Obstetrics/Gynaecology (NEW) Flashcards

(59 cards)

1
Q

Chlamydia trachomatis background

A

Epidemiology

  • most common bacterial infection
  • > more common in women
  • risk factors
  • > young adult (<25yrs)
  • > new/multiple sex partner
  • > partner with chlamydia
  • > infrequent condom use
  • > previous STD
  • > urban
  • coinfection common
  • > gonorrhoea
  • > trichomonas
  • > m genitalium

Aetiology

  • sexual transmission
  • > cervix < - > urethra (approx 75% partners affected)
  • > urethra < - > rectum (transmission rate much lower)
  • infects
  • > columnar epithelial cells cervix
  • > urethra
  • > bartholins glands
  • > fallopian tubes
  • > anus
  • does not infect squamous cells of vagina

Pathophys

  • structure
  • > gram negative bacteria
  • > obligate intracellular organism
  • life cycle
  • > spore like elementary body attaches to epithelium
  • > enter and surround by vacuole (inclusion)
  • > transforms to larger/metabolically active reticulate body
  • > replicates over 3 days
  • > transforms back into elementary bodies
  • > cell rupture and spread
  • incubation period up to 2 weeks
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2
Q

chlamydia trachomatis syndromes

A

Women

  • cervicitis
  • > vast majority asymptomatic
  • urethritis
  • > 50% of infections
  • PID and sequelae
  • pregnancy
  • > premature rupture of membranes
  • > preterm birth
  • > low birth weight
  • > chorioamnionitis

Men

  • urethritis
  • epididymitis
  • > unilateral pain/tenderness
  • > hydrocele
  • > swollen epididymis

Common to men and women

  • conjunctivitis
  • > by direct inoculation with genital secretions
  • > erythematous injection of conjunctiva
  • > non purulent
  • reactive arthritis
  • > acute onset several weeks post infection
  • > asymmetric, oligoarticular
  • > enthesitis
  • > dactylitis
  • > inflammatory lower back pain
  • reiters syndrome (classic triad)
  • > arthritis
  • > conjunctivitis/uveitis
  • > urethritis/cervicitis
  • proctitis
  • > pain
  • > discharge
  • > bleeding
  • > tenesmus
  • > constipation
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3
Q

Miscarriage (<20 weeks) background

A

Epidemiology

  • early pregnancy loss (first trimester)
  • > 10% clinically recognisable pregnancies
  • early second trimester loss (<20 weeks)
  • > less than 1% of pregnancies
  • almost half of parous women have EPL

Risk factors (ADIPOSE)

  • Age
  • > maternal
  • > possible paternal
  • Diabetes
  • > euglycaemia risk is baseline
  • Infection
  • > CMV
  • > syphilis
  • > parvovirus B19
  • Previous miscarriage
  • > OR for 1 = 1.5
  • > OR for 2 = 2.2
  • Obesity
  • Substances
  • > medications
  • > alcohol, smoking, cocaine
  • Exposures
  • > lead/arsenic
  • > air pollution
  • > radiation

Aetiologies

  • chromosomal abnormalities
  • > approx 3/4 of miscarriages
  • uterine abnormalities
  • > ashermans syndrome
  • > fibroids
  • > polyps
  • direct trauma
  • > violent
  • > iatrogenic (chorionic villus sampling)
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4
Q

Miscarriage (<20 weeks) evaluation

A

Hx

  • confirm pregnancy
  • > LMP
  • > pregnancy test results
  • bleeding
  • > clots
  • > tissue
  • pain
  • > cramping
  • > shoulder tip
  • loss of pregnancy symptoms
  • syncope
  • > hypovolaemia
  • infection
  • > fever
  • > purulent discharge
  • obstetric hx
  • > previous pregnancies
  • > previous miscarriages
  • > assisted conception
  • gynaecological hx
  • > surgeries
  • > significant conditions
  • previous investigations
  • > US
  • > b HCG

Exam

  • vitals
  • > fever/tachycardia/hypotension = infection
  • > tachycardia/hypotension = hypovolaemia
  • > bradycardia/hypotension = tissue in cervical canal
  • abdo
  • > tenderness/guarding
  • > distension
  • > enlarged uterus
  • speculum
  • > bleeding from cervix
  • > open os
  • > tissue in cervical canal
  • bimanual
  • > cervical motion tenderness
  • > uterine tenderness in infection
  • > adnexal mass

Investigations

  • b HCG
  • > urine
  • > serum
  • FBC
  • blood group and antibodies
  • > transfusion
  • > sensitising event
  • Coags
  • Consider
  • > MSU
  • > STD
  • Initial transvaginal ultrasound
  • > IUP
  • > ectopic pregnancy
  • > absence of findings (PUL/complete miscarriage)
  • > GTD
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5
Q

Suspected miscarriage investigation pathway

A

Intrauterine pregnancy

  • Confirmation
  • > yolk sac/embryo within gestational sac in endometrial cavity
  • Viable
  • > fetal heart present
  • Non viable incomplete miscarriage
  • > loss of cardiac tones in confirmed intrauterine
  • > MSD >25mm, no yolk sac/embryo
  • > CRL >7mm w no cardiac tones
  • Viability cannot be assess (MSD <25mm)
  • > repeat TVU when MSD expected to be 25mm
  • > assume MSD grows 1mm/day

Ectopic

  • Confirmed
  • > gestational sac with yolk sac/embryo at ectopic site
  • > adnexal mass/empty uterus/free fluid
  • > consider heterotopic
  • Likely
  • > pseudosac
  • > complex extra ovarian adnexal mass
  • > tubal donut sign
  • > adnexa ring of fire sign on doppler

PUL

  • DDx
  • > early IUP/non viable IUP
  • > ectopic
  • b HCG >3500 w. no findings
  • > almost certainly ectopic
  • > proceed with treatment
  • b HCG >2000 w. no findings
  • > ectopic/multiple gestation
  • > consider serum progesterone (low = non viable)
  • > expectant treatment as ectopic justifiable
  • > consider repeat TVU in 3 days (MSD visible at 3mm )
  • b HCG <2000 w. no findings
  • > repeat b HCGs over 48 hrs
  • serial b HCGs
  • > doubled = probably viable
  • > falling = likely unviable (including aborted ectopic)
  • > suboptimal rise (determined by initial level ) = ectopic or non viable IUP
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6
Q

Miscarriage psych management

A

Breaking bad news

  • setting
  • > as soon as possible
  • > ideally both parents present
  • > offer and facilitate presence of support person
  • > minimise waiting times
  • > private, preferably away from maternity wards
  • principles
  • > provide as much information as possible
  • > don’t speculate
  • > talk about ‘baby’ or use name if given

Counselling

  • principles
  • > allow time for questions, grief and discussion
  • > discuss potential experience of grief/depression
  • memories
  • > offer to provide momento (eg. US picture)
  • > offer to see baby (prepare them for image)
  • supports
  • > discuss personal supports
  • > mental health services
  • > medicare pregnancy support counselling services
  • consider
  • > risk factors for psychological morbidity
  • > suicide risk (leading cause of maternal mortality)
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7
Q

Miscarriage general management

A

Disposal of fetal tissue

  • if state requirements for birth registration met
  • > death certificate
  • > cremation or burial
  • birth registration requirements not met
  • > early pregnancy loss certificate can be provided
  • > hospital cremation
  • > private funeral director
  • > burial on private property

Histopath

  • products of conception sent to laboratory
  • > confirm pregnancy
  • > exclude ectopic
  • > exclude GTD
  • collection
  • > during surgery/inpatient miscarriage
  • > provide labelled specimen jar if expectant at home

Safety net

  • seek emergency assistance
  • > severe pain
  • > shoulder tip pain
  • > soaking more than 1 pad every hour
  • > syncope
  • > fever
  • return of period
  • > resolution of complications/completion of care
  • ongoing bleeds (>2 weeks)
  • > incomplete delivery
  • > GTD
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8
Q

Expectant management non-viable pregnancy

A

Indications

  • > patient preference
  • > incomplete miscarriage

Contraindications

  • > later than first trimester
  • > unstable
  • > evidence of infection
  • > high risk of haemorrhage or coagulopathy
  • > suspected GTD

Risks

  • > 20% unsuccessful
  • > prolonged bleeding
  • > high rate of unplanned admission
  • > low and comparable infection rate (2-3%)
  • > 2% risk of transfusion

Benefit

  • > similar success rate as medical management
  • > avoid medication/surgery
  • > managed at home

Follow up with GP/EPAS

  • > repeat b HCG in a week
  • > US if b HCG decrease <90%
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9
Q

Medical management non viable pregnancy

A

Indications

  • > patient preference
  • > incomplete miscarriage

Contraindications

  • > later than first trimester
  • > unstable
  • > evidence of infection
  • > high risk of haemorrhage or coagulopathy
  • > prostaglandin allergy

Risks

  • > heavier and prolonged bleeding than surgical
  • > 20% unsuccessful
  • > low and comparable infection rate (2-3%)
  • > 1% risk of transfusion

Benefits
->faster process than expectant

Procedure

  • > outpatient/day procedure
  • > misoprostol per vagina single dose
  • > analgesia and anti-emetics

Expect

  • > bleeding within 24 hrs
  • > bleeding heavier than menses
  • > cramping pain
  • > pain and bleeding gradual get worse
  • > peaks for 2-4 hours
  • > occasional bleeding/dull ache/cramping for 2 weeks
  • > SE = diarrhoea and vomitting

Follow up with EPAS

  • > b HCG day 1 and 8 (confirm levels falling)
  • > US if b HCG decrease <90%
  • > repeat dose after 2-7 days if no response
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10
Q

surgical management non viable pregnancy

A

Indication

  • first/early second trimester
  • patient preference
  • unstable/severe haemorrhage
  • evidence of infection
  • suspected GTD
  • unsuccessful medical/expectant management

Contraindication
-no absolute

Risks

  • standard procedure/anaesthesia risks
  • low and comparable infection rate (2-3%)
  • complications 1-2%

Benefits

  • shorter time to completion
  • lower rate unplanned hospital admissions
  • lowest rate of blood transfusion

Procedure

  • misoprostol PV 4hrs pre op
  • dilation and curettage (suction recommended)
  • general anaesthetic in OR

Follow up

  • GP if ongoing concerns
  • no b HCG or US
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11
Q

Clinical manifestations and diagnosis pregnancy

A

Hallmarks signs/symptoms

  • typical presentation
  • > within 8 wks gestation
  • > hx of sex without contraception
  • common
  • > amenorrhea
  • > nausea +/- vomiting (until 10 weeks)
  • > breast enlargement/tenderness
  • > fatigue
  • > urinary frequency

Additional hx

  • Neuro
  • > mood changes
  • > difficulty sleeping
  • > orthostatic presyncope
  • > carpal tunnel
  • Skin
  • > hyperpigmentation
  • > palmar erythema
  • > spider angiomas
  • Abdo
  • > mild uterine cramping
  • > adnexal discomfort
  • > bloating
  • > constipation
  • > GORD
  • > food cravings and aversions
  • Genitourinary
  • > bleeding
  • > nocturia
  • Resp
  • > nasal congestion
  • > SOB

Exam

  • uterus above symphysis after 12 wks
  • vulva/vaginal/cervix mucous
  • > congested and bluish after 12 weeks
  • breasts
  • > areolar darkens
  • > veins more visible

B HCG

  • serum vs urine
  • > serum much more sensitive and quantitative
  • > urine rapid, cheap but quantitative
  • serum
  • > can detect 1-2 mili IU
  • > level >5IU confirms pregnancy
  • > earliest detected 2 weeks after first day LMP
  • normal trajectory starts
  • > double every 48hrs for first month
  • > starts to decline after 10 weeks
  • > plateaus for second and third trimester

TVU

  • gestational sac
  • > 4-5 weeks
  • yolk sac
  • > 5-6 weeks
  • fetal pole w cardiac activity
  • > 6 weeks
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12
Q

Gonorrhoea background

A

Epidemiology

  • approx 5/10,000 gen pop
  • > 200 times more common in ATSI
  • risk factors
  • > ATSI
  • > MSM
  • > under 25yrs
  • > new/multiple sex partners
  • > partner with STD
  • > inconsistent condom use
  • > past STD

Aetiology

  • penetrative sex
  • > oral
  • > vagina
  • > rectum
  • transmission rate
  • > male to female = 60%
  • > female to male = 25%

Pathophys

  • attaches to mucosal epithelium
  • chromosomal plasticity
  • > evades immune system
  • > high rate of antimicrobial resistance
  • > reinfection common
  • incubation period
  • > approx 3 days in men
  • > longer in women
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13
Q

Gonoccocal syndromes

A

Women

  • cervicitis
  • > most common
  • > usually asymptomatic
  • urethritis
  • > almost always with cervicitis
  • > usually asymptomatic
  • PID and sequelae
  • bartholinitis
  • > with cervicitis
  • > perilabial pain and discharge
  • > oedematous/tender labia
  • pregnancy
  • > PPROM
  • > premature delivery
  • > low birth weight
  • > chorioamnionitis

Men

  • urethritis
  • prostatitis
  • > lower back pain
  • > dysuria
  • > frequency/urgency
  • epididymitis/orchitis uncommon

Both

  • proctitis
  • > pain
  • > discharge/bleeding
  • > tenesmus/constipation
  • pharyngitis
  • > oral sex
  • > pharyngitis
  • > exudate
  • > cervical lymphadenopathy
  • conjunctivitis
  • > by direct inoculation with anogenital secretions
  • > hyperacute (symptoms within 12 hrs)
  • > copious purulent discharge
  • > red and irritated
  • > chemosis/swollen eyelids
  • > preauricular lymphadenopathy
  • > sight threatening
  • purulent arthritis (disseminated disease)
  • > acute onset
  • > distal/asymmetric/oligoarticular arthritis)
  • > otherwise well
  • arthritis-dermitis syndrome (disseminated disease)
  • > several weeks post infection
  • > flu like illness with fever
  • > asymmetric, migratory polyarthritis
  • > tenosynovitis
  • > pustular/vesicular lesions on extremities
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14
Q

Initial antenatal visit

A

Hx

  • obstetric Hx
  • edinburgh post natal depression scale
  • genetic counselling
  • > aneuploidy screening
  • > carrier screening

Advice

  • potential teratogens
  • lifestyle
  • > smoking, drinking, drugs
  • > diet and supplements
  • > exercise
  • > general restrictions
  • infection prevention
  • > immunisation
  • > precautions
  • ongoing care
  • > care team
  • > frequency of visits
  • > antenatal education courses available

Exam

  • height, weight, BMI
  • BP
  • Uterine
  • > size
  • > consistency
  • > position

Ultrasound

  • confirm
  • > pregnancy
  • > number
  • > location
  • > cardiac tones
  • GA
  • morphological anomalies
  • > poor sensitivity

Bloods

  • FBC
  • > haemoglobin (anaemia)
  • > MCV (thalassaemia/iron deficiency)
  • > platelets (thrombocytopenia)
  • Blood group and antibodies
  • MSU
  • > dipstick for proteinuria
  • > midstream culture
  • Diabetes screening
  • > random glucose
  • > HbA1c if high risk
  • Rubella
  • > antibody titre
  • Varicella
  • > documented previous chickenpox/shingles
  • > previous vaccination
  • Syphilis
  • > trepanemal assay
  • Chlamydia/gonorrhoea
  • > high risk
  • > under 25
  • HIV
  • > EIA + western blot
  • HBV
  • > HBVsAg

Consider

  • CMV
  • > if contact with lots of children
  • HCV
  • > if high risk
  • TSH
  • > if high risk
  • sickle cell and thalasaemia screeing
  • > if high risk

Cervical screening
-if due

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15
Q

Determining GA

A

Best estimates

  • US is best estimate of EDD if
  • > before 22 weeks
  • > discrepancy with LMP larger than expected for GA
  • most accurate estimate of EDD overall
  • > CRL during first trimester
  • accepted/unchanged EDD
  • > earliest sonographic assessment made

Ultrasound

  • indications
  • > offered to all before 22 weeks
  • > irregular periods
  • > LMP unknown
  • > conception with hormonal contraception
  • > uterine size differs from LMP
  • technique
  • > TVU preferred during first trimester
  • > TAU for remainder
  • limitations
  • > multiple gestation
  • > morphology abnormalities
  • initial scan in first trimester
  • > use CRL
  • initial scan in second/third trimester
  • > BPD, HC, AC, FL

Clinical assessment

  • Naegele’s rule
  • > minus 3 months + 7 days
  • > assumes 28 day period with fertilisation on 14th
  • Uterine size (archaic)
  • > 8 = plum/10 = orange/12 = grapefruit
  • > above symphysis at 12/at umbilicus at 20
  • > cm above umbilicus after 20
  • > invalid with fibroids, obesity, twins, retroverted
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16
Q

Aneuploidy screening

A

Combined first trimester screening

  • timing
  • > 11-13+6 weeks
  • components
  • > NT = >95th centile
  • > PAPP-A = low
  • > b HCG = high
  • > maternal age
  • > gestational age
  • conditions tested (66% of all aneuploidies)
  • > trisomy 21 (Down)
  • > trisomy 13 (Patau)
  • > trisomy 18 (Edwards)
  • performance for 21
  • > sensitivity = 85%
  • > FPR = 5%
  • soft markers increase sensitivity/specificity
  • > nasal bone/DV waveform/tricuspid flow
  • confounders
  • > maternal weight
  • > smoking
  • > IVF
  • report of results
  • > risk of disease

Cell free DNA

  • timing
  • > from 10 weeks
  • > consider as secondary screen
  • components
  • > maternal serum taken
  • > fetal fraction and number of sequence specific chromosomes = presence of aneuploidy
  • > offer early anatomy US @ 11-13 weeks
  • conditions
  • > autosomal trisomies (21/13/18)
  • > sex chromosome aneuploidies
  • > micro deletions (diGeorge) not recommended
  • unable to provide a result in approx 5%
  • > early GA
  • > suboptimal collection
  • > low FF in obese mothers/fetal karyotype/IVF
  • private cost approx $400
  • trisomy 21 performance
  • > sensitivity = 99%
  • > specificity = 99%
  • > PPV = 90%
  • causes of inaccuracies
  • > placental mosaicism
  • > maternal mosaicism
  • > vanishing twin
  • > copy number variants
  • > maternal cancer
  • report of results
  • > positive/negative
  • > high risk/low risk

Second trimester testing

  • maternal serum screening (PPV = 3%)
  • > at 15-20 weeks
  • > maternal age
  • > AFP
  • > b HCG
  • > UE3
  • > Inhibin
  • cfDNA (from 10 weeks)
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17
Q

Initial antenatal genetic counselling

A

Discuss

  • patient hx
  • > concerns
  • > family hx
  • > risk factors
  • genetic conditions
  • > information on common genetic conditions
  • > risks for pregnancy, baby and beyond
  • > concept of phenotypic variability
  • genetic testing
  • > description of available tests
  • > benefits and limitations of different tests
  • > screening vs diagnosis
  • > risk of unexpected findings without solutions
  • > private costs
  • implications
  • > continue or terminate pregnancy
  • > palliate baby with terminal illness
  • > timing and restriction of abortion methods
  • supports and further information
  • > referral to genetic counselling
  • > written information
  • > support groups

Aneuploidies

  • screening tests
  • > combined first trimester screening
  • > second trimester screening
  • > cell free DNA
  • diagnostic tests
  • > amiocentesis
  • > chorionic villus sampling

Carrier screening

  • pre-conception screening preferred
  • > pre-implantantion genetic testing etc
  • monogenic diseases tested
  • > fragile X
  • > cystic fibrosis
  • > spinal muscular atrophy
  • > haemoglobinopathies
  • most adults +ive for 3 severe recessive disorders
  • > most are autosomal
  • couples or sequential screening
  • extended panel
  • > offered to at risk groups
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18
Q

Down syndrome prenatal diagnostic tests

A

Indications

  • > patient preference (before screening)
  • > postive genetic screen

Relative contraindication

  • > alloimmunisation
  • > HIV
  • > Hep B/C

Amniocentesis

  • timing
  • > from 15 weeks gestation
  • > before = high risk adverse outcomes
  • procedure
  • > withdraw amniotic fluid using needle
  • > ultrasound guidance
  • post procedure care
  • > uterine cramping normal
  • > spotting/amniotic fluid leak immediately after
  • risks
  • > rupture of membranes
  • > indirect fetal injury (talipes/respiratory)
  • > direct fetal injury (rare
  • > fetal loss = 0.5% (1/200)
  • > infection (rare)

Chorionic villus sampling

  • timing
  • > from 11 weeks
  • > before = high risk complications
  • procedure
  • > tertiary institute
  • > ultrasound guided
  • > transabdominal/transcervical approach
  • > placental tissue aspirated into syringe
  • > mild pain
  • post procedure care
  • > no exercise or sex 24hrs
  • > some light spotting is normal
  • risks
  • > fetal loss approx 1% (1/100)
  • > transverse limb reduction defects
  • > sampling failure
  • > vaginal bleeding
  • > infection (rare)

Assessment of sample

  • extremely low false negative rate
  • > variants of unknown significance in 5%
  • methods
  • conventional karyotyping
  • FISH
  • chromosomal microarray
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19
Q

Diet advice initial antenatal visit

A

Diet

  • opportunity for intervention
  • > importance of well balanced diet
  • > referral to dietician/written information
  • caloric intake
  • > no need for increase in first trimester
  • > increase is only small in second/third trimester
  • > eating for two is misnomer
  • avoid
  • > raw/smoked meats/fish (listeria/toxoplasmosis)
  • > soft cheeses/pate (listeria)
  • > unpasteurised milk/cheese (brucellosis)
  • > large predatory fish (mercury)
  • > high caffeine intake
  • > sugar sweetened beverages (childhood obesity)
  • > artificial sweeteners appear safe
  • vegetarian
  • > balanced diet probably ok
  • > supplement vitamin D/E and iron
  • vegan
  • > also deficient in calcium, B12, omega 3 fatty acids
  • low carbohydrate
  • > deficient in folate

Supplements

  • multivitamin
  • > may not be needed in well nourished mothers
  • > prudent to presribe empirically
  • goals
  • > iron 30mg
  • > calcium 1000mg
  • > vitamin D 600IU
  • > folic acid 0.4-0.8mg (increase with gestation)
  • iodine
  • > adequate intake avoids hypothyroidism
  • > 250mcg recommended
  • > may be replete is consuming fortified foods (eg salt)
  • > excess intake can cause fetal goiter
  • vitamin A
  • > main concern is excess intake (teratogenic)
  • > avoid supplements containing >1500mcg
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20
Q

Lifestyle advice initial antenatal visit

A

Substance use

  • Alcohol
  • > FASD = neurodevelopmental/ID/craniofacial
  • > possibly preterm/LBW/IUGR
  • > consider withdrawal and thiamine
  • Smoking
  • > approx 1.5 x miscarriage/still birth/SIDs
  • > approx 3x PPROM/preterm/LBW/abruption
  • Cannabis
  • > approx 3x perinatal morbidity/mortality
  • > risk of preterm/low birth weight
  • > long term neurodevelopment delay/ADHD
  • Amphetamines
  • > approx 3x fetal/neonatal death and preterm
  • > many other obstetric complications
  • Cocaine
  • > approx 3x preterm and LBW
  • > placental abruption
  • Opioid
  • > broad range of obstetric/neonatal complications
  • > heroin = Rh/HIV/IE/Hep B/C risk
  • > methadone substitution recommended

Exercise

  • standard exercise prescription
  • > controls gestational weight gain
  • > less lower back pain
  • > potential reduction pre-eclampsia/GD
  • small risk
  • > trauma leading to abruption
  • caution
  • > high intensity for long duration
  • > high level in IUGR/threatened pre term

Infection control

  • Influenza vaccine
  • > at any stage if during winter
  • DPT booster
  • > in third trimester
  • STDs
  • > advise barrier method if high risk
  • CMV and parvovirus
  • > good hand hygiene
  • > caution around children
  • Varicella
  • > pre conception vaccination
  • > IvIg available if unvaccinated exposure
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21
Q

Labour protraction/arrest background

A

Epidemiology
-approx 20% labours

Aetiology

  • risk factors
  • > highest risk in nullips
  • > abnormal pregnancy/fetal abnormality
  • > short stature/obesity/macrosomia/post term
  • > neuraxial anaesthesia

Pathophys

  • hypocontractile uterus
  • > diagnoses by palpation/tocodynamometry
  • > weak/infrequent (<3-4/10)/short (<50seconds)
  • cephalo-pelvic disproportion
  • > usually due to malposition (extension/OP/OT)
  • > floating head at 7cm
  • non occiput anterior positioning
  • > length of labour/caesarian risk correlates with rotation
  • > often start OT/OP and rotate
  • bandl’s ring
  • > rare complication of second stage
  • > hourglass contracture between upper/lower uterus
  • neuraxial anaesthesia
  • > does not impact on first stage
  • > longer second stage/more oxytocin and instrumentation
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22
Q

Evaluation and management prolonged labour

A

Review 3 P’s

  • Power
  • > uterine contractility
  • > maternal effort
  • Passenger
  • > presentation/position
  • > physical abnormalities
  • Passageway
  • > history of pelvic trauma etc
  • > maternal size, known anatomical abnormalities

Additional signs

  • CTG
  • > baseline/variability/accelerations/decelerations
  • liquor
  • > clear = reassuring
  • > bloody = normal if clears
  • > meconium stained = mature or distressed baby
  • obstructive signs
  • > caput
  • > moulding (significant override of sutures)
  • > haematuria (irritation of bladder)

Latent first stage protraction

  • definition
  • > no accepted threshold
  • > can be many hours or days
  • management
  • > counselling on normality/reduce anxiety
  • > therapeutic rest if tired (morphine <20mg)
  • > oxytocin if ready
  • > neuraxial anaesthesia

Active first stage protraction

  • definition
  • > dilating <1cm/hr after 6cm
  • > more than 7hrs for 4 to 5cm
  • > more than 4hrs for 5 to 6cm
  • high dose oxytocin (vs low dose)
  • > increased tachysystole (avoid in VBAC)
  • > decreased caesarian/increased vaginal delivery
  • > similar maternal/neonatal outcomes
  • amniotomy
  • > chemical stimulation/mechanical advantage
  • > contraindicated when not engaged (cord prolapse)
  • > best evidence when combined with oxytocin

Active first stage arrest

  • definition
  • > 6cm with ruptured membranes plus
  • > no change >4hrs with good contractions
  • > no change >6hrs with inadequate contractions
  • management
  • > caesarian section

Second stage

  • failure to progress
  • > 2hrs for nulip (95th = 3.5hrs)
  • > 1hr for multip (95th = 2hrs)
  • > longer for neuraxial anaesthesia
  • consider oxytocin after 60-90mins
  • consider passive decent
  • > one hour without pushing if high station
  • consider manual rotation manoeuvres
  • consider operative delivery
  • > fetal/maternal demise with high change of success
  • consider need for caesarian
  • > failure to progress
  • > denies or contraindication for operative delivery
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23
Q

management first stage labour

A

Initial assessment

  • review
  • > pregnancy/complications/fetal wellbeing
  • > routine bloods/Rh/GBS/STDs
  • vitals
  • > BP/HR/temp
  • > frequency/quality/duration contractions
  • > fetal heart rate
  • abdo
  • > lie (longitudinal/transverse/oblique)
  • > presentation (cephalic/breech)
  • digital exam
  • > baseline cervix status (dilation and effacement)
  • > integrity of membranes
  • > presence of bleeding
  • > position (occiput position)
  • > > station (-5 to +5/ischial spines = 0)
  • investigations
  • > UA for protein (pre-eclampsia) if membranes intact

General management

  • fluid and foods
  • > avoid foods where possible
  • > clear fluids improve outcome (consider anaesthetic risk)
  • > consider dextrose/fluid infusion
  • infection prophylaxis
  • > GBS
  • > no need for empiric antibiotics
  • positioning and activity
  • > no evidence for any preference
  • > move and position as comfortable
  • pain control
  • >
  • fetal heart rate monitoring (low risk)
  • > consider 30 mins external continuous upon admission
  • > intermittent auscultation preferred
  • > every 30 mins during active first stage
  • > every 15 mins second stage
  • > intermittent auscultation
  • fetal heart rate monitoring (high risk)
  • > continuous external from admission
  • additional monitoring
  • > external tocodynamometry
  • > cervical progress every 4 hrs
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24
Q

Intrapartum fetal heart rate monitoring

A

Types of monitoring

  • External fetal heart rate
  • > continuous doppler on maternal abdo
  • > intermittent auscultation (90s during + 30s post)
  • Internal fetal heart rate
  • > bipolar spiral electrode on fetal scalp
  • > less noise, more accurate RR
  • Continuous compared to intermittent auscultation
  • > no difference in death or long term neuro outcomes
  • > more caesarians and instrumental/less vaginal births

FHR signals

  • Normal baseline
  • > 110-160
  • Baseline bradycardia
  • > hypothermia/oxaemia/glycaemia/thyroidism
  • > heart block
  • Baseline tachycardia
  • > infection/maternal fever
  • > hyperthyroid
  • > anaemia
  • > catecholamines
  • > arrhythmia
  • > hypoxaemia
  • HRV
  • > normal =5-25bpm
  • > presence of normal variability is reassuring
  • > absence/reduced is poor predictor of acidaemia/hypoxia
  • Accelerations (>+15 for 15s)
  • > presence is reasurring
  • > absence is poor predictor of acidaemia/hypoxia
  • Early decelerations (normal response to fetal head compression
  • > with peak of uterine peak contractions
  • Late deceleration
  • > occur post peak uterine contraction
  • > fetal hypoxia due to constriction of uterine arteries
  • > insignificant when with good variability and accelerations
  • > recurrence with minimal variability/accelerations is bad
  • Variable decelerations
  • > due to cord compression
  • > initial compression of umbilical veins = increase FHR
  • > compression of umbilical artery follows = decrease FHR
  • > uterine relaxation = effects occur in reverse
  • > concerning, requires close attention
  • Prolonged deceleration (due to fetal hypoxia of any cause
  • > up to 2 mins = non reassuring
  • > more than 3 mins = abnormal
  • > more than 10 mins = new baseline (severe hypoxia)
  • Sinusoidal pattern
  • > 3-5 cycles/minute for 20 minutes with no variability
  • > severe hypoxia or fetal anaemia
  • > rare and very concerning
25
Operative delivery
- operative delivery indications - >maternal exhaustion/prolonged second stage - >engaged/position known/cephalic/adequate anaesthesia - >consider for maternal/fetal compromise - operative delivery containdications - >three prior attempts - >extremely premature - >bone or bleeding disorder - >face or brow presentation/unengaged/unknown - >cephalopelvic disproportion
26
POCS background
Epidemiology -approx 10% of women of reproductive age Aetiology - unknown - heritability = approx 75% - >multiple genes contributing small risk - environmental - >obesity and hyperinsulinaemia - >congenital adrenal hyperplasia and androgenism Pathophys - Functional ovarian hyperandrogenism - >dysregulated LH driven thecal androgen production - >causes hirsutism - >high androgens = increased primary follicle recruitment - >increased synergism with FSH = premature luteinization - >increased recruitment + premature luteinization = PCOM + oligo-anovulation - Insulin resistant hyperinsulinism - >causes and worsened by obesity - >sensitises theca cells to LH = increased androgens - High LH - >androgen excess disturbs sex steroid inhibition of LH - >high insulin decreases SHBG by liver - Excess adrenal androgens - >enhanced responsiveness to ACTH - >similar action to ovarian androgens
27
PCOS evaluation
Hx - often presents in puberty - hirsutism/acne/alopecia - oligo-anovulation - >primary amenorrhoea (no menarche by 15) - >secondary amenorrhoea (no menses for three cycles) - >oligomenorrhoea = <9 menses/year (less during puberty) - >AUB = menses <21 apart/ >7 days long/ very heavy - weight gain - infertility - medications associated with hirsutism? Exam - HTN - hyperandrogenism - >male hair growth/loss - >acne - >deep voice/clitoromegaly/increased muscle mass - obesity - acanthosis nigricans - abdo exam - >adrenal tumour - pelvic exam - >ovarian tumour Investigations - Androgens (day 3 follicular phase) - >total and free (SHBG) testosterone - >dehydroepiandrosterone sulfate (DHEA-S) - >androstenedione (A4) - 17 hydroxyprogesterone - >early morning during (day 3 follicular phase ) - >anytime if amenorrhea - >low rules out non classic congenital adrenal hyperplasia - Luteal phase (7 days before menses) progesterone - >high levels = ovulation - Rule out other causes oligomenorrhoea/anovulation - >b HCG = pregnancy - >prolactin = prolactinoma - >TSH = hypothyroidism - >LH:FSH = >3 in PCOS, low in hypothalamic disease - Tranvaginal ultrasound (if criteria not already met) - >PCOM = ovarian volume >10mL/12 follicles in either - Additional tests - >GTT - >lipids Diagnosis - 2/3 (all three for puberty) of Rotterdam criteria - >oligo/an-ovulation (present for 2yrs if pubertal) - >PCOM - >clinical or biochemical hyperandrogenism - exclude other causes
28
Hirsutism ddx
PCOS + CODEIN - Cushings - >disease (corticotroph adenoma) - >syndrome (adrenocortical tumour) - Ovarian tumour - >sertoli-leydig - >theca-granulosa - Endocrine - >hypothyroidims - >prolactinoma - >acromegaly - Idiopathic - Non classical congenital adrenal hyperplasia
29
Primary amenorrhoea background
Epidemiology -<0.1% Aetiology - Hypothalamus - >constitutionally delayed growth and puberty - >idiopathic hypogonadotropic hypogonadism - >Kallman's syndrome - Pituitary - >prolactinoma - Ovaries - >PCOS - >primary hypogonadism (Turner's/injury/insult) - >androgen insensitivity syndrome - Uterus/cervix/vagina - >mullerian agenesis - >transverse vaginal septae - >imperforate hymen - Adrenal - >NCCAH - Thyroid - >hypothyroidism - Systemic (functional hypothalamic amenorrhoea) - >anorexia nervosa - >excessive weight gain/loss - >stress - >female athlete triad
30
Menopause background
Epidemiology - average is 51yrs - >5% <45 - >5% >55 Aetiology - family history of age - smoker = earlier - hysterectomy with persevered ovaries = earlier Pathophys - several million oocytes present by approx GA 15 - primary follicles form at this time - continuous follicular atresia - >begins in utero - >steady decline in oocytes over lifespan - late reproductive (40's) - >lower inhibin and progesterone - >declining fertility - >ovulatory cycles with shorter follicular phase - perimenopause - >significant depletion of oocytes - >variable length (yrs) - >high FSH/low inhibin/low AMH - >highly variable estrogen and low luteal progesterone - >irregular/anovulatory periods - menopause - >process continues until 12 months of amenorrhea - post menopause
31
Evaluation peri/menopause
Clinical manifestations - late productive - >infertility - perimenopause - >irregular menses - >prolonged time between cycles - >occasionally heavier bleeding - hot flash (most common symptom) - >can begin in late reproductive - >most common late peri/early post - poor sleep - >often due to hot flushes or anxiety/depression - depression - >mostly perimenopausal - vaginal atrophy - >dryness - >irritation - >dyspareunia - dyspareunia - >decreased lubrication - >vagina is shorter, narrower and less elastic Complications of oestrogen withdrawal - cardiovascular disease - >increase in LDL - bone health - >decreased BMD and increased osteoporosis - decreased collagen content in skin - impaired balance - central adiposity ``` bHCG Consider -FSH -TSH -prolactin ```
32
Primary amenorrhoea evaluation
Hx - no menarche by age 15 +/- pubarche - Hypothalamus - >pubertal development (constitutional delay) - >stress/weight gain and loss/eating/ exercise - >anosmia - Pituitary - >headaches - >blurred/loss vision or diplopia - >galactorrhea - Ovaries - >stature relative to family (Turners) - >hirsutism/acne/weight (PCOS) - Uterus - >cyclical pelvic pain (anatomical abnormality) - Adrenals - >neonatal crisis (NCCAH) - Additional - >family hx of delayed puberty (constitutional) - >medications Exam - height/weight/BMI - inspect - >acne/hirsutism/pigmentation/virilisation - >syndromic features - >pubertal development - >outflow tract abnormalities - consider - >neuro exam for pituitary mass - >bi manual for outflow tract abnormalities bHCG TSH prolactin FSH and estradiol -high FSH/low estradiol = primary ovarian failure (Turners) -low FSH/low estradiol = hypothalamic failure Ultrasound pelvis -presence/absence of uterus/ovaries/cervix Consider - Karyotyping - >if uterus present/high FSH = Turners - >if uterus absent = 46 XX (genesis)/46XY (androgen insensitivity syndrome) - Androgens (PCOS) - >presence of hirsutism/acne/virilisation - MRI brain (sellar mass) - >if uterus present/low FSH/no breast development - >no mass = constitutional/functional hypothalamic/idiopathic hypogonadotropic hypogonadism
33
Background secondary amenorrhoea
Epidemiology -approx 3% Aetiology - Hypothalamus - >weight loss/athlete triad/anorexia - Pituitary - >prolactinoma (inhibits GnRH) - Thyroid - >hypothyroid (high TRH increase prolactin release) - Ovaries - >PCOS - >premature ovarian failure (radiation/chemo/fragile X/autoimmunity) - Uterus - >pregnancy - >ashermans Hx - pregnancy risk/symptoms - hypothalamus - >stress/eating/exercise - >medications (COCP/antipsychotics/metaclopramide) - pituitary - >headache/vision changes/galactorrhoea - ovaries - >hirsutism/acne/virilisation - >menopause symptoms - uterus - >bleeding/infection/curretage Exam - height/weight/BMI - inspect - >virilisation/pigmentation - >galactorrhoea - >vaginal atrophy ``` bHCG FSH and estradiol ->both low = hypothalamus/pituitary disease ->FSH high/estradiol low = POI prolactin TSH ``` Consider - PCOS testing - karyotyping if FSH high - MRI brain if FSH/estradiol low - progestin challenge if normal labs - >10mg medroxyprogesterone for 10 days - >absence of bleeding supports ashermans
34
PCOS treatment
Desiring fertility - weight loss - >ovulation in approx 80% - >may take 6-9 months - metformin - >500mg TDS titrated over 4-6wks - >1500-2000mg once daily extended release - >take with food - >may take 6-9 months to worse - >may be less effective in overweight/obese - fertility pharm - IVF - laparoscopic drilling - >pregnancy in approx 50% - >similar efficacy to fertility pharm/less multiple pregancy - >no evidence for POI Not desiring fertility/hyper-androgenism - weight loss - >less effective - COCP - >anything but levonorgestrel - Eflornithine cream BD - >effective in about 1/4 by 2 months - >can cause local reactions/acne - Spirinolactone (anti-androgen) - >50-100mg BD - >combine with OCP (teratogenic) - Consider adding metformin to OCP/spirinolactone Not desiring fertility/oligo-amenorrhoea - weight loss - >returns ovulation in up to 80% - >may take 6-9 months - OCP - >progestogen protects endometrium - >avoid levonorgestrel - progesterone (protect endometrium) - >mini pill - >Mirena
35
GBS infection
Epidemiology - 10-20% colonisation of vagina/rectum - >neonatal colonisation rate = 40-50% - >early infection rate = 0.5-0.05% Aetiology - Risk factors - >prematurity - >prolonged rupture of membranes (>18hrs) - >maternal fever - >heavy maternal colonisation - >low level maternal/fetal serotype specific Ig - >previous infant with early GBS disease - Neonatal infection - >intra-amniotic infection (with intact membranes) - >passage through birth canal - >contact with outside environment Pathophys - early onset <24hrs - >sepsis (most common) - >pneumonia - >meningitis - late onset <90 days - >fever/bacteraemia (most common) - >meningitis - >septic arthritis/osteomyelitis - >cellulitis - mortality - >overall = 3% - >pre-term early = 30% - morbidity - >CP - >ID - >seizures - >hearing/vision loss
36
GBS colonisation screening and management
Screening - rectovaginal swap/culture for all women - >false negative approx 5% - timing - >general = 35-37wks - >high risk for preterm = 3-5wks prior to EDD - exceptions - >GBS bacteruria/previous infant GBS = empiric rx Labour management - Intrapartum antibiotics - >IV penicillin G or ampicillin - >at least 4hrs prior to delivery - >reduces risk of early disease by 80% - >risk of late onset unchanged - Indication for intrapartum antibiotics - >GBS+/GBS bacteruria - >previous early GBS disease - >unknown status + preterm labour/PPROM/prolonged rupture of membranes/intrapartum maternal fever Scenarios - Caesarian - >not indicated for GBS+ - >abx not indicated for caesarian with intact membranes - Intrapartum procedures - >no indication for change in practice if intrapartum abx - PROM at term - >GBS+ = induction + intrapartum antibiotics - >GBS unknown = culture and risk assessment - Preterm labour GBS unknown - >intrapartum antibiotics until culture -ive - PPROM GBS unknown - >consider 48hrs of antibiotics - >take cultures - >intrapartum antibiotics - PPROM GBS+ - >if >34wks = induction + intrapartum antibiotics - >if <34wks = normal PPROM management
37
Caesarian section request
Compared to normal vaginal delivery - Positives - >delivery date known - >avoids post-term neonatal mortality increase - >avoids risk of emergency caesarian - >lower rate urinary and bowel incontinence - >lower rate pelvic organ prolapse/perineal tear - >lower rate HIE/birth injury/asphyxia - >less vertical transmission HIV/HSV - Negatives - >higher rate TTN/RDS (only if <39 weeks) - >higher neonatal mortality - >longer hospitalisation/recovery time - Same - maternal mortality rate - post partum sexual function - pain 4 months post partum Complications (HOISTED) - Haemorrhage - >approx 1L - >less than 5% need transfusion - Obstructed bowel (ileus) - >15% - Infection - >2% - Surgical error (rare) - >bowel/bladder perforation - >laceration to baby - Thrombosis (stroke/MI/VTE) - >3x vaginal delivery risk - >0.25% for VTE - Endometritis - Death - >less than 0.1% Anaesthetic risk - neuraxial - general Long term risk - abnormal placentation - >placenta accreta/previa/abruption - adhesions - hernias - nerve pain around scar VBAC - uterine rupture - >TOLAC = 0.5% (< if previous successful delivery) - >twice as high as risk with repeat caesar - outcome of rupture - >1/3rd hysterectomy - >neonatal death <3% - neonatal - >mortality 2-3x higher with TOLAC (very low) - >resus 2x higher with TOLAC
38
Caesarian section timing
Categories - 1 = immediate threat to maternal/fetal life (30mins) - 2 = compromise with no threat to life (1hr) - 3 = earlier than planned without compromise - 4 = maternal request - >possible if harm/benefit understood by patient Timing of planned/maternal request - before 39 wks - >increased risk of blood transfusion - >higher rates RDS/TTN - >higher neonatal mortality - at 39 wks - >approx 10% will require emergency CD prior to 39wks - >emergency has 2x risk of complications - after 39 wks - >increase perinatal mortality - >macrosomia - >dysmaturity syndrome
39
IUGR background
Epidemiology -approx 10% births Aetiology - Fetal - >genetic abnormality - >TORCH infections - Placenta - >pre-eclampsia - >abruption - Maternal (ACHINGS) - >age (extremes of) - >CKD - >HTN - >Insulin resistance - >nutritional deficiency - >genetics (previous SGA or personally SGA) - >SLE - Exposures - >teratogenic meds - >alcohol/smoking/cocaine/heroin/marujuana Pathophys - Foetal response to compromised nutrient supply - >redirect blood flow to brain/heart/adrenals - >reduces overall size/fat/BMD/glycogen stores - >reduces renal blood flow and oligohydramnios - >preserve brain growth - >accelerate lung maturation - >increased RBCs - >decrease - Symmetric - >proportional reduction of body components - >chromosomal or infection - >occurs early in gestation - Asymmetric (majority) - >weight/abdominal size reduced more than length/HC - >adaptation to pathological stressor - >occurs later in gestation
40
IUGR evaluation
Hx - PC - >unwell lately? - >headaches/vision changes - >loss of blood or fluid - >pain? - >fetal movements - This pregnancy - >any complications - >scans (morph + aneuploidy) + serology - Past obstetric - >G/P - >G/A and route - >small babies - >HTN/diabetes - Past medical - >any chronic illnesses - Allergies - Medications - Supplements and food avoidance - Social - >Smoking/drinking/drugs - >contact with children - >proximity for follow Exam - Height/weight/BMI - BP - Abdo palp - Fundal height - Doppler Confirm diagnosis with ultrasound - Urgent CTG - SGA - >weight below 10th centile in second trimester - >may be constitutional or restricted growth - >consider AC/AFI/growth velocity Determine cause - Fetal survey - >doppler (umbilical/uterine/middle cerebral arteries) - >BPP - Anatomy scan - >if abnormal, consider cell free DNA for aneuploidy - >if negative, consider amniocentesis for microarray - Infection workup - >maternal CMV/rubella/varicella seropositivity
41
IUGR management
Monitoring - Usually monitored as outpatients - Weight - >review every 2 weeks if concerned - >consider velocity (normal in constitutional) - US doppler - >umbilical artery most useful - >review every 2 weeks if first two are normal - >review weekly if abnormal or concerned - >reduced/absent end-diastolic flow = consider delivery - BPP or NST with AFI - >not needed if mild - >twice weekly if severe - >daily if abnormal doppler Delivery consideration - Issue - >pre term delivery has high mortality/morbidity - >each day in utero between 26-29wks increases survival up to 2% - >mortality in IUGR rises sharply at time (placental insufficiency) - GRIT trial - >randomised to immediate or delayed delivery - >when obstetrician was uncertain - >immediate group = fewer stillbirths/more neonatal deaths - >long term neurodevelopment outcome similar - DIGITAT trial - >randomised to spontaneous/expectant at term - >spontaneous had lower birth weight - >same adverse events/same caesarian rate/long term developmental outcomes - Consider - >dopplers/BPP/NST/risk factors - >gestational age - >patient preference - >need for caesarian delivery if poor dopplers - >corticosteroids and magnesium sulfate Intrapartum - Issues - >intrapartum heart rate abnormalities - >birth asphyxia/HIE - >meconium aspiration - >polycythaemia - >hypothermia - >hypoglycaemia - Approach - >continuous fetal heart monitoring - >low threshold for emergency caesarian - >neontal support present - >umbilical blood gas and glucose at birth Long term - catch up growth - CVD/diabetes/renal disease/neurodevelopment
42
ectopic pregnancy background
Epidemiology - approx 1% of all pregnancies - up to 15% of first trimester bleeding Aetiology - risk factors (ASEPTIC) - >age (older) - >smoking - >ectopic pregnancy in previous pregnancy - >PID - >tubal abnormalities - >infertility and IVF - >contraception failure (IUD/COP) Pathophys - anatomic sites - >fallopian tubes (more than 95%) - >ovarian - >interstitial - >abdominal - >cervical - >hysterectomy scar - >intramural - >heterotopic
43
Evaluation ectopic pregnancy
Hx - onset of symptoms usually after 8 weeks gestation - vaginal bleeding - lower abdo pain - >sharp or dull (not crampy) - >diffuse or localised - pregnancy related symptoms - rupture - >acute severe pain - >severe bleeding - >syncope - >shoulder tip pain - >tenesmus = blood in pouch of douglas - review risk factors - review surgical/medical fitness Exam - often unremarkable - vitals - >assess for shock - >postural hypotension - abdo - >tenderness - >acute abdomen in rupture - speculum - >source of bleeding - pelvic - >adnexal mass/tenderness - >cervical motion tenderness with rupture Investigations - unstable - >FAST scan for intraperitoneal haemorrhage - b HCG (urine or serum) - >confirms pregnancy - FBC - >anaemia - >baseline for methotrexate - blood group and antibodies - >hold if significant bleeding - >sensitising event (anti D) - EUCs and LFTs - >methotrexate baseline - Transvaginal ultrasound Transvaginal ultrasound - Confirms ectopic - >gestational sac with yolk sac/embryo at ectopic site - >adnexal mass/empty uterus/free fluid - Suggests ectopic - >pseudosac - >complex extra ovarian adnexal mass - >tubal donut sign - >adnexa ring of fire sign on doppler - >consider heterotopic - Suggests rupture - >fluid in morrisons or douglas' pouch - Absence of findings - >follow PUL protocol
44
medical management ectopic pregnancy
Indications - >patient preference - >stable - >b HCG <5000 - >no cardiac tones / ectopic mass <3-4cm Contraindications - >unstable - >evidence of threatened rupture - >viable IUP/heterotopic - >liver/renal/pulmonary disease - >immunosuppression or peptic ulcers - >abnormal FBC, EUCs, LFTs - >breastfeeding Risks - approx 1/3 experience side effects - >stomatitis - >conjunctivitis - treatment failure approx 20% Benefits - >avoids surgical complications - >similar efficacy to surgery when adequate doses given - >similar fertility outcomes to surgery - >similar risk as surgery of further ectopic pregnancies Procedure -IM single dose Monitoring - b HCG on days 4 and 7 - b HCG weekly until 0 - inadequate decrease - >repeat dose (no more than three total) Advice - >avoid conception for 4 months - >avoid folic acid supplements and NSAIDs - >avoid sunlight - >mild pain at 1 week is common - >severe pain needs to be investigated
45
surgical management ectopic pregnancy
Indications - any b HCG level - unstable - rupture or impending rupture - heterotopic ectopic - methotrexate contraindications - methotrexate failure Contraindications -no absolute Risks -surgical and anaesthetic risks Procedure - salpingectomy vs salpingostomy - >similar rate of future fertility - > salpingostomy = higher rate of retained/future ectopics - laparoscopic vs laparotomy - >laparoscopic preferred - >laparoscopic = less blood loss, faster operation, recovery and discharge - >consider laparotomy for interstitial or unstable Follow up - salpingostomy - >GP 3 weeks post op - >weekly b HCG until negative - >insufficient b HCG decrease = methotrexate - salpingectomy - >post op b HCG unnecessary if histopath confirmed - future conception - >no solid data - >0-3 months common
46
expectant management ectopic pregnancy
Indications - asymptomatic - no TVU findings of ectopic pregnancy - low (<1500) and decreasing b HCG - aware of risks - access to emergency treatment and close follow up Contraindications -any of indications absent Risks -rupture can occur with low and falling b HCG Benefits - similar success rate (80%) to medical management - similar treatment time as medical management Procedure - b HCG every 48hrs for 8 days - >then weekly until negative - abandon expectant management if - >any symptoms - >b HCG not decreasing - avoid conception until sonographic resolution
47
Rh incompatability
Epidemiology - Rh -ive - >15% of caucasians - >7% africans - incompatibility in 10% pregnancies Aetiology - Rh -ive mother - Rh +ive baby - >inherited from father Pathophys - sensitising event - >occurs in majority of pregnancies - >fetomaternal haemorrhage (most placental insults) - >passage of fetal cells across placenta - formation of maternal anti-D Ig - >formation of memory B lymphocytes - >future challenge leads to plasma cell Ig production - haemolytic disease of the new born - >maternal Ig cross placenta attache to fetal RBC - >RBCs sequestered in spleen and destroyed - >extramedullary haematopoeisis - >hepatosplenomegaly/pHTN/HF/cerebral hypoxia - >hydrops fetalis/intrauterine death Screening for incompatibility - blood group, Rh status, antibodies - >first antenatal visit - >Rh -ive repeated at 24-28wks - >after any sensitising event Diagnosing incompatibility - if mother Rh antibody +ive - >paternal blood group - Paternal zygosity if Rh +ive (PCR for RHD genes) - >if homozygous = fetus Rh +ive - >if heterozygous = 50% chance fetus Rh +ive - Amiocentesis (>15wks) or cfDNA (>10wks) if heterozygous Monitoring incompatability - Baby Rh +ive - >serial (monthly) maternal indirect coombs - If antibody titre rises above critical threshold - >doppler MCA for severe anaemia ever 1-2wks - If suspected sensitising event - >rosette test = presence of fetal RBC in maternal blood Sensitisation prevention - Rh incompatibility diagnosed - >maternal Ig present = no benefit of anti-D - >routine prophylaxis = anti-D at 28wks - >fetomaternal haemorrhage = anti-D - >sensitising procedure = anti-D 72hrs prior - >delivery = additional anti-D 72hrs prior - Dosage - >Kleihauer test/flow cytometry = %fetal RBC
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Diabetes pregnancy background
Epidemiology - GD = approx 10% pregnancies - pre-existing = 2% pregnancies Aetiology - pre-existing - GD risk factors - >older age - >personal hx - >family hx - >obesity - >physical inactivity - >high GI/low fibre diet - >smoking - >PCOS Pathophys GD - relative insulin resistance normal part of pregnancy - >ensures adequate glucose delivery to fetus - >most marked resistance in 3rd trimester - diabetogenic hormones released by placenta - >growth hormone - >prolactin - >lactogen - >progesterone - GD develops when maternal beta cells are overwhelmed Shared complications - short term - >LGA = preterm/caesarian/instrumental/dystocia/injury - >polyhydramnios = BPD/preterm/malposition - >pre-eclampsia - >neonate = hypoglycaemia/jaundice/CMP/cardiac/resp - long term - >increased risk of T2DM - >child = obesity/metabolic syndrome/diabetes Pre-existing complications - Congenital defects - >2-4%x base (incidence apex 5%) - >CCHD/neural tube defects - IUGR - Pre-eclampsia/HTN - Miscarriage - Aggravates underlying micro/macrovascular disease - DKA more common - >occurs at higher BGL - >more lethal for mother (fetal demise also common)
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Diabetes pregnancy evaluation and non BGL management
Screening - first antenatal visit - >all women - >low risk GD = BGL/high risk GD = GTT - >pre-existing = HbA1c/UACR/GFR/TSH/fundoscopy - 24-28wks - >all women GTT Diagnosis - GTT - >NBM for 8hrs prior - >fasting glucose - >75g glucose - >glucose at 1 hr - >glucose at 2hrs - GDM criteria - >fasting = >5.1 - >1hr = >10.0 - >2hr = >8.5 - pre-existing diabetes - >if diagnostic criteria met <1st trimester 1st trimester - Pre-existing - >cease ACEI/ARB - >low dose aspirin after 12wks - >higher folic acid supplementation 2nd trimester -morph/neural tube scan at 20wks 3rd trimester - GD and good control/lifestyle only - >fetal movements may be sufficient - >growth scans close to term - Poor control/pre-existing - >NST/ST/BPP from 32 wks - >serial growth scans from 32 wks - >increase insulin if steroids given Labour - Timing - >consider induction after 39/before 40wks - Route - >consider delivery at term for macrosomia - >consider caesarian for macrosomia >4.5kg - Intrapartum - >maternal glucose monitoring (fetal hypoglycaemia) - >continuous FHR - Post partum - >neonatal glucose monitoring - >loss of insulin resistance with placental delivery - >monitor glucose for 24-72hrs (unrecognised T2DM)
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Diabetes pregnancy BGL management
Diet - referral to dietician - >caloric needs individualised - >determined by baseline and GA - best evidence for low GI diet (vs low carb/calorie restricted) - >less insulin requirements - >lower birth weights - some evidence for increasing folic acid supplementation Exercise - moderate intensity exercise - >increased muscle mass = increased insulin sensitivity - >lower blood glucose levels - >less insulin requirements Insulin therapy - after lifestyle trial for 2-4wks - trial intermediate acting basal insulin at bedtime - >approx 6 units - assess fasting BGL over week - >more than 3 > 5 = increase by 2 units - >more than 3 > 6 = increase by 4 units - >more than 3 > 8 = increase by 6 units - avoid prolonged fasting at night - >paradoxically raises morning fasting levels - consider adding pre-prandial rapid acting bolus - >split approx 50% of total daily dose across meals Glucose self monitoring - 4x daily - >fasting/waking - >post prandial (1-2hrs) - log in book Glucose targets - fasting <5.3 - 1hr post prandial <7.8 - 2hr post prandial <6.7
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Causes cervicitis
Infectious - endocervix - >chlamydia (most common overall) - >gonorrhoea - ectocervix - >HSV - >trichomonas - other - >tuberculosis - >mycoplasma genitalium - >GAS Non infectious - mechanical - >condoms/diaphragms/tampons - >surgical instrumentation - chemical - >latex - >douching - >spermicides - systemic disease - >bechets - >lichen planus
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evaluation cervicitis
Hx - mucopurulent discharge - abnormal bleeding - >post coital - >intermenstrual - dyspareunia - vulvovaginal irritation/pruritis/burning - with concomitant urethritis - >dysuria - absence - >abdo/pelvic pain - >fever - presence of risk factors Exam - abdo - >tenderness? - speculum - >erythematous/oedematous vulva (may be normal) - >erythematous/tender vagina - >oedematous/erythematous/friable cervix with discharge - typical lesions - >strawberry cervix = trichomoniasis - >ulcerations/vesicles = HSV - bimanual to exclude PID - >cervical motion/uterine/adnexal tenderness? Investigations - b HCG - NAAT - >men = first catch urine/urethral swab - >women = first catch urine/self swab/endocervical swab - Culture (gonorrhoea sensitivity) - >thayer martin/charcoal enriched swab - >male = clinician urethral - >female = endocervical - Gram stain (provisional dx from gram -ive diplococci) - >male urethritis only (clinician collected) - Consider if typical lesions - >HSV serology - Consider if high risk/STI confirmed - >HIV - >syphilis - >Hep B/C Empiric management - if concern for PID in high risk - >empiric PID treatment - if high risk - >consider empiric chlamydia treatment Gonorrhoea management - targeted antibiotics - >ceftriaxone 500mg IM single dose - test of cure unnecessary - contact tracing/prophylactic treatment - >sexual partners for past 2 months - avoid sex for 7 days - >post treatment of index patient and partner Chlamydia management - targeted antibiotics - >azithromycin 1g oral single dose - >doxycycline 100mg oral BD 1 week - test of cure at 3 weeks - >pregnant - >PID - contact tracing/prophylactic treatment - >sexual partners for past 6 months - avoid sex for 7 days - >post treatment of index patient and partner
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PID background
Epidemiology - most common gynaecological reason for hospitalisation - risk factors - >under 25 - >multiple partners/new partner - >infrequent condom use - >previous STD/partner with STD Aetiology - majority - >chlamydia - >gonorrhoea - occassionaly - >mycoplasma genitalium - >gram negative enterics - >haemophilus influenzae Pathophys - infection of cervix with chlamydia/gonorrhoea - >disruption of protective barrier - >ascent of micro-organisms - complications - >recurrence - >chronic pain - >tuba-ovarian abscess - >hydro-salpinx - >ectopic pregnancy - >infertility (<20%) - >fitz-hugh curtis syndrome
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PID evaluation
Hx - may be asymptomatic - lower abdo pain - >often bilateral - >worse with jarring movements - >may have RUQ pain - nausea/vomiting - abnormal vaginal bleeding - >intermenstrual - >post-coital - >menorrhagia - mucopurulent discharge Exam - fever - abdo - >tenderness (bilateral) - >rebound tenderness/bowel sounds? - speculum - >discharge at endocervix - bi-manual - >cervical motion tenderness - >uterine tenderness - >adnexal tenderness - Beta HCG - Vaginal discharge wet mount - >absence of WCC has negative predictive value - Endocervical swab - >NAAT for gonorrhoea/chlamydia - >culture for gonorrhoea - FBC - CRP/ESR - Consider - >blood cultures - >US of fallopian tubes/ovaries/endometrium (severe) - >CT (peritonitis/equivocal US) - >laparoscopy (complicated/resistant/ddx suspected) - If high risk - >HIV/HBV/HCV/syphilis
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PID management
Empiric management - criteria - >high risk - >lower abdo pain/positive bi-manual - regime - >cetriaxone 500mg IM single dose - >azithromycin 1g oral single dose - >metronidazole 500mg BD for 10 days Additional - Analgesia - Patient education - >causes/risks/prevention - >prognosis/complications - >avoid intercourse for 7 days post treatment - Insufficient evidence for removal of IUD - Disposition - >generally outpatient - >inpatient if resistant/severe/complications - Safety net - >reassess in 24-48hrs - >present to hospital if its gets worse - Contact tracing - >any partner within 60 days = investigation - >no partner within 60 days = last partner - >consider empiric treatment - Test of cure - >repeat chlamydia/gonorrhoea within 3 months
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Menopause treatment
Opportunity for general health check - cst - mammogram - smoking/alcohol advice - cvd risk factors - weight control Non pharm - exercise and weight loss - >CVD risk - avoid alcohol/caffeine/spicy foods - >VMS - layered clothes/cool water/sprays - >VMS Intact uterus (including post-ablation) HRT - Perimenopausal (need contraception) - >low dose OCP - >Mirena + oestrogen - >cyclical HRT + barrier - 1-5 years post menopause - >continuous combined HRT - >Mirena + oestrogen - >Tibolone (no progestogen needed) - Over 5 years post menopause - >continuous very dose combined HRT - >Mirena + very low dose oestrogen - >caution with Tibolone - >vaginal oestrogen alone for genitourinary No uterus HRT - Under 5 years amenorrhoea - >oestogen alone - >tibolone - Over 5 years - >low dose oestrogen alone - >caution with tibolone - Hx endometriosis - >consider adding progestogen (poor evidence) Non hormonal - Indication - >HRT contraindicated - >significant mood component - >personal choice - Effect - >significant reduction of VMS (less than HRT) - Options - >paroxitine - >venlafaxine - >clonidine Urogenital symptoms only
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Infertility background
Epidemiology - fecundability - >85% over 12 months regular unprotected sex - >25% in first 3 months, then decreases Aetiology - Risk factors - >age >35 - >obesity/low BMI - >smoking - >previous STD Pathogenesis - Female factors (1/3rd) - >diminished ovarian reserve with age (majority) - >oligo/anovulation (PCOS/prolactin/hypogonadism/hypothalamus) - >tubal (post infection/endometriosis/pelvic adhesions) - >uterine (adhesions/mullerian abnormalities) - >smoking/obesity - Male factors (10%) - >oligo/azoospermia (majority idiopathic) - >primary/secondary hypogonadotrophinism - >congenital testicular disorder (klinefelter/cryptochordism) - >acquired testicular disorder (infection/drugs/exposure) - Combined factors (1/3rd) - Idiopathic 5%
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Female factor infertility evaluation
Hx - Menstrual hx - >regular menses/moliminal symptoms = ovulatory - >long = anovulation - >short = anovulation/endometrial dysfunction - Sexual hx - >timing and regularity - >dyspareunia (PID/endometriosis/adhesions/uterine abnormality) - Hypothalamus - >stress/weight loss/exercise - >anosmia - Pituitary - >headache/vision changes/nipple discharge - Ovaries - >acne/hirsuitism/overweight/irregular periods - >SLE/UC - Tubes - >pelvic surgery/STD - >endometriosis/pelvic pain/menorrhagia/dysmenorrhea - Uterus - >procedures/instrumentation - Social - >smoking - >alcohol and substances - >stress/mood/psychiatric disorders - >occupational exposure Exam - height/weight/BMI - inspection - >hirsutism/acne - >galactorrhea - >secondary sex characteristics/syndromic features - pelvic - >abnormal shape uterus - >nodular pouch of douglas (endometriosis) - >adnexal mass/tenderness Assess ovulation - serum progesterone - >7 days before menses - >ovulation if high - urine LH sticks - >serial assessments at home - >predicts ovulation approx 24hrs in advance - serial ultrasounds - >usually restricted to during treatment - if anovulatory - >FSH/LH (hyper/hypogonadotrophic hypogonadism) - >androgens (PCOS) - >TSH - >prolactin - >karyotyping Anatomical assessment - Imaging - >transvaginal ultrasound (uterine/tubal/ovarian morph) - >hysterosalpingography (uterine/tubal path) - >saline infusion sonography (uterine path) - >MRI (uterine path pre-op planning) - Surgical - >laparoscopy (endometriosis/adhesions) with chromotubation (tubal patency) - >hysteroscopy (uterine path) Ovarian reserve testing - Basal FSH on day 3 - >less than 2 = hypogonadotrophinism - >greater than 10 = possible reduced ovarian reserve - >greater than 30 = menopausal/ovulatory surge - Antral follicle count on day 3 - >transvagianl ultrsound - >less than 4 indicates diminished reserve - AMH on any day - >less than 1 ng/mL indicates diminished reserve
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Infertility management
Non pharm - Diet - >limited evidence - >beneficial for future pregnancy - Weight loss - >high BMI or PCOS - Weight gain - >athlete/low BMI/anorexia - Reduce smoking/drinking/substances - Psychology support - >high stress associated with infertility - >stress/psychological morbidity risk factor for infertility Ovarian stimulation - Clomiphene - >indicated for normogonodotrophic ovulatory dysfunction - >ineffective in hypogonadotrophic hypogonadism - Letrozole - >indicated for normogonadotrophic ovulatory dysfunction - Gonadotrophin therapy - >failed first line treatment - >hypogonadotrophic hypogonadism Tubal abnormalities - IVF - >failed ovulation treatment - >tubal abnormality - >male infertility - >uterine abnormalities with surrogate - Tubal patency improving procedures - >distal occlusion may be treated/proximal should not - >fimbrioplasty (lysis of adhesions/dilation of strictures) - >neosalpingostomy (new tubal opening) Uterine abnormalities - Setate - >some evidence for surgical intervention - Fibroids - >consider surgery if other treatments failed - >best evidence for submucosal - Polyps - >polypectomy for large endometrial polyps Specific aetiologies - Endometriosis - >first line = IVF - >surgical ablation of impants/adhesiolysis - PCOS additional treatments - >ovarian stimulation - >metformin - >ovarian drilling - Hyperprolactinaemia - >bromocriptine