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Erschienen in: Gynecological Surgery 1/2018

Open Access 01.12.2018 | Review Article

Elective uterine artery embolization prior to laparoscopic resection of interstitial pregnancy: two cases and literature review

verfasst von: Iris Verbeeck, Francesca Donders, Pieter-Jan Buyck, Dirk Timmerman, Andries Van Holsbeeck, Sandra A Cornelissen, Anne-Sophie Van Rompuy, Lien Van den Haute, Sylvie Gordts, Carla Tomassetti, Jan Deprest

Erschienen in: Gynecological Surgery | Ausgabe 1/2018

Abstract

Background

Interstitial pregnancies (IP) can be treated medically or surgically. The most common complication remains hemorrhage. The risk of that may be reduced by elective uterine artery embolization (UAE) prior to surgery, which we applied in two consecutive cases with high vascularization on ultrasound. We also reviewed larger series (n ≥ 10) on medical as well as surgical management of IP on success and complication rates and reviewed the entire literature on UAE.

Results

A gravida 5 (two ectopic pregnancies treated by salpingectomy) para 1 (cesarean section complicated by a niche, earlier repaired) presented with an asymptomatic IP. Primary treatment consisted of systemic methotrexate (MTX). Because of raising β-hCG and persisting heart activity 1 week later, she was referred for surgery (β-hCG = 59,000 IU/L; CRL = 10.5 mm). Another gravida 5 para 3 presented with an asymptomatic evolutive IP on dating ultrasound. Because of the size (CRL = 24.5 mm), thin overlaying myometrium, and high β-hCG (121,758 IU/L), we opted for primary surgery. Both IPs were highly vascularized with high flow rates. To prevent bleeding, a bilateral UAE was performed. The surgery was nearly bloodless.
In the literature, a wide range of treatment regimens for IP is reported. Larger series report a success rate of 76% for primary systemic MTX, 88% for primary local medical treatment, and 94% for primary surgery. It was not possible to determine reliable hemorrhage or rupture rates following MTX administration. As to laparoscopic surgery, the blood transfusion rate for bleeding was 9% while the conversion rate for hemorrhage was 2%. The use of UAE to reduce the risk for hemorrhage before (n = 2) or after (n = 19) MTX administration was reported in 21 cases. This failed in two cases (90% success rate), and one patient required transfusion (5%). Two cases treated with UAE and primary surgery were reported, yet the exact indication for embolization was not elaborated. Alternative hemostatic techniques during surgical management have been proposed to reduce blood loss and operating time, yet individual outcomes were not identifiable.

Conclusion

We report on the use of elective UAE prior to laparoscopic resection of IP, because of signs of strong vascularization on ultrasound. This strategy coincided with a nearly bloodless operation. Literature review suggests that this is one of the effective methods to reduce blood loss intra-operatively.
Abkürzungen
EP
Ectopic pregnancy
IP
Interstitial pregnancy
IVF
In vitro fertilization
KCL
Potassium chloride
MTX
Methotrexate
UAE
Uterine artery embolization

Background

Ectopic pregnancy (EP) is any type of pregnancy in which the fertilized ovum implants outside the uterine cavity. The vast majority of EPs are situated in the fallopian tube, typically in the ampullary region (70%), less likely in the isthmic (12%), fimbrial (11%), or interstitial part (2–4%). Other uncommon locations include ovarian (1–3%), abdominal (< 1%), cervical (< 1%), rudimentary horn (< 0.5%), and cesarean scar pregnancies (1–3%) [14].
In 1989, EPs occurred at an estimated prevalence of 1–2% worldwide. This is two to three times higher than in 1970 [5]. The increase is presumably related to an increased prevalence of risk factors directly or indirectly leading to decreased tubal passage. The prevalence has since not significantly changed [6, 7].
Pregnancies that are situated in the interstitial portion of the fallopian tube are referred to as interstitial [8, 9]. The intramural or interstitial part of the tube is approximately 0.7 mm wide and 1–2 cm long, often with a tortuous course [8]. Interstitial pregnancies (IPs) are also referred to as “cornual,” though some reserve this entity to pregnancies located within a rudimentary horn of an abnormal uterine cavity [8, 9]. While the generic risk factors displayed in Table 1 may also apply, specific risk factors to this type of EP are previous ipsilateral or bilateral salpingectomy, previous EP, in vitro fertilization, and tubal damage from previous EP [8]. Historically, the mortality rate of this condition was around 2.5%, which is approximately seven times higher than that of EPs in general. It is assumed that this can be explained by the greater expansion capacity at this location, the richer vascularization of the area, eventually leading to life-threatening hemorrhage when rupture occurs [8].
Table 1
Risk factors of ectopic pregnancy [1923]
Highly increased risk (OR = 4–40)
Moderately increased risk (OR = 2–20)
 Previous tubal surgery
 Infertility
 Documented tubal pathology
 Previous genital infections
 History of EP
 Multiple sexual partners
 In-utero exposure to DES
 
 Use of IUD [22, 23]
 
Minimally increased risk (OR = 1-4)
Other risk factors
 Previous pelvic/abdominal surgery
 Age (> 35–40 years)
 Cigarette smoking
 Assisted reproductive technologies
 Vaginal douching
 Anatomical uterine abnormality
 Early age at first intercourse
 Non-Caucasian
 Prior spontaneous or medically induced abortion
OR odds ratio, EP ectopic pregnancy, DES diethylstilbestrol, IUD intra-uterine device
There is to our knowledge no consensus on the best treatment modality of IP. Herein, we provide a literature review which we did on the occasion of treating two patients with uterine artery embolization (UAE) immediately prior surgical treatment, because of an anticipated high risk for bleeding.

Two cases

A 28-year-old gravida 5 para 1 was referred for a second opinion on an evolutive IP. She had a history of a primary cesarean section for vasa previa, a spontaneous first trimester miscarriage, two EPs treated by salpingectomy, and a hysteroscopic cesarean scar niche repair. The latter niche repair was done because of ultrasound signs of fluid in the niche before starting in vitro fertilization (IVF) treatment. On hysteroscopy, blood and debris were confirmed and a repair was performed 4 months prior to the index event (IP). Control hysteroscopy 1 month after the procedure showed normal findings. The index pregnancy was by IVF. On early scan at 6 + 6 weeks, an IP was suspected. We confirmed this at 7 + 1 weeks to be a left IP with a gestational sac of 19 × 20 mm, CRL of 6.8 mm, β-hCG of 38,000 IU/L, and heart activity. There was no abdominal fluid. The referring center opted for a single-dose methotrexate (MTX) protocol (75 mg; 50 mg/m2). She presented on day one post-injection with stinging and cramping abdominal pain, yet without hemodynamic impact or peritoneal signs. On day six post-injection, she was referred because of raising β-hCG and persisting heart activity, spotting, along with intermittent abdominal pain. Figure 1 displays the ultrasound, β-hCG, and hemoglobin findings over the reporting period. We decided to proceed with surgical intervention yet opted for prior bilateral UAE during the same general anesthesia to reduce the risk for hemorrhage based on the apparent high vascularization around the pregnancy. Access was gained through the right femoral artery with catheterization of the left internal iliac artery followed by selective catheterization of the left uterine artery. Polyvinyl particles (Contour 250-350, Boston Scientific, Diegem, Belgium) were injected under 3D angiography control. The same procedure was followed on the contralateral side. Then, a laparoscopic cornual resection was performed and the uterine defect was closed in two layers using Vicryl 2-0 (Fig. 2). Blood loss was negligible, yet operating time was 140 min. Histopathology confirmed an IP. She was discharged on day two, and β-hCG became unmeasurable 4 weeks later. She had a withdrawal bleeding 3 weeks after the operation and had another period 5 weeks later. A waiting period of at least 6 months [10, 11] was advised to allow maximal healing of the uterus. She conceived 8 months after the IP in the first IVF cycle. She presented again with right fossa pain at 5 + 3 weeks, yet ultrasound confirmed an intracavitary position without any signs of IP.
A 32-year-old gravida 5 para 3 spontaneously conceived. She was referred because on elective dating ultrasound at 9 + 2 weeks a right evolutive IP was found. She had a history of a spontaneous first trimester miscarriage and three uncomplicated term vaginal deliveries. On ultrasound, the surrounding myometrium was 2.2 mm which was strongly vascularized (Fig. 3). Because of the size (CRL = 24.5 mm), the thin myometrial layer, and a β-hCG of 121,758 IU/L, we advocated immediate surgery, yet because of the vascularization we first offered bilateral UAE. Polyvinyl particles (Contour 355-500, Boston Scientific; Embosphere 500-700 and 700-900, Merit Medical, Brussels, Belgium) and spongostan plugs (Ethicon, Diegem, Belgium) were used (Fig. 4). On laparoscopy, a 6-cm pregnancy in the right uterine horn was observed. The pregnancy was removed by cornuostomy, and the myometrial defect was sutured in three layers (first V-loc 2-0, second and third Vicryl 2-0). Blood loss was negligible, and operating time was 180 min. Two months later she still had some brown vaginal discharge. Ultrasound showed normal findings with a strong proliferative endometrium along with a corpus luteum on the left ovary and a normal looking scar at the resection site. β-hCG was 3.2 IU/L.
Both patients explicitly consented to have their history being reported in the literature.

Methods

For the literature review, we searched the PubMed on this matter, published until February 2018, using the following key terms “Pregnancy, Interstitial”[Mesh], “Therapeutics”[Mesh], “Interstitial Pregnancy,” and “Pregnancy Treatment” (953 papers). Sources of relevant articles in the references were screened as well (> 100 papers). All English-, French-, Dutch- and German-language articles were retrieved and screened on title and abstract for relevance (Appendix 1, 2, 3, 4, 5, and 6). Articles in which the location of the EP was unclear or in which the outcome was not clearly specified or objectively measured were excluded. We empirically decided to further discuss outcomes of series with 10 patients or more as to have reasonable denominators for calculating overall outcomes. The only exception to that was Table 4, which displays the entire published experience with UAE. There was not a single series with ≥ 10 patients treated with UAE.

Results

There is considerable experience with primary systemic medical therapy in asymptomatic hemodynamically stable patients with IP. Table 2 summarizes studies describing ten or more patients with IP treated by primary systemic MTX. Dosing and regimen of MTX are inconsistent, and success rates are typically over 70%, except in one series [12]. In case of failure (persisting β-hCG leading to additional treatment), surgery was offered, except in one series by Hiersch et al., where second-line local MTX was combined with UAE. Out of five patients, two still required surgery as a third step. Tanaka et al. described 33 cases treated with a very consistent scheme of slowly intravenously injected, yet a fixed dose MTX. The success rate was 94%; two patients required surgery. The opposite was true in the experience of Kim et al. (n = 30) administering intramuscular MTX, yet with an inconsistent dosing regimen. Sixteen (53%) required additional surgery.
Table 2
Primary systemic MTX treatment of interstitial pregnancy
Author
N
Initial β-hCG
Systemic MTX treatment
Hospital stay
Negative β-hCG
Success
Jermy et al. [24]
17
32–31,381
50 mg/m2 IM
0–40
3–13
16/17
Hiersch et al. [25]
14
15,764
1 mg/kg/d IM on day 1, 3, 5, 7
N/A
N/A
9/14
 
3
< 2500
50 mg/m2 IM
1
N/A
3/3
Tanaka et al. [26]
33
230–106,634
100 mg IV + 200 mg IV
1–4
3–19
31/33
Kim et al. [12]
5
375–102,970
1 mg/kg/d IM on day 1, 3, 5, 7
N/A
N/A
14/30
 
24
 
50 mg/m2 IM
N/A
N/A
 
 
1
 
100 mg IV in bolus followed by 200 mg IV
N/A
N/A
 
N number of cases, β-hCG mIU/ml, MTX methotrexate, IM intramuscular, IV intravenous, hospital stay days, negative β-hCG weeks
Local injection of MTX, potassium chloride (KCL), etoposide, and actinomycin D under laparoscopic, ultrasound, or hysteroscopic guidance have all been reported as effective (Table 3 and Appendix 2). These injections are usually given into the gestational sac, occasionally in the surrounding myometrium or locally intra-arterial. These are invasive procedures, compared to systemic MTX. Benifla et al. used MTX for IP locations and KCl for heterotopic presentations, out of concerns for teratogenicity. Of the three eutopic pregnancies associated to a heterotopic location, two were eventually lost. Further details on outcomes are missing. The calculated success rate was 88%. Treatment failures were not offered a second MTX injection, yet successfully managed by surgery.
Table 3
Primary local medical treatment of interstitial pregnancy
Author
N
Initial β-hCG
Local medical treatment
Hospital stay
Negative β-hCG
Complications
Success
Benifla et al. [27]
2
16,000–43,000
MTX 1 mg/kg + SMTX
3
6 (1/2)
Bleeding 1/2
1/2
 
6
360–10,000
MTX 1 mg/kg
3
1–3
6/6
 
3a
15,000–25,205
KCL 2 mEq in 2 ml volume
3
a
Miscarriage 2/3
3/3
Cassik et al. [28]
23
102–69,820
MTX 25 mg
N/A
3–14
21/23
Framarino et al. [29]
14
2800–3200
MTX 25 mg
N/A
Max. 8
14/14
N number of cases, β-hCG mIU/ml, (S)MTX (systemic) methotrexate, KCL potassium chloride, hospital stay days, negative β-hCG weeks
aHeterotopic pregnancy
Table 4 displays reports on patients managed with selective UAE combined with any administration regimen of MTX. The actual indication for secondary UAE was refusal of surgery (Ophir et al., Yang et al.; each n = 1) or not mentioned (Deruelle et al., Tamarit et al., Berretta et al., Hiersch et al.). Primary UAE combined with MTX was either part of a standard protocol (n = 9; Krissi et al.) or because of the suspicion of increased risk for hemorrhage (n = 1; Valsky et al.). The paper does however not mention how that increased risk was estimated. Table 4 also includes two cases managed by UAE followed immediately by planned surgery (either laparoscopic or hysteroscopic). The argument for UAE was made based on increased vascularization on 3D CT angiography. In one of those two cases, a subsequent spontaneous conception and cesarean delivery of a healthy baby at 37 weeks was reported. Overall success rate in all the series in this table is 91%.
Table 4
Primary and secondary treatment of interstitial pregnancy with elective UAE
Author
N
Initial
β-hCG
Initial treatment
β-hCG
pre- UAE
Treatment
Hospital stay
Negative β-hCG
Complications
Success
Valsky et al. [30]
1
11,695
MTX + UAE
N/A
5
1/1
Takeda et al. [31]
1
95,365
UAE + CR
8
6
1/1
Krissi et al. [32]
9
1667–46,923
UAE + S/LMTX
13
8
9/9
Takeda et al. [33]
1
44,917
UAE + TE + SMTX
N/A
13
1/1
Ophir et al. [34]
1
33,689
SMTX
51,098
UAE
7
8
1/1
Deruelle et al. [35]
1
17,785
SMTX
20,458
UAE
6
10
1/1
Yang et al. [17]
1
29,454
SMTX
35,654
UAE
6
4
1/1
Tamarit et al. [36]
2
4394–8970
SMTX
8689–10,164
UAE + LMTX
1
10
2/2
Berretta et al. [37]
1
49,997
SMTX
59,494
UAE
11
10
1/1
Hiersch et al. [25]
5
15,383
SMTX
N/A
UAE + LMTX
N/A
N/A
Transfusion 1/5
Rupture 2/5
3/5
N number of cases, β-hCG mIU/ml, S/LMTX systemic/local methotrexate, UAE uterine artery embolization, CR cornual resection (laparoscopic), TE transcervical evacuation (under laparoscopic guidance), hospital stay days, negative β-hCG weeks
Table 5 displays the experience with primary surgery, typically by minimally invasive access. Success rate was 94%; transfusion need was 9%. Primary laparotomy was performed for tubal rupture, in case of severe adhesions (Tulandi et al.) or because of surgeon’s preference (Hwang et al.). Conversions were because of significant hematoperitoneum or because of uncontrolled bleeding perioperatively (n = 7; 2%).
Table 5
Primary surgical treatment of interstitial pregnancy
Author
N
Initial β-hCG
Surgical treatment
Duration
Rupture
Hospital stay
Negative β-hCG
Complications
Success
Moon et al. [38]
3
1320–24,700
Laparoscopic CS°
52
No
N/A
N/A
3/3
 
18
28.5–305,100
Laparoscopic CS°°
U:28; R:82
3/18
N/A
N/A
17/18
 
3
4469–13,000
Laparoscopic CS°°°
35
No
N/A
N/A
3/3
Tulandi et al. [39]
13
11,471
Laparotomic CR
N/A
9/13
N/A
N/A
Transfusion 7/13
13/13
 
8
2087
Laparoscopic CR
N/A
5/11
N/A
N/A
Transfusion 2/11
7/8
 
3
2087
Laparoscopic CS
N/A
5/11
N/A
N/A
Transfusion 2/11
3/3
MacRae et al. [40]
3
3150–38,000
Laparoscopic CS
N/A
1/3
2
N/A
3/3
 
8
0–21,352
Laparoscopic CR
N/A
3/8
2
N/A
Conversion: 1/8
7/8
Ng et al. [41]
53
N/A
Laparoscopic CS if IP 1–2 cm° Laparoscopic CR if IP ≥ 3 cm°
67 (mean)
8/53
2
3
Conversion: 1/53
Transfusion: 8/53
44/53
Moon et al. [14]
20
177–39,508
Laparoscopic CS°
N/A
2/20
N/A
N/A
19/20
Hwang et al. [42]
54
12,741
Laparotomic CR
71
19/54
6
N/A
Transfusion 25/54
54/54
 
34
12,905
Laparoscopic CR
81
8/34
5
N/A
Transfusion 13/34
34/34
Cai et al. [43]
15
N/A
Laparoscopic CS°
30–80
N/A
2–5
2–5
15/15
 
7
3000–32,000
TE, LG and HG
45–90
No
N/A
2–5
Perforation: 2/7
5/7
Zuo et al. [44]
16
14,696
Laparoscopic CR
25–120
No
3–4
N/A
Rupture: 1/16
16/16
Ahn et al. [45]
6
17,797–69,303
TE, UG
N/A
N/A
2–8
N/A
5/6
 
9
20,319–50,271
Laparoscopic CR
N/A
N/A
4–7
N/A
Transfusion: 1/9
9/9
Douysset et al. [46]
13
369–45,780
Laparoscopic CR
N/A
9/18
5
N/A
Transfusion: 4/18
11/13
 
5
369–45,780
Laparoscopic CS
N/A
9/18
5
N/A
Transfusion: 4/18
4/5
Watanabe et al. [47]
12
998–55,820
Laparoscopic CS°
61–160
2/12
N/A
N/A
12/12
 
1
69
Laparoscopic CS°
N/A
Yes
N/A
N/A
1/1
Kim et al. [11]
13*
N/A
Laparoscopic CR
40–145
2/13
2–7
N/A
Rupture 1/11
Transfusion: 2/13
Miscarriage: 1/13
13/13
Nikodijevic et al. [48]
13
16,687
Laparoscopic CR
N/A
N/A
N/A
4–8
Conversion: 5/13
Transfusion: 4/13
13/13
Nirgianakis et al. [49]
10
27,634
Laparoscopic CR~
115
N/A
3
N/A
Transfusion: 3/10
10/10
Wang et al. [50]
38
25,150
Laparoscopic CS°
71
11/38
3
N/A
35/38
Lee et al. [51]
53
575–64,831
Laparoscopic CR
77
N/A
N/A
N/A
49/53
 
22
1454–62,422
Laparoscopic CS, °
59
N/A
N/A
N/A
21/22
N number of cases, β-hCG mIU/ml, CR cornual resection, CS cornuostomy, IP interstitial pregnancy, TE transcervical evacuation, HG under hysteroscopic guidance, LG under laparoscopic guidance, R ruptured, UR unruptured, duration minutes, hospital stay days, negative β-hCG weeks
Hemostatic technique: °vasopressin, °°endoloop, °°°encircling suture, *heterotopic pregnancy

Discussion

Today the diagnosis of EP is usually made by ultrasound. In high-risk patients or countries where access to early ultrasound is easy, the diagnosis can be made prior to the development of symptoms. This allows careful planning of management. We surgically managed two cases of IP, which both were initially asymptomatic. One had typical risk factors and the other one did not. One had prior MTX therapy, and the second one had a very high β-hCG level. Both the ultrasound examination raised the suspicion of a highly vascularized lesion. Therefore, we decided to perform primarily bilateral UAE and surgery in the same anesthesia. This is different than the cases managed in Table 4. Though it is impossible to prove that UAE reduces the risk for hemorrhage, it seems that our surgery in both cases was nearly bloodless. Treatment was apparently also effective given that β-hCG levels fell as expected.
When systematically searching the literature, a gap of knowledge is identified on the use of UAE or in a broader perspective, the management of IP. This is probably because of the rarity of the condition. The data around do neither allow a proper meta-analysis, so that we limited ourselves to summarize the findings in somewhat larger series for each management option. There is quite some experience with primary medical therapy in asymptomatic hemodynamically stable patients. In analogy to other ectopic locations [13], the variability of MTX administration protocols is wide, including systemic single shot (either promptly or slowly infused), repetitive doses, and local administration [13]. Medical therapy has also been combined with UAE, mostly successful, yet Hiersch et al. reports on two cases where second line local MTX treatment combined with UAE failed. In those, we would guess the patient would have had more benefit of surgery.
Our literature review learns that the most frequent complication of surgery is hemorrhage, either with or without transfusion. The overall transfusion rate in IP is not judgeable since no reference to that outcome was made in any of the medically treated cases. However, 9% of laparoscopically managed IPs required blood transfusion. Therefore, it seems logical to take measures to reduce that risk. Surgically, one can use prophylactic coagulation by electrosurgery or ligation of the feeding artery, yet this may compromise viability of the tissue. Alternatively, vasoconstrictors have been described to reduce blood loss and operating time, yet they may have their own side effects and have only been reported to be effective for IPs with an average β-hCG of 10,000–25,000 IU/L [8, 14, 15]. Conversely, these are very cheap agents.
Modern invasive radiologic techniques are becoming increasingly popular, and those services become more widely accessible even in a semi-acute setting. Embolization techniques have found their place in modern obstetrics and gynecology. The experience with uterine myomas is meanwhile very large, and subsequent conception seems to be possible and relatively safe [16]. Torre et al. described an insignificant change in fertility rate and ovarian reserve after UAE for uterine fibroids in women with no other infertility factors [16]. Krissi et al. reported on the subsequent fertility after MTX administration with UAE in the treatment IP. Out of five women who tried to conceive, four did so, and three delivered successfully. Disadvantages of UAE are the higher cost in comparison to vasopressin, the longer duration of anesthesia, the more complicated logistics, and the additional local morbidity (e.g. ischemic pain, Asherman syndrome) [17, 18].

Conclusions

We report on the use of elective UAE prior to laparoscopic resection of IP, which coincided with a nearly bloodless operation. A literature search shows a wide variety of treatment options, yet most cases seem to be following the typical approach to EP. The overall success rate of surgical treatment of IP is higher than that of medical treatment. When performing laparoscopy, good hemostatic techniques are recommended since the operation takes place in a strongly vascularized region [8, 14, 15]. Our experience with two cases of UAE is yet another approach. It seems safe and reliable and does not preclude future conception.

Availability of data and materials

Search results and supplementary tables are available on line. The dataset is available with the primary author.

Authors’ information

JD was a fundamental clinical researcher for the Fonds Wetenschappelijk Onderzoek Vlaanderen (2001–2016). He is now funded by the Great Ormond Street Hospital Charity Fund, London, UK.
Both patients explicitly consented to have their history being part of a case report. This study is approved by the Education-Support Committee of The University of Leuven (OBC MP001948). The Education-Support Committee (OBC) evaluates master’s thesis projects as mandated by the Research Ethics Committee of the KU/UZ Leuven.

Competing interests

The authors declare that they no competing interests.

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Anhänge

Appendix 1

Table 6
Primary systemic MTX treatment of interstitial pregnancy
Author
N
Initial β-hCG
Systemic MTX treatment
Hospital stay
Negative β-hCG
Complications
Success
Tanaka et al. [52]
1
64,000
30 mg IM day 0 + 15 mg/d IM 5 days, 3 cycles
N/A
3
Liver function ↓
1/1
Benifla et al. [27]
2
364–5340
15 mg/d IM for 5 days
3
3 (1/2)
1/2
 
2
430–450
1 mg/kg/d IM for 4 days
3
3–6
2/2
Hajenius et al. [53]
8
410–81,000
1 mg/kg/d IM on day 1, 3, 5, 7
N/A
7–21
8/8
Galimberti and Jones [54]
1
7072
50 mg/m2 IM
N/A
N/A
0/1
Bernardini et al. [55]
1
12,470
100 mg IM
N/A
14
1/1
Fisch et al. [56]
1
102,000
50 mg/m2 IM on day 1, 3, 5, 7
11
7
0/1
Sagiv et al. [57]
1
28,166
2 × 75 mg IM
4
N/A
0/1
Lalchandani et al. [58]
1
12,338
400 mg/w IV for 8 weeks
N/A
8
1/1
Verity et al. [59]
1
1060
2 × 75 mg IM
N/A
7
1/1
 
1
5560
2 × 50 mg/m2 IM, 48 h apart
N/A
8–9
1/1
 
1
3510
1 mg/kg IM, 2 doses
N/A
4
1/1
 
1
9070
1 mg/kg IM, 1 dose
6–7
1/1
Advincula and Senapati [60]
1
62,889
N/A
N/A
N/A
N/A
0/1
Jermy et al. [24]
17
32–31,381
50 mg/m2 IM°
0–40
3–13
16/17
Ophir et al. [34]
1
33,689
50 mg/m2 IM°
7
8
0/1
Reid and Buddha [61]
1
4680
50 mg/m2 IM
N/A
7
1/1
Rodriguez et al. [62]
7
1592–75,868
50 mg/m2 IM°
N/A
2–15
7/7
Tulandi et al. [39]
4
2627–6739
50 mg/m2 IM
N/A
7 (2/4)
2/4
Cassik et al. [28]
5
793–41,150
2 × 50 mg/m2 IM, 48 h apart
N/A
3–7
Obstipation 2/5
Neuropathy 1/5
Mild ↓ liver 1/5
4/5
Deruelle et al. [35]
1
17,785
2 × 1 mg/kg IM
6
10
0/1
Klemm et al. [63]
3
11,743–22,134
1 mg/kg/d IV on day 1, 3, 5, 7; 2 cycles
N/A
N/A
3/3
Araujo et al. [64]
1
4815
50 mg IM
N/A
N/A
0/1
Yang et al. [17]
1
29,454
1 mg/kg IM
6
4
0/1
Fujioka et al. [65]
1
11,430
50 mg/m2 IM
N/A
N/A
0/1
Api and Api [66]
1
11,706
1 mg/kg IM
1
1
0/1
Günenç et al. [67]
1
8314
2 × 1 mg/kg IM
N/A
N/A
0/1
Tamarit et al. [36]
2
4394–8970
2 × 50 mg IM
1
10
0/2
Kato et al. [68]
1
90,000
50 mg/m2 IM
N/A
N/A
0/1
Lee et al. [69]
1
3029
4 × 1 mg/kg IM
3
N/A
0/1
Gomez et al. [70]
2
3724–4116
70–75 mg + oral Mifepristone
2
5–7
2/2
Monia et al. [71]
3
3000–111,633
1–4× IM
N/A
2–6 (2/3)
2/3
Szylit et al. [72]
1
21,281
2 × 50 mg/m2 IM, 48 h apart
N/A
N/A
0/1
Ahn et al. [45]
1
4478
Multiple doses
4
N/A
1/1
Berretta et al. [37]
1
49,997
2 × 80 mg IM
11
N/A
0/1
Sagiv et al. [73]
4
4304–28,166
50 mg/m2 IM°
N/A
N/A
1/4
Surbone et al. [74]
3
2974–15,022
1 mg/kg IM
N/A
N/A
2/3
Fritz et al. [75]
1
8200
50 mg/m2 IM
N/A
N/A
0/1
Hiersch et al. [25]
14
15,764
1 mg/kg/d IM on day 1, 3, 5, 7
N/A
N/A
9/14
 
3
< 2500
50 mg/m2 IM
1
N/A
3/3
Horne et al. [76]
5
2458–9730
50 mg/m2 IM°
N/A
10
5/5
Meddeb et al. [77]
1
6320
Single dose
N/A
N/A
PTD
0/1
Corioni et al. [78]
1
8681
1 mg/kg IM
11
9
1/1
Kim et al. [79]
1
35,890
Every 2 days for 4 weeks
N/A
17
Pseudocyst
1/1
Singh et al. [80]
1
89,000
1 mg/kg IM, 3 doses
21
12
1/1
Tanaka et al. [26]
33
230–106,634
100 mg IV in bolus followed by 200 mg IV
1–4
3–19
31/33
Nikodijevic et al. [48]
2
19,563
N/A
N/A
4
3/3
Kahramanoglu et al. [81]
1
1263
50 mg/m2 IM
7
6
1/1
Kim et al. [12]
5
375–102,970
1 mg/kg/d IM on day 1, 3, 5, 7
N/A
N/A
N/A
14/30
 
24
 
50 mg/m2 IM
N/A
N/A
N/A
 
 
1
 
100 mg IV in bolus followed by 200 mg IV
N/A
N/A
N/A
 
N number of cases, β-hCG mIU/ml, MTX methotrexate, IM intramuscular, IV intravenous, hospital stay days, negative β-hCG weeks, PTD persistent trophoblastic disease
°With a second injection, if β-hCG decrease is less than 15% from days 4 to 7

Appendix 2

Table 7
Primary local medical treatment of interstitial pregnancy
Author
N
Initial β-hCG
Local medical treatment
Hospital stay
Negative β-hCG
Complications
Success
Timor-Tritsch et al. [82]
1*
14,100
KCL 0.5 ml of 2 mEq/ml cornual
N/A
6 (*)
Miscarriage
1/1
1
1400
MTX 25 mg cornual
4
5
1/1
Benifla et al. [27]
2
16,000–43,000
MTX 1 mg/kg intrasaccular, UG1
3 (1/2)
6 (1/2)
Bleeding 1/2
1/2
 
6
360–10,000
MTX 1 mg/kg intrasaccular, UG/LG
3
1–3
6/6
 
3*
15,000–25,205
KCL 2 mEq in 2 ml volume intrasaccular
3
*
Miscarriage 2/3
3/3
Baker et al. [83]
1*
18,423
MTX 12.5 mg with 1 ml of 20% KCL
0
*
1/1
Wilkinson et al. [84]
1
10,500
MTX 40 mg
N/A
N/A
1/1
Lin et al. [85]
1
3256
MTX 50 mg with diluted vasopressin
2
2
1/1
Oyawoye et al. [86]
1*
78,685
MTX
N/A
*
1/1
Verity et al. [59]
1
5780
MTX 50 mg, LG2
N/A
9
1/1
 
1
5578
MTX 50 mg, LG
N/A
4
1/1
Tulandi et al. [39]
2
2627–6739
MTX, LG
N/A
7 (1/2)
1/2
2
 
MTX
N/A
7
2/2
Cassik et al. [28]
23
102–69,820
MTX 25 mg, UG3
N/A
3–14
21/23
Chou et al. [87]
1
6413
KCL 2.5 mEq, UG
N/A
12
1/1
Narang and Kalu [88]
2
3700–40,000
MTX 50 mg/m2
N/A
N/A
2/2
Andrés et al. [89]
3
6193–21,999
MTX 50 mg intrasaccular, UG4
1
4–10
Leukopenia 1/3
2/3
Monia et al. [71]
2
7909–64,000
MTX 20–40 mg5
N/A
2
2/2
 
1
8400
MTX 60 mg
N/A
4
1/1
Surbone et al. [74]
6
2974–15,022
MTX 1 mg/kg
N/A
N/A
5/6
Swank et al. [90]
1
90,504
MTX 50 mg5
7
7
1/1
Douysset et al. [46]
2
369–45,780
N/A
N/A
N/A
2/2
Framarino et al. [29]
14
2800–3200
MTX 25 mg
N/A
Max. 8
14/14
Yu et al. [91]
4*
N/A
MTX 1 mg/kg
N/A
N/A
4/4
Maçães et al. [92]
1
2776
MTX 25 mg with 2 mEq KCL
N/A
8
1/1
Leggieri et al. [93]
1
5055
MTX 25 mg
4
3
1/1
Nikodijevic et al. [48]
3
19,563
MTX5
N/A
4
2/2
 
1
 
MTX
N/A
N/A
N/A
0/1
Kim et al. [12]
2
2292–59,090
MTX 1 mg/kg
N/A
N/A
N/A
7/8
 
6
 
MTX 1 mg/kg5
N/A
N/A
N/A
 
N number of cases, β-hCG mIU/ml, KCL potassium chloride, MTX methotrexate, UG under ultrasound guidance, LG under laparoscopic guidance, hospital stay days, negative β-hCG weeks
*Heterotopic pregnancy: 1: MTX 1 mg/kg/d IM 3 days after, 2: MTX 50 mg IM on days 2 and 4, 3: in viable pregnancies + KCL intracardially (5/23), 4 MTX 50 mg/m2IM (2/3 patients), 5: systemic MTX

Appendix 3

Table 8
Secondary/tertiary systemic/local medical treatment of interstitial treatment
Author
N
Initial
β-hCG
Initial treatment
Medical treatment
Hospital stay
Negative β-hCG
Complications
Success
Fisch et al. [56]
1
102,000
SMTX
MTX 50 mg intrasaccular
11
7
1/1
Moon et al. [38]
1
47,200
Laparoscopic CS
MTX
N/A
N/A
N/A
1/1
Tulandi et al. [39]
1
2086
Laparoscopic CR
MTX
N/A
N/A
N/A
1/1
Takeda et al. [94]
1
16,100
Laparoscopic CS
MTX
30
N/A
N/A
1/1
Araujo et al. [64]
1
4815
SMTX
LMTX (50 mg), UG
N/A
N/A
1/1
Fujioka et al. [65]
1
11,430
SMTX
Dactinomycin 12 μg/kg IV
N/A
N/A
1/1
MacRae et al. [40]
1
7237
Laparoscopic CR
SMTX
N/A
N/A
N/A
1/1
Ng et al. [41]
9
N/A
Laparoscopy
SMTX
N/A
N/A
N/A
9/9
Sahoo et al. [95]
1
12,000
Laparoscopy
SMTX
N/A
N/A
1/1
Moon et al. [14]
1
9836
Laparoscopic CS
SMTX
N/A
N/A
N/A
1/1
Kato et al. [68]
1
90,000
SMTX
LMTX (25 mg)
N/A
6
1/1
Surbone et al. [74]
1
N/A
LMTX
SMTX
N/A
N/A
N/A
0/1
Douysset et al. [46]
2
N/A
Laparoscopic CR
MTX
N/A
N/A
N/A
2/2
 
1
N/A
Laparoscopic CS
MTX
N/A
N/A
N/A
1/1
Poon et al. [96]
2
3658–89,968
Expectant
LMTX
N/A
N/A
N/A
2/2
Wang et al. [50]
1
N/A
Laparoscopic CS
MTX 20 mg IM for 5 days
N/A
4
1/1
Lee et al. [51]
5
N/A
Laparoscopy
MTX multiple dose regimen
N/A
N/A
5/5
N number of cases, β-hCG mIU/ml, (S/L)MTX (systemic/local) methotrexate, CR cornual resection, CS cornuostomy, IM intramuscular, IV intravenous, UG under ultrasound guidance, hospital stay days, negative β-hCG weeks

Appendix 4

Table 9
Primary surgical treatment of interstitial pregnancy
Author
N
Initial β-hCG
Surgical treatment
Operating time
Rupture
Hospital stay
Negative β-hCG
Complications
Success
Steadman [97]
1
N/A
Resection of GT
N/A
Yes
7
N/A
Transfusion
1/1
Bickerstaff [98]
1
N/A
CR
N/A
N/A
N/A
N/A
1/1
Farabow et al. [99]
1
N/A
Laparotomic CR
N/A
Yes
N/A
N/A
Transfusion
1/1
Iuchtman and Grunstein [100]
2
N/A
Laparotomic resection of GT
N/A
Yes
8
N/A
N/A
2/2
Hill et al. [101]
1
N/A
Laparoscopic resection of GT°
N/A
No
2
4–5
1/1
Reich et al. [102]
1
16,300
Laparoscopic CR
N/A
Yes
2
3
Transfusion
1/1
de Boer et al. [103]
1
N/A
Laparotomic CS
N/A
No
N/A
N/A
1/1
Pelosi [104]
1
N/A
Laparoscopic CR
45
N/A
1
N/A
1/1
Laury [105]
1
2450
Laparoscopic CS
N/A
No
0
N/A
1/1
Sherer et al. [106]
1*
N/A
Laparoscopic CR
N/A
Yes
3
*
Transfusion
1/1
Tulandi et al. [107]
4
4700–14,500
Laparoscopic CR°
N/A
No
N/A
N/A
5/5
 
1
8000
Laparoscopic SS°
N/A
No
N/A
N/A
1/1
Woodland et al. [108]
1
11,061
Laparoscopic CR°
N/A
No
1
N/A
1/1
Katz and Lurie [109]
1
6300
Laparoscopic CS°
N/A
No
N/A
N/A
1/1
Grobman and Milad [110]
1
32,827
Laparoscopic CS°
N/A
No
N/A
6
1/1
Kasum et al. [111]
1*
5450
Laparoscopic resection of GT
N/A
Yes
N/A
*
1/1
Crvenkoviæ et al. [112]
1
8800
Laparoscopic CR°
60
No
4
2
1/1
Rahimi [113]
1
3672
Laparoscopic CS°
N/A
No
1
2
1/1
Moon et al. [38]
3
28.5–305,100
Laparoscopic CS°
52
No
N/A
N/A
3/3
 
18
 
Laparoscopic CS°°
U:28; R:82
3/18
N/A
N/A
17/18
 
3
 
Laparoscopic CS°°°
35
No
N/A
N/A
3/3
Vicino et al. [114]
1
21,800
Laparoscopic CR
N/A
No
N/A
2
1/1
Ayoubi et al. [115]
1*
N/A
Laparotomic resection of GT
N/A
Yes
N/A
*
1/1
Dumesic et al. [116]
1*
N/A
Laparotomic CR
N/A
Yes
N/A
N/A
Transfusion
Miscarriage
1/1
Kun and Tung [117]
1
N/A
Laparotomic resection of GT
N/A
Yes
6
N/A
1/1
Osuga et al. [118]
3
14,352–19,457
Laparoscopic CR
N/A
N/A
N/A
N/A
3/3
Sagiv et al. [57]
1
N/A
Laparoscopic CS
N/A
Yes
1
N/A
Transfusion
1/1
DeWitt and Abbott [119]
1
N/A
CR
N/A
Yes
3
N/A
Transfusion
1/1
Sills et al. [120]
1*
N/A
Laparoscopic CS
< 60
No
3
*
 
1/1
Chang et al. [121]
1*
63,300
Laparotomic resection of GT
N/A
N/A
N/A
*
1/1
Habek et al. [122]
2
N/A
Laparotomic hysterectomy
N/A
Yes
8
N/A
Transfusion 1/2
2/2
Izquierdo et al. [123]
1
2500
CR
N/A
N/A
3
N/A
1/1
Katz et al. [124]
2
3467–9800
TE, LG and HG
N/A
No
N/A
N/A
2/2
Yoo et al. [125]
4
39,245
Laparoscopic CS°
54
No
2
4
4/4
Gezer and Mutlu [126]
1
N/A
Laparoscopic CS
N/A
No
1
N/A
1/1
Grimbizis et al. [127]
1
821
Laparoscopic CR
N/A
Yes
1
3
1/1
Lee et al. [128]
1
45,000
Laparotomic CS
N/A
No
7
N/A
1/1
Savvidou et al. [129]
1
27,724
Laparoscopic resection of GT
N/A
Yes
4
3
Transfusion
Conversion
1/1
Thakur et al. [130]
2
3356–17,735
TE, LG and UG
N/A
No
2
N/A
2/2
 
2
 
TE, LG and UG
N/A
No
N/A
N/A
2/2
Tulandi et al. [39]
13
11,471
Laparotomic CR
N/A
9/13
N/A
N/A
Transfusion 7/13
13/13
 
8
2087
Laparoscopic CR
N/A
5/11
N/A
N/A
Transfusion 2/11
7/8
 
3
 
Laparoscopic CS
N/A
5/11
N/A
N/A
Transfusion 2/11
3/3
Zhang et al. [131]
3
8593–16,820
TE, LG
< 18
No
3 (max)
4
3/3
Huang et al. [132]
4
39,933–74,551
Laparoscopic CS
N/A
No
N/A
4
4/4
Kumakiri et al. [133]
1
9460
Laparoscopic CR°
84
No
2
4
1/1
Ross et al. [134]
2
23,480–45,780
TE, UG1
N/A
No
2
4–8
2/2
Takeda et al. [94]
2
4250–15,500
Laparoscopic CR
44–98
Yes
6–11
N/A
Transfusion 2/2
2/2
 
1
16,100
Laparoscopic CS
75
Yes
30
N/A
Transfusion
0/1
Ko et al. [135]
1
1356
Laparoscopic resection of GT
N/A
No
1
1
1/1
Lee et al. [136]
1
N/A
Laparotomic CS
N/A
No
3
N/A
1/1
Oliver et al. [137]
5
14,874
TE, LG and UG
N/A
No
N/A
N/A
5/5
Lialios et al. [138]
1*
N/A
Laparoscopic CR
N/A
Yes
2
*
1/1
Qin et al. [139]
1*
N/A
Laparoscopic CR°°
N/A
No
N/A
*
1/1
Sherer et al. [140]
1
N/A
Laparotomic resection of GT
N/A
Yes
3
N/A
1/1
Casadio et al. [141]
1
9383
Laparoscopic CR
40
No
2
5
1/1
Cheng et al. [142]
1
59,959
Laparoscopic CS
N/A
No
6
5
1/1
Choi et al. [143]
8
3400–74,060
Laparoscopic CS°
35–80
No
N/A
2–5
8/8
Duong et al. [144]
1
N/A
Laparotomic resection of GT
N/A
Yes
7
N/A
Transfusion
1/1
MacRae et al. [40]
3
3150–38,000
Laparoscopic CS
N/A
1/3
2
N/A
3/3
 
8
0–21,352
Laparoscopic CR
N/A
3/8
2
N/A
Conversion 1/8
7/8
Ng et al. [41]
53
N/A
Laparoscopic CS if IP 1–2 cm°; Laparoscopic CR if IP 3 cm or more°
67 (mean)
8/53
2
3
Conversion 1/53
Transfusion 8/53
44/53
Pluchino et al. [145]
1
N/A
Laparoscopic CS
N/A
Yes
2
N/A
1/1
Moon et al. [14]
20
177–39,508
Laparoscopic CS°
N/A
2/20
N/A
N/A
19/20
Pan et al. [146]
1
79,194
Bilateral CR (bilateral IP)
N/A
No
10
N/A
1/1
Pistofidis et al. [147]
1
18,900
Laparoscopic resection of GT
N/A
Yes
2
N/A
1/1
Tinelli et al. [148]
3
7600–12,500
Laparoscopic CS
45 (mean)
1/3
1
2
3/3
Vignali et al. [149]
3
431–3252
Laparoscopic CR
36–60
No
1
N/A
3/3
Walid et al. [150]
1
N/A
Laparoscopic resection of GT°
N/A
N/A
N/A
N/A
1/1
Yan [151]
1
3600
Laparoscopic resection of GT°
60
No
N/A
N/A
1/1
Aust et al. [152]
1*
N/A
Laparoscopic CR
N/A
No
0
*
Miscarriage
1/1
Cerviño et al. [153]
1
20,940
TE, UG2
N/A
No
N/A
5
1/1
Chachan et al. [154]
1*
N/A
Laparoscopic CS
N/A
No
1
*
1/1
Hwang et al. [42]
54
12,741
Laparotomic CR
71
19/54
6
N/A
Transfusion 25/54
54/54
 
34
12,905
Laparoscopic CR
81
8/34
5
N/A
Transfusion 13/34
Bowel injury 1/34
34/34
Lazard et al. [155]
2
4900–14,720
Laparoscopic CR
25–35
No
2–3
2–3
2/2
Lodhi et al. [156]
1
6041
Laparoscopic CR
N/A
No
2
N/A
1/1
 
1
N/A
Laparoscopic CR
N/A
Yes
2
N/A
Transfusion
1/1
Yamamoto et al. [157]
1
N/A
Laparoscopic CR°
N/A
No
1
N/A
1/1
Ahsan Akhtar et al. [158]
1
16,740
Laparoscopic CR
25
No
1
3
1/1
Cai et al. [43]
15
N/A
Laparoscopic CS°
30–80
N/A
2–5
2–5
15/15
 
7
3000–32,000
TE, LG, and HG
45–90
No
N/A
2–5
Perforation 2/7
5/7
Cucinella et al. [159]
5
1286–20,680
Laparoscopic CR°°°°
31–46
No
N/A
3–4
5/5
Garavaglia et al. [160]
1
2173
Laparoscopic CS
N/A
N/A
N/A
N/A
1/1
Muglu et al. [161]
1
N/A
Laparoscopic resection of GT
N/A
N/A
N/A
N/A
1/1
Rheinboldt et al. [162]
1
7787
Laparoscopic CR
N/A
N/A
N/A
N/A
1/1
Zuo et al. [44]
16
14,696
Laparoscopic CR
25–120
No
3–4
N/A
Rupture 1/16
16/16
Ahn et al. [45]
6
17,797–69,303
TE, UG
N/A
No
2–8
N/A
5/6
 
9
20,319–50,271
Laparoscopic CR
N/A
N/A
4–7
N/A
Transfusion 1/9
9/9
MacKenna et al. [163]
1
5820
Laparoscopic CR°
N/A
No
1
2
1/1
Mooij and Van Dillen [164]
1
N/A
Laparotomic resection of GT
N/A
N/A
N/A
N/A
N/A
1/1
Sagiv et al. [73]
3
3282–13,260
Laparoscopic CR
N/A
N/A
N/A
N/A
3/3
 
2
21,930–88,270
Laparoscopic CS
N/A
N/A
N/A
N/A
2/2
Surbone et al. [74]
2
2974–15,022
Laparoscopic CR
N/A
N/A
N/A
N/A
Conversion 1/2
2/2
Warda et al. [165]
1
N/A
Laparoscopic CS°
N/A
No
N/A
N/A
1/1
Wright et al. [166]
3
1455–27,052
TE, UG1
N/A
No
N/A
6–12
3/3
Zhang and Yuan [167]
2
2808–14,030
Laparoscopic CR°
45–95
No
6–7
< 1
2/2
Chandran [168]
1
N/A
Laparotomic CR
N/A
No
5
N/A
1/1
Douysset et al. [46]
13
369–45,780
Laparoscopic CR
N/A
9/18
5
N/A
Transfusion 4/18
11/13
 
5
 
Laparoscopic CS
N/A
9/18
5
N/A
Transfusion 4/18
4/5
Garretto et al. [169]
1
26,476
Laparoscopic CR
N/A
No
1
N/A
1/1
Manea et al. [11]
2
2238–8915
Laparoscopic resection of GT
N/A
Yes
N/A
N/A
2/2
 
1
6892
Laparoscopic CR~
N/A
Yes
N/A
N/A
1/1
Nezhat et al. [170]
1
N/A
TE°, UG + LG
N/A
No
1
5
1/1
Wang et al. [171]
8
636–13,310
Laparoscopic CS°
40–100
No
2
N/A
8/8
 
1
N/A
Laparoscopic CS°
N/A
No
2
N/A
1/1
Warda et al. [172]
4
N/A
Laparoscopic CS°
N/A
No
N/A
N/A
4/4
Watanabe et al. [47]
12
998–55,820
Laparoscopic CS, °
61–160
2/12
N/A
N/A
12/12
 
1
69
Laparoscopic CS°
N/A
Yes
N/A
N/A
1/1
Yu et al. [91]
4*
N/A
Laparotomic resection of GT
N/A
N/A
N/A
*
Miscarriage 1/4
4/4
Ansari et al. [173]
1
65,000
Laparoscopic CS°
78
No
0
12
1/1
Afifi et al. [174]
2
3890–17,445
Laparoscopic CS°, °°°°°
55–65
1/2
1
1–2
2/2
Faioli et al. [10]
3
10,119–18,765
Laparoscopic CR
28
No
N/A
3
3/3
Grindler et al. [175]
1
39,745
TE, UG
N/A
No
0
N/A
1/1
Jeon et al. [176]
9*
N/A
Laparotomy
N/A
N/A
N/A
N/A
N/A
9/9
Kim et al. [177]
13*
N/A
Laparoscopic CR
40–145
2/13
2–7
N/A
Rupture 1/11
Transfusion 2/13
Miscarriage 1/13
13/13
Mallick et al. [178]
2
2304–14,480
Laparoscopic CS
N/A
1/2
0
N/A
2/2
 
2
N/A
Laparoscopic CS
N/A
No
1
N/A
2/2
Nikodijevic et al. [48]
13
16,687
Laparoscopic CR
N/A
N/A
N/A
4–8
Conversion 5/13
Transfusion 4/13
13/13
Nirgianakis et al. [49]
10
27,634
Laparoscopic CR~
115
N/A
3
N/A
Transfusion 3/10
10/10
Said [179]
4
N/A
Laparoscopic resection of GT~
40–60
N/A
2
N/A
4/4
 
1*
N/A
Laparoscopic resection of GT
N/A
Yes
N/A
*
1/1
Wang et al. [50]
38
25,150
Laparoscopic CS°
71
11/38
3
N/A
35/38
Xu et al. [180]
1
N/A
Resection of GT
N/A
Yes
N/A
N/A
Transfusion
1/1
Kahramanoglu et al. [81]
1
> 10,000
Laparotomic resection of GT
N/A
Yes
3
N/A
Transfusion
1/1
1
9277
TE, UG
N/A
No
0
4
1/1
1
N/A
TE, LG
N/A
No
1
1
1/1
Lee et al. [51]
53
575–64,831
Laparoscopic CR3
77
N/A
N/A
N/A
49/53
 
22
1454–62,422
Laparoscopic CS, °
59
N/A
N/A
N/A
21/22
N number of cases, β-hCG mIU/ml, CR cornual resection, CS cornuostomy, TE transcervical evacuation, SS salpingostomy, GT gestational tissue, R ruptured, U unruptured, UG under ultrasound guidance, LG under laparoscopic guidance, HG under hysteroscopic guidance, IP interstitial pregnancy, operating time minutes, hospital stay days, negative β-hCG weeks
*Heterotopic pregnancy, hemostatic technique: °vasopressin, °°endoloop, °°°encircling suture, °°°°“Purse-string” suture, °°°°°stitch at the uterine fundus and in the mesosalpinx, ~local injection of diluted adrenaline (1/4)—1: MTX 50 mg/m2 IM; 2: MTX 1 mg/kg IM; 3: +/− postoperative prophylactic MTX

Appendix 5

Table 10
Secondary/tertiary surgical treatment of interstitial pregnancy
Author
N
Initial β-hCG
Initial treatment
Surgical treatment
Operating time
Rupture
Hospital stay
Negative β-hCG
Complication
Success
Benifla et al. [27]
1
5340
SMTX
Laparotomic CR
N/A
N/A
N/A
N/A
N/A
1/1
 
1
43,000
LMTX
Laparotomic CR
N/A
Yes
N/A
N/A
N/A
1/1
Galimberti and Jones [54]
1
7072
SMTX
Laparotomy
N/A
N/A
N/A
N/A
1/1
Hamada et al. [181]
1
8000
Expectant
Laparotomic HE
N/A
No
N/A
N/A
1/1
Sungurtekin and Uyar [182]
1
31,737
SMTX
Laparotomy
N/A
No
N/A
N/A
1/1
Bremner et al. [183]
1
92
Expectant
Laparoscopic CS
N/A
No
0
N/A
Ileus
1/1
Sagiv et al. [57]
1
28,166
SMTX
Laparoscopic CS
N/A
Yes
4
N/A
1/1
Advincula et al. [60]
1
62,889
SMTX
Laparotomic CR
N/A
N/A
N/A
N/A
1/1
Coric et al. [184]
1
1770
Expectant + aspiration
Laparoscopic CR
60
No
5
N/A
1/1
Jermy et al. [24]
1
> 10,000
SMTX
Laparotomy
N/A
No
N/A
N/A
1/1
Tulandi et al. [39]
2
2627–6739
SMTX
Laparoscopy
N/A
No
N/A
N/A
N/A
2/2
 
1
 
LMTX
Laparotomy
N/A
No
N/A
N/A
N/A
1/1
Cassik et al. [28]
1
41,150
SMTX
Laparotomic CR
N/A
N/A
N/A
N/A
N/A
1/1
2
102–69,820
LMTX
N/A
N/A
N/A
N/A
N/A
N/A
2/2
Api and Api [66]
1
18,654
SMTX
Laparoscopic CS
N/A
No
1
1
1/1
Günenç et al. [67]
1
8314
SMTX
Laparoscopic CS
N/A
No
N/A
5
1/1
Lee et al. [69]
1
14,273
SMTX
Laparoscopic CR
90
No
3
N/A
1/1
Lodhi et al. [156]
1
19,714
MTX
Laparoscopic CR
N/A
No
2
N/A
1/1
Andrés et al. [89]
1
6193
LMTX
Laparoscopy
N/A
Yes
N/A
N/A
1/1
Monia et al. [71]
1
94,000
SMTX
Laparoscopic CR
N/A
N/A
N/A
N/A
1/1
Szylit et al. [72]
1
21,281
SMTX
Laparoscopic CR
N/A
N/A
2
N/A
1/1
Sagiv et al. [73]
2
4304–4987
SMTX
Laparoscopic CR
N/A
N/A
N/A
N/A
2/2
 
1
28,166
SMTX
Laparoscopic CS
N/A
N/A
N/A
N/A
1/1
Surbone et al. [74]
1
N/A
SMTX
Laparoscopic CS
N/A
N/A
N/A
N/A
N/A
1/1
 
1
N/A
L/SMTX
Laparoscopic CS
N/A
N/A
N/A
N/A
N/A
1/1
Fritz et al. [75]
1
8200
SMTX
TE, LG
N/A
No
0
3
1/1
Hiersch et al. [25]
2
15,383
SLMTX + UAE
N/A
N/A
Yes
N/A
N/A
2/2
Meddeb et al. [77]
1
6320
SMTX
Laparoscopic CR
N/A
No
N/A
N/A
PTD
1/1
Tanaka et al. [26]
2
8500–63,000
SMTX
N/A
N/A
Yes
N/A
N/A
2/2
Nikodijevic et al. [48]
1
19,563
LMTX
N/A
N/A
No
N/A
N/A
1/1
Wang et al. [50]
2
176-N/A
Surgery
Repeat laparoscopy
N/A
Scar
Day 3
3–4
2/2
N number of cases, β-hCG mIU/ml, (S/L)MTX (systemic/local) methotrexate, UAE uterine artery embolization, CR cornual resection, CS cornuostomy, HE hysterectomy, operating time minutes, hospital stay days, negative β-hCG weeks, PTD persistent trophoblastic disease

Appendix 6

Table 11
Recurrent interstitial pregnancy and its treatment
Author
N
β-hCG
Treatment 1st IP
Success
β-hCG
Treatment 2nd IP
Success
β-hCG
Treatment 3rd IP
Success
Sungurtekin and Uyar [182]
1
32
SMTX
1/1
31,737
SMTX
0/1
Sagiv et al. [57]
1
15,400
LMTX
1/1
2577
Laparoscopic CS°
1/1
Vilos [185]
1
12,000
Laparoscopic CR
1/1
4700
Laparoscopic CR
1/1
Sahoo et al. [95]
1
N/A
Laparotomy
1/1
N/A
Laparoscopy
0/1
N/A
Laparoscopic CR
1/1
Siow and Ng [186]
2
N/A
Laparoscopic CS
2/2
N/A
Laparoscopic CR
2/2
 
1
N/A
Laparoscopy
1/1
N/A
Laparoscopic CR
1/1
 
1
N/A
Laparoscopic CR
1/1
N/A
Laparoscopic CR
1/1
N/A
Laparoscopic CR
1/1
N number of cases, β-hCG mIU/ml, IP interstitial pregnancy, S/LMTX systemic/local methotrexate, CR cornual resection, CS cornuostomy
Hemostatic technique: °vasopressin
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Metadaten
Titel
Elective uterine artery embolization prior to laparoscopic resection of interstitial pregnancy: two cases and literature review
verfasst von
Iris Verbeeck
Francesca Donders
Pieter-Jan Buyck
Dirk Timmerman
Andries Van Holsbeeck
Sandra A Cornelissen
Anne-Sophie Van Rompuy
Lien Van den Haute
Sylvie Gordts
Carla Tomassetti
Jan Deprest
Publikationsdatum
01.12.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Gynecological Surgery / Ausgabe 1/2018
Print ISSN: 1613-2076
Elektronische ISSN: 1613-2084
DOI
https://doi.org/10.1186/s10397-018-1049-1

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