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Rev. Bras. Anestesiol. vol.64 número2

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REVISTA

BRASILEIRA

DE

ANESTESIOLOGIA

OfficialPublicationoftheBrazilianSocietyofAnesthesiology www.sba.com.br

SCIENTIFIC

ARTICLE

The

comparison

of

levobupivacaine

in

continuous

or

single

dose

spinal

anesthesia

for

transurethral

resection

of

prostate

surgery

Yunus

Baydilek

a

,

Bülent

Serhan

Yurtlu

b,∗

,

Volkan

Hanci

c

,

Hilal

Ayo˘

glu

b

,

Rahs

¸an

Dilek

Okyay

b

,

Gulay

Erdo˘

gan

Kayhan

d

,

Hüsnü

Tokgöz

e

,

Görkem

Mungan

f

,

Is

¸ıl

Özkoc

¸ak

b

aClinicofAnesthesiologySaniKonuko˘gluHospital,Gaziantep,Turkey

bDepartmentofAnesthesiologyandReanimation,BulentEcevitUniversity,Zonguldak,Turkey

cDepartmentofAnesthesiologyandReanimation,C¸anakkaleOnsekizMartUniversity,C¸anakkale,Turkey dDepartmentofAnesthesiologyandReanimation,InonüUniversity,Zonguldak,Turkey

eDepartmentofUrology,BulentEcevitUniversity,Zonguldak,Turkey

fDepartmentofBiochemistry,BulentEcevitUniversity,Zonguldak,Turkey

Received1May2012;accepted20March2013 Availableonline11October2013

KEYWORDS

Levobupivacaine;

Continuousspinal

anesthesia;

Spinalanesthesia;

Transurethral

prostateresection

Abstract

Background: Theaimofthestudyistocomparetheefficacyoflevobupivacaineinduced con-tinuousspinalanesthesia(CSA)versussingledosespinalanesthesia(SDSA)inpatientswhoare plannedtoundergotransurethralprostateresection.

Methods:Sixtyyearsorolder,ASAI---IIorIII,50patientswereincludedinthestudy.12.5mg 0.5%levobupivacainewere administered intrathecallyinSDSAgroup.InCSA group,initially 2mLof0.25%levobupivacainewereadministeredthroughspinalcatheter.Inordertoachieve sensoryblocklevelatT10dermatome,additional1mLof0.25%levobupivacainewere adminis-teredthroughthecatheterinevery10min.Hemodynamicparametersandblockcharacteristics wererecorded.Preoperativeandpostoperativebloodsamplesofthepatientsweredrawnto determineplasmacortisoneandplasmaepinephrinelevels.

Results:CSA techniqueprovidedbetterhemodynamicstability comparedtoSDSAtechnique particularly90minafterintrathecaladministration.Theriseinsensoryblocklevelwasrapidand thetimetoreachsurgicalanesthesiawasshorterinSDSAgroup.Motorblockdevelopedfasterin SDSAgroup.InCSAgroup,similaranesthesialevelwasachievedbyusinglowerlevobupivacaine doseandwhichwas relatedtofasterrecovery. Although,bothtechniqueswereeffective in preventing surgical stress respond,postoperative cortisonelevels were suppressed more in SDSAgroup.

Correspondingauthor.

E-mail:syurtlu68@gmail.com(B.S.Yurtlu).

0104-0014/$–seefrontmatter©2013SociedadeBrasileiradeAnestesiologia.PublishedbyElsevierEditoraLtda.Allrightsreserved.

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Conclusion:CSAtechniquewith0.25%levobupivacainecanbeusedasaregionalanesthesia methodforelderlypatientsplannedtohaveTUR-Poperation.

©2013SociedadeBrasileiradeAnestesiologia.PublishedbyElsevier EditoraLtda.Allrights reserved.

Introduction

Anesthesia is appliedin 10---20% of urologic interventions.

Anesthetic methods chosen within general principles are

topical,regionalandgeneral.1,2Mostpatientswithbladder

obstructioncausedbybenignprostatichyperplasiaare suc-cessfullytreatedbytransurethralresectionoftheprostate (TUR-P).3TUR-Pisoftenperformedonolderpatientswith

impaired renal function, cardiovascular and respiratory problems.Researchhas foundmany sideeffects ofTUR-P includingbleeding,transurethralresectionsyndrome(TUR), bladderperforation,hypothermia,intraoperativeandearly postoperative occurrence of disseminated intravascular coagulation,with high reportedmorbidity rates. To mini-mizehemodynamicchangesinthesepatientsitisimportant toprovidestableanesthesia.Generalanesthesiamaymake identification ofcomplications such asTUR syndromeand bladderperforation difficult,so regionalanesthesiaisthe preferredmethodinsuitableTUR-Pcases.4---7

Single-dose spinal anesthesia (SDSA) is widely used in theseinterventionsthough it hasthe disadvantage ofnot providingtherequireddurationinoperationsthatrunlonger thanexpected.Withthecontinuousspinalanesthesia(CSA) technique,localanestheticdosecanrepeated,thusmaking itpossibletousethisspinalanesthesiamethodinoperations withlongduration.8---12 AnotheradvantageofCSAisthatit

enablestotitrate thedose oflocalanestheticthus allow-ingbettercontrolofsensoryandmotorblocklevel,norisk oflocalanesthetictoxicityandprovidingshorterrecovery periods.ComparedtoSDSA,itsmostimportantadvantage isthatitprovidesperfecthemodynamicstability. Further-more,spinalcathetermaybeinsertedinregionalanesthesia preparationroombeforetheoperation,thuspreventingloss oftimebetweenoperations.10,13,14

Levobupivacaine,abupivacaineSisomercommonlyused in spinal anesthesia (SA), has less side effects on the cardiovascular (CVS) and central nervous systems (CNS) than bupivacaine with similar effective onset time and duration.7,15---17 Although levobupivacaine use in various

regionalanesthesia techniques have been reported previ-ously, description of its use in CSA is limited. We have hypothesizedthatlevobupivacaineprovidesbetter hemody-namicstabilitywhenusedinCSAcomparedtoSDSA.Inorder totest thishypothesis, patients scheduled tohave TUR-P operationwereadministeredeither SDSAor CSA with lev-obupivacaine; hemodynamics,sensory-motor block levels, anestheticqualityandcomplicationswerecompared.

Materials

and

methods

After receiving permission from Bulent Ecevit University Medical Faculty Hospital Ethics Committee (06.12.2007,

Decisionno.2007/09/17),thisresearchwascarriedoutin theDepartmentofAnesthesiologyandReanimationbetween December2007andJune2008.Fiftypatientsovertheage of60scheduledtohaveelectiveTUR-PinterventionsatASA I---IIIriskgroupswereincludedinthestudyafterreadingthe informedconsentform.Thepatientswererandomizedinto eithercontinuousspinalanesthesiagroup(GroupCSA,n:25) orsingle-dosespinalanesthesiagroup(GroupSDSA,n:25)by randomizednumberstable.

Exclusion criteria were refusing to be included in the study,allergiestotheresearchdrugs,severecardiacfailure (unstablecoronaryarterydisease,2ndand3rddegreeheart block, congestive heart failure, ventricular tachyarrhyth-mia) and valvular heart disease (serious aortic stenosis), coagulation abnormalities, low molecular weight heparin administrationintheprevious12h,intakeofnon-steroidal anti-inflammatorydrugwithinthe24h,historyofalcoholor drugaddiction,presenceofneurologicdisordersor psychi-atricdisease.

All the patients were premedicated with 0.03mg/kg midozolam (Dormicum®) intramuscularly 30min prior to

their arrival tooperation theater. Patients were takento thepreoperativepreparationunitandweremonitored (non-invasive bloodpressure, heartrate andperipheral oxygen saturation while breathing room air) these values were recorded as control values. Patients were given 4 l/min oxygen through a mask, a 20G cannula was inserted for intravenous accessand10mL/kg0.09% salinewasinfused within 30min, afterwards the rate was set at 5mLkg/h. Bloodsamplestaken fromeach patientwhile opening the veinwascentrifugedtoseparatedplasmafromserumand storedinafreezerat−20◦C.

Allpatients had lumbar puncture underaseptic condi-tions, while sitting, between L3---4 or L 2---3 according to anesthesist’s preference. The lumbar puncture level was recorded.Skinandsubcutaneous2mL2%lidocaine(Aritmal®

5mLampoule)infiltrationanesthesiawasgivenwitha22G needle.AnesthesiawasbegunforGroupCSAwith2mL0.25% levobupivacaine after a 22G spinal catheter (Spinocath®)

wasplaced2---3cmintotheintrathecal interval.Afterthe 10thminifthelevelofsensoryblockhadnotreachedT10, anextra1mL0.25%levobupivacainewasgiventhroughthe catheter, this was repeated at 10min intervals until T10 blocklevelwasreached.Thetotaldoseoflevobupivacaine wasrecorded.

Spinal anesthesia was induced in group SDSA patients with12.5mg(2.5mL)0.5%levobupivacaineinjectedintothe intrathecalintervalwitha22GQuinkeneedle.

Aftertheinjectionbloodpressure,heartrate,SpO2,

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15and45min.(MBS:0noparalysis,patientcanfullyflexfoot andknee;1Canonlymovekneeandfoot,cannotliftstraight leg;2cannotbendknee,canonlymovefoot;3full paraly-sis.)After45minthepatientsweretakentotheoperating room.

In both groups the time fromthe injection to sensory block level reachingdermatome T10 wasrecordedas the surgical anesthetic duration.It wasplanned thatpatients whoreacheddermatomeT10andabovesensoryblocklevel gave permission for the operation. After spinal injection untilMBS1wasreachedwasdenotedthemotorblock ini-tiation time.Fromthe injection topeakdermatome that is sensoryblock level reached maximum dermatome, was called the peak dermatome time. From the start of the surgicalproceduretotheendwastheoperationduration.

Sensoryblocklevelwascheckedusingthepin-pricktest (needle prick). Sensory block level was assumed to have reachedthedermatomewhenthepatientnolongerfeltthe needleprick.

Whenmeanarterialbloodpressure(MAP)decreased20% fromthe basal level hypotensionwasdiagnosed and5mg ephedrine HCL(Osel drugs) wasadministered. Heart rate below 50beatsper min wasaccepted asbradycardia and 0.5mgatropine(atropine1mLamp,Drogsan)was adminis-tered.Totalliquidsgiventothepatient,aswellasephedrine andatropinedoseswererecorded.

Patientstakentotheoperatingtheaterweremonitored usinganADUanestheticmonitor(Datex-Ohmeda®S/5

Anes-theticMonitor)for5-leadsurfaceelectrocardiogram(ECG, DII),SpO2andnon-invasivearterialbloodpressure.

After the operation finished the CSA group had the catheter removed. Both groups were given a PCA unit (AbbotPainManagementProvider)withivmorphine(bolus dose:2mg,lock-outtime30min)forpostoperative analge-sia.Fromintrathecal injectiontofirstuseofthePCA was recordedasthefirstanalgesicduration.

Following intrathecal injectionall patients were moni-tored at 50, 60, 70, 80, 90, 100, 110, 120, 150, 180min and 4, 6, 9, 12, 15, 18 and 24h. Values for blood pressure, heart rate, SpO2, VRS (verbal pain evaluation

scoring), sensory block level, MBS score, PCA machine requests (Dem), number of times drugs were adminis-teredbyPCA (Del)andtotal morphinegivenbyPCA were recorded.

Degree of painwasevaluated usingVRS (0:nopain; 1 slightpain;2moderate pain;3severe pain;4 verysevere pain; 5 unbearable pain). From peak dermatome sensory blockuntilitregressedtwolevelswasrecordedasthe sec-ond dermatome reductionduration. Fromspinal injection toMBSscoreof 0 wasrecordedasBromage scale 0 dura-tion.Eighthoursaftertheoperationbloodsamplesfromall patients werecentrifugedtoseparateserumfromplasma andstoredinafreezerat−20◦C.Attheendoftheresearch serumcortisolandplasmaadrenalinelevelsinpreoperative andpostoperativeblood samplesweremeasuredusingthe ELISAmethod.

Statisticalanalysis

SPSS11.5programwasusedforstatisticalanalysisofdata. The data was analyzed for normal distribution using the

Table1 Demographicdata(mean±SD).

Group GroupCSA

(n=25)

GroupSDSA (n=25)

p

Age(year) 71.04±6.62 70.68±5.68 0.838 Weight(kg) 79.6±11.39 80.24±11.06 0.841 Operationtime

(min)

50.00±7.79 51.44±8.78 0.543

ASA(I/II/III) 3/13/9 2/15/8 0.818

Kolmogorov Smirnoff test. The Mann Whitney U test was

usedtocomparethefollowingcontinuousdatafromthetwo

groups:operationduration,height,weight,age,blood

pres-sure,heartrate,sensoryblocklevel,highestsensoryblock

level, sensory block dermatome T10 time, sensory block

twosegmentregressiontime,MBS,VRS,timeoffirst

anal-gesicdose, total analgesic use,PCA requests andnumber

oftimesdrugs wereadministeredbyPCADel/Demvalues,

totalatropineandephedrineuse,andcortisolandadrenalin

levels.To analyzetherepetition of thesedata withinthe

groups the Wilcoxon test was used. The chi-square test

was used to analyze frequency (%) results of ASA

physi-calclassification, lumbar puncture level, nausea-vomiting

andsideeffects.Descriptivestatisticsforthedatasuchas

meanand standard deviation (mean±SD),mode and

fre-quency (number and %) were determined. Graphs of the

changesindifferencebetweenthegroupsagainsttimewere

constructed. A value of p<0.05 was accepted as

signifi-cant.

Results

Thestudycomprisedatotalof50patientsin2groups,all

patientscompletedtheprotocol.

Demographicdata

Therewerenostatisticallysignificantdifferencesbetween

thetwogroupsin terms ofage, bodyweight,height,ASA

riskclassandoperationduration(Table1).

Hemodynamicchanges

Comparingthegroups blood pressurein the90, 100,120, 150,180minand4,6,9,12,15,18and24hafterintrathecal injectionthe CSA group was significantly higher than the SDSAgroup(p<0.05)(Fig.1).

WithintheCSAgroupbloodpressureinthe2.5,5,7.5,10, 12.5,15,20,25and30minafterintrathecalinjectionwas significantlylowerthanthecontrolvalues(p<0.05)(Fig.1). WithintheSDSAgroupwhenbloodpressurechangeswere examinedtheywerefoundtobesignificantlylowerthanthe controlvaluesatalltimes(p<0.05)(Fig.1).

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102

96

90

84

Group CSA mmHg

p≤0.05 (between group CSA and group SDSA)

p≤0.05 (significant difference compared with group CSA control values)

p≤0.05 (significant difference compared with group SDSA control values)

Control 0. min 2.5. min 5. min 7.5 min 10. min 15 min 20 min 25 min 30 min 35 min 40 min 45 min 50 min 60 min 70 min 80 min 90 min 100 min 110 min 120 min 150 min 180 min

4 h 6 h 9 h 12 h 15 h 18 h 24 h

12.5 min

Group SDSA

Figure1 Changesinmeanarterialbloodpressure(MAP).*p<0.05(betweenGroup CSAandGroupSDSA).†p<0.05(significant

differencecomparedwithGroupCSAcontrolvalues).‡p<0.05(significantdifferencecomparedwithGroupSDSAcontrolvalues).

Group CSA

HR (beat/min)

76

Time 72

68

64

60

p≤0.05 (significant difference compared with group CSA control values)

p≤0.05 (significant difference compared with group SDSA control values)

Control 0. min 2.5. min 5. min 7.5 min 10. min 15 min 20 min 25 min 30 min 35 min 40 min 45 min 50 min 60 min 70 min 80 min 90 min 100 min 11

0 min

120 min 150 min 180 min 4 h 6 h 9 h

12 h 15 h 18 h 24 h

12.5 min

Group SDSA

Figure2 Changesinheartrate(HR).†p<0.05(significantdifferencecomparedwithGroupCSAcontrolvalues).p<0.05

(signifi-cantdifferencecomparedwithGroupSDSAcontrolvalues).

Anestheticproperties

LumbarpuncturewasperformedatL2---L3intervalin8and atL3---L4intervalin17patientsintheCSAgroup;6patients hadlumbarpuncture at L2---L3intervaland19patients at L3---L4intervalintheSDSAgroup.Therewasnostatistically significantdifferenceinlumbarpuncturelevelbetweenthe twogroups(p>0.05).

Comparing the groups modified Bromage scores (MBS) from5to120minvaluesweresignificantlyhigheringroup SDSAthaningroupCSA(p<0.05)(Fig.3).

Comparingthegroupssensoryblocklevelsat2.5,5,7.5, 10,12.5,15,20,25,30and35minafterintrathecalinjection theSDSAgroupvaluesweresignificantlyhigherthantheCSA group(p>0.05)(Fig.4).

Nostatisticallysignificantdifferencewasfoundbetween VRS scores for the groups (p>0.05). Average peak der-matome valueswereT8for theCSA group andT7for the SDSA group. There was no significant difference between thetwogroupspeakdermatomevalues(p>0.05).

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Group CSA

MBS

3

2

0 1

Time

Control 0. min 2.5. min 5. min 7.5 min 10. min 15 min 20 min 25 min 30 min 35 min 40 min 45 min 50 min 60 min 70 min 80 min 90 min 100 min 110 min 120 min 150 min 180 min 4 h 6 h 9 h

12 h 15 h

12.5 min

Group SDSA

p≤0.05 (between group CSA and group SDSA)

Figure3 MBSchangesinthegroups.*p<0.05(betweenGroupCSAandGroupSDSA).

Table2 BlockTimes(min)(mean±SD).

Blocktimes GroupCSA(n=25) GroupSDSA(n=25) p

Timetoreachpeakdermatome 31.64±11.94 25.10±5.89 0.019*

Twosegmentregressiontime 79.28±18.66 90.08±14.66 0.030* Surgicaloperationtime 18.56±6.31 13.08±4.34 0.010*

Motorblockstarttime 13.04±7.10 6.04±2.30 0.000*

TimetoreachMBS0 170.28±51.32 186.04±35.13 0.211

Firstanalgesictime 268.88±94.52 253.60±92.46 0.566

* p<0.05(betweenGroupCSAandGroupSDSA).

timeintheSDSAgroupwassignificantlyshorterthaninthe CSA group. At thesame timethe twosegmentregression timewas significantlylonger in group SDSA than in group CSA(p<0.05)(Table2).Nosignificantdifferencewasfound

between the twogroups MBS0 and first use of analgesia times(p>0.05)(Table2).

GroupSDSAusedasignificantlyhigherdoseof levobupi-vacainethangroupCSA(p<0.05).Therewasnostatistically

p≤0.05 (between group CSA and group SDSA) Group CSA

Level

Th5

Th

L1

L5

S4

Time

Control 0. min 2.5. min 5. min 7.5 min 10. min 15 min 20 min 25 min 30 min 35 min 40 min 45 min 50 min 60 min 70 min 80 min 90 min 100 min 110 min 120 min 150 min 180 min

4 h 6 h 9 h

15 h

12 h

12.5 min

Group SDSA

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Table3 Totaldrugsandliquidsgiven(mean±SD).

Totals GroupCSA(n=25) GroupSDSA(n=25) p

Totallevobupivacaine 8.70±1.63 12.50±0.00 0.000*

Totalmorphine 8.00±3.78 6.96±2.83 0.278

Totalephedrine 0.20±1.00 1.20±3.31 0.160

Totalatropine 0.02±0.1 0.04±0.13 0.561

Totalliquids 1290.20±180.01 1337.60±148.86 0.315

* p<0.05(betweenGroupCSAandGroupSDSA).

Table4 Preoperativeandpostoperativeadrenalinandcortisollevels(mean±SD).

Group GroupCSA(n=22) GroupSDSA(n=22) p

PreopAdrenalin 249.90±62.63 265.40±70.90 0.446

PostopAdrenalin 190.04±52.63† 180.76±54.770.570

PreopCortisol 168.95±85.51 134.22±51.07 0.111

PostopCortisol 127.51±57.10† 89.37±32.98‡,* 0.010

* p<0.05(betweenGroupCSAandGroupSDSA).

p<0.05(significantdifferencecomparedwithGroupCSAcontrolvalues).

p<0.05(significantdifferencecomparedwithGroupSDSAcontrolvalues).

p≤0.05 (between group CSA and group SDSA) Group CSA

Number of requests

14

12

10

8

6

4

2

0 50 min

60 min

70 min

80 min

90 min

100 min

110 min

120 min

150 min

180 min

4h 6 h 9 h 12 h 15 h 18 h 24 h

Time Group SDSA

Figure5 AveragenumberofrequestsfromthePCAunit.*p<0.05(betweenGroupCSAandGroupSDSA).

significantdifferencebetweenthetwogroupsaverage con-sumption of morphine, ephedrine, atropine and liquids (p>0.05)(Table3).

Nodifference wasfound in thenumber of dosesgiven bythetwogroupsPCAmachines (p>0.05).Comparingthe numberofrequeststothePCA machinesat9,18and24h theCSA group requestswere significantlyhigher thanthe SDSAgroup(p<0.05)(Fig.5).

No significant difference was found between the two groupsplasmaadrenalinelevels(p>0.05)(Table4).

Withineachgrouppostoperativeplasmaadrenalinlevels weresignificantlylowerthanthepreoperativecontrollevels (p<0.05)(Table4).

Comparingthegroups’postoperativeserumcortisol lev-els,theSDSAgrouplevelsweresignificantlylowerthanthe CSAgrouplevels(p<0.05)(Table4).

Within both groups postoperativeserum cortisol levels were significantly lower than preoperative control levels (p<0.05)(Table4).

Comparingsideeffectsinbothgroups,whiletherewasno differencebetweenthegroupsintermsofnausea,vomiting, respiratorydepression,headacheandrash,lowerbackpain in group CSA wassignificantly greaterthan in group SDSA (p<0.05)(Table5).

Table5 Sideeffects(n,%).

Group GroupCSA

(n=25)

GroupSDSA (n=25)

p

Nausea: 0 2(8%) 0.153

Vomiting: 0 0 1.000

Respiratorydepression: 0 0 1.000

Headache: 0 1(4%) 0.317

Lowerbackpain: 9(36%) 2(8%) 0.018*

Rash: 0 0 1.000

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Discussion

This study compared continuous spinal anesthesia with single-dose spinal anesthesia using levobupivacaine in geriatric patients undergoing transurethral urologic inter-ventions. We found that continuous spinal anesthesia provided better hemodynamic stability, shorter recovery periodsandequalanestheticquality.

Inolderpatientsincreasesinhealthproblemscombined with suppressed physiologic compensatory mechanisms meansthathemodynamic instabilitylinkedtospinal anes-thesia may bemore seriousand lastlonger. Rapid spread of sympathetic block in spinal anesthesia may cause an increase in morbidity, especially in older patients with reduced cardiovascular adaptation mechanisms.18 One of

the most important factors tobe awareof in patients of increased age and with accompanying diseases is hemo-dynamicstability. Inaprospective studyoncardiacarrest linkedtoanesthesiaBibouletetal.19 determinedthemost

importantfactorsincardiacarrestinpatientsover84and withan ASA risk factor of 3and above.They found inap-propriate anesthetic doses, hypovolemiaand hypoxia due todifficultykeepingtheairwayopen werethemost com-monreasonsfor cardiacarrest.Especiallyin patientswho are older, or have cardiovascular and respiratory system problems,evenlowdosesmayresultingreateranesthetic levels,sotechniquessuchasCSAwhichallowthepossibility of dose titrationshouldbe givenpreference comparedto SDSA.20

Favareletal.,21 inastudycomparingCSAandSDSAuse

of 0.5% hyperbaric bupivacaine, showed that blood pres-sure loweredlessin theCSA groupcomparedtotheSDSA group.The researchersfound thattheCSA grouphadless hemodynamicchangesandthattheslowerstartof segmen-talblockandslowdevelopmentofsympatheticblockmade adaptation easier.21 DeAndres etal.22 used 0.5% isobaric

bupivacaineintheircomparisonofCSAandSDSAandfound hypotensionduetotherepeateddoseintheCSAgroupdid notneedvasopressordrugswhiletheincidenceof hypoten-sionintheSDSAgroupwasgreater.

Klimschaetal.18 compared0.5%isobaricbupivacainein

CSA, SDSA and epiduralanesthesia. Bloodpressure in the CSAgroupdidnotreduce,incontinuousepidural anesthe-sia therewasa 15±3% reduction anda 19±2% decrease intheSDSAgroup.AcomparisonofSDSAwithCSAbyReisli etal.23foundasignificantreductioninbloodpressureinthe

SDSAgroupcomparedtotheCSAgroup.Labailleetal.24used

low dose 0.125% isobaric bupivacaine withCSA technique toprovideeffectiveanesthesiawithminimalhemodynamic changesinolderpatients. Minvilleetal.25 comparedSDSA

andCSA withlow dose bupivacaine in plannedhip opera-tionsinpatientsover75years.Occurrenceofhypotension intheCSA groupwas31%and68%intheSDSAgroup; seri-ous hypotensionwas 8% in the CSA group and 51% in the SDSA group. In the CSA group 4.5±2mg ephedrine was consumed, compared with 11±2mg in the SDSA group. TheyfoundtheCSAgroupwashemodynamicallymore sta-ble.

HoweverPitkanenetal.26comparedCSAandSDSA

tech-niquesinplannedhipandkneeoperationsin40patientsand foundnosignificantdifferenceinhemodynamicstabilityof thegroups.

This studyfound both groupshad lowerbloodpressure than the control values. In the CSA group 4% of patients developedhypotensioncomparedto12%intheSDSAgroup, subsequentlythedoseof ephedrineusedwaslowerinthe CSAgroup.ThelowerbloodpressureintheSDSAgroup com-paredtothe CSAgroup is similartoresults fromprevious studies. Results from the use of levobupivacaine for CSA showedthatit providesmore hemodynamic stabilitythan bupivacaineinCSA,inagreementwithpreviouslypublished research.

Patients under spinal anesthesia show a reduction in heartratedue topreganglion fiberblockage anda reduc-tionin left atriumpressure.8 Shenkman et al.27 usedlow

dosesoflocalanestheticwiththeCSAtechniquetoprovide goodcontrolofhemodynamicsandthisadvantageoverthe SDSAtechniquemadeitsuitableforuseinolderandmore highriskpatients.Theyfoundamaximumreductioninheart rateof7.2%using0.1%bupivacaineforCSAinASAIII---IVrisk grouppatients.The researchersfound thatusingCSA they couldmodifythesensoryblocklevelinacontrolledfashion andreduce the risk of hemodynamic instability.27 Favarel

etal.21 found nosignificantdifferencein heartrateusing

hyperbaricbupivacainefor CSAandSDSA.Similarresearch findingnosignificantdifferenceinheartratewhenusingCSA comparedtoSDSAisavailable.18,25,28Thisstudyfoundno

sig-nificantdifferenceinheartratebetweentheCSAandSDSA groupsatanytimeinterval,similartotheliterature.

Research evaluating CSA using levobupivacaine are limited. The only research in literature by Sell et al.14

foundtheminimumeffectivedose oflocalanestheticwas 11.7mgusinglevobupivacaine for CSA in hipreplacement operations.Ourstudyfoundanaveragedoseof8.7mg lev-obupivacaineprovidedsufficientanesthesia.Weareofthe opinionthat the differencemaybedue todemographics, position,intendedblocklevelandothersuchfactors.

This study found the time to reach dermatome T10 sensory block level was significantly longer in the CSA group than the SDSA group. This is similar to times to reachsensory block levels that allow surgery in previous research.21,22,29Whiletherewasnosignificantdifferencein

peakdermatome,thetimefortheCSAgrouptoreachpeak dermatome was significantly longer. This result conforms withpreviousstudies.18,28

Comparing Bromage scale evaluations of motor block leveltheCSA group wassignificantlylowerthan theSDSA group. While motor block is a desirable characteristic in surgeries suchas orthopedics, it delays neurologic evalu-ationpostoperatively and obstructs mobilization. Forthis reasonanearlyendtomotorblockisadesirableproperty. Thelowerdegree of,andearlyendto,motorblockinthe CSAgroupcouldbeseenasanadvantage.

SDSAgrouppatientsrequiredanaverageof12.5mg lev-obupivacainecomparedto8.7mgfortheCSAgroup.Though theCSA group usedless local anesthetic, sufficient anes-theticlevel,similartotheSDSAgroup,wasachieved.

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groupcomparedtothe SDSAgroup.Itmayalsobedue to thelowerlocalanestheticdoseandlowernerveblocklevel intheCSAgroup.

It is known that epidural and spinal anesthesia at dif-ferentlevelssuppressestheneuroendocrinestressresponse better than general anesthetic. Highlevel spinal block is necessary to suppress the andrenergic response.30 Seitz

et al.31 found cortisol increased during surgery in lower

extremity operations using general anesthetic, while the epiduralanestheticgrouphadlowerlevelscomparedto val-uesfrombeforesurgery.Pfugetal.32foundhigherlevelsof

adrenalinpostoperativelycomparedtocontrolvalues.Low levelspinalanesthesiapreventsthisincrease,thehighlevel spinalanestheticgrouphadvalueslowerthanthecontrols. WhileMolleretal.33foundnodifferenceincortisollevelsin

thelatepostoperativeperiodcomparingspinalandgeneral anesthesia, during surgery and in the early postoperative periodcortisol levelswere lower in the spinal anesthesia group.Comparingthe postoperativeplasmaadrenalinand serumcortisollevelsinbothgroupsinthisstudy,bothgroups had lower levels compared to control values. The SDSA grouppostoperativeserumcortisollevelsweresignificantly lower.ThehighernerveblocklevelintheSDSAgroupmay be responsible for greater suppression of afferent neural impulsesoriginatinginthesplanchnicsympatheticnerves.

In conclusion continuous spinal anesthesia using 0.25% concentrationlevobupivacainetoprovideregional anesthe-siafortransurethralprostateresectionoperationsinolder patientscanbeusedsafely.

Conflict

of

interest

Theauthorsdeclarenoconflictsofinterest.

References

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Imagem

Table 1 Demographic data (mean ± SD).
Figure 1 Changes in mean arterial blood pressure (MAP). *p &lt; 0.05 (between Group CSA and Group SDSA)
Figure 3 MBS changes in the groups. *p &lt; 0.05 (between Group CSA and Group SDSA).
Figure 5 Average number of requests from the PCA unit. *p &lt; 0.05 (between Group CSA and Group SDSA).

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