Perinatal outcomes in women with multiple sclerosis exposed to disease-modifying drugs

被引:41
作者
Lu, E. [1 ,2 ,3 ]
Dahlgren, L. [4 ]
Sadovnick, A. D. [1 ,2 ,5 ]
Sayao, A. [1 ,2 ]
Synnes, A. [6 ]
Tremlett, H. [1 ,2 ,3 ]
机构
[1] Univ British Columbia, Fac Med, Div Neurol, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 2B5, Canada
[3] Univ British Columbia, Fac Med, Expt Med Program, Vancouver, BC V6T 2B5, Canada
[4] Univ British Columbia, Dept Obstet & Gynaecol, Fac Med, Vancouver, BC V6T 2B5, Canada
[5] Univ British Columbia, Dept Med Genet, Fac Med, Vancouver, BC V6T 2B5, Canada
[6] Univ British Columbia, Dept Pediat, Fac Med, Vancouver, BC V6T 2B5, Canada
基金
加拿大健康研究院;
关键词
birth; disease modifying therapies; glatiramer acetate; interferon-beta; multiple sclerosis; pregnancy; relapsing-remitting; INTERFERON-BETA; PREGNANCY OUTCOMES; DIAGNOSTIC-CRITERIA; GLATIRAMER ACETATE; APGAR SCORE; BIRTH; GUIDELINES; DELIVERY; THERAPY; ISSUES;
D O I
10.1177/1352458511422244
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The incidence of disease-modifying drug (DMD) exposure during pregnancy in multiple sclerosis (MS) is unknown and limited data exists regarding the potential harm of DMD exposure during pregnancy. Objective: To investigate the incidence and effect of in utero DMD exposure on perinatal outcomes. Methods: We conducted a retrospective analysis by linking two provincial, population-based databases, the British Columbia (BC) MS database with the BC Perinatal Database Registry. Delivery (duration of the second stage of labor, assisted vaginal delivery and Cesarean section) and neonatal (birth weight, gestational age, 5-minute Apgar score and congenital anomalies) outcomes were compared between women exposed and unexposed to a DMD within 1 month prior to conception and/or during pregnancy. Findings were reported as odds ratios (ORs) with 95% confidence intervals (CIs). Results: In all, 311 women with relapsing-remitting MS delivered 418 singleton babies between April 1998 and March 2009. 21/101 (21%) of births to MS women treated with DMD prior to pregnancy were exposed to a DMD. In all cases, exposure was documented as unintentional and DMD treatment was stopped within 2 months of gestation. The overall incidence of exposure was 21/418 (5%). DMD exposure was associated with a trend towards a greater risk of assisted vaginal delivery compared to the DMD naive groups (OR = 3.0; 95% CI: 1.0-9.2). All other comparisons of perinatal outcomes were unremarkable. Conclusion: The incidence of DMD exposure was relatively low and no cases were intentional. Further studies are needed to ascertain the safety of DMD exposure during pregnancy in MS.
引用
收藏
页码:460 / 467
页数:8
相关论文
共 38 条
[1]   Pregnancy and fetal outcomes after interferon-β exposure in multiple sclerosis [J].
Amato, M. P. ;
Portaccio, E. ;
Ghezzi, A. ;
Hakiki, B. ;
Zipoli, V. ;
Martinelli, V. ;
Moiola, L. ;
Patti, F. ;
La Mantia, L. ;
Mancardi, G. L. ;
Solaro, C. ;
Tola, M. R. ;
Pozzilli, C. ;
De Giglio, L. ;
Totaro, R. ;
Lugaresi, A. ;
Di Tommaso, V. ;
Paolicelli, D. ;
Marrosu, M. G. ;
Comi, G. ;
Pellegrini, F. ;
Trojano, M. .
NEUROLOGY, 2010, 75 (20) :1794-1802
[2]   Naegele's rule: a reappraisal [J].
Baskett, TF ;
Nagele, F .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2000, 107 (11) :1433-1435
[3]  
Bayer HealthCare, BET INT BET 1B
[4]  
Biogen Idec, AV INT BET LA
[5]   The impact of the increasing number of multiple births on the rates of preterm birth and low birthweight: An international study [J].
Blondel, B ;
Kogan, MD ;
Alexander, GR ;
Dattani, N ;
Kramer, MS ;
Macfarlane, A ;
Wen, SW .
AMERICAN JOURNAL OF PUBLIC HEALTH, 2002, 92 (08) :1323-1330
[6]   The reproductive effects of beta interferon therapy in pregnancy - A longitudinal cohort [J].
Boskovic, R ;
Wide, R ;
Wolpin, J ;
Bauer, DJ ;
Koren, G .
NEUROLOGY, 2005, 65 (06) :807-811
[7]  
British Columbia Ministry of Health Services, DIS MOD DRUG COV MUL
[8]  
British Columbia Perinatal Health Program, BRIT COL PER DAT REG
[9]   The continuing value of the apgar score for the assessment of newborn infants. [J].
Casey, BM ;
McIntire, DD ;
Leveno, KJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (07) :467-471
[10]   Enhancement of Chemokine Expression by Interferon Beta Therapy in Patients With Multiple Sclerosis [J].
Cepok, Sabine ;
Schreiber, Herbert ;
Hoffmann, Steve ;
Zhou, Dun ;
Neuhaus, Oliver ;
von Geldern, Gloria ;
Hochgesand, Sonja ;
Nessler, Stefan ;
Rothhammer, Veith ;
Lang, Michael ;
Hartung, Hans-Peter ;
Hemmer, Bernhard .
ARCHIVES OF NEUROLOGY, 2009, 66 (10) :1216-1223