Rufe talla

Baya ga haɗin gwiwar Apple tare da Johnson & Johnson don nazarin da nufin rage haɗarin bugun jini, kamfanin kuma ya yarda da FDA, ko Hukumar Abinci da Magunguna, cewa fasalin Gano Fibrillation (AFIb) akan Apple Watch a ƙarƙashin wasu yanayi ba ya aiki kamar yadda ya kamata.

Kamfanin ya ce Apple Watch ba zai iya tantancewa da kuma gargadi game da fibrillation baí Atrial fibrillation idan bugun zuciya ya wuce bugun 120 a minti daya. A wannan yanayin, agogon na iya gazawae 30 az60 % na lokuta, wanda ba shakka ba ne maras iyaka. Bisa ga Cibiyar Mayo Clinic, yawan ciwon zuciya a cikin AFib yana tsakanin 100 da 175 bugun minti daya, kuma a cikin binciken 2015, matsakaicin ƙwayar zuciya na marasa lafiya ya kasance a kusa da 109.

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An kuma tabbatar da ƙarancin amincin Apple Watch ta hanyar bincike kan rukunin marasa lafiya waɗanda aka yi wa tiyatar zuciya. Ya tabbatar da agogony kashedin fibrillation kawai ae 34 daga cikin 90 lokuta, don haka daidaito ya kasance kawai 41%. A wani binciken, agogon ya gaza 1/3 na lokaci. Daga karshe ko da Apple da kansa yayi kashedin cewa agogon baya faɗakarwa akai-akai kuma bazai faɗakar da ku game da fibrillation ba. Amma hanyar da aka gabatar da fasalin na iya ba da ra'ayi na ƙarya ita dogara.

Amma Apple yana cikin hadarin azabtarwa? Wataƙila akwai ƙungiyoyin da ke zargin kamfanin da tallan karya. Amma daga FDA A bayyane babu abin da ke cikin haɗari ga Apple. Me yasa? Domin Apple bai nemi takardar shedar wannan fasalin ba. Idan ya yi hakan zai sa a kashe shi ban da bukatar mai yawa kudi da watanni masu yawa na gwaje-gwajen da ba za a iya yin su a asirce ba, domin da kyar kayayyakin Apple ba za a iya boye su ba.

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