| 4 | 1/1 | 返回列表 |
| 查看: 619 | 回復(fù): 3 | |||
| 本帖產(chǎn)生 1 個 翻譯EPI ,點擊這里進行查看 | |||
houxuezhi521木蟲 (初入文壇)
|
[求助]
求一段翻譯,真心翻譯不明白,主要是前半部分 謝謝
|
||
|
Only 1 study, a post hoc subgroup analysis of the Efficacy and Safety of Subcutaneous Enoxaparin in Non–Q-wave Coronary Events (ESSENCE) and Thrombolysis in Myocardial Infarction (TIMIIIB) trials, provided data from a controlled environment in patients with CKD. Although renal impairment was an exclusion criterion in the 2 trials, approximately 2% of the combined study population had CKD stage 4 or 5 (no renal replacement therapy). This analysis showed that the rate of major hemorrhage in patients with CKD was significantly greater than in those with no renal impairment, regardless of whether UFH or enoxaparin was administered (6.6% versus 1.1%; P<0.0001). However, numbers were small (UFH, n=74; enoxaparin, n=69) compared with the overall study sample size (n=6,969), as was the number of major bleeds in the CKD group (UFH, 4 patients; enoxaparin, 5 patients). UFH has been in clinical use since 1937, and there are no published trials comparing complication rates in patients with normal renal function and those with CKD. However, an authoritative review of the relevant literature was published in 1993 and remains valid today. It concludes that use of UFH in therapeutic dosages (>15,000 IU/d) typically is marked by average daily frequencies of fatal, major, and minor bleeding of 0.05%, 0.8%, and 2%, respectively |
|
本帖內(nèi)容被屏蔽 |
|
非冠狀動脈粥樣硬化波冠狀動脈研究中,一項關(guān)于皮下注射依諾肝素的療效和安全性分析(ESSENCE)和其在心肌梗死(TIMIIIB)試驗中溶血作用的研究,僅有一項關(guān)于患有CKD患者的控制環(huán)境的研究提供相關(guān)數(shù)據(jù)。 盡管在兩組實驗中腎功能損害是一個不予考慮的條件,仍有接近2%的綜合研究人群處于CKD的第四或者第五階段(無腎臟替代療法)。分析結(jié)果表明,無論是否使用依諾肝素,患有CKD的患者大出血的比例要明顯高于無腎臟替代療法的患者。(6.6% :1.1%; P<0.0001)。但是,相對于全體樣本數(shù)為6969,數(shù)據(jù)量較。ㄆ胀ǜ嗡兀74例;依諾肝素, 69例),其中CKD組大出血的患者數(shù)(普通肝素,4例;依諾肝素, 5例)。 普通肝素自1937年起在臨床應(yīng)用,尚無公開的實驗比較腎臟功能正常患者和患有CKD患者的并發(fā)癥比率。但是,1993年一家相關(guān)權(quán)威機構(gòu)發(fā)表的觀點現(xiàn)今仍具有權(quán)威性。其結(jié)論包括:在普通肝素的常用治療劑量(> 15,000 IU/天)下,致命,大量和少量出血每日平均頻率分別為0.05%,0.8%,和2%。 |
木蟲 (著名寫手)
|
樓上翻譯提供了很好的參考。但是,有幾個地方錯了。 僅有一項研究提供了可控環(huán)境下慢性腎。–KD)病人的數(shù)據(jù),該研究針對非Q波冠脈事件中皮下注射依諾肝素鈉療效和安全性(ESSENCE)以及心肌梗死(TIMIIIB)臨床試驗進行了事后亞組分析。在2項臨床試驗中,盡管腎功能損害是排除標(biāo)準(zhǔn),仍有約2%的聯(lián)合試驗人群處于CKD4期或5期(無腎臟替代療法)。分析結(jié)果顯示,不管使用普通肝素還是依諾肝素,CKD患者大出血的比例要明顯高于無腎功能損害的患者(6.6% :1.1%; P<0.0001)。但是,相比整體樣本大。╪=6969),樣本數(shù)較。ㄆ胀ǜ嗡,74例;依諾肝素, 69例),CKD組中大出血患者的樣本數(shù)也。ㄆ胀ǜ嗡,4例;依諾肝素, 5例)。 普通肝素自1937年開始臨床應(yīng)用,尚無公開的臨床試驗對腎功能正;颊吆虲KD患者的并發(fā)癥比率進行比較。但是,1993年一篇相關(guān)文獻的權(quán)威綜述依然有效,文章結(jié)論指出,在普通肝素的常用治療劑量(> 15,000 IU/天)下,致死、大量和少量出血的平均日頻率分別為0.05%、0.8%和2%。 |

| 4 | 1/1 | 返回列表 |
| 最具人氣熱帖推薦 [查看全部] | 作者 | 回/看 | 最后發(fā)表 | |
|---|---|---|---|---|
|
[考研] 070305高分子化學(xué)與物理 304分求調(diào)劑 +5 | c297914 2026-03-28 | 5/250 |
|
|---|---|---|---|---|
|
[考研] 283求調(diào)劑 +3 | A child 2026-03-28 | 3/150 |
|
|
[考研] 化學(xué)0703 調(diào)劑 306分 一志愿211 +4 | 26要上岸 2026-03-28 | 4/200 |
|
|
[考研] 321求調(diào)劑 +6 | 材料cailiao 2026-03-21 | 6/300 |
|
|
[考研] 數(shù)一英一271專碩(085401)求調(diào)劑,可跨 +4 | 前行必有光 2026-03-28 | 5/250 |
|
|
[考研] 081200-314 +3 | LILIQQ 2026-03-27 | 4/200 |
|
|
[考研] 085405 考的11408求各位老師帶走 +3 | Qiu學(xué)ing 2026-03-28 | 3/150 |
|
|
[考研] 291求調(diào)劑 +6 | HanBeiNingZC 2026-03-24 | 6/300 |
|
|
[考研] 285求調(diào)劑 +4 | AZMK 2026-03-27 | 7/350 |
|
|
[考研] 265求調(diào)劑11408 +3 | 劉小鹿lu 2026-03-27 | 3/150 |
|
|
[考研] 考研化學(xué)308分求調(diào)劑 +10 | 你好明天你好 2026-03-23 | 12/600 |
|
|
[考研] 305求調(diào)劑 +5 | 哇盧卡庫 2026-03-26 | 5/250 |
|
|
[考研] 一志愿鄭大085600,310分求調(diào)劑 +5 | 李瀟可 2026-03-26 | 5/250 |
|
|
[論文投稿] Journal of Mechanical Science and Technology +3 | Russ_ss 2026-03-25 | 5/250 |
|
|
[考研] 085600 材料與化工 329分求調(diào)劑 +9 | Mr. Z 2026-03-25 | 9/450 |
|
|
[考研] 生物技術(shù)與工程 +3 | 1294608413 2026-03-25 | 4/200 |
|
|
[考研] 284求調(diào)劑 +15 | Zhao anqi 2026-03-22 | 15/750 |
|
|
[考研] 300分,材料,求調(diào)劑,英一數(shù)二 +5 | 超贊的 2026-03-24 | 5/250 |
|
|
[有機交流]
20+3
|
FENGSHUJEI 2026-03-23 | 5/250 |
|
|
[考研] 292求調(diào)劑 +4 | 鵝鵝鵝額額額額?/a> 2026-03-24 | 4/200 |
|