Effect on mother and child of eculizumab given before caesarean section in a patient with severe antiphospholipid syndrome A case report

被引:46
作者
Gustavsen, Alice [1 ,2 ]
Skattum, Lillemor [3 ]
Bergseth, Grethe [4 ,5 ]
Lorentzen, Bjorg [6 ]
Floisand, Yngvar [7 ]
Bosnes, Vidar [8 ]
Mollnes, Tom Eirik [1 ,2 ,9 ]
Barratt-Due, Andreas [1 ,2 ,10 ]
机构
[1] Oslo Univ Hosp, Dept Immunol, Oslo, Norway
[2] Univ Oslo, KG Jebsen IRC, Oslo, Norway
[3] Lund Univ & Clin Immunol & Transfus Med, Sect Microbiol Immunol & Glycobiol, Dept Lab Med, Lund, Region Skane, Sweden
[4] Nordland Hosp Bodo, Res Lab, Oslo, Norway
[5] Univ Tromso, KG Jebsen TREC, Oslo, Norway
[6] Oslo Univ Hosp, Sect Med Immunol, Dept Obstet, Oslo, Norway
[7] Oslo Univ Hosp, Sect Med Immunol, Dept Haematol, Oslo, Norway
[8] Oslo Univ Hosp, Sect Med Immunol, Dept Immunol, Oslo, Norway
[9] Norwegian Univ Sci & Technol, Ctr Mol Inflammat Res, Trondheim, Norway
[10] Oslo Univ Hosp, Div Emergencies & Crit Care, Oslo, Norway
关键词
antiphospholipid syndrome; complement; eculizumab; pregnancy; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; TASK-FORCE REPORT; COMPLEMENT-SYSTEM; PREGNANCY; ANTIBODIES; MANAGEMENT; ACTIVATION;
D O I
10.1097/MD.0000000000006338
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Antiphospholipid syndrome (APS) in pregnancy may trigger the life-threatening catastrophic antiphospholipid syndrome ( CAPS). Complement activation is implicated in the pathogenesis, and inhibition of complement factor C5 is suggested as an additional treatment option. Patient concerns, diagnosis and interventions: We present a pregnant patient treated with the C5-inhibitor eculizumab due to high risk of developing devastating APS-related complications. The complement inhibitory effects of the treatment were examined both in the patient and the premature infant. Outcomes: Complement activity in the mother recovered considerably faster than anticipated; however, no new thrombosis or CAPS developed during the last week of pregnancy or postpartum. Blood sampling from the umbilical vein and artery, and from the infant after delivery showed low complement activity; however, only 0.3% of the eculizumab concentration detected in the mother, consistent with low placental passage of eculizumab. Lessons: The data underscore the importance of close monitoring of complement inhibition and individualizing dosage regimens in pregnant patients receiving eculizumab. We document how traditional functional complement activity tests cannot assess the effect of eculizumab in premature infants due to the very low levels of complement factors detected in this infant born in gestational week 33. Only trace amounts of eculizumab passed the placenta. In conclusion, complement C5 inhibition might be a safe candidate treatment option for APS during pregnancy and delivery, and additionally, enables prolongation of pregnancy with important weeks.
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页数:4
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