Lymphatic dysfunction in critical illness

被引:2
|
作者
Burke, Edmund
Datar, Sanjeev A.
机构
[1] Univ Calif San Francisco, Dept Pediat, Div Crit Care Med, San Francisco, CA USA
[2] Benioff Childrens Hosp, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
chylothorax; image-directed percutaneous embolization; lymphatic dysfunction in critical illness; plastic bronchitis; sirolimus; ubenimex; CONGENITAL HEART-DISEASE; ACUTE LUNG INJURY; RAT MESENTERIC LYMPHATICS; SEVERE ACUTE-PANCREATITIS; PULMONARY BLOOD-FLOW; THORACIC-DUCT; PLASTIC BRONCHITIS; NITRIC-OXIDE; CONTRACTILE ACTIVITY; MR LYMPHANGIOGRAPHY;
D O I
10.1097/MOP.0000000000000623
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose of reviewThe essential role of the lymphatic system in fluid homeostasis, nutrient transport, and immune trafficking is well recognized; however, there is limited understanding of the mechanisms that regulate lymphatic function, particularly in the setting of critical illness. The lymphatics likely affect disease severity and progression in every condition, from severe systemic inflammatory states to respiratory failure. Here, we review structural and functional disorders of the lymphatic system, both congenital and acquired, as they relate to care of the pediatric patient in the intensive care setting, including novel areas of research into medical and procedural therapeutic interventions.Recent findingsThe mainstay of current therapies for congenital and acquired lymphatic abnormalities has involved nonspecific medical management or surgical procedures to obstruct or divert lymphatic flow. With the development of dynamic contrast-enhanced magnetic resonance lymphangiography, image-directed percutaneous intervention may largely replace surgery. Because of new insights into the mechanisms that regulate lymphatic biology, pharmacologic inhibitors of mTOR and leukotriene B4 signaling are each in Phase II clinical trials to treat abnormal lymphatic structure and function, respectively.SummaryAs our understanding of normal lymphatic biology continues to advance, we will be able to develop novel strategies to support and augment lymphatic function during critical illness and through convalescence.
引用
收藏
页码:332 / 337
页数:6
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