Inkcazo eneenkcukacha
1.I-SARS-CoV-2 Antigen Rapid Test Kit (Uvavanyo lweMathe) yeyokusetyenziswa kuphela kwi-in vitro diagnostic.Olu vavanyo kufuneka lusetyenziselwe ukukhangela ii-antigens ze-SARS-CoV-2 kwisampulu ye-saliva yabantu.
2.I-SARS-CoV-2 Antigen Rapid Test Kit (Uvavanyo lwe-saliva) iya kubonisa kuphela ubukho be-SARS-CoV-2 kumzekelo kwaye ayifanelanga isetyenziswe njengeyona ndlela yokufumanisa usulelo lwe-SARS-CoV-2.
3. Ukuba iimpawu ziyaqhubeka, ngelixa iziphumo ezivela kwi-SARS-COV-2 Rapid Test ziziphumo ezingalunganga okanye ezingaphindi zisebenze, kucetyiswa ukuba kwenziwe isampulu yesigulane kwakhona kwiiyure ezimbalwa kamva.
4.Njengazo zonke iimvavanyo zokuxilonga, zonke iziphumo kufuneka zitolikwe kunye nolunye ulwazi lwekliniki olukhoyo kugqirha.
5.Ukuba isiphumo sovavanyo sibi kwaye iimpawu zeklinikhi ziqhubeka, uvavanyo olongezelelweyo usebenzisa ezinye iindlela zeklinikhi ziyacetyiswa.Isiphumo esibi asikuthinteli nangaliphi na ixesha ukuba nokwenzeka kosulelo lwe-SARS-CoV-2.
6. Iimpembelelo ezinokuthi zibe kho zezitofu zokugonya, unyango lwe-antiviral, i-antibiotics, i-chemotherapeutic okanye i-immunosuppressant iyeza azikavavanywa kuvavanyo.
7.Ngenxa yeyantlukwano ekhoyo phakathi kweendlela, kucetyiswa kakhulu ukuba, phambi kokutshintsha ukusuka kobunye ubuchwephesha ukuya kolandelayo, amaphononongo onxibelelaniso lweendlela enziwe ukuze afaneleke umahluko wethekhinoloji.Isivumelwano sekhulu leepesenti phakathi kweziphumo akufuneki silindeleke ngenxa yomahluko phakathi kobuchwepheshe.
8.Ukusebenza kusekwe kuphela ngeendidi zesampulu ezidweliswe kusetyenziso olucetyiweyo.Ezinye iintlobo zesampulu azikavavanywa kwaye akufuneki zisetyenziswe nolu vavanyo