Bishop Rebecca C, Jonk Kaitlyn M, Migliorisi Alessandro, Austin Scott M, Mullins Emma C, Wilkins Pamela A
Department of Veterinary Clinical Medicine, University of Illinois Urbana-Champaign, Urbana, Illinois, USA.
Equine Vet J. 2025 May;57(3):766-773. doi: 10.1111/evj.14413. Epub 2024 Sep 3.
Polycythaemia and coagulopathy are identified risk factors for non-survival in critically ill horses. Assessment of coagulation is recommended for critical care monitoring but may be affected by concurrent polycythaemia.
To evaluate the effects of induced polycythaemia on coagulation parameters as measured by a point-of-care viscoelastic coagulation device (VCM Vet™).
Prospective interventional study.
Healthy adult horses (n = 7) were given 6 mcg/kg of phenylephrine IV over 15 min to induce transient polycythaemia. Samples for packed cell volume (PCV), total solids (TS), complete blood count (CBC), activated partial thromboplastin time (PTT), prothrombin (PT) and VCM Vet™ viscoelastic testing were collected at baseline (T0), 5 min (T1) and 2 h (T2) post-phenylephrine infusion. Splenic volume was measured by transabdominal ultrasonography. VCM Vet™ and plasma-based coagulation parameters, splenic volume and haematologic values were compared within and between time points.
Splenic volume decreased from T0 (11.5 ± 4.8 L) to T1 (6.1 ± 2 L, p = 0.04) and returned to baseline volume by T2 (12.1 ± 3.9 L, p = 0.8), consistent with phenylephrine-induced splenic contraction. PCV increased from T0 (37% ± 4%) to T1 (56.3% ± 5.3%; p < 0.001) and returned to baseline at T2 (41.6% ± 3.6%; p = 0.1). A10 and A20 (amplitude at 10 and 20 min, VCM units) were decreased from T0 (12.6 ± 1.6, 18.9 ± 5) to T1 (5.4 ± 1.9, 7.6 ± 2.4; both p < 0.001) and remained lower than baseline at T2 (9.3 ± 2.1, 12.7 ± 3; both p = 0.01). PT and PTT remained within reference ranges with no significant difference over time (p = 0.5 and 0.09, respectively). PCV was negatively correlated with CFT (R = -0.61, p = 0.003), A10 (R = -0.9, p < 0.001) and A20 (R = -0.87, p < 0.001).
Small sample size, limited to healthy mares.
Phenylephrine-induced polycythaemia was associated with hypocoagulable viscoelastic traces using the VCM Vet™ device without effect on plasma-based coagulation assessments or platelet number. Further investigation of viscoelastic testing is needed in horses with increased PCV due to clinical illness.
红细胞增多症和凝血病是危重病马死亡的已知危险因素。建议对危重病马进行凝血功能评估以进行重症监护监测,但可能会受到并发红细胞增多症的影响。
评估通过即时粘弹性凝血装置(VCM Vet™)测量的诱导性红细胞增多症对凝血参数的影响。
前瞻性干预研究。
对7匹健康成年马静脉注射6 mcg/kg去氧肾上腺素,持续15分钟,以诱导短暂性红细胞增多症。在去氧肾上腺素输注前(T0)、输注后5分钟(T1)和2小时(T2)采集样本,检测血细胞比容(PCV)、总固体(TS)、全血细胞计数(CBC)、活化部分凝血活酶时间(PTT)、凝血酶原时间(PT)以及进行VCM Vet™粘弹性检测。通过经腹超声测量脾脏体积。比较各时间点内及各时间点间的VCM Vet™和基于血浆的凝血参数、脾脏体积及血液学值。
脾脏体积从T0时的(11.5±4.8 L)降至T1时的(6.1±2 L,p = 0.04),并在T2时恢复至基线体积(12.1±3.9 L,p = 0.8),这与去氧肾上腺素诱导的脾脏收缩一致。PCV从T0时的(37%±4%)升至T1时的(56.3%±5.3%;p < 0.001),并在T2时恢复至基线(41.6%±3.6%;p = 0.1)。A10和A20(10分钟和20分钟时的振幅,VCM单位)从T0时的(12.6±1.6,18.9±5)降至T1时的(5.4±1.9,7.6±2.4;均p < 0.001),并在T2时仍低于基线(9.3±2.1,12.7±3;均p = 0.01)。PT和PTT保持在参考范围内,随时间无显著差异(分别为p = 0.5和0.09)。PCV与CFT(R = -0.61,p = 0.003)、A10(R = -0.9,p < 0.001)和A20(R = -0.87,p < 0.001)呈负相关。
样本量小,仅局限于健康母马。
使用VCM Vet™装置时,去氧肾上腺素诱导的红细胞增多症与低凝性粘弹性痕迹相关,对基于血浆的凝血评估或血小板数量无影响。对于因临床疾病导致PCV升高的马匹,需要进一步研究粘弹性检测。