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P135 Altered hemostatic balance towards procoagulant state in pregnant women with systemic lupus erythematosus
  1. Daniele Lini1,
  2. Iva Gunnarsson2,
  3. Nida Soutari3,
  4. Sanja Lalic-Cosic4,
  5. Andrea MC Nicholas2,
  6. Roza Chaireti5,6,
  7. Katarina Bremme7,
  8. Franco Franceschini1,
  9. Elisabet Svenungsson2,
  10. Laura Andreoli1# and
  11. Aleksandra Antovic2#
  1. *the authors contributed equally
  2. # the authors contributed equally
  3. 1ASST Spedali Civili of Brescia and University of Brescia, Rheumatology and Clinical Immunology Unit, Dept. of Clinical and Experimental Sciences, Brescia, Italy
  4. 2Karolinska Institutet Dept. of Medicine Solna, Division of Rheumatology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden
  5. 3Karolinska Institutet and Clinical Chemistry, Karolinska University Hospital, Dept. of Molecular Medicine and Surgery, Stockholm, Sweden
  6. 4University of Belgrade, Dept. of Medical Biochemistry, Faculty of Pharmacy, Belgrade, Serbia
  7. 5Karolinska Institutet, Dept. of Molecular Medicine and Surgery, Stockholm, Sweden
  8. 6Karolinska University Hospital, Dept. of Hematology, Stockholm, Sweden
  9. 7Karolinska Institutet, Dept. of Women’s and Children’s Health, Stockholm, Sweden

Abstract

Objectives This study aimed to investigate hemostatic variables in pregnant patients with Systemic Lupus Erythematosus (SLE) in relation to preeclampsia (PE), antiphospholipid antibody (aPL) status and the use of thromboprophylaxis.

Methods Pregnant patients with SLE were sampled during the first and the third trimester for analysis of fibrinogen, D-dimer and global hemostatic variables, i.e. overall coagulation potential (OCP), overall haemostatic potential (OHP) and overall fibrinolysis potential (OFP). Pregnant healthy women with and without PE were sampled during the third trimester of gestation and used as controls (HC).

Results Twenty-two pregnant SLE patients, 80 pregnant HC without PE, and 42 pregnant HC with PE were included. All SLE patients received prophylaxis with low dose acetylsalicylic acid (LDASA). Low molecular weight heparin (LMWH) was given to 8 SLE patients (36,4%), of which 5 had aPL positivity, 1 antiphospholipid syndrome (APS), 1 had previous neurological manifestation and 1 had previous miscarriage. Disease characteristics, pregnancy features and investigated variables from the third trimester are reported in table 1.

Fibrinogen and D-dimer levels increased throughout pregnancies in SLE patients, while no differences were found compared to controls in the third trimester. OCP and OHP were significantly increased in SLE patients during the 3rd trimester of pregnancy, compared to HC (figure 1). However, in 2/8 SLE patients treated with LMWH, global hemostatic variables were undetectable, both were triple aPL positive and on therapeutic dosages of LMWH.

PE occurred in 4 SLE patients (18.2%); 2 were treated with LMWH (1 patient with APS with therapeutic and one aPL carrier with 1 prophylactic dosage). No thrombotic or major bleeding events occurred.

Conclusions All SLE patients displayed a hypercoagulable state throughout pregnancy, as demonstrated by the global hemostatic variables, except for two patients treated with therapeutic LMWH. Furthermore, in this pilot study almost 20% of pregnant women with SLE suffered PE despite ongoing LDASA prophylaxis. Larger longitudinal studies of hemostatic variables are needed to clarify the role of the procoagulant condition shown, and the benefits of thromboprophylactic treatment.

Acknowledgements The study was performed by grants provided by King Gustaf V:s memorial fund and ALF funding from Region Stockholm.

Abstract P135 Figure 1

Levels of OCP, OHP and OFP in SLE patients during pregnancy and in comparison to controls. Red circles represent patients with preeclampsia. C- control pregnant women without preeclampsia, C+PE control pregnant women with preeclampsia, T1 – first trimester during pregnancy in SLE patients, T3 – third trimester during pregnancy in SLE patients. 25th and 75th percentile of reference range of respective variable in healthy non-pregnant individuals

Abstract P135 Table 1

Characteristics and coagulation parameters of SLE patients and HC. Continuous variables are expressed as mean±SD. g, i, I, n=p<0.05; a, b, c, d, e, f, h, m=p<0.01. (*) Prophylactic dose; (#) Anticoagulant dose. Abbreviations: aPL: antiphospholipid antibodies; APS: antiphospholipid syndrome; LDASA: low dose acetylsalicylic acid; LMWH: low molecular weight heparin; NA: not applicable; OCP: overall coagulation potential; OFP: overall fibrinolysis potential; OHP: overall haemostatic potential

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