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This document explores the implications of name-based notification in public health surveillance, focusing on HIV/AIDS reporting. It discusses historical contexts, critical issues, ethical considerations,
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How to fill out The Role of Name-Based Notification in Public Health and HIV Surveillance

01
Identify and gather all relevant information regarding the individual being reported.
02
Fill out the notification form with accurate personal details, including name, address, and demographic information.
03
Include specific health information related to the individual's HIV status and any relevant medical history.
04
Ensure all information complies with local laws and regulations regarding confidentiality and data protection.
05
Submit the completed notification to the appropriate public health authority promptly.

Who needs The Role of Name-Based Notification in Public Health and HIV Surveillance?

01
Public health officials responsible for monitoring and controlling HIV transmission.
02
Healthcare providers who diagnose and treat individuals with HIV.
03
Researchers studying the epidemiology of HIV and its impacts on public health.
04
Policy makers developing strategies to improve health outcomes in HIV-affected communities.
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HIV Diagnoses ing to the latest CDC data, in 2022, 37,981 people aged 13 and older received an HIV diagnosis in the U.S. and 6 territories and freely associated states. The annual number and rate of HIV diagnosis in 2022, compared to 2018, remained stable.
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Everyone between the ages of 13 and 64 should get tested for HIV at least once. People with certain risk factors should get tested more often. You should get tested at least once a year if: You're a man who has had sex with another man.
The CDC Classification System for HIV Infection is the medical classification system used by the United States Centers for Disease Control and Prevention (CDC) to classify HIV disease and infection.
HIV surveillance brings together information from a range of sources to: estimate how many people are living with HIV; understand who is being infected and why; and. assess the impact of HIV prevention, testing, and treatment services across different population groups.
In 2022, over 80% of people with diagnosed HIV were linked to care within one month of diagnosis. Only 76% had received some care, 54% were retained in care, and 65% had achieved viral suppression in 2022. These data highlight the need for continued prevention and care efforts to reach the national goal of ending HIV.
“Data to Care” (D2C) is a public health strategy that uses surveillance and other data to improve continuity of HIV care for persons with HIV (PWH) by identifying those who are in need of medical care or other services and facilitating linkage to these services.
CDC is a critical part of the U.S. government-wide effort to promote global health security. CDC works with countries around the world to detect and respond to emerging infectious disease outbreaks and stop them at their source to prevent further spread.

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The Role of Name-Based Notification in Public Health and HIV Surveillance is to facilitate the tracking and monitoring of HIV cases to ensure effective public health responses, improve disease prevention strategies, and allocate resources where they are most needed.
Healthcare providers, laboratories, and facilities that diagnose or treat individuals with HIV are typically required to file the Name-Based Notification to ensure accurate reporting and data collection for public health purposes.
To fill out the Name-Based Notification, healthcare providers must accurately complete a standardized reporting form that includes patient identifiers, diagnosis details, and relevant demographic information while ensuring compliance with confidentiality regulations.
The purpose of Name-Based Notification is to enhance surveillance efforts, identify patterns of HIV transmission, guide intervention strategies, and ultimately reduce the incidence and prevalence of HIV within the community.
Reported information typically includes the patient's name, date of birth, gender, race, ethnicity, address, date of diagnosis, and any other relevant clinical information as required by local public health laws.
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