Reply to “Letter to the Editor: Pitfalls in Calculating the Incidence of GBS During the Pandemic”

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY European Journal of Neurology Pub Date : 2025-02-11 DOI:10.1111/ene.70069
Lorena Martín-Aguilar, Luis Querol
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We are aware that one important limitation of our study is the inaccurate codification because diagnoses are not confirmed later from discharge in each hospital, but GBS misdiagnosis rates are low and likely remain stable across all studied years. Furthermore, the literature indicates that SARS-CoV-2 GBS does not exhibit any clinical characteristics that differ from those of classic GBS [<span>1, 2</span>].</p><p>Additionally, pre-pandemic GBS incidences in Spain are completely aligned with previous reports on GBS incidence, which provides reassurance on the solidity of the findings and the codification choices.</p><p>On the other hand, we agree with Finsterer's statement that the decrease in incidence in 2021 may be due to preventive measures and we discussed this point in our article. Besides, this is why the incidence in 2021 was high in December but low in January. If we look at Figure 2, we can see that GBS incidences in January, February, and March of 2021 are considerably lower than in the same months in 2018–2020, which coincides with the first winter after the pandemic, when the prevention measures were stricter, and masks were widely used. We also agree that some mild cases may not be hospitalized due to restriction measures.</p><p>Also, we cannot differentiate between GBS associated with SARS-CoV-2 infection and GBS associated with vaccination because data on previous infections or vaccines at the individual level are lacking in the database we used. The effect of the SARS-CoV-2 vaccination was indeed studied, but it was withdrawn from publication following the recommendations of the journal's reviewers because the interval between vaccination and GBS onset was not available and the vaccination in Spain mostly occurred with mRNA-based vaccines (not associated with an increased GBS risk [<span>3, 4</span>]). Nonetheless, readers can review the results of vaccines and GBS in the preprint published on medRxiv [<span>5</span>]. The results illustrate that mass vaccination of the Spanish population has not increased the incidence of GBS significantly at the population level, which reinforces the population-wide safety of vaccine administrations even if a minor increase in vaccine-associated GBS is present. To improve this point, it would be very interesting to have epidemiological surveillance systems that include vaccination data at the individual level in our country.</p><p>To conclude, we do not see any pitfall or mistake in calculating GBS incidences; our article has some limitations due to the nature of the data extracted from a coded database with no clinical purpose. Implementation of real-time nationwide registries with individualized information would help to understand post-infectious disorders such as GBS.</p><p>L.Q. received research grants from Instituto de Salud Carlos III—Ministry of Economy and Innovation (Spain), CIBERER, Fundació La Marató, GBS-CIDP Foundation International, UCB and Grífols, received speaker or expert testimony honoraria from CSL Behring, Novartis, Sanofi-Genzyme, Merck, Annexon, Alnylam, Biogen, Janssen, Lundbeck, ArgenX, UCB, LFB, Octapharma and Roche, serves at Clinical Trial Steering Committee for Sanofi-Genzyme and Roche and is Principal Investigator for UCB’s CIDP01 trial. 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引用次数: 0

Abstract

We read Finsterer's letter with interest. No pitfalls were encountered in calculating GBS incidences, but our study presents limitations already discussed in the original article.

First, Finsterer suggests including other codes than G61.0 for GBS diagnosis, such as polyradiculitis, radiculopathy, or polyneuropathy, because SARS-CoV-2 GBS can have different clinical manifestations than classic GBS. If we include those pathologies and considering that this is a retrospective study performed through a database designed to inform Public Health policies that does not allow clinical chart review, we would be including infiltrative polyradiculitis, mechanic radiculopathies, and diabetic polyneuropathies in the calculation of GBS incidences. We are aware that one important limitation of our study is the inaccurate codification because diagnoses are not confirmed later from discharge in each hospital, but GBS misdiagnosis rates are low and likely remain stable across all studied years. Furthermore, the literature indicates that SARS-CoV-2 GBS does not exhibit any clinical characteristics that differ from those of classic GBS [1, 2].

Additionally, pre-pandemic GBS incidences in Spain are completely aligned with previous reports on GBS incidence, which provides reassurance on the solidity of the findings and the codification choices.

On the other hand, we agree with Finsterer's statement that the decrease in incidence in 2021 may be due to preventive measures and we discussed this point in our article. Besides, this is why the incidence in 2021 was high in December but low in January. If we look at Figure 2, we can see that GBS incidences in January, February, and March of 2021 are considerably lower than in the same months in 2018–2020, which coincides with the first winter after the pandemic, when the prevention measures were stricter, and masks were widely used. We also agree that some mild cases may not be hospitalized due to restriction measures.

Also, we cannot differentiate between GBS associated with SARS-CoV-2 infection and GBS associated with vaccination because data on previous infections or vaccines at the individual level are lacking in the database we used. The effect of the SARS-CoV-2 vaccination was indeed studied, but it was withdrawn from publication following the recommendations of the journal's reviewers because the interval between vaccination and GBS onset was not available and the vaccination in Spain mostly occurred with mRNA-based vaccines (not associated with an increased GBS risk [3, 4]). Nonetheless, readers can review the results of vaccines and GBS in the preprint published on medRxiv [5]. The results illustrate that mass vaccination of the Spanish population has not increased the incidence of GBS significantly at the population level, which reinforces the population-wide safety of vaccine administrations even if a minor increase in vaccine-associated GBS is present. To improve this point, it would be very interesting to have epidemiological surveillance systems that include vaccination data at the individual level in our country.

To conclude, we do not see any pitfall or mistake in calculating GBS incidences; our article has some limitations due to the nature of the data extracted from a coded database with no clinical purpose. Implementation of real-time nationwide registries with individualized information would help to understand post-infectious disorders such as GBS.

L.Q. received research grants from Instituto de Salud Carlos III—Ministry of Economy and Innovation (Spain), CIBERER, Fundació La Marató, GBS-CIDP Foundation International, UCB and Grífols, received speaker or expert testimony honoraria from CSL Behring, Novartis, Sanofi-Genzyme, Merck, Annexon, Alnylam, Biogen, Janssen, Lundbeck, ArgenX, UCB, LFB, Octapharma and Roche, serves at Clinical Trial Steering Committee for Sanofi-Genzyme and Roche and is Principal Investigator for UCB’s CIDP01 trial. The other authors report no disclosures.

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回复“致编辑的信:大流行期间计算GBS发病率的陷阱”
我们饶有兴趣地读了芬斯特的信。在计算GBS发病率时没有遇到陷阱,但我们的研究提出了在原始文章中已经讨论过的局限性。首先,Finsterer建议将G61.0以外的其他编码纳入GBS诊断,如多根性脊髓炎、神经根病或多神经病变,因为SARS-CoV-2 GBS可能具有与经典GBS不同的临床表现。如果我们纳入这些病理,并考虑到这是一项通过数据库进行的回顾性研究,该数据库旨在为公共卫生政策提供信息,不允许临床图表审查,我们将在计算GBS发病率时包括浸润性多根炎、机械性神经根病和糖尿病性多神经病变。我们意识到,我们研究的一个重要局限性是不准确的编纂,因为每家医院的诊断在出院后都没有得到证实,但GBS的误诊率很低,并且在所有研究年份都保持稳定。此外,文献表明SARS-CoV-2 GBS不表现出与经典GBS不同的任何临床特征[1,2]。此外,西班牙大流行前的吉兰-巴雷综合征发病率与以前关于吉兰-巴雷综合征发病率的报告完全一致,这为调查结果的可靠性和编纂选择提供了保证。另一方面,我们同意Finsterer的说法,2021年发病率的下降可能是由于预防措施,我们在文章中讨论了这一点。此外,这也是2021年12月发病率高、1月发病率低的原因。从图2可以看出,2021年1月、2月和3月的GBS发病率明显低于2018-2020年同期,而2018-2020年正好是大流行后的第一个冬天,当时的预防措施更加严格,口罩也被广泛使用。我们也同意,一些轻微病例可能因限制措施而无法住院。此外,我们无法区分与SARS-CoV-2感染相关的GBS和与疫苗接种相关的GBS,因为我们使用的数据库中缺乏以往感染或疫苗的数据。确实研究了SARS-CoV-2疫苗接种的效果,但根据该杂志审稿人的建议,该研究被撤回,因为无法获得疫苗接种与GBS发病之间的间隔时间,而且西班牙的疫苗接种主要是基于mrna的疫苗(与GBS风险增加无关[3,4])。尽管如此,读者可以在medRxiv[5]上发表的预印本中回顾疫苗和GBS的结果。结果表明,西班牙人口的大规模疫苗接种并没有在人口水平上显著增加GBS的发病率,这加强了疫苗接种在人口范围内的安全性,即使存在与疫苗相关的GBS的轻微增加。为了改善这一点,在我国建立包括个人层面疫苗接种数据的流行病学监测系统将是非常有趣的。总而言之,我们在计算GBS发生率时没有发现任何缺陷或错误;由于从没有临床目的的编码数据库中提取的数据的性质,我们的文章有一些局限性。实施具有个性化信息的实时全国登记将有助于了解诸如gbslq之类的感染后疾病。获得了西班牙经济与创新研究院、CIBERER、Fundació La Marató、GBS-CIDP国际基金会、UCB和Grífols的研究资助,获得了CSL Behring、诺华、赛诺菲-健赞、默克、Annexon、Alnylam、Biogen、Janssen、Lundbeck、ArgenX、UCB、LFB、Octapharma和罗氏的演讲或专家证词荣誉,担任赛诺菲-健赞和罗氏的临床试验指导委员会成员,并担任UCB CIDP01试验的首席研究员。其他作者没有披露任何信息。
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
European Journal of Neurology
European Journal of Neurology 医学-临床神经学
CiteScore
9.70
自引率
2.00%
发文量
418
审稿时长
1 months
期刊介绍: The European Journal of Neurology is the official journal of the European Academy of Neurology and covers all areas of clinical and basic research in neurology, including pre-clinical research of immediate translational value for new potential treatments. Emphasis is placed on major diseases of large clinical and socio-economic importance (dementia, stroke, epilepsy, headache, multiple sclerosis, movement disorders, and infectious diseases).
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