{"id":150,"date":"2020-09-21T08:37:03","date_gmt":"2020-09-21T05:37:03","guid":{"rendered":"https:\/\/atbs.bk-ninja.com\/suga\/?p=150"},"modified":"2021-12-13T21:04:49","modified_gmt":"2021-12-13T18:04:49","slug":"covid-19-tedavisinde-kullanilmakta-olan-antiviral-ilaclar","status":"publish","type":"post","link":"https:\/\/www.klimik.org.tr\/koronavirus\/covid-19-tedavisinde-kullanilmakta-olan-antiviral-ilaclar\/","title":{"rendered":"KL\u0130M\u0130K Derne\u011fi&#8217;nden Eri\u015fkinlerde COVID-19\u2019un Antiviral Tedavisi \u0130\u00e7in \u00d6neriler-1"},"content":{"rendered":"<div id=\"accordions-2840\" class=\"accordions-2840 accordions\" data-accordions={&quot;lazyLoad&quot;:true,&quot;id&quot;:&quot;2840&quot;,&quot;event&quot;:&quot;click&quot;,&quot;collapsible&quot;:&quot;true&quot;,&quot;heightStyle&quot;:&quot;content&quot;,&quot;animateStyle&quot;:&quot;swing&quot;,&quot;animateDelay&quot;:1000,&quot;navigation&quot;:true,&quot;active&quot;:999,&quot;expandedOther&quot;:&quot;no&quot;}>\n                <div id=\"accordions-lazy-2840\" class=\"accordions-lazy\" accordionsId=\"2840\">\n                    <\/div>\n\n    <div class=\"items\"  style=\"display:none\" >\n    \n            <div post_id=\"2840\" itemcount=\"0\"  header_id=\"header-1600776263290\" id=\"header-1600776263290\" style=\"\" class=\"accordions-head head1600776263290 border-none\" toggle-text=\"\" main-text=\"\u00d6ZET\">\n                                    <span id=\"accordion-icons-1600776263290\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600776263290\" class=\"accordions-head-title\">\u00d6ZET<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600776263290 \">\n                <p>COVID-19 genellikle hafif-orta seyirli olmakla birlikte, olgular\u0131n yakla\u015f\u0131k %10-15\u2019inde a\u011f\u0131r ve %1 kadar\u0131nda \u00e7ok a\u011f\u0131r veya \u00f6l\u00fcmc\u00fcl seyredebilmektedir.\u00a0 Bu nedenlerle etkili bir antiviral tedavisinin bulunmas\u0131 t\u00fcm bilim d\u00fcnyas\u0131n\u0131n en b\u00fcy\u00fck \u00f6nceli\u011fidir. Bu derlemede, COVID-19\u2019un antiviral tedavisinde yeniden konumland\u0131r\u0131larak t\u00fcm d\u00fcnyada yayg\u0131n olarak kullan\u0131lan ila\u00e7lar\u0131n ba\u015f\u0131nda gelen hidroksiklorokin, favipiravir, remdesivir ve lopinavir-ritonavirin tedavideki etkinli\u011fi ve g\u00fcvenilirli\u011fi bu konuda yay\u0131mlanm\u0131\u015f \u00e7al\u0131\u015fmalar analiz edilerek de\u011ferlendirilmi\u015ftir.<\/p>\n<p>G\u00fcncel in vitro\/in vivo ve randomize kontroll\u00fc klinik \u00e7al\u0131\u015fmalar, ayaktan veya yatan, hafif\/orta\/a\u011f\u0131r seyirli COVID-19 olgular\u0131n\u0131n tedavisinde hidroksiklorokinin etkili olmad\u0131\u011f\u0131n\u0131 g\u00f6stermi\u015ftir. Hidroksiklorokin, aksini bildiren yeni randomize kontroll\u00fc klinik \u00e7al\u0131\u015fma sonu\u00e7lar\u0131 olmad\u0131k\u00e7a COVID-19\u2019un asemptomatik, hafif, orta, a\u011f\u0131r formlar\u0131n\u0131n tedavisinde veya profilaksisinde kullan\u0131lmamal\u0131d\u0131r.\u00a0 Hidroksiklorokin, \u00f6zellikle QT\u2019yi uzatan azitromisin gibi di\u011fer ila\u00e7larla birlikte kullan\u0131ld\u0131\u011f\u0131nda hayat\u0131 tehdit edebilecek kardiyotoksik istenmeyen etkilere neden olabilir.<\/p>\n<p>Favipiravirin COVID-19 tedavisindeki etkisini ara\u015ft\u0131ran az say\u0131da hasta i\u00e7eren 3 randomize kontroll\u00fc klinik \u00e7al\u0131\u015fmada, bu ajan\u0131n viral klirense ve\/veya baz\u0131 klinik sonu\u00e7lara olumlu etkilerinin olabilece\u011fi bildirilmi\u015ftir. Bu nedenle, favipiravirin \u00f6zellikle pn\u00f6monili ve\/veya riskli COVID-19 olgular\u0131n\u0131n tedavisinde kullan\u0131labilece\u011fi d\u00fc\u015f\u00fcn\u00fclmektedir. Ancak devam etmekte olan randomize kontroll\u00fc klinik \u00e7al\u0131\u015fmalar\u0131n sonu\u00e7lar\u0131 yak\u0131ndan izlenmeli, optimal dozunun ve tedavi s\u00fcresinin belirlenebilmesi i\u00e7in in vitro ve ek klinik \u00e7al\u0131\u015fmalar yap\u0131lmal\u0131d\u0131r. Favipiravirin COVID-19 tedavisinde veya di\u011fer indikasyonlarla kullan\u0131m\u0131 s\u0131ras\u0131nda ciddi istenmeyen etkileri tan\u0131mlanmam\u0131\u015ft\u0131r.<\/p>\n<p>Remdesivir SARS-CoV-2\u2019ye kar\u015f\u0131 in vitro ve in vivo hayvan deneylerinde etkili bulunmu\u015f, 1647 COVID-19 hastas\u0131n\u0131 i\u00e7eren iki randomize kontroll\u00fc \u00e7al\u0131\u015fmada (RK\u00c7\u2019de) klinik sonu\u00e7lara baz\u0131 olumlu etkileri oldu\u011fu g\u00f6sterilmi\u015ftir. Bu nedenlerle remdesivirin orta\/a\u011f\u0131r seyirli COVID-19 pn\u00f6monilerinde kullan\u0131labilece\u011fi d\u00fc\u015f\u00fcn\u00fclmektedir. Yeni klinik \u00e7al\u0131\u015fma sonu\u00e7lar\u0131na g\u00f6re kullan\u0131m indikasyonlar\u0131 tekrar de\u011ferlendirilmelidir.\u00a0 Remdesivirin COVID-19 tedavisinde kullan\u0131m\u0131 s\u0131ras\u0131nda geli\u015fen ciddi istenmeyen etki bildirilmemi\u015ftir.<\/p>\n<p>COVID-19 tedavisinde lopinavir\/ritonavirin etkinli\u011fini ara\u015ft\u0131ran az say\u0131daki RK\u00c7\u2019nin sonu\u00e7lar\u0131 birbiriyle uyumsuzdur, 86 hasta i\u00e7eren bir RK\u00c7\u2019de bu ajan\u0131n etkisiz oldu\u011fu, 199 hasta i\u00e7eren bir RK\u00c7\u2019de belirgin olmasa da baz\u0131 olumlu etkilerinin olabilece\u011fi, birinde ise ribavirin ve interferonla kombine kullan\u0131lmas\u0131 halinde olumlu etkilerinin oldu\u011fu bildirilmi\u015ftir. Bu klinik \u00e7al\u0131\u015fmalar\u0131n genellikle az olgu say\u0131l\u0131 ve plasebo kontroll\u00fc olmas\u0131ndan hareketle ek \u00e7al\u0131\u015fmalar\u0131n gerekli oldu\u011fu d\u00fc\u015f\u00fcn\u00fclmektedir.<\/p>\n<p>Lopinavir\/ritonavirin SARS-CoV-2 \u00fczerine etkisini ara\u015ft\u0131ran in vitro \u00e7al\u0131\u015fma say\u0131s\u0131 azd\u0131r, sonu\u00e7lar yetersizdir, ek \u00e7al\u0131\u015fmalar gereklidir. Di\u011fer ila\u00e7lar\u0131n olas\u0131 yan etkiler nedeniyle kullan\u0131lamad\u0131\u011f\u0131 orta a\u011f\u0131r seyirli COVID-19 ge\u00e7irmekte olan gebe hastalarda Lpn\/rtnvr bir se\u00e7enek olabilir. Lopinavir\/ritonavirin COVID-19 tedavisinde, \u00f6zellikle kombinasyon rejiminin bir par\u00e7as\u0131 olarak klinik \u00e7al\u0131\u015fmalar i\u00e7inde yer alacak \u015fekilde kullan\u0131lmas\u0131 d\u00fc\u015f\u00fcn\u00fclebilir.<\/p>\n<p>Salg\u0131n\u0131n ba\u015flamas\u0131n\u0131n \u00fczerinden 8 ay ge\u00e7mi\u015f olmas\u0131na ra\u011fmen halen COVID-19\u2019a kar\u015f\u0131 etkili oldu\u011fu kesin olarak g\u00f6sterilmi\u015f bir antiviral tedavi yoktur. COVID-19\u2019a etkili bir antiviral bulmak amac\u0131yla yap\u0131lan klinik \u00e7al\u0131\u015fmalarda en \u00e7ok incelenen ve tedavide yeniden konumland\u0131r\u0131larak (repurposing) kullan\u0131lan ajanlar, etkili tedavi bulunmas\u0131 konusunda zaman kayb\u0131na neden olmu\u015f olabilir.\u00a0 SARS-CoV-2\u2019ye \u00f6zg\u00fc yeni antivirallere acilen gereksinim vard\u0131r. Mevcut kaynaklar\u0131n yeni ajanlar\u0131n ara\u015ft\u0131r\u0131lmas\u0131na, geli\u015ftirilmesine ve \u00e7al\u0131\u015f\u0131lmas\u0131na ayr\u0131lmas\u0131 en ak\u0131lc\u0131 yakla\u015f\u0131m olacakt\u0131r.<\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"1\"  header_id=\"header-1600776266850\" id=\"header-1600776266850\" style=\"\" class=\"accordions-head head1600776266850 border-none\" toggle-text=\"\" main-text=\"G\u0130R\u0130\u015e\">\n                                    <span id=\"accordion-icons-1600776266850\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600776266850\" class=\"accordions-head-title\">G\u0130R\u0130\u015e<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600776266850 \">\n                <p>Salg\u0131n\u0131n ba\u015flamas\u0131n\u0131n \u00fczerinden 8 ay ge\u00e7mesine ra\u011fmen halen COVID-19\u2019a kar\u015f\u0131 etkinli\u011fi kesin olarak g\u00f6sterilmi\u015f bir anti-viral tedavi yoktur ve tedavinin esas\u0131n\u0131 optimal bir destek tedavisi olu\u015fturmaktad\u0131r. COVID-19 genellikle hafif-orta seyirli bir hastal\u0131k olmakla birlikte, olgular\u0131n yakla\u015f\u0131k %10-15\u2019inde a\u011f\u0131r seyredebilmektedir. %0.6-1 aras\u0131nda oldu\u011fu hesaplanan infeksiyon \u00f6l\u00fcm oran\u0131yla, bu oran\u0131n <%0.1 oldu\u011fu gripten en az 5-10 kat daha \u00f6l\u00fcmc\u00fcl bir infeksiyon hastal\u0131\u011f\u0131d\u0131r (Mallapaty, S., 2020). Bu nedenlerle etkili bir anti-viral tedavisinin bulunmas\u0131 t\u00fcm bilim d\u00fcnyas\u0131n\u0131n en b\u00fcy\u00fck \u00f6nceli\u011fidir ve halen bu konuda \u00e7ok say\u0131da klinik ara\u015ft\u0131rma devam etmekte, klinik \u00e7al\u0131\u015fma kay\u0131t sistemlerine kaydedilmi\u015f toplam 1303 \u00e7al\u0131\u015fmada 381 farkl\u0131 ajan\/m\u00fcdahale ara\u015ft\u0131r\u0131lmakta, tek ba\u015f\u0131na hidroksiklorokin bu \u00e7al\u0131\u015fmalar\u0131n 113\u2019\u00fcnde denenmektedir. Bu \u00e7al\u0131\u015fmalar\u0131n %8\u2019i bitmi\u015f, %54\u2019\u00fc devam etmektedir (Hojer Karise, A.P., 2020, Malik, S., 2020).\n\nSonu\u00e7lanm\u0131\u015f olan \u00e7al\u0131\u015fmalardan elde edilen veriler, herhangi bir antiviralin t\u00fcm COVID-19 hastalar\u0131n\u0131n tedavisinde \u00f6nerilebilmesi i\u00e7in yeterli kan\u0131t sa\u011flayamamaktad\u0131r. Normalde yeni bir viral hastal\u0131\u011fa, in vitro laboratuvar testleri, hayvan deneyleri ve Faz I, II, III klinik \u00e7al\u0131\u015fmalardan olu\u015fan, uzun y\u0131llar s\u00fcren ara\u015ft\u0131rmalarla tedavi bulunabilmektedir. Ancak COVID-19 gibi a\u011f\u0131r seyirli, \u00f6l\u00fcmc\u00fcl hastal\u0131klarda, \u201cyeniden konumland\u0131rma\u201d (repurposing) denilen ve insanlarda daha \u00f6nce ba\u015fka hastal\u0131klar\u0131n tedavisi i\u00e7in ruhsatland\u0131r\u0131lm\u0131\u015f, bu indikasyonlarda yayg\u0131n bir \u015fekilde kullan\u0131lm\u0131\u015f, g\u00fcvenli oldu\u011fu g\u00f6sterilmi\u015f, in vitro olarak etken mikroorganizmaya (\u00f6rn.SARS-CoV\u2019ye) etkili oldu\u011fu belirlenmi\u015f ajanlar, yukar\u0131da belirtilmi\u015f \u00e7al\u0131\u015fma a\u015famalar\u0131n\u0131 ge\u00e7meden\u00a0 kullan\u0131labilmektedir. Bu derlemede, COVID-19\u2019un antiviral tedavisinde yeniden konumland\u0131r\u0131larak \u00a0t\u00fcm d\u00fcnyada yayg\u0131n olarak kullan\u0131lan ila\u00e7lar\u0131n ba\u015f\u0131nda gelen hidroksiklorokin, favipiravir, remdesivir ve lopinavir-ritonavirin\u00a0 bu hastal\u0131\u011f\u0131n tedavisindeki etkinli\u011fi ve g\u00fcvenilirli\u011fi, \u00a018 Eyl\u00fcl 2020 tarihine kadar bu konuda yay\u0131mlanm\u0131\u015f ba\u015fta RK\u00c7\u2019ler olmak \u00fczere klinik \u00e7al\u0131\u015fmalar g\u00f6zden ge\u00e7irilerek,\u00a0 ek olarak bu ajanlar\u0131n SARS-CoV-2\u2019ye kar\u015f\u0131 olan etkinlikleri konusunda yap\u0131lm\u0131\u015f in vitro\u00a0 veya in vivo \u00e7al\u0131\u015fmalar da analiz edilerek de\u011ferlendirilmi\u015ftir.\n<\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"2\"  header_id=\"header-1600776373704\" id=\"header-1600776373704\" style=\"\" class=\"accordions-head head1600776373704 border-none\" toggle-text=\"\" main-text=\"H\u0130DROKS\u0130KLOROK\u0130N\">\n                                    <span id=\"accordion-icons-1600776373704\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600776373704\" class=\"accordions-head-title\">H\u0130DROKS\u0130KLOROK\u0130N<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600776373704 \">\n                <p>Klorokin ve hidroksiklorokin, 50 y\u0131ldan beri s\u0131tma tedavisinde kullan\u0131lan aminokinolinlerdir. Antimalaryal etkilerinin yan\u0131nda immunomod\u00fclat\u00f6r etkileri de bulunmas\u0131 nedeniyle, SLE, romatoid artrit gibi otoimmun hastal\u0131klar\u0131n tedavisinde de uzun y\u0131llardan beri kullan\u0131lmaktad\u0131r. Her ikisi de immun aktivasyonda rol\u00fc olan belli h\u00fccresel fonksiyonlar\u0131 ve molek\u00fcler yolaklar\u0131, k\u0131smen h\u00fccrelerin endozom\/fogozomlar\u0131nda birikip lokal pH\u2019y\u0131 y\u00fckselterek inhibe edebilir (Schrezenmeie, E., 2020). COVID-19 salg\u0131n\u0131 ba\u015flad\u0131\u011f\u0131nda hidroksiklorokinin bu mekanizmalarla, h\u00fccre i\u00e7ine endozomla al\u0131nan SARS-CoV-2\u2019ye de etkili olabilece\u011fi d\u00fc\u015f\u00fcn\u00fclm\u00fc\u015ft\u00fcr. \u00a0Ek olarak\u00a0\u00a0 COVID-19 salg\u0131n\u0131n\u0131n ba\u015flang\u0131c\u0131nda b\u00f6brek kaynakl\u0131 Vero E6 h\u00fccrelerinde yap\u0131lan in vitro \u00e7al\u0131\u015fmalarda, klorokin ve hidroksiklorkinin SARS-CoV-2\u2019ye kar\u015f\u0131 olduk\u00e7a etkili oldu\u011fu da g\u00f6sterilmi\u015ftir (Liu, J., 2020; Wang, M., 2020; Lu, C.C., 2020; Yao, X., 2020; Barlow, A., 2019). Hem bu veriler, hem de daha \u00f6nce farkl\u0131 indikasyonlarla yayg\u0131n bir \u015fekilde kullan\u0131lm\u0131\u015f ve insanlarda g\u00fcvenli\u011fi g\u00f6sterilmi\u015f olmas\u0131 nedeniyle hidroksiklorokin, \u00f6l\u00fcmc\u00fcl bir hastal\u0131k olan ve etkili bir tedavisi bulunmayan COVID-19 hastal\u0131\u011f\u0131n\u0131n tedavisi amac\u0131yla \u00fclkemiz dahil olmak \u00fczere t\u00fcm d\u00fcnyada yayg\u0131n bir \u015fekilde kullan\u0131lm\u0131\u015ft\u0131r ve halen bir \u00e7ok \u00fclkede kullan\u0131m\u0131na devam edilmektedir. Ancak salg\u0131n\u0131n ba\u015flang\u0131c\u0131ndan itibaren ge\u00e7en 8 ayl\u0131k s\u00fcre\u00e7te hidroksikorokin\/klorokonin SARS-CoV-2\u2019ye etkisi, COVID-19 hastal\u0131\u011f\u0131n\u0131n tedavisindeki yeri ve COVID-19 hastalar\u0131nda kullan\u0131l\u0131rken kar\u015f\u0131la\u015f\u0131lan, \u00f6zellikle kardiyotoksik istenmeyen etkileri konusunda gerek hakemli dergilerde gerek preprint platformlarda \u00e7ok say\u0131da klinik \u00e7al\u0131\u015fma yay\u0131mlanm\u0131\u015f ve hidroksiklorokinin COVID-19 tedavisindeki yerini yeniden g\u00f6zden ge\u00e7irmeyi zorunlu k\u0131lm\u0131\u015ft\u0131r.<\/p>\n<p><strong><u>Hidroksiklorokin\/Klorokinin SARS-CoV-2\u2019ye Etkisini Ara\u015ft\u0131ran Yeni in vitro ve Hayvan Deneyleri Sonu\u00e7lar\u0131<\/u><\/strong><\/p>\n<p>Klorokin ve hidroksiklorokinin SARS-CoV-2\u2019ye kar\u015f\u0131 esas antiviral etkinli\u011finin, endozomal pH\u2019y\u0131 y\u00fckselterek, virusun h\u00fccreye giri\u015fini inhibe etmesinden kaynakland\u0131\u011f\u0131 d\u00fc\u015f\u00fcn\u00fclmekteydi. Ancak ge\u00e7mi\u015fte yap\u0131lm\u0131\u015f \u00e7al\u0131\u015fmalarda insan koronaviruslar\u0131n\u0131n farkl\u0131 h\u00fccre tiplerinde pH\u2019ya ba\u011f\u0131ml\u0131 olan ve olmayan farkl\u0131 giri\u015f mekanizmalar\u0131 kullanabildi\u011fi g\u00f6sterilmi\u015fti (Shirato, K., 2018).<\/p>\n<p>Bu ajanlar\u0131n SARS-CoV-2\u2019ye kar\u015f\u0131 antiviral etkisini g\u00f6steren \u00e7al\u0131\u015fmalar b\u00f6brek kaynakl\u0131 Vero h\u00fccrelerinde yap\u0131lm\u0131\u015ft\u0131.\u00a0 COVID-19 salg\u0131n\u0131 ba\u015flad\u0131ktan sonra yap\u0131lan bir \u00e7al\u0131\u015fmada, SARS-CoV-2\u2019nin Vero h\u00fccrelerine girmesine endozomal pH\u2019ya ba\u011f\u0131ml\u0131 bir proteaz olan katepsinin arac\u0131l\u0131k etti\u011fi, \u00e7ok d\u00fc\u015f\u00fck seviyede katepsin i\u00e7eren havayolu epitel h\u00fccrelerine girmesine ise pH\u2019dan ba\u011f\u0131ms\u0131z, plazma membran\u0131ndaki serin proteaz TMPRSS2\u2019nin arac\u0131l\u0131k etti\u011fi g\u00f6sterildi (Hoffmann, M., 2020).\u00a0 Bu verilerle klorokin ve hidroksiklorokinin insan hava yolu h\u00fccrelerinde etkili olmayabilece\u011fini d\u00fc\u015f\u00fcnen ara\u015ft\u0131r\u0131c\u0131lar\u0131n k\u0131sa s\u00fcre \u00f6nce yay\u0131mlad\u0131\u011f\u0131 bir di\u011fer in vitro \u00e7al\u0131\u015fmada da klorokin ve hidroksiklorokin, TMPRSS2 negatif olan Vero h\u00fccrelerinde SARS-CoV-2 spike\u2019yla h\u00fccreye giri\u015fi inhibe edebilirken, TMPRSS-2 pozitif akci\u011fer h\u00fccre dizisi olan Calu-3 h\u00fccrelerinde ve TMPRSS2 eklenmi\u015f Vero h\u00fccrelerinde bu giri\u015fi inhibe edememi\u015ftir. Ayn\u0131 \u00e7al\u0131\u015fmada bununla uyumlu olacak \u015fekilde klorokin, Vero h\u00fccrelerinde SARS-CoV-2 infeksiyonunu etkili bir \u015fekilde engelleyebilirken, TMPRSS2 eklenmi\u015f Vero h\u00fccrelerinde ve TMPRSS-2 pozitif akci\u011fer h\u00fccre dizisi olan Calu-3 h\u00fccrelerinde SARS-CoV-2 infeksiyonununu engelleyememi\u015ftir. Bu bulgularla, klorokin ve hidroksiklorokinin hedefinde olan viral aktivasyon yola\u011f\u0131n\u0131n, solunum yolu h\u00fccrelerinde \u00e7al\u0131\u015fmad\u0131\u011f\u0131 ve dolay\u0131s\u0131yla \u00a0bu ajanlar\u0131n \u00a0hastal\u0131\u011f\u0131n tedavisinde veya \u00f6nlenmesinde etkili olmas\u0131n\u0131n pek m\u00fcmk\u00fcn olamayaca\u011f\u0131 sonucuna var\u0131lm\u0131\u015f\u00a0 (Hoffmann, H., 2020), bu bulgular ba\u015fka \u00e7al\u0131\u015fmalarda da do\u011frulanm\u0131\u015ft\u0131r (Maisonnasse, P., 2020)\u00a0 Ek olarak mevcut klinik kullan\u0131mdaki dozlarda elde edilen serbest plazma hidroksiklorokin konsantrasyonunun belirlenmi\u015f EC50 seviyelerinin \u00e7ok alt\u0131nda kald\u0131\u011f\u0131 ve bu dozlarda SARS-CoV-2\u2019ye kar\u015f\u0131 antiviral bir etkinlik g\u00f6stermesinin m\u00fcmk\u00fcn olmayaca\u011f\u0131 bildirilmi\u015ftir (Fan, \u00a0J., 2020).<\/p>\n<p>Son olarak makaklarda yap\u0131lan bir \u00e7al\u0131\u015fmada, SARS-CoV-2 infeksiyonundan \u00f6nce veya sonra, erken veya ge\u00e7 d\u00f6nem ba\u015flanan d\u00fc\u015f\u00fck veya y\u00fcksek doz, tek ba\u015f\u0131na veya azitromisinle kombine hidroksiklorokinin, tedavi verilmemi\u015f hayvanlarla kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131nda, kanda ve akci\u011ferlerde y\u00fcksek konsantrasyonlara ula\u015fmas\u0131na ra\u011fmen, solunum yollar\u0131nda viral klirense, klinik ve radyolojik iyile\u015fmeye etkisi g\u00f6sterilememi\u015ftir. Tek ba\u015f\u0131na veya azitromisinle birlikte hidroksiklorokin verilen hayvanlarda ALT seviyeleri belirgin olarak daha y\u00fcksek saptanm\u0131\u015f, hidroksiklorokin tedavisi lenfopeniyi ve BT\u2019de pulmoner lezyonlar\u0131 da engelleyememi\u015ftir. Sonu\u00e7lar\u0131n daha \u00f6nce ba\u015fka viral infeksiyonlarda da bildirildi\u011fi gibi in vitro klasik testlerin sonu\u00e7lar\u0131yla in vivo deneylerin uyumsuz olabilece\u011fini g\u00f6sterdi\u011fi, bu durumun klorokine in vitro olarak duyarl\u0131yken klinik \u00e7al\u0131\u015fmalar\u0131nda etkisiz bulunan grip, dang ve \u00e7ikungunyayla benzerlik g\u00f6sterdi\u011fi ifade edilmi\u015ftir (Maisonnasse, P., 2020).<\/p>\n<p><strong><u>COVID-19 Tedavisinde Hidroksiklorokin\/Klorokinin Etkisini Ara\u015ft\u0131ran Kontrol Gruplu Klinik Ara\u015ft\u0131rmalar\u0131n Sonu\u00e7lar\u0131<\/u><\/strong><\/p>\n<p><strong><em>Randomize Kontroll\u00fc Klinik \u00c7al\u0131\u015fmalar\u0131n Sonu\u00e7lar\u0131<\/em><\/strong><\/p>\n<p>Hastal\u0131klar\u0131n tedavisinde etkili olan ajanlar\u0131 belirlemede RK\u00c7\u2019ler, en g\u00fc\u00e7l\u00fc kan\u0131tlar\u0131 sa\u011flayan \u00e7al\u0131\u015fmalard\u0131r. Hidroksiklorokin\/klorokinin COVID-19\u2019da etkinli\u011fini ara\u015ft\u0131ran ve sonu\u00e7lar\u0131 bug\u00fcne kadar a\u00e7\u0131klanm\u0131\u015f olan toplam 10 RK\u00c7\u2019ye ula\u015f\u0131lm\u0131\u015ft\u0131r (Horby, P.W.,\u00a0 2020; Mitja\u0300, O., 2020; Cavalcanti, A.B., 2020; Skipper, C.P., 2020; Chen, J., 2020; Tang, W., 2020; Mitja\u0300, O., 2020; Chen, Z., 2020; Huang, M., 2020; Chen, L., 2020). Bu 10 \u00e7al\u0131\u015fman\u0131n 6652 hasta i\u00e7eren\u00a0 yedisinde (Horby, P.W.,\u00a0 2020; Mitja\u0300, O., 2020; Cavalcanti, A.B., 2020; Skipper, C.P., 2020; Chen, J., 2020; Tang, W., 2020; Mitja\u0300, O., 2020) [be\u015fi hakemli dergilerde yay\u0131mlanm\u0131\u015f (Mitja\u0300, O., 2020; Cavalcanti, A.B., 2020; Skipper, C.P., 2020; Chen, J., 2020; Tang, W., 2020), ikisi preprint olarak\u00a0 bildirilmi\u015f (Horby, P.W.,\u00a0 2020; 2020; Mitja\u0300, O., 2020)] bu ajanlar\u0131n viral klirense ve\/veya hastal\u0131\u011f\u0131n klinik sonu\u00e7lar\u0131na (iyile\u015fme taburcu olma, \u00f6l\u00fcm oranlar\u0131 gibi) herhangi bir olumlu etkisinin olmad\u0131\u011f\u0131 bildirilirken, 178 hasta i\u00e7eren \u00fc\u00e7\u00fcnde (Chen, Z., 2020; Huang, M., 2020; Chen, L., 2020) [biri hakemli dergilerde yay\u0131mlanm\u0131\u015f (Chen, Z., 2020), ikisi preprint olarak\u00a0 bildirilmi\u015f (Huang, M., 2020; Chen, L., 2020)] viral klirense ve\/veya hastal\u0131\u011f\u0131n klinik sonu\u00e7lar\u0131na (iyile\u015fme taburcu olma, \u00f6l\u00fcm oranlar\u0131 gibi) baz\u0131 olumlu etkilerinin oldu\u011fu bildirilmi\u015ftir (<span style=\"color: #ff0000;\"><a style=\"color: #ff0000;\" href=\"https:\/\/www.klimik.org.tr\/koronavirus\/wp-content\/uploads\/2020\/09\/Supplementary-material_Tablo_1.pdf\" target=\"_blank\" rel=\"noopener\">Tablo 1<\/a>)<\/span>. Olumlu etki bildiren bu \u00fc\u00e7 \u00e7al\u0131\u015fma hem \u00e7ok az say\u0131da hasta i\u00e7ermesi, hem baz\u0131 y\u00f6ntemsel sorunlar bar\u0131nd\u0131rmas\u0131 (kotrol grubunda yer alan hastalar\u0131n da antiviral kullanmas\u0131 gibi) hem de genellikle hakemli dergilerde yay\u0131mlanmam\u0131\u015f olmas\u0131 nedeniyle kan\u0131t g\u00fcc\u00fc zay\u0131f \u00e7al\u0131\u015fmalarken, olumlu etki bildirmeyenlerde kontrol grubunda antiviral kullan\u0131lmam\u0131\u015f olmas\u0131, vaka say\u0131lar\u0131n\u0131n y\u00fcksekli\u011fi ve genellikle etki fakt\u00f6r\u00fc y\u00fcksek hakemli dergilerde yay\u0131mlanm\u0131\u015f olmalar\u0131 nedeniyle kan\u0131t g\u00fcc\u00fc daha y\u00fcksektir. \u00c7al\u0131\u015fmalar\u0131n detaylar\u0131 <a href=\"https:\/\/www.klimik.org.tr\/koronavirus\/wp-content\/uploads\/2020\/09\/Supplementary-material_Tablo_2.pdf\" target=\"_blank\" rel=\"noopener\"><span style=\"color: #ff0000;\">Tablo 2<\/span><\/a>\u2019de verilmi\u015ftir.<\/p>\n<p>K\u0131sa s\u00fcre \u00f6nce preprint olarak sonu\u00e7lar\u0131 a\u00e7\u0131klanan bir \u00e7al\u0131\u015fmada \u00a0COVID-19\u2019da hidroksiklorokin\/klorokinle yap\u0131lm\u0131\u015f, tamamlanm\u0131\u015f, b\u0131rak\u0131lm\u0131\u015f veya devam etmekte olan toplam 26 RK\u00c7\u2019nin (16\u2019s\u0131 yay\u0131mlanmam\u0131\u015f, be\u015fi yay\u0131mlanm\u0131\u015f, be\u015fi preprint) h\u0131zl\u0131 meta-analizi yap\u0131lm\u0131\u015f; hidroksiklorokin (24 \u00e7al\u0131\u015fma) alan 3020 hastan\u0131n 499\u2019unun (%16.5), kontrol grubunda yer alan 4639 hastan\u0131nsa 874\u2019\u00fcn\u00fcn (%18.8) hayat\u0131n\u0131 kaybetti\u011fi belirlenmi\u015f ve\u00a0 \u00a0birle\u015fik OR 1.08 (%95 CI, 0.99-1.18, p = 0.07) olarak hesaplanarak \u00a0COVID-19 hastalar\u0131nda hidroksiklorokin ve klorokinin s\u00fcrvi \u00fczerine olumlu bir etkisi olmad\u0131\u011f\u0131 sonucuna ula\u015f\u0131lm\u0131\u015ft\u0131r (Axfors C., 2020).<\/p>\n<p><strong><em>G\u00f6zlemsel Klinik \u00c7al\u0131\u015fmalar\u0131n Sonu\u00e7lar\u0131 <\/em><\/strong><\/p>\n<p>Hastal\u0131klar\u0131n tedavisinde etkili olan ajanlar\u0131 belirlemede g\u00f6zlemsel \u00e7al\u0131\u015fmalar, RK\u00c7\u2019lere g\u00f6re daha zay\u0131f kan\u0131tlar sa\u011flayabilmektedir. Hidroksiklorokin\/klorokinin COVID-19\u2019da etkinli\u011fini kontrol grubuyla kar\u015f\u0131la\u015ft\u0131rarak ara\u015ft\u0131ran ve sonu\u00e7lar\u0131 bug\u00fcne kadar a\u00e7\u0131klanm\u0131\u015f olan toplam 14 g\u00f6zlemsel \u00e7al\u0131\u015fmaya ula\u015f\u0131lm\u0131\u015ft\u0131r \u00a0(Mahe\u0301vas, M., 2020;\u00a0 Geleris, J., 2020; Rosenberg, E.S., 2020; Ip, A., 2020; Sbidian, E., 2020; Yu, B., 2020; Huang, 2020; Membrillo, F.J., 2020; Esper, R.B., 2020; Lagier, J.C., 2020; Gu\u00e9rin, V., 2020; Arshad, A., 2020; Catteau, L., 2020; Castelnuovo, A.D., 2020). Bu 14 \u00e7al\u0131\u015fman\u0131n 10 141 hastay\u0131 i\u00e7eren be\u015finde (Mahe\u0301vas, M., 2020;\u00a0 Geleris, J., 2020; Rosenberg, E.S., 2020; Ip, A., 2020; Sbidian, E., 2020) [d\u00f6rd\u00fc hakemli dergilerde yay\u0131mlanm\u0131\u015f (Mahe\u0301vas, M., 2020;\u00a0 Geleris, J., 2020; Rosenberg, E.S., 2020; Ip, A., 2020), biri preprint olarak bildirilmi\u015f<sup> (<\/sup>Sbidian, E., 2020)] hidroksiklorokin\/klorokinin viral klirense ve\/veya hastal\u0131\u011f\u0131n klinik sonu\u00e7lar\u0131na (iyile\u015fme taburcu olma, \u00f6l\u00fcm oranlar\u0131 gibi) herhangi bir olumlu etkisinin olmad\u0131\u011f\u0131 bildirilirken, 19 635 hastay\u0131 i\u00e7eren dokuzunda (Yu, B., 2020; Huang, 2020; Membrillo, F.J., 2020; Esper, R.B., 2020; Lagier, J.C., 2020; Gu\u00e9rin, V., 2020; Arshad, A., 2020; Catteau, L., 2020; Castelnuovo, A.D., 2020) [\u00fc\u00e7\u00fc hakemli dergilerde yay\u0131mlanm\u0131\u015f (Arshad, A., 2020; Catteau, L., 2020; Castelnuovo, A.D., 2020), alt\u0131s\u0131 preprint olarak bildirilmi\u015f (Yu, B., 2020; Huang, 2020; Membrillo, F.J., 2020; Esper, R.B., 2020; Lagier, J.C., 2020; Gu\u00e9rin, V., 2020)] viral klirense ve\/veya hastal\u0131\u011f\u0131n klinik sonu\u00e7lar\u0131na (iyile\u015fme taburcu olma, \u00f6l\u00fcm oranlar\u0131 gibi) baz\u0131 olumlu etkilerinin oldu\u011fu bildirilmi\u015f (<a href=\"https:\/\/www.klimik.org.tr\/koronavirus\/wp-content\/uploads\/2020\/09\/Supplementary-material_Tablo_1.pdf\" target=\"_blank\" rel=\"noopener\"><span style=\"color: #ff0000;\">Tablo 1<\/span><\/a>). \u00c7al\u0131\u015fmalar\u0131n detaylar\u0131 <a href=\"https:\/\/www.klimik.org.tr\/koronavirus\/wp-content\/uploads\/2020\/09\/Supplementary-material_Tablo_2.pdf\" target=\"_blank\" rel=\"noopener\"><span style=\"color: #ff0000;\">Tablo 2<\/span><\/a>\u2019de verilmi\u015ftir.<\/p>\n<p>Kan\u0131t seviyesi daha y\u00fcksek olan randomize kontroll\u00fc klinik \u00e7al\u0131\u015fmalardan elde edilen veriler, ayaktan veya yatan,hafif\/orta\/a\u011f\u0131r seyirli COVID-19 olgular\u0131nda hidroksiklorokinin etkili olmad\u0131\u011f\u0131n\u0131 d\u00fc\u015f\u00fcnd\u00fcrmektedir. \u00a0Bu nedenle, olumlu etki bildirmeyen, \u00e7ok hasta say\u0131s\u0131 i\u00e7eren RK\u00c7 sonu\u00e7lar\u0131n\u0131n a\u00e7\u0131klanmas\u0131yla salg\u0131n\u0131n ba\u015flang\u0131c\u0131nda COVID-19 tedavisi i\u00e7in hidroksiklorokine acil kullan\u0131m onay\u0131 veren ABD, Fransa gibi bir \u00e7ok \u00fclke bu onay\u0131 geri \u00e7ekmi\u015ftir. 20 Haziran 2020\u2019de, ABD\/NIH COVID-19 tedavisinde hidroksiklorokinin etkisini ara\u015ft\u0131ran \u00e7al\u0131\u015fmas\u0131n\u0131 ara analizlerde etkisiz \u00e7\u0131kt\u0131\u011f\u0131 i\u00e7in sonland\u0131rm\u0131\u015ft\u0131r (National Institute of Health, 2020). \u00a0 Son olarak 4 Temmuz 2020\u2019de DS\u00d6 de organize etti\u011fi SOLIDARITY \u00e7al\u0131\u015fmalar\u0131ndan hidroksiklorokin ve standard tedavinin kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131 \u00e7al\u0131\u015fmay\u0131, \u00f6n sonu\u00e7larda hastaneye yat\u0131r\u0131lm\u0131\u015f COVID-19 olgular\u0131nda hidroksiklorokinin, standard tedaviyle kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131nda herhangi bir mortalite azalmas\u0131na yol a\u00e7mad\u0131\u011f\u0131 g\u00f6r\u00fcld\u00fc\u011f\u00fc i\u00e7in sonland\u0131rm\u0131\u015ft\u0131r. Bu \u00e7al\u0131\u015fmada hidroksiklorokin alan grupta mortalitenin daha y\u00fcksek oldu\u011funu g\u00f6steren kan\u0131tlar bulunmad\u0131\u011f\u0131, ancak g\u00fcvenlik sorunuyla ilgili baz\u0131 i\u015faretlerin oldu\u011fu bildirmi\u015ftir (World Health Organisation, 2020).<\/p>\n<p><strong><em>Asemptomatik COVID-19 Hastalar\u0131nda Hidroksiklorokin Kullan\u0131m\u0131 <\/em><\/strong><\/p>\n<p>Asemptomatik olgularda hidroksiklorokin kullan\u0131m\u0131n\u0131 ara\u015ft\u0131ran sadece bir adet RK\u00c7\u2019ye ula\u015f\u0131lm\u0131\u015ft\u0131r. Bu \u00e7al\u0131\u015fmada, semptomu olmayan, temas sonras\u0131 SARS-CoV-2 pozitifli\u011fi belirlenmi\u015f\u00a0 toplam 314 hastan\u0131n, hidroksiklorokin verilmi\u015f 158\u2019inde 35 (%22) semptomatik COVID-19 geli\u015firken, kontrol grubunda yer alan tedavi verilmemi\u015f 156 hastan\u0131n 21\u2019inde (%18.6) semptomatik COVID-19 geli\u015fmi\u015f (RR 0.96 %95GA: 0.58-1.58), hidroksiklorokin asemptomatik PCR pozitif hastalarda da etkisiz bulunmu\u015ftur (Mitj\u00e0, O., 2020) Ek olarak yukar\u0131da da belirtilen g\u00fcncel in vitro veriler, hidroksiklorokinin akci\u011fer h\u00fccrelerine SARS-CoV-2 giri\u015fini inhibe etmedi\u011fini g\u00f6stermi\u015ftir, dolay\u0131s\u0131yla salg\u0131n ba\u015flang\u0131c\u0131nda hidroksiklorokinin in vitro olarak SARS-CoV-2\u2019ye etkili oldu\u011fu g\u00f6sterildi\u011fi i\u00e7in ak\u0131lc\u0131 olabilece\u011fi d\u00fc\u015f\u00fcn\u00fclen asemptomatik olgularda hidroksiklorokin kullan\u0131m\u0131 g\u00fcncel bilimsel verilerle dayanaks\u0131z hale gelmi\u015ftir. Mevcut bilimsel kan\u0131tlar asemptomatik olgularda rutin hidroksiklorokin kullan\u0131m\u0131n\u0131 desteklememektedir.<\/p>\n<p><strong><em>Temas \u00d6ncesi ve Temas Sonras\u0131 COVID-19 Profilaksisinde Hidroksiklorokin Kullan\u0131m\u0131<\/em> <\/strong><\/p>\n<p>Hidroksiklorokinin COVID-19 hastal\u0131\u011f\u0131n\u0131n temas \u00f6ncesi veya sonras\u0131nda profilaktik kullan\u0131m\u0131 konusunda sonu\u00e7lar\u0131 a\u00e7\u0131klanm\u0131\u015f iki adet RK\u00c7 vard\u0131r (Mitj\u00e0, O., 2020; Boulware, D.R., 2020). \u00a0Bu \u00e7al\u0131\u015fmalarda hidroksiklorokinin temas sonras\u0131 profilakside etkili olmad\u0131\u011f\u0131 bildirilmi\u015ftir. Ayr\u0131ca yukar\u0131da belirtilen ve hidroksiklorokinin solunum yolu epitelinde SARS-CoV-2 infeksiyonunu engellemedi\u011fini g\u00f6steren in vitro \u00e7al\u0131\u015fma da profilaktik kullan\u0131m\u0131n ak\u0131lc\u0131 olmad\u0131\u011f\u0131n\u0131 d\u00fc\u015f\u00fcnd\u00fcrmektedir. Mevcut bilimsel kan\u0131tlar COVID-19 hastal\u0131\u011f\u0131ndan korunmada rutin profilaktik hidroksiklorokin kullan\u0131m\u0131n\u0131 desteklememektedir.<\/p>\n<p><strong><u>Hidroksiklorokinin COVID -19 Tedavisinde Kullan\u0131m\u0131 S\u0131ras\u0131nda G\u00f6zlenen \u0130stenmeyen Etkileri<\/u><\/strong><\/p>\n<p>Hidroksiklorokinin COVID-19 d\u0131\u015f\u0131nda kullan\u0131ld\u0131\u011f\u0131 d\u00f6nemlerde de kardiyotoksik etkilerinin <em>olabilece\u011fi<\/em> bilinmekteydi. Bu etki, myositlerdeki hERG potasyum kanallar\u0131n\u0131 inhibe ederek, ventrik\u00fcler repolarizasyonu uzatmas\u0131na ba\u011fl\u0131d\u0131r. Bilindi\u011fi gibi QT uzamas\u0131 olanlarda, \u00f6zellikle cQT >500 ms olanlarda Torsades-de-Pointes (TdP) riski 2-3 kat daha y\u00fcksektir (<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?sort=date&term=Stevenson+A&cauthor_id=32817375\">Stevenson<\/a>, \u00a0A.,\u00a02020). DS\u00d6\u2019n\u00fcn \u00a0\u00a0130 \u00fclkeden toplam 21 milyon istenmeyen ila\u00e7 etkisi bildirimini i\u00e7eren farmakovijilans veritaban\u0131nda (VigiBase) hidroksiklorokin, azitromisin veya bunlar\u0131n kombinasyonlar\u0131 i\u00e7in \u00a0COVID-19 \u00f6ncesi d\u00f6nemde bildirilmi\u015f\u00a0 kardiyotoksik etkilerinin incelendi\u011fi bir \u00e7al\u0131\u015fmada, hem hidroksiklorokin hem azitromisin i\u00e7in QT uzamas\u0131 ve\/veya TdP dahil ventrik\u00fcler ta\u015fikardi bildiriminin di\u011fer ilcalardan belirgin olarak daha y\u00fcksek oldu\u011fu \u00a0, kombinasyonda bu riskin daha da artt\u0131\u011f\u0131,\u00a0 bu bildirimlerden baz\u0131lar\u0131n\u0131n \u00f6l\u00fcmle sonu\u00e7land\u0131\u011f\u0131,\u00a0 ek olarak hidroksiklorokinin \u00a0ileti hastal\u0131klar\u0131yla (AV ve dal bloklar\u0131) ve kalp yetmezli\u011fiyle \u00a0de ili\u015fkili oldu\u011fu g\u00f6r\u00fclm\u00fc\u015ft\u00fcr (Nguyen, L.S., 2020).<\/p>\n<p>COVID-19 hastalar\u0131nda hidroksiklorokin\/klorokin kardiyotoksisitesini ara\u015ft\u0131ran \u00e7al\u0131\u015fmalarda, bu ilac\u0131n uygunland\u0131\u011f\u0131 hastalar\u0131n %11-23\u2019\u00fcnde >500 ms\u2019den fazla olmak \u00fczere QT uzamas\u0131, %0-d\u00f6rd\u00fcnde ventrik\u00fcler aritmi ve bir olguda TdP geli\u015fti\u011fi, azitromisinle kombinasyonda bu riskin daha y\u00fcksek oldu\u011fu bildirilmi\u015ftir (<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?sort=date&term=Stevenson+A&cauthor_id=32817375\">Stevenson<\/a>, A.,\u00a02020).<\/p>\n<p>28 Mart 2020 tarihinde COVID-19\u2019da hidroksiklorokin ve klorokin i\u00e7in acil kullan\u0131m onay\u0131 (EUA) yay\u0131mlayan FDA, 24 Nisan 2020\u2019de farmakovijilans ajans\u0131na bu ila\u00e7larla ilgili bildirilen \u00f6l\u00fcm dahil kardiyotoksik istenmeyen etkiler nedeniyle, bu ila\u00e7lar\u0131n hastane d\u0131\u015f\u0131nda kullan\u0131lmamas\u0131n\u0131 da \u00f6nererek bir g\u00fcvenlik uyar\u0131s\u0131 yay\u0131mlad\u0131 ve kendisine yap\u0131lm\u0131\u015f bu etkilerin sonu\u00e7lar\u0131n\u0131 daha sonra payla\u015faca\u011f\u0131n\u0131 bildirdi.\u00a0 FDA, COVID-19 tedavisinde hidroksiklorokinin etkinli\u011fini ara\u015ft\u0131ran \u00e7ok olgu say\u0131l\u0131 RK\u00c7 sonu\u00e7lar\u0131nda etkinlik belirlenmedi\u011fi i\u00e7in 15 Haziran 2020\u2019de hidroksiklorokinin EUA\u2019s\u0131n\u0131 geri \u00e7ekmi\u015ftir. 15 Temmuz 2020\u2019de ise COVID-19 tedavisi veya profilaksisi amac\u0131yla hidroksiklorokin\/ klorokin kullan\u0131lan hastalarda geli\u015fen ve farmakovijilans ajans\u0131na bildirilen veya literat\u00fcrde yay\u0131mlanm\u0131\u015f istenmeyen ila\u00e7 etkilerinin analizini yay\u0131mlam\u0131\u015ft\u0131r: Buna g\u00f6re bu konuda toplam 385 bildirim olup (hidroksiklorokin i\u00e7in 347, klorokin i\u00e7in 38) ve da\u011f\u0131l\u0131mlar\u0131 \u015fu \u015fekildedir (Food and Drug Administration, 2020):<\/p>\n<ul>\n<li>109 kardiyak ciddi istenmeyen etki\n<ul>\n<li>80 (%73) QT uzamas\u0131<\/li>\n<li>4 (%4) Torsades de Pointes (TdP)<\/li>\n<li>92 (%84) olgu QT\u2019yi uzatan ba\u015fka ila\u00e7lar da kullanmakta<\/li>\n<li>14 (%13) ventrik\u00fcler aritmi, ventrik\u00fcler ta\u015fikardi veya ventrik\u00fcler fibrilasyon<\/li>\n<li>25 (%23)\u2019i hayat\u0131n\u0131 kaybetmi\u015f, \u00f6l\u00fcmlerin istenmeyen etkiye ba\u011fl\u0131 olup olmad\u0131\u011f\u0131 belirtilmemi\u015f, 22\u2019sinde QT\u2019yi uzatan ba\u015fka ila\u00e7lar\u0131n da oldu\u011fu bildirilmi\u015f<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<ul>\n<li>113 nonkardiyak ciddi istenmeyen etki\n<ul>\n<li>%59 hepatit\/karaci\u011fer enzim veya bilirubin y\u00fcksekli\u011fi<\/li>\n<li>%5 Akut b\u00f6brek hasar\u0131\/yetmezli\u011fi<\/li>\n<li>%4 methemoglobinemi: 2\u2019si \u00f6l\u00fcmle sonu\u00e7lanan<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>K\u0131sa s\u00fcre \u00f6nce yay\u0131mlanm\u0131\u015f bir meta-analizde de COVID-19 hastalar\u0131nda hidroksiklorokin+azitromisinin birlikte kullan\u0131m\u0131n\u0131n mortalite oran\u0131nda art\u0131\u015fla (Relatif Risk: 1.27, %95 CI: 1.04-1.54, n=7 \u00e7al\u0131\u015fma) ba\u011flant\u0131l\u0131 oldu\u011fu, tek ba\u015f\u0131na hidroksiklorokin kullan\u0131m\u0131nda ise mortalite art\u0131\u015f\u0131 g\u00f6r\u00fclmedi\u011fi (Relatif Risk: 0.83, %95 CI: 0.65-1.06, n=17 \u00e7al\u0131\u015fma) bildirilmi\u015ftir (Fiolet, T., 2020).<\/p>\n<p><strong><em>Sonu\u00e7<\/em><\/strong><\/p>\n<p><strong><em>G<\/em><\/strong><strong><em>\u00fcncel in vitro\/in vivo \u00e7al\u0131\u015fmalar ve <\/em><\/strong><strong><em>randomize kontroll\u00fc klinik \u00e7al\u0131\u015fmalar, <\/em><\/strong><strong><em>ayaktan veya yatan, <\/em><\/strong><strong><em>hafif\/orta\/a\u011f\u0131r seyirli COVID-19 olgular\u0131n\u0131n tedavisinde <\/em><\/strong><strong><em>hidroksiklorokinin etkili olmad\u0131\u011f\u0131n\u0131 g\u00f6stermi\u015ftir. Hidroksiklorokin aksini bildiren yeni RK\u00c7 sonu\u00e7lar\u0131 olmad\u0131k\u00e7a COVID-19\u2019un asemptomatik, hafif, orta, a\u011f\u0131r formlar\u0131n\u0131n tedavisinde veya profilaksisinde kullan\u0131lmamal\u0131d\u0131r.\u00a0\u00a0 <\/em><\/strong><\/p>\n<p><strong><em>Hidroksiklorokin kullan\u0131m\u0131n\u0131n hayat\u0131 tehdit edebilecek kardiyotoksik istenmeyen etkileri oldu\u011fu, bu etkilerin \u00f6zellikle QT\u2019yi uzatan azitromisin gibi di\u011fer ila\u00e7larla birlikte kullan\u0131ld\u0131\u011f\u0131nda belirgin olarak artt\u0131\u011f\u0131 s\u00f6ylenebilir<\/em><\/strong>.<\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"3\"  header_id=\"header-1600777320887\" id=\"header-1600777320887\" style=\"\" class=\"accordions-head head1600777320887 border-none\" toggle-text=\"\" main-text=\"COVID-19\u2019UN ANT\u0130V\u0130R\u0130AL TEDAV\u0130S\u0130NDE RNA SENTEZ\u0130 \u0130NH\u0130B\u0130T\u00d6RLER\u0130\">\n                                    <span id=\"accordion-icons-1600777320887\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600777320887\" class=\"accordions-head-title\">COVID-19\u2019UN ANT\u0130V\u0130R\u0130AL TEDAV\u0130S\u0130NDE RNA SENTEZ\u0130 \u0130NH\u0130B\u0130T\u00d6RLER\u0130<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600777320887 \">\n                <p>Genellikle n\u00fckleotid veya n\u00fckleozid analo\u011fu olan bu ila\u00e7lar RNA\u2019ya ba\u011f\u0131ml\u0131 RNA polimeraz (RdRp) taraf\u0131ndan substrat olarak alg\u0131lanarak ya RNA zincirinin erken sonlanmas\u0131na, ya hatal\u0131 genomik veya mRNA sentezlenmesine ya da e\u015fde\u011feri nativ n\u00fckleotidlerin sitoplazmadaki seviyelerini t\u00fcketip RdRp\u2019nin uygun \u00e7al\u0131\u015fma ortam\u0131n\u0131n bozulmas\u0131na yol a\u00e7arak antiviral etki g\u00f6sterir. (Valle, C., 2020). T\u00fcm d\u00fcnyada COVID-19 tedavisinde yayg\u0131n olarak kullan\u0131lan favipiravir ve remdesivir bu grup ila\u00e7lardand\u0131r.<\/p>\n<p>SARS-CoV-2\u2019nin nsp12\u2019si olan RdRp hem genomik, hem de mRNA sentezini yapar. Koronavirus RdRp kompleksi di\u011fer viral RdRp\u2019den en az 10 kat daha aktiftir, hem \u00e7ok y\u00fcksek n\u00fckleotid dahil etme hem de y\u00fcksek hata oran\u0131na sahiptir. Bu \u00f6zellikleriyle SARS-CoV\u2019un a\u015fil topu\u011fu olabilece\u011fi dolay\u0131s\u0131yla n\u00fckleozid analoglar\u0131n\u0131n COVID-19 tedavisinde \u00fcmit verici adaylar oldu\u011fu d\u00fc\u015f\u00fcn\u00fclmektedir. Ancak n\u00fckleozid\/n\u00fckleotid analoglar\u0131n\u0131n koronaviruslarda kullan\u0131m\u0131nda \u00f6nemli bir sorun vard\u0131r: Koronaviruslarda ekson\u00fckleaz ad\u0131 verilen (nsp14 ExoN) ve RNA\u2019da do\u011frulama okumas\u0131 yaparak hatal\u0131 k\u0131s\u0131mlar\u0131 uzakla\u015ft\u0131ran bir enzim bulunmaktad\u0131r. In vitro \u00e7al\u0131\u015fmalarda SARS-CoV-2 polimeraz\u0131n\u0131n replikasyon s\u0131ras\u0131nda ribavirini zincire soktu\u011funu, ancak sonras\u0131nda nsp14ExoN\u2019un yapt\u0131\u011f\u0131 kontrol s\u0131ras\u0131nda ribavirini saptayarak zincirden \u00e7\u0131kard\u0131\u011f\u0131 g\u00f6sterilmi\u015ftir. Bu nedenle SARS-CoV-2\u2019ye etki edecek bir n\u00fckleotid\/n\u00fckleozid analo\u011funun bu ekson\u00fckleazlara diren\u00e7li olmas\u0131 etkinlik a\u00e7\u0131s\u0131ndan olduk\u00e7a \u00f6nemlidir (Shannon, A., 2020).<\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"4\"  header_id=\"header-1600777387000\" id=\"header-1600777387000\" style=\"\" class=\"accordions-head head1600777387000 border-none\" toggle-text=\"\" main-text=\"FAV\u0130P\u0130RAV\u0130R\">\n                                    <span id=\"accordion-icons-1600777387000\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600777387000\" class=\"accordions-head-title\">FAV\u0130P\u0130RAV\u0130R<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600777387000 \">\n                <p>Bir guanozin p\u00fcrin n\u00fckleotid analo\u011fu olan favipiravir (T-705; 6-floro-3-hidroksi-2- pyrazinkarboksamid), h\u00fccre i\u00e7inde fosforibozilasyona u\u011frayarak favipiravir ribofuranosil-5B-trifosfat (Favipiravir- RTP) olarak adland\u0131r\u0131lan aktif formuna d\u00f6n\u00fc\u015f\u00fcr. Favipiravir-RTP RdRp\u2019n\u0131n potent bir inhibit\u00f6r\u00fcd\u00fcr, ancak hem DNA\u2019ya ba\u011f\u0131ml\u0131 RNA polimeraza hem de DNA polimeraza etkisizdir, bu nedenle sadece RNA viruslar\u0131na etkili olup, DNA viruslar\u0131na ve insan h\u00fccrelerine etki g\u00f6stermez.\u00a0 Sadece oral formu olan favipiravir, a\u011f\u0131zdan al\u0131nd\u0131ktan sora karaci\u011ferde aldehid oksidazla (AO) metabolize edilir, olu\u015fan inaktif metaboliti T-705M1 b\u00f6breklerden at\u0131l\u0131r.<\/p>\n<p>Kararl\u0131 kan d\u00fczeyine ula\u015ft\u0131\u011f\u0131nda (1-2 g\u00fcn s\u00fcrer) daha g\u00fc\u00e7l\u00fc antiviral etki g\u00f6sterdi\u011fi i\u00e7in erken ba\u015flanan tedavinin daha uygun olabilece\u011fi d\u00fc\u015f\u00fcn\u00fclmektedir.<\/p>\n<p>RdRp\u2019nin katalitik b\u00f6lgesi farkl\u0131 RNA viruslar\u0131 aras\u0131nda korunmu\u015f oldu\u011fu i\u00e7in in vitro \u00e7al\u0131\u015fmalarda influenza, arenaviruslar, bunyaviruslar ve flaviviruslar gibi bir\u00e7ok RNA virusuna kar\u015f\u0131 geni\u015f antiviral etkinli\u011fi g\u00f6sterilmi\u015ftir. Japonya\u2019da epidemik yeni influenza su\u015flar\u0131n\u0131n tedavisinde onayl\u0131d\u0131r. Ebola tedavisinde etkili olabilece\u011fiyle ilgili yay\u0131nlar bulunmaktad\u0131r<\/p>\n<p>\u0130ndikasyonlu oldu\u011fu grip tedavisinde \u00f6nerilen dozu birinci g\u00fcn: 1600 mg x 2; 2-5. g\u00fcn: 600 mg x 2\/g\u00fcn \u015feklindedir. 2014 Afrika Ebola salg\u0131n\u0131 s\u0131ras\u0131nda yap\u0131lan bir \u00e7al\u0131\u015fmada birinci g\u00fcn: 2400 mg -2400mg-1200 mg; 2-7. (veya 10.) g\u00fcn: 1200 mg x 2\/g\u00fcn \u015feklinde kullan\u0131lm\u0131\u015ft\u0131r. COVID-19 i\u00e7in kullan\u0131ld\u0131\u011f\u0131 \u00e7al\u0131\u015fmalarda en s\u0131k; birinci g\u00fcn 1800 mg x 2, 2-14. g\u00fcn 800mg x 2 \/g\u00fcn \u015feklinde kullan\u0131lm\u0131\u015f olmakla birlikte, birinci g\u00fcn: 1600 mg x 2; 2-5. (veya 14.) g\u00fcn: 2 x 600 mg\/g\u00fcn, \u015feklinde de kullan\u0131lm\u0131\u015ft\u0131r. \u00dclkemizde de en s\u0131k gripte belirtildi\u011fi \u015fekilde kullan\u0131lm\u0131\u015ft\u0131r<\/p>\n<p>(<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?sort=date&term=Madelain+V&cauthor_id=26798032\">Madelain<\/a>, V.,\u00a02016; Du, Y.X., 2020; Furuta, Y., 2020; Coomes, E.A., 2020).<\/p>\n<p>Tayland\u2019da favipiravir kullan\u0131lm\u0131\u015f 63 do\u011frulanm\u0131\u015f COVID-19 hastas\u0131nda yedinci g\u00fcndeki klinik iyile\u015fmeye olumsuz etki eden fakt\u00f6rler aras\u0131nda y\u00fckleme dozunun <45 mg\/kg\/g\u00fcn olmas\u0131 da yer alm\u0131\u015ft\u0131r. Bu nedenle COVID-19 tedavisinde favipiravirin uygun y\u00fckleme ve idame dozlar\u0131n\u0131n belirlenmesi, tedavi ba\u015far\u0131s\u0131n\u0131 etkileyebilece\u011fi i\u00e7in olduk\u00e7a \u00f6nemlidir Rattanaumpawan, P., 2020). Hayvanlarda embriyonik letalite ve teratojenik oldu\u011fu g\u00f6steilmi\u015ftir, gebede kullan\u0131lmamal\u0131d\u0131r, ayr\u0131ca s\u00fcte de ge\u00e7er, emzirilmeye ara verilmelidir. Kullanan erkeklerin de yedi g\u00fcn s\u00fcreyle korunmas\u0131 \u00f6nerilmektedir. <a href=\"https:\/\/www.klimik.org.tr\/koronavirus\/wp-content\/uploads\/2020\/09\/Supplementary-material_Tablo_3.pdf\" target=\"_blank\" rel=\"noopener\"><span style=\"color: #ff0000;\">Tablo 3<\/span><\/a>\u2019de favipiravirin istenmeyen etkileri ve di\u011fer ila\u00e7larla etkile\u015fimleri verilmi\u015ftir.<\/p>\n<p><strong>\u00a0<\/strong>Favipiravirin Vero E6 h\u00fccrelerinde yap\u0131lm\u0131\u015f d\u00f6rt in vitro \u00e7al\u0131\u015fmas\u0131nda SARS-CoV-2\u2019yi inhibe etti\u011fi EC50 de\u011ferleri y\u00fcksek olup, s\u0131ras\u0131yla 61.88 \u03bcM, >100 \u03bcM, >100 \u03bcM ve 207 \u03bcM \u015feklinde saptanm\u0131\u015ft\u0131r. Bu durumun klinik \u00f6nemi, mevcut dozlarla virusu inhibe edebilecek seviyelere ula\u015f\u0131lamamas\u0131 \u00f6nemli soru i\u015faretleri olu\u015fturmaktad\u0131r (Choy, K.T., 2020; Wang, M., 2020; Lou, Y., 2020). Ancak k\u0131sa s\u00fcre \u00f6nce yap\u0131lm\u0131\u015f bir di\u011fer in vitro \u00e7al\u0131\u015fmada favipiravirin, RNA zincirinin terminasyonuna, RNA sentezinin yava\u015flat\u0131lmas\u0131na ve letal mutageneze yol a\u00e7arak antiviral etki g\u00f6sterdi\u011fi g\u00f6r\u00fclm\u00fc\u015f, bu \u00e7al\u0131\u015fmada favipiravirli ortamdaki viruslarda mutasyon say\u0131s\u0131n\u0131n \u00fc\u00e7 kat daha y\u00fcksek oldu\u011fu ve favipiravir kullan\u0131m\u0131n\u0131n infekte h\u00fccrede C-U ve G-A de\u011fi\u015fikliklerini ind\u00fckledi\u011fi \u00a0belirlenmi\u015ftir (Shannon, A., 2020).<\/p>\n<p><strong><u>COVID-19\u2019un Antiviral Tedavisinde Favipiravir Kullan\u0131m\u0131 Konusunda Yap\u0131lm\u0131\u015f Klinik \u00c7al\u0131\u015fmalar<\/u><\/strong><\/p>\n<p><strong><em>Randomize Kontroll\u00fc Klinik \u00c7al\u0131\u015fmalar <\/em><\/strong><\/p>\n<p>\u00c7in\u2019de 236 do\u011frulanm\u0131\u015f COVID-19 pn\u00f6monisi olan hastada yap\u0131lm\u0131\u015f standard tedaviye ek olarak favipiravir veya arbidol\u00fcn kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131 RK\u00c7\u2019de, favipiravir grubunda a\u011f\u0131r olmayan olgularda yedinci g\u00fcnde iyile\u015fme oran\u0131 belirgin olarak daha y\u00fcksek, \u00f6ks\u00fcr\u00fc\u011f\u00fcn azalmas\u0131 ve ate\u015f d\u00fc\u015fme s\u00fcresi de belirgin olarak daha k\u0131sa bulunmu\u015ftur. Gruplar aras\u0131nda mortalite, oksijen deste\u011fi veya mekanik ventilasyon gereksinim oranlar\u0131n\u0131n farkl\u0131 olmad\u0131\u011f\u0131, Favipiravir grubunda esas olarak hiper\u00fcrisemi (%17) olmak \u00fczere istenmeyen ila\u00e7 etkilerinin daha y\u00fcksek oranda g\u00f6r\u00fcld\u00fc\u011f\u00fc bildirilmi\u015ftir (Chen, C., 2020).<\/p>\n<p>Yine \u00c7in\u2019de 29 do\u011frulanm\u0131\u015f COVID-19 tan\u0131s\u0131 olan hastalarda yap\u0131lm\u0131\u015f bir di\u011fer RK\u00c7\u2019de, standard olarak lopinavir\/ritonavir, darunavir\/kobisistat veya arbidol+ interferon-\u03b1 inhalasyonu alan hastalar favipiravir (10 hasta, 1600 veya 2200 mg y\u00fckleme, 3X600 mg\/g\u00fcn idame, <14 g\u00fcn) veya baloksavir (10 hasta) veya sadece standard tedavi alacak \u015fekilde randomize edilmi\u015f. Ond\u00f6rd\u00fcnc\u00fc g\u00fcnde viral klirens (s\u0131ras\u0131yla %70, %77, %100) ve klinik iyile\u015fme s\u00fcresi (s\u0131ras\u0131yla 14, 14 ve 15 g\u00fcn) gruplar aras\u0131nda farkl\u0131 bulunmam\u0131\u015ft\u0131r. Bu \u00e7al\u0131\u015fmada yap\u0131lm\u0131\u015f in vitro analizlerde favipiravirin 100 mM\u2019de bile antiviral etkisinin olmad\u0131\u011f\u0131 g\u00f6r\u00fclm\u00fc\u015f, d\u00f6rd\u00fcnc\u00fc ve yedinci g\u00fcnde favipiravirin plazma konsantrasyonu bu \u00e7al\u0131\u015fmada belirlenmi\u015f EC50 (>15.7 g\/mL) de\u011ferinden d\u00fc\u015f\u00fck saptanm\u0131\u015f ve mevcut dozlarda antiviral etki g\u00f6stermesinin m\u00fcmk\u00fcn olmad\u0131\u011f\u0131 belirtilmi\u015f (Lou, Y., 2020). Ancak favipiravirde, ana ilac\u0131n plazma seviyesi de\u011fil, aktif metabolitin h\u00fccre i\u00e7i konsantrasyonunun antiviral etkinlikle ba\u011flant\u0131l\u0131 oldu\u011fu ve viral dinamik modellemelerde, viral replikasyonu etkileyen ila\u00e7lar\u0131n, viremi pikinden sonra ba\u015flanmas\u0131 halinde, ilac\u0131n etkinli\u011finden ba\u011f\u0131ms\u0131z olarak s\u0131n\u0131rl\u0131 bir etkisinin olaca\u011f\u0131 g\u00f6sterilmi\u015f oldu\u011fundan farkl\u0131 dozlar ve erken ba\u015flaman\u0131n etkili olabilece\u011fi belirtilmi\u015ftir (Madelain, V., 2020).<\/p>\n<p>Rusya\u2019da, orta \u015fiddetli do\u011frulanm\u0131\u015f 60 COVID-19 olgusunda yap\u0131lm\u0131\u015f RK\u00c7\u2019de standard tedavi alan hastalar (%75 hidroksiklorokin) ya d\u00fc\u015f\u00fck doz favipiravir [birinci g\u00fcn, 1600 mg x2, 2-14.g\u00fcn 600mg x2\/g\u00fcn (20 hasta)], ya y\u00fcksek doz favipiravir [birinci g\u00fcn 1800 mg x2, 2-14. g\u00fcn 800 mg X2 (20 hasta)] ya da standard bak\u0131m (20 hasta) alacak \u015fekilde randomize edilmi\u015f. Favipiravir kullan\u0131lan hastalarda be\u015finci g\u00fcnde viral klirens (%62.5\u2019e, %30, p=0.018), ate\u015f d\u00fc\u015fme s\u00fcresi (iki g\u00fcne d\u00f6rt g\u00fcn, p=0.007) ve 15. g\u00fcnde toraks BT\u2019de iyile\u015fme oran\u0131 (%90\u2019a %80, p=0.283) belirgin olarak daha iyi bulunmu\u015f. \u00a0D\u00fc\u015f\u00fck doz favipiravir alan grupta 2 hasta kaybedilirken, di\u011fer gruplarda kay\u0131p olmam\u0131\u015f. D\u00fc\u015f\u00fck doz favipiravir grubunun 13\/20 (%65)\u2019si, y\u00fcksek doz favipiravir ve standard tedavi gruplar\u0131n\u0131nsa 17\/20 (%85)\u2019si 15. g\u00fcnde taburcu edilmi\u015f ve\/veya DS\u00d6 klinik skorlamas\u0131nda 2\u2019ye ula\u015fm\u0131\u015f (p=0.375).\u00a0 Tedaviye yan\u0131t verenlerde verilmi\u015f ortalama favipiravir y\u00fckleme dozu 43.9 mg\/kg (IQR 40.0-47.1) iken, be\u015finci g\u00fcnde PCR pozitif olanlarda bu de\u011fer 39.1 mg\/kg (IQR 35.6-43.9)\u2019m\u0131\u015f. Y\u00fcksek dozlarda istenmeyen etkilerde art\u0131\u015f g\u00f6r\u00fclmemi\u015f, ciddi istenmeyen etki olmam\u0131\u015f. Bu sonu\u00e7larla esas \u00e7al\u0131\u015fmada y\u00fckleme dozunun kiloya ba\u011fl\u0131 olmas\u0131na (44 mg\/kg) ve tedavi s\u00fcresinin 10 g\u00fcn olmas\u0131na karar verilmi\u015f (Ivashchenko, A.A. 2020).<\/p>\n<p>Son olarak Hindistan\u2019da, do\u011frulanm\u0131\u015f 150 hafif-orta COVID-19 olgusunda yap\u0131lm\u0131\u015f faz 3 RK\u00c7 (FambiFlu) \u00e7al\u0131\u015fman\u0131n sonu\u00e7lar\u0131 bas\u0131n yoluyla payla\u015f\u0131lm\u0131\u015ft\u0131r. Bu \u00e7al\u0131\u015fmada hastalar standard tedaviye ek olarak tan\u0131dan itibaren ilk 48 saatte favipiravir (birinci g\u00fcn 1800x2; 2-14 g\u00fcn: 800mg x2) veya sadece standard tedavi alacak \u015fekilde randomize edilmi\u015f. Favipiravir kolunda viral klirensin, istatistiksel olarak anlaml\u0131 olmasa da %28.6 daha h\u0131zl\u0131 oldu\u011fu, klinik d\u00fczelme s\u00fcresinin (\u00fc\u00e7 g\u00fcne be\u015f g\u00fcn) belirgin olarak daha k\u0131sa ve d\u00f6rd\u00fcnc\u00fc g\u00fcnde iyile\u015fme oran\u0131n\u0131n (%69.8\u2019e %44.9) belirgin olarak daha y\u00fcksek oldu\u011fu g\u00f6r\u00fclm\u00fc\u015f (p =0.029 ve 0.019) (Glenmark, 2020).<\/p>\n<p><strong><em>G\u00f6zlemsel \u00c7al\u0131\u015fmalar<\/em><\/strong><\/p>\n<p>Japonya\u2019da COVID-19 nedeniyle favipiravir verilmi\u015f 2158 hastan\u0131n geriye d\u00f6n\u00fck de\u011ferlendirildi\u011fi bir \u00e7al\u0131\u015fmada, hafif olgular\u0131n %87.8\u2019inde, orta \u015fiddetli olgular\u0131n %84.5\u2019inde, a\u011f\u0131r olgular\u0131nsa %60.3\u2019\u00fcnde 14. g\u00fcnde klinik durumun d\u00fczeldi\u011fi g\u00f6r\u00fclm\u00fc\u015f, mortalite oranlar\u0131n\u0131n da s\u0131ras\u0131yla %5.1, %12.7 ve %31.7 oldu\u011fu bildirilmi\u015ftir. Hastalar\u0131n %25\u2019inde istenmeyen ila\u00e7 etkisi bildirildi\u011fi ve hiper\u00fcrisemi (%16), karaci\u011fer fonksiyonlar\u0131nda anormallik (%7), d\u00f6k\u00fcnt\u00fc (%1.4), akut b\u00f6brek hasar\u0131 (%0.7) ve bulant\u0131-kusman\u0131n (%0.7) en s\u0131k bildirilen istemeyen ila\u00e7 etkisi oldu\u011fu g\u00f6r\u00fclm\u00fc\u015ft\u00fcr.\u00a0\u00a0 Doz %93\u2019\u00fcnde birinci g\u00fcn 1800 mg X2, sonra 800 mg x2, %5\u2019inde birinci g\u00fcn 1600mg x2, sonra 600mg x2, ortalama 11 g\u00fcn verilmi\u015ftir (Favipiravir Observational Study Group, 2020).<\/p>\n<p>Hafif-orta seyirli COVID-19 pn\u00f6monisi olan 80 hastada yap\u0131lm\u0131\u015f retrospektif vaka \u2013kontrol \u00e7al\u0131\u015fmas\u0131nda favipiravir + inhaler IFN-\u03b1 alan 35 hasta, lopinavir\/r+inhaler IFN-\u03b1 alan 45 hastayla kar\u015f\u0131la\u015ft\u0131r\u0131lm\u0131\u015f. \u00a0Demografik \u00f6zellikleri ve komorbiditeleri benzer olan hastalardan favipiravirli tedavi alanlarda viral klirens ortalama d\u00f6rt g\u00fcnken, lopinavir\/r grubunda 11. g\u00fcn olarak belirlenmi\u015f\u00a0 (P < 0.001). Favipiravir viral klirens i\u00e7in ba\u011f\u0131ms\u0131z g\u00f6sterge olarak saptanm\u0131\u015f ve <7 g\u00fcnde viral klirens olanlarda akci\u011fer BT\u2019de iyile\u015fme oran\u0131 da daha y\u00fcksek bulunmu\u015f. Ayr\u0131ca 14. g\u00fcnde AC g\u00f6r\u00fcnt\u00fclemesinde d\u00fczelme favipiravir grubunda %91\u2019ken di\u011fer grupta %62 olarak bulunmu\u015f (P = 0.004) (Cai, Q., 2020).\n\nFavipiravir konusunda yap\u0131lm\u0131\u015f klinik \u00e7al\u0131\u015fmalar genellikle az olgu say\u0131l\u0131, plasebo kontroll\u00fc olmamas\u0131 nedeniyle sorunludur ve ek \u00e7al\u0131\u015fmalar gereklidir. \u015eu anda COVID-19 tedavisinde favipiraviri ara\u015ft\u0131ran clinicaltrials.com\u2019da kay\u0131tl\u0131 21 RK\u00c7 vard\u0131r. \u00dclkemizde de i\u00e7inde favipiravirin hidroksiklorokinle kombine olarak veya tek ba\u015f\u0131na yer ald\u0131\u011f\u0131 bir RK\u00c7 \u00e7al\u0131\u015fmas\u0131na da \u015fu ana kadar 745 hasta randomize edilmi\u015f olup, \u00f6n\u00fcm\u00fczdeki aylarda sonu\u00e7lar\u0131n\u0131n a\u00e7\u0131klanmas\u0131 beklenmektedir.\n\n<strong><em>Sonu\u00e7<\/em><\/strong><\/p>\n<p><strong><em>Favipriavirin COVID-19 tedavisindeki etkisini ara\u015ft\u0131ran, toplam 450 hasta i\u00e7eren 3 RK\u00c7\u2019de ve 80 hastal\u0131k 1 g\u00f6zlemsel \u00e7al\u0131\u015fmada, bu ajan\u0131n kar\u015f\u0131la\u015ft\u0131r\u0131lan di\u011fer ajanlara veya standard tedaviyle kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131nda viral klirense ve\/veya baz\u0131 klinik sonu\u00e7lara olumlu etkilerinin olabilece\u011fi bildirilirken, 29 hasta i\u00e7eren bir RK\u00c7\u2019de olumlu bir etkisinin olmad\u0131\u011f\u0131 bildirilmi\u015ftir. Bu verilerle, favipiravirin \u00f6zellikle pn\u00f6monili ve\/veya riskli COVID-19 olgular\u0131n\u0131n tedavisinde kullan\u0131labilece\u011fi d\u00fc\u015f\u00fcn\u00fclmektedir. Ancak devam etmekte olan randomize kontroll\u00fc klinik \u00e7al\u0131\u015fmalar\u0131n sonu\u00e7lar\u0131 yak\u0131ndan izlenmeli, g\u00fcncel verilerle kullan\u0131m \u00f6nerileri tekrar de\u011ferlendirilmelidir. <\/em><\/strong><\/p>\n<p><strong><em>Favipiravirin COVID-19 tedavisinde veya di\u011fer indikasyonlarla kullan\u0131m\u0131 s\u0131ras\u0131nda ciddi istenmeyen etkileri tan\u0131mlanmam\u0131\u015ft\u0131r. <\/em><\/strong><\/p>\n<p><strong><em>In vitro \u00e7al\u0131\u015fmalarda SARS-CoV-2\u2019ye kar\u015f\u0131 y\u00fcksek konsantrasyonlarda etkili olabilen favipiravirin COVID-19 tedavisindeki dozunun da \u00f6zellikle a\u011f\u0131r olgularda olmak \u00fczere gripte uygulanandan daha y\u00fcksek ve daha uzun s\u00fcreli olmas\u0131 ak\u0131lc\u0131d\u0131r, ancak kesin bir sonuca varabilmek i\u00e7in bu konuda da ek \u00e7al\u0131\u015fmalar gereklidir. <\/em><\/strong><\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"5\"  header_id=\"header-1600777470625\" id=\"header-1600777470625\" style=\"\" class=\"accordions-head head1600777470625 border-none\" toggle-text=\"\" main-text=\"REMDESIVIR (GS-5734)\">\n                                    <span id=\"accordion-icons-1600777470625\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600777470625\" class=\"accordions-head-title\">REMDESIVIR (GS-5734)<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600777470625 \">\n                <p>Adenozin bir n\u00fckleozid analo\u011fu olan remdesivir 2014\u2019de Ebola virusu i\u00e7in geli\u015ftirilmi\u015ftir. Monofosforamidat bir \u00f6n ila\u00e7t\u0131r, h\u00fccre i\u00e7inde aktif formuna (GS-441524) metabolize olur, RdRp taraf\u0131ndan substrat olarak alg\u0131lanarak zinciri sonland\u0131r\u0131r. \u00a0Koronaviruslarda bulunan ve viral do\u011frulama okumas\u0131 (proof reading) yapan ekson\u00fckleazlara diren\u00e7lidir, ancak in vitro bir \u00e7al\u0131\u015fmada ExoN\u2019u olmayan su\u015flarda daha etkili oldu\u011fu, virusun bu geninde mutasyonla remdesivir direnci olabilece\u011fi ve y\u00fcksek dozlarla bu diren\u00e7le ba\u015fa \u00e7\u0131k\u0131labilece\u011fi g\u00f6sterilmi\u015ftir (Agostini, M.L., 2020).<\/p>\n<p>Geni\u015f spektrumlu bir anti-viral olup Ebola ve Marburg gibi filoviruslara, Nipah, Hendra ve RSV gibi paramiksoviruslara ve koronaviruslar\u0131n hepsine in vitro etkilidir. SARS-CoV, MERSCoV ve SARS-CoV-2\u2019ye 0.09 \u03bcM, 0.18 \u03bcM ve 0.77 \u03bcM gibi d\u00fc\u015f\u00fck EC seviyelerinde etkili bulunmu\u015ftur (Agostini, M.L., 2020; Amirian, E.S, 2020).<\/p>\n<p>Remdesivirin ilk ge\u00e7i\u015f hepatik ektraksiyonu y\u00fcksek olmas\u0131 nedeniyle oral biyoyararlan\u0131m\u0131n\u0131n d\u00fc\u015f\u00fck olmas\u0131 beklenmektedir. Sulfobutileter-siklodekstrin (SBECD)\u2019le form\u00fcle edilmi\u015ftir. \u00a0SBECD\u2019nin orta-a\u011f\u0131r b\u00f6brek yetmezli\u011finde birikerek renal vakuolasyona yol a\u00e7abildi\u011fi g\u00f6sterilmi\u015f oldu\u011fundan klirensi <30 ml\/dk olanlarda ve di\u011fer SBECD i\u00e7eren ila\u00e7larla birlikte verilirken dikkat edilmelidir (Sheahan, T.P, 2020). REmdesivirn dozu, istenmeyen ila\u00e7 etkileri gibi di\u011fer \u00f6zellikleri <a href=\"https:\/\/www.klimik.org.tr\/koronavirus\/wp-content\/uploads\/2020\/09\/Supplementary-material_Tablo_4.pdf\" target=\"_blank\" rel=\"noopener\"><span style=\"color: #ff0000;\">Tablo 4<\/span><\/a>\u2019de verilmi\u015ftir.<\/p>\n<p>Remdesivirin in vivo fare\/makak modellerinde MERS\u2019e kar\u015f\u0131 profilaktik ve terap\u00f6tik etkisi g\u00f6sterilmi\u015ftir. \u00a0In vivo fare modelinde SARS\u2019a kar\u015f\u0131, profilaktik ve erken ba\u015flanmas\u0131 halinde terap\u00f6tik etkisi g\u00f6sterilmi\u015ftir (Amirian E.S., 2020).<\/p>\n<p>Remdesivirin in vivo makak modelinde SARS-CoV-2 \u2018ye etkili oldu\u011fu g\u00f6sterilmi\u015ftir. Bu \u00e7al\u0131\u015fmada 12 makak SARS-CoV-2 ile infekte edildikten sonra 12 saat i\u00e7inde alt\u0131s\u0131na remdesivir, alt\u0131s\u0131na placebo verilmi\u015f, remdesivir alanlarda dispne, takipne, akci\u011ferlerde lezyon geli\u015fimi ve virus y\u00fck\u00fc belirgin olarak daha d\u00fc\u015f\u00fck bulunmu\u015ftur. Bu veriler remdesivirin erken ba\u015flanmas\u0131 gerekti\u011fini d\u00fc\u015f\u00fcnd\u00fcrmektedir (Williamson, B.N., 2020).<\/p>\n<p><strong><u>Cov\u0131d-19\u2019un Antiviral Tedavisinde Remdesivir Kullan\u0131m\u0131 Konusunda Yap\u0131lm\u0131\u015f Klinik \u00c7al\u0131\u015fmalar<\/u><\/strong><\/p>\n<p><strong><em>Randomize Kontroll\u00fc Klinik \u00c7al\u0131\u015fmalar <\/em><\/strong><\/p>\n<p>Remdesivirin COVID-19\u2019da etkinli\u011fini ara\u015ft\u0131ran \u00c7in\u2019de yap\u0131lm\u0131\u015f ilk RK\u00c7\u2019de a\u011f\u0131r pn\u00f6monisi (O2sat<%94, paO2\/FiO2<300) ve semptomlar\u0131n\u0131n s\u00fcresi \u226412 g\u00fcn olan, 237 do\u011frulanm\u0131\u015f COVID-19 olgusunda remdesivir (158 hasta) veya plasebo (79 hasta) ve ayn\u0131 zamanda lopinavir\u2013ritonavir, interferon ve kortikosteroidler verilmi\u015ftir. Bu \u00e7al\u0131\u015fmada klinik iyile\u015fme s\u00fcresi, 28 g\u00fcnl\u00fck mortalite ve istenmeyen ila\u00e7 etkisi oranlar\u0131n\u0131n gruplar aras\u0131nda fark g\u00f6stermedi\u011fi, ayn\u0131 \u015fekilde \u00fcst ve alt solunum yolu \u00f6rneklerindeki viral y\u00fck\u00fcn de gruplar aras\u0131nda benzer oldu\u011fu bildirilmi\u015ftir (Wang, Y., 2020). \u00a0Remdesivirle ilgili ikinci RK\u00c7 1063 do\u011frulanm\u0131\u015f a\u011f\u0131r COVID-19 olgusunda ABD\u2019de yap\u0131lm\u0131\u015ft\u0131r. Bu \u00e7al\u0131\u015fmada olgular\u0131n 538\u2019ine remdesivir, 521\u2019ine ise plasebo uygulanm\u0131\u015f; klinik iyile\u015fme s\u00fcresinin remdesivir grubunda 11, plasebo grubunda 15 g\u00fcn, aradaki fark\u0131n istatistiksel olarak anlaml\u0131 oldu\u011fu bildirilmi\u015ftir (p<0.001). Mortalite oran\u0131 da remdesivir grubunda daha d\u00fc\u015f\u00fck olmakla birlikte (%7.1\u2019e %11.9) aradaki fark\u0131n istatistiksel olarak anlaml\u0131 olmad\u0131\u011f\u0131 g\u00f6r\u00fclm\u00fc\u015ft\u00fcr (p=0.059) (Beigel, J.H., 2020).\n\nBu \u00e7al\u0131\u015fman\u0131n verilerinin a\u00e7\u0131klanmas\u0131ndan sonra ABD FDA, a\u011f\u0131r olas\u0131\/do\u011frulanm\u0131\u015f COVID-19 hastalar\u0131 i\u00e7in (SpO2 \u2264 %94) remdesivire acil kullan\u0131m onay\u0131 vermi\u015f, tedavi s\u00fcresinin ent\u00fcbe olanlarda 10 g\u00fcn, olmayanlarda be\u015f g\u00fcn olabilece\u011fini bildirmi\u015ftir. Arkas\u0131ndan\n\nAmerikan Ulusal COVID-19 Rehberi\u2019nde de remdesivir COVID-19 tedavisinde ayn\u0131 indikasyonlarla yerini alm\u0131\u015ft\u0131r (National Institute of Health, 2020).\n\nCOVID-19\u2019da uygun remdesivir tedavi s\u00fcresini belirlemek \u00fczere 397 hastada yap\u0131lan bir \u00e7al\u0131\u015fmada, be\u015f veya 10 g\u00fcn remdesivirle tedavi edilen hastalarda klinik sonu\u00e7lar ve istenmeyen ila\u00e7 etkileri a\u00e7\u0131s\u0131ndan fark g\u00f6r\u00fclmemi\u015ftir (Gilead Sciences, Inc, 2020).\nSon olarak ABD, Avrupa, Asya\u2019da O2 ihtiyac\u0131 olmayan pn\u00f6monili do\u011frulanm\u0131\u015f\u00a0\u00a0 COVID-19 tan\u0131l\u0131 584 hastada yap\u0131lm\u0131\u015f \u00e7ok merkezli RK\u00c7\u2019de, hastalar be\u015f g\u00fcn remdesivir (197), 10 g\u00fcn remdesivir (199) ve standard bak\u0131m (200) alacak \u015fekilde randomize edilmi\u015ftir.\u00a0 Onbirinci g\u00fcndeki klinik durum standard grupla kar\u015f\u0131la\u015ft\u0131r\u0131ld\u0131\u011f\u0131nda be\u015f g\u00fcn remdesivir alan grupta belirgin olarak daha iyiyken, 10 g\u00fcn remdesivir alan grupta farkl\u0131 bulunmam\u0131\u015ft\u0131r (p s\u0131ras\u0131yla 0.02 ve 0.18). Mortalite ve istenmeyen ila\u00e7 etkileri gruplar aras\u0131nda benzer bulunmu\u015ftur (Spinner, C.D., 2020).\n\n<strong><em>Sonu\u00e7<\/em><\/strong><\/p>\n<p><strong><em>Remdesivir SARS-CoV-2\u2019ye kar\u015f\u0131 in vitro ve in vivo hayvan deneylerinde olduk\u00e7a etkili bulunmu\u015f, 1647 COVID-19 hastas\u0131n\u0131 i\u00e7eren 2 RK\u00c7\u2019de klinik sonu\u00e7lara baz\u0131 olumlu etkisi g\u00f6sterilmi\u015f, 237 hasta i\u00e7eren bir RK\u00c7\u2019de ise klinik sonu\u00e7lara herhangi bir olumlu etkisi g\u00f6sterilmemi\u015ftir. \u00a0Ek klinik \u00e7al\u0131\u015fma sonu\u00e7lar\u0131 gereklidir. <\/em><\/strong><\/p>\n<p><strong><em>Remdesivirin COVID-19 s\u0131ras\u0131nda kullan\u0131m\u0131 s\u0131ras\u0131nda ciddi istenmeyen etkisi bildirilmemi\u015ftir. <\/em><\/strong><\/p>\n<p><strong><em>T\u00fcm veriler bir arada de\u011ferlendirildi\u011finde remdesivirin orta\/a\u011f\u0131r seyirli COVID-19 pn\u00f6monilerinde kullan\u0131labilece\u011fi d\u00fc\u015f\u00fcn\u00fclm\u00fc\u015ft\u00fcr. Yeni klinik \u00e7al\u0131\u015fma sonu\u00e7lar\u0131na g\u00f6re kullan\u0131m indikasyonlar\u0131 tekrar de\u011ferlendirilmelidir.\u00a0 <\/em><\/strong><\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"6\"  header_id=\"header-1600777496917\" id=\"header-1600777496917\" style=\"\" class=\"accordions-head head1600777496917 border-none\" toggle-text=\"\" main-text=\"COVID-19\u2019UN ANT\u0130V\u0130R\u0130AL TEDAV\u0130S\u0130NDE PROTEAZ \u0130NH\u0130B\u0130T\u00d6RLER\u0130\">\n                                    <span id=\"accordion-icons-1600777496917\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600777496917\" class=\"accordions-head-title\">COVID-19\u2019UN ANT\u0130V\u0130R\u0130AL TEDAV\u0130S\u0130NDE PROTEAZ \u0130NH\u0130B\u0130T\u00d6RLER\u0130<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600777496917 \">\n                <p>Koronaviruslar\u0131n ana proteaz\u0131 \u00e7ok iyi korunmu\u015f olup, SARS-CoV-2\u2019nin ana proteaz\u0131, \u00a0SARS\u2019\u0131nkiyle %96 benzerlik g\u00f6stermektedir. Koronavirus proteaz\u0131, virus konak h\u00fccresine girdikten sonra sentezlenen poliproteini par\u00e7alayarak yap\u0131sal olmayan (RNA polimeraz, ekson\u00fckleaz vb) proteinlerinin olu\u015fmas\u0131n\u0131 sa\u011flar. Bu nedenle virus \u00e7o\u011falmas\u0131nda kritik bir rol\u00fc vard\u0131r ve SARS-CoV-2 i\u00e7in i\u00e7in potansiyel ila\u00e7 hedefi olarak \u00f6nerilmi\u015ftir (Xu, Z., 2020; McKeea, D.L., 2020)<\/p>\n<p>COVID-19 tedavisi amac\u0131yla en yayg\u0131n kullan\u0131lan proteaz inhibit\u00f6r\u00fc, HIV infeksiyonunun tedavisinde uzun y\u0131llardan beri kullan\u0131lmakta olan lopinavir\/ritonavir olmu\u015ftur.<\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"7\"  header_id=\"header-1600777520530\" id=\"header-1600777520530\" style=\"\" class=\"accordions-head head1600777520530 border-none\" toggle-text=\"\" main-text=\"LOP\u0130NAV\u0130R\/R\u0130TONAV\u0130R\">\n                                    <span id=\"accordion-icons-1600777520530\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600777520530\" class=\"accordions-head-title\">LOP\u0130NAV\u0130R\/R\u0130TONAV\u0130R<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600777520530 \">\n                <p>Lopinavir, booster olarak yer alan ritonavirle birlikte HIV tedavisinde kullan\u0131lan bir proteaz inhibit\u00f6r\u00fcd\u00fcr. Daha \u00f6nce yap\u0131lm\u0131\u015f in vitro \u00e7al\u0131\u015fmalarda, lopinavir\/ritonavirin kabul edilebilir EC50 seviyeleriyle SARS-CoV\u2019a etkili oldu\u011fu, ribavirinle kombine edildi\u011finde sinerjik etkinlik g\u00f6sterdi\u011fi bildirilmi\u015ftir. Vero-E6 h\u00fccrelerinde yap\u0131lan \u00e7al\u0131\u015fmalarda lopinavir\/ritonavirin SARS-CoV-2\u2019ye 26.63\u03bcM\u2019l\u00fck EC50 seviyesiyle etkili oldu\u011fu g\u00f6sterilmi\u015ftir (Choy, K.T., 2020). Hayvan deneylerinde MERS ve SARS\u2019a etkili oldu\u011fu (Chan, J.F.W., 2015), MERS ve SARS hastalar\u0131nda yap\u0131lm\u0131\u015f baz\u0131 g\u00f6zlemsel \u00e7al\u0131\u015fmalarda da \u00e7e\u015fitli klinik sonu\u00e7lara olumlu etkisinin g\u00f6r\u00fcld\u00fc\u011f\u00fc (Chan, K.S.,2003; Chu, C.M., 2004), MERS\u2019te temas sonras\u0131 profilakside etkili olabilece\u011fi bildirilmi\u015ftir (Park, S.Y., 2019; Yao, T.T., 2020).<\/p>\n<p><strong><u>COVID-19\u2019un Antiviral Tedavisinde Lopinavir\/ritonavir Kullan\u0131m\u0131 Konusunda Yap\u0131lm\u0131\u015f Klinik \u00c7al\u0131\u015fmalar<\/u><\/strong><\/p>\n<p><strong><em>Randomize Kontroll\u00fc Klinik \u00c7al\u0131\u015fmalar <\/em><\/strong><\/p>\n<p>\u00c7in\u2019de 86 hafif\/orta do\u011frulanm\u0131\u015f COVID-19 olgusunda yap\u0131lm\u0131\u015f bir RK\u00c7\u2019de, 34 hasta lopinavir-ritonavir, 35 hasta arbidol, 17 hastaysa antiviral tedavi verilmeyecek \u015fekilde randomize edilmi\u015f; viral klirens s\u00fcresi, klinik tabloda a\u011f\u0131rla\u015fma oranlar\u0131, yedinci g\u00fcnde ate\u015fsiz olma ve BT\u2019de d\u00fczelme oranlar\u0131 gruplar aras\u0131nda benzer bulunmu\u015ftur (Li, Y., 2020).<\/p>\n<p>\u00c7in\u2019de 199 do\u011frulanm\u0131\u015f a\u011f\u0131r pn\u00f6monili COVID-19 hastas\u0131nda yap\u0131lm\u0131\u015f bir di\u011fer RK\u00c7\u2019de ise 99 hastaya standard tedaviye ek olarak Lop\/r, 100\u2019\u00fc ise sadece standard tedavi verilmi\u015f, klinik iyile\u015fme s\u00fcresi gruplara aras\u0131nda benzer (HR1.24; %95 [CI], 0.90-1.72) bulunmu\u015ftur. 28 g\u00fcnl\u00fck mortalite Lop\/r grubunda (%19.2), kontrol grubundan (%25) ( -5.8 y\u00fczdelik azalma, %95 CI\u221217.3-5.7) daha d\u00fc\u015f\u00fck olakla birlikte aradaki fark\u0131n istatistiksel olarak anlaml\u0131 olmad\u0131\u011f\u0131 bildirilmi\u015ftir. Farkl\u0131 d\u00f6nemlerde viral RNA belirlenme oranlar\u0131 da iki grupta benzer bulunmu\u015ftur. \u0130lk 12 g\u00fcnde tedavi verilebilenler ayr\u0131 de\u011ferlendirildi\u011finde klinik iyile\u015fme Lop\/r grubunda \u00a0daha h\u0131zl\u0131 olmu\u015f (16 g\u00fcne kar\u015f\u0131l\u0131k 17 g\u00fcn) ve mortalitenin de daha belirgin olarak azald\u0131\u011f\u0131 (%19\u2019a kar\u015f\u0131l\u0131k %27) g\u00f6r\u00fclm\u00fc\u015ft\u00fcr. Lop\/r grubunda gastrointestinal istenmeyen etkiler daha fazla g\u00f6r\u00fcl\u00fcrken ciddi istenmeyen etki g\u00f6r\u00fclmemi\u015f, hastalar\u0131n %13.8\u2019inde Lop\/r\u2019nin istenmeyen etkileri nedeniyle tedavi erkenden sonland\u0131r\u0131lm\u0131\u015ft\u0131r (Cao, B., 2020).<\/p>\n<p>Bu \u00e7al\u0131\u015fman\u0131n sonu\u00e7lar\u0131 de\u011ferlendirildi\u011finde, Lop\/r grubunda mortalitenin daha az g\u00f6r\u00fclmesinin \u00a0\u00f6nemli olabilece\u011fi, Lop\/r\u2019nin\u00a0 hastal\u0131\u011f\u0131n erken d\u00f6nemlerinde ba\u015flanmas\u0131n\u0131n daha ak\u0131lc\u0131 olabilece\u011fi, Lop\/r\u2019nin SARS-CoV-2\u2019yi inhibe eden konsantrasyonlar\u0131n\u0131n g\u00f6receli y\u00fcksek olmas\u0131 nedeniyle sinerjik kombinasyonlar\u0131n \u00a0ak\u0131lc\u0131 olabilece\u011fi d\u00fc\u015f\u00fcn\u00fclm\u00fc\u015ft\u00fcr (Baden, L.R., 2020).<\/p>\n<p>Hong-Kong\u2019da izlenmi\u015f 127 do\u011frulanm\u0131\u015f COVID-19 olgusunda yap\u0131lm\u0131\u015f bir di\u011fer RK\u00c7\u2019de 34 hastaya tek ba\u015f\u0131na Lop\/r, 34 hastayaysa Lop\/r, interferin-beta-1b ve ribavirin kombinasyonu verilmi\u015ftir. Tedavi ba\u015flama s\u00fcresi semptomlar\u0131n ba\u015flang\u0131c\u0131ndan itibaren ortalama be\u015f g\u00fcn, tedavi s\u00fcresi ise 14 g\u00fcn olan bu \u00e7al\u0131\u015fmada, kombinasyon grubunda viral klirens s\u00fcresi (7\u2019ye kar\u015f\u0131l\u0131k 12 g\u00fcn, p=0.010), NEWS skorunun s\u0131f\u0131r olma s\u00fcresi (4\u2019e kar\u015f\u0131l\u0131k 8 g\u00fcn, p<0.001) ve toplam hastanede yat\u0131\u015f s\u00fcresi (dokuza kar\u015f\u0131 14.5 g\u00fcn, p=0.16) daha k\u0131sa,\u00a0 \u00fc\u00e7\u00fcnc\u00fc g\u00fcndeki SOFA skoru da daha d\u00fc\u015f\u00fck (0\u2019a kar\u015f\u0131 1, p=0.010) bulunmu\u015ftur. Tedavinin semptomlardan sonraki ilk yedi g\u00fcnden \u00f6nce ba\u015flanmas\u0131 halinde t\u00fcm sonu\u00e7lar\u0131n ge\u00e7 ba\u015flananlardan daha iyi oldu\u011funun bildirildi\u011fi bu \u00e7al\u0131\u015fmada istenmeyen ila\u00e7 etkileriyse genellikle bulant\u0131 ve ishal olmak \u00fczere gruplar aras\u0131nda benzermi\u015f (%48 vs %49) (Hung, I.F.N., 2020).\n\nABD\/IDSA COVID-19 Tedavi Rehberi\u2019nde, Lop\/r\u2019in sadece klinik \u00e7al\u0131\u015fmalar kapsam\u0131nda kullan\u0131lmas\u0131, kesin bir yarg\u0131da bulunabilmek i\u00e7in ek \u00e7al\u0131\u015fmalara gereksinim oldu\u011fu vurgulanm\u0131\u015ft\u0131r (Bhimraj, A., 2020).\n\n<strong><em>Sonu\u00e7<\/em><\/strong><\/p>\n<p><strong><em>COVID-19 tedavisinde Loinavir\/ritonavirin etkinli\u011fini ara\u015ft\u0131ran 86 hasta i\u00e7eren bir RK\u00c7\u2019de bu ajan\u0131n etkisiz oldu\u011fu, 199 hasta i\u00e7eren bir RK\u00c7\u2019de baz\u0131 olumlu etkilerinin olabilece\u011fi, birinde ise ribavirin ve interferonla kombine kullan\u0131lmas\u0131 halinde olumlu etkilerinin oldu\u011fu bildirilmi\u015ftir. Bu klinik \u00e7al\u0131\u015fmalar\u0131n genellikle az olgu say\u0131l\u0131 ve plasebo kontroll\u00fc olmad\u0131\u011f\u0131 g\u00f6r\u00fclm\u00fc\u015f, ek \u00e7al\u0131\u015fmalar\u0131n gerekli oldu\u011fu d\u00fc\u015f\u00fcn\u00fclm\u00fc\u015ft\u00fcr.\u00a0 <\/em><\/strong><\/p>\n<p><strong><em>Lopinavir\/ritonavirin SARS-CoV-2 \u00fczerine etkisini ara\u015ft\u0131ran in vitro \u00e7al\u0131\u015fma say\u0131s\u0131 azd\u0131r, sonu\u00e7lar yetersizdir, ek \u00e7al\u0131\u015fmalar gereklidir. <\/em><\/strong><\/p>\n<p><strong><em>Lopinavir\/ritonavirin COVID-19 tedavisinde, \u00f6zellikle kombinasyon rejiminin bir par\u00e7as\u0131 olarak klinik \u00e7al\u0131\u015fmalar i\u00e7inde yer alacak \u015fekilde kullan\u0131lmas\u0131 d\u00fc\u015f\u00fcn\u00fclebilir. <\/em><\/strong><\/p>\n<p>COVID-19 salg\u0131n\u0131n ba\u015flamas\u0131ndan itibaren ge\u00e7en 8 ayl\u0131k s\u00fcre\u00e7te etkinli\u011fi kesin olarak g\u00f6sterilmi\u015f bir antiviral halen yoktur. \u00a0Bu ama\u00e7la yap\u0131lan klinik \u00e7al\u0131\u015fmalarda en \u00e7ok incelenen ve tedavide yeniden konumland\u0131r\u0131larak (repurposing) kullan\u0131lan ajanlar, etkili tedavi bulunmas\u0131 konusunda zaman kayb\u0131na neden olmu\u015f olabilir. \u00a0SARS-CoV-2\u2019ye \u00f6zg\u00fc yeni antivirallere acilen gereksinim vard\u0131r, mevcut kaynaklar\u0131n yeni ajanlar\u0131n ara\u015ft\u0131r\u0131lmas\u0131na, geli\u015ftirilmesine ve \u00e7al\u0131\u015f\u0131lmas\u0131na ayr\u0131lmas\u0131 en ak\u0131lc\u0131 yakla\u015f\u0131md\u0131r.<\/p>\n            <\/div>\n    \n            <div post_id=\"2840\" itemcount=\"8\"  header_id=\"header-1600777621015\" id=\"header-1600777621015\" style=\"\" class=\"accordions-head head1600777621015 border-none\" toggle-text=\"\" main-text=\"KAYNAKLAR\">\n                                    <span id=\"accordion-icons-1600777621015\" class=\"accordion-icons\">\n                        <span class=\"accordion-icon-active accordion-plus\"><i class=\"fas fa-chevron-up\"><\/i><\/span>\n                        <span class=\"accordion-icon-inactive accordion-minus\"><i class=\"fas fa-chevron-right\"><\/i><\/span>\n                    <\/span>\n                    <span id=\"header-text-1600777621015\" class=\"accordions-head-title\">KAYNAKLAR<\/span>\n                            <\/div>\n            <div class=\"accordion-content content1600777621015 \">\n                <p>1.Agostini ML, Andres EL, Sims AC, <em>et al<\/em>. \u00a0Coronavirus susceptibility to the antiviral remdesivir (GS-5734) is mediated by the viral polymerase and the proofreading exoribonuclease. <em>mBio<\/em>. 2018; 9 (2): e00221-18.<\/p>\n<p>2. Amirian ES, Levy JK. Current knowledge about the antivirals remdesivir (GS-5734) and GS-441524 as therapeutic options for coronaviruses. <em>One Health<\/em>. 2020; 9: 100128.<\/p>\n<p>3. Arshad A, Kilgore P, Chaudhry ZS, <em>et al<\/em>. Treatment with Hydroxychloroquine, Azithromycin, and Combination in Patients Hospitalized with COVID-19. <em>Int J Infect Dis<\/em>. 2020; 97: 396-403.<\/p>\n<p>4. Axfors C, Schmitt AM, Janiaud P, <em>et al<\/em>. Mortality outcomes with hydroxychloroquine and chloroquine 2 in COVID-19: an international collaborative meta-analysis of randomized trials. <em>medRxiv<\/em>. doi: https:\/\/doi.org\/10.1101\/2020.09.16.20194571.<\/p>\n<p>5. Baden LR, Rubin EJ. Covid-19\u2013The search for effective therapy. <em>N Engl J Med<\/em>. 2020; 382 (19): 1851-2.<\/p>\n<p>6. Barlow A, Landolf KM, Barlow B, <em>et al<\/em>. Review of emerging pharmacotherapy for the reatment of coronavirus disease 2019. <em>Pharmacotherapy<\/em>. 2020; 40 (5): 416-37.<\/p>\n<p>7. 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In vitro antiviral activity and projection of optimized dosing design of hydroxychloroquine for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). <em>Clin Infect Dis<\/em>. 2020; 71 (15): 732-9.<\/p>\n<p>84. Yao TT, Qian JD, Zhu Y, Wang Y,\u00a0Wang GQ. A systematic review of lopinavir therapy for SARS coronavirus and MERS coronavirus\u2013A possible reference for coronavirus disease\u201019 treatment option. <em>J Med Virol<\/em>. 2020; 92 (6): 556-63.<\/p>\n<p>85. Yu B, Li C, Chen P, <em>et al<\/em>. \u00a0Hydroxychloroquine application is associated with a decreased mortality in critically ill patients with COVID-19. <em>medRxiv<\/em>. 2020. doi: https:\/\/doi.org\/10.1101\/2020.04.27.20073379.<\/p>\n            <\/div>\n    <\/div>\n\n\n\n            <\/div>\n","protected":false},"excerpt":{"rendered":"<p>COVID-19 genellikle hafif-orta seyirli olmakla birlikte, olgular\u0131n yakla\u015f\u0131k %10-15\u2019inde a\u011f\u0131r ve %1 kadar\u0131nda \u00e7ok a\u011f\u0131r veya \u00f6l\u00fcmc\u00fcl (&#8230;)<\/p>\n","protected":false},"author":1,"featured_media":722,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[5],"tags":[],"_links":{"self":[{"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/posts\/150"}],"collection":[{"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/comments?post=150"}],"version-history":[{"count":15,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/posts\/150\/revisions"}],"predecessor-version":[{"id":5321,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/posts\/150\/revisions\/5321"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/media\/722"}],"wp:attachment":[{"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/media?parent=150"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/categories?post=150"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.klimik.org.tr\/koronavirus\/wp-json\/wp\/v2\/tags?post=150"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}