Which report is essential in identifying high-risk patients for preventive care programs?

The disease registry report is critical for identifying high-risk patients for preventive care programs because it systematically compiles data about individuals diagnosed with specific conditions. These reports allow healthcare providers to monitor trends, track outcomes, and assess the prevalence of diseases within a particular population. By flagging individuals who are at greater risk based on their health status, the registry enables targeted outreach and interventions aimed at improving preventive care.

In contrast, the other types of reports serve different purposes. Patient feedback reports focus on patient experiences and satisfaction, which, while important for improving care delivery, do not specifically highlight high-risk populations. The access to care report evaluates how easily patients can obtain necessary medical services, but it does not provide insights into the health risks of patients themselves. Lastly, wellness program reports concentrate on the effectiveness and participation rates of wellness initiatives rather than directly identifying high-risk patients. Thus, the disease registry report stands out as the most relevant tool for identifying those who may benefit from preventive care programs.