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So people who have Medicare mostly fee for service in a dementia diagnosis should have access to a care, essentially a care navigator for the duration of their condition, or at least the duration of the program. Eric 26:16 I would also say, having tried to find a primary care doctor out there in the wild, you can’t.
Additionally, it’s a way of documenting decline that captures the patient’s physical, emotional, and spiritual needs. Furthermore, documenting decline is not only for ensuring quality care but also for meeting Medicare documentation requirements for hospice eligibility and recertification. I’ll be honest.
First, like all nurses, hospice nurses are required to document ALL patientcare. Inaccurate and inconsistent documentation is a red flag and could have a negative impact on your patients, your license, and your agency. Therefore, your documentation should tell the patient’s story. Documentation is king!! Conclusion.
As we think about palliative rehab and Eric: Sarguni, some of your research is you have these patients, many of them don’t receive future cancer treatments, these cancer patients that are going to SNFs. And a lot of them never actually improve their ADLs once they’re sent to SNF. That’s the problem. Eric: Yeah.
I was working in home Health back when it was first introduced back in 2010, as a way for c m s to not only create structured penalties for hospitals with excessive readmissions, but also to reward and incentivize those providers for effective care coordination and collaboration with post-acute providers across the care continuum.
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