24. HAEMOSTATIC MEASURES
⢠Duringanysurgicalprocedure complete
hemostasismustbeachievedbefore closureof
wound .
⢠Direct control of bleeding at site of injury isbest
method
⢠Surgicalbleeding mostof timesiscausedby
ineffective local hemostasis
29. SUTURES & LIGATION
⢠Whenlargepulsatile artery needs
ligation , nonâabsorbablemateriallike
3-0 blacksilkispreferred
⢠Smallvesselscanbeligatedwith 3-0
catgut/g polygalactin
⢠Thepresenceof nonâ absorbable
material in aninfectedwoundcanlead
to extrusion/ sinustract formation
⢠Largearterieswith pulsations( ECA)
shouldhavedoubletransfixation suture
passedthroughvesselwall to prevent
slippage
30. HALFLIFEOFSUTUREMATERIAL
⢠â Timerequired for the tensile strengthof material
to reducehalf of its original value â
⢠Dissolutiontime istime elapsesbefore the thread
iscompletely dissolved
⢠Ex-Half Lifeof vicryl is7-14 days
⢠Tensilestrengthremained after 14 daysisonly 20-
30 %
31. EMBOLIZATIONOFVESSELS
⢠With the help of angiography,
exactbleedingpoint canbe
localized
⢠Agentsusedare â steelcoils,
polyvinyl alcoholfoam, gelfoam
, siliconspheres, methyl
methacrylate
⢠Theyare placedvia catheter
superselectivelyinto bleeding
vesselusuallyvia femoral artery
33. ARGON BEAM COAGULATOR
⢠Representsnew form of
electrocautery & ismore
effective than standard
cautery
⢠In thiscoagulatornonpolar
current istransmitted to
tissuesthroughthe flow of
argongas
34. ⢠Thisallowsbleedingfrom vesselswith diameter <3 mm, to becontrolled
without useof hemostats/ ligatures
⢠Tipisheld approximately 1 cmfrom tissue,flow of argongasclears
surgicalsite of fluidsto allow current to be focuseddirectly ontissuewith
decreased carbonization
⢠Thereisformation of 1-2 mmof escher( scarproducedbythermal burn or
corrosive/ gangrene) that coversthe bleedingsurface& remains
attached to tissueswith tendencyto rebleed
⢠Possibilityof gasembolismbut canbe eliminated bynot placing
handpiecetip in direct contactwith tissues
36. CAUTERY
⢠Heat activated hemostasisby
denaturation of proteinswhich
resultsin coagulationof large
area of tissues
⢠In cauterizationheat is
transmitted oninstrumentsby
conductiondirectly into tissues
⢠Whenelectrocauteryunit isnot
available , dental burnisherlike
instrument heated& applied
directly onbleeding point
⢠ELECTROCAUTERYâ Heat occurs
byinductionfrom alternating
current
37. CHEMICAL METHODS
⢠LOCALAGENTSâ
⢠1. astringents& stypticsâ
⢠Monselâssolutionâ containsferric
subsulphate& it actson
precipitating proteins
⢠Effective in arrestingcapillary
bleeding & postextractionbleeding
in medullary bone
⢠Silvernitrate istoxic, carcinogenic
& ferric chloride canbe usedin
minimal capillary bleeding
38. TANNICACID
⢠(i) Also precipitates
proteins and causes
clot formation
⢠(ii) more helpfulas
homeremedy
⢠(iii) Patient askedto
bite onfolded tea bag
in caseof post
extraction bleeding
39. BONEWAX( Beeswax +salicylicacid)
⢠Bleedingoccuringfrombony
canalisdifficult to occludeasit
isconfinedwithin canal
⢠Smallquantity of bonewaxcan
be applied
⢠It actsbymechanicalocclusion,
but largequantitiescancause
foreignbodygranuloma
formation & infection
⢠Thisshouldbeused judiciously
41. GELFOAM
â˘
â˘
â˘
â˘
â˘
â˘
â˘
Made from gelatin & isspongelike
Hasnointrinsic hemostaticaction
Main hemostatic activity is related to large
surface area , which comes in contact with
blood& further swellsonabsorbing blood
Exertspressure& actsasscaffoldfor fibrin
network
Absorbedby phagocytosis
Shouldbe moistenedin salineor thrombin
solution prior to application
It will harbour microbeswhichin turn will
cause alveolar osteitis & delayin repair
42. OXYCEL
⢠Oxidizedcellulose& anapplication releases
celluloseacidâ markedaffinity for Hbâ artificial
clot
⢠Shouldbeapplieddry asacidformedduring
wetting process, it activates thrombin orother
hemostaticagent
⢠Acidproducedalsoinhibitsepithelization ,thusit is
not usedover epithelial surfaces
43. SURGICEL
⢠Glucosepolymer based,sterile knitted fabric prepared by
controlled oxidation or regenerated cellulose
⢠Localaction isbybindingof Hbto oxycelluloseallowing dressing
to expandinto gelatinousmass,whichactsasscaffoldfor clot
formation & stabilization
⢠Canbe applied dry or soakedinthrombin
⢠Removedbyliquefaction & phagocytosisoverthe period of one
weekto one month
⢠Doesnot inhibit epithelization & canbeusedonepithelial
surfaces
45. TOOTHETTE
⢠Asmallpieceof Surgicel( haemostatic cellulose) wrapped arounda
Toothette (a pink spongeona stickusedto provide moistureto patients
who are unable to swallow)
⢠Thehaemostatic matrix canbedelivered directly to a bleedingsocketasit
clingswell to the sponge
⢠Thespongeitself canthen beeasilybitten downonbythe patient and
mouldsto the socket,in contrastto the uncomfortable bulkinessof gauze.
⢠Anaddition Toothette isthat it canbe safelyplacedin the woundby the
patient or clinicianwith advantage of reabsorption
47. ADRENALINE
⢠Applied topically causesvasoconstriction
⢠Extensiveapplicationor undiluted prep shouldbe
carefully usedâ systemic action
⢠Applied in guage( 1:1000) overoozingsite , canalso
beinjected with LA(1:80,000 to 1:2,00,000)
⢠Shouldnot beusedin hypertensives
⢠Vasoconstrictoreffect isreversibleâ watch for
recurrence
48. FERACCYLUM
⢠Localhemostatic & antisepticagent
⢠Hemostaticeffect â Basedonthe formation of synthetic complex
consistingof itâs adductwith plasmaprotein principally albumin
( this complex get brokendownoverperiod of time )
Contraindications-concomitantuse of ferrocrylum with epsilonamino
caproicacidinterferes with the formation of feracrylum albumin clot
Specialprecaution â not for parenteral use& shouldbe usedwithout dilution
Indication â adjunct to conventional hemostatic procedurein varied surgical
procedures, dental extractions & oral surgeries
Dose-undiluted solution to beapplied directly or pouredoverbleeding
surface
52. ⢠.
⢠Themilitary variant is extensively used by the DefenseForcesworldwide.
Thisbattlefield proven technology is used to manage gunshotwoundsand
blastinjuries. It comesin camouflaged,ruggedmetal pouchpacking for
easycarrying and withstand extreme temperature.
53. Axiostat isa sterile, non-absorbablehaemostaticdressingintended to controlbleedingwithin
minutesof applicationbyproviding anactive mechanical barrier to the woundsite.
54. SYSTEMIC AGENTS
⢠WHOLE BLOODâ
- Freshwhole bloodâ containsall factors
- Necessaryto type & crossmatchbloodbeforetransfusion
- Must be checkedfor HCV, HIV,HbsAg
- Banked blood
- Poorsourceof platelets
- FactorII /VII/ IX/ XIare(+)
- Oneunit of platelet conc.Has more viable platelets than oneunit of fresh
whole bloodbut isaninadequate source of factor VIII
55. PLATELET RICH PLASMA
â˘
â˘
â˘
â˘
â˘
â˘
Advisableto increaseplatelet level of
rangeof 50,000 â 1,00,000 /ul to
provideprotection
Canbe collectedfrom donatedwhole
blood& directly from patients via
plasmapheresis
Platelet conc.Arevariable for 3 days
whenstoredat roomtemperature
Variability decreaseson refrigeration
Must beinfusedquicklyvia short I/V
transfusionsetwith nofilter
Oneunit PRPraisescountby7,000 -
10,000 /ul
57. CRYOAPRECIPITATE
⢠15 ml vial containsâ 100 u
factor VIII
⢠250 mgfibrinogen & factor
XIII & vonwillebrandfactor
⢠Storedat -30 degree celcius
⢠Eachbag is from one donor
& isnot treated for inactive
viruses
⢠Thususeisassociatedwith
riskof viral transfer
58. TRASYLOL
â˘
â˘
â˘
Polypeptide obtained from
bovine parotid gland, it acts
primarily asplasmin
inhibitor , alsoinhibits
trypsin , chymotrypsin,
kallikrein & plasminogen
activation to some degree
Suppliedasâ 1000 & 500
kallikrein inhibitoryunits
/ml
Givenasâ singletransfusion
in doseof 5000-10,000 KIU
IV
68. ⢠Acuteretrobulbar hemorrhage â associatedwith zygomatic
complexfractures
⢠Midface fracturesfracuresor ocular trauma
⢠Most commonlyit occurspostâ operatively followingreduction
of zygomaticfracture , orbital floor or oroantral surgery
⢠Clinicalfeatures â proptosis, opthalmoplegia , decreasedvisual
acuity, tenseglobewith dilating pupil & pale opticdisc
⢠Treatment â
⢠Decompressionâ medical / surgical
69. SURGICAL DECOMPRESSION
⢠EitherdecreasedLA/ GA
⢠If followingorbital surgeryexistingincisioncanbe used
⢠Otherwiselateral brow incisionisused
⢠Otherwiselateral orbital rim & peri-orbitalincised
- Deepenedto lateral orbital rim & peri- orbitalincised
- Peri-orbital elevated proceedingposteriorly, if subperiostealhematomais
present
- It isevacuatedwith suction
- If nosubperiostealhematomathen periorbital isincised& intra â coronalspace
openedbyblunt dissection-anyhematomaisevacuatedâ softcorrugateddrain
placed& incisionclosedduringinterrupted sutures
70. POSTâ OPERATIVECARE
⢠Recoveryof visionisdramatic , drain removed
when drainage ceased
⢠Medical measurescanbecontinued with oral
acetazolamide500 mgODor BD& oral
prednisolone 60 mg/day
⢠If proptosispersistsor intraocular pressure
remainshigh
71. MAXILLOFACIALHEMORRHAGE
⢠Bleedingfrom facial lacerationsusuallyceasespontaneouslyor
canbe controlled by pressure
⢠Transectionof branchesof ECAwill require clamping& ligation
⢠It isusuallyaccessiblethroughwoundin a clean laceration
⢠But, in gunshotwoundcontrol maybe difficult
⢠Similarly in comminuted fracturesof midface , control of primary
hemorrhage from nose& mouth maysometimesbe impossible
bylocal measures
⢠Secondaryhemorrhage isalsodifficult to deal with simple
methods
72. ARRESTOFHAEMORRHAGE-
1. PRESSUREâ usinggauzeswabs, digital pressureor
occlusal pressureby patients
2. Clamping& ligation â vesselthat isaccessiblewithin
a wound
3. Staysuturesâ temporary suturesacrossthe wound
which2-0 /3-0 blacksilk
4. Arterial ligation â when localmeasuresalone fail to
control bleeding, ligation of branchesECAmaybe
necessaryunderideal surgicalconditionsin theatres
74. GREATERPALATINE ARTERY
⢠Runsanteriorly from the greater
palatine foramen in the submucosa
of the hardpalate
⢠Incisionoverthe palate shouldbe
made parallel
⢠Bleedingiscopious& application of
clampis difficult
⢠Haemorrhagecanbecontrolled by
a pressurepackwhichiskept in a
placebytie oversuturesfor 24 to
48 hrs
75.
76. SUBLINGUALARTERY
⢠Canoccuraccidentallybyslippingof sharpinstrument , duringimplant placement
⢠May lead to largesublingualhematomawhich, if not controlled,cancompromiseairway& maybelifethreatening
⢠Isasmallartery & localclamping& electrocauteryusuallycontrolsthebleeding
⢠Mostlyisabranchof lingual artery , but maybeabranchof submentalartery (10%)
⢠Sosometimesligationof lingual artery maynot stopbleeding& facialartery needsto beligated
78. â˘
â˘
â˘
â˘
â˘
â˘
â˘
⢠Submandibularcurvillinear incisionistakenfrom the gonial
angleto mentalregion, extendinginferolaterallyoverlying
hyoid bone
Theskin, platysma& deepfasciaare incised& lowerpole
of the submandibularglandisexposed
TheglandislIfted upwards& tendon of digastricmuscle
exposed
Mylohyoid & hyoglossusare areidentified
Hypoglossalisfoundat the posteriorborder of mylohyoid
muscle
Fibresof hyoglossuswithin the lingualtriangleare
seperatedbluntly& the gapbetweenthese fibres,lingual
artery isidentified& ligated
Ligationcanalsodoneat itâs originfrom ECA
EvenbyligatingECAbleedingcanstill continue becauseof
anastomosis
79. FACIALARTERY
â˘
â˘
â˘
â˘
â˘
Isthird anterior branchof ECA
Ligatedat the point whereit crosseslowerborder
of mandible anterior to massetermuscle,
accompaniedbyfacial veinwhichliesposteriorto
it
Marginal mandibularbranchof facial nerve crosses
superficiallyover facialvessels
Toprevent damage to this nerve submandibular
incision is given one to two cmbelow the lower
border of mandible.
Theskinsubcutaneoustissue, platysma & deep
fasciaare cut& retractedupwards& the artery lies
anterior to masseter muscle
⢠It isisolated, tied &cut
80. MAXILLARYARTERY
â˘
â˘
â˘
Terminalbranchof ECA&
situated deep sodirect
ligation isdifficult
Transâ antral approachis
used, it isat riskduringTMJ
surgery,asit liesmedial to
condylar neck
Direct pressurewith packing
, cancontrol the bleeding in
majority of casesor ligation
of ECAhasto be done
82. External carotid artery
â˘
â˘
â˘
â˘
â˘
â˘
Extensiveanastomosisof all branchesof
ECAoccursacrossthe midline, the
unilateral ligation doesnot stop
hemorrhage completelyandwill not give
bloodlessfield
ECACanbeligatedat two placesfirst in
the carotidtriangle
Arrestsbleedingfrom all the branches
exceptsuperiorthyroid artery
Secondlyretromandibularfossa, bleeding
exclusivelyfrom maxillary artery
Indicationsâ Haemorrhage from
maxillofacialregionnot controlledby
localmeasures
Anesthesiaâ generalanesthesia
86. Procedure
1
â˘
â˘
â˘
â˘
. UsingEpistatsâ
Insert epistat into eachnostril ,aiming
for a fingertip inserted into mouth to
backof soft palate , soposteriorcuffis
restingin nasopharynx
Inflate posterior cuff with upto 10 ml of
saline ;withdraw epistat until resistance
felt at nasopharyngealwall
Inflate anterior cuffwith 30 mlsaline
Suctioncathterscanbeinserted through
the central lumento aid in cleaning
debrisfrom nasopharynx
89. ⢠Insert 12- 14 guagefoley catheterwith 20 ml balloonsinto the nose,aimingagain
for the fingertip
⢠Inflate balloonwhencatheteruntil the balloonoccludesagainstchoana
⢠Pullbackoncatheter until ballonoccludesagainst choana
⢠Tiecatheterstogetherafter passingbehindheadopposite& releaseperiodically
to prevent ischemicnecrosis
⢠Insert bismuth, iodoform ,paraffin paste5 cmribbonguazepacksinto nosein
front of balloons& foleyâs catheter
⢠In patients with baseof skullfractureâ riskof enteringcranialcavity â foleys or
epistat shouldbedirected caudally
⢠Massivebleedingcontrolledbycompressionof maxillaagainstcranialbasewith
splints
⢠Lastresort- Ligationof ipsilateral ECAor its branch
90. BLOOD DONATION
⢠Theaverageadult hasabout 10 unitsof bloodin hisbody.Roughly1 unit isgivenduringa
donation.
⢠Ahealthy donormaydonate red bloodcellsevery 56 days,or doublered cellsevery 112
days.
⢠Ahealthy donormaydonate platelets asfew as7 daysapart, but a maximumof 24times
91. Blood Transfusion
⢠Introduction-
⢠FirstdescribedbyRichardlower ( 1666) in animals& in man( 1667 ) usingcalfâs
blood
⢠Firstsuccessfulmanto mantransfusionwasreported byJBlundell,in 1818 , an
obstetrician
⢠Landsteiner in 1930 first observed agglutination of human red cells byserum
belonging to other individuals & described the ABOgroups according to two
types of agglutinogens
⢠Thefourth groupABwasdescribedbyphysicianDecastelliin 1902
⢠WhenRequiredâ one540 ml bloodraisesHb1 gm%. If Hb<6gm%, blood
transfusionisdesirable
⢠If major operationsto be performed Hbmustbe>10 gm%
97. Demerits
⢠Techniqueisnot easy
⢠Cannotbegivenimmediately without grouping&
crossmatching
⢠Storageisdifficult , cannotbeusedafter 3 weeks
⢠Storedat 4 degreeCwith 3.8 %NaCitrate in a
ratio of 9:1
⢠Transfusionassociated reactions
98. RATEOFBLOODTRANSUSION
Begungenerallyat 2 to 3 ml per minute & increasedasfollows
1. For elective transfusion into normal circulatory system infus
8-10 ml per minute with 60-80 minutes per transfusion ( 40-
50 drops/min)
2. In embarrassedcardiovascularsystemespeciallyin elderly 4
5 ml per minute ( 30 min/transfusion)
3. In acutehypovolumia infuseat maximumobtainable rate
until systolicbloodpressureis100 mmof Hg(200 drops
/min)