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低氧血症与阿司匹林在地中海贫血中的作用

Hypoxaemia and the effect of aspirin in thalassaemia.

作者信息

Fucharoen S, Youngchaiyud P, Wasi P

出版信息

Southeast Asian J Trop Med Public Health. 1981 Mar;12(1):90-3.

PMID:7256361
Abstract

Blood gas analysis of arterial blood was performed in 34 patients with beta o-thalassaemia/haemoglobin E disease and homozygous beta o-thalassaemia. Among the 22 splenectomised patients 19 had PaO2 lower than the normal expected value, and 18 of these had PaO2 lower than 80 mmHg. Of the 12 non-splenectomised patients 5 had PaO2 lower than the expected normal value but only in one case it was lower than 80 mmHg. After aspirin or Persantin administration there was a definite rise in the PaO2 in 10 out of 12 patients. The hypoxaemia is believed to occur from increased platelet aggregation leading to pulmonary artery occlusion. The rise of the arterial PaO2 after aspirin administration indicates that the observed hypoxaemia is due to reversible platelet aggregation in the majority of cases.

摘要

对34例β地中海贫血/血红蛋白E病患者和纯合子β地中海贫血患者进行了动脉血气分析。在22例脾切除患者中,19例的动脉血氧分压(PaO2)低于正常预期值,其中18例低于80 mmHg。在12例未行脾切除的患者中,5例的PaO2低于预期正常值,但只有1例低于80 mmHg。给予阿司匹林或潘生丁后,12例患者中有10例的PaO2有明显升高。据信,低氧血症是由于血小板聚集增加导致肺动脉阻塞所致。阿司匹林给药后动脉PaO2升高表明,在大多数情况下,观察到的低氧血症是由于可逆性血小板聚集引起的。

相似文献

1
Hypoxaemia and the effect of aspirin in thalassaemia.低氧血症与阿司匹林在地中海贫血中的作用
Southeast Asian J Trop Med Public Health. 1981 Mar;12(1):90-3.
2
Pulmonary artery obstruction in thalassaemia.地中海贫血中的肺动脉梗阻
Southeast Asian J Trop Med Public Health. 1980 Dec;11(4):516-23.
3
Hypoxemia in thalassemia.地中海贫血中的低氧血症。
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Increased circulating platelet aggregates in thalassaemia.
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Aspirin resistance in children and young adults with splenectomized thalassemia diseases.脾切除的儿童和青年地中海贫血疾病患者的阿司匹林抵抗
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Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension.
慢性输血对合并肺动脉高压的血红蛋白 E/β 地中海贫血的益处。
Int J Gen Med. 2014 Aug 19;7:411-6. doi: 10.2147/IJGM.S66610. eCollection 2014.
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Haemoglobinopathies in southeast Asia.东南亚的血红蛋白病。
Indian J Med Res. 2011 Oct;134(4):498-506.
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Protein C and Protein S: causative factor for developing a hemorrhagic infarct in a HbE/Beta thalassemia child.蛋白 C 和蛋白 S:导致 HbE/β 地中海贫血儿童发生出血性梗死的原因。
Indian J Pediatr. 2010 Mar;77(3):316-7. doi: 10.1007/s12098-009-0297-5. Epub 2010 Jan 20.