Patient resources
We publish a large number of patient information leaflets and resources across the whole range of our clinical expertise. Leaflets remain on this website whilst under review, which could take up to four months.
Popular patient resources
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Safer Sleep Protective Factors Tool for Parent/Carer (External Link)
An external leaflet about Safer Sleep Protective Factors
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Screening for retinopathy of prematurity (External Link)
Patient information leaflet about Screening for retinopathy of prematurity
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Screening tests for you and your baby (External Link)
External link about screening tests for you and your baby. Includes Arabic, Bengali, Chinese, French, Latvian, Lithuanian, Polish, Portuguese, Punjabi, Romanian, Somali and Urdu
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Sex and contraception after birth (External Link)
Patient information leaflet about sex and contraception after birth.
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Taking care of your emotional wellbeing before, during and after pregnancy
Information for patients
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The insertion of a Shirodkar (high vaginal) cervical suture (cerclage)
Information about the insertion of a Shirodkar (high vaginal) cervical suture (cerclage).
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Information for patients
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Transvaginal ultrasound scan (TVS) in early pregnancy
Information for patients
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This resource is provided by Leeds Children's Hospital
General information
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Type 2 Diabetes Prevention (Video)
Patient information video about Type 2 Diabetes Prevention. Includes Arabic, Kurdish, Romanian, Tigrinya and Urdu translations.
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Unable to perform Combined Screening due to fetal position or gestational age
Information for patients
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Vaginal Bleeding and Pelvic Pain in early pregnancy
Information for patients
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Patient information leaflet about Your antenatal genetic test explained - Prenatal invasive testing following a higher chance screening result
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Patient information leaflet about Your antenatal genetic test explained - Prenatal invasive testing following an unexpected finding on your ultrasound scan
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Patient information leaflet about Your antenatal genetic test explained - Prenatal invasive testing where there is a family history of a known genetic condition