I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
September 22, 2019, 09:12:25 PM

Login with username, password and session length
Search:     Advanced search
528708 Posts in 33238 Topics by 12317 Members
Latest Member: Caregivingsister
* Home Help Search Login Register
+  I Hate Dialysis Message Board
|-+  Dialysis Discussion
| |-+  Advocacy
| | |-+  AHA proposed Meaningful Use Stage 2: a month to provide hospital discharge info
0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: AHA proposed Meaningful Use Stage 2: a month to provide hospital discharge info  (Read 3807 times)
natnnnat
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1281


WWW
« on: May 02, 2012, 08:50:45 PM »

A friend regularly forwards me updates from e-Patients.net,
e-Patients.net is the Society for Participatory Medicine Blog. The Society also publishes the Journal of Participatory Medicine.
Their byline is "because health professionals can't do it alone".


Recent update reads as follows:

Quote
American Hospital Association declares war on patient empowerment. Please act.
________________

The headline above is unusually strong wording, but emails and blogs have been ablaze today with outrage at the comment letter submitted Monday by the American Hospital Association regarding the proposed regulations for Meaningful Use Stage 2. The AHA has effectively said it is neither interested in, nor capable of, giving families the information they need to care for the sick after hospitalization.

And they say Federal rules should support their position. This would utterly disempower the efforts of patients and families to engage responsibly in their families’ care.

We must speak up. This is a call to action.

Perhaps the AHA has unwittingly revealed why American hospitals are inept at discharge planning: they don’t have a grip on this vital information. We already know that 20% of Medicare patients return to the hospital within a month (NEJM 2009). The industry describes this with the delightful term “bounceback.” Families call it upsetting, distressing, heartbreaking.

The issue at hand: current regulations for Meaningful Use Stage 1 (already in force) require that we be given our records within four days, but now the AHA says that’s impossible (“not feasible,” in their words) and they want thirty days.  A month.  (The iHealthBeat article links to the AHA’s 68 page letter (PDF).)

Here’s what that means, specifically: when you or a relative is discharged from the hospital, instead of giving you your information promptly – to inform and empower good home care – they want to be allowed to spend that whole month gathering the information that might let you prevent readmission.

See the full post at:
http://e-patients.net/archives/2012/05/american-hospital-association-declares-war-on-patient-empowerment-please-act.html

where there are also options for registering your opinion regarding this issue, URLs and so forth, and some interesting comments.

« Last Edit: May 02, 2012, 09:11:03 PM by natnnnat » Logged

Natalya – Sydney, Australia
wife of Gregory, who is the kidney patient: 
1986: kidney failure at 19 years old, cause unknown
PD for a year, in-centre haemo for 4 years
Transplant 1 lasted 21 years (Lucy: 1991 - 2012), failed due to Transplant glomerulopathy
5 weeks Haemo 2012
Transplant 2 (Maggie) installed Feb 13, 2013, returned to work June 17, 2013 average crea was 130, now is 140.
Infections in June / July, hospital 1-4 Aug for infections.

Over the years:  skin cancer; thyroidectomy, pneumonia; CMV; BK; 14 surgeries
Generally glossy and happy.

2009 - 2013 PhD research student : How people make sense of renal failure in online discussion boards
Submitted February 2013 :: Graduated Sep 2013.   http://godbold.name/experiencingdialysis/
Heartfelt thanks to IHD, KK and ADB for your generosity and support.
Pages: [1] Go Up Print 
« previous next »
 

Powered by MySQL Powered by PHP SMF 2.0.15 | SMF © 2017, Simple Machines Valid XHTML 1.0! Valid CSS!