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    find Author "WANG Yu" 82 results
    • Establishing Medical Risk Monitoring and Early Warning System for Quality Improvement and Patient Safety

      Release date:2016-08-25 03:34 Export PDF Favorites Scan
    • Establishing M edical Risk M onitoring and Precaution System for Quality Improvement and Patient Safety

      Release date:2016-09-07 02:17 Export PDF Favorites Scan
    • Current status and perspectives of neoadjuvant therapy for locally advanced thyroid cancer

      Patients with locally advanced thyroid cancer often face challenges in achieving radical surgery during initial diagnosis. This has become a significant hurdle in the treatment of thyroid cancer. With the continuous development of systemic therapy for thyroid cancer, several studies have demonstrated that neoadjuvant therapy can shrink tumors in some patients, thereby increasing the chances of complete resection and improving prognosis. Targeted therapy plays a crucial role as a core component of neoadjuvant treatment. Simultaneously, the potential efficacy of immunotherapy has gained attention, showing promising prospects. We aim to summarize the research progress and existing issues regarding neoadjuvant therapy for locally advanced thyroid cancer. We look forward to more high-quality clinical studies providing robust evidence for neoadjuvant therapy in locally advanced thyroid cancer, expanding the breadth of treatment options.

      Release date:2024-11-27 03:04 Export PDF Favorites Scan
    • Study on sensorless suction detection method based on the intrinsic parameter of rotary left ventricular assist devices

      The rotary left ventricular assist device (LVAD) has been an effective option for end-stage heart failure. However, while clinically using the LVAD, patients are often at significant risk for ventricular collapse, called suction, mainly due to higher LVAD speeds required for adequate cardiac output. Some proposed suction detection algorithms required the external implantation of sensors, which were not reliable in long-term use due to baseline drift and short lifespan. Therefore, this study presents a new suction detection system only using the LVAD intrinsic blood pump parameter (pump speed) without using any external sensor. Three feature indices are derived from the pump speed and considered as the inputs to four different classifiers to classify the pumping states as no suction or suction. The in-silico results using a combined human circulatory system and LVAD model show that the proposed method can detect ventricular suction effectively, demonstrating that it has high classification accuracy, stability, and robustness. The proposed suction detection system could be an important part in the LVAD for detecting and avoiding suction, while at the same time making the LVAD meet the cardiac output demand for the patients. It could also provide theoretical basis and technology support for designing and optimizing the control system of the LVAD.

      Release date:2019-06-17 04:41 Export PDF Favorites Scan
    • RESEARCH PROGRESS OF C TERMINAL PROPEPTIDE OF COLLAGEN TYPE II

      Objective To review the research progress of C terminal propeptide of collagen type II (CTX-II), a osteoarthritis (OA) biomarker. Methods Domestic and international l iterature about CTX-II was reviewed extensively and summarized. Results CTX-II is investigated broadly and has the best performance of all currently available biomarkers. CTX-II is a truly useful biomarker for early diagnosis, prognosis, and measurement of treatment response in OA. Conclusion Single CTX-II may be not sufficient for early diagnosis and prognosis of OA, so a combination of CTX-II and other biomarkers or diagnosis methods is needed.

      Release date:2016-08-31 05:41 Export PDF Favorites Scan
    • Clinical Research on Constant Infusion of Propofol for Conscious Sedation under Combined Spinal-epidural Anesthesia

      【摘要】 目的 探討腰硬聯合麻醉復合丙泊酚恒速輸注清醒鎮靜的可行性、理想的藥物劑量、術中知曉情況以及麻醉質量和效果。 方法 收集2009年3-12月480例美國麻醉醫師協會(ASA)Ⅰ~Ⅲ級擬在腰硬聯合麻醉下行下腹部、會陰部、下肢手術的患者480例,隨機分為咪達唑侖組(M組)、丙泊酚Ⅰ組(PA組)、丙泊酚Ⅱ組(PB組)、丙泊酚Ⅲ組(PC組),每組各120例。四組患者均于腰2-3或腰3-4行腰硬聯合麻醉,蛛網膜下腔注入輕比重0.2 %布比卡因12~15 mg,麻醉平面確切后,M組予以咪達唑侖0.04~0.06 mg/kg,PA組先予以負荷量丙泊酚0.50 mg/kg再以2.00 mg/(kg?h)劑量持續泵注,PB組予以負荷量丙泊酚0.75 mg/kg再以3.00 mg/(kg?h)劑量持續泵注,PC組予以負荷量丙泊酚1.00 mg/kg再以3.75 mg/(kg?h)劑量持續泵注。觀察患者給藥前(T0)、給藥1(T1)、3(T2)、5(T3)、10(T4)、30(T5)、60 min(T6)各時點血流動力學平均動脈血壓(MAP)、心率(HR)的變化、腦電雙頻指數(BIS)值及鎮靜評分、術中所看到的圖片的回憶及不良反應。 結果 各組在給予鎮靜藥后MAP、HR均有所下降,但測量值的變化在正常范圍內;在T3時間點,各組BIS值及鎮靜/警醒OAA/S評分降低,與T0比較,差異有統計學意義(Plt;0.05);與其他3組比較,在T4、T5、T6時點PC組BIS值與OAA/S評分降低,差異有統計學意義(Plt;0.05),PC組的鎮靜遺忘滿意率高于其他3組;各組間未見發生嚴重的舌后墜、呼吸暫停和血氧飽和度(SpO2)lt;90%。 結論 在下腹部、下肢手術中,應用腰硬聯合麻醉復合1.00 mg/kg負荷量的丙泊酚繼而以3.75 mg/(kg?h)劑量持續泵注,可取得良好的鎮靜效果,不良反應小。【Abstract】 Objective To investigate the feasibility, ideal dose, intra-operative awareness as well as the quality and effectiveness of constant infusion of propofol under combined spinal-epidural anesthesia (CSEA) for conscious sedation. Methods A total of 480 patients at ASA grade Ⅰ-Ⅲ to be operated in the lower abdomen, perineum and lower limbs under CSEA from March to December 2009 were randomly divided into four groups: midazolam group (M group), propofol group Ⅰ (PA group), propofol group Ⅱ (PB group), and propofol group Ⅲ (PC group), with 120 patients in each group. All four groups of patients underwent CSEA at L2-3 or L3-4 and accepted pinal injection of 12-15 mg of 0.2% hypobaric bupivacaine. After the anesthetic plane was confirmed, patients in M group accepted 0.04-0.06 mg/kg of midazolam; patients in PA group accepted propofol at a loading dose of 0.50 mg/kg followed by continuous infusion at a dose of 2.00 mg/(kg?h); patients in PB group accepted propofol at a loading dose of 0.75 mg/kg followed by continuous infusion at a dose of 3.00 mg/(kg?h); patients in PC group accepted propofol at a loading dose of 1.00 mg/kg followed by continuous infusion at a dose of 3.75 mg/(kg?h). The change of hemodynamics including the mean arterial pressure (MAP) and the heart rate (HR), bispectral index (BIS) values, sedation scores, memory of pictures seen during operation and adverse effects before drug administration (T0), at minute 1 (T1), 3 (T2), 5 (T3), 10 (T4), 30 (T5) and 60 (T6) after drug administration were observed. Results MAP and HR decreased in all the four groups after administration of sedatives, but the changes of measured values were within normal ranges. BIS value and the Observer’s Assessment of Alertness and Sedation (OAA/S) scale decreased in all groups at T3, compared with those at T0 (Plt;0.05). Compared with the other 3 groups, BIS valueand OAA/S scale were significantly lower in PC group at T4, T5 and T6 (Plt;0.05), and the satisfaction rate of sedation and amnesia was much higher. No serious glossocoma, apnea and SpO2 below 90% was observed in all the four groups. Conclusion During the surgery of lower abdomen and lower limbs, application of CSEA combined with propofol at a loading dose of 1.00 mg/kg followed by continuous infusion at a dose of 3.75 mg/(kg?h) can achieve a good sedative effect, with little side effect.

      Release date:2016-09-08 09:24 Export PDF Favorites Scan
    • Relationship Between Using Proton Pump Inhibitors and the Hospital-acquired Pneumonia in Critical Patients

      【摘要】 目的 〖JP2〗研究質子泵抑制劑(PPI)是否為危重患者發生醫院獲得性肺炎的危險因素。 方法 收集2002年6月-2009年6月收治的198例重癥患者資料,分為使用PPI組(96例)和未使用PPI組(102例)。采用logistic回歸分析PPI使用情況和醫院獲得性肺炎的關系。 結果 使用PPI組肺炎的發生率較高(26.9%),尤其是PPI使用時間超過7 d者(37.5%)。在不同的多變量logistic回歸模型中,分別用APACHE Ⅱ評分和入住重癥監護室原因校正后,使用PPI以及使用天數均是醫院獲得性肺炎發生的危險因素(P=0.031,OR=2.230,95%CI:1.957~2.947;P=0.002,OR=1.824,95%CI:1.457~2.242)。 結論 長時間應用PPI可能是增加ICU患者發生醫院獲得性肺炎的一種風險因素。【Abstract】 Objective To identify whether proton pump inhibitors (PPI) is a risk factor of hospital-acquired pneumonia (HAP) in critical patients. Methods The clinical data of the critical patients admitted to ICU from June 2002 to June 2009 were retrospectively analyzed. A total of 198 patients were divided into two groups: 96 in PPI group and 102 in non-PPI group. The relationship between PPI and HAP was analyzed by logistic regression. Results The patients in PPI group had a higher risk of HAP (26.9%), especially who were treated with PPI more than 7 days (37.5%). Adjusted by APACHE Ⅱ score and reason for admission to ICU, PPI therapy and the using duration of PPI were both the risk factors of HAP in different multiple logistic models (P=0.031, OR=2.230, 95%CI: 1.957-2.947; P=0.002, OR=1.824, 95%CI: 1.457-2.242). Conclusion Long-term use of PPI is a risk factor of HAP.

      Release date:2016-09-08 09:51 Export PDF Favorites Scan
    • Short-term effectiveness of accurate decompression via foraminoplasty in treatment of lumbar lateral recess stenosis

      Objective To discuss the effectiveness and the safety of accurate decompression via foraminoplasty in treating lumbar lateral recess stenosis patients who accompanied by disk-flavum ligamentum space and bony lateral recess stenosis, and to analysis the short-term effectiveness of the surgical procedures. Methods Forty-five lumbar lateral recess stenosis patients accompanied by disk-flavum ligamentum space and bony lateral recess stenosis were treated by accurate decompression via foraminoplasty between January 2013 and January 2016. There were 29 males and 16 females with a median age of 58 years (range, 42-82 years). The disease duration was 3-96 months (mean, 24.4 months). The lesion segment included L4, 5 in 36 cases and L5, S1 in 9 cases. The visual analogue scale (VAS) score of low back pain and leg pain at preoperation and last follow-up were recorded, and the modified Macnab criteria was used to evaluate the effectiveness at last follow-up. Postoperative CT and MRI were reviewed to evaluate the stability and decompression of the lumbar spine. Results All operations were successfully completed. All the 45 patients were followed up 3-18 months (median, 11 months). Dural tear occurred in 2 cases during operation, bone graft removed into the spinal canal in 1 case, postoperative low back pain occurred in 5 cases, and there was no nerve root injury, hematoma formation, or other complications. The leg pain VAS score at last follow-up (0.6±1.2) was significantly improved when compared with preoperative score (5.7±1.4) (t=8.981, P=0.001); and the low back pain VAS scores showed no significant difference between preoperation and last follow-up (1.5±1.3vs. 1.7±1.4;t=0.535, P=0.585). According to the modified Macnab criteria, the results were excellent in 20 cases, good in 22 cases, fair in 2 cases, and poor in 1 case at last follow-up, and the excellent and good rate was 93.3%. Conclusion Accurate decompression via foraminoplasty is an effective, safe, and less invasive way for treating lumbar recess stenosis patients accompanied by disk-flavum ligamentum space and bony lateral recess stenosis.

      Release date:2017-11-09 10:16 Export PDF Favorites Scan
    • Anesthetic Treatment of Radiofrequency Maze Procedure during Valve Replacement

      目的:本文回顧性分析總結32例心臟瓣膜置換術同期改良迷宮術患者的麻醉處理。方法:32例瓣膜病合并心房顫動患者,ASA分級Ⅱ-Ⅳ級,心功能ⅢⅣ級,采用以芬太尼為主的全身麻醉,術中以硫酸鎂和艾司洛爾調控應激反應,復溫后多聯合使用多巴胺或(和)多巴酚丁胺5~10μg/kg·min、硝酸甘油或硝普鈉0. 5~5μg/kg·min等血管活性藥物以達到擴張血管增強心肌收縮力、降低心臟負荷、維持循環穩定的目的。停機后預防性安置心外膜起搏導線,使用異丙腎上腺素后心率仍慢者,及時運用臨時起搏,保證有效的心肌收縮和穩定的心率。結果:射頻消融時間為32±5分鐘,主動脈阻斷時間89±12分鐘; 體外循環時間109±20分鐘。心臟自動復跳29例, 電除顫復跳3例, 32例患者術后均為竇性心律。5例患者使用臨時起搏器。結論:完善的術前準備和圍術期重視心肺功能的支持治療, 合理調控應激反應等措施是手術成功的重要基礎。

      Release date:2016-09-08 10:01 Export PDF Favorites Scan
    • The Effect of Hypoxic Preconditioning on Old Rat Model of Postoperative Fatigue Syndrome Caused by Excision of Bilateral Accessory and Hysterectomy

      目的:研究缺氧預處理對老年大鼠子宮及雙附件切除術后疲勞是否有改善作用,并通過對比觀察超氧化物歧化酶及丙二醛水平的變化,初步探討缺氧預處理的作用機制。方法:將老年大鼠分為空白對照組、對照組、缺氧預處理三組。空白對照組為假手術組,對照組為子宮及雙附件切除術組, 缺氧預處理組為缺氧預處理加子宮及雙附件切除術組。對比觀察缺氧預處理對大鼠體力活動及血清超氧化物歧化酶和丙二醛水平的影響。結果:空白對照組、對照組、缺氧預處理三組大鼠懸尾不動時間分別為:(21±3)s,(83±10)s,(44±5)s,各組間比較Plt;0.05。三組SOD活性分別為:(131.23±5.31)U/L,(36.12±9.68)U/L,(73.01±9.82)U/L,各組間比較Plt;0.05。三組MDA水平分別為:(9.78±1.26)μmol/L,(29.87±3.13)μmol/L,(15.98±2.21)μmol/L,各組間比較Plt;0.05。結論:缺氧預處理可提高老年大鼠的抗氧化能力,對老年大鼠子宮及雙附件切除術后疲勞綜合征有明顯的改善作用。

      Release date:2016-09-08 10:02 Export PDF Favorites Scan
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