Diagnosis and Management of Ectopic Pregnancy



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Am Fam Physician. 2005 Nov 1;72(9):1707-1714.

  Patient information: See related handout on ectopic pregnancy, written by the authors of this article.

Ectopic pregnancy is a high-risk condition that occurs in 1.9 percent of reported pregnancies. The condition is the leading cause of pregnancy-related death in the first trimester. If a woman of reproductive age presents with abdominal pain, vaginal bleeding, syncope, or hypotension, the physician should perform a pregnancy test. If the patient is pregnant, the physician should perform a work-up to detect possible ectopic or ruptured ectopic pregnancy. Prompt ultrasound evaluation is key in diagnosing ectopic pregnancy. Equivocal ultrasound results should be combined with quantitative beta subunit of human chorionic gonadotropin levels. If a patient has a beta subunit of human chorionic gonadotropin level of 1,500 mIU per mL or greater, but the transvaginal ultrasonography does not show an intrauterine gestational sac, ectopic pregnancy should be suspected. Diagnostic uterine curettage may be appropriate in patients who are hemodynamically stable and whose beta subunit of human chorionic gonadotropin levels are not increasing as expected. Appropriate treatment for patients with nonruptured ectopic pregnancy may include expectant management, medical management with methotrexate, or surgery. Expectant management is appropriate only when beta subunit of human chorionic gonadotropin levels are low and declining. Initial levels determine the success of medical treatment. Surgical treatment is appropriate if ruptured ectopic pregnancy is suspected and if the patient is hemodynamically unstable.

Ectopic pregnancy is any pregnancy that occurs outside the uterine cavity. Pregnancies in the fallopian tube account for 97 percent of ectopic pregnancies: 55 percent in the ampulla; 25 percent in the isthmus; 17 percent in the fimbria; and 3 percent in the abdominal cavity, ovary, and cervix.1

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendationEvidence ratingReferences

A physician should not rely on any combination of physical examination findings to exclude ectopic pregnancy.

B

1,1013

Ultrasound examination should be part of the initial evaluation of possible ectopic pregnancy.

C

10,14,15,18

If transvaginal ultrasonography does not detect intrauterine pregnancy, presumptive ectopic pregnancy is virtually certain when the serum beta subunit of human chorionic gonadotropin level is 1,500 mIU per L (1,500 IU per mL) or greater.

C

10,15,17


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For more information about the SORT evidence rating system, see page 1639 or http://www.aafp.org/afpsort.xml.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

View Table

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendationEvidence ratingReferences

A physician should not rely on any combination of physical examination findings to exclude ectopic pregnancy.

B

1,1013

Ultrasound examination should be part of the initial evaluation of possible ectopic pregnancy.

C

10,14,15,18

If transvaginal ultrasonography does not detect intrauterine pregnancy, presumptive ectopic pregnancy is virtually certain when the serum beta subunit of human chorionic gonadotropin level is 1,500 mIU per L (1,500 IU per mL) or greater.

C

10,15,17


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For more information about the SORT evidence rating system, see page 1639 or http://www.aafp.org/afpsort.xml.

The rate of ectopic pregnancies in North America climbed from less than 0.5 percent of all pregnancies in 1970 to 2 percent in 1992.13 Ruptured ectopic pregnancy accounts for 10 to 15 percent of all maternal deaths.1,2 Fortunately, after the advent of transvaginal ultrasonography and beta subunit of human chorionic gonadotropin (beta-hCG) tests, the incidence of rupture and case-fatality rates declined from 35.5 deaths per 10,000 ectopic pregnancies in 1970 to 3.8 per 10,000 in 1989.2 Management options for ectopic pregnancy include expectant management, medical treatment, and surgery.

Risk Factors

Risk factors most strongly associated with ectopic pregnancy include previous ectopic pregnancy, tubal surgery, and in utero diethylstilbestrol (DES) exposure. A history of genital infections or infertility and current smoking increase risk.3,4 Contraceptive use reduces the annual risk for intrauterine and ectopic pregnancy5,6 ; however, previous intrauterine device use may increase risk. Table 1 lists common risk factors for ectopic pregnancy.4,5 [corrected]

TABLE 1

Risk Factors for Ectopic Pregnancy

Risk factorNumber of studiesOdds ratio*

Previous tubal surgery

3

21.0

Previous ectopic pregnancy

10

8.3

In utero diethylstilbestrol exposure

5

5.6

Previous genital infections

24

2.4 to 3.7

Infertility

9

2 to 2.5

Current smoking

6

2.3

Previous intrauterine device use

16

1.6


*—A higher odds ratio indicates a stronger risk factor.

Information from references 4 and 5.

TABLE 1   Risk Factors for Ectopic Pregnancy

View Table

TABLE 1

Risk Factors for Ectopic Pregnancy

Risk factorNumber of studiesOdds ratio*

Previous tubal surgery

3

21.0

Previous ectopic pregnancy

10

8.3

In utero diethylstilbestrol exposure

5

5.6

Previous genital infections

24

2.4 to 3.7

Infertility

9

2 to 2.5

Current smoking

6

2.3

Previous intrauterine device use

16

1.6


*—A higher odds ratio indicates a stronger risk factor.

Information from references 4 and 5.

Diagnosis

Ectopic pregnancy is most common in women of reproductive age who present with abdominal pain and vaginal bleeding approximately seven weeks after amenorrhea.1,2,7 These findings are nonspecific and are common in patients who may miscarry.1  Table 2 lists the common differential diagnosis of ectopic pregnancy.

TABLE 2

Differential Diagnosis of Ectopic Pregnancy*

Acute appendicitis

Miscarriage

Ovarian torsion

Pelvic inflammatory disease

Ruptured corpus luteum cyst or follicle

Tubo-ovarian abscess

Urinary calculi


*—Listed alphabetically.

TABLE 2   Differential Diagnosis of Ectopic Pregnancy*

View Table

TABLE 2

Differential Diagnosis of Ectopic Pregnancy*

Acute appendicitis

Miscarriage

Ovarian torsion

Pelvic inflammatory disease

Ruptured corpus luteum cyst or follicle

Tubo-ovarian abscess

Urinary calculi


*—Listed alphabetically.

CLINICAL EXAMINATION

A normal or slightly enlarged uterus, vaginal bleeding, pelvic pain with manipulation of the cervix, and a palpable adnexal mass significantly increase the likelihood of an ectopic pregnancy. Significant abdominal tenderness suggests ruptured ectopic pregnancy, especially in a patient with hypotension who presents with guarding and rebound tenderness.

Physicians can categorize hemodynamically stable patients as high, intermediate, or low risk for ectopic pregnancy (Table 37,8) based on clinical examination findings.7 Clinical examinations are not diagnostic because up to 30 percent of patients with ectopic pregnancies have no vaginal bleeding, 10 percent have a palpable adnexal mass, and up to 10 percent have negative pelvic examinations.1,7 The overall likelihood of ectopic pregnancy is 39 percent in a patient with abdominal pain and vaginal bleeding but no other risk factors.9 The probability of ectopic pregnancy increases to 54 percent if the patient has other risk factors (e.g., history of tubal surgery, ectopic pregnancy, or pelvic inflammatory disease; in utero DES exposure; or an intrauterine device in situ at the time of conception).9 Physicians should remember that no combination of physical examination findings can reliably exclude ectopic pregnancy.1,1013

TABLE 3

Determining Ectopic Pregnancy Risk*

PresentationRisk groupEstimated risk of ectopic pregnancy (%)

Peritoneal irritation or cervical motion tenderness

High

29

No fetal heart tones; no tissue at cervical os; pain present

Intermediate

7

Fetal heart tones or tissue at cervical os; no pain

Low

< 1


*—Based on a relatively low prevalence of ectopic pregnancy (7.7 percent) in an emergency department setting in patients with positive beta subunit of human chorionic gonadotropin levels, abdominal pain, or vaginal bleeding.

Information from references 7 and 8.

TABLE 3   Determining Ectopic Pregnancy Risk*

View Table

TABLE 3

Determining Ectopic Pregnancy Risk*

PresentationRisk groupEstimated risk of ectopic pregnancy (%)

Peritoneal irritation or cervical motion tenderness

High

29

No fetal heart tones; no tissue at cervical os; pain present

Intermediate

7

Fetal heart tones or tissue at cervical os; no pain

Low

< 1


*—Based on a relatively low prevalence of ectopic pregnancy (7.7 percent) in an emergency department setting in patients with positive beta subunit of human chorionic gonadotropin levels, abdominal pain, or vaginal bleeding.

Information from references 7 and 8.

DIAGNOSTIC TESTS

Diagnostic tests for ectopic pregnancy include a urine pregnancy test; ultrasonography; beta-hCG measurement; and, occasionally, diagnostic curettage. In the past, some physicians have used serum progesterone levels as well.2,14  Table 4 summarizes the accuracy rates of diagnostic tests for ectopic pregnancy.1,1417

TABLE 4

Diagnostic Tests for Detecting Ectopic Pregnancy

Diagnostic testSensitivity (%)Specificity (%)

Transvaginal ultrasonography with beta-hCG level greater than 1,500 mIU per mL (1,500 IU per L)

67 to 100

100 (virtual certainty)

Beta-hCG levels do not increase appropriately

36

63 to 71

Single progesterone level to distinguish ectopic pregnancy from nonectopic pregnancy

15

> 90

Single progesterone level to distinguish pregnancy failure from viable intrauterine pregnancy

95

40


Beta-hCG = beta subunit of human chorionic gonadotropin.

Information from references 1 and 14 through 17.

TABLE 4   Diagnostic Tests for Detecting Ectopic Pregnancy

View Table

TABLE 4

Diagnostic Tests for Detecting Ectopic Pregnancy

Diagnostic testSensitivity (%)Specificity (%)

Transvaginal ultrasonography with beta-hCG level greater than 1,500 mIU per mL (1,500 IU per L)

67 to 100

100 (virtual certainty)

Beta-hCG levels do not increase appropriately

36

63 to 71

Single progesterone level to distinguish ectopic pregnancy from nonectopic pregnancy

15

> 90

Single progesterone level to distinguish pregnancy failure from viable intrauterine pregnancy

95

40


Beta-hCG = beta subunit of human chorionic gonadotropin.

Information from references 1 and 14 through 17.

Ultrasonography is the diagnostic test of choice, with limitations largely based on availability and the gestational age of the pregnancy.3,14,18 Ectopic pregnancy is suspected if transabdominal ultrasonography does not show an intrauterine gestational sac and the patient’s beta-hCG level is greater than 6,500 mIU per mL (6,500 IU per L) or if transvaginal ultrasonography does not show an intrauterine gestational sac and the patient’s beta-hCG level is 1,500 mIU per mL (1,500 IU per L) or greater.2,19  Ultrasound findings that suggest ectopic pregnancy are listed in Table 5.9 [corrected] More than one half of women with ectopic pregnancy have beta-hCG levels less than 2,000 mIU per mL (2,000 IU per L) at presentation. Therefore, it may be difficult to determine by ultrasonography alone whether an empty uterus indicates early pregnancy or ectopic pregnancy.2,7

TABLE 5

Transvaginal Ultrasound Findings in Ectopic Pregnancy

FindingLR*

Ectopic cardiac activity

> 100 (diagnostic)

Ectopic gestational sac

23

Ectopic mass and fluid in pouch of Douglas

9.9

Fluid in pouch of Douglas

4.4

Ectopic mass

3.6

No intrauterine gestational sac

2.2

Normal adnexal region

0.55

Intrauterine gestational sac

0.07


LR = likelihood ratio.

*—An LR greater than 5 is moderately strong evidence of ectopic pregnancy; an LR greater than 10 is strong evidence of ectopic pregnancy; and an LR less than 0.1 is strong evidence against ectopic pregnancy.

Information from reference 9.

TABLE 5   Transvaginal Ultrasound Findings in Ectopic Pregnancy

View Table

TABLE 5

Transvaginal Ultrasound Findings in Ectopic Pregnancy

FindingLR*

Ectopic cardiac activity

> 100 (diagnostic)

Ectopic gestational sac

23

Ectopic mass and fluid in pouch of Douglas

9.9

Fluid in pouch of Douglas

4.4

Ectopic mass

3.6

No intrauterine gestational sac

2.2

Normal adnexal region

0.55

Intrauterine gestational sac

0.07


LR = likelihood ratio.

*—An LR greater than 5 is moderately strong evidence of ectopic pregnancy; an LR greater than 10 is strong evidence of ectopic pregnancy; and an LR less than 0.1 is strong evidence against ectopic pregnancy.

Information from reference 9.

Beta-hCG levels may assist in interpreting ultrasound findings. In a normal intrauterine pregnancy, these levels would increase by at least 53 percent every two days, peaking at a level greater than 100,000 mIU per mL (100,000 IU per L).1,20 Beta-hCG levels alone cannot differentiate between ectopic and intrauterine pregnancy, and serial beta-hCG levels that do not increase appropriately in a woman with suspected ectopic pregnancy are only 36 percent sensitive and approximately 65 percent specific for detection of ectopic pregnancy.14,15 It also is important to note that ruptured and unruptured ectopic pregnancies have been identified at beta-hCG levels less than 100 mIU per mL (100 IU per L) and greater than 50,000 mIU per mL (50,000 IU per L).1

Serum progesterone levels can detect pregnancy failure and identify patients at risk for ectopic pregnancy, but they are not diagnostic of ectopic pregnancy. Sensitivity for diagnosis of ectopic pregnancy is very low (15 percent); therefore, 85 percent of patients with ectopic pregnancy will have normal serum progesterone levels.9 Algorithms for diagnosing ectopic pregnancy that include progesterone levels miss more ectopic pregnancies and require more surgeries than do algorithms without progesterone.9,10,14,16,17

Diagnostic uterine curettage may detect chorionic villi. If chorionic villi are not detected, ectopic pregnancy should be suspected. Curettage should only be considered when beta-hCG levels are falling or when levels are elevated and ultrasonography does not show intrauterine pregnancy.2,14 Diagnostic uterine curettage could terminate a desired pregnancy.

RECOMMENDED DIAGNOSTIC STRATEGY

The American College of Emergency Physicians and the American College of Obstetricians and Gynecologists have issued guidelines for using ultrasonography and beta-hCG levels to evaluate patients with suspected ectopic pregnancy.14,15 Figures 1 and 2 are algorithms based on these guidelines.1,14,15,17,20

Initial Diagnosis of Suspected Ectopic Pregnancy

Figure 1.

Algorithm for the initial diagnosis of suspected ectopic pregnancy. (beta-hCG = beta subunit of human chorionic gonadotropin.)

Information from references 1,14,15,17, and 20.

View Large

Initial Diagnosis of Suspected Ectopic Pregnancy


Figure 1.

Algorithm for the initial diagnosis of suspected ectopic pregnancy. (beta-hCG = beta subunit of human chorionic gonadotropin.)

Information from references 1,14,15,17, and 20.

Initial Diagnosis of Suspected Ectopic Pregnancy


Figure 1.

Algorithm for the initial diagnosis of suspected ectopic pregnancy. (beta-hCG = beta subunit of human chorionic gonadotropin.)

Information from references 1,14,15,17, and 20.

Diagnosing Suspected Ectopic Pregnancy Following Transvaginal Ultrasonography

Figure 2.

Algorithm for diagnosing suspected ectopic pregnancy following transvaginal ultrasonography. (beta-hCG = beta subunit of human chorionic gonadotropin.)

Information from references 1,14,15,17, and 20.

View Large

Diagnosing Suspected Ectopic Pregnancy Following Transvaginal Ultrasonography


Figure 2.

Algorithm for diagnosing suspected ectopic pregnancy following transvaginal ultrasonography. (beta-hCG = beta subunit of human chorionic gonadotropin.)

Information from references 1,14,15,17, and 20.

Diagnosing Suspected Ectopic Pregnancy Following Transvaginal Ultrasonography


Figure 2.

Algorithm for diagnosing suspected ectopic pregnancy following transvaginal ultrasonography. (beta-hCG = beta subunit of human chorionic gonadotropin.)

Information from references 1,14,15,17, and 20.

When evaluating patients for suspected ectopic pregnancy, physicians should take a history and perform a physical examination; then they should determine the patient’s risk stratification (Table 37,8) and order transvaginal ultrasonography.10,18 If a low-risk patient’s ultrasonography is negative for intrauterine pregnancy, and she is hemodynamically stable and has a beta-hCG level less than 1,500 mIU per mL, the physician should take another beta-hCG measurement after 48 hours. Patients with a nondiagnostic transvaginal ultrasonography result and a beta-hCG level of 1,500 mIU per mL or greater are at an increased risk for ectopic pregnancy and may need a surgical consultation or uterine evacuation procedure. If a patient’s condition is unstable, immediate surgical consultation is needed, and a uterine evacuation procedure may be considered. If chorionic villi are absent, ectopic pregnancy is likely.

Combined transvaginal ultrasonography and serial quantitative beta-hCG measurements are approximately 96 percent sensitive and 97 percent specific for diagnosing ectopic pregnancy. Therefore, transvaginal ultrasonography followed by quantitative beta-hCG testing is the optimal and most cost-effective strategy for diagnosing ectopic pregnancy.9,10,21

Treatment

EXPECTANT MANAGEMENT

Expectant management is between 47 and 82 percent effective in managing ectopic pregnancy.22,23 A good candidate for expectant management has a beta-hCG level less than 1,000 mIU per mL (1,000 IU per L) and declining, an ectopic mass less than 3 cm, no fetal heartbeat, and has agreed to comply with follow-up requirements.

MEDICAL TREATMENT

Methotrexate, a folic acid antagonist, is a well-studied medical therapy. Methotrexate deactivates dihydrofolate reductase, which reduces tetrahydrofolate levels (a cofactor for deoxyribonucleic acid and ribonucleic acid synthesis), thereby disrupting rapidly-dividing trophoblastic cells.24 Other therapeutic agents include hyperosmolar glucose, prostaglandins, and mifepristone (Mifeprex).24

Protocols for methotrexate therapy include single-dose and multiple-dose regimens (Table 624). Although no studies have compared the protocols, the single-dose regimen is easier to administer and is used more often. In a 2003 meta-analysis24 of methotrexate therapies, 20 studies examined the single-dose regimen, and six examined the multiple-dose regimen. The single-dose regimen created fewer side effects but was slightly less effective, with a crude overall success rate of 88 percent compared with the multiple-dose regimen’s 93 percent success rate. Methotrexate, regardless of the protocol, had an overall 89 percent crude success rate.24 Side effects of methotrexate include bone marrow suppression, elevated liver enzymes, rash, alopecia, stomatitis, nausea, and diarrhea. The time to resolution of the ectopic pregnancy is three to seven weeks after methotrexate therapy.

TABLE 6

Methotrexate Therapy Protocols

ProtocolSingle doseMultiple dose

Medication

50 mg per square meter of body surface methotrexate IM

Alternate every other day: 1 mg per kg methotrexate IM and 0.1 mg per kg leucovorin*

Laboratory values

LFTs, CBC, and renal function at baseline

LFTs, CBC, and renal function at baseline

Beta-hCG at baseline, day 4, and day 7

Beta-hCG at baseline, day 1, day 3, day 5, and day 7 until levels decrease

Repeat medication

Repeat regimen if beta-hCG level does not decrease by 15 percent between day 4 and day 7

Repeat regimen (for up to four doses of each medication) if beta-hCG level does not decrease by 15 percent with each measurement

Follow-up

Beta-hCG level weekly, and continue regimen until no longer detected

Beta-hCG level weekly, and continue regimen until no longer detected


*—Leucovorin protects cells from folic acid antagonists.

IM = intramuscular; LFT = liver function test; CBC = complete blood count; beta-hCG = beta subunit of human chorionic gonadotropin.

Adapted with permission from Barnhart KT, Gosman G, Ashby R, Sammel M. The medical management of ectopic pregnancy: a meta-analysis comparing “single dose” and “multidose” regimens. Obstet Gynecol 2003;101:779.

TABLE 6   Methotrexate Therapy Protocols

View Table

TABLE 6

Methotrexate Therapy Protocols

ProtocolSingle doseMultiple dose

Medication

50 mg per square meter of body surface methotrexate IM

Alternate every other day: 1 mg per kg methotrexate IM and 0.1 mg per kg leucovorin*

Laboratory values

LFTs, CBC, and renal function at baseline

LFTs, CBC, and renal function at baseline

Beta-hCG at baseline, day 4, and day 7

Beta-hCG at baseline, day 1, day 3, day 5, and day 7 until levels decrease

Repeat medication

Repeat regimen if beta-hCG level does not decrease by 15 percent between day 4 and day 7

Repeat regimen (for up to four doses of each medication) if beta-hCG level does not decrease by 15 percent with each measurement

Follow-up

Beta-hCG level weekly, and continue regimen until no longer detected

Beta-hCG level weekly, and continue regimen until no longer detected


*—Leucovorin protects cells from folic acid antagonists.

IM = intramuscular; LFT = liver function test; CBC = complete blood count; beta-hCG = beta subunit of human chorionic gonadotropin.

Adapted with permission from Barnhart KT, Gosman G, Ashby R, Sammel M. The medical management of ectopic pregnancy: a meta-analysis comparing “single dose” and “multidose” regimens. Obstet Gynecol 2003;101:779.

Patient selection is important in the medical management of ectopic pregnancy. The lower the beta-hCG levels at initiation of treatment, the higher the success rate of methotrexate therapy (Table 7).26 In addition to having a beta-hCG level less than 15,000 mIU per mL (15,000 IU per L), a candidate for medical treatment must be reliable and able to follow-up daily if necessary.15 Surgical management may be considered if a patient does not meet these criteria. Women with certain medical conditions (e.g., liver disease with a transaminase level two times greater than normal, renal disease with a creatinine level greater than 1.5 mg per dL [133 μmol per L], immune compromise with a white blood cell count less than 1,500 per mm3 [1.5 3 109 per L] and platelets less than 100,000 3 103 per mm3 [100 3 109 per L], significant pulmonary disease) are not candidates for methotrexate.27

TABLE 7

Methotrexate Therapy Success Rate at Different Baseline Beta-hCG Levels

Initial beta-hCG level (mIU per mL)Success rate (%)

Less than 1,000 (1,000 IU per L)

98

1,000 to 1,999 (1,000 to 1,999 IU per L)

93

2,000 to 4,999 (2,000 to 4,999 IU per L)

92

5,000 to 9,999 (5,000 to 9,999 IU per L)

87

10,000 to 14,999 (10,000 to 14,999 IU per L)

82

15,000 or greater (15,000 or greater IU per L)

68


Beta-hCG = beta subunit of human chorionic gonadotropin.

Adapted with permission from Lipscomb GH, McCord ML, Stovall TG, Huff G, Portera SG, Ling FW. Predictors of success of methotrexate treatment in women with tubal ectopic pregnancies. N Engl J Med 1999;341:1976.

TABLE 7   Methotrexate Therapy Success Rate at Different Baseline Beta-hCG Levels

View Table

TABLE 7

Methotrexate Therapy Success Rate at Different Baseline Beta-hCG Levels

Initial beta-hCG level (mIU per mL)Success rate (%)

Less than 1,000 (1,000 IU per L)

98

1,000 to 1,999 (1,000 to 1,999 IU per L)

93

2,000 to 4,999 (2,000 to 4,999 IU per L)

92

5,000 to 9,999 (5,000 to 9,999 IU per L)

87

10,000 to 14,999 (10,000 to 14,999 IU per L)

82

15,000 or greater (15,000 or greater IU per L)

68


Beta-hCG = beta subunit of human chorionic gonadotropin.

Adapted with permission from Lipscomb GH, McCord ML, Stovall TG, Huff G, Portera SG, Ling FW. Predictors of success of methotrexate treatment in women with tubal ectopic pregnancies. N Engl J Med 1999;341:1976.

Patients treated with methotrexate have been shown to have the same quality of life after methotrexate treatment compared with patients who had surgical treatment. Women experienced more pain, had less energy, and had worse health perception during the first few weeks after treatment with methotrexate, but they had the same quality of life after 16 weeks.28

SURGICAL TREATMENT

Before the advent of laparoscopy, laparotomy with salpingectomy (removal of the fallopian tube through an abdominal incision) was the standard therapy for managing ectopic pregnancy. Laparoscopy with salpingostomy, without fallopian tube removal, has become the preferred method of surgical treatment. Laparoscopy has similar tubal patency and future fertility rates as medical treatment.25 Salpingostomy has an estimated 8 to 9 percent failure rate, which can be managed with methotrexate.

Follow-Up and Prognosis

During treatment, physicians should examine patients at least weekly and sometimes daily. Serial beta-hCG measurements should be taken after treatment until the level is undetectable. If the levels fail to decline, the patient can be treated with a second course of methotrexate or with methotrexate post-surgery. Surgical intervention is necessary if beta-hCG levels increase.

The prognosis is good for patients who receive appropriate treatment. With proper patient selection, success rates approach 82 percent for expectant management, 90 percent for medical management, and 92 percent for surgical management.22,23,26

FUTURE FERTILITY AND RISK OF RECURRENCE

Approximately 30 percent of women treated for ectopic pregnancy later have difficulty conceiving. The overall conception rate is approximately 77 percent regardless of treatment.3 Rates of recurrent ectopic pregnancy are between 5 and 20 percent, but the risk increases to 32 percent in women who have had two consecutive ectopic pregnancies.2,3

The Authors

ANNE-MARIE LOZEAU, M.D., M.S., is assistant professor of family medicine in the Department of Family Medicine at the University of Wisconsin Medical School-Madison. She received her medical degree at Dartmouth Medical School, Hanover, N.H., and completed a residency in family medicine at the University of Wisconsin Medical School-Madison.

BETH POTTER, M.D., is assistant professor of family medicine in the Department of Family Medicine at the University of Wisconsin Medical School-Madison. She received her medical degree from Rush Medical College, Chicago, and completed a residency in family medicine at the University of Wisconsin Medical School-Madison.

Address correspondence to Anne-Marie Lozeau, M.D., M.S., 3209 Dryden Dr., Madison, WI 53704 (e-mail: alozeau@wisc.edu). Reprints are not available from the authors.

Author disclosure: nothing to disclose.

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