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两性霉素B快速静脉输注:一项初步研究。

Rapid intravenous infusion of amphotericin B: a pilot study.

作者信息

Cruz J M, Peacock J E, Loomer L, Holder L W, Evans G W, Powell B L, Lyerly E S, Capizzi R L

机构信息

Section on Oncology, Wake Forest University, Bowman Gray School of Medicine, Winston-Salem, North Carolina 27103.

出版信息

Am J Med. 1992 Aug;93(2):123-30. doi: 10.1016/0002-9343(92)90040-i.

Abstract

PURPOSE

The administration of amphotericin B in the conventional prolonged infusion over 4 to 6 hours is complicated by the acute toxicities of fevers and chills in 50% to 90% of patients and the chronic toxicities of increased creatinine levels and hypokalemia in 60% to 80% of patients. To determine the safety and toxicity of rapid infusions, we conducted a prospective, nonrandomized study in patients with clinical indications for antifungal therapy.

PATIENTS AND METHODS

Twenty-five granulocytopenic adults with acute leukemia and myelodysplastic syndromes were enrolled in a phase I trial using four sequentially shorter infusion durations: a standard infusion over 4 hours (n = 3) and shortened infusion durations at 3 hours (n = 3), 2 hours (n = 4), and 1 hour (n = 15). Toxicity was assessed by daily examinations of study subjects by one of the study investigators, by documentation of all infusion-related fevers and chills, and by daily monitoring of serum levels of creatinine, potassium, magnesium, and aspartate aminotransferase.

RESULTS

Temperatures greater than 38 degrees C occurred in 16 of 25 (64%) patients, but only two had temperatures exceeding 40 degrees C. Chills were observed in 13 of 25 (56%) patients, but only one had severe symptoms. Serum creatinine increased more than 0.5 mg/dL (44.20 mumol/L) above the pretreatment baseline in 17 of 25 (68%) patients, and the absolute creatinine level was greater than or equal to 2.0 mg/dL (176.8 mumol/L) in 10 of 25 (40%) patients. Serum potassium levels dropped below the normal limit of 3.5 mEq/L (3.5 mmol/L) in all patients, but no patient had potassium levels below 2.5 mEq/L (2.5 mmol/L). Intravenous potassium supplementation was administered to all patients and exceeded 100 mEq/d in 12 of 25 (48%) patients.

CONCLUSIONS

Rapid infusions of amphotericin B are safe, are associated with similar toxicity as prolonged infusions, and facilitate inpatient care by decreasing nursing time needed for administration and minimizing scheduling conflicts with other necessary intravenous medications. Shorter infusions also facilitate outpatient and home administration of amphotericin B.

摘要

目的

常规4至6小时长时间输注两性霉素B时,50%至90%的患者会出现发热和寒战等急性毒性反应,60%至80%的患者会出现肌酐水平升高和低钾血症等慢性毒性反应,使治疗变得复杂。为了确定快速输注的安全性和毒性,我们对有抗真菌治疗临床指征的患者进行了一项前瞻性、非随机研究。

患者与方法

25名患有急性白血病和骨髓增生异常综合征的粒细胞减少成人患者参与了一项I期试验,采用了四种依次缩短的输注时长:标准的4小时输注(n = 3)以及缩短至3小时(n = 3)、2小时(n = 4)和1小时(n = 15)的输注时长。由一名研究调查员对研究对象进行每日检查,记录所有与输注相关的发热和寒战情况,并每日监测血清肌酐、钾、镁和天冬氨酸转氨酶水平,以此评估毒性。

结果

25名患者中有16名(64%)体温超过38摄氏度,但只有两名患者体温超过40摄氏度。25名患者中有13名(56%)出现寒战,但只有一名有严重症状。25名患者中有17名(68%)血清肌酐较治疗前基线水平升高超过0.5mg/dL(44.20μmol/L),25名患者中有10名(40%)肌酐绝对水平大于或等于2.0mg/dL(176.8μmol/L)。所有患者血清钾水平均降至正常下限3.5mEq/L(3.5mmol/L)以下,但没有患者钾水平低于2.5mEq/L(2.5mmol/L)。所有患者均接受了静脉补钾,25名患者中有12名(48%)补钾量超过100mEq/d。

结论

快速输注两性霉素B是安全的,其毒性与长时间输注相似,且通过减少给药所需护理时间并最大限度减少与其他必要静脉用药的给药时间冲突,方便住院治疗。较短的输注时间也便于两性霉素B的门诊和居家给药。

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