HITEQ Resources & Events

This Guide provides focused documentation to assist users of NextGen software to improve the process of assessing, documenting, tracking, and following up on colorectal cancer screening. The Guide gives particular attention to assessment of personal and family risk and the tracking and follow-up of screening results that are not addressed in the standard NextGen guidance documents. This work aims to improve health center compliance with HRSA Uniform Data Systems (UDS) colorectal cancer screening (CRCS) through the development and implementation of workflows that produce accurate and reliable structured data and enable proactive outreach and timely follow-up with patients due for CRCS or follow-up testing. This optimization enables health centers to harness broader evidence-based strategies to improve CRCS compliance, and ultimately, health outcomes.

This webinar described the Health Resources and Services Administration's (HRSA) Health Center Program and its engagement in Ending the HIV Epidemic (EHE), as well as opportunity for collaboration between Center for AIDS Research (CFAR) programs and health centers to advance the goals of EHE. This webinar described where Federally Qualified Health Centers (FQHCs) are located, how they are funded, and provided a case study of how they have responded to the EHE funding initiative.

Privacy and confidentiality concerns are currently limiting the inclusion of behavioral health data in electronic health information exchange efforts. ONC has provided a number of tools and recommendations to address some of these concerns.

The January 2019 issue of The 405(d) Post from HHS includes a feature article from their Task Group Members discussing the importance of cybersecurity for small practices. Take a look to learn more. Also, visit the spotlight section to learn more about endpoint protections, new HHS resources and cybersecurity news stories the 405(d) team is tracking. Click here, or access from the resource links below!

Join the HITEQ Center, in collaboration with the National Council for Behavioral Health, for a webinar on Documentation Tips when using the Collaborative Care Model for the Treatment of Depression and Anxiety in Primary Care. The webinar provided a brief overview and benefits of the collaborative care model as well as information specific to each of the main staff roles. The role-specific nuances of documentation were highlighted, including considerations for tracking data such as clinical activities accomplished with each patient during the month.