ABSTRACT
OBJECTIVES: To examine if the COVID-19 pandemic is associated with a differential effect over a 2-year time period in relation to its psychological and social impact on patients with established anxiety disorders. METHODS: Semi-structured interviews were conducted with 21 individuals attending the Galway-Roscommon Mental Health Services in Ireland with an ICD-10 diagnosis of an anxiety disorder. Interviews occurred at three time-points over a 2-year period to determine the impact of the COVID-19 pandemic and associated restrictions on anxiety and depressive symptoms, social and occupational functioning, and quality of life. RESULTS: No statistical difference in symptomatology was noted between the three time-points in relation to anxiety symptoms as measured utilising psychometric rating scales (Beck Anxiety Inventory (BAI), Hamilton Anxiety Rating Scale (HARS) or Likert Scale measures). The greatest impact of COVID-19 at all time-points related to social functioning and quality of life. Significant variability was noted for individual participants. Qualitative analysis noted a tentative optimism for the future in the setting of vaccination and societal re-opening. Fear of re-emerging anxiety symptoms with the removal of societal restrictions was noted. CONCLUSIONS: No significant overall change in symptomatology or functioning over time was noted for individuals with pre-existing anxiety disorders, however variability was demonstrated, with some individuals describing ongoing anxiety, social isolation and concern for their future. A strong theme of hope for the future and less concern regarding the COVID-19 pandemic was evident; however tailored supports including the utilisation of tele-psychiatry is suggested, particularly for those experiencing increased anxiety with the removal of societal restrictions.
Subject(s)
COVID-19 , Humans , Pandemics , Quality of Life , Anxiety Disorders/epidemiology , Anxiety Disorders/psychology , AnxietyABSTRACT
OBJECTIVES: To examine if the COVID-19 pandemic is associated with a differential effect over time in relation to its psychological and social impact on patients with established anxiety disorders. METHODS: Semi-structured interviews were conducted with 24 individuals attending the Galway-Roscommon Mental Health Services with an International Classification of Diseases (ICD)-10 diagnosis of an anxiety disorder at two time points (six months apart) to determine the impact of the COVID-19 restrictions on anxiety and depressive symptoms, social and occupational functioning and quality of life. RESULTS: No statistical difference in symptomatology was noted between the two time points in relation to anxiety symptoms as measured by utilising psychometric rating scales (BAI and HARS) or utilising a Likert scale. The greatest impact of COVID-19 at both time points is related to social functioning and quality of life. Significant variability was noted for individual participants. Qualitative analysis noted social isolation, concern for the participants' future and increased difficulty managing anxiety with ongoing restrictions. CONCLUSIONS: No significant overall change in symptomatology or functioning over time was noted for individuals with pre-existing anxiety disorders. Variability was, however, demonstrated between individuals, with some individuals describing ongoing anxiety, social isolation and concern for their future. Identifying those with ongoing symptoms or distress and providing multidisciplinary support to this cohort is suggested.
Subject(s)
COVID-19 , Anxiety/epidemiology , Anxiety Disorders , Humans , Pandemics , Quality of Life , SARS-CoV-2ABSTRACT
The emergence of the COVID-19 pandemic has presented the addiction services with an unprecedented set of challenges. Opioid users are particularly vulnerable because of their high level of pre-existing health problems and lifestyle factors. In order to minimise their risks to self and to others in the current Covid-19 crisis, addiction services sought to urgently identify vulnerable individuals, and induct them into opioid substitution treatment (OST) promptly. Additionally, several guidelines were created and regularly updated by the health and safety executive (HSE) for any healthcare staff working with opioid users. These include guidance documents, to facilitate prompt induction of patients onto the OST programme, the prescribing of naloxone to all patients at risk of overdose, eConsultation, medication management for those in self-isolation, and the delivery of injecting equipment. The guidance documents and resources will provide a template for a new way of working for the sector during these challenging times and into the future.
Subject(s)
COVID-19 , Opioid-Related Disorders , Humans , Opiate Substitution Treatment , Opioid-Related Disorders/drug therapy , Opioid-Related Disorders/epidemiology , Pandemics , SARS-CoV-2ABSTRACT
The Women, Co-occurring Disorders, and Violence Study (WCDVS) was a multi-site cooperative study to evaluate new service models for women with co-occurring mental health and substance use disorders and a history of physical and/or sexual abuse. Despite common features in the service interventions and evaluation procedures, diversity across the nine sites plus differences introduced by non-random assignment led to numerous methodological challenges. This article describes the design, measurement, and analysis decisions behind the WCDVS and lays the foundation for understanding participant-level outcomes and service costs. This article also describes the study population, as recruited and following attrition at the 6-month follow-up, in order to address the threat of selection bias to inferences drawn from this multi-site study.
Subject(s)
Alcoholism/epidemiology , Child Abuse, Sexual/statistics & numerical data , Spouse Abuse/statistics & numerical data , Stress Disorders, Post-Traumatic/epidemiology , Substance-Related Disorders/epidemiology , Violence/statistics & numerical data , Women's Health Services/supply & distribution , Adult , Alcoholism/rehabilitation , Child , Child Abuse, Sexual/economics , Child Abuse, Sexual/rehabilitation , Comorbidity , Data Interpretation, Statistical , Female , Follow-Up Studies , Health Care Costs/statistics & numerical data , Health Services Needs and Demand/economics , Health Services Needs and Demand/statistics & numerical data , Health Services Research , Humans , Middle Aged , Outcome Assessment, Health Care/statistics & numerical data , Research Design , Spouse Abuse/economics , Spouse Abuse/prevention & control , Stress Disorders, Post-Traumatic/rehabilitation , Substance-Related Disorders/rehabilitation , United States , Violence/economics , Violence/prevention & control , Women's Health Services/economics , Women's Health Services/organization & administrationABSTRACT
BACKGROUND: A previous report of 5,782 trauma patients demonstrated higher mortality among those transported by emergency medical services (EMS) than among their non-EMS-transported counterparts. HYPOTHESIS: Trauma patients who are transported by EMS and those who are not differ in the injury-to-hospital arrival time interval. DESIGN: Prospective cohort-matched observation study. SETTING: Level I trauma center, multidisciplinary study group. PATIENTS: All non-EMS patients were matched with the next appropriate EMS patient by an investigator who was unaware of the outcome and mode of transport. Every 10th EMS patient with an Injury Severity Score (ISS) of 13 or greater was also randomly enrolled. Matching characteristics included age, ISS, mechanism of injury, head Abbreviated Injury Score, and presence of hypotension. An interview protocol was developed to determine the time of injury. Interview responses from patients, witnesses, and friends were combined with data obtained from police, sheriff, and medical examiner reports. MAIN OUTCOME MEASURES: Time to the hospital, mortality, morbidity, and length of stay. RESULTS: A total of 103 patients were enrolled (38 non-EMS, 38 EMS matched, 27 random EMS). Injury time was estimated using all available data made on 100 patients (97%). Independent raters agreed in 81% of cases. Deaths, complications, and length of hospital stay were similar between the EMS- and non-EMS-transported groups. Although time intervals were similar among the groups overall, more critically injured non-EMS patients (ISS > or = 13) got themselves to the trauma center in less time than their EMS counterparts (15 minutes vs 28 minutes; P<.05). CONCLUSIONS: A multidisciplinary approach can be utilized, and an interview protocol created to determine actual time of injury. Critically injured non-EMS-transported patients (ISS > or =13) arrived at the hospital earlier after their injuries.
Subject(s)
Critical Care , Emergency Medical Services , Multiple Trauma/therapy , Adolescent , Adult , California , Cohort Studies , Critical Care/statistics & numerical data , Emergency Medical Services/statistics & numerical data , Female , Hospital Mortality , Humans , Injury Severity Score , Length of Stay/statistics & numerical data , Male , Middle Aged , Multiple Trauma/mortality , Outcome and Process Assessment, Health Care , Patient Care Team , Prospective Studies , Time and Motion Studies , Trauma Centers/statistics & numerical dataABSTRACT
The present study utilized a longitudinal design to assess whether self-consistency or self-enhancement motives are predictive of future smoking onset. Participants were 1,222 nonsmoking 5th through 8th graders who were followed into the next academic year. The results showed that teens who were above the median in similarity between their self-image and smoker stereotype on coolness, sociability, and intelligence were almost twice as likely to show smoking onset at the 2nd measurement. This is supportive of a self-consistency motive for adolescent smoking. The results of this study provide an important extension to previous cross-sectional research in this area.