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The physician looking after the woman will carefully assess the effect of the disease, including on her lungs, the gut, pancreas (risk of diabetes) and heart, before giving a considered and informed advice.
This is a difficult area. One consideration is the inevitably limited life-
The second issue is the possibility of the child being affected. The mother will definitely pass on the rogue gene. It may be important to check whether the partner carries the gene. About 5% of the white population carries the gene, so the chance among this population group is relatively high. The rate among those of African or Oriental ancestry is much lower.
A test to check the status of her partner is available but it detects only about 70% of the carriers, and therefore there is still a risk of a carrier being missed.
It is possible for pregnancy to worsen cystic fibrosis symptoms. It is therefore imperative that a careful eye is kept on the pregnant woman through the course of the pregnancy. Pregnancy with cystic fibrosis is regarded and always managed as high risk.
Physiotherapy and antibiotics are the mainstay of cystic fibrosis management. These will continue to be needed during pregnancy. Penicillin or a form of cephalosporin commonly used to prevent infection are safe.
Also inhalational drugs to help dilate the lungs (bronchodilators) will almost certainly be required on a regular basis. All these are known to be safe.
Other maternal complications such as respiratory or heart failure may also prompt preterm delivery.
If labor is to be induced, it will be done the same as for everybody else. Prostaglandin
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