Mais conteúdo relacionado Saf1. Aspirin or anticoagulants for treating recurrent miscarriage in
women without antiphospholipid syndrome (Review)
Kaandorp S, Di Nisio M, Goddijn M, Middeldorp S
This is a reprint of a Cochrane review, prepared and maintained by The Cochrane Collaboration and published in The Cochrane Library
2009, Issue 1
http://www.thecochranelibrary.com
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review)
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
2. TABLE OF CONTENTS
HEADER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
ABSTRACT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
PLAIN LANGUAGE SUMMARY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
BACKGROUND . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
OBJECTIVES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
METHODS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
RESULTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
DISCUSSION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
AUTHORS’ CONCLUSIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
ACKNOWLEDGEMENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
CHARACTERISTICS OF STUDIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
DATA AND ANALYSES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Analysis 1.1. Comparison 1 Aspirin versus placebo, Outcome 1 Live-birth rate. . . . . . . . . . . . . . 16
Analysis 2.1. Comparison 2 Enoxaparin versus aspirin, Outcome 1 Live-birth rate. . . . . . . . . . . . . 17
Analysis 2.2. Comparison 2 Enoxaparin versus aspirin, Outcome 2 Preterm delivery. . . . . . . . . . . . 17
Analysis 2.3. Comparison 2 Enoxaparin versus aspirin, Outcome 3 Obstetric complications; pre-eclampsia. . . . . 18
Analysis 2.4. Comparison 2 Enoxaparin versus aspirin, Outcome 4 Obstetric complications; intrauterine growth
restriction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
APPENDICES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
FEEDBACK . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
WHAT’S NEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
HISTORY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
CONTRIBUTIONS OF AUTHORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
DECLARATIONS OF INTEREST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
DIFFERENCES BETWEEN PROTOCOL AND REVIEW . . . . . . . . . . . . . . . . . . . . . 22
INDEX TERMS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) i
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
3. [Intervention Review]
Aspirin or anticoagulants for treating recurrent miscarriage in
women without antiphospholipid syndrome
Stef Kaandorp1 , Marcello Di Nisio2 , Mariette Goddijn3 , Saskia Middeldorp4
1 Obstetrics
and Gynaecology, Academic Medical Center, Amsterdam, Netherlands. 2 Department of Vascular Medicine, F4-138,
Academic Medical Center, Amsterdam, Netherlands. 3 Center for Reproductive Medicine, Department of Obstetrics and Gynecology,
Academic Medical Center (H4-205), Amsterdam, Netherlands. 4 Department of Clinical Epidemiology, Department of General Internal
Medicine, Leiden University Medical Center (LUMC), Leiden, Netherlands
Contact address: Stef Kaandorp, Obstetrics and Gynaecology, Academic Medical Center, Meibergdreef 9, P.O. Box 22660, Amsterdam,
1100 DD, Netherlands. s.p.kaandorp@amc.uva.nl.
Editorial group: Cochrane Pregnancy and Childbirth Group.
Publication status and date: New search for studies and content updated (no change to conclusions), published in Issue 1, 2009.
Review content assessed as up-to-date: 29 April 2008.
Citation: Kaandorp S, Di Nisio M, Goddijn M, Middeldorp S. Aspirin or anticoagulants for treating recurrent miscarriage in
women without antiphospholipid syndrome. Cochrane Database of Systematic Reviews 2009, Issue 1. Art. No.: CD004734. DOI:
10.1002/14651858.CD004734.pub3.
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
ABSTRACT
Background
Since hypercoagulability might result in recurrent miscarriage, anticoagulant agents could potentially increase the live-birth rate in
subsequent pregnancies in women with either inherited thrombophilia or unexplained recurrent miscarriage.
Objectives
To evaluate the efficacy and safety of anticoagulant agents, such as aspirin and heparin, in women with a history of at least two
miscarriages without apparent causes other than inherited thrombophilia.
Search methods
We searched the Cochrane Pregnancy and Childbirth Group’s Trials Register (April 2008), the Cochrane Central Register of Controlled
Trials (The Cochrane Library 2007, Issue 1), MEDLINE (January 1966 to March 2007), and EMBASE (1980 to March 2007). We
scanned bibliographies of all located articles for any unidentified articles.
Selection criteria
Randomised and quasi-randomised controlled trials that assessed the effect of anticoagulant treatment on the live-birth rate in women
with a history of at least two miscarriages (up to 20 weeks of amenorrhoea) without apparent causes other than inherited thrombophilia
were eligible. Interventions included aspirin, unfractionated heparin, and low molecular weight heparin for the prevention of miscarriage.
One treatment could be compared with another or with placebo.
Data collection and analysis
Two authors assessed the trials for inclusion in the review and extracted the data. We double checked the data.
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 1
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
4. Main results
Two studies (189 participants) were included in the review. In one study, 54 pregnant women with recurrent miscarriage (RM) but no
detectable anticardiolipin antibodies were randomised to low-dose aspirin or placebo. RM was defined as three or more consecutive
miscarriages (occurring before 22 weeks’ gestational age (based on last menstrual period)). Similar live-birth rates were observed with
aspirin and placebo, both 81% (risk ratio (RR) 1.00, 95% confidence interval (CI) 0.78 to 1.29). In the other study, 107 women with
consecutive recurrent miscarriage without any apparent cause and no hereditary thrombophilia were randomised between enoxaparin
and aspirin. Here RM was stated as three or more consecutive first trimester miscarriages or at least two consecutive second trimester
miscarriages. Similar live birth rates were observed with enoxaparin and aspirin, respectively 82% and 84% (RR 0.97, 95% CI 0.81 to
1.16).
Authors’ conclusions
There is a paucity in studies on the efficacy and safety of aspirin and heparin in women with a history of at least two miscarriages
without apparent causes other than inherited thrombophilia. The two reviewed trials studied different treatments and only one study
was placebo-controlled. Neither of the studies showed a benefit of one treatment over the other. Therefore, the use of anticoagulants
in this setting is not recommended. However, large randomised placebo-controlled trials are still urgently needed.
PLAIN LANGUAGE SUMMARY
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome
Two studies (189 women) were included in the review. There is Insufficient evidence to say if anticoagulants help women with recurrent
miscarriage without antiphospholipid syndrome.
Recurrent miscarriage (RM) is associated with inherited blood clotting disorders that could interfere with the placental blood circulation.
Anticoagulant drugs for women with RM and such an underlying blood clotting problem may help, although these drugs may also
cause excessive bleeding. Judgement if anticoagulants help women with RM in the absence of antiphospholipid syndrome is not possible
because of the lack of sufficient evidence from the reviewed trials on this subject.
BACKGROUND
an evaluation of etiologic causes ((American College of Obstetrics
Recurrent miscarriage (RM) is devastating for women and their and Gynecology (ACOG 2001); Dutch Society of Obstetrics and
families, while up to 15% of all clinically recognised pregnancies Gynecology (NVOG 2007)). However, the risk of a miscarriage
end in miscarriage (miscarriage before the 20th week of gesta- after two or three consecutive miscarriages is almost similar (Regan
tional age) (Everett 1997; Huisjes 1984). Approximately 5% of 1988). Adequate characterisation of miscarriages and patients in
women experience two or more miscarriages, whereas RM, de- RM studies is most important and, favourably, would be the same
fined as three or more first trimester miscarriages, may affect as to make studies mutually comparable (Christiansen 2006). In this
many as 1% to 2% of women of reproductive age (Clifford 1994; review we decided to use the broad definition of RM: two or more
Cook 1995; Stirrat 1990). The definition of RM remains the sub- miscarriages (up to 20 weeks of amenorrhoea).
ject of debate. The World Health Organization (WHO) defines
miscarriage as a pregnancy ending in the death or expulsion of
the fetus or the embryo before the 20th week of gestational age Miscarriage is associated with relevant maternal morbidity like
(WHO 1977). Often RM is defined as three or more consecutive bleeding and infection and, sometimes, maternal death (NHMRC
miscarriages. According to recent European Society for Human 2001), particularly in low-income countries (Goyaux 2001).
Reproduction & Embryology (ESHRE) guidelines, RM is tradi- Moreover, miscarriage, especially if recurrent, might cause impor-
tionally defined as three or more consecutive miscarriages occur- tant psychological and emotional distress that can be further com-
ring before 20 weeks’ amenorrhoea (Jauniaux 2006). Some guide- plicated by feelings of anxiety and depression as well as social with-
lines use the definition of two or more miscarriages for offering drawal (Lee 1996).
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 2
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
5. Several factors may be involved in the aetiology of recurrent mis- nancy outcomes may result from placental infarctions and throm-
carriage. Women experiencing recurrent miscarriage may have an botic changes in decidual microvessels with possible placental in-
underlying medical condition such as carrier status of a struc- sufficiency and fetal death (Infante-Reviard 1991; Lockshin 1999).
tural chromosome abnormality (Braekeleer 1990; Franssen 2005), Heparin and low-dose aspirin seem to be effective and safe in re-
antiphospholipid syndrome, or other blood clotting disorders ducing miscarriage rates in women with antiphospholipid anti-
generally referred to as thrombophilias (Preston 1996). Factors body syndrome with significantly better pregnancy outcome than
less strongly associated with RM are anatomic abnormalities of low-dose aspirin alone (rate of live births of 71% to 80% ver-
the uterus, hyperhomocysteinemia and endocrine abnormalities sus 42% to 44% respectively, an absolute risk difference of 0.36)
(Christiansen 2005). (Kutteh 1996; Rai 1997), though findings have not always been
consistent (Farquharson 2002). Both the therapy for recurrent
Thrombophilia are a diverse group of coagulation disorders as-
miscarriage associated with the antiphospholipid syndrome and
sociated with a predisposition to thrombosis and thus increased
other possible therapies currently considered for the prevention of
risk for thrombotic events as deep vein thrombosis and pulmonary
recurrent miscarriage (as progesterone and immunotherapy) are
embolism. These hypercoagulable states can be either acquired, as
the topics covered in other Cochrane reviews (Empson 2005; Haas
for instance the antiphospholipid syndrome, or inherited as the
2008; Porter 2006).
factor V Leiden mutation (which results in a decreased capacity to
inactivate activated factor V by the protein C system, also known The prognosis in subsequent pregnancies of women with recur-
as activated protein C (APC) resistance), the deficiency of physio- rent miscarriage without antiphospholipid antibody syndrome is
logical anticoagulants like protein C, protein S and antithrombin the live-birth rate of approximately 50% to 89% (Brigham 1999;
and the prothrombin G20210A gene mutation (resulting in in- Lindqvist 2006; Rai 2000; Stirrat 1990). For women with recur-
creased concentrations of prothrombin in plasma) or an elevated rent miscarriage and underlying thrombophilic disorders, these
level of factor VIII-ac. figures range from 63% to 80% (Preston 1996; Rai 2000). The
differences between studies can probably be explained by differ-
A growing body of evidence has implicated thrombophilia in
ences in the populations of women participating in the studies.
adverse obstetrical events (such as intrauterine growth restric-
tion, miscarriage, severe pre-eclampsia, and placental abruption) The use of anticoagulants in pregnancy needs to be carefully moni-
(Kupferminc 1999; Middeldorp 2007) and there is also reason- tored and evaluated for safety since it can carry risks for the mother
able evidence to suggest that some cases of recurrent miscarriage and the fetus. In contrast to coumarin derivatives, neither unfrac-
are associated with thrombosis of placental vessels and infarction. tionated heparin nor low molecular weight heparin cross the pla-
Firstly, microthrombi are a common finding in the placental vas- centa and therefore do not have the potential to cause fetal bleeding
culature of women with recurrent miscarriage (Rushton 1988). and teratogenicity (Ginsberg 2001). The maternal risks associated
Secondly, placental thrombosis and infarction have been described with heparin administration are uncommon but potentially seri-
in association with certain thrombophilic defects (Dizon 1997; ous and include bleeding, heparin-induced thrombocytopenia and
Rai 1996), but other pathophysiological pathways than thrombo- heparin-induced osteopenia with fractures. Moreover, heparin ad-
sis could also be involved, since adverse pregnancy outcomes can ministration may cause pain and slight bruising at injection sites.
occur in women with thrombophilia in the absence of placental There is accumulating evidence that low molecular weight heparin
thrombosis (Mousa 2000). Thirdly, thrombophilic defects are sig- is at least as effective and safe as unfractionated heparin with po-
nificantly more prevalent amongst women with such pregnancy tential advantages during pregnancy, since they cause less heparin-
complications (Rai 1995; Rey 2003). A meta-analysis showed that induced thrombocytopenia, can be administered once daily, and
the magnitude of the association between thrombophilia and fe- are associated with a lower risk of heparin-induced osteoporosis
tal loss varies according to the timing of fetal loss (Rey 2003). (Ginsberg 2001; Sanson 1999). Based on current evidence, low-
In particular, first trimester recurrent miscarriage was associated dose aspirin (less than 150 mg/d) during the second and third
with factor V Leiden, APC resistance, and prothrombin G20210A trimesters appears to be safe, while the safety of higher doses of
mutation, while late non-recurrent fetal loss was associated with aspirin and/or aspirin ingestion during the first trimester remains
factor V Leiden, prothrombin G20210A mutation, and protein S uncertain (Ginsberg 2001). The use of heparin in pregnancy has
deficiency. Also, family studies showed that women with heredi- been covered in another Cochrane review (Walker 2003).
tary thrombophilia, especially those with combined defects or an-
In clinical practice, women with recurrent miscarriage associated
tithrombin deficiency, have an increased risk of miscarriage and
with inherited thrombophilia or recurrent miscarriage without any
intrauterine fetal death compared to women without these defects
other apparent predisposing disorder are frequently seeking advice
(Meinardi 1999; Preston 1996; Sanson 1996).
about the indication for anticoagulant treatment. Some clinicians
The antiphospholipid syndrome is associated both with vascu- tend to extrapolate the beneficial effect of anticoagulant therapy
lar thrombosis and pregnancy complications (including recurrent in women with antiphospholipid antibody syndrome and recur-
miscarriage and premature delivery) (Levine 2002). Adverse preg- rent miscarriage to all women with recurrent miscarriage without
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 3
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
6. apparent cause or with inherited thrombophilia; whether there is Types of outcome measures
evidence for this is the objective of this review.
Primary outcomes
OBJECTIVES Live-birth rate
The objective of this review was to determine whether anticoag-
ulant treatment improves pregnancy outcome in women with a
Secondary outcomes
history of at least two miscarriages without apparent causes other
than inherited thrombophilia. 1. Preterm delivery of a live infant between 24 and 28 weeks’
gestational age
2. Preterm delivery of a live infant between 28 and 32 weeks’
gestational age
METHODS
3. Preterm delivery of a live infant between 32 and 37 weeks’
gestational age
4. Obstetric complications (pregnancy associated
Criteria for considering studies for this review hypertension, pre-eclampsia, intrauterine growth retardation)
5. Congenital malformations
6. Admission to special care
Types of studies 7. Side effects of the drug used, both for the mother and the
Randomised controlled trials and quasi-randomised controlled tri- baby (maternal and/or neonatal bleeding, heparin-induced
als that assessed the effect of anticoagulant treatment on improv- thrombocytopenia, heparin-induced osteopenia, pain and
ing the live-birth rate in women with a history of at least two bruising at injection sites, allergic reactions to heparin, and
miscarriages without apparent causes other than inherited throm- teratogenicity)
bophilia. 8. Thromboembolic complications
Types of participants
Search methods for identification of studies
Participants were pregnant women or women who were actively
trying to become pregnant with a history of at least two mis-
carriages without apparent causes other than inherited throm-
bophilia. Studies that included women with apparent causes (other Electronic searches
than familial thrombophilia) of recurrent miscarriage (antiphos- We searched the Cochrane Pregnancy and Childbirth Group’s Tri-
pholipid syndrome; uterine abnormalities; patients’ or their part- als Register by contacting the Trials Search Co-ordinator (April
ners’ karyotype abnormalities; endocrine and toxic factors (dia- 2008).
betes mellitus); miscarriage due to documented fetal malforma- The Cochrane Pregnancy and Childbirth Group’s Trials Register
tion or the result of an infectious complication) have been in- is maintained by the Trials Search Co-ordinator and contains trials
cluded only if the results from women with a history of at least two identified from:
miscarriages without apparent causes other than inherited throm- 1. quarterly searches of the Cochrane Central Register of
bophilia could be extracted to be analysed separately. According Controlled Trials (CENTRAL);
to the WHO definitions and ESHRE guidelines, the term miscar- 2. weekly searches of MEDLINE;
riage referred to a miscarriage occurring before the 20th week of 3. handsearches of 30 journals and the proceedings of major
amenorrhoea. For the studies included in the review, the respective conferences;
definition for recurrent miscarriage is reflected. The study popu- 4. weekly current awareness alerts for a further 44 journals
lations are described whenever possible with regard to number of plus monthly BioMed Central email alerts.
miscarriages, gestational age of the miscarriages, and maternal age. Details of the search strategies for CENTRAL and MEDLINE,
the list of handsearched journals and conference proceedings, and
the list of journals reviewed via the current awareness service can
Types of interventions be found in the ‘Specialized Register’ section within the edito-
The interventions included were aspirin, unfractionated heparin, rial information about the Cochrane Pregnancy and Childbirth
and low molecular weight heparin for the prevention of miscar- Group.
riage. One treatment could be compared with another or with Trials identified through the searching activities described above
placebo. Combinations of therapy could be used. are each assigned to a review topic (or topics). The Trials Search
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 4
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
7. Co-ordinator searches the register for each review using the topic unaware of the assigned intervention. We assessed other aspects of
list rather than keywords. study quality in the studies which fulfilled the inclusion criteria.
In addition, we searched the Cochrane Central Register of Con-
trolled Trials (The Cochrane Library 2007, Issue 1), MEDLINE We included all trials in the initial analyses and carried out sen-
(January 1966 to March 2007), and EMBASE (1980 to March sitivity analyses to explore the effect of trial quality. We repeated
2007) using the search strategy listed in Appendix 1. analyses taking into account factors that could have introduced
bias, such as the inclusion of quasi-randomised studies, high levels
of exclusions which were unbalanced between the groups, or other
Searching other resources insecure allocation concealment. We interpreted any differences
cautiously and only used them to generate hypotheses. Despite
We scanned bibliographies of all located articles for any unidenti-
this quality assessment, we did not exclude any study on the ba-
fied articles.
sis of quality. We carried out statistical analyses using the Review
We did not apply any language restrictions.
Manager software (RevMan 2000), with results presented as sum-
mary relative risks. We calculated risk ratios using a fixed-effect
model (Mantel-Haenszel method).
Data collection and analysis In the case of homogenous data, we expressed summary statistics
as risk difference (RD) and we used the number needed to treat
Two review authors independently reviewed titles and abstracts
(1/RD) to express the final results of the review.
from the database searches to determine whether the inclusion
We applied tests of heterogeneity between trials to assess the sig-
criteria were satisfied. We made decisions regarding inclusion
nificance of any differences between trials (I2 method, significant
separately and compared results. We resolved any disagreements
if greater than 0.3) and explored possible causes of any hetero-
through discussion. Two authors independently reviewed the full
geneity. If we detected heterogeneity, we planned to perform sub-
text of identified articles, including those where there was disagree-
group analyses for the main outcomes by individual quality crite-
ment in the initial title or abstract scanning, to ensure that the
ria to assess the effect of poorer quality studies on the magnitude
inclusion criteria were met. Where necessary, we contacted trial
of the estimate of effect. If data were available, we also planned
authors for additional information.
to perform subgroup analysis to compare outcomes in: (1) dif-
Two authors independently extracted the study characteristics us-
ferent inherited thrombophilic disorders; (2) preconceptional or
ing an agreed format and data from included studies, including as-
periconceptional anticoagulant use; (3) type of anticoagulant(s)
sessments of quality. We resolved any disagreements by consensus
used (e.g. single drug, combination of anticoagulant agents); (4)
and, if necessary, by involvement of a third author. If we could not
dose of anticoagulant(s); (5) duration of anticoagulant use; and
reach agreement, we excluded the item until further information
(6) women with a history of three or more miscarriages or two or
was available from the trialists. One author scanned conference
more miscarriages.
proceedings and included them if adequate information could be
We assessed publication bias using the funnel plot. Symmetry
obtained either from the abstract or from personal communica-
would be expected in the absence of any bias, although situations
tion. One author identified articles from other sources (experts or
other than publication bias may result in asymmetry. We would
reference lists) as possibly eligible and then two authors indepen-
have explored any anomaly, but it was anticipated that the number
dently assessed them for inclusion, as above. Blinding of authors,
of eligible studies might be too few to allow adequate assessment.
journal of origin, or institutions did not occur. Two authors in-
dependently assessed the abstracts of non-English articles, which
had to be translated, to ascertain if they met the inclusion criteria.
We obtained a translation of the full article of those that met the
criteria.
We assessed the validity of each included trial according to the RESULTS
criteria outlined in the Cochrane Reviewers’ Handbook (Clarke
2002). These include generation of randomisation sequence; al-
location concealment; blinding of subject, investigator, and out-
come assessor; less than 20% loss to follow up; and analysis by
Description of studies
intention to treat. Where the method of allocation concealment See: Characteristics of included studies; Characteristics of excluded
was unclear, we attempted to contact authors to provide further studies; Characteristics of ongoing studies.
details. Allocation concealment was judged adequate (A), unclear Details for the trials included are in the ’Characteristics of included
(B), inadequate (C), or not used (D), depending on the conceal- studies’.
ment schemes used. Blinding was considered double or single if We included two studies (189 women) (Dolitzky 2006; Tulppala
both the physician and the participant or only one of them were 1997) in this review. For the study by Tulppala (Tulppala 1997), we
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 5
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
8. extracted data on the subgroup of women fulfilling the inclusion Given the paucity of data, we were unable to carry out the sensi-
criteria of the review. tivity and subgroup analysis as planned. In the study by Dolitzky
Dolitzky 2006 evaluated the effect of aspirin or low-molecular- et al (Dolitzky 2006), 54 patients were randomized to enoxaparin
weight heparin in women with unexplained RM. RM was defined and 50 patients to aspirin. The mean age did not differ between
as three or more consecutive first trimester miscarriages or at least the enoxaparin and aspirin groups, respectively 31.73 +/- 5.3 and
two consecutive second trimester miscarriages. The objective was 30.65 +/- 6.18. Also the number of previous miscarriages did not
to compare the effect of aspirin and enoxaparin on live-birth rate. differ between the enoxaparin and aspirin groups, respectively 3.8
Women were only included if there was no apparent cause for the +/- 1.4 and 3.9 +/- 1.4. The number lost to follow up was three
miscarriages including absence of hereditary thrombophilia (fac- (2.8%). Both groups had similar live birth rates, 82% in the enoxa-
tor V Leiden, prothrombin mutation (G20210A), homozygous parin group and 84% in the aspirin group. The RR for enoxa-
MTHFR mutation, deficiency of protein C,S or antithrombin). parin versus aspirin was 0.97 (95% CI 0.81 to 1.16). In a post-hoc
The treatment with enoxaparin (40 mg/day) or aspirin (100 mg/ analysis of women who had no live children (primary aborters),
day) was started from the time of detection of a fetal heart beat women allocated to enoxaparin had a non-significantly increased
at 6 to 12 weeks gestation. Of the 107 included women, 54 re- live birth, 94% as compared to 81% in those who had been al-
ceived enoxaparin, 50 aspirin and 3 were lost to follow up. Besides located to aspirin. The number of preterm deliveries and cases
the primary outcome measure of live-birth rate secondary out- of intrauterine growth restriction did not differ between the two
comes like preterm delivery, intrauterine growth restriction, and groups. Pre-eclampsia was found in three women in the aspirin
pre-eclampsia were reported. group and in none in the enoxaparin group. Placental doppler
blood flow studies were similar in both groups. No maternal side
Tulppala 1997 evaluated the effect of low-dose aspirin (50 mg/ effects were seen. In the aspirin group, one infant was born with a
day) on live-birth rate in pregnant women with preceding RM necrotic testis and one had a convulsion caused by hypoglycaemia.
with or without detectable anticardiolipin antibodies and no other In each group, one baby with a congenital anomaly was found.
apparent cause for their previous miscarriages. RM was defined as One fetus was detected with tricuspid insufficiency (the pregnancy
three or more consecutive miscarriages (occurring before 22 weeks was terminated) in the aspirin group and one infant had an im-
of gestational age). Aspirin was compared to placebo, with med- perforate hymen in the enoxaparin group.
ication started as soon as a home urinary pregnancy test became For the study by Tulppala et al (Tulppala 1997), we extracted data
positive. From this trial, we extracted data for the 54 women neg- for the subgroup of women fulfilling the inclusion criteria of the
ative for anticardiolipin antibodies. Of these, 27 were assigned to review. We could not extract data on mean age or mean number
aspirin and 27 to placebo. Secondary outcomes, such as preterm of miscarriages in the obstetric history in both groups. Fifty-four
delivery, obstetric complications, and bleeding rate could not be pregnant women with recurrent miscarriage without detectable
extracted separately for the group of women with negative anti- anticardiolipin antibodies were randomised to low-dose aspirin
cardiolipin antibodies. or placebo. In both groups, 81% of the pregnancies resulted in a
Overall, we excluded 18 studies from the review. We have provided live birth (RR 1.00, 95% CI 0.78 to 1.29). We could not extract
the reasons for exclusion in the ’Characteristics of excluded studies’ data on secondary outcomes, such as preterm delivery, obstetric
table. complications, or bleeding rate.
Risk of bias in included studies
Details for the two included studies are in the ’Characteristics DISCUSSION
of included studies’ table. The study by Dolitzky 2006 was not The results of this systematic review show a paucity of published
blinded and not placebo controlled. The randomisation method intervention trials with anticoagulants in women with unexplained
was clearly described with adequate concealment of allocation. recurrent miscarriage without antiphospholipid antibodies. We in-
The study by Tulppala 1997 was a double-blind, placebo-con- cluded only two randomised controlled trials in this review; in one
trolled trial. The method of randomisation was not stated and of them we could include data of only a small subgroup of women
concealment of allocation was not clear. fulfilling the inclusion criteria of the review (Tulppala 1997). Nei-
ther study, one using low-dose aspirin and placebo (Tulppala 1997)
and one comparing enoxaparin with aspirin (Dolitzky 2006),
showed improvement of gestational outcome. Therefore, the use
Effects of interventions of either aspirin or low-molecular-weight heparin to prevent mis-
We have included two trials, involving 189 participants, in this carriage in women with two or more miscarriages without appar-
review. ent causes other than inherited thrombophilia, is not based on evi-
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 6
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
9. dence and should be discouraged. Currently, properly randomised Implications for research
controlled trials using placebo or no treatment arms are ongoing.
From a public health perspective, even a moderate benefit from
aspirin or anticoagulants in this high-risk group of women might
be worthwhile, and large studies of strong methodological quality
AUTHORS’ CONCLUSIONS are awaited to clarify the real risk-benefit of such an approach.
Moreover, the inclusion of a placebo or no-treatment arm in these
Implications for practice studies is necessary since it would provide an adequate control to
There is a paucity in evidence on the efficacy and safety of aspirin the active treatment and allows assessing a risk-benefit ratio.
and heparin in women with a history of at least two miscarriages
without apparent causes other than inherited thrombophilia. The
two reviewed trials studied different treatments and only one study
was placebo-controlled. None of the studies showed an effect of
one treatment over the other. Therefore, the use of anticoagulants ACKNOWLEDGEMENTS
in this setting is not recommended. However, large, randomised,
placebo-controlled trials are urgently needed. Louisette Peters was an author on the first version of this review.
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10. American Journal of Obstetrics and Gynecology 2004;191(6 Sorensen 2000 {published data only}
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Grandone E, Brancaccio V, Colaizzo D, Sciannamé N,
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in primary early recurrent aborters with an impaired
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Sarig 2003 {published data only} Braekeleer 1990
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2005;83:821–39. Haas DM, Ramsey PS. Progestogen for preventing
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Collaboration, 2000. ∗
Indicates the major publication for the study
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 10
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
13. CHARACTERISTICS OF STUDIES
Characteristics of included studies [ordered by study ID]
Dolitzky 2006
Methods Open label, random allocation with adequate concealment.
Participants Women (n = 107) with a history of three or more consecutive fetal losses in the first trimester or at least
two second trimester fetal losses in whom no cause for their previous pregnancy losses was found
Interventions Subcutaneous enoxaparin (40 mg/daily) versus aspirin (100 mg/daily) from the time of detection of a
fetal heart beat
Outcomes Primary: live birth rates. Secondary: intrauterine growth restriction, birth weight, uterine and umbilical
blood flow, pre-eclampsia, haemorrhage, thrombocytopenia, allergic reactions and congenital malforma-
tions
Notes
Risk of bias
Item Authors’ judgement Description
Allocation concealment? Yes A - Adequate
Tulppala 1997
Methods Double-blind, placebo-controlled.
Participants Women (n = 82) with a history of at least 3 consecutive miscarriages in whom no obvious cause for their
previous pregnancy losses was found
Interventions Aspirin (50 mg/daily) versus placebo, started as soon as a urinary pregnancy test became positive
Outcomes To assess the effect of low-dose aspirin on PGI2 and TXA2 production and on the rate of abortion in
pregnant women with recurrent spontaneous abortion with or without detectable anticardiolipin anti-
bodies
Notes Participants included in the present review: subcategory of 54 women negative for anticardiolipin anti-
bodies
Risk of bias
Item Authors’ judgement Description
Allocation concealment? Unclear B - Unclear
PGI2: prostacyclin 2
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 11
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
14. TXA2: thromboxane A2
Characteristics of excluded studies [ordered by study ID]
Study Reason for exclusion
Bar 2000 Data for women without apparent causes of recurrent pregnancy loss other than inherited thrombophilia
cannot be extracted to be analysed separately
Bar 2001 Data for women without apparent causes of recurrent pregnancy loss other than inherited thrombophilia
cannot be extracted to be analysed separately. Uncontrolled trial
Bick 2000 Non-randomised, uncontrolled trial.
Brenner 2000 Non-randomised trial, historical controls.
Brenner 2005 Data for women without apparent causes of recurrent pregnancy loss other than inherited thrombophilia
cannot be extracted to be analysed separately
Carp 2003 Non-randomised trial, historical controls.
Grandone 2002 Non-randomised trial. Data for women without apparent causes of recurrent pregnancy loss other than
inherited thrombophilia cannot be extracted to be analysed separately
Gris 1995 Moroxydine chloride is not an intervention of interest in this review
Gris 2004 Not all included women had recurrent miscarriage; also women with one miscarriage with a gestational
age of 10 or more weeks were included
Li 2003 Non-randomised trial.
Ogasawara 2001 Non-randomised trial. Data for women without apparent causes of recurrent pregnancy loss other than
inherited thrombophilia cannot be extracted to be analysed separately
Rai 2000 Non-randomised trial.
Reznikoff-Etievant 1999 Non-randomised trial.
Sarig 2003 Data for women without apparent causes of recurrent pregnancy loss other than inherited thrombophilia
cannot be extracted to be analysed separately
Sarto 2001 Non-randomised trial, historical controls.
Sorensen 2000 Non-randomised, uncontrolled trial. Data from women without apparent causes of recurrent pregnancy
loss other than inherited thrombophilia cannot be extracted to be analysed separately
Tzafettas 2002 Non-randomised, uncontrolled trial.
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 12
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
15. (Continued)
Younis 2000 Non-randomised, uncontrolled trial.
Characteristics of ongoing studies [ordered by study ID]
ALIFE study
Trial name or title Anticoagulants for living fetuses study
Methods
Participants Women with at least two or more pregnancy losses without apparent causes other than inherited throm-
bophilias
Interventions Aspirin (100 mg/day) + nadroparine 2850 IE/day versus aspirin (100 mg/day) versus placebo. Medication is
started preconceptional or with a gestation less than 6 weeks. Nadroparine is started when there is a fetal hart
beat (+/- 6 weeks)
Outcomes Primary outcome is live birth rate, secondary outcomes are prevalence of adverse pregnancy outcomes:
preeclampsia, HELLP, intrauterine growth restriction, premature delivery, congenital malformations, throm-
boembolic and hemorrhagic complications, thrombocytopenia, allergic reactions
Starting date 2004
Contact information Dr. S.Middeldorp, Leiden University Medical Center, departments of Clinical Epidemiology and General
Internal Medicine C9-P, PO Box 9600, 3500 RC Leiden, The Netherlands. e-mail: alife@amc.uva.nl
Notes Trial register number:
ISRCTN 58496168
ETHIGII
Trial name or title Effectiveness of dalteparin therapy as intervention in recurrent pregnancy loss
Methods
Participants Women with a history with at least two early pregnancy losses (< 12 wks) or one late pregnancy loss (> 12
wks) without apparent causes other than inherited thrombophilias
Interventions Dalteparin (5000 IE/day) + two tablets multivitamin/day versus only two tablets multivitamin/day. Inclusion
between 5 and 8 weeks’ gestation and foetal heart activity
Outcomes Primary outcome is an ongoing pregnancy at 24 weeks of gestation. Secondary outcomes: preterm delivery,
placental insufficiency, intrauterine growth restriction, preeclampsia, abruptio placentae, structural anomalies,
thromboembolic events, side effects of dalteparin
Starting date 13-11-2006
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 13
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
16. ETHIGII (Continued)
Contact information Prof E.Schleussner, department of Obstetrics, Friedrich Schiller University, Bachstr. 18 Jena, Germany
Notes Trial register number:
ISRCTN
53717039
SPIN study
Trial name or title The Scottish Pregnancy Intervention study
Methods
Participants Women with at least two or more consecutive early pregnancy losses without apparent causes
Interventions Low molecular weight heparin versus aspirin + intense surveillance versus intense surveillance only. Inclusion
until 7 weeks of gestation
Outcomes Primary outcome is live birth rate; secondary outcomes are: preeclampsia, intrauterine growth retardation,
premature delivery, congenital malformations, admission to special care, side effects of the drug, thromboem-
bolic complications
Starting date 01-06-2004
Contact information Dr. P. Clark, Scottish National Blood Transfusion Service, East of Scotland Blood Transfusion Centre,
Ninewells Hospital, Dundee, DD1 9SY, United Kingdom
Notes Trial register number:
ISRCTN
06774126
TIPPS study
Trial name or title Thrombophilia in Pregnancy Prophylaxis Study
Methods
Participants Pregnant women with confirmed thrombophilia.
Interventions Dalteparin versus no medication. Inclusion until 17 weeks of gestation
Outcomes Primary objective is to identify if low-molecular-weight heparin prophylaxis in thrombophilic women reduces
the relative risk in venous thromboembolism, pre-eclampsia, intrauterine growth restriction, and foetal loss
Starting date 01-07-2000
Contact information Dr Marc Rodger, The Ottawa hospital, 1053 Carling Ave, CEP F650, Canada
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 14
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
17. TIPPS study (Continued)
Notes Trial register number:
ISRCTN
87441504
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 15
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
18. DATA AND ANALYSES
Comparison 1. Aspirin versus placebo
No. of No. of
Outcome or subgroup title studies participants Statistical method Effect size
1 Live-birth rate 1 54 Risk Ratio (M-H, Fixed, 95% CI) 1.0 [0.78, 1.29]
Comparison 2. Enoxaparin versus aspirin
No. of No. of
Outcome or subgroup title studies participants Statistical method Effect size
1 Live-birth rate 1 104 Risk Ratio (M-H, Fixed, 95% CI) 0.97 [0.81, 1.16]
2 Preterm delivery 1 104 Risk Ratio (M-H, Fixed, 95% CI) 0.93 [0.28, 3.01]
3 Obstetric complications; 1 104 Risk Ratio (M-H, Fixed, 95% CI) 0.13 [0.01, 2.50]
pre-eclampsia
4 Obstetric complications; 1 104 Risk Ratio (M-H, Fixed, 95% CI) 2.78 [0.12, 66.75]
intrauterine growth restriction
Analysis 1.1. Comparison 1 Aspirin versus placebo, Outcome 1 Live-birth rate.
Review: Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome
Comparison: 1 Aspirin versus placebo
Outcome: 1 Live-birth rate
Study or subgroup Aspirin Placebo Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
Tulppala 1997 22/27 22/27 100.0 % 1.00 [ 0.78, 1.29 ]
Total (95% CI) 27 27 100.0 % 1.00 [ 0.78, 1.29 ]
Total events: 22 (Aspirin), 22 (Placebo)
Heterogeneity: not applicable
Test for overall effect: Z = 0.0 (P = 1.0)
0.1 0.2 0.5 1 2 5 10
Favours placebo Favours aspirin
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 16
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
19. Analysis 2.1. Comparison 2 Enoxaparin versus aspirin, Outcome 1 Live-birth rate.
Review: Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome
Comparison: 2 Enoxaparin versus aspirin
Outcome: 1 Live-birth rate
Study or subgroup enoxaparin aspirin Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
Dolitzky 2006 44/54 42/50 100.0 % 0.97 [ 0.81, 1.16 ]
Total (95% CI) 54 50 100.0 % 0.97 [ 0.81, 1.16 ]
Total events: 44 (enoxaparin), 42 (aspirin)
Heterogeneity: not applicable
Test for overall effect: Z = 0.34 (P = 0.73)
0.01 0.1 1 10 100
Favours aspirin Favours enoxaparin
Analysis 2.2. Comparison 2 Enoxaparin versus aspirin, Outcome 2 Preterm delivery.
Review: Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome
Comparison: 2 Enoxaparin versus aspirin
Outcome: 2 Preterm delivery
Study or subgroup Enoxaparin aspirin Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
Dolitzky 2006 5/54 5/50 100.0 % 0.93 [ 0.28, 3.01 ]
Total (95% CI) 54 50 100.0 % 0.93 [ 0.28, 3.01 ]
Total events: 5 (Enoxaparin), 5 (aspirin)
Heterogeneity: not applicable
Test for overall effect: Z = 0.13 (P = 0.90)
0.01 0.1 1 10 100
Favours enoxaparin Favours aspirin
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 17
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
20. Analysis 2.3. Comparison 2 Enoxaparin versus aspirin, Outcome 3 Obstetric complications; pre-eclampsia.
Review: Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome
Comparison: 2 Enoxaparin versus aspirin
Outcome: 3 Obstetric complications; pre-eclampsia
Study or subgroup enoxaparin aspirin Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
Dolitzky 2006 0/54 3/50 100.0 % 0.13 [ 0.01, 2.50 ]
Total (95% CI) 54 50 100.0 % 0.13 [ 0.01, 2.50 ]
Total events: 0 (enoxaparin), 3 (aspirin)
Heterogeneity: not applicable
Test for overall effect: Z = 1.35 (P = 0.18)
0.01 0.1 1 10 100
Favours enoxaparin Favours aspirin
Analysis 2.4. Comparison 2 Enoxaparin versus aspirin, Outcome 4 Obstetric complications; intrauterine
growth restriction.
Review: Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome
Comparison: 2 Enoxaparin versus aspirin
Outcome: 4 Obstetric complications; intrauterine growth restriction
Study or subgroup enoxaparin aspirin Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
Dolitzky 2006 1/54 0/50 100.0 % 2.78 [ 0.12, 66.75 ]
Total (95% CI) 54 50 100.0 % 2.78 [ 0.12, 66.75 ]
Total events: 1 (enoxaparin), 0 (aspirin)
Heterogeneity: not applicable
Test for overall effect: Z = 0.63 (P = 0.53)
0.1 0.2 0.5 1 2 5 10
Favours treatment Favours control
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 18
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
21. APPENDICES
Appendix 1. Search Strategy
Cochrane Central Register of Controlled Trials (The Cochrane Library 2007, Issue 1), MEDLINE (January 1966 to April 2008), and
EMBASE (1980 to March 2007), adapted for each database.
1 randomized controlled trial.pt.
2 randomized controlled trials/
3 controlled clinical trial.pt.
4 random allocation/
5 comparative study/
6 1 or 2 or 3 or 4 or 5
7 clinical trial.pt.
8 clinical trials/
9 (clin$ adj trial$).tw
10 random$.tw
11 7 or 8 or 9 or 10
12 6 or 11
13 miscarriage$.tw
14 recurrent miscarriage$.tw
15 abortion spontaneous/
16 recurrent abortion$.tw
17 abortion habitual/
18 spontaneous pregnancy loss$.tw
19 recurrent pregnancy loss$.tw
20 early pregnancy loss$.tw
21 early pregnancy bleeding$.tw
22 habitual fetal loss$.tw
23 fetal death/
24 fetal resorption/
25 stillbirth.tw
26 13 or 14 or 15 or 16 or 17 or 18 or 19 or 20 or 21 or 22 or 23 or 24 or 25
27 aspirin/
28 heparin/
29 low-molecular-weight heparin/
30 anticoagulants/
31 anticoagulant agent/
32 antithrombotic$.tw
33 27 or 28 or 29 or 30 or 31 or 32
34 12 and 26
35 33 and 34
Lines 1, 3 and 7 were omitted in the search of EMBASE as it does not have a .pt. field.
Lines 1-12 were not used for the search of CENTRAL
The “/” refers to MeSH, medical subject headings, and (tw) to text word in the title or abstract.
The $ is a truncation character which allows all possible suffix variations of the root word.
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 19
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
22. FEEDBACK
Cundiff, September 2007
Summary
Since aspirin was ineffective compared with placebo in increasing live births, it should not be used as the control treatment in randomised
trials for this indication.
The trial of low molecular weight heparin (enoxaparin) versus low dose aspirin (n = 20) is much too small to assess the risk of potential
adverse effects, such as heparin induced thrombocytopenia with thrombosis and bleeding. Observational or population based studies
should be used to help assess these hazards. Major, fatal, and intracranial bleeding should be included in the primary or secondary
endpoints.
Rebound hypercoagulability after heparin withdrawal [1, 2] should also be assessed by follow up for at least two months after delivery.
Due to potential risks to the mother and baby, heparin or low molecular weight heparin should not be used for this indication outside
randomised trials.
The background section cites the prognosis in subsequent pregnancies of women without antiphospholipid antibody syndrome who
have recurrent pregnancy loss ranges from 50% to 80%. Consequently, in this patient population, the chances for a healthy live baby
within three pregnancies would range from 87.5% to 99.2% (i.e. 1 - [0.50 x 0.50 x 0.50] = .875 and [1 - 0.20 x 0.20 x0.20] = .992).
Given the risks of heparin and the potential for harm if tens of thousands of women have heparin treatment during pregnancy, the
main endpoint in the recommended randomised trial, of anticoagulant versus placebo, should be a live healthy baby in up to three
pregnancies rather than in a single pregnancy.
There is an undisclosed financial conflict of interest in this review, as one of the review authors, Dr. Middledorp, was also one of
the Matisse investigators, who investigated fondaparinux supported by a grant from NV Organon (The Netherlands) and Sanofi-
Synthelabo (France) [3].
References
1. Granger CB, Miller JM, Bovill EG, et al. Rebound increase in thrombin generation and activity after cessation of intravenous heparin
in patients with acute coronary syndromes. Circulation 1995; 91(7):1929-1935.
2. Low-molecular-weight heparin during instability in coronary artery disease, Fragmin during Instability in Coronary Artery Disease
(FRISC) study group. Lancet 1996; 347(9001):561-568.
3. The Matisse Investigators. Subcutaneous Fondaparinux versus Intravenous Unfractionated Heparin in the Initial Treatment of
Pulmonary Embolism. N Engl J Med 2003; 349(18):1695-1702.
(Summary of comment from David K Cundiff, September 2007)
Reply
We agree aspirin was ineffective compared with placebo in increasing live births, and so should not be used as the control treatment
in randomised trials assessing anticoagulants for women with recurrent miscarriage. As we describe in ’Implications for research’, the
inclusion of a placebo or no treatment arm in these studies is necessary to provide an adequate control for active treatment.
We also agree that trials in this field are generally too small to assess the risk of rare but potentially serious adverse effects. Observational
and population-based studies are useful to assess these hazards; however this review is limited to randomised trials.
Following recurrent miscarriage, the calculation that the chance of having a healthy live baby within three pregnancies ranges from
87.5% to 99.2% is probably slightly optimistic. It does not take account of the fact that the chance of a successful pregnancy declines
after each miscarriage, thus the chance of live birth will also decline.
The proposal that a live healthy baby in up to three pregnancies, rather than in one, would be a better endpoint is interesting. However,
the primary outcome of a live birth in a single pregnancy in a well-designed randomised placebo controlled trial will allow better
assessment of possible hazards of the intervention. Also, we doubt whether couples with recurrent miscarriage would regard a healthy
baby after three pregnancies as the ideal outcome.
Finally, although Dr. Middeldorp has been involved in trials of anticoagulants for venous thrombosis that were sponsored by pharma-
ceutical companies, this does not necessarily lead to a conflict of interest. She has published papers in which she has opposed the use of
anticoagulants for the prevention of pregnancy loss or pregnancy complications. She is also principle investigator of the ALIFE study
that is assessing the efficacy and safety of aspirin, and aspirin combined with low-molecular-weight heparin, compared with placebo
(International Standard Randomised Controlled Trial Number Register: 58496168).
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 20
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
23. (Reply from Stef Kaandorp, November 2007)
Contributors
Feedback: David K Cundiff
WHAT’S NEW
Last assessed as up-to-date: 29 April 2008.
Date Event Description
30 April 2008 New search has been performed Search updated. Scope of review changed, resulting in a
previously included study being excluded (Gris 2004).
Please see ’Differences between protocol and review’ for
further details
Authors replied to feedback.
30 April 2008 New citation required but conclusions have not changed Changes to scope of review and team of authors.
11 January 2008 Amended Converted to new review format.
HISTORY
Protocol first published: Issue 2, 2004
Review first published: Issue 2, 2005
Date Event Description
13 November 2008 Feedback has been incorporated Feedback from David K Cundiff added.
CONTRIBUTIONS OF AUTHORS
Stef Kaandorp updated the search and wrote the revised review. Mariette Goddijn commented on the revision.
Marcello Di Nisio wrote the first and the revised drafts of the protocol and review, and commented on the draft of the updated review.
Saskia Middeldorp supervised the development of the review in all of its phases.
Louisette Peters commented on the drafts of the first version of this review.
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 21
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
24. DECLARATIONS OF INTEREST
Drs Kaandorp, Goddijn, and Middeldorp are involved in the running randomised controlled trial ÄLIFE study. This trial is assessing
the efficacy and safety of aspirin, and aspirin combined with low-molecular-weight heparin, compared with placebo for the prevention
of pregnancy loss in women with recurrent miscarriage (International Standard Randomised Controlled Trial Number Register:
58496168). Besides being the principal investigator of the ALIFE study, Dr. Middeldorp has also been and is involved in phase 2
and phase 3 trials that assessing the efficacy and safety of anticoagulant drugs for the indication of venous thrombosis or superficial
thrombophlebitis. These trials were or are being sponsored by various pharmaceutical companies.
DIFFERENCES BETWEEN PROTOCOL AND REVIEW
For this update, we decided to limit our systematic review to women with recurrent miscarriage only. In the first version of the review
also women with one later intrauterine fetal death were included. However, given the presumed differences in etiology and different
prognosis, we judged it not appropriate to pool results of interventions in these different patient populations. This decision has resulted
in the exclusion of a trial (Gris 2004) in which a subgroup had been included in the former version of the review.
INDEX TERMS
Medical Subject Headings (MeSH)
Abortion, Habitual [∗ drug therapy; etiology]; Anticoagulants [∗ therapeutic use]; Antiphospholipid Syndrome [complications]; Aspirin
[therapeutic use]; Heparin, Low-Molecular-Weight [therapeutic use]; Pregnancy Complications, Hematologic [∗ drug therapy; etiology];
Randomized Controlled Trials as Topic; Thrombophilia [complications; ∗ drug therapy]
MeSH check words
Female; Humans; Pregnancy
Aspirin or anticoagulants for treating recurrent miscarriage in women without antiphospholipid syndrome (Review) 22
Copyright © 2009 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.