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        find Keyword "方案" 85 results
        • Cisplatin versus Other Platinum Combined with Etoposide in Treatment of Small Cell Lung Cancer: A Meta-analysis

          ObjectiveTo systematically review the efficacy and safety of cisplatin combined with etoposide versus other platinum combined with etoposide in the treatment of small cell lung cancer (SCLC). MethodsWe searched PubMed, The Cochrane Library (Issue 8, 2013), MEDLINE (Ovid), CNKI, VIP and WanFang Data to collect randomized controlled trials (RCTs) concerning the efficacy and safety of cisplatin combined with etoposide (the cisplatin group) versus other platinum combined with etoposide (the control group) for SCLC. The search was up to August 2013. Two reviewers screened literatures according to the inclusion and exclusion criteria, extracted data and assessed the methodological quality of included studies. And then, meta-analysis was performed by using RevMan 5.2 software. ResultsA total of 6 RCTs involving 684 patients were included. The results of meta-analysis showed that there were no significant differences in disease control rate (DCR) (RR=1.03, 95%CI 0.91 to 1.17, P=0.63), overall response rate (ORR) (RR=1.04, 95%CI 0.97 to 1.11, P=0.33), occurrence of leukocytopenia (RR=0.97, 95%CI 0.81 to 1.17, P=0.77), decreased hemoglobin (RR=0.89, 95%CI 0.61 to 1.31, P=0.56) between the cisplatin group and the control group. Occurrence of thrombocytopenia was lower (RR=0.49, 95%CI 0.38 to 0.63, P<0.000 01) while occurrence of nausea and vomiting was higher (RR=1.80, 95%CI 1.40 to 2.31, P<0.000 01) in the cisplatin group. ConclusionCurrent evidence shows that the clinical efficacy of cisplatin combined with etoposide for SCLC is equal to other platinum combined with etoposide, but it has a certain advantage in decreasing the aggregative rate of platelets, while the gastrointesnial reaction patients should avoid using cisplatin combined with etoposide.

          Release date:2016-10-02 04:54 Export PDF Favorites Scan
        • Pay attention to the correct diagnosis and rational treatment of ciliary body tumors

          Ciliary body tumor is a rare intraocular tumor. Due to its unique anatomical location, its correct diagnosis and reasonable treatment are very difficult problems. In terms of diagnosis and differential diagnosis, ophthalmologists need to fully utilize the role of slit lamp microscope and transillumination experiment to capture secondary changes in the anterior segment caused by hidden ciliary body tumors, such as monocular localized cataract, lens indentation, and pigment dissemination, etc. Ophthalmological imaging methods, especially ultrasound biomicroscopy, can achieve the purpose of early detection and early diagnosis. According to the size, location and morphological characteristics of the tumor, a reasonable treatment plan is formulated. Since ciliary body tumors are mostly benign, the recurrence rate of local resection is low, which can satisfy the pathological diagnosis and preserve part of the patient's vision. Therefore, eye-preserving treatment should be advocated. However, enucleation remains the treatment of choice for tumors that are too large to be treated with local excision or radiation, eyes with refractory glaucoma, and tumors that do not respond to radiation therapy.

          Release date:2022-04-12 05:14 Export PDF Favorites Scan
        • 以問題為基礎的教學模式下精細化教學方案在臨床教學中的應用

          目的 探討以問題為基礎(problem-based learning,PBL)的教學模式下精細化教學方案在消化內科臨床護理教學中的應用效果。 方法 選取 2013 年 7 月—2015 年 7 月在成都上錦南府醫院消化內科實習的護理學生 136 名,采用隨機數字表法將護生分為試驗組(71 例)和對照組(65 例),試驗組在 PBL 教學模式下精細化教學目標開展臨床教學工作,對照組采用傳統的方法帶教,比較兩種教學方式對臨床教學質量的影響。 結果 試驗組在理論成績、操作技能方面 [(92.52±3.83)、(95.48±2.67)分] 優于對照組 [(88.72±2.66)、(91.45±2.95)分],差異有統計學意義(P<0.05)。且 PBL 教學模式下精細化教學目標的教學方法能培養學生的臨床思維能力及學習主動性,提高護生的語言表達能力及解決實際問題的能力。 結論 PBL 教學模式下精細化教學方案,能有效提高護理教學質量。

          Release date:2017-08-22 11:25 Export PDF Favorites Scan
        • Effects of Vitamin K2 Plus 5-Fluorouracil on Proliferation,Migration,and Invasiveness of Hepatocellular Carcinoma Cells

          ObjectiveTo investigate effects of vitamin K2 in combination with 5-fluorouracil (5-FU) on proliferation, migration, and invasiveness of hepatocellular carcinoma cells in vitro. MethodsHuman hepatocellular carcinoma PLC/RAF/5 cells were cultured in vitro and exposed to vitamin K2 (10 μmol/L) and 5-FU (10 μg/mL) alone or in combination for 24 h. The cell proliferation, migration, and invasiveness were measured by CCK-8 assay, wound-scratch assay, and Matrigel invasion chamber assay, respectively. ResultsThe abilities of proliferation, migration, and invasion of PLC/RAF/5 cells were significantly decreased after either alone vitamin K2 or 5-FU treatment (all P<0.05) as compared with the control cells, and above effects were further enhanced by the vitamin K2 in combination with 5-FU treatment as compared with either alone drug treatment (all P<0.05). ConclusionCombination use of vitamin K2 and 5-FU might be an effective method for inhibiting growth, migration, and invasiveness of hepatocellular carcinoma cells.

          Release date:2016-11-22 10:23 Export PDF Favorites Scan
        • Analysis of Time and Causes of Death of 211 Cerebral Hemorrhage Patients

          目的:分析腦出血死亡時間及死因,找出腦出血不同死亡時間的主要死因,為制定腦出血不同時間的相應救治措施提供依據。方法:回顧性總結分析211 例腦出血死亡病例的死亡時間、主要死因,找出不同死亡時間對應的主要死因。 結果: (1)死亡時間:≤3 天 91 例、4~7天 52 例、8~14 天 42 例、15~21 天18 例、22~28 天 7 例、≥ 29 天 1 例。(2)死亡原因:169 例死于腦疝及中樞性呼吸、循環衰竭;20例死于肺部感染;10 例死于消化道出血;4 例死于多器官功能衰竭;4 例死于心臟病變(如心臟猝死、心肌梗塞、心功能衰竭);其它4例(痰窒息、腎功能衰竭、肝功能衰竭)。(3)不同死亡時間主要死亡原因:≤3 天 90 例死于腦疝及中樞性呼吸、循環衰竭,僅 1 例死于消化道出血;4~7 天47 例死于腦疝及中樞性呼吸、循環衰竭,3 例死于肺部感染,死于心臟病變及其它各1例;8~14 天 29 例死于腦疝及中樞性呼吸、循環衰竭,8 例死于肺部感染,2 例死于消化道出血,死于心臟病變、多器官功能衰竭、其它各 1 例;15~21 天 7 例死于肺部感染,5 例死于消化道出血,3 例死于腦疝及中樞性呼吸、循環衰竭,死于心臟病變、多器官功能衰竭、其它各1例;22~28天死于消化道出血、肺部感染各2 例,死于心臟病變、多器官功能衰竭、其它各1 例,已無死于腦疝及中樞性呼吸、循環衰竭者;29 天后死于多器官功能衰竭1 例。結論: 腦出血死亡時間不同,其主要死亡原因不同。臨床應該針對不同死亡時間的主要死因制定相應救治方案,以降低死亡率。

          Release date:2016-09-08 10:00 Export PDF Favorites Scan
        • How Allocation Concealment Is Handled in Cochrane Reviews

          Objective ① To document the way in which allocation concealment is described and coded for studies included in Cochrane Reviews.②To feed back any gaps or miscodings to individual review groups.③ To suggest changes and expansions to advice on how to code and describe allocation concealment methods.Methods The coding and description of methods of allocation concealment for studies included in all 1 596 reviews on issue 1, 2003 of The Cochrane Library are being extracted.So far results are available for 10.8% (173/1 596) of reviews containing 1 844 studies, from 10 Collaborative Review Groups (CRGs).Discrepancies, and inconsistencies with the Cochrane Reviewers’ Handbook, are being documented and analysed.Results The current coding of the adequacy of allocation concealment in studies included in Cochrane reviews is not likely to be very accurate.This is due to failure to describe methods of allocation concealment (38.6% of the sample of 1 844 studies) as well as miscoding (at least an additional 9.2%).The most common method for studies coded A was some variation of envelope use (133/675-19.7% of all A codes). The most common "method" for studies coded B was method unclear or not described in the report of the study (426/665, 64% of all B codes).Conclusions Since adequate allocation concealment is so important in protecting against bias in randomised controlled trials, it needs to be accurately coded and described.We need to improve how this is done for studies included in Cochrane Reviews.Since over half the studies coded as D were likely to have been where reviewers omitted to enter a code, the default should be changed from D to "code not supplied".Structural changes to RevMan are suggested-ideally the addition of a separate new study quality assessment table with fixed headings as well as the facility to enter free text.Suggestions for improving coding in particular reviews will be fed back to CRGs in the next stages of this project.Suggestions for additions to the Cochrane Reviewers’ Handbook are also made.

          Release date:2016-09-07 02:27 Export PDF Favorites Scan
        • 影響我院門診患者滿意度的因素分析及解決方案

          目的:分析影響門診患者滿意度的因素,并提出有針對性的解決方案。方法:2008年隨機對筆者所在醫院門診患者滿意度問卷調查2000例,患者需求、基本情況隨機問卷調查1000例,對調查統計結果進行分析。結果:2008年度筆者所在醫院門診患者綜合滿意度為85.24%,其中滿意度最低的單項為掛號、等候時間及服務態度;收集的主要批評意見包括(按意見多少排序):掛號難;檢查、就診等候時間長;部分工作人員服務態度差等。結論:影響醫院門診患者滿意度的主要因素包括:掛號難(號源不能滿足需求)、等候時間長以及部分工作人員服務態度差等問題。筆者對此提出了相應的解決方案。

          Release date:2016-09-08 10:00 Export PDF Favorites Scan
        • Interventions to screen for human immune-deficiency virus among people donating blood[Protocol]

          Background AIDS (acquired immune deficiency syndrome) has become the most devastating disease which humankind has ever encountered. Human immune-deficiency virus (HIV) is transmitted through blood, sexual behavior and mother-to-baby, with more efficient transmission through blood transfusion. HIV risk among blood transfusion was severe due to lack of effective and correctly applied screening method and rigorous management, especially in some developing countries. Since the first HIV screening reagent was approved by FDA to screen the blood in 1985, the fourth generation test has been produced till now. Initially, HIV test was primarily used to screen the blood supply, it also became an important aspect of HIV prevention, especially screening among people donating blood. Today, HIV testing is seen as an integral part of both the nation’s prevention and treatment efforts. Objective To assess the effectiveness of any intervention tests for HIV screening among people donating blood, and find appropriate tests for HIV screening to decrease the risk of HIV transmission by blood transfusion. Search strategy MEDLINE, Cochrane Controlled Trials Register (CENTRAL/CCTR), AIDSLINE, EMBASE, CBM were be searched with the terms: "HIV", "AIDS", "screening", "test", "blood donor", "blood bank" and the detailed screening method. The websites of WHO, UNAIDS, CDC, FDA, and their related links were searched. Letters were mailed to various agencies and experts in this field to acquire unpublished reports. Inclusion criteria RCT and CCT for screening HIV among blood. donors will be included. Observational studies such as cohort studies, cased-control studies, and historical controlled studies will be used for sensitivity analysis. Method of the review According to the principles of Cochrane Review, selection of trials for inclusion, quality assessment of studies, data extraction and syntheses were conducted by reviewers.

          Release date:2016-08-25 03:17 Export PDF Favorites Scan
        • Treatment and progress of cutaneous neurofibroma

          ObjectiveTo summarize current widely-used therapies for cutaneous neurofibroma (cNF) and related research progress. MethodsBased on extensive investigation of domestic and foreign research, the existing treatment of cNF, including the indications, effectiveness and trials of targeted drugs were reviewed. ResultscNF is a hallmark feature of neurofibromatosis type 1 and has a dramatic negative impact on patient appearance and quality of life. At present, there is no standard management of cNF. Invasive treatment is a commonly-used treatment. Surgical removal gives excellent cosmetic results, but it is difficult for multiple tumors; CO2 laser ablation, laser photocoagulation, electro-drying, and radiofrequency ablation are effective in treating lots of cNF at one time. Although fast and effective, these therapies can lead to depigmentation, hyperpigmentation, or extensive scarring. There is no targeted drug approval for cNF, and a series of studies have been carried out on the Ras-MEK pathway, Ras-mTOR pathway, receptor tyrosine kinase, et al. ConclusionThe treatment of cNF has developed rapidly in recent years and has broad prospects, but the individualization and precision of the treatment still needs further clinical research.

          Release date:2022-09-30 09:59 Export PDF Favorites Scan
        • Improvement of different resistance training regimens on blood lipids and insulin resistance in patients with type 2 diabetes mellitus: a network meta-analysis

          Objective To assess the improvement of different resistance training regimens on blood lipid metabolism and insulin resistance in patients with type 2 diabetes mellitus (T2DM). Methods PubMed, ProQuest, Embase, Web of Science, China National Knowledge Infrastructure, Wanfang, and VIP databases were searched to collect randomized controlled trials of resistance training intervention to improve blood lipids and insulin resistance in patients with T2DM. The search time range was from the establishment of the databases to May 2023. Two reviewers assessed the risk of bias of the included studies using the Physiotherapy Evidence Database scale, and performed a network meta-analysis of the extracted data using Stata 16.0 software. Results In the end, 24 articles were included, and a total of 983 participants were enrolled. The result of network meta-analysis showed that high-frequency and moderate-intensity resistance exercise significantly improved the levels of insulin resistance [standardized mean difference=?1.71, 95% confidence interval (CI) (?2.75, ?0.67)], triglycerides [weighted mean difference (WMD)=?0.27 mmol/L, 95%CI (?0.51, ?0.04) mmol/L], and total cholesterol [WMD=?0.16 mmol/L, 95%CI (?0.20, ?0.12) mmol/L], but had no significant effect on improving the level of high-density lipoprotein [WMD=0.05 mmol/L, 95%CI (?0.02, 0.11) mmol/L] or low-density lipoprotein [WMD=?0.20 mmol/L, 95%CI (?0.42, 0.03) mmol/L]. The results of cumulative probability ranking showed that high-frequency and moderate-intensity resistance exercise was the best in improving insulin resistance, triglycerides, high-density lipoprotein and low-density lipoprotein levels. Conclusion Based on current evidence, high-frequency and moderate-intensity resistance exercise may be the best resistance exercise regimen to improve insulin resistance and lipid metabolism in patients with T2DM.

          Release date:2024-02-29 12:03 Export PDF Favorites Scan
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