Or) ame eae
Cur x
‘Blood bank accrediation ~ tool for
quality improvement
‘inspection to eeticetanstision related
reaction
Events on quality management
Preventing Blood Transtusion Errors
‘through Process Excellence
Fecueing Chances OF O/oss
(Contamination During The Blood
Component issue Process
Managing Donor Retention
After Adverse events
Mode! Bio0d Bank
BIGUAIAMIAeereditation - A tool for quality improvement
‘Accreditation is a process in which certiication of competency,
authority, or credbiltys presented.
\With increase in population and development of more advanced
medical and surgical procedures, the need for blood is ever
increasing. There is no substitute for blood andits safety cannot be
Underscored or underemphasized. Blood banking is integral part
cot health care requires uniform standards to deliver quality blood
and products
‘Quality is the ongoing process of building and sustaining
relationships by assessing, anticipating, anc futling stated and
implied needs:
‘Accreditation provides a format to ensure work flow processes and reproducibility of
results and hence improve qualty. This is also ensured by participating in the External
quality assurance programs where theresuls are compared with other testing labs.
Blood Bank Accreditation program being used a tool for quality improvement wil promote
the highest standards of cre for both patents anc denors in all aspects of blood banking
andtransfusion medicine.
Pet
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Special Coverage
| blood transhsion is a special kind of
transplantation andlor meal theepeute
Intention tat cares wah # grat Donets
and sks 1o the feopient I inwches the
rsfor of hing tssuo om one person to
nother and hus a ecpient ofa ranctsion
Tay experence an adverse reacton to the
rodvet dung or aerthevanstsion.
Bacterial contamination occurs in
approximately 112.3000 patelet concetrates
(Pcs) and may Induce ‘sepsis. In
‘approximately one in six recipients ofthe contaminated product."
‘Mirada eartamaton accounted forthe this mast commen caure of
lrancusion associated fatalities reported to the US Food and Org
‘cmistaon between 2008 and 2008."
‘Adverse reactions occur n 1 to 6 percent of al blond vanstusions and aro
‘more froquont (10 porcen) in patents with hematologic and encologic
‘eordere Keeping the above in in ki mperaive to ensure tal blood
‘ranauson rests inthe ltmate benetothe repent whi reducing the
bt deupam canes
Need of SOP's for Pre-Release Visual Inspection
to Reduce Transfu
n Related Reactions
tiskol adverse anstison reaction
\Veualinapacton lore isuance ofthe blood component isthe est sep,
‘whlch would contibute in mirimizng vanetsion related reacions. THs
Can be acheved a Standard Operating Procedure (SOP) i formals
andimplemonted
The folowing point shouldbe bome in mind in effecting the saest pre
release ieunlaapecton process
1. Vieibity: Inspection of the Hood products should take place in a
wlkitare.
2 Memolyss: Te degree ot Hemoyis shouldbe ascertained keepingtne
Pemstiiekeisinmd
{Red Cell Contamination relevant platelets plsma Beryoprociptate
44 Bacterial Contamination: Some of the atiibutes of bacteal
contamination ae a ubbies, dk purple to tek coloration red
ols cots & fon ctandsete
5. Pantoulate mator: Vibe the form o large to smal colored masses
‘hatdonot sips wih gents anipulsten
‘Accepable lous of emoyss a8
NA
| Sonegegnecttenctes
‘contamination
Hemotyis ‘come at ony spose
AASB commends
Red eo wa AASB racomrnende so cormaine | Yet stander of coepabity
ontamintion| Cea eon Es cma desea
pera a ens wh pena SSSR Wei.
teers ood componoTs wih Dona af acepibi fo wanton.
acter
‘Blood Components are not acceptable for tansusion
~ Blood components contaning cats / bn sands should not be ranshises
+ Blood components conning ela’ aggregates should not be vanstaed
Pariulate * Vine Parteuate Maer (WPM), Blood components contsing WPM are ceptable fr tanstuBen.
mater WEN may isspate wth a change n temperature
‘ee Herolyss, Linea, bacterial | + Discoloration ato eters (ew), | + Oisenloraton due 1 ietens
contamination ‘fal contraceptives (Green iain’ | (yelow, ofl contraceptives
Discoloration ‘erlarge quatites of carols (Green, vlamin or lroe
(orange) areal! accaptanl or
traneusion
quanies of sare (orange)
20 al accopiabl for wanstusion,
Ife above is adhered io, complications Ike Tanstusion related Hemolyeis ftl sepc reactions due to baci contarinaton may be minimized.
“Relerences are not pete ce to space consi, ordeals plese contact he author on Emal lt: chasba.cr@gmal.com
24th Regional Congress (ISBT)
1 Became 2013, Koda rur Mela
2012 World Stem Goll Summit
“rsh Dee 2012, Farin USA
‘ot Annual SCT Moti
Ee crt ibe
‘own ive——
Process Excellence
Preventing Blood Transfusion Errors through
Process Excellence
Introduction:
‘Awell defined blood transfusion service
with excellent processes benefts the
patient who avails ofthe service as well
{as the overall organization. Many
serious rsks of blood transfusion have
been identiied which includes. near
miss events that can result in patent
adverse outcomes
SHOT UK 2011 reports that annually
near miss events comprise of 1rd of
the total and include wrong blood in tube (WBIT) and patient
Identiication errors. In fact, half of the adverse events were
preventable errors
Established Organizational Processes to prevent Errors:
1. Standardized transfusion order forms
‘The use ofa pre-printed, controlled blood request form should be
used to monitor and encourage ctnically appropriate transfusions.
‘Common practices observed today are incomplete request forms,
land forms forwarded by Nurses on verbal orders of clinicians. It
remains the responsibilty of the clinicians to forward the blood
requests a the practice of accepting incomplete, inaccurate and
legible requests could lead to potential legal implications. To
encourage compliance the Blood Bank should not release blood
products untithe deficiency ismet
2. Uniform Blood Sample collection process
‘2. Use two separate identiiers for patient identification eg: Full
Name and registration number
'. Collec from only one patient at atime This reduces the isk ot
Patient identification error and wrong blood in tube (WBIT), a
‘major cause of ABO incompatible transfusions
Label the sample at the Patient bedside The practice of
{generating labels atthe nursing stations after leaving the
patient room, could lead to labeling errors when mutiple
‘amples ae collected. Sample collection should involve only
‘one patient at atime, abeled a patent bed side, after patient
dentiicaion processiscomplete
3. Rejection of incorrectly labelled samples
‘Samples for type and cross match that reach the blood bank with
{an incorrect label or which do not correspond with blood request
form must be rejected and subjected to root cause analysis as a
potentalnearmiss event
4. Blood group confirmatory check
I the patient was groupedireceived transfusion previously, a
Fistoric blood group confirmation is performed trom previous
records. I previously not grouped, a second sample is requested
for testing priorto release ofblooc unt. A bedeice group check ust
prior to star of ransfusion should be established asthe final check
toprevent ABO mismatch transfusions
5. Pre-ransfusion checklist
Repeat emphasis on theneed forthe correctblood unitto reach the
‘correct patient is vial to reduce risk of incompatible reactions,
‘Good processes involve the use ofa pre-ranstusion checklist al
the bedside to ensure a final check betore stat of transtusion,
‘performed by two separate individuals. the processisinterrupted,
the fnal check using the
checklist is repeated trom
the beginning. Bloos
safety is enhanced when
the 8 rights of transfusion
acminstation are applies
for every unit: Right
product, Right patient,
Right dose, Fight Time,
Right reason, Right site,
Right documentation and
Fightresponse
Rights of Transfusion
6. Incidentreporting of Near miss events
Incident reporting provides opportunity for process improvement
by investigation and staff education withthe ultimate aim that the
‘event should not repeat itself. This involves documenting the
incident and reporting tothe hospital quality committee to ensure
preventive actions/processes are implemented to correct the
system that allowed the error to occur
7, Transfusion audits
“Transfusion verication audits can be conductedin allcinical areas
that provide transfusions to help ensure independent double
‘checks on the process. A hospital Transtusion Nurse/ Oicer can
‘be appointed to work with the blood bank management and
‘suppor clinicians inthe safe and effective use of blood. Their ole
includes active promotion of good transfusion practice by
facitaing vanstusion auait, feedback, incident reporting, folow
up of errorsinear miss, encourage education and training and
{acitae implementation of new technologies that enhance patent
safely
Conclusion:
‘Subjecting all errorsinear miss events to appropriate review,
Investigation, and root cause analysis isan essential element for
Improving tanstusion safety. With continuous training and
‘management support, the blood transfusion practice has the
‘potential to improve practices in the safe administration of Bi003,
Prevention of transfusion errors is the need of the hour and
through established processes this goalis now not beyond our
reach
“Relorences arnt rind dueto apace canst frdelalplease contactthe
‘uor on ma ear abbas
1657 : Sir Christopher Wren first injected some fluids into the circulation of animalsProcess Excellence
Reducing Chances Of Cross Contamination
During The Blood Component Issue Process
‘The primary function of @ blood
transtusion seni is to provide an
‘effective component of optimum
‘quality to the patent while ensuring
the safety ofthe donor. In order to
‘achieve this goal the blood bank
personnel must be vigilant at every
step ofthe process so that qualty is
‘maintained romeinto ven
eee
Contamination of a blood component may occur at any of the
stages from the colection process, component preparation, and
storage to the issue process. This article focuses on the risk of
‘105s: contamination during theissue process.
‘The issue process involves the following steps
1 Evaluation oftnerequistion form
2.Planning and revival ofthe components requested
3.Completing the serological testing ( as per blood bank
‘uietines)
4.Final processing the components
“+ Thawing Fresh Frozen PlasmalGryoprecipitate
+ Pooling of Components
‘Lab SideLeucodepletion
6.Completion of cocumentation and nal issue
‘The final processing of components is the stage at which
Contamination of the blood components is likely. Water baths)
thawers used for thawing plasma are a source of bacterial cross
Contamination of plasma. The most commonly found organisms
are Pseudomonas cepacia and Pseudomonas aeruginosa. (1.2)*
‘The cause ofthis contamination s that blood bags often have leaky
‘seals, camaged tubing or micro-punctures which have been linked
to bacterial contamination.(3} The water inthe thawer provide a
‘medium forthe transfer of bacterial contaminants from one bag to
another and the plasma leaked from a blood bag provides a
‘medium for bacterial growth. Over-wrapping of plasma bags
reduces the risk of contamination provided the right types of plastic
‘over wraps are usedin he corect manner.
‘The use of simple plastic bags or repeated use ofthe same over
\wrap is not advocated asitis ineffective. n spite ofthe reduced risk
(of bacterial cross contamination there is a residual risk of micro
tears and leakage in the plastic over-wraps. The proper cleaning
{and disinfection ofthe thawing baths along with sending samples
& Transfusion Medicine Chronicles
1666 : Richard Lower performs the first successful transfusion,
‘ofthe water from bath for culture at regular intervals is roquirod to
prevent bacterial contamination of plasma. An SOP (Standard
‘Operating Procedure) regarding use of the plasma thawed is
imperative to this end. There have been repeated efforts 10
‘overcome the inherent disadvantages of wet plasma thawers. He
“The use of microwaves to thaw plasma has also been tied but
there use declined due to reports of overheating and generation of
hotspois.[4;5]* There have been efforts torevivethis method thas
not caught on due the inherent disadvantage of the short
microwaves (p00r penetration and preferential absorption by the
liquid phase of plasma).[6.7]" Racio frequency (RF) heating of
fresh frozen plasma has also been tried as an altemative to
microwave thawing and shown some promise.7]* A plasma
thawer using heated air is being marketed by a German
manufacturer but there are no studies in pub med on its
efficacy (7)*
Recently Plasma thawers withthe water and plasma segregated by
the use of plastic bladders filed with heated water streamed
through them have been introduced into the market and may
provide a safer way to thaw plasma. There efficacy, saety profile
‘and exgonomics needs to be studied before using them becomes
standard practic.
Pooling and making aliquots of components are also procedures
‘raught with the risks of contamination and should be dane in a
sterile environment using a sterile connecting device. fan open
‘system is used the platelet component must be issued for use
within 4 hrs and RBCs within 24 hrs (Canadian Blood Services
Guidelines from the website). There Is also a risk of one of the
Platelets components being contaminated with bacteria, Efforts
are being made to develop a quick and reliable system to test for
bacterial contamination prior toissue, (8, 9,10]*
Hiab side leucodeplation is done using an open system, it should
be done ina clean environment using all aseptic precautions and
the components must be issued within ahs or platelets and within
‘2th for red cals. the intervening time the components should
be stored at optimally (Blood bank retigerator at 4°C for red cells
‘andina plateletincubator cum agitator at 22-C fr platelets)
Blood safety is a prictity issue for transfusion specialists. Bacterial
‘contamination is an important complication and an impediment to
safe blood supply. An effective quality management plan and
‘tit adherence to guidelines and SOPs is required to prevent
bacteria contamination of bioos components
‘fearences era notaries auetossac constant dea pleaeconactthe
‘utoron Ena es meensbaipsicnomai.eom
albeit on an animalDonor safety is of paramount importance
{uring blood donation ane is assured. nso
far as can be, by donor selection
‘uidoines, SOPs, acoquataly tained stat
and appropiate facies. Despite these
‘measures, varous acverse events and
‘eaters ean and do occu dung ane ater
Diood donation. These complications can
be a negative experience for. donors
Preventing them musta riety,
[Complications rested to blood donation
‘ocur in about 1% of all whole blood
oration procedures 2. i wel recognized that contain categories of
donors have higher reactionratas 3.
Deseription and classification: Adverse events and reactions can
‘manesnemsetvesin sevora ways. The Working Group on Completions
Related to Blocd Donation, a joint working group ofthe Iterational
‘Society of Blood Transfusion an the European Haemovigance Network
was esabished fr thispurpose. They classy complcationsinttwo main
Categenes: those wih predominantly local symptoms anc those seth
predominantly generazedsymptons
‘Complications mainly with neal symptoms. These complications are
rectly caused themsertoncl he nonce.
(s) Complications mainly characterized by the occurrence of
loodouicethevessls
+ Hematoma, Arter puncture, Delayedbeeding
(&) Compeatons mainly character by pin,
+ Nerveertation Nowe injury, Fendoninry, Panta rm
(©) Otrerkindsotestegores wath oa! symptoms
+ Theombophiebitis, ley ea
‘8: Complications main with generalized symptoms.
+ Vasovagalreacton:
+ Complicatons elated io aphacesis:
+ Cirate reacion, Hemelyss, Generatzed allergic reacton, Air
emboism
Provention strategies
Several sategies can be used to reduce the risk of complications
occurring dringardaterbiood donation
Preventionottype A) complications
[Needle techniques: Good neecie inserion techriques reduce the
‘requancy and seventy Type A complications Jorgensen and Sorensen
ietheotowing advice on needeinseron techniques’.
+ Alsaysmovethenescleforwardinasiow ongoing movement
+ Tbe noodles not inserted inthe vein at ho fret stom is rot
asable to do a second ty by moving tho neeco @ Ite Bit
backwards, change crocion anc tren move foward agalninanew
recon, az te wil ineease the rik of inure and occurence of
haomatoma,andthereby hock asevere complication.
+ Nove ty to inset the needle twice, using the same puncture ste.
Instoad ty the thorar,
+ Nove ask fr or va hep inserton was not a succes, as hs wll,
aways incudeatryinanew drecion.
Prevention otype (8) complications
Type 8 compteations, characterized pradominanty as generaizod
‘symptoms such as vasovagal reactions, require diferent precautionary
‘measures. Jorgenson and Soreneon idently the folowng generally
_aecoptod but nt evidence-based pracicos™
+ Gontie treatment of the donor, provcing rorostmants before
andaterdonatontoredieethe rst vasovagsreactons.
‘+ Observing the donor during and after donation, treating the
donor a ompleaton ooo and making sure the donor
{eal absolitely wellbore leaving thebiood session,
“+ Gwung ack fo the donor an secendary bleeding, cn, rest
‘and retum to work aer the donation. Aeking the donor to
Contacthebiood onertsymatomsrbocevt
+ Applying pressure to tne venepuncture sie and it necessary a
pressure bancage fa naomaioma s dowiopig,
“Tne preventon techniques ortyp 8 complcatons sted below have been
suggestedincovera studios.
‘+ Musele tension: whon a donor makes ropeated and ehyihmic
Contractions. wih the major muscle groups in his arms and
logs, the blood fw to the brain can be inroased in order
preventsinting
+ Distracting the donor during the bleeding procedure.
Watchingamoviecould reduce sressinadoncr
+ Water or caffeine loading. Several studies have reported
fewer complications when donors dink water or cofles before
thelr donation "=
Management
‘Adequate management of complications during biood sessions
several goal Fs, tis esantalfrthe heath and walbsingof donors
Second, proper management of complications helps 10 abeate the
negative fects complications mayhaveon dover motvaton andon donot
‘elu rales. Employees must be prepared and equipped to hance the
‘most requent completions. Protocls, training, ist aid equipment and
nar counseling are imperave. Some donors who have had severe
‘complications maybe advsedincttedenate again,
+ Stafftraining
+ Managing emergencies
* Donor counseling: ls an essential element of good donor
care that each donor who suffers @ complication of donation
Degivenspecticadviceabautthecomplicaton.
+ Donor advice: Donors should be advised on measures they should
take topreventine complication from geting worse
Donor fllow-up: This snot ony an essential element cf good danor care,
bulls basic good customer relalonships” As the compicaion may have @
negative seston acdonorsmolvationtomake& subsequent donation The
Toow.up ofthe donor and the provision of adequate infomation play 29,
impotantolein encouraging the donor tocontnueto dona
Eftecton donor motivation-next donation
‘Aogatve experience during 100d donation can havea negative tect on
donor motkation. Several suces have shown that experiencing &
‘ompleaton during te bleeding procedure isan important factor that
reves donors am making asubsequentconaton 1,14. France tal 15
found mater ign vasovagaleactiosin hoi bioo¢ donors ne tknood
atreturing for ane donation reduced by 20% ost tne donors ard by
‘33% for expotencod donors, For moderate and sovere vasovagél
‘complications retumrates reduced by 50%. Gorin and Petereenfoundthat
the more severe a compilation, the lower the rotun rato 16. Adequate
hanging ofa complication therefore, serves multiple goals: ensuring the
donors heath andretainingte dor ora subsequent donation
hlerences ere not printed se tospace consti. for dean plese conet he
sure on Era vormssh1803