Severe premenstrual syndrome — DFSRH MCQ
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Correct answer: E — Transdermal estradiol with a 52 mg levonorgestrel intrauterine device
Transdermal estradiol can improve both psychological and physical symptoms of PMS. Because this woman has an intact uterus, adequate progestogenic opposition is required to prevent estrogen-induced endometrial hyperplasia. Estradiol used for PMS is not itself contraceptive. A 52 mg levonorgestrel intrauterine device addresses both requirements: it provides highly effective contraception and can provide endometrial protection during systemic estrogen use. A copper intrauterine device provides effective contraception but no progestogenic endometrial protection, so option C is inadequate. An etonogestrel implant is contraceptive, but it is not the recommended method of providing endometrial protection with systemic estrogen, making C inappropriate. A 52 mg levonorgestrel intrauterine device alone provides contraception and local progestogen but is not an established treatment for the prospectively confirmed cyclical psychological and physical symptoms described; omitting the planned estradiol therefore makes D unsuitable. Barrier contraception does not provide the requested highly effective contraception and, like a copper device, does not oppose estrogen at the endometrium, so E is incorrect.
Reference: Managing premenstrual syndrome (PMS) (March 2018; current RCOG document accessed August 2026) — https://www.rcog.org.uk/media/mcreb5ix/pi-managing-premenstrual-syndrome-pms.pdf FSRH Guideline: Intrauterine Contraception (March 2023, amended version accessed August 2026) — https://www.fsrh.org/Common/Uploaded%20files/documents/fsrh-clinical-guideline-intrauterine-contraception-mar-23-amended.pdf Premenstrual Syndrome, Management (Green-top Guideline No. 48) (Second edition 2016; reviewed May 2023) — https://www.rcog.org.uk/guidance/browse-all-guidance/green-top-guidelines/premenstrual-syndrome-management-green-top-guideline-no-48/