血液学恶性肿瘤患者发热性中性粒细胞减少症的定义、诊断和处理

A. Vidović, D. Šefer, J. Rajić, Tara Gunjak, V. Milošević, S. Jovanović
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引用次数: 0

摘要

强化化疗/放疗治疗癌症,特别是血液系统恶性肿瘤,会导致细胞损伤和炎症反应抑制,从而增加中性粒细胞减少和发热发作的风险。绝对中性粒细胞计数< 1 ?109/L为中性粒细胞减少症,绝对中性粒细胞计数< 0.5 ?109/L还是< 1 ?109/L,预计将降至< 0.5 ?在接下来的48小时内,109/L为严重中性粒细胞减少,而绝对中性粒细胞计数< 0.1 ?109被称为深度中性粒细胞减少症。发热发作通常定义为口腔温度> 38.3?C或连续两次读数> 38.0?C持续时间超过1小时。虽然有可能是非感染引起的发热性中性粒细胞减少症,但大多数发作是由感染引起的。发热性中性粒细胞减少症是一种需要及时处理的临床急症。尽管近年来治疗取得了进展,但发热性中性粒细胞减少症仍然是化疗中常见的并发症,可导致严重的临床结果,包括死亡。经验性抗菌治疗的管理已经成功地管理发热性中性粒细胞减少症,因为它的推出50年前。广谱抗生素的广泛应用,有效地降低了发热性中性粒细胞减少症患者的死亡率。中性粒细胞减少患者在接受广谱抗菌治疗4-7天后仍处于发热状态,这是侵袭性真菌感染的高风险。两性霉素B或Caspofungin对持续发热的中性粒细胞减少患者和其他高危患者进行抗真菌治疗已显示可将侵袭性真菌感染的风险降低50 - 80%,真菌感染相关死亡率风险降低23- 45%。脂质制剂可提高传统制剂的治疗比率
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Febrile neutropenia in patients with hematological malignancies - definition, diagnosis and management
Intensive chemotherapy/radiotherapy in cancer, especially with hematologic malignancies, causes cellular injury and suppression of inflammatory responses, which increase the risks of neutropenia and febrile episodes. Absolute neutrophil count < 1 ? 109/L is considered neutropenia, with absolute neutrophil count < 0.5 ? 109/L or < 1 ? 109/L that is expected to decrease to < 0.5 ? 109/L in the next 48 hours considered severe neutropenia, while absolute neutrophil count < 0.1 ? 109 is referred as profound neutropenia. Febrile episodes are usually defined as oral temperature > 38.3?C or two consecutive readings > 38.0?C lasting more than 1 hour. Although there is the possibility of non-infection-caused febrile neutropenia, most episodes are caused by infections. Febrile neutropenia is a clinical emergency that requires prompt management. Despite advances in therapy in recent years, febrile neutropenia remains a common complication in chemotherapy causing serious clinical results, including death. The administration of empirical antibacterial therapy has been successful in the management of febrile neutropenia since its launching 50 years ago. The wide application of broad-spectrum antibiotics has effectively decreased the mortality of febrile neutropenia patients. Neutropenic patients who remain febrile despite 4-7 days of broad-spectrum antibacterial therapy are at a high risk of invasive fungal infection. Empirical antifungal therapy with Amphotericin B or Caspofungin in persistently febrile neutropenic patients and other high-risk patients has shown to reduce the risk of invasive fungal infection by 50 - 80% and the risk of fungal infection-related mortality by 23- 45%. Lipid formulations which improve the therapeutic ratio of the traditional formulation are available
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