Pregnancy & Labour Flashcards

1
Q

How many trimesters in pregnancy?

A

3

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2
Q

When is loss of pregnancy common and when does a foetus become viable ?
[pic]

A

 Spontaneous loss of pregnancy in the first trimester is very common (1/3rd of all) but after that, loss is minimal.

 The end of the 2nd trimester [∼24w] marks the limit of infant survival (after this, the child is viable).
o Modern care can push this back to 22 weeks.

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3
Q

What is term

A

 Term (39-40 weeks) is expected delivery time and is stated as (40 weeks) since LMP.

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4
Q

Maternal Changes - When do abdominal changes become apparent?

A

Abdominal changes in the mother only become apparent during the 2nd trimester +.

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5
Q

Main maternal changes

A

Increased:

  • Weight
  • Blood clotting
  • Vaginal mucus
  • Hormonal levels
  • Body temp
  • Breast size

Altered:

  • Appetite
  • Joints
  • Fluid balance
  • Immune system
  • Brain function
  • Emotions

Decreased BP
Morning sickness

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6
Q

Start of Pregnancy?

- IVF timings and significance

A

 Pregnancy is counted from the first day of the last menstrual period (LMP), with other events dated from this time.

 IVF pregnancy timing – fertilisation occurs 2-3 days before:
o There will be a difference in time of 2-2.5w from the gestational age (GA, derived from LMP) and the GA in an IVF pregnancy – this can make a large difference when determining viability (22 vs 24 weeks for example).

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7
Q

Reasons for maternal changes - Increased weight

A

(+10-15kg) – baby, placenta, amniotic fluid, increased fluid retention, increased stores.

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8
Q

Maternal changes - Increased Hormone levels

A

o hCG – peaks 1st trimester and decreases thereafter.

o All other hormones (progesterone, oestrogens, placental lactogen) – slowly increase as the pregnancy progresses.

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9
Q

Importance of progesterone in pregnancy?

- progesterone antagonist effects

A

 Progesterone is key to maintaining the pregnancy – progesterone antagonists  loss of pregnancy at ALL gestational ages.

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10
Q

Importance of hCG?

A

hCG = a functional homologue of LH produced in pregnancy and drives production of oestrogens and progesterones from corpus luteum.

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11
Q

Progesterone source?

A

Progesterone source:
o Fertilisation → 8 weeks’ gestation – corpus luteum source via hCG.
o 8+ weeks – placenta supplies progesterone.
 The change-over = “Luteo-placental shift”.

For understanding: hCG = a functional homologue of LH produced in pregnancy and drives production of oestrogens and progesterones from corpus luteum.

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12
Q

Oestrogen source?

A

o Fertilisation → Luteo-placental shift – corpus luteum (via hCG)
o 8+ weeks – complex interplay between foetal/maternal adrenals and placenta

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13
Q

Explain oestrogen source at

8+ weeks – (complex interplay between foetal/maternal adrenals and placenta)?

A

 Human placenta – does not express the enzymes needed to convert pregnenolone → androgens so this occurs in foetal adrenals.
• The weak androgen produced (DHEA) is sulphated to give DHEA-S which is inactive (so female foetus is not exposed to androgens).
• DHEA-S goes to the placenta to be converted to 17β-oestradiol.

 High levels of oestriol are produced by a parallel mechanism including hydroxylation of DHEA-S in foetal liver to give 16OH-DHEA-S.

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14
Q

FSH and LH throughout pregnancy?

A

 High steroid levels supress HPG-axis → low FSH and LH throughout.

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15
Q

Maternal change:

Reasons for Increased blood clotting tendency?

A

Protective against losing blood at delivery.

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16
Q

Decreased blood pressure lowest when and significance?

A

Is lowest during 2nd trimester and is why pregnant women should not stand for long.

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17
Q

Reasons for Increased basal body temperature?

A

possibly by role of progesterone. Also, mediated by increased foetal size.

18
Q

Increased breast size- when and why?

A

Changes start in 1st trimester and continue throughout – due to all hormones!

19
Q

Increased vaginal mucus - nature of mucus?

A

Increased vaginal mucus – more clear mucus produced.

20
Q

“Morning sickness” link and what is severe version called?

A

 “Morning sickness” – affects 80%, more severe version is “Hyperemesis gravidarium”. Unknown cause but maybe linked to hCG levels being high in the first trimester.

21
Q

Reasons for Altered brain function?

A

Due to high levels of steroids, such as progesterone.

22
Q

Reasons for Altered appetite

A

Due to +height of fundus, stomach may be impinged and mother may need smaller meals

23
Q

Reasons for Altered fluid balance and urination frequency?

A

 Altered fluid balance and urination frequency – as kidney functions change → ~50%+ in plasma fluid volume by term. Increasing abdominal size also puts pressure on bladder so more frequent urination.

24
Q

Reasons for Altered emotional state?

A

Due to hormone levels and can vary in people (e.g. happy  post-natal depression).

25
Q

Reasons for Altered joints?

A

Changes in pelvis to make connections more flexible to permit child-birth.

26
Q

Altered immune system – 2 main points should be considered?

A

o Production of factors – supress the maternal immune system from the utero-placental interface. This results in a reduction of Th1 responses and increased Th2 responses.

o Placenta cells expresses unusual HLA – placental HLA are almost invariant (HLA-G has 5 known sequence variants – normal HLA-A and others have millions of variants) and very simple. This is thought to identify the tissue as human but due to its simplicity, no other information is given. HLA-G can also supress some leucocytes and down-regulate maternal immune responses.

27
Q

Define conceptus, embryo, foetus, infant?

A

o Conceptus – everything resulting from the fertilised egg.
o Embryo – the baby up to week 8 of development.
o Foetus – the baby for the rest of pregnancy.
o Infant – applied after delivery typically.

28
Q

Timings in embryology v.s pregnancy?

A

 Again, remember that timings used to discuss embryology are usually from point of fertilisation, 2 weeks after LMP timings used in timings of pregnancy – the embryology timings are PF – Post-Fertilisation.

29
Q

Weights of the foetus in the 3 trimesters and the viable weight range?

A

o First trimester – 50g.
o Second trimester – 1050g – viable at 500-820g stage (21-24 weeks).
o Third trimester – 2100g.

30
Q

Chromosomal abnormalities?

A

o Too few sex chromosomes – Turner’s syndrome – 45 X0.
o Too many sex chromosomes – Klienfelter’s syndrome – 47 XXX, 47 XYY, etc.
o Too few autosomes – non-viability, as does 45 Y0 [no x chromosome – one is essential]
o Too many autosomes – Downs Syndrome – trisomy 21.

31
Q

Most risks to the pregnancy occur when?

- main risks in 3rd trimester

A

 Most risks to the pregnancy occur in the first trimester of pregnancy.

The main risks associated with pregnancy in the 3rd trimester is to do with the birth:
o There are 4 main organs (lungs, digestive system, immune system and brain) that have limited use in utero so late development is logical but problems developing here become apparent at birth.
 This also may cause problems with pre-term birth.

32
Q

Placental Functions

A

Separation between maternal and fetal vascular system
Exchange nutrients and waste products
Biosynthesis
Immunoregulation of whole of pregnancy [ensures no rejection of conceptus]
Connection: placenta must anchor the pregnancy in place

SEBIC

33
Q

Anatomy of the Placenta
[insert digram]
- what is the primary sub-unit and what does it provide
- Foetal Veins and arteries in placenta
- What are Cotyledons and decidua

[insert pic]

A

 Primary subunit is the placental villus that has the branches.
o This provides a large surface area for exchange between the maternal and foetal vascular systems.

 Note that the veins contain oxygenated blood and the arteries contain deoxygenated blood as the placenta carries out a parallel function to the lungs during pregnancy.
 Note the separation of the maternal and foetal systems despite being near.

 Cotyledons – the maternal surface of the placenta is sub-divided into cotyledons. Each contains one or more villi.
(The gaps between cotyledon contains maternal tissue = decidua)

34
Q

Development of the Placenta?

A

Approx. 9 days PF, the conceptus is completely implanted in the maternal endometrium.

  1. IMPLANTATION of conceptus into endometrial epithelium.
  2. Trophoblast layer of the conceptus forms 2 layers → cytotrophoblast (CTB, inner) and syncytiotrophoblast (STB, outer layer)
    - Note: Placenta originates from the cytotrophoblasts layer.
  3. STB sends out PROJECTIONS to embed onto the endometrium +
    LACUNAE → form in STB gets filled with maternal blood.
  4. CTB expansion into STB → PRIMARY CHORIONIC VILLI
  5. Mesoderm line (fill) these villi → SECONDARY CHORIONIC VILLI.
  6. Embryonic blood vessels form in the mesoderm → TERTIARY CHORIONIC VILLI

[Cytotrophoblasts proliferate into the syncytium to form a columnar structure which becomes a villous structure]

  1. CTB cells from the villi grow towards the decidua (maternal tissue between cotyledon) and form a CTB SHELL . This has plugs.
  2. ~6th week → the villi reach maternal spiral arteries → CTB invade the spiral arteries → SPIRAL ARTERY REMODELLING i.e. arteries become wide bore = greater exchange of nutrients
  3. ~10-12th week → CTB plugs breakdown and placenta exposed to full maternal blood flow.

[note: decidual gland hypertrophy supplies nutrients during 1st trimester - not maternal blood - maternal blood when plugs breakdown that block spinal arteries]
- The source of the nutrients (glands: histotrophic) rather than maternal blood (haemotrophic) is different

35
Q

~10-12th week  CTB plugs breakdown and placenta exposed to full maternal blood flow - subsequent risk of miscarriage?

A

If the placenta is not anchored properly, the increased pressure as it is exposed to the maternal blood supply can lead to a detach and a miscarriage.

36
Q

The cytotrophoblast (ctb) cells remodel the spiral arteries during the 1st trimester [what happens]?

A

 The remodelling converts the narrow bore spiral vessels into wide-bore vessels to transport more volumes of blood.
o The ctb cells replace the vascular endothelium and VSMCs which is important as it means the vessels here cannot respond to vasoconstrictors.
 The placenta has no nerves so can be cut without harm

37
Q

Regulation of Growth/Development of the placenta?

A

 Placenta regulates its own growth/development through autocrine functions.
 The maternal decidua mainly seems to restrain (modulate) placental growth/development so the placenta is optimal both for the baby and mother.

38
Q

Maternal Risks in pregnancy?

A

Most risks to the mother lie in delivery and labour.

Risks:
o Remodelling of the spiral arteries means that vessels can lose relatively large amounts of blood after delivery – this should be limited by contractions of the uterus after the placenta has been delivered.
o Placenta must be checked carefully to make sure all has been delivered as it is quite inflexible and any left in the uterus may lead to ineffective uterine contractions.

39
Q

Risks to infant in pregnancy and after ?

A

o Most severe risk is in defects in the gametes – chromosome irregularities.
- Loss of any autosome is not compatible with life  miscarriage.
- Changes in sex chromosomes is generally less severe (loss is more serious than gain).
• Turners is a loss of a sex chromosome and leads to infertility.

o Infants born before 32w GA are at the greatest risk due to incomplete development of the 4 organs (brain, lungs, digestive and immune systems)

40
Q

Risks associated with The placenta?

A

o Most serious problem is incomplete anchorage in the 1st trimester. Possibly due to:
 Developmental problems.
 Detachment in the late 1st trimester.

Note: Placental delivery after baby delivery is importnat.

41
Q

Define Stillbirth?

A

 Stillbirth – death of the infant within the uterus, so that it is delivered without signs of life.
o Some definitions include the viability limit (23w) so any dead births before this are miscarriages and any after this are stillbirths.

42
Q

Detection of stillbirth?

A

 Detection – via monitoring of foetal wellbeing:
o Ultrasound – monitor foetal movements.
o Foetal blood flow assessment – Doppler ultrasound.