关于 "Omicron 时代血液恶性肿瘤患者感染严重急性呼吸综合征冠状病毒 2:血清阴性和血清阳性患者的呼吸衰竭、机械通气需求和死亡率 "的评论

EJHaem Pub Date : 2024-07-12 DOI:10.1002/jha2.976
Hinpetch Daungsupawong, Viroj Wiwanitkit
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引用次数: 0

摘要

亲爱的编辑,我们想就 "Omicron 时代血液系统恶性肿瘤患者的严重急性呼吸系统综合征冠状病毒 2 感染:血清阴性和血清阳性患者的呼吸衰竭、机械通气需求和死亡率[1]"一文谈谈看法。在这项回顾性单中心分析中,研究人员根据严重急性呼吸系统综合征冠状病毒2(SARS-CoV-2)血清学对患者进行了比较,以研究2022年1月至2023年3月期间感染SARS-CoV-2的血液恶性肿瘤(HM)患者的预后。在112名参与研究的患者中,39%的患者SARS-CoV-2血清反应呈阴性。将血清阴性患者与血清阳性患者进行比较后发现,前者年龄更大,患淋巴肿瘤的可能性更高,服用过抗 CD20 药物,病情更严重。此外,Kaplan-Meier 研究显示,COVID-19 检测呈阴性的患者更有可能出现呼吸衰竭,需要机械通气,并死于病毒。这项研究采用了回顾性方法,可能会在数据收集和分析方面造成偏差和限制,这也是其缺点之一。此外,研究仅在一家医疗机构进行,这也限制了研究结果在其他人群中的广泛应用。此外,112 名患者的样本量可能不足以得出确定的结论,尤其是在比较血清阴性和血清阳性 HM 患者的治疗结果时。此外,该研究并未调查任何可能影响患者结果的混杂因素。开展更大规模的多中心前瞻性研究来验证该研究的结果并提高结果的普遍性,可能是该领域下一步的研究方向之一。此外,分析各种治疗方法对感染 SARS-CoV-2 的 HM 患者预后的影响可能会为临床实践提供有价值的信息。此外,研究血清反应阴性的 HM 患者的免疫反应及其对疾病预后和进展的影响可能有助于破译 COVID-19 在这一特定人群中的潜在过程。最后但并非最不重要的一点是,研究COVID-19对HM患者的长期影响,如复发的可能性和后期后遗症,可能会为患者管理和治疗后护理提供重要数据:Hinpetch Daungsupawong。构思、监督和批准 (50%):作者声明无利益冲突。作者未因此项工作获得任何特定资助。作者已确认本次提交的论文不需要伦理批准声明。作者已确认本次提交的论文不需要患者同意声明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comment on “Severe acute respiratory syndrome coronavirus 2 infection in patients with hematological malignancies in the Omicron era: respiratory failure, need for mechanical ventilation and mortality in seronegative and seropositive patients”

Dear Editor,

We would like to share ideas on the publication “Severe acute respiratory syndrome coronavirus 2 infection in patients with hematological malignancies in the Omicron era: respiratory failure, need for mechanical ventilation and mortality in seronegative and seropositive patients [1].” Researchers compared patients based on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serology in order to examine the outcomes of hematologic malignancy (HM) patients with SARS-CoV-2 infection from January 2022 to March 2023 in this retrospective single-center analysis. Of the 112 patients in the research, 39% had a negative serology for SARS-CoV-2. Comparing seronegative individuals to seropositive patients, the findings showed that the former were older, had a higher likelihood of a lymphoid neoplasm, had anti-CD20 medication, and had a more severe illness. Additionally, a Kaplan–Meier study revealed that patients who tested negative for COVID-19 were more likely to experience respiratory failure, require mechanical ventilation, and die from the virus.

This study's retrospective approach, which can create biases and restrictions in data collection and analysis, is one of its drawbacks. Furthermore, the research was carried out at a single facility, which can restrict how broadly the results can be applied to other demographics. Additionally, it is possible that the sample size of 112 patients was insufficient to make firm conclusions, particularly when comparing the outcomes of HM patients who were seronegative and those who were seropositive. Furthermore, the study did not look into any confounding factors that might have affected the patients' results.

Conducting a bigger multicenter prospective study to validate the results of this study and improve the generalizability of the results could be one of the next directions for this area of research. Furthermore, analyzing the effects of various treatment modalities on outcomes in SARS-CoV-2-infected HM patients may offer insightful information for clinical practice. Furthermore, investigating the immune response and its impact on illness outcomes and progression in seronegative HM patients may aid in deciphering the underlying processes of COVID-19 in this particular cohort. Last but not least, examining the long-term consequences of COVID-19 for HM patients, such as the likelihood of relapse and late sequelae, may yield crucial data for patient management and post-treatment care.

Ideas, writing, analyzing, and approval (50%): Hinpetch Daungsupawong. Ideas, supervision, and approval (50%): Viroj Wiwanitkit.

The authors declare no conflicts of interest.

The authors received no specific funding for this work.

The authors have confirmed that ethical approval statement is not needed for this submission.

The authors have confirmed that patient consent statement is not needed for this submission.

The authors have confirmed that clinical trial registration is not needed for this submission.

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