COVID-19 restrictions in Ukraine on mental health for OPWH and support the need to screen for psychiatric and substance use disorders, potentially using telehealth strategies.

3.
PLoS One ; 16(12): e0260251, 2021.
Article in English | MEDLINE | ID: covidwho-1546950

ABSTRACT

There continue to be conflicting data regarding the outcomes of people with HIV (PWH) who have COVID-19 infection with most studies describing the early epidemic. We present a single site experience spanning a later timeframe from the first report on January 21, 2020 to January 20, 2021 and describe clinical outcomes and predictors of hospitalization among a cohort of PWH in an urban center in Connecticut, USA. Among 103 PWH with controlled HIV disease, hospitalization occurred in 33% and overall mortality was 1%. HIV associated factors (CD4 count, HIV viral suppression) were not associated with hospitalization. Chronic lung disease (OR: 3.35, 95% CI:1.28-8.72), and cardiovascular disease (OR: 3.4, 95% CI:1.27-9.12) were independently associated with hospitalization. An increasing number of non-communicable comorbidities increased the likelihood of hospitalization (OR: 1.61, 95% CI:1.22-2.13).


Subject(s)
COVID-19/diagnosis , HIV Infections/pathology , Hospitalization/statistics & numerical data , Adult , Age Factors , Aged , CD4 Lymphocyte Count , COVID-19/complications , COVID-19/virology , Cardiovascular Diseases/complications , Comorbidity , Connecticut , Female , HIV Infections/complications , HIV Infections/mortality , Humans , Male , Middle Aged , Noncommunicable Diseases/epidemiology , Odds Ratio , Retrospective Studies , Risk Factors , SARS-CoV-2/isolation & purification
4.
Nutrients ; 13(10)2021 Sep 23.
Article in English | MEDLINE | ID: covidwho-1438683

ABSTRACT

The body of knowledge on alcohol use and communicable diseases has been growing in recent years. Using a narrative review approach, this paper discusses alcohol's role in the acquisition of and treatment outcomes from four different communicable diseases: these include three conditions included in comparative risk assessments to date-Human Immunodeficiency Virus (HIV)/AIDS, tuberculosis (TB), and lower respiratory infections/pneumonia-as well as Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) because of its recent and rapid ascension as a global health concern. Alcohol-attributable TB, HIV, and pneumonia combined were responsible for approximately 360,000 deaths and 13 million disability-adjusted life years lost (DALYs) in 2016, with alcohol-attributable TB deaths and DALYs predominating. There is strong evidence that alcohol is associated with increased incidence of and poorer treatment outcomes from HIV, TB, and pneumonia, via both behavioral and biological mechanisms. Preliminary studies suggest that heavy drinkers and those with alcohol use disorders are at increased risk of COVID-19 infection and severe illness. Aside from HIV research, limited research exists that can guide interventions for addressing alcohol-attributable TB and pneumonia or COVID-19. Implementation of effective individual-level interventions and alcohol control policies as a means of reducing the burden of communicable diseases is recommended.


Subject(s)
Alcoholism/epidemiology , COVID-19/epidemiology , Global Burden of Disease/statistics & numerical data , HIV Infections/epidemiology , Respiratory Tract Infections/epidemiology , Tuberculosis/epidemiology , Communicable Diseases/epidemiology , Comorbidity , Humans , Risk , SARS-CoV-2
5.
J Subst Abuse Treat ; 129: 108387, 2021 10.
Article in English | MEDLINE | ID: covidwho-1174394

ABSTRACT

OBJECTIVE: The COVID-19 pandemic has exacerbated health disparities, particularly among at-risk people with opioid use disorder (OUD). We sought to characterize the direct and indirect impacts of COVID-19 on this group to understand how the pandemic has affected this group, this group's public health response to COVID-19, and whether there were differences by race/ethnicity. METHODS: This study recruited its sample from a drug treatment setting in the northeast region of the United States. We surveyed 110 individuals on methadone as treatment for OUD and assessed COVID-19-related impacts on their health behaviors and other indices of social, physical, and mental well-being, including sexual health behaviors, substance use, mental health status, health care access, income, and employment. RESULTS: Our findings highlight overall increases in depression, anxiety, loneliness, and frustration among the sample of people with OUD; the study also observed decreases in financial stability. Significant differences between groups indicated a greater financial burden among racial-ethnic minorities; this subgroup also reported greater direct adverse effects of COVID-19, including being more concerned about contracting COVID-19, not being able to get a COVID-19 test, and knowing someone who had died from COVID-19. A greater proportion of Whites indicated increases in alcohol consumption and non-prescription drug use than did racial-ethnic minorities. CONCLUSIONS: Treatment providers must be vigilant in managing direct and indirect outcomes of COVID-19 among people with OUD. Findings highlight the need to develop culturally competent, differentiated interventions in partnership with community-based organizations to meet the unique challenges that the COVID-19 pandemic presents for people in treatment for OUD.


Subject(s)
COVID-19 , Opioid-Related Disorders , Ethnicity , Humans , Opioid-Related Disorders/epidemiology , Pandemics , SARS-CoV-2 , United States
6.
Clin Lymphoma Myeloma Leuk ; 20(11): 720-723, 2020 11.
Article in English | MEDLINE | ID: covidwho-614242
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