St.Jude Medical PRT-23 Mode D'emploi page 89

INNEhåLLSFÖRTECKNING
bESKRIVNING .......................................................................................................................................................................2
Portico™-klaff ................................................................................................................................................................2
Portico™ transfemoralt införingssystem ("införingssystemet") ..............................................................................2
Portico™ transfemoralt /alternativt ingångspåskjutningsystem ("påskjutningssystem") ....................................3
INDIKaTIONER ......................................................................................................................................................................3
KONTRaINDIKaTIONER ......................................................................................................................................................3
VaRNINGaR ..........................................................................................................................................................................4
FÖRSIKTIGhETSåTGÄRDER ..............................................................................................................................................4
Försiktighetsåtgärder före implantation ......................................................................................................................4
Försiktighetsåtgärder vid implantation .......................................................................................................................4
Försiktighetsåtgärder efter implantation .....................................................................................................................4
MR-SÄKERhET (MaGNETRESONaNS) .............................................................................................................................4
1,5 T radiofrekvensuppvärmning (RF) .........................................................................................................................4
3,0 T RF-uppvärmning ...................................................................................................................................................4
MR-artefakter ..................................................................................................................................................................4
Övrigt ..............................................................................................................................................................................5
MÖJLIGa bIVERKNINGaR ..................................................................................................................................................5
NÖDVÄNDIGa MaTERIaL/UTRUSTNING ...........................................................................................................................5
FÖRPaCKNING OCh FÖRVaRING ......................................................................................................................................5
Klaff .................................................................................................................................................................................5
Införingssystem/påskjutningssystem ..........................................................................................................................6
bRUKSaNVISNING ...............................................................................................................................................................6
hantering före implantation ..........................................................................................................................................6
Framtagning av klaffen ur den yttre förpackningen ..................................................................................................6
Framtagning av klaffen ur förvaringsbehållaren ........................................................................................................6
Sköljning av klaffen .......................................................................................................................................................6
Förberedelse av klaffen i påskjutningssystemet ........................................................................................................6
Påskjutning av klaffen till införingssystemet ............................................................................................................7
Implantation av klaffen ..................................................................................................................................................8
PaTIENTREGISTRERING .....................................................................................................................................................8
INDIVIDUaLISERING aV bEhaNDLINGEN ........................................................................................................................8
Patientrådgivningsinformation ....................................................................................................................................8
aVFaLLShaNTERING ..........................................................................................................................................................8
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