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TREATMENT OF SCABIES IN PREGNANCY

Date of issue: February 2018, Version: 3

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A corresponding patient information leaflet on TREATMENT OF SCABIES IN PREGNANCY is available.

Scabies is a highly infectious skin condition caused by the burrowing mite Sarcoptes scabiei. It causes intense pruritus, particularly at night, and can lead to secondary bacterial infection.

Topical insecticides for the treatment of scabies include permethrin and malathion. Although neither are licensed for use during pregnancy or breastfeeding, the available pregnancy safety data do not provide evidence that either product poses an increased risk to the fetus, however the data are too limited to state that there is no risk. Treatment of scabies should not be withheld on account of pregnancy.

Exposure to topical scabies treatments at any stage in pregnancy would not usually be regarded as medical grounds for termination of pregnancy or any additional fetal monitoring. However, other risk factors may be present in individual cases which may independently increase the risk of adverse pregnancy outcome. Clinicians are reminded of the importance of consideration of such factors when performing case-specific risk assessments.

This is a summary of the full UKTIS monograph for health care professionals and should not be used in isolation. The full UKTIS monograph and access to any hyperlinked related documents is available to NHS health care professionals who are logged in.

If you have a patient with exposure to a drug or chemical and require assistance in making a patient-specific risk assessment, please telephone UKTIS on 0344 892 0909 to discuss the case with a teratology specialist.

If you would like to report a pregnancy to UKTIS please click here to download our pregnancy reporting form. Please encourage all women to complete an online reporting form.

Disclaimer: Every effort has been made to ensure that this monograph was accurate and up-to-date at the time of writing, however it cannot cover every eventuality and the information providers cannot be held responsible for any adverse outcomes of the measures recommended. The final decision regarding which treatment is used for an individual patient remains the clinical responsibility of the prescriber. This material may be freely reproduced for education and not for profit purposes within the UK National Health Service, however no linking to this website or reproduction by or for commercial organisations is permitted without the express written permission of this service. This document is regularly reviewed and updated. Only use UKTIS monographs downloaded directly from UKTIS.org to ensure you are using the most up-to-date version.