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        west china medical publishers
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        find Keyword "插管" 73 results
        • 術前選擇性動脈灌注化療治療結直腸癌24例報告

          Release date:2016-08-29 09:16 Export PDF Favorites Scan
        • 緊急氣管插管后張力性氣胸一例

          Release date:2019-12-12 04:12 Export PDF Favorites Scan
        • Establishment of prolonged veno-venous extracorporeal membrane oxygenation support model in large animals

          ObjectiveTo explore the safety and feasibility of the establishment method and management strategy of prolonged support model with veno-venous extracorporeal membrane oxygenation (V-V ECMO) under dual lumen cannula (DLC) in conscious sheep.MethodsThree adult male sheep were selected. An Avalon Elite DLC was inserted into the superior vena cava, right atrium, and inferior vena cava through the right jugular vein and was connected with centrifugal pump and oxygenator to establish the extracorporeal membrane oxygenation circuit. All the 3 sheep were transferred into the monitoring cage after operation and were ambulatory after anesthesia recovery. Hemodynamic parameters and extracorporeal membrane oxygenation performance were measured every day.ResultsAll three sheep survived to the end of the experiment (7 days). In the whole process of the experiment, the basic vital signs of the experimental sheep were stable, and no serious bleeding or thrombotic events occurred. During the experiment, hemoglobin concentration and platelet count were relatively stable, plasma free hemoglobin was maintained at a low level, extracorporeal membrane oxygenation flow rate was stable, and oxygenation performance of oxygenator was good.ConclusionProlonged V-V ECMO model in conscious sheep under DLC is feasible and stable.

          Release date:2022-09-20 08:57 Export PDF Favorites Scan
        • Non-intubated, intravenous anesthesia with spontaneous ventilation versus routine intravenous anesthesia in video-assisted thoracoscopic surgery: A randomized controlled trial

          Objective To compare the feasibility and safety of video-assisted thoracoscopic surgery (VATS) under non-intubated, intravenous anesthesia with spontaneous ventilation. Methods A total of 80 patients undergoing VATS (48 wedge resections, 8 sympathectomies, 24 pleural biopsies) between January 2015 and June 2017 were included. Those patients were randomized into two groups. The 40 patients were enrolled as a treatment group (19 males and 21 females at age of 23.3±10.2 years) and received surgery under non-intubated intravenous anesthesia with spontaneous ventilation. And the other 40 patients were enrolled as a control group (21 males and 19 females at age of 22.2±9.9 years) and received surgery under routine intravenous anesthesia with intubated ventilation. Results Comparing with the control group, the patients of the treatment group had lower white blood cell count (5.8×109±2.4×109 vs. 7.3×109±3.6×109, P<0.001), lower gastrointestinal adverse reaction rate (7.5%vs. 27.5%, P=0.002), lower sore throat rate (5.0% vs. 30.0%, P<0.001), lower cough grade (0.9±0.3vs 2.1±0.5, P<0.050), shorter drainage time (1.8±1.6 dvs. 3.7±1.8 d, P<0.050) and shorter hospital stay (2.3±1.8 dvs. 5.8±2.3 d, P<0.050). Conclusion Video-assisted thoracoscopic surgery under non-intubated, intravenous anesthesia with spontaneous ventilation is safe and feasible, which also has certain advantages in reducing the postoperative complications and promoting patients' quick recovery from surgery.

          Release date:2018-05-02 02:38 Export PDF Favorites Scan
        • Application of noninvasive ventilation in patients with unplanned extubation in intensive care unit

          ObjectiveTo investigate the application value of noninvasive ventilation (NIV) performed in patients with unplanned extubation (UE) in intensive care unit (ICU).MethodsThis was a retrospective analysis. The clinical data, application of NIV, reintubation rate and prognosis of UE patients in the ICU of this hospital from January 2014 to December 2018 were reviewed, and the patients were assigned to the control group or the NIV group according to the application of NIV after UE. The data between the two groups were compared and the application effects of NIV in UE patients were evaluated.ResultsA total of 66 UE patients were enrolled in this study, including 44 males and 22 females and with an average age of (64.2±16.1) years. Out of them, 41 patients (62.1%) used nasal catheter or mask for oxygenation as the control group, 25 patients (37.9%) used NIV as the NIV group. The Acute Physiology andChronic Health EvaluationⅡ score of the control group and the NIV group were (18.6±7.7) vs. (14.8±6.3), P=0.043. The causes of respiratory failure in the control group and the NIV group were as follows: pneumonia 16 patients (39.0%) vs. 7 patients (28.0%), postoperative respiratory failure 7 patients (17.1%) vs. 8 patients (32.0%), chronic obstructive pulmonary disease 8 patients (19.5%) vs. 6 patients (24.0%), others 5 patients (12.2%) vs. 4 patients (16.0%), heart failure 3 patients (7.3%) vs. 0 patients (0%), nervous system diseases 2 (4.9%) vs. 0 patients (0%), which showed no significant difference between the two groups. Mechanical ventilation time before UE were (12.5±19.8) vs (12.7±15.2) d (P=0.966), PaO2 of the control group and the NIV group before UE was (114.9±37.4) vs. (114.4±46.3)mm Hg (P=0.964), and oxygenation index was (267.1±82.0) vs. (257.4±80.0)mm Hg (P=0.614). Reintubation rate was 65.9% in the control group and 24.0% in the NIV group (P=0.001). The duration of mechanical ventilation was (23.9±26.0) vs. (21.8±26.0)d (P=0.754), the length of stay in ICU was (34.4±36.6) vs. (28.5±25.8)d (P=0.48). The total mortality rate in this study was 19.7%. The mortality rate in the control group and NIV group were 22.0% and 16.0% (P=0.555).ConclusionPatients with UE in ICU may consider using NIV to avoid reintubation.

          Release date:2019-11-26 03:44 Export PDF Favorites Scan
        • 經口與經鼻氣管插管在急診搶救中的應用對比分析

          目的對比經口氣管插管和經鼻氣管插管在急診搶救的優缺點。 方法回顧分析2010年1月-2013年1月155例急救氣管插管患者,其中80例患者為明視經口氣管插管(KC組),75例患者為明視經鼻氣管插管(BC組),比較兩組患者的一次插管成功率、插管時間、并發癥以及患者耐受性等。 結果KC組和BC組一次插管成功率分別為86.2%和88.0%,差異無統計學意義(P>0.05);KC組平均插管時間為(50±20)s,BC組平均插管時間(74±22)s,差異有統計學意義(P<0.05);插管過程中出現的并發癥發生率KC組明顯多于BC組,而患者耐受性BC組明顯好于KC組。 結論經口氣管插管操作簡單、快速,適合急診搶救。但經鼻氣管插管對患者體位要求低,并發癥較低以及患者耐受性較好,值得推廣。

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        • 1,3-β-D葡聚糖檢測對尿路插管所致真菌感染的診斷價值

          【摘要】 目的 探討尿路插管所致真菌感染患者的血漿和尿液中1,3-β-D葡聚糖檢測的臨床意義。 方法 將2009年1-5月47例尿路插管所致真菌感染患者設為試驗組,50例正常健康體檢者設為對照組,分別檢測其血漿和尿液中1,3-β-D葡聚糖的水平。 結果 試驗組與對照組比較,血漿及尿液中1,3-β-D葡聚糖含量差異有統計學意義(Plt;0.001);試驗組的尿液和血漿中1,3-β-D葡聚糖含量比較,有統計學意義(Plt;0.05),尿液中的1,3-β-D葡聚糖含量高于血漿。 結論 血漿和尿液1,3-β-D葡聚糖水平檢測可作為診斷泌尿系統真菌感染的可靠指標,且尿液樣本的診斷價值高于血漿。

          Release date:2016-09-08 09:50 Export PDF Favorites Scan
        • Total Arch Replacement with Proximal Lengthening Grafted Stent and Modified Inno-minate Artery Cannula for Stanford A Aortic Dissection

          ObjectiveTo evaluate the short-term result of proximal lengthening grafted stent and modified innominate artery cannula for Stanford A aortic dissection. Method We retrospectively analyzed the clinical data of 21 patients with Stanford A aortic dissection in our hospital between December 2012 and January 2015. There were 16 males and 5 females at a mean age of 57 years. All 21 patients underwent total arch replacement with proximal lengthening grafted stent and modified innominate artery cannula invented by our center. Result The mean operation time of 21 patients was 187.0±31.1 minutes, the mean cardiopulmonary bypass time was 116.0±32.0 minutes, the mean aortic block time was 87.0±23.0 minutes, the mean selective cerebral perfusion (SCP) time was 23.0±3.9 minutes, the mean breathing machanical ventilation time was 19.0±6.0 hours, and the mean intensive care unit stay time was 3.0±0.9 days. All patients had a good recovery after surgery. There was no death or severe complications. ConclusionThe technique of total arch replacement with proximal lengthening grafted stent and modified innominate artery cannula for Stanford A aortic dissection is effective, easy, and safe. The short-term result is satisfying.

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        • Thrombolysis infusion via microcatheter treating central retinal artery occlusion

          ObjectiveTo investigate the therapeutic effects of thrombolysis infusion via microcatheter on the treatment of central retinal artery occlusion(CRAO). MethodsUrokinase (UK) was directly infused via ophthalmic artery (OA) by microcatheter (6 patients) or via intravenous (7 patients) to dissolve the thrombus. The patency of the artery was evaluated by fundus fluorescein angiography (FFA), and the effect of fibrinolytic activity on the systemic changes was observed by blood biochemical examination simultaneously. ResultsIn 6 patients in the microcatheter group, 5 had completely and 1 had partly reopened OA on the morrow of UK infusion with the patency rate of 83.33%, while in 7 patients in vein group, 3 completely reopened, 2 partly reopened and 2 obstructed OA were found with the patency rate of 42.86%. The difference between the two groups was significant. No obvious change of index of blood coagulation system was found in catheter group, which had great disparity compared with the vein group.ConclusionUrokinase infusion via microcatheter in CRAO has better therapeutic impact and smaller effect on systemic action. (Chin J Ocul Fundus Dis, 2005,21:16-19)

          Release date:2016-09-02 05:52 Export PDF Favorites Scan
        • 胃網膜動脈插管區域性化療治療晚期胃癌

          Release date:2016-08-29 03:20 Export PDF Favorites Scan
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