Grauberger Jennifer, Kerezoudis Panagiotis, Choudhry Asad J, Alvi Mohammed Ali, Nassr Ahmad, Currier Bradford, Bydon Mohamad
Mayo Clinic Neuro-Informatics Laboratory, Rochester, Minnesota2Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota.
Department of Surgery, Mayo Clinic, Rochester, Minnesota.
JAMA Surg. 2017 Jun 21;152(6):e170544. doi: 10.1001/jamasurg.2017.0544.
Predictive factors associated with increased risk of medical malpractice litigation have been identified, including severity of injury, physician sex, and error in diagnosis. However, there is a paucity of literature investigating informed consent in spinal surgery malpractice.
To investigate the failure to obtain informed consent as an allegation in medical malpractice claims for patients undergoing a spinal procedure.
DESIGN, SETTING, AND PARTICIPANTS: In this retrospective cohort study, a national medicolegal database was searched for malpractice claim cases related to spinal surgery for all years available (ie, January 1, 1980, through December 31, 2015).
Failure to obtain informed consent and associated medical malpractice case verdict.
A total of 233 patients (117 [50.4%] male and 116 [49.8%] female; 80 with no informed consent allegation and 153 who cited lack of informed consent) who underwent spinal surgery and filed a malpractice claim were studied (mean [SD] age, 47.1 [13.1] years in the total group, 45.8 [12.9] years in the control group, and 47.9 [13.3] years in the informed consent group). Median interval between year of surgery and year of verdict was 5.4 years (interquartile range, 4-7 years). The most common informed consent allegations were failure to explain risks and adverse effects of surgery (52 [30.4%]) and failure to explain alternative treatment options (17 [9.9%]). In bivariate analysis, patients in the control group were more likely to require additional surgery (45 [56.3%] vs 53 [34.6%], P = .002) and have more permanent injuries compared with the informed consent group (46 [57.5%] vs 63 [42.0%], P = .03). On multivariable regression analysis, permanent injuries were more often associated with indemnity payment after a plaintiff verdict (odds ratio [OR], 3.12; 95% CI, 1.46-6.65; P = .003) or a settlement (OR, 6.26; 95% CI, 1.06-36.70; P = .04). Informed consent allegations were significantly associated with less severe (temporary or emotional) injury (OR, 0.52; 95% CI, 0.28-0.97; P = .04). In addition, allegations of informed consent were found to be predictive of a defense verdict vs a plaintiff ruling (OR, 0.41; 95% CI, 0.17-0.98; P = .046) or settlement (OR, 0.01; 95% CI, 0.001-0.15; P < .001).
Lack of informed consent is an important cause of medical malpractice litigation. Although associated with a lower rate of indemnity payments, malpractice lawsuits, including informed consent allegations, still present a time, money, and reputation toll for physicians. The findings of this study can therefore help to improve preoperative discussions to protect spinal surgeons from malpractice claims and ensure that patients are better informed.
已确定与医疗事故诉讼风险增加相关的预测因素,包括损伤严重程度、医生性别和诊断错误。然而,关于脊柱手术医疗事故中知情同意的文献却很少。
调查在脊柱手术医疗事故索赔中,未获得知情同意这一指控情况。
设计、背景和参与者:在这项回顾性队列研究中,检索了一个全国性法医学数据库,以获取所有年份(即1980年1月1日至2015年12月31日)与脊柱手术相关的医疗事故索赔案例。
未获得知情同意情况及相关医疗事故案件判决结果。
共研究了233例接受脊柱手术并提起医疗事故索赔的患者(117例[50.4%]男性和116例[49.8%]女性;80例未被指控未获得知情同意,153例称存在缺乏知情同意情况)(总体平均[标准差]年龄为47.1[13.1]岁,对照组为45.8[12.9]岁,知情同意组为47.9[13.3]岁)。手术年份与判决年份之间的中位间隔为5.4年(四分位间距为4 - 7年)。最常见的知情同意指控是未解释手术风险和不良反应(52例[30.4%])以及未解释替代治疗方案(17例[9.9%])。在双变量分析中,与知情同意组相比,对照组患者更有可能需要额外手术(45例[56.3%]对53例[34.6%],P = 0.002)且有更多永久性损伤(46例[57.5%]对63例[42.0%],P = 0.03)。在多变量回归分析中,永久性损伤在原告胜诉后更常与赔偿金支付相关(比值比[OR]为3.12;95%置信区间为1.46 - 6.65;P = 0.003)或和解相关(OR为6.26;95%置信区间为1.06 - 36.70;P = 0.04)。知情同意指控与不太严重(暂时性或情感性)损伤显著相关(OR为0.52;95%置信区间为0.28 - 0.97;P = 0.04)。此外,发现知情同意指控可预测辩护胜诉与原告胜诉(OR为0.41;95%置信区间为0.17 - 0.98;P = 0.046)或和解(OR为0.01;95%置信区间为0.001 - 0.15;P < 0.001)。
缺乏知情同意是医疗事故诉讼的一个重要原因。尽管与较低的赔偿金支付率相关,但包括知情同意指控在内的医疗事故诉讼仍会给医生带来时间、金钱和声誉方面的损失。因此,本研究结果有助于改善术前讨论,保护脊柱外科医生免受医疗事故索赔,并确保患者得到更充分的信息告知。