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RevBrasAnestesiol.2017;67(5):538---540

REVISTA

BRASILEIRA

DE

ANESTESIOLOGIA

PublicaçãoOficialdaSociedadeBrasileiradeAnestesiologia

www.sba.com.br

CLINICAL

INFORMATION

Postpartum

hemorrhage

and

pregnancy

induced

hypertension

during

emergency

lower

segment

cesarean

section:

dexmedetomidine

to

our

rescue

Uma

Hariharan

BhagwanMahavirHospital,RajivGandhiCancerInstituteandResearchCentre,DelhiGovernmentHealthServices, NewDelhi,India

Received6November2014;accepted23December2014 Availableonline1October2015

KEYWORDS

Dexmedetomidine; Obstetricanesthesia; Pregnancy-induced hypertension; Post-partum hemorrhage; Emergencycesarean section

Abstract Dexmedetomidineisahighlyselective␣-2agonistwhichhasrecently

revolution-izedouranesthesiaandintensivecarepractice.Anobstetricpatientpresentedforemergency cesareandeliveryundergeneralanesthesia,withpre-eclampsiaandpostpartumhemorrhage.In carefullyselectedcaseswithrefractoryhypertensionandpostpartumhemorrhage, dexmedeto-midinecanbeusedforimprovingoverallpatientoutcome.Itwasbeneficialincontrollingboth thebloodpressureanduterinebleedingduringcesareansectioninourpatient.

©2015SociedadeBrasileiradeAnestesiologia.PublishedbyElsevierEditoraLtda.Thisisan openaccessarticleundertheCCBY-NC-NDlicense( http://creativecommons.org/licenses/by-nc-nd/4.0/).

PALAVRAS-CHAVE

Dexmedetomidina; Anestesiaobstétrica; Hipertensãoinduzida pelagravidez; Hemorragia pós-parto; Cesarianade emergência

Hemorragiapós-partoehipertensãoinduzidapelagravidezdurantecesarianade emergênciaemsegmentouterinoinferior:dexmedetomidinaparanossoresgate

Resumo Dexmedetomidinaéum␣2-agonistaaltamenteseletivo querecentemente

revolu-cionou a nossa prática de anestesia e tratamento intensivo. Uma paciente obstétrica foi admitida paracesariana deemergência sobanestesia geral,com pré-eclâmpsiae hemorra-giapós-parto.Emcasoscuidadosamenteselecionadoscomhipertensãorefratáriaehemorragia pós-parto,dexmedetomidinapodeserusadaparamelhoraroresultadogeraldapaciente.O fár-macofoibenéficonocontroletantodapressãoarterialquantodosangramentouterinodurante cesarianaemnossapaciente.

©2015SociedadeBrasileiradeAnestesiologia.PublicadoporElsevierEditoraLtda.Este ´eum artigoOpen Accesssobumalicenc¸aCCBY-NC-ND( http://creativecommons.org/licenses/by-nc-nd/4.0/).

E-mail:[email protected]

http://dx.doi.org/10.1016/j.bjane.2014.12.002

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Postpartumhemorrhageandpregnancyinducedhypertension 539

Introduction

Eversincedexmedetomidinehasbeenapprovedforhuman use by the FDA in 1999, its indications and ramifications in anesthesia and intensive care has been increasing. Its useinobstetricanesthesiahasbeendelayeddueconcerns regarding maternal and fetal effects. In view of its sev-eral advantageous effects, it has been used in cesarean sections for controlling blood pressure response to intu-bation and as an alternative agent for labor analgesia as an IVPCA (intravenous patient controlled analgesia). We presentacaseofPIHforemergencycesareansectionunder general anesthesia, where dexmedetomidine wasused to controlherrefractoryhypertension,uterotonicity,stabilize hemodynamics,prevention of postoperative shivering and supplementpostoperativeanalgesia.

Case

report

A30yearold,70kg,primigravidapresentedtothe obstet-ric emergency in labor, with uncontrolled blood pressure andnon-reassuring fetalheartrate at 38weeksperiodof gestation.She wasadiagnosedcaseofpregnancyinduced hypertension(PIH)onalpha-methyl-dopatherapy.Shewas postedforemergencycesareansectioninviewofpersistent fetaldecelerations.Thepatientrefusedanykindof neurax-ialblockinviewofpreviousbacksurgeryforlumbarslipped diskandrecurrent back achesince 2years.On preopera-tive evaluation,blood pressure(B.P) was200×102mmHg; pulseratewas120beatsper minute,regular, normal vol-ume;bilateralpedaledema waspresent withnoevidence ofcongestivecardiacfailure.Intravenous(I.V.)Magnesium sulphatetherapy wasstarted preoperativelybythe obste-triciansforseizureprophylaxis.TherewerenosignsofCNS (Central Nervous System) irritation, visual defects, coag-ulopathy or renal dysfunction. Invasive arterial line was institutedpre-inductionforbeat-to-beatpressure monitor-ing. Due to patient refusal, standard general anesthesia withpreoxygenation,rapidsequenceinductionandcricoids pressure was planned after aspiration prophylaxis and appropriatemonitoring.Tominimizehypertensiveresponse tolaryngoscopyandintubation, I.V.preservativefree Lig-nocainehydrochloride2%(2mL)andI.V.Labetololinfusion (5mg.min−1) were given. Modified Cormack and Lehane

gradingwas2B.

Despitealltheabovemeasuresandsingleattemptgentle laryngoscopicintubation,theB.Pwasnotcontrolled.Post intubationB.P.was198×100mmHgandPulserate118min, when O2+ N2O+ Isoflurane inhalational agent werestarted for maintenance of anesthesia. Induction delivery inter-valwas4min.Immediatelyoncordclamping,loadingdose (70␮g.h−1 over 10min) of dexmedetomidine wasstarted, followed by maintenance dose of 35␮g.h−1 I.V. infusion (alongwithsyntocinoninfusion).B.Pandpulseratestarted tostabilizeandnormalize.

Deliveryofthebabyandplacentawasfollowedby post-partum hemorrhage (PPH). Despite meticulous attention tohemostasis,syntocinoninfusion,decreasinginhalational anestheticagentandprostadin injection,uterinebleeding wasnot controlled.Dexmedetomidine alsohas uterotonic effects, which was beneficial in controlling this PPH.

Once B.P was controlledand the uterus contractedafter dexmedetomidineinfusion,uterinebleedingwasalso con-trolled.Theapgarscoresofthebabywerenormalatbirth, 1and5min.Afterensuringadequatehemostasis,followed byuterineand skin closure,preparations for reversaland extubationweremade.Dexmedetomidineinfusionwas con-tinued on maintenance dose. On return of spontaneous respiration andtrain-of- fourresponses onneuromuscular monitoring,reversal wasgivenand thepatient extubated whenfullyawake.

Patientmaintainedhervitalswellandherpostoperative B.P was132×80mmHg and pulserate 88beats/min. Pain managementwasdone with multi-modal analgesia (intra-venousparacetamol infusion1g,intramuscular diclofenac injection75mgandincisionsitelocalanestheticinfiltration) alongwithdexmedetomidineinfusion(30mcg.h−1).

Patientwasshiftedtoa highdependency care unitfor observation and monitoring. After 2h, dexmedetomidine infusionwasslowlytapered-offandstoppedafter1h.Inthe meanwhile, her B.P remained within normal limits.After stopping dexmedetomidine infusion, B.P. was controlled withlowdoseintravenouslabetolol(5mgslowI.V.boluses over 1min) asand whenrequired (labetolol wasrequired onlytwice in 24h) andlater withoral amlodepine (10mg twicedailyfromnextday).Thenewbornwasputtobreast feedingwithin4hofbirthandtakencare-offinthenursery. Patient was shifted to ward with normal vitals the next day (after removing arterial line) and later discharged, withoralantihypertensivetherapyandadvisedforregular follow-upwiththeobstetrician.

Discussion

Dexmedetomidine hydrochloride is a highly selective ␣-2 receptor1 agonist (

␣-1 to ␣-2 ratio is 1:1600) with vari-ousapplicationsin anesthesiaandintensivecare. Itisthe S-enantiomer of medetomidine,2 with empirical formula

C13H16N2.

It is given in a loading dose3 of 1

␮g.kg−1.h−1 over 10min, followed by maintenance intravenous infusion of 0.2---0.7␮g.kg−1.h−1. It produces4 sedation, sympa-tholysis, cardiovascular stability, anxiolysis, analgesia, neuroprotection and anesthesia-sparing effects. Its pur-portedadvantages5includeminimalrespiratorydepression,

renoprotection, quick offset and cardioprotection. The mainside effectsincludedry mouth, nausea,hypotension and bradycardia. Its reluctant use in obstetrics is due to concerns regarding possible maternal and fetal effects.6

Dexmedetomidineislipophilicanditsplacentalextraction is high. Hence its fetal transfer through the placenta is minimal.Inanimalexperiments,dexmedetomidinehasnot beenfoundtocauseadversefetaleffects.7Ithasbeenused

inobstetricsforcontrolofB.Pduringcesareansectionand forlaboranalgesia.Isolatedcasereportshaveassertedthe safety of dexmedetomidine in obstetric anesthesia.8 Our

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540 U.Hariharan

The uterine bleeding got controlled only after starting dexmedetomidineinfusion.PPHisadevastating complica-tionduringdelivery.Wedidnotpreferusingnitroglycerine forB.Pcontrolduetoitsuterinerelaxanteffects.

Inhalational anesthetics could also confound PPH, henceIsoflurane concentration wasdecreased onstarting dexmedetomidine infusion. Once the B.P was controlled withdexmedetomidine, thebleedersalsostopped oozing. Timely control of PPH is this case could be due to the combined effects of B.P control and uterotonicity. This uterotoniceffect of dexmedetomidine needs tobe inves-tigated and researched further. Bloodtransfusion and its attendantcomplicationscouldbeavoidedinpatientswith PPH.Analgesiawasalsosupplementedbydexmedetomidine infusion both intra- and postoperatively. Her hyperten-sion was also under control in the postoperative period. Dexmedetomidine was used only after cord clamping, so the question of fetal effects does not arise in this case, ashighlightedbythenormalapgarscores.Invasivearterial andneuromuscular monitoring was usedalong with other standard monitoring devices in this patient.She also was observedpostoperativelyinan intensivecareunitfor 24h andthentransferredout.

Conclusions

Thoughitistooambitioustoroutinelyrecommendtheuse ofdexmedetomidineinobstetricanesthesia,itsunparalled multipurposeuseinsedation,cardiovascularstability, anal-gesiaandbloodpressurecontrolcannotbeignored.Weneed tobecautiousasthereisapossibilityofmaternal hypoten-sionandfetalbradycardia.

Since its placental extraction is high, its fetal effects areusuallynegligible.Itsplacentalretention ratiois high (Maternal to Fetal Index/Ratio 0.77) and it also directly potentiatestheamplitudeandrateofuterinecontractions. ItsuterotoniceffectandefficacyinPPH,needstobestudied furtherinlargerandomizedtrialsbeforebeingputto tangi-bleclinicaluse.Incarefullyselectedcaseswithrefractory

hypertensionandpost-partumhemorrhage, dexmedetomi-dinecanbeusedforimprovingoverallpatientoutcome.It was beneficialin controllingboth the blood pressure and uterinebleedingduringcesareansection,aswellasfor anal-gesiainourpatient.Suchcasesofpatientrefusalor some relative contraindicationto regionalanesthesia for emer-gencyoperativedeliverymayposeachallengeforthe anaes-thesiologists,especiallywhencomplicatedbyPIHorPPH.

Conflicts

of

interest

Theauthordeclaresnoconflictsofinterest.

References

1.AantaaR,JalonenJ.Perioperativeuseofalpha-2-adrenoceptor agonists and the cardiac patient. Eur J Anaesthesiol. 2006;23:361---72.

2.GertlerR, Brown HC,Mitchel DH,et al. Dexmedetomidine: a novelsedative-analgesicagent.BUMCProc.2001;14:13---21.

3.CoursinDB,MaccioloniGA.CurrOpinCritCare.2001;7:221---6.

4.NairAS,Sriprakash K.Dexmedetomidineinpregnancy: review of literature and possible use. J Obstet Anesth Crit Care. 2013;3:3---6.

5.El Tahan MR, Mowafi HA, Al Sheikh IH, et al. Efficacy of dexmedetomidine in suppressing cardiovascular and hormonal responses to general anesthesia for caesarean section: a dose---responsestudy.IntJObstetAnesth.2012;21:222---9.

6.SiaTA,SngLB.Intravenousdexmedetomidineforobstetric anaes-thesiaandanalgesia:convertingachallengeintoanopportunity. IntJObstetAnesth.2009;18:204---6.

7.AlaKokkoTI,PienimakiP,LampelaE,etal.Transferof cloni-dineanddexmedetomidineacrosstheisolatedperfusedhuman placenta.ActaAnaesthesiolScand.1997;41:313---9.

8.Palanisamy A, Klickovich RJ, Ramsay M, et al. Intravenous dexmedetomidineasanadjunct forlabouranalgesiaand cae-sareandeliveryanaesthesiainaparturientwithtetheredspinal cord.IntJObstetAnesth.2009;18:258---61.

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