Documente Academic
Documente Profesional
Documente Cultură
Approved
Version
Date of First Issue
Review Date
Date of Issue
EQIA
Author / Contact
24/01/10
2.3
09/06/2008
30/06/2016
01/07/2014
Yes
Dr Christopher Brammer, Consultant Haematologist
Group / Committee
Final Approval
Version 2.3
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Consultation Process:
Distribution:
Dr David Watts
Dr Christopher Brammer
Dr Martyn Hawkins
Mr Stephen McBurney
Members of Hospital Transfusion Team; Hospital Transfusion
Committee; Consultant Gastroenterologists; Intensive Care
Consultants
Intranet
Change of Record
Date
Author
23.6.09 Dr C
Brammer
Nature of Change
Removal of reference to 500ml units of
4.5% HAS replacing with 500ml units of
4% HAS.
Reference
Pages 4 and 5
Page 6
Page 6
1.6.11
Dr C
Brammer
Pages 4, 5 and 6
1.3.12
Dr C
Brammer
Page 6
Page 5
18.5.12 Dr C
Brammer
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Forth Valley Guidelines for the Usage of Human Albumin Solution (HAS) in
the context of the clinical complications of chronic liver disease
viral hepatitis
alcoholic liver disease
autoimmune liver disease e.g. PBC / PSC
haemochromatosis
NASH
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Day 3: 1g HAS / kg
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For all the indications detailed above, clinical guidance is provided by the
Consultant Gastroenterologists, who will indicate which of the above products,
and how much, is required for each individual patient. Medical staff responsible
for the care of the patient should then request HAS directly from the FVRH
Pharmacy department by completing a pharmacy indent request, available on the
ward, with the following information:
Full name, date of birth and CHI number for the patient
Product required and volume (number of bottles) to be issued
Location of patient and time when HAS is required
For all indications not included in these guidelines, the request will be redirected
to the duty consultant haematologist for authorization. The Hospital Transfusion
Committee will monitor and audit HAS issue and use.
HAS will be issued from the pharmacy on a daily basis as required it is not
appropriate to store HAS in the ward area. A small emergency stock of HAS will
be held in ITU and the Pharmacy dept. emergency fridge (which the bed coordinator has access to). At the end of the clinical episode, any HAS which has
not been infused to the named patient must be destroyed as clinical waste. It is
not acceptable to infuse a product issued to a named patient into any other
individual.
References:
1.Arroyo V, Gines P, Gerbes AL, Dudley FJ, Gentilini P, Laffi G, Reynolds TB,
Ring-Larsen H, Scholmerich J. Definition and diagnostic criteria of refractory
ascites and hepatorenal syndrome in cirrhosis. International Ascites Club.
Hepatology. 1996 Jan; 23(1):164-76.
2. Wong F, Blendis L. New challenge of hepatorenal syndrome: prevention and
treatment. Hepatology 2001 Dec; 34(6):1242-51.
3. Arroyo V, Guevara M, Gines P. Hepatorenal syndrome in cirrhosis:
pathogenesis and treatment. Gastroenterology 2002 May; 122(6):1658-76.
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Further references:
British Society of Gastroenterology Guidelines for the management of ascites
in cirrhosis. Gut 2006
http://www.bsg.org.uk/bsgdisp1.php?id=6831b1e0bcbd40a30f82&h=1&sh=1&i=1
&b=1&m=00023
Gines et al. The management of ascites in adult patients with cirrhosis.
N Engl J Med. 2004 Apr 15; 350(16):1646-54.
Runyon BA et al Management of adult patients with ascites caused by cirrhosis
Hepatology. 1998 Jan; 27(1):264-72.
Runyon BA American Association for Study of Liver Disease Practice
Guideline. Management of adult patients with ascites due to cirrhosis
Hepatology 2004 39(3):1-16
https://www.aasld.org/eweb/docs/practiceguidelines/ascites.pdf
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