St.Jude Medical PRT-23 Mode D'emploi page 159

SADRŽAJ
OPIS .......................................................................................................................................................................................2
bioproteza Portico™ .....................................................................................................................................................2
Transfemoralni sustav za isporuku Portico™ ("Sustav za isporuku") ....................................................................2
Sustav za uvođenje s transfemoralnim/alternativnim pristupom ("Sustav za uvođenje") Portico™ ...................3
INDIKaCIJE ...........................................................................................................................................................................3
KONTRaINDIKaCIJE ............................................................................................................................................................3
UPOZORENJa .......................................................................................................................................................................4
MJERE OPREZa ...................................................................................................................................................................4
Mjere opreza prije ugradnje ..........................................................................................................................................4
Mjere opreza prilikom ugradnje ....................................................................................................................................4
Mjere opreza nakon ugradnje .......................................................................................................................................4
SIGURNOST SNIMaNJa MaGNETSKOM REZONaNCIJOM (MR) ...................................................................................4
Radiofrekvencija zagrijavanja 1,5 T (RF) .....................................................................................................................4
3,0 T RF zagrijavanja .....................................................................................................................................................4
MR artefakti ....................................................................................................................................................................4
MOGUĆE NUSPOJAVE ........................................................................................................................................................4
POTREbNI MaTERIJaLI/OPREMa ......................................................................................................................................5
PAKIRANJE I ČUVANJE .......................................................................................................................................................5
bioproteza ......................................................................................................................................................................5
Sustav za isporuku/sustav za uvođenje ......................................................................................................................5
UPUTE Za UPORabU ..........................................................................................................................................................5
Rukovanje prije ugradnje ..............................................................................................................................................6
Vađenje bioproteze iz vanjskog pakiranja ...................................................................................................................6
Vađenje bioproteze iz spremnika za čuvanje ..............................................................................................................6
Ispiranje bioproteze .......................................................................................................................................................6
Komprimiranje bioproteze u sustavu za uvođenje .....................................................................................................6
Uvođenje bioproteze u sustav za isporuku .................................................................................................................6
Ugradnja bioproteze ......................................................................................................................................................8
REGISTRaCIJa PaCIJENTa ................................................................................................................................................8
INDIVIDUALNI PRISTUP LIJEČENJU ..................................................................................................................................8
Informacije o savjetovanju pacijenta ...........................................................................................................................8
ODLaGaNJE .........................................................................................................................................................................8
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