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1
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84910657153
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Bipolar disorder, affective psychosis, and schizophrenia in pregnancy and the post-partum period
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Jones I, Chandra PS, Dazzan P, Howard LM. Bipolar disorder, affective psychosis, and schizophrenia in pregnancy and the post-partum period. Lancet. 2014;384(9956):1789–99. doi:10.1016/s0140-6736(14)61278-2.
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Risk of recurrence in women with bipolar disorder during pregnancy: prospective study of mood stabilizer discontinuation
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Viguera AC, Whitfield T, Baldessarini RJ, Newport DJ, Stowe Z, Reminick A, et al. Risk of recurrence in women with bipolar disorder during pregnancy: prospective study of mood stabilizer discontinuation. Am J Psychiatry. 2007;164(12):1817–24. doi:10.1176/appi.ajp.2007.06101639.
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Bipolar II postpartum depression: detection, diagnosis, and treatment
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PID: 1988423
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Sharma V, Burt VK, Ritchie HL. Bipolar II postpartum depression: detection, diagnosis, and treatment. Am J Psychiatry. 2009;166(11):1217–21. doi:10.1176/appi.ajp.2009.08121902.
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Sensitivity and specificity of the Mood Disorder Questionnaire as a screening tool for bipolar disorder during pregnancy and the postpartum period
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Frey BN, Simpson W, Wright L, Steiner M. Sensitivity and specificity of the Mood Disorder Questionnaire as a screening tool for bipolar disorder during pregnancy and the postpartum period. J Clin Psychiatry. 2012;73(11):1456–61. doi:10.4088/JCP.12m07856.
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Saving mothers’ lives: reviewing maternal deaths to make motherhood safer: 2006–2008. The eighth report of the confidential enquiries into maternal deaths in the United Kingdom
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Cantwell R, Clutton-Brock T, Cooper G, Dawson A, Drife J, Garrod D, et al. Saving mothers’ lives: reviewing maternal deaths to make motherhood safer: 2006–2008. The eighth report of the confidential enquiries into maternal deaths in the United Kingdom. BJOG. 2011;118 Suppl 1:1–203. doi:10.1111/j.1471-0528.2010.02847.x.
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7
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0033950655
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Risk of recurrence of bipolar disorder in pregnant and nonpregnant women after discontinuing lithium maintenance
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COI: 1:STN:280:DC%2BD3c7jslKrtQ%3D%3D, PID: 1067138
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Viguera AC, Nonacs R, Cohen LS, Tondo L, Murray A, Baldessarini RJ. Risk of recurrence of bipolar disorder in pregnant and nonpregnant women after discontinuing lithium maintenance. Am J Psychiatry. 2000;157(2):179–84.
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Bergink V, Armangue T, Titulaer MJ, Markx S, Dalmau J, Kushner SA. Autoimmune encephalitis in postpartum psychosis. Am J Psychiatry. 2015:appiajp201514101332
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9
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Screening for bipolar disorder during pregnancy
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PID: 2596860
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Merrill L, Mittal L, Nicoloro J, Caiozzo C, Maciejewski PK, Miller LJ. Screening for bipolar disorder during pregnancy. Arch Womens Ment Health. 2015;18(4):579–83. doi:10.1007/s00737-015-0527-y.
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Miller, L.J.6
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10
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PID: 2019839
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Chessick CA, Dimidjian S. Screening for bipolar disorder during pregnancy and the postpartum period. Arch Womens Ment Health. 2010;13(3):233–48. doi:10.1007/s00737-010-0151-9.
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Chessick, C.A.1
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11
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Screening for postpartum bipolar disorder: validation of the Mood Disorder Questionnaire
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Sharma V, Xie B. Screening for postpartum bipolar disorder: validation of the Mood Disorder Questionnaire. J Affect Disord. 2011;131(1–3):408–11. doi:10.1016/j.jad.2010.11.026.
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Sharma V, Pope CJ. Pregnancy and bipolar disorder: a systematic review. J Clin Psychiatry. 2012;73(11):1447–55. doi:10.4088/JCP.11r07499.
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14
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84869197635
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Risks of adverse pregnancy and birth outcomes in women treated or not treated with mood stabilisers for bipolar disorder: population based cohort study
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Boden R, Lundgren M, Brandt L, Reutfors J, Andersen M, Kieler H. Risks of adverse pregnancy and birth outcomes in women treated or not treated with mood stabilisers for bipolar disorder: population based cohort study. BMJ. 2012;345, e7085. doi:10.1136/bmj.e7085.
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Management of bipolar disorder during pregnancy and the postpartum period
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Yonkers KA, Wisner KL, Stowe Z, Leibenluft E, Cohen L, Miller L, et al. Management of bipolar disorder during pregnancy and the postpartum period. Am J Psychiatry. 2004;161(4):608–20.
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16
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Lithium placental passage and obstetrical outcome: implications for clinical management during late pregnancy
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Newport DJ, Viguera AC, Beach AJ, Ritchie JC, Cohen LS, Stowe ZN. Lithium placental passage and obstetrical outcome: implications for clinical management during late pregnancy. Am J Psychiatr. 2005;162(11):2162–70.
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17
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Letter: Lithium, Ebstein’s anomaly, and other congenital heart defects
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19
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84903643234
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Pregnancy outcome following in utero exposure to lithium: a prospective, comparative, observational study
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PID: 24781368, This is a prospective, comparative observational study evaluating the risk of major malformations associated with lithium exposure during pregnancy. Lithium exposure was associated with an increased rate of cardiovascular anomalies (5/123 [4.1%] compared with 4/711 [0.6%] in the non-teratogenic exposure group), however this risk was no longer statistically significant after excluding malformations which resolved spontaneously
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Diav-Citrin O, Shechtman S, Tahover E, Finkel-Pekarsky V, Arnon J, Kennedy D, et al. Pregnancy outcome following in utero exposure to lithium: a prospective, comparative, observational study. Am J Psychiatry. 2014;171(7):785–94. doi:10.1176/appi.ajp.2014.12111402. This is a prospective, comparative observational study evaluating the risk of major malformations associated with lithium exposure during pregnancy. Lithium exposure was associated with an increased rate of cardiovascular anomalies (5/123 [4.1%] compared with 4/711 [0.6%] in the non-teratogenic exposure group), however this risk was no longer statistically significant after excluding malformations which resolved spontaneously.
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Diav-Citrin, O.1
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Arnon, J.5
Kennedy, D.6
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Kozma C. Neonatal toxicity and transient neurodevelopmental deficits following prenatal exposure to lithium: another clinical report and a review of the literature. Am J Med Genet A. 2005;132A(4):441–4. doi:10.1002/ajmg.a.30501.
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84860531133
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Fetal, neonatal and developmental outcomes of lithium-exposed pregnancies
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PID: 22000820, This observational retrospective cohort study evaluated the growth and neurodevelopment of 15 children exposed to lithium in pregnancy at 3–15 years and found that lithium exposure was not associated with adverse effects on growth and cognitive development
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van der Lugt NM, van de Maat JS, van Kamp IL, Knoppert-van der Klein EA, Hovens JG, Walther FJ. Fetal, neonatal and developmental outcomes of lithium-exposed pregnancies. Early Hum Dev. 2012;88(6):375–8. doi:10.1016/j.earlhumdev.2011.09.013. This observational retrospective cohort study evaluated the growth and neurodevelopment of 15 children exposed to lithium in pregnancy at 3–15 years and found that lithium exposure was not associated with adverse effects on growth and cognitive development.
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Early Hum Dev
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Hovens, J.G.5
Walther, F.J.6
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22
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Pharmacotherapy for mood disorders in pregnancy: a review of pharmacokinetic changes and clinical recommendations for therapeutic drug monitoring
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COI: 1:CAS:528:DC%2BC2cXjsVKmsbY%3D, PID: 24525634, This paper reviews the pharmacokinetic changes of antidepressants and mood stabilizers during pregnancy, discusses the implications for clinical and therapeutic drug monitoring, and offers clinical recommendations
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Deligiannidis KM, Byatt N, Freeman MP. Pharmacotherapy for mood disorders in pregnancy: a review of pharmacokinetic changes and clinical recommendations for therapeutic drug monitoring. J Clin Psychopharmacol. 2014;34(2):244–55. doi:10.1097/jcp.0000000000000087. This paper reviews the pharmacokinetic changes of antidepressants and mood stabilizers during pregnancy, discusses the implications for clinical and therapeutic drug monitoring, and offers clinical recommendations.
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J Clin Psychopharmacol
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Bergink V, Kushner SA. Lithium during pregnancy. Am J Psychiatry. 2014;171(7):712–5. doi:10.1176/appi.ajp.2014.14030409.
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Viguera AC, Newport D, Ritchie J, Stowe Z, Whitfield T, Mogielnicki J, et al. Lithium in breast milk and nursing infants: clinical implications. Am J Psychiatry. 2007;164(2):342–5.
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25
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Lithium and artificial breastmilk; or is maternal breastfeeding better?
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COI: 1:STN:280:DC%2BC3MjksVCkug%3D%3
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Marin Gabriel MA, Olza Fernandez I, Donoso E, Gutierrez Cruz N. Lithium and artificial breastmilk; or is maternal breastfeeding better? An Pediatr (Barc). 2011;75(1):67–8. doi:10.1016/j.anpedi.2010.12.007.
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Marin Gabriel, M.A.1
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Three cases of lithium exposure and exclusive breastfeeding
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Bogen DL, Sit D, Genovese A, Wisner KL. Three cases of lithium exposure and exclusive breastfeeding. Arch Womens Ment Health. 2012;15(1):69–72. doi:10.1007/s00737-012-0257-3.
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Tomson T, Battino D. Antiepileptic treatment in pregnant women: morphological and behavioural effects. Handb Exp Pharmacol. 2011;205:295–315. doi:10.1007/978-3-642-20195-0_15.
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84858076955
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Valproate and the risk for congenital malformations: is formulation and dosage regime important?
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Mawhinney E, Campbell J, Craig J, Russell A, Smithson W, Parsons L, et al. Valproate and the risk for congenital malformations: is formulation and dosage regime important? Seizure. 2012;21(3):215–8. doi:10.1016/j.seizure.2012.01.005.
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Baker GA, Finnell RH, Kalayjian LA, Liporace JD, Loring DW, Mawer G, Pennell PB, Smith JC, Wolff MC, Group NS. In utero antiepileptic drug exposure: fetal death and malformations.[see comment]
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35
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Severe fetal valproate syndrome: combination of complex cardiac defect, multicystic dysplastic kidney, and trigonocephaly
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84876564424
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Prenatal valproate exposure and risk of autism spectrum disorders and childhood autism
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COI: 1:CAS:528:DC%2BC3sXnsVKksb4%3D, PID: 23613074, This Danish population based study found that prenatal exposure to valproate was associated with an increased risk of autism spectrum disorder and childhood autism; the 508 children exposed to valproate had an absolute risk of 4.42 % (95 % CI, 2.59–7.46 %) for autism spectrum disorder (adjusted HR, 2.9 [95 % CI, 1.7–4.9]) and an absolute risk of 2.50 % (95 % CI, 1.30–4.81 %) for childhood autism (adjusted HR, 5.2 [95 % CI, 2.7–10.0]
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Christensen J, Gronborg TK, Sorensen MJ, Schendel D, Parner ET, Pedersen LH, et al. Prenatal valproate exposure and risk of autism spectrum disorders and childhood autism. JAMA. 2013;309(16):1696–703. doi:10.1001/jama.2013.2270. This Danish population based study found that prenatal exposure to valproate was associated with an increased risk of autism spectrum disorder and childhood autism; the 508 children exposed to valproate had an absolute risk of 4.42 % (95 % CI, 2.59–7.46 %) for autism spectrum disorder (adjusted HR, 2.9 [95 % CI, 1.7–4.9]) and an absolute risk of 2.50 % (95 % CI, 1.30–4.81 %) for childhood autism (adjusted HR, 5.2 [95 % CI, 2.7–10.0]).
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