Naing Cho, Whittaker Maxine A
College of Public Health, Medical and Veterinary Sciences, Division of Tropical Health and Medicine, James Cook University, Townsville, Australia.
Cochrane Database Syst Rev. 2017 Jun 20;6(6):CD011375. doi: 10.1002/14651858.CD011375.pub2.
Pressure ulcers, also known as bed sores, pressure sores or decubitus ulcers develop as a result of a localised injury to the skin or underlying tissue, or both. The ulcers usually arise over a bony prominence, and are recognised as a common medical problem affecting people confined to a bed or wheelchair for long periods of time. Anabolic steroids are used as off-label drugs (drugs which are used without regulatory approval) and have been used as adjuvants to usual treatment with dressings, debridement, nutritional supplements, systemic antibiotics and antiseptics, which are considered to be supportive in healing of pressure ulcers. Anabolic steroids are considered because of their ability to stimulate protein synthesis and build muscle mass. Comprehensive evidence is required to facilitate decision making, regarding the benefits and harms of using anabolic steroids.
To assess the effects of anabolic steroids for treating pressure ulcers.
In March 2017 we searched the Cochrane Wounds Specialised Register; the Cochrane Central Register of Controlled Trials (CENTRAL); Ovid MEDLINE (including In-Process & Other Non-Indexed Citations); Ovid Embase and EBSCO CINAHL Plus. We also searched clinical trials registries for ongoing and unpublished studies, and scanned reference lists of relevant included studies as well as reviews, meta-analyses and health technology reports to identify additional studies. There were no restrictions with respect to language, date of publication or study setting.
Published or unpublished randomised controlled trials (RCTs) comparing the effects of anabolic steroids with alternative treatments or different types of anabolic steroids in the treatment of pressure ulcers.
Two review authors independently carried out study selection, data extraction and risk of bias assessment.
The review contains only one trial with a total of 212 participants, all with spinal cord injury and open pressure ulcers classed as stage III and IV. The participants were mainly male (98.2%, 106/108) with a mean age of 58.4 (standard deviation 10.4) years in the oxandrolone group and were all male (100%, 104/104) with a mean age of 57.3 (standard deviation 11.6) years in the placebo group. This trial compared oxandrolone (20 mg/day, administered orally) with a dose of placebo (an inactive substance consisting of 98% starch and 2% magnesium stearate) and reported data on complete healing of ulcers and adverse events. There was very low-certainty evidence on the relative effect of oxandrolone on complete ulcer healing at the end of a 24-week treatment period (risk ratio RR) 0.81, 95% confidence interval (CI) 0.52 to 1.26) (downgraded twice for imprecision due to an extremely wide 95% CI, which spanned both benefit and harm, and once for indirectness, as the participants were mostly male spinal cord injury patients). Thus, we are uncertain whether oxandrolone improves or reduces the complete healing of pressure ulcers, as we assessed the certainty of the evidence as very low.There was low-certainty evidence on the risk of non-serious adverse events reported in participants treated with oxandrolone compared with placebo (RR 3.85, 95% CI 1.12 to 13.26) (downgraded once for imprecision and once for indirectness, as the participants were mostly male spinal cord injury patients). Thus, the treatment with oxandrolone may increase the risk of non-serious adverse events reported in participants.There was very low-certainty evidence on the risk of serious adverse events reported in participants treated with oxandrolone compared with placebo (RR 0.54, 95% CI 0.25 to 1.17) (downgraded twice for imprecision due to an extremely wide 95% CI, which spanned both benefit and harm, and once for indirectness, as the participants were mostly male spinal cord injury patients). Of the five serious adverse events reported in the oxandrolone-treated group, none were classed by the trial teams as being related to treatment. We are uncertain whether oxandrolone increases or decreases the risk of serious adverse events as we assessed the certainty of the evidence as very low.Secondary outcomes such as pain, length of hospital stay, change in wound size or wound surface area, incidence of different type of infection, cost of treatment and quality of life were not reported in the included trial.Overall the evidence in this study was of very low quality (downgraded for imprecision and indirectness). This trial stopped early when the futility analysis (interim analysis) in the opinion of the study authors showed that oxandrolone had no benefit over placebo for improving ulcer healing.
AUTHORS' CONCLUSIONS: There is no high quality evidence to support the use of anabolic steroids in treating pressure ulcers.Further well-designed, multicenter trials, at low risk of bias, are necessary to assess the effect of anabolic steroids on treating pressure ulcers, but careful consideration of the current trial and its early termination are required when planning future research.
压疮,也被称为褥疮、压力性溃疡或压疮,是由于皮肤或其下组织或两者的局部损伤而形成的。这些溃疡通常出现在骨隆突处,是影响长期卧床或坐轮椅人群的常见医学问题。合成代谢类固醇被用作非处方药(未经监管批准使用的药物),并已被用作敷料、清创、营养补充剂、全身用抗生素和防腐剂等常规治疗的辅助药物,这些被认为有助于压疮的愈合。考虑使用合成代谢类固醇是因为它们能够刺激蛋白质合成并增加肌肉量。需要全面的证据来辅助关于使用合成代谢类固醇的利弊的决策。
评估合成代谢类固醇治疗压疮的效果。
2017年3月,我们检索了Cochrane伤口专业注册库;Cochrane对照试验中央注册库(CENTRAL);Ovid MEDLINE(包括在研及其他未索引的引用文献);Ovid Embase和EBSCO CINAHL Plus。我们还检索了临床试验注册库以查找正在进行和未发表的研究,并浏览了相关纳入研究以及综述、荟萃分析和卫生技术报告的参考文献列表以识别其他研究。在语言、出版日期或研究背景方面没有限制。
比较合成代谢类固醇与替代治疗或不同类型合成代谢类固醇在治疗压疮方面效果的已发表或未发表的随机对照试验(RCT)。
两位综述作者独立进行研究选择、数据提取和偏倚风险评估。
该综述仅包含一项试验,共有212名参与者,均为脊髓损伤且患有III期和IV期开放性压疮。参与者主要为男性(98.2%,106/108),氧雄龙组的平均年龄为58.4岁(标准差10.4),安慰剂组均为男性(100%,104/104),平均年龄为57.3岁(标准差11.6)。该试验将氧雄龙(20毫克/天,口服给药)与一剂安慰剂(一种由98%淀粉和2%硬脂酸镁组成的无活性物质)进行比较,并报告了溃疡完全愈合的数据和不良事件。在24周治疗期结束时,关于氧雄龙对溃疡完全愈合的相对效果,证据确定性非常低(风险比RR 0.81,95%置信区间(CI)0.52至1.26)(因95%CI极宽,涵盖了有益和有害两种情况,因不精确性被降级两次,且因参与者大多为男性脊髓损伤患者,因间接性被降级一次)。因此,我们不确定氧雄龙是改善还是降低了压疮的完全愈合,因为我们将证据的确定性评估为非常低。与安慰剂相比,在接受氧雄龙治疗的参与者中报告的非严重不良事件风险的证据确定性较低(RR 3.85,95%CI 1.12至13.26)(因不精确性和间接性各降级一次,因为参与者大多为男性脊髓损伤患者)。因此,氧雄龙治疗可能会增加参与者报告的非严重不良事件风险。与安慰剂相比,在接受氧雄龙治疗的参与者中报告的严重不良事件风险的证据确定性非常低(RR 0.54,95%CI 0.25至1.17)(因95%CI极宽,涵盖了有益和有害两种情况,因不精确性被降级两次,且因参与者大多为男性脊髓损伤患者,因间接性被降级一次)。在氧雄龙治疗组报告的5例严重不良事件中,试验团队均未将其归类为与治疗相关。由于我们将证据的确定性评估为非常低,所以不确定氧雄龙是增加还是降低了严重不良事件的风险。纳入试验未报告疼痛、住院时间、伤口大小或伤口表面积变化、不同类型感染的发生率、治疗成本和生活质量等次要结局。总体而言,本研究中的证据质量非常低(因不精确性和间接性被降级)。当研究作者认为无效性分析(中期分析)表明氧雄龙在改善溃疡愈合方面并不优于安慰剂时,该试验提前终止。
没有高质量证据支持使用合成代谢类固醇治疗压疮。需要进一步进行设计良好、偏倚风险低的多中心试验来评估合成代谢类固醇治疗压疮的效果,但在规划未来研究时需要仔细考虑当前试验及其提前终止的情况。