Stengel Dirk, Bauwens Kai, Rademacher Grit, Ekkernkamp Axel, Güthoff Claas
Centre for Clinical Research, Department of Trauma and Orthopaedic Surgery, Unfallkrankenhaus Berlin, Berlin, Germany.
Cochrane Database Syst Rev. 2013 Jul 31(7):CD004446. doi: 10.1002/14651858.CD004446.pub3.
Ultrasonography is regarded as the tool of choice for early diagnostic investigations in patients with suspected blunt abdominal trauma. Although its sensitivity is too low for definite exclusion of abdominal organ injury, proponents of ultrasound argue that ultrasound-based clinical pathways enhance the speed of primary trauma assessment, reduce the number of computed tomography scans and cut costs.
To assess the effects of trauma algorithms that include ultrasound examinations in patients with suspected blunt abdominal trauma.
We searched the Cochrane Injuries Group's Specialised Register, CENTRAL (The Cochrane Library), MEDLINE (OvidSP), EMBASE (OvidSP), CINAHL (EBSCO), publishers' databases, controlled trials registers and the Internet. Bibliographies of identified articles and conference abstracts were searched for further elligible studies. Trial authors were contacted for further information and individual patient data. The searches were updated in February 2013.
randomised controlled trials (RCTs) and quasi-randomised trials (qRCTs).
patients with blunt torso, abdominal or multiple trauma undergoing diagnostic investigations for abdominal organ injury.
diagnostic algorithms comprising emergency ultrasonography (US).
diagnostic algorithms without ultrasound examinations (for example, primary computed tomography [CT] or diagnostic peritoneal lavage [DPL]).
mortality, use of CT and DPL, cost-effectiveness, laparotomy and negative laparotomy rates, delayed diagnoses, and quality of life.
Two authors independently selected trials for inclusion, assessed methodological quality and extracted data. Where possible, data were pooled and relative risks (RRs), risk differences (RDs) and weighted mean differences, each with 95% confidence intervals (CIs), were calculated by fixed- or random-effects modelling, as appropriate.
We identified four studies meeting our inclusion criteria. Overall, trials were of moderate methodological quality. Few trial authors responded to our written inquiries seeking to resolve controversial issues and to obtain individual patient data. We pooled mortality data from three trials involving 1254 patients; relative risk in favour of the US arm was 1.00 (95% CI 0.50 to 2.00). US-based pathways significantly reduced the number of CT scans (random-effects RD -0.52, 95% CI -0.83 to -0.21), but the meaning of this result is unclear. Given the low sensitivity of ultrasound, the reduction in CT scans may either translate to a number needed to treat or number needed to harm of two.
AUTHORS' CONCLUSIONS: There is currently insufficient evidence from RCTs to justify promotion of ultrasound-based clinical pathways in diagnosing patients with suspected blunt abdominal trauma.
超声检查被视为对疑似钝性腹部创伤患者进行早期诊断性检查的首选工具。尽管其敏感性对于明确排除腹部器官损伤而言过低,但超声检查的支持者认为,基于超声的临床路径可提高初次创伤评估的速度,减少计算机断层扫描(CT)的次数并降低成本。
评估在疑似钝性腹部创伤患者中采用包含超声检查的创伤诊疗方案的效果。
我们检索了Cochrane损伤组专业注册库、Cochrane系统评价数据库(Cochrane图书馆)、医学期刊数据库(OvidSP)、荷兰医学文摘数据库(OvidSP)、护理学与健康照护数据库(EBSCO)、出版商数据库、对照试验注册库以及互联网。对已识别文章的参考文献和会议摘要进行检索,以寻找更多符合条件的研究。与试验作者联系以获取更多信息及个体患者数据。检索于2013年2月更新。
随机对照试验(RCT)和半随机试验(qRCT)。
遭受钝性躯干、腹部或多处创伤且正在接受腹部器官损伤诊断性检查的患者。
包含急诊超声检查(US)的诊断方案。
不进行超声检查的诊断方案(例如,初次CT检查或诊断性腹腔灌洗[DPL])。
死亡率、CT和DPL的使用情况、成本效益、剖腹手术及阴性剖腹手术率、延迟诊断以及生活质量。
两位作者独立选择纳入试验,评估方法学质量并提取数据。尽可能合并数据,并根据情况采用固定效应模型或随机效应模型计算相对风险(RR)、风险差值(RD)及加权均数差值,各指标均给出95%置信区间(CI)。
我们识别出四项符合纳入标准的研究。总体而言,试验的方法学质量中等。很少有试验作者回复我们旨在解决争议问题及获取个体患者数据的书面询问。我们合并了三项涉及1254例患者的试验的死亡率数据;支持超声检查组的相对风险为1.00(95%CI 0.50至2.00)。基于超声的诊疗路径显著减少了CT扫描的次数(随机效应RD -0.52,95%CI - \alpha.83至-0.21),但该结果的意义尚不清楚。鉴于超声检查的敏感性较低,CT扫描次数的减少可能意味着每治疗或每伤害2例患者就会出现1次变化。
目前随机对照试验中尚无充分证据支持推广基于超声的临床路径用于诊断疑似钝性腹部创伤患者。