What are your questions about the ending of the PHE?
Hi all,
We have been trying to get CDC to come onto our SI calls to talk to the community about what to expect with the ending of the COVID-19 public health emergency. They have asked what types of questions folks have. Could you please let us know what some of your questions are? I am attaching the latest set of talking points that are distributed by CDC - these were also sent out earlier today to the SI steering committee.
Also I have a few additional questions:
1) Do you receive these talking points through another means (e.g., from anyone in your health department or from CDC)?
2) Do you attend the Regional meetings that CDC holds with STLT health authorities? If not, do you get notes or materials shared with you from those calls?
Many thanks!
We have been trying to get CDC to come onto our SI calls to talk to the community about what to expect with the ending of the COVID-19 public health emergency. They have asked what types of questions folks have. Could you please let us know what some of your questions are? I am attaching the latest set of talking points that are distributed by CDC - these were also sent out earlier today to the SI steering committee.
Also I have a few additional questions:
1) Do you receive these talking points through another means (e.g., from anyone in your health department or from CDC)?
2) Do you attend the Regional meetings that CDC holds with STLT health authorities? If not, do you get notes or materials shared with you from those calls?
Many thanks!
One question we would love to see addressed is how this impacts reporting from skilled nursing facilities. Some of our facilities report through NHSN - but a large number report directly to us in NC I think there is a CMS requirement for skilled nursing facilites to continue with full (line level) reporting of positives through the end of the year. But it would be great to have clarity on that point. I'm not sure how the nursing home data reported to us gets routed once it is sent on.
As a side note - I think the talking points document is very helpful.
One question area is looking at communications. How will CDC and other federal agencies communicate changes in federal data direct data collection activities? How will messaging regarding differences between federal and state/other jurisdictional levels be addressed so that it is clear regarding specifically what reporting or other practices are being altered.
Can STLTs receive a consolidated list of changes before they are announced to providers so that we can be involved appropriately in any transition activities?
For some individuals, vaccinations for COVID-19 through major pharmacy chains may not be suitable, such as where transportation is lacking or there are medical conditions that require special attention. How will vaccines be made available for these populations?
Thanks!
Steve
Steve Eichner
Health Information Technology Lead
Texas Department of State Health Services
steve.eichner@dshs.texas.gov<mailto:steve.eichner@dshs.texas.gov>; www.dshs.texas.gov<http://www.dshs.texas.gov/>
Phone: 512.221.5632
I think Steve's point above is a good one -- if we could get a consolidated list then we can evaluate how State regulations impact.
Do we know what conclusions are being drawn about hospitalization data? The document says that CDC is working with CMS and ASPR on which data elements remain critical. Hospitalization data has been an ongoing need for us and I fear with reduced cadence and requirements that it will become less reliable and helpful.
I will let you know if others have questions as I share the summary document.
Thank you for advocating for us all!
Angela Herbert
DMI Business Lead & Interim DMI Director
Nebraska DHHS
to answer question 2: I don't attend the regional meetings or get notes. I would like to. It has been a struggle to remind folks to include the Informatics staff who are managing the reporting systems and who also have experience in epi and/or IT. We get left out and that is a mistake. It always works better when we are at the table as early as possible so any planning for updates, case report design, lab data capture, etc. can be reviewed by the people who know the data systems and how the data collection and reporting work (and who are doing the work to make all of that happen). :-)
Here are the questions I sent (paraphrased) and the initial responses from my supervisor. Do not take these answers as final - some items are still being discussed. Items in brackets or as Note are my addendums.
Q1: When can we stop requiring negative SARS-CoV-2 lab results to be processed/sent. Ans. We are updating the reportable diseases list to remove negative labs; exact date TBD.
Q2: Can we drop the requirement for providers to report results and just have them focus on case reports. Those reports can include the tests they've done onsite - we have a new web portal nearing completion for that. Similar question for colleges, mobile clinics, etc. If we are going to a flu reporting model, is there a plan to build a CLI network of providers? Ans. I’m not sure we can do this yet [drop provider onsite test reporting]; it is a requirement of them being a “lab” [HHS] so I don’t think I want to do that quite yet. However, they will only need to report positive results.
Note: My take is when HHS requirements drop then we should drop provider reporting of test results or modify for just urgent care/ED plus lab - again TBD
Q3: I would like to stop sending data to CELR as soon as feasible. At this point we are primarily sending negative results. CDC can still get our positive result numbers from our open data portal. (and I just thought of this - the COVID and GenV2 HL7 messages). Ans. I think we need more information from CDC on this one. We won’t have negatives to send to them; the ODP data [CT's open data portal where we publish our COVID-19 data including test results] will go away June 1 and it sounds like they might be modifying the CCLs so they really won’t be able to scrape much longer after the end of the PHE.
Note: We will publish COVID-19 results on a weekly basis like we do influenza results. Note #2: I would like to see a discussion on how CELR worked because I think there was a wide variation on getting it to work and how it worked, as well as some limitations on the CELR side for data deduplication, how to update with 'catch up' data, etc. That may be helpful for future planning purposes.
I had some questions about the utility of having nursing homes report positive test results given they must report outbreaks. That is being discussed.
I hope you don't regret asking Annie, but thanks for being sure the communities are in the loop!
Nancy L Barrett, ID Informatics HIS Program Lead, CT DPH