成人小说亚洲一区二区三区,亚洲国产精品一区二区三区,国产精品成人精品久久久,久久综合一区二区三区,精品无码av一区二区,国产一级a毛一级a看免费视频,欧洲uv免费在线区一二区,亚洲国产欧美中日韩成人综合视频,国产熟女一区二区三区五月婷小说,亚洲一区波多野结衣在线

立即打開(kāi)
首支HIV家庭自檢器上市背后的“丑聞”

首支HIV家庭自檢器上市背后的“丑聞”

Roger Parloff 2012-07-11
7月3日,美國(guó)食品和藥物管理局批準(zhǔn)了全球首支HIV病毒“家用快速自檢器”的發(fā)售。事實(shí)上,24年前FDA就接到過(guò)類似的審批申請(qǐng),但卻出于種種考慮,拒絕受理。FDA之前對(duì)HIV家庭自檢器的禁令人為地導(dǎo)致這種設(shè)備的上市推遲了24年,其間是否導(dǎo)致了數(shù)千名本可避免感染HIV的患者最終感染了艾滋???

????盡管如此,F(xiàn)DA拒絕一切HIV自檢設(shè)備的研究、甚至不允許研究HIV自檢的可行性的做法依然十分不妥。為什么就不能允許研究人員做些測(cè)試,看看圍繞著家庭自檢的那些疑慮是否合理呢?為什么連醫(yī)療器械公司只是研究一下這個(gè)問(wèn)題、想減輕艾滋病的風(fēng)險(xiǎn)也不允許呢?說(shuō)得好聽(tīng)些,這條禁令屬于“家長(zhǎng)式作風(fēng)”。只是因?yàn)閾?dān)心有些人會(huì)對(duì)家庭自檢的檢測(cè)結(jié)果做出不理智的極端情緒反應(yīng)就剝奪了所有人選擇家庭自檢的權(quán)力,強(qiáng)迫大家都去醫(yī)院做檢測(cè)。(有些門(mén)診既不夠私密,收費(fèi)也高,也不方便,而且很多去了門(mén)診檢測(cè)的人要么沒(méi)有獲得任何心理輔導(dǎo),要么也只是被馬馬虎虎地敷衍幾句,沒(méi)有多大價(jià)值。)

????雖然FDA的禁令在1988年看起來(lái)似乎還有些道理,但隨著時(shí)間的推移卻變得越來(lái)越站不住腳。隨著治療艾滋病的藥物不斷涌現(xiàn),人們對(duì)艾滋病的恐慌也不再那么歇斯底里,政治上的阻力也日漸減輕,在很多情況下甚至傾向于支持HIV自檢。因此在17年后,也就是2005年,F(xiàn)DA終于取消了禁令,開(kāi)始考慮接受HIV家用測(cè)試器械的申請(qǐng)。又過(guò)了7年,OraQuick自檢器終于走完了漫長(zhǎng)的審批流程,在上周獲批上市發(fā)售。

????需要指出的是,雖然統(tǒng)計(jì)數(shù)據(jù)表明,OraQuick在上市后的第一年就可能阻止4,000多起HIV傳播,這個(gè)數(shù)據(jù)實(shí)際上很模糊。實(shí)際可能更少,也可能更多。不過(guò)不管真實(shí)數(shù)據(jù)如何,我們都需要記住,由于FDA長(zhǎng)期以來(lái)對(duì)家庭快速自檢的反對(duì),導(dǎo)致了OraQuick自檢器仍然不是最先進(jìn)的檢測(cè)方法。這種方法已經(jīng)被醫(yī)療專業(yè)人士使用了8年了。FDA表示OraQuick的“窗口期”是90天,也就是說(shuō)患者在感染90天內(nèi),檢測(cè)結(jié)果可能不會(huì)呈陽(yáng)性。按今天的標(biāo)準(zhǔn),這個(gè)窗口開(kāi)得有些大。今天還有其它快速的檢測(cè)方法——它們也已經(jīng)獲得了FDA的批準(zhǔn)——不過(guò)也只能用于臨床測(cè)試。它們的窗口期只有12到26天左右。

????窗口期對(duì)于HIV傳播非常重要,因?yàn)槿藗冊(cè)谑状胃腥綡IV病毒之后的傳染性是最強(qiáng)的。據(jù)信,超過(guò)一半的HIV傳播都是由患者在被感染的60到90天內(nèi)傳播給下一個(gè)受害者的。

????所以如果OraQuick真的能在今年阻止4,000起新增HIV感染的話,不妨想象一下,如果上周獲批的是一種目前最先進(jìn)的檢測(cè)技術(shù),會(huì)有多少人因此從HIV的魔爪下逃過(guò)一劫。

????再想象一下,如果在五年前,有任何一種HIV快速家庭檢測(cè)方法獲批的話,又有多少人會(huì)幸免于難。

????那么10年前呢?

????或是15年前。

????或是20年前。

????或是24年前。

????這就是我所說(shuō)的“丑聞”。

????譯者:樸成奎

????Still, the approach the FDA took—to reject out of hand all research into even the feasibility of rapid home testing—was ill-advised. Why not allow researchers to do trials to see if the apprehensions surrounding home testing were empirically justified? Why discourage medical device companies from even exploring the question and trying to mitigate the dangers? At best, the ban was paternalistic. Out of concern that some people might respond emotionally and irrationally to the extremely valuable information a home test could provide, everyone was deprived of that option and forced to go to a clinic instead. (This was so even though clinics were not private, more expensive, less convenient, and plenty of people who went to them ended up receiving no counseling or perfunctory counseling of uncertain value.)

????And even if the FDA's ban on considering home testing kits might have been defensible in 1988, it became less so as each year passed—as drugs become available to treat AIDS, as fears became less hysterical, and as political opposition abated and, in many cases, morphed into support. Yet the years did pass—17 of them—before the FDA in 2005 effectively lifted its ban and started considering applications for HIV home testing kits. It then took another seven years for the OraQuick test to wend its way to the approval finish line—the journey it completed last week.

????To be sure, the statistics suggesting that OraQuick might avert more than 4,000 HIV infections in its first year are squishy. It could be less. It might be more. But whatever the true figure turns out to be, we need to remember that even the OraQuick test, because of the FDA's long opposition to home rapid tests, is not a state-of-the-art procedure. It's been in use by healthcare professionals for eight years already. The FDA says that OraQuick's "window period" is 90 days, meaning that infected people should not expect to see a positive result if they were infected less than 90 days before they give themselves that test. By today's standards, that's a wide window. There are other rapid tests available today—which have already won FDA approval, though, again, only for use at clinics—which have window periods as short as 12-26 days.

????Window periods are important, since people are most infectious right after they are first exposed to the HIV virus. More than half of HIV transmissions are believed to pass from an infected person to a new victim during the infected person's first 60 to 90 days of exposure.

????So if OraQuick might avert 4,000 new infections this year, imagine the number that could have been prevented if a state-of-the-art test had been approved last week.

????And now imagine the number that could have been averted if a rapid home test of any description had been approved five years ago.

????Or ten.

????Or 15.

????Or 20.

????Or 24.

????That's the scandal.

掃描二維碼下載財(cái)富APP
粗大黑人巨精大战欧美成人| 国产日韩精品欧美一区灰灰| 亚洲熟女乱综合一区二区| 国产乱了真实在线观看| 97人伦影院A级毛片| 美女哺乳久久精品免费视频| 久久精品国产亚洲AV果冻传媒| 极品尤物一区二区三区| 亚洲精品无码永久在线观看| 迈开腿让我看一下小鸡蛋视频| 国产香蕉一区二区三区在线视频| 精品毛片拥有数百万视频创作者| 日本免码va在线看免费最| 久久99精品国产99久久| 精品午夜久久福利大片免费| 亚洲中文无码h在线观看| 精品久久久久久久久久久aⅴ| 国产成人无码视频一区二区三区| 激情综合亚洲色婷婷五月app| 无码人妻一区二区三区精品视频| a级毛片100部免费观看| av无码免费岛国动作片片段| 玩弄丰满少妇视频| 国产人人干人人透免费看| 国产色无码专区在线观看| 亚洲日韩精品无码专区加勒比海| 2024国内精品久久久久精品k8| 四虎永久在线精品免费一区二区| 日韩欧美精品日韩综合| 免费无码av片在线观看中文| 亚洲国产成人片在线观看直播| 亚洲AV片不卡无码在线a | 亚洲一区精品视频在线| 国产亚洲第一午夜福利合集| 日韩人妻一区二区| 国产亚洲日韩欧美另类| 亚洲AV乱码久久精品蜜桃| 色窝窝无码一区二区三区| 欧美 亚洲 有码中文字幕| 久久久婷婷五月亚洲97号色| 国产欧美精品一区二区三区四区|