• Nenhum resultado encontrado

Avaliação dos resultados do uso do hialuronato de sódio intra-articular no pós-operatório da artroscopia do joelho

N/A
N/A
Protected

Academic year: 2017

Share "Avaliação dos resultados do uso do hialuronato de sódio intra-articular no pós-operatório da artroscopia do joelho"

Copied!
7
0
0

Texto

(1)

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

Original

Article

Results

evaluation

of

the

use

of

intra-articular

sodium

hyaluronate

in

the

post-operative

knee

arthroscopy

,

夽夽

Ayrton

de

Paula

Pereira

Junior

a

,

Ricardo

Pozzi

Fasolin

a

,

Felipe

Ayusso

Correa

Sossa

a

,

Ozorio

de

Almeida

Lira

Neto

b

,

Marcelo

Schmidt

Navarro

c

,

Antonio

Milani

a,b,∗ aDepartamentodeOrtopedia,HospitalIfor,SãoBernardodoCampo,SP,Brazil

bDepartamentodeOrtopediaeTraumatologia,UniversidadeFederaldeSãoPaulo,SãoPaulo,SP,Brazil cDisciplinadeOrtopedia,FaculdadedeMedicinadoABC,SantoAndré,SP,Brazil

a

r

t

i

c

l

e

i

n

f

o

Articlehistory:

Received3September2012 Accepted7December2012

Keywords: Arthroscopy Knee

Hyaluronicacid Viscosuplementation

a

b

s

t

r

a

c

t

Objective:to evaluate the efficacy of hyaluronic acid in the post-operative of knee arthroscopy.

Methods:wehaveevaluated49patientsundergoingarthroscopicprocedurewiththeuseof intra-articularhyaluronicacid(Group1)and49patientsundergoingarthroscopicprocedure withouttheuseofhyaluronicacid(Group2).PatientswereevaluatedbasedontheVisual AnalogueScale,householdanalgesia,assessmentoftheRangeofMotionwithagoniometer, andtheLysholmquestionnaire.

Results:therewerenosubstantialadverseeffectsoneithergroup.

Conclusion: theuseofhyaluronicacidinthepost-operativeofkneearthroscopyisjustified due/becauseitleadstoadecreaseinpainintheearlystage,enablingfasterrecoveryofthe patient.

©2014SociedadeBrasileiradeOrtopediaeTraumatologia.PublishedbyElsevierEditora Ltda.Allrightsreserved.

Avaliac¸ão

dos

resultados

do

uso

do

hialuronato

de

sódio

intra-articular

no

pós-operatório

da

artroscopia

do

joelho

Palavras-chave: Artroscopia Joelho

Ácidohialurônico Viscossuplementac¸ão

r

e

s

u

m

o

Objetivo:avaliaraeficáciadousodoácidohialurôniconopós-operatóriodeartroscopiade joelho.

Métodos:foramavaliados49pacientessubmetidosaoprocedimentoartroscópico associ-ado aousodoácidohialurônico intra-articular(GrupoI) e49 pacientessubmetidosao procedimentoartroscópicosemusodoácido hialurônico(GrupoII).Ospacientesforam avaliadoscombasenaEscalaVisualAnalógicadedor(EVA),analgesiadomiciliar,amplitude domovimentodojoelhocomgoniômetroenoquestionárioLysholm.

Resultados: nãoocorreramefeitosadversossignificativosemnenhumdosdoisgrupos.

Pleasecitethisarticleas:dePaulaPereiraJuniorA,FasolinRP,SossaFAC,deAlmeidaLiraNetoO,NavarroMS,MilaniA.Avaliac¸ãodos resultadosdousodohialuronatodesódiointra-articularnopós-operatóriodaartroscopiadojoelho.RevBrasOrtop.2014;49:37–43.

夽夽

StudyconductedattheHospitalIfor,SãoBernardodoCampo,SP,Brazil.

Correspondingauthor.

E-mail:pilot@osite.com.br(A.Milani).

2255-4971/$–seefrontmatter©2014SociedadeBrasileiradeOrtopediaeTraumatologia.PublishedbyElsevierEditoraLtda.Allrightsreserved.

(2)

Conclusão:ousodoácidohialurôniconopós-operatóriodeartroscopiadejoelhoéjustificado porlevaraumadiminuic¸ãodadornafaseinicialepossibilitarumarecuperac¸ãomaisrápida dopaciente.

©2014SociedadeBrasileiradeOrtopediaeTraumatologia.PublicadoporElsevier EditoraLtda.Todososdireitosreservados.

Introduction

Theuseofintra-articularmedicationintheimmediate post-operativeperiodintheareaofarthroscopickneesurgeriesis controversial,withprospectsfornewbehaviorsandroutines, andwithauthorsforandagainsttheuseofhyaluronicacid post-operatively.1,2

A knee arthroscopy is a medicalprocedure moreusual inthe UnitedStates ofAmerica (USA), and iseffective for symptomreliefinpatientswithintra-articularloosebodies, chondralinjuryandmeniscalpathology.2

Theperformanceofhumanjointsisstrictlyrelatedtothe viscoelasticpropertiesofsynovialfluid,whichdeterminesthe strengthtransmission,lubricationandprotectionofarticular cartilage.Thisviscoelasticitydependsontheconcentrationof hyaluronicacidinthesinovialfluid.3

Other actions of hyaluronic acid would be an anti-inflammatoryeffect(decreasedgeneexpressionofcytokines, prostaglandinproduction,andintra-articularconcentrationof metalloproteinases)andanalgesic(inhibitionofnociceptors), stabilization ofcartilaginous matrix,chondrocyte prolifera-tion,increasedproductionoftypeIIcollagenanditsdecreased degradation.4–6

Someauthorsbelievethatexogenoushyaluronicacidalso stimulates the production of endogenous hyaluronic acid, whichwouldexplainitslong-termeffect.7Withrespecttothe

analgesiceffectofintra-articularhyaluronicacid,itisbelieved that,initially,itwouldbesmallerthantheintra-articular cor-ticosteroidinjection,butwithpersistenceforlongerperiods.8

Anothersourceofdebateisthediscussionregardingthe numberofdosesofhyaluronicacidtobeeffective,butthere wasnodifferenceinthecomparisonbetweenthreeandsix dosesatweeklyintervals.9

Some authors claim that, during an arthroscopic knee surgery,adecreaseinintra-articularhyaluronicacid concen-trationmay occur and,as immediatetherapy, recommend intra-articular applications of sodium hyaluronate 20mg after surgery, and subsequently four injections at weekly intervals.10

Theaimofthisstudywastocomparetheresultsoftheuse ofintra-articularsodiumhyaluronateinagroupofpatients undergoingarthroscopicsurgeryduetomeniscallesions ver-susresultsobservedinagroupofpatientsnottreatedbythis complementarytherapy.

Materials

and

methods

Ninety-eight patients with meniscal lesions were studied. ThesepatientsweretreatedfromMarchtoNovember2005by arthroscopicsurgerywithpartialmeniscectomyofthemedial meniscus,alwaysbythesamesurgicalteam.

Their agesrangedfrom 18to65 years(mean:34 years). Sixty-five(63%)weremenand33(37%),women.

Theparticipantswererandomlydividedintotwogroups of49.Thefirstgroupwastreatedwithintra-articularsodium hyaluronate20mg(Polireumim, TRBPharma) inthe imme-diatepost-operativeperiodand,subsequently,withaweekly applicationforfourconsecutiveweeks.Inthesecondgroup, thistreatmentwasnotdone.Thesurgeonwasunawareofthe grouptowhicheachpatientbelonged,havingbeeninformed onlyafterskinsuture,atthetimeofcompletion(ornot)ofthe infiltration(Table1).

Allpatientswererehabilitatedaccordingtothesame pro-tocol,withevaluationsafterthree,eight,15,30and60days, andwereinstructedtoreturntosportpracticeafter60daysof surgery.

Allpatientsunderwentthesamesurgicaltechnique,with theuseofonlytwoinfrapatellarportals(medialandlateral) and,onaverage,withjointinfusion(6Lofsaline0.9%),using aninfusionpumpatameanpressureof50mmHg.All ran-domizedpatientsshowednosignificantchangesincartilage and,inthis study,onlycasesofOuterbridgegradeIand II chondropathy(Table1)wereincluded.

Allpatientswereanesthetizedbysubarachnoidblockwith bupivacaine0.5%associatedwithglucose12.5to15mg, with-outopioids.Apneumatictourniquetwasalsoused,withan averagetimeof35min.

Afterhospitaldischarge(mean:12haftertheintervention), bothgroupsweretreatedwithcephalexin500mgPO6/6hfor sevendaysand,incaseofpain,dipyrone50dropstothelimit of6/6h.Theuseofanalgesicswascontrolledinaform,in whichthepatienthadtocheckthedateandtimeofuseuntil theeighthday.

InGroup1,afterskinsuturetheinfiltrationsweremadein thelateralsuprapatellararea,(onceaweekforfour consec-utiveweeks).Besidesthecontrolontheformwiththedate andtimeofuseofanalgesics,patientsunderwentVAS.Inall reviews,therangeofmotionofthekneewasalsomeasured witha goniometer;theLysholm questionnairewasapplied inthepreoperatoryonthe dayofsurgeryandonthe 15th, 30thand60thdayspost-operatively.Allevaluationswere per-formedbythe sameexaminerwho didnotknowatwhich groupthepatientbelonged.

Toavoidbiasintheresultsbecause ofthepainof infil-tration,theassessmentsinthe8th,15thand30thdayswere alwaysmadebeforethisprocedure.

Inthestatisticalanalysis,analysisofvariancewithtwo fac-torsand repeatedmeasuresonthetimefactorwere made, assuming a first-order autoregressive correlation matrix betweentimepoints.11Aftertheanalysis,Tukeymultiple

com-parisonsweremade12toseebetweenwhichgroupsortime

pointsoccurreddifferencesinscales.

(3)

Table1–Characterizationofsample.

Variables n=98 Group1=49 Group2=49

Age(years)–mean(SD) 34(12.1) 36(11.3) 33(12.1)

Minimum–maximum 18–65 20–65 18–61

Gender–n(%)

Female 33(37) 15(30.6) 18(36.7)

Male 65(63) 34(69.4) 31(63.3)

Operatedsite–n(%)

Right 58(59.2) 26(53) 32(65.3)

Left 40(40.8) 23(47) 17(34.7)

Chondrallesionan(%)

Withoutlesion 43(43.9) 22(44.9) 21(42.9)

GradeI 31(31.6) 14(28.6) 17(34.7)

GradeII 24(24.5) 13(26.5) 11(22.4)

a Outerbridge.

Results

ConsideringtheassessmentsbyVAS,theresultssuggestmore rapidreductionofpaininGroup1versusGroup2.Theanalysis showedthatthemeanbehaviorofVASwasstatistically differ-entbetweengroupsovertheevaluationtimepoints(p<0.001) (Fig.1).

Incomparingthedifferentevaluationtimepoints,thedata

inTable2showthatbothgroupshadameanreductioninVAS

withstatisticalsignificanceatallevaluationtimepoints,when comparedto the previous timepoint (p<0.001),but inthe eighthand15thdays,Group1showed,onaverage,statistically lowerVASversusGroup2(p<0.001andp<0.001)andinother timepoints,therewasnostatisticallysignificantdifferencein VASbetweengroups(p>0.05)(Table2).

Withrespecttotheneedforuseofhomeanalgesia,there was no statistical difference between the groups until the eighthday.

Withregardtoassessmentsmadewiththegoniometer,it wasobservedthatafter15daystheGroup1hadgreaterrange ofmotionversusGroup2.After30days,thisdifferencecould stillbeobserved,toalesserextent,butwithoutstatistical sig-nificance.Intheassessmentmadeonthe60thday,theresults weresimilarinbothgroups.

0 1 2 3 4 5 6 7 8

0 10 20 30 40 50 60 70

Dia

VAS

Groups 1 Groups 2

Fig.1–Graphicalrepresentationofthemeanprofilesand respectivestandarderrorsofVAS,accordingtogroups.

IntheevaluationwiththeLysholmquestionnaire (excel-lent:patientsbetween95and100points,good:94–84;regular: 83–65,andpoorscore:<64),wenotedinthepreoperativethat theGroups1and2hadanaverageof46and48points, respec-tively,classifiedthenaspoor(Table3).

Table 3shows that inboth Groups(1 and 2), themean

Lysholmscoredecreasedstatisticallyfromthepreoperatoryto 15dayspost-operatively(p=0.003andp<0.001,respectively), with“poor”ratinginbothgroups.However,intheevaluation ofthequestions,wefoundthatthelargestdifferencebetween groupswasobservedintheitems “pain”and “swelling”,in whichtheGroup1hadbetterresultsversusGroup2.Inother questions,theresultsweresimilarbetweengroups.

Inthe30thdaytheresultsshowedthegreateststatistical differencebetweengroups.Group1averaged90points, clas-sifiedasgood,andGroup2averaged77points,classifiedas regular. Weperceived agreater difference inthe questions about claudication,instability, swelling and squatting, and noticedthat,justasthatinthe15thday,theswellingwasalso animportantfactor.

Atthelastevaluationperiod,60daysafterthesurgery,the twogroupsdifferedstatistically,with94pointsinGroup1and 90pointsinGroup2,bothclassifiedasgood.Inthisevaluation, werealizedthatthetwogroupsdifferedprimarilyintheitem “climbing stairs”,but withoutstatisticaldifferencebetween values.

IntheallocationoftheresultsoftheLysholmetal. ques-tionnaireonagraph,earlierimprovementoffunctioninGroup 1versusGroup2wasnotedinallassessments(p<0.001)(Fig.2). Inthisstudy,somecomplicationsoccurred:eightpatients inGroup1reportedaneedforanalgesiaafterinfiltration.Insix ofthesecases,twopatientsrequiredonlyonedoseofdipyrone 50drops,andintwoofthem,twodaysofdipyrone50drops 8/8hwererequired.

Noneofthepatientshadpost-operativeinfections,joint stiffness,orscarchanges.

Discussion

(4)

Table2–ResultofmultiplecomparisonsofVASamonggroupsandtimepoints.

Group/timepoint Comparison Meanestimated

difference

Standarderror tvalue gL p

Group1 3days–8days 3.86 0.10 38.60 384 <0.001

3days–15days 5.20 0.13 41.05 384 <0.001

3days–30days 6.22 0.14 44.25 384 <0.001

3days–60days 7.02 0.15 47.27 384 <0.001

8days–15days 1.35 0.10 13.48 384 <0.001

8days–30days 2.37 0.13 18.67 384 <0.001

8days–60days 3.16 0.14 22.49 384 <0.001

15days–30days 1.02 0.10 10.21 384 <0.001

15days–60days 1.82 0.13 14.33 384 <0.001

30days–60days 0.80 0.10 7.97 384 <0.001

Group2 3days–8days 2.27 0.10 22.67 384 <0.001

3days–15days 4.33 0.13 34.12 384 <0.001

3days–30days 6.37 0.14 45.26 384 <0.001

3days–60days 7.06 0.15 47.55 384 <0.001

8days–15days 2.06 0.10 20.63 384 <0.001

8days–30days 4.10 0.13 32.35 384 <0.001

8days–60days 4.80 0.14 34.09 384 <0.001

15days–30days 2.04 0.10 20.42 384 <0.001

15days–60days 2.73 0.13 21.57 384 <0.001

30days–60days 0.69 0.10 6.94 384 <0.001

3days Group1–Group2 −0.10 0.16 −0.64 384 >0.999

8days Group1–Group2 −1.69 0.16 −10.59 384 <0.001

15days Group1–Group2 −0.98 0.16 −6.12 384 <0.001

30days Group1–Group2 0.04 0.16 0.26 384 >0.999

60days Group1–Group2 −0.06 0.16 −0.38 384 >0.999

matrixandispresentinhighconcentrationsincartilageand synovialfluid.10

Some authors claimthat sodium hyaluronate, which is a defined fraction of hyaluronic acid, has analgesic and anti-inflammatoryproperties,contributestothe normaliza-tion of fluidity or viscoelasticity of the synovial fluid and totheactivation oftissueregenerationintheaffected car-tilage, and restores the functional balance of the joint. Therefore, they recommend its use for the treatment of osteoarthritis.4,13,14

Somestudieshavereportedthat,inadditiontorelieving painandimprovingfunction,theuseofhyaluronicacidcould

alterthecourseofosteoarthrosisandimprove qualitatively and quantitativelythearticularcartilage.Theseindications are based on studies of imaging such as X-ray and MRI, in which therewas an increase incartilage volume and a decrease injoint space afterthe treatment versus placebo. Thesebenefitsarealsobasedonthebestqualityofthematrix andonahigherdensityofchondrocytesinbiopsystudiesafter theimplementationoftreatment.4

Inanimalstudies,Plaasetal.15concludedthathyaluronic

acid suppresses synovialhyperplasia and the development ofperiarticularfibrosis,andprotectagainstcartilageerosion, andalsoactstorelievepainintheshortterm(dilutionofjoint

Table3–ResultofmultiplecomparisonsofLysholmquestionnaireamonggroupsandtimepoints.

Group/timepoint Comparison Meanestimated

difference

Standarderror tvalue gL p

Group1 Pre–15days 1.10 0.28 3.92 288 0.003

Pre–30days −43.47 0.33 −133.55 288 <0.001

Pre–60days −47.76 0.34 −140.79 288 <0.001

15days–30days −44.57 0.28 −158.49 288 <0.001

15days–60days −48.86 0.33 −150.11 288 <0.001

30days–60days −4.29 0.28 −15.24 288 <0.001

Group2 Pre–15days 12.02 0.28 42.74 288 <0.001

Pre–30days −28.88 0.33 −88.72 288 <0.001

Pre–60days −41.84 0.34 −123.34 288 <0.001

15days–30days −40.90 0.28 −145.43 288 <0.001

15days–60days −53.86 0.33 −165.47 288 <0.001

30days–60days −12.96 0.28 −46.08 288 <0.001

Pre Group1–Group2 −1.73 0.35 −5.01 288 <0.001

15days Group1–Group2 9.18 0.35 26.54 288 <0.001

30days Group1–Group2 12.86 0.35 37.16 288 <0.001

(5)

0 10 20 30 40 50 60 70 80 90 100

-10 0 10 20 30 40 50 60 70

Dia

Lysholm

Group 1 Group 2

Fig.2–Graphicalrepresentationofthemeanprofilesand respectivestandarderrorsofLysholmquestionnaire, accordingtogroups.

fluid)andinthelongterm(blockingofpainreceptors),and improvethegaitpatternoftheosteoarthrosisknee.

Currently,theuseofintra-articularhyaluronicacidisalso widelydiscussedbecauseofthedifferentformulations,with differentmolecular weightsand theresultsofsome meta-analyses.Thesestudiesalsodifferintheparameterusedand furtherincreasethediscussionastotheeffectivenessofits use.16

Huanget al.,13inarandomized,double-blind,

multicen-terstudy,evaluatedinonesampleofthe Asianpopulation theuseofintra-articularhyaluronicacidversusplacebo.These authorsfoundstatisticallysignificantimprovementin reduc-ingthepainandinthekneefunction,especiallyafterthefifth weekoftreatment.Thesebenefitshaveremainedeffectivefor upto25weeks.Inthesubjectiveevaluation,favorableresults withitsusealsowerenoted.Regardingtheconsumptionof acetaminophenandthevolumeofjointfluid,therewasno statisticallysignificantdifferenceforanygroup.11

Theseresultsare consistentwiththe study by Navarro-Sarabiaetal.,17inwhichtherewasastatisticallysignificant

difference in favor of hyaluronic acid in the categories of painrelief,improvedfunctionandoverallimprovementofthe patientversusplacebo.

Bannuruetal.,14inameta-analysiscomparativeoftheuse

ofintra-articularhyaluronic acidversus placebo, concluded thathyaluronicacidiseffectiveasearlyasthefourthweek oftreatment, with peak effectiveness at eight weeks, and remainingbeneficialforupto24weeks.Theseauthors eval-uatedtheeffectivenessforpainrelief,improvedfunctionand decreasedjointstiffness.

Leeetal.18believethattheanalgesiceffectofhyaluronic

acid in the first five weeksis equal tothat ofplacebo. In their prospective and randomized study, the authors con-cludedthattheuse ofcetorolac associatedwithhyaluronic acidshowedmorerapidanalgesiaversusmonotherapywith hyaluronic acid. In the fifth week this analgesia achieved equalintensityinbothgroups(hyaluronicacidwith cetoro-lac×hyaluronicacidalone).

Butit isworthbearinginmindthattheaforementioned studies evaluate the hyaluronic acid in the treatment of

osteoarthrosis;hence,itisinterestingtoquotethem,because they discuss the efficacy ofhyaluronicacid as ameans of improvingfunctionandpain.

Regardingtheuseofhyaluronicacidinthepost-operative ofarthroscopy,ForsterandStraw19comparedpainand

func-tion in activities of daily living in patients with isolated arthroscopy versus arthroscopy associated with hyaluronic acid.Theseauthorsconcludedthattherewasimprovement offunctionwiththeuseofHA,butwithoutdifferenceinthe categoryofpain.

Heybeli et al.1 compared pain and function in patients

with 40–65yearsold with mildtomoderate osteoarthrosis and whounderwent arthroscopywithand withoutthe use ofhyaluronicacid(HA)post-operatively.Therewasno statis-ticallysignificant differencewithrespecttopain,but there wasimprovementinfunctioninpatientswhousedHA.Inour study,weobservedthesameresultwithrespecttofunction improvement,mainlyuntilthe30thday,bothbytheLysholm questionnaireandbythegoniometermensuration.However, withregardtopain,untilthethirddaytheresultsconfirmthe literature,withnodifferencewiththeuseofthemedication inquestion;thereafter,patientstreatedwithhyaluronicacid hadlesspainversuscontrolgroup,andthisanalgesiaachieved equalintensityinthe30thday-evaluationandfromthenon.

Hempfling10 also contrasted isolated arthroscopy versus

arthroscopyassociatedwithHAinthe itemsofnightpain, pain when walking, and ability to walk 100 meters with-out pain. A clear symptomatic improvement occurred in bothgroups,comparedwithpreoperativevalues;butinthe group using HA this improvement lasted longer. In our study, therewas alsosignificant improvementin pain and function versus preoperative assessments, but this differ-ence wasobservedintheinitialevaluations.Afterthe60th day,animportantdifferencebetweentheratingsofGroups 1 and 2 was not observed, which can be justified by the lack ofassessmentof patientsover a longer period, when maybe we could observe results equivalent to the litera-ture.

In2007,Ulucayet al.20comparedtheuse ofthreetypes

of HA in women40–60 years old with mild osteoarthrosis and degenerative meniscal lesion,after arthroscopy. These authors concluded that HA is effective therapy for these patients.

Alsoin2008,Atay etal.21 comparedthe effectofHAof

high and lowmolecular weight versus placebo interms of pain,stiffnessandfunctionalabilityatsixand12monthsafter arthroscopicdebridementinpatientswithmildtomoderate osteoarthrosis. Aftersix months,there was nostatistically significantdifference,butthisoccurredafter12months.The authorsconcludedthattheuseofHAresultsbeneficialand improves the effectivenessof treatment, regardless of the substance’shighorlowmolecularweight.Inourstudy,pain improvement wasobserved untilthe 15th day, withbetter rangeofmotionandfunctionalcapacityuntilthe30thday. There was nostatistical differencefor theitems evaluated fromthe60thday.

Waddell andBert,2 inasystematicreviewconductedin

(6)

decreasepainandimprovethefunctionofasignificant num-berofpatientspost-operatively.Inourstudy,theimprovement ofpain,function,andrangeofmotioninpatientswhowere treatedwithHAinfiltrationwasobserved.Theimprovement ofpainisobserved intheinitialstage, especiallyuntilthe 15thday;ontheotherhand,thefunctionandrangeofmotion improvedafterthisperiod.Webelieveinadirectrelationwith thiseffect:withlesspain,thepatientcanachieveafaster reha-bilitation,withmorequality,besidesafasterreturntohis/her dailyfunctions.

When interpreting more deeply the Lysholm question-naire,ourresultsdemonstrated,intheinitialevaluation,that although both groups were classified as poor, the superi-ority of the patients in Group 1 was justifiedby the best assessmentsin relation topain and swelling.This finding corroboratestheresultsofVASandcanbeexplainedbythe analgesic and anti-inflammatory effect of hyaluronic acid.

4,13,14

Inthe30thdayevaluation,wefoundthegreatestdifference betweenGroups1and2:90and77points,respectively.The maindifferencesareintheitem“swelling”,againbecausethe anti-inflammatoryeffectofHA.Asof“claudication”, “instabil-ity”and“squatting”,webelievethat,bythistime,withamore effectivetherapy and because ofalower intensity ofpain, itispossiblethatthepatientbesubmittedtomoreintense demands and achieve an earlier gain ofmuscle mass and proprioception.Thiswouldfacilitatetheactivitiesabove eval-uated.Fromthe 30th,the painwassimilarinbothgroups, andintheassessmentofthe60thdaybothgroupswere clas-sifiedasgood,withstatisticalsuperiorityinGroup1versus Group2(94×90,respectively).Thissuperioritywasduetothe

improvedabilitytoclimbstairsbyGroupHApatients,likely duetothebettermusclereservesacquired inthe initial60 days.

Conclusion

Giventhesubjective parametersevaluated, webelievethat theuseofintra-articularinfiltrationsofsodiumhyaluronate 20mgin proceduresof arthroscopicsurgery ofthe knee is fullyjustified,asthispracticeleadstoadecreaseinpainin theinitialphase,enablesfasterpatientrecoveryand gener-atesafasterreturnandbetterqualitytotheactivitiesofdaily living.

Ourstudyhassomelimitations:theshortperiodof eval-uation ofpatients (wewere unable toverify the effects of hyaluronicacidinthemediumandlongterm),andalsothe factofthesubjectivityoftheevaluationofpatients’function. Thisimpliesthatperhapsanisokineticevaluationwithcybex couldbetterdemonstrateamuscledifferencesbetweenthe twogroupsofindividuals.Webelievethatthis isthemain causeofimprovementofthefunctiononthe60thday. Unfor-tunately,wecould notproceedwiththis optionforlackof money.

Conflicts

of

interest

Theauthorsdeclarenoconflictsofinterest.

r

e

f

e

r

e

n

c

e

s

1.HeybeliN,DoralMN,AtayOA,LeblebiciogluG,UzumcugilA.

Intra-articularsodiumhyaluronateinjectionsafter

arthroscopicdebridementforosteoarthritisoftheknee:a

prospective,randomized,controlledstudy.ActaOrthop

TraumatolTurc.2008;42(4):221–7.

2.WaddellDD,BertJM.Theuseofhyaluronanafterarthroscopic

surgeryoftheknee.Arthroscopy.2010;26(1):105–11.

3.CarulliC,MatassiF,CivininiR,MorfiniM,TaniM,Innocenti

M.Intra-articularinjectionsofhyaluronicacidinduce

positiveclinicaleffectsinkneesofpatientsaffectedby

haemophilicarthropathy.Knee.2013;20(1):36–9.

4.RezendeMU,CamposGC.Viscossuplementac¸ão.RevBras

Ortop.2012;47(2):160–4.

5.ConrozierT,JeroschJ,BeksP,KemperF,Euller-ZieglerL,

BailleulF,etal.Prospective,multi-centre,randomized

evaluationofthesafetyandefficacyoffivedosingregimens

ofviscosupplementationwithhylanG-F20inpatientswith

symptomatictibio-femoralosteoarthritis:apilotstudy.Arch

OrthopTraumaSurg.2009;129(3):417–23.

6.PavelkaK,UebelhartD.Efficacyevaluationofhighlypurified

intra-articularhyaluronicacid(Sinovial®)hylanG-F20

(Synvisc®)inthetreatmentofsymptomaticknee

osteoarthritis.Adouble-blind,controlled,randomized,

parallel-groupnon-inferioritystudy.OsteoarthritisCartil.

2011;19(11):1294–300.

7.BaggaH,BurkhardtD,SambrookP,MarchL.Longtermeffects

ofintraarticularhyaluronanonsynovialfluidinosteoarthritis

oftheknee.JRheumatol.2006;33(5):946–50.

8.ClarkeS,LockV,DuddyJ,SharifM,NewmanJH,KirwanJR.

Intra-articularhylanG-F(Synvisc®)inthemanagementof

patellofemoralosteoarthritisoftheknee(POAK).Knee.

2005;12(1):57–62.

9.PetrellaR,PetrellaM.Aprospective,randomized,

double-blind,placebocontrolledstudytoevaluatethe

efficacyofintraarticularhyaluronicacidforosteoarthritisof

theknee.JRheumatol.2006;33(5):951–6.

10.HempflingH.Intra-articularhyaluronicacidafterknee

arthroscopy:atwo-yearstudy.KneeSurgSportsTraumatol

Arthrosc.2007;15(5):537–46.

11.SingerJM,AndradeDF.Analysisoflongitudinaldata.In:Sen

PK,RaoCR,editors.Handbookofstatistics:

bio-environmentalandpublichealthstatistics.Amsterdam:

NorthHolland;2000.p.115–60.

12.NeterJ,KutnerMH,NachtsheimCJ,WassermanW.Applied

linearstatisticalmodels.4thed.Illinois:RichardD.Irwing;

1996.

13.HuangTL,ChangCC,LeeCH,ChenSC,LaiCH,TsaiCL.

Intra-articularinjectionsofsodiumhyaluronate(Hyalgan®)in

osteoarthritisoftheknee.Arandomized,controlled,

double-blind,multicentertrialintheAsianpopulation.BMC

MusculoskeletDisord.2011;12:221–8.

14.BannuruRR,NatovNS,DasiUR,SchmidCH,McAlindonTE.

Therapeutictrajectoryfollowingintra-articularhyaluronic

acidinjectioninkneeosteoarthritis–meta-analysis.

OsteoarthritisCartil.2011;19(6):611–9.

15.PlaasA,LiJ,RiescoJ,DasR,SandyJD,HarrisonA.

Intraarticularinjectionofhyaluronanpreventscartilage

erosion,periarticularfibrosis,andmechanicalallodyniaand

normalizesstancetimeinmurinekneeosteoarthritis.

ArthritisResTher.2011;13(2):R46.

16.CurranMP.Hyaluronicacid(Supartz®).Areviewofitsusein

osteoarthritisoftheknee.DrugsAging.2010;27(11):925–41.

17.Navarro-SarabiaF,CoronelP,CollantesE,NavarroFJ,DeLa

SernaAR,NaranjoA,etal.A40-monthmulticentre,

(7)

andcarry-overeffectofrepeatedintra-articularinjectionsof

hyaluronicacidinkneeosteoarthritis:theAMELIAproject.

AnnRheumDis.2011;70(11):1957–62.

18.LeeSC,RhaDW,ChangWH.Rapidanalgesiconsetof

intra-articularhyaluronicacidwithketorolacinosteoarthritis

oftheknee.JBackMusculoskeletRehabil.2011;24(1):31–8.

19.ForsterMC,StrawR.Aprospectiverandomizedtrial

comparingintra-articularHyalganinjectionandarthroscopic

washoutforkneeosteoarthritis.Knee.2003;10(3):291–3.

20.UlucayC,AltintasF,UgutmenE,BeksacB.Theuseof

arthroscopicdebridementandviscosupplementationinknee

osteoarthritis.ActaOrthopTraumatolTurc.2007;41(5):

337–42.

21.AtayT,AslanA,BaydarML,CeylanB,BaykalB,KirdemirV.

Theefficacyoflow-andhigh-molecular-weighthyaluronic

acidapplicationsafterarthroscopicdebridementinpatients

withosteoarthritisoftheknee.ActaOrthopTraumatolTurc.

Imagem

Table 1 – Characterization of sample.
Table 3 – Result of multiple comparisons of Lysholm questionnaire among groups and time points.
Fig. 2 – Graphical representation of the mean profiles and respective standard errors of Lysholm questionnaire, according to groups.

Referências

Documentos relacionados

Objetivo: Verificar a prevalência de hábitos parafuncionais de mordida e não mordida bem como sinais e sintomas de disfunções temporomandibulares em adolescentes com

In the periods of 0-21, 0-28 and 0-35 days of age, birds fed the antibiotic again presented higher weight gain values, but only as compared with the control group (P&lt;0.05) and

The results demonstrated in Table I showed that the samples CP24 and CP48 in the refrigeration condition (8 °C ± 1) had no statistical difference compared to their control at

Furthermore, there were statistical signiicant changes between control group and IPC group in values of the last point of reperfusion (P&lt;0.05*) but in comparison

In animals treated with the laser, vasodilation was notable at every post-treatment time-point compared with control animals, although at days 2 and 4 the differences were

Aerobic power, as measured by AnT, showed a significant increase (p&lt;0.05) for the ET and IT groups in comparison to the CO group and to the PRE time point; the interval training

No setor de suinocultura do Departamento de Zootecnia da Universidade Federal de Lavras (UFLA), foram conduzidos dois experimentos com a finalidade de verificar o efeito

With regard to the average germination time ( AT ), the wild poinsettia diaspores showed a significant increase when treated with the aqueous leaf extracts of all the donor