Session Information
Session Type: ACR Poster Session A
Session Time: 9:00AM-11:00AM
Background/Purpose: To assess the safety and efficacy of anakinra in pregnant FMF patients.
Methods: Six FMF patients, treated with anakinra during pregnancy were monitored for side effects, fetal and maternal outcomes.
Results: We present six FMF patients who were treated with Anakinra 100 mg/d sc during pregnancy due to severe protracted febrile myalgia in 4, thrombocytopenia in 1 and amyloidosis in 1. One of these patients has been previously reported (1). No anakinra-related adverse event was observed either in the mother-to-be or the fetus during pregnancy and delivery. One patient had an incision-site infection after c-section and one of the babies developed thrombocytopenia as his mother, and improved after treatment with IVIG. Four of these six patients gave birth to healthy babies and two are still pregnant . During the anakinra treatment, all patients recieved anakinra together with cholchicine, except one patient with thrombocytopenia was solely on Anakinra throughout pregnancy. No flare was observed in 3 out of 4 patients in whom Anakinra was was stopped after delivery. Pregnancy-related features are listed in Table 1.
Conclusion:
Anakinra promises to be a safe alternative in pregnant FMF patients who have active disease despite colchicine or intolerant and also can be given transiently during pregnancy and successfully stopped after delivery, as in our patients.
References:.
1) Lachman HJ, et al. Anti IL-1 therapies and pregnancy outcome. Pediatric Rheumatology 2013, 11 (Suppl 1) :A269
Table 1. Pregnancy-related outcomes
Case |
Maternal Age |
Anakinra Relation to pregnancy |
USGs |
Weeks at delivery or currrent gestational age |
Gender of the baby/fetus |
Mode of the delivery |
1st minute APGAR |
Follow-up duration after birth (months) |
Complications after birth |
1 |
33
|
started at 21st GW and used continiously until birth |
normal |
Birth at 36th GW |
boy |
C/S |
8 |
34 |
No |
2 |
28 |
started at 12th GW and used until birth |
normal |
Birth at 40th GW |
girl |
vaginal |
10 |
22 |
No |
3 |
31 |
Conceived on Anakinra (have been on Anakinra since 2012), discontinued at 29th GW, reintroduced at 33th GW due to symptom flare. |
normal |
Birth at 38th GW |
boy |
C/S |
6 |
4 |
Methicillin-Sensitive Staphylococcus Aureus incision-site infection (treated with Tygecycline) in mother |
4 |
24 |
started at 15th GW and used until birth |
normal |
Birth at 38th GW |
boy |
Vaginal |
8 |
4 |
thrombocyte count of the baby was low (23,000/mm3) (After three courses of IVIG, it was increased to 95,000/mm3 and a month later to 269,000/mm3) |
5 |
32 |
started at 16th GW, still using |
normal |
At 22nd GW |
Twin girls |
|
|
|
|
6 |
25 |
Started at 23th GW, still on Anakinra at 29th GW |
normal |
At 29th GW |
girl |
|
|
|
|
To cite this abstract in AMA style:
Ozdogan H, Ugurlu S, Ergezen B. How Safe IT Is to TREAT Pregnant FMF Patients with Anakinra ? [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/how-safe-it-is-to-treat-pregnant-fmf-patients-with-anakinra/. Accessed .« Back to 2015 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/how-safe-it-is-to-treat-pregnant-fmf-patients-with-anakinra/