review33.com:談天說地:［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊

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[#1] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊 https://lihkg.com/thread/2177872/page/1 美國知名藥廠 Abbott 雅培宣布，BinaxNOW 測試套裝已獲美國 FDA 緊急使用授權，最快 15 分鐘即知測試結果外，測試套裝售價更只是低至 US$5（約 HK$39）。另外品牌還推出 NAVICA 免費 iOS 及 Android 手機 app 配合 BinaxNOW 測試套裝使用，當中將為測試報告呈陰性反應的用家發出數碼健康通行證，而該通行證會附顯示測試日期結果，方便在手機上查看，且能在每次進行測試後都作出更新，得知最新健康狀況。品牌 CEO Robert B. Ford 表示，我們設計 BinaxNOW 測試套裝和 NAVICA 應用程式是想提供全面測試方案，幫助市民對自己的健康和生活建立更大信心。品牌指 BinaxNOW 測試套裝，測出確診新冠肺炎的機率為 97.1％，呈陰性結果的機率為 98.5％左右。當中操作原理是檢測冠狀病毒表面的微量蛋白，而非病毒本身的基因排序。雖然當中準確性或會較低，但有研究人員認為，使用頻繁、廉價、較不準確的檢測或為控制新冠肺炎大流行的最佳方法。據 FDA 聲明提及，BinaxNOW 測試套裝可供專業醫療保健人員使用，可在急症室、診所，甚至學校等地方進行檢測。只要將測試者鼻腔樣本置於 BinaxNOW 測試卡中，當呈現一條彩色線的話，就代表檢測呈陽性反應。 https://ezone.ulifestyle.com.hk/article/2736373		blackspin 正式會員 219.xxx.xxx.89	2020-08-28 13:14

[#2] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
大陸一定唔會俾佢合格使用。

AndyTKO

正式會員
14.xxx.xxx.74

2020-08-28 13:25

[#3] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
#2 依家香港都未必批

olddude

正式會員
218.xxx.xxx.94

2020-08-28 13:28

[#4] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
搶人生意，罪大惡極！

最後修改時間: 2020-08-28 13:30:23

AndyTKO

正式會員
14.xxx.xxx.74

2020-08-28 13:30

[#5] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
佢老母，香港機場測試要十幾個鐘先有結果，人地唔使一個鐘搞掂。

juno123

正式會員
27.xxx.xxx.93

2020-08-28 13:34

[#6] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
打擊收集市民DNA樣本計劃，又一確鑿證據美帝忘我之心不死！！

hnm

正式會員
220.xxx.xxx.100

2020-08-28 13:37

[#7] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
禾屌吖！同禾以前驗孕一樣咁easy！

AndyTKO

正式會員
14.xxx.xxx.74

2020-08-28 13:40

[#8] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
#7

技術上有d似，小心人家用驗孕棒插你鼻腔就當ok。

bigleung

正式會員
220.xxx.xxx.177

2020-08-28 13:44

[#9] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
"雖然當中準確性或會較低" ?

- 測出確診新冠肺炎的機率為 97.1％ (Sensitivity)
- 呈陰性結果的機率為 98.5％ (Specificity)。

假設香港人現有0.6%人中招 , 100萬人去做, 6,000個中招嘅可以檢測出5,826個，假陰性係174宗，

979,090個健康者，假陽性只得 14,910宗，仲可以即時做多次覆檢！

想知香港全民檢測點樣比較呢？ ^-^

最後修改時間: 2020-08-28 14:22:14

bankguy

正式會員
212.xxx.xxx.18

2020-08-28 14:19

[#10] ［完爆華大基因］雅培 BinaxNOW 測試套裝鼻腔就得 15分鐘完成準確率97% 港紙39蚊
FDA approves inexpensive COVID-19 test that provides results in 15 minutes

Abbott Diagnostics will make 50 million monthly tests by October
Pat Ralph HeadshotBY PAT RALPH
PhillyVoice Staff

The U.S. Food and Drug Administration has authorized a COVID-19 test that produces a rapid result using the same technology as pregnancy tests.

The BinaxNOW test, manufactured by Abbott Diagnostics Scarborough Inc., only costs $5 and produces results within 15 minutes. It's the first coronavirus test where results can be read directly from a testing card.

A health care provider first swabs the patient's nose and then twirls the sample on the card with a testing regent added. If one line appears on the card, the test result is negative. Two lines indicate a positive test result.

The FDA's emergency use authorization requires health care providers to administer the test. It can be conducted at approved point-of-care locations on patients suspected of COVID-19 within seven days of symptom onset.

The test relies on antigens to determine its results, unlike the molecular tests that detect the virus's genetic material. Antigen tests produce faster results, but they generally are not as accurate as molecular tests.

Because of the decreased sensitivity, patients who receive negative test results may need to confirm those results via a molecular test, the FDA said. But the advantage of antigen tests is that they catch positive cases faster, potentially preventing additional people from being exposed to the virus.

According to Abbott, the test accurately diagnoses a positive case 97.1% of the time and correctly diagnoses a negative case 98.5% of the time.

"This new COVID-19 antigen test is an important addition to available tests because the results can be read in minutes, right off the testing card," said Dr. Jeff Shuren, director of the FDA's Center for Devices and Radiological Health.

"This means people will know if they have the virus in almost real-time. Due to its simpler design and the large number of tests the company anticipates making in the coming months, this new antigen test is an important advancement in our fight against the pandemic."

Abbott is currently shipping out about 1 million tests per day. By October, the manufacturer intends to make 50 million tests available on a monthly basis.

The company said it has invested hundreds of millions of dollars into two new facilities to scale up the BinaxNOW test.

Abbott also has developed a corresponding mobile app, Navica, which allows people to store, access and display their test results with organizations that accept results.

If test results are negative, the app will display a digital health pass via a QR code. If test results are positive, patients receive a message to self-quarantine and contact their doctor.

"We intentionally designed the BinaxNOW test and Navica app so we could offer a comprehensive testing solution to help Americans feel more confident about their health and lives," Abbott CEO Robert B. Ford said. "BinaxNOW and the Navica app give us an affordable, easy-to-use, scalable test and a complementary digital health tool to help us have a bit more normalcy in our daily lives."

This is the sixth test that Abbott has launched in the U.S. during the COVID-19 pandemic. The company has provided more than 27 million COVID-19 diagnostics to date, including 14 million detection tests and 13 million antibody tests.

https://www.phillyvoice.com/abbott-binaxnow-covid-19-test-rapid-results-fda-authorization-coronavirus/

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Abbott soars 10% after its 15-minute COVID-19 test wins FDA approval.

最後修改時間: 2020-08-28 14:41:46

bankguy

正式會員
212.xxx.xxx.18

2020-08-28 14:37