The additional value of ovarian hyperstimulationin intrauterine insemination for couples withan abnormal postcoital test and a poor prognosis:a randomized clinical trial
Pieternel Steures, Jan Willem van der Steeg, M.D.,Peter G. A. Hompes, M.D., PhPatrick M. M. Bossuyt, J. Dik F. Habbema, Marinus J. C. Eijkemans, M.Sc., Ph.D.,Caroline A. M. Koks, Petra Boudrez, M.D.,Fulco van der Veen, M.D., Ph.D.,
a Department of Obstetrics and Gynecology, Vrije Universiteit Medical Center, Amsterdam; b Center for Reproductive Medicine,Academic Medical Center, Amsterdam; c Department of Public Health, Erasmus MC, University Medical Center Rotterdam,Rotterdam; d Department of Clinical Epidemiology and Biostatistics, Academic Medical Center, Amsterdam; e Department ofObstetrics and Gynecology, Ma´xima Medical Center, Veldhoven; and f Department of Obstetrics and Gynecology, Vie Curie,Venlo, the Netherlands
Objective: To assess the effectiveness of controlled ovarian hyperstimulation (COH) in intrauterine insemination(IUI) for subfertile couples with an abnormal postcoital test and a poor prognosis. Design: Randomized clinical trial. Setting: Twenty-four fertility centers in the Netherlands. Patient(s): Subfertile couples with a well-timed nonprogressive PCT and additional factors that reduce fertility. Intervention(s): Couples were randomly allocated to three cycles of IUI with COH or three cycles of IUI withoutCOH. Main Outcome Measure(s): Ongoing pregnancy within three IUI cycles. Result(s): We randomly allocated 132 couples to IUI with COH, and 133, to IUI without COH. We observed 33pregnancies (25%) in the couples allocated to IUI with COH, of which 28 were ongoing (21%), vs. 28 pregnancies(21%) in the couples allocated to IUI without COH, of which 23 were ongoing (17%; relative risk of an ongoingpregnancy, 1.2; 95% confidence interval, 0.75 to 2.0). Two multiple pregnancies occurred in the IUI with COHgroup, and one, in the IUI without COH group. Conclusion(s): In couples with an abnormal PCT and a poor prognosis, IUI with COH leads to pregnancy ratescomparable to those for IUI without COH. We propose to perform IUI without COH in couples with an abnormalPCT. (Fertil SterilÒ 2007;88:1618–24. Ó2007 by American Society for Reproductive Medicine.)
Key Words: Intrauterine insemination, cervical factor, subfertility, postcoital test, randomized
Intrauterine insemination (IUI) is a common treatment in un-
trolled ovarian hyperstimulation carries the risk of multiple
explained subfertile couples as well as in male subfertility
pregnancies. It poses a burden to the couple and is costly be-
and cervical-factor subfertility. It can be performed with or
cause of the use of gonadotropins and the need for monitoring
without controlled ovarian hyperstimulation (COH). Con-
of follicular development and growth . These drawbacksare warranted only by a substantial gain in ongoing-preg-nancy rate from using IUI with COH compared with IUI
Received July 24, 2006; revised and accepted January 22, 2007.
This randomized controlled trial is registered in the Dutch Trial Register
In cases of unexplained subfertility, IUI is not effective
when the couple’s spontaneous-pregnancy likelihood is
Supported by grant 945-12-002 from ZonMw, the Netherlands Organiza-
>30% in the next 12 months . When IUI is performed in
tion for Health Research and Development, the Hague, the Netherlands.
Presented orally at the Conjoint Annual Meeting of the American Society
unexplained subfertile couples, COH doubles the pregnancy
for Reproductive Medicine and the Canadian Fertility and Andrology
Society, ASRM/CFAS 2005, Montreal, Quebec, Canada, October15–19, 2005.
In cases of male subfertility, IUI improves pregnancy rates.
Reprint requests: Pieternel Steures, M.D., Center of Reproductive Medi-
Intrauterine insemination without COH has been proven to be
cine, Room H4-213, Department of Obstetrics and Gynecology, Aca-
equally effective as IUI with COH and should therefore be the
demic Medical Center, Meibergdreef 9, 1105 AZ Amsterdam, theNetherlands (FAX: 31-20-6963489; E-mail:
first choice of treatment but couples with less severe
Fertility and Sterilityâ Vol. 88, No. 6, December 2007
Copyright ª2007 American Society for Reproductive Medicine, Published by Elsevier Inc.
semen defects benefit from the addition of COH . In none
taneous ongoing pregnancy in the next 12 months, resulting
of the studies on IUI in male subfertility was the prognosis of
Consenting eligible couples were randomly allocated to
In cases of cervical-factor subfertility, IUI appears to be ef-
IUI with COH or to IUI without COH for three cycles, with-
fective in couples with an isolated cervical factor without ad-
out a prespecified time horizon. The randomization sequence
ditional factors that reduce fertility . The incremental
was computer generated in balanced-block multiples of two
value of COH in IUI in couples with a cervical factor has
or four, stratified by center. Sealed opaque envelopes were
been reported in only one retrospective study, which showed
prepared by an independent individual. Clinicians in the par-
a nonsignificant increase in pregnancy rate after the use of
ticipating centers unsealed the first-in-order envelope after
COH (odds ratio, 1.4; 95% confidence interval [CI], 0.85 to
enrolling a couple. The inclusion was then confirmed by
2.2) To prevent undertreatment and overtreatment with
COH, this low level of evidence needs to be confirmed or re-
Cycle monitoring, detection and/or induction of ovulation,
jected in a randomized clinical trial.
as well as semen preparation and insemination regimens were
At present, there are no randomized clinical trials on the
performed according to hospital-specific protocols. The
incremental value of COH in IUI in cervical-factor subfertil-
study recommended for IUI with COH the use of FSH for
ity and male subfertility, taking into account the prognosis of
COH. In general, a baseline transvaginal sonography was
the couple. Therefore, we aimed to assess whether COH in
performed on cycle day 3 to exclude ovarian cysts of size
IUI is of additional value in couples with an abnormal post-
>20 mm. Thereafter, the women started with daily SC injec-
coital test (PCT) resulting from a cervical factor or a male
tions of FSH (Gonal F; Serono Benelux BV, Den Haag, the
factor and with a poor prognosis of an ongoing spontaneous
Netherlands or Puregon; Organon, Oss, the Netherlands) or
pregnancy because of additional factors that reduce fertility.
human menopausal gonadotropin (Menopur; Ferring, Hoofd-dorp, the Netherlands) in doses of 75 IU, until transvaginalsonography showed at least one follicle with a diameter of16 mm. Doses were adjusted in a range from 50 IU to 150
IU, depending on the ovarian response. The aim of mild ovar-
The study was performed between June 1, 2002 and July 1,
ian hyperstimulation was to obtain multifollicular growth.
2005 in 24 fertility centers in the Netherlands. The study
Ovulation was then induced by the administration of 5,000
was approved by the local ethics committee of each partici-
or 10,000 IU of hCG (Pregnyl, Organon), and women were
inseminated 36 to 40 hours later. The administration ofhCG was withheld, and IUI was not performed, if there
In couples who had an unfulfilled wish for a child and had
were present more than three follicles with a diameter of
R1 year with regular unprotected intercourse and in whom
R16 mm, or five follicles with a diameter of R12 mm.
the woman had a regular cycle, a basic fertility workup wasperformed. This was done according to the guidelines of
Semen samples were processed within 1 hour after ejacu-
the Dutch Society of Obstetrics and Gynaecology and in
lation by using a density gradient centrifugation, followed by
the same way as reported in our study on the effectiveness
a washing step with culture medium. The volume of semen
of IUI with COH in unexplained subfertility
that was inseminated varied between 0.3 mL and 0.5 mL.
After completion of the basic fertility workup, in couples
In the IUI cycles without COH, ovulation detection was
with an abnormal (negative) PCT, in other words, a well-
performed with urine LH tests (a semi-quantitative monoclo-
timed, nonprogressive PCT that was caused by a cervical fac-
nal antibody–based kit; OvuQuick, Quid, San Diego, CA)
tor or a male factor, the prognosis was calculated for a
with a detection level of 40 IU, or by transvaginal sonogra-
spontaneous ongoing pregnancy resulting in a live-born child
phy. If ovulation was detected with LH tests, patients tested
in the next 12 months. A spontaneous pregnancy was defined
their urine samples once or twice per day, starting on an indi-
as a pregnancy that occurred without treatment. The progno-
vidually calculated cycle day. Women were inseminated 20 to
sis was calculated according to the prediction model of
30 hours after the endogenous LH surge had been detected in
Hunault et al. by using a computer program or a paper
the urine sample. In case follicular growth was monitored by
score list . This model incorporates the variables of fe-
transvaginal sonography, hCG (Pregnyl, Organon) was ad-
male age, duration of subfertility, primary or secondary sub-
ministered when the dominant follicle had a diameter of
fertility, referral status, and percentage of progressive motile
R16 mm. Women were inseminated 36 to 40 hours thereaf-
semen. Each variable is converted into a point score. The total
ter. Semen was processed and inseminated in the same way as
point score of each couple corresponds to a prognosis for
spontaneous ongoing pregnancy. The computer model can
Couples were followed until an ongoing pregnancy oc-
curred. If pregnancy had not occurred, follow-up ended after
the third IUI cycle or at drop out. If a pregnancy miscarried,
Couples with an abnormal PCT were invited to join the
follow-up continued until the next pregnancy, or the last of
study if the model indicated a prognosis of %30% of a spon-
The primary endpoint was ongoing pregnancy within three
a number needed to treat, both with their 95% CI. We plotted
IUI cycles. Ongoing pregnancy was defined as the presence
Kaplan-Meier curves to visualize the time to pregnancy in the
of fetal cardiac activity at transvaginal sonography at a gesta-
two groups, and we compared these curves by using a log
tional age of R12 weeks. Secondary endpoints were clinical
pregnancies, miscarriages, ectopic pregnancies, multiple
We performed additional analyses in which we evaluated
pregnancies, and live birth. Clinical pregnancy was defined
the pregnancy rate per IUI cycle with or without COH and ex-
as the presence of a yolk sac at transvaginal sonography at
pressed the treatment effect as relative risk and number
a gestational age of 7 weeks. Miscarriage was defined as non-
needed to treat. We compared the effectiveness of IUI with
vital pregnancy, either seen at transvaginal sonography or as
COH with that of IUI without COH in the subgroup of cou-
a result of the loss of a visible pregnancy.
ples with a total motile sperm count (TMC) of R10 million
We designed our study as a noninferiority trial. Our hy-
and in the subgroup of couples with a TMC of <10 million
pothesis was that IUI without COH would not be inferior to
(severe male subfertility). In the IUI with COH group, we
IUI with COH. If this were to be true, IUI without COH
also assessed the relation between follicular growth patterns
would be the preferred strategy. We considered IUI without
COH not to be inferior to IUI with COH if we could excludethat the pregnancy rate without COH was R12.5% lower, us-ing a 5% significance level. A smaller difference was judged
to be clinically irrelevant, because the cost and adverse ef-
In total, 657 consecutive couples with an abnormal PCT and
fects of COH would outweigh the slight increase in preg-
a poor prognosis of a spontaneous ongoing pregnancy in the
nancy rate. Assuming an 18% ongoing-pregnancy rate after
next year were registered in one of the participating centers.
three cycles of IUI, 117 couples had to be enrolled in each
Informed consent was obtained from 272 couples (41%),
group to achieve an 80% level of power.
among whom 136 couples were randomly allocated to IUIwith COH and 136 couples to IUI without COH ().
All pregnancies occurring within the three IUI cycles were
included in the analyses, as well as spontaneous pregnancies
Seven randomized couples had to be excluded from the
occurring before or between these IUI cycles. The treatment
analyses who did not meet the inclusion criteria because
effect of IUI with COH was expressed as relative risk and as
they had a positive PCT, a short duration of subfertility
Flowchart of trial population, with inclusion and outcome. Ong ¼ ongoing.
Steures. Value of COH in IUI for an abnormal PCT. Fertil Steril 2007.
(<12 mo), or two-sided tubal occlusion, known at the time of
cies were ongoing, and one miscarried. After IUI, 26 preg-
nancies (20%) occurred. Twenty-two of these pregnancieswere ongoing, 3 miscarried, and 1 was an ectopic pregnancy.
The baseline characteristics of the two groups were com-
There were 2 twin pregnancies. Of the 28 ongoing pregnan-
parable All women included in the study had their
cies, all 26 singleton pregnancies (100%) resulted in a live
tubes assessed before randomization by chlamydia antibody
birth of one child; 1 twin pregnancy resulted in the live birth
test (CAT), hysterosalpingography, or diagnostic laparoscopy
of both children; and in the other twin pregnancy, one child
(DLS). In 101 women (77%) allocated to IUI with COH and
was healthy and the other one died. Eighteen couples did
107 women (80%) allocated to IUI without COH, tubal func-
not complete three IUI cycles because of the burden of the
tion had been assessed by hysterosalpingography or laparos-
treatment, insurance problems, personal reasons, or having
copy before randomization. In 8 women (7.9%) and 9 women
switched earlier to IVF (13.6%). The latest IUI cycle took
(8.4%), respectively, one-sided tubal occlusion was found. In
the follow-up time for three IUI cycles, two and five women,respectively, underwent a hysterosalpingography or laparos-
In the group allocated to IUI without COH, three women
copy. In these women, both tubes were patent. Taken to-
(2%) conceived spontaneously before the start of IUI. All
gether, 103 women (78%) allocated to IUI with COH and
three pregnancies were ongoing. One hundred and twenty
112 women (84%) allocated to IUI without COH underwent
eight couples started IUI. Three women (2%) conceived
a hysterosalpingography or laparoscopy, among whom 8
spontaneously between IUI cycles. These pregnancies were
women (7.8%) and 9 women (8.0%), respectively, had one-
all ongoing. After IUI, 22 pregnancies (17%) occurred. Sev-
enteen of these pregnancies were ongoing, four miscarried,
Pregnancy data are summarized in Complete fol-
and one was an ectopic pregnancy. There was one twin preg-
low-up was obtained for all couples. In the group allocated to
nancy. Finally, of the 23 ongoing pregnancies, 21 singleton
IUI with COH, three women (2%) conceived spontaneously
pregnancies resulted in a live birth of one child, one singleton
before the start of IUI. All pregnancies were ongoing. In
pregnancy resulted in an intrauterine fetal death, and the twin
124 couples, IUI was started. Four women (3%) conceived
pregnancies resulted in the live birth of both children. Ten
spontaneously between IUI cycles. Three of these pregnan-
couples did not complete three IUI cycles because of burden
Mean duration of subfertility, y (min–max)
a Data available at time of randomization in 117 and 115 women in the IUI with COH group and expectant-management
b Data available at time of randomization in 64 and 65 women in the IUI with COH group and expectant-management
c Data available at time of randomization in 100 and 101 women in the IUI with COH group and expectant-management
d Data available at time of randomization in 72 and 66 women in the IUI with COH group and expectant-management
e Data available at time of randomization in 29 and 41 women in the IUI with COH group and expectant-management
Steures. Value of COH in IUI for an abnormal PCT. Fertil Steril 2007.
In the group allocated to IUI with COH, 325 IUI cycles
were started, of which 43 cycles (13%) were canceled. Thepregnancy rate per started cycle was 8.0%, with an ongo-
Kaplan Meier curves: time to ongoing pregnancy.
ing-pregnancy rate of 6.8% per started cycle. In 23 IUI cycles
(7.1%), COH was performed with antiestrogenic medication(clomiphene citrate). In these IUI cycles, two ongoing preg-
nancies occurred (8.7% per started cycle). In the group allo-cated to IUI without COH, 345 IUI cycles were started, ofwhich 34 cycles (9.9%) were canceled. The pregnancy rate
per started cycle was 6.4%, with an ongoing-pregnancy rateof 4.9% per started cycle. When calculations were performed
at a cycle level, the relative risk was 1.4 (95% CI, 0.74 to 2.5). The number of cycles needed to treat for COH was 54 to
achieve one additional ongoing pregnancy (95% CI, 18 toinfinity).
The pregnancies in relation to the TMC for IUI with and
without COH are shown in . The effectiveness of
IUI with COH in couples with a TMC of R10 million was
not different from that in the total group (relative risk, 1.25;95% CI, 0.93 to 1.7). Multifollicular growth was registered
Steures. Value of COH in IUI for an abnormal PCT. Fertil Steril 2007.
in 230 (82%) of the 282 inseminated cycles. Multifolliculargrowth, defined as more than one follicle with a diameter
of the treatment, insurance problems, personal reasons, or
of 10 mm, occurred in 62% of the inseminated cycles with
having switched earlier to IVF (7.5%). The latest IUI cycle
COH. In 38% of the inseminated cycles with COH, more
took place within 6 months of follow-up.
than one follicle with a diameter of 15 mm was present atthe time of hCG injection. The pregnancies in relation to
In total, 33 pregnancies (25%) occurred in the group allo-
the follicular growth for the group allocated to IUI with
cated to IUI with COH, and 28 pregnancies (21%), in the
COH are shown in No clear differences in the preg-
group allocated to IUI without COH ). The miscarriage
nancy rates were seen between the cycles with monofollicu-
rates in both groups were 15% and 18%, respectively. The
number of ongoing pregnancies in the IUI with and withoutCOH groups were 28 (21%) and 23 (17%), respectively, re-sulting in a relative risk of 1.2 (95% CI, 0.75 to 2.0). The cor-
responding absolute risk difference was þ4% (95% CI, –6%
This is the first randomized clinical trial that evaluated the ad-
to þ13%), corresponding with a number needed to treat of 26
ditional value of COH in IUI in couples with an abnormal
(95% CI, 10 to infinity). The Kaplan-Meier curves showed no
PCT. Our data show an almost similar effect of IUI with
significant difference in the time to pregnancy in both groups
and without COH in these couples. The estimates of treat-
ment effect were not different in couples with a TMC of
Pregnancies in relation to the TMC for IUI with and without COH. Note: All data are n (%) unless otherwise indicated.
Steures. Value of COH in IUI for an abnormal PCT. Fertil Steril 2007.
Pregnancies after IUI with COH in relation to follicular growth.
Steures. Value of COH in IUI for an abnormal PCT. Fertil Steril 2007.
>10 million and in couples with a TMC of <10 million, but
lower pregnancy rate can be explained by the prognostic pro-
because the study was not powered for the additional analysis
file of the couple. In the retrospective study, couples with cer-
of the relation between pregnancies and the total motile
vical-factor subfertility were included independently of their
sperm count, this result should be interpreted with caution.
prognosis, whereas in the present study, only couples witha poor prognosis were included.
A strength of this study is that we used the prognostic pro-
file of each couple, in addition to their diagnosis, as an inclu-
The 4% difference in pregnancy rate that we found means
sion criterion. This way, we included both couples with an
that COH should not be applied in couples with an abnormal
abnormal PCT and a long duration of their subfertility, as
PCT. Because the 95% CI ranged from À6% to 13%, a bene-
well as couples with an abnormal PCT and poor semen qual-
ficial effect of COH cannot be excluded completely. How-
ity or couples with an advanced maternal age. This approach
ever, in clinical decision making, the risks of these two
led to a selection of a more specific and homogeneous group
treatment policies also should be taken into account. In
from the prognostic profile. Because the treatment effect in
case of multifollicular growth, which is the primary aim of
subfertile couples may be dependent not only on diagnosis
COH, there is a risk of multiple pregnancy, and couples are
but also on prognosis, documenting the prognostic profile
forced to trade off between the risks of a multiple pregnancy
of the included couples makes our study results easy to inter-
and cancellation of the IUI cycle, the latter obviously imply-
pret and to generalize for each fertility clinic .
ing no pregnancy at all. Moreover, the risk of multiple preg-nancies cannot always be foreseen, because in IUI with COH,
There are some possible limitations of this study. We erro-
these pregnancies also can arise from borderline or small fol-
neously included seven couples who did not meet the inclu-
licles in cycles that are not canceled on the basis of existing
sion criteria. These couples were distributed equally over
guidelines. In contrast, IUI without COH bears no increased
the two treatment policies, and therefore either inclusion or
medical risk at a lower financial cost.
exclusion would not affect the results and conclusion or ourstudy. Because the aim of this trial was to assess whether ad-
The PCT has been abandoned in many guidelines. How-
dition of COH is effective in subfertile couples with a nega-
ever, performing the PCT enables identification of couples
tive PCT and at least one patent tube, we believe that
with a cervical factor and avoids misclassifying these couples
postrandomization exclusion is a better option than leaving
as having unexplained infertility. This misdiagnosis would
lead to the use of IUI with COH, which increases costs andthe risk of multiple pregnancies, without increasing chances
Another limitation may be the fact that the study protocol
recommended FSH for COH, but in 7.1% of IUI cycles, COHwas performed with anti-estrogenic medication (clomiphene
In conclusion, IUI with COH, in couples with an abnormal
citrate). However, in a Cochrane review, no significant differ-
PCT and a poor prognosis, leads to pregnancy rates that are
ence in live birth rates per couple after IUI with FSH and IUI
comparable to those obtained by using IUI without COH. In-
with anti-estrogenic medication was found Although
trauterine insemination without COH should be the treatment
this study had a protocol for the performance of the PCT
and the treatment of IUI, the very fact that 24 centers partic-ipated in the trial may have affected the results. Nevertheless,this limitation is relative because this multicenter approach
reflects the performance of the PCT and the effectiveness of
1. Fauser BCJM, Devroey P, Macklon NS. Multiple birth resulting from
IUI in daily fertility practice. The ongoing-pregnancy rate
ovarian stimulation for subfertility treatment. Lancet 2005;365:
per started IUI cycle with or without COH of 6.8% and
2. Steures P, van der Steeg JW, Hompes PG, Habbema JD, Eijkemans MJ,
4.9%, respectively, is lower than the 10% and 13% that
Broekmans FJ, et al. Intrauterine insemination with controlled ovarian
were described elsewhere in a retrospective study This
hyperstimulation versus expectant management for couples with
unexplained subfertility and an intermediate prognosis: a randomised
clinical trial. Lancet 2006;368:216–21.
3. Guzick DS, Sullivan MW, Adamson GD, Cedars MI, Falk RJ,
The CECERM (Collaborative Effort for Clinical Evaluation
Peterson EP, et al. Efficacy of treatment for unexplained infertility. Fertil
in Reproductive Medicine) study group investigators and
4. Guzick DS, Carson SA, Coutifaris C, Overstreet JW, Factor-Litvak P,
their participating centers in the Netherlands are as follows:
Steinkampf MP, et al. Efficacy of superovulation and intrauterine insem-
Y.M. van Kasteren (Medisch Centrum Alkmaar, Alkmaar)
ination in the treatment of infertility. National Cooperative ReproductiveMedicine Network. N Engl J Med 1999;340:177–83.
P. F. M. van der Heijden (Twenteborg Ziekenhuis, Almelo)
5. Cohlen BJ, Vandekerckhove P, te Velde ER, Habbema JDF. Timed inter-
W. A. Scho¨ls (Meander Medisch Centrum, Amersfoort)
course versus intra-uterine insemination with or without ovarian hyper-
M. H. Mochtar (Academisch Medisch Centrum, Amsterdam)
stimulation for subfertility in men. Cochrane Database Syst Rev
H. R. Verhoeve (Onze Lieve Vrouwe Gasthuis, Amsterdam)
P. G. A. Hompes (Vrij Universiteit Medisch Centrum,
6. Cohlen BJ, te Velde ER, van Kooij RJ, Looman CW, Habbema JDF. Con-
trolled ovarian hyperstimulation and intrauterine insemination for treat-
ing male subfertility: a controlled study. Hum Reprod 1998;13:1553–8.
L. J. van Dam (Gelre Ziekenhuis, Apeldoorn)
7. Steures P, van der Steeg JW, Hompes PGA, Bossuyt PMM, Habbema
A. V. Sluijmer (Wilhelmina Ziekenhuis, Assen)
JDF, Eijkemans MJC, et al. Effectiveness of intrauterine insemination
R. E. Bernardus (Ziekenhuis Gooi-Noord, Blaricum)
in subfertile couples with an isolated cervical factor: a randomized clin-
J. P. Do¨rr (Westeinde Ziekenhuis, Den Haag)
ical trial. Fertil Steril. In press.
8. Steures P, van der Steeg JW, Verhoeve HR, van Dop PA, Hompes PGA,
P.J.Q. van der Linden (Ziekenhuis Deventer, Deventer)
Bossuyt PMM, et al. Does ovarian hyperstimulation in intrauterine in-
J. M. Burggraaff (Scheper Ziekenhuis, Emmen)
semination for cervical factor subfertility improve pregnancy rates?
G. J. E. Oosterhuis (Medisch Spectrum Twente, Enschede)
M. H. Schouwink (Sint Anna Ziekenhuis, Geldrop)
9. Dutch Society of Obstetrics and Gynaecology. Guideline—basic fertility
P. X. J. M. Bouckaert (Atrium Medisch Centrum, Heerlen)
work-up. 2004. NVOG-richtlijn no. 1.
10. Hunault CC, Habbema JDF, Eijkemans MJC, Collins JA, Evers JL, te
F. M. C. Delemarre (Elkerliek Ziekenhuis, Helmond)
Velde ER. Two new prediction rules for spontaneous pregnancy leading
J. H. Schagen-Van Leeuwen (St. Antonius Ziekenhuis,
to live birth among subfertile couples, based on the synthesis of three pre-
vious models. Hum Reprod 2004;19:2019–26.
J. A. M. Kremer (UMC St. Radboud, Nijmegen)
11. van der Steeg JW, Steures P, Eijkemans MJ, Habbema JD, Hompes PG,
H. J. H. M. Van Dessel (TweeSteden Ziekenhuis, Tilburg/
Broekmans FJ, et al. Pregnancy is predictable: a large-scale prospectiveexternal validation of the prediction of spontaneous pregnancy in subfer-
tile couples. Hum Reprod 2007;22:536–42.
F. J. M. Broekmans (UMC Utrecht, Utrecht)
12. Habbema JDF, Collins J, Leridon H, Evers JLH, Lunenfeld B,
C. A. M. Koks (Ma´xima Medisch Centrum, Veldhoven)
Velde ERT. Towards less confusing terminology in reproductive medi-
P. Bourdrez (Vie Curi Medisch Centrum, Venlo/Venray)
cine: a proposal. Fertil Steril 2004;82:36–40.
W. W. J. Riedijk (Zaans Medisch Centrum, Zaandam)
13. Athaullah N, Proctor M, Johnson NP. Oral versus injectable ovulation in-
duction agents for unexplained subfertility. Cochrane Database Syst Rev
A Summary of Some Useful Plants in the Páramo of Nudo del Azuay Jessica A. Werner Round River Conservation Studies, Cuenca, Ecuador (Department of Biology, Colby College, Waterville, ME) April, 2010 Abstract: The data was gathered about the edible or useful plants in the páramo of Nudo del Azuay. Information was gathered on 31 plant species, 24 were identified to at least family and 17
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