Kosmidis H V, Bouhoutsou D O, Varvoutsi M C, Papadatos J, Stefanidis C G, Vlachos P, Scardoutsou A, Kostakis A
Department of Oncology, Children's Hospital, A. Kyriakou, Athens, Greece.
Pediatr Hematol Oncol. 1991 Apr-Jun;8(2):171-8. doi: 10.3109/08880019109033445.
Vincristine overdose (7.5 mg/m2) was accidentally administered to 3 children with acute lymphoblastic leukemia. Treatment included double-volume exchange transfusion, phenobarbital administered prophylactically, and folinic acid rescue 18 mg every 3 hours for 16 doses. Vincristine levels were also assayed and showed a dramatic decline in postexchange levels in the 2 patients who survived and an almost unchanged value in the patient who succumbed. Early signs of toxicity in the 2 survivors were peripheral neuropathy (day 4), bone marrow toxicity (day 5), gastrointestinal toxicity (days 6 and 7), and hypertension (days 7 and 8). Marrow aplasia lasted for 4 and 10 days, peripheral neuropathy for 15 and 42 days, gastrointestinal toxicity for 3 and 5 days, and hypertension for 5 and 14 days. The 2 children were discharged on days 13 and 16 and cytostatic therapy was restarted on days 18 and 25. Both are alive without evidence of leukemia. The third patient developed liver and marrow toxicity on day 3 and died on day 9. Postmortem examination showed leukemia infiltration of the liver and spleen.
3名急性淋巴细胞白血病患儿意外过量使用了长春新碱(7.5mg/m²)。治疗措施包括双倍量换血输血、预防性使用苯巴比妥以及每3小时给予18mg亚叶酸钙解救,共16剂。还检测了长春新碱水平,结果显示,2名存活患者换血后的水平显著下降,而死亡患者的水平几乎未变。2名幸存者的早期毒性迹象包括周围神经病变(第4天)、骨髓毒性(第5天)、胃肠道毒性(第6天和第7天)以及高血压(第7天和第8天)。骨髓再生障碍持续了4天和10天,周围神经病变持续了15天和42天,胃肠道毒性持续了3天和5天,高血压持续了5天和14天。这2名患儿分别于第13天和第16天出院,并于第18天和第25天重新开始细胞毒性治疗。两人均存活,无白血病迹象。第三名患者在第3天出现肝脏和骨髓毒性,于第9天死亡。尸检显示肝脏和脾脏有白血病浸润。