Authors: Dr Sashika Samaranayaka, Department of Dermatology, Middlemore Hospital, New Zealand; Hon A/Prof Paul Jarrett, Dermatologist, Middlemore Hospital and Department of Medicine, The University of Auckland, New Zealand. Copy edited by Gus Mitchell. January 2022
Psoriasis is a chronicinflammatory skin condition usually characterised by well-demarcated red and scalyplaques on typical parts of the body including the knees, elbows, and lower back.
It can occur on any part of the body and different types of psoriasis are recognised. Pustular psoriasis of pregnancy (impetigo herpetiformis) is a rare variant of pustular psoriasis, usually occurring in the third trimester.
Psoriasis in pregnancy
Psoriasis is common in women of reproductive age as three-quarters of patients develop the disease before reaching their 4th decade. It tends to persist lifelong and will generally fluctuate in severity.
For many pregnant women (33–60%), psoriasis improves during pregnancy but for a minority the disease may flare (25%). In the postpartum period, flaring of psoriasis is common (65%).
The severity of psoriasis during pregnancy can improve during pregnancy (40–60%), worsen (10–20%), or remain stable in the remainder.
What are the clinical features of psoriasis in pregnancy?
There are no differences in the clinical features of psoriasis during pregnancy apart from the variation in severity for the individual woman pre-, during, and post-pregnancy.
Some topical and systemic treatments may harm the baby, so care is needed. The effect of some treatments is unknown. Phototherapy is useful and there is increasing evidence for the use of biologics. Oral photochemotherapy (PUVA) has theoretical mutagenic risk, although detailed studies have not substantiated this, but it is best avoided in pregnancy
Consult the national or regional guidelines on the safety of medicines during pregnancy. For example, in New Zealand sources such as the drug datasheet and New Zealand formulary may be referred to.
Narrowband ultraviolet light (nUVB) is considered to be safe for pregnant patients. Phototherapy depletes folate so supplementation is recommended.
Systemic medications
Ciclosporin (cyclosporin) appears to be safe in pregnancy and is used for moderate to severe psoriasis.
Acitretin must be avoided during pregnancy as it is highly teratogenic and avoided three years prior to conception.
Methotrexate must be avoided during pregnancy as it is highly teratogenic and an abortifactant.
Apremilast has not been studied in pregnancy and should not be taken.
Biologics
There are no controlled studies of the use of biologics in pregnant patients. However, there is increasing evidence for the safe and effective use of biologics in moderate to severe psoriasis treatment during pregnancy. Stopping these agents during pregnancy carries a risk of moderate to severe psoriasis flaring. There is less data about some of the newer agents.
Many monoclonalantibodies used in the treatment of psoriasis actively cross the placental barrier especially in the third trimester after organogenesis is complete, resulting in therapeutic levels in the baby. However, certolizumab (a pegylated tumournecrosis alpha inhibitor), crosses the placental barrier passively and is present in negligible or low concentrations in the baby because of its molecular structure, which lacks an Fc moiety. Etanercept (fusion protein including the Fc receptor) is also present in infants at low levels. If it is safe to do so, some dermatologists withhold the biological agent for the last 8 weeks of pregnancy so that infants are born with negligible levels of the administered drug.
Vaccination of infants
Great care needs to be taken with biologics that cross the placental barrier and vaccinating the newborn infant with live/attenuated vaccines including the Bacillus Calmette-Guérin (BCG) vaccine. There is significant potential for harm or death from live/attenuated vaccines in the infant who are immunocompromised due to them having therapeutic levels of the biological agent that their mother is receiving. There are stand down periods in which the infant must not be vaccinated with these agents; this is commonly 6 months or longer.
New agents
There are a number of new agents being developed for psoriasis including janus kinase (JAK) inhibitors and tyrosine kinaseinhibitors. There is insufficient evidence to base a recommendation at present for their use in pregnancy and they should be avoided.
What is the outcome for psoriasis in pregnancy?
Many women will only need topical treatments. However, for those women who require systemic treatment such as those with extensive psoriasis, careful judgement needs to be exercised. A balance of the significant adverse effects of untreated psoriasis on maternal wellbeing and conception against the potential risk of systemic agent use must be sought.
References
Boggs JME, Griffin L, Ahmad K, Hackett C, Ramsay B, Lynch M. A retrospective review of pregnancies on biologics for the treatment of dermatological conditions. Clin Exp Dermatol. 2020;45(7):880–3. doi:10.1111/ced.14263 Journal
Pottinger E, Woolf RT, Exton LS, Burden AD, Nelson-Piercy C, Smith CH. Exposure to biological therapies during conception and pregnancy: a systematic review. Br J Dermatol. 2018;178(1):95–102. doi:10.1111/bjd.15802. Journal
Tirelli LL, Luna PC, Cristina E, Larralde M. Psoriasis and pregnancy in the biologic era, a feared scenario. What do we do now?. Dermatol Ther. 2019;32(6):e13137. doi:10.1111/dth.13137. Journal
Rademaker M, Agnew K, Andrews M, et al. Psoriasis in those planning a family, pregnant or breast-feeding. The Australasian Psoriasis Collaboration. Australas J Dermatol. 2018;59(2):86–100. doi:10.1111/ajd.12641. Journal
Vena GA, Cassano N, Bellia G, Colombo D. Psoriasis in pregnancy: challenges and solutions. Psoriasis (Auckl). 2015;5:83–95. Published 2015 May 18. doi:10.2147/PTT.S82975. Journal