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脊髓刺激器导致医疗事故诉讼的原因分析

Analysis of reasons for medical malpractice litigation due to spinal cord stimulator.

作者信息

Kejriwal Sameer, Weldon Edward, Carter Davis, Agonias Keinan, Razzouk Jacob, Bohen Daniel, Ramos Omar, Danisa Olumide, Cheng Wayne

机构信息

John A Burns School of Medicine, Honolulu, HI, USA.

School of Medicine, Loma Linda University, Loma Linda, CA, USA.

出版信息

Interv Pain Med. 2023 Dec 15;2(4):100376. doi: 10.1016/j.inpm.2023.100376. eCollection 2023 Dec.

Abstract

STUDY DESIGN

Retrospective cohort study.

INTRODUCTION

Malpractice claims analysis is performed by several specialties to improve quality of patient care and to identify areas where physicians can improve their practice to mitigate the incidence of committing malpractice. The Food and Drug Administration has flagged over 80,000 injuries caused by spinal cord stimulator (SCS), making them the 3rd most flagged medical device. This study analyzed malpractice claims due to SCS by querying two legal databases widely used in medicolegal research.

METHODS

Westlaw Edge and VerdictSearch were queried for malpractice cases filed between the years 2000 and 2022 using the keywords "spinal cord stimulator." Case inclusion criteria was defined as a plaintiff's basis of litigation resting on a claim of medical malpractice due to SCS. Additional data collected included date of case hearing, plaintiff sex and age, defendant specialty, verdict ruling, location of the filed claim, payment or settlement amount, and sustained injuries.

RESULT

Of the 1773 reviewed cases, 45 cases were included and categorized as battery or implantable pulse generator malfunction (35.56 %), lead complications (28.89 %), surgical complications (20.00 %), and miscellaneous (15.56 %). Four (8.89 %) cases resulted in settlement, 11 (24.44 %) in a plaintiff verdict, and 30 (68.00 %) resulted in a defendant verdict. Claims filed due to infection related to SCS were more likely to result in a defendant verdict ( = .047), whereas claims filed due to neurological deficit were more likely to result in a plaintiff verdict ( = .020). The average settlement amount for the 4 cases is $1,975,309.61.

CONCLUSION

Our findings suggest obtaining adequate neuroimaging preoperatively with MRIs, disclosing neurological risks specifically paralysis on informed consent, and evaluating radiography intraoperative and postoperatively with anterior-posterior (AP) and lateral x-ray films to ensure proper SCS placement are practices that may mitigate malpractice due to SCS. Battery defects and lead complications were the most common grounds for SCS-related malpractice claims.

摘要

研究设计

回顾性队列研究。

引言

多个专业领域进行医疗事故索赔分析,以提高患者护理质量,并确定医生可改进其医疗行为以降低医疗事故发生率的领域。美国食品药品监督管理局已标记出超过80000起因脊髓刺激器(SCS)导致的伤害事件,使其成为被标记次数第三多的医疗设备。本研究通过查询两个在法医学研究中广泛使用的法律数据库,分析了因SCS引发的医疗事故索赔。

方法

使用关键词“脊髓刺激器”在Westlaw Edge和VerdictSearch中查询2000年至2022年期间提交的医疗事故案件。案件纳入标准定义为原告的诉讼依据是因SCS导致的医疗事故索赔。收集的其他数据包括案件听证日期、原告性别和年龄、被告专业、裁决结果、索赔提交地点、赔偿或和解金额以及所遭受的伤害。

结果

在1773例审查案件中,45例被纳入并分类为殴打或植入式脉冲发生器故障(35.56%)、导线并发症(28.89%)、手术并发症(20.00%)和其他(15.56%)。4例(8.89%)案件达成和解,11例(24.44%)原告胜诉,30例(68.00%)被告胜诉。因与SCS相关的感染提起的索赔更有可能导致被告胜诉(P = 0.047),而因神经功能缺损提起的索赔更有可能导致原告胜诉(P = 0.020)。这4起案件的平均和解金额为1975309.61美元。

结论

我们的研究结果表明,术前通过磁共振成像(MRI)获得足够的神经影像学检查结果,在知情同意书中明确披露神经风险尤其是瘫痪风险,并在术中及术后通过前后位(AP)和侧位X线片评估影像学情况以确保SCS正确放置,这些做法可能会减少因SCS导致的医疗事故。电池缺陷和导线并发症是与SCS相关的医疗事故索赔最常见的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05e2/11372987/17436441e725/gr1.jpg

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