Sean - thank you for the response - I agree this is huge. So much so, that I 
couldn't quite believe my eyes and wanted a confirmation [😊]    We were 
concerned about spending time struggling to get compliance for a complicated 
piece of documentation; this change allows us to focus more on the clinical 
care with the documentation more easily following.


I'm also very relieved to see that plasmalyte will count towards the 30ml/kg. 
We were failing a lot of cases due to plasmalyte given after 1-2 L NS. Was 
always curious why it wasn't included before, and am happy that it's now a 
non-issue.


Thanks also to the many others who have chimed in on this thread - all are very 
helpful.  I'm very grateful for this resource.


Joe


Joseph Clement, MS, RN, CCNS
Clinical Nurse Specialist
San Francisco General Hospital
ph: 628 206-6174
pg: 415 327-0220
office: H5841


________________________________
From: Townsend, Sean, M.D. <[email protected]>
Sent: Wednesday, August 24, 2016 3:51 PM
To: Clement, Joseph (DPH)
Cc: [email protected]
Subject: Re: [External] [Sepsis Groups] SEP-1 Specification Manual for January 
2017 Discharges

You are correct in your reading.  The LIP can now attest to the reperfusion 
assessment without giving greater detail.  What is more, nursing documentation 
and a nursing exam can be the basis of that attestation.  The only requirement 
is that the one exam item LIP has to do as part of that attestation is a 
cardiopulmonary exam.

This is huge. I hope you appreciate the change.  Our goal wasn't to make people 
document but rather to conduct an exam and satisfy themselves that the patient 
was perfusing adequately.

As regards antibiotic acceptable delay the provider has to state a delay of 45 
minutes or longer would have transpired.

Sean

On Aug 24, 2016, at 1:49 PM, Clement, Joseph (DPH) 
<[email protected]<mailto:[email protected]>> wrote:


Hello,


I'm reviewing the updated specification manual 5.2 for SEP-1, that will go into 
effect 1/1/17, and I have a few questions - I wonder if others are further 
along than me.

https://www.qualitynet.org/dcs/ContentServer?c=Page&pagename=QnetPublic%2FPage%2FQnetTier3&cid=1228775749207<https://na01.safelinks.protection.outlook.com/?url=https%3a%2f%2fwww.qualitynet.org%2fdcs%2fContentServer%3fc%3dPage%26pagename%3dQnetPublic%252FPage%252FQnetTier3%26cid%3d1228775749207&data=01%7c01%7ctownsesr%40sutterhealth.org%7c9dad663bd1fe4129e4c108d3cc602cd1%7caef453eadaa243e0be62818066e9ff63%7c0&sdata=Lfj7WQvlpCs3T%2b0LsrjWZtrnfLyK42X5rtVyK7r924w%3d>


[] The manual says that MD attestation of reassessment, VS review, skin 
assessment, cardiopulmonary exam, and peripheral pulse exams are acceptable. It 
also says that "performing, or attesting to performing a physical examination, 
perfusion (re-perfusion) assessment, or sepsis (severe sepsis or septic shock) 
focused exam is acceptable."

At the risk of asking an obvious question, I just want to make sure I am 
getting this right.  If the MD signs something that says "I attest to having 
performed a severe sepsis re-perfusion exam at XX:XX", then this would meet the 
measure requirement?


[] I see that a new element was added "Blood Culture Collection Acceptable 
Delay" - but I'm not clear from the manual what constitutes an acceptable 
delay.  Am I missing something?  Can anybody clarify?


Thanks in advance!


Joe


Joseph Clement, MS, RN, CCNS
Clinical Nurse Specialist
San Francisco General Hospital
ph: 628 206-6174
pg: 415 327-0220
office: H5841
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