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化疗相关性发热还是感染性发热?

Chemotherapy-related fever or infection fever?

机构信息

Department of Pediatric Hematology and Oncology, Karadeniz Technical University, Trabzon, Turkey.

出版信息

Support Care Cancer. 2021 Apr;29(4):1859-1862. doi: 10.1007/s00520-020-05670-z. Epub 2020 Aug 12.

DOI:10.1007/s00520-020-05670-z
PMID:32789623
Abstract

BACKGROUND

The present study investigates the reason for the onset of fever after chemotherapy (CT) for cancer with the aim of reducing unnecessary medical care.

METHODS

A total of 37 consecutive cycles of CT for cancer were analyzed retrospectively from the files of patients. Fever was defined as a temperature of ≥ 38 °C lasting for 1 h.

RESULTS

The study sample included 23 males and 14 females (aged 8.43 ± 5.04 [min-max]). Fever was observed in all 37 cycles of chemotherapy agent (CA), which included cytarabine (ARA-C), dacarbazine, cyclophosphamide, irinotecan, adriamycin, etoposide, ifosfamide, cisplatin, and methotrexate. Fever was recorded within the first 12 h following treatment with ARA-C (45.9%), dacarbazine (16.2%), or cyclophosphamide (8.1%). A physical examination of the patients yielded normal results, C-reactive protein (CRP) and procalcitonin (PCT) values were within the normal range, the median absolute neutrophil count (ANC) was 3200/uL (0.00-16.340/uL), and a median sedimentation (ESR) level of 10 mm/h (2-59) was determined. All fevers were accepted as having resulted from CT based on the above criteria. Paracetamol and diphenhydramine were administered and the patients' treatments were continued.

CONCLUSION

Febrile episodes occurring within the first 6 h following treatment were considered to constitute an adverse drug reaction after CT for the treatment of cancer. While ARA-C fever has been previously reported on in the literature, it should be kept in mind that CT fever can be seen with different CA. Physicians should be aware of this aspect of chemotherapy-associated fever and avoid unnecessary examinations and treatments, including antibiotics.

摘要

背景

本研究旨在减少不必要的医疗护理,探讨癌症化疗(CT)后发热的原因。

方法

回顾性分析了 37 例连续的癌症 CT 治疗周期的病历。发热定义为体温≥38°C 持续 1 小时。

结果

本研究样本包括 23 名男性和 14 名女性(年龄 8.43±5.04[最小-最大])。37 个化疗药物(CA)周期均出现发热,包括阿糖胞苷(ARA-C)、达卡巴嗪、环磷酰胺、伊立替康、阿霉素、依托泊苷、异环磷酰胺、顺铂和甲氨蝶呤。阿糖胞苷(45.9%)、达卡巴嗪(16.2%)或环磷酰胺(8.1%)治疗后 12 小时内记录到发热。患者体格检查结果正常,C 反应蛋白(CRP)和降钙素原(PCT)值在正常范围内,中位绝对中性粒细胞计数(ANC)为 3200/uL(0.00-16.340/uL),中位血沉(ESR)水平为 10mm/h(2-59)。根据上述标准,所有发热均被认为是 CT 引起的。给予对乙酰氨基酚和苯海拉明,并继续治疗患者。

结论

治疗后 6 小时内发生的发热被认为是癌症 CT 治疗后的药物不良反应。虽然文献中已有关于 ARA-C 发热的报道,但应注意不同 CA 也可能出现 CT 发热。医生应了解这一化疗相关发热的方面,避免不必要的检查和治疗,包括抗生素。

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