Medical Abortion at all Gestations

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Presentation transcript:

Medical Abortion at all Gestations Professor Emeritus Allan Templeton, University of Aberdeen

EBCOG Statement The provision of safe abortion is crucial to the public health of all communities. WHO advises that the choice of abortion should be readily available to women in all national healthcare systems. EBCOG considers that its universal availability in all countries in Europe is fundamental to women’s health and well-being. Medical abortion is one of the safest procedures in medical practice, with minimal morbidity and mortality, and as such there appears to be no good reason to restrict the licensing of mifepristone and misoprostol. EBCOG recommends that training in abortion care is mandatory and is included in the curriculum for anyone training in the specialty of gynaecology and obstetrics.

Rates of termination by age of woman 2005 – 2014

Development of medical methods of induced abortion with mifepristone and prostaglandin 1984 Mifepristone alone 1985 Mifepristone and Prostaglandin 1987 Mifepristone and vaginal prostaglandin 1991 Mifepristone and oral prostaglandin 1991 Reduced doses of mifepristone 1995 Mifepristone and vaginal misoprostol 2000 Medical methods at all gestations 2002 Mifepristone and sublingual misoprostol

Outcome of medical abortion (10291 women) <7 8-9 10 11 12 13 14-15 16-17 18-19 >19 Evac 1.8 1.7 3.8 4.8 6.4 6.0 4.7 4.1 2.2 Incomp 1.3 1.1 2.6 2.7 3.2 2.5 3.5 3.9 3.0 1.5 FH 0.2 0.7 2.8 0.3 0.0 Emerg 0.5 0.4 0.8 1.2

Abortions in Scotland by Gestation 1968-2014

Comparison of mifepristone and misoprostol

Mifepristone, PG and uterine contractility Bygdeman & Swahn 1985

Uterine contractility Uterine contractility* in response to PGE2 in 20 women treated with RU486 PG Dose Control 0.05 0.1 0.15 6 49 45 122 24 hours 50 300 356 529 36 hours 222 711 806 1023 48 hours 175 502 636 910 *Montevideo units Swahn and Bygdeman, 1988

Misoprostol alone Higher total dose is needed Less effective (failed and continuing) Induction-to-abortion interval longer 80-90% within 24 hours More side-effects. Gemzell-Danielsson and Lalitkumar, 2008

Cervical Preparation with misoprostol before Surgery reduces incomplete abortion Misoprostol Placebo RR(CI) n=2427 n=2431 Complications (%) 2 4 0.7(0.5-0.96) Incomplete Ab (n) 19 55 0.3(0.2-0.6) Meirik et al 2012

Early Medical Abortion using mifepristone 200mg then vaginal misoprostol 800ugs <49 Days n = 2879 (46%) 49 – 63 Days n = 3396 (54%) n % Evacuations 51 1.8 81 2.4 Missed/Incomplete 40 1.4 1.5 FH Present 2 0.1 13 0.4 Emergency 6 0.2

Sublingual misoprostol as effective as vaginal but with slightly more side effects (for medical abortion up to 13 weeks) Hamoda et al, 2004

Outcome of medical abortion at home among 1001 women Complete 993 (99.2) Missed / incomplete 6 (0.6) FH present _ Emergency 2 (0.2)

Abortions at Home, Aberdeen 2003-2015

Late First Trimester Medical Abortion in 2228 Women Gestation in Days 64 – 70 (n=1037) 71 – 77 (n=584) 78 – 84 (n=389) 85-91 (n=209) Evacuation 3.2 5.1 7.5 6.7 ( Missed/Incomplete 2.2 3.1 4.2 3.8 FH Present 0.7 1.7 2.6 2.9 Emergency 0.3 0.8 1.0 )

Outcome among 10-13 weeks since change Review % Change Complete 95.0 97.3 Missed/Incomplete 2.8 1.3 FH present 1.7 Emergency 0.5

Second trimester regimen Mifepristone 200 mgs 36 – 48 hours later Misoprostol 0.8 mgs vaginal (sublingual) Then according to bleeding Misoprostol 0.4 mgs vaginal/sublingual/oral Up to a total of 5 doses (15 hours)

Doses of PG used in second trimester Surg evac (%) 2.3 2.7 5.9 17.1 23.1

Second trimester medical abortion (n=1002) Cumulative success No. % Day 1 970 97.1 Day 2 989 99.0 Day 3 999 99.9

Second day Repeat mifepristone 200 mgs evening then repeat misoprostol regimen If Third Day , no additional mifepristone then gemeprost 1 mg , 5 doses

Second trimester recent (n = 1244) Weeks 13-14 14-15 15-17 17-19 > 19 n 383 236 282 219 124 Complete % 98 92 95 Incomplete % 1.0 6.3 3.5 3.6 1.6 Positive FH % 0.4 Emergency % 1.3 1.1 1.4 0.8

Women who would opt for same method Weeks Medical Surgical % % <6 100 ) 7 90 ) 87 8 69 ) 9 66 ) 10-13 70 79 13-20 53 100 From Henshaw 1993, Ashok 2002, Kelly 2010

Women approached but not randomised 67% had strong preference for surgical wanting to be asleep less traumatic psychologically less painful 33% had strong preference for medical not wanting to be asleep shorter time to wait Kelly et al, 2010

Analgesia use among 4343 women having medical abortion

Antibiotic Policy All women are screened for chlamydia and gc If positive given azithromycin (can use doxycycline) If 18 years and under - given prophylactic azithromycin All women get metronidazole 800mgs at time of abortion

Prevention of Subsequent Unintended Pregnancy Immediate insertion of IUCD is safe and acceptable (Grimes et al 2003) Significantly fewer subsequent abortions (Goodman et al 2008, Heikinheimo et al 2008, Roberts et al 2010) Immediate insertion has higher rate of use at six months (Bednarek et al 2011)

First-trimester Abortion • Up to 9 weeks’ gestation, a choice of medical or surgical abortion should be offered, since both are safe and effective. (Medical at home or surgical without GA but with misoprostol pre-treatment) • Medical abortion is associated with more pain and bleeding, and it carries a slightly higher risk of incomplete abortion (2 to 5%, vs. 1% with surgical abortion). • Surgical abortion may be associated with an increased risk of serious, but very rare, complications requiring major surgery. • Women can be reassured that the current evidence indicates that neither method of abortion is associated with an increased risk of harm to their future reproductive health or to their future mental health, as compared with continued pregnancy. • The insertion of an intrauterine device at the time of the abortion is the best reversible method of contraception to prevent another unintended pregnancy.

EBCOG Position Statement The provision of safe abortion is crucial to the public health of all communities. WHO advises that the choice of abortion should be readily available to women in all national healthcare systems. EBCOG considers that its universal availability in all countries in Europe is fundamental to women’s health and well-being. Medical abortion is one of the safest procedures in medical practice, with minimal morbidity and mortality, and as such there is no reason to restrict the licensing of mifepristone and misoprostol. EBCOG recommends that training in abortion care is mandatory and is included in the curriculum for anyone training in the specialty of gynaecology and obstetrics.