Maternal medicine Flashcards
What is the incidence of PE in pregnant women in the UK?
a) 1.5 per 10,000 maternities
b) 1.5 per 10,000 births
c) 1.3 per 10,000 maternities
d) 1.3 per 100,000 maternities
e) 2.0 per 10,000 births
C
Regarding PE in pregnancy
a) the risk is higher in the second trimester
b) risk is 9 times higher than in non-pregnant women
c) Heritable thrombophilias account for 15% of PEs in pregnancy
d) Women are 5 times more at risk postpartum than antenatally
e) mortality is lower in obese women
a) risk increases with GA
b) RR in pregnant is 4-5 times higher than non-pregnant
c) account for 20-50%
d) True. RR 5x the antenatal risk
e) false. 60% of deaths between 2003 and 2008 were obese
D
Which of the following can cross the placenta?
a)Heparin
b)IgA
c)IgG
d)IgM
e)Insulin
C
A 25-year-old women who is 10 weeks pregnant has anti-D antibodies in her booking bloods. What is the reliable method available at this gestation to determine the fetal RhD antigen status?
a-Amniocentesis
b-Fetal blood sampling
c-Maternal blood for cell-free fetal DNA
d-Partner’s blood for rhesus status
e-Ultrasound with middle cerebral artery Doppler
C
A RhD antigen-negative woman in her first pregnancy has been involved in a road traffic accident at 29 weeks of gestation without any vaginal bleeding but with trauma to the abdomen. She had received routine antenatal prophylaxis with 1500 units at 28 weeks. What is the most appropriate management?
aAdminister 1500 IU anti-D and take bloods for Kleihauer
b-Administer 1500 IU anti-D
c-Administer 500 IU anti-D and take bloods for Kleihauer
d-Administer 500 IU anti-D
e-Take bloods for Klieihauer
C
A woman in her second pregnancy who is RhD antigen negative and has anti-D levels of 4 IU/ml has an antepartum haemorrhage at 24 weeks of gestation. What is the most appropriate management with regards to anti-D?
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Do not administer anti-D
Take Kleihauer to guide the dose of anti-D to give
Do not administer
A RhD-negative women has a caesarean section; cell salvage is used intraoperatively. What is the most appropriate management?
Administer anti-D 1500 units intramuscularly prior to reinfusing the blood
Take a cord blood group and if the fetus is found to be RhD negative, administer 1500 units intramuscularly after reinfusion of the blood
Take a cord blood group and if the fetus is found to be RhD negative, administer 500 units intramuscularly after reinfusion of the blood
Take a cord blood group and if the fetus is found to be RhD positive, administer 1500 units intramuscularly after reinfusion of the blood
Take a cord blood group and if the fetus is found to be RhD positive, administer 500 units intramuscularly after reinfusion of the blood
D
A women in her fourth pregnancy is known to have anti-K antibodies. She is now at 22 weeks of gestation. What is the best management to investigate if anaemia is present in the fetus?
All of the below
Amniocentesis optical density for bilirubin concentration
Maternal blood titre to quantify antibodies
MCA pulsatility index (PI)
Middle cerebral artery (MCA) peak systolic velocity (PSV)
E
You have been asked to review the notes of a 31-year-old nulliparous woman who is now 12 weeks pregnant. She is fit and healthy with a BMI of 24. In the past she had surgical management for a missed miscarriage at 10 weeks of gestation.
The results of her booking bloods have been phoned through to the clinic and are as follows:
blood group: A Rhesus negative
antibody screen: anti-D antibodies present at 3 IU/ml.
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Continue midwifery-led care
Measure serum antibody levels every 2 weeks
Measure serum antibody levels every 4 weeks
No action required
Perform a Kleihauer blood test only
Refer the woman to tertiary fetal medicine unit
Retest for antibodies at 28 weeks
Wait until delivery and test the baby’s blood group
Antibodies every 4 weeks
A 23-year-old multiparous woman at 29 weeks of gestation is referred to the antenatal clinic measuring large for dates (symphysio–fundal height = 34 cm).
In her previous pregnancy, she had recurrent antepartum haemorrhage and had a normal delivery at 37 weeks of gestation of a baby girl weighing 2.9 kg.
So far, this pregnancy has progressed as expected with dating and anomaly scans both reporting no anomolies. However, at booking she was noted to have elevated anti-D levels (blood group = AB Rhesus negative). At 16 weeks of gestation, anti-D was 3 IU/ml and at 20 weeks of gestation it was 4 IU/ml. She missed her 24-week blood test due to a family holiday.
She had an ultrasound scan that showed polyhydramnios, fetal ascites and generalised fetal edema.
A serum antibody screen performed last week shows anti-D levels of 18 IU/ml.
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Continue midwifery-led care
Measure serum antibody levels every 2 weeks
Measure serum antibody levels every 4 weeks
No action required
Perform a Kleihauer blood test only
Refer the woman to tertiary fetal medicine unit
Retest for antibodies at 28 weeks
Wait until delivery and test the baby’s blood group
Question 3 (1 point)
refer to FMU
A 27-year-old primiparous woman attends for external cephalic version at 38 weeks of pregnancy. Ultrasound confirms a normally grown singleton adopting a flexed breech position, the amniotic fluid index is normal.
Her BMI is 26 and blood group is O-negative. She received routine antenatal anti-D prophylaxis (1500 IU intramuscularly) at 28 weeks of gestation.
Question 3 options:
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Continue midwifery-led care
Measure serum antibody levels every 2 weeks
Measure serum antibody levels every 4 weeks
No action required
Perform a Kleihauer blood test only
Refer the woman to tertiary fetal medicine unit
Retest for antibodies at 28 weeks
Wait until delivery and test the baby’s blood group
500IU
A 22-year-old primparous woman who is 34 weeks pregnant presents at the antenatal clinic. She is RhD negative with a RhD-positive fetus on cell-free fetal DNA. She attended hospital 1 week ago with an antepartum haemorrhage but did not receive anti-D.
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Continue midwifery-led care
Measure serum antibody levels every 2 weeks
Measure serum antibody levels every 4 weeks
No action required
Perform a Kleihauer blood test only
Refer the woman to tertiary fetal medicine unit
Retest for antibodies at 28 weeks
Wait until delivery and test the baby’s blood group
500IU
A 34-year-old RhD-negative women is at 22 weeks of gestation in her second pregnancy and just completed an intrauterine platelet transfusion for alloimmunisation to platelets
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Continue midwifery-led care
Measure serum antibody levels every 2 weeks
Measure serum antibody levels every 4 weeks
No action required
Perform a Kleihauer blood test only
Refer the woman to tertiary fetal medicine unit
Retest for antibodies at 28 weeks
Wait until delivery and test the baby’s blood group
500IU
A 31-year-old nulliparous women who is 16 weeks pregnant. At her booking bloods she was found to be O RhD negative with anti-c antibodies. The anti-c level is reported as 5 IU/ml.
Administer anti-D 1500 IU intramuscularly
Administer anti-D 250 IU intramuscularly
Administer anti-D 500 IU intramuscularly
Continue midwifery-led care
Measure serum antibody levels every 2 weeks
Measure serum antibody levels every 4 weeks
No action required
Perform a Kleihauer blood test only
Refer the woman to tertiary fetal medicine unit
Retest for antibodies at 28 weeks
Wait until delivery and test the baby’s blood group
measure every 4 weeks (below 7.5)
How much higher is the overall prevalence of PE in pregnancy in comparison to antenatally?
a) 2x
b) 4x
c) 5x
d) 7x
e) 10x
- overall prevalence 10x higher
- Incidence 1.3/10,000 mternities or 1-2/1000
- RIsk is 20x higher in the puerperium in comparison to non-pregnant; 5x higher than in antenatal
E
About LMWH
a) Anit-Xa levels are recommended in women with a previous DVT in pregnancy
b) It increases PPH risk in vaginal deliveries by 1.5X
c) Recurrence risk of PE on LMWH is 1.15%
d) LMWH induces less osteoporosis than UFH
e) A twice daily treatment dose is more effective than once daily
- Anti-Xa levels should be considered in: weight <50kg or >90kg; renal impairment or recurrent VTE only
- It does not increase PPH in VD. In comparison to UFH, it decreases haemorrhage, recurrence, extension and mortality
- CORRECT. It is lower than with UFH
- There is no evidence for one or the other
D
A 30- year-old nulliparous woman attended the obstetric medicine clinic for pre-pregnancy counselling. She was diagnosed with mitral stenosis eight years ago and had insertion of mechanical heart valve at mitral position two years ago. She is on lifelong anti-coagulation with warfarin (4 mg/day).
What is the most effective anticoagulation regimen during pregnancy to prevent valve thrombosis?
Continue warfarin throughout pregnancy with INR monitoring every four weeks
Continue warfarin throughout pregnancy with INR monitoring twice weekly
Continue warfarin throughout pregnancy with INR monitoring weekly or every two weeks
Therapeutic LMWH between positive pregnancy test - 20 weeks followed by warfarin
Therapeutic LMWH throughout pregnancy
Continue warfarin throughout pregnancy with INR monitoring weekly or eve
ou have been asked to prescribe the therapeutic dose of LMWH for a 25-year-old woman who gave birth vaginally 6 hours ago. She had a DVT 6 weeks ago. Her labour was induced at 40 weeks because of recurrent episodes of reduced fetal movement. She needed syntocinon for slow progress in first stage and used Entonox, diamorphine and epidural for analgesia.
When is the safest time to restart her on LMWH after removing the epidural catheter (there is no concerns with bleeding)?
2 hours
3 hours
4 hours
6 hours
8 hours
LMWH should not be given for 4 hours after the use of spinal anaesthesia or after the epidural catheter has been removed, and the epidural catheter should not be removed within 12 hours of the most recent injection.
4 hours
A woman, aged 41, gives birth to her first baby by emergency caesarean section complicated by 1.2 litre PPH. She makes a straightforward recovery. Her booking weight was 98 kg with BMI 35. She is a smoker of 10 cigarettes a day. She has no personal or family history of VTE or thrombophilia. What dose and duration of enoxaparin should she be advised to take?
40 mg SC, once a day, for 10 days
40 mg SC, once a day, for 6 weeks
60 mg SC, once a day, for 10 days
60 mg SC, once a day, for 3 months
60 mg SC, once a day, for 6 weeks
All women should have a risk assessment for VTE carried out at booking, during any admission or change in circumstances during pregnancy and postnatally. This woman has several risk factors for VTE, namely emergency caesarean section, PPH, age, raised BMI and smoking status. She requires an increased daily dose of low molecular weight heparin due to her booking weight. She requires an extended course of LMWH due to the number of risk factors. Each trust will have a scoring system for VTE to enable accurate scoring of VTE risk.
60 mg SC, once a day, for 6 weeks
A woman with BMI 42, aged 36, with 3 previous normal births, has a straightforward pool birth in midwifery led care. When should she receive her first prophylactic dose of postnatal low molecular weight heparin?
12 hours after birth
2 hours after birth
4 hours after birth
6 pm that evening
As soon as possible
As this woman has had a straightforward birth, with no use of regional analgesia, she is able to receive her first dose of LMWH straight after delivery. Use of LMWH following regional analgesia should be guided by discussion with anaesthetic colleagues.
As soon as possible
A 34 year old had an emergency caesarean section for failure to progress with an epidural top up. Estimate blood loss was 600ml. She is transferred to recovery with the epidural catheter in situ for post operative analgesia. There have been delays in transferring women to the post-natal ward. Shortly before transferring to the post-natal ward you are told that the patient has already received prophylactic LMWH which was given 4 hours after her caesarean section. What would you advise regarding the removal of the epidural catheter?
Remove the epidural catheter immediately and transfer to the post-natal ward
Remove the catheter 4 hours after the caesarean section
Remove the catheter 12 hours after the caesarean section
Remove the catheter 12 hours after the last dose of LMWH
Remove the catheter 8 hours after the last dose of LMWH
At least 12 hours should pass after the prophylactic dose of LWMH and the introduction or removal of and epidural or spinal catheter.
Remove the catheter 12 hours after the last dose of LMWH
A 26-year-old woman is 24 weeks pregnant in her second pregnancy. She is admitted with a swollen right leg. A provisional diagnosis of DVT is made and is awaiting duplex ultrasound of the leg. She needs to be commenced on anticoagulation.
Anti-Xa activity
Chest X-ray
FBC, coagulation screen, liver and renal function test
Ultrasound should be repeated on day 3 and day 7
Ventilation perfusion scan/CTPA
FBC, coagulation screen, liver and renal function test
A 31-year-old woman is 6 days postnatal. She had a emergency caesarean section for fetal distress. She is admitted with shortness of breath, chest pain and haemoptysis. Her chest X-ray is normal.
Anti-Xa activity
Chest X-ray
FBC, coagulation screen, liver and renal function test
Ultrasound should be repeated on day 3 and day 7
Ventilation perfusion scan/CTPA
V/Q / CTPA