/
Article  Artikel Severe hypoxaemia in fieldanaesthetis Article  Artikel Severe hypoxaemia in fieldanaesthetis

Article Artikel Severe hypoxaemia in fieldanaesthetis - PDF document

calandra-battersby
calandra-battersby . @calandra-battersby
Follow
405 views
Uploaded On 2015-04-28

Article Artikel Severe hypoxaemia in fieldanaesthetis - PPT Presentation

Physiological monitoring of white rhinoc eros anaesthetised with etorphine hydro chloride M99 reveals physiological alterations including hypertension tachycardia acidaemia and respiratory depression with hypoxia and hyper capnia 258 The addition o ID: 55989

Physiological monitoring white

Share:

Link:

Embed:

Download Presentation from below link

Download Pdf The PPT/PDF document "Article Artikel Severe hypoxaemia in fi..." is the property of its rightful owner. Permission is granted to download and print the materials on this web site for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.


Presentation Transcript

Article — Artikel, J PRaathand LKleinSafeandreliableanaesthesiaofrhinocerosisanimportanttoolforhealthcareofbothcaptiveandfree-ranginganimalsandforconservation-basedprogrammes.Physiologicalmonitoringofwhiterhinocerosanaesthetisedwithetorphinehydrochloride(M99)revealsphysiologicalalterations,includinghypertension,tachycardia,acidaemiaandrespiratorydepressionwithhypoxiaandhyper.TheadditionofazaperonetoM99decreasedbloodpressureinaseriesof6animals.Manyreportsrecommendoxygen(O a ,indicatingamildtomoderatemetabolicacidosis.Therhinoceroswerealsohypertensive(systolicbloodpressure=21.861±5.465kPa(164±41mmHg))andtachycardic(HR=107±31/min).Followingnasaltrachealintubationandinsufflation,the%OandPincreasedwhilebloodpHandPremainedunchanged.Trachealintubationviathenoseisnotdifficult,andwhenoxygenisinsufflated,theP blindfoldedandearplugswereinsertedToensurethesafetyoftherhinocerosduringthisstudy,20–50mgnalorphine(Lethidrone,Wellcome)and/or100–400mgDoxapramHCL(Dopram-V,FortDodgeAnimalHealth,FortDodge,Iowa50501USA)wereadministeredintravenously(i.v.),atthediscretionoftheveterinarianincharge(JPRorDG)toreverseapnoeabothbeforeandduringthedata-Arterialbloodgases(ABG)werecollectedfollowingcatheterisationoftheauriculararterylocatedontheinsideofthepinna,usinga22gaugecatheter(Jelco,Critikon,SA,JohnsonandJohnson(Pty)Ltd.SA).Thesampleswerecollectedanaerobicallyintoheparinisedsyringes,whichweresealedandstoredoniceuntilanalysedwithin3hoursofcollection.Thecatheterwasmaintainedwithaheparinsalineflushand1–2m ofbloodwaswithdrawnanddiscardedpriortocollectionoftheABGsample.Arterialhaemoglobinoxygensaturation(%O)andbaseexcess(BE)werecalculatedaccordingtostandardhumanformulae.SampleswerecollectedpriortoadministrationofOandatvariousintervalsduringOistration.Samplesfromcontrolanimals(4fromtheKrugerParkand3fromMpumalangaParks)werealsocollectedatvariousintervalsduringthemonitoringTrachealintubationwasaccomplishedwithanequinenasogastrictube(0.9or1.4cminternaldiameter)(KalayjianIndustries,Inc,LongBeach,CA90806,USA)passedalongtheventralfloorofthenasalcavitytoavoidthenasalturbinates.Oncethetubewasintheposteriorpharynx,theoperatorlistenedforanexhalationandthenadvancedthetubeintothetracheatoapproximatelythelevelofthetrachealbifurcation(Fig.1).Thetubeneverenteredtheoesophagusduringthisstudy,butonoccasionwasreflectedbytheposteriorpharyngealwallandcameouttheothernostril.Trachealintubationwasverifiedbylisteningtotheairpassingthroughthetubeduringrespiration.Oxygenwasadministeredatarateof15–30 /mindependingonthesizeofThedata-gatheringperiodvariedamonganimalssinceitwasrelatedtothetimerequiredtocrateeachanimal.When2animalswereanaesthetisedsimulta-neously,1animalwaschosentobecratedlast,thusobtainingalongermonitoringperiod.Thecontrolanimalswereselectedrandomly.Systolicbloodpressurewasmeasuredindirectlyfromthetail(Dinamap,CritikonInc.Tampa,Florida33607USA).Respirationratewasobtainedbyfeelingtheexpirationofairandaheartratewasobtainedusingastethoscope.RectaltemperaturewastakentocalibratetheFollowingthemonitoringperiodintheKrugerParkrhinoceros,M99effectswereantagonisedwitheither6–7.5mgdiprenorphine(M50-50,C-Vet)or25–40mgnalorphinei.v.andeachanimalwasdirectedtothecrateusingthepre-placedropesafteritregaineditsfeet.In10rhinocerositwaspossibletoobtainanABGsamplefromthearterialcatheterintheauriculararteryaftertheanimalwasstandinginthecrate.The3controlrhinocerosfromMpumalangaweregiven40–80mgnaltrexonei.v.andallowedtorecover and return to their habitat.RESULTSNomortalityorpost-anaestheticmor-bidityoccurredintherhinocerosthatTheresultsofphysiologicalmonitoringofrhinocerosthatreceivedOmentationandthecontrolsaresummarisedinTable1.Physiologicaldatawerenotrecordedforallanimalsstudied.NotethatthemeansofallABGparametersexceptthePandthe%Oaresimilarinthegroups.Bothgroupsshowedrespi-ratoryandmetabolicacidosis,hypercapnia,tachycardia,decreasedrespiratory rate and moderate hypertension.ThesummaryofallABGsamplescollectedoverthemonitoringperioddividedintothegroupthatreceivedOsupplementationandthenon-supple Fig.1:Drawingofarecumbentrhinocerosshowingtheplacementofthenasotrachealtubepassingthroughthelarynxintothetrachea,withthetubeattachedtoanoxygentankwithaflow.Table1:SummaryofthephysiologicalmonitoringandarterialbloodgasvaluesfrombothO-supplementedandcontrolanimals.Meanvaluesforallparameters(exceptPand%O,whichincreasedmarkedlyinthesupplementedanimals)arecomparableandshow BEHeart rateRespiration rateSystolic BP( %)(kPa)(kPa)(mmol/ (mmol/ )(per min)(per min)(kPa)Suppl.Mean887.14813.8639.46423.5–5.8104924.93SD150.0978.2652.6664.24.43837.7338393939393915131.47Mean577.2065.0658.66523.7–3.71061024.93SD180.0781.4661.6004.85.03233.20 3636363632367101.07 mentedcontrolgroupareshowninTable2.Time0showsvaluesobtainedfromthe1stABGsamplecollectedinbothgroups,andservesasabaselineforboththecontrolanimalsandtheanimalsthatreceivedOfollowingTime0.ThePandthe%OvaluesincreasedrapidlyandmarkedlyfollowingOsupple-mentationwhiletherhinocerosthatdidnotreceiveOremainedveryhypoxae-micthroughoutthemonitoringperiod,withonlyaslightelevationat30min.TheverylowPvalues,combinedwithacidosis,resultedinseverehaemoglobindesaturationwithinitial%Obelow50%recordedinthe7controlanimalsbreathingambientair,whileduringOsupplementation,30of39samplesshowedthe%Otobegreaterthan90 %andinonly1samplewas%Obelow80%.ThepHandPinbothgroupsshowedconsistentacidaemiaandhypercapnoeathroughoutthemonitoringperiod.Baseexcessremainedbelow0mmol/ exceptforthe20–25minmonitoringperiodinthenon-supplementedrhinoceros(0.3mmol/ ),indicatingthatmetabolicacidosispersistedthroughouttherecumbentperiod.Themeanbicarbonatevalueintheanaesthetisedrhinocerosrangedbetween22and28mmol/ (Table2),reflectingthedecreaseduetometabolicacidosis,combinedwiththeincreaseresultingfromhypercapnoeaduetoanaesthetic-inducedrespiratoryArterialbloodgasvaluesfrom2subadultfemalerhinocerosinthisstudyduringthemonitoringperiodandinitialrecoveryareshowninFig.2(anOplementedanimal)andFig.3(acontrolanimal)withthePandthe%OplottedandtheotherABGvalueslistedinthetablebelowthechart.Figure2plotsPand%OandP,beforeandduringOsupplementation.Theand%OincreasedrapidlyduringsupplementationwhilethePmainedelevated.TheABGvaluesfromthestandinganimalfollowingthereversalbyM99showedadropinbothPandPwhilethepHandBEincreased,indicatingapartialcorrectionofboththerespiratoryandthemetabolicacidosis.Figure3showsthat,inthenon-Oplementedanimal,hypoxiaandhypercapnoeapersisteduntiltheanimalwasstandingafterreversal.Bothanimalswerealsoacidoticduringrecumbency,withtheABGvaluesreturningtowardsnormalbythetimetheanimalswereFigure4showstheinitialeffectofOTable2:SummaryofthearterialbloodgasvaluesduringthemonitoringperiodfromO-supplementedandcontrolanimals.Time0combinestheinitialsampleonthesupplementedanimalsandcontrolanimals.FollowingtheoxygensupplementationtheriseinP Time 0OsupplementationNo O First 10 min11–20 min20–40 minFirst 10 min11–20 min20–35 minpHaMean7.1757.1337.1427.2137.2467.2447.246SD0.0760.1140.0820.0360.0510.0840.067(%)Mean49848995626970SD161715323138(kPa)Mean4.66612.79715.33013.5974.9325.4655.599SD1.2007.86510.1313.3331.8661.6000.933(kPa)Mean8.2659.7319.7318.3989.3318.5318.931SD1.6003.3332.2660.5330.9331.2002.000 )Mean22232425282427SD4542533 )Mean–6.4–6.77–5.7–3.2–0.26–1.40.3SD4.275.33.41.93.495.732.7Sample time (min)Mean71528101724SD3370.133 2119146555 ChartandassociatedtableshowingtheresultsofarterialbloodgasvaluesofasubadultfemalerhinocerosthatreceivedOsupplementationviaanasotrachealtube.NotetherapidinitialriseofboththePand%Ooncesupplementationbegan.Whentheanimalwasstandinginthecratethearterialbloodgasvaluesstartedtoreturntowardsnormality. supplementationonanadultrhinoceros.TheOsupplementationwasdiscontin-uedfor4minat14minwitharesultantdecreaseofbothPand%O,whichincreasedrapidlyagainonceOmentationwasresumed.ThisillustratestherapidchangesthatoccurintheABGAcommonprocedureistheadministra-tionofnalorphine(10–30mg)i.v.towhiterhinoceroswithin10minofrecum-bency.Theobjectiveistoimprovethesafetyoftheprocedurebylighteningtheopioidanaesthesiaandimprovingrespi-ration,whichisobservedclinically.Twelveanimalsthatreceivednalorphineweremonitored.Follow-updata,within10minofinjection,showedverylittleimprovementinthephysiologicalparam-eterscomparedtothe5controlanimalsthatdidnotreceivenalorphineorOsupplementation(Table3).Themajorphysiologicalalterationspersisted.Whennalorphinewasgiventhenetchangein,afteranaverageof7minutes,wasanincreaseof0.93kPa(7mmHg)from4.27 to 5.20 kPa (32 to 39 mm Hg).Table4showstheABGvaluesof10rhinoceros,includingtheanimalsinFigs2and3,sampledatvarioustimeswhentheywerestandingintheircratesafterhavingreceivedtheantagonisttoM99.TheABGvaluesreturnedtowardsnormalwithinanaverageofabout3minThisstudydocuments5observations:1)rhinocerosanaesthetisedwithdosesofM99andazaperoneappropriateforfree-rangingconditionsexperiencesevererespiratorydepressionandhypoxaemia,moderatehypercapnia,andcombinedrespiratoryandmetabolicacidosis.2)Tenrhinocerosrequiredadministrationofnalorphinewithinthefirst10mintoensuretheirsafety,whiletheresultantmonitoringwithin10minofadministrationshowedlittlephysiologicalimprovement.3)Healthyrhinoceroscantoleratetheseseverephysiologicalalterationsforshortperiodsduringfieldanaesthesiawiththeseagents.4)TrachealintubationandinsufflationwillrapidlyandmarkedlyimproveoxygenationasshownbyPandthe%O,butdoesnotaffecthypercapnoeaormetabolicacidosis.5)FollowingantagonismofM99andtheendofrecumbencytheABGvaluesrap-idly return towards normal levels.Therespiratorydepressionandresultanthypoxiaisprobablydueto4factors:1)thehighdoseofM99requiredtoshortentheinductiontimewhenanaesthetisingananimalunderfieldconditions;2)whiterhinocerosareverysensitivetoopioidssuchasM99;3)alargeanimalrecumbentwhileanaesthetisedissubjecttophysiologicalalterationsthatleadtocardiopulmonarydepression,ashasbeenshownindomesticanimalsandhumans;4)alargerecumbentanimalwilldevelopaperfusion/Therealsoseemstobevariationbetweenwhiteandblackrhinoceroses,withtheformerbeingmuchmoresensitivetotherespiratorydepressanteffectsofInthegroupofwhiterhinocerosunderstudy,thenegativeBEvaluesindicatesomedegreeofmetabolicacidosis.FormulaeusedintheinstrumentsoftwareforthecalculationofBEarebasedontherelationshipofpHtoPinhumans,withthe‘normal’rangeforBEcentredaroundavalueof0mmol/ .Usingtheseformulae,normaldomesticherbivorestypicallyhaveBEvaluesabove0,from+4to+8mmol/ ,dependingonthespecific Fig.3:ChartandassociatedtableshowingtheresultsofarterialbloodgasvaluesofasubadultfemalerhinoceroscontrolthatdidnotreceiveOsupplementation.NotehypoxiawithlowPand%OandhypercapniawithelevatedP,whichpersisteduntilthe Fig.4:ChartandassociatedtableshowingtheresultsofarterialbloodgasvaluesofanadultfemalerhinocerosthatinitiallyreceivedOsupplementation.Thesupplementationwasdiscontinuedfor4minuteswithamarkeddropinboththePand%O,which bloodgasanalyser(LK,pers.obs.,2003).Althoughnormalvaluesforunrestrained,free-rangingwhiterhinocerosarenotavailable,itislikelythattheiracid-basebalanceissimilartootherherbivoresandthatthenegativeBEvaluesreportedhererepresentatruemetabolicacidosis.Metabolicacidosisintheseanimalsprobablyresultedfromlacticacidaccumulationduetomuscleactivitybeforeandafterdarting,andhypoxaemiaduringtherecumbentperiod.ThepersistenceofmetabolicacidosiseveninthoseanimalsthatreceivedOsupplementationmaybeduetothemuscleactivityandrigidity,whichtypicallyaccompaniesrestraintArterialhaemoglobinoxygensaturationvaluesintheserhinoceroswerecalculated,alsousingformulaebasedontheOaffinityandBohreffect(effectofachangeinpHontheP50(Patwhichthehaemoglobinishalf-saturatedwith))ofnormaladulthumanhaemoglobin.DomestichorseshaveaP50of3.33kPa(25mmHg),similartohumansandthereforethe%Ovaluescalculatedfromhumanformulaearereasonablyaccurate.Noreportsofrespiratorycharacteristicsofwhiterhinoceroshaemoglobinusingwholebloodcouldbefoundintheliterature,butresultsof1studyoftheeffectsofvariousanionsandotherfactorsontheOaffinityofwhiterhinoceroshaemoglobininsolutionsuggestedthattheP50mightbe2.67kPa(20mm Hg).Ifthisisthecase,thenthetrue%Ointherhinocerosinthisstudymaybesomewhathigherthanthevaluesreportedherealthoughstillprofoundlydesaturatedinthoseanimalsdidnotre-Nasaltrachealintubationisnotadifficultprocedureinthefield.TheinsufflationwithOimprovesthesafetyoftheprocedurebyincreasingthePthe%O,butdoesnotcorrecttheacidosisorhypercapnia,whichhasalsobeenreportedinwapiti.GivingOdoesnotseemtoworsentherespiratorydepressionbyremovinghypoxicrespiratorydrive,sincesignificantincreasesinPwerenotdetectedduringOmentation.Caremustbetaken,wheninsufflatingoxygenthoughanasotrachealtubeorcatheter,toensurethatthetubeisinthetrachea,andnottheoesophagus.Insufflationofoxygenintotheoesophaguscanresultingastricrupture,whichhasoccurredinhorses(LK,pers.obs.,2003),butinthisstudywedidnotpassthetubeintotheprobablythankstopharyngealMethodstocorrecttheacidosisandhypercapnoeawouldincludeIPPV,whichwouldbedifficultinthefield,sinceitwouldrequireplacementofacuffedendotrachealtubeandalarge-capacityventilator,or2demandvalvesjoinedinparallelwithalargersourceofcom-pressedOthanrequiredforinsufflationasusedinthisstudy.EvenwithIPPVinlargespecies,hypoxiamaypersistinsomeindividualsduetoventilation/perfusiondisparity,andhypercapnoeapersistsbecauseofinsufficienttidalandminuteWeacknowledgethecooperationandlogisticalsupportgivenbytheSouthAfricanNationalParksandMpumalangaParksBoard.WealsoacknowledgethegeneroussupportofBritishAirways,FriendsoftheNationalZoo(FONZ)andtheShirleySichelFund.TheauthorsalsothankJJvanAltena,JohanMalanandMariusKrugerfortechnicalsupportwithaspecialthankstothehelicopterpilotsoftheKrugerNationalParkwhoseskillandeffort helped make this study possible.1.BaumannR,MazurG,BraunitzerG1984Oxygenbindingpropertiesofhemoglobinfromthewhiterhinoceros(-GLU)andthe tapir.RespirationPhysiology2.Cornick-SeahornJL,MikotaSK,SchaefferDO,RanglackGS,BoatrightSB.1995Isofluraneanesthesiainarhinoceros.JournalofAmericanVeterinaryMedicalAssociationTable3:Effectofreceivingnalorphinein12rhinoceroscomparedto5animalsthatdidnotreceivenalorphineorOsupplementation.Note RespirationHeart rateP(per min)(per min)(kPa)(kPa)(%) Time:T = 010 minT = 010 minT = 010 minT = 010 minT = 010 min12 Nalorphine10101381159.609.604.675.477175 5Controls911113879.209.205.205.207479 Table4:Arterialbloodgasvaluesfrom10rhinoceroswhiletheywerestandinginacrateafterreversalofM99.Notethatallvaluesare Arterial samples Total time downSample after upS(min)(min)(%)(kPa)(kPa)(mmol/ )(mmol/ 121877.2798.2657.87826.9–0.34912827.2387.5988.22525.4–2.5211907.2669.4648.34527.61.0217907.2709.4648.47828.30.3414867.3167.7317.55828.21.2601917.3159.0646.57225.4–0.8413827.3046.9326.23823.5–2.6353767.3065.9996.09223.0–2.9261887.2928.5318.13128.70.8291927.3409.9987.50529.72.9 Mean33.53.486.57.2938.2917.50526.7–0.3SD14.63.65.10.0301.2530.8932.31.91=1010101010101010 3.DunlopCI,HodgsonDS,CambreRC,KennyDE,MartinHD1994CardiopulmonaryeffectsofthreeprolongedperiodsofisofluraneanesthesiainanadultJournalofAmericanVeterinaryMedicalAssociation4.HeardDJ,JacobsonER,BrockKA1986EffectsofoxygensupplementationonbloodgasvaluesinchemicallyrestrainedjuvenileAfricanelephants.JournaloftheAmericanVeterinaryMedicalAssociation5.HeardDJ,OlsenJH,StoverJ1992Cardiopulmonarychangesassociatedwithchemicalimmobilizationandrecumbencyinawhiterhinoceros(CeratoheriumsimumJournalofZooandWildlifeMedicine6.HattinghJ,KnoxCM,RaathJP1994Arterialbloodpressureandbloodgascompositionofwhiterhinocerosesunderetorphineanaesthesia.SouthAfricanJournalofWildlifeResearch7.KockMD,MorkelP,AtkinsonM,FogginC1995Chemicalimmobilizationoffree-rangingwhiterhinoceros(simumsimum)inHwangeandMatoboNationalParks,Zimbabwe,usingcombinationsofetorphine(M99),fentanyl,xylazine,anddetomidine.JournalofZooandWildlife8.LeBlancPH,EickerSW,CurtisM,BeehlerB1987Hypertensionfollowingetorphineanaesthesiainarhinoceros(Dicerossimus).JournalofZooandWildlifeMedicine9.McDonellW1996RespiratorySystem.InThurmonJC,TranquilliWJ,BensonGJLumbandJones’veterinaryanesthesia.Williams & Wilkins, Baltimore: 115–14710.PaoloP,CrociM.RavaganI,TrediciS,PedotoA,LissoniA,GattinoniL1988Theeffectsofbodymassonlungvolume,respiratorymechanics,andgasexchangeduringgeneralanesthesia.Anesthesiaand11.QuandtJE,RobinsonEP1996Nasotrachealintubationincalves.JournaloftheAmericanVeterinaryMedicalAssociation12.RaathJP1999Anesthesiaofwhiterhinoceroses.InFowlerME,MillerRE(eds)Zooandwildlifemedicinecurrenttherapy4.13.ReadMR,CaulkettNA,SymingtonA,yTK2001Treatmentofhypoxemiaduringxylazine-tiletamine-zolazepanimmobilizationofwapiti.CanadianVeterinaryJournal14.RieboldTW,EngelHN,GrubbTL,AdamsJG,HuberMJ,SchmotzerWB1994OrotrachealandnasotrachealintubationinJournaloftheAmericanVeterinaryMedicalAssociation15.RogersPS1993Chemicalcaptureofthewhiterhinoceros(Ceratotheriumsimum).InMcKenzieAA(ed.)ThecaptureandcaremanWildlifeDecisionSupportServiceandSouthAfricanVeterinaryFoundation,Pretoria, South Africa: 512–52816.SomaLR1980Equineanesthesia:causesforreducedoxygenandincreasedcarbondioxidetensions.CompendiumofContinuingLargeAnimalSupplement17.WebbAI1984Nasalintubationinthefoal.JournaloftheAmericanVeterinaryMedical