...
首页> 外文期刊>The annals of pharmacotherapy >Topical phenytoin treatment of stage II decubitus ulcers in the elderly.
【24h】

Topical phenytoin treatment of stage II decubitus ulcers in the elderly.

机译:苯妥英钠局部治疗老年Ⅱ期褥疮。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

OBJECTIVE: To compare the healing of stage II decubitus ulcers with topically applied phenytoin sodium with two other standard topical treatment procedures in a long-term care setting; and to assess the extent of systemic absorption after topical application in the phenytoin group. METHODS: Forty-seven nursing home patients with stage II decubitus ulcers were chosen for this study. The patients were matched for age, gender, and size and severity of wounds, and randomly assigned to each treatment group. Clinical assessment of decubitus ulcers was performed at the beginning of treatment and at each dressing change. Ulcers were examined for the presence of healthy granulation tissue, reduction in surface dimensions, and time to healing. Two phenytoin sodium plasma concentrations were to be obtained on all patients in the phenytoin group. RESULTS: Topical phenytoin therapy resulted in a shorter time to complete healing and formation of granulation tissue when compared with DuoDerm dressings or triple antibiotic ointment applications (p < or = 0.05). The mean +/- SD time to healing in the phenytoin group was 35.3 +/- 14.3 days compared with 51.8 +/- 19.6 and 53.8 +/- 8.5 days for the DuoDerm and triple antibiotic ointment groups, respectively. Healthy granulation tissue in the phenytoin group appeared within two to seven days in all subjects. Patients in the standard treatment groups required six to 21 days to produce new granulation tissue. Serum phenytoin sodium concentrations were nondetectable. No patient withdrew from the study secondary to adverse treatment effects. CONCLUSIONS: Both the phenytoin and standard treatment groups showed progress over the study period. However, the phenytoin group demonstrated more rapid results in all aspects of ulcer healing.
机译:目的:比较在长期护理环境中局部应用苯妥英钠和其他两种标准局部治疗方法对Ⅱ期褥疮的愈合情况;并评估苯妥英钠局部应用后的全身吸收程度。方法:本研究选择了47例II期褥疮性溃疡疗养院患者。根据年龄,性别,伤口的大小和严重程度对患者进行匹配,并随机分配至每个治疗组。在治疗开始和每次换药时都要进行褥疮的临床评估。检查溃疡是否存在健康的肉芽组织,表面尺寸减小以及恢复时间。苯妥英钠组的所有患者均应获得两个苯妥英钠血浆浓度。结果:与DuoDerm敷料或三联抗生素软膏应用相比,局部苯妥英钠治疗缩短了完成肉芽组织愈合和形成的时间(p <或= 0.05)。苯妥英钠组的平均+/- SD治愈时间为35.3 +/- 14.3天,而DuoDerm和三联抗生素软膏组分别为51.8 +/- 19.6天和53.8 +/- 8.5天。在所有受试者中,苯妥英钠组的健康肉芽组织出现在两到七天内。标准治疗组的患者需要6至21天才能产生新的肉芽组织。血清苯妥英钠浓度未检出。没有患者因不良治疗而退出研究。结论:苯妥英钠和标准治疗组在研究期间均显示出进展。然而,苯妥英钠组在溃疡愈合的各个方面均显示出更快的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号