Ilulissat Hospital, Ilulissat, Greenland.
Department of Emergency Medicine, University of Colorado School of Medicine, Denver, USA.
Cochrane Database Syst Rev. 2020 Dec 20;12(12):CD012980. doi: 10.1002/14651858.CD012980.pub2.
Frostbite is a thermal injury caused when tissue is exposed to sub-zero temperatures (in degrees Celsius) long enough for ice crystals to form in the affected tissue. Depending on the degree of tissue damage, thrombosis, ischaemia, necrosis (tissue death), gangrene and ultimately amputation may occur. Several interventions for frostbite injuries have been proposed, such as hyperbaric oxygen therapy, sympathectomy (nerve block), thrombolytic (blood-thinning) therapy and vasodilating agents such as iloprost, reserpine, pentoxifylline and buflomedil, but the benefits and harms of these interventions are unclear.
To assess the benefits and harms of the different management options for frostbite injuries.
On 25 February 2020, we searched the Cochrane Central Register of Controlled Trials (CENTRAL) in the Cochrane Library, Ovid MEDLINE(R), Ovid MEDLINE(R) In-Process & Other Non-Indexed Citations, Ovid MEDLINE(R) Daily and Ovid OLDMEDLINE(R), Embase (OvidSP), ISI Web of Science: Science Citation Index Expanded (SCI-EXPANDED), Conference Proceedings Citation Index-Science (CPCI-S), as well as trials registers. Shortly before publication, we searched Clinicaltrials.gov, the World Health Organization (WHO) International Clinical Trials Registry Platform, OpenGrey and GreyLit (9 November 2020) again. We investigated references from relevant articles, and corresponded with a trial author.
We included randomised controlled trials (RCTs) that compared any medical intervention, e.g. pharmacological therapy, topical treatments or rewarming techniques, for frostbite injuries to another treatment, placebo or no treatment.
Two authors independently extracted data. We used Review Manager 5 for statistical analysis of dichotomous data with risk ratio (RR) with 95% confidence intervals (CIs). We used the Cochrane 'Risk of bias' tool to assess bias in the included trial. We assessed incidence of amputations, rates of serious and non-serious adverse events, acute pain, chronic pain, ability to perform activities of daily living, quality of life, withdrawal rate from medical therapy due to adverse events, occupational effects and mortality. We used GRADE to assess the quality of the evidence.
We included one, open-label randomised trial involving 47 participants with severe frostbite injuries. We judged this trial to be at high risk of bias for performance bias, and uncertain risk for attrition bias; all other risk of bias domains we judged as low. All participants underwent rapid rewarming, received 250 mg of aspirin and 400 mg intravascular (IV) buflomedil (since withdrawn from practice), and were then randomised to one of three treatment groups for the following eight days. Group 1 received additional IV buflomedil 400 mg for one hour per day. Group 2 received the prostacyclin, iloprost, 0.5 ng to 2 ng/kg/min IV for six hours per day. Group 3 received IV iloprost 2 ng/kg/min for six hours per day plus fibrinolysis with 100 mg recombinant tissue plasminogen activator (rtPA) for the first day only. The results suggest that iloprost and iloprost plus rtPA may reduce the rate of amputations in people with severe frostbite compared to buflomedil alone, RR 0.05 (95% CI 0.00 to 0.78; P = 0.03; very low-quality evidence) and RR 0.31 (95% CI 0.10 to 0.94; P = 0.04; very low-quality evidence), respectively. Iloprost may be as effective as iloprost plus rtPA at reducing the amputation rate, RR 0.14 (95% CI 0.01 to 2.56; P = 0.19; very low-quality evidence). There were no reported deaths or withdrawals due to adverse events in any of the groups; we assessed evidence for both outcomes as being of very low quality. Adverse events (including flushing, nausea, palpitations and vomiting) were common, but not reported separately by comparator arm (very low-quality evidence). The included study did not measure the outcomes of acute pain, chronic pain, ability to perform activities of daily living, quality of life or occupational effects.
AUTHORS' CONCLUSIONS: There is a paucity of evidence regarding interventions for frostbite injuries. Very low-quality evidence from a single small trial indicates that iloprost, and iloprost plus rtPA, in combination with buflomedil may reduce the need for amputation in people with severe frostbite compared to buflomedil alone. However, buflomedil has been withdrawn from use. High quality randomised trials are needed to establish firm evidence for the treatment of frostbite injuries.
冻伤是一种由于组织暴露在零下温度(摄氏度)下足够长的时间而导致组织中形成冰晶的热损伤。根据组织损伤的程度,可能会发生血栓形成、缺血、坏死(组织死亡)、坏疽,最终导致截肢。已经提出了几种用于冻伤损伤的干预措施,如高压氧治疗、交感神经切除术(神经阻断)、溶栓(血液稀释)治疗和血管扩张剂如前列环素、利血平、己酮可可碱和布法罗美迪尔,但这些干预措施的益处和危害尚不清楚。
评估不同管理选项对冻伤损伤的益处和危害。
2020 年 2 月 25 日,我们检索了考科兰图书馆中的 Cochrane 对照试验中心注册库(CENTRAL)、Ovid MEDLINE(R)、Ovid MEDLINE(R)在处理中及其他非索引引文、Ovid MEDLINE(R)每日和 Ovid OLDMEDLINE(R)、Embase(OvidSP)、ISI Web of Science:科学引文索引扩展版(SCI-EXPANDED)、会议论文集引文索引-科学(CPCI-S),以及试验注册处。在出版前,我们再次检索了 Clinicaltrials.gov、世界卫生组织(WHO)国际临床试验注册平台、OpenGrey 和 GreyLit(2020 年 11 月 9 日)。我们调查了相关文章的参考文献,并与一位试验作者进行了通信。
我们纳入了将任何医学干预措施(如药理学治疗、局部治疗或复温技术)与另一种治疗、安慰剂或不治疗进行比较的随机对照试验(RCT),用于冻伤损伤。
两位作者独立提取数据。我们使用 Review Manager 5 对二分类数据进行了统计分析,采用风险比(RR)和 95%置信区间(CI)。我们使用 Cochrane“风险偏倚”工具来评估纳入试验中的偏倚。我们评估了截肢率、严重和非严重不良事件发生率、急性疼痛、慢性疼痛、日常生活活动能力、生活质量、因不良事件退出医学治疗的比例、职业影响和死亡率。我们使用 GRADE 评估证据质量。
我们纳入了一项开放性随机试验,涉及 47 名严重冻伤患者。我们认为该试验存在高偏倚风险,表现在实施偏倚方面,以及在失访偏倚方面存在不确定风险;所有其他风险偏倚领域我们都认为是低风险。所有参与者都接受了快速复温,接受了 250 毫克阿司匹林和 400 毫克静脉内(IV)布法罗美迪尔(现已不再使用),然后随机分配到以下三个治疗组中的一个,接受为期八天的治疗。第 1 组额外接受 IV 布法罗美迪尔 400 毫克,每天一小时。第 2 组接受前列环素,依前列醇,0.5 至 2 纳克/千克/分钟 IV 治疗,每天六小时。第 3 组接受 IV 依前列醇 2 纳克/千克/分钟,每天六小时,加纤维蛋白溶解,第 1 天用 100 毫克重组组织型纤溶酶原激活剂(rtPA)。结果表明,与单独使用布法罗美迪尔相比,依前列醇和依前列醇加 rtPA 可能降低严重冻伤患者的截肢率,RR 0.05(95%CI 0.00 至 0.78;P = 0.03;极低质量证据)和 RR 0.31(95%CI 0.10 至 0.94;P = 0.04;极低质量证据)。依前列醇可能与依前列醇加 rtPA 一样有效降低截肢率,RR 0.14(95%CI 0.01 至 2.56;P = 0.19;极低质量证据)。各组均无报告因不良事件而死亡或退出,我们评估这两个结局的证据质量均为极低质量。不良事件(包括潮红、恶心、心悸和呕吐)很常见,但未按比较组分别报告(极低质量证据)。纳入的研究未测量急性疼痛、慢性疼痛、日常生活活动能力、生活质量或职业影响的结局。
目前关于冻伤损伤干预措施的证据有限。一项来自单一小型试验的极低质量证据表明,与单独使用布法罗美迪尔相比,依前列醇和依前列醇加 rtPA 联合布法罗美迪尔可能降低严重冻伤患者的截肢需求。然而,布法罗美迪尔已不再使用。需要高质量的随机试验来确定冻伤损伤治疗的可靠证据。