Public health surveillance
(Redirected from Clinical surveillance)
Public health surveillance is the ongoing systematic collection, analysis, and interpretation of health-related data essential to planning, implementation, and evaluation of public health practice. This closely integrated process involves steps to ensure that the data are used in public health action to prevent and control the occurrence or spread of diseases.
Definition[edit | edit source]
Public health surveillance is defined by the World Health Organization (WHO) as "the continuous, systematic collection, analysis and interpretation of health-related data needed for the planning, implementation, and evaluation of public health practice."
History[edit | edit source]
The concept of public health surveillance has its roots in the practice of disease surveillance in 19th century Europe. It was initially used to monitor the spread of infectious diseases like cholera, tuberculosis, and diphtheria. The practice has since evolved and expanded to include surveillance of non-communicable diseases and the monitoring of trends in health behaviors, health services, and environmental hazards.
Types of Surveillance[edit | edit source]
Public health surveillance can be divided into two main types: passive surveillance and active surveillance. Passive surveillance involves the regular collection of health data by health care providers, while active surveillance involves a more proactive approach, with health officials contacting health care providers or the population to collect data.
Uses[edit | edit source]
Public health surveillance is used to monitor and control disease outbreaks, identify changes in health practices and the health status of populations, guide public health policy and strategies, and respond to public health emergencies. It is also used to evaluate the effectiveness of public health interventions and measures.
Challenges[edit | edit source]
Despite its importance, public health surveillance faces several challenges. These include the need for timely and accurate data, the need for adequate resources and trained personnel, and the need to balance public health needs with individual privacy rights.
See also[edit | edit source]
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