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Antiphospholipid antibodies and pregnancy loss

Author: john   Add date: 09/12/2008   Publishing date: 03/01/2014   Hits: 1
Total 3 pages, Current page:1, Jump to page:
 
Systematic review
Results
Comment

What's worse than being asked a question to which you don't know the answer (or even understand the question)? It could be having only half of the answer, but not knowing which half. Such a position could arise with treatments for antiphospholipid antibodies in pregnancy.

Antiphospholipid antibodies are antibodies directed against several phospholipids in the body. There is an association between antiphospholipid antibodies in the circulation and pregnancy loss, and between 3% and 7% of pregnant women have the antibodies. In low risk pregnancies, the antibodies are associated with a nine-fold increase in pregnancy loss, while in high risk pregnancies with at least three previous losses, they are associated with a 90% risk of further pregnancy loss.

The mechanism of pregnancy loss is thought to be through thrombosis of placental vessels, though this is a complicated, and perhaps controversial area. The important question is whether there are effective treatments. A new systematic review [1] begins to answer that.

Systematic review


The searching strategy for this review was impressive, using the usual electronic databases, plus the Cochrane controlled trials register, plus hand-searching of specialist journals and abstracts of relevant symposia. Trials sought were those that sought to prevent pregnancy loss in pregnant women with a history of at least one previous loss and serological evidence of antiphospholipid antibodies. The primary outcome sought from the trials was pregnancy loss, though many others, including birth weight, prematurity and even issues around maternal bone mineral density were looked for.

Results


There were 10 randomised or quasi-randomised trials included with 627 women, and their design and results are given in detail in the review. In most trials women had at least two and often three previous miscarriages, and both treatments and the results of serology tests are described. Trials were not large, though, with 90 women being the biggest, and some were very small. Trial design was generally adequate, most being properly randomised, some blind, and with intention to treat analysis and 100% follow up in all. The biggest difficulty was the plethora of different treatments used, from aspirin alone, to heparin plus aspirin, prednisolone plus aspirin or intravenous immunoglobulin.

In direct comparisons, aspirin alone was no better than placebo or usual care, with the important qualification that these were small trials with only 70 women in total, and with what appeared to be a lowish rate of loss without treatment. Heparin and aspirin was better than aspirin in two trials with 140 patients, with a relative risk of loss of 0.45 (95% CI 0.29 to 0.70) and number needed to treat of 3.2 (2.1 to 6.3). A trial of high dose heparin versus low dose heparin, both with aspirin, showed no difference, and with rates of pregnancy loss consistent with the comparisons of heparin plus aspirin with aspirin.

 
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