Hemovigilance Pasien

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HEMOVIGILANCE

PASIEN

Dr Errisa Maisuritadevi Mara, M.Sc., Sp.PK


Apa Itu Haemovigilance ?
Untuk Pasien ....
REAKSI TRANSFUSI
adverse reaction
adalah "respons atau efek yg tidak diinginkan" pada pasien
terkait dg pemberian transfusi darah atau komponen
darah.
• Dapat terjadi akibat dari suatu insiden, tetapi tidak selalu

NHSN manual: biovigilance component protocol hemovigilance module, June 2011.


Guidelines and procedures for monitoring hemovigilance. http://www.cdc.gov/nhsn/bio.html.
Transfusion Related Activities
Adverse KEJADIAN YG TIDAK DIHARAPKAN yg terjadi
event sebelum, selama atau setelah transfusi darah.
= KTD Termasuk insiden dan adverse reactions.

Adverse Respons atau efek yg tidak diinginkan pd pasien yg


reaction terkait dg pemberian transfusi darah. Dapat terjadi
= EFEK akibat dari suatu insiden, tetapi tidak selalu
SAMPING
INSIDEN Setiap error atau accident yg dapat mempengaruhi
kualitas atau efikasi transfusi pd pasien.
Dapat menimbulkan reaksi yg merugikan pada
recipient transfusi.

Near miss Any error OR a subset of incidents that is discovered


before the start of the transfusion and that could
have led to a wrongful transfusion or to a adverse
reaction in a transfusion recipient
SEVERITY Adverse reaction
GRADE
1 Non severe -- the recipient may have required medical intervention (e.g. symptomatic
treatment) but lack of such would not result in permanent damage or impairment of a
body function.

2 Severe- needs medical intervention or prolongation of


hospitalisation, or both

3 Life threatening; required major intervention following the transfusion


(vasopressors, intubation, transfer to intensive care) to prevent death

4 Death as a result of adverse transfusion reaction


HOTSPOTS FOR ERRORS
“WRONG BLOOD”
CLINICAL DECISION
What can go wrong? Why it goes wrong?
 Unnecessary transfusion or  Inadequate clinical assessment
failure to give necessary
 Lack of transfusion knowledge or
transfusion
failure to follow guideline
 Wrong component or dose
 Unaware of importance of
prescribed
information & consent
 Patient was not informed &
consent not obtain
SPECIMEN COLLECTION
What can go wrong? Why it goes wrong?
 Patient was not identified  Do not follow SOP for specimen
correctly collection
 Pre transfusion specimen taken  Staff takes shortcut
from wrong patient
 Request form/ sample tube was
wrongly labeled
ISSUING/DELIVERY OF BLOOD
What can go wrong? Why it goes wrong?
 Wrong unit selected  Patient ID details not properly
 Blood delivered to wrong checked
location  SOP was not followed
 Wrong storage
LABORATORY ERROR

What can go wrong? Why it goes wrong?


 Wrong ABO/ Rh grouping  Patient sample and request not
 RBC alloantibodies not detected checked for consistency and
completeness
 Error in crossmatch & wrong unit
issued  Error in testing procedure or
recording of result
 Poor staff training or failure to
comply with SOP
EVERY ONE MATTERS

Transfuse One Unit

Re-assess the patient

Don’t increase the RISKS


if NO BENEFIT
The Serious Hazard of Transfusion (SHOT) scheme
showed that approximately 70% of IBCT event errors
take place in clinical areas, the most frequent error
being failure of the final patient ID check at the bedside.

(Serious Hazards of Transfusion (SHOT) 2007)


SINGLE UNIT TRANSFUSION

WHAT
Transfuse one unit, then re-assess the patient for clinical
symptoms before transfusing another
 Every unit is a new clinical decision
 Base decision on patient symptoms, not only on haemoglobin
level
SEROLOGY
REAKSI TRANSFUSI
Risks and problems in the different key processes in the context of a
blood transfusion in a HOSPITAL
Actions and measures
http://haemovigilanceindo.com

Mari Bergabung

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