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急性呼吸窘迫综合征行异基因造血干细胞移植受者院内死亡的危险因素:基于 2023 年急性呼吸窘迫综合征新定义的回顾性研究。

Risk factors for in-hospital mortality in recipients of allogeneic hematopoietic stem cell transplantation with acute respiratory distress syndrome: a retrospective study based on the 2023 new definition of acute respiratory distress syndrome.

机构信息

Department of Emergency, The Fourth Affiliated Hospital of Soochow University (Suzhou Dushu Lake Hospital, Medical Center of Soochow University), No.9 Chongwen Road, Suzhou, Jiangsu, China.

Department of Pulmonary and Critical Care Medicine, The Fourth Affiliated Hospital of Soochow University (Suzhou Dushu Lake Hospital, Medical Center of Soochow University), Suzhou, Jiangsu, China.

出版信息

BMC Pulm Med. 2024 Aug 13;24(1):391. doi: 10.1186/s12890-024-03195-3.

Abstract

INTRODUCTION

ARDS (acute respiratory distress syndrome) is the most severe form of acute hypoxic respiratory failure. Most studies related to ARDS have excluded patients with hematologic diseases, let alone allogeneic hematopoietic stem cell transplantation (allo-HSCT) recipients. Numerous patients experiencing severe hypoxic respiratory failure do not meet the Berlin definition due to the limitations of diagnosis and treatment. A new definition of ARDS, remove some diagnosis restrictions, was proposed in 2023. Based on the 2023 new definition of ARDS, we investigated the clinical features of ARDS in allo-HSCT recipients and reported risk factors for in-hospital mortality in allo-HSCT recipients defined by the Berlin definition and the new definition of ARDS respectively.

METHODS

From Jan 2016 to Dec 2020, 135 allo-HSCT recipients identified with the new definition and 87 identified with the Berlin definition at three teaching hospitals were retrospectively included in this study. Variables (demographic information, characteristics of hematologic disease and ARDS episode, laboratory tests and SOFA score) with P < 0.05 in univariate logistic regression analysis were included in multivariate stepwise logistic regression analysis. Adjusted odds ratios (ORs) and 95% confidence intervals (95% CIs) were reported.

RESULTS

Under the new definition, SOFA score (OR = 1.351, 95% CI: 1.146-1.593, P < 0.01) were found as an independent risk factor for in-hospital mortality in ARDS after allo-HSCT, while SpO2/FiO2 (OR = 0.984, 95% CI: 0.972-0.996, P < 0.01) was a protective factor. The infusion of peripheral-derived stem cells was found to be a protective factor against in-hospital mortality in post-transplantation ARDS compared with the infusion of bone marrow-derived stem cells (OR = 0.726, 95% CI: 0.164-3.221, P = 0.04). Under the Berlin definition, PaO2/FiO2 (OR = 0.977, 95% CI: 0.961-0.993, P = 0.01, lactate (OR = 7.337, 95% CI: 1.313-40.989, P < 0.01) and AST (OR = 1.165, 95% CI: 1.072-1.265, P < 0.01) were independently associated with in-hospital mortality.

CONCLUSION

These prognostic risk factors we found in allo-HSCT recipients may contribute to closer monitoring and ARDS prevention strategies. These findings require confirmation in prospective, large sample size studies.

摘要

介绍

ARDS(急性呼吸窘迫综合征)是最严重的急性低氧性呼吸衰竭形式。大多数与 ARDS 相关的研究都排除了患有血液疾病的患者,更不用说接受异基因造血干细胞移植(allo-HSCT)的患者了。许多经历严重低氧性呼吸衰竭的患者由于诊断和治疗的限制,不符合柏林定义。2023 年提出了一种新的 ARDS 定义,该定义取消了一些诊断限制。基于 ARDS 的 2023 年新定义,我们研究了 allo-HSCT 受者中 ARDS 的临床特征,并分别报告了根据柏林定义和 ARDS 的新定义定义的 allo-HSCT 受者住院死亡率的危险因素。

方法

本研究回顾性纳入了 2016 年 1 月至 2020 年 12 月在三所教学医院接受 allo-HSCT 的 135 名符合新定义和 87 名符合柏林定义的患者。单变量逻辑回归分析中 P 值<0.05 的变量(人口统计学信息、血液疾病和 ARDS 发作特征、实验室检查和 SOFA 评分)被纳入多变量逐步逻辑回归分析。报告调整后的优势比(OR)和 95%置信区间(95%CI)。

结果

在新定义下,SOFA 评分(OR=1.351,95%CI:1.146-1.593,P<0.01)被发现是 allo-HSCT 后 ARDS 住院死亡率的独立危险因素,而 SpO2/FiO2(OR=0.984,95%CI:0.972-0.996,P<0.01)是保护因素。与输注骨髓源性干细胞相比,输注外周源性干细胞被发现是移植后 ARDS 住院死亡率的保护因素(OR=0.726,95%CI:0.164-3.221,P=0.04)。在柏林定义下,PaO2/FiO2(OR=0.977,95%CI:0.961-0.993,P=0.01)、乳酸(OR=7.337,95%CI:1.313-40.989,P<0.01)和 AST(OR=1.165,95%CI:1.072-1.265,P<0.01)与住院死亡率独立相关。

结论

我们在 allo-HSCT 受者中发现的这些预后危险因素可能有助于更密切的监测和 ARDS 预防策略。这些发现需要在前瞻性、大样本量研究中得到证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac2/11321144/02b02d2c8a43/12890_2024_3195_Fig1_HTML.jpg

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