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Adolescent girls undergoing medical abortion have lower risk of haemorrhage, incomplete evacuation or surgical evacuation than women above 18 years old

Authors:
Prognosis
30 Evidence-Based Medicine February 2012 | volume 17 | number 1 |
10.1136/ebm.2011.100064
Family Practice, The University
of British Columbia (UBC),
Vancouver, British Columbia,
Canada
Correspondence to:
Ellen R Wiebe
Family Practice, The University of
British Columbia (UBC),
1013-750 West Broadway,
Vancouver, BC V5Z-1H9,
Canada;
ellenwiebe@gmail.com
Cohort study
Adolescent girls undergoing medical abortion have lower
risk of haemorrhage, incomplete evacuation or surgical
evacuation than women above 18 years old
Ellen R Wiebe
Context
Medical abortions induced with mifepristone and
misoprostol are common, and yet there have been only
a few small studies in patients below 18 years. This study
was done to determine the short-term adverse effects of
medical abortion in younger and older women.
Methods
This was a population-based retrospective cohort
study using the Finnish abortion register from 2000
to 2006. The only exclusions were abortions over 20
weeks, and only the  rst-induced abortion was anal-
ysed for each woman. The main outcome measures
were the incidence of adverse events (haemorrhage,
infection, incomplete abortion, surgical evacuation,
psychiatric morbidity, injury, thromboembolic disease
and death) among adolescent (<18 years) and older
(≥18 years) women through record linkage of Finnish
registries. The data from the abortion were linked
to data from inpatient and outpatient visits for
42 days postprocedure. Diagnoses of adverse events
were based on the 1985 report by the Royal College of
General Practicioners/Royal College of Obstetritions
and Gynaecologists (RCGP/RCOG).1
Findings
Data from 3024 adolescents and 24 006 adults were
analysed. The rate of chlamydia infections was higher in
the adolescent cohort (5.7% vs 3.7%, p<0.001). The rates
of adverse events for adolescents and adults, respec-
tively, were 12.8% and 15.4% (haemorrhage), 2% and 2%
(infection), 7% and 10.2% (incomplete abortion), 11%
and 13% (surgical evacuation) and 0.1% and 0% (psy-
chiatric morbidity). There were two deaths in the adult
group. The risks of haemorrhage (adjusted OR (AOR)
0.87, 95% CI 0.77 to 0.99), incomplete abortion (AOR
0.69, 95% CI 0.59 to 0.82) and surgical evacuation (AOR
0.78, 95% CI 0.67 to 0.90) were lower in the adolescent
cohort. In subgroup analyses of primigravid women, the
risks of incomplete abortion (AOR 0.68, 95% CI 0.56 to
0.81) and surgical evacuation (AOR 0.75, 95% CI 0.64
to 0.88) were lower in the adolescent cohort. In logistic
regression, duration of gestation was the most important
risk factor for infection, incomplete abortion and surgi-
cal evacuation.
Commentary on: Niinimäki M, Suhonen S, Mentula M, et al. Comparison of rates of adverse events
in adolescent and adult women undergoing medical abortion: population register based study. BMJ
2011;342:d2111.
Commentary
This study credibly answers the research question and
reassures us that medical abortions are as safe for
adolescents as they are for adults. The subgroup analy-
sis of the primigravid women is the most important, as
we know that primigravid patients have fewer incom-
plete abortions.2 These  nding are consistent with the
ndings from previous studies with smaller numbers of
adolescents.3 4
We are indebted to the researchers of countries like
Finland who have access to national registers that can
yield such rich data. In North America and many other
countries, it would not be possible to do this study, where
population-based data are much more limited, and sam-
ples may not be representative of populations and may
miss complications because of lack of follow-up when
doing clinical trials.
The main problem with extrapolating from the
results of this study to other settings comes from under-
standing the demographics of the patients, the medi-
cal protocols used and the de nitions of adverse events
in Finland. North America is much more ethnically
diverse than Finland. In addition, different protocols
are used elsewhere; a survey of the National Abortion
Federation,5 whose members provide about half of all
abortions in the USA and Canada, indicated that most
medical abortions were performed with 200 mg of
mifepristone followed 1–2 days later by home admin-
istration of 800 μg misoprostol vaginally in 2001. In
Finland, the protocol was mifepristone 600 mg followed
by clinic-administered 200 μg misoprostol orally. Most
importantly, the de nitions of adverse events can dif-
fer. For example, in this study, infection was de ned
as a hospital/clinic visit with a diagnosis of infection
compared with the Planned Parenthood de nition of
“fever accompanied by pelvic pain and was treated with
intravenous antibiotics either in an emergency depart-
ment or inpatient unit.”3
As these very important population-based studies
coming from countries with excellent registries cannot be
replicated in countries without such registries, we need to
have a more complete understanding of the implications
of differing demographics, protocols and de nitions of
adverse events in order to apply the results of registry
studies such as this one widely.
Competing interests None.
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Prognosis
31
Evidence-Based Medicine February 2012 | volume 17 | number 1 |
References
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determinant of success rate in medical abortion: a retrospective
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gemeprost. Contraception 2000;62:297–303.
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Article
Full-text available
To compare medical abortion practised at home and in clinics in terms of effectiveness, safety and acceptability. A systematic search for randomized controlled trials and prospective cohort studies comparing home-based and clinic-based medical abortion was conducted. The Cochrane Central Register of Controlled Trials, EMBASE, MEDLINE and Popline were searched. Failure to abort completely, side-effects and acceptability were the main outcomes of interest. Odds ratios and their 95% confidence intervals (CIs) were calculated. Estimates were pooled using a random-effects model. Nine studies met the inclusion criteria (n = 4522 participants). All were prospective cohort studies that used mifepristone and misoprostol to induce abortion. Complete abortion was achieved by 86-97% of the women who underwent home-based abortion (n = 3478) and by 80-99% of those who underwent clinic-based abortion (n = 1044). Pooled analyses from all studies revealed no difference in complete abortion rates between groups (odds ratio = 0.8; 95% CI: 0.5-1.5). Serious complications from abortion were rare. Pain and vomiting lasted 0.3 days longer among women who took misoprostol at home rather than in clinic. Women who chose home-based medical abortion were more likely to be satisfied, to choose the method again and to recommend it to a friend than women who opted for medical abortion in a clinic. Home-based abortion is safe under the conditions in place in the included studies. Prospective cohort studies have shown no differences in effectiveness or acceptability between home-based and clinic-based medical abortion across countries.
Article
From 2001 through March 2006, Planned Parenthood health centers throughout the United States provided medical abortion (abortion by means of medication) principally by a regimen of oral mifepristone followed 24 to 48 hours later by vaginal misoprostol. In response to concern about serious infections, in early 2006 Planned Parenthood changed the route of misoprostol administration from vaginal to buccal and required either routine provision of antibiotics or universal screening and treatment for chlamydia; in July 2007, Planned Parenthood began requiring routine treatment with antibiotics for all medical abortions. We performed a retrospective analysis assessing the rates of serious infection after medical abortion during a time when misoprostol was administered vaginally (through March 2006), as compared with rates after a change to buccal administration of misoprostol and after initiation of additional infection-reduction measures. Rates of serious infection dropped significantly after the joint change to buccal misoprostol from vaginal misoprostol and to either testing for sexually transmitted infection or routine provision of antibiotics as part of the medical abortion regimen. The rate declined 73%, from 0.93 per 1000 abortions to 0.25 per 1000 (absolute reduction, 0.67 per 1000; 95% confidence interval [CI], 0.44 to 0.94; P<0.001). The subsequent change to routine provision of antibiotics led to a further significant reduction in the rate of serious infection - a 76% decline, from 0.25 per 1000 abortions to 0.06 per 1000 (absolute reduction, 0.19 per 1000; 95% CI, 0.02 to 0.34; P=0.03). The rate of serious infection after medical abortion declined by 93% after a change from vaginal to buccal administration of misoprostol combined with routine administration of antibiotics.
Article
Little is known about clinical implementation of medical abortion in the United States following approval of mifepristone as an abortifacient by the Food and Drug Administration (FDA) in 2000. We collected information regarding medical abortion practices of National Abortion Federation (NAF) members for the year 2001. Questionnaires were mailed to 337 active US NAF member facilities. A total of 258 facilities responded (77%); 252 nonhospital facilities were included in the analysis. Most of these facilities (87%) offered medical abortion in 2001, providing an estimated 28,400 medical abortions, approximately 52% of medical abortions in the US that year. Over 75% began offering mifepristone/misoprostol abortions within 5 months of the start of mifepristone distribution. Almost all (99%) reported using mifepristone/misoprostol regimens, with most offering one or more evidence-based alternative regimens (83%); a few (4%) used the FDA-approved regimen. After FDA approval of mifepristone, NAF member facilities rapidly adopted evidence-based mifepristone/misoprostol regimens.
Article
The antiprogesterone mifepristone in combination with a suitable prostaglandin provides an effective method for induction of abortion in early pregnancy up to 63 days of gestation. The combination of 600 mg mifepristone followed by 1 mg of gemeprost vaginal pessary 48 h later is one of the standard regimens in practice, which is registered in several countries in Europe. In 1995, we reduced the doses for both mifepristone and gemeprost to 200 mg and 0.5 mg respectively, as this was shown to decrease significantly the incidence of side effects whilst maintaining a high efficacy. In this article, we report our experience with this regimen in routine clinical practice by analysing 3161 consecutive medical abortions retrospectively. Twelve case notes (0.4%) were not available, and for 310 (9.8%) women, the outcome was not known with certainty as they did not return for their follow up visit. Of the remaining 2839 women, 2732 (96.2%) had a complete abortion following their treatment. One-hundred-two (3.6%) women required an evacuation of the uterus: for incomplete abortion in 63 (2.2%) and ongoing pregnancy in 39 (1.4%). Three women had to undergo surgery for ectopic pregnancies. The surgical intervention rate was significantly higher at gestation of >49 days compared to < or = 49 days (5.7% vs. 2.6%, p = 0.002) and at >56 days than among those at < or = 56 days (6.7% vs. 3.1%; p <0.001). However, for incomplete abortion a significant increase was only seen at gestation >49 days compared to < or = 49 days (3% vs. 1.6%, p = 0.017). The incidence of ongoing pregnancies increased significantly only after 56 days of gestation compared to < or = 56 days (3.8% vs. 0.9%; p <0.001). Parity was related to the outcome with parous women having significantly more incomplete/ongoing abortions compared to nulliparous women (5.4% vs. 2.0%; p <0.001), although parous women did present earlier in pregnancy for termination than nulliparous women (p = 0.01). The incidence of complications was low: 165 (5.8%) women were given antibiotics for presumed genital infection and severe haemorrhage occurred in 11 (0.4%) women, of whom only two required blood transfusion. In summary, the recommended regimen with the reduced doses of mifepristone and gemeprost is highly effective, meeting the anticipated efficacy with a complete abortion rate of >95%. We have concluded from the data that gestation and parity are strong predictors for clinicians to anticipate the probability of a successful medical termination of pregnancy.
Joint study of the Royal College of General Practitioners and the Royal College of Obstetricians and Gynaecologists
Induced abortion operations and their early sequelae. Joint study of the Royal College of General Practitioners and the Royal College of Obstetricians and Gynaecologists. J R Coll Gen Pract 1985;35:175-80.