Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 37
Filter
1.
PLoS One ; 13(8): e0201437, 2018.
Article in English | MEDLINE | ID: mdl-30110350

ABSTRACT

Lesbian, gay, bisexual, trans, and/or queer (LGBTQ) people face barriers to accessing mental health care; however, we know little about service experiences of low income LGBTQ people. In this qualitatively-driven mixed methods study, over 700 women and/or trans people completed an internet survey, of whom 12 LGBTQ individuals living in poverty participated in interviews. Low income LGBTQ respondents saw more mental health professionals and had more unmet need for care than all other LGBTQ/income groups. Narrative analysis illustrated the work required to take care of oneself in the context of extreme financial constraints. These findings highlight the mechanisms through which inadequate public sector mental health services can serve to reproduce and sustain both poverty and health inequities.


Subject(s)
Health Services Accessibility , Mental Disorders/epidemiology , Mental Health Services , Poverty , Sexual and Gender Minorities , Adult , Female , Humans , Male , Mental Disorders/therapy , Middle Aged , Ontario
2.
Health Soc Care Community ; 25(3): 1139-1150, 2017 05.
Article in English | MEDLINE | ID: mdl-28098398

ABSTRACT

This article uses an intersectionality lens to explore how experiences of race, gender, sexuality, class and their intersections are associated with depression and unmet need for mental healthcare in a population of 704 women and transgender/gender liminal people from Ontario, Canada. A survey collecting demographic information, information about mental health and use of mental healthcare services, and data for the Everyday Discrimination Scale and the PHQ-9 Questionnaire for Depression was completed by 704 people via Internet or pen-and-paper between June 2011 and June 2012. Bivariate and regression analyses were conducted to assess group differences in depression and discrimination experiences, and predictors of depression and unmet need for mental healthcare services. Analyses revealed that race, gender, class and sexuality all corresponded to significant differences in exposure to discrimination, experiences of depression and unmet needs for mental healthcare. Use of interaction terms to model intersecting identities and exclusion contributed to explained variance in both outcome variables. Everyday discrimination was the strongest predictor of both depression and unmet need for mental healthcare. The results suggest lower income and intersections of race with other marginalised identities are associated with more depression and unmet need for mental healthcare; however, discrimination is the factor that contributes the most to those vulnerabilities. Future research can build on intersectionality theory by foregrounding the role of structural inequities and discrimination in promoting poor mental health and barriers to healthcare.


Subject(s)
Depression/epidemiology , Sexual and Gender Minorities/psychology , Social Discrimination , Female , Health Services Needs and Demand , Humans , Mental Health Services , Ontario/epidemiology
3.
J Womens Health (Larchmt) ; 26(2): 116-127, 2017 02.
Article in English | MEDLINE | ID: mdl-27898255

ABSTRACT

BACKGROUND: Previous studies have found that transgender, lesbian, and bisexual people report poorer mental health relative to heterosexuals. However, available research provides little information about mental health service access among the highest need groups within these communities: bisexual women and transgender people. This study compared past year unmet need for mental health care and untreated depression between four groups: heterosexual cisgender (i.e., not transgender) women, cisgender lesbians, cisgender bisexual women, and transgender people. MATERIALS AND METHODS: This was a cross-sectional Internet survey. We used targeted sampling to recruit 704 sexual and gender minority people and heterosexual cisgendered adult women across Ontario, Canada. To ensure adequate representation of vulnerable groups, we oversampled racialized and low socioeconomic status (SES) women. RESULTS: Trans participants were 2.4 times (95% confidence intervals [CI] = 1.6-3.8, p < 0.01) and bisexual people 1.8 times (95% CI = 1.1-2.9, p = 0.02) as likely to report an unmet need for mental healthcare as cisgender heterosexual women. Trans participants were also 1.6 times (95% CI = 1.0-27, p = 0.04) more likely to report untreated depression. These differences were not seen after adjustment for social context factors such as discrimination and social support. CONCLUSION: We conclude that there are higher rates of unmet need and untreated depression in trans and bisexual participants that are partly explained by differences in social factors, including experiences of discrimination, lower levels of social support, and systemic exclusion from healthcare. Our findings suggest that the mental health system in Ontario is not currently meeting the needs of many sexual and gender minority people.


Subject(s)
Depression/epidemiology , Health Services Needs and Demand , Healthcare Disparities/statistics & numerical data , Mental Health Services , Sexual and Gender Minorities/psychology , Transgender Persons/psychology , Adult , Aged , Cross-Sectional Studies , Female , Humans , Internet , Logistic Models , Male , Middle Aged , Ontario , Social Class , Surveys and Questionnaires , Young Adult
4.
J Sex Med ; 13(11): 1765-1772, 2016 11.
Article in English | MEDLINE | ID: mdl-27693265

ABSTRACT

INTRODUCTION: Spironolactone and cyproterone acetate (CPA) are the two main antiandrogen medications used in feminizing hormone therapy in transgender women. Previous studies have suggested that these two agents might have opposite effects on high-density lipoprotein (HDL) level when used in this context, and limited data have suggested CPA increases prolactin more than spironolactone. AIM: To compare the effects of spironolactone and CPA on HDL and prolactin serum concentrations in transgender women. METHODS: A retrospective chart review was conducted at three clinical sites in Toronto, Ontario, Canada. Patients were selected if they (i) identified as a transgender woman, (ii) had newly started spironolactone or CPA with estrogen or restarted spironolactone or CPA after a washout period of at least 6 months, and (iii) had not used other antiandrogens within the previous 6 months. MAIN OUTCOME MEASURES: HDL and prolactin concentrations between the two treatment groups at baseline and at 12 months. RESULTS: Eighty-two patients were included in the spironolactone group and 31 patients were included in the CPA group. Baseline HDL and prolactin levels were not significantly different between the two groups. At 12 months, HDL increased by 0.10 mmol/L (SD = 0.24) in the spironolactone group but decreased by 0.07 mmol/L (SD = 0.21) in the CPA group (P = .002). The difference remained significant after adjusting for baseline HDL, use of lipid-lowering drugs, and age. The change in prolactin was +3.10 µg/L (SD = 5.70) in the spironolactone group and +11.8 µg/L (SD = 8.63) in the CPA group (P < 0.001). This difference also remained significant after adjusting for baseline prolactin level. CONCLUSION: These data suggest that spironolactone use in transgender women increases HDL levels and that CPA has the opposite effect. CPA also is associated with a larger increase in prolactin. These factors should be considered when choosing between these two antiandrogen agents.


Subject(s)
Androgen Antagonists/therapeutic use , Cyproterone Acetate/therapeutic use , Lipoproteins, HDL/drug effects , Prolactin/drug effects , Spironolactone/therapeutic use , Transsexualism/drug therapy , Adult , Canada , Cyproterone/therapeutic use , Drug Therapy, Combination , Estrogens/therapeutic use , Female , Humans , Lipoproteins, HDL/metabolism , Male , Prolactin/metabolism , Retrospective Studies , Sex Reassignment Surgery/methods , Transgender Persons
5.
Dis Colon Rectum ; 59(9): 836-42, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27505112

ABSTRACT

BACKGROUND: High-grade intraepithelial neoplasia is known to progress to invasive squamous-cell carcinoma of the anus. There are limited reports on the rate of progression from high-grade intraepithelial neoplasia to anal cancer in HIV-positive men who have sex with men. OBJECTIVES: The purpose of this study was to describe in HIV-positive men who have sex with men with perianal high-grade intraepithelial neoplasia the rate of progression to anal cancer and the factors associated with that progression. DESIGN: This was a prospective cohort study. SETTINGS: The study was conducted at an outpatient clinic at a tertiary care center in Toronto. PATIENTS: Thirty-eight patients with perianal high-grade anal intraepithelial neoplasia were identified among 550 HIV-positive men who have sex with men. INTERVENTION: All of the patients had high-resolution anoscopy for symptoms, screening, or surveillance with follow-up monitoring/treatment. MAIN OUTCOME MEASURES: We measured the incidence of anal cancer per 100 person-years of follow-up. RESULTS: Seven (of 38) patients (18.4%) with perianal high-grade intraepithelial neoplasia developed anal cancer. The rate of progression was 6.9 (95% CI, 2.8-14.2) cases of anal cancer per 100 person-years of follow-up. A diagnosis of AIDS, previously treated anal cancer, and loss of integrity of the lesion were associated with progression. Anal bleeding was more than twice as common in patients who progressed to anal cancer. LIMITATIONS: There was the potential for selection bias and patients were offered treatment, which may have affected incidence estimates. CONCLUSIONS: HIV-positive men who have sex with men should be monitored for perianal high-grade intraepithelial neoplasia. Those with high-risk features for the development of anal cancer may need more aggressive therapy.


Subject(s)
Anal Canal/pathology , Anus Neoplasms/pathology , Carcinoma in Situ/pathology , Carcinoma, Squamous Cell/pathology , HIV Infections/complications , Homosexuality, Male , Precancerous Conditions/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Anus Neoplasms/diagnosis , Anus Neoplasms/epidemiology , Anus Neoplasms/etiology , Carcinoma in Situ/diagnosis , Carcinoma in Situ/epidemiology , Carcinoma in Situ/etiology , Carcinoma, Squamous Cell/diagnosis , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/etiology , Disease Progression , Follow-Up Studies , Humans , Incidence , Male , Middle Aged , Neoplasm Grading , Precancerous Conditions/diagnosis , Precancerous Conditions/epidemiology , Precancerous Conditions/etiology , Prospective Studies , Risk Factors , Young Adult
6.
BMC Health Serv Res ; 15: 336, 2015 Aug 20.
Article in English | MEDLINE | ID: mdl-26290068

ABSTRACT

BACKGROUND: Given that immigration has been linked to a variety of mental health stressors, understanding use of mental health services by immigrant groups is particularly important. However, very little research on immigrants' use of mental health service in the host country considers source country. Newcomers from different source countries may have distinct experiences that influence service need and use after arrival. This population study examined rates of use of primary care and of specialty services for non-psychotic mental health disorders by immigrants to Ontario Canada during their first five years after arrival. Service use by recent immigrants in broad source region groups representing all world regions was compared to use by age-matched Canadian-born or long term immigrants (called long term residents). METHOD: This matched population-based cross-sectional study assessed likelihood of any use and counts of visits for each of primary care, psychiatric care and hospital care (emergency department visits or inpatient admissions) for non-psychotic mental health disorders from 1993-2012. Adult immigrants living in urban Ontario (n = 912,114) were categorized based on their nine world regions of origin. Sex-stratified conditional logistic regression models and negative binomial models were used to compare service use by immigrant region groups to their age-matched long term residents. RESULTS: Immigrant were more or less likely to access primary mental health care compared to age-matched long term residents, depending on their world region of origin. Regarding specialty mental health care (psychiatry and hospital care), immigrants from all regions used less than long term residents. Across the three mental health services, estimates of use by immigrant region groups compared to long term residents were among the lowest for newcomers from East Asian and Pacific (range: 0.16-0.82) and among the highest for persons from Middle East and North Africa (range: 0.56-1.23). CONCLUSION: This population-based study showed lower use of mental health services by recent immigrants than long-term immigrants or native born individuals, with variation in immigrants' use linked to world region of origin and type of mental health care. Variation across source region groups underscores the importance of identifying underlying individual characteristics that affect service use to make services more responsive to newcomers.


Subject(s)
Emigrants and Immigrants , Mental Health Services/statistics & numerical data , Adult , Cross-Sectional Studies , Emergency Service, Hospital , Female , Health Services Needs and Demand , Humans , Logistic Models , Male , Mental Disorders/therapy , Middle Aged , Ontario/epidemiology , Primary Health Care/statistics & numerical data , Young Adult
7.
Ann Fam Med ; 13(4): 343-6, 2015.
Article in English | MEDLINE | ID: mdl-26195679

ABSTRACT

PURPOSE: Reports of bupropion misuse have increased since it was first reported in 2002. The purpose of this study was to explore trends in bupropion prescribing suggestive of misuse or diversion in Ontario, Canada. METHODS: A serial cross-sectional study was conducted of Ontarians aged younger than 65 years who received prescriptions under Ontario's public drug program from April 1, 2000, to March 31, 2013. We determined the number of potentially inappropriate prescriptions in each quarter, defined as early refills dispensed within 50% of the duration of the preceding prescription, as well as potentially duplicitous prescriptions, defined as similarly early refills originating from a different prescriber and different pharmacy. We replicated these analyses for citalopram and sertraline, antidepressants not known to be prone to abuse. RESULTS: We identified 1,780,802 prescriptions for bupropion, 3,402,462 for citalopram, and 1,775,285 for sertraline. Rates of early refills for bupropion declined during the study from 4.8% to 3.1%. In the final quarter, rates of early refills for bupropion were more common than for citalopram (3.1% vs 2.2%) (P <.001) but not for sertraline (3.1% vs 2.9%) (P =.16). Potentially duplicitous prescriptions for bupropion increased dramatically, from <0.05% of all prescriptions in early 2000 to 0.47% in early 2013 and by the final quarter were more common than both citalopram (0.11%) and sertraline (0.12%) (P <.001). CONCLUSIONS: Although no marked differences were seen for early refills of bupropion relative to its comparators, potentially duplicitous prescriptions have increased dramatically in Ontario, suggesting growing misuse of the drug.


Subject(s)
Antidepressive Agents/administration & dosage , Bupropion/administration & dosage , Inappropriate Prescribing/statistics & numerical data , Prescription Drug Misuse/statistics & numerical data , Citalopram/administration & dosage , Cross-Sectional Studies , Female , Humans , Male , Ontario , Pharmacies , Sertraline/administration & dosage
8.
J Subst Abuse Treat ; 57: 30-5, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26014916

ABSTRACT

We aimed to examine pharmacologic, demographic and medical comorbidity risk factors for opioid-related mortality among patients currently receiving methadone for an opioid use disorder. We conducted a population-based, nested case-control study linking healthcare and coroner's records in Ontario, Canada, from January 31, 1994 to December 31, 2010. We included social assistance recipients receiving methadone for an opioid use disorder. Within this group, cases were those who died of opioid-related causes. For each case, we identified up to 5 controls matched on calendar quarter. The primary analysis examined the association between use of psychotropic drugs (benzodiazepines, antidepressants or antipsychotics) and opioid-related mortality. Secondary analyses examined the associations between baseline characteristics, health service utilization, comorbidities and opioid-related mortality. Among 43,545 patients receiving methadone for an opioid use disorder, we identified 175 (0.4%) opioid-related deaths, along with 873 matched controls. Psychotropic drug use was associated with a two fold increased risk of opioid-related death (adjusted odds ratio (OR) 2.0; 95% confidence interval (CI) 1.2 to 3.5). Specifically, benzodiazepines (adjusted OR 1.6; 95% CI 1.1 to 2.5) and antipsychotics (adjusted OR 2.3; 95% CI 1.5 to 3.5) were independently associated with opioid-related death. Other associated factors included chronic lung disease (adjusted OR 1.7; 95% CI 1.2 to 2.6), an alcohol use disorder (adjusted OR 1.9; 95% CI 1.2 to 3.2), mood disorders (adjusted OR 1.8; 95% CI 1.0 to 3.2), and a history of heart disease (adjusted OR 5.3; 95% CI 2.0 to 14.0). Psychotropic drug use is associated with opioid-related death in patients receiving methadone. Mindfulness of these factors may reduce the risk of death among methadone recipients.


Subject(s)
Analgesics, Opioid/therapeutic use , Methadone/therapeutic use , Opiate Substitution Treatment/statistics & numerical data , Opioid-Related Disorders/mortality , Adult , Case-Control Studies , Female , Humans , Male , Middle Aged , Ontario/epidemiology , Risk Factors
9.
BMJ Open ; 5(3): e006690, 2015 Mar 13.
Article in English | MEDLINE | ID: mdl-25770230

ABSTRACT

OBJECTIVE: While newcomers are often disproportionately concentrated in disadvantaged areas, little attention is given to the effects of immigrants' postimmigration context on their mental health and care use. Intersectionality theory suggests that understanding the full impact of disadvantage requires considering the effects of interacting factors. This study assessed the inter-relationship between recent immigration status, living in deprived areas and service use for non-psychotic mental health disorders. STUDY DESIGN: Matched population-based cross-sectional study. SETTING: Ontario, Canada, where healthcare use data for 1999-2012 were linked to immigration data and area-based material deprivation scores. PARTICIPANTS: Immigrants in urban Ontario, and their age-matched and sex-matched long-term residents (a group of Canadian-born or long-term immigrants, n=501,417 pairs). PRIMARY AND SECONDARY OUTCOME MEASURES: For immigrants and matched long-term residents, contact with primary care, psychiatric care and hospital care (emergency department visits or inpatient admissions) for non-psychotic mental health disorders was followed for 5 years and examined using conditional logistic regression models. Intersectionality was investigated by including a material deprivation quintile by immigrant status (immigrant vs long-term resident) interaction. RESULTS: Recent immigrants in urban Ontario were more likely than long-term residents to live in most deprived quintiles (immigrants--males: 22.8%, females: 22.3%; long-term residents--both sexes: 13.1%, p<0.001). Living in more deprived circumstances was associated with greater use of mental health services, but increases were smaller for immigrants than for long-term residents. Immigrants used less mental health services than long-term residents. CONCLUSIONS: This study adds to existing research by suggesting that immigrant status and deprivation have a combined effect on recent immigrants' care use for non-psychotic mental health disorders. In settings where immigrants are over-represented in deprived areas, policymakers focused on increasing immigrants' access of mental health services should broadly address the influence of structural and cultural factors beyond the disadvantage.


Subject(s)
Emigrants and Immigrants , Emigration and Immigration , Mental Disorders/therapy , Mental Health Services/statistics & numerical data , Patient Acceptance of Health Care , Poverty , Residence Characteristics , Adolescent , Adult , Aged , Cross-Sectional Studies , Female , Health Services Accessibility , Humans , Logistic Models , Male , Middle Aged , Ontario , Primary Health Care , Socioeconomic Factors , Vulnerable Populations , Young Adult
10.
Can Fam Physician ; 61(6): 538-543, 2015 Jun.
Article in English | MEDLINE | ID: mdl-30207979

ABSTRACT

OBJECTIVE: To explore family physicians' attitudes toward prescribing naloxone to at-risk opioid users, as well as to determine the opportunities and challenges for expanding naloxone access to patients in family practice settings. DESIGN: One-hour focus group session and SWOT (strengths, weaknesses, opportunities, and threats) analysis. SETTING: Workshop held at the 2012 Family Medicine Forum in Toronto, Ont. PARTICIPANTS: Seventeen conference attendees from 3 Canadian cities who practised in various family practice settings and who agreed to participate in the workshop. METHODS: The workshop included an overview of information about naloxone distribution and overdose education programs, followed by group discussion in smaller focus groups. Participants were instructed to focus their discussion on the question, "Could this [overdose education and naloxone prescription] work in your practice?" and to record notes using a standardized discussion guide based on a SWOT analysis. Two investigators reviewed the forms, extracting themes using an open coding process. MAIN FINDINGS: Some participants believed that naloxone could be used safely among family practice patients, that the intervention fit well with their clinical practice settings, and that its use in family practice could enhance engagement with at-risk individuals and create an opportunity to educate patients, providers, and the public about overdose. Participants also indicated that the current guidelines and support systems for prescribing or administering naloxone were inadequate, that medicolegal uncertainties existed for those who prescribed or administered naloxone, and that high-quality evidence about the intervention's effectiveness in family practice was lacking. CONCLUSION: Family physicians believe that overdose education and naloxone prescription might provide patients at risk of opioid overdose in their practices with broad access to a potentially lifesaving intervention. However, they explain that there are key barriers currently limiting widespread implementation of naloxone use in family practice settings.

11.
Healthc Policy ; 10(1): 31-45, 2014.
Article in English | MEDLINE | ID: mdl-25410694

ABSTRACT

PURPOSE: To examine service use by adults with serious mental illness (SMI) rostered in new primary care models: enhanced fee-for-service (FFS), blended-capitation (CAP) and team-based capitation (TBC) models with and without mental health workers (MHW) in Ontario. METHODS: This cross-sectional study used administrative health service databases to compare use of mental health and general health services among persons with SMI enrolled in new models (n = 125,233). RESULTS: Relative to persons rostered in enhanced FFS, those in CAP and TBC had fewer mental health primary care visits (adjusted rate ratios and 95% confidence limits: CAP: 0.77 [0.74, 0.81]; TBC with MHW: 0.72 [0.68, 0.76]; TBC with no MHW: 0.81 [0.72, 0.93]). Compared to patients in enhanced FFS, those in TBC models also had more mental health hospital admissions (TBC with MHW: 1.12 [1.05, 1.20]; TBC with no MHW: 1.22 [1.05, 1.41]). Patterns of use of general services were similar. CONCLUSION: Further attention to financial incentives in capitation that influence care of persons with SMI is necessary to determine if they are aligned with aims of primary care reform.


Subject(s)
Mental Disorders/therapy , Mental Health Services/statistics & numerical data , Cross-Sectional Studies , Databases, Factual , Female , Humans , Male , Models, Theoretical , Multivariate Analysis , Ontario , Primary Health Care
12.
Open Med ; 8(4): e136-46, 2014.
Article in English | MEDLINE | ID: mdl-25426182

ABSTRACT

BACKGROUND: Most Canadian newcomers are admitted in the economic, family, or refugee class, each of which has its own selection criteria and experiences. Evidence has shown various risks for mental health disorders across admission classes, but the respective service-use patterns for people in these classes are unknown. In this study, we compared service use for nonpsychotic mental health disorders by newcomers in various admission classes with that of long-term residents (i.e., Canadian-born persons or immigrants before 1985) in urban Ontario. METHODS: In this population-based matched cross-sectional study, we linked health service databases to the Ontario portion of the Citizenship and Immigration Canada database. Outcomes were mental health visits to primary care physicians, mental health visits to psychiatrists, and emergency department visits or hospital admissions. We measured service use for recent immigrants (those who arrived in Ontario between 2002 and 2007; n = 359 673). We compared service use by immigrants in each admission class during the first 5 years in Canada with use by age- and sex-matched long-term residents. We measured likelihood of access to each service and intensity of use of each service using conditional logistic regression and negative binomial models. RESULTS: Economic and family class newcomers were less likely than long-term residents to use primary mental health care. The use of primary mental health care by female refugees did not differ from that of matched long-term residents, but use of such care by male refugees was higher (odds ratio 1.14, 95% confidence interval 1.09-1.19). Immigrants in all admission classes were less likely to use psychiatric services and hospital services for mental health care. Exceptions were men in the economic and family classes, whose intensity of hospital visits was similar to that of matched long-term residents. INTERPRETATION: Immigrants in all admission classes generally used less care for nonpsychotic disorders than longterm residents, although male refugees used more primary care. Future research should examine how mental health needs align with service use, particularly for more vulnerable groups such as refugees.


Subject(s)
Emigrants and Immigrants/statistics & numerical data , Mental Health Services/statistics & numerical data , Primary Health Care/statistics & numerical data , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Cross-Sectional Studies , Female , Humans , Language , Male , Middle Aged , Ontario , Refugees/statistics & numerical data , Sex Factors , Socioeconomic Factors , Time Factors , Young Adult
13.
J Obstet Gynaecol Can ; 36(2): 146-153, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24518914

ABSTRACT

OBJECTIVE: To determine what recommendations lesbian, gay, bisexual, trans, and queer (LGBTQ) people have for provision of assisted human reproduction (AHR) services to their communities. METHODS: Using a semi-structured guide, we interviewed a purposeful sample of 66 LGBTQ-identified individuals from across the province of Ontario who had used or had considered using AHR services since 2007. RESULTS: Participants were predominantly cisgender (non-trans), white, same-sex partnered, urban women with relatively high levels of education and income. Participants made recommendations for changes to the following aspects of AHR service provision: (1) access to LGBTQ-relevant information, (2) adoption of patient-centred practices by AHR service providers, (3) training and education of service providers regarding LGBTQ issues and needs, (4) increased visibility of LGBTQ people in clinic environments, and (5) attention to service gaps of particular concern to LGBTQ people. CONCLUSION: Many of the recommendations made by study participants show how patient-centred models may address inequities in service delivery for LGBTQ people and for other patients who may have particular AHR service needs. Our results suggest that service providers need education to enact these patient-centred practices and to deliver equitable care to LGBTQ patients.


Objectif : Chercher à connaître les recommandations que formuleraient les personnes lesbiennes, gaies, bisexuelles, transgenres et allosexuelles (LGBTQ) en ce qui concerne l'offre de services de procréation assistée (PA) à leurs communautés. Méthodes : En utilisant un guide semi-structuré, nous avons interviewé un échantillon choisi à dessein de 66 personnes s'identifiant comme étant LGBTQ et provenant de partout dans la province de l'Ontario qui avaient utilisé ou qui avaient envisagé d'utiliser des services de PA depuis 2007. Résultats : Les participantes étaient principalement des femmes cisgenres (non transgenres), blanches, ayant une partenaire du même sexe et vivant en milieu urbain qui comptaient des niveaux relativement élevés de scolarité et de revenu. Les participantes ont formulé des recommandations visant l'apport de modifications aux aspects suivants de l'offre de services de PA : (1) accès à des renseignements pertinents pour les personnes LGBTQ, (2) adoption de pratiques axées sur la patiente par les fournisseurs de services de PA, (3) formation et éducation des fournisseurs de services à l'égard des enjeux et des besoins des personnes LGBTQ, (4) accroissement de la visibilité des personnes LGBTQ en milieu clinique et (5) octroi d'une attention aux lacunes en matière de services qui préoccupent particulièrement les personnes LGBTQ. Conclusion : Bon nombre des recommandations formulées par les participantes à l'étude illustrent la façon dont l'adoption de modèles axés sur la patiente pourrait combler les inégalités en ce qui concerne l'offre de services aux personnes LGBTQ et à d'autres patientes pouvant avoir des besoins particuliers en matière de PA. Nos résultats semblent indiquer que des ressources éducatives devraient être mises à la disposition des fournisseurs de services pour leur permettre de mettre en œuvre de telles pratiques axées sur les patientes et d'offrir des soins équitables aux patientes LGBTQ.


Subject(s)
Minority Groups , Reproductive Techniques, Assisted , Sexuality , Adult , Bisexuality , Female , Health Services Accessibility , Health Services Needs and Demand , Healthcare Disparities , Homosexuality, Female , Homosexuality, Male , Humans , Income , Male , Middle Aged , Ontario , Surveys and Questionnaires , Transgender Persons , Transsexualism , White People
14.
Open Med ; 7(1): e9-20, 2013.
Article in English | MEDLINE | ID: mdl-23687535

ABSTRACT

BACKGROUND: In Ontario, Canada, the patient-centred medical home is a model of primary care delivery that includes 3 model types of interest for this study: enhanced fee-for-service, blended capitation, and team-based blended capitation. All 3 models involve rostering of patients and have similar practice requirements but differ in method of physician reimbursement, with the blended capitation models incorporating adjustments for age and sex, but not case mix, of rostered patients. We evaluated the extent to which persons with mental illness were included in physicians' total practices (as rostered and non-rostered patients) and were included on physicians' rosters across types of medical homes in Ontario. METHODS: Using population-based administrative data, we considered 3 groups of patients: those with psychotic or bipolar diagnoses, those with other mental health diagnoses, and those with no mental health diagnoses. We modelled the prevalence of mental health diagnoses and the proportion of patients with such diagnoses who were rostered across the 3 medical home model types, controlling for demographic characteristics and case mix. RESULTS: Compared with enhanced fee-for-service practices, and relative to patients without mental illness, the proportions of patients with psychosis or bipolar disorders were not different in blended capitation and team-based blended capitation practices (rate ratio [RR] 0.91, 95% confidence interval [CI] 0.82-1.01; RR 1.06, 95% CI 0.96-1.17, respectively). However, there were fewer patients with other mental illnesses (RR 0.94, 95% CI 0.90-0.99; RR 0.89, 95% CI 0.85-0.94, respectively). Compared with expected proportions, practices based on both capitation models were significantly less likely than enhanced fee-for-service practices to roster patients with psychosis or bipolar disorders (for blended capitation, RR 0.92, 95% CI 0.90-0.93; for team-based capitation, RR 0.92, 95% CI 0.88-0.93) and also patients with other mental illnesses (for blended capitation, RR 0.94, 95% CI 0.92-0.95; for team-based capitation, RR 0.93, 95% CI 0.92-0.94). INTERPRETATION: Persons with mental illness were under-represented in the rosters of Ontario's capitation-based medical homes. These findings suggest a need to direct attention to the incentive structure for including patients with mental illness.


Subject(s)
Insurance, Health, Reimbursement , Mentally Ill Persons , Patient-Centered Care/statistics & numerical data , Adolescent , Adult , Aged , Capitation Fee , Confidence Intervals , Cross-Sectional Studies , Fee-for-Service Plans , Female , Humans , Male , Middle Aged , Odds Ratio , Ontario/epidemiology , Patient-Centered Care/economics , Sex Distribution , Young Adult
15.
Int J Telemed Appl ; 2012: 945745, 2012.
Article in English | MEDLINE | ID: mdl-23193395

ABSTRACT

Shoulder disorders are common, debilitating, and represent a considerable burden on society. As primary contact practitioners, physiotherapists play a large role in the management and rehabilitation of people with these conditions. For those living outside of urban areas, however, access to physiotherapy can be limited. The aim of this study was to evaluate the validity and reliability of using a telerehabilitation system to collect physical examination findings and correctly identify disorders of the shoulder. Twenty-two participants with 28 shoulder disorders were recruited and underwent a face-to-face physical examination and a remote telerehabilitation examination. Examination findings and diagnoses from the two modes of assessment were used to determine validity and reliability of the new method. Diagnostic agreement and agreement on individual findings between the two methods were found to be consistent with the reliability of conventional assessment methods. This study provides important preliminary findings on the validity and reliability of musculoskeletal examinations conducted via telerehabilitation.

16.
J Telemed Telecare ; 18(7): 413-8, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23086982

ABSTRACT

We examined the validity and reliability of a physiotherapy examination of the elbow, using telerehabilitation. The patho-anatomical diagnoses, systems diagnosis and physical examination findings of face-to-face physiotherapy examinations were compared with telerehabilitation examinations. Ten participants attended a single session, during which they were interviewed, a face-to-face physical examination was performed and a remote physical examination was conducted, guided by an examiner at a different location via a telerehabilitation system. Conventional face-to-face physiotherapy physical examination test results, diagnoses and systems diagnoses were compared to those produced by an examiner using the telerehabiliation system. There was substantial agreement for systems diagnosis (73%; P = 0.013) for validity and almost perfect agreement for intra-rater reliability (90%; P = 0.001). The inter-rater reliability had a weaker and non-significant agreement (64%; P = 0.11). Physical examination data demonstrated >68% agreement across all three datasets, between the examination methods. Performing a telerehabilitation physical examination to determine a musculoskeletal diagnosis of the elbow joint complex is both valid and reliable.


Subject(s)
Elbow/abnormalities , Musculoskeletal Diseases/diagnosis , Physical Examination/methods , Remote Consultation/methods , Adult , Female , Humans , Internet/statistics & numerical data , Male , Palpation/standards , Peripheral Nervous System , Physical Therapy Modalities , Reproducibility of Results
17.
Arch Womens Ment Health ; 14(3): 175-85, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21311926

ABSTRACT

Few studies have examined whether rural residence is associated with increased or decreased risk for postpartum depression (PPD). To address this research gap, this pilot study examined rates of depressive symptoms and perceived social support among women living in rural (population <10,000), semi-rural (population 10,000-20,000), and urban (downtown Toronto, population approximately 2.5 million) areas. Women were consecutively recruited at 25-35 weeks gestation from midwifery clinics and hospital-based prenatal care practices in two catchment areas and asked to complete a demographic questionnaire including postal code. On the basis of their responses, rural, semi-rural, and urban mothers were contacted by telephone at 36 weeks gestation (baseline) and 6-8 weeks postpartum (primary outcome). During each assessment, participants completed standardized measures of social connectedness, mental health, and health service utilization, including the Edinburgh Postnatal Depression Scale (EPDS) and the Medical Outcome Study Social Support Scale. A total of 87 participants [N = 23 rural (R), N = 23 semi-rural (SR), N = 41 urban (U)] were recruited into the study. There were no statistically significant differences between groups in mean EPDS scores during pregnancy (U = 7.1, SR = 5.3, R = 5.3, p = 0.15) or at 6 weeks postpartum (U = 5.3, SR = 4.4, R = 4.2, p = 0.43). The proportion of women with EPDS scores >12 similarly did not differ between groups. There were few statistically significant differences between groups on indicators of social connectedness; however, urban women reported significantly lower scores on measures of social network diversity and social capital than either the semi-rural or rural groups. This pilot study is limited by its small sample size; however, our data do not support the hypothesis that there are clinically important differences in risk for PPD associated with rural residence. Further studies examining potential relationships between indicators of social connectedness and perinatal mental health may be warranted.


Subject(s)
Attitude to Health , Depression/epidemiology , Life Change Events , Mothers/statistics & numerical data , Pregnancy Complications/epidemiology , Rural Population/statistics & numerical data , Adult , Catchment Area, Health , Depression/diagnosis , Female , Health Status , Humans , Interpersonal Relations , Mothers/psychology , Ontario/epidemiology , Pilot Projects , Pregnancy , Pregnancy Complications/diagnosis , Prenatal Care/methods , Social Support , Socioeconomic Factors , Urban Population/statistics & numerical data , Young Adult
18.
Health Soc Work ; 35(3): 191-200, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20853646

ABSTRACT

To date, there is little evidence to inform social work practice with lesbian and bisexual women who are trying to conceive (TTC). The authors report a preliminary examination of the mental health experiences of lesbian and bisexual women who are TTC, through a comparison with lesbian and bisexual women in the postpartum period (PP). Thirty-three lesbian and bisexual women (TTC, n = 15; PP, n = 18) completed standardized questionnaires assessing symptoms of depression and anxiety as well as relationship satisfaction and perceived social support. Qualitative interviews were also conducted to further investigate the experience of TTC. No significant differences were found between groups on any of the dependent variables. Analysis of qualitative data highlighted the challenges for lesbian and bisexual women who are TTC, particularly in terms of difficulty conceiving, lack of support during the conception process, and heterosexism in the fertility system. Women perceived these challenges to conception as having emotional consequences. The findings from this study begin to elucidate the unique context of TTC for lesbian and bisexual women, and they highlight the importance of culturally competent social work practice with this population.


Subject(s)
Bisexuality/psychology , Homosexuality, Female/psychology , Mental Health , Reproductive Techniques, Assisted/psychology , Adult , Anxiety , Case-Control Studies , Depression , Female , Humans , Ontario , Social Support , Social Work , Spouses/psychology
19.
Can J Public Health ; 101(3): 255-8, 2010.
Article in English | MEDLINE | ID: mdl-20737821

ABSTRACT

OBJECTIVES: Previous large-scale population studies have reported that gay and bisexual men may be at increased risk for health disparities. This study was conducted to determine whether health status and health risk behaviours of Canadian men vary based on sexual orientation identity. METHODS: Utilizing the Canadian Community Health Survey data (Cycle 2.1, 2003; n = 49,901), we conducted multivariable logistic regression to assess the independent effects of sexual orientation on health status and health risk behaviours. For all multivariate models, we calculated odds ratios, p-values, standard errors, and 95% confidence intervals (CIs) using the bootstrap re-sampling procedure recommended by Statistics Canada. RESULTS: When compared to heterosexual men, gay and bisexual men did not report more respiratory conditions; had lower rates of obesity and overweight BMI; and reported more mood/anxiety disorders, and a history of lifetime suicidality. Gay and bisexual men did not report higher rates of daily smoking or risky drinking, however, gay men reported an almost six-fold increase in STD diagnoses when compared to heterosexual men. CONCLUSION: This study represents the largest-known population-based data analysis on health risks and behaviours among men of varying sexual orientations. These findings raise important concerns regarding the impact of sexual orientation on mental and sexual health. Limitations of this data set, including those associated with measurement of sexual orientation, are discussed. Further research is required to understand the mechanisms that influence these health resiliencies and disparities.


Subject(s)
Health Status , Risk-Taking , Sexual Behavior , Adult , Bisexuality , Canada , Cross-Sectional Studies , Homosexuality, Male , Humans , Interviews as Topic , Logistic Models , Male , Middle Aged
20.
Women Health ; 49(5): 353-67, 2009.
Article in English | MEDLINE | ID: mdl-19851942

ABSTRACT

The current study sought to determine whether health status and health risk behaviors of Canadian women varied based on sexual identity. This was a cross-sectional analysis of data from the Canadian Community Health Survey: cycle 2.1, a national population-based survey designed to gather health data on a representative sample of over 135,000 Canadians including 354 lesbian respondents, 424 bisexual women respondents, and 60,937 heterosexual women respondents. Sexual orientation was associated with disparities in health status and health risk behaviors for lesbian and bisexual women in Canada. Bisexual women were more likely than lesbians or heterosexual women to report poor or fair mental and physical health, mood or anxiety disorders, lifetime STD diagnosis, and, most markedly, life-time suicidality. Lesbians and bisexual women were also more likely to report daily smoking and risky drinking than heterosexual women. In sum, sexual orientation was associated with health status in Canada. Bisexual women, in particular, reported poorer health outcomes than lesbian or heterosexual women, indicating this group may be an appropriate target for specific health promotion interventions.


Subject(s)
Health Status , Mental Health/statistics & numerical data , Sexuality/statistics & numerical data , Adult , Alcohol Drinking , Canada , Chi-Square Distribution , Cross-Sectional Studies , Female , Health Surveys , Humans , Middle Aged , Odds Ratio , Regression Analysis , Risk-Taking , Smoking , Surveys and Questionnaires , Women's Health
SELECTION OF CITATIONS
SEARCH DETAIL
...