医学
血友病
养生
重症监护医学
预防性治疗
血友病A
梅德林
儿科
外科
政治学
法学
出处
期刊:Haemophilia
[Wiley]
日期:2014-04-08
卷期号:20 (5): 607-615
被引量:55
摘要
Summary Prophylaxis is considered optimal care for children and adults with severe haemophilia A because of its proven ability to reduce joint and other bleeding episodes. However, a ‘one size fits all’ approach to prophylaxis is not ideal, potentially leading to over‐treatment in some individuals and under‐treatment in others. Moreover, a generic plan fails to take into account a patient's lifestyle and personal preferences. This article reviews the factors contributing to bleeding risk and joint damage and uses case studies to illustrate how these contributors can be weighed to individualize the prophylactic regimen, thereby increasing the likelihood of therapeutic success.
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