Professional Documents
Culture Documents
It is
the result of a flaw in human reproductive physiology that allows the conceptus to
implant and mature outside the endometrial cavity, which ultimately ends in death of the
fetus. Without timely diagnosis and treatment, ectopic pregnancy can become a life-
threatening situation.
Ectopic pregnancy currently is the leading cause of pregnancy-related death during the
first trimester in the United States, accounting for 9% of all pregnancy-related deaths. In
addition to the immediate morbidity caused by ectopic pregnancy, the woman's future
ability to reproduce may be adversely affected as well.
[ CLOSE WINDOW ]
The survival rate in the early 19th century was dismal. One report demonstrated only 5
patients of 30 surviving the abdominal operation. Interestingly, the survival rate in
patients who were left untreated was 1 of 3.
In the beginning of the 20th century, great improvements in anesthesia, antibiotics, and
blood transfusion contributed to the decrease in the maternal mortality rate. In the early
half of the 20th century, 200-400 deaths per 10,000 cases were attributed to ectopic
pregnancy. In 1970, the Centers for Disease Control and Prevention (CDC) began to
record the statistics regarding ectopic pregnancy, reporting 17,800 cases. By 1992, the
number of ectopic pregnancies had increased to 108,800. Concurrently, however, the
case-fatality rate decreased from 35.5 deaths per 10,000 cases in 1970 to 2.6 per 10,000
cases in 1992.
Problem
Ectopic pregnancy is derived from the Greek word ektopos, meaning out of place, and it
refers to the implantation of a fertilized egg in a location outside of the uterine cavity,
including the fallopian tubes, cervix, ovary, cornual region of the uterus, and the
abdominal cavity. This abnormally implanted gestation grows and draws its blood supply
from the site of abnormal implantation. As the gestation enlarges, it creates the potential
for organ rupture because only the uterine cavity is designed to expand and accommodate
fetal development. Ectopic pregnancy can lead to massive hemorrhage, infertility, or
death.
Frequency
Since 1970, the frequency of ectopic pregnancy has increased 6-fold, and it now occurs in
2% of all pregnancies. An estimated 108,800 ectopic pregnancies in 1992 resulted in
58,200 hospitalizations with an estimated cost of $1.1 billion.
Etiology
Multiple factors contribute to the relative risk of ectopic pregnancy. In theory, anything
that hampers the migration of the embryo to the endometrial cavity could predispose
women to ectopic gestation. The most logical explanation for the increasing frequency of
ectopic pregnancy is previous pelvic infection; however, most patients presenting with an
ectopic pregnancy have no identifiable risk factor. The following risk factors have been
linked with ectopic pregnancy:
After one ectopic pregnancy, a patient incurs a 7- to 13-fold increase in the likelihood of
another ectopic pregnancy. Overall, a patient with prior ectopic pregnancy has a 50-80%
chance of having a subsequent intrauterine gestation, and a 10-25% chance of a future
tubal pregnancy.
Prior tubal surgery has been demonstrated to increase the risk of developing ectopic
pregnancy. The increase depends on the degree of damage and the extent of anatomic
alteration. Surgeries carrying higher risk of subsequent ectopic pregnancy include
salpingostomy, neosalpingostomy, fimbrioplasty, tubal reanastomosis, and lysis of
peritubal or periovarian adhesions.
Conception after previous tubal ligation increases a women's risk of developing ectopic
pregnancies. Thirty-five to 50% of patients who conceive after a tubal ligation are
reported to experience an ectopic pregnancy. Failure after bipolar tubal cautery is more
likely to result in ectopic pregnancy than occlusion using suture, rings, or clips. Failure is
attributed to fistula formation that allows sperm passage. Ectopic pregnancies following
tubal sterilizations usually occur 2 or more years after sterilization, rather than
immediately after. In the first year, only about 6% of sterilization failures result in ectopic
pregnancy.
Ovulation induction with clomiphene citrate or injectable gonadotropin therapy has been
linked with a 4-fold increase in the risk of ectopic pregnancy in a case-control study. This
finding suggests that multiple eggs and high hormone levels may be significant factors.
One study has demonstrated that infertility patients with luteal phase defects have a
statistically higher ectopic pregnancy rate than patients whose infertility is caused by
anovulation. The risk of ectopic pregnancy and heterotopic pregnancy (ie, pregnancies
occurring simultaneously in different body sites) dramatically increases when a patient
has used assisted reproductive techniques to conceive, such as in vitro fertilization (IVF)
or gamete intrafallopian transfer (GIFT). In a study of 3000 clinical pregnancies achieved
through in vitro fertilization, the ectopic pregnancy rate was 4.5%, which is more than
double the background incidence. Furthermore, studies have demonstrated that up to 1%
of pregnancies achieved through IVF or GIFT can result in a heterotopic gestation,
compared to an incidence of 1 in 30,000 pregnancies for spontaneous conceptions.
Increasing age
The highest rate of ectopic pregnancy occurs in women aged 35-44 years. A 3- to 4-fold
increase in the risk for developing an ectopic pregnancy exists compared to women aged
15-24 years. One proposed explanation involves the myoelectrical activity in the
fallopian tube, which is responsible for tubal motility. Aging may result in a progressive
loss of myoelectrical activity along the fallopian tube.
Smoking
Cigarette smoking has been shown to be a risk factor for developing an ectopic
pregnancy. Studies have demonstrated elevated risk ranging from 1.6-3.5 times that of
nonsmokers. A dose-response effect also has been suggested. Based on laboratory studies
in humans and animals, researchers have postulated several mechanisms by which
cigarette smoking might play a role in ectopic pregnancies. These mechanisms include
one or more of the following: delayed ovulation, altered tubal and uterine motility, or
altered immunity. To date, no study has supported a specific mechanism by which
cigarette smoking affects the occurrence of ectopic pregnancy.
Other
Other risk factors associated with increased incidence of ectopic pregnancy include
previous diethylstilbestrol (DES) exposure, a T-shaped uterus, prior abdominal surgery,
failure with progestin-only contraception, and ruptured appendix.
Pathophysiology
Most ectopic pregnancies are located in the fallopian tube (see Media file 1).
[ CLOSE WINDOW ]
Sites and frequencies of ectopic pregnancy. By Donna M. Peretin, RN. (A)
Ampullary, 80%; (B) Isthmic, 12%; (C) Fimbrial, 5%; (D) Cornual/Interstitial, 2%;
(E) Abdominal, 1.4%; (F) Ovarian, 0.2%; (G) Cervical, 0.2%.
The most common site is the ampullary portion of the tube, where over 80% occur. The
next most common sites are the isthmic segment of the tube (12%), the fimbria (5%), and
the cornual and interstitial region of the tube (2%). Nontubal sites of ectopic pregnancy
are a rare occurrence, with abdominal pregnancies accounting for 1.4% of ectopic
pregnancies and ovarian and cervical sites accounting for 0.2% each.
Presentation
The classic clinical triad of ectopic pregnancy is pain, amenorrhea, and vaginal bleeding.
Unfortunately, only 50% of patients present typically. Patients may present with other
symptoms common to early pregnancy, including nausea, breast fullness, fatigue, low
abdominal pain, heavy cramping, shoulder pain, and recent dyspareunia. Astute clinicians
should have a high index of suspicion for ectopic pregnancy in any woman who presents
with these symptoms and who presents with physical findings of pelvic tenderness,
enlarged uterus, adnexal mass, or tenderness.
Remember, however, that only 40-50% of patients with an ectopic pregnancy present
with vaginal bleeding, 50% have a palpable adnexal mass, and 75% may have abdominal
tenderness. Approximately 20% of patients with ectopic pregnancies are
hemodynamically compromised at initial presentation, which is highly suggestive of
rupture. Fortunately, using modern diagnostic techniques, most ectopic pregnancies may
be diagnosed prior to rupturing.
Indications
Medical therapy
Surgical therapy
Within the last 2 decades, a more conservative surgical approach to unruptured ectopic
pregnancy using minimally invasive surgery has been advocated to preserve tubal
function (see Surgical Therapy). Laparoscopy has become the recommended approach in
most cases. Laparotomy is usually reserved for patients who are hemodynamically
unstable or patients with cornual ectopic pregnancies. It also is a preferred method for
surgeons inexperienced in laparoscopy and in patients where laparoscopic approach is
difficult (eg, secondary to the presence of multiple dense adhesions, obesity or massive
hemoperitoneum). In a patient who has completed childbearing and no longer desires
fertility, in a patient with a history of an ectopic pregnancy in the same tube, or in a
patient with severely damaged tubes, total salpingectomy is the procedure of choice.
Expectant management
Candidates for successful expectant management are asymptomatic and have no evidence
of rupture or hemodynamic instability. Furthermore, they should portray objective
evidence of resolution, such as declining bhCG levels. They must be fully compliant and
must be willing to accept the potential risks of tubal rupture.
Relevant Anatomy
See Pathophysiology.
Contraindications
Medical therapy
A bhCG level of greater than 15,000 IU/L, fetal cardiac activity, and free fluid in the cul-
de-sac on US (presumably representing tubal rupture) are contraindications to medical
therapy with methotrexate. Other contraindications to the use of methotrexate include
documented hypersensitivity to methotrexate; breastfeeding; immunodeficiency;
alcoholism; alcoholic liver disease or any liver disease; blood dyscrasias; leukopenia;
thrombocytopenia; anemia; active pulmonary disease; peptic ulcer disease; and renal,
hepatic, or hematologic dysfunction.
Surgical therapy
Surgical treatment in cases in which the pregnancy is located on the cervix, ovary, or in
the interstitial or the cornual portion of the tube is often associated with increased risk of
hemorrhage, often resulting in hysterectomy or oophorectomy. In these cases, treatment
with methotrexate is an especially attractive option.
An ectopic (tubal) pregnancy is one that is not normal. In a normal pregnancy, the
fertilized egg is implanted in the uterus. In an ectopic pregnancy, the fertilized egg is
implanted in places other than in the uterus. Some examples of this include the Fallopian
tubes, cervix, abdomen, and ovaries. At first glance, this may not seem like that big of a
deal. However, once you consider that the role of the uterus is to house a fertilized egg
and it is designed to grow and expand, you can begin to understand the problems and
complications that can arise. Other parts of the body such as the abdomen are not
designed to grow and expand as the fetus grows.
Actually, there are no known causes of ectopic pregnancy. It is unclear why the egg
would implant itself someplace other than the uterus. The pathophysiology of ectopic
pregnancy is such that the normal process of egg implantation is somehow disturbed.
However, there are some factors that can put a woman at increased risk of ectopic
pregnancy such as their age, problems with the fallopian tubes such as prior surgery or
inflammation, if the woman already experienced an ectopic pregnancy, and invitro-
fertilization can all put someone at risk for it.
The symptoms of ectopic (tubular) pregnancy can take a while to develop or the woman
may not experience any at all. However, as the fetus starts to grow and expand, problems
can arise. The uterus is designed for this concept. However, other parts are not. As a
result, symptoms such as pain in the area where the egg implanted itself and mild vaginal
bleeding can be early warning signs. A major problem, or symptom, of ectopic (tubal)
pregnancy is internal bleeding that is usually related to a hemorrhaging of the area where
the fetus is developing. This can prove serious and fatal if not treated.
If any of those symptoms are present, it is wise to see a doctor so they can properly
diagnose whether or not an ectopic pregnancy condition is present. There are a few ways
that it can be determined. The doctor may diagnose an ectopic pregnancy via ultrasound.
Another way to tell is because the hCg level will be elevated in the woman who has an
ectopic pregnancy. To determine if the ectopic pregnancy is in the fallopian tube or
pelvis, a laparoscopy or a laparotomy can be done so the doctor can see if the fetus is
developing there.
There are a few treatment options for ectopic pregnancy and the path taken will largely
depend on whether or not the woman wants to have anymore children. A drug called
methotrexate can be taken to cause a miscarriage. In some cases, it is not a good idea to
let this kind of pregnancy continue. Surgery can also be done to remove the developing
fetus. In general, it is very difficult and very dangerous to let this condition continue. If
an ectopic pregnancy does occur, it can affect the future ability to have children so swift
treatment is necessary.
As soon as a woman becomes pregnant, it is important to report any symptoms that occur
to a doctor. They will be able to help determine if these symptoms are normal or if they
determine an ectopic pregnancy. There are some treatment options and it is important to
contact the doctor to figure out what to do.
MORTALITY
Despite the increased frequency of ectopic pregnancy, the case mortality rate has declined
from 3.5 deaths per 1000 ectopic pregnancies in 1970 to 0.4 deaths per 1000 ectopic
pregnancies in 1985. Although ectopic pregnancies accounted for only 1.5% of the total
gestations in 1984 and 1985, they accounted for 14% of maternal deaths in 1984 and 11%
in 1985.20
Ectopic pregnancy confers a greater risk of maternal mortality than either childbirth or
legal abortion. An extrauterine gestation is 50 times more likely to result in a maternal
death than a first-trimester abortion and 10 times more likely than delivery in the third
trimester.21
A study of the clinical aspects of ectopic pregnancy mortality in the United States has
shown that the most frequent direct causes of death are hemorrhage, infection, and
anesthetic complications. Of women dying from hemorrhage, 70% did not undergo
surgery. In 50% of women, the condition was misdiagnosed or confused with other
pathology such as gastrointestinal disorders, intrauterine pregnancies, spontaneous
abortions, PID, sequelae of induced abortion, and psychiatric disorders. In 70% of cases,
patients had either called or visited a physician within 1 week of development of
symptoms. Diagnostic delay could be ascribed to physician delay in 53% of cases and to
combined patient and physician delay in 8% of cases. In 5% of cases, the physician made
the diagnosis but did not act promptly enough to prevent maternal death. The site of
implantation was also important, as interstitial and nontubal ectopic pregnancies account
for only 5–10% of all ectopic pregnancies, but for 20% of all fatalities.22
PATHOPHYSIOLOGY
The mechanisms responsible for ectopic implantation are unknown. The four main
possibilities are an anatomic obstruction to the passage of the zygote, an abnormal
conceptus, abnormalities in the mechanisms responsible for tubal motility, and
transperitoneal migration of the zygote.
Anatomic distortion and obstruction of the fallopian tube are widely believed to be
responsible for most ectopic implantations. Obstruction could result from PID, salpingitis
isthmica nodosa,5 tubal endometriosis, or postsurgical fibrosis.23 Scarring of the
endosalpinx could lead to diverticuli formation, in which the zygote could be trapped, or
to simple obstruction of the tubal passage. Support for the contribution of an anatomic
cause is the demonstration of histologic and gross evidence of past infection in 30–50%
of cases of ectopic gestation.3, 24 Other researchers studying the isthmic portion of the
fallopian tube, however, have failed to demonstrate significant pathology (e.g., fibrosis,
chronic inflammation of endometriosis) associated with ectopic pregnancy.25 This
observation suggests the contribution of nonanatomic factors to the etiology of ectopic
pregnancy. Functional causes could include a defective conceptus, abnormalities in the
motility of the fallopian tube, or transperitoneal migration.
Tubal motility seems to be influenced by the hormonal milieu. The suspicion that some
cases of ectopic pregnancy may be due to endocrine abnormalities stems from clinical
observations that have suggested an association in patients using a progesterone-only pill,
an IUD,13, 15, 16 or human menopausal gonadotropins for ovulation induction.28, 29 It has
been suggested that high estrogen levels noted in cases of hyperstimulation with human
menopausal gonadotropins interfere with tubal transport. An alternative explanation is
that an increased number of eggs are released (superovulation) in hyperstimulated
patients, resulting in an increased risk of ectopic implantation. In contrast, subnormal
estrogen levels subsequent to vigorous exercise and dietary fads have been hypothesized
to contribute to increased ectopic rates in today's more health-conscious society.30
Recent SART data from 2001 show that ectopic pregnancy occurs in 1.8% of recipients
of embryo transfer during in vitro fertilization and up to 4.3% in patients undergoing
zygote intrafallopian transfer (ZIFT).33 Indeed, the first pregnancy reported in humans
with this technique was an ectopic pregnancy.34 Postulated mechanisms include the
inadvertent injection of embryos into the fallopian tube, uterine irritability stimulating the
contractile portion of the tube secondary to cervical and uterine manipulation, and a
gravitational effect. It has been suggested that this inadvertent injection or migration of
embryos into the fallopian tubes occurs more often than realized. A diseased tube is less
likely than a normal tube to propel the embryo back into the uterus.35 In addition, infertile
women undergoing gamete and zygote intrafallopian transfer should be counseled
regarding at least a theoretic increased risk of tubal gestation.36
Of all ectopic pregnancies, 97% occur in the fallopian tube (tubal), 2.5% in the uterine
cornu, and the remaining 2% in various other locations including the cervix, abdomen,
and ovary (Fig. 2). The majority of tubal pregnancies are located in the ampullary portion
of the tube. Coexistence of an intrauterine and a tubal pregnancy (heterotopic) was
initially reported to occur in 1:30,000 ectopic pregnancies, and the occurrence of bilateral
ectopic pregnancy in the same cycle is even rarer.37, 38, 39 With the increased use of
ovulation induction, the reported incidence of heterotopic pregnancy has increased to
reports of 0.3%.40
Schermers49 reviewed the symptoms in 3970 ectopic pregnancies reported in the literature
and found pain to be the most common presenting symptom, occurring in 96.3% of the
patients; irregular bleeding was second, occurring in 74.1% of the patients. Other
symptoms included shoulder pain, gastrointestinal symptoms, and syncope. Also reported
as the second most common sign was adnexal tenderness, occurring in 85–95% of
patients. The irregular vaginal bleeding might not be a result only of a breakdown of the
endometrium, but of blood flowing from the fallopian tube into the uterine cavity and out
the cervical os as well.
Other findings also include the Arias–Stella phenomenon and decidual casts (Fig. 3).
These are rare occurrences and are more a curiosity than a helpful adjunct in diagnosing
an ectopic pregnancy. Physical findings, although helpful, are inconsistent other than in
the case of hemorrhagic shock, and a pelvic mass is palpable in only approximately 50%
of cases.50 This leads to a need for more objective criteria.
DIAGNOSIS
Patients clinically suspected of having ectopic pregnancy fall into two major categories:
those who have an acute abdomen and in whom immediate surgery is indicated, and those
who are clinically stable and in whom adjunctive diagnostic procedures can be
performed.
Patients with a surgical abdomen are evaluated in the emergency room with a rapid
pregnancy test and potentially a culdocentesis. A positive culdocentesis in a patient with a
positive pregnancy test result has been reported to correspond with ectopic pregnancy in
99.2% of cases.51
Patients who will benefit most from a culdocentesis are those in whom a clinical
suspicion of ectopic pregnancy exists, and who present at a time when expeditious
diagnosis is desired and when sophisticated diagnostic modalities, such as
ultrasonography and sensitive human chorionic gonadotropin (hCG) assays, cannot be
obtained without significant delay. Under these circumstances, culdocentesis is an
inexpensive, rapid, and easily performed means of patient evaluation that often provides
the impetus for immediate intervention.
In clinically stable patients, the approach to the evaluation is based on the combined use
of sensitive pregnancy testing, ultrasound examination, and/or laparoscopy. hCG testing
is used to screen for pregnancy, and ultrasonography is employed to locate it.52
Evaluation of the patient begins with a sensitive and rapid pregnancy test. Blood and
urine pregnancy tests have been used to screen for ectopic pregnancy. Advances in
technologies of enzyme-linked immunoassay and monoclonal antibodies to the β subunit
have promoted the evolution of rapid, inexpensive, and similar qualitative urinary
pregnancy tests. However, we prefer to use the sensitive blood pregnancy testing in the
form of a radioimmunoassay against β-hCG. We recommend an assay with a sensitivity
of 2.5 mIU/mL because with this system the false-negative rate is 0.5%. The
radioreceptor assay, with a sensitivity of 200 mIU/mL, is not suitable for screening
because its false-negative rate ranges between 6% and 12%, which is unacceptably high
for a life-threatening condition.53, 54
A negative blood pregnancy test virtually rules out pregnancy and thus an ectopic
gestation. A positive qualitative hCG result requires further investigation, mainly a
determination of the hCG titer and an ultrasonographic examination (either abdominal or
vaginal) of the pelvis.
A positive diagnosis of ectopic pregnancy can be made if fetal motion is demonstrated
outside the uterus. Unfortunately, this is a rare and late finding, and awaiting its
appearance would delay the diagnosis and conceivably increase the risk of tubal rupture.
In practice, ultrasonography is used to identify an intrauterine pregnancy, which would
render the simultaneous presence of an ectopic pregnancy extremely unlikely (1:30,000).
Confirmation of the presence of an intrauterine pregnancy can be made by identifying
either a gestational sac or a fetal pole within the endometrial cavity.
Ultrasonographically, ectopic pregnancies can show a single-ring sac due to the presence
of blood within the endometrial cavity in association with a significant decidual reaction.
This appearance has been shown to occur in 10–20% of all cases (Fig. 4).55, 56, 57, 58, 59, 60, 61,
62, 63
Nyberg and colleagues64 and Bradley and associates65 have proposed morphologic criteria
to distinguish the pseudogestational sac of ectopic pregnancy from the gestational sac of
a normal intrauterine pregnancy. They have described the normal intrauterine gestational
sac as having a double contour produced by the decidua capsularis and the decidua
parietalis. The pseudogestational sac of an ectopic pregnancy has only a single ring. The
researchers have reported that 98.3% of all patients with a double-ring sac had an
intrauterine pregnancy and 64 of 68 patients with a single-ring sac had ectopic
pregnancies.
The traditional abdominal ultrasonographic criterion used for the diagnosis of ectopic
pregnancy is failure to visualize a gestational sac in the uterus of patients with more than
6 weeks of amenorrhea. The problem with this criterion is that one third of patients with
ectopic pregnancy do not know the date of their last menstrual period, and in others
irregular bleeding makes interpretation of the menstrual history difficult.
It has been established that the sac of a normal intrauterine pregnancy becomes visible
with abdominal ultrasonography when the hCG titer is greater than 6500 mIU/mL. When
levels are higher than this, the absence of a sac is associated with an ectopic pregnancy in
86% of cases. This criterion has a sensitivity of 100%, a specificity of 96%, and a
negative predictive value of 100%.51 The absence of a sac at levels less than 6000
mIU/mL is a nondiagnostic finding and should not lower or raise the suspicion of ectopic
pregnancy.66, 67 Management of these patients depends on the clinical situation, however,
if transvaginal ultrasonography is available, it should be employed. If a patient remains
clinically stable, serial hCG determinations are useful. Additionally, management can be
based upon ultrasonographic findings of the adnexa and clinical suspicion. Romero and
colleagues68 prospectively evaluated 220 patients who were suspected of having ectopic
pregnancy and who had hCG titers less than 6000 mIU/mL and abdominal
ultrasonographic adnexal findings. The demonstration of a noncystic mass, alone or
associated with cul-de-sac fluid, was an indication for diagnostic laparoscopy.
Vaginal scanning has proved to be more accurate than abdominal scanning in detecting
ectopic pregnancies (90% vs 80%) and cul-de-sac fluid (77% vs 46%) and in discerning
whether the tubal pregnancy has ruptured (76% vs 50%).69 In the transvaginal
ultrasonographic evaluation of pregnancy, Bernaschek and associates,70 using a 5-MHz
transducer, proposed a “discriminatory zone” of an hCG titer of 750 mIU/mL (second
International Standard) for the detection of an intrauterine gestational sac. Unfortunately,
using this proposed criterion and similar ultrasonographic equipment, Fossum and
associates71 may have inadvertently surgically investigated several pregnancies that
proved to be normal intrauterine gestations (Fig. 6). If an hCG titer exceeds 2000
mIU/mL, we now expect to detect an intrauterine gestational sac using transvaginal
ultrasonography.
We recommend laparoscopy or dilation and curettage (D&C) for patients with subnormal
quantitative increases of hCG. Curettage productive of trophoblastic tissue confirms an
abnormal intrauterine pregnancy and completion of therapy. Approximately 30% of
patients with abnormally rising quantitative hCG values will have an abnormal
intrauterine pregnancy. The remainder will be ectopics. Unfortunately, this test is limited
by a false-negative rate of up to 20%.77 Endometrial biopsy with pipelle is even less
sensitive than D&C for detection of chorionic villi with a sensitivity somewhere between
30 and 60%.78, 79
Normal increments in hCG are monitored until hCG titers exceed either 2000 or 6500
mIU/mL, at which time either transvaginal or transabdominal ultrasonography,
respectively, may be performed. The presence or absence of a gestational sac above these
hCG levels should be supportive either of an ectopic or an intrauterine gestation. A good
algorithm for the management of ectopic pregnancy is shown below (see Fig. 7).
SURGICAL MANAGEMENT
The ultimate decision regarding surgical management depends on a patient's desire for
future fertility. However, it is important to note that whatever procedure is performed, the
pregnancy rate after an ectopic pregnancy may be decreased by 40–70%.47 If a patient is
not interested in future fertility, the appropriate surgical procedure is salpingectomy.
Additional indications for salpingectomy include recurrent ectopic pregnancy in the same
tube, a severely damaged tube, prior unsuccessful conservative surgery, and uncontrolled
bleeding.80 If a patient does desire future fertility, however, much data from the past few
years support performing conservative surgery in a majority of these cases. Conservative
options vary from expression of a tubal abortion through the distal end of the tube to
linear salpingostomy to segmental resection and secondary anastomosis of an isthmic
ectopic pregnancy.
A majority of ectopic pregnancies are associated with contralateral tubal disease, such as
salpingitis. The fact that clinical assessment and evaluation of the contralateral tube
during the initial surgery correlates poorly with postoperative hysterosalpingographic
findings underscores the importance of intraoperative conservative management
whenever feasible.81 It is not recommended that a test of tubal patency be done during the
operation for an ectopic pregnancy in order to evaluate the status of the contralateral tube.
The information provided can be erroneous because decidual reaction around the cornual
portion might give a false impression of an occluded tube. The possibility of introducing
infection into an already compromised pelvis is also an important consideration.
In 1955, Jeffcoate88 suggested that in conjunction with a salpingectomy, which is still the
most commonly employed surgical treatment for ectopic pregnancy, an oophorectomy on
the ipsilateral side be done as well. The theory behind this is that all ovulations would be
into the good tube; this discounts the importance of transmigration. There are no data that
justify this conjecture. Several reports have shown that there is no advantage in
performing a salpingo-oophorectomy compared with salpingectomy in terms of
pregnancy rates and repeat ectopic pregnancies in those patients.89 Considering the
successful pregnancy rates with in vitro fertilization and embryo transfer, every effort
must be maintained to conserve as much ovarian tissue as possible in any eventuality.
Table 3. Choice of surgical treatment and subsequent fertility among 151 fatients with
ectopic pregnancy
No. of subsequent
pregnancies
(% in parentheses) Incidence of sterility
No. of
Surgical treatment patients Intrauterine Repeat ectopic
Conservative 47 39 (83) 3 (6.4) 175
Radical 104 75 (72.1) 6 (5.8) 225
There are no substantial data to support the role of cornual resection in conjunction with a
salpingectomy. The theoretic rationale is to prevent interstitial implantation. A review of
the literature by Kalchman and Meltzer98 demonstrated only 75 cases of interstitial
pregnancy following a salpingectomy, leading to the conclusion that this is a rare
occurrence and should not dictate surgical technique. Hallatt has suggested that the
procedure has some inherent risks secondary to increased bleeding at the time of the
original surgery and the possibility of a rupture in the course of a subsequent intrauterine
pregnancy.89 Uterotubal fistula formation after this procedure is also a possibility.
Therefore, for aesthetic reasons, only a small, shallow cornual resection should be
performed.
The primary difference between a salpingostomy and a salpingotomy is that, in the latter,
the fallopian tube is closed by primary intention. Stromme99 was the first to describe
salpingotomy. This procedure involves an antimesenteric incision over the ectopic
pregnancy, excising the products of conception and closing the tube in either one or two
layers with fine suture material after hemostasis is achieved. The sutures used should be
interrupted. Other reports have modified this technique but still espouse primary closure
of the tube.91, 94 Anecdotal reports of tuboperitoneal fistulas subsequent to salpingostomy,
but not salpingotomy, support performance of the latter procedure.100
Blood testing demonstrates the disappearance of β-hCG levels over time (Fig. 8.)106
Ectopic pregnancies that occur in the isthmic portion of the tube present a different entity
entirely. A recent histopathologic comparison of ampullary and isthmic ectopic
pregnancies noted preservation of the ampullary muscularis in 85% of the former cases
and only a 43% preservation rate of the muscularis in isthmic pregnancies. The disruption
of the tubal wall was also more extensive in isthmic pregnancies.107 This is why patients
with isthmic ectopic pregnancies are believed to be the only ectopic pregnancy patients
who develop a tuboperitoneal fistula after linear salpingostomy (Fig. 9). Therefore,
segmental resection is most commonly recommended.108
The option then becomes to close the tube by primary intention, which has been done
successfully by Stangel and colleagues,109 or to perform a second procedure and do an
anastomosis at that time. The major advantage of doing an anastomosis at the time of
resection of the ectopic pregnancy is that the wide lumen of the tube facilitates the
anastomosis. However, edema and the presence of blood may increase the chance of
infection. Normal intrauterine pregnancies are achieved regardless of the mode of
anastomosis employed. It is recommended that patients waiting for a secondary
anastomosis be placed on birth control pills so that they do not form an ectopic pregnancy
in the blind distal portion of the tube that has been created (Fig. 10).110 In either event, the
anastomosis is performed in two layers using the operating microscope. Four to six 8-0
polyglycolic acid or polydioxanone sutures are placed approximating the muscularis. The
serosa is then loosely opposed with running 6-0 Vicryl or PDS sutures (Fig. 11).
Fig. 10. Transmigration of sperm to the contralateral
horn of the tube, resulting in an ectopic
pregnancy.(Cartwright PS, Entman SS: Repeat ipsilateral
tubal pregnancy following partial salpingectomy: A case
report. Fertil Steril 42:647, 1984. Reproduced with
permission of the publisher, The American Fertility
Society)
Fig. 11. Isthmic anastomosis following segm
for an ectopic pregnancy.
With the move toward laparoscopic conservative surgery, it is of interest to note Smith
and colleagues'111 similar postoperative tubal patency rates when microsurgical
anastomosis was compared with linear salpingostomy in the treatment of isthmic ectopic
gestation at the time of laparotomy. Pouly and associates85 accordingly treated 22 isthmic
ectopic pregnancies by laparoscopic linear salpingostomy, yielding a 54.5% subsequent
intrauterine pregnancy rate. DeCherney and Boyers,112 however, showed that treating
isthmic pregnancy with linear salpingostomy by laparotomy resulted in subsequent
occlusion of the tube in three of four patients.
A rare form of ectopic pregnancy occurs in the infundibular portion of the tube between
the fimbria and the ampulla. These are usually treated by “milking or squeezing” the
pregnancy out through the distal end. Schermers49 reported a higher incidence of delayed
hemorrhage after the milking-out procedure. This experience has been substantiated by
Bruhat.82 Success rates are also lowest with this procedure; therefore, these patients also
should have a linear salpingostomy rather than “milking out.”
This entity is different from a tubal abortion, in which the products of conception are
already partially or completely extruded from the fimbriated end of the fallopian tube.
This process can be completed, if necessary, simply by removing the remaining products
of conception.
ADJUNCTIVE THERAPY
NONOPERATIVE MANAGEMENT
At this time, expectant management should be considered an option only for patients with
extreme surgical risk, falling hCG titers, or in a research setting.
The use of drug therapy for ectopic pregnancy was first reported in 1982, in a patient
with an interstitial pregnancy who refused surgery.116 Since then, many investigators have
reported the successful treatment of selected patients using a variety of agents, including
parenteral methotrexate, intratubal or intra-amniotic methotrexate, and intratubal osmotic
agents.117, 118, 119, 120, 121 To date, there have not been a significant number of reports of
successful treatment of ectopic pregnancy using mefipristone (RU-486).
At this time, parenteral (intramuscular) methotrexate is the best studied and most
accepted agent for the medical treatment of ectopic pregnancy. Methotrexate is a folic
acid antagonist that interferes with the synthesis of DNA. It is most commonly
administered intramuscularly, though reports of oral administration are available.122
Patients receiving medical therapy must be hemodynamically stable and desire future
fertility. Contraindications include a ruptured ectopic, ectopic mass greater than 3.5 cm,
fetal cardiac activity, high level hCG value (10,000 IU), breastfeeding,
immunodeficiency, elevated creatinine or liver function tests, alcoholism, and active
pulmonary or gastrointestinal disease.
In 1993, Stovall117 reported a prospective study of 120 women treated with a single dose
(50 mg/m2) of intramuscular methotrexate. In this series, the author reported a success
rate of 94%, with subsequent tubal patency rates similar to those quoted for conservative
surgical treatment. Pregnancy rates were nearly 80%, with approximately 88% of these
being intrauterine. There were no adverse effects of methotrexate therapy reported in this
series; however, there have been recent reports of tubal rupture and hematosalpinx after
methotrexate therapy.123, 124 Overall, the outcome of medical treatment of ectopic
pregnancy closely approximates results obtained surgically, and there is evidence to
support a significant improvement in cost-effectiveness.125 Lipscomb et al. in 1998
reported on 315 patients treated with single-dose methotrexate and reported a success rate
of 90.1%.126
There has been some controversy over the use of single-dose versus multiple-dose
methotrexate. Direct comparisons of the two therapies have so far found no significant
difference.87 A recent study described higher ipsilateral tubal obstruction (as noted by
hysterosalpingogram) in patients treated with multiple-dose versus single-dose regimens.
This may be attributable to preexisting obstruction or the potential for tubal harm with a
multiple dose of methotrexate.127 Additionally, there is some concern for the long-term
effects of methotrexate on ovarian function, in that chemotherapy for gestational
trophoblastic tumors may hasten menopause by 3 years.128 Although the harm with
multiple-dose therapy has not been proven, there does not appear to be any additional
benefit over single-dose therapy.
Once a patient is treated with medical therapy for ectopic pregnancy, she must be
followed closely to ensure resolution. Day 1 is considered the day of administration of
methotrexate. Follow-up hCG levels should be obtained on days 4 and 7, with an
expected 15% drop between the two latter values. Thereafter, hCG values should be
followed weekly until negative.
Treatment failure is indicated by a less than 15% drop in hCG values between days 4 and
7, worsening abdominal pain concerning for rupture, and increasing or plateauing hCG
values after the first week of therapy. If the patient is hemodynamically stable, a second
injection of methotrexate can be given with weekly follow-up. A second dose may be
required in at least 11% of patients. Tubal rupture may occur in up to 8% of patients
requiring subsequent surgery.129
Patients should be counseled regarding the side effects of medical therapy. These can
include nausea and vomiting, abdominal pain, diarrhea, stomatitis, dizziness, and rarely
neutropenia or reversible alopecia.130
Conservative surgical treatment can be carried out without lowering the chance of a
subsequent intrauterine pregnancy or raising the incidence of an extrauterine pregnancy.
A review of the literature summarizing 467 cases operated on for ectopic pregnancy is
summarized in Table 4.131 Of these patients, 46% had a subsequent intrauterine pregnancy
and 12% had a repeat ectopic pregnancy. These results do not differ greatly from older
statistics based on the results after radical surgery. DeCherney and Oelsner131 reviewed
1630 cases treated radically and found a 41% intrauterine pregnancy rate and a 14%
repeat extrauterine pregnancy rate. It is hoped that over time, with the use of modern
microsurgical techniques, the intrauterine pregnancy rate will increase and the repeat
ectopic pregnancy rate will decrease in these patients.
These statistics do not hold, however, for patients who have had two or more ectopic
pregnancies. In these patients, the incidence of repeat ectopic pregnancy approximates
that of a subsequent intrauterine gestation.132, 133 An unanswered question at this point
remains: How many conservative procedures for an ectopic pregnancy can a patient
undergo before her reproductive future is compromised to the point where in vitro
fertilization is the only viable alternative (Table 5)?132, 133
With the advent of effective medical therapy for ectopic pregnancy, there exist a wide
variety of available treatment choices. A recent review compared laparoscopic
salpingostomy, multiple-dose methotrexate, single-dose methotrexate, and expectant
management. The authors concluded that there was no significant clinical difference
between the four groups with subsequent intrauterine pregnancy rates varying from 52-
61% and subsequent ectopic pregnancy rates ranging from 8–13%. However, successful
resolution with expectant management appeared lower at 68% (compared with 87–93%
for other therapies).134 Therefore it seems reasonable to conclude that treatment choice
should be based upon physician comfort and patient characteristics.
CONCLUSION
During the past decade, the incidence of ectopic pregnancy has noticeably increased.
Although 50% of ectopic pregnancies are attributable to infection, the remainder remain
unexplained. Clinical findings such as adnexal tenderness, irregular bleeding, and
abdominal pain still represent reliable but imperfect clues that a patient has an ectopic
pregnancy. It is the advent of newer diagnostic techniques, including laparoscopy, serial
β-hCG testing, and transvaginal ultrasonography, that has allowed for the earlier
diagnosis of ectopic pregnancy. Previously, 85% of ectopic pregnancies were diagnosed
as ruptured and 15% as unruptured.135 Today, this ratio is reversed. The diagnosis of many
cases of small, unruptured ectopic pregnancies has led to a reversal from surgical
management to medical management with methotrexate especially in patients desirous of
future fertility. The hallmark of improved diagnostic management remains the β-hCG
test, with failure to achieve a normal slope of increase during the early stages of gestation
heralding an ectopic pregnancy or an inevitable abortion.136