Pregnancy and Infant Outcomes in Multiple Sclerosis: Findings From the Global MAPLE-MS Pharmacovigilance Program.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Kerstin Hellwig, Hugh H Tilson, Sandra Thiel, Kathryn Ball, Joerg Seebeck, Muriel Danten, Nancy Dubois, Meritxell Sabidó
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引用次数: 0

Abstract

Background and objectives: With its use being contradicted during pregnancy, limited information exists concerning pregnancy and infant outcomes on exposure to cladribine tablets before or during pregnancy in women with multiple sclerosis (MS). In this study, we assess cumulative pregnancy exposure to cladribine tablets and prevalence of pregnancy and infant outcomes in women with MS exposed during pregnancy or within 6 months before conception and pregnancies fathered by men with MS exposed within 6 months before conception.

Methods: MAPLE-MS, a 10-year enhanced pharmacovigilance program, uses a global patient safety database to assess pregnancy outcomes potentially associated with cladribine tablets exposure in MS. Data collection began after the first approval of cladribine tablets (August 22, 2017). The primary outcome is the prevalence of major congenital anomalies (MCAs) in offspring. Secondary outcomes include other pregnancy outcomes (live birth, elective termination, spontaneous abortion, ectopic pregnancy, and stillbirth).

Results: In this Year 7 interim analysis, of 383 pregnancies analyzed, 336 (87.7%) involved maternal exposure to cladribine tablets and 47 (12.3%) were associated with paternal exposure. In the maternal exposure group, MCA prevalence (excluding genetic anomalies) in pregnancies with known outcomes was 1.1% (95% confidence interval [CI] 0.0-6.7; an atrial septal defect). Prevalence of live births in the maternal exposure group was 57.3% (95% CI 49.5-64.8). Secondary outcomes in the maternal exposure group were elective terminations (21.0% [95% CI 15.3-28.1]), spontaneous abortions (20.4% [95% CI 14.8-27.4]), and ectopic pregnancies (1.3% [95% CI 0.1-4.8]). In the paternal exposure group, no cases of MCA were observed in live births with known outcomes. Prevalence of live births was 81.3% (95% CI 56.2-94.2). Spontaneous abortions occurred in 12.5% (95% CI 2.2-37.3) and stillbirths in 6.3% (95% CI 0.0-30.3) of cases.

Discussion: Results are limited by the small number of pregnancies with known outcomes. Of pregnancies with known outcomes, the majority resulted in live births, with low frequencies of elective terminations and stillbirths reported. Since 2017, a single MCA (atrial septal defect) has been reported to the global patients' safety database. The results align with published estimates from the general population and MS patient cohorts.

多发性硬化症的妊娠和婴儿结局:来自全球MAPLE-MS药物警戒项目的发现
背景和目的:由于在妊娠期间使用氯吡嗪存在矛盾,有关多发性硬化症(MS)妇女妊娠前或妊娠期间暴露于氯吡嗪片的妊娠和婴儿结局的信息有限。在这项研究中,我们评估了在怀孕期间或怀孕前6个月内暴露于MS的女性以及怀孕前6个月内暴露于MS的男性的妊娠和婴儿结局的累积妊娠暴露率。方法:MAPLE-MS是一项为期10年的强化药物警戒项目,使用全球患者安全数据库来评估ms患者接触克拉昔滨片剂可能与妊娠结局相关的数据收集始于克拉昔滨片剂首次获批后(2017年8月22日)。主要结果是主要先天性异常(MCAs)在后代中的患病率。次要结局包括其他妊娠结局(活产、选择性终止妊娠、自然流产、异位妊娠和死产)。结果:在今年7年级的中期分析中,分析了383例妊娠,336例(87.7%)涉及母亲接触克拉德里滨片,47例(12.3%)与父亲接触克拉德里滨片有关。在母体暴露组中,已知结局妊娠的MCA患病率(不包括遗传异常)为1.1%(95%可信区间[CI] 0.0-6.7;房间隔缺损)。产妇暴露组的活产率为57.3% (95% CI 49.5-64.8)。产妇暴露组的次要结局是选择性终止妊娠(21.0% [95% CI 15.3-28.1])、自然流产(20.4% [95% CI 14.8-27.4])和异位妊娠(1.3% [95% CI 0.1-4.8])。在父亲接触组中,没有观察到已知结局的活产MCA病例。活产率为81.3% (95% CI 56.2-94.2)。自然流产占12.5% (95% CI 2.2-37.3),死产占6.3% (95% CI 0.0-30.3)。讨论:由于已知结局的妊娠数量少,结果有限。在已知结局的妊娠中,大多数是活产,选择性终止妊娠和死产的发生率较低。自2017年以来,已向全球患者安全数据库报告了单个MCA(房间隔缺损)。该结果与来自普通人群和多发性硬化症患者队列的公开估计一致。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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