St.Jude Medical PRT-23 Mode D'emploi page 81

INDhOLDSFORTEGNELSE
bESKRIVELSE ......................................................................................................................................................................2
Portico™ hjerteklap .......................................................................................................................................................2
Portico™ transfemoralt indføringssystem ("Indføringssystem") .............................................................................2
Portico™-påsætningssystem til transfemoral/alternativ adgang ("Påsætningssystem") .....................................3
INDIKaTIONER ......................................................................................................................................................................3
KONTRaINDIKaTIONER ......................................................................................................................................................3
aDVaRSLER .........................................................................................................................................................................4
FORhOLDSREGLER ............................................................................................................................................................4
Forholdsregler før implantation ...................................................................................................................................4
Forholdsregler ved implantation ..................................................................................................................................4
Forholdsregler efter implantation ................................................................................................................................4
SIKKERhED I FORbINDELSE MED MR-SKaNNING .........................................................................................................4
1,5 T radiofrekvens (RF) opvarmning. .........................................................................................................................4
3,0 T RF-opvarmning .....................................................................................................................................................4
MR-artefakter ..................................................................................................................................................................4
MULIGE bIVIRKNINGER ......................................................................................................................................................5
NøDVENDIGE MaTERIaLER/NøDVENDIGT UDSTyR ......................................................................................................5
EMbaLLERING OG OPbEVaRING .....................................................................................................................................5
hjerteklap ........................................................................................................................................................................5
Indføringssystem/påsætningssystem .........................................................................................................................6
bRUGSaNVISNING ...............................................................................................................................................................6
håndtering før implantation ..........................................................................................................................................6
Udtagning af klappen fra den udvendige emballage .................................................................................................6
Udtagning af klappen fra opbevaringsbeholderen .....................................................................................................6
Skylning af hjerteklappen .............................................................................................................................................6
Komprimering af klappen i påsætningssystemet ......................................................................................................6
Påsætning af klappen på indføringssystemet ...........................................................................................................7
Implantation af klappen .................................................................................................................................................8
PaTIENTREGISTRERING .....................................................................................................................................................8
INDIVIDUaLISERING aF bEhaNDLING .............................................................................................................................8
Oplysninger om patientrådgivning .............................................................................................................................8
bORTSKaFFELSE ................................................................................................................................................................8
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