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Peripheral nerve stimulation - Outcome Medical of Georgia

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<strong>Peripheral</strong> <strong>nerve</strong> <strong>stimulation</strong> in thetreatment <strong>of</strong> intractable painJAMESN. CAMPBELL M.D. AND DONUN M. LONG M.D. PH.D.Department <strong>of</strong> Neurosurgery. JohnsHopkinsHospital. Baltimore. Maryland<strong>Peripheral</strong> <strong>nerve</strong> stimulating deviceswere implanted for pain control in 33 patiewith variety <strong>of</strong> disabling chronic pain conditionswhich had persisted despite ustmedical and surgical therapy. The implantswere placed on major <strong>nerve</strong>sthe area<strong>of</strong> the patientspain.innervatiRecordswere obtained <strong>of</strong> each patientsstatedfrom pain produced by <strong>nerve</strong> <strong>stimulation</strong> along with assessments<strong>of</strong> narcowithdrawal ability to return to work sleep pattern and relief from depression. Bason these five criteria 17 patientswere judged to be treatment failureswhile eighttientshad excellentwereresultsand seven had intermediate results. Twelve <strong>of</strong> the failurin patientswith either low back pain with sciatica or pain from metastaticease. The most dramatic successesoccurred in patientswith peripheral <strong>nerve</strong> trauirThe incidence <strong>of</strong> complicationshas been low and two patientshave usedstimulator foryearswithout adverse effects. Techniques<strong>of</strong> peripheral stimulator itplantation possible mechanisms<strong>of</strong> action and conclusionsregarding peripheral net<strong>stimulation</strong> in the treatment <strong>of</strong> chronic pain are discussed.rdKEYWORDSintractable pain <strong>nerve</strong> <strong>stimulation</strong>0.THE optionsfor treatment <strong>of</strong> intractable pain are few. Until recent yearsthey have been confined to psychotherapy narcoticsor variousneural ablative promethod has provedcedures. None <strong>of</strong> these methodssatisfactory for long-term patient management. The finding <strong>of</strong> Wall and Sweee in1967 that percutaneoussensory <strong>nerve</strong> electrical <strong>stimulation</strong> could produce hypesthesiasdistal to the point <strong>of</strong> <strong>stimulation</strong> thereforeencouraged interest in the possibility thatneural <strong>stimulation</strong> could be used to treat intractable pain. The two most common techniquesdescribed are transcutaneouselectrical <strong>stimulation</strong> and spinal cord <strong>stimulation</strong>viaelectrodes placed over the dorsal columns.317Transcutaneous<strong>stimulation</strong> has the. disadvantage <strong>of</strong> being cumbersome moreoveradequate<strong>stimulation</strong> <strong>of</strong> the involved ncrvcproducesdiscomfort referred to the overing skin. Spinal cord <strong>stimulation</strong> has the diadvantage <strong>of</strong> requiring major operation.addition there are <strong>of</strong>ten difficultieswith ide.placement <strong>of</strong> the electrodesand di.turbingly high number <strong>of</strong> long-term technicfailuresoccur due in part to scar formaticaroundpainthe clectrodes.3third method <strong>of</strong> neural <strong>stimulation</strong> fccontrol involvesimplantation<strong>of</strong> peripFera <strong>nerve</strong> stimulatorsPNS. Bipolar dcctrodesare attached tothe field <strong>of</strong> innervation containswhichmajor <strong>nerve</strong>s<strong>of</strong> whicthe regionpain arisesand are then connected toradi<strong>of</strong>requency receiver placed under thskin. The electrodescan then be activatedtransmitting device connected to an antenntaped in place over the receiver.In the following report we describe thresults obtained in series<strong>of</strong> 23 patientswhi692 J.Neurwurg. Volume 45 December. 1973015


J.N. Campbell and I. M. Longdirected at the assessment <strong>of</strong> five variablesI. Each patientsown impression <strong>of</strong> howmuch pain relief he was receiving fromuse <strong>of</strong> the stimulator device2. Patterns<strong>of</strong> drug use3. Sleeping habits4. Activity level5. Psychological well-being.In addition inquiriesas to patternsstimulator use and adverse effectswere made.Follow-up information was also obtainedon nine <strong>of</strong> 10 patientswith PNS implantationdone at the University <strong>of</strong> Minnesota. Patientchartsandinformation obtained from the patientspersonal physician were used assources<strong>of</strong> thisinformation.Summary <strong>of</strong> PatientsJohnsHopkinsHospital Seriessummary<strong>of</strong> the resultsfor each patientis contained in Table along with thepatientsdiagnosistype <strong>of</strong> stimulator implanted and length <strong>of</strong> follow-up period. Anexcellent result is defined by the followingcriteriaI. The patient must continue to require theuse <strong>of</strong> the stimulator for pain relief thusallpatientswith<strong>of</strong>spontaneousremission are excluded. Only one patient had spontaneousremission andthispatient was consideredtreatment failure by other criteria.2. Analgesic use must be confined to occasional use <strong>of</strong> Tylenol acetaminophen oraspirin.3. All patientsmust have been able toresume their usual occupation or at lcast beactive at level compatible with their neurological deficit.4. All patientswho previously had beendepressed because <strong>of</strong> their pain must have hadan improvement in mood.5. Sleep disturbance previously associatedwith pain must have ceased.6. Each patient must have felt that use <strong>of</strong>the peripheral <strong>nerve</strong> stimulator providedmore than 50% relief <strong>of</strong> his pain.Of the 23 patientsfour were judged to havehad excellent results. Another five patientsmet some <strong>of</strong> these criteria and were judged tobe partial successes. The remaining 14 patientswere treatment failures. Eleven <strong>of</strong> thetreatmentfailuresoccurred in patientswithlow back pain syndrome with sciatica or painfrom metastatic disease. One <strong>of</strong> the treatmentfailureswas in patient Case who had hadtraumatic amputation <strong>of</strong> hs thumb withresulting dysesthesias.Trials<strong>of</strong> percutaneous<strong>stimulation</strong> preoperatively had failed torelieve his pain however because <strong>of</strong> hisdesperate situation brachial plexusstimulator was implanted although thechancefor successwas thought to be poor.One <strong>of</strong> the four partial successpatientsCase had had <strong>nerve</strong> trauma in the handand had undergone number <strong>of</strong> handoperations. He had two distinct types<strong>of</strong> painthe worse being sharp jabbing pain and theother burning dysesthesia. The stimulatorrelieved the former pain and allowed him toreturn to work. Subsequent to the stimulatorimplantation he had sympathectomy andinternal neurolysis<strong>of</strong> the median <strong>nerve</strong> whichhas relieved his second type <strong>of</strong> pain. He isnow able to resume normal life without use<strong>of</strong> analgesicsbut requiresthe use <strong>of</strong> thestimulator to control the sharp jabbing painto which he is still subject.Another partial successwas patient whohad had excellent resultsfor monthsbutthen developed an incomplete radial <strong>nerve</strong>palsy and partial return <strong>of</strong> pain in the areasdistal to the brachial plexus<strong>stimulation</strong>device. Thispatient is currently in the hospital undergoing diagnostic evaluation. Theother partial successeswere in patientswithlow back pain sciatica tvho claimed substantial pain relief with use <strong>of</strong> the stimulatorbut who were unable to resume normal livesbecause <strong>of</strong> remaining pain.Two <strong>of</strong> the excellent resultsoccurred in patientswith peripheral <strong>nerve</strong> trauma which hadfailed to improve despite multiple operations. Another was in patient with brachialneuritissecondary to radiation therapy forbreast carcinoma. The fourth case was inpatient who continued to have severe armpain following removal <strong>of</strong> cervical rib causing brachial plexuscompression.There was one infection which occurred inthe area where the receiver had been implanted on the anterior chest wall. The patientCase had had radical mastectomyandradiation therapy to thisarea and the infection probably resulted from poor healing. Shehas done well after relocation <strong>of</strong> the receiver.There was one noninfectioustissue reaction.Thiscomplication presumably reflectsanidiosyncratic reaction to the PNS implant as694J. iVcurosurg. Volume 45 lkcenbcr. /9763016


Nerve stiniulation for intractable painTABLEResults<strong>of</strong> peripheral <strong>nerve</strong> stimulator imp/at in 23 patientstoLiushe1tsStimulatorAge SexDiagnosisNo.Location155 brachial arm pain after cervicalrib removalComplications32 brachial crush injury to elbow relict foryr thenwrist weaknessRu1tFollow-Upmosnone excellent 12andreturnpartial painpartialsuccess1327 brachial ringer injury to hand none partial12adthetor51 brachial traumatic amputation<strong>of</strong> thumb71 brachial brachial plexitisradiotherapyfromfornoneinfectionremovedPNSthensuccessfailureexcellenttotortndich33 medianbreasttraumaticcarcinoma<strong>of</strong> forefinger37 median wrist crush withamputationmedian <strong>nerve</strong> injuryreimplantednoninfectiotisnonetissue reactiontechnicalfailureexcellent1017 NI ulnar elbow crush with ulnar none excellent 12jsetheambut10 5711 54<strong>nerve</strong> injury60 sciatic metastasisto spinebilateralsciaticsciaticcoloniccarcinomametastasisto spine hiphypernephromametastasisto hipadrenalcarcinoma12 33 sciatic hyperesthesia leg paincausenone failure 12nonefailure17nonefailure13none failure II13 56 sciatic foot pain cause none failure 1514 43 sciatic low back pain syndromewith sciatica15 38 sciatic low back pain syndromewith sciatica16 42sciatic low back pain syndromewith sciatica17 56sciatic low back pain syndromewith sciatica18 43 Nt sciatic low back pain syndromewith sciaticanonenonenonenonesoreness<strong>of</strong> receiverin areapartialsuccesspartialsuccesspartialsuccess14failure 12failure 1419 32 NI sciatic low back pain syndromewith sciatica20 53 sciatic low back pain syndromesciatica21 78 sciatic low back pain syndromewith sciatica22 38 sciatic low back pain syndromeWith sciatica23 51 sciatic low back pain syndromenone failure 13none failure 16none failure 13none failure 12none failure 16withsciaticat.ntr.a.no source <strong>of</strong> contamination could be found.Another patient had considerable tendernessin the area <strong>of</strong> the receiver leading to removal<strong>of</strong> the implant. There were no objective signs<strong>of</strong> inflammation.The use <strong>of</strong> the stimulator by patientseither the excellentor partial successcategoryinchanged little from the time immediatelyafter implantation to the time <strong>of</strong> follow-upexamination. Almost all <strong>of</strong> the patientsusedthe device more than 12 hoursday. All usedsufficientpower output to produce light-tosttong buzzing sensation which radiated tothe area <strong>of</strong> pain.693I. iVeurosurg. Volume 45 December. /976ac.scr 4L ..


J.N. Campbell and D. Ni. LorTABLEResults<strong>of</strong> peripheral tierve stimulator irnplanta in the University <strong>of</strong> tIhnesuta .ccriesAgeSnrnuIiturDiagnosisComplicationsResultFollow-U47 NI uhiar gunshot wound innone excellent 68elbow ulnar palsy42 ulnar ulnar pain fromnone excellent 63olecranon fracture42 ulnar tardy ulnar palsy none excellent 4641 ulnar tardy ulnar palsy none xccllent 5419 sciatic hip dislocationsciaticinjurynone partial 44successnone failure 4459 sciatic spine injurysciatic palsy31 brachial traumatic amputation<strong>of</strong> arm stump pain57 brachial traumatic amputation<strong>of</strong> arm stump pain64 sciatic amputation above theknee vascular diseaseneuropathy stumpinfectionremovedPNSthen failurerecent 44reimplantedwire disconnected initially excellentrcimplantedlost to follow-upmuscle movement failure 48with <strong>stimulation</strong>10 63 sciatic andfemoralpainleg trauma stump pain none failure 54Patientswere asked to characterize theirpain in terms<strong>of</strong> variouscharacteristicssuchas steady pulsating hot burning heavypressing aching. Patientsin either the partialsuccessor excellent category more <strong>of</strong>tencharacterized their pain as sharp and stabbing six patientsas compared to patientsinthe failure group one patient. Two patientsin the excellent result group had hypercsthesiasas major problem and thesedisappeared with <strong>stimulation</strong>. Power outputrequirementsfrom the transmitter did notincrease with time as has been noted withdorsal column <strong>stimulation</strong>5t although thefollow-up period is too short for thistoconclusive.Muscle cramping from <strong>stimulation</strong> did notoccur in any <strong>of</strong> the patientsin either <strong>of</strong> thesuccessgroups. Furthermore these patientsdid not find the <strong>stimulation</strong> distracting butrather that with the reduction in pain theyhad better ability to concentrate. Pain relieflastedfor variousbelengths<strong>of</strong> time after given<strong>stimulation</strong> period. In three patientsthe painbegan again as soon as <strong>stimulation</strong> stoppedin twootherspainreturned within 30 to 60minutesand in four otherspain returnedtohours.Patientsdenied that the <strong>stimulation</strong> interfercd with walking coordination sexualinfunctioning driving sensation or musculstrength. These patientsreported no tissuejuryresult.<strong>of</strong>in the stimulated limbanalgesia.or elsewhereUniversity <strong>of</strong> Minnesota SeriesIn 1973 series<strong>of</strong> 10patientswithchror<strong>nerve</strong> injury treated with PNS implantsdescribed. At that time six patientsjudged to have excellent resultswhilehad good resultsand two were treatmefailures. Now yearslater one <strong>of</strong>patientsin the excellent result serieshas belost to follow-up while another has becomcfailure.Thislatter patient who hadtraumatic arm amputation continuedreceive <strong>stimulation</strong> into the painful areano longer obtainspain relief. The longefollow-up period is in two <strong>of</strong> the patientswiexcellentweresultswho have now been using.nar <strong>nerve</strong> stimulatorsfor yearsand cctinue to obtain complete pain relief. Theresultsarc summarized in Table 2.DiscussionThe best predictor for successin usingPNS implant in the treatment <strong>of</strong> intractabpain was the patientsdiagnosis. No patietreated with sciatic implant for the low ba696 J. Neurosurg. Volume 45 December 19sois


Nerve <strong>stimulation</strong> for intratctuble puzupain syndrome had an excellent result.Patientswith pain front ntetastatic diseasealso did poorly. Patientswith chronicperipheral <strong>nerve</strong> injury had the best results.withfoursix patientshaving excellenthaving partial success.resultsandhigh failure rate occurred in patientswith low back pain syndrome despitesuccessfultrialswithpercutaneoustion. The reason for thismay be relatedstimulato theobservation noted by the present authorsandothers12 that for <strong>stimulation</strong> to provide painrelief it must be applied to an area proximaltQ the source <strong>of</strong> the pain. Thusbipolar<strong>stimulation</strong> <strong>of</strong> the sciatic <strong>nerve</strong> in patientswith the low back pain syndrome would beexpectedto fail since the source <strong>of</strong> the pain isproximal to the area stimulated. The temporarythe other handtrials<strong>stimulation</strong> may onsucceed since thisis done withunipolar <strong>stimulation</strong> which allowsfor greatercurrent spread. In support <strong>of</strong> thispreliminary work has shown that in suchpatientspercutaneousbipolar epidural<strong>stimulation</strong>may be completely effective inrelieving sciatic pain when the electrodesareplaced over the ipsilateral LA L-5 or S-I<strong>nerve</strong>rootsunder fluoroscopic control.The first reported use <strong>of</strong> permanentperipheral <strong>nerve</strong> implantsfor pain controlwas made by Sweet and \Vepsc in 1968however these resultshave not beenpublished and detailed follow-up data are notavailable. Picaza et at reported that 20 out<strong>of</strong> 23 patientshad excellent resultsafterfollow-up period ranging from to 20months. Ninepatientsin their serieshadlowback pain syndrome. The <strong>stimulation</strong> wasapplied to an area remote from the location<strong>of</strong> pain in nine patients. The reason for thediscrepancyour own is not clear.in resultsbetween their seriesandThe mechanism by which peripheral <strong>nerve</strong><strong>stimulation</strong>relievesis still pain uncertain.Campbell and Taub confirmed that normalhuman subjectshad sensory lossduringtranscutaneous<strong>nerve</strong> <strong>stimulation</strong> in the distribution <strong>of</strong> the stimulated <strong>nerve</strong>. Thischangebegan with decreased touch sensation at lowlevels<strong>of</strong> <strong>stimulation</strong> and progressed toanalgesia with levelshigher<strong>of</strong> <strong>stimulation</strong>.The development <strong>of</strong> analgesia was associatedwith loss<strong>of</strong> the A-delta elevation in the compound action potential recording whichsuggeststhat peripheral axonal blockadewas responsible for the observed analgesia.Thishypothesiswas supported by work <strong>of</strong>Torehj rk and l-lallin2 who showed thatrepeated electrical <strong>stimulation</strong> <strong>of</strong> humanperipheralin<strong>nerve</strong>sresulted in excitation failurefibersfollowed to lesser extent by excitation failure in fibers. That electrical<strong>stimulation</strong> may relieve clinical pain by thismechanism was shown by Wall and Gutnick.24Experimentally induced neuromasinratswere shown to have an abundance <strong>of</strong>hyperirritable small myelinated fibersrecording techniquesdid not allow for recording from fibersthat showedprolongedsilentperiodsafter brief antidromic tetanus.mechanism by whichelectrical <strong>stimulation</strong>may selectively block small fiber activity wasdescribed by Accornero at. who showedthat eathodal current can stimulate both largeandselectivelysmall fiberswhile the anodal currentaxonal blockadeinactivates the smaller fibers. Thehypothesisis in keeping withthe observation that electrical <strong>stimulation</strong>must be applied to an area proximal to thesource <strong>of</strong> pain and to <strong>nerve</strong> <strong>of</strong> which theperipheral field <strong>of</strong> innervation includessite <strong>of</strong> origin <strong>of</strong> the pain.Alternatively peripheral <strong>nerve</strong> <strong>stimulation</strong>themay inhibit pain perception by way <strong>of</strong> centralnervoussystem effects. There are numerousexamples<strong>of</strong> inhibitory and facilitatory interactions<strong>of</strong> sensory stimuli. It is postulatedthat electrical <strong>stimulation</strong> <strong>of</strong> peripheral<strong>nerve</strong> may block more distal nociceptive inputby inhibitory action at the dorsal horn brainstem thalamusor even the parietal cortex.The gate theory proposed by Melzackand Wall in 1965L0 representsspecifichypothesisinvolving thisgeneral mechanism.Thisproposal along with increasing Westernawareness<strong>of</strong> the application <strong>of</strong> acupuncturein China led to the popularization <strong>of</strong> electrical <strong>stimulation</strong> techniquesfor the treatment <strong>of</strong> pain. In the gate theoryit isproposed that electrical <strong>stimulation</strong> activateslarge fiber activity in peripheral <strong>nerve</strong>swhichinducessuppression <strong>of</strong> transmission <strong>of</strong> largeand small fiber activity to high C145 structuresand thereby blockspain perception.The specific assumptions<strong>of</strong> thishypothesishave not been supported by subsequent investigationsa.3.s.2.at and Wall himself hasstated The least and perhapsthe bestthatcan be said for the 1965 paper was that itprovoked discussion and experiment. Thet.ti1. Nvurocurg. Volunt- 45 December. /976 697301


J. N. Campbell and D. M. Longrote <strong>of</strong> central effects as meansby whichelectrical <strong>stimulation</strong> relievespain thereforeremainsunsettled.Conclusionsas to the role <strong>of</strong> peripheral<strong>nerve</strong> <strong>stimulation</strong> in the treatment <strong>of</strong> chronicpain can only be made tentatively. In selectgroup<strong>of</strong> patientsin thisseriesthismode <strong>of</strong>treatment has provided relatively safeeffective means<strong>of</strong> controlling pain. Thissuccessis evidenced by pain relief imin lifeprovementsstyle cessation <strong>of</strong> narcoticintake normalization <strong>of</strong> sleep-wake cyclesand improvement in psychological well-beingwith no disturbance <strong>of</strong> other neurologicalfunctions. The most promising group <strong>of</strong>patientsfor thismode <strong>of</strong> treatmentappearstobe those with peripheral <strong>nerve</strong> injurieswhich the <strong>stimulation</strong> can be attached to theaffected <strong>nerve</strong> at point proximal to the site<strong>of</strong> injury. The incidence <strong>of</strong> complicationsappearsto be relatively low. The use <strong>of</strong> sciatic<strong>nerve</strong> stimulatorsin the treatment <strong>of</strong> the lowback pain syndrome and painfrom metastaticdisease is not advocated for in our seriesthesepatientshave done poorly. Futureresearch will be directed toward determiningthe safety <strong>of</strong> thistechnique and its mechanism<strong>of</strong> action and toward better definition <strong>of</strong>the patient population that will respondfavorably to its use.References1. Accornero Bini Manfredi Differential block <strong>of</strong> cutaneous<strong>nerve</strong> fiberswith triinangularly shaped electrical impulses. Presented at the First World Congress<strong>of</strong> theInternational Association for the Study <strong>of</strong>Pain Florence Italy September 19752. Bessou Perl ER Response <strong>of</strong> cutaneoussensory unitswith unmyelinated fibersto noxiousstimuli. Neurophysiol 321025104319693. Campbell 3M Local analgesia froni percutaneouselectrical <strong>stimulation</strong> andperipheral mechanism. M.D. thesisUniversity 1973Yale4. Campbell 3M. Taub Local analgesia fromelectrical <strong>stimulation</strong>.percutaneousperipheral mechanism. Arch Neurul 23347350 19735. Hodge Ci ir Potential changesinside centralafferentterminals secondary to <strong>stimulation</strong><strong>of</strong>large- and small-diameter peripheral <strong>nerve</strong>fibers. Neurophysiol 353043 19726. Long DM Electrical <strong>stimulation</strong> for rclicf <strong>of</strong>pain from chronic <strong>nerve</strong> injury. Neurosurg3971S722 19737. Long DM External electrical <strong>stimulation</strong> astreatmcnt <strong>of</strong> chronic pain. Minn Med 57195198. 19748. Long DM Erickson DE Stimulation <strong>of</strong> theposterior<strong>of</strong>1975intractablecolumns<strong>of</strong> the spinal cord for reliefpain. Surg Neurol 41341419. Manfredi Modulation <strong>of</strong> sensory projectionsin anterolateral column <strong>of</strong> cat spinal cordby peripheral afferents<strong>of</strong> different size. Archhal Biol 10872lOS1970 Eng10. Melzack Wall PD Pain mechanismsnew theory. Science 150971979 196511. Mendell Properties and distribution <strong>of</strong>.peripherally evoked presynaptic hyperpolarization in cat lumbar spinalcord. PhyslolLond 226769792 197212. Meyer GA FieldsIlL Causalgia treated byselectivelarge<strong>nerve</strong>. Brain 95163168 1972fibre <strong>stimulation</strong> <strong>of</strong> peripheral13. Nashold BS Jr Friedman Dorsal column<strong>stimulation</strong> for control <strong>of</strong> pain. Preliminaryreport on 30 patients. Neurosurg36590597 197214. Picaza JA Cannon BW Hunter SE ct alPain suppression by peripheral <strong>nerve</strong> <strong>stimulation</strong>. Part I. Observationswith implanteddevices. Surg Neurol 4115126 197515. Pineda Dorsal column <strong>stimulation</strong> and itsprospects. Surg Neurol 4157163 197516. Shealy CM Dorsal column <strong>stimulation</strong> optimization <strong>of</strong> application. Surg Neurol4142145 197517. Shealy CM Mortimer JT HagforsNR Dosal column clectroanalgesia. Neurosurg32560564 197018. Sweet WH Wepsic JO Stimulation <strong>of</strong> theposteriorcontrolcolumns<strong>of</strong> the spinal cord for painindicationsClin Neurosurg 212783 10 1974techniquesand results.19. Sweet WH Wcpsic JO Treatment <strong>of</strong> chronicpain by <strong>stimulation</strong> <strong>of</strong> fibers<strong>of</strong> primaryafferent neurons. Trans Am Neurol Asset93103107 196820. Taub Electrical <strong>stimulation</strong> for the relief <strong>of</strong>pain two lessonsin technological zealotry.Perspect Biol Med 19125135 Autumn 197521. Torebjork HE Hallin RO Responseshuman and fibersto repeatedinelectrical intradermal <strong>stimulation</strong>. Neurol NeurosurgPsychiatry 37653664 197422. Wngman III Price DD Respntses<strong>of</strong> dorsalhorn celis<strong>of</strong> Af. mulatto to cutaneousand aural <strong>nerve</strong> and fiber stimuli. Neurophysiul32802817 196923. Wall PD Dorsal horn electrophysiology inIggo ed Handbook <strong>of</strong> Sensory PhysiologyVolume Soniatosensory System. BerlinSpringer-Vcrlag 1973 pp 253270698J.Peurosurg. Volume 43 0fjnbcr.1976


ItNerve <strong>stimulation</strong> or intractabic pattiWaIl PD Gutnick Ongoing activity inperipheral<strong>nerve</strong>sthe physiology and phar.macology <strong>of</strong> impulsesoriginating from Adtlres.c eprin nqziesrs to Donlin NT. Longneuron. Exp Neurol 43580593 1974 M.D. Department <strong>of</strong> Neurosurgery Johns\ValI PD. Sweet %VH Temporary abolition <strong>of</strong> HopkinsHospital 601 North Broadway.pain in man. Science 155108109 1967 Baltimore Maryland 21205.illiiIVeurosurg. Volume 45 December. 197621El

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