Antiphospholipid syndrome natural history, complications and prognosis: Difference between revisions
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==Complications== | ==Complications== | ||
The complications of APS are described in a systemic order which are as follows: | |||
Thrombotic complications: | |||
Neurological complications: | |||
Preganancy related complications: | |||
Pulmonary complications: | |||
Hematological complications: | |||
Cardiac involvement: | |||
Cutaneous complications: | |||
Renal disease: | |||
Adrenal involvement: | |||
Ocular manifestations: | |||
Gastrointestinal complications: | |||
==Prognosis== | ==Prognosis== |
Revision as of 22:30, 2 April 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Feham Tariq, MD [2]
Overview
Natural History
Complications
The complications of APS are described in a systemic order which are as follows: Thrombotic complications: Neurological complications: Preganancy related complications: Pulmonary complications: Hematological complications: Cardiac involvement: Cutaneous complications: Renal disease: Adrenal involvement: Ocular manifestations: Gastrointestinal complications:
Prognosis
The prognosis of antiphospholipid syndrome is as follows:
- It is associated with increased mortality and morbidity.
- The mean age of death is 59 years.
- Main causes of death in the order of percentage include the following:
- Thrombosis (31%)
- Sepsis (27%)
- Malignancy (14%)
- Hemorrhage (11%)
- Systemic lupus erythematosus involvement (8%)
- Catastrophic APS