OBGYN Flashcards

1
Q

VTE in pregnancy
Patients are either started on LMWH immediately, at 28 weeks, or non-medical (mobilisation) depending on their risk score. VTE prophlaxis is continued for 6weeks/3mo after (LMWH/DOAC).

Requirements for:
1. Starting immediately and referring to experts
2. Considering starting immediately
2. Starting at 28 weeks
3. Non-medical

A
  • High risk (previous VTE; not related to major surgery).
  • Intermediate risk (medical comorbidity, high-risk thrombophilia, previous surgery+/-VTE, any admission). And those with 4+ general RFs.
  • 3+
  • <3.

General risk factors
* Age >35
* Parity >3
* BMI >30
* IVF
* Immobility
* Smoker
* Gross varicose veins
* FHx of VTE
* Multiple pregnancy
* Smoker
* Low risk thrombophilia

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2
Q

Gestational HTN, Anaemia, DM.

  • Gestational HTN
  • Anaemia of pregnancy
  • Gestational diabetes

Also
* Pre-existing HTN

A
  • HTN after 20 weeks with BP of >140 systolic of >90 diastolic. or increase by 15mmHg diastolic or 30 systolic. Labetalol/Nifedipine + weekly Monitoring (bloods, urine dipstick, growth scans). Admit for observation if BP >160/110.
  • Hb <110 at booking (12wk) or <105 at 28 wks. Ferrous Sulfate.
  • fasting glucose >5.6 or 2hr gluocse >7.8. Exercise/diet 2 weeks –> Metformin –> Insulin

> 140/90 before 20 weeks; advise changing teratogenic meds (ACE-I/ARBs/thiazides) –> Labetaolol/Nifedipine

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3
Q

Diabetes and birth
* gestational
* gestational + complications
* pre-exisiting

A
  • up to 40+6
  • elective birth <37 weeks
  • advised elective birth 37-38+6 (induced/C-section)
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4
Q

Pre-eclampsia
Mild/moderate/severe
* typical triad
* Diagnosis
* Investigations
* Investigation to rule out pre-eclampsia (20-35 weeks)
* Criteria for admission
* symptoms/signs
* management - medication (1st, 2nd, 3rd line). What is first line to swap to after birth?
* prevention for women (1 high risk factor or 2 moderate)
* screening (2)
* complications (3)

A
  • HTN, oedema, proteinuria
  • HTN >140/90 past 20 wks + 1 of proteinuria (>30mg/mmo urine Protein:creatine ration) or end organ dysfunction (renal failure - rising CRP; liver failure - deranged LFTs; hamatological markers - low Plt)
  • Urine PCR/urinalysios; U&E,LFT, coag
  • PlGF: low levels in P-E (produced by placenta to stimulate growth of new vessels) -
  • Admit high clinical suspicion for pre-eclampsia or BP >160/110
  • Abdominal pain, headache, visual disturbance (blurry), hyperreflexia, N+V, leg swelling

Management
* 1st line - Labetalol.
* 2nd line - Nifedipine.
* 3rd line - Methyldopa.
* After birth –> Enalapril (note CCB if black)
* If <24 wk ? termination. Otherwise - monitor and anticipate early delivery.

Prevention
* Aspirin 75-150mg from 12 wks

Screening
- Doppler (20wk)
- Ratio of dFlt-1:PIGF; used to rule out PE
Comps
- Maternal: eclampsia, stroke, end-organ damage inc. HELLP/DIC
- Fetal compromise; stillborn; IUGR; prem

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5
Q

RIsk factors for aspirin prophylaxis for pre-eclampsia:
high risk - 1 of (3)
moderate risk - 2 or more (6)

A

HIGH RISK - OFFER AT 12 WEEKS, if either:
* known hypertension or hypertensive disease in previous pregnancy
* auto-immune disease (inc.DM)
* chronic kidney disease

MODERATE RISK - OFFER AT 12 WEEKS IF 1+ RISK FACTOR
- Nulliparity
- extreme obese (BMI >35 at first visit)
- FHx of P/E
- Multiple pregnancy
- >40
- Pregnancy interval >10 years

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6
Q

Causes of jaundice in pregnancy
* Intrahepatic cholestasis
* Acute fatty liver

Which is found in 1%, due to increased reproductive hormones –> stasis of bile acids?*
* Symptoms
* It can lead to…
* Inv findings
* Mx - symptomatic? delivery? if PT deranged?

A
  • Intrahepatic cholestasis
  • Severe pruritus, dark urine/pale greasy stools, jaundice.
  • Placental insufficiency. Complications for mother (malabsorption, liver failure) and fetus (FGR, stillbirth).
  • Deranged LFTs, raised bile acids, Abdo U/S - blockage within ducts + inflamm.
  • Ursodeoxycholic acid
  • IOL (37wk)
    • monitoring/follow-up of LFTs.
  • If pt deranged –> Vitamin K

Acute fatty liver
- rare, T3 or just after delivery
- raised ALT; deranged clotting; abdo pain, jaundice, N+V etc
- like hepatitis with ascites
- obstetric emergency - requires immediate admission and delivery
- more likely differential is HELLP

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7
Q

2nd stage of labour (pushing) involves…
Every Day Fine Infants Enter Engage and Excited

A

Engagement - largest diameter of head is within the pelvis.
Descent
Flexion
Internal rotation
Extension
External rotation
Expulsion

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8
Q

Labour
Define FTP in
* 1st stage - onset of contractions until 10cm dilatation.
* (latent: irregular contractions, cervical effacement and dilatation –> 4cm. Active: regular contractions, –> 10cm).
* 2nd stage - until delivery of baby.
* (passive and active)
* 3rd stage - until delivery of placenta / membranes.
* (active or physiological.)

A

FTP
1. <2cm dilation in 4hr (nulliparous) or slow to progress (multiparous)
2. Active stage >2hr (nulli); >1hr (multi)
3. Physiological >60m. Active >30m.

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9
Q

Indications for active mx of 3rd stage of labour (3)
What does it involve?

A
  • FTP (>60 mins physiological mx)
  • Prevention of PPH
  • Patient choice
  • Oxytocin (Syntocin) & cord traction
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10
Q

Prevention of PTL
Diagnosis, investigation for:
* PPROM
* PTL w/ intact membranes

Prevention options:
* 16-24 wks (3)
* 16-28wks (1)
* 24-32 wks - drugs used for tocolysis (2). Extra indications if suspected labour before 34 wk (1) 36 wk (1).

A
  • Pooling of amniotic fluid within vagina + positive IGTBP-1 or PAM-G1
  • Contractions w/o ROM; cervical shortening less than 15mm. Confirmed with fetal fibronectin >50g/ml if >30wks.

Prevention 16-24 wks
* Cervical cerclage (if <25mm)
* progesterone pessary/gel
14-28 wks
* rescue cerclage - dilatation without ROM.
14-32 wks: tocolysis
* Nifedipine (1) or Atosiban
* MgSo4 + close monitoring
* Betamethasone IM x2 (24hrs apart)

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11
Q

Fetal monitoring
low risk (intermittent auscultation in 2nd/3rd stage) and high risk (CTG).
CTG indications - fetal distress/RFM, pre-eclampsia, maternal raised tachycardia meconium passed + use of oxytocin during labour etc.
* Interpreting a cardiotocogram: DRCBRAVADO.
* Risk statification? - for further intervention/alert senior.
* What is the most concerning finding on an ECG?
* SHort episodes of loss of baseline variability- most common cause?

Concerning features
- Loss of baseline variability (prolonged) <5bpm variation in heartrate from baseline
- Late decellerations (after contraction)
- Variable decelerations (no coordination with contraction) or prolonged

A
  • Define Risk
  • Contractions = 3-4/10 minutes = normal.not progressing/hyperstimulation
  • Baseline rate = brady (< 100); tachy (>160)
  • Variability = how much heart rate changes along baseline rate: normal 5-25
  • Accelerations - signs of baby moving; good sign
  • Decelerations -
  • Early- start at same time as uterine contraction,
  • Late - begins after contraction starts, recovers as contraction ends
  • Variable - no association with uterine contraction at all
  • Prolonged - >3minutes: abnormal
  • Overall impression - risk stratify into normal, suspicious, pathological, requiring urgent attention

Causes of;
* Reduced variability - baby sleeping, maternal opiate use (or hypoxia)
* Early decc - normal; head compression by uterus
* Late decc - abnormal: maternal hypotension, pre-eclampsia, uterine hyperstimulation
* Varibale or prolonged decc - umbilical cord compression

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12
Q

Mx for fetal bradycardia
3 mins
6 mins
9 mins
12 mins

A
  • Alert senior
  • Move to theatre
  • Prep for delivery
  • Deliver within 3 mins (15 mins)

eg peristent fetal bradycarida (reduced BPM on ctg) - urgent c-section category 1

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13
Q

IOL
* Indications for IOL (Bishop score) - takes into account which factors (5)?
* Bishops >9 means? Bishops <5?
* 2 initial methods for manual ROM (2)
* If above fail (no labour within 24hrs) what happens next? (1)
* Main risk associated with prostaglandins/oxytocin
* Main risk of ARM

A

Bishop = cervical position, effacement, dilatation, consistency + fetal station (-3 –>2)
>9 = labour likely to happen spontenously.
<5 = labour unlikely to start without induction. Indication for IOL. Note less than 3 means IOL is unlikely to be successful.
1. Cervical ripening methods:* Prostaglandins (*Propess or Prostin) or Balloon (24hrs). Cervical membrane sweep as adjunct.
2. Artificial ROM (amiotomy) +/-oxytocin (+ epidural if given oxytocin due to increased frequency and strength of contractions)
Risks
- Uterine hyperstimulation –> fetal distress/uterine rupture/emergnecy section. >5 contractions /10 mins
- Cord prolapse

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14
Q

C-section Categories 1-4 and time frame for delivery (categories 1 and 2)

A
  1. Life-threatening maternal & fetal compromise; deliver within 30 mins
  2. Non LF M&F compromise; within 75 mins
  3. Stable M&F, but section reqd.
  4. Elective
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15
Q

Vaginal delivery after C-section (VDAC)
* Success rate
* Contraindications (2)

A
  • 72-75%
  • Classical C-section scar (longitudinal), previous uterine rupture
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16
Q

Perineal tears (1-4) & mx

A
  1. Superficial - skin only –> conservative
  2. Deep; skin + perineal muscle –> suture on ward
  3. Extends to anal sphincter –> theatre
  4. Extends to anal mucosa/rectum –> theatre
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17
Q

PPH:
Can be prevented by active mx of 3rd stage (IM oxytocin); tranexamic acid in C-section, antenatal control.
* define minor and major (moderate, severe).
* Define primary vs secondary
* Causes of PPH: Primary - 4 Ts (what is most common) and Secondary (2)

A

Bleeding within the 3rd stage of labour (after vaginal delivery or C-section).
* Minor = 500-1000ml
* Major = >1000 (moderate); >2000(severe)
* Primary = within 24 hrs of birth
* Secondary = 24hrs –> 12wks post birth

Causes
- Tone - Uterine atony (failure of uterus to vasoconstrict after delivery)
- Tissue - RPOC; retained placental tissue
- Trauma - e.g. during C-section, instrumental delivery
- Thrombin - existing bleeding disorder
Typically cause secondary (24hours - 6 weeks)
- RPOC or infection (endometritis)

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18
Q

PPH Emergency Mx
- initial
- stopping bleeding (mechanical, medical, surgical)
- Rare complication of PPH

A
  1. Resus; A-E (oxygen)
  2. 2 x grey cannula (bloods - FBC, U&E, coag screen)
  3. cross match 4 units blood
  4. IV crystalloid (warmed) and blood resus (+ FFP if nec)
    If severe –> active major haemorrhage protocol –> 4 units O neg blood
    Stopping bleeding
    Mechanical - uterine compression (10mins) & catheterisation
    Medical -
  5. Oxytocin IM–> IV.
  6. Ergometrine - unless hx of HTN
  7. Carboprost - unless hx of asthma
  8. Misoprostol
    +/- Tranexamic acid
    Surgical -
    1.** Intrauterine Bakir catheter (balloon tamponade)**
    2.Alternatives: B-Lynch suture, uteirne artery ligation, hysterectomy (last resort)
    Sheehan’s syndrome = anterior pituitary avascular necrosis.
    Massive blood loss –> reduced perfusion to anterior pituitary –> depleting TSH, FSH, LH, ACTH, prolactin, GH. Mx with hormone replacement.
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19
Q

HELLP syndrome

A
  • Complication of pre-eclampsia - can lead to DIC
  • Haemolysis, Elevated Liver enzymes, Low Plt
  • Abdominal pain (R sided - liver inflammation) N+V, HTN
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20
Q

Requirments for forceps delivery: FORCEPS.
* And contra-indications for instrumental delivery in general?
* Indications for forceps delivery (3)
* Preterm births can have instrumental delivery but only one type - which is it?
* Advantage for forceps?

A
  • Fully diated cervix
  • OA/OP position
  • ROM
  • Cephalic presentation
  • Engagement (of fetal head within pelvis)
  • Pain relief
  • Sphincter empty - catheter

CIs for instrumental
* cervix not dilated, non engagement, large fetal head

Indications for forceps
* 2nd stage - FTP or maternal/fetal distress
* Control of ehad in breech delivery

type of instrumental for prem
* Forceps (can’t use venthouse suction cup on preterm; risk of cephalohaematoma etc)

advantage
* Forceps doesn’t require maternal effort and has a higher success rate.

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21
Q

Breech
* 3 main types
* Mx options at 36 weeks
* Is vaginal birth possible with breech presentation?
* Complications

A
  • Complete (hips flexed, knees flexed), Frank (hips flexed, knees extended), footling (one hip extended; foot/buttock presenting part)
  • ECV + Terbutaline (uterine muscle relaxant) at 36wk. If fails or CIed (e.g. past C-section/haemorrhage) –> C-section.
  • Vaginal birth possible but not advised (?hands off approach, or other manouvres e.g. Lovsette’s/MSV)
  • Cord prolapse, asphyxia, ICH, DDH (requires US at 6 weeks)
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22
Q

Shoulder dystocia
* Main risk factor
* Signs (3)
* Immediate mx: call for help; advise to stop pushing, don’t pull. Episiotomy.
* Manouvres (1st line & other options)
* Complications

A
  • Macrosomia; maternal DM
  • Turtle neck sign; failure of rotation
  • McRobert’s (knee flexion) + suprapubic pressure
  • Rubin’s & screw manouvres
  • Posterior shoulder pressure
  • Hypoxia, Erb’s palsy, PPH etc.
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23
Q

Cord-prolapse:
can result in fetal hypoxia and death. Risk factors - ARM, polyhydramnios, multiple pregnancy, breech presentation, PROM (waters break before fetus has moved into birth canal). Can be diagnosed by:
1. Abnormal CTG (fetal bradycardia) and palpable cord in vagina
2. VIsible cord beyond level of introitus
Mx(3) - 3 initial management steps before definitive delivery
Alternatives to that method of delivery?
What else can help to reduce uterine contractions?
What can help to elevate presenting part of fetus from crushing the cord?

A
  1. Presenting part of fetus pushed back into uterus to avoid compression.
  2. If cord below introitus –> minimal handling; keep cord warm and moist.
  3. All-4s OR left lateral position –> C section
  • Alternative - instrumental delivery if head is low and cervix fully dilated
  • Tocolytics
  • Retro-filling bladder with saline
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24
Q

The puerperium
* 3 physical changes after birth
* Typical blood finding 1/7 after
* Sign of post-partum endometritis, and risk factors (2)
* What is the normal pattern of postpartum thyroiditis?

A
  • Uterine involution (6-8wk, cramps)
  • Lochia (discharge: blood, endometrial tissue, mucus: dark red–> brown –> yellow; 6-8wk; avoid tampons)
  • Leucocytosis
  • Foul smelling lochia + abdominal pain, menorrhagia + fever. ERPC (for RPOC) & C-section. Mx with abx community/hospital.
  • 3mo -Throtoxicosis –> 6mo -hypothyroid –> 1yr - return to normal. Treat like normal with meds.
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25
Q

Puerperium: contraception
* Lactational amenorrhoea can be used as form of contraception until how many months postpartum?
* When will women who are bottle-feeding have periods return?
* How long is contraception not required for? Aka fertility returns when?
* Why are oestrogen containing methods avoided during the first 6 weeks of breast-feeding?
* List types of contraception recommended for after birth/after day 21?
- When can the OCP be safely prescribed if benefits outweigh risks (UKMEC2)?

A
  • 6mo
  • 3wks (ish)
  • 3wks
  • Excess oestrogen (natural levels raised due to BF + exogenous from pill) –> increased risk of ovarian/breast cancer/VTE.
  • Types:
    1. Lactational amenorrhoea (6mo)
    2. Progesterone - POP, Implant, Mirena (IUS), IUD
    Note coils can be put in 48hr after birth;POPs/implants at any time.
  • COCP is UKMEC4 when breast-feeding <6weeks, but UKMEC2 between 6 weeks and 6 months
26
Q

Retained productions of conception
Retained after miscarriage, termination or birth. RF - placenta accreta.
* Key sign:
* U/S –> Mx
* Key complications (2)

A
  • “Offensive lochi with no involution”
  • ERPC, dilatation and currettage
  • Post-partum endometritis.
  • Asherman’s syndrome: uterine adhesions –> reduced fertilty
27
Q

Ectopic - 6-8wks amenorrhoea –> lower abdominal pain +/- vaginal bleeding. Shoulder tip pain & cervical excitation.
Mx Criteria (includes presence of fetal heart beat, beta-hCG level, size of pregnancy, and presenting symptoms) for:
- Conservative = expectant mngmnt + follow-up.
- Medical = Methotrexate (IM) + follow-up
- Surgery = lap salpingectomy (removal of the tube - best) or salpingotomy (if risk factors for infertility aka the other tube is damaged; may also require methotrexate) or other surgery.

A

Conservative: expectant management + betahcg followup (should decrease)
* able to follow-up, x rupture, x severe pain, betahCG less than 1500, no fetal heartbeat, <35mm

Medical
* beta-hcg < 5000 + confirmed evidence on TV U/S, <35mm, no fetal heartbeat

Surgical
* beta-hcg >5000, rupture (e.g. shoulder tip pain), visible heart beat, >35mm

28
Q

Miscarriage: bleeding & crampy abdominal pain following period of amenorrhoea
Define:
– Threatened/viable
Non-viable types:
- Silent/missed
- Inevitable
- Incomplete
- Complete
- Anembryonic

  • Which 3 features are visible on TV/US as the pregnancy progresses? E.g. which is checked first –> second –> third?
  • Which patients are referred to EPAU?
  • Mx - depends on type of miscarriage but generally
  • what needs to be done at 3 weeks
  • How does the mx differ for TOP?
A
  • Bleeding, closed cervix
  • No bleeding/minimal sx not usually painful, closed cervix normally-* aka fetus is not viable but no symptoms of expulsion*
  • heavy bleeding, open cervix
  • With RPOC, open cervix
  • Without RPOC, closed cervix, empty uterine cavity
  • Gestational sac without embryo

TVUS
Normal development:
Mean sac diameter –»25mm - confirm failed pregnancy, if less - repeat scan in 14 days
fetal pole & CRL –> 7mm –>
fetal heartbeat

Referral to EPAU - after 6wks gestation –> pregnancy test, U/S confirm. Repeat pregnancy test 3 weeks later.
Mx - Misoprostol (oxytocin analogue, stimulate contractions, oral, vaginal or sublingual) +/- “surgery” (outpatient vacuum aspiration or surgicery)
Missed miscarriage - hasn’t yet started contractions = mifepristone and misoprostol.
Pregnancy test at 3 weeks.
Mx for TOP - Mifepristone (relaxes cervix) + Misoprostol.
Surgical currettage (<14 wks) –> dilatation & evacuation (<24 weeks) –> + KCl if >22wks.

29
Q

Hydatidiform mole
* Distinguish partial from complete
* Which signs may indicate a molar
* Mx

A
  • Partial - may have some fetal tissue; 69 chromsomes (triploid). Complete = no fetal tissue; 46 chromsomes (diploid).
  • Severe morning sickness, uterus enlargement, heavy vaginal bleeding, abnormally high beta-hCG –> thyrotoxicosis
  • evacuation of uteru ( –> referral for follow-up)
30
Q

Placenta
- “low-lying”
- praevia
- accreta
- increta
- percreta
- abruption

A
  • close to but not over internal os - within 20mm
  • placenta first - placenta over internal os
  • placenta attaches too deeply to uterine wall
  • attachment to uterine muscle
  • placenta invades through uterus (–> bladder/other organs)
  • placenta seperates from wall of uterus - EMERGENCY
31
Q

Placenta praevia
many pregnancies will have a low-lying placenta at 16-20 week scan, only 0.5% have placenta praevia at delivery
* Presentation
* RFs
* Investigation if not picked up on 20 week scan
* Grading (I-IV minor to major)
* Management from 20 weeks
* presents in a similar way to

A
  • Painless bleeding (spotting to massive haemorrhage)
  • Multiple pregnancy, multiparity
  • TVUS
  • lower seg –> internal os–> covers internal os not dilated–> covers internal os when dilated
  • further scans 32 and 36, steroids for fetal lung maturation, planned delivery 36-37 weeks C-section, unless PP grade I
  • similar to placenta accreta
32
Q

Placental abruption
* Causes - unknown but associated factors:
* Presentation
* Define concealed or revealed
* Management
* Complications

A

Cocaine use, multiparity, increasing maternal age, proteinuric htn, trauma

  • Shock (out of keeping with visual loss), abdo pain, tender/tense uterus “woody abdomen”
    **sudden onset abdominal pain, bleeding and tense abdomen **
  • Concealed = os closed, revealed = open
  • may have normal BP
  • treat as major haemorrhage.
  • immediate C-section/deliver vaginally depending on fetus alive/dead and GA/presence of distress
  • shock, DIC, renal failure, PPH. Fetal IUGR, hypoxia, death
33
Q

Fibroids/uterine leiomyoma - benign growths of uterine tissue, can present with menorrhagia/dysmenorrhoea/dyspareuna/subfertility or asx. Generally regress postmenopause.
* Risk factors (general; due to increased oestrogen exposure)
* Ix
* Mx (depends on size) -
- If <3cm/asymptomatic : medical mx; of menorrhagia secondary to fiborids
- If >3cm: medical and/or surgery

A
  • Age, ethnicity (50% in black women)
  • Increased exposure (x3) = early menarche, exogenous hormone use (COCP), pregnancy
  • TVUS
    Small - treat as menorrhagia:
    contraceptive methods
  • (1st line Mirena –> COCP; POP),
    non-contraceptive
  • tranexamic acid- antifibrinolytic;
  • mefanemic acid - NSAID; reduce bleeding+pain
  • Large - refer to gynae for further mx:
  • medical - GnRH agonists (short-term treatment)
  • surgical: endometrial ablation, fibroid resection (–>hysteroscopy), myomectomy (lap/hysterectomy), uterine artery embolisation
34
Q

Endometriosis
ectopic endometrial tissue outside uterus - metaplastic development of embryonic cells destined to be endometrial tissue (ovaries - choclate cyst; uterine muscle - adenomyosis; bladder/bowel; lymph nodes )
* RFs
* Typical presentation
* Main complication
* Ix & gold standard diagnostic test
* Mx is similar to that of fibroids - medical/surgical - depend on whether patient is planning to conceive.
* Medical treatments may be used as a trial before establishing a definitive diagnosis. How do the medical treatments work?

A
  • RFs from increased exposure to oestrogen (early menarche, late menopause, short cycle, pregnancy). Genetic element. Unknown aetiology.
  • Cyclical pelvic pain , dyspareunia, menorrhagia +/- cyclical bleeding from other sites
  • Subfertility (e.g. endometriomas damaging eggs)
  • TVUS. GS = laparoscopic surgery w. lesion biopsy
  • Medical = contraceptive methods to manage dysmenorrhoea (NSAIDs/pct–> hormonal management: OCP, POP, +/- Mirena, GnRH agonist etc)
  • Contraceptive methods like OCP and POP stop ovulation & reduce endomtrial thickening; Mirena to reduce bleeding (less retrograed menstruation) GnRH stop production of sex hormones (menopause like state).
  • Surgical = ablation/excision of lesions / hysterectomy & BSO
35
Q

Post-menopausal bleeding
* List common causes of PMB specific
* Guidelines -

A
  1. Atrophic vaginitis
    1. HRT related (periods/spotting)
  2. Endometrial hyperplasia (+/- atypia)
  3. Endometrial cancer (or other gynae ca)
    + general (fibroids, polyps, trauma, bleeding disorder)

All women >55 with PMB must be referred to gynae for a TVUS within 2 weeks (for endometrial ca)

36
Q

Ovarian torsion
- sudden onset unilateral pelvic pain +/- N,V + palpable mass
-aetilogy
- ix
- sign on TVUS
- immediate mx

A
  • Large cyst/tumour in the adnexa
  • TVUS
  • Whirlpool sign (free fluid in pelvis)
  • lap surgery (definitive diangosis) - detorsion or oophorectomy (untwist or remove the ovary; depending on extend of ischemia/necrosis)
37
Q

Causes of pelvic pain

A
  • Ovarian pathology - torsion, ruptured cyst
  • Cervical pathology - cervical ectropion, polyps
  • Bleeding - menorrhagia, fibrois, endometriosis
  • Sexually acquired - STI/PID
  • Non-gynae - appendicitis, IBS, diverticulitis, UTI
  • Early pregnancy - ectopic, miscarriage
38
Q

Pelvic Organ Prolapse
* Types (4)
* RFs (congenital, lifestyle, acquired)
* Grading 0-4 (POP-Q) - depends on level of prolapse relateive to introitus (entrance of vagina)
* Mx (cons, med, surg)

A
  • uterine, vault (top of uterus), cystocele (anterior vaginal wall) rectocele (posterior)
  • Congenital: spina bifida. Lifestyle = obesity. Acquired: multiparity, vaginal deliveres.
  • Grading 0-4 = normal, lowest part of prolapse is 1cm above introitus, within 1cm, 1cm below introitus, full descent with eversion of vagina
  • Lifestyle changes (weight loss) & treat sx (urinary incontinence)
  • Medical: pessary - simple, ring or Gellhorn (removal every 4 months)
  • Surgery: obliterative - colpocleisis; reconstruction - sacro-colpopexy (suspension of vagina to sacrum using mesh) colporrhaphy (repair)
39
Q

Female incontience
Urge/stress
Distinguish the types
Conservative/medical/surgical for both

A

Urge
- overactive bladder; detrusor instability
- 1st line - bladder retraining (6wks)
- Anticholinergic (Oxybutinin or Mirabegron), or anti-muscarinics (Tolteradine/ Danifenacin)
- Botox injection, percutaneous sacral nerve stimulation, augmentation cystoplasty, urinary diversion –> urostomy

Stress - pelvic floor weakness; leakage under pressure
- exercise, weight loss, pelvic floor training (Kegel’s)
- SNRI (Duloxetine - sphincter constriction)
- Slings / colposuspension (supports urethra), intramural urethral bulking, artificial urinary sphincter

40
Q

Amenorrhoea
Primary - causes
Secondary - causes
Investigations - bedside (1) and bloods (4)

A

Primary
No secondary sexual characteristics
* Chromosomal disorder- Turner’s (45XO)
* HPG axis dysfunction - stress/anorexia etc

With -
* Physiological - e.g. imperforate hymen
* Endocrine - PCOS, hypo/hyperthyroid, Cushing’s, hyperprolacitnaemia, congenital adrenal hyperplasia
……+ same causes as for secondary

Secondary
* Pregnancy, lactation, menopause
* HPG axis dysfunction - chronic illness, stress, weight loss, excessive exercise
* Iatrogenic (exogenous hormone use)
* PCOS, Cushing’s, androgen-secreting tumours

Investigations
- Bedside - pregnancy test/ blood beta-HCG
- Bloods - gonadotrophins (LH, FSH).
Low LH/FSH - hypothalamic cause; raised levels - ovarian cause. Normal = weight loss/exercise.
- Prolactin - ?hyperprolactinaemia from stress/drugs
- Androgens - raised in PCOS or tumours
- TFTs - exclude thyroid dysfunction

41
Q

Diagnostic criteria for PCOS: 2/3 of criteria:
Typical blood findings in PCOS
- LH/FSH ratio
- Testosterone
- Sex hormone binding globulin

A

Criteria (Rotterdam)
* Features/biochemical evidence of hyperandrogenism - hirsutism, acne, raised testosterone
* Oligomenorrhoea
* Evidence of polycystic ovaries on TVUS

Bloods - Hormone profile (LH, FSH, testosterone, SHBG)
* Raised, 2:1 or 3:1
* Normal/elevated
* Normal/low

Pathophysiology; largely unknown - theory related to:
**Insulin resistance –> Low SHBG; and reduced follicle maturation - low FSH, and subsequent androgen-producing cyst formation*
–> anovulation (disproportionately high LH to FSH)
shbg binds to oestrogen, testosterone and dihydrotestosterone; if there are low levels of it then there are increased levels of unbound, active forms of testosterone and Dihydro –> features of PCOS

42
Q

Emergency contraception - time window from UPSI
* Levonorgestrel (Levonelle) -synthetic progesterone
* Ulipristal (EllaOne) - progresterone receptor modulator
* IUD (copper coil)

Which requires double dose for increased BMI (over 26 or over 70kg) and has a 1% risk of vomiting?

Dose of Levonorgestrel?

A
  • Within 72hrs of UPSI (3 days)
  • Within 120hrs (5 days)
  • Within 120hrs/5days from UPSI, or 5 days from expected time of ovulation (LMP-14 days). Can remain, or be removed after next period.

Levonorgestrel- repeat dose if vomiting within 3 hrs.
1.5mg for 1 dose

43
Q

Emergency contraception
Why is it important to know what day in the cycle the UPSI happened?

A
  • Because oral emergency contraception is not effective after ovulation
  • Pt requires coil - can be fitted up to 5 days after UPSI
44
Q

STIs
Chlamydia
- type of bacteria
- epidemiology, % asymptomatic
- complications (4)
- types A-C cause
- types D-K cause
- risk factor for types L1-L2
- national screening prgramme age and method
- treatment

A
  • gram -ve
  • most common STI in developing world
  • 70% asx
  • cause of infertility
  • A-C: ocular
  • D-K: genital
  • can lead to PID, SARA and Fitz-Hugh-Curtis syndrome (complication of severe PID adhesion formation between liver capsule and abdominal wall)
  • MSM - lymhogranuloma venereum (note painless ulcer)
  • National Screening Programme- <25 sexually active, yearly, or more often if multiple partners, self swab (LVS)
  • Doxycycline
45
Q

Vaginal discharge/STIs
* Risk factors
* Vaginal / endocervical causes of abnormal discharge
* General sx (male/female)
* Investigations (female)
* Mx
* What does a pH >4.5 indicate?
* What does a pH <4.5 indicate?

A

15-24; MSM; recurrent partner; not using barrier protection.
Vaginal
candidiasis, vaginal trichomoniasis, BV
endocervical
chlaymida, gonorrhoea
General sx
Female - discharge, pelvic pain/dyspareunia, IMB/PCB.
Male - testicular pain, swelling, dysuria (epidymo-orchitis)
…. also;
Ulcers - herpes, syphillis (chancre), lymphogranuloma venereum (complication of chlamydia in MSM)
Ix
Bedside: Swabs x2
- HVS, ECS –> MC&S (+NAAT for chlamyida/gonorrhoea specificalyl)
- Discharge pH test (distinguish vaginal causes)
- >4.5= trichomonas and BV
- <4.5 = candidiasis (because acid is fun) - more acidic
Mx
- referral to GUM
- Abx (+/ abx for partners? and follow-up)
- fruther advice re sexual health

46
Q

STIS: Gonorrhea
- type of bacterium
- male/female?
- presentation
- management
- complication & presentation

A
  • gram -ve diplococcus
  • men asx (mostly), women 50/50
  • yellow/green discharge
  • IM Ceftriaxone + empirical abx for sexual partners + Follow-up (test of cure)
  • Notable complication - disseminated gonococcal infection –> rash, arthralgia, tenosynovitis, systemic sx
47
Q

Trichomoniasis
* type of organism
* endemic to
* found in where in males/females
* finding on speculum
* presentation
* ph
* management

A
  • protoza (flagella)
  • developing countries, low prevalence in UK
  • vaginal (F) urethral (M)
  • “strawberry cervix” - microhaemorrhages
  • yellow/green discharge + fishy odour + usual
  • pH >4.5
  • Metronidazole
48
Q

Genital herpes
-caused by
-presentation
- how is it spread
- risks if contracted when pregnant
- treatment if recurrent or pregnant, otherwise symptomatic management

A
  • HSV2
  • ulcerations, flu-sx, dysuria
  • remains latent
  • can only be spread during sex when lesions present
  • NAAT
  • risk of neonatal infection if contract when pregnant
  • Aciclovir - if recurrent/pregnant. Sx management.
49
Q

Syphillis
* 3 stages
* antibody testing for ….
*

A
  • chancre (painless genital ulcer) + painless lymphadenopathy –> rash (snail tract ulcers, condylomata lata - genital lesions –> gummas (granulomatous lesions of skin and bones afecting any organ) - aortic aneurysm, tabes dorsalis, Argyll-Robertson pupil
  • t palladium
50
Q

Menopause; perimenopausal (irregular bleeding) –> menopausal (amenorrhoea); median age 51. Generally benefits>risks for women less than 60 (reduced osteoporotic risk) but risks (endometrial ca, breast, VTE) increase as age increase. Continue for 1 year at least to reduce sx recurrence.

  • most common sx and non HRT treatment for it?
  • what are the UKMEC guidelines for the COCP during menopause, after 40 and post-menopausal?
  • what can HRT contain (3)?
  • What formulations are available?
  • Indication for cyclical/continuous HRT?
  • How do women come off HRT?
A

Vasomotor sx (hot fluses, insomnia, night sweats, headache) - Clonidine - alpha adrenergic agonist; Gabapentin - headache. SSRIs for hot flushes.
COCP in over 40s
* During menopause: beneficial for sx
* After 40: UKMEC2 (benefits>risks)
* Post-menopause: stop, change to POP
* 55: don’t require contraception
HRT contents
* oestrogen
* +/- progesterone (as unopposed oestrogens increase risk of endometrial ca)
* +/- testosterone (Tibolone contrains all 3)
Formulations
* Gel
* Patch (if VTE risk)
* Pessary
* PO tablet
Cyclical/continuous
* Cyclical if peri - had period within 1 year
* Continuous if not (post)
Stopping HRT
* gradually reduce HRT to reduce symptom occurrence in the short-term.

51
Q

HRT
Contra-indications (4/5)
What can be prescribed instead?

A
  • Current or past breast cancer/oestrogen-sensitive cancer
  • Past PE (VTE risk)
  • Undiagnosed vaginal bleeding
  • Untreated endometrial hyperplasia

Venlafaxine/Fluoxetine for symptom relief / Clonadine

52
Q

HRT: Risks
1. CVD
2. Breast ca
3. Ovarian ca
4. Endometrial ca (oestrogen-only HRT)
5. VTE/ Stroke
6.

A
53
Q

Ovarian cancer
Often presents late with abdominal bloating, change in bowel habit, early satiety, AUB + systemic sx.
* Types (3 + metastasis)
* Risk factors (M, NM, others)
* Protective factors (3)
* Epidemiology (2)
Referral - 2WW >55 with ascites, aabdominal/pelvic mass. >40 with any suspcious features for further inv.
* Ix (4)
* FIGO staging (4)
* Mx - medical, surgical (2)
*

A

Types
* dermoid (e.g. terotomas: raised b-hCG and AFP)
* epithelial cell - majority
* sex stromal cell - rare/benign/malingnant
* Krukenberg - mets in ovary from GI “signet cells”
Risk factors
* NM: FHx (BRCA1,BRCA2)
* M: Smoking, obesity, Clomifene use
* Increased no of ovulations - early menarche, late menopause, nulliparity
Protective - reduced no. of ovulations
* OCP
* pregnancy
* breast-feeding
Ix
* CA-125
* TVUS
* Gold-standard: biopsy
* CT/MRI pelvis (staging)
FIGO
1 - confined to ovary/ovaries. 2. - spread within pelvix. 3 - outside pelvis. 4 - metastasis (liver mets).
Mx
Tumour debulking surgery; TAH & BSO. May require adjuvant chemotherapy (platinum based - Carboplatin & Paclitaxel).

54
Q

Endometrial hyperplasia - precancerous condition causing thickening of the endomtrium
- types
- gold standard ix
- % risk of becoming cancerous
- treatment

A
  • With/without Atypia
  • 5%
    hysteroscopy with endometrial biopsy
  • progestogens (IUS, oral) for endometrial hyperplasia without atypia; hysterectomy advised with atypia
55
Q

Endometrial cancer
Guidelines - Post menopausal bleeding –> 2WW refer to gynae for TVUS. Or >55 with unexplained discharge/visible haematuria (raised Plt, anaemia, elevated glucose) –> TVUS.
* Risk factors (exposure to UO; M; NM)
* Protective factors
* Why is Tamoxifen a risk factor?
* Ix (TVUS, Hysteroscopy with endomtrail biopsy/pipelle –>CT/MRI for staging). What is the cut off for endometrial wall thickeness?
* FIGOstaging 1 - 4: refers to level of invasion of cancer
* Mx: 1,2,3,4

A

Risk factors
* Exposure to unopposed oestrogens - obesity, early menarche, late menopause, anovulation- PCOS (not ovulating; no CL producing progesterone), nulliparity (because in pregnancy there is increase in both hormones)
* NM: Lynch syndrome, endometrial hyperplasia (5%), DM (insulin stimulates endomtrial cells)
* Tamoxifen - anti-oestrogenic effect in breast tissue but oestrogenic effect in endomtrium
Protective
* COCP - as it contains a progesterone
* increased pregnancies - oestrogen & progesterone
* Smoking (anti-oestrogenic)
* FIGO
1. confined to uterus
2. in uterus and cervix
3. within pelvis (e.g. invades tubes, vagina etc)
4. beyong pelvis/bladder or rectum
Ix
- TVUS greater than 4mm thickeness –> further ix
Mx
1. Total hysterectomy with bilateral salpingo-ooperectomy (removal uterus, tubes and ovaries)
2. Radial hysterectomy (uterus + vaginal tissue + lymph nodes)
3. Maximal debulking surgery +/- chemo
4. Like 3 +/- chemo or palliaitve

56
Q

Cervical screening
* Age range and frequency
* Basics - 3 methods of testing
* % of women with HPV in lifetime
* Exceptions (which women require annual/additional screening?)
* Can you request after 65?
* How long do pregnant women have to wait?
What happens if:
1. +ve hrHPV & normal cytology?
2. ……now negative hrHPV (after 12mo)?
3……., or, now positive hrHPV (after 12mo)?
4. ……now positive hrHPV (aka 3 positive hrHPVs in 24mo)?
5. ….. noe negative hrHPV (aka 2 positives, 1 neg in 24 mo)?

A
  • 15-49 3 yrly, 50-64 5 yrly
  • Test (hrHPV), cytology (abnormal cells), colposcopy (CIN - dysplasia grades I-III).
  • Between 1/2 and 1/4
  • HIV - annual. Immunocompromised - additional.
  • Yes, if havent had one since 50.
  • 3 mo post partum.
    1. Repeat in 12 mo
    2. Return to normal recall
    3. Repeat in 12 mo
    4. Colposcopy
    5. Return to normall recall
57
Q

Cervical cancer - majority SCC (squamocolumnar junction withi transformation zone); 99.7% of cancers caused by **>2 yr infection with hr-HPV **
* Epidemiology
* Most are detected by screening. If suspected clinically –> 2WW referrral. What test is diagnostic?
* FIGO (I-IV;split into A/B - summary)
* Mx (depends on stage)
* Type of chemo
* What can be used in combination with other therapies for metastatic or rrecurrent cance?

A
  • Most common tumour of female genital tract, 2nd most common cancer in women. Peaks in 30s and >70s.
  • Biopsy
    FIGO
    1. Confined to cervix
    2. Spread to upper 2/3 vagina
    3. Spread to lower 2/3 vagina and within pelvis
    4. Spread to bladder/rectum or mets
    Mx
    Managment depends on FIGO staging but generally includes surgery +/- radiotherapy or chemotherapy.
    Surgeries (from lower to higher stage) include:
  • Trachelectomy (fertility preserving, removal of cervix and upper vagina)
  • Radical Hysterectomy (uterus, vagina, cervix, ligaments) +/- BSO
  • Chemo: cisplatin based
58
Q

Vulval cancer; 80% SCC; majority in >65s, rare
* risk factors
* pre-malignant condition - 2 types
* FIGO stating –> mx options

A
  • lichen sclerosis, HPV infection, immunosuppression, age
  • VIN - “usual”: younger, hPV related. “differentiated” - older women with chronic dermatological condition, not HPV.
  • chemo, radio, surgery (depends on size of lesion)
59
Q

Diagnosis for premature ovarian failure

A

Under 40
Irregular periods
FSH in perimenopausal range

60
Q

Isolated oesophageal atresia
- sign on ultrasound

A
  • polyhdramnios
  • absent stomach
  • dilated proximal oesophageal pouch in neck/mediastinum

fetus drinks amniotic fluid