Department of Haematology, Royal Brompton Hospital, London, United Kingdom.
Department of Haematology, Imperial College Healthcare NHS Trust, London, United Kingdom.
Crit Care Med. 2020 May;48(5):e371-e379. doi: 10.1097/CCM.0000000000004261.
To ascertain: 1) the frequency of thrombocytopenia and heparin-induced thrombocytopenia; 2) positive predictive value of the Pretest Probability Score in identifying heparin-induced thrombocytopenia; and 3) clinical outcome of heparin-induced thrombocytopenia in adult patients receiving venovenous- or venoarterial-extracorporeal membrane oxygenation, compared with cardiopulmonary bypass.
A single-center, retrospective, observational cohort study from January 2016 to April 2018.
Tertiary referral center for cardiac and respiratory failure.
Patients who received extracorporeal membrane oxygenation for more than 48 hours or had cardiopulmonary bypass during specified period.
None.
Clinical and laboratory data were collected retrospectively. Pretest Probability Score and heparin-induced thrombocytopenia testing results were collected prospectively. Mean age (± SD) of the extracorporeal membrane oxygenation and cardiopulmonary bypass cohorts was 45.4 (± 15.6) and 64.9 (± 13), respectively (p < 0.00001). Median duration of cardiopulmonary bypass was 4.6 hours (2-16.5 hr) compared with 170.4 hours (70-1,008 hr) on extracorporeal membrane oxygenation. Moderate and severe thrombocytopenia were more common in extracorporeal membrane oxygenation compared with cardiopulmonary bypass throughout (p < 0.0001). Thrombocytopenia increased in cardiopulmonary bypass patients on day 2 but was normal in 83% compared with 42.3% of extracorporeal membrane oxygenation patients at day 10. Patients on extracorporeal membrane oxygenation also followed a similar pattern of platelet recovery following cessation of extracorporeal membrane oxygenation. The frequency of heparin-induced thrombocytopenia in extracorporeal membrane oxygenation and cardiopulmonary bypass were 6.4% (19/298) and 0.6% (18/2,998), respectively (p < 0.0001). There was no difference in prevalence of heparin-induced thrombocytopenia in patients on venovenous-extracorporeal membrane oxygenation (8/156, 5.1%) versus venoarterial-extracorporeal membrane oxygenation (11/142, 7.7%) (p = 0.47). The positive predictive value of the Pretest Probability Score in identifying heparin-induced thrombocytopenia in patients post cardiopulmonary bypass and on extracorporeal membrane oxygenation was 56.25% (18/32) and 25% (15/60), respectively. Mortality was not different with (6/19, 31.6%) or without (89/279, 32.2%) heparin-induced thrombocytopenia in patients on extracorporeal membrane oxygenation (p = 0.79).
Thrombocytopenia is already common at extracorporeal membrane oxygenation initiation. Heparin-induced thrombocytopenia is more frequent in both venovenous- and venoarterial-extracorporeal membrane oxygenation compared with cardiopulmonary bypass. Positive predictive value of Pretest Probability Score in identifying heparin-induced thrombocytopenia was lower in extracorporeal membrane oxygenation patients. Heparin-induced thrombocytopenia had no effect on mortality.
确定:1)血小板减少症和肝素诱导的血小板减少症的频率;2)在识别肝素诱导的血小板减少症中,预测试验概率评分的阳性预测值;3)与体外循环相比,接受静脉-静脉或静脉-动脉体外膜氧合的成年患者的肝素诱导的血小板减少症的临床结局。
2016 年 1 月至 2018 年 4 月期间的单中心回顾性观察队列研究。
心脏和呼吸衰竭的三级转诊中心。
接受体外膜氧合超过 48 小时或在此期间接受体外循环的患者。
无。
回顾性收集临床和实验室数据。前瞻性收集预测试验概率评分和肝素诱导的血小板减少症检测结果。体外膜氧合和体外循环队列的平均年龄(±标准差)分别为 45.4(±15.6)和 64.9(±13)(p<0.00001)。体外循环的中位持续时间为 4.6 小时(2-16.5 小时),而体外膜氧合的中位持续时间为 170.4 小时(70-1008 小时)。与体外循环相比,整个体外膜氧合过程中中度和重度血小板减少症更为常见(p<0.0001)。体外循环患者在第 2 天血小板减少症增加,但在第 10 天,83%的患者血小板计数正常,而 42.3%的体外膜氧合患者血小板计数正常。体外膜氧合患者在停止体外膜氧合后也遵循类似的血小板恢复模式。体外膜氧合和体外循环中肝素诱导的血小板减少症的发生率分别为 6.4%(19/298)和 0.6%(18/2998)(p<0.0001)。静脉-静脉体外膜氧合(8/156,5.1%)与静脉-动脉体外膜氧合(11/142,7.7%)患者肝素诱导的血小板减少症的发生率无差异(p=0.47)。体外循环和体外膜氧合患者肝素诱导的血小板减少症的预测试验概率评分的阳性预测值分别为 56.25%(18/32)和 25%(15/60)。体外膜氧合患者有或无肝素诱导的血小板减少症(分别为 6/19,31.6%和 89/279,32.2%)的死亡率无差异(p=0.79)。
血小板减少症在开始体外膜氧合时已经很常见。与体外循环相比,静脉-静脉和静脉-动脉体外膜氧合中肝素诱导的血小板减少症更为常见。预测试验概率评分在识别肝素诱导的血小板减少症中对体外膜氧合患者的阳性预测值较低。肝素诱导的血小板减少症对死亡率没有影响。