Beginning on December 1st, 2023 providers enrolled in the Adult Vaccine Program will be required to submit temperature logs through a portal in REDCap, similar to how temperature logs were submitted for the COVID-19 Vaccine Program. Providers that are dual enrolled in both the Childhood Vaccine Program and Adult Vaccine Program will also be required to submit temperature logs for both programs through the REDCap portal. Providers only enrolled in the Childhood Vaccine Program will have the option to submit temperature logs through the REDCap portal as well. The primary and back up vaccine coordinator at each location will receive an automated email on December 1st that will prompt you to upload your temperature logs for the prior calendar month of November. Beginning on January 1, 2024 this new temperature log submission process will be required for all enrolled providers in the Childhood Vaccine Program and the Adult Vaccine Program. Please be sure to attend this month's CVP training session (below) on Navigating Temperature Log Submission in REDCap to learn more.
Please join us for a very important training session to learn how your clinic can submit temperature logs through the REDCap portal, rather than submitting them through email.
Topic: Navigating Temperature Log Submission in REDCap
Date: November 16, 2023 Time: 12:00 pm (noon) Intended Audience: AVP and CVP enrolled Providers and Vaccine Coordinators
Join the Training Session Webinar ID: 851 4240 2545 Passcode: 673609
COVID Vaccine Inventory in the WAIIS is a quick reference guide that may be helpful in managing '23-'24 COVID-19 vaccine inventory in the WAIIS.
Nirsevimab Documentation in the WAIIS is a reference guide that shows how to document and manage Nirsevimab inventory in the WAIIS.
IMPORTANT: The documentation for Nirsevimab differs from other immunizations because a patient could receive identical injections twice in the same day. Administering two doses to a patient on the same day can also affect Nirsevimab inventory counts in the WAIIS. Contact IIS.training@doh.wa.gov if you have questions.
Click here to access the IIS Training Materials Portal.
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If you have staff who are new to using the Washington State Immunization Information System (WAIIS), you can access the recording, slides, and FAQ from a recent New User Training through the IIS Webinars web page. This training provides an overview of what an IIS is, information about the WAIIS, and a demonstration of how to search and add patients to the system, enter vaccines, and access a patient’s vaccination history.
The next WAIIS virtual training will occur on November 15, 2023 at 11:00am. The topic is “Adding and Editing Patient and Immunization Information in the WAIIS”. You can register here or through the link on the IIS Training Materials Portal. If you have any questions or training topic suggestions for future webinars, please contact IIS.Training@doh.wa.gov.
Important Information: Ensuring Correct Dosing of Moderna COVID-19 Vaccine (2023-2024 Formula) to Individuals 6 months through 11 years (0.25mL)
FDA released important information to ensure correct administration of the Moderna COVID-19 Vaccine (2023-2024 Formula) for individuals 6 months through 11 years.
The announcement advises that providers who administer the Moderna COVID-19 Vaccine (2023-2024 Formula) to individuals ages 6 months through 11 years should ensure that the correct volume of the vaccine (0.25 mL) is withdrawn from the vial and administered to the recipient. Providers should discard the vial and excess volume after extracting a single 0.25mL dose. Excess volume should not be used to administer an additional dose. Additionally, never combine partial doses from multiple vials to make one dose for a patient.
FDA shared this information after learning some healthcare providers may not recognize that the single dose vial of Moderna COVID-19 Vaccine (2023-2024 Formula) contains more than 0.25 ml of the vaccine and may be withdrawing the entire contents of the vial to administer to an individual. FDA has not identified any safety risks associated with administration of the higher dose in individuals 6 months through 11 years of age, and no serious adverse events related to this issue have been identified.
For additional information, see the FDA announcement, updated Moderna fact sheet, and the vaccine administration resources listed at the end of this email.
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