Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, United States of America.
Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, United States of America.
Gynecol Oncol. 2018 Dec;151(3):433-437. doi: 10.1016/j.ygyno.2018.10.006. Epub 2018 Oct 16.
Our objective was to determine the safety and efficacy of acute normovolemic hemodilution (ANH) to reduce the requirement for allogenic red blood cell (RBC) transfusions in patients undergoing primary cytoreduction for advanced ovarian cancer.
Patients undergoing primary cytoreduction for advanced ovarian cancer were enrolled in a prospective trial assessing ANH at time of surgery. Intraoperative blood withdrawal was performed to a target hemoglobin of 8.0 g/dL. A standardized transfusion protocol first using autologous then allogenic blood was applied intraoperatively and throughout hospitalization according to institutional guidelines. The primary endpoint was to determine the overall rate of allogenic RBC transfusions in the intra- and postoperative periods. A predetermined allogenic RBC transfusion rate <35% was deemed a meaningful reduction from a 50% transfusion rate in historical controls.
Forty-one patients consented to participate. Median blood withdrawn during ANH was 1650 mL (range, 700-3000). Cytoreductive outcomes were as follows: 0 mm, 30 (73%); 1-10 mm, 8 (20%); and >10 mm, 3 (7%) residual disease. Estimated blood loss was 1000 mL (range, 150-2700). Fourteen patients (34%) received allogenic RBC transfusions intra- or postoperatively, meeting the primary endpoint. No patients were transfused outside protocol guidelines. The rate of ≥grade 3 complications (20%) and anastomotic leaks (7%) were similar to historical controls and met predefined safety thresholds.
For patients with advanced ovarian cancer undergoing primary cytoreductive surgery, ANH appears to reduce allogenic RBC transfusion rates versus historical controls without increasing perioperative complications. Further evaluation of the technique is warranted.
本研究旨在确定急性等容血液稀释(ANH)在降低接受初次肿瘤细胞减灭术的晚期卵巢癌患者异体红细胞(RBC)输注需求方面的安全性和有效性。
本前瞻性试验纳入了在手术期间接受初次肿瘤细胞减灭术的晚期卵巢癌患者,以评估 ANH。术中以目标血红蛋白 8.0 g/dL 为标准进行血液采集。根据机构指南,术中及住院期间采用标准化输血方案,首先使用自体血,然后使用异体血。主要终点是确定围手术期异体 RBC 输注的总发生率。预定的异体 RBC 输注率<35%被认为是相对于历史对照的 50%输注率有显著降低。
41 例患者同意参与研究。ANH 期间平均采血 1650 mL(范围 700-3000)。肿瘤细胞减灭术结果如下:0 mm,30 例(73%);1-10 mm,8 例(20%);>10 mm,3 例(7%)有残留疾病。估计失血量为 1000 mL(范围 150-2700)。14 例(34%)患者在围手术期输注了异体 RBC,达到了主要终点。没有患者违反方案指南进行输血。≥3 级并发症(20%)和吻合口漏(7%)的发生率与历史对照相似,且符合预定的安全阈值。
对于接受初次肿瘤细胞减灭术的晚期卵巢癌患者,ANH 似乎可以降低与历史对照相比的异体 RBC 输注率,而不会增加围手术期并发症。需要进一步评估该技术。