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ntroduction to Chron

part 1 module introduction to Chronic

TermDefinition
Chronic Illness A long-term health condition that persists over time, such as heart disease or diabetes.
Acute Illness: A health condition with a sudden onset and typically short duration.
Epidemiology: The study of how diseases spread and impact populations.
Morbidity: The rate of disease within a specific population.
Incidence: The number of new cases of a disease in a population during a specific time.
Prevalence: The total number of existing cases of a disease in a population at a given time.
Mortality: The death rate from a specific disease or within a population.
Cancer: A group of diseases characterized by the uncontrolled growth and spread of abnormal cells.
Diabetes: A chronic condition that affects how the body turns food into energy, leading to high blood sugar.
Cardiovascular Diseases: Conditions affecting the heart and blood vessels, such as heart disease and stroke.
Chronic Respiratory Diseases: Long-term diseases of the airways and other structures of the lungs, like asthma and COPD.
Indigenous Peoples: The original inhabitants of a land, who in Canada face significant health disparities.
Colonization: The process of establishing control over Indigenous peoples and their lands, with lasting negative impacts.
Intergenerational Trauma: Trauma that is passed down from one generation to the next.
Cultural Genocide: The deliberate destruction of the cultural heritage of a people.
Residential Schools: Government-sponsored schools aimed at assimilating Indigenous children, a source of trauma.
Structural Racism: Societal patterns and policies that create unequal outcomes based on race.
Social Determinants of Health: The social and economic conditions that influence health, such as income and education.
Health: A state of complete physical, mental, and social well-being, not just the absence of disease.
Disease: A medical condition diagnosed from a pathophysiological perspective.
Illness: The personal, lived experience of having a disease, including symptoms and suffering.
Signs: Objective, observable evidence of a disease.
Symptoms: Subjective feelings reported by the patient, such as pain.
Comorbidity: The presence of two or more unrelated disorders in the same person at the same time.
Multimorbidity: The presence of two or more chronic medical conditions in the same person.
Determinants of Health: The broad range of personal, social, economic, and environmental factors that influence health.
Lifestyle Factors: Personal behaviors that affect health, such as diet and exercise.
Social Environment: The social context, including relationships and community, that influences health behaviors.
Income: The amount of money a person or household earns, which impacts access to resources for health.
Education: A person's level of schooling, which is linked to better health outcomes.
Poverty: The state of having little or no money and few resources, a major risk factor for poor health.
Socioeconomic Disadvantage: Having a lower social and economic position, which increases health risks.
Risk Factors: Attributes or exposures that increase the likelihood of developing a disease.
Background Risk Factors: Non-modifiable factors like age, sex, and genetics.
Behavioural Risk Factors: Modifiable habits like smoking or poor diet.
Intermediate Risk Factors: Conditions like high blood pressure that result from other risks and lead to disease.
Community-Level Factors: Social and economic conditions in a community that affect health, like poverty and pollution.
Modifiable Risk Factors: Risk factors that can be changed or controlled.
Nonmodifiable Risk Factors: Risk factors that cannot be changed, like age or family history.
Hypertension: The medical term for high blood pressure.
Hyperlipidemia: High levels of lipids (fats) in the blood, such as cholesterol.
Overweight: Having more body weight than is considered normal or healthy for a certain height.
Obesity: A complex disease involving an excessive amount of body fat.
Prediabetes: A condition where blood sugar levels are higher than normal but not yet high enough for a diabetes diagnosis.
Prevention: Actions aimed at eradicating, delaying, or minimizing the impact of disease.
Genetics: The study of genes and their role in inheritance and disease.
Aging: The process of growing older, which increases the risk of chronic illness.
Disability: A complex interaction between a person's health condition and their environment, leading to limitations.
Medical Model of Disability: Views disability as a problem caused by a disease or trauma, requiring medical treatment.
Social Model of Disability: Views disability as a problem created by societal barriers and attitudes.
Biopsychosocial Model of Disability: An integrated model that combines medical and social perspectives.
Psychosocial Dimensions: The emotional, social, and mental aspects of living with a chronic illness.
Illness Behaviour: The ways in which individuals perceive, evaluate, and act upon their symptoms.
Sick Role: The socially recognized set of rights and obligations linked to being ill.
Self-Efficacy: A person's belief in their own ability to succeed in specific situations.
Mastery: The feeling of being in control of one's life and circumstances.
Vicarious Experience: Learning by observing others perform a behavior.
Verbal Persuasion: Being encouraged by others to believe in one's own capabilities.
Physiological States: Bodily states, such as stress or fatigue, that can influence self-efficacy.
Affective States: Emotional states or moods that can influence self-efficacy.
Health-Related Hardiness (HRH): A personality characteristic that helps people cope with chronic illness.
Mood Disorders: A category of mental health problems, including depression and anxiety.
Fatigue: Extreme tiredness resulting from mental or physical exertion or illness.
Stigma: A mark of disgrace associated with a particular circumstance, quality, or person.
Quality of Life: The general well-being of an individual or society
Health-Related Quality of Life (HRQL): An assessment of how a person's health affects their quality of life.
Caregiving: The act of providing assistance to someone who is ill or disabled.
Informal Caregiver: A person who provides care without pay, often a family member.
Caregiver Burden: The physical, emotional, and financial strain experienced by caregivers.
Conceptual Models: Theoretical frameworks used to understand an experience, like chronic illness.
Illness Trajectory: The experiential pathway a person follows as they live with an illness.
Crisis Phase: The initial stage of an illness trajectory, often involving diagnosis and acute treatment.
Chronic Phase: The long-term stage of living with and managing an illness.
Terminal Phase: The final stage of an illness trajectory as a person nears the end of life.
Shifting Perspectives Model: A model that views living with chronic illness as an ongoing process where focus shifts between illness and wellness.
Self-Management: The daily tasks individuals undertake to control their chronic illness and its impact.
Adherence: The extent to which a patient's behavior matches agreed recommendations from a healthcare provider.
Self-Care: The practice of individuals taking responsibility for their own health and well-being.
Chronic Care Model: A model for improving care for chronic illness by focusing on six system elements.
Self-Management Support: Helping patients and families to acquire the skills and confidence to manage their health.
Clinical Information Systems: Organized systems to manage patient data and support care.
Delivery System Redesign: Changing how care is delivered to better meet patient needs.
Decision Support: Providing clinicians with information and tools to guide evidence-based care.
Health Care Organization: The structure and culture of a healthcare system that supports high-quality care.
Community Resources: Assets and services in the community that can support patient health.
Advocacy: The act of supporting or recommending a cause or course of action on behalf of others.
Code of Conduct: A set of rules outlining the social norms, responsibilities, and proper practices for a group.
Culturally Safe: An environment that is spiritually, socially, and emotionally safe for people, respecting their identity.
Inclusive Practice: Providing care that respects the diversity of patients and ensures equal access.
Discrimination: The unjust or prejudicial treatment of different categories of people.
Health Inequities: Unfair and avoidable differences in health status seen within and between countries.
Created by: user-1992883
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