This site provides an overview of acquired coagulopathy in the postoperative setting, and specifically explores the less-recognized phenomenon of iatrogenic immune-mediated coagulopathy (IMC) in surgical patients. This site is intended for healthcare professionals.
What is a coagulopathy?
Coagulopathy stems from defective function in one or more elements of the inherent clotting mechanisms, and is distinct from hemorrhage related to direct vascular breach during surgery or other pathologies.
Coagulopathy is defined as a disease affecting the coagulability of blood, including:
- Hemorrhagic or thrombotic disorders: These disorders generally involve excessive bleeding (hemorrhage) or excessive clot formation leading to vascular obstruction (thrombosis).
- Inherited or acquired disorders: Inherited disorders are congenital conditions that individuals are born with and are transmitted by inheritance. Some examples include: hemophilia and von Willebrand disease. Acquired disorders are conditions that are not congenital but have developed after birth. Some causes include: liver disease, vitamin K deficiency, disseminated intravascular coagulation and immune-mediated coagulopathy.
Postoperative coagulopathy is a complex medical disorder with a variety of causes and health effects. Identifying a coagulopathy requires assessments of the components and function of normal coagulation. A thorough patient assessment and medical history are also required, and consultation with specialists may be needed to diagnose and develop a management plan. This site provides resources and information, but is not intended to replace appropriate medical evaluation and judgment.