The group of individuals sharing common characteristics or health-related factors, often used in healthcare to analyze, study, and tailor interventions or policies.

Demographics:

Statistical data related to the characteristics of a patient population, including age, gender, ethnicity, socioeconomic status, and other relevant factors.

Health Disparities:

Differences in health outcomes and access to healthcare services among various segments of the patient population, often associated with social, economic, or environmental factors.

Risk Stratification:

The process of categorizing individuals within a patient population based on their health risks, allowing for targeted interventions and personalized care plans.

Vulnerable Populations:

Subgroups within the patient population that may face increased health risks or barriers to healthcare access, such as the elderly, low-income individuals, or those with chronic conditions.

Patient Cohort:

A subgroup of the patient population sharing specific characteristics or experiencing similar health conditions, often studied as a unit in research or quality improvement initiatives.

Patient-Centered Outcomes:

Measures focused on the impact of healthcare interventions from the perspective of the patient, providing insights into the effectiveness of treatments within a specific patient population.

Population Health Management:

Strategies and interventions aimed at improving the health outcomes of a defined patient population, often involving proactive care, preventive measures, and health education.

Epidemiology:

The study of the distribution and determinants of health-related events, diseases, and conditions within a patient population, informing public health practices.

Social Determinants of Health:

External factors, such as education, housing, and employment, that influence the health outcomes of individuals within a patient population.

Inclusion Criteria:

Specific characteristics or conditions that individuals must possess to be included in a study or clinical trial, shaping the composition of the patient population under investigation.

Exclusion Criteria:

Factors or conditions that disqualify individuals from participating in a study or clinical trial, influencing the homogeneity of the patient population being studied.