重症监护病房中的中性粒细胞败血症:不同中性粒细胞减少原因导致的临床表现和预后差异

Aleece MacPhail, C. Dendle, Monica Slavin, R. Weinkove, Michael Bailey, D. Pilcher, Zoe McQuilten
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引用次数: 0

摘要

中性粒细胞脓毒症患者通常需要入住重症监护病房(ICU)。中性粒细胞减少性败血症患者亚群之间的差异尚未得到很好的描述。 研究嗜中性粒细胞增多性败血症合并血液恶性肿瘤、转移性实体癌或未确诊癌症患者的临床结局。 对2000年1月至2022年12月期间在澳大利亚或新西兰入住重症监护病房、主要入院诊断为败血症且白细胞总数小于1.0 × 109cells/L的所有患者进行回顾性队列研究。 我们确定了8617名入住ICU的中性粒细胞败血症患者(血液恶性肿瘤n=4660;转移性实体癌n=1034;无癌症n=2800)。血液恶性肿瘤患者较年轻(中位数为 61.5 岁),慢性并发症发生率较低(4.7%),通常从病房进入重症监护室(67.4%)。机械通气率为20.2%,院内死亡率为30.6%。转移性实体癌患者年龄较大(中位数为 66.3 岁),慢性并发症发生率较高(9.9%),通常从急诊科进入重症监护室(50.8%)。机械通气率为16.9%,院内死亡率为42.4%。无癌症记录的患者机械通气率(41.7%)和死亡率(46.3%)最高。中性粒细胞减少症与实体癌或无癌症患者的死亡率密切相关,但不会增加血液恶性肿瘤患者的风险(OR 0.98,95% CI 0.90-1.06,p = 0.60)。 中性粒细胞减少性败血症合并血液恶性肿瘤、转移性实体癌或未确诊癌症的患者构成了三个不同的临床群体。管理方法也应相应调整。
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Neutropenic sepsis in the Intensive Care Unit: differences in clinical profile and outcomes according to the cause of neutropenia
Neutropenic sepsis frequently requires admission to an Intensive Care Unit (ICU). Differences between subgroups of patients with neutropenic sepsis are not well characterised. To investigate clinical outcomes among patients with neutropenic sepsis and haematological malignancy, metastatic solid cancer, or no cancer diagnosis. Retrospective cohort study of all patients admitted to ICU in Australia or New Zealand between January 2000 and December 2022 with a primary admission diagnosis of sepsis and total white cell count <1.0 × 109cells/L. We identified 8,617 ICU admissions with neutropenic sepsis (Haematological malignancy n = 4,660; metastatic solid cancer n = 1,034; no cancer n = 2,800). Patients with haematological malignancy were younger (median 61.5 years) with low rates of chronic comorbidities (4.7%), and were usually admitted to ICU from the ward (67.4%). Mechanical ventilation rates were 20.2% and in-hospital mortality was 30.6%. Patients with metastatic solid cancers were older (median 66.3 years), with higher rates of chronic comorbidities (9.9%), and were usually admitted to ICU from the emergency department (50.8%). Mechanical ventilation rates were 16.9% and in-hospital mortality was 42.4%. Patients with no documented cancer had highest rates of mechanical ventilation (41.7%) and mortality (46.3%). Neutropenia was independently associated with mortality among patients with solid cancers or no cancer, but did not confer increased risk among patients with haematological malignancy (OR 0.98, 95% CI 0.90–1.06, p = 0.60). Patients with neutropenic sepsis and haematological malignancy, metastatic solid cancer, or no cancer diagnosis constitute three distinct clinical groups. Management approaches should be tailored accordingly.
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