FEMALE INFERTILITY:
Endometriosis
Fertil Steril 2002 Oct;78(4):750-6
Cycle-specific and cumulative fecundity in patients
with endometriosis who are undergoing controlled ovarian
hyperstimulation-intrauterine insemination or in vitro
fertilization-embryo transfer.
Dmowski WP, Pry M, Ding J, Rana N.
Institute for the Study and Treatment of Endometriosis,
Oak Brook, Illinois, USA. wpdmowski@oakbrookfertility.com
OBJECTIVE: To compare controlled ovarian hyperstimulation-intrauterine
insemination (COH-IUI) or IVF-ET pregnancy rates per cycle
(PR) and cycle and cumulative fecundity (f and cf) with
COH-IUI or IVF-ET in endometriosis. DESIGN: Retrospective
analysis. SETTING: Endometriosis research institute. PATIENT(S):
Women with endometriosis and infertility (n = 313) who
underwent consecutive COH-IUI (202 patients, 648 cycles),
IVF-ET (111 patients, 139 cycles), or IVF-ET after failed
COH-IUI (56 patients, 68 cycles). INTERVENTION(S): None.
MAIN OUTCOME MEASURE(S): Crude PR and life table-estimated
f and cf. RESULT(S): With COH-IUI, 69 patients conceived;
65 conceived with IVF-ET; and 30 conceived with IVF-ET
after COH-IUI (PR 11%, 47%, and 44%). With COH-IUI, six-cycle
cf was 41%, and f for cycles 1-6 was 15%, 12%, 8%, 7%,
7%, and 0. With IVF-ET, three-cycle cf was 73%, whereas
f for cycles 1-3 was 47%, 27%, and 33%. First-cycle f
with IVF-ET was significantly higher than cf of six COH-IUI
cycles. When the data were stratified according to the
stage of endometriosis and women's age, the benefit of
IVF over COH was even more pronounced. Prior COH-IUI failure
did not adversely affect IVF-ET outcome. CONCLUSION(S):
In endometriosis, PR, f, and cf are significantly higher
with IVF-ET than COH-IUI, especially in stage IV and in
women >38 years of age. Considering adverse effects of
prolonged ovarian stimulation on endometriosis, IVF-ET
should be the first-line approach in the management of
infertility in this disease. If COH-IUI is attempted,
it should not exceed three to four cycles.
J Med Assoc Thai 2001 Jun;84 Suppl 1:S371-6
Effects of contaminated endometriotic contents on quality
of oocytes. Suwajanakorn S, Pruksananonda K, Sereepapong
W, Ahnonkitpanit V, Chompurat D, Boonkasemsanti W, Virutamasen
P.
Department of Obstetrics and Gynecology, Faculty of
Medicine, Chulalongkorn University, Bangkok, Thailand.
The mechanism of infertility associated with endometriosis
is poorly understood. There is evidence supporting that
women with ovarian endometriosis have a lower pregnancy
rate than women with peritoneal lesions only. This study
aimed to evaluate the effects of endometriotic contents
contamination while retrieving oocytes on oocytes' quality.
Thirty-eight infertile patients with endometriotic cysts
from January 1993 to June 2000 were enrolled in this study.
There were no statistically significant differences among
the quality of oocytes and embryos from the contaminated,
non-contaminated, and control group. However, the fertilization
rate and pregnancy rate were impaired by the contamination
of endometriotic contents. We conclude that ovarian endometriosis
should be treated before starting in vitro fertilization
program in order to increase the pregnancy outcome.
J Reprod Med 2002 Oct;47(10):801-8
Impact of endometriosis on implantation. Data from
the Wilford Hall Medical Center IVF-ET Program. Hickman
TN.
Division of Reproductive Endocrinology and Infertility,
Department of Obstetrics and Gynecology, Wilford Hall
Medical Center, Lackland Air Force Base, Texas, USA. timothy.hickman@jhu.edu
OBJECTIVE: To investigate the effect of endometriosis
on implantation. STUDY DESIGN: In a retrospective cohort
study, 149 consecutive in vitro fertilization retrieved
cycles were analyzed. Patients with endometriosis (n =
27, 31 cycles) were compared with a control group with
tubal infertility (n = 104, 118 cycles). The main outcome
measure was implantation rate (gestational sac per transferred
embryo). RESULTS: The patients in the tubal infertility
group were slightly younger and tended to have a better
response to stimulation and increased number of oocytes
retrieved than did the patients in the endometriosis group;
however, there were no differences in fertilization rates,
number of embryos transferred or clinical pregnancy rates
per cycle between the endometriosis group and tubal infertility
group. The overall clinical pregnancy rate per cycle was
similar for women in the endometriosis and tubal infertility
groups (54.8% and 55.1%, respectively). The implantation
rate was not different in the endometriosis versus tubal
infertility group (28% [28/100] and 29.8%, [108/363],
respectively; P = .75, relative risk = .94, 95% confidence
interval .66, 1.34). CONCLUSION: For women undergoing
in vitro fertilization-embryo transfer with endometriosis,
the implantation rate is not markedly different from that
for women undergoing in vitro fertilization-embryo transfer
with tubal infertility.