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find Keyword "敷料" 45 results
  • DEVELOPMENT RESEARCH OF BIOLOGICAL DRESSING

    ObjectiveTo review the research progress of modern biological dressings. MethodsThe related literature at home and abroad was reviewed, analyzed, and summarized in the progress of biological dressing situation and various types of biological dressing research. ResultsCompared with the traditional dressing, the biological dressing can greatly promote wound healing. Biological dressings are mainly divided into the natural materials, artificial synthetic materials, and drug loaded dressings. The natural material dressings are mainly the alginate dressing, this kind of dressing can promote wound healing, which has been confirmed by a large number of studies. The artificial synthetic materials include film dressings, liquid, water colloids, gels, and foam, each has its own advantages and disadvantages, which can be chosen according to need. The drug dressing can play the role of drug loading, and further promote the wound healing; using microcapsule technology to construct the dressing and choosing Chinese medicine as drugs is the research direction of load. ConclusionThe experiment and clinical application of biological dressing are many types, clinical application prospect is wide, but each has its own advantages and disadvantages, further study is needed to improve its efficacy.

    Release date:2016-08-25 10:18 Export PDF Favorites Scan
  • 湿性敷料在骨科Ⅱ期压疮治疗中的效果评价

    目的 比较湿性敷料与传统纱布敷料在Ⅱ期压疮治疗中的效果差异。 方法 2009年9月-2011年12月将50例骨科Ⅱ期压疮患者随机分为观察组(26例,30处压疮)和对照组(24例,24处压疮),分别使用湿性敷料和传统纱布敷料,观察2周后的治疗效果及患者感受。 结果 观察组治疗6~10 d,治愈25处,显效3处,无效2处;对照组治疗10~14 d,12处治愈,2处显效,8处无效,2例加重。观察组治愈时间明显少于对照组,治疗效果优于对照组,患者疼痛感受程度低于对照组,差异有统计学意义(P<0.05)。门诊随访1个月,无1例复发。 结论 湿性敷料有利于伤口愈合,且患者舒适度较高,值得临床推广使用。

    Release date:2021-06-23 07:35 Export PDF Favorites Scan
  • 水胶体敷料用于PICC置管后局部皮肤的观察

    目的:了解不同水胶体敷料用于PICC置管术后穿刺局部皮肤过敏的发生情况。 方法: 将PICC置管患者随机分为水胶体敷料组及透明敷贴组,实验组穿刺局部皮肤使用水胶体敷料,对照组常规使用3 M透明敷贴,比较两组患者穿刺局部皮肤过敏的发生率。 结果: 水胶体敷料组患者局部皮肤过敏的发生率(3.3%)低于3M透明敷贴组(24.1%)(P<0.05)。 结论: 水胶体敷料用于PICC置管术后穿刺局部皮肤的固定皮肤过敏的发生率低于3 M透明敷贴组。

    Release date:2016-08-26 02:21 Export PDF Favorites Scan
  • CLINICAL STUDY ON TOPICAL Bismuth Subgallate/Borneol (SuileTM) DRESSING FOR TREATMENT OF DIABETIC FOOT ULCERS

    Objective To evaluate the efficacy and safety of Bismuth Subgallate/Borneol (SuileTM) (BSB) dressing in the treatment of diabetic foot ulcers. Method s A two-center, randomized controlled parallel-group comparison study was conducted. Between September 2005 and November 2006, 35 patients with nonhealing diabetic foot ulcer (Wagner 2-3 grade) were recruited and divided randomly into the test group (BSB group, n=25) and control group (IG group, n=10). There was no significant difference in general data between 2 groups (P gt; 0.05). Based on the comprehensive therapy of diabetic foot, ulcers were topically treated by SuileTM dressing and Intrasite gel in the BSB group and IG group, respectively. The ulcer area was measured once a week. Ulcer bleeding was observed and acceptance of the dressing was inquired each week. Results Of the patients, 22 patients in the BSB group and 8 in the IG group completed the clinical trial. Intention to treat (ITT) analysis indicated that the results were excellent in 19 (76%) cases, good in 3 cases (12%), fair in 1 case (4%), and poor in 2 cases (8%) in the BSB group. In the IG group, the results were excellent in 8 cases (80%) cases, fair in 1 case (10%), and poor in 1 case (10%). Per-protocol (PP) analysis showed that the results were excellent in 19 cases (86%) and good in 3 cases (14%) in the BSB group, and were excellent in 8 cases (100%) in the IG group. The results of ITT and PP analysis all showed no significant difference between 2 groups (P gt; 0.05). The change trend of ulcer areas in the BSB group was similar to that in the IG group. There was no significant difference in the hemostatic effect between 2 groups (P gt; 0.05) and the patients were more likely to accept BSB dressings. Conclusion BSB dressings is an effective, safe, and generally well-tolerated therapy dressing in the treatment of diabetic foot ulcers.

    Release date:2016-08-31 04:24 Export PDF Favorites Scan
  • APPLICATION OF DAMAGE CONTROL SURGERY STRATEGY IN TREATMENT OF BURN-TRAUMA COMBINED INJURY

    Objective To explore the appl ication of damage control surgery (DCS) strategy in the treatment of severe burn-trauma combined injury. Methods From January 2004 to December 2009, 28 patients with severe burn-trauma combined injury received salvage treatment according to DCS, including 12 cases of burn combining injury at 2 sites, 6 cases ofburn combining injury at 3 sites, and 10 cases of burn combining injury at 4 sites or above. There were 18 males and 10 females with a median age of 39.5 years (range, 8-56 years). The burn area was 15% to 56% of total body surface area. The injury severity score a (ISS) was 25 to 56, and the traumatic index was 17 to 24. Lethal triad syndrome occurred in all patients. Of them, 16 cases were on admission immediatly after first-aid, and 12 cases were thansferred from other hospitals. The time from injury to hospital ization was 20 minutes to 36 hours. All patients were treated by immediate fluid resuscitation and emergent operation to control hemorrhage and contaminations. Biological dressings were used to seal the wounds provisionally. The systemic therapy was carried out as soon as the vital signs of the patients became stable. Results In 26 survivors, 23 achieved wound heal ing by first intention, 3 had a l ittle residual wound at discharge. The hospital ization days were 31 to 398 days (62 days on average). However, 1 patient died of multiple organ failure, another 1 patient died of severe cerebral trauma with refractory shock. Conclusion The DCS strategy is effective in reducing mortal ity of patients with severe burn-trauma combined injury.

    Release date:2016-08-31 05:48 Export PDF Favorites Scan
  • EXPERIMENTAL STUDY OF THE EFFECT OF CHITOSAN/ALGINATE DRESSINGS ON WOUND IMMERSED IN SEAWATER/

    To observe the effect of chitosan/alginate (CTS/ALG) dressings on wound immersed in seawater. Methods Twenty-five healthy SD rats weighing 250-300 g were used to establ ish skin wound model through cutting 1.8 cm circle-shaped wound along spine bilaterally. The left side served as experimental group, and the right side as control group. The wounds were immersed in the prepared artificial seawater for 1 hour, then the experimental group was treated with CTS/ALG dressings, while the control group was treated with sterile gauze. Gross observation was performed andwound heal ing time was recorded. At 3, 5, 7, 10 and 12 days after operation, 2 cm × 2 cm skin tissues including the wounds were removed and underwent HE staining and immunohistochemistry staining using Envision method. Histological change of wound and expression of EGF receptor (EGFR) and bFGF were observed. Results In the experimental group, wound inflammatory response was sl ight and incrustation shrinked faster, while the incrustation in the control group shrinked slowly. The wound heal ing time of the experimental group and the control group was (11.68 ± 0.57) and (12.51 ± 0.54) days, respectively, suggesting there was a significant difference between two groups (P lt; 0.05). In the experimental group, granulation tissue prol iferation, cell infiltration, collagen tissue prol iferation, wound shrinkage and epithel ization appeared at 3 days after operation; regularly l ined collagen tissue, complete epithel ization and occurrence of skin appendages were observed at 10 days after operation; complete wound heal ing was noted at 12 days after operation; while in the control group, at the corresponding time point, late cell infiltration and epithel ization were observed and granulation tissue with ulcer was noted. Immunohistochemistry observation: high expression of bFGF in vascular endothel ial cells and interstitial fibroblasts and high expression of EGFR in vascular endothel ial cells were observed in the experimental group at 3 and 5 days after operation, and their expressions were low at 7, 10 and 12 days after operation; while in the control group, there were no or low expression of bFGF and EGFR at the same time point. Conclusion CTS/ALG dressings can promote the heal ing of wound immersed in seawater, but its mechanism needsfurther study.

    Release date:2016-09-01 09:07 Export PDF Favorites Scan
  • EXPERIMENTAL STUDY ON HYDROGEL DRESSING IN VEIN INJURY PREVENTION AND TREATMENT

    Objective To observe the efficacy of hydrogel dressings in preventing and treating vein injury of rabbits so as to provide a experimental evidence for cl inical appl ication. Methods Twenty-four healthy large-eared Japanese rabbits (48 ears) were choosen, weighing (2.15 ± 0.15) kg, and divided into 3 groups randomly. The vein injury models were made byintravenously infusing 20% mannite (2.5 mL/kg). The sites of puncture were treated with hydrogel dressings (group A, n=8) and 25%MgSO4 (group B, n=8) 5 minutes after infusion. The sites of puncture were not treated as a blank control (group C, n=8). The tissue specimens were collected from the auricular veins at 24 hours after mannite infusion for histological observation by HE staining. The injury of the vessel wall, hemorrhage around the vessels, infiltration of inflammatory cells, and disturbance of circulation were observed to evaluate the injury degree of vein. Results There existed redness and congestion in the injured veins of each group. HE staining showed that in both groups A and B, the vessel wall was sl ightly injured and hemorrhage around the vessel was mild. There existed infiltration of inflammatory cells in the vessel wall and surrounding tissues. There also existed congestion and thrombus in the vessel lumen in these two groups. While in group C, the injury of vessel wall was severe, and schistic bleeding in the surrounding tissue of the vessel was existed. The severe congestion and thrombus in the vessel lumen was observed. There was no significant difference among three groups in the extent of vein wall injury and hemorrhage around the vessel (P gt; 0.05). The degree of infiltration of inflammatory cells and circulatory disturbance in both groups A and B were significantly less than that of group C (P lt; 0.05); but there was no significant difference between groups A and B (P gt; 0.05). Conclusion Hydrogel dressing is helpful to prevent vein injury of rabbits induced by mannite.

    Release date:2016-09-01 09:08 Export PDF Favorites Scan
  • CLINICAL STUDY ON APPLICATION OF BOVINE AMNION ON BURN WOUNDS

    Objective To observe clinical effects of burn wounds treatment with bovine amnion and to screen the best method of preparing and storing of bovine amnion. Methods From January 2004 to January 2005,We selected randomly 58 patients with superficial Ⅱ° wound, deepⅡ° wound, autografting area for removal of eschars and tangential excision, fetching skin area or residual burn wound . Using auto-control, every burn wound was divided into 3 parts and was treated with 3 dressings: bovine amnion dealt with by 0.1% chlorhexidine(group A), bovine amnion dealt with by 0.4% glutaraldehyde(group B) and vaseline gauze dressing(group C as control). The clinical effects were compared between different groupsand the method of preparing and storing bovine amnion was evaluated. Results The dressing texture of group A was softer than that of group B, and its flexibility was fine. The pretreatment was not necessary for dressing in group A. When the dressing was used on burn wounds in groups A and B, painwas slight, but pain was obvious in group C; healing time in groups A and B was much less than that in group C, showing statistically significant difference(P<0.01). There was no statistically significant difference in healing time between groups A and B (P>0.05). The infection ratio of burn wound in deepⅡ° wound and residual burn wound of groups A and B is much lower than that of group C, showing statistically significant difference (P<0.05); in theother burn wounds there was no significant difference (P>0.05). There was no statistically significant difference between groups A and B (P>0.05). Conclusion Bovine amnion could make benefit on burn wounds healing, reduce infection ratio of burn wounds, could be used on different kinds of burn wounds. The clinical effect between bovine amnion dealt with by glutaraldehyde and by chlorhexidine is similar. Whereas the latter is more easy to be popularized. 

    Release date:2016-09-01 09:26 Export PDF Favorites Scan
  • 新型敷料用于颈部淋巴结核溃疡型伤口的疗效观察

    目的 观察讨论新型敷料用于颈部淋巴结核溃疡型伤口的疗效。 方法 选择2008年9月-2013年2月24例颈部淋巴结核溃疡型伤口患者为研究对象,使用新型银离子敷料德湿银和天然藻酸钙纤维敷料德湿康对其颈部淋巴结核溃疡伤口进行换药治疗,于第1次换药后的第3、9、18、30天,对伤口进行评估。 结果 经10次换药后,16例患者的伤口痊愈,6例伤口创面愈合3/4,2例伤口创面愈合1/2。 结论 新型敷料用于治疗颈部淋巴结核溃疡型伤口疗效好,值得推广。

    Release date:2016-09-07 02:34 Export PDF Favorites Scan
  • The Use of PELNAC in Repairing the Wounds Caused by Plastic Surgery

    目的 探讨瘢痕或皮肤肿瘤切除后创面使用皮能快愈敷料(PELNAC,商品名:皮耐克)结合自体刃厚皮覆盖的治疗效果。 方法 回顾分析2010年1月-2013年1月收治的两组瘢痕或皮肤肿瘤切除术后创面分别使用不同皮片覆盖的治疗效果。A组6例,采用PELANC与自体刃厚皮片复合移植;B组10例,采用自体中厚皮片移植修复。随访近期、远期,对比评估两组创面存活的皮片外观,弹性;供皮区愈合情况。 结果 两组患者皮片完全成活,外观好,弹性佳,较术前明显改善。与B组相比,A组供皮区愈合时间短,愈合后色素沉着轻微,无明显疤痕形成。 结论 采用PELNAC与自身刃厚皮片复合移植修复瘢痕或肿瘤切除后创面,既能够显著改善外观、功能,达到理想的创面修复效果,又不会造成供皮区的继发性瘢痕增生,是一种理想的创面修复方式。

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