About: Qualitative

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : Qualitative Goto Sponge NotDistinct Permalink

Attributs	Valeurs
type	Concept
rdfs:label	Qualitative
skos:inScheme	http://hub.abes.fr/referentiel/bmjarticlecategories
is Subject of	Inpatients had mostly negative experiences of seclusion during short term treatment in a mental health facility General practitioners often used emotional responses for “referrals away” and intellectual decision making for “referrals to” in patients with mild depression and/or anxiety Dying patients with cancer reflected on implications of euthanasia Different attitudes towards mental health revealed in a survey of nurses across five European countries; more positive attitudes found in Portugal, in women and in those in senior roles Becoming a long term survivor of AIDS involved 5 dimensions of adapting Parental perception of stress during a child's health crisis was represented by 4 dimensions Patients' experiences of healing a venous ulcer were described as “forever healing” which affected their activities and treatment Discovering a sense of difference was the main experience of growing up with cystic fibrosis Integrating hearing loss was a complex and dynamic process for patients Adults with chronic low back pain felt frustrated, unsupported, and powerless with healthcare, social, and legal systems Teenage mothers with oppressive pasts created new family caregiving traditions Adolescents from different socioeconomic backgrounds had different attitudes about teen pregnancy People at high risk for STDs used a variety of primary and secondary prevention strategies Women with polycystic ovarian syndrome had excess hair, irregular or absent menstruation, and infertility and felt freakish, abnormal, and not proper women Patients with heart failure had inadequate information about the disease and lacked the tools for optimal self care The media contributed to the knowledge and decision making of patients throughout their cancer experiences Young women described the benefits of having advance supplies of emergency contraception but emphasised its use as a “last resort” rather than an alternative form of contraception Patient-provider communication about sexuality and intimacy after a cancer diagnosis was described in terms of unmet needs and mismatched expectations Families with loved ones on mechanical ventilation in the ICU found a way to face “living with dying” Loss of continuity and lack of closure in therapeutic relationships were associated with feelings of abandonment at the transition to end of life care Following bereavement, poor health is more likely in carers who perceived that their support from health services was insufficient or whose family member did not die in the carer's preferred place of death Families with children diagnosed with cancer used various strategies to create a new normal routine Review: patients living with diabetes mellitus focus on learning to balance by assuming control for the management of their illness Fatigue in HIV infection was perceived as a barometer of disease progression Nurses and family caregivers of elderly relatives engaged in 4 evolving types of relationships Chronic pain affected the way individuals viewed their bodies, their relationships with others, and their sense of time The experiences of patients with rheumatoid arthritis admitted to hospital focused on 5 interrelated themes Stories of both agency and acceptability were identified in accounts of HIV infected individuals having unprotected sex Individuals taking combination therapies for HIV or AIDS faced barriers to remaining in, or returning to work Parents of adult children with schizophrenia dealt with societal objections in order to provide the necessary care 3 themes described how self care management was learned and experienced by patients with chronic illness Promotion of physical activity and healthy food choices was hampered by competitiveness, lack of quality food, easy access to non-nutritious food, and time constraints Patients used the internet to transform their cancer experiences Facilitated advance care planning in end stage renal disease positively enhanced patients’ hope Resilience was not necessarily a healthy concept for adolescents in inner city vocational high schools 5 categories of coping described how people who were admitted to hospital for psychotic disorders used narrative to integrate their self with their illness Patients with terminal illness and their healthcare providers preferred a dosed and gradual process of truth-telling Women kept up appearances and developed multiple coping strategies to deal with menopause Adolescent girls and boys differed in how they incorporated diabetes into their identities and how they managed the illness Patients who attempted suicide emphasised they wanted to be well cared for and receive understanding and confirmation Parents' perceptions of obtaining a diagnosis of childhood cancer can include experiences of disputes and delays Older people perceived health as going and doing something meaningful Living with untreated localised prostate cancer was seen as living under a dark shadow Women with ovarian cancer described waiting for recurrence, facing the diagnosis of recurrence, managing treatment related concerns, and attempting to regain control Review: mothers with HIV infection worked hard to protect their children and preserve a positive maternal identity Mothers’ decisions about MMR vaccination were framed by their children’s vulnerabilities and wider social trends Perceived barriers and benefits were factors in decision making about colorectal screening Patterns of tobacco use became an integral component of intimate partner relationships Patients with recently diagnosed hypertension described risk in terms of acceptance and denial narratives, which served as personal frameworks of coping Adolescents managed their asthma or diabetes in gendered ways with the aim of projecting different gendered identities Physically injured patients described several forms of post-traumatic concerns Peer relationships were important to the experience of thriving in some, but not all, nursing home residents Men experienced and responded to the embodied and emotional effects of prostate cancer in different ways Decision making between women and their caregivers during labour ranged from being unilateral to joint and was associated with various emotions Adults with chronic lung disease had fatigue with laboured breathing that interfered with daily living, but coped well Helping, mutual sharing, committing, and benefiting described the peer advisor experience of providing social support Patients in stroke units have better outcomes, but receive less personal nursing care People with enduring mental health problems described the importance of communication, continuity of care, and stigma The lived experience of men with erectile dysfunction was reflected in the themes of loss and being alone with it Arthritis symptoms, information sources, and a constantly shifting threshold of risk-benefit ratios influenced elderly patients’ decisions about total joint replacement The complex self perceptions and relationships of patients who attended free clinics affected their attendance and ability to benefit from care Conflicts within and between patients and health professionals characterised poorly controlled diabetes Inpatients felt that pressure ulcers had emotional, mental, physical, and social effects on quality of life because nurses did not adequately treat or manage their pain or discomfort Therapists of patients who committed suicide reported a wide range of emotional responses Carers living with stroke survivors who were incontinent had minimal social interaction and felt socially isolated Nurses’ triage assessments were affected by patients’ behaviours and stories and their perceived credibility Patients with cancer believed that chemotherapy had to “hurt” or “cause side effects” to be effective Survey of people with type 2 diabetes shows the majority prefer diabetes education to be given during regular diabetes check-ups; other education preferences and opinions on self-care vary depending on patient characteristics Environmental issues affected women's caring Review: research on chronic illness has shifted towards viewing the individual as empowered and a partner in the health management process Women's decisions to seek evaluation of self discovered breast symptoms occurred in a complex social context Dealing with a family member who has a mental illness was a long term, frustrating, and confusing process before acceptance occurred Men's experiences of coping with their wives' breast cancer involved focusing on the cancer and treatment and focusing on family to keep life going Inpatients had mostly negative experiences of seclusion during short term treatment in a mental health facility Parents’ accounts of their children’s respiratory symptoms showed a range of interpretations Gender, age, religion, and tradition influenced the smoking attitudes and behaviour of Bangladeshi and Pakistani adults Adolescents struggled to maintain a sense of control over their cigarette smoking through a 4 phase cycle Expressed desire for hastened death by patients with advanced cancer had several meanings and uses “Multiple margins” (being older, a woman, or a visible minority) constrained older women’s access to Canadian health care Review: delays in help seeking for cancer symptoms related to recognition and interpretation of symptoms and fear of consultation and were affected by gender and sanctioning of help seeking Review: meta-analysis of qualitative studies generated recommendations for healthcare professionals meeting with women who had experienced intimate partner violence People with cardiovascular disease identified 5 areas of medication-related problems that influenced adherence and informed decision making Young children experienced marked insecurity and grief after parental divorce and perceived legal professionals as exacerbating difficulties Women’s experiences of myocardial infarction were described in terms of gradual onset, not having chest pain, and responding to symptoms CAM therapies were used as treats and as alternative, complementary, and conventional treatments Parents experienced cycles of defining and managing adversity in caring for a child with a chronic progressive illness Commonalities were found in meanings, situations, and life experiences of women who survived breast cancer The experience of giving up smoking was described as encompassing 7 major categories Homeless people preserved former identities, devalued current identities, and envisioned a non-homeless future Practitioners' actions inhibited patient participation in self care decision making Gate keeping and legitimisation were central in the interactions between informal carers of older people and healthcare workers Women associated vaginal symptoms with disease and sexual infidelity The experiences of children and adolescents living with ADHD were reflected in 6 themes The experiences of women who survived an attempt on their lives by an intimate partner represented a wide spectrum of previous violence and control issues in the relationship Adolescents’ conceptualisations of depression (a helpful label, chronic medical problem, or personality characteristic) affected their attitudes and decisions about treatment Parents of young people with mental health problems experienced a deskilling and had to learn to reskill themselves 4 themes described the sexual concerns and educational needs of patients with an implantable cardioverter defibrillator

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata