Bergrath S, Rörtgen D, Skorning M, Fischermann H, Beckers S K, Mutscher C, Brokmann J C, Rossaint R
Bereich Notfallmedizin, Lehrstuhl und Klinik für Anästhesiologie, Universitätsklinikum Aachen, Rheinisch-Westfälische Technische Hochschule (RWTH), Pauwelsstr. 30, 52074 Aachen, Deutschland.
Anaesthesist. 2011 Mar;60(3):221-9. doi: 10.1007/s00101-010-1790-y. Epub 2010 Sep 19.
BACKGROUND: The aim of this study was to examine documentation quality in physician staffed emergency medical services (EMS). This study compared simulated on-site care with the associated patient records written by EMS physicians. METHODS: For this study two standardized simulated case scenarios, ST segment elevation myocardial infarction (STEMI) and major trauma with traumatic brain injury were designed by an expert committee. Overall 29 EMS teams each consisting of 1 EMS physician and 2 paramedics ran through the scenarios on high fidelity patient simulators and each scenario was videotaped. The scenarios were stopped after 12 min for STEMI and after 14 min for major trauma independent of the actions carried out and each EMS physician then had 10 min to document this initial phase on standardized protocol sheets. The videotaped scenarios were analyzed by two independent investigators. Documentation of predefined contents and all drug dosages were checked against the simulated on-site care. The data were evaluated and classified as correct, incorrect or missing documentation although action performed. RESULTS: Written consent for data analysis was provided by 28 teams. Overall 20 parameters and actions in the STEMI scenario and 16 in the major trauma scenario as well as all drug dosages were evaluated. For the scenario STEMI 469 actions were analyzed of which 271 (58%) were correct, 94 (20%) incorrect and 104 (22%) had missing documentation. A total of 140 medications were administered of which 31 (22%) were documented incorrectly and 14 (10%) were not documented. For major trauma 401 actions were analyzed of which 244 (61%) were correct, 101 (25%) incorrect and 56 (14%) had missing documentation. In this scenario the teams administered 138 medications of which 31 (22%) were documented incorrectly and 16 (12%) were not documented. Infused amounts of crystalloids and colloids were mostly documented correctly in this case (35 correct /6 incorrect/8 not documented). Documentation of several clinical parameters was carried out predominantly correctly, e.g. initial blood pressure (STEMI: 25/2/1, major trauma: 21/4/2) and initial ECG rhythm (STEMI: 27/0/1, major trauma: 26/0/1). Documentation of other clinically relevant parameters was often performed incorrectly: 12-lead ECG in STEMI (5/9/12) and capnometry in major trauma (9/4/7). No team used a pain scale to assess the level of pain in the STEMI scenario but 12 EMS physicians documented an accordant value (numerical rating scale) on the patient records. Furthermore some parameters could be identified where documentation was mostly missing although they were measured, e.g. onset of symptoms in STEMI (5/4/15) and reduced level of consciousness and bradypnea in major trauma (9/2/17). CONCLUSION: Patient safety can be reduced if relevant preclinical data are not transmitted correctly to the admitting hospital. Therefore there is a need to improve documentation quality in EMS. Electronic documentation, training of EMS staff and quality management programs might offer solutions. Because of the small sample size further studies are needed to evaluate the validity of these results.
背景:本研究旨在检查配备医师的紧急医疗服务(EMS)中的文件记录质量。本研究将模拟现场护理与EMS医师编写的相关患者记录进行了比较。 方法:对于本研究,一个专家委员会设计了两个标准化模拟病例场景,即ST段抬高型心肌梗死(STEMI)和伴有创伤性脑损伤的严重创伤。总共29个EMS团队,每个团队由1名EMS医师和2名护理人员组成,在高保真患者模拟器上完成这些场景,每个场景都进行了录像。对于STEMI,在12分钟后停止场景;对于严重创伤,在14分钟后停止场景,与所采取的行动无关。然后,每位EMS医师有10分钟时间在标准化协议表上记录这一初始阶段。两名独立研究人员对录像的场景进行了分析。将预定义内容和所有药物剂量的记录与模拟现场护理进行核对。对数据进行评估,并根据所采取的行动将其分类为正确、不正确或记录缺失。 结果:28个团队提供了数据分析的书面同意书。总共评估了STEMI场景中的20个参数和行动以及严重创伤场景中的16个参数和行动以及所有药物剂量。对于STEMI场景,分析了469项行动,其中271项(58%)正确,94项(20%)不正确,104项(22%)记录缺失。总共使用了140种药物,其中31种(22%)记录错误,14种(10%)未记录。对于严重创伤,分析了401项行动,其中244项(61%)正确,101项(25%)不正确,56项(14%)记录缺失。在这个场景中,团队使用了138种药物,其中31种(22%)记录错误,16种(12%)未记录。在这种情况下,晶体液和胶体液的输注量大多记录正确(35项正确/6项错误/8项未记录)。几个临床参数的记录大多正确,例如初始血压(STEMI:25/2/1,严重创伤:21/4/2)和初始心电图节律(STEMI:27/0/1,严重创伤:26/0/1)。其他临床相关参数的记录经常不正确:STEMI中的12导联心电图(5/9/12)和严重创伤中的二氧化碳描记法(9/4/7)。在STEMI场景中,没有团队使用疼痛量表来评估疼痛程度,但有12名EMS医师在患者记录上记录了相应的值(数字评分量表)。此外,可以确定一些参数,尽管进行了测量,但大多记录缺失,例如STEMI中的症状发作(5/4/15)以及严重创伤中的意识水平降低和呼吸过缓(9/2/17)。 结论:如果临床前相关数据未正确传输到收治医院,患者安全可能会降低。因此,需要提高EMS中的文件记录质量。电子记录、EMS工作人员培训和质量管理计划可能会提供解决方案。由于样本量小,需要进一步研究来评估这些结果的有效性。
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