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Treating hypoxemic patients with SARS-COV-2 pneumonia: Back to applied physiology

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Treating hypoxemic patients with SARS-COV-2 pneumonia: Back to applied physiology

BENDJELID, Karim, GIRAUD, Raphaël

BENDJELID, Karim, GIRAUD, Raphaël. Treating hypoxemic patients with SARS-COV-2

pneumonia: Back to applied physiology. Anaesthesia Critical Care & Pain Medicine , 2020, vol. 39, no. 3, p. 389-390

DOI : 10.1016/j.accpm.2020.04.003 PMID : 32305591

Available at:

http://archive-ouverte.unige.ch/unige:143204

Disclaimer: layout of this document may differ from the published version.

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Editorial

Treating hypoxemic patients with SARS-COV-2 pneumonia:

Back to applied physiology

Asmedicaldoctors,wearefacingterribleandunprecedented challengesin theprovisionofmedical caretopatients infected withSARS-CoV-2pneumonia(severeacuterespiratorysyndrome coronavirus2).IntensiveCareUnitsaroundtheworldarestraining as demand for intubation and mechanical ventilation (MV) continuesits ever-upward curve.In this regard,as intensivists, wewouldliketosharesomethoughtsonhowappliedphysiology mightrelatetoSARS-CoV-2pneumonia(pneumonitis).

Wewilldescribeourexperienceindealingwithpatientswho wereintubatedandventilatedwithpositivepressureMV.Upto thisday,wehaveadmitted89patientsintoourcriticalcareunitof which92%neededinvasiveMV(uptothisday26patientshave been discharged). During the first two days of mechanical ventilation,themajoritysurprisinglyexhibitedgoodlungcompli- ance with preserved lung mechanics and diffuse and bilateral groundglassareasonComputedTomographyandcoalescentB2 linesonbedsidelungultrasound[1].Itappearsthatattheinitial stage, SARS-CoV-2 pneumonia induces high permeability-type pulmonaryoedema witha large capillaryleaksyndrome and a significant venous admixture (poorly aerated-perfused lung regions) concomitant with a loss of hypoxic vasoconstriction (Euler-Liljestrandmechanism)[2].Thus,theobservedbenefitafter intubationandpositivepressureMV,attheearlystageofSARS- CoV-2 pneumonia, does not seem to be related to the usual recruitmentoflungvolumebutmainlytoa decreasein venous return,rightventricularoutput,transpulmonarybloodflowand finallyintrapulmonaryshunt[3,4].Thepositiveimpactofreverse TrendelenburgpositioningonSaO2values,inselectedpatients,can bespectacular.

However,somepatientswithahistoryoflungdisease,and/or latebacterialsuperinfection,orfollowing48hoursofMVthereby inducingheterogeneousmechanicalstress,willpresentatypical inflammatory ARDS phenotype with large consolidations pre- dominatingindependentlowerlobes[5].Thepresentcondition

generates large areas of true pulmonary shunt (non-aerated/

perfusedlungregions),thatfurtherworsenoxygenation,decrease respiratory complianceandmayrequireahigherPEEP,a lower tidalvolume,prone positioning, neuromuscularblockingagents and,fortheworstcases,VV-ECMO.Obviously,thissecondpheno- type,moretypicalofclassicalARDS,willneedalongerMVperiod.

Interestingly, the initial, high permeability-type pulmonary oedema phenotype that characterises SARS-CoV-2 pneumonia with apparently preserved lung mechanics, while undergoing positivepressureMV,mayshifttothetypicalARDSphenotypein absenceoftimelyweaningMV.

Acloserlookatthepathophysiologyofthishypoxemicalveolar state reveals that a decrease in venous admixture induced by decreasing in transpulmonary blood flow may be obtained mechanically (PPV), chemically (nitroglycerin in cardiogenic pulmonary oedema), by body posture (reverse Trendelenburg positioning)oracombinationofthese.However,whencapillary hydrostatic pressure is low or normal as observed in high permeability-typepulmonaryoedema,amedicationlikealmitrine bismesylate,that promoteshypoxic pulmonaryvasoconstriction [6],mayimprovehypoxemiaresultingfromSARS-CoV-2pneumo- nia. Indeed, there are several studies indicating that upon intravenousadministration,almitrineiseffectiveinhumanARDS byincreasingarterialPO2iftheriseinpulmonaryarterypressureis adequately supported bytherightventricle and cardiacoutput does not fall [7]. Unfortunately, almitrine is not available in Switzerland.

ItisnotablethatpatientswithsevereSARS-Cov-2pneumonia tendtobeelderlyand/orhavelimitedorgansfunctionalreserve.In thisregard,wemaythinkthatitisunfortunatetobeforcedtotreat selected clinically stable patients with temporary hypoxemia (silent hypoxemia) using invasive MV to decrease their initial venousadmixture,wheninsteadwecouldpotentiallytreatthem bydecreasingtranspulmonarybloodflow(almitrine,continuous positiveairwaypressure[CPAP],reverseTrendelenburgposition- ing,fluiddepletion...).Indeed,in-hospitalmortalityreportedfrom Wuhan was very high among patients requiring invasive mechanicalventilation,ofwhombetween62%and97%ofpatients died[8].

Thepresentmessagehighlightsthatthemortalityisveryhigh among patients with severe SRAS-CoV-2 pneumonia who are underorrequiringMV[8].Thus,anytherapyandproceduresthat could prevent intubation and MV, or enhance MV weaning, withoutfurtherdeteriorationofthepatient’sparlousstatewould AnaesthCritCarePainMedxxx(2020)xxx–xxx

ARTICLE INFO

Keywords:

Hypoxemia Venousadmixture Shunt

SARS-CoV-2pneumonia GModel

ACCPM-649;No.ofPages2

Pleasecitethisarticleinpressas:Bendjelid K,Raphae¨ G.TreatinghypoxemicpatientswithSARS-COV-2pneumonia:Backtoapplied physiology.AnaesthCritCarePainMed(2020),https://doi.org/10.1016/j.accpm.2020.04.003

https://doi.org/10.1016/j.accpm.2020.04.003

2352-5568/C 2020Socie´te´ franc¸aised’anesthe´sieetdere´animation(Sfar).PublishedbyElsevierMassonSAS.Allrightsreserved.

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bewelcome.Thepresentapproachseemsrationalinasituation wherewearefacingterriblechallengesintheprovisionofICUbeds andventilators[9].Allproceduresseemjustifiedaslongastheydo notobscureclinicaldetectionoftheneedfor MVanddoes not increase the transmission dynamics of COVID-19 by aerosol- generating procedures (in absenceof protective equipment for healthcareprofessionals).

AsincerethanksyoutoDrJohnVogel,ConsultantinIntensive CareandAnaesthesiaatEalingHospitalNHSTrustforhisdiligent proofreadingofthepresentmanuscript.

Disclosureofinterest

Theauthordeclaresthathehasnocompetinginterest.

References

[1]ChungM,BernheimA,MeiX,ZhangN,HuangM,ZengX,etal.CTimaging featuresof2019novelcoronavirus(2019-nCoV).Radiology2020;295:202–7.

[2]MarshallBE,HansonCW,FraschF,MarshallC.Roleofhypoxicpulmonary vasoconstriction inpulmonary gasexchange and blood flow distribution.

Pathophysiology.IntensiveCareMed1994;20:379–89.

[3]BendjelidK.Rightatrialpressure:determinantorresultofchangeinvenous return?Chest2005;128:3639–40.

[4]SiegenthalerN,GiraudR,CourvoisierDS,WiklundCU,BendjelidK.BMCEffects ofacutehemorrhageonintrapulmonaryshuntinapigmodelofacuterespira- torydistress-likesyndrome.BMCPulmMed2016;16:59.

[5]BernheimA,MeiX,HuangM,YangY,FayadZA,ZhangN,etal.ChestCTFindings inCoronavirusDisease-19(COVID-19):relationshiptodurationofinfection.

Radiology2020200463.http://dx.doi.org/10.1148/radiol.2020200463.

[6]PapazianL,RochF,BregeonA,ThirionF,GaillatX,SauxV,etal.Inhalednitric oxideandvasoconstrictorsinacuterespiratorydistresssyndrome.AmJRespir CritCareMed1999;160:473–9.

[7]Gallart L, LuQ, Puybasset L, Umamaheswara Rao GS, CoriatP,Rouby JJ.

Intravenousalmitrinecombinedwithinhalednitricoxideforacuterespiratory distresssyndrome.TheNOAlmitrineStudyGroup.AmJRespirCritCareMed 1998;158:1770–7.

[8]WeissP,MurdochDR.ClinicalcourseandmortalityriskofsevereCOVID-19.

Lancet2020[Onlineaheadofprint.DOI:10.1016/S0140-6736.20.30633-4].

[9]TruogRD,MitchellC,DaleyGQ,TruogRD,etal.Thetoughesttriageallocating ventilators in a pandemic.N Engl J Med 2020. http://dx.doi.org/10.1056/

NEJMp2005689[Onlineaheadofprint.Articleinpress].

KarimBendjelida,b,c,*,GiraudRaphae¨a,b,c

aIntensivecaredivision,universityhospitals,Geneva,Switzerland

bGenevahaemodynamicresearchgroup,Geneva,Switzerland

cFacultyofmedicine,Geneva,Switzerland

*Correspondingauthorat:Intensivecaredivision,university hospitals,Geneva,Switzerland E-mailaddress:karim.bendjelid@hcuge.ch(K.Bendjelid).

Availableonlinexxx Editorial/AnaesthCritCarePainMedxxx(2020)xxx–xxx

2 GModel

ACCPM-649;No.ofPages2

Pleasecitethisarticleinpressas:Bendjelid K,Raphae¨ G.TreatinghypoxemicpatientswithSARS-COV-2pneumonia:Backtoapplied physiology.AnaesthCritCarePainMed(2020),https://doi.org/10.1016/j.accpm.2020.04.003

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