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Abstract

Objective: This is a case illustration of the challenges in managing a patient with central post stroke pain secondary to right thalamic bleed. We describe in detail the events of this case management and the challenges that we had encountered. Method: We report a case of a 68-year-old lady who had right thalamic bleed secondary to hypertensive crisis in 2015 and was further complicated with central post stroke pain over the hemiparetic side. In our report, we describe in detail the challenges in managing the patient to improve her function to achieve a better quality of life. Conclusion: This article illustrates the importance of a multidisciplinary approach and knowledge of various methods in managing a patient with central post stroke pain.
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BangladeshJournalofMedicalScienceVol.18No.02April’19
Case report:
Challenges in Managing A Patient With Central Post-Stroke Pain
Mazatulfazura SF Salim1, Muhammad Haz Hana2, Tan Yew Chin3, Nur Karyatee Kassim4, Mazlina
Mazlan5
Abstract :
Objective:Thisisacaseillustrationofthechallengesinmanagingapatientwithcentralpost
strokepain secondary toright thalamic bleed.Wedescribeindetail the eventsof this case
managementandthechallengesthatwehadencountered. Method:Wereportacaseofa68-year-
oldladywhohadrightthalamicbleedsecondarytohypertensivecrisisin2015andwasfurther
complicatedwithcentralpoststrokepainoverthehemipareticside.Inourreport,wedescribein
detailthechallengesinmanagingthepatienttoimproveherfunctiontoachieveabetterquality
of life. Conclusion:Thisarticleillustratestheimportanceofamultidisciplinaryapproachand
knowledgeofvariousmethodsinmanagingapatientwithcentralpoststrokepain.
Correspondence to: Dr Muhammad Haz Hana, Senior Lecturer / Rehabilitation Medicine Specialist,
Rehabilitation Medicine Unit, School of Medical Sciences, UniversitiSainsMalaysia16150KubangKerian,
Kelantan, Malaysia. Email:drmdhaz@usm.my
Bangladesh Journal of Medical Science Vol. 18 No. 02 April’19. Page : 416-418
DOI: https://doi.org/10.3329/bjms.v18i2.40717
Case presentation:
A68-years-oldladywithuncontrolled hypertension
sustained a right thalamic bleed in 2015. She was
premorbidly well prior to the cerebrovascular
accident.Shedevelopedanacuteonsetofleftsided
hemiparesis,hemisensorylosswithneuropathicpain
overherleftupperlimb.Thepoweroftheaected
limbs were 4/5 according to Medical Research
Councilgradingscalewithevidenceofmildspasticity
overtheleftbicep,andgastrocnemius/soleusmuscle
complex with Modied Ashworth Scale of 1. She
was still able to ambulate indoor independently
usingquadripodandperformsomesimpledomestic
activities of daily living. The major problem that
aectedherdailylifewastheneuropathicpainover
theleftupperlimb.
She described the pain as burning and pricking
in nature, which was severe enough to disturb her
activitiesofdailylivingwithNumericalRatingScale
(NRS)of 7 to8over 10. The painwas continuous
throughout the day and frequently at night, which
causedserioussleepdisturbance.Thepainwasfelt
overthe entire aspect of thewhole leftupper limb
andoccasionallyspreadtoherleftfaceandneck.She
deniedanyhyperalgesiaorallodynia.
She was started on Amitryptiline 25mg daily two
weeksafter thepain onset. However,there was no
improvementintheNRSpainscoreafterstartingthe
medicationforalmostamonth.Increasingthedoseup
till50mgdailydidnotbringforthanyimprovement
1. Dr Mazatulfazura SF Salim, MBBCh BAO, MMed (Rehab Med) Lecturer / Rehabilitation Medicine
Specialist,DepartmentofMedicine,FacultyofMedicineandHealthSciences,UniversitiPutraMalaysia,
43400Serdang,Selangor,Malaysia.fazurasf@upm.edu.my
2. DrMuhammadHazHana,MBBS,MMed(Rehab Med.)SeniorLecturer/RehabilitationMedicine
Specialist,RehabilitationMedicineunit,SchoolofMedicalSciences,UniversitiSainsMalaysia,16150
KubangKerian,Kelantan,Malaysia.drmdhaz@usm.my
3. Dr Tan Yew Chin, MD, MMed (Neurosurgery) Senior Lecturer / Neurosurgeon & Pain Specialist,
DepartmentofNeurosciences,SchoolofMedical Sciences Universiti Sains Malaysia,16150Kubang
Kerian, Kelantan, Malaysia. drtanyc@usm.my
4. Dr Nur Karyatee Kassim MBBS, MPath (Chemical Pathology) Senior Lecturer/ Chemical Pathologist
Basic Sciences Unit, School of Dental Sciences, Universiti Sains Malaysia, 16150 Kubang Kerian,
Kelantan,Malaysia.karyatee@usm.my
5. Associate Professor Dr Mazlina Mazlan, MD, MMed (Rehab Med.) Associate Professor / Rehabilitation
MedicineSpecialist.DepartmentofRehabilitationMedicine,FacultyofMedicine,UniversityofMalaya,
59100KualaLumpur,Malaysia.mazlinamazlan@ummc.edu.my
412
CentralPost-strokePain
too.Wewereabitcautiousnottoincreasethedosage
furtherasthispatienthaspre-existingcardiovascular
disease. We then stopped the Amytripiline
and changed the medication to Gabapentin, an
anticonvulsant.  She only showed signicant pain
reliefwithGabapentin600mgtds,wherebyherNRS
scoreimproved to4 over 10. However, the patient
experiencedintolerablesideeectsatthisdose,where
shefelt lightheadedness andsleepyduring daytime
and was unable to perform her normal activities
of daily living. She became frustrated and started
to display depressive symptoms such as persistent
low mood and lost of interest in daily activities.
Nonethelesswedidnotstartheronanymedications,
as her PHQ-9 score was only 5, which indicated
mild depression.  We then reduced the Gabapentin
dosage to 300mg tds and incorporated counseling
andpsychologicalmanagementto address thepain.
Theseinvolvedcognitivebehavioralapproachsuch
as breathing and relaxation therapy and distraction
techniques.However,these techniques require high
commitmentfromthepatienttopracticethemdaily.
WehadeducatedMadamHonthesignicantroleof
psychologicalapproachbesidesthepharmacological
managementintreatingthepainandemphasizedon
the importance of applying the technique correctly
and regularly. The managing team had failed to
convinceher topractice those techniquesregularly
eventhoughmultipletherapysessionswerearranged.
Besides, she also underwent acupuncture as an
alternativetreatmenttomanageherpain.Shestopped
afterseveralsessionsandclaimedthatitdidnothelp
torelieveherpain.HerNRSscorewasmaintained
at 6 over 10, which, according to the patient, was
notthedesirablescore.SinceGabapentinseemedto
work,wecontinuedthemedicationwithalowerdose
of300mgtds and encouragedhertocomplyonthe
breathing,relaxationanddistractiontechniques.
After 6 months of initiating treatment for the
neuropathicpain,theNRSpainscorewasstill6to
7 over 10. The patient felt dissatised and started
todeterioratein her dailyfunction.She wished for
theneuropathic pain to be completelytreated. Due
to the therapy resistance, we oered her electrical
neurostimulation therapy for further reduction of
painbutshe refused.Shehaddecidedto continue
withtheGabapentin300mgtdsonlyeventhoughit
controlsthepainsuboptimally.
Ethical Clearance:
Thiscasereportwassubmittedforpublicationafter
gettingEthicalapprovalfromtheEthicsCommittee
of the School of Medical Sciences, Universiti
Sains Malaysia, 16150 Kubang Kerian, Kelantan,
Malaysia.
Discussion:
Centralpoststrokepainbelongstoagroupofchronic
paindisordersthataretermedcentralneuropathicpain
becausethepainisduetoalesionordysfunctionof
the central nervous syste1.Neuropathicorcentralpain
hasbeen estimatedtooccurinupto8%ofpatients
aftera strokeduring 1 year follow up.About18%
of stroke patients with somatosensory disturbances
developed central post stroke pain2. In clinical
practice,the treatment ofpatientswith central post
strokepainisoftenbasedontrialanderroruntilpain
reliefisfound.Ourcasepresentedhereshowedsome
challengesinoptimizingthepain.Thereisageneral
consensusthatamitriptylineisthedrugofrstchoice,
butnotallpatientsreportaresponse3.Thetricyclic
antidepressantamitriptylinegivenat75mgdailywas
found to be eective in improving the pain scores
in10outof15patientswithcentralpoststrokepain
versus1of15inaplacebogroupofadouble-blinded
placebo-controlled study at 2 weeks and 4 weeks
from the start of treatment4.Amitriptylineisusually
startedat10 or 25mg/dayand titrated up to75mg/
day.OurpatientdidnotrespondtoAmitryptilineat
50mgdailyhoweverwedidnotincreasethedosage
furtherasourpatienthadapreexistingcardiovascular
disease.Thus,wehadtotryonanothertypeofdrug,
which is Gabapentin, the anticonvulsant group.
Although the ecacy of Gabapentin on peripheral
and central neuropathic pain is well documented.
It is associated with side-eects such as dizziness,
decreasedintellectualperformance,somnolence,and
nausea5.Thesesideeectshavecausedourpatientto
beunabletoperformherdailyactivitiesandthedose
hadtobereducedtoasub-optimaldose.
Besides medical therapy, the psychological
approachesalsoplaysimportantrole.Dierentcoping
strategies have been recommended and used for
post-strokepainsuppression.Cognitivebehavioural
therapy including breathing, relaxation and
distractiontechniquesmayhelptomodifynegative
thoughts related to pain. This can help patients to
increasetheir activitylevel andfunctioning, which
inturncanhelpimprovemood,sleepandqualityof
life.Inthecasewepresentedabove,thepatientfailed
to apply the techniques taught to her in her daily
activitiesdespitereassuranceontheeectivenessof
thepsychologicalapproach.
Acupuncture is a complementary and alternative
medical modality.The World Health Organization
(WHO) in 2002 released a report entitled
413
MazatulfazuraSFSalim,MuhammadHazHana,TanYewChin,NurKaryateeKassim,MazlinaMazlan
“Acupuncture:Review andAnalysisof Reportson
Controlled Clinical Trials”. This report states that
acupuncturecanberegardedasthemethodofchoice
fortreatingmanychronicallypainfulconditions.For
poststrokecomplications,therewereonlyevidences
on eectiveness of acupuncture for shoulder pain
after stroke6. For central post stoke pain, there are
stilllowevidencesthatacupunctureshowssignicant
eect7.In the casepresented here, acupuncturedid
nothelpinalleviatingthepain.
Other non-pharmacological treatment, including
repetitive transcranial magnetic stimulation
(rTMS), deep brain stimulation (DBS) and motor
cortex stimulation (MCS) has been reported in
case series and brief reports, but there are no
controlled trials in this eld. Due to low-quality
evidence, recommendations for MCS and DBS are
“inconclusive”inthetreatmentofcentralpoststroke
pain. Therefore, it is recommended that electrical
neurostimulation should be considered in drug-
resistantcentralpoststroke pain patients only8. We
suggested a trial of electrical neurostimulation to
our patient since she did not respond optimally to
pharmacological treatment, psychological therapy
and alternative treatment.
Inconclusion,managingcentralpoststrokepainwas
indeed very challenging and there is a great need to
identifybettertreatmentregimes. However,holistic
approach, including medical and psychological
togetherwithpatient’sparticipationandcommitment
towardstreatment oeredare theonly current best
practiceinmanagingcentralpoststrokepain.
Conict of interest: None declared
Authors’ Contributions:
Datagatheringandideaownerofthisstudy:Salim
MSF,HanaMH
Studydesign:SalimMSF,HanaMH,TanYC
Data gathering: Salim M SF, Mazlan M
Writingandsubmittingmanuscript:SalimMSF,
HanaMH
Editingandapprovalofnaldraft:SalimMSF,
HanaMH,TanYC
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A double-blind, 3-phase, cross-over, placebo-controlled trial of the pain-relieving effect of amitriptyline and carbamazepine was carried out in 15 patients with central post-stroke pain (CPSP) but without signs of depression. Treatment was given, in randomized order, for periods of 4 weeks, separated by 1 week wash-out. The final doses were 75 and 800 mg/day, respectively, for amitriptyline and carbamazepine. The treatment effects were assessed by daily ratings of pain intensity on a 10-step verbal scale and at the end of each treatment period by a global rating of the analgesic effect on a 5-step verbal scale. For the assessment of depression the Comprehensive Psychopathological Rating Scale (CPRS) was used. Amitriptyline produced a statistically significant reduction of pain when compared to placebo. According to the global rating, 10 of the 15 patients were responders to this drug. The effect could already be noticed during the second treatment week and it appeared to be correlated to the plasma concentration, since the median total ami- and nortriptyline concentrations were 497 and 247 nmol/l, respectively, for responders and non-responders. The early onset, together with the fact that the patients were not depressed, nor did they obtain reduced scores on ratings of depressive symptoms and signs, provides strong support for the conclusion that the pain relief was not caused by an antidepressive effect. Five of the 14 patients treated with carbamazepine reported some pain relief, but the effect did not reach statistical significance when compared to placebo. No correlation was found between effect and plasma concentration. In general, the patients tolerated the planned final dose of amitriptyline well. No final dose reduction was necessary. Carbamazepine caused more side effects and the final dose had to be reduced in 4 patients. However, only 1 patient had to be taken off medication, on day 25, due to drug interaction.
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New studies of the treatment of neuropathic pain have increased the need for an updated review of randomized, double-blind, placebo-controlled trials to support an evidence based algorithm to treat neuropathic pain conditions. Available studies were identified using a MEDLINE and EMBASE search. One hundred and five studies were included. Numbers needed to treat (NNT) and numbers needed to harm (NNH) were used to compare efficacy and safety of the treatments in different neuropathic pain syndromes. The quality of each trial was assessed. Tricyclic antidepressants and the anticonvulsants gabapentin and pregabalin were the most frequently studied drug classes. In peripheral neuropathic pain, the lowest NNT was for tricyclic antidepressants, followed by opioids and the anticonvulsants gabapentin and pregabalin. For central neuropathic pain there is limited data. NNT and NNH are currently the best way to assess relative efficacy and safety, but the need for dichotomous data, which may have to be estimated retrospectively for old trials, and the methodological complexity of pooling data from small cross-over and large parallel group trials, remain as limitations.
MMed (Rehab Med) Lecturer / Rehabilitation Medicine Specialist, Department of Medicine, Faculty of Medicine and Health Sciences
  • Dr Mazatulfazura
  • S F Salim
  • Bao Mbbch
Dr Mazatulfazura SF Salim, MBBCh BAO, MMed (Rehab Med) Lecturer / Rehabilitation Medicine Specialist, Department of Medicine, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia. fazurasf@upm.edu.my