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新日本产科弥散性血管内凝血诊断标准的有效性、可靠性和有效性。

Effectiveness, reliability, and validity of new Japanese diagnostic criteria for obstetrical disseminated intravascular coagulation.

机构信息

Department of Obstetrics and Gynecology, Kansai Medical University, Shinmachi 2-5-1, Hirakata, Osaka, 573-1010, Japan.

Department of Obstetrics and Gynecology, Maternal and Child Health Center, Aiiku Hospital, Tokyo, Japan.

出版信息

Sci Rep. 2024 Jul 30;14(1):17677. doi: 10.1038/s41598-024-68298-7.

Abstract

Since July 2022, obstetrical disseminated intravascular coagulation (DIC) in Japan has been diagnosed based on the new criteria (tentative version), which assesses the main underlying disease, fibrinogen level, and fibrin/fibrinogen degradation products or D-dimer level. In June 2024, the tentative version underwent minor revision and the final version was released. The previous Japanese criteria assessed underlying disease, clinical symptoms, and various laboratory findings. This study aimed to prove the effectiveness, reliability, and validity of the new criteria (final version). We analyzed 212 women with singleton pregnancies who delivered after 22 gestational weeks and experienced blood loss ≥ 1000 mL during vaginal delivery or ≥ 2000 mL during cesarean section. Those with missing laboratory findings before receiving blood transfusion at delivery were excluded. In the obstetrical DIC group, the frequency of fibrinogen levels < 150 mg/dL was significantly higher than in the control group (90% vs. 5%, p < 0.0001), as was the frequency of scores ≥ 8 according to the previous Japanese criteria (100% vs. 10%, p < 0.0001). Cronbach alpha was 0.757 and Spearman's rank-order correlation was 0.558 between the new and previous criteria. In conclusion, we proved the effectiveness, reliability, and validity of the Japanese new criteria (final version) to diagnose obstetrical DIC.

摘要

自 2022 年 7 月起,日本采用新的(暂定版)诊断标准来诊断产科弥散性血管内凝血(DIC),该标准评估主要基础疾病、纤维蛋白原水平、纤维蛋白/纤维蛋白原降解产物或 D-二聚体水平。2024 年 6 月,暂定版进行了细微修订,并发布了最终版。以前的日本标准评估基础疾病、临床症状和各种实验室发现。本研究旨在证明新(最终版)标准的有效性、可靠性和有效性。我们分析了 212 名单胎妊娠的妇女,这些妇女在 22 孕周后分娩,且在阴道分娩时出血量≥1000mL 或剖宫产时出血量≥2000mL。在分娩前接受输血前缺少实验室发现的患者被排除在外。在产科 DIC 组中,纤维蛋白原水平<150mg/dL 的频率明显高于对照组(90% vs. 5%,p<0.0001),根据以前的日本标准,评分≥8 的频率也明显更高(100% vs. 10%,p<0.0001)。新和旧标准之间的 Cronbach alpha 为 0.757,Spearman 秩相关系数为 0.558。总之,我们证明了日本新(最终版)标准诊断产科 DIC 的有效性、可靠性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be11/11291721/e63506b60413/41598_2024_68298_Fig1_HTML.jpg

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