Male and Female Sterilisation FSRH Sep 2014 Flashcards

1
Q

failure rate of tubal occlusion by intra-fallopian micro-insert

A

1 in 500 at 5 years of follow-up

this includes cases
- where luteal-phase pregnancy (- ve pregnancy test at time of sterilization doesn’t exclude)
- non-adherence with post-procedural instructions was
documented.

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2
Q

contraindication of Hysteroscopic sterilisation with micro-inserts

A

-documented proven patch test for nickel allergy

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3
Q
  • If tubal occlusion performed at same time as a caesarean section, counselling and agreement should be given how much in advance of procedure.
A

at least 2 weeks in advance of the procedure.

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4
Q

Clinicians should modify their technique if their overall failure attributable to

  • technical failure,
  • recanalisation and
  • non-compliance with additional contraception is how much?
A

more than 1%.

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5
Q

Optimal timing to schedule the first PVSA.

A

12 weeks post-vasectomy (Postal sample acceptable if Royal Mail standards are met)

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6
Q

In which cases special clearance given to cease using additional contraception

A
  • when less than 100 000 non-motile sperm/ml are observed in a fresh semen sample post-vasectomy.
    (In a small proportion of men non-motile sperm will persist following vasectomy.)
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7
Q

When the vasectomy should be considered a failure.

A

If motile sperm are observed in a fresh sample 7 months post-procedure,

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8
Q

If more than 100 000 non-motile sperm/ml are observed in a fresh sample 7 months after vasectomy,

A

clinical judgement and/or local protocols may be used to determine whether or not the procedure should be deemed a failure.

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9
Q

failure rate of vasectomy has an associated

A

approximately 1 in 2000 (0.05%) after clearance has been given. several years

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10
Q

lifetime risk of laparoscopic tubal occlusion failure, using a mix of occlusion methods,

A

1 in 200.

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11
Q

failure rate of Filshie clip, at 10 years.

A

2–3 per 1000 procedures at 10 years.

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12
Q

Incidence of unsuccessful placement of intra-fallopian implants is reported as ranging, following up to two attempts in an outpatient setting.

A

between 0% and 19%

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13
Q

When & how confirmatory imaging test should be undertaken after the insertion of intra-fallopian micro-inserts.

A
  • 3 months
  • X-ray or TVUSS in first instance, followed by HSG in selected patients where X-ray or TVUSS cannot confirm satisfactory placement.
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