Malformation risk of new anti-epileptic drugs in women with epilepsy; observational data from the Kerala registry of epilepsy and pregnancy (KREP)

被引:19
作者
Thomas, Sanjeev, V [1 ,2 ]
Jeemon, Panniyammakal [1 ,3 ]
Pillai, Rajit [1 ,2 ]
Jose, Manna [1 ,2 ]
Lalithakumari, Arya M. [1 ,2 ]
Murali, Sruthy [1 ,2 ]
Sanalkumar, Arjun [1 ,2 ]
Salini, Reshma A. [1 ,2 ]
Pavithran, Veena [1 ,2 ]
机构
[1] Sree Chitra Tirunal Inst Med Sci & Technol, Dept Neurol, Kerala Registry Epilepsy & Pregnancy, Trivandrum, Kerala, India
[2] Sree Chitra Tirunal Inst Med Sci & Technol, Dept Neurol, Trivandrum 695011, Kerala, India
[3] Sree Chitra Tirunal Inst Med Sci & Technol, AMCHSS, Trivandrum, Kerala, India
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2021年 / 93卷
关键词
Birth defect; Teratogenicity; Antiseizure medicine; Major congenital malformation; Epilepsy; ILAE COMMISSION; POSITION PAPER; CLASSIFICATION;
D O I
10.1016/j.seizure.2021.10.015
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: : We aim to report the major congenital malformation (MCM) rates for new and old anti-epileptic drugs (AED) exposures during the first trimester of pregnancy in women with epilepsy (WWE). Methods: : We extracted relevant data on drug exposure and malformation rate from the records of a prospective observational registry (Kerala Registry of Epilepsy and Pregnancy) for all completed pregnancies between 1998 and 2019. A comprehensive and uniform criterion with detailed guideline was used for assessment of malformations. We employed generalised linear model to generate adjusted incidence rate ratios (aIRR) of MCM in AED exposed group as compared to AED unexposed group, after adjustment for age and educational status of mothers' and epilepsy classification. Results: : The unadjusted MCM rate was 6.2% for all the infants included in the study (148/2328); 4.7% for the unexposed group (16/340), and 6.6% for the exposed group (132/1988). The aIRR of MCM as compared to unexposed group was similar for all monotherapies; lamotrigine (0.50; 95% CI 0.07-3.68), levetiracetam (1.16; 0.43-3.11), oxcarbazepine (1.61; 0.62-4.21) valproate (1.71, 0.93-3.19), phenytoin (1.21, 0.51-2.90), carbamazepine (0.99, 0.54-1.82), and phenobarbitone (1.20, 0.52-2.74). However, the point estimates suggest least risk with lamotrigine and highest risk with valproate. Polytherapy with high-dose valproate carried significantly higher risk of MCM as compared to the unexposed group (aIRR=4.12; 2.18-7.79, p<0.001). The aIRR of GTCS during pregnancy was 1.63 (95% CI 1.12-2.37, p = 0.011) for monotherapy with new AEDs (lamotrigine, levetiracetam or oxcarbazepine) as compared to old AEDs (phenobarbitone, phenytoin, carbamazepine, or valproate). Conclusion: : The MCM risk was significantly higher for polytherapy with high dose valproate. It did not differ substantially between different AED monotherapies although point estimate was lowest with lamotrigine. Pregnant women on new AEDs report higher likelihood of GTCS than women on old AEDs during pregnancy.
引用
收藏
页码:127 / 132
页数:6
相关论文
共 22 条
[1]   PROPOSAL FOR REVISED CLASSIFICATION OF EPILEPSIES AND EPILEPTIC SYNDROMES [J].
不详 .
EPILEPSIA, 1989, 30 (04) :389-399
[2]  
[Anonymous], 2018, PRAC REC NEW MEAS AV
[3]   PROPOSAL FOR REVISED CLINICAL AND ELECTROENCEPHALOGRAPHIC CLASSIFICATION OF EPILEPTIC SEIZURES [J].
BANCAUD, J ;
HENRIKSEN, O ;
RUBIODONNADIEU, F ;
SEINO, M ;
DREIFUSS, FE ;
PENRY, JK .
EPILEPSIA, 1981, 22 (04) :489-501
[4]   Pregnancy registries in epilepsy [J].
Beghi, E ;
Annegers, JF .
EPILEPSIA, 2001, 42 (11) :1422-1425
[5]   Treatment of epilepsy in light of the most recent advances [J].
Beghi, Ettore ;
Giussani, Giorgia .
LANCET NEUROLOGY, 2019, 18 (01) :7-8
[6]   Trends, patterns and predictive factors of infant and child mortality in well-performing and underperforming states of India: a secondary analysis using National Family Health Surveys [J].
Bhatia, Mrigesh ;
Dwivedi, Laxmi Kant ;
Ranjan, Mukesh ;
Dixit, Priyanka ;
Putcha, Venkata .
BMJ OPEN, 2019, 9 (03)
[7]   Prevalence of Congenital Anomalies in an Indian Maternal Cohort: Healthcare, Prevention, and Surveillance Implications [J].
Bhide, Prajkta ;
Gund, Pooja ;
Kar, Anita .
PLOS ONE, 2016, 11 (11)
[8]   Malformation risks of antiepileptic drug monotherapies in pregnancy: updated results from the UK and Ireland Epilepsy and Pregnancy Registers [J].
Campbell, E. ;
Kennedy, F. ;
Russell, A. ;
Smithson, W. H. ;
Parsons, L. ;
Morrison, P. J. ;
Liggan, B. ;
Irwin, B. ;
Delanty, N. ;
Hunt, S. J. ;
Craig, J. ;
Morrow, J. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2014, 85 (09) :1029-1034
[9]   France bans sodium valproate use in case of pregnancy [J].
Casassus, Barbara .
LANCET, 2017, 390 (10091) :217-217
[10]   Prevalence trends and individual patterns of antiepileptic drug use in pregnancy 2006-2016: A study in the five Nordic countries, United States, and Australia [J].
Cohen, Jacqueline M. ;
Cesta, Carolyn E. ;
Furu, Kari ;
Einarsdottir, Kristjana ;
Gissler, Mika ;
Havard, Alys ;
Hernandez-Diaz, Sonia ;
Huybrechts, Krista F. ;
Kieler, Helle ;
Leinonen, Maarit K. ;
Li, Jiong ;
Reutfors, Johan ;
Schaffer, Andrea ;
Selmer, Randi ;
Yu, Yongfu ;
Zoega, Helga ;
Karlstad, Oystein .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2020, 29 (08) :913-922