UK Medical Eligibility Criteria (UKMEC) for combined oral contraceptive use

Combined oral contraceptive: Issues for current users article
Issue 12 Contents
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UKMEC Category 1 – Unrestricted Use
Age – menarche to <40 years
Parity – nulliparous and parous
Breastfeeding – >6 months postpartum
Postpartum – >21 days if not breastfeeding
Post-abortion – immediately first and second trimester, and post-septic
Past ectopic pregnancy
History of pelvic surgery
Minor surgery without immobilisation
Varicose veins
Non-migrainous headaches – mild or severe
Epilepsy – and not using liver enzyme-inducers
Depressive disorders
Vaginal bleeding – unsuspicious irregular, heavy or prolonged
Endometriosis
Benign ovarian tumour
Severe dysmenorrhoea
Gestational trophoblastic neoplasia – when hCG is normal
Cervical ectropion
Breast disease – benign breast disease or a family history of breast cancer
Endometrial or ovarian cancer
Uterine fibroids – with or without distortion of the uterine cavity
PID – current; or past history of, with or without subsequent pregnancy
STI – current, vaginitis or increased risk of STI
HIV/AIDS – risk of HIV/AIDS, current HIV not using antiretroviral therapy
Schistosomiasis, pelvic and non-pelvic tuberculosis, malaria
Diabetes – history of gestational disease
Thyroid disorders
Viral hepatitis – carrier
Anaemias – thalassaemia, iron deficiency
Raynaud’s disease – primary without lupus anticoagulant
UKMEC Category 2 – Benefits generally outweigh risks
Age – ≥40 yearsa
Breastfeeding – between 6 weeks and 6 months postpartum and partially breastfeeding (medium to low)
Smoking
– aged <35 years, or aged ≥35 years and stopped smoking ≥1 year ago
Obesity – BMI ≥30–34 kg/m2
History of high blood pressure during pregnancy
Family history of VTE in a first-degree relative aged ≥45 years
Major surgery without prolonged immobilisation
Superficial thrombophlebitis
Known hyperlipidaemias – e.g. common hypercholesterolaemia or familial combined hyperlipidaemia
Valvular and congenital heart disease – uncomplicated
Migraine headaches – without aura in women aged <35 years
Vaginal bleeding – suspicious for serious condition before evaluation
CIN and cervical cancer
HIV/AIDS – current HIV using antiretroviral therapy, or current AIDS and using HAART
Diabetes – NIDDM and IDDM, non-vascular disease
Gallbladder disease – asymptomatic or treated with a cholecystectomy
History of cholestasis – pregnancy-related
Inflammatory bowel disease
Sickle cell disease
Raynaud’s disease
– secondary without lupus anticoagulant
Non-liver enzyme-inducing antibiotics
Highly active antiretroviral therapy (HAART)
UKMEC Category 3 – Risks generally outweigh benefitsb
Breastfeeding – between 6 weeks and 6 months postpartum and fully or almost fully breastfeeding
Postpartum – <21 days postpartum
Smoking – aged ≥35 years and smoking <15 cigarettes per day, or stopped smoking <1 year ago
Obesity – BMI 35–39 kg/m2
Cardiovascular disease – multiple risk factors for arterial cardiovascular disease
Hypertension – elevated blood pressure >140 to 159 mmHg systolic or >90 to 94mmHg diastolic
Family history of VTE in a first-degree relative aged <45 years

Immobility (unrelated to surgery) – e.g. wheelchair use, debilitating illness
Known hyperlipidaemias – e.g. familial
hypercholesterolaemia
Migraine headaches – without aura in women aged ≥35 years; or a past history of migraine with aura at any age
Breast disease – past history of breast cancer and no evidence of recurrence for 5 years; carriers of known gene mutations associated with breast cancer (e.g. BRCA1); undiagnosed mass
Diabetes – with nephropathy/ retinopathy/ neuropathy; or other vascular disease or diabetes of >20 years’ duration (category given will depend on disease severity)
Gallbladder disease – symptomatic medically treated or current
History of cholestasis – past COC-related
Cirrhosis – mild compensated disease
Drugs which induce liver enzymes – e.g. rifampicin, rifabutin, St John’s Wort, griseofulvin and certain anticonvulsants (i.e. phenytoin, carbamazepine, barbiturates, primidone, topiramate, oxcarbazepine)
UKMEC Category 4 – Unacceptable health risk and should not be used
Breastfeeding – <6 weeks postpartum
Smoking – aged ≥35 years and smoking ≥15 cigarettes per day
Obesity
– BMI ≥40 kg/m2
Cardiovascular disease – multiple risk factors for arterial cardiovascular disease
Hypertension – blood pressure ≥160 mmHg systolic and/ or ≥95 mmHg diastolic; or vascular disease
VTE – current (on anticoagulants) or past history
Major surgery with prolonged immobilisation
Known thrombogenic mutations
Current and history of ischaemic heart disease
Stroke
Valvular and congenital heart disease – complicated by pulmonary hypertension, atrial fibrillation, history of subacute bacterial endocarditis
Migraine headaches – with aura at any age
Gestational trophoblastic neoplasia – when hCG is abnormal
Breast disease – current breast cancer
Diabetes – with nephropathy, retinopathy, neuropathy or other vascular disease, or diabetes of >20 years’ duration (category given will depend on disease severity)
Viral hepatitis – active disease
Cirrhosis – severe decompensated disease
Liver tumours – benign and malignant
Raynaud’s disease – secondary with lupus anticoagulant and thus a tendency to thrombosis
a Age ≥40 years: women may use COC until age 50 years if there are no medical contraindications.
b Definition of UKMEC 3 – the risks generally outweigh the benefits but the method can be considered for use with clinical judgement and/ or specialist referral if other methods are unacceptable.
AIDS, acquired immune deficiency syndrome; BMI, body mass index; CIN, cervical intraepithelial neoplasia; HAART, highly active antiretroviral therapy; hCG, human chorionic gonadotrophin; HIV, human immunodeficiency virus; IDDM, insulin-dependent diabetes; NIDDM, non-insulin-dependent diabetes; PID, pelvic inflammatory disease; STI, sexually transmitted infection; TB, tuberculosis; VTE, venous thromboembolism.

Reference

Faculty of Sexual and Reproductive Health Care Clinical Effectiveness Unit. First prescription of combined oral contraceptive. Available from: www.fsrh.org. Accessed February 2008

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