Kathryn Graham

ORCID: 0000-0002-5245-5491
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About
Contact & Profiles
Research Areas
  • Blood groups and transfusion
  • Erythrocyte Function and Pathophysiology
  • Pregnancy-related medical research
  • Assisted Reproductive Technology and Twin Pregnancy
  • Maternal and Perinatal Health Interventions
  • Parvovirus B19 Infection Studies
  • Pregnancy and preeclampsia studies
  • Birth, Development, and Health
  • Gestational Diabetes Research and Management

Royal Prince Alfred Hospital
2014-2019

Westmead Hospital
2019

Aim To determine the feasibility of a multicentre randomised controlled trial ( RCT ) to investigate whether digital rotation fetal head from occiput posterior OP position in second stage labour reduces risk operative delivery (defined as caesarean section CS or instrumental delivery). Methods We conducted study between December 2010 and 2011 tertiary referral hospital Australia. A transabdominal ultrasound was performed early on women with cephalic, singleton pregnancies position. Those...

10.1111/ajo.12192 article EN Australian and New Zealand Journal of Obstetrics and Gynaecology 2014-03-16

Haemolytic disease of the fetus and newborn (HDFN) is associated with red cell antibodies. Anti-M usually results in a mild haemolysis rarely clinically significant. There no established consensus on management pregnancies anti-M. A case recurrent HDFN maternal M alloimmunisation was identified at tertiary hospital Australia. We collected patient neonate's clinical pathological data interpreted available literature. This first literature fetal hydrops setting alloimmunisation. Neonate...

10.1136/bcr-2019-230552 article EN BMJ Case Reports 2019-07-01

Background The Fetal Medicine Foundation developed a multiple logistic regression algorithm for risk prediction of delivering small gestational age neonate. Aim To validate this in an Australian population. Methods At the combined first trimester screen participants’ medical histories, demographic data, mean arterial pressure, uterine artery pulsatility index and pregnancy‐associated plasma protein‐A were assessed. After delivery, neonate at <37 or ≥37 weeks gestation was retrospectively...

10.1111/ajo.12951 article EN Australian and New Zealand Journal of Obstetrics and Gynaecology 2019-01-24
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