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31.
螺旋CT三维重建成像在先天性高肩胛症手术方式选择中的作用 总被引:4,自引:2,他引:2
[目的]探讨螺旋CT三维重建技术在先天性高肩胛症分度和手术方式选择中的作用。[方法]22例先天性高肩胛症术前应用螺旋CT对病变部位进行扫描并三维重建,测量以肩胛骨肩胛冈内侧缘为参照点,两侧肩胛骨高度差。根据测量结果依据Cavendish分度将其分类,并根据三维重建成像选择不同的矫形手术术式。[结果]本组22例病人,随访2—4年,外观及功能均有不同程度的改善,未出现神经、血管和椎体等的损伤。[结论]根据螺旋CT扫描和三维重建检查结果,术前即可直观的明确先天性高肩胛症的病变程度,相互关系,伴发畸形,患侧肩胛骨与正常对侧肩胛骨的外观差异等,便于手术操作方案的制定,避免了手术操作的盲目性,减少医源性并发症的发生。 相似文献
32.
Teruyuki Usuba Yutaka Suzuki Akira Kuramochi Hisao Tajiri Katsuhiko Yanaga 《Digestive endoscopy》2007,19(1):18-21
Background: Buried bumper syndrome (BBS) is a rare complication of percutaneous endoscopic gastrostomy (PEG). Along with the widespread use of the button‐type kit, BBS is encountered frequently. Methods: In the present study, we examined causes and treatments for BBS among 1400 patients who had undergone PEG. Results: The causes of BBS after PEG were classified into two categories: early causes consisted of wound infection, inappropriate size of kit and severe lordosis, while late causes were inappropriate exchange of kit, rough management or weight gain. The treatments for BBS could be determined by the degree of wound infection, fistula and burial of the bumper. Conclusion: We prepared a flowchart for replacement, by which BBS can be managed safely and quickly without surgical or endoscopic intervention. 相似文献
33.
M. I. James 《European journal of plastic surgery》1989,12(2):258-260
A technique is presented which allows the rapid precise harvesting of split-skin grafts in rats. This technique uses the skin
which would have been discarded in the formation of an open wound as a donor site thus reducing the overall assault on the
animal. 相似文献
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本实验用自制纯钛两段式种植体,以一次手术法植入到狗的下颌前磨牙区,观察5个月,结果表明,观察期间内牙龈无炎症,种植体稳固,X线片显示种植体周围无透射区,镜下可见种植体表面与牙龈之间形成上皮附着样结构,与骨组织之间大多呈骨性愈合。提示了两段式种植体有两种设计和手术方式可供选择。骨内部分在开放的环境中也可达到骨性愈合。 相似文献
36.
应用蒙特卡洛法仿真辐射式金属换热器内的辐射传热过程,建立了换热器综合传热的数学模型,利用概率论原理,把辐射能迁移过程仿真为一定累积概率分面下的随机过程,该模型能较好地反映换热器内传热过程的真实情况,可以计算出换热器内烟气、筒壁、空气的温度和壁面热流分布,以及研究烟气进口温度、换热器筒径和狭逢宽度对换热效果的影响。 相似文献
37.
C. J. Bowden W. D. Figg N. A. Dawson O. Sartor R. J. Bitton M. S. Weinberger Donna Headlee Eddie Reed C. E. Myers M. R. Cooper 《Cancer chemotherapy and pharmacology》1996,39(1-2):1-8
Introduction: Suramin is a synthetic polysulfonated naphthylurea which has been used for the treatment of African trypanosomiasis and onchocerciasis,
but since the mid-1980s has received attention as a possible antiretroviral and antineoplastic agent. Objective: This clinical trial of suramin was undertaken as a phase I/II study in patients with hormone-refractory prostate cancer,
with the hypothesis that the intensity of therapy with suramin could be increased significantly if measures were undertaken
to maintain the plasma concentrations of the drug under 300 μg/ml. Methods: We report the clinical results of this trial, wherein patients were treated at three different targeted plasma suramin concentrations
(275, 215 and 175 μg/ml) for varying periods of time (2, 4 or 8 weeks), with delivery of the drug by continuous intravenous
infusion. Results: The major toxicity observed in this trial was neurologic, consisting of a motor and sensory peripheral neuropathy that resulted
in both paresis and paralysis of the limbs. Nearly all of this severe (CTEP grade III, IV) neurologic toxicity was observed
in the patients treated at a plasma suramin concentration of 275 μg/ml for 4 or more weeks. A single patient treated at 215 μg/ml
for 8 weeks developed moderate (CTEP grade III) proximal lower extremity weakness, and no patient treated at 175 μg/ml developed
this toxicity. The second most common toxicity observed was infection of the central venous catheter. The overall response
rate for all of the evaluable patients was 17% (13 of 75 patients). In addition, prostate-specific antigen (PSA)-defined responses
were observed in six patients receiving therapy at 175 μg/ml, but these responses were confounded by cessation of therapy
with flutamide during suramin treatment. Conclusions: In summary, although plasma suramin concentrations were maintained below 300 μg/ml, neurologic toxicity nonetheless occurred
with high frequency in patients treated at 275 μg/ml for 4 or more weeks. Therapy at 215 and 175 μg/ml was in general well
tolerated, but central venous catheter-related infection, as well as the inconvenience and expense of continuous infusional
therapy, make this method of drug delivery impractical. Only moderate antitumor activity was observed during this trial, but
it is possible that both continuation of flutamide and flutamide withdrawal during suramin therapy confounded the assessment
of suramin’s activity in hormone-refractory prostate cancer.
Received: 9 June 1995/Accepted: 18 March 1996 相似文献
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电位滴定法测定胰激肽释放酶活力测试条件探讨 总被引:8,自引:0,他引:8
本文用FIP推荐的方法,以具有国际单位的参照品为标样,滴定液为0.01mol/LNaOH标准溶液,考查了以BAEE为底物的电位滴定法测定胰激肽释放酶活力的实验条件,通过正交试验得出直观和方差分析的结果,依据酶活力单位高、SD和RSD%较小的原则,求出酶活力测定的最适条件是:酶反应温度为25℃;缓冲液为0.0015mol/LNa2B4O7-0.25mol/LNaCL-2×10(-4)mol/LEDTA,pH为8.00;反应液中酶浓度为0.48IU/ml;底物浓度为5×10(-3)mol/L;胰蛋白酶抑制剂浓度为125μg/ml。胰激肽释放酶活力测定的实验数据的相对标准偏差小于5%。 相似文献