Jovaisa Tomas, Norkiene Ieva, Karjagin Juri, Golubovska Iveta, Gambickas Lukas, Kalinauskaite Migle, Kauzonas Evaldas, Wijayatilake Dhuleep
Clinic of Anesthesiology, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Clinic of Anesthesiology and Intensive Care, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Med Sci Monit. 2020 Oct 5;26:e925905. doi: 10.12659/MSM.925905.
BACKGROUND International application of existing guidelines and recommendations on anesthesia-specific informed consent is limited by differences in healthcare and legal systems. Understanding national and regional variations is necessary to determine future guidelines. MATERIAL AND METHODS Anonymous paper surveys on their practices regarding anesthesia-specific patient informed consent were sent to anesthesiologists in Estonia, Latvia, and Lithuania. RESULTS A total of 233 responses were received, representing 36%, 26%, and 24% of the practicing anesthesiologists in Lithuania, Latvia, and Estonia, respectively. Although 85% of responders in Lithuania reported using separate forms to secure patient informed consent for anesthesia, 54.5% of responders in Estonia and 50% in Latvia reported using joint forms to secure patient informed consent for surgery and anesthesia. Incident rates were understated by 14.2% of responders and overstated by 66.4% (P<0.001), with the latter frequently quoting incident rates that are several to tens of times higher than those published internationally. Physicians obtaining consent in the outpatient setting were more satisfied with the process than those obtaining consent on the day of surgery, with 62.5% and 42.6%, respectively, agreeing that the informed consent forms provided a satisfactory description of complications (P=0.03). Patients were significantly less likely to read consent information when signing forms on the day of surgery than at earlier times (8.5% vs. 67.5%, P<0.001). Only 46.2% of respondents felt legally protected by the current consent process. CONCLUSIONS Anesthesia-specific informed patient consent practices differ significantly in the 3 Baltic states, with these practices often falling short of legal requirements. Efforts should be made to improving information accuracy, patient autonomy, and compliance with existing legal standards.
背景 现有麻醉特定知情同意指南和建议在国际上的应用受到医疗保健和法律体系差异的限制。了解国家和地区差异对于确定未来指南很有必要。材料与方法 向爱沙尼亚、拉脱维亚和立陶宛的麻醉医师发送了关于其麻醉特定患者知情同意做法的匿名纸质调查问卷。结果 共收到233份回复,分别占立陶宛、拉脱维亚和爱沙尼亚执业麻醉医师的36%、26%和24%。尽管立陶宛85%的受访者报告使用单独的表格来确保患者对麻醉的知情同意,但爱沙尼亚54.5%的受访者和拉脱维亚50%的受访者报告使用联合表格来确保患者对手术和麻醉的知情同意。14.2%的受访者低估了事件发生率,66.4%的受访者高估了事件发生率(P<0.001),后者经常引用比国际公布的事件发生率高出几倍到几十倍的发生率。在门诊环境中获取同意的医生对该过程的满意度高于在手术当天获取同意的医生,分别有62.5%和42.6%的医生认为知情同意书对并发症的描述令人满意(P=0.03)。与早期相比,患者在手术当天签署表格时阅读同意信息的可能性显著降低(8.5%对67.5%,P<0.001)。只有46.2%的受访者认为当前的同意过程能提供法律保护。结论 波罗的海三国在麻醉特定患者知情同意方面的做法存在显著差异,这些做法往往不符合法律要求。应努力提高信息准确性、患者自主性并遵守现有法律标准。