dc.contributor.author |
Sutharsiny, Y. |
|
dc.contributor.author |
Darshani, W. M. N. |
|
dc.contributor.author |
Moratuwagama, H. M. D. |
|
dc.contributor.author |
Costa, Y. |
|
dc.contributor.author |
Williams, H. S. A. |
|
dc.contributor.author |
Kularatne, W. M. M .T. |
|
dc.date.accessioned |
2019-02-06T09:15:06Z |
|
dc.date.available |
2019-02-06T09:15:06Z |
|
dc.date.issued |
2018 |
|
dc.identifier.citation |
Proceedings of the Sri Lanka Medical Association, Anniversary Academic Sessions. 2018; 63(sup 1): 134 |
en_US |
dc.identifier.issn |
0009875 |
|
dc.identifier.uri |
http://repository.kln.ac.lk/handle/123456789/19858 |
|
dc.description |
Poster presentation Abstract (PP146), 131st Annual Scientific Sessions, Sri Lanka Medical Association, 26th-29th July 2018 Colombo, Sri Lanka |
en_US |
dc.description.abstract |
INTRODUCTION & OBJECTIVES: The British Committee for Standards in Haematology (BCSH) provides guidelines for use of fresh frozen plasma (FFP). Inappropriate use and non-compliance with guidelines for FFP have been reported.This audit is to reinforce guidelines and avoid inappropriate use. The objectives are to check -
l.The indications ofFFP use
2.Calculation of dose according to weight of patient
3.Checking of coagulation (PT/APTT) before and after FFP
METHODS: Data was collected from blood bank requests for 4 months. Details were collected from a questionnaire from patients and BHTs following transfusion.RESULTS: Of 50 patients, 11 were neonates and 4 children. Indications were liver disease with abnormal coagulation (40%), DIC and severe sepsis (20%), liver disease with normal coagulation awaiting surgery (10%), and massive bleeding (8%). 14% of neonates required FFP for resuscitation and to treat sepsis.Though weight was measured in 41(82%), adequate dose was administered to 14 (28%), overestimated in 26%, and underestimated in 28%. Pre and post transfusion coagulation was done in 33 (66%) and 17 (34%) respectively. Seven (14%) had coagulation tests within 3 hours. None of the patients had informed consent, risks and benefits informed prior to transfusion. CONCLUSION: All FFP is used according to guidelines. Documentation of volume of FFP used requires improvement as ambiguity of ml or units. Each unit of FFP varies· from 180ml - 230ml. Requirement of post transfusion coagualation within 3 hours is to be emphasized. Requirement of informed consent prior to transfusion of blood products is stressed. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Sri Lanka Medical Association |
en_US |
dc.subject |
FFP |
en_US |
dc.title |
Rational use of FFP at North Colombo Teaching Hospital: An audit |
en_US |
dc.type |
Conference abstract |
en_US |