Esposito Thomas J, Ingraham Angela, Luchette Fred A, Sears Benjamin W, Santaniello John M, Davis Kimberly A, Poulakidas Stathis J, Gamelli Richard L
Division of Trauma, Critical Care and Burns, Department of Surgery, The Burn and Shock Trauma Institute, Loyola University Medical Center, Maywood, Illinois 60153, USA.
J Trauma. 2005 Dec;59(6):1314-9. doi: 10.1097/01.ta.0000198375.83830.62.
Performance of digital rectal examination (DRE) on all trauma patients during the secondary survey has been advocated by the Advanced Trauma Life Support course. However, there is no clear evidence of its efficacy as a diagnostic test for traumatic injury. The purpose of this study is to analyze the value of a policy mandating DRE on all trauma patients as part of the initial evaluation process and to discern whether it can routinely be omitted.
Prospective study of patients treated at a Level I trauma center. Clinical indicators other than DRE (OCI) denoting gastrointestinal bleeding (GIB), urethral disruption (UD), or spinal cord injury (SCI) were sought and correlated with DRE findings suggesting the same. Impression of the examining physician as to the need and value of DRE was also studied. Patients with a Glasgow Coma Scale Score (GCS) of 3 and pharmacologically paralyzed were excluded from the SCI analyses. UD analysis included only males.
In all, 512 cases were studied (72% male, 28% female) ranging in age from 2 months to 102 years. Thirty index injuries were identified in 29 patients (6%), 17 SCI (3%), 11 GIB (2%), and 2 UD (0.4%). DRE findings agreed positively or negatively with one or more OCI of index injuries in 93% of all cases (92% seeking SCI, 90% seeking GIB, 96% seeking UD). Overall, negative predictive value of DRE was the same as that of OCI, 99% (SCI 98% versus 99%, GIB, 97% versus 99%, UD both 100%). Positive predictive value for DRE was 27% and for OCI 24% (SCI 47% versus 44%, GIB 15% versus 18%, UD 33% versus 6%). Efficiency of DRE was 94% and OCI was 93%. For confirmed index injuries, indicative DRE findings were associated with 41% and OCI 73% (SCI 36% versus 79%, GIB 36% versus 73%, UD 50% versus 100%). OCIs were present in 81% of index injury cases. In all index injury cases where OCIs were absent, positive DRE findings were also absent. DRE was felt to give additional information in 5% of all cases and change management in 4%. In cases where the clinician felt DRE was definitely indicated (29%) it reportedly gave no additional information in 85% and changed management in 11%.
DRE is equivalent to OCI for confirming or excluding the presence of index injuries. When index injuries are demonstrated, OCI is more likely to be associated with their presence. DRE rarely provides additional accurate or useful information that changes management. Omission of DRE in virtually all trauma patients appears permissible, safe, and advantageous. Elimination of routine DRE from the secondary survey will presumably conserve time and resources, minimize unpleasant encounters, and protect patients and staff from the potential for further harm without any significant negative impact on care and outcome.
高级创伤生命支持课程提倡在二次评估时对所有创伤患者进行直肠指检(DRE)。然而,尚无明确证据表明其作为创伤性损伤诊断检查的有效性。本研究的目的是分析一项政策的价值,该政策要求对所有创伤患者进行DRE作为初始评估过程的一部分,并确定是否可以常规省略该项检查。
对一家一级创伤中心治疗的患者进行前瞻性研究。寻找除DRE之外表示胃肠道出血(GIB)、尿道断裂(UD)或脊髓损伤(SCI)的临床指标(OCI),并将其与提示相同情况的DRE结果进行关联分析。还研究了检查医师对DRE必要性和价值的看法。格拉斯哥昏迷量表评分为3分且使用药物麻痹的患者被排除在SCI分析之外。UD分析仅包括男性患者。
共研究了512例患者(男性占72%,女性占28%),年龄从2个月至102岁。29例患者(6%)发现30处索引损伤,其中17例SCI(3%),11例GIB(2%),2例UD(0.4%)。在所有病例的93%中,DRE结果与索引损伤的一项或多项OCI呈阳性或阴性一致(寻求SCI的病例中为92%,寻求GIB的病例中为90%,寻求UD的病例中为96%)。总体而言,DRE的阴性预测值与OCI相同,均为99%(SCI分别为98%和与99%,GIB分别为97%和99%,UD均为100%)。DRE的阳性预测值为27%,OCI为24%(SCI分别为47%和与44%,GIB分别为15%和18%,UD分别为33%和与6%)。DRE的效率为94%,OCI为93%。对于确诊的索引损伤,提示性DRE结果与41%相关,OCI与73%相关(SCI分别为36%和与79%,GIB分别为36%和与73%,UD分别为50%和与100%)。81%的索引损伤病例存在OCI。在所有不存在OCI的索引损伤病例中,也不存在阳性DRE结果。在所有病例的5%中,DRE被认为可提供额外信息,在4%的病例中可改变治疗方案。在临床医生认为肯定需要进行DRE的病例中(29%),据报告85%的病例未提供额外信息,11%的病例改变了治疗方案。
在确认或排除索引损伤方面,DRE与OCI相当。当出现索引损伤时,OCI更有可能与之相关。DRE很少提供能改变治疗方案的额外准确或有用信息。几乎对所有创伤患者省略DRE似乎是可行的、安全的且有益的。从二次评估中取消常规DRE大概可节省时间和资源,减少不愉快的接触,并保护患者和工作人员免受进一步伤害的可能性,而对治疗和结果没有任何重大负面影响。