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Updated: Sep 16, 2025

Isolation of Leukocytes from the Murine Tissues at the Maternal-Fetal Interface
Published on: May 21, 2015
Beyond pregnancy in systemic autoimmune diseases: a focus on postpartum experience from a referral centre
Dina Zucchi1, Benedetta Ciribè1, Francesca Monacci2
1Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Objective:
To evaluate the incidence and types of complications occurring within 60 days postpartum in patients with systemic autoimmune diseases (SAD), focusing on disease flares and other clinical events.
Methods:
This is a retrospective analysis of prospectively collected data from a single-centre cohort. Variables included demographic and clinical features, pregnancy treatments, disease course, postpartum visit attendance, complications and breastfeeding data.
Results:
A total of 253 pregnancies were included. Most diagnoses were connective tissue diseases (CTDs, 80.2%), followed by inflammatory arthritis (14.2%) and vasculitis (5.5%). A postpartum visit was performed in 234 patients (92.5%). Postpartum complications occurred in 50 patients (19.8%), including 42 flares (16.6%) and 12 other complications (4.7%). Flares included 20 articular, five mucocutaneous, five renal, four hematological, three parotid swelling, two deep venous thromboses in aPL-positive patients, two uveitis relapses and one myositis. Flares were associated with active disease during pregnancy (P < 0.01). Inflammatory arthritis showed the highest flare rate (41.7% vs 12.0% in CTD, P < 0.01), though severe flares occurred only in CTD or vasculitis. Other complications included six hypertension cases, four postpartum hemorrhages (two on LDA/LMWH), one Clostridium difficile infection and one ICU admission for severe hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome. Non-flare complications did not differ by diagnosis. At postpartum visit, 147 patients (58.5%) were breastfeeding. Of the 42 with flares, four were contraindicated to breastfeed due to therapies. The others who did not breastfeed did so by choice or unrelated reasons.
Conclusions:
The postpartum period is high-risk in SAD patients. Follow-up should extend beyond pregnancy, with multidisciplinary care to manage disease activity and breastfeeding-related treatment restrictions.
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