Department of Nephrology, Kitasato University School of Medicine, Japan.
Intern Med. 2023 Oct 1;62(19):2803-2811. doi: 10.2169/internalmedicine.0507-22. Epub 2023 Feb 15.
Objective Allergic reactions are a severe complication of plasma exchange (PEx). Few reports have analyzed allergic reactions during PEx using fresh-frozen plasma (FFP) as a replacement solution. We therefore clarified the relationship between risk and exacerbation factors that lead to the onset of PEx-related allergic reactions, particularly PEx, using FFP, and examined whether or not allergic reactions were predictable. Methods This retrospective study included 88 consecutive patients who underwent PEx with FFP as a replacement solution at Kitasato University Hospital. The patients were grouped according to the presence of allergic reactions and compared. Data were analyzed using the χ test, Mann-Whitney U test, and a binomial logistic analysis. Statistical analyses were performed using EZR software program, version 1.54, with p<0.05 considered statistically significant. Results There were 44 allergic reaction cases. The average time to the onset of an allergic reactions was 63.5 (45-93) minutes. The allergic reaction-onset group had significantly higher average albumin (Alb) levels than did the non-allergic reaction-onset group. The binomial logistic analysis identified Alb levels as independent risk factors for allergic reactions. The receiver operating characteristic analysis identified an Alb level ≥3.4 g/dL as a risk factor for allergic reactions (area under the curve: 0.731; 95% confidence interval: 0.622-0.84). Conclusion Allergic reaction onset occurred approximately one hour after PEx initiation in the critical period. A serum Alb level ≥3.4 g/dL was identified as a risk factor for predicting allergic reactions. Patients with Alb levels ≥3.4 g/dL at the first PEx should be monitored for allergic reaction symptoms.
过敏反应是血浆置换(PEx)的严重并发症。很少有报道分析使用新鲜冷冻血浆(FFP)作为替代溶液时 PEx 中的过敏反应。因此,我们阐明了导致 PEx 相关过敏反应(尤其是 PEx)发作的风险和加重因素之间的关系,并检查了过敏反应是否可以预测。
这项回顾性研究包括在桂由大学医院接受 PEx 并用 FFP 作为替代溶液的 88 例连续患者。根据是否存在过敏反应将患者分组并进行比较。使用卡方检验、Mann-Whitney U 检验和二项逻辑分析进行数据分析。使用 EZR 软件程序(版本 1.54)进行统计分析,p<0.05 被认为具有统计学意义。
有 44 例过敏反应病例。过敏反应发作的平均时间为 63.5(45-93)分钟。过敏反应发作组的平均白蛋白(Alb)水平明显高于非过敏反应发作组。二项逻辑分析确定 Alb 水平是过敏反应的独立危险因素。受试者工作特征分析确定 Alb 水平≥3.4 g/dL 是过敏反应的危险因素(曲线下面积:0.731;95%置信区间:0.622-0.84)。
过敏反应发作发生在 PEx 开始后的关键时期约 1 小时。血清 Alb 水平≥3.4 g/dL 被确定为预测过敏反应的危险因素。首次 PEx 时 Alb 水平≥3.4 g/dL 的患者应监测过敏反应症状。