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find Keyword "重度" 97 results
  • EFFECT OF LOW-DOSE CYCLOPHOSPHAMIDE ON THE APOPTOSIS OF LUNG PARENCHYMA CELLS IN THE EARLY SEVERE BURN STAGE IN RATS

    Objective To study the effect of low-dose cyclophosphamide (CY) on apoptosis of lung parenchyma cells in the early severe burn stage in rats. Methods Ninety clean SD male rats were randomly divided into 3 groups: the normal group (n=10), the experimental group (n=40) and the burn group (n=40). The model of degree III with 30% burn area was made in the experimental group and the burn group. CY (2 mg/kg) was injected into the abdominal cavity right after burn in the experimental group. No treatment was done in the normal group and burn group. Lung tissues were obtained at 3, 6, 12and 24 hours, respectively, after burn, and were observed by HE staining. Apoptosis of lung parenchyma cells was observed by TUNEL. Results Lung tissues were observed under the opticalmicroscopy in the normal group: the pulmonary structure was clear, and there were no inflammatory cells and exudation in the alveolar space and bronchial lumen. Besides, a few RBCs were seen. Pathological changes of lung tissues were observed under the opticalmicroscopy in the burn group: alveolar septum was obviously widened; alveolar wall was destroyed; interstitial edema and atelectasis occurred; and pathological lesion was gradually aggravated as time passed by. The pathological lesion of lung tissues mentioned above in the experimental group was better than those in the burn group. Compared with the normal group, the apoptosis ratio of lung parenchyma cells continuously increased in the burn group from the 3 hour after burn, and reached the peak at 12 hours. There were significant differences between the two groups (P lt; 0.05). However, in the experimental group, the apoptosis ratio of lung parenchyma cells increased at 3 hours after burn, cut down to normal at 6 and 12 hours, respectively, and notably decreased at 24 hours. There were significant differences between the experimental group and the normal group (P lt; 0.05). Compared with the burn group, the apoptosisrate of lung parenchyma cells in the experimental group began to decrease strikingly from the 6 hours after burn, and there were significant differences between the two groups (P lt; 0.05). Conclusion Low-dose CY can restrain the apoptosis of lung parenchyma cells in the early severe burn stage in rats and alleviate the injury of the lung.

    Release date:2016-09-01 09:19 Export PDF Favorites Scan
  • 老年重度颅脑损伤急性期呼吸道护理

    目的 探讨老年重度颅脑损伤患者急性期呼吸道临床护理方法及要点,以提高护理水平。 方法 对2009年11月-2010年7月收治的28例老年重度颅脑损伤急性期患者在治疗基础上,重点对其呼吸道进行特别护理,采用及时畅通呼吸道、加强早期气道湿化、应用多种排痰方法、人工气道护理及呼吸机的早期使用等措施,为患者生命的救治发挥了重要作用。 结果 6例(21.4%)恢复良好,2例(7.1%)伴功能障碍,1例(3.6%)呈植物生存状态,6例(21.4%)自动放弃,13例(46.4%)死亡。 结论 老年重度颅脑损伤急性期患者病情危重,加强呼吸道护理,能改善呼吸功能,降低肺部感染发生,防止继发性脑损害。

    Release date:2016-09-08 09:18 Export PDF Favorites Scan
  • Analysis of clinical and inflammatory characteristics and risk factors of severe asthma

    Objective To explore the clinical and inflammatory characteristics and risk factors of severe asthma to improve clinicians' awareness of the disease. Methods The general information of patients with asthma who visited the Department of Respiratory Medicine, the First Hospital of Shanxi Medical University from May 2018 to May 2021, as well as the diagnosis and treatment of asthma, personal history, comorbidities, auxiliary examination, asthma control test (ACT) score were collected. A total of 127 patients were included, including 40 in the severe asthma group and 87 in the mild-to-moderate asthma group. Chi-square test, independent sample t test and logistic regression were used to analyze the clinical characteristics, inflammatory markers and risk factors of severe asthma. Results Compared with the patients with mild to moderate asthma, the patients with severe asthma were more older (51.0±12.0 years vs 40.7±12.8 years, P<0.05), had more smokers (32.5% vs. 14.9%, P<0.05), and more males (67.5% vs. 40.2%, P<0.05). The patients with severe asthma got poor FEV1%pred [(56.1±23.8)% vs. (93.2±18.0)%, P<0.05] and FEV1/FVC [(56.7±13.2)% vs. (75.8±9.0)%, P<0.05)], and more exacerbations in the previous year (2.7±3.1 vs. 0.1±0.4, P<0.05), lower ACT score (14.4±3.7 vs. 18.0±5.0, P<0.05), and higher blood and induced sputum eosinophil counts [(0.54±0.44)×109/L vs. (0.27±0.32)×109/L, P<0.05; (25.9±24.2)% vs. (9.8±17.5)%, P<0.05]. There was no significant difference in the proportion of neutrophils in the induced sputum or FeNO between the two groups (P>0.05). Analysis of related risk factors showed that smoking (OR=2.740, 95%CI 1.053 - 7.130), combined with allergic rhinitis (OR=14.388, 95%CI 1.486 - 139.296) and gastroesophageal reflux (OR=2.514, 95%CI 1.105 - 5.724) were risk factors for severe asthma. Conclusions Compared with patients with mild to moderate asthma, patients with severe asthma are characterized by poor lung function, more exacerbations, and a dominant eosinophil inflammatory phenotype, which is still poorly controlled even with higher level of treatment. Risk factors include smoking, allergic rhinitis, and gastroesophageal reflux, etc.

    Release date:2023-12-07 04:39 Export PDF Favorites Scan
  • 小剂量利尿剂在中-重度胰腺炎中的作用评价

    目的探讨小剂量利尿剂在中-重度胰腺炎治疗中的作用。 方法回顾性分析2012年1月-2013年8月62例中-重度胰腺炎患者病历资料。入院后立即给予积极液体复苏及综合治疗,使24 h尿量达到1 000 mL以上,有46例患者在24~48 h内出现呼吸>24次/min,心率>100次/min。根据患者是否使用利尿剂分为2组,对照组22例患者给予限制液体量和滴速,利尿剂组24例患者在上述方案基础上同时给予小剂量利尿剂,并统计分析两组患者的出入量、治愈率、并发症、住院周期。 结果两组平均24 h入量为利尿剂组(1 076.67±88.99)mL、对照组(1 140.45±133.75)mL,差异无统计学意义(P>0.05);平均24 h尿量为利尿剂组(1 219.17±242.05)mL、对照组(1 038.18±171.54)mL,差异有统计学意义(P<0.05)。利尿剂组24例患者短期内心率、呼吸恢复正常,其局部并发症发生率为4.2%,全身并发症的发生率为12.5%,治愈好转率为91.7%,平均住院时间为(13.88±3.79)d; 22例对照组患者其局部并发症发生率为27.3%,全身并发症的发生率为40.9%,治愈好转率为63.9%,平均住院时间为(19.09±4.68)d;除局部并发症发生率差异无统计学意义(P>0.05),其余指标组间差异均有统计学意义(P<0.05)。 结论小剂量利尿剂在中-重度胰腺炎治疗中能有效地减少并发症发生,提高疗效,缩短住院周期。

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  • Efficacy of Procedure for Prolapse and Hemorrhoids in the Treatment of Large Severe Circumferential Hemorrhoids (Report of 38Cases)

    目的 探讨吻合器痔上黏膜环切术(PPH)对巨大型Ⅲ、Ⅳ度环状痔的临床应用价值。方法 采用美国强生公司生产的痔疮吻合器对38例巨大型Ⅲ、Ⅳ度环状痔患者进行手术,并分析其临床资料。结果 患者平均手术时间19 min,术后平均住院2.8 d,术后10例肛门疼痛较剧者使用了镇痛剂(其中6例加切了外痔),13例有轻度疼痛,15例无疼痛。术后9例1~6 d有便血,其中1例为大出血,出血量约1 000 ml,均经保守治疗后好转。随访1~19个月,患者无大便失禁、肛周感染、脓肿及肛门狭窄发生。结论 PPH治疗巨大型Ⅲ、Ⅳ度环状痔具有手术时间短、住院时间少、痛苦小、恢复快、疗效显著、并发症少的优势。

    Release date:2016-08-28 04:44 Export PDF Favorites Scan
  • The surgical treatment strategy and perioperative management of patients with heart valve disease complicated with severe chronic heart failure

    ObjectiveTo summarize the individualized selection of surgical treatment strategies and the key points of perioperative management for patients with heart valve disease complicated with severe chronic heart failure.MethodsThe clinical characteristics of 5 male patients with valvular heart disease complicated with severe chronic heart failure (CHF) were analyzed retrospectively from June 2017 to October 2018 in Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, with an average age of 60.21 years.ResultsFive patients were given angiotensin receptor and neprilysin inhibitor (ARNI)-based anti-heart failure treatment after admission. The operation mode of these patients was decided to be valve replacement under cardiopulmonary bypass after individualized evaluation of patients’ improving symptoms. Three patients were treated with intra-aortic balloon pump (IABP) and continuous renal replacement therapy (CRRT) early after operation to assist patients in improving cardiac function. Five patients recovered oral anti-heart failure after awakening. All patients were discharged smoothly 2 weeks after operation.ConclusionIndividualized evaluation is needed for the choice of operation timing and mode, standardized preoperative treatment for heart failure, shortening the aortic blocking time during cardiopulmonary bypass, and early application of left ventricular adjuvant drugs or instruments are all important measures to help patients recover smoothly.

    Release date:2019-09-18 03:45 Export PDF Favorites Scan
  • Short-term results of transcatheter aortic valve replacement using Venus A-Plus valve delivery system in patients with severe aortic stenosis: A retrospective cohort study

    Objective To evaluate the short-term efficacy of transcatheter aortic valve replacement (TAVR) using Venus A-Plus valve delivery system in patients with severe aortic stenosis. Methods The clinical data of patients undergoing TAVR in our hospital from August 2018 to March 2022 were collected and divided into a Venus A-PLUS and a Venus A group according to the type of valve delivery system used. The perioperative data of the two groups were compared. ResultsA total of 121 patients were included, including 70 patients in the Venus A-Plus group (45 males and 25 females with a mean age of 67.81±6.62 years), and 51 patients in the Venus A group (33 males and 18 females with a mean age of 68.25±7.01 years). All patients underwent TAVR, and the postoperative hemodynamic features (left ventricular ejection fraction, mean cross-valve pressure difference, peak flow rate) were significantly improved (P<0.05). There was no statistical difference in surgical success rate, all-cause mortality, conversion to thorax opening, midvalve placement, moderate or above perivalvular regurgitation, new left bundle branch block or new right bundle branch block between the two groups (P>0.05). Conclusion TAVR with Venus A-Plus valve delivery system in patients with severe aortic stenosis is satisfactory, safe and reliable.

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  • Modified vertebral-carotid transposition treating stenosis at V1 segment of vertebral artery

    ObjectiveTo investigate the treatment of modified vertebral-carotid transposition (VCT) in patients with severe stenosis or occlusion at V1 segment of vertebral artery.MethodsA retrospective study of 13 patients with severe stenosis or occlusion at V1 segment of vertebral artery treated by modified VCT in our hospital from October 2016 to December 2018 was done. There were 10 males and 3 females with an average age of 70.5±7.1 years.ResultsThe operation was successful in this series of patients. The follow-up duration was 1-3 years. The stenosis degree of the V1 segment of the vertebral artery decreased from 86.8%±7.5% to 17.4%±14.5%. All patients achieved remission of symptoms after the surgery. Temporary peripheral nerve injury occurred in 6 patients. Four patients with neurological complications relieved during follow-up. The patency rate was 100.0% at postoperative 1 and 3 years. There was no perioperative death, stroke or re-intervention.ConclusionModified VCT can precisely restore the distal blood flow of patients with severe stenosis or occlusion at V1 segment of vertebral artery, and relieve their symptoms.

    Release date:2022-03-18 02:44 Export PDF Favorites Scan
  • Treatment of 32 Cases of Severe Hemorrhoids Underwent PPH with Local Anesthesia

    目的 探讨在局部麻醉下行痔上黏膜环形切除钉合术(procedure for prolapse and hemorrhoids,PPH)治疗重度内痔的可行性及临床应用价值。方法 笔者所在医院科室从2005年起对32例Ⅲ度及Ⅳ度脱垂性内痔(含1例混合痔)患者均采用苯巴比妥+氢溴酸东莨菪碱+利多卡因肛管直肠环形局部浸润麻醉行PPH术,对其麻醉效果、手术时间、术中及术后疼痛、尿潴留、术后感染、肛门狭窄、住院时间、治疗满意度等进行分析。结果 32例患者均顺利完成手术,有1例术中改行低位连续硬膜外麻醉,1例辅加镇静剂及镇痛剂。术后28例对疼痛能耐受,4例需镇痛药物;1例患者有肛门坠胀感;所有患者伤口均一期愈合,无尿潴留、术后感染、出血、肛门狭窄等并发症发生;31例对疗效满意,有1例感肛门坠胀,行温水坐浴及痔疮膏纳肛治疗1周后缓解。住院时间3~6d,平均4d。32例患者均进行有效随访,随访时间2~4个月,平均3个月,无大便失禁或复发,肛门控便能力均可。结论 局部麻醉下行PPH术治疗重度内痔是一种安全可行的手术方法,麻醉操作护理简单,疗效确切,术后并发症少,术后恢复快,并可减少医疗费用。

    Release date:2016-09-08 10:25 Export PDF Favorites Scan
  • 结核性肠梗阻伴重度营养不良患者的围术期治疗策略:附5例报道

    目的探讨结核性肠梗阻伴重度营养不良患者围术期治疗策略。方法回顾性分析2022年12月至2023年8月期间在甘肃省中医院普通外科治疗的5例结核性肠梗阻患者的诊断、治疗过程及预后。结果5例患者在入院时均明确诊断为结核性肠梗阻,均伴重度营养不良及体能异常,在中位38 d的预康复后手术治疗,以粘连松解及肠排列术为基础(其中4例行回肠造口术),中位总手术时间为8 h。5例患者中只有1例术后发生肠瘘(为未行肠造口患者),经对症治疗后痊愈出院。中位总住院时间62 d,中位术后住院时间43 d;术后中位随访16个月,3例患者于1年时顺利回纳造口,随访期间未发生肠梗阻;5例患者于1年后体能异常者均恢复正常。结论预康复、肠造口及肠梗阻导管在结核性肠梗阻伴重度营养不良患者围术期治疗中至关重要,可明显提高治愈率及减少术后并发症发生。

    Release date:2025-03-25 11:18 Export PDF Favorites Scan
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