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Management

of

dengue

hemorrhagic

fever

in

a

secondary

level

hospital

in

Bangladesh:

A

case

report

Yasmin

Jahan

a,

*,

Atiqur

Rahman

b

a

GraduateSchoolofBiomedical&HealthSciences,HiroshimaUniversity,Japan

b

DivisionAgeingandSocialChange(ASC),ISV,LinköpingUniversity,Sweden

ARTICLE INFO Articlehistory: Received8June2020

Receivedinrevisedform18June2020 Accepted18June2020

Keywords:

Denguehemorrhagicfever Management

Secondaryhospital Bangladesh

ABSTRACT

Dengueisanimportanttropicalinfectioncausedbyanarbovirus.Asamosquitoborneinfection,this diseaseiswidelyspreadinseveraltropicalendemiccountriesandthisimpliestheglobalimportanceof this infection. In this specific case report, the author discussedthe case management of dengue hemorrhagicfever(DHF).A42-year-oldpatientcametoasecondarylevelhospitalwithcomplaintsof diffuseabdominalpain(moreincentralregion)continuallyfor3days.Basedonhisclinicalinvestigations thepatientwasdiagnosedbyDHFandmanagedwithintravenouslyadministeredfluidresuscitationas hehadahistoryofvomiting,closemonitoringofvitalstatus,andgaveconservativetreatment.Although, theplasmaleakagehadconcernedthedoctorsaboutdevelopingDSS.Butafterseeinghisbloodreport, whenthedoctorsfoundthatthepatient’splateletcountwasraisedgraduallyandnootherassociated signsthentheydecidedtogivehimdischargefromthehospital.Preventionandcontrolofdengueand DHF hasbecome more urgent and the available vaccine is still limited. Hence, effective disease prevention programs, education of themedical communityto ensure effective casemanagement, community-basedintegratedmosquitocontrolarenecessary.

©2020PublishedbyElsevierLtd.ThisisanopenaccessarticleundertheCCBY-NC-NDlicense(http:// creativecommons.org/licenses/by-nc-nd/4.0/).

Introduction

Dengue fever (DF) is a mosquito borne (family Flaviviridae, genus Flavivirus) disease of humans considered as a temporal worldwide public health concern [1]. The disease is now hyperendemicbothintropicalandsubtropicalregionscirculating all four serotypes (DENV-1 to DENV-4) [2]. Globally, almost 4 billionpeoplefromatleast128countriesareundertherisk[3]and estimated50milliondengueinfectionsareoccurringeachyear[4]. TheWorldHealthOrganizationdeclaredSouthAsiaasanendemic areaforthediseaseduetofavorabledisseminationenvironmentof Aedesaegypti,themaindenguevector[5].

Theclinicalspectrumofdenguediseasemanifestationsranges fromasymptomatic to symptomatic forms like dengue hemor-rhagicfever(DHF)anddengueshocksyndrome(DSS)[6]. Most commonlydeterminedsignsandsymptomsofDFincludeshigh fever,myalgia,arthralgia,severeheadache,retroorbitalpainand maculopapular rash. In exception, dengue patientsmight have nonspecific symptoms like nausea, vomiting, cough, dizziness,

diarrhea[7].Sometimes,itcanbeasymptomaticorself-limitingDF toseveredenguecharacterizedbyplasmaleakage(DHF),(grades1 and2)thatcanleadtoalife-threateningsyndrome(DSS),(grades3 and4)[5].Furthermore,subjectswhodevelopDHFaccompanied byDSShave3–5%higherchanceofdeath[8].Wepresentacase reportofapatientwithDHFattemptingtodiscloserelatedsigns, symptomsandtreatments.

Casereport

A42-year-oldpatientcametoasecondarylevelhospitalwith complaints of diffuse abdominal pain (more in central region) continuallyfor3days.Onadmissiontothemedicalward,hewas afebrile(37.4degreecentigrade),withapulserateof92beatsper minute anda bloodpressureof105/65mmHg.Hedidnothave history of fever at thetime of admission. On inspectionof his abdomen,reddishdiscolorationwasfound(Fig.1)and noother localizedcomplaintswerereportedexceptanabdominal tender-nessjustupperabdomenonpalpation.

Aftertakingapropernarrativehistory,thepatientletinform abouthis3dayscontinualfever.Firstdayitwashighgrade(39.5 degreecentigrade);andlowgrade(38.3degreecentigrade)inthe next two days. Initially, he had visited to a local primary care hospitalduetosymptomslikevomiting,losemotionanddiffuse

* Correspondingauthorat:GraduateSchoolofBiomedicalandHealthSciences, HiroshimaUniversity,Kasumi1-2-3Minami-ku,Hiroshima,734-8553,Japan.

E-mailaddress:d160207@hiroshima-u.ac.jp(Y.Jahan).

https://doi.org/10.1016/j.idcr.2020.e00880

2214-2509/©2020PublishedbyElsevierLtd.ThisisanopenaccessarticleundertheCCBY-NC-NDlicense(http://creativecommons.org/licenses/by-nc-nd/4.0/).

IDCases21(2020)e00880

ContentslistsavailableatScienceDirect

IDCases

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abdominalpain,therefore,beenadvisedtodosomeinvestigations. Resultsof the investigationswere as follows:platelets 32,000/ mm3; white blood cell count 3400/mm3 (neutrophils 40 %;

lymphocyte43%);hematocrit36%;hemoglobin11.6g/dl;blood picture– leukopenia,lymphocytosis,andthrombocytopenia.No abnormalities were shown in his ultrasonogram of whole abdomen.But hisphysical conditionwas deteriorating, and he hadbeenreferredtoasecondaryhospital.

Theon-dutydoctorofsecondaryhospitalprimarilypredicted the patient might have acute hemorrhagic pancreatitis due to tendernessonpancreaticregionregardlessofhispreviousreports. Basedonthissymptom,thedoctorhadstartedmanagementand advisedforroutinebloodinvestigationssoonerafterthe admis-sion.Resultsoftheinvestigationswereasfollows:whitebloodcell count9700/mm3(neutrophils54%,lymphocytes40%);hematocrit

42.9 %; hemoglobin 11.7g/dl, platelet 22,000/mm3; peripheral

bloodpicture–thrombocytopenia;antidengueIgMwaspositive (done on 4th day of fever-on admission day); random blood glucosewas 5.8mmol/l,alaninetransaminase39 IU/mL; serum creatinine 1.3mg/dl; serum electrolytes: serum sodium (Na) 126.4mmol/l;serumpotassium(K)4.29mmol/l;serumchloride (Cl)93.2mmol/l;serumamylase82IU/L(normalupto95);urinary amylase650IU/L(normalupto490);bloodgroupwasABpositive; ultra-sonogram of whole abdomen showed moderate ascites, prominent pancreas, mild to moderate pleural effusion (as an

abnormalchestfinding)andhisurinaryoutputwasnormal.There wasnohistoryofbleedingmanifestations.Astheplateletcounts werebelowinrespecttonormalrange,doctorsmadetheclinical diagnosis of dengue hemorrhagic fever. Due to a history of vomiting,thepatientwasmanagedwithintravenously adminis-teredfluidresuscitation,closemonitoringofvitalstatus,andgave conservative treatment. Besides, the plasma leakage was a concernedofthedoctorsindevelopingDSS.

Onnextday,thereportsofrepeatbloodinvestigationsadvised by thedoctors were: platelet 20,000/mm3; serum electrolytes:

serumsodium(Na)130.1mmol/l;serumpotassium(K)4.30mmol/ l;serumchloride(Cl)91.3mmol/l.Hewasadvisedtoarrangeblood donors (for fresh frozen plasma) since his platelet count was deteriorating gradually even though the vital signs were completelynormal.

Similarly,theplateletcountwasdoneagainateveningresulted around 50,000/mm3. He had no fever and stomach pain was

likewisedieddownsteadily.Doctorscompletedanultra-sonogram ofwholeabdomenanditdemonstratednonoteworthyvariations from the norm. At that point they proceeded with similar treatmentlikeplateletcountonceaday,forthefollowing2days. Whentheyfoundthepatient’splateletcountwasraisinggradually (70,000/mm3and 110,000/mm3)and nootherassociated signs,

theydecidedtogivehimdischargefromthehospital(Table1). Discussion

OnlyacountablenumberofcasereportsinrespecttoDHFhave beendocumentedinmedicalliterature.Pathophysiologyofsevere clinicalmanifestationobservedinDHFremainspoorlyunderstood, sinceacommonbeliefissecondaryinfectionputthesubjectsat great risk of DHF [8]. Besides, vasculopathy, deficiency and dysfunction of platelets and defects in the blood coagulation pathwaysaretheattributedfactors[9].

The clinicalcourseof DHFischaracterized bythree phases: Febrile,leakage,andconvalescentphase.Theinitialfebrileillness ismarkedbyamorbilliformrashandhemorrhagictendencies[10]. Thefeverpersistsfor2daysto1weekandthendropstonormalor subnormallevelswhenthepatienteitherconvalescesoradvances totheplasmaleakagephase.Highplasmaescapecasesaremarked byfrankshockwithlowpulsepressure,cyanosis,hepatomegaly, pleuralandpericardialeffusions,andascites.Hence,highclinical

Fig.1.Bandshapedskinrashontheabdomen.

Table1

Investigationsreportandvitalsignsrecordedfromadmissiontodischargeday.

Investigations Day0 Day1 Day2 Day3

Whitebloodcellcount 9700/mm3

Hematocrit 42.9% 47% – –

Hemoglobin 11.7g/dl – 12.1g/dl –

Platelet 22,000/mm3 Atmorning-20,000/mm3

Atnight-50,000/mm3

70,000/mm3 110,000/mm3

Randombloodglucose 5.8mmol/l 4.8mmol/l – –

Anti-dengueIgM Positive – – –

Serumelectrolytes Na-126.4mmol/l K-4.29mmol/l Cl-93.2mmol/l Na-130.1mmol/l K-4.30mmol/l Cl-91.3mmol/l – –

Serumamylase 82IU/L 76IU/L – –

Alaninetransaminase 39IU/mL – – –

Serumcreatinine 1.3mg/dl – – –

urinaryamylase 650IU/L 530IU/L Ultra-sonogramofwhole

abdomen

moderateascites,prominentpancreas,mildtomoderate pleuraleffusion(asanabnormalchestfinding)

– nonoteworthyvariation wasfound

– Urinaryoutput normal normal normal normal VitalSigns

Temperature 37.4degreecentigrade 37.1degreecentigrade 36.7degreecentigrade 37.0degreecentigrade Pulserate 92beats/minute 84beats/minute 80beats/minute 82beats/minute Bloodpressure 105/65mmHg 110/70mmHg 110/65

mmHg

112/73 mmHg 2 Y.Jahan,A.Rahman/IDCases21(2020)e00880

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suspicionandclosemonitoringofpatientareimportantforearly diagnosisandmanagementofsuchcases.Managementisusually conservative.

DHFisfrequentlyseenduringasecondarydengueinfection.An interviewwiththepatientdidnotrevealthatapreviousdengue viralinfectionhadoccurred.Aroundthattime,thefeverbeginsto subside(usually3–7daysaftersymptomonset),thepatienthad developedwarning signsofseverediseaselikeabdominalpain, persistent vomiting, change in temperature (from fever to afebrile).In ourcase report,the patientwas closely monitored withacautionofdevelopinghemorrhagicmanifestations,or/and changesinmentalstatus(irritability,confusion,orobtundation). Conclusion

The factors associated with dengue transmission include demographic and societalchangeslike uncontrolledpopulation growth,unplannedurbanization,substandardhousing,crowding, anddeteriorationinwater,sewer,andwastemanagementsystems. Alongwiththese,lackofpublichealthawareness,andappropriate diseasehavecreatedidealconditionsforincreasedtransmissionof mosquito-borne diseases especially in tropical and subtropical developing countries like Bangladesh. Nonetheless, prevention andcontrolofdengueandDHFhasbecomemoreurgentwiththe expanding geographic distribution and increased disease inci-denceinthepastdecades.Thereisaneedforunderstandingthe changingepidemiologythroughcontinuousmonitoring,including extendingthesurveillanceareasandaddressingthechallengesto reducetheimpactofthediseaseonpublichealth.Itmaybevery challengingtorootupthediseasefromthesupplysidedepending oneconomicconditionofthecountry.Along-terminvestmentis neededtoachievebehavioralchangesintheurbanpopulationto jointhefightagainsttheAedesmosquitoes.

Byfar,onedenguevaccine(Dengvaxia),developedbySanofi Pasteur,hasbeenapprovedbytheWorldHealthOrganizationand licensed in 20 countries[11]. The vaccineis only available for peoplelivinginsomedengueendemiccountriesyettobeavailable commerciallyfortravelers.Currently,theCDCandIndianresearch organizationsarecollaborating[12],tocomeforwardtoinitiate and coordinate a large-scale randomized clinical trial of the dengue vaccine in Bangladesh. Further studies are needed to explore. Finally, this case report urges a need for up taking awarenessonpossibleoccurrenceofserioussecondarybacterial infectionsrelatedtodengueviralinfection,especiallyinpatients with prolonged fever (more than 5 days) and highlights the likelihoodofshockoccurringcommonlyinDHF.

Fundingsource Nofundingsources.

Ethicalapproval

Informedconsentwasobtainedfromthepatienttopublishthe case.

Authorsstatement

The authorshave statedthat theyhave addressedallissues mentionedinthereviewers'commentsverycarefullyandmade the necessary corrections accordingly in the text with track changes.YJwrotethefirstdraftofthemanuscriptandARcritically reviewed andrevisedthe manuscript.Alltheauthors read and approvedthefinalpaper.

DeclarationofCompetingInterest

The authors declare that they have no known competing financial interests or personal relationships that could have appearedtoinfluencetheworkreportedinthispaper.

References

[1]WorldHealth Organization (WHO). Dengue and Severe Dengue. 2019. . Availablefrom:[Cited12January2020]https://www.who.int/news-room/ fact-sheets/detail/dengue-and-severe-dengue.

[2]CentersforDiseaseControlandPrevention(CDC).AboutDengue:WhatYou NeedtoKnow.2012..Availablefrom:[Cited14January2020]https://www. cdc.gov/dengue/about/index.html.

[3]FritzellC,RoussetD,AddeA,KazanjiM,VanKerkhoveMD,FlamandC.Current challengesandimplicationsfordengue,chikungunyaandZikaseroprevalence studiesworldwide:ascopingreview.PLoSNeglTropDis2018;12(7)e0006533. [4]AkhtarN,SaeedK,RafiqN,KhanN.Prevalenceofdengueserotype(DENV-2)in

Pakistan.JGenesCells2016;2(1):8.

[5]WorldHealthOrganization(WHO).DengueHaemorrhagicFever:Diagnosis, Treatment,PreventionandControl.2nded.WorldHealthOrganization;1997.. Availablefrom:[Cited2February2020]https://apps.who.int/iris/handle/ 10665/41988.

[6]KumarA,MondalS,SethiP,ManchandaS,BiswasA,WigN.Spontaneous iliopsoashaematomainapatientwithdenguehaemorrhagicfever(DHF):a casereport.JVectorBorneDis2017;54(1):103.

[7]FernandesC,PerezL,PerezD.Uncommonoralmanifestationsofdengueviral infection.BrazJOtorhinolaryngol2016;463:1–3,doi:http://dx.doi.org/ 10.1016/j.bjorl.2016.10.001.

[8]MahmoodS,HafeezS,NabeelH,ZahraU,NazeerH.Corrigendumto“Does comorbidityincreasetheriskofdenguehemorrhagicfeveranddengueshock syndrome?”.IntSchResNotices20172725850.

[9]WorldHealthOrganization(WHO).ReportonGlobalSurveillanceof Epidemic-proneInfectiousDiseases-Dengueanddenguehaemorrhagicfever.2019.. Availablefrom[Cited15February2020]https://www.who.int/csr/resources/ publications/surveillance/dengue.pdf?ua=1.

[10]KalayanaroojS.Clinicalmanifestationsandmanagementofdengue/DHF/DSS. TropMedHealth2011;39(4Suppl):83–7.

[11]WorldHealthOrganization(WHO).Immunization,VaccinesandBiologicals. 2018..Availablefrom[Cited16June2020]https://www.who.int/ immunization/research/development/dengue_q_and_a/en/.

[12]DubeyAP,AgarkhedkarS,ChhatwalJ,NarayanA,GangulyS,WartelTA,etal. Immunogenicityandsafetyofatetravalentdenguevaccineinhealthyadultsin India:arandomized,observer-blind,placebo-controlledphaseIItrial.Hum VaccinImmunother2016;12(2):512–8.

References

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