Department of Anaesthesiology, Heinrich-Heine-University, Moorenstrasse 5, D-40225, Düsseldorf, Germany.
BMC Anesthesiol. 2012 Aug 8;12:19. doi: 10.1186/1471-2253-12-19.
Approximately 90 haemoglobinopathies have been identified that result in abnormally high oxygen affinity. One of these is haemoglobinopathy York (HbY), first described in 1976. HbY causes an extreme leftward shift of the oxygen dissociation curve with the P50 value changing to 12.5 - 15.5 mmHg (normal value 26.7 mmHg), indicating that approximately half of the haemoglobin is not available as oxygen carrier. Patients with haemoglobinopathies with increased oxygen affinity could suffer from the risk developing ischaemic complications due to a lack of functional oxygen carriers. This is, to best of our knowledge, the first case report on a patient with HbY published in connection with anesthesia.
A 42-year-old female with a severe headache and Glasgow coma scale (GCS) of 15 was admitted to the neurosurgical intensive care unit with a ruptured, right sided ICA aneurysm with consecutive subarachnoid haemorrhage [Fisher III, World Federation of Neurosurgical Societies (WFNS) I)]. The medical history of the patient included an erythrocytosis (Hb 17.5 g/dl) on the base of a high-oxygen-affinity haemoglobinopathy, called Hb York (HbY). With no time available to take special preoperative precautions, rapid blood loss occurred during the first attempt to clip the aneurysm. General transfusion procedures, according to the guidelines based on haemoglobin and haematocrit values, could not be applied due to the uncertainty in the oxygen carrier reduction. To maintain tissue oxygen supply, clinical indicators of ischaemia were instead utilized to gauge the appropriate required blood products, crystalloids and colloids replacements. Despite this, the patient survived the neurosurgical intervention without any neurological deficit.
Family members of patients with HbY (and other haemoglobinopathies with increased oxygen affinity) should undergo clinical assessment, particularly if they are polycythaemic. If the diagnosis of HbY is confirmed, they should carry an "emergency anaesthesiology card" in order to avert perioperative risks arising from their "hidden" anemia.
已发现约 90 种血红蛋白病会导致氧亲和力异常升高。其中一种是血红蛋白病约克(HbY),于 1976 年首次描述。HbY 导致氧离解曲线向左极移动,P50 值变为 12.5-15.5mmHg(正常值为 26.7mmHg),表明大约一半的血红蛋白不能作为氧载体。由于缺乏功能性氧载体,氧亲和力增加的血红蛋白病患者可能有发生缺血性并发症的风险。据我们所知,这是首例与麻醉相关的 HbY 患者病例报告。
一名 42 岁女性,因右侧颈内动脉破裂伴连续蛛网膜下腔出血[Fisher III 级,世界神经外科学联合会(WFNS)Ⅰ级]头痛剧烈,格拉斯哥昏迷评分(GCS)为 15,入住神经外科重症监护病房。该患者既往有红细胞增多症(Hb 17.5g/dl),基础为高氧亲和力血红蛋白病,称为 Hb York(HbY)。由于没有时间采取特殊的术前预防措施,第一次试图夹闭动脉瘤时就迅速失血。根据基于血红蛋白和血细胞比容值的指南,不能进行常规输血程序,因为氧载体减少的不确定性。为了维持组织氧供应,相反利用缺血的临床指标来判断适当的所需血液制品、晶体和胶体替代物。尽管如此,患者在没有任何神经功能缺损的情况下幸存下来。
HbY(和其他氧亲和力增加的血红蛋白病)患者的家属应接受临床评估,特别是如果他们有红细胞增多症。如果确诊为 HbY,他们应携带“紧急麻醉学卡片”,以避免因“隐匿性”贫血引起的围手术期风险。