UPDATE: Ropa Specimen Collection Tube Conservation Strategies

Iyo US Food and Drug Administration (FDA) inoziva kuti United States iri kusangana nekukanganisika kukuru mukupihwa kwemachubhu akati wandei eropa (kudhonza ropa) nekuda kwekuwedzera kwekudiwa panguva yeCCIDID-19 yehutano hweveruzhinji uye matambudziko ekupa kwevatengesi. .Iyo FDA iri kuwedzera rondedzero yekushomeka kwemidziyo yekurapa kuti ibatanidze ese machubhu ekuunganidza eropa.Iyo FDA yakambopa tsamba kune vehutano nevashandi vemurabhoritari munaChikumi10, 2021, nezve kushomeka kwemachubhu e-sodium citrate yeropa remuenzaniso (chiedza chebhuruu pamusoro).

Recommendations

Iyo FDA inokurudzira vatapi vehutano, vatungamiriri vemarabhoritari, phlebotomists, uye vamwe vashandi vanofunga zvinotevera nzira dzekuchengetedza kudzikisira kuunganidzwa kweropa kushandiswa kwechubhu uye kuchengetedza kunaka uye kuchengetedzeka kwekuchengeta varwere:

• Ita zvinotorwa ropa chete zvichionekwa sezvinofanirwa kurapwa. Deredza ongororo pakushanya kweutano uye kuongororwa kweallergy kune idzo chete dzakanangana nenzvimbo dzakanangana dzechirwere kana kwadzichachinja marapirwo emurwere.

• Bvisa zvakapetwa kaviri bvunzo kuti udzivise kutorwa ropa kusiri madikanwa.

• Rega kuedza kakawanda kana kuwedzera nguva pakati pebvunzo pose pazvinogoneka.

• Funga nezvekuwedzera kuongororwa kana kugovera sampuli pakati pemadhipatimendi emurabhoritari kana zvienzaniso zvakambounganidzwa zviripo.

• Kana uchida chubhu yekurasa, shandisa rudzi rwechubhu ine huwandu hukuru huripo panzvimbo yako.

• Funga nezvepfungwa yekuongororwa kwekuchengetedza isingade kushandisa machubhu ekuunganidza eropa (lateral flow tests).

FDA Zviito

Musi wa19 Ndira, 2022, FDA yakagadziridza rondedzero yekushomeka kwemidziyo yekurapa kuti ibatanidze ese machubhu ekuunganidza eropa (makodhi ezvigadzirwa GIM neJKA).Chikamu 506J cheFederal Food, Drug, and Cosmetic Act (FD&C Act) chinoda kuti FDA ichengetedze ruzhinji-rinowanikwa, runyorwa rwezvishandiso izvo FDA yakaronga kuve iri kushomeka.

Kare, pa:

• Musi wa10 Chikumi, 2021, FDA yakawedzera sodium citrate (yebhuruu pamusoro) machubhu pasi pemakodhi echigadzirwa akafanana (GIM neJKA) kurondedzero yekushomeka kwemidziyo yekurapa panguva yeCOVID-19 yehutano hweveruzhinji.

• Chikunguru 22, 2021, FDA yakapa Emergency Use Authorization kuna Becton Dickinson yeimwe sodium citrate blood specimen (light blue top) machubhu ekuunganidza anoshandiswa kuunganidza, kutakura, uye kuchengeta masampuli eropa kuti aongorore coagulation kuti zvinyatso zivikanwa nekurapa coagulopathy muvarwere. nevanozivikanwa kana vanofungidzirwa kuti COVID-19.

Iyo FDA inoenderera mberi nekutarisa mamiriro aripo kuti ibatsire kuona kuti kuongororwa ropa kunoramba kuripo kune varwere uko kuongororwa kunodiwa.Iyo FDA ichazivisa veruzhinji kana ruzivo rutsva rwakakosha rwuripo.

 

 


Nguva yekutumira: Aug-12-2022