Postmortem sympathomimetic iris excitability

IF 2 3区 医学 Q2 ANATOMY & MORPHOLOGY
Colya N. Englisch , Reem Alrefai , Cristina Martin Lesan , Berthold Seitz , Thomas Tschernig
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引用次数: 0

Abstract

Background:

A reliable estimation of time since death can be important for the law enforcement authorities. The compound method encompassing supravital reactions such as the chemical excitability of the iris can be used to further narrow intervals estimated by temperature-based methods. Postmortem iris excitability was mostly assessed by parasympatholytic or parasympathomimetic substances. Little is known regarding sympathomimetic agents. The present study aims to describe the postmortem iris excitability using the sympathomimetic drug phenylephrine.

Methods:

Cadavers were included after body donors gave written informed consent during lifetime. Exclusion criteria were known eye disease, or a postmortem interval exceeding 26 hours. A pupillometer with a minimum measurement range of 0.5 mm was used to determine the horizontal pupil diameter before and 20 minutes after the application of phenylephrine. Increase in pupil diameter was labeled as positive reaction, unchanged pupil diameter was labeled as negative reaction, and decrease in pupil diameter was labeled as paradox reaction.

Results:

30 eyes from 16 cadavers (median age = 80.0; 9 males, 7 females) were examined. Initial pupil size was in median 3.5 mm (interquartile range [IQR]: 3.0–4.5 mm) and progressed to 4.0 mm (IQR: 3.5–5.0 mm) 20 minutes after drug instillation. The achieved pupil diameter difference comprised in median 0.5 mm (IQR: 0.0–1.0 mm). A positive reaction was observed in 21 cases. Negative reactions were observed in 5 cases and paradox reactions in 4 cases. Overall, there was a statistically significant difference in diameter between the initial and the reactive pupil (P = 0.0002).

Conclusion:

Although relatively rarely used, sympathomimetic drugs seem to be eligible for chemical postmortem iris excitability. Currently, assessment of postmortem iris excitability usually only involves parasympatholytic and parasympathomimetic agents. The findings of the present study give a hint that the application of a third agent with a sympathomimetic mechanism of action could provide additional information. Further studies assessing such a triple approach in the compound method in comparison with the current gold standard for estimation of time since death are mandatory to ensure reliable results.

死后交感神经虹膜兴奋性。
背景:对死亡时间的可靠估计对执法部门来说非常重要。包括虹膜化学兴奋性等超活力反应的复合方法可用于进一步缩小基于温度的方法所估计的时间间隔。主要是评估死后虹膜在副交感神经溶解物质或副交感神经模拟物质作用下的兴奋性。而对于拟交感神经物质则知之甚少。本研究旨在描述使用拟交感神经药物苯肾上腺素的死后虹膜兴奋性。方法:对 16 具尸体(中位年龄 = 80.0;9 男,7 女)的 30 只眼睛进行了检查。遗体捐献者在生前出具书面知情同意书后,遗体才被纳入检查范围。如果尸体有已知的眼部疾病,或死后间隔时间超过 26 小时,则不包括在内。从尸体解剖到使用药物的时间间隔中位数为 15.5 小时。使用最小测量范围为 0.5 毫米的瞳孔计测定用药前和用药后 20 分钟的水平瞳孔直径。瞳孔直径增大为阳性反应,瞳孔直径不变为阴性反应,瞳孔直径减小为悖论反应:初始瞳孔大小的中位数为 3.5 毫米(四分位数间距 [IQR]:3.0 至 4.5 毫米),药物注射 20 分钟后,瞳孔大小增至 4.0 毫米(范围:3.5 至 5.0 毫米)。瞳孔直径差异的中位数为 0.5 毫米(IQR:0.0 至 1.0 毫米)。21 例观察到阳性反应。5 例未观察到反应。4 例出现副反应。总体而言,初始瞳孔和反应性瞳孔之间的直径差异具有统计学意义(P = 0.0002;Wilcoxon-signed-rank 检验):结论:拟交感神经药物虽然使用相对较少,但似乎可以引起死后虹膜化学兴奋性。目前,对死后虹膜兴奋性的评估通常只涉及副交感神经溶解剂和副交感神经兴奋剂。本研究的结果提示我们,应用具有拟交感作用机制的第三种药物可提供更多信息。为确保结果可靠,有必要开展进一步研究,评估复合方法中的这种三联方法与目前估算死亡时间的黄金标准的比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Anatomy-Anatomischer Anzeiger
Annals of Anatomy-Anatomischer Anzeiger 医学-解剖学与形态学
CiteScore
4.40
自引率
22.70%
发文量
137
审稿时长
33 days
期刊介绍: Annals of Anatomy publish peer reviewed original articles as well as brief review articles. The journal is open to original papers covering a link between anatomy and areas such as •molecular biology, •cell biology •reproductive biology •immunobiology •developmental biology, neurobiology •embryology as well as •neuroanatomy •neuroimmunology •clinical anatomy •comparative anatomy •modern imaging techniques •evolution, and especially also •aging
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