TY - JOUR
T1 - Disease-Modifying Drugs and Family Planning in People with Multiple Sclerosis
T2 - A Consensus Narrative Review from the Gulf Region
AU - Alroughani, Raed
AU - Inshasi, Jihad
AU - Al-Asmi, Abdullah
AU - Alkhabouri, Jaber
AU - Alsaadi, Taoufik
AU - Alsalti, Abdullah
AU - Boshra, Amir
AU - Canibano, Beatriz
AU - Ahmed, Samar Farouk
AU - Shatila, Ahmed
N1 - Funding Information:
All authors participated in the closed meeting that gave rise to this article, which was organised by Merck Serono Middle East FZ-Ltd, United Arab Emirates, an affiliate of Merck KGaA, Darmstadt, Germany. Jihad Inshasi, Abdullah Al-Asmi, and Jaber Alkhabouri declared no additional duality of interest. Additional duality of interest declarations are as follows. Raed Alroughani received honoraria as a speaker and for serving in scientific advisory boards from Bayer, Biogen, Merck, Novartis, Roche, and Sanofi. AA-A received honoraria for serving on scientific advisory boards from Merck, Novartis, Roche, and Sanofi, and also received travel reimbursement from, Biologix, Sanofi, Merck, Roche, Bayer and Novartis. Ahmed Shatila received honoraria for lectures from Sanofi-Genzyme, Merck, Genpharm, Roche, Novartis, Boehringeringer Ingelheim, and Biologix, and for advisory boards from Sanofi-Genzyme, Roche, Novartis, Pfizer, and Biologix, and received financial support for registration, accommodation and travel for conferences provided by Sanofi-Genzyme, Merck, Genpharm, Roche, Novartis, and Biologix. Beatriz Canibano has received travel, speaker and consultant honoraria from Merck, Novartis, Biologix, Roche and Sanofi. Taoufik Alsaadi has received speaker fees from Newbridge, Novartis, Eli Lilly, GlaxoSmithKline, Janssen-Cilag, LivaNova, Lundbeck, Merck, Pfizer, Hikma, Sanofi, has received consultancy fees from Cyberonics, Eli Lilly, LivaNova, Lundbeck, Merck, Pfizer, Hikma, Novartis, Sanofi; and has received research grants from Novartis, Biogen, GlaxoSmithKline, Cyberonics, Schwartz, Pfizer, UCB, Astra, Merck, and Elan Pharmaceuticals; Taoufik Alsaadi holds no shares in, nor has any ongoing financial relationship with, any pharmaceutical company. Samar Farouk Ahmed reported no additional duality of interest. Amir Boshra is an employee of Merck Serono Middle East FZ-Ltd, United Arab Emirates, an affiliate of Merck KGaA, Darmstadt, Germany.
Funding Information:
Merck Serono Middle East FZ-Ltd, United Arab Emirates, funded the Rapid Service Fee for this review. Medical writing support was provided by Dr Mike Gwilt of GT Communications, funded by Merck Serono Middle East FZ-Ltd, United Arab Emirates, an affiliate of Merck KGaA, Darmstadt, Germany. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. All authors participated in the closed meeting that gave rise to this article, which was organised by Merck Serono Middle East FZ-Ltd, United Arab Emirates, an affiliate of Merck KGaA, Darmstadt, Germany. Jihad Inshasi, Abdullah Al-Asmi, and Jaber Alkhabouri declared no additional duality of interest. Additional duality of interest declarations are as follows. Raed Alroughani received honoraria as a speaker and for serving in scientific advisory boards from Bayer, Biogen, Merck, Novartis, Roche, and Sanofi. AA-A received honoraria for serving on scientific advisory boards from Merck, Novartis, Roche, and Sanofi, and also received travel reimbursement from, Biologix, Sanofi, Merck, Roche, Bayer and Novartis. Ahmed Shatila received honoraria for lectures from Sanofi-Genzyme, Merck, Genpharm, Roche, Novartis, Boehringeringer Ingelheim, and Biologix, and for advisory boards from Sanofi-Genzyme, Roche, Novartis, Pfizer, and Biologix, and received financial support for registration, accommodation and travel for conferences provided by Sanofi-Genzyme, Merck, Genpharm, Roche, Novartis, and Biologix. Beatriz Canibano has received travel, speaker and consultant honoraria from Merck, Novartis, Biologix, Roche and Sanofi. Taoufik Alsaadi has received speaker fees from Newbridge, Novartis, Eli Lilly, GlaxoSmithKline, Janssen-Cilag, LivaNova, Lundbeck, Merck, Pfizer, Hikma, Sanofi, has received consultancy fees from Cyberonics, Eli Lilly, LivaNova, Lundbeck, Merck, Pfizer, Hikma, Novartis, Sanofi; and has received research grants from Novartis, Biogen, GlaxoSmithKline, Cyberonics, Schwartz, Pfizer, UCB, Astra, Merck, and Elan Pharmaceuticals; Taoufik Alsaadi holds no shares in, nor has any ongoing financial relationship with, any pharmaceutical company. Samar Farouk Ahmed reported no additional duality of interest. Amir Boshra is an employee of Merck Serono Middle East FZ-Ltd, United Arab Emirates, an affiliate of Merck KGaA, Darmstadt, Germany. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors. Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study. This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
Funding Information:
Medical writing support was provided by Dr Mike Gwilt of GT Communications, funded by Merck Serono Middle East FZ-Ltd, United Arab Emirates, an affiliate of Merck KGaA, Darmstadt, Germany.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Most disease-modifying drugs (DMDs) are contraindicated in pregnancy. Management of MS is especially challenging for pregnant patients, as withdrawal of DMDs leave the patient at risk of increased disease activity. We, a group of experts in MS care from countries in the Arab Gulf, present our consensus recommendations on the management of MS in these patients. Where possible, a patient planning pregnancy can be switched to a DMD considered safe in this setting. Interferon β now can be used during pregnancy, where there is a clinical need to maintain treatment, in addition to glatiramer acetate. Natalizumab (usually to 30 weeks’ gestation for patients with high disease activity at high risk of relapse and disability progression) may also be continued into pregnancy. Cladribine tablets and alemtuzumab have been hypothesised to act as immune reconstitution therapies (IRTs). These drugs provide a period of prolonged freedom from relapses for many patients, but the patient must be prepared to wait for up to 20 months from initiation of therapy before becoming pregnant. If a patient becomes pregnant while taking fingolimod, and requires continued DMD treatment, a switch to interferon β or natalizumab after a variable washout period may be prescribed, depending on the level of disease activity. Women who wish to breastfeed should be encouraged to do so, and interferon β may also be used during breastfeeding. There is a lack of data regarding the safety of using other DMDs during breastfeeding.
AB - Most disease-modifying drugs (DMDs) are contraindicated in pregnancy. Management of MS is especially challenging for pregnant patients, as withdrawal of DMDs leave the patient at risk of increased disease activity. We, a group of experts in MS care from countries in the Arab Gulf, present our consensus recommendations on the management of MS in these patients. Where possible, a patient planning pregnancy can be switched to a DMD considered safe in this setting. Interferon β now can be used during pregnancy, where there is a clinical need to maintain treatment, in addition to glatiramer acetate. Natalizumab (usually to 30 weeks’ gestation for patients with high disease activity at high risk of relapse and disability progression) may also be continued into pregnancy. Cladribine tablets and alemtuzumab have been hypothesised to act as immune reconstitution therapies (IRTs). These drugs provide a period of prolonged freedom from relapses for many patients, but the patient must be prepared to wait for up to 20 months from initiation of therapy before becoming pregnant. If a patient becomes pregnant while taking fingolimod, and requires continued DMD treatment, a switch to interferon β or natalizumab after a variable washout period may be prescribed, depending on the level of disease activity. Women who wish to breastfeed should be encouraged to do so, and interferon β may also be used during breastfeeding. There is a lack of data regarding the safety of using other DMDs during breastfeeding.
KW - Breastfeeding
KW - Disease-modifying drugs
KW - Family planning
KW - Multiple sclerosis
KW - Pregnancy
UR - http://www.scopus.com/inward/record.url?scp=85086744344&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85086744344&partnerID=8YFLogxK
U2 - 10.1007/s40120-020-00201-8
DO - 10.1007/s40120-020-00201-8
M3 - Review article
C2 - 32564333
AN - SCOPUS:85086744344
SN - 2193-8253
VL - 9
SP - 265
EP - 280
JO - Neurology and Therapy
JF - Neurology and Therapy
IS - 2
ER -