KCI V.A.C.Via Instructions For Use Manual page 195

Negative pressure wound therapy system
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INDHOLDSFORTEGNELSE
Advarsler og vigtig information til brugerne ................................................................................................................................... 196
Sikkerhedsinformation om V.A.C.® Terapi ............................................................................................................................................ 197
Indikationer ........................................................................................................................................................................................................... 197
Kontraindikationer ............................................................................................................................................................................................ 198
Advarsler ................................................................................................................................................................................................................. 198
Forholdsregler ..................................................................................................................................................................................................... 202
Overvejelser før brug af V.A.C.® Terapi i hjemmeplejen ............................................................................................................. 204
Vejledning i brug af V.A.C.Via™ Terapisystem .................................................................................................................................. 205
Terapienhedens komponenter ................................................................................................................................................................. 205
V.A.C.Via™ Terapisystemets forbindingsmateriale .................................................................................................................... 205
Sårrevision .............................................................................................................................................................................................................. 206
Anlæggelse af V.A.C.® GranuFoam™ Spiralforbinding ................................................................................................................. 208
Anlæggelse af V.A.C.® GranuFoam™ Spiralforbinding ved incisionshåndtering......................................................... 209
Klargøring af incisionsstedet ...................................................................................................................................................................... 209
Smertelindringsudstyr og dræn ............................................................................................................................................................... 209
Anlæggelse af forbinding på incisionsstedet .................................................................................................................................. 209
Anlæggelse af V.A.C.® Avanceret film .................................................................................................................................................... 210
Anlæggelse af SensaT.R.A.C.™ Pad........................................................................................................................................................... 211
Isætning af V.A.C.Via™ Beholderen .......................................................................................................................................................... 212
Igangsætning af behandlingen ................................................................................................................................................................ 213
Fejlsøgning af enheden ................................................................................................................................................................................. 214
Terapiens varighed ........................................................................................................................................................................................... 215
............................................................................................................................................................................ 215
Fjernelse af forbindingen ............................................................................................................................................................................. 215
Fjernelse og udskiftning af beholderen .............................................................................................................................................. 216
Lækager ................................................................................................................................................................................................................... 216
..................................................................................................................................................... 217
Alarmer .................................................................................................................................................................................................................... 217
Batteriopladning ................................................................................................................................................................................................ 219
Vigtige oplysninger, der skal diskuteres med patienterne ...................................................................................................... 220
Daglig brug ........................................................................................................................................................................................................... 220
Bortskaffelse af enheden .............................................................................................................................................................................. 220
Symbolforklaring .......................................................................................................................................................................................... 221
Specifikationer ..................................................................................................................................................................................................... 222
Kontaktoplysninger .......................................................................................................................................................................................... 224
195

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