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首页> 外文期刊>Haemophilia: the official journal of the World Federation of Hemophilia >The impact of haemarthropathy on the QoL of Korean severe haemophilia A patients: The critical level of haemarthropathy for the QoL
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The impact of haemarthropathy on the QoL of Korean severe haemophilia A patients: The critical level of haemarthropathy for the QoL

机译:血液病对韩国严重A型血友病患者QoL的影响:QoL的严重血液病水平

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摘要

The minimum goal of secondary prophylaxis may be to delay the progression of haemarthropathy below a critical level over which it has a great impact on the QoL of haemophilia patients. However, the critical level of haemarthropathy may be different across countries. For these reasons, the impact of haemarthropathy on the QoL in Korean haemophilia A patients was investigated. Depending on observed Pettersson scores of 27 severe haemophilia A patients, they were divided into three groups, P (Pettersson score) ≤10, P11~19 and P ≥ 20 groups. The QoL of each patient, assessed by the SF36, was compared between the groups. In addition, the changes in the QoL of the patients were observed according to the changes of Pettersson scores to find out the critical level of arthropathy. None of the scores of the SF36 scales were different between the P ≤ 10 and P11~19 groups. In contrast, the scores of PF and MH scales were significantly different between the P11~19 and P ≥ 20 groups. When changes in the scores of each scale in the SF36 were observed according to changes in Pettersson scores, the average P score of 13.0 ± 2.7 was thought to be the critical level of haemarthropathy because above that level, haemarthropathy and physical and mental health of the patients rapidly deteriorated. The progression of haemarthropathy to the critical level should be delayed as long as possible to prevent or to delay a rapid deterioration of the QoL of Korean patients with haemophilia.
机译:二级预防的最小目标可能是将血栓形成的进展延迟到对血友病患者的QoL有很大影响的临界水平以下。但是,不同国家的严重血栓形成程度可能有所不同。由于这些原因,研究了韩国人A型血友病患者中血液病对QoL的影响。根据观察到的27位严重A型血友病患者的Pettersson评分,将他们分为三组:P(Pettersson评分)≤10,P11〜19和P≥20组。在两组之间比较由SF36评估的每位患者的QoL。另外,根据Pettersson评分的变化观察患者的QoL变化,以找出临界的关节病水平。 P≤10和P11〜19组的SF36量表得分均无差异。相比之下,P11〜19和P≥20组的PF和MH量表得分明显不同。当根据Pettersson分数的变化观察到SF36中每个量表的分数变化时,平均P分数13.0±2.7被认为是严重的血液病水平,因为高于该水平,则血液病以及该人群的身心健康患者迅速恶化。应当尽可能延迟将血友病进展至临界水平,以防止或延迟韩国血友病患者的QoL迅速恶化。

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