IC 10: Advanced Techniques in Needle Aponeurotomy and ...
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IC 10: Advanced Techniques in Needle
Aponeurotomy and Collagenase -Going
Beyond the MP Joint
Moderator(s): Gary M. Pess, MD
Faculty: Gary M. Pess, MD, Charles J. Eaton, MD, Keith Denkler, MD
Session Handouts
Thursday, September 05, 2019
74TH ANNUAL MEETING OF THE ASSH
SEPTEMBER 5 – 7, 2019
LAS VEGAS, NV
822 West Washington Blvd
Chicago, IL 60607
Phone: (312) 880-1900
Web: www.assh.org
Email: [email protected]
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IC10
AdvancedTips,PearlsandTechniquesforNeedleAponeurotomy
(NAandPNF)
GaryM.Pess,MD
MedicalDirector,CentralJerseyHandSurgery
ClinicalSeniorInstructor,DepartmentofOrthopedicSurgery,DrexelUniversity
SchoolofMedicine
[email protected](Feelfreetoemailmewithdifficultcasesorquestions)
Adaptedfrom:
Pess,GaryM.:“MinimallyInvasiveTreatmentofDupuytrenContracture”,InG.R.Scuderi,A.J.Tria(eds.),MinimallyInvasiveSurgeryinOrthopedics,SpringerInternationalPublishing,Switzerland,2015
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ABSTRACT
Dupuytrendiseaseisabenigninheritedfibromatosisofthefasciaofthehandand
fingers.Itleadstoprogressivecontracture,whichaltershandfunction.Thereisnoknown
“cure”forDupuytrencontracture.
Dupuytrencontractureistraditionallytreatedwithopensurgicalprocedures,most
commonlypartialpalmarfasciectomy.Therearenumerousproblemsassociatedwith
openfasciectomy.Regionalorgeneralanesthesiaisoftenrequired.Recurrenceratesvary
from12%-73%andthereisasignificantcomplicationratereportedbetween3.9to39%.
Itiscommonforpatientstorequireanextendedperiodoutofworkandawayfromsports
andanextensivecourseofpostoperativehandtherapyisoftennecessary.Evenafter
meticulousremovalofdiseasedfascia,thediseaseandcontracturecanrecur.
Needleaponeurotomy(NA/PNF)andClostridiumHistolyticumCollagenase(CCH,
Xiaflex,Xiapex)injectionarenewminimallyinvasivemethodsusedtotreatDupuytren
contracture.Comparedtofasciectomy,theyhavealowercomplicationrateandrecovery
ismorerapid.Patientscanreturntoworkandsportsmorequickly.Theseprocedurescan
beperformedunderlocalanesthesiainanofficeorclinicsetting.Theoverallcostislower,
however,recurrenceratesarehigherthanwithopensurgery.
Thisinstructionalcourseexaminesthehistoryofminimallyinvasivetreatmentand
theanatomyandphysicalexaminationofthepathologiccords.Reportedoutcomes,
efficacyandrecurrenceratesarereviewed.Precisestep-by-steptechniquesfor
performingNAandCCHarepresented.Emphasisisplacedonaccuracy,maximizing
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correctionandminimizingpotentialcomplications.Tipsandpearlsfromtheauthor’s
fifteen-yearexperiencearediscussed.
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INTRODUCTION:
Dupuytrendiseaseisabenignfibromatosisofthefasciaofthehandandfingers.It
beginswithapalpablemassornodule.Thisisusuallylocatedbetweentheproximal
palmarcreaseanddistalpalmarcrease,butthenodulemayfirstpresentinthefinger.
Enlargementofthenodule,leadstothedevelopmentofpathologiccordswhichthicken
andcontract,causingcontractureofthemetacarpophalangeal(MP)andproximal
interphalangeal(PIP)joints.Otherareasaffectedincludethedistalinterphalangeal(DIP)
jointandwebspaces.
Dupuytrendiseaseisaninheriteddisorderthatisautosomaldominantwith
variablepenetrance1.ItismostcommonlyseeninolderCaucasianmalesofEuropean
descent,butcanbefoundinpeopleofallbackgrounds.Thereisahigherincidencewith
advancingageandthepeakageinthemalesisinthe50’s2.Thereisa3.5:1–9:1maleto
femaleratio3.Thediseaseappearslaterinwomenthanmen,withwomencatchingupto
menintheir80’s.TheoverallprevalenceofDupuytrencontractureisuncertain,butis
believedtorangefrom0.2%to56%4,5.EstimatedincidenceintheUSArangesfrom1-7%6.
Itisoftenmisdiagnosedandundertreated.
Themostcommonlyaffecteddigitsaretheringfingerandlittlefinger(50-60%),
followedbythethumb,middlefinger,andindexfinger7.Dupuytrencontractureisusually
bilateral,withanincidenceof42-98%8.Thediseasemayalsobeassociatedwithectopic
lesions,includingGarrod’snodules(dorsalPIPjointfibromatosis),Peyronie’sdisease,and
Ledderhose’sdisease4,9,10.Huestondescribedthisgroupoffibroproliferativediseasesas
Dupuytrendiasthesis11,12.Herecognizedthatriskfactorsincludingearlyageofonset
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(<age50),bilaterality,strongfamilyhistoryandectopiclesionspredisposeapatienttoa
poorerprognosiswithrapidprogressionandhigherrecurrenceaftertreatment.More
recentstudieshaveconcludedthattheworstoutcomeswereassociatedwithplantar
fibromatosis,Garrod’snodules,radialsidedinvolvement,earlyonset(<age50),malesex
andthesmallfingerrequiringsurgery13,14.
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HISTORYOFMINIMALLYINVASIVETREATMENT
HenryCline15proposedtreatmentofthecontracturein1777.Heusedabladeto
sectionthecontractedcords,performingafasciotomyoraponeurotomy.Cooper
(1822)16,performedapercutaneousfasciotomy,usingapointedbistourytodividethe
pathologicalcords.Percutaneousprocedureswerecommonlyusedthroughoutthe1800’s
andweredocumentedbyAdams17(1892).Openexcisionoftheabnormalfasciabecame
thestandardtreatmentaftertheintroductionofgeneralanesthesiainthemid1800’s.
Fergusson(1842)19proposedtreatmentbyopenexcisionofthediseasedfasciaand
Goyrand(1883)18performedalimitedfasciectomy.
Luck(1959)20reintroducedsubcutaneousfasciotomyfortheinvolutionaland
residualstagesofDupuytrendisease.Usingafasciatome,hesectionedthefibrouscords
subcutaneouslyatmultiplelevelsinthepalm.Fortheinvolutionalstage,healso
recommendedopenresectionofthepalmarnodules.
LermusiauxandDebeyre(1972)21describedusinganeedle,ratherthanaknife,to
dividethecords.Needlefasciotomywaslessinvasivethanopenfasciectomy,andpatients
hadaquickerrecoveryoffunction.Badois,Lermusiaux,MasseandKuntz(1993)22,
Foucher,MedinaandNavarro(2003)23,andvanRijssenandWerker
(2006)24subsequentlyreportedontheuseoffasciotomy,anditsacceptance
increased.ThishasbeensupportedinrecentyearswiththeworkofEaton(2011)25,Pess,
PessandPess(2012)26,DiazandCurtin(2014)27,Morhart(2014)28andMcMillanand
Binhammer(2014)29.
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Collagenaseclostridiumhistolyticum(CCH,Xiaflex,Xiapex)isanenzymatic
treatmentforadultpatientswhohaveapalpablecord.HurstandBadalamentestudied
CCHextensively,firstinvitroonexcisedDupuytrencords(1996)30andtheninPhaseIII
clinicaltrial(2007)31.Thiswasfollowedbydouble-blind,placebo-controlledmulticenter
trialsCORDI(2008),CORDII(2009),JOINTI(2013),JOINTII(2013),CORDLESS(2013)
andtheMULTICORDstudy(2015)32-37.XiaflexwasapprovedforuseintheUnitedStates
onFebruary2,2010.ThesBLAwasapprovedonOctober20,2014,allowingthe
treatmentofuptotwojointsinasingletreatmentvisitandpermittingdelayed
manipulation24–72hoursafterinjection.Useofcollagenaseisrestrictedtoclinicians
whohaveundergonethethree-steptraining,enrollmentandregistrationprocedurewith
themanufacturer.
ThecurrentdrugisapredeterminedmixtureofAUX1andAUX2collagenasethat
cleavescollagenmoleculesatdifferentlocations.AUX1andAUX2worksynergisticallyto
providehydrolyzingactivityandrapidlydegradecollagen.CCHislessactiveagainstType
IVcollagen,whichisfoundinthebasementmembraneofbloodvesselsandthe
perineuriumofperipheralnerves.
Non-surgicaltreatmentsforDupuytrencontractureincludesplinting,handtherapy,
radiationtherapy38,intralesionalsteroidinjections39,40andCCHinjection.Minimally
invasiveproceduresincludeneedleaponeurotomy(NA)/percutaneousneedle
fasciotomy(PNF).
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OPENSURGICALPROCEDURES
The“GoldStandard”fortreatmentofpatientswithDupuytrencontractureis
fasciectomyandsurgeryisstillthemostcommonintervention.Opensurgicalprocedures
includestandardlimitedfasciectomy,segmentalfasciectomy,radicalfasciectomy,
dermofasciectomyandopenfasciotomy11,41-48.
Therearenumerousproblemsassociatedwithopenfasciectomy.Regionalor
generalanesthesiaisoftenrequired.Recurrenceratesvaryfrom12%-73%26.Thereisa
significantcomplicationratereportedbetween3.9and39%49.Seriouscomplications
includingdelayedwoundhealing,hematoma,scarpain,infection,dysesthesia,nerve
laceration,arteriallaceration,PIPjointdislocationandCRPS.Itiscommonforpatientsto
requireanextendedperiodoutofworkandawayfromsports.Anextensivecourseof
postoperativehandtherapyisoftennecessarytodecreasesensitivityofscarsand
maximizepost-operativerangeofmotionandstrength.Somepatientsneverregainfull
flexion.ThetotalcostoftreatmentishigherthanNAorCCH50.
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ANATOMYandPHYSICALEXAMINATIONofCORDS
Dupuytrendiseaseconsistsofacombinationofnodules,skinpitsandcords.
Commoncordsinclude:
1)Pretendinouscord–originatesfrompretendinousband,beginsproximaltothe
proximalfingercrease,contractstheMPjointoffingersorthumb.
2)Centralcord–locatedmidlinebetweenneurovascularbundlesanddistaltothe
proximalfingercrease,isacontinuationofthepretendinouscord,contractsthePIPjoint.
3)Lateralcord–composedofdiseasedlateraldigitalfascia,locatedsuperficialto
neurovascularbundle,contractsPIPjoint.
4)Retrovascularcord–locateddeeptoneurovascularbundle,cancontractboththe
PIPandDIPjoints.
5)Natatorycord-contractsthe2nd,3rdand4thwebspaces.
6)Commisuralcords(proximalanddistal)-contractsthe1stwebspace,maybe
rope-likeinconsistency.
7)Abductordigitiminimicord-contractsthelittlefingerMPandPIPjoints.Can
displacetheneurovascularbundleinavolar,midlineanddistaldirection.
8)Spiralcord–contractsPIPjoint-usuallyacombinationofpretendinouscord,
diseasedlateraldigitalfasciaandGrayson’sligament.Candisplaceneurovascularbundle
inavolar,midlineanddistaldirection.
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INDICATIONSFORTREATMENT
Thereisno“cure”forDupuytrencontracture,nomatterwhattreatmentischosen51.
Oncepresent,thecontracturedoesnotresolvespontaneously.Achievingperfectionisnot
necessary,especiallywhentreatingadiseasethathasasignificantrecurrencerate.
Patientsappreciateimprovementoffunctionandincreaseinrangeofmotion,even
withoutachievingfullextension.Whensevere,long-standingcontracturesarepresent,the
patient’sexpectationsneedtoreasonable.
WhenperformingminimallyinvasiveproceduresforDupuytrencontracture,treat
early.Sinceminimallyinvasivetreatmentshavealowermorbidityandrisk,theold
paradigmofwaitingforanMPorPIPcontractureof30°doesnotpertain.Thehighest
efficacyandlowestrecurrenceratesareinpatientswiththeearlydiseaseandminimal
arthrofibrosisofthePIPjoint.Ifacontracturerecurs,minimallyinvasivetreatments
shouldberepeatedearly.
Priortoperforminganyprocedure,adiagramofthehandisusedtochartnodules,
cords,previoussurgicalincisionsandskingrafts,rangeofmotionanddegreeof
contracture.Allabnormalcordsshouldbeidentifiedbypalpationandillustratedwitha
marker.Theunderlyingpathologyshouldbevisualizedinathree-dimensionalpattern,
whichisnecessarytoplanneedleentrancepointsandsitesforCCHinjection.Skincreases
shouldbeavoidedforbothneedleinsertionandCCHinjection.TheideallocationsforCCH
injectionsandNAinsertionareareaswherethecordismaximallybowstringed,which
increasesthedistancebetweenthecordandtheflexortendonsandneurovascular
bundles.Suppleskin,whenavailable,isoptimalforneedleplacement.Careshouldbe
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takentoavoidtheneurovascularbundlewhenaspiralorADMcordispresent.Only
pathologiccordsarereleased.Scarredandcontractedskinfrompreviousopensurgery
andskingraftingarenottreated.
Step-by-steptechniqueisdescribedinthefollowingsection.Thisisdesignedtogive
guidanceandprovideknowledgetoallowmostfingercontractures(includingPIPjoint
contractures)tobetreatedwitheitherNAorCCH.
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TECHNIQUE:
NEEDLEAPONEUROTOMY(NA)/PERCUTANOUSNEEDLEFASCIOTOMY(PNF)
Needle aponeurotomy is performed in an outpatient treatment room under local anesthesia
with the patient recumbent26. For patients who require anesthesia, light monitoredanesthesia
care(MAC)sedation can be utilized in a surgery center setting. If anesthesia is used, an
experienced anesthesiologist is essential, so that it can be assured that the patient remains
responsive to stimuli. Constant communication with the patient is mandatory.
The patient’s hand is prepped with antiseptic solution. A stack of folded towels is placed
under the hand to aid in extension of the MP and PIP joints. Portal sites are carefully chosen
between skin creases in areas of definite cords and are marked with a surgical marker. The
injections sites may need to be modified after releasing the MP joint. The center of the cord is
normally used as the needle entrance site, but 2 parallel insertion sites, radial and ulnar, may be
used for wider cords > 5mm52.
Intradermal anesthesia is performed with <1cc lidocaine 1% plain injected in the area of the
palmar portals, prior to the release of any cords. Only the dermis is penetrated and injection is
performed as the needle is withdrawn. This syringe is placed aside.
A 5cc syringe is filled with 3cc lidocaine 1% plain and 1cc methylprednisolone acetate
injectable suspension 40mg (Depo-Medrol, Pharmacia & Upjohn Co., New York, NY).
Corticosteroids are not used for patients with diabetes mellitus. Short 25-gauge, 16-mm (5/8-in)
length needles are used exclusively. Use of larger needles is not recommended. A tourniquet is
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not applied. Patients are asked to stop anticoagulation, if possible, but blood thinners are not
considered a contraindication to the procedure.
Eachtimeaportalisentered,0.1ccofthelidocaine/corticosteroidmixisinjectedinto
thelocalarea,andtheneedleisusedasascalpeltoreleasethecordatmultiplelevelsfrom
proximaltodistal.A“pinchandpoke”techniqueisemployed.Thecordispalpatedand
thenpinchedbetweenthefingertips.Theneedleisalignedperpendiculartothecord.The
fingerisflexedandextendedimmediatelyaftereachneedleinsertiontoconfirmthatthe
needleisnotplacedwithintheflexortendon.Insertionportalsaremadeattheareasof
maximumbowstringingofapalpablecord.Areasfarthestfromtheneurovascularbundle
areselectedandthepatientsareconstantlyaskediftheyfeelanyelectricshocks.Portals
arespaced5mmapartandskincreasesareavoided11.NoDopplerorultrasoundisused.
Careistakentonotpushtheneedleintoodeep.Mostcordsarelessthan4mmfromthe
skin,sotheneedlecanremainfairlysuperficial.Thedistancebetweenhuboftheneedle
andtheskiniswatchedcloselyatalltimes.
Toconfirmagoodportalsite,applytractionandlookforblanching51.Ifthediseased
cordistighterthantheskin,theskinwillusuallynotblanchwithtraction.Blanchingmay
indicatethattheskiniscontractedandtheremaynotbeanunderlyingcordpresentto
release.Blanchingwilladvancedistallywhentheunderlyingcordhasbeenadequately
released.
Threemaneuversareused:perforate,slice,andclear.Anupanddownperforationof
thecordisperformedwiththeneedleorientedvertically.Agentlependulumside-to-side
slicingmotionisusedwiththeneedletipperpendiculartothecord’slongitudinalaxis.
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Divisionofthecordprogressesfromsuperficialtodeep.Itcansometimeshelptopushthe
cordagainsttheneedlewhileslicing.Thethree-dimensionalanatomyofthecordshould
bekeptinmindatalltimes.Inareasofpitting,atangentialclearingmotionorsubcision
isemployedtoseparatethecordandnodulefromthedermis.Thishelpstolowerthe
incidenceofskintears.Acracklyfeelingisnotedasthefibersarereleased.Theneedle
shouldbechangedfrequentlytomaintainsharpness(~15-25).Gentleextensiontension
isplacedonthecordduringtherelease,andthenpassiveextensionisusedtorupturethe
cords.Apopmaybeheardorfelt.Thefingeristhenmanipulatedinabduction,adduction,
pronationandsupinationtoreleaseallcords.Unaffectedadjacentfingersshouldalsobe
manipulated,sincethiscanhelpdisruptanyresidualcords.
Natatorycordsarereleasedbyorientingtheneedleparalleltothelongitudinalaxisof
thefinger(perpendiculartothetransverseaxisofthecord).Thecordisthenreleased
withaslicingmotion,movingproximallytodistally.Thereleasedcordismassagedto
helpdisruptremainingdeepfibers.Massagingisalsousefulfornarrowlateralcords.
Aftercompletingthereleasedistally,thepalmandfingerarereassessedforresidual
cords.Eachofthesecordsisreleased,againworkinginaproximaltodistaldirection.A
PIPjointcontracturemaystillpersistevenafterallcordsarereleased.Thereisoftena
non-palpablecentralcordpreventingreleaseofthePIPcontracture.Apalmarreleaseof
thiscordcanbeperformedinthemidline,proximaltomiddlefingercrease.Itiscriticalto
stayverysuperficialandavoidenteringtheflexortendonsheath.Ahiddenretrovascular
cordcanbefoundthroughmeticulouspalpationandiseasilyreleased.
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Releasingthetransverseretinacularligaments,bothradiallyandulnarly,canhelp
correctadifficultPIPjointcontracture.Theligamentisreleasedinatransversedirection,
stayingdorsaltotheneurovascularbundles.
Subcision,usingabent25or18gaugeneedle,freesuptetheredskinandcreases.It
alsoallowsmoreskinmobility.Thereleaseisdonesuperficiallyoverthecentralcordat
theMPandPIPjointcreases.
AfixedBoutonnièredeformityleftuntreatedleadstorapidrecurrenceafterNA.
Releasetheterminalextensortendonusinga25gaugeneedleoverthemiddlephalanx
head.Enterbothradiallyandulnarlyforcompletereleaseandhavethepatientactively
flextheDIPjointtoconfirmrelease.
DIPjointcontracturescanalsobereleasedbycarefullystayingsuperficialandavoiding
theneurovascularbundlesandFDPtendon.
InpatientswithseverePIPjointcontractures,anerveblock(wristordigital)and/or
PIPjointinjectionwithlidocaine1%plainisusedforsupplementaryanesthesia.Thisis
performedafterNAiscompletedtohelpreducepainduringtheextensionprocedure.
Afterallpossiblecordshavebeenreleased;nodulesareinjectedwiththemixtureof
lidocaine and corticosteroid28.
Alightdressingwithgauzebandageisapplied,andremovalofthebandageisallowed
thatevening.Asplintisfittedimmediatelypost-procedureandnightuseisrecommended
forthreetofourmonths.Eventhoughasplintisrecommended,thereisnoscientific
evidencesupportingtheuseofapost-proceduresplint53.Patientsareinstructedto
exerciseathome5-10minutestwiceadayfor4weeks.Writteninstructionsareprovided,
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includingspecificactiverangeofmotionexercisesinflexion,extension,abductionand
adductionandgentlepassivestretching.Itisrecommendedthatpatientsavoidheavy
graspingforthefirst2weeks.Therapyisnotneededinmostinstances.Handtherapywith
splintingcanbeorderedforresidualcontracturesandtotreatPIPjointsthathave
regainedfullpassiveextension,buthavearesidualactiveextensionlag(centralslip
laxity)54.
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AUTHOR’STIPSANDPEARLSNEEDLEAPONEUROTOMY
-Flexandextendfingeraftereachneedleinsertiontoconfirmneedlenotinflexortendon-Maintaintensiononcord-Theneedleisalignedwiththebevelperpendiculartocord-Releaseperpendiculartothelongitudinalaxisofthecord-Changeneedlesfrequently-Chooseareasofmaximumbowstringforinsertion.SelectareasfarthestfromNVbundle.-Communicationwithpatientisnecessary-repeatedlyaskpatientiftheyfeelelectricshocks-Usuallycenterofcord,butsidebysideportalsforthickcords>5mm-Releaseproximallytodistally,allowingeasierandsaferreleaseofPIPjoint-Manipulatefingerinextension,adduction,abduction,pronationandsupination-Manipulateunaffectedadjacentfingerstoo-Massagecordswiththumbtohelpdisruptcord(especiallyusefulfornarrowlateralcordsandnatatorycords)-ForresidualPIPjointcontractures,releasethenon-palpablecentralcord,retrovascularcordandthetransverseretinacularligaments-InjectthePIPjointwithanesthesiapriortomanipulatingseverecontractures-ReleasetheterminalextensortendontotreataBoutonièrredeformity
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OUTCOMES,EFFICACYANDRECURRENCE
PublishedreportsontheresultsoffasciectomyandNAuseavarietyofdefinitionsof
bothcorrectionofcontractureandrecurrence26,55.Thetimingofevaluationofthe
outcomealsovariesgreatly.Thismakesitdifficulttocompareresults.Standardizingthe
reportingofresultsinthefuturewillallowamoremeaningfulcomparisonofdifferent
treatmentsforDupuytrencontracture.Efficacyshouldbedefinedascorrectionofthe
affectedjointto≤5°within90daysoftheprocedure.Recurrenceshouldbedefinedas
>=20°lossofpostprocedurecorrection.MPandPIPjointefficacyandrecurrenceshould
beevaluatedindividuallysincePIPjointshavealowertreatmentefficacyrateandahigher
recurrencerate56.
TheFrenchexperiencewithNAhasbeenreportedbyseveralgroupsofsurgeons
andrheumatologists.Badois,Lermusiaux,MasseandKuntz(1993)published,inFrench,
theresultsofNA22.Therewerenomajorcomplications,thoughtherewasaskinbreakin
16%,digitaldysesthesiain2%,andinfectionin2%.Bleton,MarcireauandAlmot(1997)
documentedtheresultsofaprospectivestudyofNA57.Allcomplicationswereminor
includingskintearin4%,temporaryparesthesiain2%andsuperficialinfectionin1%.
Lermusiaux,Lellouche,BadoisandKunz(1997)relatedtheresultsofalargenumberof
NAprocedures58.Animprovementofover70%wasobservedin81%ofhands.The
complicationratewas0.05%forbothtendonanddigitalnerveinjuries.Foucher,Medina
andNavarro(2003)reporteda79%gaininextensionfortheMPjointand65%forthe
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PIPjoint23.Therewasonedigitalnerveinjury.Asubgroupof100patientshada
recurrencerateof58%aftermeanfollow-upof3.2years.
VanRijssenandWerker(2006),describedapost-procedureimprovementof71%
(fromaverageof62°to18°)24.Therecurrenceratewas65%.Theirdefinitionof
recurrencewasanincreaseinthepassiveextensiondeficitof>30°.Twopatientshad
diminishedsensibility(3%).Therewerenoflexortendoninjuries.
VanRijssen,LindenandWerker(2012),reportedtheresultsofrandomized,
controlledstudy,whichcomparedtheoutcomeofNA/PNFandlimitedfasciectomyafter5
years.The5-yearrecurrenceratewas85%.Howeverpatientswhorecurredstill
preferredPNFoverfasciectomyforrepeattreatment59.
Pess,PessandPess(2012)reportedanextensiveseriesof1,013fingerstreated
withaminimumfollow-upof3years26.Therewasanimmediatepost-procedure
correctionofMPandPIPjointcontracturesfrom35°to1°and50°to6°respectively.At
finalfollow-up,themeanMPandPIPjointcontractureswere11°and35°.Thedifference
incorrectionwasstatisticallysignificantforMPvs.PIPjointsandforageunder55,
comparedto55andover.Successfulcorrectiontoaresidualcontractureof≤5°,after1
procedure,wasachievedin98%ofMPjointsand67%ofPIPjoints.Recurrencewas
definedasanincreaseofcontracture>20°,comparedtopost-procedurecorrection.
Minimumfollow-upwas3years(range3.0-6.2years).Therecurrenceratewas20%for
MPjointsand65%forPIPjoints.Animprovementofextension≥50%oftheinitial
contracturewasmaintainedatfinalfollow-upin75%ofMPjointsand33%ofPIPjoints.
Complicationswererare,exceptforskintears,whichoccurredin3.4%ofdigits.Alltears
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healedwithoutanyinterventionotherthanlocalwoundcare.Therewasatemporary
neuropraxiain1.2%ofpatients,andapresumednervelacerationin0.1%(ulnardigital
nerveoflittlefinger).Therewerenoknowninstancesofarteriallaceration,tendon
rupture,pulleyrupture,hematoma,infection,orcomplexregionalpainsyndrome,andno
patientwashospitalized.
McMillanandBinhammer29(2015)comparedthelong-termresultsof54patients
whounderwentNAcombinedwithaseriesoftriamcinoloneacetonideinjections(Sandoz
CanadaInc.,Boucherville,Quebec)orwhounderwentNAalone.Theinjectionsweregiven
immediatelypost-NAandagainat6weeksand3monthslater.MeanTotalActive
ExtensionDeficit(TAED)wassignificantlylessinneedleaponeurotomytriamcinolone
acetonidepatientsat6monthsandbetween13and24months.Meantimetoretreatment
andmeanTAEDimmediatelypriortoretreatmentdidnotdiffersignificantlybetween
groups.Kaplan-Meiersurvivalestimatesdemonstratedasignificantlyhigherpercentage
ofNAgrouppatientsexpectedtoreturnforretreatmentby24months,butnotby36
months.
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COMPLICATIONS
SideeffectsareuncommonafterNA.Themostcommoncomplaintsarepain,
swellingandecchymosis.Analgesicscanbeofferedtopatients.
SkintearsarerelativelycommonafterNAwithanincidenceof~3-4%.Tearsare
treatedinitiallywithpressureandelevation.Patientsareinstructedinlocalwoundcare
anddressingchanges.Anyexposedtendoniskeptmoistuntilthewoundgranulates,
becauseifitdoesn’tdry,itwon’tdie.Skingrafts,rotationflapsandothertypesofcoverage
arenotnecessary.Allskintearshealwithin2-6weeks.
Seriouscomplicationsoccurinfrequently.Infectionisusuallysuperficialandcanbe
treatedwithoralantibiotics.Transientneurapraxiaismorecommonthancompletenerve
laceration.Tendonruptureandarteriallacerationarerare.
CONCLUSIONThereisnocureforDupuytrencontracture.Nomatterwhatprocedureischosen,
thediseasemayrecur.Untilageneticordisease-modifyingtreatmentcanbefound,
minimallyinvasivetreatmentsshouldbeconsidered.Thesetechniquesoffera
combinationofexcellentefficacy,significantimprovementofrangeofmotion,low
complicationrateandquickrecovery.
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BIBLIOGRAPHY
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21. LermusiauxJL,DebeyreN.LetraitementmedicaldelamalidiedeDupuytren,Rhumatologique.Paris:Expansion
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26. PessGM,PessRM,PessRA.ResultsofneedleaponeurotomyforDupuytrencontractureinover1,000fingers.JHand
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27. DiazR,CurtinC.NeedleaponeurotomyforthetreatmentofDupuytren’sdisease.HandClin.2014;30:33-38.
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29. McMillanC,BinhammerP.SteroidinjectionandneedleaponeurotomyforDupuytrendisease:Longtermfollow-upof
arandomizedcontrolledtrialJHandSurg.(Am)2014;39(10):1942-1947.
30. BadalamenteMA,HurstLC.EnzymeinjectionasanonoperativetreatmentforDupuytren’sdisease.DrugDelivery
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31. BadalamenteMA,HurstLC.Efficacyandsafetyofinjectablemixedcollagenasesubtypesinthetreatmentof
Dupuytren’scontracture.JHandSurg.(Am)2007;32:767-774.
32. HurstLC,BadalamenteMA,HentzVR,HotchkissRN,KaplanFT,MealsRA,SmithTM,RodzvillaJ.Injectable
collagenaseclostridiumhistolyticumforDupuytren’scontracture.NEnglJMed.2009;361:968-979.
33. GilpinD,ColemanS,HallS,HoustonA,Karrasch,JonesN.Injectablecollagenaseclostridiumhistolyticum:anew
nonsurgicaltreatmentforDupuytren’sdisease.JHandSurg.(Am)2010;35(12):2027-2038.
34. WattAJ,CurtinCM,HentzVR.CollagenaseinjectionasnonsurgicaltreatmentofDupuytren’sdisease.JHandSurg.
(Am)2010;35(4):534-539.
35. WitthautJ,JonesG,SkrepnikN,KushnerH,HoustonA,LindauT.Efficacyandsafetyofcollagenaseclostridium
histolyticuminjectionforDupuytren’scontracture:short-termresultsfrom2open-labelstudies.JHandSurg.(Am)
2013;38(1):2-11.
36. PeimerCA,BlazarP,ColemanS,Kaplan,FT,Smith,T,Tursi,JP,Cohen,B,Kaufman,GJ,LindauT.Dupuytren’s
contracturerecurrencefollowingtreatmentwithcollagenaseclostridiumhistolyticum(CORDLESSstudy):3-year
data.JHandSurg.(Am)2013;38(1):12-22.
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37. Gaston,G;Larsen,SE;Pess,GM;Coleman,S;Dean,B;Cohen,BM;Kaufman,GJ;Tursi,JP;Hurst,LC.Theefficacyand
safetyofconcurrentcollagenaseclostridiumhistolyticuminjectionsfortwoDupuytrencontracturesinthesame
hand,aprospectivemulticentercenter.JHandSurg.(Am)2015;40:1963-1971.
38. SeegenschmiedtMH,KeilholzL,WielputzM,SchubertC,FehlauerF.Longtermoutcomeofradiotherapyforearly
stageDupuytren’sdisease:aphaseIIIclinicalstudy.In:EatonC,SeegenschmiedtMH,BayatA,GabbianiG,WerkerP,
WachW,editors.Dupuytren’sdiseaseandrelatedhyperproliferativedisorders:principals,researchandclinical
perspectives.Berlin:Spring-Verlag;2012.p.349-371.
39. KetchumLD,DonahueTK.TheinjectionofnodulesofDupuytren’sdiseasewithtriamcinoloneacetonide.JHandSurg.
2000;25(6):1157-1162.
40. McMillanC,BinhammerP.SteroidinjectionandneedleaponeurotomyforDupuytrendisease:arandomized
controlledstudy.JHandSurg.(Am)2012;37(7):1307-1312.
41. McIndoeA,BeareRLB:ThesurgicalmanagementofDupuytren’scontracture.AmJSurg.1958;95:197-203.
42. McCashCR:TheopenpalmtechniqueinDupuytren’scontracture.BrJPlastSurg.1964;17:271-280.
43. GelbermanRH,AmielD,RudolphRM,VanceRM.Dupuytrencontracture.Anelectronmicroscopic,biochemical,and
clinicalcorrelativestudy.JBoneJointSurg.(Am)1980;62:425-432.
44. HuestonJT:DermofasciectomyforDupuytren’sdisease.BullHospJtDis.1984;44:224-232.
45. KetchumLD,HixsonFP:Dermofasciectomyandfull-thicknessgraftsinthetreatmentofDupuytren’scontracture.J
HandSurg.[Am]1987;12:659-663.
46. DiasJJ,BraybrookeJ.Dupuytrencontracture:anauditoftheoutcomesofsurgery.JHandSurg.2006;31B:514-521.
47. UllahAS,DiasJJ,BhowalB.Doesa'firebreak'full-thicknessskingraftpreventrecurrenceaftersurgeryforDupuytren
contracture?:aprospective,randomisedtrial.JBoneJointSurg.(Br)2009;91:374-378.
48. HurstLC.:Dupuytren’scontracture.WolfeSW,HotchkissRN,PedersonWC,KozinSH.InGreen’sOperativeHand
Surgery.6thed.Philadelphia:ElsevierChurchillLivingstone;2011.p.141-158.
49. DenklerK.SurgicalcomplicationsassociatedwithfasciectomyforDupuytren’sdisease:a20-yearreviewofthe
Englishliterature.PlasticSurg.2010:10:116-133.
50. DongaP.,DeKovenM.,KaplanFT.,TursiJP,LeeWC.Costsofcollagenaseclostridiumhistolyticumandfasciectomyfor
Dupuytren’scontracture.AmJPharmBenefits2015;7(1):24-31.
51. BayatA,McGroutherDA.ManagementofDupuytren’sdisease–clearadviceforanelusivecondition.AnnRCollSurg
Engl.2006;88(1):3-8.
52. HenryM.Dupuytren’sdisease:currentstateoftheart.Hand.2014;9:1-8.
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53. SkirvenTM,BachouraA,JacobySM,CulpRW,OstermanAL.Theeffectofatherapyprotocolforincreasingcorrection
ofseverelycontractedproximalinterphalangealjointscausebyDupuytrendiseaseandtreatedwithcollagenase
injection.JHandSurg.2013;38(4):684-689.
54. WerkerPMN,PessGM,vanRijssenAL,DenklerK.CorrectionofcontractureandrecurrenceratesofDupuytren
contracturefollowinginvasivetreatment:theimportanceofcleardefinitions.JHandSurg.2012;37(10):2095-2105.
55. FeliciN,MarcoccioI,GiuntaR,HaerleM,LeclercqC,PajardiG,WillebrandS,GeorgescuAV,PessG.Dupuytren
contracturerecurrenceproject:reachingconsensusonadefinitionofrecurrence.HandhirMikrochirPlastChir.
2014;46:350-354.
56. BletonR,MarcireauD,AlmotJY.TreatmentofDupuytrenDiseasebypercutaneousneedlefasciotomy.InSafferP,
AmadioPC,FoucherG,editors.CurrentPracticeinHandSurgery.London:MartinDunitz,1997:187-193.
57. LermusiauxJL,LelloucheH,BadoisF,KuntzD.HowshouldDupuytrencontracturebemanagedin1997?RevRhum.
(EnglEd)1997;64:775-776.
58. vanRijssenAL,LindenH,WerkerPN.Five-yearresultrsofarandomizedclinicaltrialontreatmentofDupuytren’s
disease:Percutaneousneedlefasciotomyversuslimitedfasciectomy.PlastReconstrSurg.2012;129:469-477.
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IC10: Anatomy and Analysis of Dupuytren Cords 2019‐09‐05
Bibliography and additional materials at https://dupuytrens.org/ASSH2019 1
ICL 10Anatomy and Analysis of
Dupuytren Cords
Charles Eaton MD
Financial/Commercial Disclosure: None
Bibliography and more: https://Dupuytrens.org/ASSH2019
The Palmar Fascia
Part of a 3D soft tissue scaffold
•Anchors skin to skeleton•Redistributes shear forces•Provides secure grip
Soft tissue strain is a Dupuytren trigger
1
2
3
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IC10: Anatomy and Analysis of Dupuytren Cords 2019‐09‐05
Bibliography and additional materials at https://dupuytrens.org/ASSH2019 2
SuperficialTransverse
IntermediateLongitudinal
4
5
6
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IC10: Anatomy and Analysis of Dupuytren Cords 2019‐09‐05
Bibliography and additional materials at https://dupuytrens.org/ASSH2019 3
DeepTransverse
Nodule Locations v. Cord Locations
NODULES CORDS
2300 previously untreated patientsDigital Nodules more central, Cords more lateral
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9
10
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IC10: Anatomy and Analysis of Dupuytren Cords 2019‐09‐05
Bibliography and additional materials at https://dupuytrens.org/ASSH2019 4
Central
BowstringsCentralNear NVBDisplaces NVB
Spiral
BowstringsCentral (Prox)Lateral (Distal)Near NVBDisplaces NVB
Retrovascular
BowstringsLateralNear NVBDisplaces NVBMore common if > 45°
Lateral
BowstringsLateralNear NVBDisplaces NVB
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12
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IC10: Anatomy and Analysis of Dupuytren Cords 2019‐09‐05
Bibliography and additional materials at https://dupuytrens.org/ASSH2019 5
Doppler Spiral Locations70 Previously Untreated Patients
Cord Length and Location vs. Angle
•Dupuytren affects cords, not joints.
•We measure joint angles, not cords.
•How do length changes affect angles?
Central CordsLateral Cords
Cord Location and Angular Contracture
For the same length change, angles change
• Lateral = 2X Central
•PIP=2X MCP
Central CordsLateral Cords
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IC10: Anatomy and Analysis of Dupuytren Cords 2019‐09‐05
Bibliography and additional materials at https://dupuytrens.org/ASSH2019 6
Contribution to overall contracture
MCP PIP
Central Central
Spiral orLateral
Spiral orLateral
Retrovascular
Retrovascular
AccessoryCollateral
Multiple Structures:Each additional 45°increases chancesof an additionaltethering structure
2013 Trickett
17
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Tips on Dupuytren Contracture Incision, Excision, and Dissolve
Keith Denkler Clinical Professor of Surgery, Division of Plastic Surgery, UCSF
Larkspur, Marin County, California
Disclaimer/Conflicts of Interest
I participate in Endo Pharmaceuticals speaker panel.
However, this talk is my own talk about my way of treating those with Dupuytren Disease.
Endo did not assist or review any of this talk.
Historical Treatments: Needle, Collagenase, or Surgery
1777 Closed fasciotomy Cline
1831 Open fasciotomy Dupuytren
1834 Fasciectomy Goyrand
2010 Collagenase. Only new treatment in over 100 years.
The Treatment
Needle does not remove tissue but can change the biology of the contracture
Enzyme dissolves tissue
Fasciectomy removes tissue
I perform all three treatments for Dupuytren Contracture
My wide-awake fasciectomy for Dupuytren contracture published in 2005
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I was also part of the original prospective study on epinephrine use in the hand 2005
Needle aponeurotomy
Experience since 2004 in over 7,000 digits
Collagenase
Experience in over 1,600 digits
Surgery
Start small or start grand.
Surgery is the best chance of long term improvement without recurrence
But has the highest complication rate and longest recovery
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Lesser treatments such as needle or enzyme can also have excellent long term results
Above: A five-year result from one needle aponeurotomy to Stage IV Dupuytren contracture of the little
and ring finger
Above: A seven-year follow-up before and after needle aponeurotomy
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Fasciectomy Removes Tissue and Leaves a Volume Deficit
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Above: My own five-year fasciectomy/allograft follow-up
Subcision
Release of vertical fibers to the skin from the underlying cord
Also can be used to release adherent Grayson’s or Cleland’s ligaments laterally
Can use local anesthesia hydro-dissection and an 18-gauge needle.
Stay immediately subdermal.
Illustration of Skin Fibers to be released by Subcision
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From Zancolli and Cozzi, Atlas of Surgical Anatomy of the Hand. 1992
Demonstration of Superficial Subcision at the PIP Joint
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Choosing the right procedure (Incise, Excise, or Dissolve) for the right patient
Young patient
Careful burning bridges
This 41-year-old patient above has had 27 procedures (fusions, skin grafts, and fasciectomies) in the past
31 years on this right hand
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Above another view of the same patient after 27 surgical procedures
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Above: The left hand has had one collagenase and one needle treatment
Above: Two months after needle aponeurotomy and fat grafting
Patients with no Insurance
Have to keep it simple so consider needle aponeurotomy
Collagenase has an assistance programs which is helpful
Mixing
There will be left over collagenase in the vial
0.90 mg in the vial and 0.58 used
0.32 can be used in other areas or wasted
Document full use of the vial, or wastage in your medical record
Wastage in two vial treatment is .64 mg or enough for a full treatment
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Medicare does not want docs treating a patient with two vials and using the leftover (and
charging) in another patient.
Mixing
Entire vial contains 0.9mg of collagenase
For MP joint cord dilution: 0.9mg collagenase/ 0.39ml diluent = 2.30 mg/ml (dose of 0.58 mg =
0.25ml)
For PIP joint cord dilution: 0.9mg collagenase/ 0.31ml diluent = 2.9 mg/ml (dose of 0.58mg = 0.20ml)
Pre Numbing
Cold pack as seen below
Ethyl chloride
Frozen needle helps for one pass
Vibration seen below can distract
Topical anesthetics work less well on the hand
Literature
Wrist block lessens pain[1]
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Numbing
I always pre-numb upstream with a proximal block or wrist block
Have used digital block liposomal bupivacaine for pre-numbing and for extension before 72 hours
I use lidocaine with epinephrine, then 1: 200,000 bupivicaine
For manipulation I tend to use 0.5 cc lido with epinephrine 1: 200,000 mixed 50/50 with 2% lidocaine
Numbing before collagenase and manipulation.[1, 2]
From Sanjuan-Cervero, R. et al 2017
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Manipulation
24 to 72 hours is on label recommendation.
One week is very good with level II evidence by Mickelson et al.
Two weeks has also been used in my practice.
Recurrent Dupuytren Contracture after Previous Fasciectomy Treated with Collagenase
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Above, green outlines the previous incisions. Blue are the multiple low dose (0.1mg) injection
collagenase including DIP contracture
Above One-year follow-up after the one injection
The Severe PIP Stage IV Contracture Treated with Collagenase
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Above: Before treatment with one vial 0.9 of collagenase to little and ring fingers
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Above: Markings for injection of collagenase
Above: Before manipulation
Above: Immediately after injection and not tip is still pink
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Above: At two-month follow-up
Severe PIP after Previous Fasciectomy
Above: Markings for this patient who had been advised to consider amputation due to recurrent
disease and severe recontracture
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Above: One week after injection collagenase
Above: Immediately after manipulation
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Above: Two-month follow-up photos from home
Efficacy Table
Five-year recurrence with definition as 30-degree increase in passive extension deficit
Combined MCP Joint PIP joint Needle aponeurotomy >30 ° recurrence
84.9 ° (63% at 3 years)
57 ° 70 °
Fasciectomy >30 ° recurrence
20.9 ° 21 ° 21 °
Collagenase > 30 ° recurrence
32 ° 26 ° 46 °
Collagenase > 20 ° degree recurrence
47 ° 39 ° 66 °
From: van Rijssen, et al 2011 5-year results of randomized clinical trial on treatment in Dupuytren's disease: percutaneous
needle fasciotomy versus limited fasciectomy
Peimer, C. et al 2015 Dupuytren Contracture Recurrence Following Treatment with Collagenase Clostridium histolyticum
Collagenase does not dissolve all
Lalonde[3]
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Severe PIP Joint and Collagenase
Severe PIP Contractures of the little and ring fingers before collagenase
At one month following collagenase
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Previous radiation
Plastic surgeons often perform surgery in heavily radiated breast tissue after cancer
Anatomy of the finger
One month is possible (long distance commute patient)
Injected, returned, and manipulated/injected at one month, then repeat
Longest six weeks (patient forgot) with some popping
Where Can You Needle with Enzyme
Proximal to distal palmar crease
Natatory cords and superficial subcision
Proximal to distal palmar crease
And thumb web
Nerves are not at risk
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Second Stretch
Early recurrence of PIP contracture in up to the first month after injection/manipulation can be
re-stretched. Further popping and improvement can occur
Followed by re-splinting and PT/OT.
PIP Joint in Dupuytren’s Disease
Tonkin, Burke and Watson.[4]
Adding Needle to Collagenase
Value in the thumb web cords and natatory cords due to lack of nerves
Subcision of superficial skin bands from the cord to the skin is safe and
Proximal cords at the Distal Palmar Crease released by needle allow for further traction distally
Thumb Web
Collagenase
Steenbeek[5]
Needle
Boutonniere Contractures
Small doses of collagenase can be used as a tenotomy for boutonniere
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Above: 0.01mg or 0.055 cc of fluid for an MCP dose used for Boutonniere
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Results Collagenase Fowler Tenotomy for Boutonniere in 13 patients (5.7-month average F/U)
One single injection of small dose collagenase proximal to DIP joint for tenotomy at time of
treatment for Dupuytren contracture of MCP joint and PIP joint with boutonniere
DIP hyperextension of 27.3 improved to 8.8 degrees
An 18.5-degree improvement
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DIP range of motion improved from 28.5 to 35.8 degrees
Ana 7.3-degree improvement
Results submitted to AAHS meeting Jan. 2018
DIP Flexion Contractures
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REFERENCE ON DIP PUBLISHED
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DIP collagenase by Fei et al.
Improved extension to less than 5 degree PED in 17/21 patients at 2.6 month followup.[6]
FEI DIP collagenase[6]
DURability collagenase werker at 2 years.[5]
Dip collagenase.
Severe PIP and DIP Contractures Using Small Border Doses of Distal Collagenase
Forty-five year old male with MCP 0 PIP -70 DIP -50 degree contractures
Markings of 0.60 mg of collagenase proximal in three doses
And .3 mg in three doses along the ulnar cord
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After manipulation using lidocaine with epinephrine block
At twenty-month follow-up
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Coumadin
Patients on blood thinners can stop the medication at risk of a stroke, a disastrous problem
Risk of blood thinners and collagenase is localized hematoma treatable with evacuation.
Labels says use with caution and does not prohibit
Patients with abnormal coagulation: Use with caution, including in patients who have
received anticoagulant medications other than low dose aspirin within 7 days of the injection.
Coumadin: Delay manipulation
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Above, before collagenase, delayed manipulation till four weeks, and immediately after manipulation
Patient on Coumadin daily.
Coumadin
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DIP Joint Collagenase
Small doses are necessary and can be used on the radial or ulnar sides
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Fat Grafting
Can provide fire break and add padding via living fat grafts
And can provide new stem cells that can teach and help the "injured" fibrotic cells of Dupuytren disease
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Fat Grafting of Hovius and Khouri: PALF
Equipment is inexpensive
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Local infiltration blunt needle, manual harvesting needle, separation stand, and injection needle
Micro Fat is injected with around 1mm injection ports
Nano Fat can be injected with 30-gauge needle
Diamondplasty
At time of fasciotomy as named by Colville 1983
Before needle aponeurotomy and Diamondplasty
Aponeurotomy skin tears sutured horizontally “Diamondplasty”
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Result at suture removal
Diamondplasty
Can treat scars that are at right angles to the creases and much easier than Z-plasty
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The Severe PIP Joint
Joints do not fuse, they need release
Andrew in 1991 studied 7 amputated Dupuytren PIP joint averaging 95 degrees of contracture
Excision of all Dupuytren cords and tissue did not open the joints
PIP joints in 5s required release of the accessory collateral ligaments to straighten which can be done
with a needle via closed capsulotomy
Release of the volar plate straightened the last two.
Needle PIP Joint Capsulotomy
Release of Transverse Retinacular Ligament
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Can assist with releasing contracture and allowing the extensor apparatus to elevate dorsally.
NA Severe Contracture Release Markings
Below: Are the midaxillary markings for PIP capsulotomy and the arrows pointing to release of the
transverse retinacular ligament. Also shown is subcision of proximal palmar tissue to mobilize skin.
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Staged Treatment
Preliminary fasciotomy followed by touch up collagenase
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NA Technique
Stromberg[7]
Satisfaction
Patient[8]
Thoughts
Onabotulinumtoxin A to reduce contracted FDS or FDP during recovery from collagenase or
needle aponeurotomy and take tension off PIP joint flexion
Successful treatment of Dupuytren proximal interphalangeal joint (PIP) joint contractures remains a
problem. Options for treatment include presurgical fasciotomy, preliminary soft-tissue distraction,
checkrein ligament release, joint capsulotomies, release of the digital flexor sheath, joint pinning,
tendon lengthening, and early hand therapy.
Onaotulinum toxin A, already FDA approved for muscle spasticity of the fingers after stokes (30-50 u)
has a role in weakening the contracted flexor digitorum sublimis muscle found in longstanding, severe
PIP joint Dupuytren contractures.
METHODS
Four patients with more than 60-degree Dupuytren PIP joint contractures that failed previous
treatments were administered one dose 10 to 20 u of botulinum toxin administered to the sublimis
muscle of the involved PIP finger contracture during their treatment. For NA it was at the time of the
procedure and for collagenase it was at the time of the initial administration of collagenase.
RESULTS
Patient Finger Treatment
Dose Botulinum Toxin
PIP Before
PIP After Gain PIP F/u Months
Prev. Treatments
1 L Little NA 10 u FDS -100 -25 75 8 Prev. NA
2 R Little (2) Treatments of Collagenase
20 u FDS -90 -15 75 5 Prev. NA
3 R Little NA 20 u FDS -70 -25 45 5 Prev. NA
4 R Little NA + Fat Graft
20 u FDS -60 -25 35 2.5 Prev. NA
Average -80 -22.5 57.5 5.1
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Significant improvement in little finger severe PIP contractures at early follow-up
CONCLUSION
Onabotulinum toxin A injections into the sublimis tendon helps PIP contractures during the early
postoperative stage. Botulinum toxin may be used with all three techniques for release of Dupuytren
contracture: Fasciotomy, fasciectomy, and collagenase. With collagenase, an on-label repeat treatment
would be of benefit during the period (approx. four months) of botulinum toxin effect.
Fig. 1 Eight-month F/U after NA and 20u Botulinum toxin to R little FDS
Fig. 2 PIP -100 to PIP -25-degree PIP with full passive extension (not shown).
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Fig. 3 Three month follow-up after NA/Fat grafting and 20 u Botulinum to FDS left little finger
1. Sanjuan-Cervero, R., et al., Pain Associated With Treatment of Dupuytren Contracture With Collagenase Clostridium histolyticum. J Hand Surg Am, 2017. 42(2): p. e109-e114.
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2. Nordenskjold, J., et al., Benefit of Local Anesthesia in Reducing Pain during Collagenase Injection for Dupuytren's Contracture. Plast Reconstr Surg, 2017. 140(3): p. 565-569.
3. Lalonde, D.H., Discussion: Collagenase Clostridium Histolyticum for Dupuytren Contracture: Comparing Single and Concurrent Injections. Plast Reconstr Surg, 2019. 143(4): p. 788e-789e.
4. Tonkin, M.A., F.D. Burke, and J.P. Varian, The proximal interphalangeal joint in Dupuytren's disease. J Hand Surg Br, 1985. 10(3): p. 358-64.
5. Steenbeek, L.M., M.M. Dreise, and P.M.N. Werker, Durability of Collagenase Treatment for Dupuytren Disease of the Thumb and First Web After at Least 2 Years' Follow-Up. J Hand Surg Am, 2018.
6. Fei, T.T., et al., Collagenase Clostridium histolyticum for the Treatment of Distal Interphalangeal Joint Contractures in Dupuytren Disease. J Hand Surg Am, 2019. 44(5): p. 417 e1-417 e4.
7. Stromberg, J., Percutaneous Needle Fasciotomy for Dupuytren Contracture. JBJS Essent Surg Tech, 2019. 9(1): p. e6.
8. Buckwalter V, J.A., et al., Needle Aponeurotomy Versus Collagenase Injections for Dupuytren Disease: A Review of the Literature and Survey of Patient-Reported Satisfaction, Recurrence, and Complications After Needle Aponeurotomy. Journal of Hand Surgery Global Online, 2019. 1(2): p. 91-95.