Causes of oligohydramnios?
From head down:
1.Postdates
2. IUGR
3.Chromosomal anomalies
4. Duodenal atresia
5.Renal agenesis/dysgenesis
6.Polycystic kidneys
7.Urinary tract obstruction
8.PPROM
9.Fetal infection
List causes of Intrauterine demise?
There are maternal, placental and fetal causes.
Maternal:
- DM
- HTNsive disorders
- HbSS
- autoimmune diseases: SLE, thyroid disease, antiphospholipid antibody syndrome
- thrombophilias ( apa, prot c/s deficiency, factor v Leiden…)
- maternal infection (septicaemia, hypotension)
Placental:
- IUGR
- Placental infarction
- placental abruption
- feto-maternal haemorrhage (can occur with ECV)
- twin-to-twin transfusion syndrome
Foetal
- chromosomal abnormalities
- congenital abnormalities
- fetal viral and bacterial infections: TORCH, listeriosis, parvovirus
- immune haemolytic disease
- cord accidents (cord prolapse)
- fetal metabolic disorders
What are the causes of non-immune hydrops?
** all are causes of intrauterine demise!!*
What are the side effects of tranexamic acid?
Nausea, vomiting, diarrhea, disturbance in colour vision
Which progesterone can virilize a female foetus?
Gestrinone
Patients should use barrier contraception
How does phaeochromoxytoma present in pregnancy?
What is the fetal loss rate associated with phaeochromocytoma?
15-50%
How is phaeo diagnosed?
Urinary vanil-lyl-mandelic acid
T/F. Phaeo causes preeclampsia?
FALSE
Which drugs may exacerbate myasthenia Gravis?
T/F. In pts with APA/antiphospholipid antibody syndrome ASA alone improves live birth rates?
False. ASA + heparin improves live birth rates
T/F. Thrombocytopenia is not a recognized complication of APA?
False
Increased thrombus formation uses up platelets
T/F. Acute hydramnios and broad ligament haematoma are causes of prerenal renal failure?
False. They cause postrenal renal failure by compressing and obstructing the ureters.
How does phenylketonuria affect the foetus?
Phenylpyruvate products cross the placenta and deposit in foetal brain tissue.
What kind of inheritance is assoc with phenylketonuria?
Autosomal recessive
Risk of foetus being affected if mother has phenylketonuria?
1 in 4 (25%), if partner is a carrier
If partners not a carrier. All children would be carriers
What is phenylketonuria?
An autosomal recessive condition that causes deficiency of phenylalanine hydroxylase
Treatment for PKU
Diet low in phenylalanine and tryptophan for 20days/ into adulthood.
Has a GOOD outcome.
Patient with a viable intrauterine pregnancy presents with mild abdominal pain and difficulty passing urine for the past 12 hrs. Vitals are stable and abd exam shows a distended lower abdomen.
Justify your next step.
Immediately catheterize and reassure. It is common for patients with a retroverted uterus to have acute urinary retention in the early weeks of gestation.
Patient presents with a heterotopic pregnancy at 10 weeks gestation. Live intrauterine gestation and ectopic w/o cardiac activity. Justify your next step?
Offer laparoscopic salpingectomy as it is a minimally invasive procedure. It will allow for removal of the ectopic pregnancy with minimal disturbance to the uterus. Thus allowing the intrauterine pregnancy to continue.
Next step for a patient with a spontaneous, viable 7 week, quadruplet pregnancy?
Extensive counselling about the risk of pregnancy to both mother and the fetuses.
- Counsel about selective fetal reduction.
What is Wernicke’s encephalopathy and what are the features?
Wernicke’s encephalopathy is a medical emergency that occurs due to thiamine deficiency.
What is the mortality rate of Wernickes encephalopathy? What happens if it progresses?
10-15%
Can progress to KORSAKOFF’s encephalopathy
— causes 1. Antegrade & retrograde amnesia, b.Confabulation
Treatment for Wernicke’s encephalopathy?
Vitamin B1/thiamine:
50mg po tds or
200mg IV od x 3/7 or
Pabrinex contains 250mg thiamine
— and also: riboflavin, pyridoxine, nicotinamide and vit C