Humm K R, Chan D L
Department of Clinical Science and Services, The Royal Veterinary College, London, AL97TA, UK.
J Small Anim Pract. 2020 May;61(5):285-291. doi: 10.1111/jsap.13124. Epub 2020 Mar 4.
To: (1) assess the frequency of crossmatch incompatibility in naïve feline blood transfusion recipients using two crossmatching methods, (2) measure the effect of crossmatch incompatibility on change in packed cell volume following transfusion, (3) assess the frequency of acute transfusion reactions and errors in blood transfusions in cats and (4) assess the impact of crossmatch incompatibility on the likelihood of transfusion reactions.
Cats being administered a first AB-matched transfusion in a veterinary teaching hospital were prospectively recruited for this observational study. A slide agglutination method and a commercial test were both used for major and minor crossmatching. We measured increase in packed cell volume at 12 hours after transfusion relative to the mass of red blood cells given per recipient bodyweight and recorded transfusion reactions.
A total of 101 cats was included. Crossmatch incompatibility was common using the slide agglutination method (27% and 10% major and minor incompatibility, respectively), but less common with the commercial test (major and minor incompatibility both 4%). Crossmatch incompatibility with any method was not associated with less effective transfusion in terms of change in packed cell volume. Transfusion reactions occurred in 20 cats, most commonly febrile non-haemolytic transfusion reactions (n = 9) and haemolytic transfusion reactions (n = 7). The commercial test appeared to be most specific for predicting haemolytic transfusion reactions.
Transfusion reactions were fairly common but not associated with increased mortality. Use of crossmatch-compatible blood did not lead to a greater increase in PCV at 12 hours. The commercial test may predict a haemolytic transfusion reaction.
(1) 使用两种交叉配血方法评估初次接受输血的猫科动物受血者交叉配血不相容的频率;(2) 测量交叉配血不相容对输血后红细胞压积变化的影响;(3) 评估猫输血时急性输血反应和错误的频率;(4) 评估交叉配血不相容对输血反应可能性的影响。
前瞻性招募在兽医教学医院接受首次AB血型匹配输血的猫进行这项观察性研究。玻片凝集法和一种商业检测方法均用于主次交叉配血。我们测量了输血后12小时相对于每位受血者体重给予的红细胞质量的红细胞压积增加量,并记录了输血反应。
共纳入101只猫。使用玻片凝集法时交叉配血不相容情况常见(主要和次要不相容分别为27%和10%),但商业检测方法中较少见(主要和次要不相容均为4%)。就红细胞压积变化而言,任何一种方法的交叉配血不相容均与输血效果不佳无关。20只猫发生了输血反应,最常见的是发热性非溶血性输血反应(n = 9)和溶血性输血反应(n = 7)。商业检测方法似乎对预测溶血性输血反应最具特异性。
输血反应相当常见,但与死亡率增加无关。使用交叉配血相容的血液在12小时时并未导致红细胞压积有更大幅度的增加。商业检测方法可能预测溶血性输血反应。