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成人继发性噬血细胞性淋巴组织细胞增生症患者早期死亡预后模型研究。

A Study on Early Death Prognosis Model in Adult Patients with Secondary Hemophagocytic Lymphohistiocytosis.

机构信息

Department of Hematology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

Department of General Medicine, Beijing Friendship Hospital, Capital Medical University, Beijing, China.

出版信息

J Healthc Eng. 2022 Jul 1;2022:6704859. doi: 10.1155/2022/6704859. eCollection 2022.

Abstract

BACKGROUND

The mortality risks for secondary hemophagocytic lymphohistiocytosis in the induction stage and investigated prognostic factors need to be further discussed.

OBJECTIVE

The aim of this study is to establish a clinical model for predicting early death in adult patients with secondary hemophagocytic lymphohistiocytosis. . The baseline characteristics, laboratory examination results, and 8-week survival rate of 139 adult sHLH patients diagnosed from January 2018 to December 2018 were analyzed retrospectively, and a prognostic model was constructed with low-risk (score 0-2), medium-risk (score 3), and high-risk (score ≥ 4) as parameters. . Univariate analysis confirmed that early death was not related to the type of HLH but significantly related to the patient's response to first-line treatment. The peripheral blood cell count was significantly decreased, C-reactive protein was higher, glutamyl transpeptidase and total bilirubin were higher, albumin was significantly lower, urea nitrogen was higher, hypocalcemia and hyponatremia, deep organ hemorrhage and D-dimer increased, cardiac function damage and HLH central involvement, sCD25 increased, and EB virus infection were predictive factors of early death. In the multivariate model, patients' response to first-line treatment was a good predictor of overall survival, and hypocalcemia and deep organ bleeding were associated with poor survival. The risk factors were scored and graded according to the risk ratio. The 8-week overall survival rates of the low-risk group (82 cases), medium-risk group (36 cases), and high-risk group (21 cases) were 85.4%, 52.8%, and 23.8%, respectively ( < 0.001).

CONCLUSIONS

The early death of sHLH patients is closely related to some laboratory examination results. Attention should be paid to identify high-risk patients, choose effective first-line induction therapy, achieve deep remission as soon as possible, prevent deep organ bleeding, correct electrolyte disorders, and improve the early survival rate of sHLH patients.

摘要

背景

继发性噬血细胞性淋巴组织细胞增多症(sHLH)诱导期的死亡率风险及相关预后因素仍需进一步探讨。

目的

本研究旨在建立预测成人 sHLH 患者早期死亡的临床模型。

方法

回顾性分析 2018 年 1 月至 2018 年 12 月诊断的 139 例成人 sHLH 患者的基线特征、实验室检查结果和 8 周生存率,并采用低危(评分 0-2)、中危(评分 3)和高危(评分≥4)作为参数构建预后模型。

结果

单因素分析结果显示,早期死亡与 HLH 类型无关,但与患者对一线治疗的反应显著相关。外周血白细胞计数显著降低,C 反应蛋白升高,谷氨酰转肽酶和总胆红素升高,白蛋白显著降低,血尿素氮升高,低钙血症和低钠血症,深器官出血和 D-二聚体升高,心脏功能损害和 HLH 中枢受累,可溶性 CD25 升高,EB 病毒感染是早期死亡的预测因素。多因素模型中,患者对一线治疗的反应是总生存期的良好预测因素,低钙血症和深器官出血与生存不良相关。根据风险比对危险因素进行评分和分级。低危组(82 例)、中危组(36 例)和高危组(21 例)的 8 周总生存率分别为 85.4%、52.8%和 23.8%(<0.001)。

结论

sHLH 患者的早期死亡与某些实验室检查结果密切相关。应注意识别高危患者,选择有效的一线诱导治疗,尽快达到深度缓解,预防深器官出血,纠正电解质紊乱,提高 sHLH 患者的早期生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9bc/9270127/1257be712eaf/JHE2022-6704859.001.jpg

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