• Nenhum resultado encontrado

Rev. bras. ortop. vol.49 número6

N/A
N/A
Protected

Academic year: 2018

Share "Rev. bras. ortop. vol.49 número6"

Copied!
8
0
0

Texto

(1)

w w w . r b o . o r g . b r

Review

Article

Cartilage

lesions

and

ankle

osteoarthrosis:

review

of

the

literature

and

treatment

algorithm

,

夽夽

Alexandre

Leme

Godoy

Santos

a,∗

,

Marco

Kawamura

Demange

a

,

Marcelo

Pires

Prado

b

,

Tulio

Diniz

Fernandes

a

,

Pedro

Nogueira

Giglio

a

,

Beat

Hintermann

c

aInstituteofOrthopedicsandTraumatology,SchoolofMedicine,UniversityofSãoPaulo(USP),SãoPaulo,SP,Brazil

bOrthopedicsandRehabilitationCenter,HospitaldoCorac¸ão,SãoPaulo,SP,Brazil

cDepartmentofOrthopedics,Kantonsspital,Liestal,Switzerland

a

r

t

i

c

l

e

i

n

f

o

Articlehistory:

Received21October2013

Accepted21October2013

Availableonline11November2014

Keywords:

Osteoarthritis Ankle Osteotomy Arthroplasty Arthrodesis

a

b

s

t

r

a

c

t

Themainetiologyofankleosteoarthrosisispost-traumaticanditsprevalenceishighest

amongyoungindividuals.Thus,thisdiseasehasagreatsocioeconomicimpactandgivesrise

tosignificantlossesofpatients’qualityoflife.Theobjectiveofitstreatmentistoeliminate

painandkeeppatientsactive.Therefore,thetreatmentshouldbestagedaccordingtothe

degreeofdegenerativeevolution,etiology,jointlocation,systemiccondition,bonequality,

lower-limbalignment,ligamentstabilityandage.Thetreatmentalgorithmisdividedinto

non-surgicaltherapeuticmethodsandoptionsforsurgicaltreatment.Jointpreservation,

jointreplacementandarthrodesissurgicalprocedureshavepreciseindications.Thisarticle

presentsareviewonthistopicandaproposalforatreatmentalgorithmforthisdisease.

©2014SociedadeBrasileiradeOrtopediaeTraumatologia.PublishedbyElsevierEditora

Ltda.Allrightsreserved.

Lesão

de

cartilagem

e

osteoartrose

do

tornozelo:

revisão

da

literatura

e

algoritmo

de

tratamento

Palavras-chave:

Osteoartrite Tornozelo Osteotomia Artroplastia Artrodese

r

e

s

u

m

o

A principal etiologia da osteoartrose (OA) do tornozelo é pós-traumática e sua maior

prevalência estáentreindivíduosjovens;assim,essadoenc¸aapresentagrandeimpacto

socioeconômicoesignificativoprejuízonaqualidadedevidadospacientes.Oobjetivodo

tratamentoéeliminaradoremanterospacientesativos.Dessaforma,otratamentodeve

serestagiadodeacordocomograudeevoluc¸ãodadegenerac¸ão,aetiologia,alocalizac¸ão

articular,acondic¸ãosistêmica,aqualidadeóssea,oalinhamentodomembroinferior,a

estabilidadeligamentareaidade.Oalgoritmodetratamentoédivididonasmodalidades

Pleasecitethisarticleas:Santos ALG,Demange MK,Prado MP,Fernandes TD,GiglioPN,HintermannB.Lesão decartilageme

osteoartrosedotornozelo:revisãodaliteraturaealgoritmodetratamento.RevBrasOrtop.2014;49:565–572.

夽夽

WorkdevelopedattheInstituteofOrthopedicsandTraumatology,SchoolofMedicine,UniversityofSãoPaulo(USP),SãoPaulo,Brazil.

Correspondingauthor.

E-mail:alexandrelemegodoy@gmail.com.br(A.L.G.Santos).

http://dx.doi.org/10.1016/j.rboe.2014.11.003

(2)

deterapianãocirúrgicasenasopc¸õesdetratamentocirúrgico.Ascirurgiasdepreservac¸ão

articular,ascirurgiasdesubstituic¸ãoarticulareasartrodesesapresentamindicac¸ões

pre-cisas.Opresenteartigoapresentaumarevisãosobreotemaeumapropostadealgoritmo

detratamentoparaessadoenc¸a.

©2014SociedadeBrasileiradeOrtopediaeTraumatologia.PublicadoporElsevier

EditoraLtda.Todososdireitosreservados.

Introduction

Osteoarthrosis(OA) isasyndrome characterizedby

degen-eration of the joint cartilage, alterations to subchondral

bone,intra-articularinflammatoryalterationsand

periartic-ularbonegrowth,andit causespainandfunctionallossin

theaffectedlimb.1–3Thereisstillnoeffectivecureforthis

syn-drometoday,throughanymethodsforprevention,diminution

ofitsprogressionortreatmentofsymptomsthathavebeen

proposed.1,2,4,5

OAaffects15%oftheworldwideadultpopulation,which

makesit a disease ofhigh socioeconomicimpact both for

individualsandforallofsociety.6Forexample,intheUnited

States,thisrepresentsannualcostsof60billiondollarsforthe

directtreatment.1,6,7

Themostimportantuniversalriskfactorsareage,

exces-sive joint loading, joint injuries, fractures and ligament

injuries.1,6

OAofthetibiotarsaljointispresentin4.4%ofthepatients

whoseekorthopedicattendancebecauseofOAofthelower

limbs.

Differentlyfromhipjointdegeneration(58%)andkneejoint

degeneration(67%),OAoftheankleisofprimaryorigininonly

9%ofthecases.Thesecondarycauses(rheumatoidarthritis,

hemochromatosis,hemophiliaorosteonecrosis)arepresent

in13%ofthecases.Themainetiologyispost-traumaticand

thisisthereasonfortibiotarsaljointdegenerationin78%of

thecases,whilefracturesaroundtheanklearethecausein

62%andligamentinjuriesarethecausein16%.7–9

Individualswithanklearthrosistendtobeyoungerthan

otherpatientswithjointdegenerationinthelowerlimbsand

presentfasterfunctional loss,withprogressiontothefinal

stagesofthediseasebetween10and20yearsafterthestart

ofthelesion.9

Physiopathogenesis

Avarietyofanatomicalandbiomolecularcharacteristics of

theanklearedeterminantsforunderstandingthe

susceptibil-ityofthecartilageofthisjointtodegeneration.

Thetotalareaofthetibiotarsaljointis350mm2anditis

subjectedtoaforceof500N,whilethehipandknee,withjoint

areasofrespectively1100mm2and1120mm2,aresubjected

tothesameforce.10–12Thus,thepressureonthejointcartilage

oftheanklemaybeuptothreetimesgreaterthanthepressure

ontheotherjointsofthelowerlimbs.Ontheotherhand,the

loaddistributiononthecongruentjoints,i.e.theankleand

hip,differsfromtheloaddistributionontheknee,suchthat

thecompressiveforcesaredistributedoveralargerarea.This

possiblyallowstheanklecartilagetobethinnerthanthatof

theknee.Thethicknessoftheanklejointcartilagerangesfrom

1to1.62mmandisthinnerthanthatofthehip(1.35–2mm)

andknee(1.69–2.55mm).13

Comparativebiomolecularstudiesonhumanshaveshown

thatthe anklecartilagehashigherdensity of

glycosamino-glycan sulfate and lower modulusofequilibrium, dynamic

rigidity, water componentand hydraulicpermeability than

thoseofthekneecartilage.Thepropertiesinfluencethe

capac-ity todeformundercompressionduringtheloadcycle.14,15

The way in which the collagen of the ankle cartilage is

organizedresemblesthatoftheknee,butthechondrocyte

dis-tributiondiffers.Intheankle,inthesuperficiallayerofthe

cartilage,thechondrocytesarepresentedingroups.16

Along with these characteristics, the cartilage tissueof

anklesthataresubjectedtoinjurypresentsincreased

colla-gensynthesis.Thechondrocytesoftheanklearemetabolically

more active than those of the knee and present greater

aggrecanturnoverandgreatersensitivitytoanabolicstimuli,

followedbyremovalofinterleukin-1,andgreaterresponseof

thechondrocytestoinflammatorystimuli.17–20

Thefollowingarealsodeterminantsforthe

physiopatho-genesis:poorstructuraloracquiredalignmentsofthelower

limb,muscleimbalanceandweaknessaroundthetibiotarsal

joint,age,gender,ethnicityandgeneticpredisposition.2,6

Diagnosis

and

classification

system

The clinical presentation consists ofpain in the region of

thejointinterline,withorwithoutanassociatedincreasein

volume(jointeffusion)andlimitationsontherangeofjoint

motion,functioning,workandrecreationalactivities.These

conditionsmaydiminishthequalityoflifeofindividualswith

diseaseslikehipOA,dialytickidneyfailure,congestiveheart

failureorradiculopathy.21Otherassociatedclinicalalterations

includelegmuscleatrophyandalterationstogaitpatterns,

particularlychangestokinematicsandkinetics.22–25

Theinitialinvestigationbymeansofimagingisconducted

usingradiographswithweight-bearing.Thesemayshow

dif-ferentdegreesifdiminutionofthejointspaceandformation

ofosteophytes,sclerosisandsubchondralcysts.TheMorrey

andWiedemanclassificationsystemisbasedonthese

radio-graphicfindings.26,27

Magneticresonance imaging(MRI) isthe mostsensitive

andspecificnoninvasiveimagingexaminationforevaluating

thejointcartilage.Bymeansofspecificprotocolsforimage

acquisition andanalysis,it alsoenablesaccesstothe

(3)

Determiningthepreciselocation,sizeoftheareaaffected

anddepthofthecartilaginouslesionisfundamentalin

select-ing the treatment. Thus, MRI protocols aimed toward the

cartilage andequipment withbigger magneticfields (three

tosevenTesla)provideabetterviewofthecartilageandthe

associatedlesions.29–32

New MRItechniques forstudying the cartilage,such as

volumetricquantitativeanalysis,dGEMRICmapping,T1-rho

mapping, T2 mapping and MRI using sodium-23, enable

accessto the microstructureand, indirectly, to

fundamen-talcharacteristics oftheankle cartilage,therebyimproving

thediagnosisandtreatmentofchondralandosteochondral

lesions.30–33

Recently,theSPECTtechniquemadeitpossibletocorrelate

themorphologicalandbiochemicalinformationin

investigat-ingankleOAandwasshowntobeusefulforlocatingtheactive

degeneration,especiallyinareasinwhichthenumberandthe

configurationofthejointarecomplex.34–36

Algorithm

for

staged

treatment

The decision on which treatment to use depends on the

intensity ofthe pain, functional limitation,degree ofjoint

degeneration, etiology, joint location, systemic condition,

bonequality,lower-limbalignment,ligamentstabilityandage,

followingthe stagesproposed through the treatment

algo-rithm(Fig.1).

StageI.Nonsurgicaltreatment

Nonsurgicaltreatmentismainlyindicatedforpatientswith

mildtomoderateOA,mildpain,slightfunctionallimitations,

anyetiology,good bonequality,adequate lower-limb

align-mentandstablejoints,ofanyagegroup.

Theobjectivesaretoimprovethesymptoms,maintainthe

remainingjointrangeofmotionandprovidetheconditions

forappropriatefuturesurgicaltreatment.

Bracesandinsoles

Bracesand insolesshould beusedtokeepthe jointinthe

neutral position during walking movements. Some braces

also limit ankle mobility in the sagittal plane and thus

reducethe joint instability and overloadingon the injured

cartilage.37

Although somestudies have shown satisfactory results

fromuse ofcorrectiveinsolesfortreatingknee OA(to

pro-ducevarusdeformity),38,39thishasnotbeenseenintreating

ankleOA.37,40

Analgesicsandanti-inflammatoryagents

Analgesics and anti-inflammatory agents present proven

effectsrelatingtopain,andthelatteralsoshowsadditional

reliefrelatingtoactiveOA.

However,becauseofthevarioussystemicsideeffectsand

alsobecauseprogressionofthedegenerationisnotavoided,

thesemedicationsarenotusedaslong-termsolutions.

Stage I

Stage II

Stage III

Stage IV

Nonsurgical treatment

Insoles

Modification of footwear characteristics Analgesics and anti-inflammatory agents condroprotetores

Corrective osteotomy: simple or combined Ligament repair and reconstruction Tenoplasty and tendon transfer

Corrective surgery on the osteochondral lesion arthrodiastasis

Joint preservation surgery

Three components Constrained or unconstrained Heterologous transplantation

Total ankle arthroplasty

Open or arthroscopic Single or combined Retrograde intramedullary rod Plate

Screws

Ankle arthrodesis

Fig.1–Stagedtreatmentalgorithm.

Physiotherapy

Incasesofmildtomoderateankle OA,physiotherapymay

helptopreservetherangeofmotionand mayincreasethe

dynamic jointstability throughmuscle strengthening.This

isusefuluntilthetimeoffuturetreatmentwithtotalankle

arthroplasty.8

Viscosupplementation

Interest inusing intra-articular viscosupplementationwith

hyaluronicacidintheankle,asatreatmentoptionforjoint

degeneration,hasbeenincreasingsignificantly.41

InpatientswithOA,chondrocytesandsynovialcells

pro-duce increased levels of inflammatory cytokines, such as

interleukin1␤(IL-1␤)andtumornecrosisfactoralpha

(TNF-␣).In turn,thesedecrease collagen synthesisand increase

thelevelsofcatabolicmediatorssuchasmetalloproteinases

(MMPs)andotherinflammatorymediatorslikeinterleukin8

(IL-8),interleukin6(IL-6),prostaglandinE2(PGE2)andnitric

oxide(NO).42,43Onekeyproteininthepathologicalprocessof

OAisCD44,whichisfoundonthesurfacesofchondrocytes,

synovioblastsand macrophages. CD44iscapable of

inhibi-tingthesynthesisofinflammatorycytokineswhenboundto

hyaluronicacid.44

Hyaluronic acid is an important modulator, especially

(4)

fibroblast-like synoviocytes.45 Therefore, inaddition to the

mechanicaleffectsofpromotingbetterdistributionofforces,

decreasingthepressureonthechondrocytes46andrecovering

therheologicalpropertiesofthesynovialfluid,47hyaluronic

acidactsbiochemicallytodiminishthegeneexpressionofthe

cytokinesandtheenzymesassociatedwithOA,the

produc-tionofprostaglandinsandthe intra-articularconcentration

ofmetalloproteinases.46,48

Mei-Danetal.49studied16patientswithsymptomaticOA

intheanklewhoreceivedintra-articularinjectionsof25mgof

sodiumhyaluronateforfiveconsecutiveweeks.Therewasa

20%improvementinrangeofmotionandasignificant

reduc-tion in pain, as assessed using a visual analog scale and

scoringsfortheankleandhindfoot.

Sunetal.50observedimprovementsinpainandankle

func-tioninginaseriesof50patientswithanklearthrosiswhowere

treatedwiththreeintra-articularinjectionsofhyaluronicacid

perweek.AnotherprospectivecaseseriesrevealedthatHylan

GF20waseffectiveforsignificantlyreducingthepain

associ-atedwithankleOA.Thiseffectseemedtolastevenbeyondsix

tosevenmonthsafterthetreatment.51

Thesafetyseemstobesimilartothatoftheapplications

thatarewidelyusedintreatingOAinseveralotherjoints,such

astheknee,hip,shoulderandhand.51–56

Findingsfrom meta-analyseshave suggestedthat

intra-articular viscosupplementation with hyaluronic acid can

significantlyreducepaininpatientswithankleOA,in

com-parison withthe statebefore the treatment, and that this

treatmentoptionissuperiortootherconservativetherapies

inpatientswithsymptoms.However,thereisnoconsensus

regardingthetotalnumberofinjectionsandthevolumeper

dose,inrelationtothetherapeuticresults.57

StageII.Jointpreservationsurgery

Jointpreservationsurgeryismainlyindicatedforpatientswith

moderateOApresentingdailypainofsignificantintensityand

mildtomoderatefunctionallimitation,ofpost-traumaticor

primaryetiology,withgoodbonequality,asymmetryof

lower-limbalignmentandjointinstability,inanon-elderlyagegroup

andwithoutsystemiccomorbidities.

Theobjectivesaretoreestablishthebiomechanics,

align-mentandjointstability,deceleratetheevolutionofthejoint

degeneration and postponeprocedures of a more invasive

nature.

Jointdebridement

There is controversy regarding the value of joint

debride-ment for treating ankle OA.58 Studies conducted among

patientswithkneearthrosishaveindicatedthatjointlavage

anddebridement intheabsence ofmechanicalcausesthat

would justify the procedure only provide short-term pain

relief.59,60 Thus,thereisgreater evidencethatdebridement

that addresses all the concomitant factors involved inthe

etiology of OA (removal of osteophytes and loose bodies,

resectionofscarandhypertrophicsynovialtissueandrepair

techniquesforfocalosteochondralcartilagedefects)presents

improvementsinpain,edemaandstiffnessovertheshortand

mediumterms.58,61,62

Arthroscopicjointdebridement

SpecificlesionsassociatedwithOA,suchasosteophytes,loose

bodies and chondral defects, can be treated by means of

arthroscopy. However, thesepresent worse resultsthan do

otherdiagnoses.60,61

Arthrodiastasis

Itisbelievedthatapplicationoftractiontoajointmayimprove

nutritionandtherepairproperties,throughwithdrawalofthe

load.Thisisdonebymeansofexternalfixators,whichenable

removaloftractiononthejointline,withmaintenanceofjoint

movement,whichhaspositiveeffectsonthejointfluid

pres-sure.Aldegherietal.62 describedthisprocedurein1979,for

treatingdegenerativelesionsofthehipinyoungpatients.

Somestudieshaveshownsatisfactoryresultswithtypeof

approachinsmallcaseseries,63–66 butthisoptionhastobe

understood asanon-definitive procedurethat hastheaim

ofpostponingarthroplastyor arthrodesisoftheankle. Itis

indicatedforyoungpatients.

Osteotomies

Inpatientswithasymmetryofalignmentofthelowerlimbs

(either varus or valgus) associated ankle OA, realignment

surgeryprovides analternativetofusionor arthroplastyin

selectedcases.

Osteotomies can be simple (tibia and fibula) or

com-bined (legand heel),withor withoutassociatedsoft-tissue

procedures.67

Theaimsaretotransfertheweightfromareaswith

dam-agedcartilagetoareaswithgood-qualitycartilage;toimprove

thejointcongruence;todeceleratetheprogressionoftheOA;

andtoreducethepain.

Pagenstertetal.67foundthattherewasanimprovementin

theAOFASscoreoverafive-yearfollow-upon35consecutive

patientswithpost-traumaticOAwhoweretreatedbymeans

ofrealignmentofthelegandhindfoot.

Preciseselectionofthepatientsandadequatecorrectionof

thejointalignmentanglearecrucialtosuccess.68,69

Treatmentofosteochondrallesions

Repairoffocalosteochondralcartilagedefects.

Microfractures

Themicrofracture procedureconsistsofmaking smalldrill

holes in the subchondral bone after regularization of the

lesion,inassociationwithremovalofthecalcifiedlayerofthe

jointcartilage.Thisprocedurefollowstheprincipleof

obtain-ingacoagulumformedbymesenchymalcellsoriginatingfrom

thebonemarrow.

Morerecently,somecentershavefollowedthesameline

(5)

concentratesofbonemarrowaspirate(whichcontain

mes-enchymalcells)butwithoutattackingthesubchondralbone.

Theseproceduresareunderdevelopmentandunder

evalua-tion.Thelogicbehindtheseproceduresisbasedonobtaininga

pluripotentcellcontentthatistheoreticallyataconcentration

greaterthanthroughmicrofracturing,butwithoutattacking

thesubchondralbone.Studiesonanimalshavedemonstrated

thatsuperior repairtissueisformed70 and have compared

use of bone marrow aspirate concentrate with

microfrac-turing. Furthermore, several clinical studies have reported

occurrences of significant alterations to subchondral bone

(suchasbonecystsandosteophytesinsidethelesions),after

microfractureprocedures.71,72

Thefactors indicatingapoorprognosisfrom this

proce-durecompriselesionsizegreaterthan1.5cm2,whichsignifies

diametergreaterthan1.2cm,73uncontainedlesionsand

pres-ence of cystic lesions associated with the osteochondral

lesion.74

Autologousosteochondraltransfer

Osteochondraltransferisbased onusing anosteochondral

cylinderobtainedfromalow-demandarea,usuallyfromthe

knee:inthe intercondylarregion,the lateralportionofthe

trochleaimmediatelyproximaltotheloadingareaofthe

lat-eralcondyleorthelateralcrestproximaltothetrochlea.

Thisprocedure isindicatedforlesions ofup toanarea

of 2cm2, in which either the cartilage alone is affected

or the cartilage together with the subchondralbone, as in

osteochondritisdissecans.Themainlimitingfactorfor

osteo-chondral transferconsists of morbidity inthe donor area,

whichrestrictsthequantityand sizeofthecylinderstobe

used.

Autologousimplantationofchondrocytes

Thisconsistsofcelltherapyfortreatingjointcartilagelesions

inwhichabiopsyisfirstperformedinordertoculture

chon-drocytes.This cell expansion isdone in the laboratory for

approximately six weeks. In a second surgical procedure,

debridementofthelesionandimplantationofchondrocytes

areperformed.Inthefirstgenerations,thisimplantationwas

doneusingaperiostealmembrane,butcollagenmembranes

arenowused(seededduringthesurgeryorusingcellsthat

hadpreviouslybeenculturedinthemembrane).

StageIII.Totalanklearthroplasty

Totalanklearthroplasty(TAA)ismainlyindicatedforpatients

withsevereOApresentingdailypainofsignificantintensity

andmajorfunctionallimitations,ofanyetiology,withgood

bonequality,adequatealignmentoronlymildasymmetryof

thelowerlimbsandstablejoints,inanon-elderlyagegroup

andwithoutanyseveresystemiccomorbidities.

Theaimsaretorestore thefunctional range ofmotion,

eliminatepainandimprovequalityoflife.

Thefirstdesignsfortotalankleprosthesesappearedinthe

1970s.Despitehighfailureratesexperienceswiththefirst

gen-erationsoftotalankleprostheses,75severalgroupscontinued

withtheresearchandtodayavarietyofimplantsthatcome

closetotheanatomicalandfunctionalrequirementsofthis

jointareavailable.

Thisevolutionhasresultedinimprovementoftheclinical

resultsandhasmadethisproceduremorepopularfortreating

ankleOA.76

Analysisoftheliteratureindicatesthatthemainadvance

has been the concept of “mobile support”, in which the

prosthetic components interrelatewith various degrees of

freedom,without any occurrenceofjoint constriction.The

third-generationprostheses,whichcomprisethreeelements

(tibial, talar and intermediate components), have been the

mostsuccessfulofthesesofar.77–79

However,TAAstillpresentshighcomplicationratesin

com-parisonwithkneeandhiparthroplasty.80Theintraoperative

complicationsareduetodifficultyinaligningthecomponents

and making the bonecuts and to fracturing ofthe

malle-oli.Duringthepostoperativeperiod,thecomplicationsrelate

todehiscenceofthesurgicalincisionandinfection.78,81Over

thelongterm,thegreatestcomplicationisasepticloosening

ofthetibialortalarcomponents,followedbystress

fractur-ing,capsuleretractionandretractionoftheperiarticularsoft

tissues.82

Thus,precisepatientselectionisfundamentaltothe

suc-cessofthisprocedure.

The contraindications include osteonecrosis, severe

peripheral vascular disease, peripheral neuropathy, recent

orpreviousjointinfection,severeligamentinstability,major

misalignmentofthelowerlimbandpoorbonequality.8

Thereisalsothepossibilityofperformingcompletejoint

replacementbymeansofafreshbipolargraftfromthe

tibio-tarsal joint.This procedure isa useful option forcarefully

selectedpatients,especiallyyoungandactiveindividuals.It

allowspainreliefandmaintenanceoffunctionaljoint

mobil-ity.However,furtherstudiesontheimmunologicalbehavior

of the transplanted cartilage in this type ofprocedure are

needed.83–85

StageIV.Arthrodesis

Arthrodesisismainlyindicatedforpatientswithsevere OA

presentingdailypainofsignificantintensityandmajor

func-tional limitation, of any etiology, with good bone quality,

adequate alignment ormildasymmetryofthe lowerlimbs

andstablejoints,intheelderlyandyoungadultagegroups

andwithabsenceofseveresystemiccomorbidities.

Theaimsaretoreestablishthealignmentofthelowerlimb

andeliminatethepain.

Tibiotarsalandtibiotalar-calcanealarthrodesis

Patients withadvancedankleOA without anindicationfor

totalankle arthroplastyandthosewho presentTAAfailure

formagroupthatmightbenefitfromsalvageprocedures

con-sistingoftibiotarsalortibiotalar-calcanealarthrodesis.Many

surgicaltechniquesandfixationmaterialshavealreadybeen

describedintheliterature.86–88

The choice between tibiotarsal or tibiotalar-calcaneal

arthrodesiswilldepend onthe conditionsofdegeneration,

(6)

Thisproceduregenerallyprovidesgoodfunctionalresults

andahighrateofsymptomrelief.Thereisnodoubtthat

cor-rectpositioningofthejointfusionduringtheoperationhas

adirectimpactontheclinicalresultsachieved.Thus,valgus

anglesof5◦, externalrotationangles of5-10and neutral

flexion-extensionpositionsoftheankleneedtobeachieved.89

Itsdisadvantagesincludethe timetaken afterthe

oper-ationtoreachconsolidation,painfulnonunionrates,length

discrepancies between the lower limbs, chronic edema,

implantlooseningandperi-implantfracturing.88,89

Final

remarks

AnkleOAisadiseasethatdiffersfromotherformsofarthrosis

ofthelowerlimbs.Itsmainetiologicalfactorisjointtrauma,

especiallymalleolarfractures,chronicankle instabilityand

distalfractures of the tibia. It affects young individuals in

theproductiveagegroup,whichresultsinhighpersonaland

socialcostsrelatingtothedirecttreatmentofthisdisease,

whichusuallytakesalongtime.

Thetherapeuticstrategiesarebasedonastagedtreatment

algorithmanddependonabroadspectrumofrelatedfactors.

Conflicts

of

interest

Theauthorsdeclarenoconflictsofinterest.

r

e

f

e

r

e

n

c

e

s

1. BuckwalterJA,SaltzmanC,BrownT.Theimpactof osteoarthritis.ClinOrthopRelRes.2004;427Suppl.:S6–15.

2. DivisionofAdultandCommunityHealth,NationalCenterfor

ChronicDiseasePreventionandHealthPromotion.

http://www.cdc.gov/arthritis/basics/osteoarthritis.htm

3. LawrenceRC,FelsonDT,HelmickCG,ArnoldLM,ChoiH, DeyoRA,etal.Estimatesoftheprevalenceofarthritisand otherrheumaticconditionsintheUnitedStates.PartII ArthritisRheum.2008;58(1):26–35.

4. Martel-PelletierJ,BoileauC,PelletierJP,RoughleyPJ.Cartilage innormalandosteoarthritisconditions.BestPractResClin Rheumatol.2008;22(2):351–84.

5. DeLange-BrokaarBJ,Ioan-FacsinayA,vanOschGJ, ZuurmondAM,SchoonesJ,ToesRE,etal.Synovial inflammation,immunecellsandtheircytokinesin

osteoarthritis:areview.OsteoarthrCartil.2012;20(12):1484–99.

6. FelsonDT.Theepidemiologyofosteoarthritis:prevalenceand riskfactors.In:KuettnerKE,GoldbergVM,editors.

Osteoarthritisdisorders.Rosemont,IL:AmericanAcademyof OrthopaedicSurgeons;1995.p.13–24.

7. BrownTD,JohnstonRC,SaltzmanCL,MarshJL,Buckwalter JA.Posttraumaticosteoarthritis:afirstestimateofincidence, prevalence,andburdenofdisease.JOrthopTrauma. 2006;20(10):739–44.

8. HorisbergerM,ValderrabanoV,HintermannB.Posttraumatic ankleosteoarthritisafterankle-relatedfractures.JOrthop Trauma.2009;23(1):60–7.

9. ValderrabanoV,HorisbergerM,RussellI,DougallH, HintermannB.Etiologyofankleosteoarthritis.ClinOrthop RelatRes.2009;467(7):1800–6.

10.ChangKV,HsiaoMY,ChenWS,WangTG,ChienKL. Effectivenessofintra-articularhyaluronicacidforankle

osteoarthritistreatment:asystematicreviewand meta-analysis.ArchPhysMedRehabil.2013;94(5):951–60.

11.KimizukaM,KurosawaH,FukubayashiT.Load-bearing patternoftheanklejoint:contactareaandpressure distribution.ArchOrthopTraumaSurg.1980;96(1):45–9.

12.IhnJC,KimSJ,ParkIH.Invitrostudyofcontactareaand pressuredistributioninthehumankneeafterpartialand totalmeniscectomy.IntOrthop.1993;17(4):214–8.

13.BrownTD,ShawDT.Invitrocontactstressdistributionsin thenaturalhumanhip.JBiomech.1983;16(6):373–84.

14.ShepherdDE,SeedhomBB.Thicknessofhumanarticular cartilageinjointsofthelowerlimb.AnnRheumDis. 1999;58(1):27–34.

15.TreppoS,KoeppH,QuanEC,ColeAA,KuettnerKE, GrodzinskyAJ.Comparisonofbiomechanicaland biochemicalpropertiesofcartilagefromhumankneeand anklepairs.JOrthopRes.2000;18(5):739–48.

16.KuettnerKE,ColeAA.Cartilagedegenerationindifferent humanjoints.OsteoarthrCartil.2005;13(2):93–103.

17.HendrenL,BeesonP.Areviewofthedifferencesbetween normalandosteoarthritisarticularcartilageinhumanknee andanklejoints.Foot(Edinb).2009;19(3):171–6.

18.AurichM,SquiresGR,ReinerA,MollenhauerJA,KuettnerKE, PooleAR,etal.Differentialmatrixdegradationandturnover inearlycartilagelesionsofhumankneeandanklejoints. ArthritisRheum.2005;52(1):112–9.

19.EgerW,SchumacherBL,MollenhauerJ,KuettnerKE,ColeAA. Humankneeandanklecartilageexplants:catabolic

differences.JOrthopRes.2002;20(3):526–34.

20.KangY,KoeppH,ColeAA,KuettnerKE,HomandbergGA. Culturedhumanankleandkneecartilagedifferin

susceptibilitytodamagemediatedbyfibronectinfragments.J OrthopRes.1998;16(5):551–6.

21.ColeAA,KuettnerKE.Molecularbasisfordifferencesbetween humanjoints.CellMolLifeSci.2002;59(1):19–26.

22.SaltzmanCL,ZimmermanMB,O’RourkeM,BrownTD, BuckwalterJA,JohnstonR.Impactofcomorbiditiesonthe measurementofhealthinpatientswithankleosteoarthritis. JBoneJointSurgAm.2006;88(11):2366–72.

23.ValderrabanoV,vonTscharnerV,NiggBM,HintermannB, GoepfertB,FungTS,etal.Lowerlegmuscleatrophyinankle osteoarthritis.JOrthopRes.2006;24(12):2159–69.

24.ThomasR,DanielsTR,ParkerK.Gaitanalysisandfunctional outcomesfollowinganklearthrodesisforisolatedankle arthritis.JBoneJointSurgAm.2006;88(3):526–35.

25.NüeschC,HuberC,PagenstertG,vonTscharnerV,

ValderrabanoV.Muscleactivationofpatientssufferingfrom asymmetricankleosteoarthritisduringisometric

contractionsandlevelwalking–atime-frequencyanalysis.J ElectromyogrKinesiol.2012;22(6):939–46.

26.NüeschC,ValderrabanoV,HuberC,vonTscharnerV, PagenstertG.Gaitpatternsofasymmetricankleosteoarthritis patients.ClinBiomech(Bristol,Avon).2012;27(6):613–8.

27.MorreyBF,WiedemanGPJr.Complicationsandlong-term resultsofanklearthrodesesfollowingtrauma.JBoneJoint SurgAm.1980;62(5):777–84.

28.MuehlemanC,FogartyD,ReinhartB,TzvetkovT,LiJ,NeschI. In-laboratorydiffraction-enhancedX-rayimagingfor articularcartilage.ClinAnat.2010;23(5):530–8.

29.LangP,YoshiokaH,SteinesD,Nöbauer-HuhmannIM,Imhof H.Magneticresonancetomography(MRI)ofjointcartilage. Currentstatusofknowledgeandnewdevelopments. Radiologe.2000;40(12):1141–8.

30.LinkTM,StahlR,WoertlerK.Cartilageimaging:motivation, techniques,currentandfuturesignificance.EurRadiol. 2007;17(5):1135–46.

(7)

resonance:preliminaryresultsofdGEMRIC,zonalT2,andT2* mappingofarticularcartilage.InvestRadiol.

2008;43(9):619–26.

32.StricklandCD,KijowskiR.Morphologicimagingofarticular cartilage.MagnResonImagingClinNAm.2011;19(2):229–48.

33.ForneyM,SubhasN,DonleyB,WinalskiCS.MRimagingof thearticularcartilageofthekneeandankle.MagnReson ImagingClinNAm.2011;19(2):379–405.

34.JazrawiLM,AlaiaMJ,ChangG,FitzgeraldEF,RechtMP. Advancesinmagneticresonanceimagingofarticular cartilage.JAmAcadOrthopSurg.2011;19(7):420–9.

35.PagenstertGI,BargA,LeumannAG,RaschH,Müller-BrandJ, HintermannB,etal.SPECT-CTimagingindegenerativejoint diseaseofthefootandankle.JBoneJointSurgBr.

2009;91(9):1191–6.

36.KnuppM,PagenstertGI,BargA,BolligerL,EasleyME, HintermannB.SPECT-CTcomparedwithconventional imagingmodalitiesfortheassessmentofthevarusand valgusmalalignedhindfoot.JOrthopRes.2009;27(11): 1461–6.

37.NathanM,MohanH,VijayanathanS,FogelmanI, GnanasegaranG.Theroleof99mTc-diphosphonatebone SPECT/CTintheankleandfoot.NuclMedCommun. 2012;33(8):799–807.

38.JohnS,BongiovanniF.Bracemanagementforanklearthritis. ClinPodiatrMedSurg.2009;26(2):193–7.

39.PhamT,MaillerfertJF,HudryC,KieffertP,BourgeoisP, LechevalierD,etal.Laterallyelevatedwedgedinsolesinthe treatmentofmedialkneeosteoarthritis:atwo-year prospectiverandomizedcontrolledstudy.OsteoarthrCartil. 2004;12(1):46–55.

40.TodaY,TsukimuraN.A2-yearfollow-upofastudyto comparetheefficacyoflateralwedgedinsoleswithsubtalar strappingandin-shoelateralwedgedinsolesinpatientswith varusdeformityosteoarthritisoftheknee.OsteoarthrCartil. 2006;14(3):231–7.

41.KitaokaHB,CrevoisierXM,HarbstK,HansenD,KotajarviB, KaufmanK.Theeffectofcustom-madebracesfortheankle andhindfootonankleandfootkinematicsandground reactionforces.ArchPhysMedRehabil.2006;87(1):130–5.

42.PelletierJP,Martel-PelletierJ,AbramsonSB.Osteoarthritis,an inflammatorydisease:potentialimplicationfortheselection ofnewtherapeutictargets.ArthritisRheum.

2001;44(6):1237–47.

43.DiBattistaJA,Martel-PelletierJ,WosuLO,SandorT,AntaklyT, PelletierJP.Glucocorticoidreceptormediatedinhibitionof interleukin-1stimulatedneutralmetalloproteasesynthesisin normalhumanchondrocytes.JClinEndocrinolMetab. 1991;72(2):316–26.

44.YasudaT.HyaluronaninhibitsprostaglandinE2production viaCD44inU937humanmacrophages.TohokuJExpMed. 2010;220(3):229–35.

45.WangCT,LinYT,ChiangBL,LinYH,HouSM.Highmolecular weighthyaluronicaciddown-regulatesthegeneexpression ofosteoarthritis-associatedcytokinesandenzymesin fibroblast-likesynoviocytesfrompatientswithearly osteoarthritis.OsteoarthrCartil.2006;14(12):1237–47.

46.PeyronJG,BalazsEA.Preliminaryclinicalassessmentof Na-hyaluronateinjectionintohumanarthriticjoints.Pathol Biol(Paris).1974;22(8):731–6.

47.BaggaH,BurkhardtD,SambrookP,MarchL.Longtermeffects ofintraarticularhyaluronanonsynovialfluidinosteoarthritis oftheknee.JRheumatol.2006;33(5):946–50.

48.SasakiA,SasakiK,KonttinenYT,SantavirtaS,TakaharaM, TakeiH,etal.Hyaluronateinhibitsthe

interleukin-1beta-inducedexpressionofmatrix

metalloproteinase(MMP)-1andMMP-3inhumansynovial cells.TohokuJExpMed.2004;204(2):99–107.

49.Mei-DanO,KishB,ShabatS,MasarawaS,ShterenA,MannG, etal.Treatmentofosteoarthritisoftheankleby

intra-articularinjectionsofhyaluronicacid:aprospective study.JAmPodiatrMedAssoc.2010;100(2):

93–100.

50.SunSF,HsuCW,SunHP,ChouYJ,LiHJ,WangJL.Theeffectof threeweeklyintra-articularinjectionsofhyaluronateonpain, function,andbalanceinpatientswithunilateralankle arthritis.JBoneJointSurgAm.2011;93(18):1720–6.

51.WitteveenA,GianniniS,GuidoG,JeroschJ,LohrerH,Vannini F,etal.Aprospectivemulti-centre,openstudyofthesafety andefficacyofhylanG-F20(Synvisc)inpatientswith symptomaticankle(talo-crural)osteoarthritis.FootAnkle Surg.2008;14(3):145–52.

52.BlaineT,MoskowitzR,UdellJ,SkyharM,LevinR,Friedlander J,etal.Treatmentofpersistentshoulderpainwithsodium hyaluronate:arandomized,controlledtrial.Amulticenter study.JBoneJointSurgAm.2008;90(5):970–9.

53.SilversteinE,LegerR,SheaK.Theuseofinta-articularHylan GF-20inthetreatmentofsymptomaticosteoarthritisofthe shoulder:apreliminarystudy.AmJSportsMed.

2007;35(6):979–85.

54.FigenAyhanF,UstunN.Theevaluationofefficacyand tolerabilityofHylanGF-20inbilateralthumbbase osteoarthritis:6monthsfollow-up.ClinRheumatol. 2009;28(5):535–41.

55.SaliniV,DeAmicisD,AbateM,NataleMA,DiIorioA. Ultrasound-guidedhyaluronicacidinjectionin carpometacarpalosteoarthritis:short-termresults.IntJ ImmunopatholPharmacol.2009;22(2):455–60.

56.DeCamposGC,RezendeMU,PailoAF,FrucchiR,CamargoOP. Addingtriamcinoloneimprovesviscosupplementation:a randomizedclinicaltrial.ClinOrthopRelatRes.

2013;471(2):613–20.

57.Ogilvie-HarrisD,Sekyi-OtuA.Arthroscopicdebridementfor theosteoarthriticankle.Arthroscopy.1995;11(4):433–6.

58.JacksonR,GilbertR,SharkeyPF.Arthroscopicdebridement versusarthroplastyinosteoarthroticknee.JArthroplasty. 1997;12(4):465–70.

59.ChengJ,FerkelR.Theroleofarthroscopyinankleand subtalardegenerativejointdisease.ClinOrthopRelatRes. 1998;(349):65–72.

60.LoongTW,MitraAK,TanSK.Roleofarthroscopyinankle disorder–earlyexperience.AnnAcadMedSingapore. 1994;23(3):348–50.

61.HassounaH,KumarS,BendallS.Arthroscopicankle debridement:5-yearsurvivalanalysis.ActaOrthopBelg. 2007;73(6):737–40.

62.AldegheriR,TrivellaG,SalehM.Articulateddistractionofthe hip.Conservativesurgeryforarthritisinyoungpatients.Clin OrthopRelatRes.1994;(301):94–101.

63.PaleyD,LammBM.Anklejointdistraction.FootAnkleClin. 2005;10(4):685–98.

64.IndaDJ,BlyakherA,O’MalleyMJ.Distractionarthroplastyfor theankleusingtheIlizarovframe.TechFootAnkleSurg. 2003;2(4):249–53.

65.PloegmakersJJ,vanRoermundPM,vanMelkebeekJ, LammensJ,BijlsmaJW,LafeberFP,etal.Prolongedclinical benefitfromjointdistractioninthetreatmentofankle osteoarthritis.OsteoarthrCartil.2005;13(7):582–8.

66.PagenstertG,HintermannB,BargA,LeumannA,

ValderrabanoV.Realignmentsurgeryasalternativetreatment ofvarusandvalgusankleosteoarthritis.ClinOrthopRelat Res.2007;(462):156–68.

(8)

68.ChengY,HuangP,HongS,LinSY,LiaoCC,ChiangHC,etal. Lowtibialosteotomyformoderateanklearthritis.Arch OrthopTraumaSurg.2001;121(6):355–8.

69.KreuzPC,SteinwachsMR,ErggeletC,KrauseSJ,KonradG,Uhl M,etal.Resultsaftermicrofractureoffull-thicknesschondral defectsindifferentcompartmentsintheknee.Osteoarthr Cartil.2006;14(11):1119–25.

70.MithoeferK,WilliamsRJ3rd,WarrenRF,PotterHG,SpockCR, JonesEC,etal.Themicrofracturetechniqueforthetreatment ofarticularcartilagelesionsintheknee.Aprospectivecohort study.JBoneJointSurgAm.2005;87(9):1911–20.

71.FortierLA,PotterHG,RickeyEJ,SchnabelLV,FooLF,ChongLR, etal.Concentratedbonemarrowaspirateimproves

full-thicknesscartilagerepaircomparedwithmicrofracturein theequinemodel.JBoneJointSurgAm.2010;92(10):1927–37.

72.FurukawaT,EyreDR,KoideS,GlimcherMJ.Biochemical studiesonrepaircartilageresurfacingexperimentaldefects intherabbitknee.JBoneJointSurgAm.1980;62(1):79–89.

73.CutticaDJ,SmithWB,HyerCF,PhilbinTM,BerletGC. Osteochondrallesionsofthetalus:predictorsofclinical outcome.FootAnkleInt.2011;32(11):1045–51.

74.HintermannB.Historyoftotalanklearthroplasty.In:Total anklearthroplasty:historicaloverview,currentconcepsand futureperspectives.NewYork:Springer-Verlag;2005.p.53–63.

75.HaddadS,CoetzeeJ,EstokR,FahrbachK,BanelD,NalysnykL. Intermediateandlong-termoutcomesoftotalankle

arthroplastyandanklearthrodesis.Asystematicreviewof theliterature.JBoneJointSurgAm.2007;89(9):1899–905.

76.HintermannB.Shortandmid-termresultswithStartotal ankleprosthesis.Orthopade.1999;28(9):792–803.

77.HintermannB,ValderrabanoV,DereymaekerG,DickW.The Hintegraankle:rationaleandshort-termresultsof122 consecutiveankles.ClinOrthopRelRes.2004;(424):57–68.

78.NeryC,FernandesTD,RéssioC,FuchsML,Godoy-SantosAL, OrtizRT.Totalanklereplacement:Brazilianexperiencewith theHintegraprosthesis.RevBrasOrtop.2010;45(1):92–100.

79.GougouliasN,KhannaA,MaffulliN.Howsuccessfulare currentanklereplacements?:asystematicreviewofthe literature.ClinOrthopRelatRes.2010;(468):

199–208.

80.LeeK,ChoS,HurC,YoonT.Perioperativecomplicationsof Hintegratotalanklereplacement:ourinitial50cases.Foot AnkleInt.2008;29(10):978–84.

81.KarantanaA,HobsonS,DharS.TheScandinaviantotalankle replacement:survivorshipat5and8yearscomparableto otherseries.ClinOrthopRelatRes.2010;(468):

951–7.

82.BugbeeWD,KhannaG,CavalloM,McCauleyJC,GörtzS,Brage ME.Bipolarfreshosteochondralallograftingofthetibiotalar joint.JBoneJointSurgAm.2013;95(5):426–32.

83.GianniniS,BudaR,GrigoloB,BevoniR,DiCaprioF,RuffilliA, etal.Bipolarfreshosteochondralallograftoftheankle.Foot AnkleInt.2010;31(1):38–46.

84.PimentaR,CarvalhoP,AmadoP.Freshbipolarosteochondral allograftoftheankle.Reviewoftheliteratureandcasereport ofayoungpatientwithbilateralpost-traumatic

osteoarthritis.RevEspCirOrtopTraumatol.2012;56(2):120–6.

85.DemetriadesL,StraussE,GallinaJ.Osteoarthritisofthe ankle.ClinOrthopRelatRes.1998;(349):28–42.

86.CulpanP,LeStratV,PiriouP,JudetT.Arthrodesisafterfailed totalanklereplacement.JBoneJointSurgBr.

2007;89(9):1178–83.

87.CoesterL,SaltzmanC,LeupoldJ,PontarelliW.Long-term resultsfollowinganklearthrodesisforpost-traumatic arthritis.JBoneJointSurgAm.2001;83(2):

219–28.

88.FuchsS,SandmannA,SkwarA,ChylareckiC.Qualityoflife 20yearsafterarthrodesisoftheankle:astudyofadjacent joints.JBoneJointSurgBr.2003;85(7):994–8.

89.BuchnerM,SaboD.Anklefusionattributableto

Imagem

Fig. 1 – Staged treatment algorithm.

Referências

Documentos relacionados

test group was significantly greater than that of the control group and established the possibility that the DHS and antiro- tational screws can be used for osteosynthesis of

The objective of the present study was to assess the impor- tance of CT for managing fractures of the tibial plateau and compare the classification, surgical approach and type

Results: Motorcycle accidents accounted for 52.1% of the cases notified and bicycles, 7.1%.. Males predominated in both types of accidents: 81.6% and

Thus, the present study had the aim of ascertain- ing whether the proprioceptive deficit regarding JPS continues when patients with a deficient ACL are evaluated by means of a test

Thus, the objective of the present study was to use a strength reproduction test to investigate the existence of proprioceptive deficits between the injured limb and the unin-

All of them underwent computed tomo- graphy with 3D reconstruction in order to evaluate the entry point and positioning of the Rigidfix pins in relation to the joint cartilage of

using the medial joint line, anterior tibial tuberosity (ATT), tibial collateral ligament and a horizontal line parallel to the medial joint line that passes over the ATT, as

Objectives: To evaluate and compare the in vitro biomechanical results from two stitches: the Mason-Allen stitch, as modified by Habermeyer; and the locked double-tie stitch