Gynae Flashcards

1
Q

What is the path of the ureter

A

Crosses pelvic brim at level of common iliac bifurcation
Travels medial and posterior to IP vessels
Travels in lateral pelvic sidewall medial to internal iliac
Travels in medial leaf of broad ligament
Crossed by uterine artery at level of internal os
Lateral to uterosacral ligaments
Through cardinal ligament (ureteric tunnel) and into the bladder before trigone

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2
Q

What levels can the ureter be injured at and at which steps of a hysterectomy?

A

Crosses pelvic brim with ligation of IP if ovaries are being taken
As crossed by uterine artery as uterine artery is ligated at level of internal os
Lateral aspect of cardinal ligament as being taken
Lateral to uterosacrals as vaginal vault is being sutured

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3
Q

What are the branches of the internal iliac?

A

Iliolumbar
Lateral sacral
Superior gluteal

Inferior gluteal
Internal pudendal
Uterine
Middle rectal
Obturator
Vaginal and inferior vesical
Umbilical remnant and superior vesical
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4
Q

Describe Palmer’s point entry

A

Anaesthetist insert NG tube to empty stomach

Percuss to exclude hepatosplenomegaly

Landmark is 3cm below inferior costal margin in midclavicular line on the L

Insertion with a verres needle with appropriate safety checks, ensure initial pressure <8mmHg x 3

Establishment of pneumoperitoneum 20mmHg

Optical direct entry once established

Visualisation of anatomy at umbilicus

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5
Q

What are the benefits of MHT?

A

Most effective treatment for vasomotor symptoms
Improvement in genitourinary symptoms
Reduction in osteoporosis and assoc fractures
Reduction in cardiovascular disease - WoO
Reduction in T2DM onset
Reduction in colorectal cancer
Reduction in all-cause mortality - WoO

WoO = Window of opportunity

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6
Q

What are the risks of MHT?

A
VTE
Breast cancer - combined
Stroke - >60y
Cardiovascular disease - not if in WoO
Endometrial cancer - unopposed oestrogen
Gallbladder disease - oral oestrogen
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7
Q

What are risk factors for OHSS?

A
GnRH antagonist with HCG trigger
Superovulation - raised pre-treatment follicle count
Raised pre-trigger follicle count >13 over 10mm
>20 collected = 2% risk
Increased oestradiol
Fresh embryo transfer
Multiple pregnancy
Prev OHSS
Young
Lean
PCOS
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8
Q

What are classifications of OHSS?

A

MILD
Abdo distension, pain, ovary size <8cm

MODERATE
Above plus USS evidence of ascites, nausea, vomiting, diarrhoea, ovary 8-12cm

SEVERE
Clinical ascites, hydrothorax, HCT >45%, electrolyte disturbance, oliguria, Cr rise, ovary >12cm

CRITICAL
Tense ascites, large hydrothorax, HCT >55%, WCC >25, oliguria or anuria, VTE, ARDS

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9
Q

What are principles for management of OHSS?

A
Admit if severe or higher
Symptom control (but avoid NSAIDs)
Lower Hct
Fluid balance, UO monitoring, daily weighs
VTE prophylaxis
Daily electrolyte checks
Consider paracentesis
Consider dopamine infusion
Psychological support
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10
Q

What are the criteria for PCOS?

A

Chronic oligomenorrhoea or anovulation

Hyperandrogenism - clinical or biochemical

Polycystic appearing ovaries on USS
>12 as per Rotterdam
>20 as per recent criteria as USS better and would otherwise overdiagnose

AND other causes excluded

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11
Q

What is the pathophysiology of PCOS

A

Increased LH production and action
Acts on thecal cells and higher amounts of androgen production - hyperandrogenism features

Reduced insulin sensitivity and hyperinsulinaemia augments higher androgen production
- metabolic syndrome, cardiovascular disease

Hyperandrogenism leads to poor follicle maturation, cysts are follicles in arrested development - lack of dominant follicle, anovulatory cycles

Genetic contributors - as evidenced in twin studies. Autosomal dominant gene with low penetrance
Obesity contributes
Lifestyle factors
In utero hormonal exposures

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12
Q

What are methods of assessing tubal patency? State advantages and disadvantages.

A

Hysterosalpingogram

Hysterocontastsalpingography

Laparoscopic tubal dye test

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13
Q

What are the cause of azoospermia?

A

Obstructive - absent vas deferens (CF and carriers), prev infection e.g. chlamydia, vasectomy

Non-obstructive - trauma, torsion, prev mumps infection, cryptorchidism, chemotherapy, radiation therapy, medications, Kleinfelters (47 XXY), Micro-deletion Y chromosome, Hyperprolactinaemia, Kallman’s syndrome

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14
Q

What investigations should be carried out for azoospermia?

A

Clinical exam

USS – mass, varicocoele, vas deferens

STI screen

Post ejaculatory urinalysis

Testosterone, FSH, LH

PRL

  • CF screen
  • Karyotype – 47XXY
  • Microarray – Y chromosome microdeletion
  • Genetic testing should have pre-test genetic counselling
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15
Q

What are causes of vaginal fistulae?

A
*Post hysterectomy - abdominal, radical (higher risk but less common)
Obstetric - obstructed labour, invasive placentation, rectal injury, iatrogenic at CS
Malignancy
Inflammatory - IBD, severe infection
Endometriosis
Foreign body erosion - pessary
Radiation therapy
Congenital
  • Most common in developed world
    Obstetric fistulae most common in developing world
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16
Q

Surgical management of a borderline ovarian tumor?

A

Stage 1 surgery
Laparoscopic
Fertility sparing if reproductive age and no invasive disease
USO (+ cystectomy if tumors bilateral)
Controversy exists whether completion surgery upon fertility completion
Full staging if no fertility desire/okay not to retain endocrine function - benefits are diagnosing more advanced stage and occult invasion

Stage 2+
Utilise frozen sections
Washings
TAH, BSO
Omentectomy
Peritoneal inspection
Nodes not necessary
Resection all visible disease
Peritoneal biopsy
Appendicectomy (mucinous)
17
Q

Borderline ovarian tumors - risk factors for recurrence

A
Young age
Higher stage
Cystectomy > oophorectomy
Microinvasion
Invasive peritoneal implants
Micropapillary pattern
Serous type (as more likely to be bilateral)
18
Q

What are components of vaginal discharge?

A

Endometrial and tubal fluid

Cervical mucous from columnar epithelium

Vaginal + cervical squamous cells (desquamated cells)

Vaginal epithelium transudate

Fluid from Bartholin’s and Skene’s glands

Normal flora - lactobacilli predominantly

19
Q

What are Amsel criteria for BV?

A

pH >4.5
Whiff test “fishy odour” when exposed to KOH
Presence of clue cells on wet slide
Homogenous grey/white discharge coating vaginal walls

20
Q

Which organisms contribute to BV?

A
Gardnerella vaginalis
Atopobium vaginae
Mobiluncus spp
Prevotella spp
Bacteroides
Mycoplasma hominis
Peptostreptococcus
21
Q

List Fraser guidelines for prescribing of contraception in <16yo

A

May prescribe contraception as long as

  1. Understand advice being given, nature of treatment
  2. Cannot be persuaded to inform their parent/guardian
  3. Will commence/resume sexual activity regardless of prescription
  4. Physical and/or mental health is at risk without contraception or advice
  5. Provision of contraception is in their best interest, regardless of whether parent/guardian is informed
22
Q

Rate of TOP globally

A

35/1000

23
Q

Definition of a medically safe abortion

A

WHO recommended methods used by a trained operator

24
Q

Risks and complications of unsafe abortions

A
  1. Higher morbidity and mortality (bleeding, infection, genital tract trauma, RPOC)
    150,000 deaths occur annually worldwide due to unsafe abortion
  2. Later presentation for problems as stigma associated with being illegal
  3. Care for above dependent on whether they disclose provider information
  4. Further costs managing complications that ensure from provision of unsafe services
  5. Don’t get appropriate contraception
  6. Higher psychological impact if illegal – also means less likely to receive appropriate counselling which could worsen mental health
25
Q

What are LARC benefits?

A

Cheaper over 12months - woman and government as lower unintended pregnancy rate
Highest continuation rate and high satisfaction
Highest efficacy - compared to oral contraceptives risk of unintended pregnancy is 20x less
Doesn’t require daily adherence
Easily reversible
Fewer visits to health provider
Suitable any age, overall few contraindications
Immediate return to fertility once removed
Many reduce HMB

26
Q

What are barriers to LARCs?

A

Inadequate HCP knowledge
Insufficient training for insertion, removal, complication management
Concern re IUCD in nulliparous women
Lack of patient awareness re benefits, misconception re fertility, AUB
Funding barriers in primary care

27
Q

What are methods to improve uptake of LARCs?

A

Build contemporary evidence base to inform policy
Establish National guidelines
Improved funding for research
Information and education campaigns for LARCs
- NB CHOICE study promoted LARCs first and had a much higher uptake
Involve in school curriculums
Training courses for providers - insertion, removal, troubleshooting
Provide incentives for women and providers to take up