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Gynecological Surgery

, 16:2 | Cite as

The diagnosis and management of interstitial ectopic pregnancies: a review

  • Maximilian BrincatEmail author
  • Alison Bryant-Smith
  • T. K. Holland
Open Access
Review Article
  • 60 Downloads

Abstract

The objective of this article is to review the published literature on the diagnosis and management of interstitial pregnancies (IPs). IPs account for 2–6% of all ectopic pregnancies and have the potential to cause life-threatening haemorrhage resulting in a 2–5% mortality rate. There is little consensus on the best practice for diagnosing and managing interstitial pregnancies. By reviewing the published data, we set out to determine what the best evidence-based practice for the management of interstitial ectopic pregnancies is, what protocols can be used and whether this improves post-operative outcomes and future fertility rates.

Keywords

Interstitial ectopic pregnancy Methotrexate Cornuostomy Wedge resection Fertility 

Abbreviations

GS

Gestational sac

IP

Interstitial pregnancy

IVF

In vitro fertilisation

MRI

Magnetic resonance imaging

MTX

Methotrexate

RCT

Randomised control trial

TVUS

Transvaginal ultrasound scan

UTCE

Ultrasound-guided transcervical forceps extraction

β-hCG

Beta human chorionic gonadotrophin

Introduction

The diagnosis and management of interstitial pregnancies (IPs) remains challenging, largely due to the rarity of this diagnosis. Most units are likely to manage only one or two cases per year. Appropriate first line management is based on many factors, including the patient’s symptoms, timely diagnosis, size of the pregnancy, depth of surrounding myometrium, haemodynamic stability, and desires for future fertility.

There is limited evidence on interstitial pregnancies and their management with current evidence consisting of small case series with no randomised controlled trials (RCTs). This review will perform a comprehensive and systematic review of the current evidence regarding the diagnosis and management of interstitial pregnancies, to help work toward a consensus on the appropriate management of such cases.

Definition, incidence, and pathophysiology

An interstitial pregnancy (IP) occurs when the blastocyst implants in the most proximal section of the fallopian tube (called the interstitial portion), which is within the myometrium [1]. This interstitial section of the fallopian tube is approximately 0.7-mm wide and 1–2-cm long [2].

IPs may be incorrectly referred to as ‘cornual’ or ‘angular’ pregnancies. It is important to correctly differentiate between these terms, as the resultant maternal morbidity and mortality vary greatly. An ‘angular pregnancy’ occurs when an embryo is implanted medial to the utero-tubal junction, in the lateral angle of the uterine cavity, and as such is neither an ectopic pregnancy nor dangerous (Fig. 1). Cornual implantation describes those in the upper and lateral uterine cavity, whereas interstitial denotes those blastocysts implanted within the proximal intramural portion of the tube [1]. Therefore a ‘cornual pregnancy’ is any pregnancy which is implanted in the horn of a uterus, which may be one horn of a bicornuate uterus, which is not an ectopic pregnancy [3] or a non-communicating, functional rudimentary cornua of a unicornuate uterus, which is an ectopic pregnancy (Mavrelos et al. 2007). Because the term ‘cornual’ can be applied to many different types of pregnancy, it should be avoided when discussing interstitial ectopic pregnancies.
Fig. 1

US image of angular pregnancy

The incidence of ectopic pregnancies is generally increasing; there also appears to be a concurrent increase in the proportion of ectopic pregnancies that are IPs. The increase in incidence of IPs may be due to various factors, including better diagnosis, more prevalent pelvic inflammatory disease, pelvic surgery, and assisted reproductive techniques [3, 4]. IPs account for 2–6.8% of all ectopic pregnancies [5, 6, 7].

Historically IPs were diagnosed at laparotomy after rupture at the end of the first trimester or early in the second trimester, and hysterectomy rates were as high as 40% [8]. However, the outcome from this diagnosis has improved more recent case series that have estimated a mortality rate of 2–2.5%, which is seven times the average for all ectopic pregnancies [7]. The increased morbidity and mortality is due to catastrophic bleeding secondary to rupture, due to the close proximity of the gestational sac (GS) to the intramyometrial arcuate vasculature [3]. It is also likely that IPs are larger when they rupture than tubal ectopic pregnancies as the layer of overlying myometrium is able to accommodate larger pregnancies, before rupture, than the uterine tube.

Methodology

A literature search was carried out in March 2018 using key words ‘interstitial pregnancy’, ‘cornual pregnancy’ and ‘angular pregnancy’. Articles that were published from January 2000 until March 2018 were obtained from MEDLINE, EMBASE and PUBMED. This systematic search initially identified 1666 articles. After reviewing all abstracts, 86 articles were identified as being significantly related to the diagnosis and management of interstitial pregnancies.

Diagnosis

Timely diagnosis is key to the successful management of patients with IPs. Diagnosing such cases may be difficult, due to the wide spectrum of presenting symptoms and signs and difficulties distinguishing an IP from an intra-uterine or isthmic tubal ectopic pregnancy. Also, some patients may present with rupture and haemodynamic instability requiring immediate surgery before a non-invasive diagnosis may be made. Patients may present with abdominal pain and/or vaginal bleeding, may be asymptomatic or have their IP diagnosed on routine early pregnancy scan.

Risk factors for IP include previous ectopic pregnancy, tubal surgery, in vitro fertilisation (IVF), ovulation induction, or history of sexually transmitted disease [7, 9, 10] (Table 1). Hiersch et al. noted that 46% of the women with IPs treated in their hospital had conceived following assisted reproductive techniques [11]. With the incidence of IVF increasing, one expects a resultant increase in IPs. There does not appear to be a single risk factor that clearly differentiates patients with an IP from those with an ampullary or isthmic ectopic pregnancy [12].
Table 1

Risk factors for interstitial pregnancies

Risk factors

Percentage of women with an IP who have this risk factor

Previous ectopic pregnancy

22.9–54%

Previous ipsilateral or bilateral salpingectomy

22.9–54%

Conception after in vitro fertilisation

17.1–34.4%

History of sexually transmitted disease

12.5–25.0%

Since the introduction of high-resolution transvaginal ultrasonography (TVUS) and highly sensitive β-hCG assays, timely and accurate diagnosis has become possible. There is no evidence of particular serum β-hCG trends that are sensitive in differentiating IPs from either normal intrauterine pregnancies or other types of ectopic pregnancies.

Ultrasound diagnosis

Ever-improving ultrasound technology has resulted in wider utilisation of ultrasound to diagnose gynaecological conditions. TVUS has been reported to have a sensitivity of 56% at 8.2 weeks’ gestation [10], and 71.4% of patients at 6.9 weeks’ gestation [7]. MacRae et al.’s study reported 80% of IPs being correctly diagnosed on 2D-TVUS scanning [13]. There is no evidence that 3D-US is more accurate for diagnosing IPs than 2D-US; however, it is easier to demonstrate the interstitial nature of the pregnancy on 3D than 2D.

The diagnosis of IP by ultrasound is based on the following criteria: the GS is located outside the uterine cavity; the interstitial part of Fallopian tube is seen adjoining the lateral aspect of the uterine cavity and GS; and the myometrial mantle extends laterally to encircle the GS (Fig. 2) [14].
Fig. 2

US image of interstitial pregnancy

The fallopian tube’s interstitial section is best evaluated in the transverse plane at the level of the uterine fundus and appears as a thin echogenic line extending from the lateral aspect of the endometrium toward the uterine serosa [15].

Magnetic resonance imaging (MRI) and surgical diagnosis

MRI may be used in clinically stable patients whose diagnosis remains uncertain despite having a TVUS. However, referral to a tertiary centre with sufficient expertise in diagnosing and managing IPs may be preferable [16]. Despite the above advances in the radiological diagnosis of IP, a small cohort of patients will only be diagnosed with an IP at laparoscopy or laparotomy due to either the lack of sufficient ultrasound expertise or haemodynamic instability (Fig. 3).
Fig. 3

Laparoscopic view of interstitial pregnancy

Management

Historically, management of IPs included wedge resection by laparoscopic/open surgery or hysterectomy [3]. Less invasive and/or aggressive techniques may reduce the risk of intra-operative complications, whilst improving long-term fertility and obstetric outcomes. Table 2 illustrates the various management options and their associated benefits (in lighter grey) and drawbacks (in darker grey); we will discuss these options in detail below.
Table 2

Benefits and drawbacks of modes of management used in IPs

Table illustrates the various management options and their associated benefits (in lighter grey) and drawbacks (in darker grey): we will discuss these options in detail below

Conservative management (expectant and medical management)

The establishment of early pregnancy assessment units, use of high resolution TVUS and access to rapid quantitative β-hCG testing facilitate early detection of ectopic pregnancies, prior to tubal rupture [14]. Conservative management (encompassing expectant and medical management) should only be offered to patients with a radiologically diagnosed IP who are haemodynamically stable and have no obvious risks of immediate rupture, such as large GS or rapidly increasing β-hCG levels. Fastidious follow-up allows expectant or medical management to be offered as first line management in appropriate patients.

Expectant management

Spontaneous miscarriage is a common pregnancy outcome, whether the pregnancy is intra-uterine or ectopic [12]. Expectant management is an appropriate first line approach for women with an IP and declining serum β-hCG levels (irrespective of ectopic mass size and initial serum β-hCG levels) [17, 18]. Expectant management should be abandoned if there is evidence of clinical deterioration.

Retrospective case series carried out by Cassik et al. and Poon et al. at King’s College Hospital (London) reported a total of 26 cases which were initially offered expectant management (Table 3). Cassik et al. noted that there were no significant differences in success rates between expectant or medical management options (P > 0.05) [14]. However, success rates for patients given local methotrexate (21/23, 91%) may have been higher than for expectant 5/7, 71% (95%CI 29–96) due to larger numbers of patients. The authors did not find any significant differences in either the initial β-hCG levels or β-hCG resolution times between the three subgroups. They did note that the initial serum β-hCG was significantly lower in cases of successful conservative treatment, with no failures occurring when the initial β-hCG was less than 9000 IU/L. Poon et al. noted that the length of follow-up for those patients managed expectantly ranged from 7 to 141 days, with a median duration of 50.6 days [18]. Several other studies analysed expectant management, but the number of patients was too low to be able to detect significant differences in outcome [16, 19, 20].
Table 3

Studies on expectant management on IPs

Article

Location

No. of cases

Patient age (years)

Gestation (weeks)

Diameter of GS (mm)

Foetal cardiac activity present

β-hCG

Comments

Cassik et al. 2005 [14]

King’s College Hospital (London, UK)

[December 1996 to March 2003]

7

N/A

7 (4–13)

N/A

0

1799 (438–11,460)

71% success rate ((95%CI 29–96)

No significant differences in success rates between the three different management options (P > 0.05)

Poon et al. 2014 [18]

King’s College Hospital (London, UK)

[January 2004 to April 2013]

19

31.26 (18–42)

10.1

19.0 (9–49)

0

3468.0 (157–89,968)

Overall success rate 89.5% (n = 17)

Two failed cases were subsequently treated with MTX. No cases of uterine rupture.

Median follow-up 50.6 days

Medical management of tubal ectopic pregnancy

High dose intravenous/intramuscular methotrexate (MTX) with oral folic acid rescue was first proposed as a safe alternative for the management of IP in 1982 [21] (Table 4). The dose of one-off systemic MTX is calculated according to the Stovall et al. protocol: 50 mg/m2 body surface area [22].
Table 4

Combined data from current studies on medical management of interstitial ectopic pregnancy

Study

Number of patients in total

Number of patients successfully managed (local and systemic MTX)

Number of patients managed with systemic MTX

Number of patients successfully managed (systemic MTX)

Number of patients managed with local MTX

Number of patients successfully managed (local MTX)

Hafner et al. 1999 [16]

10

9

5

4

5

5

Jermy et al. 2004 [20]

18

14

18

14

N/A

N/A

Tulandi et al 2004 [44]

8

5

N/A

N/A

N/A

N/A

Cassik et al. 2005 [8]

28

24

5

4

23

21

Tang et al. 2006 [42]

11

10

11

10

N/A

N/A

Surbone et al. 2013 [38]

9

8

3

2

6

6

Hiesch et al. 2014 [17]

17

12

17

12

N/A

N/A

Framarino et al. 2014 [15]

14

14

N/A

N/A

14

14

Tanaka et al. 2015 [40]

33

31

33

31

N/A

N/A

Total

148

127

92

77

48

46

Success rate (95%CI)

 

85.81% (84.17–87.45)

 

79.98% (72.68–87.29)

 

97.83% (93.56–100)

N/A implies that the particular study did not consider patients managed with that treatment

Systemic MTX is now widely used as the first-line management for patients with tubal ectopic pregnancy who fulfil all the inclusion criteria [23]. An RCT comparing methotrexate with laparoscopic salpingostomy surgery for tubal ectopics showed that methotrexate is equally successful to salpingostomy in terms of requirement for further treatment [24]. However, current guidance is that for women with a normal contralateral tube salpingectomy is recommended due to the risk of ongoing trophoblast, increased bleeding and no proven different in future intra-uterine pregnancy rates [25]. Another RCT comparing single methotrexate with laparoscopic salpingostomy surgery concluded that single dose methotrexate was less effective than salpingostomy (65% vs. 93% respectively) [26]. However, RCTs comparing expectant management versus management with MTX did not find any significant benefit for pregnancies with β-hCG levels less than 1500 IU [27, 28].

Medical management for interstitial ectopic pregnancy

For IP, in addition to intravenous or intramuscular administration, MTX may also be injected locally either into, or close to, the GS (under TVUS or laparoscopic guidance). Doses for the local injection of MTX in the studies below ranged from 25 to 50 mg.

Cassik et al. [14] published a case series of conservatively managed IP. They found success rates for local methotrexate, systemic methotrexate and expectant management was 91%, 80% and 71% respectively although the numbers were too small to show a statistically significant difference [14]. However, the 5/35 (14.3%) of the patients managed conservatively required surgical treatment, all of whom had β-hCG levels greater than 9000 IU/L [14].

Some authors advocate local injection of MTX or potassium chloride into the GS when foetal cardiac activity is present [14, 29]: our review did not find any evidence that this is beneficial in the management of IPs. Even though Cassik et al. had a higher success rate in the local MTX group than the systemic MTX group, this was not found to be significant (P > 0.05) [14]. Of note, local MTX administration is more invasive than systemic administration and requires special facilities and trained personnel; this makes it more operator-dependent, less widely available and more costly than systemic MTX administration. Local treatment can be administered under ultrasound guidance into the gestational sac/chorionic tissue, via transvaginal route using a fine spinal needle. This needle may be advanced through the anterior fornix, through the anterior uterine wall and into the targeted area where the MTX may be delivered straight into the gestational sac and surrounding area [14].

One proposed benefit of administering MTX locally (rather than systemically) is to reduce the incidence of side-effects, such as transitory peripheral neuropathy, severe constipation, and deterioration in liver function [30]. Significant side effects were documented in 2/5 (40%) of women receiving systemic MTX in [14] study. Cassik and Hafner et al. noted that patients who received MTX injected locally into the GS did not experience any of these side effects; however, numbers were too low to show significance [14, 30].

The safety of MTX management of IP relies upon diligent follow-up and the capacity to perform expedient surgery if required. Close follow-up (such as that outlined above) is crucial, as 10–20% of patients will require either a second dose of MTX or surgery. Success rates in the studies included in this review were 85.81% (95%CI 84.17–87.45). Of note, different MTX regimens were used in these studies, including both systemic and local MTX injection: the average success rate for systemic MTX was 79.9% (95%CI 72.68–87.29), whilst for local MTX injection, it was 97.83% (95%CI 93.59–100). None of the studies reported any significant difference in the success rate between systemic and local MTX.

Our literature search did not identify the following factors as significantly affecting the efficacy of MTX management: initial β-hCG levels, GS size, gestation, maternal age, or foetal cardiac activity (Table 5). Hiersch et al. identified a higher rate of unsuccessful first-line treatment in women with two previous ectopic pregnancies (4/5 cases, 80% versus 1/12 cases; 8.3%; P = 0.01) [11].
Table 5

Studies on medical management of IPs

Paper

Location

MTX route of administration

No. of cases

Patient age (years)

Gestation (weeks)

Diameter of GS (mm)

Foetal cardiac activity (FCA) present

β-hCG (mIU/mL)

Comments

Hafner et al. 1999 [30]

King’s College Hospital (London, UK)

Prospective interventional study

2 cases of systemic MTX (2 doses 1 mg/kg IM, 48 h apart, with rescue folinic acid)

5 cases of local MTX (single 25 mg dose of MTX, TVUS-guided, injected into the GS)

3 cases: 2–4 mEq of KCL + MTX if FHR present

10

34.18

6.5 (6–9)

24.8 (9–51)

3

9574 (102–41,150)

90% success rate in total

100% success rate with local MTX therapy

80% for systemic MTX

No rupture

No difference between local and systemic MTX Rx in time taken for resolution of β-hCG

Mean 18.8 days for β-hCG to resolve (max 32 days)

All 3 FCA treated successfully

Jermy et al. 2004 [6]

St George’s University Hospital (London, UK)

[1998–2002]

Prospective observational study

Single dose MTX IM

18

32.7

5.4

30.39 (12–54)

4

6452 (32–31,381)

50% treated successfully with 1 dose of MTX

80% treated successfully with second dose of MTX

All 4 FCA cases treated successfully

No ruptures

All patients with β-hCG < 5000 IU were treated successfully with single dose MTX

Hospital stay (days) 7 (0–40)

No side effects secondary to MTX

Tulandi et al. 2004 [7]

Multi-centre

(Europe, North America, Chile)

[1999–2002]

Retrospective case series

4 cases: local MTX

4 cases: systemic MTX

8

32.6

7.9 +/− 0.9

15 +/− 9

4683 +/− 2056

62.5% success rate

37.5% required second intervention (surgical treatment)

No ruptures

FCA not a factor in treatment success

Mean interval between MTX administration and β-hCG resolution was 52.7 +/− 36.0 days

Cassik et al. 2005 [14]

King’s College Hospital (London, UK)

[1996–2003]

Retrospective case series

23 cases: local MTX injection

5 cases: systemic MTX

28

7 (4–13)

5

Local MTX: 6006 (102–69,820)

Systemic MTX: 5576 (793–41,150)

85.7% success rate overall

Local MTX: 91% success rate

Systemic MTX: 80% success rate

No significant differences in success rates between the three different management options (P > 0.05)

None of the women receiving local MTX experienced significant side-effects

1 failed case had a ruptured ectopic

Tang et al. 2006 [46]

Royal Brisbane and Women’s Hospital (Australia)

[2000–2005]

Retrospective case series

Medium-dose IV MTX (100 mg/5 min, followed by 200 mg/12 h), with oral folinic acid rescue (15 mg) on day 0

11

31

6.45 (5–8)

20.72 (10–60)

4

25,473 (1600–106,634)

91% success rate

1 case required second dose of MTX on day 17 (due to plateauing β-hCG), followed by

emergency laparotomy on day 31 for rupture

Surbone et al. 2013 [47]

University Hospital of Lausanne (Switzerland)

[2001–2011]

Retrospective case series

3 cases: single dose IM MTX

6 cases: local MTX, injected into the cornual region

9

33 (25–39)

6 (5–9)

5838 (2974–15,022)

88.9% success rate

1 case who received IM MTX required a second dose of IM MTX, followed by laparoscopic cornual resection

Hiesch et al 2014 [11]

The Helen Schneider Hospital for Women (Israel)

[2003–2013]

Retrospective case series

14 case: multi dose MTX regimen

3 cases: single dose MTX

17

32 +/− 5.8

6.5 +/− 1.3

36.0 +/− 24.1

3

15,763 +/− 25,147

70.5% success rate

All 3 patients treated with single-dose MTX were successful

5 unsuccessful cases of multi-dose MTX required selective uterine artery MTX injection

Poon et al. 2014 [18]

King’s College Hospital (London, UK)

[? years]

Retrospective case series

16 cases: local MTX

3 cases: systemic MTX

19

7.8 (6–12.6)

13.0 (10–48)

4

7131 (562–8464)

No comments

Framarino et al. 2014 [48]

Umberto I Hospital, Sapienza University (Rome, Italy)

[2007–2012]

Retrospective observational study

Local MTX (TVUS-guided)

14

31 +/− 3

6.5 +/−  1.0

2

2146 +/−  807

100% success rate, so no second line Rx needed, and no patients required hospitalisation

No reported side-effects from MTX

β-hCG levels had normalised within 2 months, but (on US) the GS disappeared more slowly (taking about 4 months)

Tanaka et al. 2015 [49]

Royal Brisbane and Women’s Hospital (Australia)

[2000–2012]

Retrospective observational study

Double dose of IV MTX

33

31.8 (21–43)

6.45

24.1

7

20,546 (230–106,634)

93.9% success rate

2 cases (6.1%) complicated by rupture

β-hCG resolution took an average of 55.6 (19 to 137) days

3 patients had side-effects from MTX

In Jermy et al.’s study, all patients with an initial serum β-hCG < 5000 were managed successfully with a single dose of systemic MTX [6] (Table 6). The key indicators of failed MTX management were insufficient reduction in β-hCG levels, abdominal pain, or rupture. 2.4% of the 167 cases experienced a ruptured ectopic pregnancy, requiring emergency surgery. The mean time taken for β-hCG levels to normalise was 47.93 days. The duration of hospital stay varied considerably, with some patients being managed as outpatients and others as inpatients: one patient was admitted for 40 days.
Table 6

Combined data from current studies on surgical management of interstitial ectopic pregnancy

Study

Number of patients in total

Success rate of combined (cornuostomy/cornual resection)

Number of patients treated by cornuostomy

Success rate of cornuostomies

Number of patients treated by cornual resection

Success rate of cornual resection

Moon et al. 2000 [41]

24

23

24

23

N/A

N/A

Tulandi et al. 2004 [7]

24

23

3

3

21

20

Choi et al. 2009 [50]

8

8

8

8

N/A

N/A

Moon et al. 2010 [37]

20

20

20

20

N/A

N/A

Watanabe et al. 2014 [38]

13

13

13

13

N/A

N/A

Liao et al. 2016 [32]

29

29

N/A

N/A

29

29

Nirgianakis et al. 2017 [43]

10

10

N/A

N/A

10

10

Total

128

126

68

67

60

59

Success rate (95%CI)

 

98.1% (95.48–100)

 

99.16% (97.51–100)

 

98.41% (95.30–100)

N/A implies that the particular study did not consider patients managed with that treatment

Patients with continuously rising β-hCG levels warrant closer surveillance, such as sonographic evaluation for signs of pregnancy progression (e.g. the development of foetal cardiac activity) or uterine/tubal rupture. Repeated MTX dosing should be considered until one is satisfied that the IP has been resolved.

Surgical management

Surgical management of IPs remains an important option, as it offers definitive treatment (Table 7). Historically, wedge resection or hysterectomy by laparotomy was the mainstays of surgical management; however, the morbidity associated with such invasive operations has led to newer, less invasive techniques being preferred.
Table 7

Studies on surgical management of IPs

Paper

Location

Mode of surgical management (cases)

No. of cases

Patient age (years)

Gestation (weeks)

Diameter of GS (mm)

Foetal cardiac activity (FCA) present

β-hCG (IU/ml)

Comments

Moon et al. 2000 [41]

Moon Hwa Hospital, Pusan

(South Korea)

[1993–1998]

Retrospective case series

Laparoscopic cornuostomy (24)

Endo-loop vs. vasopressin + electric cauterization vs. encircling suture

24

33.4 +/− 5.8

7.6

35.29

7

2652.8

95.8% success rate

75% pregnancy rate in future

No ipsilateral ectopics

Tulandi et al. 2004 [7]

Multi-centre

(Europe, North America, Chile)

[1999–2002]

Retrospective case series

Laparoscopic: cornual resection (8) vs. cornuostomy (3)

11

32.6 +/− 1.0

5.4 +/− 1.0

11 +/− 6

2086.9 +/− 698.2

90.9% success rate

1 failed primary treatment (9.1%)

Subsequent treatment: single dose/multi-dose MTX (for persistently elevated β-hCG)

Tulandi et al. 2004 [7]

Multi-centre

(Europe, North America, Chile)

[1999–2002]

Retrospective case series

Laparotomic cornual resection

13

 

7.3 +/− 0.4

14 +/− 8

 

11,471 +/− 6281

100% success rate

9 cases had tubal rupture confirmed

Choi et al. 2009 [50]

EUN Hospital (South Korea)

[? Years]

Retrospective case series

Laparoscopic cornuostomy (8)

8

7.6 +/− 1.11

33 +/− 6.7

5

3656 +/− 2573

100% success rate

Operating time 50 +/− 22 min

No major post-operative complications

β-hCG normalised by 26.5 +/− 7 days

Moon et al. 2010 [37]

Moon Hwa Hospital, Pusan

(South Korea)

[2003–2006]

Retrospective case series

Laparoscopic cornuostomy (20)

20

33.5 +/− 3.2

6.7 +/− 1.2

 

1095 (? range)

100% success rate

Time to resumption of menstrual period: 38.6 days

Hwang et al. 2011 [42]

Korea University Medical Center

(South Korea)

[1998–2009]

Case – control study

Open cornual resection (49) vs. laparoscopic cornual resection (39)

88

32.5 (19–42)

7.86 +/− 1.7

 

22 (22.5%)

12,741 +/− 103–81,351)

5 cases of laparoscopic management needed conversion to open management.

No statistical differences in operating time, estimated blood loss, blood transfusion requirements, or complications

Mean post-operative inpatients admission was 5.89 +/− 1.86 days (laparotomy) vs. 4.53 +/− 1.44 days (laparosocopy) (P = 0.0001)

Poon et al. 2014 [18]

King’s College Hospital (London, UK)

[2004–2013]

Retrospective case series

 

9

 

8.21 (5.1–11)

31.5 (13–44)

3 (33%)

9,402 (2225–75,530)

No comments

Hiersch et al. 2014 [11]

The Helen Schneider Hospital for Women (Israel)

[2003–2013]

Retrospective case series

 

7

32 +/− 5.8

10.5 +/− 5.5

2094.8 +/− 1721.3

No comments

Watanabe et al. 2014 [38]

NTT East Japan Tohoku Hospital and Sendai City Hospital (Japan)

[2000–2012]

Retrospective case series

Laparoscopic cornuostomy + MTX administration to local site (13)

13

 

7.6 +/− 1.3 weeks (5–9)

34.6 +/− 10.2

3

20,800 +/− 18,100

100% success rate

Mean operative time 107 +/− 23 min (61–160)

Mean haemoglobin drop was from 12.4 +/− 1.0 to 10.3 +/− 1.7 g/dL

No major post-operative complications

No persistent ectopic pregnancies

10/13 patients followed up

8 conceived spontaneously [average 13 months after the procedure]:

1 pregnancy ended in early miscarriage;

3 delivered by ventouse delivery, the other? 2 by elective caesarean section

Liao et al. 2016 [32]

Mennonite Christian Hospital

(? country)

[1992–2013]

Retrospective case series

Laparoscopic cornual resection (29)

29

31 (18–43)

8 (5–12 + 1)

   

Of the 10 pregnancies post-cornual resection, there were 3 cases of subsequent uterine rupture or dehiscence (30%)

71.4% of patients who were trying to conceive achieved subsequent pregnancy

No recurrent ectopic pregnancies

Nirgianakis et al. 2017 [43]

University of Bern

(Switzerland)

[2009–2015]

Retrospective case series

Laparoscopic cornual resection (10)

10

34.50 +/− 6.21

53.25 +/− 16.79 days

  

27,634 +/− 35,198

100% success rate

EBL 137.00 +/− 178.64 mL

3 patients required blood transfusions

Length of hospitalisation was 2.67 +/− 1.00 days

Women with IPs who are haemodynamically unstable and/or have an ultrasound suggestive of pregnancy rupture should undergo immediate surgical management. Patients who present with heterotopic pregnancies (one of which is both viable and wanted) should be offered surgical rather than expectant management as accurate monitoring with β-hCG levels is not possible in this situation.

Advances in laparoscopic surgery allow for less invasive and less traumatic surgical options for patients with IPs than those practised historically (i.e. laparoscopic cornual resection, rather than abdominal hysterectomy). While cornual (‘wedge’) resection preserves patients’ future fertility, it may carry the risk of uterine rupture due to the loss of myometrium and extensive uterine scarring ([31],). Liao et al. reported an incidence of subsequent uterine rupture and dehiscence after wedge resection of 30% [32]. This is considerably higher than the uterine rupture rates post myomectomies, which typically range from 0.49 to 0.70% in subsequent pregnancies [32] However, an alternate study has not shown increased risk of uterine rupture in subsequent pregnancy although, in this cohort, the caesarean rate was 60% versus 30% of patients without a history of ectopic pregnancy (P = 0.137) [33].

More recent studies favour cornuostomy over cornual resection. Cornuostomy excises the IP, while preserving uterine architecture and maintaining fertility ([34]). Cornuostomy is considered to cause less tubal damage than cornual resection and may have better pregnancy outcomes in future (including fewer cases of uterine rupture) [32]. The risk of persistent ectopic pregnancy (i.e. failed initial management) after laparoscopic salpingostomy in tubal pregnancies has been reported to be 5–20% [35]); however, our review found a 99.16% (95%CI 97.51–100) success rate in patients with IPs who underwent cornuostomy. Risk factors for recurrent IP following salpingostomy/cornuostomy include an IP < 2 cm and rapidly rising pre-operative β-hCG [36]. The smaller the gestational sac, the harder it is to ensure that the entire interstitial pregnancy has been excised, thereby increasing the risk of persistent interstitial pregnancy [37]. A larger ectopic pregnancy does not appear to be an indication for cornual resection (rather than cornuostomy): MacRae et al. and Watanabe et al. performed cornuostomies for larger interstitial GSs [13, 38]. However, this conflicts with the advice given by Cucinella who notes that cornual resection was preferred in cases of advanced gestational age and/or when ectopic size was > 4 cm in diameter [34]. Our experience is that with intra-myometrial vasopressin use for haemostasis, large and small IP can be treated laparoscopically.

Wedge resection disrupts the uterine architecture and should only be performed in cases of ruptured IP with troublesome bleeding or for patients not desiring future fertility. Similar operations (such as myomectomy) carry a risk of uterine rupture in subsequent pregnancies of 0.49–0.70% [39]: cornual resection is an accepted risk factor for uterine rupture in subsequent pregnancies [40] Cucinella et al.’s systematic review compared 156 cases of cornuostomy with 198 cases of cornual resection: the pregnancy rates in a small sample of these cases were 72% vs. 62% respectively, of which the live birth rates 48% vs. 62% in the cornuostomy and cornual resection groups, respectively. Any differences in the fertility outcomes or live birth rates between the two groups were not statistically significant [34].

Key steps in laparoscopic cornuostomy include cornual incision, removal of the products of conception, cornual repair and confirming haemostasis [41]. Prior to cornual incision, various methods to reduce intra-operative blood loss can be employed: vasopressin injection into peri-cornual area, electric cauterisation of incision area, endo-loop application to create a para-cornual tourniquet and an encircling suture around the cornu. There are concerns that electrocoagulation may damage the underlying myometrium and interfere with the revascularisation process, therefore weakening the area and theoretically increasing the risk of uterine rupture in future [37]; electrocauterisation also increases the risk of damage to surrounding organs, leading to injuries such as bowel perforation. Moon et al. concluded that the endo-loop and encircling suture methods are simple, safe, effective and nearly bloodless in achieving haemostatic control during treatment of IPs [37].

If possible, one should manage IPs using a minimally invasive approach, rather than open surgery. Tulandi et al. found that the mean volume of intra-abdominal haemorrhage encountered for the laparotomy group was 1385.7+/− 978.8 ml, compared to 460.0+/− 70.7 ml for the laparoscopy group (P value—is this significant) [7]; this difference probably reflects surgeons’ pre-operative decision-making (taking into account patients’ differing pre-operative blood loss or haemodynamic stability), rather than blood loss caused by the operative technique itself. Hwang et al. assessed 88 cases of cornual resection, performed by either laparoscopy or laparotomy: the only significant difference found between the two groups was the duration of post-operative recovery [42]. The post-operative pain, length of hospital stay, return to normal function, return to work and cosmetic advantages of a laparoscopic approach should also be considered. Nirgianakis et al. noted similar rates of surgical complications (P = 0.413) and the need for subsequent MTX treatment (P = 0.513) in patients with an IP treatment with laparoscopic cornual resection, compared to women with tubal ectopic pregnancies treated with laparoscopic salpingectomy/salpingostomy [43].

Other management options

Ultrasound-guided transcervical forceps extraction (UTCE)

As described by Ahn et al 2013, UTCE utilises a natural orifice to remove any products of conception [44]. The IP is approached through the vagina and cervical canal, then the GS is removed using small forceps (presumably through the tubal ostium), under transabdominal US guidance [44]).

Ahn et al. conducted a retrospective review of all IPs diagnosed between 1 March 2008 and 31 December 2011 at Ulsan University Hospital (South Korea). Six of the 16 IPs were managed by UTCE; these women were all haemodynamically stable at diagnosis. Five of these patients were treated successfully; one required further management. No patients had serious complications; the average drop in haemoglobin was 1.7 g/dL (0.3–2.2 g/dL). Three women went on to have successful pregnancies. The small number of patients and low power of this study means that statistically significant results cannot be easily inferred. The authors state that a potential benefit is that UTCE does not breach (and therefore weaken) the myometrium, as no incision into the myometrium is needed; however, we believe that management of IPs by this procedure would be difficult to achieve without damage to the myometrium.

Transcervical suction under laparoscopic and hysteroscopic guidance

An alternative to UTCE is transcervical suction under laparoscopic and hysteroscopic guidance. Cai et al. described how seven IPs of > 2 mm size were removed using a flexible 8F paediatric suction catheter introduced transvaginally [45]. However, two of their seven suffered from a uterine perforation and increased blood loss (> 500 ml). These complications necessitated subsequent surgical management.

Conclusion

The diagnosis and management of interstitial pregnancies remains challenging, in part due to the rarity of these cases and the paucity of evidence to guide management. The high sensitivity of US, when sufficient expertise is available, makes it the best first line investigation that one may use to diagnose IPs.

IPs should be managed in early pregnancy units that have experience in managing such cases. Conservative management (encompassing expectant and medical management) should only be offered to patients with a radiologically diagnosed IP, who are haemodynamically stable and have no obvious risks of immediate rupture, such as large gestational sac or rapidly increasing β-hCG levels. Expectant management is an appropriate first line approach for women with an IP and declining serum β-hCG levels (irrespective of ectopic mass size and initial serum β-hCG levels) [17, 18]. Expectant management should, however, be abandoned if there is any evidence of clinical deterioration. MTX has been advocated widely in the literature; however, much of the safety data is from retrospective cohort studies which may be susceptible to selection bias. The success rates for MTX management vary from 79.9% for systemic MTX to 97.83% for local MTX injection; however, the numbers in these studies were small. It needs to be remembered that failure of medical management resulting in rupture may have catastrophic consequences. For this reason, surgical management with a likely higher success rate (99.16%) is becoming more popular in centres with sufficient experience. Laparoscopic cornuostomy is preferable to wedge resection due to the decreased intra-operative blood loss, reduced distortion of uterine anatomy and possible reduction in the risk of uterine rupture in subsequent pregnancies.

Further studies using prospective data from multiple centres are required to assess the impact of the various management options on the short term complications and long term outcomes such as fertility and pregnancy/labour complications.

Notes

Funding

Not funded

Disclosure statement

The authors declare that they have no conflicts of interest and nothing to disclose.

Authors’ contributions

MB contributed to the study conception, performed the searches, reviewed titles and abstracts, reviewed full text articles, extracted data, performed data analysis and drafted the manuscripts. AB-S contributed to the study conception, review of full-text articles and data analysis as well as reviewed the manuscript for important intellectual content. TKH contributed to the study conception, providing clinical expertise on interstitial pregnancies, and reviewed the manuscript for important intellectual content. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not required

Consent for publication

Not required

Competing interests

The authors declare that they have no competing interests.

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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Department of Women’s HealthGuy’s and St Thomas’ NHS Trust, St Thomas’ HospitalLondonUK

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